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Electronic correlations and crystal structure distortions in BaBiO3

D. Korotin,V. Kukolev,A. V. Kozhevnikov,D. Novoselov,V. I. Anisimov

Published 2012 in Journal of Physics: Condensed Matter

ABSTRACT

BaBiO3 is a material where Bi4+ ions with half-filled 6s-states form an alternating set of Bi3+ and Bi5+ ions resulting in a charge ordered insulator. The charge ordering is accompanied by breathing distortion of the BiO6 octahedra (extension and contraction of the Bi–O bond lengths). Standard density functional theory (DFT) calculations fail to obtain the crystal structure instability caused by the pure breathing distortions. Combining effects of the breathing distortions and tilting of the BiO6 octahedra allows DFT to reproduce qualitatively an experimentally observed insulator with monoclinic crystal structure but strongly underestimates the breathing distortion parameter and energy gap values. In the present work we reexamine the BaBiO3 problem within the GGA + U method using a Wannier function basis set for the Bi 6s-band. Due to the high oxidation state of bismuth in this material, the Bi 6s-symmetry Wannier function is predominantly extended spatially on surrounding oxygen ions and hence differs strongly from a pure atomic 6s-orbital. That is in sharp contrast to transition metal oxides (with exclusion of high oxidation state compounds) where the major part of the d-band Wannier function is concentrated on the metal ion and a pure atomic d-orbital can serve as a good approximation. The GGA + U calculation results agree well with experimental data, in particular with experimental crystal structure parameters and energy gap values. Moreover, the GGA + U method allows one to reproduce the crystal structure instability due to the pure breathing distortions without octahedra tilting.

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