光致发光
钙钛矿(结构)
离子键合
卤化物
材料科学
扩散
离子
化学物理
光电子学
相(物质)
光谱学
分析化学(期刊)
光伏
工作(物理)
离子电导率
薄膜
分子物理学
光伏系统
作者
Sarah C. Gillespie,Jérôme Gautier,Linde M. van de Ven,Agustin O. Alvarez,Bruno Ehrler,L.J. Geerligs,Veronique S. Gevaerts,Gianluca Coletti,Erik C. Garnett
标识
DOI:10.1021/acsenergylett.5c04253
摘要
Halide perovskites exhibit coupled electronic-ionic properties that govern photovoltaic performance and stability; understanding ionic transport is, thus, essential for optimized photovoltaics. Characterizing ions with electrical techniques requires complete devices, yet electrical results are often dominated by interfacial effects over intrinsic ionic behavior. Here, localized-intensity-modulated photoluminescence spectroscopy (IMPLS) is used to optically probe ionic processes in a triple-cation, mixed-halide perovskite film. An analytical diffusion model is proposed to describe the IMPLS trends. The model indicates that mobile defects migrate laterally from high light intensity regions, with ionic diffusion coefficients extracted from IMPLS agreeing with the literature values. Moreover, spatially mapping IMPLS enables the separation of mobile and immobile defect contributions to the photoluminescence by quantifying the difference between the area-averaged photoluminescence intensity and phase shift. Ultimately, this work demonstrates that localized IMPLS provides a means to extract lateral ion diffusion coefficients while spatially distinguishing defect types across the sample.
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