Electronic structure of Fe and magnetism in the double perovskites CaFeReO and BaFeReO
arXiv:1905.04988 · doi:10.1103/PhysRevB.99.195118
Abstract
The Fe electronic structure and magnetism in (i) monoclinic CaFeReO with a metal-insulator transition at K and (ii) quasi-cubic half-metallic BaFeReO ceramic double perovskites are probed by soft x-ray absorption spectroscopy (XAS) and magnetic circular dichroism (XMCD). These materials show distinct Fe XAS and XMCD spectra, which are primarily associated with their different average Fe oxidation states (close to Fe for CaFeReO and intermediate between Fe and Fe for BaFeReO) despite being related by an isoelectronic (Ca/Ba) substitution. For CaFeReO, the powder-averaged Fe spin moment along the field direction ( T), as probed by the XMCD experiment, is strongly reduced in comparison with the spontaneous Fe moment previously obtained by neutron diffraction, consistent with a scenario where the magnetic moments are constrained to remain within an easy plane. For T, the unsaturated XMCD signal is reduced below consistent with a magnetic transition to an easy-axis state that further reduces the powder-averaged magnetization in the field direction. For BaFeReO, the field-aligned Fe spins are larger than for CaFeReO ( T) and the temperature dependence of the Fe magnetic moment is consistent with the magnetic ordering transition at K. Our results illustrate the dramatic influence of the specific spin-orbital configuration of Re electrons on the Fe local magnetism of these Fe/Re double perovskites.
7 pages, 3 figures
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