插层(化学)
钙钛矿(结构)
铯
离子交换
无机化学
图层(电子)
化学
化学工程
材料科学
离子
纳米技术
结晶学
有机化学
工程类
作者
Xiaomin Liu,Xingtao Wang,Taiyang Zhang,Yanfeng Miao,Zhixiao Qin,Yuetian Chen,Yixin Zhao
标识
DOI:10.1002/anie.202102538
摘要
Abstract The in situ formation of reduced dimensional perovskite layer via post‐synthesis ion exchange has been an effective way of passivating organic‐inorganic hybrid perovskites. In contrast, cesium ions in Cs‐based inorganic perovskite with strong ionic binding energy cannot exchange with those well‐known organic cations to form reduced dimensional perovskite. Herein, we demonstrate that tetrabutylammonium (TBA + ) cation can intercalate into CsPbI 3 to effectively substitute the Cs cation and to form one‐dimensional (1D) TBAPbI 3 layer in the post‐synthesis TBAI treatment. Such TBA cation intercalation leads to in situ formation of TBAPbI 3 protective layer to heal defects at the surface of inorganic CsPbI 3 perovskite. The TBAPbI 3 ‐CsPbI 3 perovskite exhibited enhanced stability and lower defect density, and the corresponding perovskite solar cell devices achieved an improved efficiency up to 18.32 % compared to 15.85 % of the control one.
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