The self-interaction-corrected local-spin-density approximation is used to describe the electronic structure of dioxides, REO2, and sesquioxides, RE2O3, for the rare earths, RE=Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy and Ho. The valencies of the rare earth ions are determined from total energy minimization. We find Ce, Pr, Tb in their dioxides to have the tetravalent configuration, while for all the sesquioxides the trivalent groundstate configuration is found to be the most favourable. The calculated lattice constants for these valency configurations are in good agreement with experiment. Total energy considerations are exploited to show the link between oxidation and f-electron delocalization, and explain why, among the dioxides, only the CeO2, PrO2, and TbO2 exist in nature. Tetravalent NdO2 is predicted to exist as a metastable phase - unstable towards the formation of hexagonal Nd2O3.
@article{arxiv.cond-mat/0503667,
title = {First principles study of rare-earth oxides},
author = {L. Petit and A. Svane and Z. Szotek and W. M. Temmerman},
journal= {arXiv preprint arXiv:cond-mat/0503667},
year = {2009}
}