轻稀土金属及其氧化物的n4,5级外观电位研究

T.K. Hatwar, D.R. Chopra
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引用次数: 0

摘要

外观电位光谱(APS)探测固体表面核能级结合能和局部导带状态。软x射线APS (SXAPS)和俄歇电子APS (AEAPS)分别测量x射线荧光和二次电子产率随入射电子能量的变化。我们获得了La、Ce、Pr、Nd和Sm金属及其氧化物的N4、5能级SXAPS和AEAPS光谱。这些金属的n4,5水平的AEAPS研究以前没有报道过。两种光谱的比较显示出很强的相似性。两者均表现出低于预期4d激发阈值的多重结构,并且在阈值以上出现10-20 eV宽的宽峰,随后出现强度逐渐减弱的小峰。AEAPS峰比SXAPS峰更强烈、更窄。这些数据用于了解这些光谱中核心能级激发后的衰变机制。从氧化金属中记录的光谱除了阈值的化学位移外,没有显示出任何主要的光谱特征变化。除Sm为2.5 eV外,其余金属氧化物的位移均小于1.0 eV。金属光谱和氧化物光谱的相似性表明,APS光谱主要受原子效应而非能带效应的支配。
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Appearance potential study of N4,5-level of light rare earth metals and their oxides

Appearance potential spectroscopy (APS) probes the binding energy of core levels and local conduction band states of solid surfaces. Soft X-ray APS (SXAPS) and Auger electron APS (AEAPS) respectively measure the differential X-ray fluorescence and secondary electron yields as a function of incident electron energy. We have obtained the N4,5-level SXAPS and AEAPS spectra of La, Ce, Pr, Nd and Sm metals and their oxides. The N4,5-level AEAPS studies of these metals have not been reported previously. The comparison of the two spectra shows a strong resemblance. Both exhibit multiplet structure below the expected 4d excitation threshold and a broad, 10–20 eV wide peak above threshold followed by small peaks of decreasing intensity. AEAPS peaks are more intense and narrower than SXAPS peaks. The data are used to gain an understanding of the decay mechanism following the excitation of the core levels in these spectroscopies. The spectra recorded from oxidized metals do not show any major changes in the spectral features except for the chemical shift of the threshold. The shifts for all metal oxides are less than 1.0 eV except for Sm which is 2.5 eV. The similarity of the metal and oxide spectra indicates that the APS spectra are dominated by atomic rather than band effects.

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