Simulation of anodic Pt oxide growth

A microscopic model of the growth of the thin anodic oxide film on Pt is presented. The slow step is migration of a Pt atom from the metal lattice to become a Pt(II) species. Pt(II) species can then rapidly diffuse across the surface. Sites of different types, e.g. terrace atoms or step atoms, have different reactivity, dependent on their number and type of bonds. Monte Carlo simulations are used to predict the kinetics and the surface reconstruction. The treatment of the structures of the oxide and metal is oversimplified by the assumption that they both have simple cubic unit cells with identical lattice parameters. The model predicts correctly the observed direct logarithmic growth law for potential step transients, without any change in behavior at full monolayer coverage. For cyclic voltammetry, it predicts an anodic peak on the first cycle, and plateau behavior for subsequent cycles. The reversible component is found, and interpreted in terms of a reversible reconstruction aided by the rapid surface diffusion. The height distributions predicted by this model agree with recent structural measurements, but the exact topography of the surface after multiple cycles is not reproduced.

[1]  R. Yonco,et al.  In‐situ x‐ray reflectivity study of incipient oxidation of Pt(111) surface in electrolyte solutions , 1994 .

[2]  B. Conway,et al.  Real condition of oxidized platinum electrodes. Part 2.—Resolution of reversible and irreversible processes by optical and impedance studies , 1973 .

[3]  Gregory Jerkiewicz,et al.  Surface orientation dependence of oxide film growth at platinum single crystals , 1992 .

[4]  V. Birss,et al.  Platinum oxide film formation—reduction: an in-situ mass measurement study , 1993 .

[5]  D. Harrington,et al.  An ac voltammetry study of Pt oxide growth , 1997 .

[6]  J. D. H. Donnay,et al.  Crystal data : determinative tables , 1963 .

[7]  L. Pauling,et al.  The Crystal Structures of the Tetragonal Monoxides of Lead, Tin, Palladium, and Platinum , 1941 .

[8]  B. Conway,et al.  Chloride-ion effects on the reversible and irreversible surface oxidation processes at Pt electrodes, and on the growth of monolayer oxide films at Pt , 1982 .

[9]  Z. Nagy,et al.  Oxidation-reduction-induced roughening of platinum (1 1 1) surface , 1994 .

[10]  D. Harrington,et al.  Platinum oxide growth kinetics for cyclic voltammetry , 1992 .

[11]  H. Angerstein-Kozlowska,et al.  The real condition of electrochemically oxidized platinum surfaces , 1973 .

[12]  R. Durand,et al.  Structural changes of a Pt(111) electrode induced by electrosorption of oxygen in acidic solutions: a coupled voltammetry, LEED and AES study , 1986 .

[13]  G. Tremiliosi‐Filho,et al.  Significance of the apparent limit of anodic oxide film formation at Pt: saturation coverage by the quasi two-dimensional state , 1992 .

[14]  B. Conway,et al.  A surface‐electrochemical basis for the direct logarithmic growth law for initial stages of extension of anodic oxide films formed at noble metals , 1990 .

[15]  A. Adamson Physical chemistry of surfaces , 1960 .

[16]  Patricia A. Thiel,et al.  The interaction of water with solid surfaces: Fundamental aspects , 1987 .

[17]  J. Clavilier,et al.  Electrochemical behaviour of Pt(100) in various acidic media: Part I. On a new voltammetric profile of Pt(100) in perchloric acid and effects of surface defects , 1991 .