光伏
卤化物
存水弯(水管)
光电子学
材料科学
钙钛矿(结构)
纳米技术
化学工程
化学
光伏系统
环境科学
无机化学
结晶学
电气工程
环境工程
工程类
作者
Eric T. Hoke,Daniel J. Slotcavage,Emma R. Dohner,Andrea R. Bowring,Hemamala I. Karunadasa,Michael D. McGehee
出处
期刊:Chemical Science
[Royal Society of Chemistry]
日期:2014-11-04
卷期号:6 (1): 613-617
被引量:2244
摘要
. Photoluminescence (PL) spectra of these perovskites develop a new, red-shifted peak at 1.68 eV that grows in intensity under constant, 1-sun illumination in less than a minute. This is accompanied by an increase in sub-bandgap absorption at ∼1.7 eV, indicating the formation of luminescent trap states. Light soaking causes a splitting of X-ray diffraction (XRD) peaks, suggesting segregation into two crystalline phases. Surprisingly, these photo-induced changes are fully reversible; the XRD patterns and the PL and absorption spectra revert to their initial states after the materials are left for a few minutes in the dark. We speculate that photoexcitation may cause halide segregation into iodide-rich minority and bromide-enriched majority domains, the former acting as a recombination center trap. This instability may limit achievable voltages from some mixed-halide perovskite solar cells and could have implications for the photostability of halide perovskites used in optoelectronics.
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