Abstract
Early stage oxidation of a dilute depleted uranium-molybdenum alloy was analysed in situ under UHV conditions by AES and XPS. At the equivalent of less than 300 ns at 1 atm O2, U-5Mo oxidises to form stoichiometric UO2. No molybdenum oxidation is observed. After an oxygen dose of approximately 39 L, the oxide layer approached a limiting thickness of approximately 2.4 nm. The oxidation kinetics followed a logarithmic rate law, with the best fit to the experimental data for the oxide thickness, d, being given by d = 1.26 log(0.12t + 0.56). Changes in oxygen KLL and 1s peak positions associated with transformation from chemisorbed oxygen to metal oxide were observed at similar oxygen doses of 2.3 and 2.6 L O2 by AES and XPS respectively, which opens up the possibility of using well characterised XPS chemical information to inform Auger peak shifts.