Molecular adsorption on the (0001) surfaces of rare-earth metals

被引:17
作者
Blyth, RIR
Searle, C
Tucker, N
White, RG
Johal, TK
Thompson, J
Barrett, SD
机构
[1] Univ Lecce, Dipartimento Ingn Innovaz, INFM, Natl Nanotechnol Lab, I-73100 Lecce, Italy
[2] Univ Liverpool, Surface Sci Res Ctr, Liverpool L69 3BX, Merseyside, England
[3] Univ Liverpool, Dept Phys, Liverpool L69 3BX, Merseyside, England
关键词
D O I
10.1103/PhysRevB.68.205404
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The adsorption of molecules on rare-earth (0001) thin films on W(110) at room temperature has been studied using photoemission spectroscopy. CO2 adsorbs dissociatively, up to monolayer coverage, forming a carbonate species, with clean up of adventitious hydrogen also observed. Higher coverages result in molecular adsorption. H2O and H2S on Y(0001) also adsorb dissociatively, resulting in atomic H and S, up to monolayer coverage. Higher coverages of H2O result in oxidation of the substrate to Y2O3, with formation of H2O multilayers. H2S dissociation appears to result in atomic S, adsorbed in both hollow and bridge sites. No indication of CH4 adsorption was seen on Y(0001). These results, and those from the literature, are compared to data from bulk single-crystal rare-earth (0001) surfaces in an attempt to explain the origin of certain unexplained photoemission features observed on those surfaces.
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页数:7
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