B.A. Hutchins, T.N. Rhodin, et al.
Surface Science
Reaction of chlorine with Ag surfaces has been studied at 300 K with X-ray photoelectron spectroscopy and Auger depth profiling over a wide range of Cl2 exposures. Formation of AgCl and subsurface diffusion are observed. At exposures lower than 107 L, the Ag-Cl2 reaction is logarithmic in time and the surface layer is Ag enriched. This behavior can be related to a field-assisted diffusion mechanism known from oxidation of metal surfaces. At higher exposures, however, a t1/2 time dependence of the chlorination reaction is found. The Cl penetration saturates, and a stoichiometric AgCl layer is formed on the surface. It is further observed that a solid AgCl can be reduced to metallic Ag in the surface region when bombarded by Ar+ ions. Irradiation by X-ray photons can cause more complex chemical changes on the solid surfaces. © 1987 Elsevier Science Publishers B.V.
B.A. Hutchins, T.N. Rhodin, et al.
Surface Science
A. Ney, R. Rajaram, et al.
Journal of Magnetism and Magnetic Materials
Thomas H. Baum, Carl E. Larson, et al.
Journal of Organometallic Chemistry
Corneliu Constantinescu
SPIE Optical Engineering + Applications 2009