A model for oxidation-driven surface segregation and transport on Pt-alloys studied by atom probe tomography

被引:13
作者
Bagot, P. A. J. [1 ]
Kreuzer, H. J. [2 ]
Cerezo, A. [1 ]
Smith, G. D. W. [1 ]
机构
[1] Univ Oxford, Dept Mat, Oxford OX1 3PH, England
[2] Dalhousie Univ, Dept Phys & Atmospher Sci, Halifax, NS B3H 3J5, Canada
基金
英国工程与自然科学研究理事会;
关键词
Platinum; Rhodium; Oxidation; Surface diffusion; Surface segregation; Catalysis; Atom probe tomography; Field ion microscopy; OXYGEN-INDUCED SEGREGATION; CORE-SHELL NANOPARTICLES; MONTE-CARLO SIMULATIONS; SELF-DIFFUSION; MORPHOLOGICAL-CHANGES; OXIDE FORMATION; DEPTH-PROFILES; GAS-ADSORPTION; METAL-SURFACES; SOLID-SURFACES;
D O I
10.1016/j.susc.2011.05.026
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Using a purpose-built 3D atom probe, we have previously shown that exposure to oxidising gases (NO, N2O, O-2) induces Rh surface segregation in Pt-Rh alloys, the extent of which is strongly dependent on treatment temperature, crystallographic plane and the presence of ternary alloy additions. In this paper, the segregation trends identified on three different crystallographic surfaces of Pt-Rh are analysed using thermodynamic and kinetic arguments. The segregation model we present is generic for diffusion on alloy surfaces in the presence of active gases. From it we obtain activation energies and diffusion coefficients for the processes of metal-oxide species diffusion both perpendicular to and laterally across the surface. Using these we propose a simple model for the interaction of chemically active gases with the surfaces of such alloys. Applying this understanding to sequential oxidation/reduction treatments would in principle allow improved control of the surface composition of alloy catalysts. Related applications of this model include optimisation of core-shell catalyst nanoparticles. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:1544 / 1549
页数:6
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