期刊
POLYMER CHEMISTRY
卷 8, 期 36, 页码 5496-5503出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c7py01089c
关键词
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资金
- National Key Basic Research and Development Program of China (973 program) [2014CB643504, 2015CB655001]
- National Natural Science Foundation of China [51373165, 21625403]
- Strategic Priority Research Program of Chinese Academy of Sciences [XDB12010200]
- State Key Laboratory of Luminescence and Applications [SKLA-2016-02]
For solution processability of polymer solar cells (PSCs), polymer electron donors are almost always composed of conjugated main chains and flexible alkyl side chains. In this paper, we report a polymer electron donor based on isoindigo units bearing branched oligo(ethylene glycol) (OEG) side chains, P-OEG. Compared with the control polymer bearing alkyl side chains (P-Alkyl), P-OEG exhibits not only a smaller pi-pi stacking distance and redshifted absorption spectra, but also larger surface energy for better compatibility with the [6,6]-phenyl-C-71-butyric acid methyl ester (PC71BM) electron acceptor. The PSC device of P-OEG exhibits an open-circuit voltage (VOC) of 0.73 V, short-circuit current density (J(SC)) of 13.92 mA cm(-2), and fill factor (FF) of 0.50, corresponding to the power conversion efficiency (PCE) of 5.10%. This performance is higher than that of P-Alkyl (PCE = 3.0%), which is attributed to the finer phase separation morphology of the P-OEG: PC71BM blend than that of the P-Alkyl: PC71BM blend. These results suggest that the branched OEG side chain is an effective approach to improve the PSC device performance of some polymer electron donors.
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