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Structural perturbations of epitaxial α-(Fe1-xVx)2O3 thin films driven by excess oxygen near the surface

Journal Article · · Journal of Applied Physics, 116(23):Article No. 233702
DOI:https://doi.org/10.1063/1.4903839· OSTI ID:1188913
We examine the structure and composition of phase-pure epitaxial α-(Fe1-xVx)2O3 thin films deposited on α-Al2O3(0001) substrates by oxygen-plasma-assisted molecular beam epitaxy for 0 ≤ x ≤ ~0.5. The films crystallize in the corundum lattice, with vanadium substituting for iron throughout. Vanadium cations exhibit the expected 3+ charge state in the bulk, but exhibit higher valences nearer to the surface, most likely because of excess oxygen in interstitial sites near the surface. The extent of vanadium oxidation beyond the 3+ state is inversely proportional to x. The gradation of vanadium valence with depth may have an impact on local bonding geometries, and could be highly significant in this material’s efficiency as a photocatalyst.
Research Organization:
Pacific Northwest National Laboratory (PNNL), Richland, WA (US), Environmental Molecular Sciences Laboratory (EMSL)
Sponsoring Organization:
USDOE
Grant/Contract Number:
AC05-76RL01830
OSTI ID:
1188913
Alternate ID(s):
OSTI ID: 22402808
OSTI ID: 1392580
Report Number(s):
PNNL-SA-105900; 48144; KC0304030
Journal Information:
Journal of Applied Physics, 116(23):Article No. 233702, Journal Name: Journal of Applied Physics, 116(23):Article No. 233702
Country of Publication:
United States
Language:
English

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