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首页> 外文期刊>International Journal of Quantum Chemistry >Orthorhombic superstructures within the rare earth strontium-doped cobaltate perovskites: Ln(1-x)Sr(x)CoO(3-delta) (Ln = Y3+, Dy3+-Yb3+; 0.750 <= x <= 0.875)
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Orthorhombic superstructures within the rare earth strontium-doped cobaltate perovskites: Ln(1-x)Sr(x)CoO(3-delta) (Ln = Y3+, Dy3+-Yb3+; 0.750 <= x <= 0.875)

机译:稀土锶掺杂钴酸盐钙钛矿中的斜方超结构:Ln(1-x)Sr(x)CoO(3-delta)(Ln = Y3 +,Dy3 + -Yb3 +; 0.750 <= x <= 0.875)

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A combination of electron, synchrotron X-ray and neutron powder diffraction reveals a new orthorhombic structure type within the Sr-doped rare earth perovskite cobaltates Ln(1-x) SrxCoO3-delta (Ln = Y3+, Dy3+, Ho3+, Er3+, Tm3+ and Yb3+). Electron diffraction shows a C-centred cell based on a 2 root 2a(p) x 4a(p) x 4 root 2a(p) superstructure of the basic perovskite unit. Not all of these very weak satellite reflections are evident in the synchrotron X-ray and neutron powder diffraction data and the average structure of each member of this series could only be refined based on Cmma symmetry and a 2 root 2a(p) x 4a(p) x 2 root 2a(p) cell. The nature of structural and magnetic ordering in these phases relies on both oxygen vacancy and cation distribution. A small range of solid solution exists where this orthorhombic structure type is observed, centred roughly around the compositions Ln(0.2)Sr(0.8)CoO(3-delta). In the case of Yb3+ the pure orthorhombic phase was only observed for 0.850 <= x <= 0.875. Tetragonal (14/mmm; 2a(p) x 2a(p) x 4a(p)) superstructures were observed for compositions having higher or lower Sr-doping levels, or for compounds with rare earth ions larger than Dy3+. These orthorhombic phases show mixed valence (3+/4+) cobalt oxidation states between 3.2+ and 3.3+. DC magnetic susceptibility measurements show an additional magnetic transition for these orthorhombic phases compared to the associated tetragonal compounds with critical temperatures > 330 K. (C) 2007 Elsevier Inc. All rights reserved.
机译:电子,同步加速器X射线和中子粉末衍射的组合揭示了Sr掺杂稀土钙钛矿钴酸盐Ln(1-x)SrxCoO3-δ(Ln = Y3 +,Dy3 +,Ho3 +,Er3 +,Tm3 +和Yb3 +)。电子衍射显示基于钙钛矿基本单元的2根2a(p)x 4a(p)x 4根2a(p)超结构的C中心电池。并非所有这些非常微弱的卫星反射都在同步加速器X射线和中子粉末衍射数据中显现出来,并且只能基于Cmma对称性和2根2a(p)x 4a( p)x 2个根2a(p)单元。这些阶段中结构和磁有序的性质取决于氧空位和阳离子分布。存在少量固溶体,在该固溶体中观察到这种正交结构类型,大致以成分Ln(0.2)Sr(0.8)CoO(3-δ)为中心。在Yb3 +的情况下,仅在0.850 <= x <= 0.875的情况下观察到纯正交相。对于具有较高或较低Sr掺杂水平的组合物,或稀土离子大于Dy3 +的化合物,观察到四边形(14 / mmm; 2a(p)x 2a(p)x 4a(p))上层结构。这些正交相显示出在3.2+和3.3+之间的混合价态(3 + / 4 +)钴氧化态。与临界温度> 330 K的相关四方化合物相比,直流磁化率测量显示这些正交相具有额外的磁跃迁。(C)2007 Elsevier Inc.保留所有权利。

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