钙钛矿(结构)
材料科学
异质结
碘化物
薄膜
水分
相(物质)
卤化物
图层(电子)
光电子学
相对湿度
化学物理
化学工程
无机化学
化学
纳米技术
复合材料
有机化学
工程类
热力学
物理
作者
Johannes Schlipf,Yinghong Hu,Shambhavi Pratap,Lorenz Bießmann,Nuri Hohn,Lionel Porcar,Thomas Bein,Pablo Docampo,Peter Müller‐Buschbaum
标识
DOI:10.1021/acsaem.9b00005
摘要
To increase the moisture stability of hybrid perovskite photovoltaics, a combination of three-dimensional (3D) and a thin layer of two-dimensional (2D) perovskite incorporating long-chained organic cations is often employed as photoabsorber. However, the detailed interaction between water and 3D/2D perovskite heterojunctions has not been elucidated yet. Using in situ neutron and X-ray scattering techniques, we reveal surprisingly strong water uptake into 3D/2D perovskite films despite the presence of hydrophobic bulky cations. Our results show rapid disproportionation of the initial 2D phase (number of layers, m = 5) in methylammonium lead iodide (MAPI)/2D films into lower m phases under humidity. Nevertheless, the 2D perovskite inhibits the irreversible PbI2 formation, which suggests that the suppression of I– and MA+ ion migration and consequently of MAI escape is related to the improved moisture stability of MAPI/2D perovskite films. In comparison, quadruple-cation perovskites including Rb+ exhibit poor stability toward phase segregation upon exposure to moisture regardless of the 2D perovskite layer.
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