三卤化物
碘化物
卤化物
材料科学
钙钛矿(结构)
带隙
半导体
相(物质)
甲脒
化学物理
光电子学
结晶学
无机化学
化学
有机化学
作者
Yang Zhou,Simone C. W. van Laar,Daniele Meggiolaro,Luca Gregori,Samuele Martani,Jia‐Yong Heng,Kunal Datta,Jesús Jiménez‐López,Feng Wang,E Laine Wong,Isabella Poli,Antonella Treglia,Daniele Cortecchia,Mirko Prato,Libor Kobera,Feng Gao,Ni Zhao,René A. J. Janssen,Filippo De Angelis,Annamaria Petrozza
标识
DOI:10.1002/adma.202305567
摘要
Abstract Bandgap tunability of lead mixed halide perovskites (LMHPs) is a crucial characteristic for versatile optoelectronic applications. Nevertheless, LMHPs show the formation of iodide‐rich (I‐rich) phase under illumination, which destabilizes the semiconductor bandgap and impedes their exploitation. Here, it is shown that how I 2 , photogenerated upon charge carrier trapping at iodine interstitials in LMHPs, can promote the formation of I‐rich phase. I 2 can react with bromide (Br − ) in the perovskite to form a trihalide ion I 2 Br − (I δ− ‐I δ+ ‐Br δ− ), whose negatively charged iodide (I δ− ) can further exchange with another lattice Br − to form the I‐rich phase. Importantly, it is observed that the effectiveness of the process is dependent on the overall stability of the crystalline perovskite structure. Therefore, the bandgap instability in LMHPs is governed by two factors, i.e., the density of native defects leading to I 2 production and the Br − binding strength within the crystalline unit. Eventually, this study provides rules for the design of chemical composition in LMHPs to reach their full potential for optoelectronic devices.
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