钙钛矿(结构)
材料科学
电场
纳米
晶界
光电子学
微晶
探测器
腐蚀
湿度
离子
电化学
氧气
电极
辐射
Crystal(编程语言)
铀
纳米技术
纳米线
单晶
粒子探测器
化学稳定性
钛
纳米颗粒
作者
Wenqing Zhang,Hu Wang,Jie Fu,Pengxiang Wang,H. B. Dong,Zijun Gao,Yuchuan Shao
标识
DOI:10.1021/acsenergylett.5c02178
摘要
While a high electric field enhances the sensitivity and response speed of MAPbBr3 single-crystal radiation detectors, it also triggers interfacial electrochemical corrosion and ion migration, compromising device stability. This study reveals that multivalent titanium ion (Ti4+) migration in MAPbBr3 single-crystal radiation detectors at a high electric field requires grain boundary (GBs) assistance and is confined to the polycrystalline regions, located hundreds of nanometers from the crystal surface. Consequently, device performance can be fully restored by removing the corroded surface and redepositing the electrode. Furthermore, our results also illustrate that humidity and oxygen in the atmosphere can accelerate the electrochemical reaction at the Ti/perovskite single-crystal interface, highlighting the importance of encapsulation for perovskite single-crystal-based devices.
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