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Corresponding Author

Pei-fang LIU(jtlu@whu.edu.cn)

Abstract

Based on the Fleischmann's model of nucleation and crystal growth for electrodeposition combined with the Barradas-Bosco's adsorption-nucleation model for electrochemical phase formation, the chronoamperometry was well fitted for Pt deposition on polycrystalline Au micro disc electrodes (30 μm in diameter) in different H2PtCl6 concentrations at different over-potentials. The initial stage of Pt deposition in dilute H2PtCl6 could be interpreted by the model of H2PtCl6 adsorption combined with instantaneous nucleation and two-dimensional cylindrical growth. The rate constant of the two-dimensional growth increased linearly with overpotential. Then the deposit grew layer by layer and the rate constant increased non-linearly with overpotential. In contrast to the situation in dilute solutions, Pt deposition in higher H2PtCl6 concentrations was found to follow the mechanism of adsorption-instantaneous nucleation and three-dimensional cone growth.The rate constant of perpendicular growth kperp appeared two orders of magnitude larger than that of parallel growth kparaand increased linearly with overpotential. However, the kpara increased with overpotential in S shape. Both kperpor kpara in concentrated solutions were larger than the growth rate constant in dilute solutions.

Keywords

Electrodeposition, Nucleation and crystal growth, Electrodeposition of Pt on Au, Microelectrodes

Publication Date

2004-08-28

Online Available Date

2004-08-28

Revised Date

2004-04-13

Received Date

2004-01-20

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