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Fused Nonacyclic Electron Acceptors for Efficient Polymer Solar Cells.
Dai, Shuixing; Zhao, Fuwen; Zhang, Qianqian; Lau, Tsz-Ki; Li, Tengfei; Liu, Kuan; Ling, Qidan; Wang, Chunru; Lu, Xinhui; You, Wei; Zhan, Xiaowei.
Affiliation
  • Dai S; Department of Materials Science and Engineering, College of Engineering, Key Laboratory of Polymer Chemistry and Physics of Ministry of Education, Peking University , Beijing 100871, China.
  • Zhao F; Fujian Key Laboratory of Polymer Materials, College of Materials Science and Engineering, Fujian Normal University , Fuzhou 350007, China.
  • Zhang Q; Institute of Chemistry, Chinese Academy of Sciences , Beijing 100190, China.
  • Lau TK; Department of Chemistry, University of North Carolina at Chapel Hill , Chapel Hill, North Carolina 27599-3290, United States.
  • Li T; Department of Physics, Chinese University of Hong Kong , New Territories, Hong Kong, China.
  • Liu K; Department of Materials Science and Engineering, College of Engineering, Key Laboratory of Polymer Chemistry and Physics of Ministry of Education, Peking University , Beijing 100871, China.
  • Ling Q; Department of Materials Science and Engineering, College of Engineering, Key Laboratory of Polymer Chemistry and Physics of Ministry of Education, Peking University , Beijing 100871, China.
  • Wang C; Fujian Key Laboratory of Polymer Materials, College of Materials Science and Engineering, Fujian Normal University , Fuzhou 350007, China.
  • Lu X; Institute of Chemistry, Chinese Academy of Sciences , Beijing 100190, China.
  • You W; Department of Physics, Chinese University of Hong Kong , New Territories, Hong Kong, China.
  • Zhan X; Department of Chemistry, University of North Carolina at Chapel Hill , Chapel Hill, North Carolina 27599-3290, United States.
J Am Chem Soc ; 139(3): 1336-1343, 2017 01 25.
Article in En | MEDLINE | ID: mdl-28059503
ABSTRACT
We design and synthesize four fused-ring electron acceptors based on 6,6,12,12-tetrakis(4-hexylphenyl)-indacenobis(dithieno[3,2-b;2',3'-d]thiophene) as the electron-rich unit and 1,1-dicyanomethylene-3-indanones with 0-2 fluorine substituents as the electron-deficient units. These four molecules exhibit broad (550-850 nm) and strong absorption with high extinction coefficients of (2.1-2.5) × 105 M-1 cm-1. Fluorine substitution downshifts the LUMO energy level, red-shifts the absorption spectrum, and enhances electron mobility. The polymer solar cells based on the fluorinated electron acceptors exhibit power conversion efficiencies as high as 11.5%, much higher than that of their nonfluorinated counterpart (7.7%). We investigate the effects of the fluorine atom number and position on electronic properties, charge transport, film morphology, and photovoltaic properties.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Am Chem Soc Year: 2017 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Am Chem Soc Year: 2017 Document type: Article Affiliation country:
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