X射线光电子能谱
过渡金属
结合能
谱线
氧化态
原子轨道
金属
材料科学
化学
电子结构
物理化学
化学物理
计算化学
原子物理学
物理
催化作用
核磁共振
生物化学
天文
量子力学
电子
冶金
出处
期刊:ACS Nano
[American Chemical Society]
日期:2024-05-22
卷期号:18 (22): 13973-13982
被引量:1
标识
DOI:10.1021/acsnano.4c03964
摘要
Nanomaterials based on transition-metal oxides (TMOs) that contain late 3d transition metals (e.g., Mn, Fe, Co, Ni) have diverse properties and functionality that are related to the oxidation state of constituent transition-metal (TM) cations. X-ray photoelectron spectroscopy (XPS) of TM 2p orbitals has been widely used to quantify the TM oxidation state of TMOs. However, 2p XPS spectra of late 3d TM cations usually have complicated shapes due to the charge transfer between the TM cation and oxygen ligands (anions), which makes the analysis highly nontrivial. In this article, we will examine the validity of commonly used analysis methods based on either peak fitting or the shift of binding energy (BE). The different origins of the BE shift in XPS spectra will be discussed. We will then introduce a model to reproduce the complex shapes of TM 2p spectra, based on fundamental parameters that describe the TMO electronic structure.
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