三碲化二铀U2Te3的晶体结构和磁性能

O. Tougait, M. Potel, J.C. Levet, H. Noël
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引用次数: 11

摘要

以一定量的氯化铯与这些元素按化学计量比例进行固相反应,制得U2Te3单晶。U2Te3在正交体系中结晶,空间群Pnma (no . 62),晶胞参数a = 12.175(2)Å, b = 4.370(1)Å, c = 11.828(2)Å, Z = 4。根据单晶x射线衍射数据确定结构,并对32个可变参数和1100个衍射强度的唯一数据集进行细化,最终残余因子R(F) = 0.030和Rω(F) = 0.035 [I >3σ(我)]。U原子位于两个4c不等效的晶体位置上。U(1)具有7倍Te原子配位,其配位多面体由一个顶点被分成两个位置的八面体衍生而来,U(2)具有单端三角棱柱配位。U2Te3表现出相当复杂的磁性行为,在T ~ 110 K时铁磁有序开始,在105 K以下自旋重定向。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Crystal structure and magnetic properties of the diuranium tritelluride U2Te3

Single crystals of U2Te3 were obtained by solid state reaction between the elements in stoichiometric proportions mixed with a small quantity of cesium chloride. U2Te3 crystallizes in the orthorhombic system, space group Pnma (no 62), with unit cell parameters a = 12.175(2)Å, b = 4.370(1)Å, c = 11.828(2)Å, and Z = 4. The structure was determined from single crystal X-ray diffraction data and refined to final residual factors R(F) = 0.030 and Rω(F) = 0.035 for 32 variable parameters and a unique data set of 1100 diffraction intensities [I > 3σ(I)]. The U atoms are located on two 4c non equivalent crystallographic positions. U(1) has a 7-fold coordination of Te atoms with a coordination polyhedron deriving from an octahedron in which one apex is split into two positions, and U(2) has a monocapped trigonal prismatic coordination. U2Te3 exhibits rather complex magnetic behaviour, with an onset of ferromagnetic order at T ∼ 110 K and spin reorientation below 105 K.

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