The spontaneous oxidation of a magnetite surface and shape design are major aspects of synthesizing various nanostructures with unique magnetic and electrical properties, catalytic activity, and biocompatibility. In this article, the roles of different organic modifiers on the shape and formation of an oxidized layer composed of maghemite were discussed and described in the context of magnetic and electrical properties. It was confirmed that Fe₃O₄ nanoparticles synthesized in the presence of triphenylphosphine could be characterized by cuboidal shape, a relatively low average particle size (9.6 ± 2.0 nm), and high saturation magnetization equal to 55.2 emu/g. Furthermore, it has been confirmed that low-frequency conductivity and dielectric properties are related to surface disordering and oxidation. The electric energy storage possibility increased for nanoparticles with a disordered and oxidized surface, whereas the dielectric losses in these particles were strongly related to their size. The cuboidal magnetite nanoparticles synthesized in the presence of triphenylphosphine had an ultrahigh electrical conductivity (1.02 × 10⁻⁴ S/cm at 10 Hz) in comparison to the spherical ones. At higher temperatures, the maghemite content altered the behavior of electrons. The electrical conductivity can be described by correlated barrier hopping or overlapping large polaron tunneling. Interestingly, the activation energies of electrons transport by the surface were similar for all the analyzed nanoparticles in low- and high-temperature ranges.

The Mg₆₀Cu₃₀Y₁₀ and Mg₆₅Cu₂₀Y₁₀Zn₅ bulk metallic glasses in the form of a rod 2 mm in diameter were successfully prepared by the conventional Cu-mold casting method. The addition of Zn caused the decrease in the crystallization and melting temperatures in comparison with the Mg₆₀Cu₃₀Y₁₀ alloy. The crystallization and melting temperatures are crucial factors that influence the casting process. An increase in annealing temperature leads to structural changes by the formation of the crystalline phases and lowers the compressive strength. These results obtained for the Mg-based bulk metallic glasses (Mg-BMGs) are important for some practical reasons, in particular, for developing the fabrication process. It has been shown that minor addition of an alloying element can change glass-forming ability and strength of the Mg-BMGs.

The ternary Ca₅₀Mg₂₀Cu₃₀ bulk metallic glass with thickness of 1 mm and width of 10 mm was successfully fabricated by conventional copper-mold casting method. The structural characterization of the alloy in the “as-cast” and after-annealing states was carried out using x-ray diffraction method. The corrosion behaviors of the glassy and crystalline samples were studied by electrochemical measurements and immersion tests in a 5% NaCl solution at room temperature. The amorphous alloy showed higher corrosion resistance than crystalline samples. The post-test analyses were conducted by scanning electron microscopy and energy-dispersive x-ray spectroscopy to examine the damage and chemical composition of the investigated surfaces.

Magnesium alloys are considered as potential biomaterials for use in orthopedic implantology. The main barrier to the use of Mg alloys in medicine is their overly fast and irregular degradation in body fluids. The use of protective calcium phosphate coatings to increase the corrosion resistance of Mg alloy (AM50 alloy: 4 wt.% Al, 0.3 wt.% Mn, 0.2 wt.% Zn, rest Mg) was examined in this study. The scientific goal of the study was the assessment of the influence of calcium phosphate layer morphology on the corrosion process in Ringer’s solution. Modification of the coating morphology was obtained by changing the chemical composition of the phosphatizing bath using NaOH (NaAM50 sample) or ZnSO₄ (ZnAM50 sample). In practice, a more dense and uniform coating could be obtained by the immersion of AM50 alloy in a solution containing ZnSO₄ (ZnAM50 sample). In this study, an adhesion test performed on the ZnAM50 sample indicated that the critical load was 1.35 N. XRD phase analysis confirmed that the obtained coatings included dicalcium phosphate dihydrate (CaHPO₄*2H₂O). The coatings prepared on the NaAM50 and ZnAM50 samples are effective barriers against the progress of corrosion deeper into the substrate. After 120 h immersion in Ringer’s solution, the volume of the evolved hydrogen was 5.6 mL/cm² for the NaAM50 and 3.4 mL/cm² for the ZnAM50 sample.