X射线光电子能谱
单层
纳米
接口(物质)
氢键
密度泛函理论
材料科学
化学物理
纳米技术
电子结构
化学键
固体表面
计算机科学
分子
化学
计算化学
化学工程
工程类
复合材料
有机化学
毛细管数
毛细管作用
作者
Xueqiang Zhang,Andrew J. E. Rowberg,Nitish Govindarajan,Xin He
出处
期刊:Elsevier eBooks
[Elsevier]
日期:2024-01-01
卷期号:: 92-113
被引量:1
标识
DOI:10.1016/b978-0-323-85669-0.00125-2
摘要
Probing the chemical, structural, and electronic properties of dynamically evolving H2O/solid interfaces is highly desirable due to the ubiquity of such interfaces in numerous fields. Ambient pressure X-ray photoelectron spectroscopy (APXPS) has been used in a wide range of studies to investigate the microscopic details of the H2O/solid interface, in particular, the hydrogen bond network that develops as water builds up on top of the material surface. Here, we review the fundamentals of APXPS, recent advances in the instrumentation, and its scientific applications in studying the properties of water on various surfaces. We discuss cases where the thickness of H2O layer varies between one monolayer and tens of nanometers, as the thickness of water plays a critical role in determining the properties of the interface. In addition, we discuss computational approaches based on density functional theory (DFT) that can be used to model (AP)XPS spectra, support spectral peak assignments, and provide information beyond what can be readily obtained experimentally.
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