Structural, magnetic, and dielectric tailoring of Nd3+-substituted Ni0.7Zn0.3Cr0.5Fe1.5-xNdxO4 nanoferrites

IF 4.2 4区 材料科学 Q2 MATERIALS SCIENCE, CERAMICS
A. A. Doke, K. P. Gattu, S. S. Kammar, Ahamad Imran, Ahmed Mohamed El-Toni, Y. R. Kapse, R. H. Kadam, Sagar E. Shirsath, G. H. Kale
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引用次数: 0

Abstract

Nd3+-substituted Ni0.7Zn0.3Cr0.5Fe1.5-xNdxO4 nanoferrites (0.00 ≤ x ≤ 0.05) were synthesized by the sol–gel auto-combustion route to examine how rare-earth substitution tunes the structural, dielectric, electrical, and magnetic characteristics of Ni–Zn ferrites. X-ray diffraction with Rietveld refinement confirmed the formation of a single-phase cubic spinel structure for all compositions. The larger ionic radius of Nd3+ compared with Fe3+ causes lattice expansion/local strain and indicates preferential incorporation into the octahedral B-site network, as also supported by the Bertaut-type cation-distribution analysis. TEM revealed a progressive reduction in particle size with increasing Nd content, consistent with the observed microstructural evolution. Elemental mapping/EDS supported a uniform spatial distribution of constituent elements across the investigated samples. FTIR spectra showed ferrite-related low-wavenumber metal–oxygen vibrational features, with band-shape modifications attributable to Nd-induced perturbation of the local bonding environment. Dielectric spectroscopy showed the expected dispersion of ε′ and tanδ with frequency; moreover, ε′ and dielectric loss decrease with Nd substitution, suggesting suppression of space-charge/interfacial polarization and reduced charge carrier mobility at grain boundaries. The frequency dependence of σac follows the typical ferrite response and is consistent with a hopping-assisted conduction mechanism; σac decreases with increasing Nd content, indicating inhibited hopping between localized states (e.g., Fe2+/Fe3+). Room-temperature M–H measurements confirmed soft ferrimagnetic behavior for all compositions, while the gradual reduction in saturation magnetization and coercivity with Nd incorporation is correlated with weakened A–B superexchange interactions, magnetic dilution, increased Yafet–Kittel spin canting, and modified anisotropy. Overall, Nd3+ substitution provides a viable pathway to tailor the microstructure and multifunctional response of Ni–Zn–Cr ferrites for high-frequency and low-loss magnetic/dielectric device applications.

Abstract Image

Nd3+取代Ni0.7Zn0.3Cr0.5Fe1.5-xNdxO4纳米铁氧体的结构、磁性和介电剪裁
采用溶胶-凝胶自燃烧法合成了Nd3+取代Ni0.7Zn0.3Cr0.5Fe1.5-xNdxO4纳米铁氧体(0.00≤x≤0.05),研究稀土取代对Ni-Zn铁氧体结构、介电、电学和磁性的影响。经里特费尔德细化的x射线衍射证实,所有成分均形成单相立方尖晶石结构。与Fe3+相比,Nd3+的离子半径更大,导致晶格膨胀/局部应变,并表明优先融入八面体b位网络,这也得到了bertaut型阳离子分布分析的支持。TEM显示,随着Nd含量的增加,晶粒尺寸逐渐减小,这与观察到的显微组织演变相一致。元素映射/EDS支持在所调查样品中组成元素的均匀空间分布。FTIR光谱显示出与铁氧体相关的低波数金属-氧振动特征,并且由于nd引起的局部键合环境的扰动导致了带形的改变。电介质谱显示ε′和tanδ随频率的预期色散;此外,ε′和介电损耗随Nd取代而降低,表明空间电荷/界面极化受到抑制,晶界处载流子迁移率降低。σac的频率依赖性遵循典型的铁氧体响应,符合跳变辅助传导机制;σac随Nd含量的增加而减小,表明局域态(如Fe2+/Fe3+)之间的跳变受到抑制。室温M-H测量证实了所有成分的软铁磁行为,而Nd掺入后饱和磁化强度和矫顽力的逐渐降低与A-B超交换相互作用减弱、磁稀释、Yafet-Kittel自旋倾斜增加和各向异性的改变有关。总之,Nd3+取代提供了一个可行的途径来定制Ni-Zn-Cr铁氧体的微观结构和多功能响应,用于高频和低损耗的磁/介电器件应用。
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来源期刊
Journal of Sol-Gel Science and Technology
Journal of Sol-Gel Science and Technology 工程技术-材料科学:硅酸盐
CiteScore
4.70
自引率
4.00%
发文量
280
审稿时长
2.1 months
期刊介绍: The primary objective of the Journal of Sol-Gel Science and Technology (JSST), the official journal of the International Sol-Gel Society, is to provide an international forum for the dissemination of scientific, technological, and general knowledge about materials processed by chemical nanotechnologies known as the "sol-gel" process. The materials of interest include gels, gel-derived glasses, ceramics in form of nano- and micro-powders, bulk, fibres, thin films and coatings as well as more recent materials such as hybrid organic-inorganic materials and composites. Such materials exhibit a wide range of optical, electronic, magnetic, chemical, environmental, and biomedical properties and functionalities. Methods for producing sol-gel-derived materials and the industrial uses of these materials are also of great interest.
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