Zhenan Bao
Professor of Chemical Engineering and, by courtesy, of Materials Science and Engineering and of Chemistry
Bio
Zhenan Bao joined Stanford University in 2004 and is currently holds the rank of Professor in Chemical Engineering. She is also an affiliated faculty member ofPrecourt Institute, Woods Institute, Center for Advanced Molecular Photovoltaics and Bio-X. Professor Bao received her Ph.D. degree in Chemistry from The University of Chicago in 1995 and joined the Materials Research Department of Bell Labs, Lucent Technologies. She became a Distinguished Member of Technical Staff in 2001. Professor Bao currently has more than 300 refereed publications and ~65 US patents. She served as a member of Executive Board of Directors for the Materials Research Society and Executive Committee Member for the Polymer Materials Science and Engineering division of the American Chemical Society. She is an Associate Editor for the Royal Society of Chemistry journal Chemical Science. She was an Editor for Polymer Reviews and Synthetic Metals and she serves on the international advisory board for Advanced Materials, Advanced Energy Materials, Advanced Functional Materials, Chemistry of Materials, Chemical Communications, ACS Nano, Nature Asian Materials, Materials Horizon and Materials Today. She is one of the Founders and currently sits on the Board of Directors of C3 Nano Co., located in Hayward, California. She is Fellow of AAAS, ACS, MRS, SPIE, ACS POLY and ACS PMSE. She was awarded the ACS Creative Polymer Chemistry Award in 2013 ACS Cope Scholar Award in 2011, and was selected by Phoenix TV, China as 2010 Most influential Chinese in the World-Science and Technology Category. She is a recipient of the Royal Society of Chemistry Beilby Medal and Prize in 2009, IUPAC Creativity in Applied Polymer Science Prize in 2008, American Chemical Society Team Innovation Award 2001, R&D 100 Award, and R&D Magazine Editors Choice Best of the Best new technology for 2001. She has been selected in 2002 by the American Chemical Society Women Chemists Committee as one of the twelve Outstanding Young Woman Scientist who is expected to make a substantial impact in chemistry during this century. She is also selected by MIT Technology Review magazine in 2003 as one of the top 100 young innovators for this century. She has been selected as one of the recipients of Stanford Terman Fellow and has been appointed as the Robert Noyce Faculty Scholar, Finmeccanica Faculty Scholar and David Filo and Jerry Yang Faculty Scholar.
Academic Appointments
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Professor, Chemical Engineering
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Professor (By courtesy), Materials Science and Engineering
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Professor (By courtesy), Chemistry
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Member, Bio-X
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Affiliate, Precourt Institute for Energy
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Member, Stanford Neurosciences Institute
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Affiliate, Stanford Woods Institute for the Environment
Honors & Awards
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ACS POLY Fellow, American Chemical Society (ACS) Polymer Division (POLY) (2014)
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Andreas Acrivos Award for Professional Progress in Chemical Engineering, American Institute of Chemical Engineers (AICHE) (2014)
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MRS Fellow, Materials Research Society (MRS) (2014)
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ACS Polymer Division Carl S. Marvel Creative Polymer Chemistry Award, American Chemical Society (ACS) (2013)
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Honorary Guest Professorship, Soochow University, China (2013)
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AAAS Fellow, American Association for the Advancement of Science (AAAS) (2012)
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Cheung Kong Scholar, Li Ka Shing Foundation and Chinese Ministry of Education (2012)
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Honorary Guest Professorship, Nanjing Industry University, China (2012)
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ACS Fellow, American Chemical Society (ACS) (2011)
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ACS PMSE Fellow, American Chemical Society (ACS) Polymer Science and Engineering (PMSE) division (2011)
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Most influential Chinese in the World, Science and Technology Category, Phoenix TV (2011)
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Founder, Board of Directors, C3 Nano Co. (2010-present)
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Honorary Si Yuan Chair Professorship, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing, China (2010-2013)
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David Filo and Jerry Yang Faculty Scholar, Stanford University (2009-2012)
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The Royal Society of Chemistry 2009 Beilby Medal and Prize, Stanford University (2009)
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IUPAC Award, Polymer International (2008)
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SPIE Fellow, SPIE (2008)
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50 Awards in the Innovator category, Nanotech Briefs (2007)
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Featured in Women in SPIE Optics Planner calendar, SPIE (2007)
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Ranked 4 among the Top 20 most cited authors in the field of Organic Thin Film Transistors, ISI (2007)
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Teaching Excellence Award, Stanford Society of Women Engineering (2007)
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Sloan Research Fellowship, Alfred P. Sloan Foundation (2006)
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Du Pont Science and Technology Award, DuPont (2005)
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Finmeccanica Faculty Scholar, Stanford University (2004-2008)
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Terman Fellow, Stanford University (2004-2007)
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Robert Faculty Scholar, Stanford University (2004-2005)
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Robert Noyce Faculty Scholar, Stanford University (2004-2005)
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3M Faculty Award, 3M (2004)
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Best Mentor Award, University Relations of Lucent Technologies (2003)
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Top 100 young innovators for this century, MIT Technology Review (2003)
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Zhu Kezhen Distinguished Lecturer, Zhejiang University, Hangzhou city, Zhejiang province, China (2003)
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Elizabeth Crosby Lecturer, University of Michigan, Department of Material Sciences and Engineering (2002)
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Team Innovation Award, American Chemical Society (2002)
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Eastman Lecturer, University of Akron, Department of Polymer Science (2001)
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Editor's Choice of the "Best of the Best" in new technology, R&D Magazine (2001)
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R&D 100 Award for the work on Printed Plastic Circuits for Electronic Paper Displays, R&D Magazine (2001)
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Top 10 Research Breakthroughs for work on large scale integrated circuits based on organic materials, Science Magazine (2000)
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Top 100 Young Engineers, National Academy of Engineering (2000)
Boards, Advisory Committees, Professional Organizations
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International Advisory Board, J. Am. Chem. Soc. (2015 - Present)
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Associate Editor, Chemical Science (2014 - Present)
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International Editorial Advisory Board, Advanced Materials (2013 - Present)
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International Editorial Advisory Board, Materials Horizon (2013 - Present)
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International Editorial Advisory Board, Nanoscale (2012 - Present)
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International Editorial Advisory Board, Advanced Energy Materials (2012 - Present)
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International Editorial Advisory Board, Chemical Communications (2012 - Present)
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Board of Directors, C3 Nano, Co. (2011 - Present)
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International Editorial Advisory Board, Nature Asia Materials (2011 - Present)
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International Editorial Advisory Board, ACS Nano (2011 - Present)
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International advisory board member, LG Display (2010 - Present)
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Conference Chair, Gordon Research Conference on Electronic Processes in Organic Materials (2010 - 2010)
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Board Member, National Academies Board on Chemical Sciences and Technology (2009 - 2012)
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Executive Committee Member/Member-at-Large, Division of Polymer Materials Science and Engineering, American Chemical Society (2009 - 2012)
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Associate Editor, Synthetic Metals (2009 - 2011)
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International Editorial Advisory Board, Chemistry of Materials (2006 - 2011)
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Scientific Advisory Board Member, Plastic Electronics Foundation (2006 - 2009)
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Associate Editor, Polymer Review (2004 - 2008)
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Board of Directors, Material Research Society (MRS) (2003 - 2005)
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International Editorial Advisory Board, Materials Today (2002 - Present)
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Meeting chair, Materials Research Society Spring Meeting (2002 - 2002)
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International Editorial Advisory Board, Advanced Functional Materials (2001 - 2005)
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Executive Committee Member/Member-at-Large, Division of Polymer Materials Science and Engineering, American Chemical Society (2000 - 2006)
Professional Education
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PhD, The University of Chicago (1995)
2015-16 Courses
- Equilibrium Thermodynamics
CHEMENG 110 (Win) - Special Topics in Functional Organic Materials for Electronic and Optical Devices
CHEMENG 513 (Aut, Win, Spr, Sum) -
Independent Studies (13)
- Advanced Undergraduate Research
CHEM 190 (Aut, Win, Spr, Sum) - Directed Instruction/Reading
CHEM 110 (Aut, Win, Spr) - Directed Investigation
BIOE 392 (Aut, Win, Spr) - Graduate Independent Study
MATSCI 399 (Aut, Win, Spr, Sum) - Graduate Research Rotation in Chemical Engineering
CHEMENG 399 (Aut, Win, Sum) - Graduate Research in Chemical Engineering
CHEMENG 600 (Aut, Win, Spr, Sum) - Master's Research
MATSCI 200 (Aut, Win, Spr, Sum) - Ph.D. Research
MATSCI 300 (Aut, Win, Spr, Sum) - Practical Training
MATSCI 299 (Aut, Win, Spr, Sum) - Research and Special Advanced Work
CHEM 200 (Aut, Win, Spr, Sum) - Research in Chemistry
CHEM 301 (Aut, Win, Spr, Sum) - Undergraduate Honors Research in Chemical Engineering
CHEMENG 190H (Aut, Win, Spr, Sum) - Undergraduate Research in Chemical Engineering
CHEMENG 190 (Aut, Win, Spr, Sum)
- Advanced Undergraduate Research
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Prior Year Courses
2014-15 Courses
- Equilibrium Thermodynamics
CHEMENG 110 (Win) - Micro and Nanoscale Fabrication Engineering
CHEMENG 140, CHEMENG 240 (Win) - Polymer Chemistry
CHEMENG 464 (Aut) - Special Topics in Functional Organic Materials for Electronic and Optical Devices
CHEMENG 513 (Aut, Win, Spr, Sum)
2013-14 Courses
- Equilibrium Thermodynamics
CHEMENG 110 (Win) - Micro and Nanoscale Fabrication Engineering
CHEMENG 140, CHEMENG 240 (Win) - Special Topics in Functional Organic Materials for Electronic and Optical Devices
CHEMENG 513 (Aut, Win, Spr, Sum)
2012-13 Courses
- Equilibrium Thermodynamics
CHEMENG 110 (Win) - Micro and Nanoscale Fabrication Engineering
CHEMENG 140, CHEMENG 240 (Win) - Special Topics in Functional Organic Materials for Electronic and Optical Devices
CHEMENG 513 (Aut, Win, Spr, Sum)
- Equilibrium Thermodynamics
Stanford Advisees
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Postdoctoral Faculty Sponsor
Sean Andrews, Won-Gyu Bae, Zheng Chen, Ho-Hsiu Chou, Jeremy Feldblyum, Dawei Feng, Xiaodan Gu, Desheng Kong, Tadanori Kurosawa, Min Ah Lee, Ting Lei, Franziska Lissel, Jia Liu, Nan Liu, Francisco Molina Lopez, Jinyoung Oh, Raphael Pfattner, Igor Pochorovski, Yingli Rao, Simon Rondeau Gagne, Bob Schroeder, Clementine Viellard Boutry, Sihong Wang, Yue Wang, Jie Xu -
Doctoral Dissertation Reader (AC)
Jiajun He
All Publications
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Ultra-high mobility transparent organic thin film transistors grown by an off-centre spin-coating method.
Nature communications
2014; 5: 3005-?
Abstract
Organic semiconductors with higher carrier mobility and better transparency have been actively pursued for numerous applications, such as flat-panel display backplane and sensor arrays. The carrier mobility is an important figure of merit and is sensitively influenced by the crystallinity and the molecular arrangement in a crystal lattice. Here we describe the growth of a highly aligned meta-stable structure of 2,7-dioctyl[1]benzothieno[3,2-b][1]benzothiophene (C8-BTBT) from a blended solution of C8-BTBT and polystyrene by using a novel off-centre spin-coating method. Combined with a vertical phase separation of the blend, the highly aligned, meta-stable C8-BTBT films provide a significantly increased thin film transistor hole mobility up to 43 cm(2) Vs(-1) (25 cm(2) Vs(-1) on average), which is the highest value reported to date for all organic molecules. The resulting transistors show high transparency of >90% over the visible spectrum, indicating their potential for transparent, high-performance organic electronics.
View details for DOI 10.1038/ncomms4005
View details for PubMedID 24398476
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Effects of Odd-Even Side Chain Length of Alkyl-Substituted Diphenylbithiophenes on First Monolayer Thin Film Packing Structure
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
2013; 135 (30): 11006-11014
Abstract
Because of their preferential two-dimensional layer-by-layer growth in thin films, 5,5'bis(4-alkylphenyl)-2,2'-bithiophenes (P2TPs) are model compounds for studying the effects of systematic chemical structure variations on thin-film structure and morphology, which in turn, impact the charge transport in organic field-effect transistors. For the first time, we observed, by grazing incidence X-ray diffraction (GIXD), a strong change in molecular tilt angle in a monolayer of P2TP, depending on whether the alkyl chain on the P2TP molecules was of odd or even length. The monolayers were deposited on densely packed ultrasmooth self-assembled alkane silane modified SiO2 surfaces. Our work shows that a subtle change in molecular structure can have a significant impact on the molecular packing structure in thin film, which in turn, will have a strong impact on charge transport of organic semiconductors. This was verified by quantum-chemical calculations that predict a corresponding odd-even effect in the strength of the intermolecular electronic coupling.
View details for DOI 10.1021/ja400015e
View details for Web of Science ID 000322752900031
View details for PubMedID 23822850
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Integrated Materials Design of Organic Semiconductors for Field-Effect Transistors
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
2013; 135 (18): 6724-6746
Abstract
The past couple of years have witnessed a remarkable burst in the development of organic field-effect transistors (OFETs), with a number of organic semiconductors surpassing the benchmark mobility of 10 cm(2)/(V s). In this perspective, we highlight some of the major milestones along the way to provide a historical view of OFET development, introduce the integrated molecular design concepts and process engineering approaches that lead to the current success, and identify the challenges ahead to make OFETs applicable in real applications.
View details for DOI 10.1021/ja400881n
View details for Web of Science ID 000318839300001
View details for PubMedID 23557391
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Flexible Wireless Temperature Sensors Based on Ni Microparticle-Filled Binary Polymer Composites
ADVANCED MATERIALS
2013; 25 (6): 850-855
View details for DOI 10.1002/adma.201204082
View details for Web of Science ID 000314653300006
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Stable Li-ion Battery Anodes by In-situ Polymerization of Conducting Hydrogel to Conformally Coat Silicon Nanoparticles
Nature Comm.
2013; 4: 1943
View details for DOI 10.1038/ncomms2941
- An ultra-sensitive resistive pressure sensor based on hollow-sphere microstructure induced elasticity in conducting polymer film Nature Comm. 2013
- A Flexible Bimodal Sensor Array for Simultaneous Sensing of Pressure and Temperature Adv. Mater. 2013
- Stretchable LEDs: Light-emitting electronic skin Nature Photonics 2013; 7: 769-771
- Direct Growth of Aligned Graphitic Nanoribbons from a DNA Template by Chemical Vapour Deposition Nature Comm. 2013; 4: 2402
- 25th Anniversary Article: The Evolution of Electronic Skin (E-Skin): A Brief History, Design Considerations, and Recent Progress Adv. Mat. 2013; 25: 5997-6038
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Solution coating of large-area organic semiconductor thin films with aligned single-crystalline domains
Nature Materials
2013; 12: 665-671
View details for DOI 10.1038/nmat3650
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Flexible polymer transistors with high pressure sensitivity for application in electronic skin and health monitoring
Nature Comm.
2013; 4: 1859
View details for DOI 10.1038/ncomms2832
- Ultra-High Mobility Transparent Organic Thin Film Transistors Via an Off-Center Spin-Coating Method Nature Comm. 2013
- Highly stable organic polymer field-effect transistor sensor for selective detection in the marine environment Nature Comm. 2013
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An electrically and mechanically self-healing composite with pressure- and flexion-sensitive properties for electronic skin applications
NATURE NANOTECHNOLOGY
2012; 7 (12): 825-832
Abstract
Pressure sensitivity and mechanical self-healing are two vital functions of the human skin. A flexible and electrically conducting material that can sense mechanical forces and yet be able to self-heal repeatably can be of use in emerging fields such as soft robotics and biomimetic prostheses, but combining all these properties together remains a challenging task. Here, we describe a composite material composed of a supramolecular organic polymer with embedded nickel nanostructured microparticles, which shows mechanical and electrical self-healing properties at ambient conditions. We also show that our material is pressure- and flexion-sensitive, and therefore suitable for electronic skin applications. The electrical conductivity can be tuned by varying the amount of nickel particles and can reach values as high as 40 S cm(-1). On rupture, the initial conductivity is repeatably restored with ?90% efficiency after 15 s healing time, and the mechanical properties are completely restored after ?10 min. The composite resistance varies inversely with applied flexion and tactile forces. These results demonstrate that natural skin's repeatable self-healing capability can be mimicked in conductive and piezoresistive materials, thus potentially expanding the scope of applications of current electronic skin systems.
View details for DOI 10.1038/NNANO.2012.192
View details for Web of Science ID 000312003700019
View details for PubMedID 23142944
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Hierarchical nanostructured conducting polymer hydrogel with high electrochemical activity
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
2012; 109 (24): 9287-9292
Abstract
Conducting polymer hydrogels represent a unique class of materials that synergizes the advantageous features of hydrogels and organic conductors and have been used in many applications such as bioelectronics and energy storage devices. They are often synthesized by polymerizing conductive polymer monomer within a nonconducting hydrogel matrix, resulting in deterioration of their electrical properties. Here, we report a scalable and versatile synthesis of multifunctional polyaniline (PAni) hydrogel with excellent electronic conductivity and electrochemical properties. With high surface area and three-dimensional porous nanostructures, the PAni hydrogels demonstrated potential as high-performance supercapacitor electrodes with high specific capacitance (~480 F·g(-1)), unprecedented rate capability, and cycling stability (~83% capacitance retention after 10,000 cycles). The PAni hydrogels can also function as the active component of glucose oxidase sensors with fast response time (~0.3 s) and superior sensitivity (~16.7 ?A · mM(-1)). The scalable synthesis and excellent electrode performance of the PAni hydrogel make it an attractive candidate for bioelectronics and future-generation energy storage electrodes.
View details for DOI 10.1073/pnas.1202636109
View details for Web of Science ID 000305511300024
View details for PubMedID 22645374
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2-(2-Methoxyphenyl)-1,3-dimethyl-1H-benzoimidazol-3-ium Iodide as a New Air-Stable n-Type Dopant for Vacuum-Processed Organic Semiconductor Thin Films
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
2012; 134 (9): 3999-4002
Abstract
2-(2-Methoxyphenyl)-1,3-dimethyl-1H-benzoimidazol-3-ium iodide (o-MeO-DMBI-I) was synthesized and employed as a strong n-type dopant for fullerene C(60), a well-known n-channel semiconductor. The coevaporated thin films showed a maximum conductivity of 5.5 S/cm at a doping concentration of 8.0 wt% (14 mol%), which is the highest value reported to date for molecular n-type conductors. o-MeO-DMBI-I can be stored and handled in air for extended periods without degradation and is thus promising for various organic electronic devices.
View details for DOI 10.1021/ja211382x
View details for Web of Science ID 000301550800018
View details for PubMedID 22324847
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Chemical and Engineering Approaches To Enable Organic Field-Effect Transistors for Electronic Skin Applications
ACCOUNTS OF CHEMICAL RESEARCH
2012; 45 (3): 361-371
Abstract
Skin is the body's largest organ and is responsible for the transduction of a vast amount of information. This conformable material simultaneously collects signals from external stimuli that translate into information such as pressure, pain, and temperature. The development of an electronic material, inspired by the complexity of this organ is a tremendous, unrealized engineering challenge. However, the advent of carbon-based electronics may offer a potential solution to this long-standing problem. In this Account, we describe the use of an organic field-effect transistor (OFET) architecture to transduce mechanical and chemical stimuli into electrical signals. In developing this mimic of human skin, we thought of the sensory elements of the OFET as analogous to the various layers and constituents of skin. In this fashion, each layer of the OFET can be optimized to carry out a specific recognition function. The separation of multimodal sensing among the components of the OFET may be considered a "divide and conquer" approach, where the electronic skin (e-skin) can take advantage of the optimized chemistry and materials properties of each layer. This design of a novel microstructured gate dielectric has led to unprecedented sensitivity for tactile pressure events. Typically, pressure-sensitive components within electronic configurations have suffered from a lack of sensitivity or long mechanical relaxation times often associated with elastomeric materials. Within our method, these components are directly compatible with OFETs and have achieved the highest reported sensitivity to date. Moreover, the tactile sensors operate on a time scale comparable with human skin, making them ideal candidates for integration as synthetic skin devices. The methodology is compatible with large-scale fabrication and employs simple, commercially available elastomers. The design of materials within the semiconductor layer has led to the incorporation of selectivity and sensitivity within gas-sensing devices and has enabled stable sensor operation within aqueous media. Furthermore, careful tuning of the chemical composition of the dielectric layer has provided a means to operate the sensor in real time within an aqueous environment and without the need for encapsulation layers. The integration of such devices as electronic mimics of skin will require the incorporation of biocompatible or biodegradable components. Toward this goal, OFETs may be fabricated with >99% biodegradable components by weight, and the devices are robust and stable, even in aqueous environments. Collectively, progress to date suggests that OFETs may be integrated within a single substrate to function as an electronic mimic of human skin, which could enable a large range of sensing-related applications from novel prosthetics to robotic surgery.
View details for DOI 10.1021/ar2001233
View details for Web of Science ID 000302033000005
View details for PubMedID 21995646
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Tuning charge transport in solution-sheared organic semiconductors using lattice strain
NATURE
2011; 480 (7378): 504-U124
Abstract
Circuits based on organic semiconductors are being actively explored for flexible, transparent and low-cost electronic applications. But to realize such applications, the charge carrier mobilities of solution-processed organic semiconductors must be improved. For inorganic semiconductors, a general method of increasing charge carrier mobility is to introduce strain within the crystal lattice. Here we describe a solution-processing technique for organic semiconductors in which lattice strain is used to increase charge carrier mobilities by introducing greater electron orbital overlap between the component molecules. For organic semiconductors, the spacing between cofacially stacked, conjugated backbones (the ?-? stacking distance) greatly influences electron orbital overlap and therefore mobility. Using our method to incrementally introduce lattice strain, we alter the ?-? stacking distance of 6,13-bis(triisopropylsilylethynyl) pentacene (TIPS-pentacene) from 3.33?Å to 3.08?Å. We believe that 3.08?Å is the shortest ?-? stacking distance that has been achieved in an organic semiconductor crystal lattice (although a ?-? distance of 3.04?Å has been achieved through intramolecular bonding). The positive charge carrier (hole) mobility in TIPS-pentacene transistors increased from 0.8?cm(2)?V(-1)?s(-1) for unstrained films to a high mobility of 4.6?cm(2)?V(-1)?s(-1) for a strained film. Using solution processing to modify molecular packing through lattice strain should aid the development of high-performance, low-cost organic semiconducting devices.
View details for DOI 10.1038/nature10683
View details for Web of Science ID 000298318000056
View details for PubMedID 22193105
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Siloxane-Terminated Solubilizing Side Chains: Bringing Conjugated Polymer Backbones Closer and Boosting Hole Mobilities in Thin-Film Transistors
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
2011; 133 (50): 20130-20133
Abstract
We introduce a novel siloxane-terminated solubilizing group and demonstrate its effectiveness as a side chain in an isoindigo-based conjugated polymer. An average hole mobility of 2.00 cm(2) V(-1) s(-1) (with a maximum mobility of 2.48 cm(2) V(-1) s(-1)), was obtained from solution-processed thin-film transistors, one of the highest mobilities reported to date. In contrast, the reference polymer with a branched alkyl side chain gave an average hole mobility of 0.30 cm(2) V(-1) s(-1) and a maximum mobility of 0.57 cm(2) V(-1) s(-1). This is largely explained by the polymer packing: our new polymer exhibited a ?-? stacking distance of 3.58 Å, while the reference polymer showed a distance of 3.76 Å.
View details for DOI 10.1021/ja209328m
View details for Web of Science ID 000298713600028
View details for PubMedID 22122218
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Skin-like pressure and strain sensors based on transparent elastic films of carbon nanotubes
NATURE NANOTECHNOLOGY
2011; 6 (12): 788-792
Abstract
Transparent, elastic conductors are essential components of electronic and optoelectronic devices that facilitate human interaction and biofeedback, such as interactive electronics, implantable medical devices and robotic systems with human-like sensing capabilities. The availability of conducting thin films with these properties could lead to the development of skin-like sensors that stretch reversibly, sense pressure (not just touch), bend into hairpin turns, integrate with collapsible, stretchable and mechanically robust displays and solar cells, and also wrap around non-planar and biological surfaces such as skin and organs, without wrinkling. We report transparent, conducting spray-deposited films of single-walled carbon nanotubes that can be rendered stretchable by applying strain along each axis, and then releasing this strain. This process produces spring-like structures in the nanotubes that accommodate strains of up to 150% and demonstrate conductivities as high as 2,200 S cm(-1) in the stretched state. We also use the nanotube films as electrodes in arrays of transparent, stretchable capacitors, which behave as pressure and strain sensors.
View details for DOI 10.1038/NNANO.2011.184
View details for Web of Science ID 000298248300011
View details for PubMedID 22020121
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Selective dispersion of high purity semiconducting single-walled carbon nanotubes with regioregular poly(3-alkylthiophene)s
NATURE COMMUNICATIONS
2011; 2
Abstract
Conjugated polymers, such as polyfluorene and poly(phenylene vinylene), have been used to selectively disperse semiconducting single-walled carbon nanotubes (sc-SWNTs), but these polymers have limited applications in transistors and solar cells. Regioregular poly(3-alkylthiophene)s (rr-P3ATs) are the most widely used materials for organic electronics and have been observed to wrap around SWNTs. However, no sorting of sc-SWNTs has been achieved before. Here we report the application of rr-P3ATs to sort sc-SWNTs. Through rational selection of polymers, solvent and temperature, we achieved highly selective dispersion of sc-SWNTs. Our approach enables direct film preparation after a simple centrifugation step. Using the sorted sc-SWNTs, we fabricate high-performance SWNT network transistors with observed charge-carrier mobility as high as 12?cm(2)?V(-1)?s(-1) and on/off ratio of >10(6). Our method offers a facile and a scalable route for separating sc-SWNTs and fabrication of electronic devices.
View details for DOI 10.1038/ncomms1545
View details for Web of Science ID 000297686500028
View details for PubMedID 22086341
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3,4-Disubstituted Polyalkylthiophenes for High-Performance Thin-Film Transistors and Photovoltaics
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
2011; 133 (42): 16722-16725
Abstract
We demonstrate that poly(3,4-dialkylterthiophenes) (P34ATs) have comparable transistor mobilities (0.17 cm(2) V(-1) s(-1)) and greater environmental stability (less degradation of on/off ratio) than regioregular poly(3-alkylthiophenes) (P3ATs). Unlike poly(3-hexylthiophene) (P3HT), P34ATs do not show a strong and distinct ?-? stacking in X-ray diffraction. This suggests that a strong ?-? stacking is not always necessary for high charge-carrier mobility and that other potential polymer packing motifs in addition to the edge-on structure (?-? stacking direction parallel to the substrate) can lead to a high carrier mobility. The high charge-carrier mobilities of the hexyl and octyl-substituted P34AT produce power conversion efficiencies of 4.2% in polymer:fullerene bulk heterojunction photovoltaic devices. An enhanced open-circuit voltage (0.716-0.771 eV) in P34AT solar cells relative to P3HT due to increased ionization potentials was observed.
View details for DOI 10.1021/ja207429s
View details for Web of Science ID 000296678200004
View details for PubMedID 21970371
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From computational discovery to experimental characterization of a high hole mobility organic crystal
NATURE COMMUNICATIONS
2011; 2
Abstract
For organic semiconductors to find ubiquitous electronics applications, the development of new materials with high mobility and air stability is critical. Despite the versatility of carbon, exploratory chemical synthesis in the vast chemical space can be hindered by synthetic and characterization difficulties. Here we show that in silico screening of novel derivatives of the dinaphtho[2,3-b:2',3'-f]thieno[3,2-b]thiophene semiconductor with high hole mobility and air stability can lead to the discovery of a new high-performance semiconductor. On the basis of estimates from the Marcus theory of charge transfer rates, we identified a novel compound expected to demonstrate a theoretic twofold improvement in mobility over the parent molecule. Synthetic and electrical characterization of the compound is reported with single-crystal field-effect transistors, showing a remarkable saturation and linear mobility of 12.3 and 16 cm(2)?V(-1)?s(-1), respectively. This is one of the very few organic semiconductors with mobility greater than 10 cm(2)?V(-1)?s(-1) reported to date.
View details for DOI 10.1038/ncomms1451
View details for Web of Science ID 000294806500030
View details for PubMedID 21847111
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Highly sensitive flexible pressure sensors with microstructured rubber dielectric layers
NATURE MATERIALS
2010; 9 (10): 859-864
Abstract
The development of an electronic skin is critical to the realization of artificial intelligence that comes into direct contact with humans, and to biomedical applications such as prosthetic skin. To mimic the tactile sensing properties of natural skin, large arrays of pixel pressure sensors on a flexible and stretchable substrate are required. We demonstrate flexible, capacitive pressure sensors with unprecedented sensitivity and very short response times that can be inexpensively fabricated over large areas by microstructuring of thin films of the biocompatible elastomer polydimethylsiloxane. The pressure sensitivity of the microstructured films far surpassed that exhibited by unstructured elastomeric films of similar thickness, and is tunable by using different microstructures. The microstructured films were integrated into organic field-effect transistors as the dielectric layer, forming a new type of active sensor device with similarly excellent sensitivity and response times.
View details for DOI 10.1038/nmat2834
View details for Web of Science ID 000282134700025
View details for PubMedID 20835231
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Water-stable organic transistors and their application in chemical and biological sensors
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
2008; 105 (34): 12134-12139
Abstract
The development of low-cost, reliable sensors will rely on devices capable of converting an analyte binding event to an easily read electrical signal. Organic thin-film transistors (OTFTs) are ideal for inexpensive, single-use chemical or biological sensors because of their compatibility with flexible, large-area substrates, simple processing, and highly tunable active layer materials. We have fabricated low-operating voltage OTFTs with a cross-linked polymer gate dielectric, which display stable operation under aqueous conditions over >10(4) electrical cycles using the p-channel semiconductor 5,5'-bis-(7-dodecyl-9H-fluoren-2-yl)-2,2'-bithiophene (DDFTTF). OTFT sensors were demonstrated in aqueous solutions with concentrations as low as parts per billion for trinitrobenzene, methylphosphonic acid, cysteine, and glucose. This work demonstrates of reliable OTFT operation in aqueous media, hence opening new possibilities of chemical and biological sensing with OTFTs.
View details for DOI 10.1073/pnas.0802105105
View details for Web of Science ID 000258905700009
View details for PubMedID 18711145
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Self-sorted, aligned nanotube networks for thin-film transistors
SCIENCE
2008; 321 (5885): 101-104
Abstract
To find use in electronics, single-walled carbon nanotubes need to be efficiently separated by electronic type and aligned to ensure optimal and reproducible electronic properties. We report the fabrication of single-walled carbon nanotube (SWNT) network field-effect transistors, deposited from solution, possessing controllable topology and an on/off ratio as high as 900,000. The spin-assisted alignment and density of the SWNTs are tuned by different surfaces that effectively vary the degree of interaction with surface functionalities in the device channel. This leads to a self-sorted SWNT network in which nanotube chirality separation and simultaneous control of density and alignment occur in one step during device fabrication. Micro-Raman experiments corroborate device results as a function of surface chemistry, indicating enrichment of the specific SWNT electronic type absorbed onto the modified dielectric.
View details for DOI 10.1126/science.1156588
View details for Web of Science ID 000257320800045
View details for PubMedID 18599781
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Soluble regioregular polythiophene derivatives as semiconducting materials for field-effect transistors
CHEMISTRY OF MATERIALS
1999; 11 (9): 2607-2612
View details for Web of Science ID 000082706700051
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Thermotropic Phase Transition of Benzodithiophene Copolymer Thin Films and Its Impact on Electrical and Photovoltaic Characteristics
CHEMISTRY OF MATERIALS
2015; 27 (4): 1223-1232
View details for DOI 10.1021/cm503773j
View details for Web of Science ID 000350192500013
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Ultrafast Electron Transfer at Organic Semiconductor Interfaces: Importance of Molecular Orientation
JOURNAL OF PHYSICAL CHEMISTRY LETTERS
2015; 6 (1): 6-12
View details for DOI 10.1021/jz502253r
View details for Web of Science ID 000347513700002
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High Mobility N-Type Transistors Based on Solution-Sheared Doped 6,13-Bis(triisopropylsilylethynyl)pentacene Thin Films
ADVANCED MATERIALS
2013; 25 (33): 4663-4667
Abstract
An N-Type organic thin-film transistor (OTFT) based on doped 6,13-Bis(triisopropylsilylethynyl)pentacene is presented. A transition from p-type to n-type occurrs with increasing doping concentrations, and the highest performing n-channel OTFTs are obtained with 50 mol% dopant. X-ray diffraction, scanning Auger microscopy, and secondary ionization mass spectrometry are used to characterize the morphology of the blends. The high performance of the obtained transistors is attributed to the highly crystalline and aligned nature of the doped thin films.
View details for DOI 10.1002/adma.201205098
View details for Web of Science ID 000327692700022
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Atomic layer deposition of high-k dielectrics on single-walled carbon nanotubes: a Raman study
NANOTECHNOLOGY
2013; 24 (24)
Abstract
Single-wall carbon nanotubes (SWCNTs) have great potential to become the channel material for future high-speed transistor technology. However, to realize a carbon nanotube field effect transistor (CNTFET) with excellent gate control, the high-k dielectrics between the CNT and the metal gate must have superb electrical properties and extremely high uniformity. Thus it is essential to understand the interactions between high-k materials and the SWCNTs to effectively control the transistor characteristics. In this study, we investigate the effects of atomic layer deposited (ALD) high-k dielectrics (Al2O3 and HfO2) on SWCNTs using Raman spectroscopy. We subjected the SWCNTs to various ALD cycles and studied the nucleation and growth of ALD dielectrics at defect sites using scanning electron microscopy and transmission electron microscopy images. We analyzed these samples using Raman spectroscopy and x-ray photoelectron spectroscopy. The Raman peak shifts of the G-peak and the 2D (G') peaks suggest doping and stress induced effects on the CNTs by the surrounding high-k oxide environment. Trends in the G-peak FWHM and G/D-peak ratios were identified and compared between Al2O3 and HfO2. We confirmed the ALD-deposited HfO2 is polycrystalline using x-ray diffraction and analyzed dielectric-CNT bonding states using XPS measurements. This study provides insights on the effects of ALD high-k materials on SWCNTs for future high-speed transistor applications.
View details for DOI 10.1088/0957-4484/24/24/245703
View details for Web of Science ID 000319384300021
View details for PubMedID 23696347
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p-Channel Field-Effect Transistors Based on C-60 Doped with Molybdenum Trioxide
ACS APPLIED MATERIALS & INTERFACES
2013; 5 (7): 2337-2341
Abstract
Fullerene (C60) is a well-known n-channel organic semiconductor. We demonstrate that p-channel C60 field-effect transistors are possible by doping with molybdenum trioxide (MoO3). The device performance of the p-channel C60 field-effect transistors, such as mobility, threshold voltage, and on/off ratio is varied in a controlled manner by changing doping concentration. This work demonstrates the utility of charge transfer doping to obtain both n- and p-channel field-effect transistors with a single organic semiconductor.
View details for DOI 10.1021/am3026568
View details for Web of Science ID 000317549100007
View details for PubMedID 23446111
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Scalable Synthesis of Fused Thiophene-Diketopyrrolopyrrole Semiconducting Polymers Processed from Nonchlorinated Solvents into High Performance Thin Film Transistors
CHEMISTRY OF MATERIALS
2013; 25 (5): 782-789
View details for DOI 10.1021/cm303953e
View details for Web of Science ID 000316168800017
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Scalable and Selective Dispersion of Semiconducting Arc-Discharged Carbon Nanotubes by Dithiafulvalene/Thiophene Copolymers for Thin Film Transistors
ACS NANO
2013; 7 (3): 2659-2668
Abstract
We report a simple and scalable method to enrich large quantities of semiconducting arc-discharged single-walled carbon nanotubes (SWNTs) with diameters of 1.1-1.8 nm using dithiafulvalene/thiophene copolymers. Stable solutions of highly individualized and highly enriched semiconducting SWNTs were obtained after a simple sonication and centrifuge process. Molecular dynamics (MD) simulations of polymer backbone interactions with and without side chains indicated that the presence of long alkyl side chains gave rise to the selectivity toward semiconducting tubes, indicating the importance of the roles of the side chains to both solubilize and confer selectivity to the polymers. We found that, by increasing the ratio of thiophene to dithiafulvalene units in the polymer backbone (from pDTFF-1T to pDTFF-3T), we can slightly improve the selectivity toward semiconducting SWNTs. This is likely due to the more flexible backbone of pDTFF-3T that allows the favorable wrapping of SWNTs with certain chirality as characterized by small-angle X-ray scattering. However, the dispersion yield was reduced from pDTFF-1T to pDTFF-3T. MD simulations showed that the reduction is due to the smaller polymer/SWNT contact area, which reduces the dispersion ability of pDTFF-3T. These experimental and modeling results provide a better understanding for future rational design of polymers for sorting SWNTs. Finally, high on/off ratio solution-processed thin film transistors were fabricated from the sorted SWNTs to confirm the selective dispersion of semiconducting arc-discharge SWNTs.
View details for DOI 10.1021/nn4000435
View details for Web of Science ID 000316846700086
View details for PubMedID 23402644
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Hybrid nanostructured materials for high-performance electrochemical capacitors
NANO ENERGY
2013; 2 (2): 213-234
View details for DOI 10.1016/j.nanoen.2012.10.006
View details for Web of Science ID 000318319700009
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Look fast: Crystallization of conjugated molecules during solution shearing probed in-situ and in real time by X-ray scattering
PHYSICA STATUS SOLIDI-RAPID RESEARCH LETTERS
2013; 7 (3): 177-179
View details for DOI 10.1002/pssr.201206507
View details for Web of Science ID 000318069900002
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A Comparison of the Properties of Two Structurally Equivalent but Regiochemically Different Mono-Alkylated Polybithiophenes Prepared Through AABB-Type Stille Polycondensation
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY
2013; 51 (4): 908-915
View details for DOI 10.1002/pola.26448
View details for Web of Science ID 000314150500018
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Comparison of the Photovoltaic Characteristics and Nanostructure of Fullerenes Blended with Conjugated Polymers with Siloxane-Terminated and Branched Aliphatic Side Chains
CHEMISTRY OF MATERIALS
2013; 25 (3): 431-440
View details for DOI 10.1021/cm303572d
View details for Web of Science ID 000315018500020
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High-Performance Phototransistors Based on Single-Crystalline n-Channel Organic Nanowires and Photogenerated Charge-Carrier Behaviors
ADVANCED FUNCTIONAL MATERIALS
2013; 23 (5): 629-639
View details for DOI 10.1002/adfm.201201848
View details for Web of Science ID 000314468600012
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Oriented, polymer-stabilized carbon nanotube films: influence of dispersion rheology
NANOTECHNOLOGY
2013; 24 (1)
Abstract
Thin carbon nanotube films have great potential for transparent electrodes for solar cells and displays. One advantage for using carbon nanotubes is the potential for solution processing. However, research has not been done to connect solution rheological properties with the corresponding film characteristics. Here we study the rheological properties of single-walled carbon nanotube/polythiophene composite dispersions to better understand the alignment that can be achieved during deposition. Several parameters are varied to explore the cause of the alignment and the requirements of achieving a uniform, aligned carbon nanotube/polythiophene film. By understanding the dispersions thoroughly, the film quality can be predicted.
View details for DOI 10.1088/0957-4484/24/1/015709
View details for Web of Science ID 000312272500031
View details for PubMedID 23221393
- Mechanistic Study on the Solution-Phase n-Doping of 1,3-Dimethyl-2-aryl-2,3-dihydro-1H-benzoimidazole Derivatives J. Am. Chem. Soc. 2013
- Tuning the Dirac Point in CVD-Grown Graphene through Solution Processed n-Type Doping with 2-(2-Methoxyphenyl)-1,3-dimethyl-2,3-dihydro-1H-benzoimidazole Nano Lett. 2013; 13: 1890-1897
- Effects of Odd-Even Side Chain Length of Alkyl-Substituted Diphenyl-bithiophenes on First Monolayer Thin Film Packing Structure J. Am. Chem. Soc. 2013; 135: 11006-11014
- Observation of orientation-dependent photovoltaic behaviors in aligned organic nanowires Appl. Phys. Lett. 2013; 103: 53304
- Investigation of protein detection parameters using nanofunctionalized organic field-effect transistors ACS Nano 2013; 7: 3970-3980
- High Mobility N-Type Transistors Based on Solution-sheared Doped TIPS-pentacene Thin Films Adv. Mat. 2013; 25: 4663-4667
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Toward high-mobility organic field-effect transistors: Control of molecular packing and large-area fabrication of single-crystal-based devices
MRS BULLETIN
2013; 38 (1): 34-42
View details for DOI 10.1557/mrs.2012.309
View details for Web of Science ID 000317549400011
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A review of fabrication and applications of carbon nanotube film-based flexible electronics
NANOSCALE
2013; 5 (5): 1727-1752
Abstract
Flexible electronics offer a wide-variety of applications such as flexible circuits, flexible displays, flexible solar cells, skin-like pressure sensors, and conformable RFID tags. Carbon nanotubes (CNTs) are a promising material for flexible electronics, both as the channel material in field-effect transistors (FETs) and as transparent electrodes, due to their high intrinsic carrier mobility, conductivity, and mechanical flexibility. In this feature article, we review the recent progress of CNTs in flexible electronics by describing both the processing and the applications of CNT-based flexible devices. To employ CNTs as the channel material in FETs, single-walled carbon nanotubes (SWNTs) are used. There are generally two methods of depositing SWNTs on flexible substrates-transferring CVD-grown SWNTs or solution-depositing SWNTs. Since CVD-grown SWNTs can be highly aligned, they often outperform solution-processed SWNT films that are typically in the form of random network. However, solution-based SWNTs can be printed at a large-scale and at low-cost, rendering them more appropriate for manufacturing. In either case, the removal of metallic SWNTs in an effective and a scalable manner is critical, which must still be developed and optimized. Nevertheless, promising results demonstrating SWNT-based flexible circuits, displays, RF-devices, and biochemical sensors have been reported by various research groups, proving insight into the exciting possibilities of SWNT-based FETs. In using carbon nanotubes as transparent electrodes (TEs), two main strategies have been implemented to fabricate highly conductive, transparent, and mechanically compliant films-superaligned films of CNTs drawn from vertically grown CNT forests using the "dry-drawing" technique and the deposition or embedding of CNTs onto flexible or stretchable substrates. The main challenge for CNT based TEs is to fabricate films that are both highly conductive and transparent. These CNT based TEs have been used in stretchable and flexible pressure, strain, and chemical and biological sensors. In addition, they have also been used as the anode and cathode in flexible light emitting diodes, solar cells, and supercapacitors. In summary, there are a number of challenges yet to overcome to optimize the processing and performance of CNT-based flexible electronics; nonetheless, CNTs remain a highly suitable candidate for various flexible electronic applications in the near future.
View details for DOI 10.1039/c3nr33560g
View details for Web of Science ID 000314931900002
View details for PubMedID 23381727
- A Rapid and Efficient Self-Healing Thermo-Reversible Elastomer Crosslinked with Graphene Oxide Adv. Mater. 2013; 25: 5785-5790
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Confined organization of fullerene units along high polymer chains
JOURNAL OF MATERIALS CHEMISTRY C
2013; 1 (36): 5747-5755
View details for DOI 10.1039/c3tc31158a
View details for Web of Science ID 000323578000020
- Solution-Grown Organic Single-Crystalline p-n Junctions with Ambipolar Charge Transport Adv. Mater. 2013
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A comparison of two air-stable molecular n-dopants for C-60
ORGANIC ELECTRONICS
2012; 13 (12): 3319-3325
View details for DOI 10.1016/j.orgel.2012.09.024
View details for Web of Science ID 000311681600076
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Toward mechanically robust and intrinsically stretchable organic solar cells: Evolution of photovoltaic properties with tensile strain
SOLAR ENERGY MATERIALS AND SOLAR CELLS
2012; 107: 355-365
View details for DOI 10.1016/j.solmat.2012.07.013
View details for Web of Science ID 000311270000048
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Evaluation of Solution-Processable Carbon-Based Electrodes for All-Carbon Solar Cells
ACS NANO
2012; 6 (11): 10384-10395
Abstract
Carbon allotropes possess unique and interesting physical, chemical, and electronic properties that make them attractive for next-generation electronic devices and solar cells. In this report, we describe our efforts into the fabrication of the first reported all-carbon solar cell in which all components (the anode, active layer, and cathode) are carbon based. First, we evaluate the active layer, on standard electrodes, which is composed of a bilayer of polymer sorted semiconducting single-walled carbon nanotubes and C(60). This carbon-based active layer with a standard indium tin oxide anode and metallic cathode has a maximum power conversion efficiency of 0.46% under AM1.5 Sun illumination. Next, we describe our efforts in replacing the electrodes with carbon-based electrodes, to demonstrate the first all-carbon solar cell, and discuss the remaining challenges associated with this process.
View details for DOI 10.1021/nn304410w
View details for Web of Science ID 000311521700114
View details for PubMedID 23113673
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A simple droplet pinning method for polymer film deposition for measuring charge transport in a thin film transistor
ORGANIC ELECTRONICS
2012; 13 (11): 2450-2460
View details for DOI 10.1016/j.orgel.2012.07.011
View details for Web of Science ID 000311177700035
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Manipulating the Morphology of P3HT-PCBM Bulk Heterojunction Blends with Solvent Vapor Annealing
CHEMISTRY OF MATERIALS
2012; 24 (20): 3923-3931
View details for DOI 10.1021/cm302312a
View details for Web of Science ID 000310095100012
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TIPS-pentacene crystalline thin film growth
ORGANIC ELECTRONICS
2012; 13 (10): 2056-2062
View details for DOI 10.1016/j.orgel.2012.06.019
View details for Web of Science ID 000309591200039
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Dispersion of single walled carbon nanotubes in amidine solvents
NANOTECHNOLOGY
2012; 23 (34)
Abstract
The excellent electronic and material properties of single walled carbon nanotubes (SWNTs) makes this nanomaterial very attractive for incorporation into flexible and stretchable electronics. However, the widespread application of SWNTs in electronic devices is still limited. To purify, process and place SWNTs, appropriate solvents for dispersion are needed. However, a fundamental understanding of the reasons why certain solvents are capable of dispersing SWNTs is still missing. Here we report on two new potential solvents containing amidine moieties, 1,8-diazabicycloundec-7-ene (DBU) and 1,5-diazabicyclo(4.3.0)non-5-ene (DBN). Even though these solvents' molecular structures differ by only two -CH(2)- groups, we found that DBU is capable of dispersing SWNTs, while DBN is not. We carried out density functional theory (DFT) calculations to investigate the interaction between DBU and DBN, and we elucidated the reasons for the different performances of the two solvents. DBU has a preferential edge-on interaction with the SWNT, thus allowing for a higher solvent coverage than DBN. In addition, the CH(2)-SWNT interaction present for DBU substantially increases the adsorption energy compared to DBN. Our results point to the important interplay between the interaction of pi electrons, nitrogen lone pairs and the -CH(2)- groups present in aprotic solvent molecules and the delocalized pi electrons in SWNTs.
View details for DOI 10.1088/0957-4484/23/34/344011
View details for Web of Science ID 000307812000012
View details for PubMedID 22885377
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Work function recovery of air exposed molybdenum oxide thin films
APPLIED PHYSICS LETTERS
2012; 101 (9)
View details for DOI 10.1063/1.4748978
View details for Web of Science ID 000308408100070
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Engineering the metal gate electrode for controlling the threshold voltage of organic transistors
APPLIED PHYSICS LETTERS
2012; 101 (6)
View details for DOI 10.1063/1.4739511
View details for Web of Science ID 000307862400089
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Strong and Stable Doping of Carbon Nanotubes and Graphene by MoOx for Transparent Electrodes
NANO LETTERS
2012; 12 (7): 3574-3580
Abstract
MoO(x) has been used for organic semiconductor doping, but it had been considered an inefficient and/or unstable dopant. We report that MoO(x) can strongly and stably dope carbon nanotubes and graphene. Thermally annealed MoO(x)-CNT composites can form durable thin film electrodes with sheet resistances of 100 ?/sq at 85% transmittance plain and 85 ?/sq at 83% transmittance with a PEDOT:PSS adlayer. Sheet resistances change less than 10% over 20 days in ambient and less than 2% with overnight heating to 300 °C in air. The MoO(x) can be easily deposited either by thermal evaporation or from solution-based precursors. Excellent stability coupled with high conductivity makes MoO(x)-CNT composites extremely attractive candidates for practical transparent electrodes.
View details for DOI 10.1021/nl301207e
View details for Web of Science ID 000306296200037
View details for PubMedID 22694046
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Transparent, Optical, Pressure-Sensitive Artificial Skin for Large-Area Stretchable Electronics
ADVANCED MATERIALS
2012; 24 (24): 3223-3227
Abstract
Optical pressure sensors are highly responsive and are unaffected by surrounding parameters such as electronic noise, humidity, temperature, etc. A new type of optical pressure sensor is described that demonstrates the stretchability and transparency of a polydimethylsiloxane waveguide, while also serving as a substrate. The pressure sensors are both robust and easy to fabricate over a large area.
View details for DOI 10.1002/adma.201200523
View details for Web of Science ID 000305450500009
View details for PubMedID 22641411
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Using Nitrile Functional Groups to Replace Amines for Solution-Deposited Single-Walled Carbon Nanotube Network Films
ACS NANO
2012; 6 (6): 4845-4853
Abstract
Amine-terminated self-assembled monolayers (SAMs) can be utilized to selectively adsorb semiconducting single-walled carbon nanotubes (S-SWNTs), but are not ideal. Formation of these monolayer films from silanes can be dramatically influenced by atmospheric and other processing conditions, resulting in poor-quality SAMs or irreproducible results. The surface sorting method of fabricating these semiconducting nanotube networks (SWNTnts) can become ineffective if the functionalized surface is not smooth with high amine density. However, by replacing the amine with a nitrile group, SAM formation can be made more controllable and reproducible. Upon SWNT deposition, the nitrile group was found to not only adsorb higher density SWNTnts but also sort the nanotubes efficiently, as shown by micro-Raman spectroscopy. Upon testing these SWNTnts for device performance, these thin-film transistors (TFTs) were also found to yield higher quality devices than those fabricated on amine surfaces. Overall, these results expand the applicability of surface sorting and SWNT adsorption to other organic functionalities for nanotube separation. This report provides an outline of the merits and characterization of using the nitrile functional group for the separation and adsorption of SWNTs and its integration in network TFTs.
View details for DOI 10.1021/nn300124y
View details for Web of Science ID 000305661300031
View details for PubMedID 22588018
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In Situ Hetero End-Functionalized Polythiophene and Subsequent "Click" Chemistry With DNA
MACROMOLECULAR RAPID COMMUNICATIONS
2012; 33 (10): 938-942
Abstract
It is demonstrated that bifunctionalized polythiophenes involving thiol and azide end-functional groups can be synthesized by chain-growth Suzuki-Miyaura type polymerization. The bifunctionalized polythiophenes are successfully characterized by 1H NMR, gel permeation chromatography (GPC), and matrix-assisted laser desorption ionization time-of-flight (MALDI-TOF). Furthermore, the azide end-group reacts with DNA via "click chemistry" to form a polythiophene/DNA hybrid structure, which is characterized by ESI-MS. The described synthetic approaches will lead to the synthesis of novel multi-block copolymers as well as biomolecule-based conjugated polymer structures.
View details for DOI 10.1002/marc.201100686
View details for Web of Science ID 000304192400008
View details for PubMedID 22354688
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High-Performance Transistors and Complementary Inverters Based on Solution-Grown Aligned Organic Single-Crystals
ADVANCED MATERIALS
2012; 24 (19): 2588-2591
View details for DOI 10.1002/adma.201200151
View details for Web of Science ID 000303795700008
View details for PubMedID 22461243
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Recent advances in flexible and stretchable electronics, sensors and power sources
SCIENCE CHINA-CHEMISTRY
2012; 55 (5): 718-725
View details for DOI 10.1007/s11426-012-4503-3
View details for Web of Science ID 000304248500007
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Graphene-sponges as high-performance low-cost anodes for microbial fuel cells
ENERGY & ENVIRONMENTAL SCIENCE
2012; 5 (5): 6862-6866
View details for DOI 10.1039/c2ee03583a
View details for Web of Science ID 000303251500019
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Organic Transistors with Ordered Nanoparticle Arrays as a Tailorable Platform for Selective, In Situ Detection
ACS NANO
2012; 6 (4): 3100-3108
Abstract
The use of organic transistors as sensing platforms provides a number of distinct advantages over conventional detection technologies, including their tunability, portability, and ability to directly transduce binding events without tedious and expensive labeling procedures. However, detection efforts using organic transistors lack a general method to uniquely specify and detect a target of interest. While highly sensitive liquid- and vapor-phase sensors have been previously reported, detection has been restricted either to the serendipitous interaction of the analyte molecules with the organic semiconductor or to the covalent functionalization of the semiconductor with receptor groups to enhance specificity. However, the former technique cannot be regularly relied upon for tailorable sensing while the latter may result in unpredictable decreases in electronic performance. Thus, a method to provide modular receptor sites on the surface of an organic transistor without damaging the device will significantly advance the field, especially regarding biological species detection. In this work, we utilized a block copolymer to template ordered, large-area arrays of gold nanoparticles, with sub-100 nm center-to-center spacing onto the surface of an organic transistor. This highly modular platform is designed for orthogonal modification with a number of available chemical and biological functional groups by taking advantage of the well-studied gold-thiol linkage. Herein, we demonstrate the functionalization of gold nanoparticles with a mercury-binding oligonucleotide sequence. Finally, we demonstrate the highly selective and robust detection of mercury(II) using this platform in an underwater environment.
View details for DOI 10.1021/nn204830b
View details for Web of Science ID 000303099300027
View details for PubMedID 22397363
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Controlled Conjugated Backbone Twisting for an Increased Open-Circuit Voltage while Having a High Short-Circuit Current in Poly(hexylthiophene) Derivatives
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
2012; 134 (11): 5222-5232
Abstract
Conjugated polymers with nearly planar backbones have been the most commonly investigated materials for organic-based electronic devices. More twisted polymer backbones have been shown to achieve larger open-circuit voltages in solar cells, though with decreased short-circuit current densities. We systematically impose twists within a family of poly(hexylthiophene)s and examine their influence on the performance of polymer:fullerene bulk heterojunction (BHJ) solar cells. A simple chemical modification concerning the number and placement of alkyl side chains along the conjugated backbone is used to control the degree of backbone twisting. Density functional theory calculations were carried out on a series of oligothiophene structures to provide insights on how the sterically induced twisting influences the geometric, electronic, and optical properties. Grazing incidence X-ray scattering measurements were performed to investigate how the thin-film packing structure was affected. The open-circuit voltage and charge-transfer state energy of the polymer:fullerene BHJ solar cells increased substantially with the degree of twist induced within the conjugated backbone--due to an increase in the polymer ionization potential--while the short-circuit current decreased as a result of a larger optical gap and lower hole mobility. A controlled, moderate degree of twist along the poly(3,4-dihexyl-2,2':5',2''-terthiophene) (PDHTT) conjugated backbone led to a 19% enhancement in the open-circuit voltage (0.735 V) vs poly(3-hexylthiophene)-based devices, while similar short-circuit current densities, fill factors, and hole-carrier mobilities were maintained. These factors resulted in a power conversion efficiency of 4.2% for a PDHTT:[6,6]-phenyl-C(71)-butyric acid methyl ester (PC(71)BM) blend solar cell without thermal annealing. This simple approach reveals a molecular design avenue to increase open-circuit voltage while retaining the short-circuit current.
View details for DOI 10.1021/ja210954r
View details for Web of Science ID 000302191900036
View details for PubMedID 22385287
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Contacting nanowires and nanotubes with atomic precision for electronic transport
APPLIED PHYSICS LETTERS
2012; 100 (10)
View details for DOI 10.1063/1.3692585
View details for Web of Science ID 000301655500059
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Highly Effective Separation of Semiconducting Carbon Nanotubes verified via Short-Channel Devices Fabricated Using Dip-Pen Nanolithography
ACS NANO
2012; 6 (3): 2487-2496
Abstract
We have verified a highly effective separation of semiconducting single-walled carbon nanotubes (sc-SWNTs) via statistical analysis of short-channel devices fabricated using multipen dip-pen nanolithography. Our SWNT separation technique utilizes a polymer (rr-P3DDT) that selectively interacts with and disperses sc-SWNTs. Our devices had channel lengths on the order of 300-500 nm, with an average of about 3 SWNTs that directly connected the source-drain electrodes. A total of 140 SWNTs were characterized, through which we have observed that all of the SWNTs exhibited semiconducting behavior with an average on/off current ratio of ~10(6). Additionally, we have characterized 50 SWNTs after the removal of rr-P3DDT, through which we have again observed semiconducting behavior for all of the SWNTs with similar electrical characteristics. The relatively low average on-conductance of 0.0796 ?S was attributed to the distribution of small diameter SWNTs in our system and due to the non-ohmic Au contacts on SWNTs. The largely positive threshold voltages were shifted toward zero after vacuum annealing, indicating that the SWNTs were doped in air. To the best of our knowledge, this is the first time numerous SWNTs were electrically characterized using short-channel devices, through which all of the measured SWNTs were determined to be semiconducting. Hence, our semiconducting single-walled carbon nanotube sorting system holds a great deal of promise in bringing forth a variety of practical applications in SWNT electronics.
View details for DOI 10.1021/nn204875a
View details for Web of Science ID 000301945900064
View details for PubMedID 22352426
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The effect of pH and DNA concentration on organic thin-film transistor biosensors
ORGANIC ELECTRONICS
2012; 13 (3): 519-524
View details for DOI 10.1016/j.orgel.2011.12.013
View details for Web of Science ID 000300392100024
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High-Mobility Field-Effect Transistors from Large-Area Solution-Grown Aligned C-60 Single Crystals
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
2012; 134 (5): 2760-2765
Abstract
Field-effect transistors based on single crystals of organic semiconductors have the highest reported charge carrier mobility among organic materials, demonstrating great potential of organic semiconductors for electronic applications. However, single-crystal devices are difficult to fabricate. One of the biggest challenges is to prepare dense arrays of single crystals over large-area substrates with controlled alignment. Here, we describe a solution processing method to grow large arrays of aligned C(60) single crystals. Our well-aligned C(60) single-crystal needles and ribbons show electron mobility as high as 11 cm(2)V(-1)s(-1) (average mobility: 5.2 ± 2.1 cm(2)V(-1)s(-1) from needles; 3.0 ± 0.87 cm(2)V(-1)s(-1) from ribbons). This observed mobility is ~8-fold higher than the maximum reported mobility for solution-grown n-channel organic materials (1.5 cm(2)V(-1)s(-1)) and is ~2-fold higher than the highest mobility of any n-channel organic material (~6 cm(2)V(-1)s(-1)). Furthermore, our deposition method is scalable to a 100 mm wafer substrate, with around 50% of the wafer surface covered by aligned crystals. Hence, our method facilitates the fabrication of large amounts of high-quality semiconductor crystals for fundamental studies, and with substantial improvement on the surface coverage of crystals, this method might be suitable for large-area applications based on single crystals of organic semiconductors.
View details for DOI 10.1021/ja210430b
View details for Web of Science ID 000300460600049
View details for PubMedID 22239604
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Fabrication of organic semiconductor crystalline thin films and crystals from solution by confined crystallization
ORGANIC ELECTRONICS
2012; 13 (2): 235-243
View details for DOI 10.1016/j.orgel.2011.11.005
View details for Web of Science ID 000299539100004
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Highly Conductive and Transparent PEDOT:PSS Films with a Fluorosurfactant for Stretchable and Flexible Transparent Electrodes
ADVANCED FUNCTIONAL MATERIALS
2012; 22 (2): 421-428
View details for DOI 10.1002/adfm.201101775
View details for Web of Science ID 000299251800021
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Electronic Properties of Transparent Conductive Films of PEDOT:PSS on Stretchable Substrates
CHEMISTRY OF MATERIALS
2012; 24 (2): 373-382
View details for DOI 10.1021/cm203216m
View details for Web of Science ID 000299367500018
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Micro-imprinted prism substrate for self-aligned short channel organic transistors on a flexible substrate
APPLIED PHYSICS LETTERS
2012; 100 (4)
View details for DOI 10.1063/1.3679119
View details for Web of Science ID 000300064500064
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Mechanistic Considerations of Bending-Strain Effects within Organic Semiconductors on Polymer Dielectrics
ADVANCED FUNCTIONAL MATERIALS
2012; 22 (1): 175-183
View details for DOI 10.1002/adfm.201101418
View details for Web of Science ID 000298673500021
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Wafer-Scale Fabrication and Characterization of Thin-Film Transistors with Polythiophene-Sorted Semiconducting Carbon Nanotube Networks
ACS NANO
2012; 6 (1): 451-458
Abstract
Semiconducting single-walled carbon nanotubes (SWCNTs) have great potential of becoming the channel material for future thin-film transistor technology. However, an effective sorting technique is needed to obtain high-quality semiconducting SWCNTs for optimal device performance. In our previous work, we reported a dispersion technique for semiconducting SWCNTs that relies on regioregular poly(3-dodecylthiophene) (rr-P3DDT) to form hybrid nanostructures. In this study, we demonstrate the scalability of those sorted CNT composite structures to form arrays of TFTs using standard lithographic techniques. The robustness of these CNT nanostructures was tested with Raman spectroscopy and atomic force microscope images. Important trends in device properties were extracted by means of electrical measurements for different CNT concentrations and channel lengths (L(c)). A statistical study provided an average mobility of 1 cm(2)/V·s and I(on)/I(off) as high as 10(6) for short channel lengths (L(c) = 1.5 ?m) with 100% yield. This highlights the effectiveness of this sorting technique and its scalability for large-scale, flexible, and transparent display applications.
View details for DOI 10.1021/nn203771u
View details for Web of Science ID 000299368300055
View details for PubMedID 22148677
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5,11-Conjugation-extended low-bandgap anthradithiophene-containing polymer exhibiting enhanced thin-film order and field-effect mobility
CHEMICAL COMMUNICATIONS
2012; 48 (58): 7286-7288
Abstract
Anthradithiophene was incorporated in a polymer structure by extending its conjugation from the 5,11-positions, through in situ desilylation followed by acetylenic coupling with a dibromo-monomer. The resulting polymer showed largely redshifted order in a thin film as well as order in thin film, forming lamellar structures out of the substrate plane. As a result, it exhibits field-effect hole mobilities, on the order of 0.1 cm(2) V(-1) s(-1), a ten to hundred-fold improvement as compared to previous acene-containing polymers.
View details for DOI 10.1039/c2cc32473c
View details for Web of Science ID 000305624500018
View details for PubMedID 22699310
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Themed issue on "organic optoelectronic materials''
JOURNAL OF MATERIALS CHEMISTRY
2012; 22 (10): 4134-4135
View details for DOI 10.1039/c1jm90199k
View details for Web of Science ID 000300250200001
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Impact of regioregularity on thin-film transistor and photovoltaic cell performances of pentacene-containing polymers
JOURNAL OF MATERIALS CHEMISTRY
2012; 22 (10): 4356-4363
View details for DOI 10.1039/c2jm15483h
View details for Web of Science ID 000300250200027
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A Cell-Compatible Conductive Film from a Carbon Nanotube Network Adsorbed on Poly-L-lysine
ACS NANO
2011; 5 (12): 10026-10032
Abstract
Single-walled carbon nanotubes (SWNTs) have shown promise for use in organic electronic applications including thin film transistors, conducting electrodes, and biosensors. Additionally, previous studies found applications for SWNTs in bioelectronic devices, including drug delivery carriers and scaffolds for tissue engineering. There is a current need to rapidly process SWNTs from solution phase to substrates in order to produce device structures that are also biocompatible. Studies have shown the use of surfaces covalently functionalized with primary amines to selectively adsorb semiconducting SWNTs. Here we report the potential of substrates modified with physisorbed polymers as a rapid biomaterials-based approach for the formation of SWNT networks. We hypothesized that rapid surface modification could be accomplished by adsorption of poly-L-lysine (PLL), which is also frequently used in biological applications. We detail a rapid and facile method for depositing SWNTs onto various substrate materials using the amine-rich PLL. Dispersions of SWNTs of different chiralities suspended in N-methylpyrrolidinone (NMP) were spin coated onto various PLL-treated substrates. SWNT adsorption and alignment were characterized by atomic force microscopy (AFM) while electrical properties of the network were characterized by 2-terminal resistance measurements. Additionally, we investigated the relative chirality of the SWNT networks by micro-Raman spectroscopy. The SWNT surface density was strongly dependent upon the adsorbed concentration of PLL on the surface. SWNT adsorbed on PLL-treated substrates exhibited enhanced biocompatibility compared to SWNT networks fabricated using alternative methods such as drop casting. These results suggest that PLL films can promote formation of biocompatible SWNT networks for potential biomedical applications.
View details for DOI 10.1021/nn203870c
View details for Web of Science ID 000298316700079
View details for PubMedID 22053708
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High-Mobility Air-Stable Solution-Shear-Processed n-Channel Organic Transistors Based on Core-Chlorinated Naphthalene Diimides
ADVANCED FUNCTIONAL MATERIALS
2011; 21 (21): 4173-4181
View details for DOI 10.1002/adfm.201101606
View details for Web of Science ID 000297096900021
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Improving the Performance of Lithium-Sulfur Batteries by Conductive Polymer Coating
ACS NANO
2011; 5 (11): 9187-9193
View details for DOI 10.1021/nn203436j
View details for Web of Science ID 000297143300081
View details for PubMedID 21995642
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Carrier mobility in pentacene as a function of grain size and orientation derived from scanning transmission X-ray microscopy
ORGANIC ELECTRONICS
2011; 12 (11): 1936-1942
View details for DOI 10.1016/j.orgel.2011.08.007
View details for Web of Science ID 000295830700029
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Enhancing the Supercapacitor Performance of Graphene/MnO2 Nanostructured Electrodes by Conductive Wrapping
NANO LETTERS
2011; 11 (10): 4438-4442
Abstract
MnO2 is considered one of the most promising pseudocapactive materials for high-performance supercapacitors given its high theoretical specific capacitance, low-cost, environmental benignity, and natural abundance. However, MnO2 electrodes often suffer from poor electronic and ionic conductivities, resulting in their limited performance in power density and cycling. Here we developed a "conductive wrapping" method to greatly improve the supercapacitor performance of graphene/MnO2-based nanostructured electrodes. By three-dimensional (3D) conductive wrapping of graphene/MnO2 nanostructures with carbon nanotubes or conducting polymer, specific capacitance of the electrodes (considering total mass of active materials) has substantially increased by ?20% and ?45%, respectively, with values as high as ?380 F/g achieved. Moreover, these ternary composite electrodes have also exhibited excellent cycling performance with >95% capacitance retention over 3000 cycles. This 3D conductive wrapping approach represents an exciting direction for enhancing the device performance of metal oxide-based electrochemical supercapacitors and can be generalized for designing next-generation high-performance energy storage devices.
View details for DOI 10.1021/nl2026635
View details for Web of Science ID 000295667000073
View details for PubMedID 21942427
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Stretchable, elastic materials and devices for solar energy conversion
ENERGY & ENVIRONMENTAL SCIENCE
2011; 4 (9): 3314-3328
View details for DOI 10.1039/c1ee01881g
View details for Web of Science ID 000294306900015
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Solution-Processed Graphene/MnO2 Nanostructured Textiles for High-Performance Electrochemical Capacitors
NANO LETTERS
2011; 11 (7): 2905-2911
Abstract
Large scale energy storage system with low cost, high power, and long cycle life is crucial for addressing the energy problem when connected with renewable energy production. To realize grid-scale applications of the energy storage devices, there remain several key issues including the development of low-cost, high-performance materials that are environmentally friendly and compatible with low-temperature and large-scale processing. In this report, we demonstrate that solution-exfoliated graphene nanosheets (?5 nm thickness) can be conformably coated from solution on three-dimensional, porous textiles support structures for high loading of active electrode materials and to facilitate the access of electrolytes to those materials. With further controlled electrodeposition of pseudocapacitive MnO(2) nanomaterials, the hybrid graphene/MnO(2)-based textile yields high-capacitance performance with specific capacitance up to 315 F/g achieved. Moreover, we have successfully fabricated asymmetric electrochemical capacitors with graphene/MnO(2)-textile as the positive electrode and single-walled carbon nanotubes (SWNTs)-textile as the negative electrode in an aqueous Na(2)SO(4) electrolyte solution. These devices exhibit promising characteristics with a maximum power density of 110 kW/kg, an energy density of 12.5 Wh/kg, and excellent cycling performance of ?95% capacitance retention over 5000 cycles. Such low-cost, high-performance energy textiles based on solution-processed graphene/MnO(2) hierarchical nanostructures offer great promise in large-scale energy storage device applications.
View details for DOI 10.1021/nl2013828
View details for Web of Science ID 000292849400059
View details for PubMedID 21667923
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Stretchable Organic Solar Cells
ADVANCED MATERIALS
2011; 23 (15): 1771-?
View details for DOI 10.1002/adma.201004426
View details for Web of Science ID 000289531800014
View details for PubMedID 21491510
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Aryl-Perfluoroaryl Substituted Tetracene: Induction of Face-to-Face pi-pi Stacking and Enhancement of Charge Carrier Properties
CHEMISTRY OF MATERIALS
2011; 23 (7): 1646-1649
View details for DOI 10.1021/cm200356y
View details for Web of Science ID 000289029400004
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Pentacene Based Organic Thin Film Transistors as the Transducer for Biochemical Sensing in Aqueous Media
CHEMISTRY OF MATERIALS
2011; 23 (7): 1946-1953
View details for DOI 10.1021/cm103685c
View details for Web of Science ID 000289029400039
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The Phase Behavior of a Polymer-Fullerene Bulk Heterojunction System that Contains Bimolecular Crystals
JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS
2011; 49 (7): 499-503
View details for DOI 10.1002/polb.22214
View details for Web of Science ID 000288541400003
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Solution-Shear-Processed Quaterrylene Diimide Thin-Film Transistors Prepared by Pressure-Assisted Thermal Cleavage of Swallow Tails
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
2011; 133 (12): 4204-4207
Abstract
A scalable synthesis of swallow-tailed quaterrylene diimides (STQDIs) and a method for the solution processing of sparingly soluble quaterrylene diimide (QDI) thin films are described. The pressure-assisted thermal cleavage of swallow tails yields crystalline QDI layers with electron mobility up to 0.088 cm(2) V(-1) s(-1). The developed method opens up a new route toward the solution processing of higher rylene diimides with poor solubility.
View details for DOI 10.1021/ja110486s
View details for Web of Science ID 000291715300015
View details for PubMedID 21375243
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The effect of amine protonation on the electrical properties of spin-assembled single-walled carbon nanotube networks
NANOTECHNOLOGY
2011; 22 (12)
Abstract
Amine-terminated self-assembled monolayers (SAMs) have been shown to selectively adsorb semiconducting single-walled carbon nanotubes (sc-SWNTs). Previous studies have shown that when deposited by spin coating, the resulting nanotube networks (SWNTnts) can be strongly influenced by the charge state of the amine (primary, secondary, and tertiary). When the amine surfaces were exposed to varying pH solutions, the conductivity and overall quality of the resulting fabricated networks were altered. Atomic force microscopy (AFM) topography had shown that the density of the SWNTnts was reduced as the amine protonation decreased, indicating that the electrostatic attraction between the SWNTs in solution and the surface influenced the adsorption. Simultaneously, ?-Raman analysis had suggested that when exposed to more basic conditions, the resulting networks were enhanced with sc-SWNTs. To directly confirm this enhancement, Ti/Pd contacts were deposited and devices were tested in air. Key device characteristics were found to match the enhancement trends previously observed by spectroscopy. For the primary and secondary amines, on/off current ratios were commensurate with the Raman trends in metallic contribution, while no trends were observed on the tertiary amine (due to weaker interactions). Finally, differing SWNT solution volumes were used to compensate for adsorption differences and yielded identical SWNTnt densities on the various pH-treated samples to eliminate the influence of network density. These results further the understanding of the amine-SWNT interaction during the spin coating process. Overall, we provide a convenient route to provide SWNT-based TFTs with highly tunable electronic charge transport through better understanding of the influence of these specific interactions.
View details for DOI 10.1088/0957-4484/22/12/125201
View details for Web of Science ID 000287448200001
View details for PubMedID 21317495
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Microfluidic Arrays for Rapid Characterization of Organic Thin-Film Transistor Performance
ADVANCED MATERIALS
2011; 23 (10): 1257-?
View details for DOI 10.1002/adma.201003815
View details for Web of Science ID 000288170700010
View details for PubMedID 21381125
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Syntheses of Organic Molecule-DNA Hybrid Structures
ACS NANO
2011; 5 (3): 2067-2074
Abstract
Investigation of robust and efficient pathways to build DNA-organic molecule hybrid structures is fundamentally important to realize controlled placement of single molecules for potential applications, such as single-molecule electronic devices. Herein, we report a systematic investigation of synthetic processes for preparing organic molecule-DNA building blocks and their subsequent elongation to generate precise micrometer-sized structures. Specifically, optimal cross-coupling routes were identified to enable chemical linkages between three different organic molecules, namely, polyethylene glycol (PEG), poly(p-phenylene ethynylene) (PPE), and benzenetricarboxylate, with single-stranded (ss) DNA. The resulting DNA-organic molecule hybrid building blocks were purified and characterized by both denaturing gel electrophoresis and electrospray ionization mass spectrometry (ESI-MS). The building blocks were subsequently elongated through both the DNA hybridization and ligation processes to prepare micrometer-sized double-stranded (ds) DNA-organic molecule hybrid structures. The described synthetic procedures should facilitate future syntheses of various hybrid DNA-based organic molecular structures.
View details for DOI 10.1021/nn1032455
View details for Web of Science ID 000288570600062
View details for PubMedID 21323343
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Controlling Electric Dipoles in Nanodielectrics and Its Applications for Enabling Air-Stable n-Channel Organic Transistors
NANO LETTERS
2011; 11 (3): 1161-1165
Abstract
We present a new method to manipulate the channel charge density of field-effect transistors using dipole-generating self-assembled monolayers (SAMs) with different anchor groups. Our approach maintains an ideal interface between the dipole layers and the semiconductor while changing the built-in electric potential by 0.41-0.50 V. This potential difference can be used to change effectively the electrical properties of nanoelectronic devices. We further demonstrate the application of the SAM dipoles to enable air-stable operation of n-channel organic transistors.
View details for DOI 10.1021/nl104087u
View details for Web of Science ID 000288061500043
View details for PubMedID 21323381
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Halogenated Materials as Organic Semiconductors
CHEMISTRY OF MATERIALS
2011; 23 (3): 446-455
View details for DOI 10.1021/cm102182x
View details for Web of Science ID 000286691100010
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Selective Surface Chemistry Using Alumina Nanoparticles Generated from Block Copolymers
LANGMUIR
2011; 27 (1): 445-451
Abstract
Developing orthogonal surface chemistry techniques that perform at the nanoscale is key to achieving precise control over molecular patterning on surfaces. We report the formation and selective functionalization of alumina nanoparticle arrays generated from block copolymer templates. This new material provides an alternative to gold for orthogonal surface chemistry at the nanometer scale. Atomic force microscopy and X-ray photoelectron spectroscopy confirm these particles show excellent selectivity over silica for phosphonic and carboxylic acid adsorption. As this is the first reported synthesis of alumina nanoparticles from block copolymer templates, characterizations via Fourier transform infrared spectroscopy, Auger electron spectroscopy, and transmission electron microscopy are presented. Reproducible formation of alumina nanoparticles was dependent on a counterintuitive synthetic step wherein a small amount of water is added to an anhydrous toluene solution of block copolymer and aluminum chloride. The oxidation environment of the aluminum in these particles, as measured by Auger electron spectroscopy, is similar to that of native aluminum oxide and alumina grown by atomic layer deposition. This discovery expands the library of available surface chemistries for nanoscale molecular patterning.
View details for DOI 10.1021/la104094h
View details for Web of Science ID 000285560400060
View details for PubMedID 21133369
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Thin Film Structure of Triisopropylsilylethynyl-Functionalized Pentacene and Tetraceno[2,3-b]thiophene from Grazing Incidence X-Ray Diffraction
ADVANCED MATERIALS
2011; 23 (1): 127-?
View details for DOI 10.1002/adma.201003135
View details for Web of Science ID 000285723400015
View details for PubMedID 21104808
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The Shear Flow Processing of Controlled DNA Tethering and Stretching for Organic Molecular Electronics
ACS NANO
2011; 5 (1): 275-282
Abstract
DNA has been recently explored as a powerful tool for developing molecular scaffolds for making reproducible and reliable metal contacts to single organic semiconducting molecules. A critical step in the process of exploiting DNA-organic molecule-DNA (DOD) array structures is the controlled tethering and stretching of DNA molecules. Here we report the development of reproducible surface chemistry for tethering DNA molecules at tunable density and demonstrate shear flow processing as a rationally controlled approach for stretching/aligning DNA molecules of various lengths. Through enzymatic cleavage of ?-phage DNA to yield a series of DNA chains of various lengths from 17.3 ?m down to 4.2 ?m, we have investigated the flow/extension behavior of these tethered DNA molecules under different flow strengths in the flow-gradient plane. We compared Brownian dynamic simulations for the flow dynamics of tethered ?-DNA in shear, and found our flow-gradient plane experimental results matched well with our bead-spring simulations. The shear flow processing demonstrated in our studies represents a controllable approach for tethering and stretching DNA molecules of various lengths. Together with further metallization of DNA chains within DOD structures, this bottom-up approach can potentially enable efficient and reliable fabrication of large-scale nanoelectronic devices based on single organic molecules, therefore opening opportunities in both fundamental understanding of charge transport at the single molecular level and many exciting applications for ever-shrinking molecular circuits.
View details for DOI 10.1021/nn102669b
View details for Web of Science ID 000286487300035
View details for PubMedID 21126082
- High Mobility Air-Stable Solution-Shear-Processed n-Channel Organic Transistors Based on Core-Chlorinated Naphthalene Diimides Adv. Funct. Mater. 2011; 21: 4173-4181
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Solvent additives and their effects on blend morphologies of bulk heterojunctions
JOURNAL OF MATERIALS CHEMISTRY
2011; 21 (1): 242-250
View details for DOI 10.1039/c0jm01976c
View details for Web of Science ID 000285067300031
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Synthesis of regioregular pentacene-containing conjugated polymers
JOURNAL OF MATERIALS CHEMISTRY
2011; 21 (20): 7078-7081
View details for DOI 10.1039/c1jm10643k
View details for Web of Science ID 000290167200006
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Side chain engineering of fused aromatic thienopyrazine based low band-gap polymers for enhanced charge carrier mobility
JOURNAL OF MATERIALS CHEMISTRY
2011; 21 (5): 1537-1543
View details for DOI 10.1039/c0jm02491k
View details for Web of Science ID 000286332000032
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Molecular n-type doping for air-stable electron transport in vacuum-processed n-channel organic transistors
APPLIED PHYSICS LETTERS
2010; 97 (24)
View details for DOI 10.1063/1.3527972
View details for Web of Science ID 000285481000079
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Full-Swing and High-Gain Pentacene Logic Circuits on Plastic Substrate
IEEE ELECTRON DEVICE LETTERS
2010; 31 (12): 1488-1490
View details for DOI 10.1109/LED.2010.2081336
View details for Web of Science ID 000284541400044
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2,9-Dibromopentacene: Synthesis and the role of substituent and symmetry on solid-state order
SYNTHETIC METALS
2010; 160 (23-24): 2447-2451
View details for DOI 10.1016/j.synthmet.2010.09.025
View details for Web of Science ID 000286910000011
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Fabrication and Evaluation of Solution-Processed Reduced Graphene Oxide Electrodes for p- and n-Channel Bottom-Contact Organic Thin-Film Transistors
ACS NANO
2010; 4 (11): 6343-6352
Abstract
Reduced graphene oxide (RGO) is an electrically conductive carbon-based nanomaterial that has recently attracted attention as a potential electrode for organic electronics. Here we evaluate several solution-based methods for fabricating RGO bottom-contact (BC) electrodes for organic thin-film transistors (OTFTs), demonstrate functional p- and n-channel devices with such electrodes, and compare their electrical performance with analogous devices containing gold electrodes. We show that the morphology of organic semiconductor films deposited on RGO electrodes is similar to that observed in the channel region of the devices and that devices fabricated with RGO electrodes have lower contact resistances compared to those fabricated with gold contacts. Although the conductivity of RGO is poor compared to that of gold, RGO is still an enticing electrode material for organic electronic devices possibly owing to the retention of desirable morphological features, lower contact resistance, lower cost, and solution processability.
View details for DOI 10.1021/nn101369j
View details for Web of Science ID 000284438000008
View details for PubMedID 20945927
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Dip-Pen Nanolithography of Electrical Contacts to Single Graphene Flakes
ACS NANO
2010; 4 (11): 6409-6416
Abstract
This study evaluates an alternative to electron-beam lithography for fabricating nanoscale graphene devices. Dip-pen nanolithography is used for defining monolayer graphene flakes and for patterning of gold electrodes through writing of an alkylthiol on thin films of gold evaporated onto graphene flakes. A wet gold etching step was used to form the individual devices. The sheet resistances of these monolayer graphene devices are comparable to reported literature values. This alternative technique for making electrical contact to 2D nanostructures provides a platform for fundamental studies of nanomaterial properties. The merits of using dip-pen nanolithography include lack of electron-beam irradiation damage and targeted patterning of individual devices with imaging and writing conducted in the same instrument under ambient conditions.
View details for DOI 10.1021/nn101324x
View details for Web of Science ID 000284438000015
View details for PubMedID 20945878
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In Situ, Label-Free DNA Detection Using Organic Transistor Sensors
ADVANCED MATERIALS
2010; 22 (40): 4452-4456
View details for DOI 10.1002/adma.201000790
View details for Web of Science ID 000284000900003
View details for PubMedID 20859935
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Effects of Thermal Annealing Upon the Morphology of Polymer-Fullerene Blends
ADVANCED FUNCTIONAL MATERIALS
2010; 20 (20): 3519-3529
View details for DOI 10.1002/adfm.201000975
View details for Web of Science ID 000284000200013
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Effect of Surface Chemistry on Electronic Properties of Carbon Nanotube Network Thin Film Transistors
ACS NANO
2010; 4 (10): 6137-6145
Abstract
Thin films of single-walled carbon nanotubes (SWNTs) are a viable nanomaterial for next generation sensors, transistors, and electrodes for solar cells and displays. Despite their remarkable properties, challenges in synthesis and processing have hindered integration in current electronics. Challenges include the inability to precisely assemble and control the deposition of SWNT films on a variety of surfaces and the lack of understanding of the transport properties of these films. Here, we utilize an optimized "dry transfer" technique that facilitates the complete intact transfer of SWNT films between different surfaces. We then show the effect of surface chemistry on the electronic properties of SWNT films. By isolating the effect of the surface, we gain insight into the fundamental transport properties of SWNTs on surfaces with different chemical functionalities. Thin film transistor (TFT) characteristics, corroborated with ?-Raman spectroscopy, show that by using different surface chemical functionalities it is possible to alter the electronic properties of SWNT films. This opens up another route to tune the electronic properties of integrated SWNT films.
View details for DOI 10.1021/nn1012226
View details for Web of Science ID 000283453700085
View details for PubMedID 20857943
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Driving High-Performance n- and p-type Organic Transistors with Carbon Nanotube/Conjugated Polymer Composite Electrodes Patterned Directly from Solution
ADVANCED MATERIALS
2010; 22 (37): 4204-?
Abstract
We report patterned deposition of carbon nanotube/conjugated polymer composites from solution with high nanotube densities and excellent feature resolution. Such composites are suited for use as electrodes in high-performance transistors of pentacene and C(60), with bottom-contact mobilities of > 0.5 and > 1 cm(2) V(?1) s(?1), respectively. This represents a clear step towards development of inexpensive, high-performance all-organic circuits.
View details for DOI 10.1002/adma.201001435
View details for Web of Science ID 000283392000017
View details for PubMedID 20626010
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Synthesis and characterization of soluble indolo[3,2-b]carbazole derivatives for organic field-effect transistors
ORGANIC ELECTRONICS
2010; 11 (10): 1649-1659
View details for DOI 10.1016/j.orgel.2010.07.011
View details for Web of Science ID 000281624700008
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Organic Semiconductor Growth and Morphology Considerations for Organic Thin-Film Transistors
ADVANCED MATERIALS
2010; 22 (34): 3857-3875
Abstract
Analogous to conventional inorganic semiconductors, the performance of organic semiconductors is directly related to their molecular packing, crystallinity, growth mode, and purity. In order to achieve the best possible performance, it is critical to understand how organic semiconductors nucleate and grow. Clever use of surface and dielectric modification chemistry can allow one to control the growth and morphology, which greatly influence the electrical properties of the organic transistor. In this Review, the nucleation and growth of organic semiconductors on dielectric surfaces is addressed. The first part of the Review concentrates on small-molecule organic semiconductors. The role of deposition conditions on film formation is described. The modification of the dielectric interface using polymers or self-assembled mono-layers and their effect on organic-semiconductor growth and performance is also discussed. The goal of this Review is primarily to discuss the thin-film formation of organic semiconducting species. The patterning of single crystals is discussed, while their nucleation and growth has been described elsewhere (see the Review by Liu et. al).([¹]) The second part of the Review focuses on polymeric semiconductors. The dependence of physico-chemical properties, such as chain length (i.e., molecular weight) of the constituting macromolecule, and the influence of small molecular species on, e.g., melting temperature, as well as routes to induce order in such macromolecules, are described.
View details for DOI 10.1002/adma.200903193
View details for Web of Science ID 000282793600007
View details for PubMedID 20715062
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Effects of Dispersion Conditions of Single-Walled Carbon Nanotubes on the Electrical Characteristics of Thin Film Network Transistors
ACS APPLIED MATERIALS & INTERFACES
2010; 2 (9): 2672-2678
Abstract
To facilitate solution deposition of single-walled carbon nanotubes (SWNTs) for integration into electronic devices they need to be purified and dispersed into solutions. The vigorous sonication process for preparing these dispersions leads to large variations in the length and defect density of SWNTs, affecting the resulting electronic properties. Understanding the effects of solution processing steps can have important implications in the design of SWNT films for electronic applications. Here, we alter the SWNTs by varying the sonication time, followed by deposition of sub-monolayer SWNT network films onto functionalized substrates. The corresponding electrical performance characteristics of the resulting field effect transistors (FETs) are correlated with SWNT network sorting and morphology. As sonication exposure increases, the SWNTs shorten, which not only affects electrical current by increasing the number of junctions but also presumably leads to more defects. The off current of the resulting transistors initially increased with sonication exposure, presumably due to less efficient sorting of semiconducting SWNTs as the defect density increases. After extended sonication, the on and off current decreased because of increased bundling and fewer percolation pathways. The final transistor properties are influenced by the nanotube solution concentration, density, alignment, and the selectivity of surface sorting of the SWNT networks. These results show that in addition to chirality, careful consideration of SWNT dispersion conditions that affect SWNT length, bundle diameter, and defect density is critical for optimal SWNT-FET performance and potentially other SWNT-based electronic devices.
View details for DOI 10.1021/am1005223
View details for Web of Science ID 000282017700029
View details for PubMedID 20738099
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Tuning the Optoelectronic Properties of Vinylene-Linked Donor-Acceptor Copolymers for Organic Photovoltaics
MACROMOLECULES
2010; 43 (16): 6685-6698
View details for DOI 10.1021/ma101088f
View details for Web of Science ID 000280855000023
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Anthradithiophene-Containing Copolymers for Thin-Film Transistors and Photovoltaic Cells
MACROMOLECULES
2010; 43 (15): 6361-6367
View details for DOI 10.1021/ma1001639
View details for Web of Science ID 000280743300017
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Contact engineering for organic semiconductor devices via Fermi level depinning at the metal-organic interface
PHYSICAL REVIEW B
2010; 82 (3)
View details for DOI 10.1103/PhysRevB.82.035311
View details for Web of Science ID 000280123900004
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High-Performance Air-Stable n-Type Organic Transistors Based on Core-Chlorinated Naphthalene Tetracarboxylic Diimides
ADVANCED FUNCTIONAL MATERIALS
2010; 20 (13): 2148-2156
View details for DOI 10.1002/adfm.201000425
View details for Web of Science ID 000280276900016
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Use of a 1H-Benzoimidazole Derivative as an n-Type Dopant and To Enable Air-Stable Solution-Processed n-Channel Organic Thin-Film Transistors
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
2010; 132 (26): 8852-?
Abstract
We present here the development of a new solution-processable n-type dopant, N-DMBI. Our experimental results demonstrated that a well-known n-channel semiconductor, [6,6]-phenyl C(61) butyric acid methyl ester (PCBM), can be effectively doped with N-DMBI by solution processing; the film conductivity is significantly increased by n-type doping. We utilized this n-type doping for the first time to improve the air-stability of n-channel organic thin-film transistors, in which the doping can compensate for the electron traps. Our successful demonstration of n-type doping using N-DMBI opens up new opportunities for the development of air-stable n-channel semiconductors. It is also potentially useful for application on solution-processed organic light-emitting diodes and organic photovoltaics.
View details for DOI 10.1021/ja103173m
View details for Web of Science ID 000279561200019
View details for PubMedID 20552967
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X-ray Microscopy Imaging of the Grain Orientation in a Pentacene Field-Effect Transistor
CHEMISTRY OF MATERIALS
2010; 22 (12): 3693-3697
View details for DOI 10.1021/cm100487j
View details for Web of Science ID 000278684000016
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Induced Sensitivity and Selectivity in Thin-Film Transistor Sensors via Calixarene Layers
ADVANCED MATERIALS
2010; 22 (21): 2349-2353
View details for DOI 10.1002/adma.200903305
View details for Web of Science ID 000279100200010
View details for PubMedID 20376848
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Nanotubes on Display: How Carbon Nanotubes Can Be Integrated into Electronic Displays
ACS NANO
2010; 4 (6): 2975-2978
Abstract
Random networks of single-walled carbon nanotubes show promise for use in the field of flexible electronics. Nanotube networks have been difficult to utilize because of the mixture of electronic types synthesized when grown. A variety of separation techniques have been developed, but few can readily be scaled up. Despite this issue, when metallic percolation pathways can be separated out or etched away, these networks serve as high-quality thin-film transistors with impressive device characteristics. A new article in this issue illustrates this point and the promise of these materials. With more work, these devices can be implemented in transparent displays in the next generation of hand-held electronics.
View details for DOI 10.1021/nn101092d
View details for Web of Science ID 000278888600003
View details for PubMedID 20565139
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Band structure measurement of organic single crystal with angle-resolved photoemission
APPLIED PHYSICS LETTERS
2010; 96 (22)
View details for DOI 10.1063/1.3446849
View details for Web of Science ID 000278404800029
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Parallel Fabrication of Electrode Arrays on Single-Walled Carbon Nanotubes using Dip-Pen-Nanolithography-Patterned Etch Masks
LANGMUIR
2010; 26 (9): 6853-6859
Abstract
This article presents a novel application of using dip-pen nanolithography (DPN) to fabricate Au electrodes concurrently in a high-throughput fashion through an etch resist. We have fabricated 26 pairs of electrodes, where cleanly etched electrode architectures, along with a high degree of feature-size controllability and tip-to-tip uniformity, were observed. Moreover, electrode gaps in the sub-100-nm regime have been successfully fabricated. Conductivity measurements of multiple electrodes in the array were all comparable to that of bulk Au, confirming the reliability and the low-resistance property of the electrodes. Finally, as a demonstration of electrode functionality, SWNT devices were fabricated and the electrical properties of an SWNT device were measured. Hence, our experimental results validate DPN as an effective tool in generating high-quality electrodes in a parallel manner with mild, simple processing steps at a relatively low cost.
View details for DOI 10.1021/la904170w
View details for Web of Science ID 000276969700114
View details for PubMedID 20163131
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Biomaterials-based organic electronic devices
POLYMER INTERNATIONAL
2010; 59 (5): 563-567
Abstract
Organic electronic devices have demonstrated tremendous versatility in a wide range of applications including consumer electronics, photovoltaics, and biotechnology. The traditional interface of organic electronics with biology, biotechnology, and medicine occurs in the general field of sensing biological phenomena. For example, the fabrication of hybrid electronic structures using both organic semiconductors and bioactive molecules has led to enhancements in sensitivity and specificity within biosensing platforms, which in turn has a potentially wide range of clinical applications. However, the interface of biomolecules and organic semiconductors has also recently explored the potential use of natural and synthetic biomaterials as structural components of electronic devices. The fabrication of electronically active systems using biomaterials-based components has the potential to realize a large set of unique devices including environmentally biodegradable systems and bioresorbable temporary medical devices. This article reviews recent advances in the implementation of biomaterials as structural components in organic electronic devices with a focus on potential applications in biotechnology and medicine.
View details for DOI 10.1002/pi.2827
View details for Web of Science ID 000277767500001
View details for PubMedID 20607127
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Low-voltage and short-channel pentacene field-effect transistors with top-contact geometry using parylene-C shadow masks
APPLIED PHYSICS LETTERS
2010; 96 (13)
View details for DOI 10.1063/1.3336009
View details for Web of Science ID 000276275300063
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Influence of Electrostatic Interactions on Spin-Assembled Single-Walled Carbon Nanotube Networks on Amine-Functionalized Surfaces
ACS NANO
2010; 4 (2): 1167-1177
Abstract
Preferential interactions between self-assembled monolayers (SAMs) terminated with amine functional groups and single-walled carbon nanotubes (SWNTs) were exploited to produce nanotube networks (SWNTnts) via spin coating. We provide insight into the mechanisms of this system while simultaneously demonstrating a facile approach toward controllable arrays of SWNTnts. The chirality, density, and alignment of the SWNTnt was heavily influenced by adsorption onto amine-functionalized surfaces that were exposed to varying pH solutions, as evidenced by atomic force microscopy (AFM) and Raman spectroscopy. This pH treatment altered the charge density on the surface, allowing for the examination of the contribution from electrostatic interaction to SWNT adsorption and SWNTnt characteristics. Secondary and tertiary amines with methyl substitutions were utilized to confirm that adsorption and chirality specific adsorption is largely due to the nitrogen lone pair, not the neighboring hydrogen atoms. Thus, the nature of adsorption is predominantly electrostatic and not due to van der Waals forces or localized polarization on the SWNTs. Moreover, the overall density of SWNTnts is different for the various amines, indicating that the accessibility to the lone pair electrons on the nitrogen plays a crucial role in SWNT adsorption. With greater understanding of the amine-SWNT interaction, these findings can be utilized to control SWNTnt formation for the precise integration into electronic devices.
View details for DOI 10.1021/nn901388v
View details for Web of Science ID 000274635800073
View details for PubMedID 20112967
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Energetics and stability of pentacene thin films on amorphous and crystalline octadecylsilane modified surfaces
JOURNAL OF MATERIALS CHEMISTRY
2010; 20 (13): 2664-2671
View details for DOI 10.1039/b921767c
View details for Web of Science ID 000275662400018
- Organic Thin-Film Transistors Fabricated on Resorbable Biomaterial Substrates Adv. Mater. 2010; 22: 651-655
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A Crystal-Engineered Hydrogen-Bonded Octachloroperylene Diimide with a Twisted Core: An n-Channel Organic Semiconductor
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
2010; 49 (4): 740-743
View details for DOI 10.1002/anie.200904215
View details for Web of Science ID 000274424000012
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Organic Light-Emitting Diodes on Solution-Processed Graphene Transparent Electrodes
ACS NANO
2010; 4 (1): 43-48
Abstract
Theoretical estimates indicate that graphene thin films can be used as transparent electrodes for thin-film devices such as solar cells and organic light-emitting diodes, with an unmatched combination of sheet resistance and transparency. We demonstrate organic light-emitting diodes with solution-processed graphene thin film transparent conductive anodes. The graphene electrodes were deposited on quartz substrates by spin-coating of an aqueous dispersion of functionalized graphene, followed by a vacuum anneal step to reduce the sheet resistance. Small molecular weight organic materials and a metal cathode were directly deposited on the graphene anodes, resulting in devices with a performance comparable to control devices on indium-tin-oxide transparent anodes. The outcoupling efficiency of devices on graphene and indium-tin-oxide is nearly identical, in agreement with model predictions.
View details for DOI 10.1021/nn900728d
View details for Web of Science ID 000273863400007
View details for PubMedID 19902961
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Thiophene-rich fused-aromatic thienopyrazine acceptor for donor-acceptor low band-gap polymers for OTFT and polymer solar cell applications
JOURNAL OF MATERIALS CHEMISTRY
2010; 20 (28): 5823-5834
View details for DOI 10.1039/c0jm00903b
View details for Web of Science ID 000279565900008
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Fused aromatic thienopyrazines: structure, properties and function
JOURNAL OF MATERIALS CHEMISTRY
2010; 20 (47): 10568-10576
View details for DOI 10.1039/c0jm01840f
View details for Web of Science ID 000284542600001
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Solution Assembly of Organized Carbon Nanotube Networks for Thin-Film Transistors
ACS NANO
2009; 3 (12): 4089-4097
Abstract
Ultrathin, transparent electronic materials consisting of solution-assembled nanomaterials that are directly integrated as thin-film transistors or conductive sheets may enable many new device structures. Applications ranging from disposable autonomous sensors to flexible, large-area displays and solar cells can dramatically expand the electronics market. With a practical, reliable method for controlling their electronic properties through solution assembly, submonolayer films of aligned single-walled carbon nanotubes (SWNTs) may provide a promising alternative for large-area, flexible electronics. Here, we report SWNT network TFTs (SWNTntTFTs) deposited from solution with controllable topology, on/off ratios averaging greater than 10(5), and an apparent mobility averaging 2 cm(2)/V.s, without any pre- or postprocessing steps. We employ a spin-assembly technique that results in chirality enrichment along with tunable alignment and density of the SWNTs by balancing the hydrodynamic force (spin rate) with the surface interaction force controlled by a chemically functionalized interface. This directed nanoscale assembly results in enriched semiconducting nanotubes yielding excellent TFT characteristics, which is corroborated with mu-Raman spectroscopy. Importantly, insight into the electronic properties of these SWNT networks as a function of topology is obtained.
View details for DOI 10.1021/nn900827v
View details for Web of Science ID 000272846000043
View details for PubMedID 19924882
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Interplay between Energetic and Kinetic Factors on the Ambient Stability of n-Channel Organic Transistors Based on Perylene Diimide Derivatives
CHEMISTRY OF MATERIALS
2009; 21 (22): 5508-5518
View details for DOI 10.1021/cm902531d
View details for Web of Science ID 000271756400019
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Micrometer-Sized DNA-Single-Fluorophore-DNA Supramolecule: Synthesis and Single-Molecule Characterization
SMALL
2009; 5 (21): 2418-2423
Abstract
The synthesis of single-fluorophore-bis(micrometer-sized DNA) triblock supramolecules and the optical and structural characterization of the construct at the single-molecule level is reported. A fluorophore-bis(oligodeoxynucleotide) triblock is synthesized via the amide-coupling reaction. Subsequent protocols of DNA hybridization/ligation are developed to form the supramolecular triblock structure with lambda-DNA fragments on the micrometer length scale. The successful synthesis of the micrometer-sized DNA-single-fluorophore-DNA supramolecule is confirmed by agarose gel electrophoresis with fluorescence imaging under UV excitation. Single triblock structures are directly imaged by combined scanning force microscopy and single-molecule fluorescence microscopy, and provide unambiguous confirmation of the existence of the single fluorophore inserted in the middle of the long DNA. This type of triblock structure is a step closer to providing a scaffold for single-molecule electronic devices after metallization of the DNAs.
View details for DOI 10.1002/smll.200900494
View details for Web of Science ID 000271791100011
View details for PubMedID 19517486
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Dip-Pen Nanolithography of Electrical Contacts to Single-Walled Carbon Nanotubes
ACS NANO
2009; 3 (11): 3543-3551
Abstract
This paper discusses a method for the direct patterning of Au electrodes at nanoscale resolution using dip-pen nanolithography, with proof-of-concept demonstrated by creating single-walled carbon nanotube devices. This technique enables insight into three key concepts at the nanoscale: using dip-pen nanolithography as an alternative to electron-beam lithography for writing contacts to carbon nanotubes, understanding the integrity of contacts and devices patterned with this technique, and on a more fundamental level, providing a facile method to compare and understand electrical and Raman spectroscopy data from the same isolated carbon nanotube. Electrical contacts to individual and small bundle single-walled carbon nanotubes were masked by an alkylthiol that was deposited via dip-pen nanolithography on a thin film of Au evaporated onto spin-cast, nonpercolating, and highly isolated single-walled carbon nanotubes. A wet Au etching step was used to form the individual devices. The electrical characteristics for three different single-walled carbon nanotube devices are reported: semimetallic, semiconducting, and metallic. Raman analysis on representative devices corroborates the results from AFM imaging and electrical testing. This work demonstrates a technique for making electrical contact to nanostructures of interest and provides a platform for directly corroborating electrical and optical measurements. The merits of using dip-pen nanolithography include flexible device configuration (such as varying the channel length and the number, size, and orientation of contacts), targeted patterning of individual devices with imaging and writing conducted in the same instrument under ambient conditions, and negligible damage to single-walled carbon nanotubes during the fabrication process.
View details for DOI 10.1021/nn900984w
View details for Web of Science ID 000271951200029
View details for PubMedID 19852486
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Sorted and Aligned Single-Walled Carbon Nanotube Networks for Transistor-Based Aqueous Chemical Sensors
ACS NANO
2009; 3 (10): 3287-3293
Abstract
Detecting trace amounts of analytes in aqueous systems is important for health diagnostics, environmental monitoring, and national security applications. Single-walled carbon nanotubes (SWNTs) are ideal components for both the sensor material and active signal transduction layer because of their excellent electronic properties and high aspect ratio consisting of entirely surface atoms. Submonolayer arrays, or networks of SWNTs (SWNTnts) are advantageous, and we show that topology characteristics of the SWNT network, such as alignment, degree of bundling, and chirality enrichment strongly affect the sensor performance. To enable this, thin-film transistor (TFT) sensors with SWNTnts were deposited using a one-step, low-cost, solution- based method on a polymer dielectric, allowing us to achieve stable low-voltage operation under aqueous conditions. These SWNT-TFTs were used to detect trace concentrations, down to 2 ppb, of dimethyl methylphosphonate (DMMP) and trinitrotoluene (TNT) in aqueous solutions. Along with reliable cycling underwater, the TFT sensors fabricated with aligned, sorted nanotube networks (enriched with semiconductor SWNTs) showed a higher sensitivity to analytes than those fabricated with random, unsorted networks with predominantly metallic charge transport.
View details for DOI 10.1021/nn900808b
View details for Web of Science ID 000271106100055
View details for PubMedID 19856982
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Tuning Crystalline Solid-State Order and Charge Transport via Building-Block Modification of Oligothiophenes
ADVANCED MATERIALS
2009; 21 (36): 3678-?
View details for DOI 10.1002/adma.200900836
View details for Web of Science ID 000270441700010
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Fabrication of low-cost electronic biosensors
MATERIALS TODAY
2009; 12 (9): 12-20
View details for Web of Science ID 000270568800011
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Low-voltage transistor sensors based on organic semiconductors and carbon nanotube networks
AMER CHEMICAL SOC. 2009
View details for Web of Science ID 000207861905501
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Synthesis of Acenaphthyl and Phenanthrene Based Fused-Aromatic Thienopyrazine Co-Polymers for Photovoltaic and Thin Film Transistor Applications
CHEMISTRY OF MATERIALS
2009; 21 (15): 3618-3628
View details for DOI 10.1021/cm900788e
View details for Web of Science ID 000268523300021
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Crystalline Ultrasmooth Self-Assembled Monolayers of Alkylsilanes for Organic Field-Effect Transistors
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
2009; 131 (26): 9396-9404
Abstract
Crystalline self-assembled monolayers (SAMs) of organosilane compounds such as octadecyltrimethoxysilane (OTMS) and octadecyltrichlorosilane (OTCS) were deposited by a simple, spin-casting technique onto Si/SiO(2) substrates. Fabrication of the OTMS SAMs and characterization using ellipsometry, contact angle, atomic force microscopy (AFM), grazing angle attenuated total reflectance Fourier transform infrared (GATR-FTIR) spectroscopy and grazing incidence X-ray diffraction (GIXD) are described. The characterization confirms that these monolayers exhibit a well-packed crystalline phase and a remarkably high degree of smoothness. Semiconductors deposited by vapor deposition onto the crystalline OTS SAM grow in a favorable two-dimensional layered growth manner which is generally preferred morphologically for high charge carrier transport. On the OTMS SAM treated dielectric, pentacene OFETs showed hole mobilities as high as 3.0 cm(2)/V x s, while electron mobilities as high as 5.3 cm(2)/V x s were demonstrated for C(60).
View details for DOI 10.1021/ja9029957
View details for Web of Science ID 000267633300056
View details for PubMedID 19518097
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Self-Sorted Nanotube Networks on Polymer Dielectrics for Low-Voltage Thin-Film Transistors
NANO LETTERS
2009; 9 (7): 2526-2531
Abstract
Recent exploitations of the superior mechanical and electronic properties of carbon nanotubes (CNTs) have led to exciting opportunities in low-cost, high performance, carbon-based electronics. In this report, low-voltage thin-film transistors with aligned, semiconducting CNT networks are fabricated on a chemically modified polymer gate dielectric using both rigid and flexible substrates. The multifunctional polymer serves as a thin, flexible gate dielectric film, affords low operating voltages, and provides a platform for chemical functionalization. The introduction of amine functionality to the dielectric surface leads to the adsorption of a network enriched with semiconducting CNTs with tunable density from spin coating a bulk solution of unsorted CNTs. The composition of the deposited CNT networks is verified with Raman spectroscopy and electrical characterization. For transistors at operating biases below 1 V, we observe an effective device mobility as high as 13.4 cm(2)/Vs, a subthreshold swing as low as 130 mV/dec, and typical on-off ratios of greater than 1,000. This demonstration of high performance CNT thin-film transistors operating at voltages below 1 V and deposited using solution methods on polymeric and flexible substrates is an important step toward the realization of low-cost flexible electronics.
View details for DOI 10.1021/nl900287p
View details for Web of Science ID 000268138600003
View details for PubMedID 19499894
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The Role of OTS Density on Pentacene and C-60 Nucleation, Thin Film Growth, and Transistor Performance
ADVANCED FUNCTIONAL MATERIALS
2009; 19 (12): 1962-1970
View details for DOI 10.1002/adfm.200801727
View details for Web of Science ID 000267509900015
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Precise Structure of Pentacene Monolayers on Amorphous Silicon Oxide and Relation to Charge Transport
ADVANCED MATERIALS
2009; 21 (22): 2294-?
View details for DOI 10.1002/adma.200803328
View details for Web of Science ID 000267509500006
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Cross-Linked Polymer Gate Dielectric Films for Low-Voltage Organic Transistors
CHEMISTRY OF MATERIALS
2009; 21 (11): 2292-2299
View details for DOI 10.1021/cm900637p
View details for Web of Science ID 000266708700017
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Polymer-Assisted Direct Deposition of Uniform Carbon Nanotube Bundle Networks for High Performance Transparent Electrodes
ACS NANO
2009; 3 (6): 1423-1430
Abstract
Flexible transparent electrodes are crucial for touch screen, flat panel display, and solar cell technologies. While carbon nanotube network electrodes show promise, characteristically poor dispersion properties have limited their practicality. We report that addition of small amounts of conjugated polymer to nanotube dispersions enables straightforward fabrication of uniform network electrodes by spin-coating and simultaneous tuning of parameters such as bundle size and density. After treatment in thionyl chloride, electrodes have sheet resistances competitive with other reported carbon nanotube based transparent electrodes to date.
View details for DOI 10.1021/nn9002456
View details for Web of Science ID 000267533600016
View details for PubMedID 19422197
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Isotropic transport in an oligothiophene derivative for single-crystal field-effect transistor applications
APPLIED PHYSICS LETTERS
2009; 94 (20)
View details for DOI 10.1063/1.3129162
View details for Web of Science ID 000266342800026
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Solution-processed flexible organic transistors showing very-low subthreshold slope with a bilayer polymeric dielectric on plastic
APPLIED PHYSICS LETTERS
2009; 94 (20)
View details for DOI 10.1063/1.3133902
View details for Web of Science ID 000266342800065
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Liquid-Crystalline Semiconducting Copolymers with Intramolecular Donor-Acceptor Building Blocks for High-Stability Polymer Transistors
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
2009; 131 (17): 6124-6132
Abstract
The ability to control the molecular organization of electronically active liquid-crystalline polymer semiconductors on surfaces provides opportunities to develop easy-to-process yet highly ordered supramolecular systems and, in particular, to optimize their electrical and environmental reliability in applications in the field of large-area printed electronics and photovoltaics. Understanding the relationship between liquid-crystalline nanostructure and electrical stability on appropriate molecular surfaces is the key to enhancing the performance of organic field-effect transistors (OFETs) to a degree comparable to that of amorphous silicon (a-Si). Here, we report a novel donor-acceptor type liquid-crystalline semiconducting copolymer, poly(didodecylquaterthiophene-alt-didodecylbithiazole), which contains both electron-donating quaterthiophene and electron-accepting 5,5'-bithiazole units. This copolymer exhibits excellent electrical characteristics such as field-effect mobilities as high as 0.33 cm(2)/V.s and good bias-stress stability comparable to that of amorphous silicon (a-Si). Liquid-crystalline thin films with structural anisotropy form spontaneously through self-organization of individual polymer chains as a result of intermolecular interactions in the liquid-crystalline mesophase. These thin films adopt preferential well-ordered intermolecular pi-pi stacking parallel to the substrate surface. This bottom-up assembly of the liquid-crystalline semiconducting copolymer enables facile fabrication of highly ordered channel layers with remarkable electrical stability.
View details for DOI 10.1021/ja8095569
View details for Web of Science ID 000265755800036
View details for PubMedID 19354240
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High-Performance Air-Stable n-Channel Organic Thin Film Transistors Based on Halogenated Perylene Bisimide Semiconductors
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
2009; 131 (17): 6215-6228
Abstract
The syntheses and comprehensive characterization of 14 organic semiconductors based on perylene bisimide (PBI) dyes that are equipped with up to four halogen substituents in the bay area of the perylene core and five different highly fluorinated imide substituents are described. The influence of the substituents on the LUMO level and the solid state packing of PBIs was examined by cyclic voltammetry and single crystal structure analyses of seven PBI derivatives, respectively. Top-contact/bottom-gate organic thin film transistor (OTFT) devices were constructed by vacuum deposition of these PBIs on SiO(2) gate dielectrics that had been pretreated with n-octadecyl triethoxysilane in vapor phase (OTS-V) or solution phase (OTS-S). The electrical characterization of all devices was accomplished in a nitrogen atmosphere as well as in air, and the structural features of thin films were explored by grazing incidence X-ray diffraction (GIXD) and atomic force microscopy (AFM). Several of those PBIs that bear only hydrogen or up to two fluorine substitutents at the concomitantly flat PBI core afforded excellent n-channel transistors, in particular, on OTS-S substrate and even in air (mu > 0.5 cm(2) V(-1) s(-1); I(on)/I(off) > 10(6)). The best OTFTs were obtained for 2,2,3,3,4,4,4-heptafluorobutyl-substituted PBI 1a ("PTCDI-C4F7") on OTS-S with n-channel field effect mobilities consistently >1 cm(2) V(-1) s(-1) and on-to-off current rations of 10(6) in a nitrogen atmosphere and in air. For distorted core-tetrahalogenated (fluorine, chlorine, or bromine) PBIs, less advantageous solid state packing properties were found and high performance OTFTs were obtained from only one tetrachlorinated derivative (2d on OTS-S). The excellent on-to-off current modulation combined with high mobility in air makes these PBIs suitable for a wide range of practical applications.
View details for DOI 10.1021/ja901077a
View details for Web of Science ID 000265755800047
View details for PubMedID 19354212
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Lyotropic Liquid-Crystalline Solutions of High-Concentration Dispersions of Single-Walled Carbon Nanotubes with Conjugated Polymers
SMALL
2009; 5 (9): 1019-1024
View details for DOI 10.1002/smll.200800640
View details for Web of Science ID 000266184500004
View details for PubMedID 19291730
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Flexible, plastic transistor-based chemical sensors
ORGANIC ELECTRONICS
2009; 10 (3): 377-383
View details for DOI 10.1016/j.orgel.2008.12.001
View details for Web of Science ID 000266000700001
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Correlating Carrier Type with Frontier Molecular Orbital Energy Levels in Organic Thin Film Transistors of Functionalized Acene Derivatives
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
2009; 131 (14): 5264-5273
Abstract
We investigate the relationship between the charge carrier type in organic thin film transistors (OTFTs) and molecular energy levels. We examine a series of functionalized acenes that collectively have their HOMOs range from -4.9 eV to -5.6 eV and LUMOs range from -2.8 eV to -3.7 eV, as measured by cyclic voltammetry. Placed together, these 20 molecules allow us to chart the transition from OTFTs that display only hole transport, to ambipolar, to solely electron transport. Specifically, we note that for octadecyltrimethoxysilane (OTS) treated substrates, with top contact gold electrodes, electron injection and transport occurs when the LUMO < -3.15 eV, while hole injection and transport ceases when the HOMO < -5.6 eV. Ambipolar transport prevails when molecules have HOMO/ LUMO levels within the aforementioned range. This is seen across channel lengths ranging from 50-150 microm and using only gold as electrodes. This empirical plot is the first time such a detailed study has been made on the onset of charge injection and transport for a class of organic semiconductors. It provides guidelines for future molecular design.
View details for DOI 10.1021/ja809659b
View details for Web of Science ID 000265039000053
View details for PubMedID 19317404
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Solution-processed, high-performance n-channel organic microwire transistors
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
2009; 106 (15): 6065-6070
Abstract
The development of solution-processable, high-performance n-channel organic semiconductors is crucial to realizing low-cost, all-organic complementary circuits. Single-crystalline organic semiconductor nano/microwires (NWs/MWs) have great potential as active materials in solution-formed high-performance transistors. However, the technology to integrate these elements into functional networks with controlled alignment and density lags far behind their inorganic counterparts. Here, we report a solution-processing approach to achieve high-performance air-stable n-channel organic transistors (the field-effect mobility (mu) up to 0.24 cm(2)/Vs for MW networks) comprising high mobility, solution-synthesized single-crystalline organic semiconducting MWs (mu as high as 1.4 cm(2)/Vs for individual MWs) and a filtration-and-transfer (FAT) alignment method. The FAT method enables facile control over both alignment and density of MWs. Our approach presents a route toward solution-processed, high-performance organic transistors and could be used for directed assembly of various functional organic and inorganic NWs/MWs.
View details for DOI 10.1073/pnas.0811923106
View details for Web of Science ID 000265174600009
View details for PubMedID 19299506
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Direct Patterning of Organic-Thin-Film-Transistor Arrays via a "Dry-Taping" Approach
ADVANCED MATERIALS
2009; 21 (12): 1266-?
View details for DOI 10.1002/adma.200802201
View details for Web of Science ID 000264926800009
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Controlled Deposition of Crystalline Organic Semiconductors for Field-Effect-Transistor Applications
ADVANCED MATERIALS
2009; 21 (12): 1217-1232
View details for DOI 10.1002/adma.200802202
View details for Web of Science ID 000264926800001
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Chlorination: A General Route toward Electron Transport in Organic Semiconductors
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
2009; 131 (10): 3733-3740
Abstract
We show that adding chlorine atoms to conjugated cores is a general, effective route toward the design of n-type air-stable organic semiconductors. We find this to be true for acenes, phthalocyanines, and perylene tetracarboxylic diimide (PDI)-based molecules. This general finding opens new avenues in the design and synthesis of organic semiconductors. We compared a series of fluoro- and chloro-functionalized acenes, phthalocyanines, and PDI-based molecules. The acenes synthesized showed high and balanced ambipolar transport in the top-contact organic field effect transistor (OFET) geometry. The electron-withdrawing halogen groups lowered the LUMO and the charge injection barrier for electrons, such that electron and hole transport occurred simultaneously. If the chlorine added does not distort the planarity of the conjugated core, we found that the chloro-functionalized molecules tend to have a slightly smaller HOMO-LUMO gap and a lower LUMO level than the fluoro-containing molecules, both from calculations and cyclic voltammetry measurements in solution. This is most likely due to the fact that Cl contains empty 3d orbitals that can accept pi-electrons from the conjugated core, while F does not have energetically accessible empty orbitals for such delocalization.
View details for DOI 10.1021/ja809045s
View details for Web of Science ID 000264792600065
View details for PubMedID 19243143
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Detailed Characterization of Contact Resistance, Gate-Bias-Dependent Field-Effect Mobility, and Short-Channel Effects with Microscale Elastomeric Single-Crystal Field-Effect Transistors
ADVANCED FUNCTIONAL MATERIALS
2009; 19 (5): 763-771
View details for DOI 10.1002/adfm.200801019
View details for Web of Science ID 000264502000012
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Experimental Study and Statistical Analysis of Solution-Shearing Processed Organic Transistors Based on an Asymmetric Small-Molecule Semiconductor
IEEE TRANSACTIONS ON ELECTRON DEVICES
2009; 56 (2): 176-185
View details for DOI 10.1109/TED.2008.2010580
View details for Web of Science ID 000262816800004
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Pentaceno[2,3-b]thiophene, a Hexacene Analogue for Organic Thin Film Transistors
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
2009; 131 (3): 882-?
Abstract
Hexacene and larger fused rings remain elusive targets for chemists. Here, we report a hexacene-like molecule containing six linearly fused rings, specifically a pentacene molecule fused with a terminal thiophene ring, pentaceno[2,3-b]thiophene. It can be purified and isolated as a purple-black powder at ambient conditions. This molecule has a low HOMO-LUMO gap of 1.75 eV in o-DCB and an optical band gap of 1.58 eV in thin film. Top contact organic thin film transistors (OTFTs) were made, and atomic force microscopy (AFM) reveals a dendritic thin film growth characteristic of pentacene. An OTFT mobility of 0.574 cm(2)/V s was measured for pentaceno[2,3-b]thiophene under nitrogen.
View details for DOI 10.1021/ja808142c
View details for Web of Science ID 000264791600005
View details for PubMedID 19125619
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Overestimation of the field-effect mobility via transconductance measurements and the origin of the output/transfer characteristic discrepancy in organic field-effect transistors
JOURNAL OF APPLIED PHYSICS
2009; 105 (2)
View details for DOI 10.1063/1.3029587
View details for Web of Science ID 000262970900112
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Patterning of alpha-Sexithiophene Single Crystals with Precisely Controlled Sizes and Shapes
CHEMISTRY OF MATERIALS
2009; 21 (1): 15-17
View details for DOI 10.1021/cm802806t
View details for Web of Science ID 000262266500006
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Transistor and solar cell performance of donor-acceptor low bandgap copolymers bearing an acenaphtho[1,2-b]thieno[3,4-e]pyrazine (ACTP) motif
JOURNAL OF MATERIALS CHEMISTRY
2009; 19 (5): 591-593
View details for DOI 10.1039/b819210c
View details for Web of Science ID 000262547000003
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Molecular design for improved photovoltaic efficiency: band gap and absorption coefficient engineering
JOURNAL OF MATERIALS CHEMISTRY
2009; 19 (39): 7195-7197
View details for DOI 10.1039/b915222a
View details for Web of Science ID 000270382400004
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New indolo[3,2-b]carbazole derivatives for field-effect transistor applications
JOURNAL OF MATERIALS CHEMISTRY
2009; 19 (19): 2921-2928
View details for DOI 10.1039/b900271e
View details for Web of Science ID 000265919300008
- Solution-processed, high-performance n-channel organic nanowire transistors Proc. Nat. Acad. Sci. USA 2009; 106: 6065-6070
- Chlorination: a general route towards electron transport in organic semiconductors J. Am. Chem. Soc. 2009; 131: 3733-3740
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Solution Assembly of Transistor Arrays Based on Sorted Nanotube Networks for Large-scale Flexible Electronic Applications
2009 SID INTERNATIONAL SYMPOSIUM DIGEST OF TECHNICAL PAPERS, VOL XL, BOOKS I - III
2009: 877-879
View details for Web of Science ID 000272997600227
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Material and device considerations for organic thin-film transistor sensors
JOURNAL OF MATERIALS CHEMISTRY
2009; 19 (21): 3351-3363
View details for DOI 10.1039/b816386c
View details for Web of Science ID 000266269300003
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Influence of Molecular Structure And Film Properties on the Water-Stability and Sensor Characteristics of Organic Transistors
CHEMISTRY OF MATERIALS
2008; 20 (23): 7332-7338
View details for DOI 10.1021/cm802530x
View details for Web of Science ID 000261335200021
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Oligothiophene based organic semiconductors with cross-linkable benzophenone moieties
SYNTHETIC METALS
2008; 158 (21-24): 958-963
View details for DOI 10.1016/j.synthmet.2008.06.019
View details for Web of Science ID 000262573900030
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Highly Efficient Patterning of Organic Single-Crystal Transistors from the Solution Phase
ADVANCED MATERIALS
2008; 20 (21): 4044-?
View details for DOI 10.1002/adma.200703244
View details for Web of Science ID 000261040000007
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Synthesis and characterization of pentacene- and anthradithiophene-fluorene conjugated copolymers synthesized by Suzuki reactions
MACROMOLECULES
2008; 41 (19): 6977-6980
View details for DOI 10.1021/ma800931a
View details for Web of Science ID 000259859800020
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FLEXIBLE ELECTRONICS Stretching our imagination
NATURE NANOTECHNOLOGY
2008; 3 (10): 585-586
View details for DOI 10.1038/nnano.2008.296
View details for Web of Science ID 000260314300006
View details for PubMedID 18838993
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Synthesis of DNA-organic molecule-DNA triblock oligomers using the amide coupling reaction and their enzymatic amplification
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
2008; 130 (39): 12854-?
Abstract
Precise electrical contact between single-molecule and electrodes is a first step to study single-molecule electronics and its application such as (bio)sensors and nanodevices. To realize a reliable electrical contact, we can use DNA as a template in the field of nanoelectronics because of its micrometer-scaled length with the thickness of nanometer-scale. In this paper, we studied the reactivity of the amide-coupling reaction to tether oligodeoxynucleotides (ODNs) to organic molecules and the elongation of the ODNs by the polymerase chain reaction (PCR) to synthesize 1.5 kbp dsDNA-organic molecule-1.5 kbp dsDNA (DOD) triblock architecture. The successful amide-coupling reactions were confirmed by electrospray ionization mass spectrometry (ESI-MS), and the triblock architectures were characterized by 1% agarose gel electrophoresis and atomic force microscope (AFM). Our result shows that this strategy is simple and makes it easy to construct DNA-organic molecule-DNA triblock architectures and potentially provides a platform to prepare and investigate single molecule electronics.
View details for DOI 10.1021/ja8044458
View details for Web of Science ID 000259553700009
View details for PubMedID 18763775
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Direct Patterning of Gold Nanoparticles Using Dip-Pen Nanolithography
ACS NANO
2008; 2 (10): 2135-2142
Abstract
Various methods for the patterned assembly of metal nanoparticles have been developed in order to harness their unique electrical and optical properties for device applications. This paper discusses a method for direct writing of Au nanoparticles at nanoscale resolution using dip-pen nanolithography. First, a procedure was developed for increasing the loading of Au nanoparticles onto AFM tips to prolong patterning life. AFM tips were subsequently imaged by scanning electron microscopy to determine ink coverage and to gain insight into the deposition process. Next, surface interactions, relative humidity, and writing speed were controlled to determine an optimal range of conditions for deposition. Various ink-substrate combinations were studied to elucidate the dependence of deposition on interactions between Au nanoparticles and the substrate surface; inks consisted of positively and negatively charged particles, and substrates were SiO(2) surfaces modified as hydrophilic or hydrophobic and interacted electrostatically or covalently with Au nanoparticles. Results indicate that a highly hydrophilic surface is required for Au nanoparticle deposition, unless covalent binding can occur between the Au and substrate surface. The optimal range of relative humidity for patterning was found to be 40-60%, and Au nanoparticle deposition was not sensitive to writing speeds ranging from 0.01 to 2 microm/s.
View details for DOI 10.1021/nn8005416
View details for Web of Science ID 000260503100022
View details for PubMedID 19206460
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Aging Susceptibility of Terrace-Like Pentacene Films
JOURNAL OF PHYSICAL CHEMISTRY C
2008; 112 (42): 16161-16165
View details for DOI 10.1021/jp8055224
View details for Web of Science ID 000260129400001
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Trialkylsilylethynyl-functionalized tetraceno[2,3-b]thiophene and anthra[2,3-b]thiophene organic transistors
CHEMISTRY OF MATERIALS
2008; 20 (14): 4669-4676
View details for DOI 10.1021/cm800644y
View details for Web of Science ID 000257666300022
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Self-assembly, molecular packing, and electron transport in n-type polymer semiconductor nanobelts
CHEMISTRY OF MATERIALS
2008; 20 (14): 4712-4719
View details for DOI 10.1021/cm8010265
View details for Web of Science ID 000257666300027
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High-performance organic thin-film transistors through solution-sheared deposition of small-molecule organic semiconductors
ADVANCED MATERIALS
2008; 20 (13): 2588-?
View details for DOI 10.1002/adma.200703120
View details for Web of Science ID 000257808700022
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Organic solar cells with solution-processed graphene transparent electrodes
APPLIED PHYSICS LETTERS
2008; 92 (26)
View details for DOI 10.1063/1.2924771
View details for Web of Science ID 000257424500068
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Functionalized asymmetric linear acenes for high-performance organic semiconductors
ADVANCED FUNCTIONAL MATERIALS
2008; 18 (10): 1579-1585
View details for DOI 10.1002/adfm.200701529
View details for Web of Science ID 000256846400011
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Ambipolar, high performance, acene-based organic thin film transistors
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
2008; 130 (19): 6064-?
Abstract
We present a high performance, ambipolar organic field-effect transistor composed of a single material. Ambipolar molecules are rare, and they can enable low-power complementary-like circuits. This low band gap, asymmetric linear acene contains electron-withdrawing fluorine atoms, which lower the molecular orbital energies, allowing the injection of electrons. While hole and electron mobilities of up to 0.071 and 0.37 cm2/V.s, respectively, are reported on devices measured in nitrogen, hole mobilities of up to 0.12 cm2/V.s were found in ambient, with electron transport quenched. These devices were fabricated on octadecyltrimethoxysilane-treated surfaces at a substrate temperature of 60 degrees C.
View details for DOI 10.1021/ja8005918
View details for Web of Science ID 000255620200004
View details for PubMedID 18412338
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Microstructure of oligofluorene asymmetric derivatives in orgranic thin film transistors
CHEMISTRY OF MATERIALS
2008; 20 (8): 2763-2772
View details for DOI 10.1021/cm800071r
View details for Web of Science ID 000255019300026
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Introducing organic nanowire transistors
MATERIALS TODAY
2008; 11 (4): 38-47
View details for Web of Science ID 000254691900020
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Thin film structure of tetraceno[2,3-b]thiophene characterized by grazing incidence X-ray scattering and near-edge X-ray absorption fine structure analysis
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
2008; 130 (11): 3502-3508
Abstract
Understanding the structure-property relationship for organic semiconductors is crucial in rational molecular design and organic thin film process control. Charge carrier transport in organic field-effect transistors predominantly occurs in a few semiconductor layers close to the interface in contact with the dielectric layer, and the transport properties depend sensitively on the precise molecular packing. Therefore, a better understanding of the impact of molecular packing and thin film morphology in the first few monolayers above the dielectric layer on charge transport is needed to improve the transistor performance. In this Article, we show that the detailed molecular packing in thin organic semiconductor films can be solved through a combination of grazing incidence X-ray diffraction (GIXD), near-edge X-ray absorption spectra fine structure (NEXAFS) spectroscopy, energy minimization packing calculations, and structure refinement of the diffraction data. We solve the thin film structure for 2 and 20 nm thick films of tetraceno[2,3-b]thiophene and detect only a single phase for these thicknesses. The GIXD yields accurate unit cell dimensions, while the precise molecular arrangement in the unit cell was found from the energy minimization and structure refinement; the NEXAFS yields a consistent molecular tilt. For the 20 nm film, the unit cell is triclinic with a = 5.96 A, b = 7.71 A, c = 15.16 A, alpha = 97.30 degrees, beta = 95.63 degrees, gamma = 90 degrees; there are two molecules per unit cell with herringbone packing (49-59 degree angle) and tilted about 7 degrees from the substrate normal. The thin film structure is significantly different from the bulk single-crystal structure, indicating the importance of characterizing thin film to correlate with thin film device performance. The results are compared to the corresponding data for the chemically similar and widely used pentacene. Possible effects of the observed thin film structure and morphology on charge carrier mobility are discussed.
View details for DOI 10.1021/ja0773002
View details for Web of Science ID 000253951900062
View details for PubMedID 18293975
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Evaluation of solution-processed reduced graphene oxide films as transparent conductors
ACS NANO
2008; 2 (3): 463-470
Abstract
Processable, single-layered graphene oxide (GO) is an intriguing nanomaterial with tremendous potential for electronic applications. We spin-coated GO thin-films on quartz and characterized their sheet resistance and optical transparency using different reduction treatments. A thermal graphitization procedure was most effective, producing films with sheet resistances as low as 10(2) -10(3) Omega/square with 80% transmittance for 550 nm light. Our experiments demonstrate solution-processed GO films have potential as transparent electrodes.
View details for DOI 10.1021/nn700375n
View details for Web of Science ID 000254408000014
View details for PubMedID 19206571
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Organic semiconductor-carbon nanotube bundle bilayer field effect transistors with enhanced mobilities and high on/off ratios
APPLIED PHYSICS LETTERS
2008; 92 (5)
View details for DOI 10.1063/1.2841033
View details for Web of Science ID 000253016500082
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"Air-stable n-channel organic thin-film transistors with high field-effect mobility based on N,N '-bis(heptafluorobutyl)-3,4 : 9,10-perylene diimide"(vol 91, art no 212107, 2007)
APPLIED PHYSICS LETTERS
2008; 92 (4)
View details for DOI 10.1063/1.2839368
View details for Web of Science ID 000252860400130
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Adding new functions to organic semiconductor nanowires by assembling metal nanoparticles onto their surfaces
JOURNAL OF MATERIALS CHEMISTRY
2008; 18 (44): 5395-5398
View details for DOI 10.1039/b809228c
View details for Web of Science ID 000260620300014
- High performance organic thin film transistor through solution sheared deposition of small molecule organic semiconductors Adv. Mater. 2008; 20: 2588-2594
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High-resolution measurement of the anisotropy of charge transport in single crystals
ADVANCED MATERIALS
2007; 19 (24): 4535-?
View details for DOI 10.1002/adma.200701139
View details for Web of Science ID 000252511500044
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Tunable thin-film crystalline structures and field-effect mobility of oligofluorene-thiophene derivatives
CHEMISTRY OF MATERIALS
2007; 19 (24): 5882-5889
View details for DOI 10.1021/cm0710599
View details for Web of Science ID 000251150900022
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Enhancement in open circuit voltage through a cascade-type energy band structure
APPLIED PHYSICS LETTERS
2007; 91 (22)
View details for DOI 10.1063/1.2817935
View details for Web of Science ID 000251324600089
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Selective nucleation of organic single crystals from vapor phase on nanoscopically rough surfaces
ADVANCED FUNCTIONAL MATERIALS
2007; 17 (17): 3545-3553
View details for DOI 10.1002/adfm.200700330
View details for Web of Science ID 000251537300018
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Air-stable n-channel organic thin-film transistors with high field-effect mobility based on N,N '-bis(heptafluorobutyl)3,4 : 9,10-perylene diimide
APPLIED PHYSICS LETTERS
2007; 91 (21)
View details for DOI 10.1063/1.2803073
View details for Web of Science ID 000251105500020
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Core-fluorinated rerylene bisimide dyes: Air stable n-channel organic semiconductors for thin film transistors with exceptionally high on-to-off current ratios
ADVANCED MATERIALS
2007; 19 (21): 3692-?
View details for DOI 10.1002/adma.200701478
View details for Web of Science ID 000250992000051
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Synthesis, characterization, and field-effect transistor performance of pentacene derivatives
ADVANCED MATERIALS
2007; 19 (20): 3381-?
View details for DOI 10.1002/adma.200700298
View details for Web of Science ID 000250735600053
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Selective crystallization of organic semiconductors on patterned templates of carbon nanotubes
ADVANCED FUNCTIONAL MATERIALS
2007; 17 (15): 2891-2896
View details for DOI 10.1002/adfm.200700484
View details for Web of Science ID 000250526300036
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Perylenediimide nanowires and their use in fabricating field-effect transistors and complementary inverters
NANO LETTERS
2007; 7 (9): 2847-2853
Abstract
Perylenetetracarboxyldiimide (PTCDI) nanowires self-assembled from commercially available materials are demonstrated as the n-channel semiconductor in organic field-effect transistors (OFETs) and as a building block in high-performance complementary inverters. Devices based on a network of PTCDI nanowires have electron mobilities and current on/off ratios on the order of 10(-2) cm2/Vs and 10(4), respectively. Complementary inverters based on n-channel PTCDI nanowire transistors and p-channel hexathiapentacene (HTP) nanowire OFETs achieved gains as high as 8. These results demonstrate the first example of the use of one-dimensional organic semiconductors in complementary inverters.
View details for DOI 10.1021/nl071495u
View details for Web of Science ID 000249501900055
View details for PubMedID 17696562
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Synthesis of solution-soluble pentacene-containing conjugated copolymers
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
2007; 129 (34): 10308-?
View details for DOI 10.1021/ja0725403
View details for Web of Science ID 000249035200005
View details for PubMedID 17685520
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Probing the anisotropic field-effect mobility of solution-deposited dicyclohexyl-alpha-quaterthiophene single crystals
ADVANCED FUNCTIONAL MATERIALS
2007; 17 (10): 1617-1622
View details for DOI 10.1002/adfm.200600865
View details for Web of Science ID 000248062100004
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Solution-assisted assembly of organic semiconducting single crystals on surfaces with patterned wettability
LANGMUIR
2007; 23 (14): 7428-7432
Abstract
Two efficient approaches to assembling organic semiconducting single crystals are described. The methods rely on solvent wetting and dewetting on substrates with patterned wettability to selectively direct the deposition or removal of organic crystals. Substrates were functionalized with different self-assembled monolayers (SAMs) to achieve the desired wettabilities. The assembly of different organic crystals over centimeter-squared areas on Au, SiO2, and flexible plastic substrates was demonstrated. By designing line features on the substrate, the alignment of crystals, such as CuPc needles, was also achieved. As a demonstration of the potential application of this assembly approach, arrays of single-crystal organic field-effect transistors were fabricated by patterning organic single crystals directly onto and between transistor source and drain electrodes.
View details for DOI 10.1021/1a700493p
View details for Web of Science ID 000247487200004
View details for PubMedID 17547427
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Solution deposited liquid crystalline semiconductors on a photoalignment layer for organic thin-film transistors
APPLIED PHYSICS LETTERS
2007; 90 (23)
View details for DOI 10.1063/1.2746937
View details for Web of Science ID 000247145500036
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Resistance switching in a polystyrene film containing Au nanoparticles
JAPANESE JOURNAL OF APPLIED PHYSICS PART 1-REGULAR PAPERS BRIEF COMMUNICATIONS & REVIEW PAPERS
2007; 46 (6A): 3622-3625
View details for DOI 10.1143/JJAP.46.3622
View details for Web of Science ID 000247493000070
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Correlating molecular structure to field-effect mobility: The investigation of side-chain functionality in phenylene - Thiophene oligomers and their application in field effect transistors
CHEMISTRY OF MATERIALS
2007; 19 (9): 2342-2351
View details for DOI 10.1021/cm070117n
View details for Web of Science ID 000245900100031
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Air-stable n-channel organic semiconductors based on perylene diimide derivatives without strong electron withdrawing groups
ADVANCED MATERIALS
2007; 19 (8): 1123-1127
View details for DOI 10.1002/adma.200601705
View details for Web of Science ID 000246432800017
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Non-destructive probing of the anisotropy of field-effect mobility in the rubrene single crystal
SYNTHETIC METALS
2007; 157 (6-7): 257-260
View details for DOI 10.1016/j.synthmet.2007.02.004
View details for Web of Science ID 000247520300003
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Organic single-crystal field-effect transistors
MATERIALS TODAY
2007; 10 (3): 20-27
View details for Web of Science ID 000244597300016
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Fabrication of field-effect transistors from hexathiapentacene single-crystal nanowires
NANO LETTERS
2007; 7 (3): 668-675
Abstract
This paper describes a simple, solution-phase route to the synthesis of bulk quantities of hexathiapentacene (HTP) single-crystal nanowires. These nanowires have also been successfully incorporated as the semiconducting material in field-effect transistors (FETs). For devices based on single nanowires, the carrier mobilities and current on/off ratios could be as high as 0.27 cm2/Vs and >103, respectively. For transistors fabricated from a network of nanowires, the mobilities and current on/off ratios could reach 0.057 cm2/Vs and >104, respectively. We have further demonstrated the use of nanowire networks in fabricating transistors on mechanically flexible substrates. Preliminary results show that these devices could withstand mechanical strain and still remain functional. The results from this study demonstrate the potential of utilizing solution-dispersible, nanostructured organic materials for use in low-cost, flexible electronic applications.
View details for DOI 10.1021/nl0627036
View details for Web of Science ID 000244867400023
View details for PubMedID 17288487
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Complementary inverter using high mobility air-stable perylene di-imide derivatives
APPLIED PHYSICS LETTERS
2007; 90 (9)
View details for DOI 10.1063/1.2695873
View details for Web of Science ID 000244591700107
- Structural transitions of nanocrystalline domains in regioregular poly(3-hexyl thiophene) thin films J. Poly. Sci. Part B: Poly. Phys. 2007; 45: 1303-1312
- Design, Synthesis, and Transistor Performance of Organic Semiconductors Organic Thin Film Transistors edited by Bao, Z., Locklin, J., J. CRC Press. 2007
- Probing Non-destructive probing of the anisotropy of field-effect mobility in the rubrene single crystal Syn. Met. 2007; 157: 257-260
- Solubility-driven thin film structures of regioregular poly(3-hexyl thiophene) using volatile solvents Appl. Phys. Lett. 2007; 90: 172116
- Air Stable n-Channel Organic Semiconductors for Thin Film Transistors Based on Fluorinated Derivatives of Perylene Diimides Chem. Mater. 2007; 19: 816-824
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Structure property relationships: Asymmetric oligofluorene-thiophene molecules for organic TFTs
CHEMISTRY OF MATERIALS
2006; 18 (26): 6250-6257
View details for DOI 10.1021/cm0623514
View details for Web of Science ID 000242935500028
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High-performance organic semiconductors: Asymmetric linear acenes containing sulphur
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
2006; 128 (50): 16002-16003
Abstract
Two new linear acenes with fused thiophene units have been synthesized. These acenes have conjugation lengths between anthracene and pentacene. Thin films of these linear molecules were characterized by ultraviolet spectroscopy, X-ray diffraction, atomic force microscopy (AFM), and field-effect transistor measurements. Submonolayer AFM studies show growth that greatly resembles pentacene, while thin-film growth is dendritic. Mobilites as high as 0.47 cm2 V-1 s-1 have been found for the tetraceno[2,3-b]thiophene and are as high as 0.15 cm2 V-1 s-1 for anthra[2,3-b]thiophene.
View details for DOI 10.1021/ja066824j
View details for Web of Science ID 000242825600037
View details for PubMedID 17165730
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Patterning organic single-crystal transistor arrays
NATURE
2006; 444 (7121): 913-917
Abstract
Field-effect transistors made of organic single crystals are ideal for studying the charge transport characteristics of organic semiconductor materials. Their outstanding device performance, relative to that of transistors made of organic thin films, makes them also attractive candidates for electronic applications such as active matrix displays and sensor arrays. These applications require minimal cross-talk between neighbouring devices. In the case of thin film systems, simple patterning of the active semiconductor layer minimizes cross-talk. But when using organic single crystals, the only approach currently available for creating arrays of separate devices is manual selection and placing of individual crystals-a process prohibitive for producing devices at high density and with reasonable throughput. In contrast, inorganic crystals have been grown in extended arrays, and efficient and large-area fabrication of silicon crystalline islands with high mobilities for electronic applications has been reported. Here we describe a method for effectively fabricating large arrays of single crystals of a wide range of organic semiconductor materials directly onto transistor source-drain electrodes. We find that film domains of octadecyltriethoxysilane microcontact-printed onto either clean Si/SiO(2) surfaces or flexible plastic provide control over the nucleation of vapour-grown organic single crystals. This allows us to fabricate large arrays of high-performance organic single-crystal field-effect transistors with mobilities as high as 2.4 cm(2) V(-1) s(-1) and on/off ratios greater than 10(7), and devices on flexible substrates that retain their performance after significant bending. These results suggest that our fabrication approach constitutes a promising step that might ultimately allow us to utilize high-performance organic single-crystal field-effect transistors for large-area electronics applications.
View details for DOI 10.1038/nature05427
View details for Web of Science ID 000242805400052
View details for PubMedID 17167482
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Hexathiapentacene: Structure, molecular packing, and thin-film transistors
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
2006; 128 (49): 15576-15577
Abstract
In this communication we report the electrical characteristics of hexathiapentacene (HTP) and emphasize the unusual chemical structure and molecular packing. We report field-effect mobilities as high as 0.04 cm2 V-1 s-1 and current on/off ratios of >105. With crystallographic evidence of unusually long S-S bonds compared to normal S-S bonds, we have suggested a unique resonance structure similar to trithiapentalene, which well explains the bonding characteristics of HTP. This work appears to be the first to determine its molecular structure/packing mode and to study its application in organic transistors.
View details for DOI 10.1021/ja066088j
View details for Web of Science ID 000242575300014
View details for PubMedID 17147352
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Assembly and alignment of metallic nanorods on surfaces with patterned wettability
SMALL
2006; 2 (12): 1448-1453
View details for DOI 10.1002/smll.200600275
View details for Web of Science ID 000242275800011
View details for PubMedID 17193004
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Copper hexafluorophthalocyanine field-effect transistors with enhanced mobility by soft contact lamination
ORGANIC ELECTRONICS
2006; 7 (6): 568-575
View details for DOI 10.1016/j.orgel.2006.09.003
View details for Web of Science ID 000242736700018
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High-performance organic semiconductors based on fluorene-phenylene oligomers with high ionization potentials
ADVANCED MATERIALS
2006; 18 (22): 2989-?
View details for DOI 10.1002/adma.200601608
View details for Web of Science ID 000242599600012
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High-performance microscale single-crystal transistors by lithography on an elastomer dielectric
APPLIED PHYSICS LETTERS
2006; 89 (20)
View details for DOI 10.1063/1.2388151
View details for Web of Science ID 000242100200042
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Air-stable n-channel copper hexachlorophthalocyanine for field-effect transistors
APPLIED PHYSICS LETTERS
2006; 89 (16)
View details for DOI 10.1063/1.2362976
View details for Web of Science ID 000241405200123
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High-performance organic single-crystal transistors on flexible substrates
ADVANCED MATERIALS
2006; 18 (17): 2320-?
View details for DOI 10.1002/adma.200600634
View details for Web of Science ID 000240573300024
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Optimizing the thin film morphology of organic field-effect transistors: The influence of molecular structure and vacuum deposition parameters on device performance
POLYMER REVIEWS
2006; 46 (1): 79-101
View details for DOI 10.1080/15321790500471244
View details for Web of Science ID 000240473300005
- Organic Single-Crystal Complementary Inverters Appl. Phys. Lett. 2006; 89: 222111
- Molecular conductance measurements through printed Au nanodots Appl. Phys. Lett. 2006; 89: 113107
- High Performance Organic Semiconductors Based on Fluorene-phenylene Oligomers with High Ionization Potentials Adv. Mater. 2006; 18: 2989-2992
- Patterning Organic Semiconductors Using ‘Dry’ Poly(dimethylsiloxane) Elastomeric Stamps for Thin Film Transistors J. Am. Chem. Soc. 2006; 128: 3880-3881
- Transistor Performance of Top, Rough Surface of Pentacene Measured by Laminated, Double Insulated-Gate Supported on a Poly(dimethylsiloxanes) Base Structure Appl. Phys. Lett. 2006; 88: 33502
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Effect of morphology on organic thin film transistor sensors
ANALYTICAL AND BIOANALYTICAL CHEMISTRY
2006; 384 (2): 336-342
Abstract
This review provides a general introduction to organic field-effect transistors and their application as chemical sensors. Thin film transistor device performance is greatly affected by the molecular structure and morphology of the organic semiconductor layer. Various methods for organic semiconductor deposition are surveyed. Recent progress in the fabrication of organic thin film transistor sensors as well as the correlation between morphology and analyte response is discussed.
View details for DOI 10.1007/s00216-005-0137-z
View details for Web of Science ID 000234299600004
View details for PubMedID 16328249
- Thickness Dependence of Microstructure in Semiconducting Films of an Oligofluorene Derivative J. Am. Chem. Soc. 2006; 128: 16579-12586
- High Performance Organic Semiconductors: Asymmetric Linear Acenes Containing Sulphur J. Am. Chem. Soc. 2006; 128: 160002-160003
- Control of Topography, Stress and Diffusion at Molecule-metal Interface Nanotechnology 2006; 17: 1272-1277
- Organic Single Crystals: Tools for the Exploration of Charge Transport Phenomena in Organic Materials J. Mater. Chem. 2006; 16: 329-333
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Nanowire lithography: Fabricating controllable electrode gaps using Au-Ag-Au nanowires
NANO LETTERS
2005; 5 (6): 1071-1076
Abstract
A method to fabricate nanowire electrodes possessing controllable gaps is described. The method relies on electrochemical deposition and selective chemical etching or heating to selectively remove the Ag segment of Au-Ag-Au nanowires. Because the thickness of the Ag segment directly dictates the size of the nanogap, the gap width can be easily controlled during the nanowire fabrication process. Herein, we demonstrate gaps with 2 microm, 100 nm and 20 nm widths via the above-mentioned approaches. In addition, we observed that small gaps (approximately 20 nm) can be formed through annealing Au-Ag-Au nanowires at 200 degrees C in air. Electrical contact between nanowire electrodes and contact pads is studied. Using nanowire electrodes with a 100 nm gap, we subsequently fabricate organic field effect transistors (FETs) with regioregular poly(3-hexylthiophene).
View details for DOI 10.1021/nl050581w
View details for Web of Science ID 000229729900014
View details for PubMedID 15943445
- Organic Thin Film Transistors Based on Cyclohexyl-substituted Organic Semiconductors Chem. Mater. 2005; 17: 3366-3374
- Patterned Growth of Large Oriented Organic Semiconductor Single Crystals on Self-Assembled Monolayer Templates J. Am. Chem. Soc. 2005; 127: 2164-12165
- Molecular Nano-junctions Formed with Different Metallic Electrodes Nanotechnology 2005; 16: 495-500
- Conducting AFM and 2D GIXD Studies on Pentacene Thin Films J. Am. Chem. Soc. 2005; 127: 11542-11543
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Metallic contact formation for molecular electronics: interactions between vapor-deposited metals and self-assembled monolayers of conjugated mono- and dithiols
LANGMUIR
2004; 20 (5): 1539-1542
Abstract
We present grazing-incidence Fourier transform infrared and AFM data of Au, Al, and Ti vapor-deposited onto self-assembled monolayers (SAMs) of conjugated mono- and dithiols. SAMs of 4,4'''-dimercapto-p-quaterphenyl, 4,4"-dimercapto-p-terphenyl, and 4,4'-dimercapto-p-biphenyl have reactive thiols at the SAM/vacuum interface that interact with vapor-deposited Au or Al atoms, preventing metal penetration. Conjugated monothiols lack such metal blocking groups, and metals (Au, Al) can penetrate into their SAMs. Vapor deposition of Ti onto conjugated mono- and dithiol SAMs and onto hexadecanethiol SAMs destroys the monolayers.
View details for DOI 10.1021/la0356349
View details for Web of Science ID 000189241500002
View details for PubMedID 15801409
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