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Interdiffusion of adsorbed Pb and Bi on Cu(1 0 0)
Authors:J.P. Monchoux  D. Chatain
Affiliation:a Centre de Recherche en Matière Condensée et Nanosciences,1Laboratoire propre du CNRS, associé aux Universités d’Aix-Marseille 2 et 3.1 - CNRS, Campus de Luminy - case 913, 13288 Marseille Cedex 9, France
b Now at Centre d’Elaboration de Matériaux et d’Etudes Structurales - CNRS, 29 rue Jeanne Marvig, BP 94347, 31055 Toulouse Cedex 4, France
c Department of Materials Science and Engineering, Carnegie Mellon University, Pittsburgh, PA 15213, USA
Abstract:The impingement and interdiffusion of adsorbed Pb and Bi layers spreading from separated 3D pure bulk sources on Cu(1 0 0) has been studied, at T = 513 K, by in situ scanning Auger microscopy. When the leading edges of the pure Pb and Bi diffusion profiles impinge, they both consist of low-coverage lattice gas surface alloyed phases. In these low-coverage phases, Pb displaces surface alloyed Bi and the point of intersection of the profiles drifts towards the Bi source. These features lead to the conclusion that Pb atoms are more strongly bound at surface alloyed sites in Cu(1 0 0) than Bi atoms. Once the total coverage (Pb + Bi) on the substrate reaches about one monolayer, Pb and Bi are dealloyed from the substrate, and the interdiffusion profiles become essentially symmetric. Pb and Bi mix in all proportions, with an interdiffusion coefficient of ∼10−13 m2/s. This is considerably smaller than the self-diffusion coefficients previously observed for pure Pb and Bi in their respective high-coverage phases, indicating that the mechanism of interdiffusion is different from that of self-diffusion. As interdiffusion proceeds, the point of intersection of the Pb and Bi profiles reverses its drift direction, leading to the conclusion that binding of Bi atoms to the Cu(1 0 0) substrate is stronger than that of Pb atoms in the highest-coverage surface dealloyed layers.
Keywords:Surface diffusion   Auger electron spectroscopy   Lead   Bismuth   Copper (1     0)
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