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巨磁致伸缩拉夫斯相SmFe中的结构与相变

Structure and Phase Transformation in the Giant Magnetostriction Laves-Phase SmFe.

作者信息

Liu Xiaonan, Lin Kun, Gao Qilong, Zhu He, Li Qiang, Cao Yili, Liu Zhanning, You Li, Chen Jun, Ren Yang, Huang Rongjin, Lapidus Saul H, Xing Xianran

机构信息

Argonne National Laboratory, X-Ray Science Division , Argonne, Illinois 60439, United States.

Key Laboratory of Cryogenics, Technical Institute of Physics and Chemistry, Chinese Academy of Sciences , Beijing 100190, China.

出版信息

Inorg Chem. 2018 Jan 16;57(2):689-694. doi: 10.1021/acs.inorgchem.7b02525. Epub 2017 Dec 28.

DOI:10.1021/acs.inorgchem.7b02525
PMID:29283569
Abstract

As one class of the most important intermetallic compounds, the binary Laves-phase is well-known for its abundant magnetic properties. Samarium-iron alloy system SmFe is a prototypical Laves compound that shows strong negative magnetostriction but relatively weak magnetocrystalline anisotropy. SmFe has been identified as a cubic Fd3̅m structure at room temperature; however, the cubic symmetry, in principle, does not match the spontaneous magnetization along the [111] direction. Here we studied the crystal structure of SmFe by high-resolution synchrotron X-ray powder diffraction, X-ray total scattering, and selected-area electron diffraction methods. SmFe is found to adopt a centrosymmetric trigonal R3̅m structure at room temperature, which transforms to an orthorhombic Imma structure at 200 K. This transition is in agreement with the changes of easy magnetization direction from [111] to [110] direction and is further evidenced by the inflection of thermal expansion behavior, the sharp decline of the magnetic susceptibility in the field-cooling-zero field-cooling curve, and the anomaly in the specific heat capacity measurement. The revised structure and phase transformation of SmFe could be useful to understand the magnetostriction and related physical properties of other RM-type pseudocubic Laves-phase intermetallic compounds.

摘要

作为一类最重要的金属间化合物,二元拉夫斯相以其丰富的磁性而闻名。钐铁合金体系SmFe是一种典型的拉夫斯化合物,具有很强的负磁致伸缩,但磁晶各向异性相对较弱。SmFe在室温下被确定为立方Fd3̅m结构;然而,立方对称性原则上与沿[111]方向的自发磁化不匹配。在此,我们通过高分辨率同步辐射X射线粉末衍射、X射线全散射和选区电子衍射方法研究了SmFe的晶体结构。发现SmFe在室温下采用中心对称的三角R3̅m结构,在200 K时转变为正交Imma结构。这种转变与易磁化方向从[111]向[110]方向的变化一致,并且通过热膨胀行为的拐点、场冷-零场冷曲线中磁化率的急剧下降以及比热容测量中的异常现象得到进一步证明。SmFe的修正结构和相变可能有助于理解其他RM型伪立方拉夫斯相金属间化合物的磁致伸缩及相关物理性质。

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