离子
钙钛矿(结构)
电容
光电子学
材料科学
离子键合
扩散
半导体
瞬态(计算机编程)
卤化物
光电探测器
化学物理
分析化学(期刊)
化学
物理
无机化学
计算机科学
电极
热力学
物理化学
操作系统
色谱法
有机化学
结晶学
作者
M. Schmidt,Agustín O. Alvarez,Jeroen J. de Boer,L. J. M. van de Ven,Bruno Ehrler
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2024-11-12
卷期号:9 (12): 5850-5858
被引量:24
标识
DOI:10.1021/acsenergylett.4c02446
摘要
The migration of mobile ions through the metal halide perovskite layer is still one of the main reasons for the poor stability of perovskite solar cells, LEDs, and photodetectors. To characterize mobile ions in the perovskite layer, time- and frequency-based electrical measurements are promising techniques. However, the presence of transport layers complicates their interpretation, limiting the information about mobile ions that can be extracted, and it is not clear how different features in frequency- and time-domain measurements relate to mobile ions. Here, we characterize a transport-layer-free device with capacitance frequency, capacitance transient, and current transient measurements in the dark, under illumination, and at different temperatures. We extract characteristic ionic signatures from the measurements, which we reproduce with drift-diffusion simulations for each technique. This allows us to explain the origins of the different ionic signatures, advancing our understanding of how electronic characterization techniques can be used to study the properties of mobile ions.
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