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ЖЭТФ, Том 132, Вып. 1, стр. 57 (Июль 2007)
(Английский перевод - JETP, Vol. 105, No 1, p. 46, July 2007 доступен on-line на www.springer.com )

CORRELATION ENERGIES IN DISTORTED 3d-t2g PEROVSKITE OXIDES
Solovyev I.V.

Поступила в редакцию: 17 Октября 2006

PACS: 71.10.-w, 71.15.Nc, 71.28.+d, 75.25.+z

DJVU (110.6K) PDF (309.6K)

Using an effective low-energy Hamiltonian derived from the first-principle electronic structure calculations for the narrow t2g bands of YTiO3, LaTiO3, YVO3, and LaVO3, we evaluate the contributions of the correlation energy Ec to the stability of different magnetic structures that can be realized in these distorted perovskite oxides. We consider two approximations for Ec that are based on the regular perturbation theory expansion around a nondegenerate Hartree - Fock ground state. One is the second order of the perturbation theory, which allows comparing the effects of local and nonlocal correlations. The other is the local t-matrix approach, which allows treating some higher-order contributions to Ec. The correlation effects systematically improve the agreement with the experimental data and additionally stabilize the experimentally observed G- and C-type antiferromagnetic (AFM) structures in YVO3 and LaVO3, although the absolute magnitude of the stabilization energy is sensitive to the level of approximations and is somewhat smaller in the t-matrix method. The nonlocal correlations additionally stabilize the ferromagnetic ground state in YTiO3 and the C-type AFM ground state in LaVO3. Among two inequivalent transition-metal sites in the monoclinic structure, the local correlations are stronger at the sites with the least distorted environment. Limitations of the regular perturbation-theory expansion for LaTiO3 are also discussed.

 
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