X-ray photoelectron spectroscopy studies of reactions on chromium metal and chromium oxide surfaces

微晶 铬 金属 X射线光电子能谱 多重态 谱线 氧化物 化学 分析化学(期刊) 结晶学 核磁共振 物理 天文 色谱法 有机化学
作者
Brad P. Payne,Mark C. Biesinger,N. S. McIntyre
出处
期刊:Journal of Electron Spectroscopy and Related Phenomena [Elsevier BV]
卷期号:184 (1-2): 29-37 被引量:219
标识
DOI:10.1016/j.elspec.2010.12.001
摘要

This paper reports several interrelated XPS investigations of the Cr–O system that provide additional interpretation of the Cr 2p3/2 spectra, along with more detail on the reaction mechanisms between O2 gas and H2O vapour with metallic Cr. The Cr 2p3/2 spectra of polycrystalline Cr2O3 contain multiplet structures that bear a strong resemblance to those calculated by Gupta and Sen for the free Cr3+ ion. The O/Cr ratio derived from the corrected Cr3+ and substitutional O2− intensities for all polycrystalline Cr2O3 samples was 1.5. Annealing of freshly cleaved polycrystalline Cr2O3 surfaces above 550 °C resulted in a sharpening of the multiplet structures that may be caused by the increased prevalence of the (0 0 0 1) Cr2O3 orientation on the surface. The slight difference in binding energies between the low energy (0 0 0 1) plane and the other major crystallographic orientations could contribute to the spectral broadening that is observed for the Cr 2p3/2 spectral line shapes. The Cr 2p3/2 spectrum for Cr(OH)3 was isolated from that produced by Cr2O3 and the multiplet structure was qualitatively re-assembled for that of the hydroxide. The Cr 2p3/2 and O 1s spectra of reaction products on polycrystalline metal surfaces were analysed using the above information. The oxidic portion of the Cr 2p3/2 spectra could be cleanly separated from the metallic substrate using spectral subtraction. Reactions of either O2 gas or H2O vapour both produced a thin Cr2O3 film that was deficient in Cr3+ and, depending on the reactant, showed varying concentrations of hypo-stoichiometric Cr moieties. The surface corrected O/Cr ratios calculated for all the oxidised surfaces were 1.7. There was little evidence to support the formation of Cr(OH)3 on these surfaces. For comparison, an aqueous reaction of a Ni–Cr (20%) alloy was studied where both Cr(OH)3 and Cr2O3 components could be analysed. For this example no sub-stoichiometric Cr oxide species were produced.
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