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Modification of low temperature magnetic interactions in Dy1-xEuxMnO3

机译:DY1-XEUXMNO3中低温磁相互作用的改变

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摘要

Solid solutions of rare earth ion (Eu3+) substituted DyMnO3, Dy1-xEuxMnO3 (x = 0.0-1.0) have been synthesized by ceramic method. Powder X-ray diffraction revealed single phase nature of the compounds with orthorhombic structure. Contributions from the atomic vibrations to the observation of Raman bands have been established and assigned to symmetry stretching and anti symmetry stretching, bending and tilting modes. Raman band frequencies of tilting, asymmetric stretching and bending modes were found to decrease with increasing europium concentration showing softening. Transport studies revealed that all the compounds show semiconducting nature. While the end compounds display hopping process for electrical conduction, all the substituted compounds showed activated type of conduction, and activated energy was found to reduce with increase in x. Molar susceptibility of the substituted compounds for x = 0.1, 0.3 and 0.5 revealed an antiferromagnetic transition corresponding to Mn ions. The fitted Curie-Weiss temperatures also suggested the existence of antiferromagnetic interactions in all the materials. The magnetic field dependent magnetization at various temperatures revealed paramagnetic nature down to 8 K below which hysteresis loops are observed. The presence of strong ferromagnetic correlations between Dy and Mn spins through apical oxygen ions results in the large coercive fields. For temperatures above the antiferromagnetic temperature of manganese ions (39 K) M-H curves show almost straight lines implying the absence of ferromagnetic interactions in the compounds. Different magnetic transitions: from high temperature paramagnetic state to intermediate temperature antiferromagnetic state to low temperature ferromagnetic states are observed in the M-H data.
机译:通过陶瓷方法合成了稀土离子(EU3 +)取代的DymnO3,Dy1-XexmnO 3(x = 0.0-1.0)的固溶体。粉末X射线衍射揭示了具有正交结构的化合物的单相性质。已经建立并分配了来自原子振动对拉曼带的观察的贡献,并分配到对称拉伸和抗对称拉伸,弯曲和倾斜模式。发现倾斜,不对称拉伸和弯曲模式的拉曼带频率随着铕浓度的增加显示软化而降低。运输研究表明,所有化合物都显示出半导体性质。虽然结束化合物显示电导的跳跃过程,但所有取代的化合物都显示出活化的传导类型,并且发现活性能量随X增加而减少。 X = 0.1,0.1,0.5的取代化合物的摩尔敏感性揭示了对应于Mn离子的反铁磁性转变。安装的居里 - 韦斯温度还提出了所有材料的反铁磁相互作用。各种温度下的磁场依赖性磁化揭示了下降到8k以下的顺磁性,观察到滞后环。 Dy和Mn之间的强烈铁磁性相关性通过顶端氧离子之间的旋转导致大矫顽田。对于高于高于锰离子的反铁磁温度(39 k)M-H曲线的曲线显示几乎直线,暗示了化合物中没有铁磁相互作用。在M-H数据中观察到不同磁化转换:从高温顺磁状态到中间温度的反铁磁状态,在M-H数据中观察到低温铁磁状态。

著录项

  • 来源
    《RSC Advances》 |2018年第24期|共9页
  • 作者单位

    Indira Gandhi Ctr Atom Res Mat Sci Grp HBNI Kalpakkam 603102 Tamil Nadu India;

    Indira Gandhi Ctr Atom Res Mat Sci Grp HBNI Kalpakkam 603102 Tamil Nadu India;

    Indira Gandhi Ctr Atom Res Mat Sci Grp HBNI Kalpakkam 603102 Tamil Nadu India;

    Indira Gandhi Ctr Atom Res Mat Sci Grp HBNI Kalpakkam 603102 Tamil Nadu India;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
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