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首页> 外文期刊>Solid state sciences >On the novel double perovskites A(2)Fe(Mn0.5W0.5)O-6 (A= Ca, Sr, Ba). Structural evolution and magnetism from neutron diffraction data
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On the novel double perovskites A(2)Fe(Mn0.5W0.5)O-6 (A= Ca, Sr, Ba). Structural evolution and magnetism from neutron diffraction data

机译:在新型双重钙钛矿A(2)Fe(MN0.5W0.5)O-6(A = CA,SR,BA)。 中子衍射数据的结构演化与磁力

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New A(2)Fe(Mn0.5W0.5)O-6 (A = Ca, Sr, Ba) double perovskite oxides have been prepared by ceramic techniques. X-ray diffraction (XRD) complemented with neutron powder diffraction (NPD) indicate a structural evolution from monoclinic (space group P2(1)/n) for A = Ca to cubic (Fm-3m) for A = Sr and finally to hexagonal (P6(3)/mmc) for A = Ba as the perovskite tolerance factor increases with the A(2+) ionic size. The three oxides present different tilting schemes of the FeO6 and (Mn,W)O-6 octahedra. NPD data also show evidence in all cases of a considerable anti-site disordering, involving the partial occupancy of Fe positions by Mn atoms, and vice-versa. Magnetic susceptibility data show magnetic transitions below 50 K characterized by a strong irreversibility between ZFC and FC susceptibility curves. The A = Ca perovskite shows a G-type magnetic structure, with weak ordered magnetic moments due to the mentioned antisite disordering. Interesting magnetostrictive effects are observed for the Sr perovskite below 10 K. (C) 2018 Elsevier Masson SAS. All rights reserved.
机译:新的A(2)Fe(MN0.5w0.5)O-6(A = CA,SR,BA)通过陶瓷技术制备了双钙钛矿氧化物。与中子粉末衍射(NPD)互补的X射线衍射(XRD)表明A = Sr的α= Ca至立方(FM-3M)的单斜(空间组P2(1)/ N)的结构演变,最后达到六边形(P6(3)/ mmc)对于a = ba,因为钙钛矿容差因子随着a(2+)离子尺寸而增加。三种氧化物存在FeO6和(Mn,W)O-6 octahedra的不同倾斜方案。 NPD数据还显示所有案例的证据,涉及Mn原子的Fe位置的部分占用,反之亦然。磁化性数据显示低于50 k以下的磁化转变,其特征在于ZFC和FC易感曲线之间的强不可逆转性。 A = CA PEROVSKITE显示了G型磁性结构,由于所述的ARISite排放而具有弱有序的磁矩。对于低于10 K的SR Perovskite观察到有趣的磁致伸缩效果。(c)2018 Elsevier Masson SAS。版权所有。

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