Chemical bonding and magnetic properties of gadolinium (Gd) substituted cobalt ferrite

被引:79
|
作者
Puli, Venkata Sreenivas [1 ]
Adireddy, Shiva [2 ]
Ramana, C. V. [1 ]
机构
[1] Univ Texas El Paso, Dept Mech Engn, El Paso, TX 79968 USA
[2] Tulane Univ, Dept Phys & Engn Phys, New Orleans, LA 70118 USA
基金
美国国家科学基金会;
关键词
Cobalt ferrite; Gd-substitution; Raman spectroscopy; Magnetic properties; Neel temperature; THIN-FILMS; DIELECTRIC-PROPERTIES; NICKEL FERRITE; MICROSTRUCTURE; RE; SM; NANOPARTICLES; SPINEL; TB; ND;
D O I
10.1016/j.jallcom.2015.05.031
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
Polycrystalline gadolinium (Gd) substituted cobalt ferrites (CoFe2-xGdxO4; x = 0-0.3, referred to CFGO) ceramics have been synthesized by solid state reaction method. Chemical bonding, crystal structure and magnetic properties of CFGO compounds have been evaluated as a function of Gd-content. X-ray diffraction (XRD) and Raman spectroscopic analyses confirmed the formation of inverse spinel cubic structure. However, a secondary ortho-ferrite phase (GdFeO3) nucleates for higher values of Gd-content. A considerable increase in the saturation magnetization has been observed upon the initial substitution of Gd (x = 0.1). The saturation magnetization drastically decreases at higher Gd content (x >= 0.3). No contribution from ortho-ferrite GdFeO3 phase is noted to the magnetic properties. The increase in the magnetic saturation magnetization is attributed to the higher magnetic moment of Gd3+ (4f(7)) residing in octahedral sites is higher when compared to that of Fe3+ (3d(5)) and as well due to the migration of Co2+ (3d(7)) ions from the octahedral to the tetrahedral sites with a magnetic moment aligned anti-parallel to those of rare earth (RE3+) ions in the spinel lattice. Increase in coercivity with increase in Gd3+ is content is attributed to magnetic anisotropy in the ceramics. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:470 / 475
页数:6
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