4.7 Article

Structural phase stabilization via Ba site doping with bivalent Sr, Ca and Zn ions and Fe site doping with trivalent Cr and Ga ions in the BaFe12O19 hexaferrite and its magnetic modification

Journal

CRYSTENGCOMM
Volume 24, Issue 29, Pages 5269-5288

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2ce00583b

Keywords

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Funding

  1. UGC-DAE CSR Indore [CSR-IC-ISUM-03/CRS-286/2019-20/1338]
  2. Central Instrumentation Facilities (CIF), Pondicherry University

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Doping of various ions in M-type BaFe12O19 hexaferrite has been achieved through mechanical alloying and heat treatment, resulting in changes in structural phase, crystallite size, lattice strain, and magnetic moment.
The doping of divalent Sr, Ca, and Zn ions at the Ba sites and trivalent Cr and Ga ions at the Fe sites in the M-type BaFe12O19 hexaferrite has been performed via the mechanical alloying of elemental metal oxides and post heat treatment. The structural phase in the material was studied by the analysis of the synchrotron X-ray diffraction patterns and Raman spectra. The doped samples show the M-type BaFe12O19 structure as the major phase and a small amount of hematite phase after heat treatment at 800 degrees C. This secondary phase was reduced at higher heat treatment temperatures. In addition to the M-type hexaferrite and hematite phases, the Zn-doped system-formed ZnFe2O4 and W-type hexaferrite after heat treatment at 800 degrees C and 1100 degrees C, respectively. The material shows a unique variation in crystallite size and lattice strain with the dopant and heat treatment of the samples. The X-ray photoelectron spectra confirmed that the charge states of the Fe site- (Fe, Ga, Cr) and Ba site- (Sr, Ca, Zn) doped ions are nearly +3 and +2, respectively. The hard ferrimagnetic properties of the BaFe12O19 structure have been retained in all the doped samples. The magnetic moment is noticeably changed by Fe site doping, unlike the small change noted with Ba site doping. The ferrimagnetic parameters of the samples are affected by the lattice structure regardless of whether metal doping is at the Ba and Fe sites of the M-type BaFe12O19 structure.

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