...
首页> 外文期刊>RSC Advances >Modification of low temperature magnetic interactions in Dy1?xEuxMnO3
【24h】

Modification of low temperature magnetic interactions in Dy1?xEuxMnO3

机译:Dy1?xEuxMnO3中低温磁性相互作用的修饰

获取原文
   

获取外文期刊封面封底 >>

       

摘要

Solid solutions of rare earth ion (Eu ~(3+) ) substituted DyMnO _(3) , Dy _(1? x ) Eu _( x ) MnO _(3) ( 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:陶瓷合成了稀土离子(Eu〜(3+))取代的DyMnO _(3),Dy _(1?x)Eu _(x)MnO _(3)(x = 0.0–1.0)的固溶体方法。粉末X射线衍射显示具有正交晶结构的化合物的单相性质。已经建立了从原子振动到拉曼谱带观测的贡献,并将其分配给对称拉伸和反对称拉伸,弯曲和倾斜模式。人们发现,随着,浓度的增加,拉曼带的频率出现倾斜,不对称拉伸和弯曲的模式,从而降低,从而显示出软化的趋势。运输研究表明,所有化合物均显示出半导体性质。虽然最终化合物显示出导电的跳跃过程,但所有取代的化合物均显示出活化的导电类型,并且发现活化能随x的增加而降低。对于x = 0.1、0.3和0.5,取代的化合物的摩尔磁化率显示出对应于Mn离子的反铁磁跃迁。居里-魏斯拟合温度也表明所有材料中都存在反铁磁相互作用。在各种温度下与磁场有关的磁化强度显示出低至8 K的顺磁特性,低于8 K时可观察到磁滞回线。 Dy和Mn自旋通过顶部氧离子之间存在强铁磁相关性,导致产生较大的矫顽场。当温度高于锰离子的反铁磁温度(39 K)时,M–H曲线显示几乎是直线,这意味着化合物中不存在铁磁相互作用。不同的磁跃迁:在M – H数据中观察到从高温顺磁态到中温反铁磁态再到低温铁磁态。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号