Structural, magnetic and dielectric properties of pure and nickel-doped barium nanohexaferrites synthesized using chemical co-precipitation technique

Naini Dawar, Mansi Chitkara, I. S. Sandhu, J. Jolly, S. Malhotra
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引用次数: 20

Abstract

Abstract Nickel-doped barium nanohexaferrites with the chemical formula BaNixFe(12-x)O19 are prepared using the chemical co-precipitation technique. The calcination of the samples is done at 800°C for 4 h. In order to carry out the structural analysis that includes the crystallographic and the morphological investigations, X-ray diffraction and TEM are carried out to govern the phase, structure and the size of the crystal. By the use of Debye–Scherrer equation, the size of the crystallite is calculated to be in the range of 38–100 nm. TEM results reveal the magnetoplumbite structure of the hexaferrites. The M–H curve obtained using the Vibrating Sample Magnetometer computes the magnetic parameters like saturation magnetization, coercivity, remanence and verifies the behaviour of hexaferrites as hard magnetic materials. Further, the effect of variation in calcination temperature is also investigated on the values of magnetic parameters of hexaferrites. In order to carry out the investigations on the electrical properties of hexaferrites, the two-probe method and parallel plate capacitor set-up are used. The values of relative permittivity, dielectric loss and loss tangent are computed as a function of frequency. The values of DC electrical resistance for pure and nickel-doped barium nanohexaferrites are evaluated from the slope of I–V graphs.
化学共沉淀法合成纯和掺镍钡纳米六铁氧体的结构、磁性和介电性能
摘要采用化学共沉淀法制备了化学式为BaNixFe(12-x)O19的掺镍钡纳米六铁体。样品在800°C下煅烧4小时。为了进行结构分析,包括晶体学和形态学研究,进行x射线衍射和透射电镜来控制晶体的相、结构和尺寸。利用Debye-Scherrer方程,计算出晶体的尺寸在38 ~ 100 nm之间。透射电镜结果显示了六铁体的磁铅石结构。用振动样品磁强计得到的M-H曲线计算了饱和磁化强度、矫顽力、剩余力等磁性参数,验证了六铁氧体作为硬磁性材料的性能。此外,还研究了煅烧温度的变化对六铁氧体磁性参数的影响。为了对六铁氧体的电性能进行研究,采用了双探针法和并联板电容装置。相对介电常数、介电损耗和损耗正切值作为频率的函数来计算。用I-V曲线的斜率计算了纯钡纳米六铁氧体和掺镍钡纳米六铁氧体的直流电阻。
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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来源期刊
Cogent Physics
Cogent Physics PHYSICS, MULTIDISCIPLINARY-
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