Experiments on the oxidation, at room temperature, in 5×{}10^-8 Torr oxygen, of vapor deposited films of cerium, niobium, and niobium covered by some monolayers of cerium are reported. The valence-band structure was studied by ultraviolet photoemission spectroscopy (UPS), the surface potential due to chemisorbed oxygen was measured by measuring work-function change by UPS, and oxide growth was followed by x-ray photoelectron spectroscopy. The energy level εₐ of oxygen chemisorbed on CeO₂ was determined from UPS difference spectra and found to be at 4 eV below the Fermi level εF. Comparing this with measured values of the surface potential (VS=-0.6 V) we conclude that contrary to earlier predictions, the entire value of the Mott potential VM{≡}e^-1(εF-εₐ) does not materialize as a surface potential in the course of oxidation. We found, that for the oxidation of Nb the incorporation of oxygen ions at the surface is the rate-limiting step, while in case of cerium, and niobium covered by some monolayers of cerium, the first stage of oxidation is limited by oxygen-ion diffusion, and the second stage of oxidation is limited by electron tunneling.
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Ronay et al. (1985) studied this question.
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