The optical/infrared properties of films of vanadium dioxide (VO2) and vanadium sesquioxide (V2O3) have been investigated via ellipsometry and near-normal incidence reflectance measurements from far infrared to ultraviolet frequencies. Significant ch
anges occur in the optical conductivity of both VO2 and V2O3 across the metal-insulator transitions at least up to (and possibly beyond) 6 eV. We argue that such changes in optical conductivity and electronic spectral weight over a broad frequency range is evidence of the important role of electronic correlations to the metal-insulator transitions in both of these vanadium oxides. We observe a sharp optical transition with possible final state (exciton) effects in the insulating phase of VO2. This sharp optical transition occurs between narrow a1g bands that arise from the quasi-one-dimensional chains of vanadium dimers. Electronic correlations in the metallic phases of both VO2 and V2O3 lead to reduction of the kinetic energy of the charge carriers compared to band theory values, with paramagnetic metallic V2O3 showing evidence of stronger correlations compared to rutile metallic VO2.
We report on far infrared measurements of interplane conductivity for underdoped single-crystal YBa2Cu3Oy in magnetic field and situate these new data within earlier work on two other high-Tc cuprate superconductors, La(2-x)SrxCuO4 and Bi2Sr2CaCu2O(8
+d). The three systems have displayed apparently disparate electrodynamic responses in the Josephson vortex state formed when magnetic field H is applied parallel to the CuO2 planes. Specifically, there is discrepancy in the number and field dependence of longitudinal modes observed. We compare and contrast these findings with several models of the electrodynamics in the vortex state and suggest that most differences can be reconciled through considerations of the Josephson vortex lattice ground state as well as the c-axis and in-plane quasiparticle dissipations.
