Side-Chain Engineering of Non-Fullerene Acceptors with Trialkylsilyloxy Groups for Enhanced Photovoltaic Performance

被引:0
|
作者
Wang, Qingyuan [1 ]
Chen, Qi [1 ]
Meng, Shixin [1 ]
Tian, Li [2 ]
Wang, Haiqiao [3 ]
Chen, Yu [4 ]
Liu, Zitong [5 ]
Xue, Lingwei [6 ]
Zhang, Zhi-Guo [1 ]
机构
[1] Beijing Univ Chem Technol, Beijing Adv Innovat Ctr Soft Matter Sci & Engn, State Key Lab Chem Resource Engn, Beijing 100029, Peoples R China
[2] Henan Univ Technol, Sch Mat Sci & Engn, Zhengzhou 450001, Henan, Peoples R China
[3] Beijing Univ Chem Technol, Beijing Engn Res Ctr Synth & Applicat Waterborne P, Beijing 100029, Peoples R China
[4] Chinese Acad Sci, Inst High Energy Phys, Beijing 100049, Peoples R China
[5] Lanzhou Univ, Coll Chem & Chem Engn, State Key Lab Appl Organ Chem SKLAOC, Lanzhou 730000, Gansu, Peoples R China
[6] Pingdingshan Univ, Yaoshan Lab, Pingdingshan 467000, Henan, Peoples R China
基金
北京市自然科学基金; 中国国家自然科学基金;
关键词
Organic solar cells; Non-fullerene acceptors; Oligomers; Side-chain engineering; Energy conversion; Synthesis design; Donor-acceptor systems; ORGANIC SEMICONDUCTOR;
D O I
10.1002/cjoc.202400083
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Side-chain engineering has emerged as a highly effective strategy for tailoring the aggregation behavior and charge transport properties of non-fullerene small molecule acceptors (SMAs). In this study, we designed and synthesized two SMAs, namely BTPSi-Bu and BTPSi-Pr, respectively incorporating tributylsilyloxy and triisopropylsilyloxy groups in their outer positions. Notably, BTPSi-Bu exhibited better planarity, crystallization, and favorable phase separation when paired with PM6 donor polymer compared to its counterpart, BTPSi-Pr. The resulting organic solar cells, utilizing the PM6:BTPSi-Bu blend, demonstrated a remarkable power conversion efficiency of 17.41% and a high open-circuit voltage of 0.859 V. These findings underscore the significance of integrating trialkylsilyloxy side chains into SMAs as a rational design approach for enhancing the performance of photovoltaic systems.
引用
收藏
页码:2153 / 2160
页数:8
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