Crystallographic and Magnetic Properties of Co, Zn, Ni-Zn Substituted Nano-size Manganese Ferrites Synthesized by Sol-gel Method

Kwang Mo Noh, Young Bae Lee, Woo Hyun Kwon, Jeoung Yun Kang, Won-Ok Choi, Kwang Pyo Chae
2016 Journal of Magnetics  
Cobalt-, zinc-, and nickel-zinc-substituted nano-size manganese ferrite powders, MnFe 2 O 4 , Mn 0.8 Co 0.2 Fe 2 O 4 , Mn 0.8 Zn 0.2 Fe 2 O 4 and Mn 0.8 Ni 0.1 Zn 0.1 Fe 2 O 4 , were fabricated using a sol-gel method, and their crystallographic and magnetic properties were subsequently studied. The MnFe 2 O 4 ferrite powder annealed at temperatures above 523 K exhibited a spinel structure, and the particle size increased as the annealing temperature increased. All ferrites annealed at 773 K
more » ... nealed at 773 K showed a single spinel structure, and the lattice constants and particle size decreased with the substitution of Co, Zn, and Ni-Zn. The Mössbauer spectrum of the MnFe 2 O 4 ferrite powder annealed at 523 K only showed a doublet due to its superparamagnetic phase, and the Mössbauer spectra of the MnFe 2 O 4 , Mn 0.8 Co 0.2 Fe 2 O 4 , and Mn 0.8 Zn 0.2 Fe 2 O 4 ferrite powders annealed at 773 K could be fitted as the superposition of two Zeeman sextets due to the tetrahedral and octahedral sites of the Fe 3+ ions. However, the Mössbauer spectrum of the Mn 0.8 Ni 0.1 Zn 0.1 Fe 2 O 4 ferrite powder annealed at 773 K consisted of two Zeeman sextets and one quadrupole doublet due to its ferrimagnetic and paramagnetic behavior. The area ratio of the Mössbauer spectra could be used to determine the cation distribution equation, and we also explained the variation in the Mössbauer parameters by using this cation distribution equation, the superexchange interaction and the particle size. Relative to pure MnFe 2 O 4 , the saturation magnetizations and coercivities were larger in Mn 0.8 Co 0.2 Fe 2 O 4 and smaller in Mn 0.8 Zn 0.2 Fe 2 O 4 , and Mn 0.8 Ni 0.1 Zn 0.1 Fe 2 O 4 . These variations could be explained using the site distribution equations, particle sizes and magnetic moments of the substituted ions.
doi:10.4283/jmag.2016.21.3.308 fatcat:wxueofrbnfavtjf2rdmvy2q6rq