Double perovskite oxides A2BB′O6 combining 3d and 4d or 5d transition metal ions at the B and B′ sites feature a variety of magnetic and magneto-electric properties. Targeting Ba2FeOsO6, we… Click to show full abstract
Double perovskite oxides A2BB′O6 combining 3d and 4d or 5d transition metal ions at the B and B′ sites feature a variety of magnetic and magneto-electric properties. Targeting Ba2FeOsO6, we synthesized powder samples of nonstoichiometric Ba2Fe1.12Os0.88O6 by solid-state reaction from the oxides. The crystal structure was investigated by using synchrotron powder X-ray and powder neutron diffraction. In contrast to Ca2FeOsO6 and Sr2FeOsO6, the compound adopts the hexagonal 6L perovskite structure (space group P3m1) with partial Fe–Os order at both the face-sharing B2O9 dimer and the corner sharing BO6 transition metal sites. Magnetization, neutron diffraction, and 57Fe Mossbauer spectroscopy results show that Ba2Fe1.12Os0.88O6 develops ferrimagnetic order well above room temperature at TC ≈ 370 K. The nonsaturated magnetization curve at 2 K features a magnetic moment of 0.4 μB per formula unit at 7 T and a pronounced hysteresis with a coercive field of about 2 T. Large exchange bias effects are observed wh...
               
Click one of the above tabs to view related content.