Influence of Cu2+ doping on the structure, dielectric and magnetic properties of NiFe2O4 prepared by the sol-gel method

被引:14
|
作者
Sun, Li [1 ,2 ]
Guo, Jianqin [2 ]
Zhang, Ru [2 ]
Cao, Ensi [2 ]
Zhang, Yongjia [2 ]
Hao, Wentao [2 ]
Ju, Lin [3 ]
机构
[1] Taiyuan Univ Technol, Minist Educ, Key Lab Adv Transducers & Intelligent Control Sys, Taiyuan 030024, Shanxi, Peoples R China
[2] Taiyuan Univ Technol, Coll Phys & Optoelect, Taiyuan 030024, Shanxi, Peoples R China
[3] Anyang Normal Univ, Coll Phys & Elect Engn, Anyang 455000, Peoples R China
基金
中国国家自然科学基金;
关键词
CuxNi1-xFe2O4; Sol-gel method; Ferrites; Magnetic properties; COBALT FERRITE; ELECTRICAL-PROPERTIES; NICKEL FERRITES; AUTO-COMBUSTION; ZN FERRITE; NANOPARTICLES; TEMPERATURE; ANISOTROPY; CERAMICS; BEHAVIOR;
D O I
10.1016/j.jmmm.2017.10.104
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
CuxNi1-xFe2O4 powders were prepared by the sol-gel method and the corresponding temperature dependence of microstructure, magnetic and dielectric properties of different CuxNi1-xFe2O4 samples have been investigated. Results of XRD and SEM indicate that the Cu2+ concentration played an important role in both crystal phase and particle distribution of CuxNi1-xFe2O4. The measurement of magnetic properties shows that both Cu2+ doping and sintering temperature could change the saturation magnetization and remanent magnetization in a noticeable manner, and even the magnetic material type. The Cu0.2Ni0.8Fe2O4 sample sintered at 900 degrees C had the largest saturation magnetization (34.61 emu/g), remanent magnetization (17.85 emu/g) and the lowest coercivity (0.17 kOe). The dielectric measurements show strong frequency dependence for all the samples. The peak observed in frequency dependence of dielectric loss measurements shifts to higher frequency with the increasing Cu2+ concentration and sintering temperature, indicating a Debye- like dielectric relaxation. All the results indicate that the Cu2+ doping has a significant influence on NiFe2O4 ferrites. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:545 / 551
页数:7
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