In this study, the antibacterial activity of cerium oxide nanoparticles on two Gram-negative and three Gram-positive foodborne pathogens was investigated. CeO₂ nanoparticles (CeO₂ nps) were synthesized by a Wet Chemical Synthesis route, using the precipitation method and the Simultaneous Addition of reactants (WCS–SimAdd). The as-obtained precursor powders were investigated by thermal analysis (TG–DTA), to study their decomposition process and to understand the CeO₂ nps formation. The composition, structure, and morphology of the thermally treated sample were investigated by FTIR, Raman spectroscopy, X-ray diffraction, TEM, and DLS. The cubic structure and average particle size ranging between 5 and 15 nm were evidenced. Optical absorption measurements (UV–Vis) reveal that the band gap of CeO₂ is 2.61 eV, which is smaller than the band gap of bulk ceria. The antioxidant effect of CeO₂ nps was determined, and the antibacterial test was carried out both in liquid and on solid growth media against five pathogenic microorganisms, namely Escherichia coli, Salmonella typhimurium, Listeria monocytogenes, Staphylococcus aureus, and Bacillus cereus. Cerium oxide nanoparticles showed growth inhibition toward all five pathogens tested with notable results. This paper highlights the perspectives for the synthesis of CeO₂ nps with controlled structural and morphological characteristics and enhanced antibacterial properties, using a versatile and low-cost chemical solution method.

We report a simple and efficient approach for graphene production, by electrochemical exfoliation of graphite rods, in acidic solutions. The applied bias and electrolyte concentration were optimized. The X-ray powder diffraction (XRD) patterns of nanosheets reveal the decreasing, or even the disappearance, of the graphene oxide peak by reducing the electrochemical exfoliation bias from +6 to +2.5 V. Thus, graphene with different oxidation degrees can be obtained by controlling the applied bias. An optimal graphene sample was prepared in a mixture of H₂SO₄ : HNO₃ (3 : 1 ratio; 1 M each) at a bias of +3 V. The interlayer spacing, crystallite size and the average number of layers were determined by XRD. The structural and morphological characteristics of the prepared samples were also investigated by Raman Spectroscopy, FTIR Spectroscopy, X-ray Photoelectron Spectroscopy (XPS), Transmission Electron Microscopy (TEM), Scanning Electron Microscopy (SEM), and Atomic Force Microscopy (AFM).