材料科学
钙钛矿(结构)
光降解
卤化物
光致发光
光谱学
降级(电信)
化学工程
衍射
光电子学
纳米技术
结晶学
催化作用
光学
无机化学
光催化
有机化学
化学
电信
物理
工程类
量子力学
计算机科学
作者
Natalia N. Udalova,Sergey A. Fateev,Elizaveta Nemygina,Andrea Zanetta,Giulia Grancini,Eugene A. Goodilin,Alexey B. Tarasov
标识
DOI:10.1021/acsami.1c20043
摘要
Layered lead halide perovskites (2D LHPs) are attracting considerable attention as a promising material for a new generation of solar cell devices. LHPs have been presented as a more stable alternative to the more widespread 3D bulk perovskite materials; however, a critical analysis of their photostability is still lacking. In this work, we perform a comparative study between BA2MAn-1PbnI3n+1 (BA─butylammonium and MA─methylammonium) 2D LHPs with different dimensionalities (n = 1-3) and MAPbI3 3D perovskites. We compare different stability testing protocols including photometrical determination of iodine-containing products in nonpolar solvents, X-ray diffraction, and photoluminescence (PL) spectroscopy. The resulting trends of the photostability in an inert atmosphere based on PL spectroscopy measurements demonstrate a nonmonotonic dependence of the degradation rate on the perovskite layer thickness n with a "stability island" at n ≥ 3, which is caused by a combination of antibate factors of electronic structures and chemical compositions in the family of 2D perovskites. We also identify a critical oxygen concentration in the surrounding environment that affects the mechanism and strongly enhances the rate of layered perovskite photodegradation.
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