新型共轭聚合物的设计合成及其在场效应晶体管的应用

近年来,有机场效应晶体管(OFETs)由于在柔性器件和可穿戴电子学中的潜在应用受到了学术界和工业界的普遍关注,尤其是以聚合物半导体材料构筑的晶体管性能得到了快速的发展.如何设计合成用于OFETs的高性能聚合物半导体材料,一直是我们的追求目标.然而,分子结构对迁移率的影响仍缺少系统的比较.本文综述了近年来国内外新型聚合物材料的最新进展.我们按照材料的种类以及载流子的传输类型进行了分类,对高性能聚合物材料的发展过程、材料的设计思路以及相应的FETs性能进行了系统地归纳总结.通过研究分子及分子聚集态结构与器件性能之间的关系,希望为以后设计合成新型的高性能的聚合物材料提供有益的借鉴和指导.     

高迁移率有机薄膜晶体管材料进展

对近几年来高迁移率有机薄膜晶体管材料研究的主要发展作了简要介绍和评述,讨论了高迁移率有机半导体材料存在的问题和发展方向．     

A General Method for Growing Two‐Dimensional Crystals of Organic Semiconductors by “Solution Epitaxy”

Two‐dimensional (2D) crystals of organic semiconductors (2DCOS) have attracted attention for large‐area and low‐cost flexible optoelectronics. However, growing large 2DCOS in controllable ways and transferring them onto technologically important substrates, remain key challenges. Herein we report a facile, general, and effective method to grow 2DCOS up to centimeter size which can be transferred to any substrate efficiently. The method named “solution epitaxy” involves two steps. The first is to self‐assemble micrometer‐sized 2DCOS on water surface. The second is epitaxial growth of them into millimeter or centimeter sized 2DCOS with thickness of several molecular layers. The general applicability of this method for the growth of 2DCOS is demonstrated by nine organic semiconductors with different molecular structures. Organic field‐effect transistors (OFETs) based on the 2DCOS demonstrated high performance, confirming the high quality of the 2DCOS.     

Progresses in organic field-effect transistors and molecular electronics

In the past years, organic semiconductors have been extensively investigated as electronic materials for organic field-effect transistors (OFETs). In this review, we briefly summarize the current status of organic field-effect transistors including materials design, device physics, molecular electronics and the applications of carbon nanotubes in molecular electronics. Future prospects and investigations required to improve the OFET performance are also involved. __________ Translated from Huaxue Tongbao (Chemistry), 2006, 69(6) (in Chinese)     

An Air‐Stable Semiconducting Polymer Containing Dithieno[3,2‐b:2′,3′‐d]arsole

Arsole‐containing conjugated polymers are a practically unexplored class of materials despite the high interest in their phosphole analogues. Herein we report the synthesis of the first dithieno[3,2‐b;2′,3′‐d]arsole derivative, and demonstrate that it is stable to ambient oxidation in its +3 oxidation state. A soluble copolymer is obtained by a palladium‐catalyzed Stille polymerization and demonstrated to be a p‐type semiconductor with promising hole mobility, which was evaluated by field‐effect transistor measurements.     

Anthradithiophene–thiophene copolymers with broad UV–vis absorption for organic solar cells and field‐effect transistors

New semiconducting copolymers, poly((TIPS‐ADT)‐(4,4′‐didodecyl‐2,2′‐bithiophene)) (PTADT2) and poly((TIPS‐ADT)‐(2,2′‐(4,4′‐didodecyl‐2,2′‐bithiophene)dithiophene)) (PTADT4) , produced by incorporating 5,11‐bis(triisopropylsilylethynyl) anthra[2,3‐b:7,6‐b']dithiophene (TIPS‐ADT) and alkyl‐thiophene derivatives were synthesized via Stille coupling polymerization. The optical, electrochemical, structural, field‐effect transistor, and solar cell properties of the polymers were investigated. The polymers showed good solubility at room temperature in common organic solvents due to their abundant side groups including TIPS and dodecyl side chains. Both polymers showed very broad UV absorption spectra covering the spectral range from 300 to 750 nm as a result of the combination of the different absorption ranges of the TIPS‐ADT unit (short wavelength region) and thiophene derivatives (long wavelength region). The FET device fabricated using PTADT4 containing additional unsubstituted thiophene rings as a spacer between TIPS‐ADT and thiophene derivatives showed a higher hole mobility (5.7 × 10^?4 cm²/V s) than the PTADT2 device (2.8 × 10^?5 cm²/V s), due to the improved intermolecular ordering caused by the reduced steric hindrance between bulky side chain groups. In addition, the PTADT4 :(6,6)‐phenyl‐C₇₀‐butyric acid methyl ester (PC₇₀BM) device showed an enhanced power conversion efficiency (PCE) of 1.30% compared with the PTADT2 :PC₇₀BM device (PCE of 0.55%) under AM 1.5G irradiation (100 mW/cm²). © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012     

Investigation of spacer influences in phosphorescent‐emitting nonconjugated PLED systems

An assay was introduced to clarify influences on electroluminescent behavior for RGB‐colored phosphorescent terpolymers with N,N‐Di‐p‐tolyl‐aniline as hole‐transporting unit, 2‐(4‐biphenyl)‐5‐(4‐tert‐butylphenyl)‐1,3,4‐oxadiazole (tert‐BuPBD) as electron‐transporting unit, and different iridium complexes in RGB‐colors as triplet emitting materials. All monomers were attached with spacer moieties to the “para” position of a polystyrene. Polymer light emitting diodes (PLEDs) were built to study the electro‐optical behavior of these materials. The gist was a remarkable influence of hexyl‐spacer units to the PLED performance. For all three colors only very restricted PLED performances were found. In comparison RGB‐terpolymers were synthesized with directly attached charge transport materials to the polymer backbone. For this directly linked systems efficiencies were 28 cd A^?1 @ 6 V (green), 4.9 cd A^?1 @ 5 V (red) and 4.3 cd A^?1 @ 6 V (bluish). In summary we assume that an improved charge percolation pathways regarding to the higher content of semiconducting molecules and an improved charge transfer to the phosphorescent dopand in the case of the copolymers without spacers are responsible for the better device performance comparing the copolymers with hexyl spacers. The approach of the directly connected charge transport materials at the nonconjugated styrene polymer backbone should be favored for further investigations, therefore. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 389–402, 2010     

聚合物场效应晶体管材料及其器件

导电聚合物因为可以大面积成膜、器件制作工艺简单,近年来在有机场效应晶体管的研究中受到越来越多的关注。有的聚合物场效应晶体管其性能已经可以和无定型硅晶体管相比拟。本文回顾了聚合物场效应晶体管的发展历程,概述了聚合物场效应晶体管的材料、器件制作、性能及工作机理。同时,对聚合物场效应晶体管的发展前景和目前存在的问题作了简单的总结。     

聚合物场效应晶体管材料及其器件

导电聚合物因为可以大面积成膜、器件制作工艺简单,近年来在有机场效应晶体管的研究中受到越来越多的关注.有的聚合物场效应晶体管其性能已经可以和无定型硅晶体管相比拟.本文回顾了聚合物场效应晶体管的发展历程,概述了聚合物场效应晶体管的材料、器件制作、性能及工作机理.同时,对聚合物场效应晶体管的发展前景和目前存在的问题作了简单的总结.     

二维分子晶体的研究进展

二维分子晶体具有超薄、长程有序、无晶界和缺陷密度低等优点,是构建多种高性能光电器件的理想材料.实现二维分子晶体的低成本、大面积制备是二维分子晶体走向应用的关键.目前,人们开发了多种方法,在气相和液相中实现了二维分子晶体的可控制备,并揭示了这类二维有机体系独特的光电性能.本文综述了二维分子晶体的制备方法及其在有机场效应晶...     

Length‐Independent Charge Transport in Chimeric Molecular Wires

Advanced molecular electronic components remain vital for the next generation of miniaturized integrated circuits. Thus, much research effort has been devoted to the discovery of lossless molecular wires, for which the charge transport rate or conductivity is not attenuated with length in the tunneling regime. Herein, we report the synthesis and electrochemical interrogation of DNA‐like molecular wires. We determine that the rate of electron transfer through these constructs is independent of their length and propose a plausible mechanism to explain our findings. The reported approach holds relevance for the development of high‐performance molecular electronic components and the fundamental study of charge transport phenomena in organic semiconductors.     

Organic semiconductors for solution-processable field-effect transistors (OFETs)

The cost-effective production of flexible electronic components will profit considerably from the development of solution-processable, organic semiconductor materials. Particular attention is focused on soluble semiconductors for organic field-effect transistors (OFETs). The hitherto differentiation between "small molecules" and polymeric materials no longer plays a role, rather more the ability to process materials from solution to homogeneous semiconducting films with optimal electronic properties (high charge-carrier mobility, low threshold voltage, high on/off ratio) is pivotal. Key classes of materials for this purpose are soluble oligoacenes, soluble oligo- and polythiophenes and their respective copolymers, and oligo- and polytriarylamines. In this context, micro- or nanocrystalline materials have the general advantage of somewhat higher charge-carrier mobilities, which, however, could be offset in the case of amorphous, glassy materials by simpler and more reproducible processing.