Optical absorption and luminescence of α-LiV2O5 from the Bethe Salpeter Equation

Abstract

α-LixV2O5 is obtained by intercalating Li between the layers of V2O5. The partial filling of the split-off conduction band by electron donation from Li leads to significant changes in optical properties. Here we study the electronic band structure of α-LiV2O5 using quasiparticle self-consistent (QS) GW calculations and the optical dielectric function by means of the Bethe-Salpeter Equation (BSE). The half-filling of the narrow split-off band leads to a spin-splitting and formation of magnetic moments of 0.5 μB per V which order antiferromagnetically along the chain or b-direction. The imaginary part of the dielectric function shows a very strong optical absorption band near 2 eV for polarization along the a-direction. This absorptions stems from a localized transition between the occupied V-dxy derived band, which is odd with respect to the a-mirrorplane to the higher lying empty band formed from the same V-dxy orbitals but even with respect to that mirror-plane, which explains its polarization and large oscillator strength. We relate this to a recent experimental study of cathodoluminescence (CL) in which a suppression of the lowest CL peak was observed upon addition of Li. The lowest CL peak near 1.8 eV, which lies well below the indirect absorption onset of V2O5 is proposed to be related to recombination of a self-trapped electron polaron, resulting from oxygen vacancies, with a hole at the valence band maximum and is suppressed in LiV2O5 by the strong self--absorption from the Li induced occupied band to the higher empty bands at about the same energy.

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