Interaction of O 2 with the Fe 0.84Cr 0.16(001) surface studied by photoelectron spectroscopy

Abstract

Abstract Soft X-ray photoelectron spectroscopy (SXPS; hv = 130−600 eV) employing synchrotron radiation and X-ray photoelectron spectroscopy (XPS; hv = 1486.6 eV) employing AlKα X-rays were used to study the effect of molecular oxygen adsorption (1 to 104 L) on the (001) surface of the steel-like alloy Fe0.84Cr0.16 at room temperature. The use of multiple photon energies allowed a qualitative determination of the distribution of species in the oxide film perpendicular to the surface. Prior to oxidation, Fe0.84Cr0.16samples were annealed to different temperatures to produce varying concentrations of Cr in the top few monolayers of the (001) surface. The differences between the oxide films produced on these different surfaces were determined from SXPS primarily of the Fe 3p, Cr 3p, and valence levels. Small amounts of carbidic carbon(⩽ 1 ML) that had segregated to the (001) surface of the Fe0.84Cr0.16alloy during initial sputter/anneal treatments were removed during the first ∼ 5 L O2 exposure. In general, the resistance of the Fe0.84Cr0.16(001) surface to oxidation was directly related to the initial Cr concentration at the surface. The oxide films were richer in Cr compared to the bulk concentration for the lowest O2 exposures, and became increasingly enriched in Fe for increasing exposures, in agreement with studies by other groups. The resulting mixed FeCrO film contained Cr that was in the form of Cr3+ for all exposures. The Fe was in the form of Fe2+ and Fe3+, with an increasing Fe3+/Fe2+ ratio as the O2 exposure is increased. The results indicate that for O2 exposures