纳米晶
卤化物
钙钛矿(结构)
化学
离子
溶解度
离子交换
离子键合
无机化学
动力学
材料科学
纳米技术
结晶学
物理化学
有机化学
物理
量子力学
作者
Einav Scharf,Franziska Krieg,Orian Elimelech,Meirav Oded,Adar Levi,Dmitry N. Dirin,Maksym V. Kovalenko,Uri Banin
出处
期刊:Nano Letters
[American Chemical Society]
日期:2022-05-23
卷期号:22 (11): 4340-4346
被引量:65
标识
DOI:10.1021/acs.nanolett.2c00611
摘要
The soft lattice of lead-halide perovskite nanocrystals (NCs) allows tuning their optoelectronic characteristics via anion exchange by introducing halide salts to a solution of perovskite NCs. Similarly, cross-anion exchange can occur upon mixing NCs of different perovskite halides. This process, though, is detrimental for applications requiring perovskite NCs with different halides in close proximity. We study the effects of various stabilizing surface ligands on the kinetics of the cross-anion exchange reaction, comparing zwitterionic and ionic ligands. The kinetic analysis, inspired by the "cage effect" for solution reactions, showcases a mechanism where the surface capping ligands act as anion carriers that diffuse to the NC surface, forming an encounter pair enclosed by the surrounding ligands that initiates the anion exchange process. The zwitterionic ligands considerably slow down the cross-anion exchange process, and while they do not fully inhibit it, they confer improved stability alongside enhanced solubility relevant for various applications.
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