Pinning Bromide Ion with Ionic Liquid in Lead-Free Cs2AgBiBr6 Double Perovskite Solar Cells

被引:61
|
作者
Li, Jiangning [1 ]
Meng, Xianghuan [1 ]
Wu, Zhiheng [1 ]
Duan, Yanyan [1 ]
Guo, Ruxin [1 ]
Xiao, Weidong [1 ,2 ]
Zhang, Yongshang [1 ,2 ]
Li, Yukun [1 ]
Shen, Yonglong [1 ,2 ]
Zhang, Wei [3 ]
Shao, Guosheng [1 ,2 ]
机构
[1] Zhengzhou Univ, State Ctr Int Cooperat Designer Low Carbon & Envi, Sch Mat Sci & Engn, Zhengzhou 450001, Henan, Peoples R China
[2] Zhengzhou Mat Genome Inst ZMGI, Bldg 2, Zhengzhou 450100, Peoples R China
[3] Univ Surrey, Adv Technol Inst ATI, Guildford GU2 7XH, Surrey, England
基金
欧盟地平线“2020”; 中国国家自然科学基金; 中国博士后科学基金;
关键词
energy band; ion migration; ionic liquid; lead-free double perovskites; stability; DEFECT PASSIVATION; OPTICAL-PROPERTIES; STABILITY; PERFORMANCE; EFFICIENCY; CATION;
D O I
10.1002/adfm.202112991
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Lead-free Cs2AgBiBr6 double perovskite has received widespread attention because of its non-toxicity and high thermal stability. However, intrinsic bromide ion (Br-) migration limits continuous operation of Cs2AgBiBr6-based perovskite solar cells (PSCs). Herein, an operational and simple strategy is carried out to improve the power conversion efficiency (PCE) and long-term stability of Cs2AgBiBr6-based PSCs by introducing 1-butyl-1-methylpyrrolidinium chloride (BMPyrCl) and 1-butyl-3-methylpyridinium chloride (BMPyCl) ionic liquids (ILs). The higher binding energy between Br- in Cs2AgBiBr6 and cation in IL containing pyrrole can inhibit Br- migration effectively, thereby reducing film defects and improving energy level matching. The optimized PCE of 2.22% is obtained for hole transport layer-free, carbon-based PSC, which hardly degrades at 40% +/- 5% relative humidity and 25 degrees C for 40 days. This work highlights an effective method to mitigate the halide migration in Cs2AgBiBr6 perovskite, thus providing an effective route in promoting the development of lead-free double PSCs.
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页数:8
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