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The tailoring and understanding of the metal-insulator transitions (MITs) in vanadium sesquioxide, V2O3, is of major interest for both applications and fundamental physics. V2O3 has been characterized by MIT and concurrent structural transition at ∼155 K; however, the nature of the MIT has remained more elusive. We investigated the MIT and the electronic structure (in metallic phase) of the pulsed laser deposition grown strained vanadium sesquioxide thin films on Si. The strained thin films synthesized here show the suppression (by ∼23 K) of the MIT to lower temperatures, whilst the structural transition temperature decreases only by ∼10 K. Our results systematically confirm that albeit the structural changes are crucial in V2O3, electronic transition seems to be of Mott-Hubbard type. Stabilization of the metallic phase in the strained V2O3 thin film has been manifested from resistivity data and observations of the increased crystal field and quasiparticle features.

Insulator to metal (IMT) transition (Tt ∼ 341 K) in the VO2 accompanies transition from an infrared (IR) transparent to IR opaque phase. Tailoring of the IMT and associated IR switching behavior can offer potential thermochromic applications. Here we report on effects of the W and the Tb doping on the IMT and associated structural, electronic structure and optical properties of the VO2 thin film. Our results show that the W doping significantly lowers IMT temperature (∼ 292 K to ∼ 247 K for 1.3% W to 3.7% W) by stabilizing the metallic rutile, R, phase while Tb doping does not alter the IMT temperature much and retains the insulating monoclinic, M1 , phase at room temperature. It is observed that the W doping albeit significantly reduces the IR switching temperature but is detrimental to the solar modulation ability, contrary to the Tb doping effects where higher IR switching temperature and solar modulation ability is observed. The IMT behavior, electrical conductivity and IR switching behavior in the W and the Tb doped thin films are found to be directly associated with the spectral changes in the V 3d states.

We report structural, magnetic, and dielectric properties of oxygen deficient hexagonal BaFeO3−δ. A large dielectric permittivity comparable to that of other semiconducting oxides is observed in BaFeO3−δ. Magnetization measurements indicate magnetic inhomogeneity and the system shows a paramagnetic to antiferromagnetic transition at ∼160 K. Remarkably, the temperature, at which paramagnetic to antiferromagnetic transition occurs, around this temperature, a huge drop in the dissipation factor takes place and resistivity shoots up; this indicates the possible correlation among magnetic and dielectric properties. First principle simulations reveal that some of these behaviors may be explained in terms of many body electron correlation effect in the presence of oxygen vacancy present in BaFeO3−δ indicating its importance in both fundamental science as well as in applications.

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