Synthesis and magnetic properties of nanostructured Ni1-xZnxFe2O4(x = 0.4, 0.5 and 0.6)

B. Sattibabu, T. D. Rao, T. Das, M. Chatterjee, A. Bhatnagar, S. Rayaprol, D. Das
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Abstract

Nanostructured Ni1-xZnxFe2O4(x = 0.4, 0.5 and 0.6) samples are prepared by the auto-combustion method. The compounds are formed in the cubic spinel phase without any impurity as confirmed by the XRD data. Increase in lattice parameters and volume of the unit cell with the Zn content is observed which is due to the larger ionic sizes of Zn2+ (0.74 A) and Ni2+ (0.69 A) when compared with that of Fe3+ (0.60 A). The crystallite size increased with the Zn content. FESEM analysis reveals a non-uniform size distribution in grain sizes with the Zn content. All the prepared compounds maintained (Ni, Zn) and Fe stoichiometry in the ratio close to 1:2 as observed from the EDAX measurements. Magnetic properties are investigated using a VSM magnetometer. The magnetic parameters, such as saturation magnetization (Ms), coercive field (Hc), remnant magnetization (Mr) and Bohr magneton (μB), are determined. The saturation magnetization decreases gradually with increase in the Zn concentration.
纳米结构Ni1-xZnxFe2O4(x = 0.4、0.5和0.6)的合成及其磁性能
采用自燃烧法制备了纳米结构Ni1-xZnxFe2O4(x = 0.4、0.5和0.6)样品。XRD数据证实,化合物形成于立方尖晶石相中,无杂质。由于Zn2+ (0.74 A)和Ni2+ (0.69 A)的离子尺寸比Fe3+ (0.60 A)的离子尺寸大,晶胞的晶格参数和体积随Zn含量的增加而增大。FESEM分析表明,随着锌含量的增加,晶粒尺寸呈非均匀分布。从EDAX测量中观察到,所有制备的化合物(Ni, Zn)和Fe的化学计量比接近1:2。用VSM磁强计研究了其磁性能。测定了饱和磁化强度(Ms)、矫顽力场(Hc)、剩余磁化强度(Mr)和玻尔磁子(μB)等磁性参数。随着Zn浓度的增加,饱和磁化强度逐渐降低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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