Highly efficient polymer solar cells by step-by-step optimizing donor molecular packing and acceptor redistribution

Qianqian Sun, Fujun Zhang*, Qiaoshi An, Miao Zhang, Jian Wang, Jian Zhang

*Corresponding author for this work

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Abstract

The dynamic drying process of the active layer should play a vitally important role in determining the performance of polymer solar cells (PSCs). Donor molecular packing and acceptor redistribution can be optimized by two successive post-treatments on the active layer. The blend films were freshly prepared by spin-coating method and then immediately transferred to a covered glass Petri dish to allow self-assembly of the donor molecules. The films were then treated with methanol or PFN-methanol solution to adjust the acceptor redistribution. In this study, power conversion efficiencies (PCEs) of PSCs with PffBT4T-2OD:PC71BM as the active layer were improved from 6.74% to 8.75% by employing 80 min for self-assembly and 20 s of methanol soaking. The PCE was improved even further to 9.72% by inserting a PFN interfacial layer. The performance improvement was mainly attributed to the optimized PffBT4T-2OD molecular packing during the self-assembly process, ideal vertical phase separation driven by methanol soaking and efficient charge collection by insertion of a PFN interfacial layer. The molecular packing and vertical phase separation were characterized by grazing incidence X-ray diffraction (GIXD), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS), respectively. The experimental results solidly supported the effectiveness of the step-by-step optimization strategy.

Original languageEnglish
Pages (from-to)709-716
Number of pages8
JournalPhysical Chemistry Chemical Physics
Volume19
Issue number1
DOIs
Publication statusPublished - 2017
Externally publishedYes

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Sun, Q., Zhang, F., An, Q., Zhang, M., Wang, J., & Zhang, J. (2017). Highly efficient polymer solar cells by step-by-step optimizing donor molecular packing and acceptor redistribution. Physical Chemistry Chemical Physics, 19(1), 709-716. https://doi.org/10.1039/c6cp06692e