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The enhancement of the Ce-solubility limit and saturation magnetization in the Ce0.25BixPryY2.75-x-yFe5O12 garnet synthesized by the conventional ceramic method
Dastjerdi, O. Dehghani1; Shokrollahi, H.1; Yang, H.2
2020-02-15
发表期刊Ceramics International
ISSN02728842
卷号46期号:3页码:2709-2723
摘要This paper has focused on the structural and magnetic properties of Ce0.25BixPryY2.75-x-yFe5O12(x = 0.15, 0.20, 0.25) and (y = 0.25, 0.5) prepared by the solid-state method. The structural and microstructural evaluations were carried out by the X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM) and transmission electron microscopy (TEM), Raman Spectroscopy (RS) and Fourier-transform infrared spectroscopy (FTIR). Furthermore, the magnetic properties were studied through a vibrating sample magnetometer (VSM). As it can be obtained from the XRD patterns, a single garnet phase with high purity has been formed in all samples in the sintering condition. Also, the FTIR analysis confirmed the formation of the garnet phase and related inorganic bonding. Raman spectroscopy reveals the dominant garnet phase with good incorporation of the Bi, Pr and Ce dopants into the garnet structure. XPS confirmed the presence of Ce4+ and also its value was measured from the peak areas. The results showed that the amount of Ce4+ in all the samples is lower than 10%. According to the results, by increasing the Bi content from x = 0.15 up to x = 0.25, saturation magnetization (Ms) increased from 29.31 to 37.79 emu/g, and by enhancing the Pr concentration from x = 0.25 to x = 0.5, this magnetic characteristic enhanced from 29.31 to 33.16 emu/g. Furthermore, the Ce-solubility limit was enhanced from x = 0.2 to x = 0.25 by the charge compensation mechanism. An increase in the Ce-solubility limit and also the saturation magnetization led to an enhancement in the magneto-optical and magnetic properties of YIG for telecommunication applications and memory storages, respectively. © 2019 Elsevier Ltd and Techna Group S.r.l.
关键词Bismuth metallography Cerium oxide Ferrite Fourier transform infrared spectroscopy Garnets High resolution transmission electron microscopy Magnetic properties Raman spectroscopy Scanning electron microscopy Sensors Sintering Solubility X ray diffraction X ray photoelectron spectroscopy CeO2 Charge compensation mechanism Magnetic characteristic Microstructural evaluation Sintering condition Structural and magnetic properties Telecommunication applications Vibrating sample magnetometer
DOI10.1016/j.ceramint.2019.09.261
收录类别EI ; SCIE
语种英语
WOS研究方向Materials Science
WOS类目Materials Science, Ceramics
WOS记录号WOS:000508752000017
出版者Elsevier Ltd
EI入藏号20194007486131
EI主题词Saturation magnetization
EI分类号531.2 Metallography - 701.2 Magnetism: Basic Concepts and Phenomena - 741.3 Optical Devices and Systems - 801 Chemistry - 801.4 Physical Chemistry
来源库Compendex
分类代码531.2 Metallography - 701.2 Magnetism: Basic Concepts and Phenomena - 741.3 Optical Devices and Systems - 801 Chemistry - 801.4 Physical Chemistry
引用统计
被引频次:26[WOS]   [WOS记录]     [WOS相关记录]
文献类型期刊论文
条目标识符https://ir.lut.edu.cn/handle/2XXMBERH/115436
专题理学院
通讯作者Shokrollahi, H.
作者单位1.Shiraz Univ Technol, Eletroceram Grp, Dept Mat Sci & Engn, Shiraz, Iran;
2.Lanzhou Univ Technol, Sch Sci, Lanzhou 730050, Peoples R China
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GB/T 7714
Dastjerdi, O. Dehghani,Shokrollahi, H.,Yang, H.. The enhancement of the Ce-solubility limit and saturation magnetization in the Ce0.25BixPryY2.75-x-yFe5O12 garnet synthesized by the conventional ceramic method[J]. Ceramics International,2020,46(3):2709-2723.
APA Dastjerdi, O. Dehghani,Shokrollahi, H.,&Yang, H..(2020).The enhancement of the Ce-solubility limit and saturation magnetization in the Ce0.25BixPryY2.75-x-yFe5O12 garnet synthesized by the conventional ceramic method.Ceramics International,46(3),2709-2723.
MLA Dastjerdi, O. Dehghani,et al."The enhancement of the Ce-solubility limit and saturation magnetization in the Ce0.25BixPryY2.75-x-yFe5O12 garnet synthesized by the conventional ceramic method".Ceramics International 46.3(2020):2709-2723.
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