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The oxidation of iron films at {~}25 K and the reactive formation of iron oxides in a solid oxygen matrix is investigated using synchrotron-radiation-based photoemission. For O₂ on Fe, the oxygen molecules dissociate and go into a chemisorbed state. At intermediate oxygen coverages, a disordered divalent FeO-like phase grows at the expense of the chemisorbed state. Further exposures of oxygen lead to the condensation of molecular oxygen on top of the oxide. Initial Fe depositions into a solid molecular oxygen film produce a trivalent Fe₂{O}₃$-like phase. At higher iron coverages divalent FeO-like and metallic iron phases form because the supply of ${O}₂$ for the oxide-forming reaction decreases.
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Ruckman et al. (1992) studied this question.
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