卤化物
钙钛矿(结构)
离子
热稳定性
材料科学
结构稳定性
化学
化学物理
纳米技术
无机化学
结晶学
有机化学
结构工程
工程类
作者
Preethi Susan Mathew,Junsang Cho,Prashant V. Kamat
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2024-02-21
卷期号:9 (3): 1103-1114
被引量:11
标识
DOI:10.1021/acsenergylett.4c00093
摘要
Lower dimensional or 2D halide perovskites, with their versatile structural and functional properties, are known to improve the performance and room temperature stability of perovskite solar cells. One would expect 2D perovskites to be more resistant to ion migration compared to their 3D counterparts because of the presence of bulky organic cations. However, recent findings show that ion migration indeed is prevalent in 2D halide perovskites similar to 3D perovskites. Halide ion migration in 2D perovskites manifests itself in halide ion segregation under photoirradiation as well as in halide exchange between physically paired films of 2D perovskites with different halide ions. Besides halide ion migration, cation migration of spacer cations and A-site cations is also seen when 2D/3D perovskite films are subjected to light and thermal stress. It is important to recognize the importance of ion migration while incorporating 2D perovskites in solar cells and other optoelectronic devices, as it can be detrimental for achieving streamlined performance and long-term stability. This Perspective discusses recent reports on ion migration in 2D and in 2D/3D halide perovskite films under the operational conditions (at elevated temperature and given built-in bias) and presents a few mitigating strategies.
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