Structural, dielectric relaxation and magnetic features of the (La0.8Ca0.2)0.9Bi0.1Fe1-yTiyO3 (y=0.0 and 0.1) nanoparticles

被引:7
|
作者
Benali, A. [1 ,2 ,3 ]
Bejar, M. [1 ]
Dhahri, E. [1 ]
Graca, M. P. F. [2 ]
Valente, M. A. [2 ]
Hlil, E. K. [4 ]
Costa, B. F. O. [3 ]
机构
[1] Univ Sfax, Fac Sci, Lab Phys Appl, BP 1171, Sfax 3000, Tunisia
[2] Univ Aveiro, Phys Dept, I3N, Campus Santiago, Aveiro, Portugal
[3] Univ Coimbra, CFisUC, Phys Dept, Rua Larga, P-3004516 Coimbra, Portugal
[4] Univ Grenoble Alpes, CNRS, Grenoble INP, Inst Neel, F-38000 Grenoble, France
关键词
Nanoparticle; Giant dielectric constant; Dielectric relaxation; Havriliak-Negami; Ferromagnetism; ALTERNATING-CURRENT CONDUCTIVITY; SOL-GEL; ANNEALING TEMPERATURE; ELECTRICAL-PROPERTIES; SENSING PROPERTIES; BI-SUBSTITUTION; PEROVSKITE; IMPEDANCE; RAMAN; CA;
D O I
10.1016/j.jallcom.2021.160222
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Two nanoparticle orthoferrite materials (La0.8Ca0.2)(0.9)Bi0.1Fe1-yTiyO3 (y = 0.0 and 0.1) have been successfully synthesized via the assisted ball milling solid-state reaction. The effect of Bismuth and Titanium ions insertion in A and B-sites of La0.8Ca0.2FeO3 material on structural, dielectric relaxation and magnetic properties was conducted. Structural study reveals the formation of majoritarian orthorhombic phase in both nanomaterials. Importantly, both compounds present a giant dielectric constant epsilon' and low dielectric loss tangent tg(delta). Two relaxation processes have been detected at low and high-temperature ranges. The adjustment of the imaginary parts of complex Modulus via the Havriliak-Negami formalism (H-N) confirms a Cole-Cole (grains) and Cole-Davison (grain boundaries) relaxation processes at low and high temperature regions, respectively. The magnetic study reveals the enhancement of magnetization when introducing Titanium ions in B-site which increases the Ferromagnetic interactions. It also confirms an important decrease in the Curie Weis temperature (T-C = 450 K). (C) 2021 Elsevier B.V. All rights reserved.
引用
收藏
页数:14
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