Fused Nonacyclic Electron Acceptors for Efficient Polymer Solar Cells

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...

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Veröffentlicht in:Journal of the American Chemical Society 2017-01, Vol.139 (3), p.1336-1343
Hauptverfasser: Dai, Shuixing, Zhao, Fuwen, Zhang, Qianqian, Lau, Tsz-Ki, Li, Tengfei, Liu, Kuan, Ling, Qidan, Wang, Chunru, Lu, Xinhui, You, Wei, Zhan, Xiaowei
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Sprache:eng
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Zusammenfassung: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.
ISSN:0002-7863
1520-5126
DOI:10.1021/jacs.6b12755