Vanadium
dioxide (VO2) is a strongly correlated material with 3d
electrons, which exhibits temperature-driven insulator-to-metal transition
with a concurrent change in the crystal symmetry. Interestingly, even
modest changes in stoichiometry-induced orbital occupancy dramatically
affect the electrical conductivity of the system. Here, we report
a successful transformation of epitaxial monoclinic VO2 thin films from a conventionally insulating to permanently metallic
behavior by manipulating the electron correlations. These ultrathin
(∼10 nm) epitaxial VO2 films were grown on NiO(111)/Al2O3(0001) pseudomorphically, where the large misfit
between NiO and Al2O3 were fully relaxed by
domain-matching epitaxy. Complete conversion from an insulator to
permanent metallic phase is achieved through injecting oxygen vacancies
(x ∼ 0.20 ± 0.02) into the VO2–x
system via annealing under high vacuum (∼5
× 10–7 Torr) and increased temperature (450
°C). Systematic introduction of oxygen vacancies partially converts
V4+ to V3+ and generates unpaired electron charges
which result in the emergence of donor states near the Fermi level.
Through the detailed study of the vibrational modes by Raman spectroscopy,
hardening of the V–V vibrational modes and stabilization of
V–V dimers are observed in vacuum-annealed VO2 films,
providing conclusive evidence for stabilization of a monoclinic phase.
This ultimately leads to convenient free-electron transport through
the oxygen-deficient VO2–x
thin
films, resulting in metallic characteristics at room temperature.
With these results, we propose a defect engineering pathway through
the control of oxygen vacancies to tune electrical and optical properties
in epitaxial monoclinic VO2.