钙钛矿(结构)
光电流
材料科学
正交晶系
光电子学
光致发光
光电探测器
相(物质)
半导体
薄膜
辐照
纳米技术
化学物理
化学
晶体结构
结晶学
物理
有机化学
核物理学
作者
Binbin Jin,Fei Liang,Ding Zhao,Yihan Lu,Lufang Liu,Fengjiang Liu,Zhong Chen,Gang Bi,Pan Wang,Qing Zhang,Min Qiu
出处
期刊:Nano Letters
[American Chemical Society]
日期:2022-09-13
卷期号:22 (18): 7449-7456
被引量:3
标识
DOI:10.1021/acs.nanolett.2c02368
摘要
Organic-inorganic hybrid perovskites (OIHPs) with superior optoelectronic properties have emerged as revolutionary semiconductor materials for diverse applications. A fundamental understanding of the interplay between the microscopic molecular-level structure and the macroscopic optoelectronic properties is essential to boost device performance toward theoretical limits. Here, we reveal the critical role of CH3NH3+ (MA) in the regulation of the physicochemical and optoelectronic properties of a MAPbI3 film irradiated by an electron beam at 130 K. The order-to-disorder transformation of the MA cation not only leads to a notably enhanced photoluminescence emission but also results in the suppression of the orthorhombic phase down to 85 K. Taking advantage of the regulation of MA cation dynamics, we demonstrate a perovskite photodetector with 100% photocurrent enhancement and long-term stability exceeding one month. Our study provides a powerful tool for regulating the optoelectronic properties and stabilities of perovskites and highlights potential opportunities related to the organic cation in OIHPs.
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