Jiangning LiXianghuan MengZhiheng WuYanyan DuanRuxin GuoWeidong XiaoYongshang ZhangYukun LiYonglong ShenWei ZhangGuosheng Shao
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.
Wolfgang TressMaximilian T. Sirtl
Nathan DaemJennifer DewalqueFelix LangAnthony MahoGilles SpronckCatherine HenristPierre ColsonSamuel D. StranksRudi Cloots
Mehri GhasemiLei ZhangJung‐Ho YunMengmeng HaoDongxu HePeng ChenYang BaiTongen LinMu XiaoAijun DuMiaoqiang LyuLianzhou Wang
Baoning WangNa LiLin YangChunxiang Dall’AgneseAjay Kumar JenaTsutomu MiyasakaXiaofeng Wang
Fuxiang JiJohan KlarbringFeng WangWeihua NingLinqin WangChunyang YinJ. FigueroaChristian Kolle ChristensenMartin EtterThomas EderthLicheng SunS. I. SimakIgor A. AbrikosovFeng Gao