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Franco, D. G., R. E. Carbonio, and G. Nieva. "Synthesis and structural and magnetic characterization of the frustrated magnetic system La2Ni4/3−xCoxSb2/3O6." Journal of Solid State Chemistry 207 (2013): 69–79.
Abstract: We report the synthesis of double perovskites La2Ni4/3−xCoxSb2/3O6 with x=0, 1/3, 2/3 and 1 by a solid state method. Rietveld refinements of X-ray and neutron powder diffraction data show that all samples crystallize in space group P21/n, with almost perfect occupation of the 2d octahedral site with the transition metals, while all Sb5+ are randomly distributed in a 2c octahedral site. The saturation magnetization in hysteresis loops indicates that the samples are ferrimagnetic throughout all the series. Virgin magnetization curves lie outside hysteresis loops at low temperatures and thermal evolution of Hm – defined as the inflection point of these curves – follows the de Almeida–Thouless dependence for x ≠0 . This spin glass like behavior below 30 K is also supported by thermal evolution of the coercivity, which follows an exponential law typical of magnetic clusters, not found in the pure Ni2+ perovskite, x=0 extreme.
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Franco, D. G., V. C. Fuertes, M. C. Blanco, M. T. Fernández-Díaz, R. D. Sánchez, and R. E. Carbonio. "Synthesis, structure and magnetic properties of La3Co2SbO9: A double perovskite with competing antiferromagnetic and ferromagnetic interactions." Journal of Solid State Chemistry 194 (2012): 385–391.
Abstract: The synthesis, structural characterization, and magnetic properties of La3Co2SbO9 double perovskite are reported. The crystal structure has been refined by X-ray and neutron powder diffraction data in the monoclinic space group P21/n. Co2+ and Sb5+ have the maximum order allowed for the La3Co2SbO9 stoichiometry. Rietveld refinements of powder neutron diffraction data show that at room temperature the cell parameters are a=5.6274(2) Å, b=5.6842(2) Å, c=7.9748(2) Å and β=89.999(3)°. Magnetization measurements indicate the presence of ferromagnetic correlations with TC=55 K attributed to the exchange interactions for non-linear Co2+–O–Sb5+–O–Co2+ paths. The effective magnetic moment obtained experimentally is μexp=4.38 μB (per mol Co2+), between the theoretical one for spin only (3.87 μB) and spin-orbit value (6.63 μB), indicating partially unquenched contribution. The low magnetization value at high magnetic field and low temperature (1 μB/f.u., 5 T and 5 K) and the difference between ZFC and FC magnetization curves (at 5 kOe) indicate that the ferromagnetism do not reach a long range order and that the material has an important magnetic frustration.
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