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,Ruxin Guo,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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