A Difluoro‐Monobromo End Group Enables High‐Performance Polymer Acceptor and Efficient All‐Polymer Solar Cells Processable with Green Solvent under Ambient Condition

In this paper, a difluoro‐monobromo end group is designed and synthesized, which is then used to construct a novel polymer acceptor (named PY2F‐T) yielding high‐performance all‐polymer solar cells with 15.22% efficiency. The fluorination strategy can increase the intramolecular charge transfer and i...

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Veröffentlicht in:Advanced functional materials 2021-06, Vol.31 (25), p.n/a
Hauptverfasser: Yu, Han, Luo, Siwei, Sun, Rui, Angunawela, Indunil, Qi, Zhenyu, Peng, Zhengxing, Zhou, Wentao, Han, Han, Wei, Rong, Pan, Mingao, Cheung, Andy Man Hong, Zhao, Dahui, Zhang, Jianquan, Ade, Harald, Min, Jie, Yan, He
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container_issue 25
container_start_page
container_title Advanced functional materials
container_volume 31
creator Yu, Han
Luo, Siwei
Sun, Rui
Angunawela, Indunil
Qi, Zhenyu
Peng, Zhengxing
Zhou, Wentao
Han, Han
Wei, Rong
Pan, Mingao
Cheung, Andy Man Hong
Zhao, Dahui
Zhang, Jianquan
Ade, Harald
Min, Jie
Yan, He
description In this paper, a difluoro‐monobromo end group is designed and synthesized, which is then used to construct a novel polymer acceptor (named PY2F‐T) yielding high‐performance all‐polymer solar cells with 15.22% efficiency. The fluorination strategy can increase the intramolecular charge transfer and interchain packing of the previous PY‐T based acceptor, and significantly improve photon harvesting and charge mobility of the resulting polymer acceptor. In addition, detailed morphology investigations reveal that the PY2F‐T‐based blend shows smaller domain spacing and higher domain purity, which significantly suppress charge recombination as supported by time‐resolved techniques. These polymer properties enable simultaneously enhanced JSC and FF of the PY2F‐T‐based devices, eventually delivering device efficiencies of over 15%, significantly outperforming that of the devices based on the non‐fluorinated PY‐T polymer (13%). More importantly, the PY2F‐T‐based active layers can be processed under ambient conditions and still achieve a 14.37% efficiency. They can also be processed using non‐halogenated solvent o‐xylene (no additive) and yield a decent performance of 13.05%. This work demonstrates the success of the fluorination strategy in the design of high‐performance polymer acceptors, which provide guidelines for developing new all‐PSCs with better efficiencies and stabilities for commercial applications. A novel polymer acceptor PY2F‐T with difluoro‐monobromo end groups on monomer sub‐units is synthesized, exhibiting extended absorption and stronger crystallinity compared to its non‐fluorinated counterpart (PY‐T). When employed in all‐polymer solar cells, the PY2F‐T based device yields an outstanding efficiency of 15.22% and retains a decent performance of 13.05% when processed under ambient conditions with an eco‐friendly solvent (o‐xylene, no additive).
doi_str_mv 10.1002/adfm.202100791
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The fluorination strategy can increase the intramolecular charge transfer and interchain packing of the previous PY‐T based acceptor, and significantly improve photon harvesting and charge mobility of the resulting polymer acceptor. In addition, detailed morphology investigations reveal that the PY2F‐T‐based blend shows smaller domain spacing and higher domain purity, which significantly suppress charge recombination as supported by time‐resolved techniques. These polymer properties enable simultaneously enhanced JSC and FF of the PY2F‐T‐based devices, eventually delivering device efficiencies of over 15%, significantly outperforming that of the devices based on the non‐fluorinated PY‐T polymer (13%). More importantly, the PY2F‐T‐based active layers can be processed under ambient conditions and still achieve a 14.37% efficiency. They can also be processed using non‐halogenated solvent o‐xylene (no additive) and yield a decent performance of 13.05%. 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This work demonstrates the success of the fluorination strategy in the design of high‐performance polymer acceptors, which provide guidelines for developing new all‐PSCs with better efficiencies and stabilities for commercial applications. A novel polymer acceptor PY2F‐T with difluoro‐monobromo end groups on monomer sub‐units is synthesized, exhibiting extended absorption and stronger crystallinity compared to its non‐fluorinated counterpart (PY‐T). 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source Wiley Journals
subjects Addition polymerization
all‐polymer solar cells
Charge transfer
Construction standards
Domains
fluorinated end group
Fluorination
Materials science
Morphology
Photovoltaic cells
polymer acceptors
Polymers
Solar cells
Solvents
Xylene
title A Difluoro‐Monobromo End Group Enables High‐Performance Polymer Acceptor and Efficient All‐Polymer Solar Cells Processable with Green Solvent under Ambient Condition
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