Thiazolothiazole Donor-Acceptor Conjugated Polymer Semiconductors for Photovoltaic Applications

被引:35
作者
Subramaniyan, Selvam
Xin, Hao
Kim, Felix Sunjoo
Murari, Nishit M.
Courtright, Brett A. E.
Jenekhe, Samson A. [1 ]
机构
[1] Univ Washington, Dept Chem Engn, Seattle, WA 98195 USA
关键词
FIELD-EFFECT TRANSISTORS; HIGH-ELECTRON-MOBILITY; COPOLYMER SEMICONDUCTORS; MOLECULAR-WEIGHT; CHARGE PHOTOGENERATION; HOLE MOBILITY; SOLAR-CELLS; N-CHANNEL; PERFORMANCE; STABILITY;
D O I
10.1021/ma500250j
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A series of eight new donor-acceptor conjugated copolymers based on thiazolo[5,4-d]thiazole (TT) were synthesized by Suzuki and Stile polycondensations, and their optical, electronic structure, field-effect charge transport, and photovoltaic properties were investigated. The number-average molecular weight was moderate to high (20-103 kDa) for four of the new copolymers and low (<10 kDa) for the rest. The optical band gap (1.7-2.2 eV) and the ionization potential (4.9-5.7 eV) of the copolymers could be tuned by varying the strength of the electron-donating comonomers. X-ray diffraction analysis of the neat TT polymer thin films showed that they exhibit a lamellar crystalline morphology with a (100) d-spacing of 1.449-1.881 nm. The polymers had field-effect hole mobilities of 2 X 10(-3)-3 X 10(-2) cm(2)/(V s). Although fullerene (PC71BM)-based bulk heterojunction solar cells showed that most of the new polymers had low photovoltaic power conversion efficiency (<2.4%), the standout polymer PDEHTT had a high efficiency of 5.7%. X-ray diffraction analysis and TEM imaging of PDEHTT/PC71BM blend films showed a bicontinuous nanoscale morphology with a crystalline polymer nanofiber (15-20 nm width) network.
引用
收藏
页码:4199 / 4209
页数:11
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