Domain size control in all-polymer solar cells

被引:44
|
作者
Liu, Jiangang [1 ]
Yin, Yukai [1 ]
Wang, Kang [1 ]
Wei, Puxin [1 ]
Lu, Haodong [1 ]
Song, Chunpeng [1 ]
Liang, Qiuju [1 ]
Huang, Wei [1 ]
机构
[1] Northwestern Polytech Univ, Xian 710129, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
PHASE-SEPARATION; BULK HETEROJUNCTION; AGGREGATION; MORPHOLOGY; CRYSTALLINITY; PERFORMANCE; TEMPERATURE; NUCLEATION; EFFICIENCY;
D O I
10.1016/j.isci.2022.104090
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
In all polymer solar cells (all-PSCs), the domain size is critical for device performance. In highly crystalline polymer blends, however, precisely adjusting the domain size remains a significant challenge because of the simultaneous crystallization of both components. Herein, a strategy that promotes acceptor and donor to crystallize separately was proposed. Take PBDB-T/N2200 blends for instance; the solution state and confined crystallization were combined, which induced the crystallization of N2200, and PBDB-T occurred during the film-forming process and at thermal annealing stage. This separated crystallization process lowers the driving force of phase separation without affecting the degree of crystallinity of the blends. Thus, an interpenetrating network with high crystallinity and proper domain size was obtained, which boosted the power conversion efficiency to 7.59%. Importantly, the relation between pre-aggregation and domain size was established, which may be a guide to precisely adjust the active layer's domain size in all-PSCs.
引用
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页数:17
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