Investigation of multiplet splitting of Fe 2p XPS spectra and bonding in iron compounds

电负性 铁质 X射线光电子能谱 结合能 谱线 配体(生物化学) 离子键合 离子 化学 多重态 分析化学(期刊) 结晶学 物理化学 无机化学 核磁共振 原子物理学 物理 生物化学 受体 色谱法 有机化学 天文
作者
Andrew P. Grosvenor,Brad Kobe,Mark C. Biesinger,N. S. McIntyre
出处
期刊:Surface and Interface Analysis [Wiley]
卷期号:36 (12): 1564-1574 被引量:3624
标识
DOI:10.1002/sia.1984
摘要

Abstract Ferrous (Fe 2+ ) and ferric (Fe 3+ ) compounds were investigated by XPS to determine the usefulness of calculated multiplet peaks to fit high‐resolution iron 2p 3/2 spectra from high‐spin compounds. The multiplets were found to fit most spectra well, particularly when contributions attributed to surface peaks and shake‐up satellites were included. This information was useful for fitting of the complex Fe 2p 3/2 spectra for Fe 3 O 4 where both Fe 2+ and Fe 3+ species are present. It was found that as the ionic bond character of the iron —ligand bond increased, the binding energy associated with either the ferrous or ferric 2p 3/2 photoelectron peak also increased. This was determined to be due to the decrease in shielding of the iron cation by the more increasingly electronegative ligands. It was also observed that the difference in energy between a high‐spin iron 2p 3/2 peak and its corresponding shake‐up satellite peak increased as the electronegativity of the ligand increased. The extrinsic loss spectra for ion oxides are also reported; these are as characteristic of each species as are the photoelectron peaks. Copyright © 2004 John Wiley & Sons, Ltd.
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