Fluorination-enabled optimal morphology leads to over 11% efficiency for inverted small-molecule organic solar cells

被引:599
作者
Deng, Dan [1 ]
Zhang, Yajie [1 ]
Zhang, Jianqi [1 ]
Wang, Zaiyu [2 ]
Zhu, Lingyun [1 ]
Fang, Jin [1 ,3 ]
Xia, Benzheng [1 ]
Wang, Zhen [1 ]
Lu, Kun [1 ]
Ma, Wei [2 ]
Wei, Zhixiang [1 ,3 ]
机构
[1] CAS Ctr Excellence Nanosci, Natl Ctr Nanosci & Technol, CAS Key Lab Nanosyst & Hierarch Fabricat, Beijing 100190, Peoples R China
[2] Xi An Jiao Tong Univ, State Key Lab Mech Behav Mat, Xian 710049, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
OPEN-CIRCUIT VOLTAGE; POLYMER; PERFORMANCE; ENHANCEMENT; DESIGN;
D O I
10.1038/ncomms13740
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
Solution-processable small molecules for organic solar cells have attracted intense attention for their advantages of definite molecular structures compared with their polymer counterparts. However, the device efficiencies based on small molecules are still lower than those of polymers, especially for inverted devices, the highest efficiency of which is <9%. Here we report three novel solution-processable small molecules, which contain pi-bridges with gradient-decreased electron density and end acceptors substituted with various fluorine atoms (0F, 1F and 2F, respectively). Fluorination leads to an optimal active layer morphology, including an enhanced domain purity, the formation of hierarchical domain size and a directional vertical phase gradation. The optimal morphology balances charge separation and transfer, and facilitates charge collection. As a consequence, fluorinated molecules exhibit excellent inverted device performance, and an average power conversion efficiency of 11.08% is achieved for a two-fluorine atom substituted molecule.
引用
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页数:9
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