Crystal structure and magnetic properties of the diuranium tritelluride U2Te3

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

Abstract

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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三碲化二铀U2Te3的晶体结构和磁性能
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。
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