Abstract

Experiments on single crystal Au/Ag alloy surfaces may provide insight into the physical and chemical phenomena that determine the reactivity of complex alloy surfaces such as nanoporous gold or bimetallic nanoparticles. In this study, we report the highly unexpected observation that as soon as interfacial diffusion is feasible (400K) thin gold films drastically restructure Ag(110) surfaces on the micrometer scale and create regular islands in a pattern which resembles the result of a sputter-etching process; bulk diffusion plays apparently no role during this phenomenon. Scanning tunneling microscopy (STM) reveals that the deposition of monolayer quantities of gold on the surface creates elongated islands, typically with a length of 1000nm, a width of ~50nm, and a height of ~30 lattice planes. The islands are predominantly elongated along the [1–10] direction and have a mutual distance of about 50nm. Approximately, one monolayer of gold causes the relocation of ~11ML of material. The islands are thermally unstable as further heating between 450K and 600K reduces the island structure significantly. The ‘etching’ of gold into the Ag(110) bulk material and the associated island formation can be rationalized with a simple kinetic model involving the diffusion of surface atoms only, illustrated with Monte Carlo simulations. A kinetic interpretation is also supported by the fact that those structures diminish after further annealing to higher temperatures. The observed large-scale reorganization underlines that even seemingly simple and well-defined surfaces may evolve in complex ways and that massive restructuring of surfaces can occur at temperatures well below the onset of bulk diffusion.

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