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Structural and magnetic properties correlated with cation distribution of Mo-substituted cobalt ferrite nanoparticles
被引:41
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,
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页码:246 / 251
页数:6
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