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首页> 外文期刊>The journal of physical chemistry, A. Molecules, spectroscopy, kinetics, environment, & general theory >Two-photon photoemission study of the coverage-dependent electronic structure of chemisorbed alkali atoms on a Ag(111) surface
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Two-photon photoemission study of the coverage-dependent electronic structure of chemisorbed alkali atoms on a Ag(111) surface

机译:Ag(111)表面化学吸附的碱原子与覆盖率相关的电子结构的双光子光发射研究

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摘要

We report a systematic investigation of the electronic structure of chemisorbed alkali atoms (Li-Cs) on a Ag(111) surface by two-photon photoemission spectroscopy. Angle-resolved two-photon photoemission spectra are obtained for 0-0.1 monolayer coverage of alkali atoms. The interfacial electronic structure as a function of periodic properties and the coverage of alkali atoms is observed and interpreted assuming ionic adsorbate/substrate interaction. The energy of the alkali atom σ-resonance at the limit of zero coverage is primarily determined by the image charge interaction, whereas at finite alkali atom coverages, it follows the formation of a dipolar surface field. The coverage- and angle-dependent two-photon photoemission spectra provide information on the photoinduced charge-transfer excitation of adsorbates on metal surfaces. This work complements the previous work on alkali/Cu(111) chemisorption [ Phys. Rev. B 2008, 78, 085419 ].
机译:我们通过二光子光电子能谱报告了Ag(111)表面化学吸附的碱原子(Li-Cs)的电子结构的系统研究。对于碱原子的0-0.1单层覆盖,获得了角度分辨的两个光子光发射光谱。假定离子吸附物/底物相互作用,观察并解释了界面电子结构随周期特性和碱原子覆盖度的变化。零覆盖极限处的碱原子σ共振能量主要由图像电荷相互作用决定,而在有限碱原子覆盖率下,它遵循偶极表面场的形成。取决于覆盖率和角度的双光子光发射光谱提供了有关金属表面吸附物的光诱导电荷转移激发的信息。这项工作是对先前有关碱/ Cu(111)化学吸附的工作的补充。版本B 2008,78,085419]。

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