卤化物
铅(地质)
降级(电信)
材料科学
钙钛矿(结构)
化学
环境科学
环境化学
无机化学
地质学
结晶学
计算机科学
电信
地貌学
作者
Gianluca Grimaldi,Imme Schuringa,Jaco J. Geuchies,Susan A. Rigter,T.H. Hoekstra,Jan Versluis,Juanita Hidalgo,Juan‐Pablo Correa‐Baena,Jorik van de Groep,Heejae Kim,Mischa Bonn,Bruno Ehrler
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2024-11-07
卷期号:: 5771-5779
标识
DOI:10.1021/acsenergylett.4c02300
摘要
Quasi-2D perovskites have been pivotal in recent efforts to stabilize perovskite solar cells. Despite the stability boost provided when these materials are introduced in perovskite solar cells, little is known about the intrinsic light and environmental stability of quasi-2D perovskites. In this study, we characterize the photostability of exfoliated quasi-2D perovskite single crystals in air using photoluminescence, infrared, X-ray fluorescence, and energy-dispersive X-ray spectroscopy. Photoexcitation leads to severe material loss with oxygen as a prerequisite for material breakdown. The effect can be traced to the formation of reactive oxygen species, as demonstrated by increases in the photostability under oxygen-free conditions. We show the effect of combined passivation steps, showcasing the stability enhancement offered by 2D-capping layers in combination with an oxygen-free atmosphere. Our results reveal that the stability of illuminated quasi-2D perovskites depends critically on oxygen exposure, highlighting the importance of oxygen-blocking passivation strategies for stable 2D perovskite-based devices.
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