卤化物
离子液体
溴化物
化学
钙钛矿(结构)
无机化学
相(物质)
混合(物理)
化学工程
催化作用
结晶学
有机化学
量子力学
物理
工程类
作者
Christopher Greve,Philipp Ramming,Markus Griesbach,Nico Leupold,Ralf Moos,Anna Köhler,Eva M. Herzig,Fabian Panzer,Helen Grüninger
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2023-11-07
卷期号:8 (12): 5041-5049
被引量:12
标识
DOI:10.1021/acsenergylett.3c01878
摘要
Ionic liquids, such as BMIMBF 4, are added to mixed halide perovskites to prevent halide phase segregation and increase phase stability, but exact mechanisms changing halide kinetics are currently unclear. Here, X-ray diffraction, nuclear magnetic resonance, and photoluminescence spectroscopy are used in situ under dark conditions to follow thermally driven halide mixing processes forming MAPbI 3– x Br x from physical mixtures of MAPbI 3 and MAPbBr 3 powders with and without BMIMBF 4 . Halide migration is significantly accelerated with BMIMBF 4 compared to additive-free mixtures. This is attributed to liquid-like dynamics of BMIMBF 4 at elevated temperatures, liberating defect sites at perovskite interfaces. Furthermore, the presence of BMIMBF 4 increases the activation energies for bromide migration, suggesting a changed nature of the latter. This is explained by a preferred interaction between BMIM + and bromide, indicating that the cations of the additive shuttle bromide ions between interfaces. Overall, these observations pave the way for a better understanding of halide transport in hybrid perovskites.
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