卤化物
钙钛矿(结构)
碘化物
二氯甲烷
溴化物
相(物质)
材料科学
光化学
化学
结晶学
无机化学
有机化学
溶剂
作者
Preethi Susan Mathew,Gábor Szabó,Masaru Kuno,Prashant V. Kamat
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2022-10-19
卷期号:7 (11): 3982-3988
被引量:16
标识
DOI:10.1021/acsenergylett.2c02026
摘要
Two-dimensional (2D) Ruddlesden–Popper mixed-halide perovskite films, BA2PbBr2I2, undergo phase segregation when excited with visible light to generate bromide- and iodide-rich regions, as marked by absorption and emission changes. Upon stopping illumination, the process reverses, allowing original film compositions to be restored. However, if films are in contact with dichloromethane, light irradiation causes the sequential expulsion of iodide and bromide and introduces irreversible changes to the 2D films. The sequential disappearance of I– and Br– from pristine films (BA2Pb2Br4 and BA2Pb2I4) under photoirradiation, as observed from variances in expulsion rates, reflects differences in halide ion mobilities in these films. The photoinstability of 2D films raises questions about their use in stabilizing bulk, three-dimensional (3D) perovskite solar cells through 3D/2D interfaces.
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