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Tunability of MoO(3) Thin-Film Properties Due to Annealing in Situ Monitored by Hard X-ray Photoemission
[Image: see text] The chemical and electronic structure of MoO(3) thin films is monitored by synchrotron-based hard X-ray photoelectron spectroscopy while annealing from room temperature to 310 °C. Color-coded 2D intensity maps of the Mo 3d and O 1s and valence band maximum (VBM) spectra show the ev...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6648274/ https://www.ncbi.nlm.nih.gov/pubmed/31460196 http://dx.doi.org/10.1021/acsomega.9b01027 |
Sumario: | [Image: see text] The chemical and electronic structure of MoO(3) thin films is monitored by synchrotron-based hard X-ray photoelectron spectroscopy while annealing from room temperature to 310 °C. Color-coded 2D intensity maps of the Mo 3d and O 1s and valence band maximum (VBM) spectra show the evolution of the annealing-induced changes. Broadening of the Mo 3d and O 1s spectra indicate the reduction of MoO(3). At moderate temperatures (120–200 °C), we find spectral evidence for the formation of Mo(5+) and at higher temperatures (>165 °C) also of Mo(4+) states. These states can be related to the spectral intensity above the VBM attributed to O vacancy induced gap states caused by partial filling of initially unoccupied Mo 4d-derived states. A clear relation between annealing temperature and the induced changes in the chemical and electronic structure suggests this approach as a route for deliberate tuning of MoO(3) thin-film properties. |
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