UNOCCUPIED ELECTRONIC STATES IN ADSORBATE SYSTEMS

被引:30
作者
BERTEL, E
机构
[1] Max-Planck-Institut für Plasmaphysik, EURATOM-Association, Garching, W-8046
来源
APPLIED PHYSICS A-MATERIALS SCIENCE & PROCESSING | 1991年 / 53卷 / 05期
关键词
D O I
10.1007/BF00348148
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Experimental work on unoccupied electronic states in adsorbate systems on metallic substrates is reviewed with emphasis on recent developments. The first part is devoted to molecular adsorbates. Weakly chemisorbed hydrocarbons are briefly discussed. An exhaustive inverse photoemission (IPE) study of the CO bond to the transition metals Ni, Pd, and Pt is presented. Adsorbed NO is taken as an example to demonstrate the persisting discrepancies in the interpretation of IPE spectra. Atomic adsorbates are discussed in the second part. The quantum well state model is applied to interpret the surface states in reconstructing and non-reconstructing adsorption systems of alkali metals and hydrogen. A recent controversy on the unoccupied electronic states of the Cu(110)/O p(2 x 1) surface is critically reviewed. The quantum well state model is then compared to tight binding and local-density-functional calculations of all unoccupied bands and the deficiencies of the various approaches are pointed out. Finally, the relation between the surface state model and more chemically oriented models of surface bonding is briefly discussed.
引用
收藏
页码:356 / 368
页数:13
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