钙钛矿(结构)
卤化物
碘化物
溴
分解
材料科学
相(物质)
化学工程
扩散
原位
化学稳定性
化学
扩散阻挡层
水分
矿物学
衍射
粒度
无机化学
分析化学(期刊)
作者
Adam Wincukiewicz,Małgorzata M. Brzóska,Aliaksei Bohdan,Rafał Bożek,M. Kamińska,Jacek B. Jasiński
标识
DOI:10.1016/j.solmat.2026.114278
摘要
The poor environmental stability of three-dimensional (3D) halide perovskites remains a critical barrier to their commercialization. Mixed-dimensional systems incorporating two-dimensional (2D) perovskites have shown improved stability, yet high 2D fractions often compromise optoelectronic performance. Here, we demonstrate that introducing only 0.02 (2%) 2D perovskite into methylammonium lead iodide (MAPI) films - both undoped and with 15% nominal bromine substitution - yields a pronounced enhancement in intrinsic environmental stability. Long-term (∼3000 h) in situ X-ray diffraction measurements on non-encapsulated films exposed to ambient air (∼40% relative humidity) reveal a two-to four-fold reduction in perovskite decomposition and PbI 2 formation rate, with a significant fraction of the perovskite phase remaining intact. This stabilization arises from the preferential localization of the 2D phase at film surfaces and grain boundaries, where it encapsulates 3D grains and kinetically suppresses diffusion of reactive species such as moisture and oxygen. Bromine incorporation provides an additional, though smaller, stabilizing effect. These findings identify low-fraction 2D incorporation as a highly efficient and scalable strategy for enhancing the environmental stability of hybrid perovskites.
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