New interpretations of XPS spectra of nickel metal and oxides

被引:1840
|
作者
Grosvenor, Andrew P.
Biesinger, Mark C.
Smart, Roger St. C. [1 ]
McIntyre, N. Stewart
机构
[1] Univ S Australia, ACeSSS, Mawson Lakes, SA 5095, Australia
[2] Univ Western Ontario, London, ON N6A 5B7, Canada
关键词
nickel; metals; oxides; X-ray photoelectron spectroscopy;
D O I
10.1016/j.susc.2006.01.041
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A current interpretation of XPS spectra of Ni metal assumes that the main 6 eV satellite is due to a two hole c3d(9)4s(2) (c is a core hole) final state effect. We report REELS observation in AES at low voltages of losses (plasmons and inter-band transitions) corresponding to the satellite structures in Ni metal 2p spectra. The satellite near 6 eV is attributed to a predominant surface plasmon loss. A current interpretation of Ni 2p spectra of oxides and other compounds is based oil charge transfer assignments of the main peak at 854.6 eV and the broad satellite centred at around 861 eV to the cd(9)L and the unscreened cd(8) final-state configurations, respectively (L is a ligand hole). Multiplet splittings have been shown to be necessary for assignment of Fe 2p and Cr 2p spectral profiles and chemical states. The assignments of Ni 2p states are re-examined with intra-atomic multiplet envelopes applied to Ni(OH)(2), NiOOH and NiO spectra. It is shown that the free ion inultiplet envelopes for Ni2+ and Ni3+ simulate the main line and satellite structures for Ni(OH)2 and NiOOH. Fitting the NiO Ni 2p spectral profile is not as straightforward as the hydroxide and oxyhydroxide. It may involve contributions from interatomic. non-local electronic coupling and screening effects with multiplet structures significantly different from the free ions as found for MnO. A scheme for fitting these spectra using multiplet envelopes is proposed. (c) 2006 Elsevier B.V. All rights reserved.
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页码:1771 / 1779
页数:9
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