首页> 外文期刊>Journal of magnetism and magnetic materials >Magnetic properties of larger ionic radii samarium and gadalonium doped manganese zinc ferrite nanoparticles prepared by solution combustion method
【24h】

Magnetic properties of larger ionic radii samarium and gadalonium doped manganese zinc ferrite nanoparticles prepared by solution combustion method

机译:溶液燃烧法制备较大离子半径钐和甘氨酸掺锰锌铁氧体纳米粒子的磁性

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

Nanoparticles of Mn_(0.5)Zn_(0.5)Fe_2O_4, Mn_(0.5)Zn_(0.5)Fe_(1.95)Sm_(0.05)O_4 and Mn_(0.5)Zn_(0.5)Fe_(1.9)Gd_(0.05)Sm_(0.05)O_4 ferrites are prepared by solution combustion method and characterized to comprehend their structural, microstructural and magnetic properties. The single-phase formation and spinel cubic structure of the samples analyzed by XRD method. The average crystallite sizes were found in the range 10.26 to 16.68 nm. The lattice parameters were found in the range 8.4157 to 8.4508 A. The particle size was studied by using TEM micrographs and found to be in nano range. The results are good agreements with XRD results. A strong correlation between the size of the particle with respect to the Sm~(3+) and Gd~(3+) content has been identified using TEM micrographs. The M-H loop of Mn_(0.5)Zn_(0.5)Sm_xGd_yFe_(2-(x+y))O_4 (where x = 0, y = 0; x = 0.05, y = 0; x = 0.05, y = 0.05) nanoparticles exhibit ferromagnetic nature with saturation magnetization and coercivity. The M-H loop of Mn_(0.5)Zn_(0.5)Fe_2O_4 nanoparticles exhibit a high saturation and remanent magnetization. The saturation magnetization and remanent magnetization found in the range 44.16 to 5.805 emu/g and 24.46 to 0.093 emu/g, respectively. The saturation and remanent magnetization decreases after Sm~(3+) and Gd~(3+) substitution on Fe- site in Mn_(0.5)Zn_(0.5)Fe_2O_4 is because of the distinction in the cation distribution at tetrahedral site and octahedral site. Meanwhile, experiments demonstrate that the solution combustion method has significant effect on structure and magnetic behavior of the prepared ferrite nanoparticles.
机译:Mn_(0.5)Zn_(0.5)Fe_2O_4,Mn_(0.5)Zn_(0.5)Fe_(1.95)SM_(0.05)O_4和MN_(0.5)FE_(0.5)FE_(1.9)GD_(0.05)SM_(0.05) O_4铁氧体通过溶液燃烧方法制备,其特征是理解其结构,微观结构和磁性。通过XRD方法分析样品的单相形成和尖晶石立方体结构。发现平均微晶尺寸在10.26至16.68nm的范围内。在8.4157至8.4508A范围内发现晶格参数。通过使用TEM显微照片研究粒度并发现纳米范围。结果是与XRD结果的良好协议。使用TEM显微照片鉴定了粒子尺寸与SM〜(3+)和GD〜(3+)含量之间的强关系。 MH循环的MN_(0.5)Zn_(0.5)Sm_xgd_yfe_(2-(x + y))O_4(其中x = 0,y = 0; x = 0.05,y = 0; x = 0.05,y = 0.05)纳米颗粒呈现饱和磁化和矫顽力的铁磁性质。 MN_(0.5)Zn_(0.5)Fe_2O_4纳米颗粒的M-H环形纳米颗粒表现出高饱和度和再现磁化。饱和磁化和剩余磁化在44.16至5.805埃u / g和24.46至0.093 emu / g的范围内。在Mn_(0.5)Zn_(0.5)Fe_2O_4的Fe-位点上的SM〜(3+)和GD〜(3)取代后,饱和和再搅拌磁化减小是因为四面体位点和八面体部位的阳离子分布中的区分。同时,实验表明,溶液燃烧方法对制备的铁氧体纳米颗粒的结构和磁性行为具有显着影响。

著录项

  • 来源
    《Journal of magnetism and magnetic materials》 |2021年第7期|167899.1-167899.6|共6页
  • 作者单位

    Department of Physics P.C. Jabin Science College Hubballi 580031 India;

    Department of Physics School of Engineering Presidency University Bengaluru 560064 India Materials Research Centre School of Engineering Presidency University Bengaluru 560064 India;

    Department of Physics Palamuru University Telangana 509 001 India;

    New Chemistry Unit Jawaharlal Nehru Center for Advanced Scientific Research Bangalore 560064 India;

    Department of Physics Indian Institution of Science (IISC) Bengaluru 560012 India;

    Department of Physics FMPS Ramaiah University of Applied Sciences Bengaluru 560058 India;

    Department of Engineering Physics Faculty of Engineering and Technology KBNU Kalaburagi 585101 India;

    Department of Physics P.C. Jabin Science College Hubballi 580031 India;

    Department of Physics P.C. Jabin Science College Hubballi 580031 India;

    Department of Physics Indian Institution of Science (IISC) Bengaluru 560012 India;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Ferrites; Solution combustion; Ferromagnetic nature; Saturation magnetization;

    机译:铁氧体;溶液燃烧;铁磁性质;饱和磁化;

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号