Random terpolymer based on thiophene-thiazolothiazole unit enabling efficient non-fullerene organic solar cells

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作者
Jingnan Wu
Guangwei Li
Jin Fang
Xia Guo
Lei Zhu
Bing Guo
Yulong Wang
Guangye Zhang
Lingeswaran Arunagiri
Feng Liu
He Yan
Maojie Zhang
Yongfang Li
机构
[1] Soochow University,Laboratory of Advanced Optoelectronic Materials, College of Chemistry, Chemical Engineering and Materials Science
[2] Shanghai Jiao Tong University,Department of Physics and Astronomy and Collaborative Innovation Center of IFSA (CICIFSA)
[3] eFlexPV Limited,Department of Chemistry, Hong Kong Branch of Chinese National Engineering Research Center for Tissue Restoration & Reconstruction
[4] Flat/RM B,Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Organic Solids, Institute of Chemistry
[5] 12/F,undefined
[6] Hang Seng Causeway Bay BLDG,undefined
[7] Hong Kong University of Science and Technology (HKUST),undefined
[8] Chinese Academy of Sciences,undefined
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摘要
Developing a high-performance donor polymer is critical for achieving efficient non-fullerene organic solar cells (OSCs). Currently, most high-efficiency OSCs are based on a donor polymer named PM6, unfortunately, whose performance is highly sensitive to its molecular weight and thus has significant batch-to-batch variations. Here we report a donor polymer (named PM1) based on a random ternary polymerization strategy that enables highly efficient non-fullerene OSCs with efficiencies reaching 17.6%. Importantly, the PM1 polymer exhibits excellent batch-to-batch reproducibility. By including 20% of a weak electron-withdrawing thiophene-thiazolothiazole (TTz) into the PM6 polymer backbone, the resulting polymer (PM1) can maintain the positive effects (such as downshifted energy level and reduced miscibility) while minimize the negative ones (including reduced temperature-dependent aggregation property). With higher performance and greater synthesis reproducibility, the PM1 polymer has the promise to become the work-horse material for the non-fullerene OSC community.
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