钝化
钙钛矿(结构)
材料科学
分子
能量转换效率
路易斯酸
卤化物
基础(拓扑)
光电子学
纳米技术
化学
无机化学
催化作用
结晶学
有机化学
数学分析
数学
图层(电子)
作者
Jing Wang,Jie Zhang,Yingzhi Zhou,Hongbin Liu,Qifan Xue,Xiaosong Li,Chu‐Chen Chueh,Hin‐Lap Yip,Zonglong Zhu,Alex K.‐Y. Jen
标识
DOI:10.1038/s41467-019-13909-5
摘要
Abstract All-inorganic perovskite solar cells (PVSCs) have drawn increasing attention because of their outstanding thermal stability. However, their performance is still inferior than the typical organic-inorganic counterparts, especially for the devices with p-i-n configuration. Herein, we successfully employ a Lewis base small molecule to passivate the inorganic perovskite film, and its derived PVSCs achieved a champion efficiency of 16.1% and a certificated efficiency of 15.6% with improved photostability, representing the most efficient inverted all-inorganic PVSCs to date. Our studies reveal that the nitrile (C-N) groups on the small molecule effectively reduce the trap density of the perovskite film and thus significantly suppresses the non-radiative recombination in the derived PVSC by passivating the Pb-exposed surface, resulting in an improved open-circuit voltage from 1.10 V to 1.16 V after passivation. This work provides an insight in the design of functional interlayers for improving efficiencies and stability of all-inorganic PVSCs.
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