Beyond Fullerenes: Design of Nonfullerene Acceptors for Efficient Organic Photovoltaics

被引:216
作者
Li, Haiyan [1 ,2 ]
Earmme, Taeshik [1 ,2 ]
Ren, Guoqiang [1 ,2 ]
Saeki, Akinori [3 ,4 ]
Yoshikawa, Saya [3 ]
Murari, Nishit M. [1 ,2 ]
Subramaniyan, Selvam [1 ,2 ]
Crane, Matthew J. [1 ,2 ]
Seki, Shu [3 ]
Jenekhe, Samson A. [1 ,2 ]
机构
[1] Univ Washington, Dept Chem Engn, Seattle, WA 98195 USA
[2] Univ Washington, Dept Chem, Seattle, WA 98195 USA
[3] Osaka Univ, Grad Sch Engn, Dept Appl Chem, Suita, Osaka 5650871, Japan
[4] Japan Sci & Technol Agcy JST, PRESTO, Kawaguchi, Saitama 3320012, Japan
基金
日本学术振兴会;
关键词
POLYMER SOLAR-CELLS; CHARGE SEPARATION; ELECTRON-ACCEPTOR; HIGH-PERFORMANCE; CONVERSION EFFICIENCY; SMALL-MOLECULE; HETEROJUNCTION; SEMICONDUCTORS; DONOR; DIIMIDES;
D O I
10.1021/ja508472j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
New electron-acceptor materials are long sought to overcome the small photovoltage, high-cost, poor photochemical stability, and other limitations of fullerene-based organic photovoltaics. However, all known nonfullerene acceptors have so far shown inferior photovoltaic properties compared to fullerene benchmark [6,6]-phenyl-C-60-butyric acid methyl ester (PC60BM), and there are as yet no established design principles for realizing improved materials. Herein we report a design strategy that has produced a novel multichromophoric, large size, nonplanar three-dimensional (3D) organic molecule, DBFI-T, whose pi-conjugated framework occupies space comparable to an aggregate of 9 [C-60]-fullerene molecules. Comparative studies of DBFI-T with its planar monomeric analogue (BFI-P2) and PC60BM in bulk heterojunction (BHJ) solar cells, by using a common thiazolothiazole-dithienosilole copolymer donor (PSEHTT), showed that DBFI-T has superior charge photogeneration and photovoltaic properties; PSEHTT:DBFI-T solar cells combined a high short-circuit current (10.14 mA/cm(2)) with a high open-circuit voltage (0.86 V) to give a power conversion efficiency of 5.0%. The external quantum efficiency spectrum of PSEHTT:DBFI-T devices had peaks of 60-65% in the 380-620 nm range, demonstrating that both hole transfer from photoexcited DBFI-T to PSEHTT and electron transfer from photoexcited PSEHTT to DBFI-T contribute substantially to charge photogeneration. The superior charge photogeneration and electron-accepting properties of DBFI-T were further confirmed by independent Xenon-flash time-resolved microwave conductivity measurements, which correctly predict the relative magnitudes of the conversion efficiencies of the BHJ solar cells: PSEHTT:DBFI-T > PSEHTT:PC60BM > PSEHTT:BFI-P2. The results demonstrate that the large size, multichromophoric, nonplanar 3D molecular design is a promising approach to more efficient organic photovoltaic materials.
引用
收藏
页码:14589 / 14597
页数:9
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