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Synthesis, crystal and magnetic structure of the new double perovskite Ba2MnMoO6

机译:新型双钙钛矿Ba2MnMoO6的合成,晶体和磁性结构

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We describe the preparation and characterization of a new double perovskite of formula Ba2MnMoO6. It has been obtained in polycrystalline form by thermal treatment, in a H-2/N-2 flow, of previously decomposed citrate precursors. This material has been studied by X-ray (XRD) and neutron powder diffraction (NPD): it crystallizes, at room temperature, in the cubic space group Fm3m, and shows an almost perfect ordering between Mn2+ and Mo6+ cations at the B substructure. Below T-N = 10.8 K, it experiences a long range antiferromagnetic ordering that was followed from sequential NPD data. The low-temperature magnetic structure is defined by the propagation vector k = ((1)/(2), (1)/(2), (1)/(2)). The ordered magnetic moment of Mn is found to be 4.04(8) mu(B) at 2 K, suggesting a divalent oxidation state for Mn cations, in a high spin t(2g)(3) e(g)(2) (S = 5/2) electronic configuration. [References: 19]
机译:我们描述了分子式为Ba2MnMoO6的新型双钙钛矿的制备和表征。它是通过在H-2 / N-2流中对先前分解的柠檬酸盐前体进行热处理而以多晶形式获得的。对该材料进行了X射线(XRD)和中子粉末衍射(NPD)研究:它在室温下在立方空间群Fm3m中结晶,并在B亚结构处显示Mn2 +和Mo6 +阳离子之间几乎完美的有序性。低于T-N = 10.8 K时,它将经历长距离反铁磁排序,随后从顺序NPD数据开始进行排序。低温磁性结构由传播矢量k =((1)/(2),(1)/(2),(1)/(2))定义。发现在2 K时Mn的有序磁矩为4.04(8)mu(B),表明在高自旋t(2g)(3)e(g)(2)中Mn阳离子的二价氧化态( S = 5/2)电子配置。 [参考:19]

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