Abstract

We have studied atomic chemisorption at room temperature of chlorine on Ag(110) using high-resolution electron energy loss spectroscopy (HREELS), supplemented by XPS and LEED. The ClAg vibration energy (around 25 meV) and the line-width of this loss peak show well resolved variations with both chlorine coverage and substrate temperature T. The observed shift with T is related to the anharmonicity of the potential. Based on the Morse potential we derive an anharmonicity parameter x a = 6.2 × 10 −2 for the (2 × 1)Cl-overlayer. This indicates that the anharmonicity is enhanced by about a factor of two as compared to the bulk. In contrast, we find x a < 0.2 × 10 −2 for c(4 × 2)Cl. By comparison to other data we conclude that the (2 × 1)Cl-phase is a simple overlayer, with no significant reconstruction of the topmost substrate layer.

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