甲脒
钙钛矿(结构)
卤化物
材料科学
光漂白
相(物质)
光致发光
化学物理
纳米技术
化学工程
光学
无机化学
光电子学
化学
荧光
物理
工程类
有机化学
作者
Davide Raffaele Ceratti,Yevgeny Rakita,Llorenç Cremonesi,Ron Tenne,Vyacheslav Kalchenko,Michael Elbaum,Dan Oron,M. A. C. Potenza,Gary Hodes,David Cahen
标识
DOI:10.1002/adma.201706273
摘要
Abstract Self‐healing, where a modification in some parameter is reversed with time without any external intervention, is one of the particularly interesting properties of halide perovskites. While there are a number of studies showing such self‐healing in perovskites, they all are carried out on thin films, where the interface between the perovskite and another phase (including the ambient) is often a dominating and interfering factor in the process. Here, self‐healing in perovskite (methylammonium, formamidinium, and cesium lead bromide (MAPbBr3, FAPbBr3, and CsPbBr3)) single crystals is reported, using two‐photon microscopy to create damage (photobleaching) ≈110 µm inside the crystals and to monitor the recovery of photoluminescence after the damage. Self‐healing occurs in all three perovskites with FAPbBr3 the fastest (≈1 h) and CsPbBr3 the slowest (tens of hours) to recover. This behavior, different from surface‐dominated stability trends, is typical of the bulk and is strongly dependent on the localization of degradation products not far from the site of the damage. The mechanism of self‐healing is discussed with the possible participation of polybromide species. It provides a closed chemical cycle and does not necessarily involve defect or ion migration phenomena that are often proposed to explain reversible phenomena in halide perovskites.
科研通智能强力驱动
Strongly Powered by AbleSci AI