The surface morphology and composition of MoO2 prepared via the low-temperature decomposition of a molybdenum(VI) isopropylhydroxylaminate complex, MoO2(i-C3H7NHO)2, have been studied by scanning electron microscopy, X-ray diffraction, and X-ray photoelectron… Click to show full abstract
The surface morphology and composition of MoO2 prepared via the low-temperature decomposition of a molybdenum(VI) isopropylhydroxylaminate complex, MoO2(i-C3H7NHO)2, have been studied by scanning electron microscopy, X-ray diffraction, and X-ray photoelectron spectroscopy (XPS). During the sample preparation process for XPS, the molybdenum dioxide, which has the form of nanocrystals, actively reacts with atmospheric oxygen and moisture because of the small particle size of the material. The composition of the surface layer in terms of molybdenum is 5 at % MoO2, 10 at % Mo2O5, and 85 at % MoO3, and the Eb(Mo 3d5/2) binding energy is 230.0, 231.4, and 233.1 eV, respectively. After argon ion etching of the sample surface for 45 s, the surface composition is 52 at % MoO2, 23 at % Mo2O5, and 25 at % MoO3. In addition, there are ~3 carbon atoms per Mo atom. Based on analysis of the structure of the C 2s, 2p valence electron spectra, we assume that the carbon on the sample surface is present as amorphous or nanoparticulate carbon phases. The material studied here does not become charged when exposed to an X-ray beam, which suggests that it is a weak dielectric.
               
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