X射线光电子能谱
俄歇电子能谱
氧气
低能电子衍射
上部结构
工作职能
吸附
化学
氧化物
电子衍射
分析化学(期刊)
溶解
解吸
钴
材料科学
衍射
无机化学
物理化学
核磁共振
电极
核物理学
光学
有机化学
物理
海洋学
色谱法
地质学
作者
B. Klingenberg,F. Grellner,D. Borgmann,G. Wedler
标识
DOI:10.1016/0039-6028(93)90031-e
摘要
Adsorption of oxygen on the (112̄0) surface of hexagonal cobalt at 100 and 320 K has been studied by means of low energy electron diffraction (LEED), X-ray photoelectron spectroscopy (XPS), UV photoelectron spectroscopy (UPS), change of work function (Δφ) and Auger electron spectroscopy (AES). At 100 K, adsorbed oxygen and Co3O4 features are observed, as identified by the UP spectra. During heating, a conversion into CoO takes place. This process is completed at 230 K and followed by dissolution of oxygen in the bulk at temperatures exceeding 450 K. Admission of oxygen at 320 K leads to identical results, but the total amount of adsorbed oxygen is approximately 30% lower. LEED experiments show a (1 × 3) superstructure at low coverages. After higher exposures, CoO formation, as revealed by the photoelectron data, is indicated by a changed diffraction pattern. It is concluded that an epitaxial growth of CoO(100) takes place.
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