Ab initio computation of d-d excitation energies in low-dimensional Ti and V oxychlorides

Article

关键词: HARTREE-FOCK;    WANNIER FUNCTIONS;    SYSTEM;    INSULATOR;    OXIDES;    TIOCL;    LICL;    LIF;   

DOI  :  10.1103/PhysRevB.84.235146

来源: SCIE

【 摘 要 】

Using a quantum chemical cluster-in-solid computational scheme, we calculate the local d-d excitation energies for two strongly correlated Mott insulators, the oxychlorides TiOCl and VOCl. TiOCl harbors quasi-one-dimensional spin chains made out of S = 1/2 Ti3+ ions while the electronic structure of VOCl displays a more two-dimensional character. We find in both cases that the lowest-energy d-d excitations are within the t(2g) subshell, starting at 0.34 eV and indicating that orbital degeneracies are significantly lifted. In the vanadium oxychloride, spin triplet to singlet excitations are calculated to be 1 eV higher in energy. For TiOCl, the computed d-level electronic structure and the symmetries of the wave functions are in very good agreement with resonant inelastic x-ray scattering results and optical absorption data. For VOCl, future resonant inelastic x-ray scattering experiments will constitute a direct test of the symmetry and energy of about a dozen different d-d excitations that we predict here.

【 授权许可】

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