Aggregation and morphology control enables multiple cases of high-efficiency polymer solar cells

被引:2567
作者
Liu, Yuhang [1 ]
Zhao, Jingbo [1 ]
Li, Zhengke [1 ]
Mu, Cheng [1 ]
Ma, Wei [2 ,3 ]
Hu, Huawei [1 ]
Jiang, Kui [1 ]
Lin, Haoran [1 ]
Ade, Harald [2 ,3 ]
Yan, He [1 ,4 ]
机构
[1] Hong Kong Univ Sci & Technol, Dept Chem, Kowloon, Hong Kong, Peoples R China
[2] N Carolina State Univ, Dept Phys, Raleigh, NC 27695 USA
[3] N Carolina State Univ, ORaCEL, Raleigh, NC 27695 USA
[4] HKUST Shenzhen Res Inst, Shenzhen 518057, Peoples R China
关键词
ACCEPTOR CONJUGATED POLYMER; CONVERSION EFFICIENCY; MOLECULAR-ORIENTATION; PHOTOVOLTAIC CELLS; MISCIBILITY; WEIGHT;
D O I
10.1038/ncomms6293
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Although the field of polymer solar cell has seen much progress in device performance in the past few years, several limitations are holding back its further development. For instance, current high-efficiency (>9.0%) cells are restricted to material combinations that are based on limited donor polymers and only one specific fullerene acceptor. Here we report the achievement of high-performance (efficiencies up to 10.8%, fill factors up to 77%) thick-film polymer solar cells for multiple polymer: fullerene combinations via the formation of a near-ideal polymer: fullerene morphology that contains highly crystalline yet reasonably small polymer domains. This morphology is controlled by the temperature-dependent aggregation behaviour of the donor polymers and is insensitive to the choice of fullerenes. The uncovered aggregation and design rules yield three high-efficiency (>10%) donor polymers and will allow further synthetic advances and matching of both the polymer and fullerene materials, potentially leading to significantly improved performance and increased design flexibility.
引用
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页数:8
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