Structural, spectral, rietveld refinement and cation distribution of nanoferrite NiFe2O4 doped with Mn

被引:0
|
作者
F. S. El-Sbakhy
M. I. Abdel-Ati
A. M. Abdelghany
O. M. Hemeda
机构
[1] Tanta University,Physics Department, Faculty of Science
[2] Sinai University,Physics Department, Faculty of Engineering
关键词
D O I
暂无
中图分类号
学科分类号
摘要
The spinel ferrite Ni1–xMnxFe2O4 system (x = 0.0, 0.2, 0.4, 0.6, 0.8 and 1.0) have been successfully synthesized by using the flash auto-combustion method at 600 °C for 2 h. The annealed powders were characterized by X-ray diffraction (XRD), IR spectroscopy, transmission electron microscopy and scanning electron microscopy. The structural analysis confirms the formation of spinel phase with the presence of small ratio of a secondary phases. It was noticed from the XRD data that the increasing of Mn2+ content increases the lattice parameter from 8.345 to 8.421 Å and the size of crystallite decreases from 33.63 to 27.30 nm. The theoretical density ρx and the area of crystallite surface were calculated. IR study reveals the presence of tetrahedral and octahedral absorption bands ν1andν2\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$\nu_{1} \;{\text{and}}\;\nu_{2} { }$$\end{document} with two weak bands ν1′andν2′\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$ \nu_{1}^{\prime } \;{\text{and}}\;\nu_{2}^{\prime }$$\end{document}. The morphological observations show the formation of agglomerated grains with different shapes and sizes.
引用
收藏
相关论文
共 50 条
  • [41] INDUCED FERRIMAGNETISM IN NIFE2O4
    BASHKIROV, SS
    GUBAIDULLIN, RK
    IVOILOV, NG
    CHISTYAKOV, VA
    FIZIKA TVERDOGO TELA, 1976, 18 (11): : 3200 - 3202
  • [42] Formation and characterization of NiFe2O4
    Music, S
    Balzar, D
    Popovic, S
    Gotic, M
    CzakoNagy, I
    Dalipi, S
    CROATICA CHEMICA ACTA, 1997, 70 (02) : 719 - 734
  • [43] Formation of nanocrystalline NiFe2O4
    Gotic, M
    Czako-Nagy, I
    Popovic, S
    Music, S
    PHILOSOPHICAL MAGAZINE LETTERS, 1998, 78 (03) : 193 - 201
  • [44] Study of Urbach energy and Kramers-Kronig on Mn and Zn doped NiFe2O4 ferrite nanopowder for the determination of structural and optical characteristics
    Nazari, N.
    Golzan, M. M.
    Mabhouti, Kh.
    SCIENTIFIC REPORTS, 2024, 14 (01)
  • [45] Structural and Magnetic Studies of Thermally Treated NiFe2O4 Nanoparticles
    Ghosh, Surajit
    Patel, Prayas Chandra
    Gangopadhyay, Debraj
    Sharma, Poornima
    Singh, Ranjan K.
    Srivastava, P. C.
    METALLURGICAL AND MATERIALS TRANSACTIONS A-PHYSICAL METALLURGY AND MATERIALS SCIENCE, 2017, 48A (12): : 6135 - 6141
  • [46] Structural, optical, and magnetic properties of NiO/NiFe2O4 nanocomposites
    B. Sahu
    U. K. Panigrahi
    Sujay Chakravarty
    Shamima Hussain
    P. Mallick
    Applied Physics A, 2023, 129
  • [47] Structural and magnetic investigations of Cr substituted NiFe2O4 nanostructures
    Azam, M.
    Adeela, N.
    Khan, U.
    Riaz, S.
    Iqbal, M.
    Naseem, S.
    JOURNAL OF ALLOYS AND COMPOUNDS, 2017, 698 : 228 - 233
  • [48] Structural and Electrical Properties of Mechanothermally Synthesized NiFe2O4 Nanoceramics
    Behera, C.
    Das, Piyush R.
    Choudhary, R. N. P.
    JOURNAL OF ELECTRONIC MATERIALS, 2014, 43 (09) : 3539 - 3549
  • [49] Structural and Magnetic Studies of Thermally Treated NiFe2O4 Nanoparticles
    Surajit Ghosh
    Prayas Chandra Patel
    Debraj Gangopadhyay
    Poornima Sharma
    Ranjan K. Singh
    P. C. Srivastava
    Metallurgical and Materials Transactions A, 2017, 48 : 6135 - 6141
  • [50] Structural and magnetic properties of In3+ substituted NiFe2O4
    Shirsath, Sagar E.
    Toksha, B. G.
    Jadhav, K. M.
    MATERIALS CHEMISTRY AND PHYSICS, 2009, 117 (01) : 163 - 168