BODIPY-Thiophene Copolymers as p-Channel Semiconductors for Organic Thin-Film Transistors

被引:81
作者
Usta, Hakan [1 ]
Yilmaz, M. Deniz [2 ]
Avestro, Alyssa-Jennifer [2 ]
Boudinet, Damien [1 ]
Denti, Mitchell [1 ]
Zhao, Wei [1 ]
Stoddart, J. Fraser [2 ,3 ]
Facchetti, Antonio [1 ]
机构
[1] Polyera Corp, Skokie, IL 60077 USA
[2] Northwestern Univ, Dept Chem, Evanston, IL 60208 USA
[3] Korea Adv Inst Sci & Technol, Grad Sch EEWS, Taejon 305701, South Korea
基金
美国国家科学基金会;
关键词
bodipy; polymer; organic semiconductor; transistor; FIELD-EFFECT TRANSISTORS; HIGH-MOBILITY; HIGH-PERFORMANCE; CHARGE-TRANSPORT; SOLAR-CELLS; BAND-GAP; CONJUGATED POLYMERS; BUILDING-BLOCKS; ENERGY-TRANSFER; DYES;
D O I
10.1002/adma.201300318
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The synthesis and physicochemical properties of a new class of BODIPY-based donor-acceptor π-conjugated polymers are presented. Solution-processed top-gate/bottom-contact (TG-BC) thin-film transistors on flexible plastic substrates exhibit air-stable p-channel activities with charge carrier mobilities as high as 0.17 cm2/V·s and current on/off ratios of 105-106, the highest reported to date for a BODIPY-based semiconductor. The results shown here indicate a significant charge-transport improvement (>10000×) in BODIPY-based polymeric semiconductors, demonstrating its potential in future organic optoelectronic applications. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
引用
收藏
页码:4327 / 4334
页数:8
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