Effect of site preferences on structural and magnetic switching properties of CO-Zr doped strontium hexaferrite SrCoxZrxFe(12-2x)O19

被引:97
作者
Chawla, S. K. [1 ]
Meena, S. S. [2 ]
Kaur, Prabhjoyt [1 ]
Mudsainiyan, R. K. [1 ]
Yusuf, S. M. [2 ]
机构
[1] Guru Nanak Dev Univ, Dept Chem, Amritsar 143005, Punjab, India
[2] Bhabha Atom Res Ctr, Div Solid State Phys, Bombay 400085, Maharashtra, India
关键词
M-type hexagonal ferrites; Sol-gel; Sire preference; Magnetic properties; Coercivity; SOL-GEL; DIELECTRIC-PROPERTIES; FERRITE; MOSSBAUER; PARTICLES; SRFE12O19; ZN;
D O I
10.1016/j.jmmm.2014.10.168
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The aim of this work is to investigate the correlation between the distribution of cations over five crystallographic sublattices and magnetic properties of Sr-hexaferrites in the coupled substitution of magnetic Co2+ and non-magnetic Zr4+ for Fe3+. During present work, we have synthesized a series of SrCox ZrxFe(12-2x)O19 ferrites (x=0.0, 0.2, 0.4, 0.6, 0.8 and 1.0) using sol-gel route at a much lower temperature of 800 degrees C. These compounds were characterized by TGA, FT-IR, XRD, EDS and TEM. XRD data reveal the formation of polycrystalline magnetoplubite structure for all the compounds of the series. The crystallite size of nanoparticles lies in the range of 30-55 nm. Mossbauer spectroscopy was employed to probe magnetic properties at microscopic level. Mossbauer analysis indicates that dopant ions largely prefer 12k, 4f(1) and 2b sites at x=0.2 and 0.4 levels whereas at higher concentrations substitution Lakes place at 12k and 4f(2) sites. Magnetic measurements reveal that the values of coercivity (H-c) reduced from 6082 (x=0) to 1104 Oe (x=1.0) but the net magnetization of the samples is not correlated with dopant level. The saturation magnetization (M-s) values are in the range of 64.8-56.8 emu/g. Our results suggest that magnetization and magneto-crystalline anisotropy are closely related to the distribution of Co-Zr on the five sublattices of the crystal. (C) 2014 Published by Elsevier B.V.
引用
收藏
页码:84 / 91
页数:8
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