准一维自旋链化合物Ca3Co2O6中Ge取代强化铁磁链内耦合

S. De, A. Banerjee
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引用次数: 0

摘要

利用X射线衍射(XRD)和直流磁化技术分别对Ca3Co2-XGeXO6 (X = 0.000、0.015和0.030)氧化物体系的结构和磁性进行了详细的研究。室温XRD数据的Rietveld细化表明,所有Ge掺杂化合物均与Ca3Co2O6 (CCO)呈同构关系,晶格参数无明显变化。同时,从磁化研究中可以看出,随着Ge的取代,铁磁链内偶联逐渐增加。而掺入Ge后,周围FM链的相互作用强度没有明显变化。因此,与CCO相比,链内相互作用的加强导致Ge取代化合物在高温下具有理想的一维行为。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Strengthening of ferromagnetic intrachain coupling by Ge substitution in quasi-one-dimensional spin chain compound: Ca3Co2O6
Detail study of the structural and magnetic properties of oxide systems, Ca3Co2-XGeXO6 (X = 0.000, 0.015 and 0.030), have been carried out using X-ray diffraction (XRD) and dc magnetization techniques respectively. Rietveld refinement of room temperature XRD data shows that all the Ge doped compounds are isostructural with Ca3Co2O6 (CCO) and there is no remarkable change in lattice parameters. At the same time, it is evident from magnetization study that ferromagnetic intrachain coupling gradually increases with Ge substitution. Whereas no significant modification is observed in the interaction strength of surrounding FM chains with Ge doping. Thus, the strengthening of intrachain interaction results in ideal one-dimensional behavior at high temperature in Ge substituted compounds compared to CCO.
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