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The rare earth (Yb3+) substituted W-type hexagonal ferrites with composition CaPb 2-x Yb x Fe 16 O 27 (x = 0.0, 0.5, 1.0, 1.5, 2.0) were synthesized by a facile and cost-effective sol-gel auto combustion method with post heat treatment. The synthesized hexagonal ferrites were characterized by a variety of analytical techniques, and an impedance analyzer was used to investigate the effects of Ytterbium on structural, magnetic, spectral and dielectric properties. The relationship between their impedance, structure and dielectric properties was investigated. The X-ray diffraction patterns verify the presence of single-phase W-type hexagonal ferrites. Physical properties such as D bulk (bulk density), D xrd (X-ray density), and P (porosity) of the CaPb 2-x Yb x Fe 16 O 27 W-type hexagonal ferrites were calculated. The bulk density of all the samples was decreased, and X-ray intensity was increased with the Ytterbium replacement in the W-type hexaferrite. By adding Yb3+ ions, the lattice parameters, cell volume and X-ray density were reduced due to the substitution of ytterbium with smaller ionic radii compared to the lead ion with large ionic radii. The AC-conductivity was increased from (1.523 × 10−5 to 6.699 × 10−5) Ωcm−1. The dielectric constant and tangent loss was found to decrease substantially. The magnetic properties were found to enhance by the substitution of Yb3+. The low coercivity value of Yb3+ substituted W-type hexagonal ferrites are suitable for magnetic recording media operated at a high-frequency regime. The enhancement of electrical, dielectric and magnetic characteristics suggests these materials as promising for multi-layer chip inductors (MLCIs) circuit applications. [ABSTRACT FROM AUTHOR]

Sol-gel auto combustion was used to create a sequence of soft ferrites, NixMg1-xFe1.9Sm0.1O4(x = 0.0, 0.2, 0.4 & 0.6). The XRD, FTIR, UV-vis, & four probe I-V techniques, respectively, were used to evaluate the structural, optical, and electrical properties. The cubic crystal structure was confirmed by the XRD pattern. The range of 25.71 - 33.67 nm was found to be the average crystallite size. FTIR spectra provided evidence of the tetrahedral band's existence. With the enhancement of Ni2+ concentration, Eg was determined from 2.28-3.21 eV. It was confirmed by the ranges of DC electrical resistivity that materials might be used in transformers to lessen eddy current losses. [ABSTRACT FROM AUTHOR]

M -type hexagonal ferrites with compositions Ca 1 − x CrxFe 1 2 O 1 9 at (x = 0. 1 , 0.2, 0.3, 0.4, 0.5) were successfully prepared by sol–gel auto combustion method and then immersed with polyvinyl alcohol (PVA) by ultrasound-assisted in situ emulsion technique. The results indicate that the synthesized nanoparticles were diffused homogeneously in PVA retaining the size and shape of the particle. The single-phase M -type hexagonal structure was revealed by X-ray diffraction (XRD) with extra 101 peak of PVA at 2 θ = 1 8 ∘ . The suitable signal-to-noise ratio in the high density recording media can be achieved due to the small particle size of the prepared composites as compared to pure hexaferrites. The interaction between PVA and nanoparticles was confirmed by Fourier transform infrared spectroscopy (FTIR). Scanning electron microscopy (SEM) images revealed the homogeneous distribution of grains, the crystallite size was measured from SEM (25–38 nm), and it is also in agreement as calculated from the Scherer formula. Dielectric properties were also explored in the range of 1 MHz–3 GHz frequencies. Dielectric constant and dielectric loss were found to decrease with increasing frequency and decrease with the addition of ferrite ratio in the polymer matrix. This impact is because of the grain boundary at low frequency regime. The occurrence of resonance at high frequency regime recommends the investigated samples for multilayer chip inductor. The formation of PVA-Ferrite Nanocomposites was confirmed by the FTIR in the range of 3500–400 cm–1 wavenumbers. The FTIR spectra of ferrite-polymer composites (PF3,PF5) were shown. The absorption bands in the range of 500–600 cm–1 wavenumbers are due to stretching vibrations at tetrahedral sites and absorption bands in the 400–500 cm–1 wavenumbers demonstrate the octahedral site formation in the M-type hexagonal ferrites structure. The absorption band at 1600 cm–1 is due to the stretching bands of hydroxyl group -O-H. Slight shifts in the bands were recorded due to the addition of polymer. Due to the interaction of ferrites-polymer, force constant and electron density were found to be decreased. [ABSTRACT FROM AUTHOR]