This review article provides a systematic analysis of synthesis methods, structural characteristics, and functional properties of spinel-structured ferrite nanoparticles (MFe₂O₄). The physicochemical principles, advantages, and limitations of various synthesis techniques—including co-precipitation, combustion, sol–gel, thermal decomposition, hydrothermal, solvothermal, microwave-assisted, sonochemical, electrochemical, and solid-state reaction methods—are comparatively discussed. The influence of synthesis parameters on crystal structure, morphology, and cation distribution between tetrahedral and octahedral sites, as well as on magnetic, dielectric, and optical properties, is critically analyzed. Furthermore, the capabilities of characterization techniques such as X-ray diffraction (XRD), scanning electron microscopy with energy-dispersive spectroscopy (SEM/EDS), Fourier-transform infrared spectroscopy (FTIR), FT-Raman spectroscopy, dielectric measurements, and magnetic measurements for investigating spinel ferrites are comprehensively summarized. Finally, the high potential of spinel ferrite nanoparticles for applications in electronics, microwave devices, water treatment, catalysis, sensors, and biomedical fields is highlighted.

This article reports on the synthesis and physicochemical characterization of a novel complex ferrite material, LiCr₃.₄Fe₁.₆O₈, prepared via the sol-gel method. X-ray diffraction (XRD) analysis confirmed that the synthesized compound is a single-phase material with a spinel-type structure and cubic symmetry. Raman spectroscopy was employed to investigate the vibrational modes, and the observed peaks corresponding to Fe–O and Cr–O bonds further validated the spinel-like structure of the compound. The microstructure and elemental composition were examined using scanning electron microscopy (SEM). Multiple regions of the LiCr₃.₄Fe₁.₆O₈ crystals were analyzed, revealing a homogeneous phase and providing detailed insight into the morphology and chemical composition of the surface. The synthesized ferrite particles exhibited relatively large dimensions, with sizes measured at approximately 5, 30, 100, and 200 μm. The dielectric behavior was studied to assess the material’s response to an external electric field, demonstrating its capacity for electric charge polarization. Both capacitance and electrical conductivity were found to increase with rising temperature. Electrophysical measurements were conducted using the LCR-800 system over a temperature range of 293–483 K and at frequencies of 1.5 kHz and 10 kHz. An increase in frequency to 10 kHz resulted in a decrease in the dielectric constant (ε) across the entire temperature range.

This paper presents a comprehensive investigation into the synthesis, morphological characteristics, electrical conductivity, dielectric behavior, and electrocatalytic activity of perovskite-structured iron manganite (FeMnO₃), with a specific focus on its performance in the hydrogen evolution reaction (HER). FeMnO₃(FMO) nanoparticles (NPs) were synthesized using a sol–gel-type Pechini method and characterized by X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FT-IR), and field-emission scanning electron microscopy combined with energy-dispersive X-ray spectroscopy (FESEM-EDS). XRD analysis confirmed the formation of a crystalline structure with cubic symmetry assigned to the Ia-3 space group, with an average crystallite size of 52.47 nm. FESEM images revealed a relatively uniform morphology with an average particle diameter of 55.84 nm. The redox and oxidation states of Fe and Mn can be studied by temperature-programmed oxidation (TPO-O₂) in order to understand oxygen uptake and metal oxidation processes occurring within the FMO lattice. The dielectric constant, dielectric loss, electric modulus and electrical conductivity were calculated as a function of frequency and temperature using a Novocontrol Alpha-A broadband dielectric spectrometer (Novocontrol system) coupled with the LCR-800 precision meter. The dielectric data reveal that the FMO has semiconducting behavior with dominant charge- or ionic-relaxation processes. The electrocatalytic activity toward the HER was evaluated using linear sweep voltammetry (LSV), with the working electrode modified by an FMO catalyst ink. The material exhibited significant catalytic activity within the HER potential range, and an increase in the number of cycles led to stabilized current and enhanced hydrogen evolution. These results highlight the stability of FeMnO₃ for hydrogen generation.