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Structural and thermal properties of Xe on the Pb(111) surface studied by low-energy electron diffraction

N Ferralis et al 2007 J. Phys.: Condens. Matter 19 056011 (12pp)   doi: 10.1088/0953-8984/19/5/056011  Help

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N Ferralis1, H I Li, K J Hanna, J Stevens, H Shin, F M Pan and R D Diehl2
Department of Physics, Penn State University, University Park, PA 16802, USA
1 Present address: Department of Chemical Engineering, 201 Gilman Hall, University of California, Berkeley, CA 94720-1462, USA
2 Author to whom any correspondence should be addressed
E-mail: rdiehl@psu.edu

Abstract. The growth, structures and thermodynamics of Xe adsorbed on Pb(111) were studied with low-energy electron diffraction (LEED). Measurements of equilibrium adsorption isobars indicate layer-by-layer growth for at least two layers in the temperature range 60–90 K, and an isosteric heat of adsorption of 191 ± 10 meV for the first Xe layer and 158 ± 20 meV for the second Xe layer. The monolayer has an incommensurate hexagonal structure with a lattice parameter similar to that found in bulk Xe, and its thermal expansion coefficient was measured to be 9 ± 1 × 10−4 K−1. The average overlayer–substrate spacing was determined from a constant-momentum-transfer analysis of the LEED intensities to be 3.95 ± 0.10 Å. Vibrational information was obtained from measuring the decay of the diffraction intensities as a function of temperature. The perpendicular root mean square displacement of the Xe atoms at 50 K is 0.12 ± 0.01 Å, giving an effective Debye temperature for adsorbed Xe of 37 ± 2 K. The corresponding vibrational energy for the perpendicular mode of Xe is 3.2 ± 0.3 meV.

Print publication: Issue 5 (7 February 2007)
Received 13 November 2006, in final form 2 January 2007
Published 17 January 2007

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