The synthesis of orthoferrites of the type La_1−xCe_xFeO_3+x/2, x = 0.00, 0.01, 0.03, 0.05, and 0.07, by applying a simple and effective mechanochemical transformation from the constituent oxides is presented. Physicochemical methods such as powder X-ray diffraction (XRD), transmission electron microscopy (TEM), UV–Vis spectroscopy, and Brunauer–Emmett–Teller (BET) adsorption were applied to gain information about the effect of Ce⁴⁺ content on the structural, textural, and optical properties of the samples. The catalytic activity of the samples for water decontamination was determined in a photo-Fenton-like activation of persulfate for removal of tetracycline hydrochloride as model pollutant. The presence of persulfate, PDS, considerably increased the removal efficiency under visible light illumination.

In this study, TiO₂-Fe₂O₃/polyvinylpyrrolidone (PVP) hybrids were prepared using the sol–gel method. The iron content in the synthesized samples was 10 and 20 wt%. The influence of PVP on the phase transformation, morphology and optical properties of the as-prepared hybrids was characterized by various physicochemical methods—XRD analysis, UV–Vis spectroscopy, IR spectroscopy and SEM. The obtained sol–gel powders were tested for photocatalytic activity against tetracycline hydrochloride in distilled water under ultraviolet and simulated solar light illumination. The obtained results were compared to commercial TiO₂ P25 (Evonik). The investigated samples exhibited good photocatalytic efficiency for the degradation of tetracycline hydrochloride; however, better activity was demonstrated by the 90TiO₂-10Fe₂O₃/PVP sample. The latter one displayed weak antibacterial action against E. coli ATCC 25922 in the presence of UVA light.

This study explores the sol–gel synthesis, structural characterization, and photocatalytic performance of Ho³⁺-doped TiO₂ nanopowders at two dopant levels (0.5 and 2 mol%). Transparent, homogeneous gels were prepared using titanium (IV) butoxide and holmium (III) nitrate pentahydrate in ethanol, followed by drying and optional annealing at 500 °C. X-ray diffraction confirmed anatase TiO₂ as the dominant crystalline phase, with Ho incorporation suppressing crystal growth and yielding smaller crystallite sizes than undoped TiO₂. FT-IR and UV-Vis spectroscopy verified complete hydrolysis–condensation during gel formation, while diffuse reflectance spectra revealed a red-shifted absorption edge, indicating reduced band gaps. SEM analysis showed nanoscale particles with agglomeration, which intensified after annealing. Photocatalytic activity was tested under UV irradiation using Crystal Violet (anionic dye) and Carmoisine (cationic dye). Annealed Ho-doped powders exhibited markedly higher degradation rates, with the 2 mol% sample achieving the greatest efficiency, particularly against Crystal Violet. These findings demonstrate that Ho³⁺ doping enhances TiO₂’s UV-driven photocatalytic activity by tailoring its structural and optical properties.

In this study, Fe-doped SrTiO₃ powders have been synthesized using the sol-gel approach. The effect of the Fe³⁺ doping on the degradation efficiency of SrTiO₃ toward specific pollutants was studied. The obtained samples were characterized using the following techniques: XRD, SEM-EDS, FTIR, UV-Vis, and BET. Subsequently, the samples were tested for degradation of two organic pollutants—tetracycline hydrochloride and Malachite green in distilled water under different light sources—UV light and visible light. The investigated powders exhibited good photocatalytic degradation efficiency against both pollutants. A comparison of the photocatalytic abilities of the samples under different lights has been made, which emphasizes the paper’s novelty. Undoped SrTiO₃ exhibited better photocatalytic activity for TCH both under UV and visible light irradiation in comparison to the Fe-doped. The SrTi_0.15Fe_0.85O₃ shows superior photocatalytic activity under visible light irradiation for the degradation of MG dye. The antibacterial activity has been tested against two bacterial strains, E. coli ATCC 25922 and P. aeruginosa ATCC 27853. It has been found that the antibacterial efficiency of the Fe-doped sample is greater than compared of the undoped one.

In this study, sol–gel-synthesized nanoparticles were characterized by various physicochemical techniques, including scanning electron microscopy (SEM), X-ray powder diffraction (XRD), UV-Vis spectrophotometry, and thermogravimetric analysis (DTA/TG). The as-obtained powders were tested for their antimicrobial activity against the Gram-positive bacteria Staphylococcus aureus and Enterococcus faecalis, as well as the fungal strains Candida albicans and Saccharomyces cerevisiae. Additionally, the photocatalytic performance of the samples was evaluated under simulated solar light. The results are promising for possible environmental applications. The antimicrobial assessment also revealed notable effects, with varying degrees of growth inhibition observed across the tested microorganisms. The main approach in this study consists of the combination of physicochemical characterization with antibacterial and photocatalytic evaluations, resulting in promising multifunctional materials.

In this study, pure ZnO and Ho-doped ZnO powders (1 and 2 mol % Ho) were synthesized via hydrothermal and sol–gel methods and evaluated for their tribocatalytic activity toward the degradation of paracetamol, an emerging pharmaceutical contaminant in aquatic environments. Structural, morphological, and optical properties of the obtained materials were investigated by X-ray diffraction (XRD), scanning electron microscopy coupled with energy-dispersive X-ray spectroscopy (SEM/EDS), ultraviolet–visible (UV–Vis) spectroscopy, X-ray photoelectron spectroscopy (XPS), and electron paramagnetic resonance (EPR) spectroscopy. SEM observations revealed pronounced morphology differences between the synthesis routes, with hydrothermally prepared samples exhibiting well-defined rod-like structures. XPS and EPR analyses provided evidence for successful Ho modification of ZnO and the presence of defect-related electronic states associated with Ho doping. The tribocatalytic performance was examined in distilled, tap, and mineral water using friction rods with different geometries in order to assess the influence of synthesis route, Ho concentration, and water composition. Among all the investigated materials, hydrothermally synthesized ZnO doped with 2 mol % Ho exhibited the highest tribocatalytic activity, achieving 96.91% degradation of paracetamol at an initial concentration of 15 mg/L within 24 h. The enhanced performance was attributed to improved charge separation induced by Ho modification, combined with the favorable rod-like morphology of the particles. Higher degradation efficiencies were observed in distilled water compared to tap and mineral water, indicating the important role of dissolved ions during the tribocatalytic process. These findings demonstrate that the synthesis route, Ho doping, and water composition collectively govern the tribocatalytic performance of ZnO-based materials, highlighting their potential for water purification.