离子
材料科学
化学物理
钙钛矿(结构)
热的
磁滞
卤化物
再分配(选举)
离子键合
压力(语言学)
热稳定性
金属
谱线
光谱学
分析化学(期刊)
晶体缺陷
介电谱
化学
电子迁移率
载流子密度
离子运输机
二次离子质谱
作者
Manjeet Kumar,Changzeng Ding,Jiansheng Yang,Oskar J. Sandberg,Mathias Nyman,Chang-Qi Ma,R. Österbacka
标识
DOI:10.1021/acs.jpclett.5c03513
摘要
Ion migration is a key phenomenon that influences the performance and stability of metal halide perovskite solar cells (PSCs). In this work, we systematically study how ion mobility evolves under thermal stress at 85 °C, using capacitance-frequency (C-f) spectroscopy measured in the dark. Aided by drift-diffusion simulations, we demonstrate that the measured C-f spectra cannot be reproduced using a single anion density with a unique ion mobility, particularly in the low-frequency domain where nonideal behavior emerges. A double-Gaussian distribution of anion mobilities provides a substantially better fit even for fresh devices and remains necessary after prolonged aging under thermal stress. This evolution suggests that heat stress not only influences the redistribution of mobile ions but also induces morphology-related changes, such as interface modifications and interlayer degradation, which collectively alter the electrochemical response of the device. Furthermore, the experimental hysteresis index (HI) for fresh and aged devices cannot be captured by assuming a single ion mobility, indicating that a distribution of ion mobilities is necessary to fully describe hysteresis behavior. These findings elucidate the complex ion dynamics under thermal stress and point toward the presence of distinct ionic populations contributing to device behavior, with implications for improving PSC stability.
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