Nikmanesh Hossein, Jaberolansar Elnaz, Kameli Parviz, Varzaneh Ali Ghotbi, Mehrabi Mohsen, Rostami Momammad
Department of Physics, Persian Gulf University, Bushehr 75169, Iran.
Department of Physics, Isfahan University of Technology, Isfahan 84156-83111, Iran.
Nanotechnology. 2021 Nov 5;33(4). doi: 10.1088/1361-6528/ac31e8.
This work's main purpose is to investigate the effect of Gdsubstitution on the structural, cation distribution, morphological, and magnetic characteristics of cobalt ferrite nanostructures. The nanostructures were synthesized through the sol-gel auto combustion technique. X-ray diffraction (XRD) analysis with the Rietveld refinement through the Material Analysis Using Diffraction (MAUD) program confirmed a single-phase spinel structure for lower contents of Gd. However, for higher concentrations, a trace of second phase GdFeOwas evident. The crystallite size reduction from 17 to 11 nm with Gddoping confirmed the formation of nanocrystalline Co-Gd ferrite. Cation distribution was another parameter inferred from the experimental data of XRD analyzed by the MAUD program. Fourier-transform infrared spectra confirmed the formation of spinel structure through two prominent vibrational modes observed at the desired wavelength range. FESEM analysis confirmed the data obtained from the XRD about the structure and morphology of the nano samples. Saturation magnetization () of the nano samples evaluated at 10 K showed a decreasing behavior from 94 to 86 emu gby Gddoping, while a fluctuating trend ofwas observed at room temperature. Coercive field () evaluated at 10 K reached a maximum value of about 1145 kA mfor the sample CoFeGdO, and then it decreased. At the same time,experienced no considerable change at 300 K. The possible concepts attributed to such a trend ofwere also investigated. Overall, the significant impact of Gddoping on the cobalt ferrite nanoparticles causes Gd-Co ferrite to have a desirable capacity of permanent magnet materials and storage of information with high density. As a result, this ferrite may be a proper candidate to be utilized, especially at lower temperatures.
这项工作的主要目的是研究钆替代对钴铁氧体纳米结构的结构、阳离子分布、形态和磁特性的影响。通过溶胶-凝胶自燃技术合成了纳米结构。利用衍射材料分析(MAUD)程序进行Rietveld精修的X射线衍射(XRD)分析证实,对于较低含量的钆,为单相尖晶石结构。然而,对于较高浓度,明显存在微量的第二相钆铁氧化物。钆掺杂使微晶尺寸从17纳米减小到11纳米,证实了纳米晶钴-钆铁氧体的形成。阳离子分布是从MAUD程序分析的XRD实验数据推断出的另一个参数。傅里叶变换红外光谱通过在所需波长范围内观察到的两种突出振动模式证实了尖晶石结构的形成。场发射扫描电子显微镜(FESEM)分析证实了从XRD获得的有关纳米样品结构和形态的数据。在10 K下评估的纳米样品的饱和磁化强度从94emu/g下降到86emu/g,这是由于钆掺杂导致的,而在室温下观察到波动趋势。在10 K下评估的矫顽力在样品CoFeGdO处达到最大值约1145 kA/m,然后下降。同时,在300 K下没有经历显著变化。还研究了导致这种趋势的可能原因。总体而言,钆掺杂对钴铁氧体纳米颗粒的显著影响使得钆-钴铁氧体具有永磁材料的理想性能和高密度信息存储能力。因此,这种铁氧体可能是一种合适的候选材料,特别是在较低温度下使用。