Solution-Processable Hyperbranched Conjugated Polymer Nanoparticles Based on C3h-Symmetric Benzotrithiophene for Polymer Solar Cells

被引:17
作者
Wu, Xiaofu [1 ]
Zhang, Zijian [2 ]
Hang, Hao [2 ]
Chen, Yonghong [2 ]
Xu, Yuxiang [2 ]
Tong, Hui [1 ]
Wang, Lixiang [1 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Polymer Phys & Chem, Changchun 130022, Jilin, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
benzotrithiophene; hyperbranched conjugated polymer nanoparticles; polymer solar cells; solution-processability; Stille polymerization in miniemulsions; ORGANIC PHOTOVOLTAIC DEVICES; DONOR-ACCEPTOR COPOLYMERS; INTERCHAIN AGGREGATION; TRITHIOPHENE DONOR; MOLECULAR DESIGN; BUILDING-BLOCKS; HOLE MOBILITY; BANDGAP; BENZODITHIOPHENE; DISPERSIONS;
D O I
10.1002/marc.201700001
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The development of photovoltaic polymers based on C(3)h-symmetric benzotrithiophene (C(3)h-BTT), an analogue of the well-known benzodithiophene (BDT) donor unit, has been severely limited due to difficult processability. Here the authors report the preparation of solution-processable C(3)h-BTT-based hyperbranched conjugated polymer nanoparticles (BTT-HCPNs) with tunable particle sizes via Stille miniemulsion polymerization. Compared with the corresponding star-shaped small molecule (C(3)h-BTT core with three diketopyrrolopyrrole arms, BTT-3DPP) with a wide bandgap (1.83 eV), both BTT-HCPNs show strong aggregation even in dilute solutions, leading to much-extended absorption (up to approximate to 1000 nm) and lower bandgaps (1.38 eV). The larger BTT-HCPN particle exhibits stronger aggregation and more extended absorption than the smaller one. As a result, solar cells fabricated from BTT-HCPNs/PC71BM solutions show a power conversion efficiency up to 1.51% after DIO additive treatment, much higher than that of BTT-3DPP (0.31%).
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页数:8
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