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This investigation is motivated by the surge of interest in materials, combining high spontaneous magnetization and pseudocapacitance at room temperature. Ferrimagnetic MnFe 2 O 4 offers benefits of high magnetization. However, the non-pseudocapacitive behavior, low capacitance and high resistance of MnFe 2 O 4 are limiting factors for its applications in magnetic pseudocapacitive devices. This investigation demonstrates that nearly ideal pseudocapacitive behavior can be achieved for MnFe 2 O 4 electrodes in Na 2 SO 4 electrolyte. High pseudocapacitance is observed in positive and negative potential ranges and two different charging mechanisms are proposed. High capacitance is achieved at a low impedance. The ability to achieve comparable and high areal capacitances in the positive and negative potential ranges facilitates the fabrication of a symmetric pseudocapacitive device, containing ferrimagnetic MnFe 2 O 4 as cathode and anode material for operation in enlarged voltage window of 1.6 V. The symmetric device shows capacitance of 0.92 F cm−2 at a current density of 3 mA cm−2. The individual electrodes and device show good cycling stability. The approach is based on the use of murexide and gallocyanine as redox-active dispersants and charge transfer mediators. The analysis of testing results provides an insight into the influence of chemical structure, charge and redox properties of the dispersants on the capacitive behavior. The ability to fabricate a pseudocapacitive device, containing two ferrimagnetic electrodes is promising for energy storage, water purification and novel applications based on magnetocapacitive effects. [ABSTRACT FROM AUTHOR]

Cobalt doping's influence on the structural, magnetic, and electronic properties of the double spinel LiFeCr 4 O 8 was systematically investigated. Rietveld refinement revealed a consistent increase in lattice parameter a and unit cell volume with cobalt incorporation. Magnetic susceptibility measurements indicated three distinct transitions: an increase in the ferrimagnetic transition temperature (T N), a decrease in the magnetostructural transition temperature (T MS), and an increase in the spin gap transition by cobalt doping. Through diffuse reflectance spectroscopy the direct optical band gap (E og) was obtained with values of 1.169 eV, 1.303 eV, 1.396 eV, and 1.230 eV for x = 0.0, 0.1, 0.2, and 0.5, respectively. The observed increase in E og with cobalt doping suggests a widening of the band gap, which could be beneficial for optoelectronic applications. By means of X-ray photoelectron spectroscopy (XPS) the core levels of Li 1s , Co 3p , Fe 3p , Cr 3p , Fe 2p , Cr 2p , and O 1s were identified. XPS valence band (VB) analysis revealed a decreasing intensity at binding energy BE = 0 eV with respect to x = 0.0. Density functional theory calculations with Hubbard U correction (DFT + U) confirmed a ferrimagnetic semiconductor behavior with a direct electronic band gap (E eg) of 1.085 eV. [ABSTRACT FROM AUTHOR]

Yttrium Iron Garnet (YIG) ferrites, characterized by their superior magnetic and dielectric attributes, are instrumental in advancing the development of microwave devices, particularly in enhancing high-frequency performance, integration, and miniaturization. This paper synthesizes YIG ferrite materials with the composition Bi 0.6 Y 1.4-x Ca 1+x Fe 4.5-x V 0.5 Ge x O 12 (x = 0.10 to 0.50, incrementing by 0.10) through the solid-state sintering method. It delves deeply into the mechanism by which Ca2+-Ge4+ ions substitution regulates the magnetic properties of BiV-YIG. The microstructural and magnetic properties of the samples were systematically tested and analyzed using X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), vibrating sample magnetometry (VSM), and TE106 perturbation method. At a substitution content of x = 0.50, the substitution of Ge4+ ions for the Fe3+ ions at the d-site transforms the material from ferrimagnetic to paramagnetic, and the saturation magnetization of the sample drops to 132.74 G. By calculating the ferromagnetic resonance (FMR) linewidth using the law of approach to saturation, the study elucidates the negative impact of low saturation magnetization on FMR linewidth. The mechanisms proposed in this paper provide theoretical and experimental bases for reducing the FMR linewidth of high dielectric constant Bi-substituted YIG, paving the way for developing high-dielectric, low-loss YIG ferrite materials for microwave devices. [ABSTRACT FROM AUTHOR]

We prepared ultrafine MnCo 2 O 4 particles using a facile sol–gel autocombustion method. The structural and vibrational characterizations confirmed the formation of a pure cubic spinel phase in as-synthesized MnCo 2 O 4 particles. The surface morphology analyses revealed the porous structure with an average particle size of 5 nm and uniform distribution of manganese (Mn), cobalt (Co), and oxygen (O) in the particles. We observed the presence of multiple valence states of Mn and Co, occupying both tetrahedral and octahedral sites, enhancing our insight into the material's electronic properties and structural configuration. Our magnetization studies unveiled a Curie Temperature (T C) of 185 K with ferrimagnetic ordering below T C , resulting in substantial magnetization (9.8 emu/g) and coercivity (3.46 kOe) at 2 K and weak magnetic behavior above T C. This is attributed to the finite size and surface effects. Furthermore, the incorporation of MnCo 2 O 4 nanoparticles and graphene oxide into a polyurethane foam matrix resulted in an excellent sound absorption coefficient of 90 % at 2000 Hz. This outstanding acoustic performance underscores the versatile applications of MnCo 2 O 4 nanoparticles in diverse noise mitigation applications. [Display omitted] [ABSTRACT FROM AUTHOR]

In this work, the ion-exchange technique in molten salts was investigated to introduce copper ions in a bioactive and ferrimagnetic devitrified glass. This approach aimed to develop a magnetic and bioactive material for oncologic bone implants, able to join the ability to promote bone bonding to hyperthermic therapy while simultaneously lowering the risk of developing post-surgery infections. The ion-exchange approach was developed in order to overcome experimental critical issues related to the influence of copper introduction as a starting reagent, during the material synthesis, on magnetite nucleation. The magnetic devitrified glass was prepared by melt and quenching route, followed by ion exchange in a mixture of molten sodium and copper nitrates, in three different Na/Cu molar ratios (20, 200, 2000). The obtained samples were analysed in terms of morphology, composition, ability to release heat, bioactivity and antibacterial properties. The results revealed that copper ion-exchange involved both sodium and calcium ions and the precipitation of few amounts of copper oxide aggregates occurred. The crystalline nature of the starting material and its ability to reach the temperature needed for hyperthermia, under exposition to an alternating magnetic field, were not affected. A bacteriostatic effect was obtained by samples with the highest copper amount and the copper doping did not affect the bioactivity of the glass ceramic. [ABSTRACT FROM AUTHOR]

Triboelectric nanogenerators (TENGs), which are powered by Maxwell's displacement current, have a wide range of applications, including energy harvesting and self-powered sensors. However, very little attention has been paid to the effect of the ferromagnetic medium on TENG displacement current. Herein, flexible ferrimagnetic poly(vinylidene fluoride-co-hexafluoropropylene) (P(VDF–HFP))/nickel ferrite (NiFe 2 O 4) fiber composite film based TENGs were fabricated and their performances were analysed. Highly crystalline, ferrimagnetic NiFe 2 O 4 nanofibers with high aspect ratio were prepared using electrospinning technique by systematic optimization of spinning parameters. Thereafter, the fibers were reinforced into the polymeric matrix to improve the β–phase and dielectric constant which in turn significantly enhanced the TENG performance. The β–phase enhancement in the composite films was confirmed by XRD and FTIR analysis; 77 % of the β–phase was achieved with the incorporation of NiFe 2 O 4 fiber. Morphological features were examined using SEM and AFM, which revealed more β–phase spherulite formation in the composite films. A notable increase in the dielectric properties was evidenced with the addition of NiFe 2 O 4 fibers and a maximum dielectric constant of∼26 was attained at 100 Hz. The TENG was developed using P(VDF-HFP)/NiFe 2 O 4 and nylon which generated an output voltage (V pp) and current (I pp) values of 584 V and 25 μA, respectively. Furthermore, the performance of TENG under an external magnetic field was examined, and a notable improvement in performance was observed, paving the way for the application of NiFe 2 O 4 fibers in hybrid energy harvesters and self-powered sensors. [ABSTRACT FROM AUTHOR]