煅烧
磁晶各向异性
材料科学
超顺磁性
矫顽力
微晶
铁磁性
纳米颗粒
傅里叶变换红外光谱
化学工程
铁氧体(磁铁)
分析化学(期刊)
磁各向异性
磁化
纳米技术
冶金
化学
凝聚态物理
复合材料
有机化学
工程类
物理
磁场
量子力学
催化作用
作者
Thomas Dippong,Oana Cadar,Iosif Grigore Deac,Lucian Barbu‐Tudoran,Erika Andrea Levei
标识
DOI:10.1016/j.jallcom.2023.170074
摘要
This study presents the effect of Ni2+ substitution by Co2+ on the structure, morphology and magnetic properties of CoαNi0.9-αZn0.1Fe2O4 nanoparticles calcined at different temperatures. Fourier-transform infrared spectroscopy revealed the presence of Fe-O, Co-O, Zn-O and Ni-O bonds in samples calcined at 200 °C, while the presence of the characteristic bonds of the SiO2 confirmed the embedding of CoαNi0.9-αZn0.1Fe2O4 at all calcination temperatures. Single phase poorly crystalline ferrite for samples calcined at 400 °C and ferrite accompanied by traces of Fe2SiO4 and SiO2 for samples calcined at high temperatures (800 and 1200 °C) were identified. The dependence of X-ray diffraction parameters on the Co2+ content of nanoparticles was also investigated. The increase in Co2+ content and calcination temperature led to crystallite growth from 4 to 43 nm, while the porosity decreased with the increase in Co2+ content and calcination temperature. The magnetic properties of the rectangular shape nanoparticles evolved proportionally with the particle size. The magnetization, coercivity and magnetocrystalline anisotropy increased with the increase in Co2+ content and calcination temperature. The shape of hysteresis loops indicated a superparamagnetic-like behavior of the nanoparticles calcined at 400 °C and a ferrimagnetic-like behavior at higher calcination temperatures (800 and 1200 °C). These features make the obtained nanoparticles attractive candidates for various technical applications.
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