材料科学
卤化物
溴化物
钙钛矿(结构)
离子液体
离子
热稳定性
能量转换效率
氯化物
相对湿度
化学工程
离子键合
光电子学
无机化学
催化作用
有机化学
化学
冶金
工程类
物理
热力学
作者
Jiangning Li,Xianghuan Meng,Zhiheng Wu,Yanyan Duan,Guo Ru-xin,Weidong Xiao,Yongshang Zhang,Yukun Li,Yonglong Shen,Wei Zhang,Guosheng Shao
标识
DOI:10.1002/adfm.202112991
摘要
Abstract Lead‐free Cs 2 AgBiBr 6 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 Cs 2 AgBiBr 6 ‐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 Cs 2 AgBiBr 6 ‐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 Cs 2 AgBiBr 6 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 °C for 40 days. This work highlights an effective method to mitigate the halide migration in Cs 2 AgBiBr 6 perovskite, thus providing an effective route in promoting the development of lead‐free double PSCs.
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