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The evolution of different W oxidation states and the oxide reduction mechanism of polycrystalline WO3 thin films, induced by low-energy H2+ bombardment at room temperature, was investigated in situ by X-ray photoelectron spectroscopy around W 4f and O 1s core levels and the valence band. A hydrogen tungsten bronze is formed at the beginning of the reduction process, as is evident from the development of the W5+ oxidation state and the creation of the O–H bonds. With the higher H implantation dose, reduction proceeds with the creation of H2O gas molecules, whose evolution with the bombardment time correlates with the cumulative concentration fractions of W4+, W2+, and W0 oxidation states. The generation of H2O molecules removes O atoms from the WO3 matrix, inducing the reduction of WO3 to lower oxides and, subsequently, metallic W, which is the dominant phase on the surface after 180 min of bombardment.
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Piltaver et al. (2024) studied this question.
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