Structural ordering and enhanced carrier mobility in organic polymer thin film transistors

被引:101
作者
Kinder, L [1 ]
Kanicki, J
Petroff, P
机构
[1] Univ Calif Santa Barbara, Dept Mat, Santa Barbara, CA 93106 USA
[2] Univ Michigan, Dept Elect Engn & Comp Sci, Ann Arbor, MI 48109 USA
基金
美国国家科学基金会;
关键词
organic semiconductor; liquid-crystal; transistor; thiophene; fluorene; absorption;
D O I
10.1016/j.synthmet.2004.06.024
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
We have used thermal treatment and rubbed polyimide alignment layers to produce large domains of poly(9,9-dioctylfluorene-co-bithiophene) alternating copolymer (FM). The direction of rubbing on the polyimide surface determines the orientation of these domains, allowing us to create thin-film transistors with channel lengths parallel and perpendicular to the liquid-crystal polymer director. We show that thermal annealing at 280degreesC brings F8T2 into a mesophase as observed by X-ray diffraction and differential scanning calorimetry. Polarized optical microscopy and polarized UV-vis absorption spectroscopy show that this ordered phase is associated with very large ordered domains and corresponds to a thermotropic, nematic liquid-crystal phase. We investigated thermal annealing effects on both F8T2 structural ordering and the associated anisotropic electrical properties of the thin-film transistors (TFTs). Enhanced mobility of holes is observed with ordering. Field-effect mobility parallel to the polymer backbone is as much as 6.5 times greater than the perpendicular configuration. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:181 / 185
页数:5
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