甲脒
钙钛矿(结构)
材料科学
能量转换效率
卤化物
钙钛矿太阳能电池
带隙
降级(电信)
相(物质)
化学工程
光电子学
无机化学
有机化学
化学
电子工程
工程类
作者
Xiaoxin Gao,Wen Luo,Yi Zhang,Ruiyuan Hu,Bao Zhang,Andreas Züttel,Yaqing Feng,Mohammad Khaja Nazeeruddin
标识
DOI:10.1002/adma.201905502
摘要
Abstract Organic–inorganic metal halide perovskite solar cells (PSCs) have achieved certified power conversion efficiency (PCE) of 25.2% with complex compositional and bandgap engineering. However, the thermal instability of methylammonium (MA) cation can cause the degradation of the perovskite film, remaining a risk for the long‐term stability of the devices. Herein, a unique method is demonstrated to fabricate highly phase‐stable perovskite film without MA by introducing cesium chloride (CsCl) in the double cation (Cs, formamidinium) perovskite precursor. Moreover, due to the suboptimal bandgap of bromide (Br − ), the amount of Br − is regulated, leading to high power conversion efficiency. As a result, MA‐free perovskite solar cells achieve remarkable long‐term stability and a PCE of 20.50%, which is one of the best results for MA‐free PSCs. Moreover, the unencapsulated device retains about 80% of the original efficiencies after a 1000 h aging study. These results provide a feasible approach to enhance solar cell stability and performance simultaneously, paving the way for commercializing PSCs.
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