Abstract

AbstractThe Cd underpotential deposition (UPD) process on Au(111) was analyzed by means of combined electrochemical measurements and in situ scanning tunneling microscopy (STM). In the underpotential range 300⩽ΔE (mV) ⩽400, 2D Cd islands are formed on the fcc regions of the Au(111)‐(√3 × 22) reconstructed surface without lifting the reconstruction. At lower underpotentials, the 2D Cd islands grow and, simultaneously, new 2D islands nucleate and coalesce with the previous ones forming a complete condensed Cd monolayer (ML). STM images and long time polarization experiments performed at ΔE = 70 mV demonstrate the formation of an AuCd surface alloy. At ΔE = 10 mV, the formation of the complete Cd ML is accompanied by a significant AuCd surface alloying and the kinetic results reveal two different solid‐state diffusion processes. The first one, with a diffusion coefficient D1 = 4 × 10−17 cm2 s−1, could be ascribed to the mutual diffusion of Au and Cd atoms through a highly distorted (vacancy‐rich) AuCd alloy layer. The second and faster diffusion process (D2 = 7 × 10−16 cm2 s−1) is associated with the appearance of an additional peak in the anodic stripping curves and could be attributed to the formation of another CdzAux alloy phase. Copyright © 2008 John Wiley & Sons, Ltd.

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