钙钛矿(结构)
铅(地质)
相(物质)
材料科学
螯合作用
化学工程
化学
冶金
结晶学
有机化学
地质学
地貌学
工程类
作者
Shiheng Wang,Z. L. Miao,Jing Yang,Zhenkun Gu,Pengwei Li,Yiqiang Zhang,Yanlin Song
标识
DOI:10.1002/ange.202407192
摘要
Abstract Formamidinium‐lead triiodide (FAPbI 3 ) perovskite holds promise as a prime candidate in the realm of perovskite photovoltaics. However, the photo‐active α‐FAPbI 3 phase, existing as a metastable state, is observable solely at elevated temperatures and is susceptible to degradation into the δ‐phase in ambient air. Therefore, the attainment of phase‐stable α‐FAPbI 3 in ambient conditions has become a crucial objective in perovskite research. Here, we proposed an efficient conversion process of PbI 2 into the α‐FAPbI 3 perovskites in ambient air. This conversion was facilitated by the introduction of chelating molecules, which interacted with PbI 2 to form an intermediate phase. Due to the reduced formation barrier resulting from the altered reaction pathway, this stable intermediate phase transitioned directly into α‐FAPbI 3 upon the deposition of the organic cation solution, effectively bypassing the formation of δ‐FAPbI 3 . Consequently, the ambient‐fabricated FAPbI 3 perovskite solar cells (PSCs) exhibited an outstanding power conversion efficiency of 25.08 %, along with a high open‐circuit voltage of 1.19 V. Furthermore, the unencapsulated devices demonstrated remarkable environmental stability. Notably, this innovative approach promises broad applicability across various chelating molecules, opening new avenues for further progress in the ambient air fabrication of FAPbI 3 PSCs.
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