The microcalorimetric hydrogen titration technique combined with conventional volumetric measurements has been used to reveal peculiarities of the hydrogenation of the single-phase TiZrVNbTa equiatomic high-entropy alloy. The alloy has been produced in the form of microfibers by the pendent drop melt extraction technique. Palladium coating of the fibers has been applied to enable first hydrogenation at room temperature without additional activation. An analysis of the obtained data allows us to evaluate the dependence of hydrogenation enthalpy on the hydrogen concentration in the alloy. Three concentration ranges, presumably related to the formation of the hydrogen solid solution, monohydride and dihydride phases, have been identified, and the corresponding ΔH values of about −100, −80 and −60 kJ/mol H₂, respectively, have been determined.

Composites based on Zr₆₅Cu_17.5Ni₁₀Al_7.5 metallic glass (MG) and polytetrafluoroethylene (PTFE) were prepared by ball milling. Different composites (30/70, 50/50 and 70/30) were produced. Samples for dynamic mechanical analysis and laser flash analysis were fabricated in the supercooled region of the metallic glass and viscous region of the polymer. Spark plasma sintering (SPS) was performed at the supercooled region for the metallic glass powder. Characteristics such as thermal, mechanical, and structural properties were studied. A formation of the Zr₂Cu and Zr₂Ni intermetallic was found in the metallic glass after SPS. A formation of the nanocrystalline Zr₂Cu was found in composite samples. Dynamical mechanical analysis (DMA) was used to study the mechanical behavior of the material. It was concluded that the 70/30-MG/PTFE composite sample had better thermal conductivity than the other composite samples. The thermal conductivity of the metallic glass was the highest among the samples and it increased with the MG content in composites.

Composites based on Zr₆₅Cu_17.5Ni₁₀Al_7.5/PTFE (polytetrafluoroethylene) with silane were prepared by ball milling with subsequent thermal pressing. Silanization was performed in the alcoholic solution with metallic glass powder. Different composites, 30/70 and 50/50 with silane, were prepared. During ball milling, Zr₂Cu and Zr₂Ni intermetallic phases were formed. The Zr-based metallic glass had a large supercooled region, and the melting point of the 30/70 and 50/50 composites with silane was near to the melting point of PTFE. The 50/50 composite (silane) had the highest thermal conductivity compared to the 30/70 composite samples. The incorporation of silane in metallic glass/polymer was investigated by Fourier-transform infrared spectroscopy (FTIR) and scanning electron microscope (SEM) analysis. Thermogravimetric analysis (TGA) showed the thermal stability of the composite samples up to 450–460 °C. It was also concluded that the 50/50 composite with silane has better thermal stability than the 30/70 composite with silane. The addition of silane in 30/70 and 50/50 composites increased the thermal conductivity compared to the composites without silane.

Herein we report a simple and easily scalable method for fabricating ZnO/h-BN composites with tunable photoluminescence (PL) characteristics. The h-BN support significantly enhances the ultraviolet (UV) emission of ZnO nanoparticles (NPs), which is explained by the ZnO/h-BN interaction and the change in the electronic structure of the ZnO surface. When h-BN NPs are replaced with h-BN microparticles, the PL in the UV region increases, which is accompanied by a decrease in visible light emission. The dependence of the PL properties of ZnO NPs on the thickness of h-BN carriers, observed for the first time, is explained by a change in the dielectric constant of the support. A quantum chemical analysis of the influence of the h-BN thickness on the electron density redistribution at the wZnO/h-BN interface and on the optical properties of the wZnO/h-BN composites was carried out. Density functional theory (DFT) calculations show the appearance of hybridization at the h-BN/wZnO interface and an increase in the intensity of absorption peaks with an increase in the number of h-BN layers. The obtained results open new possibilities for controlling the properties of ZnO/h-BN heterostructures for various optical applications.