共 44 条
Enhanced Performance of Bulk Heterojunction Solar Cells Using Block Copoly(3-alkylthiophene)s
被引:95
作者:

Ren, Guoqiang
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Univ Washington, Dept Chem Engn, Seattle, WA 98195 USA Univ Washington, Dept Chem Engn, Seattle, WA 98195 USA

Wu, Pei-Tzu
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Univ Washington, Dept Chem Engn, Seattle, WA 98195 USA Univ Washington, Dept Chem Engn, Seattle, WA 98195 USA

Jenekhe, Samson A.
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机构:
Univ Washington, Dept Chem Engn, Seattle, WA 98195 USA
Univ Washington, Dept Chem, Seattle, WA 98195 USA Univ Washington, Dept Chem Engn, Seattle, WA 98195 USA
机构:
[1] Univ Washington, Dept Chem Engn, Seattle, WA 98195 USA
[2] Univ Washington, Dept Chem, Seattle, WA 98195 USA
关键词:
CHARGE-TRANSPORT;
PHOTOVOLTAIC PROPERTIES;
CONJUGATED COPOLYMERS;
MICROPHASE SEPARATION;
DIBLOCK COPOLYMER;
CHAIN-LENGTH;
MORPHOLOGY;
DONOR;
METHANOFULLERENE;
NANOSTRUCTURES;
D O I:
10.1021/cm903783w
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
The photovoltaic properties, charge transport, and morphology of a series of diblock conjugated copolymers, poly(3-butylthiophene)-b-poly(3-octylthiophene) (P3BT-b-P3OT), were investigated as a functional of block composition. Bulk heterojunction solar cells comprising blends of P3BT-b-P3OT and [6,6]-phenyl-C-71-butyric acid methyl ester (PC71BM) were found to have power conversion effeciencies as high as 3.0% which represents factors of 1.6-9 enhancements compared to those of the homopolymers made under simiar conditions. Imaging of P3BT-b-P3OT/PC71BM blends by atomic force microscopy and transmission electron microscopy revealed interpenetrating network with 11-18 nm crystalline polymer domains. The zero-field spae charge limited current mobility of holes(similar to(1-3) x 10(-4) cm(2) V-1 s(-1)) was similarly enhanced in the diblock copolymer solar cells compared to the homopolymers. These results demonstrate that block conjugated copolymers offer a promising approach to advanced materials for polymer solar cells and that the block composition is an attractive means to optimize the materials.
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页码:2020 / 2026
页数:7
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