Number of the records: 1  

Neutron diffraction study of the crystal and magnetic structures of nanostructured Zn.sub.0.34./sub.Fe.sub.2.53./sub.O.sub.4./sub. ferrite

  1. 1.
    0532460 - FZÚ 2021 RIV NL eng J - Journal Article
    Belozerova, N.M. - Kichanov, S.E. - Kozlenko, D. P. - Kaman, Ondřej - Jirák, Zdeněk - Lukin, E.V. - Savenko, B. N.
    Neutron diffraction study of the crystal and magnetic structures of nanostructured Zn0.34Fe2.53O4 ferrite.
    Journal of Nanoparticle Research. Roč. 22, č. 5 (2020), s. 1-9, č. článku 121. ISSN 1388-0764. E-ISSN 1572-896X
    R&D Projects: GA ČR GA19-02584S
    Institutional support: RVO:68378271
    Keywords : neutron diffraction * magnetometry * ferrite nanoparticles * thermal decomposition
    OECD category: Condensed matter physics (including formerly solid state physics, supercond.)
    Impact factor: 2.253, year: 2020
    Method of publishing: Limited access
    https://doi.org/10.1007/s11051-020-04852-4

    The structure and magnetic arrangement of Zn0.34Fe2.53O4 in the form of spherical nanoparticles with the mean size of 14 nm, prepared by thermal decomposition method, have been studied by neutron diffraction at 10-300 K. The investigation provides detailed data on lattice parameters, interatomic bond lengths and angles, and ferrimagnetically ordered moments of iron ions in A and B crystallographic sites of the spinel structure. With a help of supplementary result of Mossbauer spectroscopy, the distribution of Zn and Fe ions between A and B sites is determined to (Fe0.823+Zn0.182+)A[Fe1.443+Fe0.272+Zn0.162+□0.13] BO4, where the B-site vacancy □0.13 quantifies the cation non-stoichiometry due to partial oxidation of the ferrite. Within a collinear model of ionic spins, this distribution agrees well with the spontaneous magnetization determined by magnetometry at 5 K of 103.6 Am2/kg equivalent to 4.22 μB per f
    Permanent Link: http://hdl.handle.net/11104/0310946

     
     
Number of the records: 1  

  This site uses cookies to make them easier to browse. Learn more about how we use cookies.