卤化物
脱质子化
材料科学
钙钛矿(结构)
铵
化学工程
无机化学
纳米技术
有机化学
离子
化学
工程类
作者
Chong Liu,Luyao Ma,Pengzhen Zhao,Yuan Li,Fengyuan Li,Zhiyu Fang,Qing Chang,Ning Jia,Pengfei Guo,Fei Guo,Zhe Liu,Ruihao Chen,Hongqiang Wang
标识
DOI:10.1002/adfm.202405735
摘要
Abstract Ammonium iodides are intensively investigated as effective interfacial passivation agents in perovskite solar cells (PSCs) while facing a major challenge of their high reactivity with perovskites that undermines the operational stability of the PSCs. Exemplified by involving rationally designed/selected peptide into the widely adopted phenethylammonium iodide (PEAI), the present work demonstrates that the bespoke peptide‐PEAI can effectively inhibit the deprotonation of ammonium iodides and thus hinder the formation of 2D perovskite, facilitating the stability enhancement in perovskite films by multi hydrogen bonding. The additional lone pair electrons provided by peptide molecules can also enhance the passivation ability of the modified layer. Attributed to the stable co‐modifier peptide‐PEAI, the small‐area FAPbI 3 ‐based PSCs yield a high efficiency of 25.02% with robust light and thermal stabilities. Moreover, the peptide‐PEAI‐based minimodules with an efficiency of 19.06% for a total area of 36 cm 2 manifested the great application potential of this co‐modification strategy in the perovskite photovoltaics.
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