铈(Ce3+)取代对Co0.9Fe2.1-xCexO4纳米铁氧体结构和频率相关电学性能的影响

IF 2.8
Y. S. Madansure, Pravin K. Gaikwad, Vishnu S. Shinde, S. R. Manegopale, Sagar E. Shirsath, S. K. Gurav
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摘要

本文研究了稀土铈(Ce3+)取代对富钴纳米铁素体结构和电学性能的影响。采用溶胶-凝胶自燃烧法合成了一系列标称成分为Co0.9Fe2.1-xCexO4 (x = 0.0, 0.025, 0.05, 0.075, 0.1)的纳米颗粒。x射线衍射(XRD)分析证实,所有成分均形成了一个单相立方尖晶石结构,随着铈含量的增加,晶格参数从8.38系统地增加到8.42 Å,表明较大的Ce3+离子成功地结合到晶格中。使用Debye-Scherrer公式估计的晶体尺寸在纳米范围内。电子显微镜研究(扫描电镜和透射电镜)显示凝聚的准球形纳米颗粒。在室温下分析了频率相关的电学特性。结果表明,随着铈浓度的增加,材料的交流电导率、介电常数(ε′)和介电损耗正切(tan δ)有系统的降低。这是由于Fe3+离子在八面体位置被Ce3+离子取代,限制了Fe2+和Fe3+离子之间的跳跃机制。介质损耗的显著降低突出了这些掺铈纳米铁氧体在高频器件应用中的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Influence of Cerium (Ce3+) Substitution on the Structural and Frequency-Dependent Electrical Properties of Co0.9Fe2.1-xCexO4 Nanoferrites

Influence of Cerium (Ce3+) Substitution on the Structural and Frequency-Dependent Electrical Properties of Co0.9Fe2.1-xCexO4 Nanoferrites

This study investigates the impact of rare-earth cerium (Ce3+) substitution on the structural and electrical properties of cobalt-rich nanoferrites. A series of nanoparticles with the nominal composition Co0.9Fe2.1-xCexO4 (where x = 0.0, 0.025, 0.05, 0.075, and 0.1) are synthesized via the sol-gel auto-combustion method. X-ray diffraction (XRD) analysis confirms the formation of a single-phase cubic spinel structure for all compositions, with the lattice parameter systematically increasing from 8.38 to 8.42 Å with rising cerium content, indicating the successful incorporation of the larger Ce3+ ions into the lattice. The crystallite size, estimated using the Debye-Scherrer formula, is found to be in the nanometer range. Electron microscopy studies (SEM and TEM) reveal agglomerated, quasi-spherical nanoparticles. The frequency-dependent electrical properties are analyzed at room temperature. Results show a systematic decrease in AC conductivity, dielectric constant (ε'), and dielectric loss tangent (tan δ) with increasing cerium concentration. This behavior is attributed to the substitution of Fe3+ ions by Ce3+ ions at the octahedral sites, which limits the hopping mechanism between Fe2+ and Fe3+ ions. The significant reduction in dielectric loss highlights the potential of these cerium-doped nanoferrites for high-frequency device applications.

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