钙钛矿(结构)
钝化
异质结
位阻效应
插层(化学)
材料科学
卤化物
无机化学
光电子学
化学工程
化学
纳米技术
结晶学
立体化学
图层(电子)
工程类
作者
Yanfeng Miao,Meng Ren,Haifei Wang,Lei Lu,Xiaomin Liu,Yuetian Chen,Yixin Zhao
标识
DOI:10.1002/anie.202312726
摘要
Abstract Compared to widely adopted low‐dimensional/three‐dimensional (LD/3D) heterostructure, functional organic cation based surface termination on perovskite can not only realize advantage of defect passivation but also prevent potential disadvantage of the heterostructure induced intercalation into 3D perovskite. However, it is still very challenging to controllably construct surface termination on organic–inorganic hybrid perovskite because the functional organic cations’ substitution reaction is easy to form LD/3D heterostructure. Here, we report using a novel benzyltrimethylammonium (BTA) functional cation with rational designed steric hindrance to effectively surface terminate onto methylammonium lead triiodide (MAPbI 3 ) perovskite, which is composed of the most unstable MA cations. The BTA cation is difficult to form a specific 1.5‐dimensional perovskite of BTA 4 Pb 3 I 10 by cation substitution with MA cation, which then provides a wide processing window (around 10 minutes) for surface terminating on MAPbI 3 films. Moreover, the BTAI surface terminated BTAI‐MAPbI 3 shows better passivation effect than BTA 4 Pb 3 I 10 ‐MAPbI 3 heterojunction. Finally, BTAI surface terminated solar cell (0.085 cm 2 ) and mini‐module (11.52 cm 2 ) obtained the efficiencies of 22.03 % and 18.57 %, which are among the highest efficiencies for MAPbI 3 based ones.
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