摘要

Ion blocking in the low keV energy range is demonstrated to be a sensitive method for probing surface adsorption sites by means of the technique of time-of-flight scattering and recoiling spectroscopy (TOF-SARS). Adsorbed atoms can block the nearly isotropic backscattering of primary ions from surface atoms in the outmost layers of a crystal. The relative adsorption site position can be derived unambiguously by simple geometrical constructs between the adsorbed atom site and the surface atom sites. Classical ion trajectory simulations using the scattering and recoiling imaging code (SARIC) and molecular dynamics (MD) simulations provide the detailed ion trajectories. Herein we present a quantitative analysis of the blocking effects produced by sub-monolayer Na adsorbed on a Cu(111) surface at room temperature. The results show that the Na adsorption site preferences are different at different Na coverages. At a coverage theta=0.25 monolayer, Na atoms preferentially populate the fcc threefold surface sites with a height of 2.7 +/- 0.1 angstrom above the 1st layer Cu atoms. At a lower coverage of theta=0.10 monolayer, there is no adsorption site preference for the Na atoms on the Cu(111) surface.

  • 出版日期2010-7-15