Induction of magnetodielectric coupling in multiferroic lanthanum ferrite by cobalt doping

IF 5.6 2区 材料科学 Q1 MATERIALS SCIENCE, CERAMICS
X.J. Téllez-Tovar , J.A. Félix-Bernabe , F. Sánchez-De Jesús , C.A. Cortés-Escobedo , A.M. Bolarín-Miró
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Abstract

This research focuses on studying the magnetodielectric coupling at room temperature in lanthanum ferrite induced by cobalt substituting iron sites. The study involved varying cobalt content from 0 to 0.1 mol, with samples synthesized via high-energy ball milling. The evolution of crystal structure, dielectric, and magnetic properties was analyzed. X-ray diffraction (XRD) and Rietveld refinement confirmed the orthorhombic single-phase structure with the Pnma space group in the doped lanthanum ferrite. Vibrating-sample magnetometry results demonstrated that cobalt doping alters the antiferromagnetic order of lanthanum ferrite, inducing ferromagnetism, with a maximum specific magnetization of 1.25 emu/g observed at 0.075 mol cobalt content. Scanning electron microscopy (SEM) analysis revealed an increase in grain size with higher cobalt content, which impacts the material's electrical and dielectric properties. The doped ferrites exhibited lower relative permittivity values compared to pure LaFeO3. Additionally, the presence of cobalt reduced the dielectric dissipation factor, attributed to minor crystal structure distortions. Notably, magnetodielectric coupling was observed in these multiferroic materials for the first time, evidenced by changes in relative permittivity under varying applied fields and frequencies. The highest magnetodielectric coupling was achieved at 0.025 mol cobalt doping, with relative permittivity values ranging from 70 to 26 across frequencies from 50 to 1000 Hz. These findings confirm that cobalt-doped lanthanum ferrites exhibit magnetodielectric coupling at room temperature, suggesting potential for expanded technological applications.

Abstract Image

钴掺杂诱导多铁氧体镧的磁介电耦合
本研究主要研究了室温下钴取代铁位引起的铁酸镧的磁介电耦合。该研究涉及改变钴含量从0到0.1 mol,样品通过高能球磨合成。分析了晶体结构、介电性能和磁性能的演变。x射线衍射(XRD)和Rietveld细化证实了掺杂镧铁氧体中存在具有Pnma空间基的正交单相结构。振动样品磁强计结果表明,钴掺杂改变了铁氧体镧的反铁磁序,产生了铁磁性,在钴含量为0.075 mol时,最大比磁化强度为1.25 emu/g。扫描电子显微镜(SEM)分析显示,随着钴含量的增加,晶粒尺寸增加,这影响了材料的电学和介电性能。与纯LaFeO3相比,掺杂铁氧体的相对介电常数值更低。此外,由于轻微的晶体结构扭曲,钴的存在降低了介电损耗因子。值得注意的是,在这些多铁性材料中首次观察到磁介电耦合,在不同的电场和频率下,相对介电常数的变化证明了这一点。在0.025 mol钴掺杂时,获得了最高的磁介电耦合,在50至1000 Hz的频率范围内,相对介电常数值为70至26。这些发现证实了钴掺杂镧铁氧体在室温下表现出磁介电耦合,表明了扩大技术应用的潜力。
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来源期刊
Ceramics International
Ceramics International 工程技术-材料科学:硅酸盐
CiteScore
9.40
自引率
15.40%
发文量
4558
审稿时长
25 days
期刊介绍: Ceramics International covers the science of advanced ceramic materials. The journal encourages contributions that demonstrate how an understanding of the basic chemical and physical phenomena may direct materials design and stimulate ideas for new or improved processing techniques, in order to obtain materials with desired structural features and properties. Ceramics International covers oxide and non-oxide ceramics, functional glasses, glass ceramics, amorphous inorganic non-metallic materials (and their combinations with metal and organic materials), in the form of particulates, dense or porous bodies, thin/thick films and laminated, graded and composite structures. Process related topics such as ceramic-ceramic joints or joining ceramics with dissimilar materials, as well as surface finishing and conditioning are also covered. Besides traditional processing techniques, manufacturing routes of interest include innovative procedures benefiting from externally applied stresses, electromagnetic fields and energetic beams, as well as top-down and self-assembly nanotechnology approaches. In addition, the journal welcomes submissions on bio-inspired and bio-enabled materials designs, experimentally validated multi scale modelling and simulation for materials design, and the use of the most advanced chemical and physical characterization techniques of structure, properties and behaviour. Technologically relevant low-dimensional systems are a particular focus of Ceramics International. These include 0, 1 and 2-D nanomaterials (also covering CNTs, graphene and related materials, and diamond-like carbons), their nanocomposites, as well as nano-hybrids and hierarchical multifunctional nanostructures that might integrate molecular, biological and electronic components.
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