离子液体
酰亚胺
铂金
X射线光电子能谱
电化学
化学
无机化学
单层
烷基
物理化学
材料科学
高分子化学
有机化学
催化作用
化学工程
电极
工程类
生物化学
作者
Fabien Krebs,Oliver Höfft,Frank Endres
出处
期刊:Coatings
[Multidisciplinary Digital Publishing Institute]
日期:2023-06-30
卷期号:13 (7): 1182-1182
被引量:6
标识
DOI:10.3390/coatings13071182
摘要
The processes at the interface between ionic liquids (ILs) and metals are a key factor for understanding especially in electrochemical deposition, nanoscale tribology applications and batteries. In the present work, the interfaces of 1-butyl-1-methylpyrrolidinium bis(trifluoromethylsulfonyl)imide ([Py1,4]TFSI) and 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide ([EMIm]TFSI) and platinum and aluminum were investigated by depositing thin IL films and studying them with X-ray photoelectron spectroscopy (XPS) in ultrahigh vacuum. It is found that there is no evidence of a decomposition reaction of either IL on platinum; however, the imidazolium cation of [EMIm]TFSI shows a strong interaction with the surface in the monolayer regime. In contrast, [Py1,4]TFSI and [EMIm]TFSI show massive decomposition on the aluminum surface without applying any electrochemical potential. The spectra for the [TFSI]− anion components show cleavage of C-F or N-S bonds in both cases. Both cleavage of a single fluorine atom and complete cleavage were observed, leading to further decomposition reactions of the anion. Consequently, new components such as AlOOH, Al(OH)3, Al2S3, Al2(SO4)3 and AlF3 appear at the interface. In addition, there is also evidence of decomposition of the cation by the splitting off hydrogen atoms or parts of the alkyl chain in both ILs.
科研通智能强力驱动
Strongly Powered by AbleSci AI