Magnetism in SrCrMoO: A combined abinitio and model study
arXiv:1608.00380 · doi:10.1103/PhysRevB.94.035132
Abstract
Using a combination of first-principles density functional theory (DFT) calculations and exact diagonalization studies of a first-principles derived model, we carry out a microscopic analysis of the magnetic properties of the half-metallic double perovskite compound, SrCrMoO, a sister compound of the much discussed material SrFeMoO. The electronic structure of SrCrMoO, though appears similar to SrFeMoO at first glance, shows non trivial differences with that of SrFeMoO on closer examination. In this context, our study highlights the importance of charge transfer energy between the two transition metal sites. The change in charge transfer energy due to shift of Cr states in SrCrMoO compared to Fe in SrFeMoO suppresses the hybridization between Cr and Mo . This strongly weakens the hybridization-driven mechanism of magnetism discussed for SrFeMoO. Our study reveals that, nonetheless, the magnetic transition temperature of SrCrMoO remains high since additional superexchange contribution to magnetism arises with a finite intrinsic moment developed at the Mo site. We further discuss the situation in comparison to another related double perovskite compound, SrCrWO. We also examine the effect of correlation beyond DFT, using dynamical mean field theory (DMFT).
8 pages, 3 figures
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