Electrodynamics near the Metal-to-Insulator Transition in V3O5
arXiv:cond-mat/0701742 · doi:10.1103/PhysRevB.75.245108
Abstract
The electrodynamics near the metal-to-insulator transitions (MIT) induced, in V3O5 single crystals, by both temperature (T) and pressure (P) has been studied by infrared spectroscopy. The T- and P-dependence of the optical conductivity may be explained within a polaronic scenario. The insulating phase at ambient T and P corresponds to strongly localized small polarons. Meanwhile the T-induced metallic phase at ambient pressure is related to a liquid of polarons showing incoherent dc transport, in the P-induced metallic phase at room T strongly localized polarons coexist with partially delocalized ones. The electronic spectral weight is almost recovered, in both the T and P induced metallization processes, on an energy scale of 1 eV, thus supporting the key-role of electron-lattice interaction in the V3O5 metal-to-insulator transition.
arXiv comment7 pages, 5 figures
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- Direct observation of the electrically triggered Insulator-Metal transition in V3O5 far below the transition temperature
- Optical properties of V2O3 in its whole phase diagram
- Optical conductivity of V4O7 across its metal-insulator transition
- Electrodynamics of BaFe2As2 from infrared measurements under pressure
- Signatures of polaronic charge ordering in optical and dc conductivity using dynamical mean field theory
- High-pressure infrared spectroscopy: tuning of the low-energy excitations in correlated electron systems