光电化学
卤化物
材料科学
金属
透视图(图形)
纳米技术
化学
电化学
无机化学
电极
计算机科学
冶金
物理化学
人工智能
作者
Zhaojian Xu,Ross A. Kerner,Leeor Kronik,Barry P. Rand
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2024-09-03
卷期号:: 4645-4654
标识
DOI:10.1021/acsenergylett.4c02033
摘要
Ion migration is a broad term used to account for the degradation of halide perovskite materials and devices. However, ion mobility is only one piece of the full picture─mobile ions/defects are first created, then transported, and eventually annihilated or immobilized. In this Perspective, we summarize emerging work that shows how tractable photochemical and Faradaic reactions provide a continuous source of ions to migrate. Furthermore, we discuss strategies to fundamentally manipulate ion migration by targeting specific electrochemical and reduction/oxidation mechanisms. This highlights the important role of defect photoelectrochemistry, as well as the soft nature of the perovskite lattice, in ion migration and self-healing. We conclude that distinguishing more detailed processes involved in "ion migration", with an emerging focus on the reactions that form mobile ionic defects, is necessary to greatly improve the stability of devices and open up more technological applications.
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