Structural and magnetic properties correlated with cation distribution of Mo-substituted cobalt ferrite nanoparticles

被引:43
作者
Heiba, Z. K. [1 ,2 ]
Mostafa, Nasser Y. [1 ,3 ]
Abd-Elkader, Omar H. [4 ,5 ]
机构
[1] Taif Univ, Fac Sci, Al Haweiah, Taif, Saudi Arabia
[2] Ain Shams Univ, Fac Sci, Dept Phys, Cairo, Egypt
[3] Suez Canal Univ, Fac Sci, Dept Chem, Ismailia 41522, Egypt
[4] King Saud Univ, Coll Sci, Dept Zool, Riyadh 11451, Saudi Arabia
[5] NRC, Elect Microscope & Thin Films Dept, Cairo 12622, Egypt
关键词
Chemical synthesis; Crystal structure; Magentisation; Microstructure; X-ray diffraction; CoFe2O4; X-RAY; COPRECIPITATION; MOSSBAUER; PARTICLES; MAGNESIUM; SURFACE;
D O I
10.1016/j.jmmm.2014.05.036
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Mo-substituted cobalt ferrite nanoparticles; CoFe2-2xMoxO4 (0.0 <= x <= 03) were prepared by a one-step solution combustion synthesis technique. The reactants were metal nitrates and glycine as a fuel. The samples were characterized using an X-ray diffraction (XRD), a transmission electron microscope (TEM) and a vibrating sample magnetometer (VSM). XRD analysis revealed a pure single phase of cubic spinel ferrites for all samples with x up to 0.3. The lattice parameter decreases with Mo6+ substitution linearly up to x=0.15, then nonlinearly for x >= 0.2. Rietvelcl analysis and saturation magnetization (M-s) revealed that Mo6+ replaced Fe3+ in the tetrahedral A-sites up to x=0.15, then it replaced Fe3+ in both A-sites and B-sites for x >= 0.2. The saturation magnetization (M-s) increases with increasing Mo6+ substitution up to x=0.15 then decreases. The crystallite size decreased while the microstrain increased with increasing Mo6+ substitution. Inserting Mo6+ produces large residents of defects and cation vacancies. (C) 2014 Elsevier B.V. All rights reserved,
引用
收藏
页码:246 / 251
页数:6
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