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Synthesis and characterization of the reduced double-layer manganite Sr3Mn2O6+x

机译:还原型双层锰矿Sr3Mn2O6 + x的合成与表征

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The oxygen-deficient Ruddlesden-Popper (RP) phase Sr3Mn2O6 crystallizes with an ordered array of oxygen vacancies to afford a structure in which the Mn3+ ions exist in a square-pyramidal environment. The MnO5 polyhedra are linked through their corners to form a structure that is related to that observed for the single-layered material, Sr2MnO3.5. The nuclear and magnetic structures of a polycrystalline sample of Sr3Mn2O6 have been determined using Rietveld analysis of neutron powder diffraction data and electron diffraction techniques. The pure Mn3+ double-layered phase crystallizes in a superstructure of the simple RP subcell: tetragonal, P4/mbm, a = 10.8686(2) Angstrom and c = 20.2051(3) Angstrom. Magnetic susceptibility studies suggest a transition at similar to 250 K to a canted antiferromagnetic ordered structure. The magnetic unit-cell consists of ferromagnetic clusters of corner-sharing MnO5 units, which are antiferromagnetically aligned to other clusters within the layers. (C) 2003 Elsevier Inc. All rights reserved. [References: 13]
机译:缺氧的Ruddlesden-Popper(RP)相Sr3Mn2O6以有序排列的氧空位结晶,从而提供其中Mn3 +离子存在于方形金字塔形环境中的结构。 MnO5多面体通过它们的角连接在一起,形成与单层材料Sr2MnO3.5观察到的结构有关的结构。使用中子粉末衍射数据的Rietveld分析和电子衍射技术已经确定了Sr3Mn2O6多晶样品的核和磁结构。纯Mn3 +双层相在简单的RP子电池的上层结构中结晶:四边形,P4 / mbm,a = 10.8686(2)埃和c = 20.2051(3)埃。磁化率研究表明,类似于250 K的过渡转变为倾斜的反铁磁有序结构。磁性单位单元由角共享MnO5单元的铁磁簇组成,这些铁磁簇与层中的其他簇反铁磁对齐。 (C)2003 Elsevier Inc.保留所有权利。 [参考:13]

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