Abstract
Cationic substitutions and sintering temperature both are crucial variables in modifying the structural and magnetic properties of M-type hexaferrites. The effect of the cationic substitutions on M-type BaFe10−xAl2MgxO19 hexaferrites is examined in the current work. An XRD analysis reveals that Fe2O3 phases are present as an impurity in all of the samples. Firstly, lattice parameters a and c show a decrease, then start increasing. The(Mr/Ms) ratio confines within a specific stable range. Morphology of the samples shows the uniform distribution of the particles throughout all the compositions.The anisotropy field-(Ha) and coercivity-(Hc) show an increase with increasing doping levels. The average grain size (D) grew continuously between 200 and 900 nm as the the doping content of Mg ascended. At a doping content of x = 0.05, the M type BaFe9.95Al2Mg0.05O19 hexaferrites shows the excellent magnetic characteristics having mB = 9.4098µB, Ms = 49.95 emu/g, Hc = 4.98 kOe, and Ha = 1.6kOe. The findings suggest that M-type hexagonal ferrite’s magnetic properties can be significantly enhanced by varying the cationic substitutions.
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The authors are thankful to the Deanship of Scientific Research at King Khalid University for funding this work through a large group Research Project under Grant Number RGP2/236/44.
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Funding was supported by Deanship of Scientific Research at King Khalid University for funding this work through a large group Research Project under Grant Number (RGP2/236/44).
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All the authors contributed equally to this work. SUA, and FA, gave the idea. MA, synthesized material, SUA, FA, FAI, MMH, EAMS, and MSH analyzed the data. EAA, and URG, formatted the initial draft. The manuscript was written through the contributions of all authors. All authors have approved the final version of the manuscript.
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Asif, S.U., Ghori, UuR., Ahsan, M. et al. Structural and magnetic influence by mg on BaFe10Al2O19 hexaferrites prepared via ceramic route for potential magnetic applications. J Mater Sci: Mater Electron 34, 2211 (2023). https://doi.org/10.1007/s10854-023-11645-7
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DOI: https://doi.org/10.1007/s10854-023-11645-7