钙钛矿(结构)
材料科学
卤化物
X射线光电子能谱
表征(材料科学)
薄膜
化学物理
通量
光谱学
化学工程
光电子学
纳米技术
光学
无机化学
化学
物理
量子力学
工程类
激光器
作者
Guillaume Vidon,Pia Dally,Mirella Al‐Katrib,Daniel S. Ory,Minjin Kim,Etienne Soret,Eva Rangayen,Marie Legrand,Alexandre Blaizot,Philip Schulz,Jean‐Baptiste Puel,Daniel Suchet,Jean‐François Guillemoles,Arnaud Etchéberry,Muriel Bouttemy,Stéfania Cacovich
标识
DOI:10.1002/adfm.202304730
摘要
Abstract Understanding the effects of X‐rays on halide perovskite thin films is critical for accurate and reliable characterization of this class of materials, as well as their use in detection systems. In this study, advanced optical imaging techniques are employed, both spectrally and temporally resolved, coupled with chemical characterizations to obtain a comprehensive picture of the degradation mechanism occurring in the material during photoemission spectroscopy measurements. Two main degradation pathways are identified through the use of local correlative physico‐chemical analysis. The first one, at low X‐Ray fluence, shows minor changes of the surface chemistry and composition associated with the formation of electronic defects. Moreover, a second degradation route occurring at higher fluence leads to the evaporation of the organic cations and the formation of an iodine‐poor perovskite. Based on the local variation of the optoelectronic properties, a kinetic model describing the different mechanisms is proposed. These findings provide valuable insight on the impact of X‐rays on the perovskite layers during investigations using X‐ray based techniques. More generally, a deep understanding of the interaction mechanism of X‐rays with perovskite thin films is essential for the development of perovskite‐based X‐ray detectors and solar for space applications.
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