卤化物
钙钛矿(结构)
金属卤化物
X射线光电子能谱
化学
卤素
金属
太阳能电池
光谱学
无机化学
分析化学(期刊)
化学工程
材料科学
结晶学
光电子学
有机化学
工程类
物理
烷基
量子力学
作者
Azat F. Akbulatov,Lyubov A. Frolova,Nadezhda N. Dremova,Ivan S. Zhidkov,В. М. Мартыненко,Sergey Tsarev,Sergey Yu. Luchkin,E.Z. Kurmaev,С. М. Алдошин,Keith J. Stevenson
标识
DOI:10.1021/acs.jpclett.9b03308
摘要
We report the first systematic assessment of intrinsic photothermal stability of a large panel of complex lead halides APbX3 incorporating different univalent cations (A = CH3NH3+, [NH2CHNH2]+, Cs+) and halogen anions (X = Br, I) using a series of analytical techniques such as UV–vis and X-ray photoelectron spectroscopy, X-ray diffraction, EDX analysis, atomic force and scanning electron microscopy, ESR spectroscopy, and mass spectrometry. We show that heat stress and light soaking induce a severe degradation of perovskite films even in the absence of oxygen and moisture. The stability of complex lead halides increases in the order MAPbBr3 < MAPbI3 < FAPbI3 < FAPbBr3 < CsPbI3 < CsPbBr3, thus featuring all-inorganic perovskites as the most promising absorbers for stable perovskite solar cells. An important correlation was found between the stability of the complex lead halides and the volatility of univalent cation halides incorporated in their structure. The established relationship provides useful guidelines for designing new complex metal halides with immensely improved stability.
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