钝化
材料科学
钙钛矿(结构)
离子键合
化学计量学
图层(电子)
碘化物
纳米技术
化学工程
无机化学
离子
物理化学
有机化学
化学
工程类
作者
Haifei Wang,Bowei Li,Fang Liu,Wenji Zhan,Menglei Feng,Jiahao Guo,Shaowei Wang,Yugang Liang,Yingping Fan,Yuetian Chen,Yanfeng Miao,Yixin Zhao
标识
DOI:10.1002/adfm.202423397
摘要
Abstract Surface termination is so far the mainstream passivating method to enhance the performance of CsPbI 3 solar cells. However, surface termination can hardly achieve effective and homogeneous passivation on large‐area CsPbI 3 films, which is one key challenge toward high‐performance inorganic perovskite solar modules (PSMs). The strong ionic bond between Cs and the Pb‐I framework in inorganic CsPbI 3 makes it difficult to construct 2D perovskite layer on film surface via post treatment, which is otherwise a classic and effectual approach for defect elimination in organic–inorganic hybrid perovskites. Herein, a novel and programmable surface reconstruction strategy is reported that can facilely tune surface termination to 2D passivation on CsPbI 3 perovskite using 2‐(1‐cyclohexenyl) ethyl ammonium iodide (CHEAI). In comparison to surface termination, the in situ formation of 2D CHEA 2 PbI 4 by adjusting the stoichiometry of CHEAI demonstrates more comprehensive passivation effects and favorable energy level alignment for CsPbI 3 films. Such 2D construction has greatly facilitated the enhancement on device performance, especially when scaling up the area. The optimal CsPbI 3 PSM (active area of 12.44 cm 2 ) based on 2D CHEA 2 PbI 4 achieves a record‐high efficiency of 19.32% (certified efficiency of 18.83%) with much improved stability, endorsing the practical promotion of this intrinsically stable perovskite material.
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