Sr 2 CoWO 6 perovskite has been prepared in polycrystalline form by solid-state reaction at 1150 °C. This material has been studied by high-resolution synchrotron X-ray and neutron powder diffraction (NPD), magnetic measurements, and differential scanning calorimetry (DSC). At room temperature, the crystal structure is tetragonal, space group I 4/ m, with a = 5.58277(1) Å and c = 7.97740(1) Å. The structure contains alternating CoO 6 and WO 6 octahedra, tilted in anti-phase by 7.24° in the basal ab plane along the [001] direction of the pseudocubic cell. This corresponds to the a 0 a 0 c - Glazer's notation as derived by Woodward for 1:1 ordering of double perovskites, consistent with space group I 4/ m . DSC and NPD measurements as a function of temperature indicate a structural transition from tetragonal to monoclinic (space group P 2 1 / n ) at 260 K. At 2 K the cell parameters are a = 5.61267(8) Å, b = 5.58753(8) Å, c = 7.8994(1) Å, and β = 90.041(3)°. The structure contains alternating CoO 6 and WO 6 octahedra, tilted in-phase by 4.77° along the [001] direction of the pseudocubic cell and in anti-phase by 5.82° along the [010] and [100] directions. This corresponds to the a - a - c + Glazer's notation as derived by Woodward for 1:1 ordering in double perovskites, consistent with space group P 2 1 / n . Magnetic and neutron diffraction measurements indicate an antiferromagnetic ordering below T N = 24 K. The magnetic moment calculated through the linear fit of the Curie−Weiss law at high temperatures (5.20 μ B ) indicates that the orbital contribution is unquenched at high temperatures, which is consistent with high-spin Co 2+ ( 4 T 1g ground state) in a quasi-regular octahedral environment. As prepared, the sample is an electrical insulator. Magnetic and electrical properties and bond valence sums are consistent with the electronic configuration Co 2+ (3d 7 )−W 6+ (5d 0 ).
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Viola et al. (2003) studied this question.
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