Among microporous storage materials copper benzene-1,3,5-tricarboxylate (CuBTC MOF, Cu₃(BTC)₂ or HKUST-1) holds the greatest potential for clean energy gases. However, its usefulness is challenged by water vapor, either in the gas to be stored or in the environment. To determine the protection potential of graphene oxide (GO) HKUST-1@GO composites containing 0–25% GO were synthesized and studied. In the highest concentration, GO was found to strongly affect HKUST-1 crystal growth in solvothermal conditions by increasing the pH of the reaction mixture. Otherwise, the GO content had practically no influence on the H₂, CH₄ and CO₂ storage capacities, which were very similar to those from the findings of other groups. The water vapor resistance of a selected composite was compared to that of HKUST-1. Powder X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), thermogravimetric (TG/DTG) and N₂ adsorption techniques were used to monitor the changes in the crystal and pore structure. It was found that GO saves the copper–carboxyl coordination bonds by sacrificing the ester groups, formed during the solvothermal synthesis, between ethanol and the carboxyl groups on the GO sheets.

Microstructure and magnetic properties of sputter deposited Co/Pd multilayered perpendicular magnetization films with amorphous C or Si seedlayer were investigated. The angstrom scale surface roughness of the seedlayer causes fine crystal grains to form in the Co/Pd multilayer and to decrease the extent of intergranular exchange coupling, while it obstructs the formation of a regular interface between Co and Pd layers. The Si seedlayer, which exhibits a surface roughness lower than the C seedlayer, yields Co/Pd multilayered films with the lowest intergranular exchange coupling and the highest coercivity. The improvement in magnetic properties of the Co/Pd film with Si seedlayer is attributable mainly to the formation of ${\mathrm{Pd}}_2\mathrm{Si}$ at the interface between the Co/Pd layer and the Si seedlayer. The ${\mathrm{Pd}}_2\mathrm{Si}$ provides suitable nucleation sites for the grain growth of Co/Pd multilayered film that can be utilized as a perpendicular magnetic recording medium.

The selective oxidation of veratryl alcohol as lignin-derived compound was studied under mild conditions, using Au-Cu catalysts synthesized from pre-formed nanoparticles with different Au:Cu molar ratios. Bimetallic catalysts show higher activity compared to monometallic counterparts, highlighting a clear synergistic effect. By comparing the physico-chemical surface properties of catalysts supported on carbon and Al₂O₃, we were able to establish a strong support effect, with alumina-based catalysts being more active than carbon-supported ones. Moreover, TEM and X-ray photoelectron spectroscopy (XPS) analyses showed a different composition of nanoparticles (NPs) and metal exposure, and we established that Au is the active phase of the reaction. The co-presence of Au and Cu species, and their different interaction with the support, enabled obtaining more than 70% conversion of veratryl alcohol to veratryl aldehyde as a unique product. Moreover, the Au₁Cu₁ supported on alumina catalyst was recovered by filtration and reused without significant loss of activity and selectivity up to four times.

In this study, the surface and textural properties as well as the catalytic performance of Ni/CeO₂ and NiIn/CeO₂ catalysts prepared by wet impregnation (WI) and deposition–precipitation (DP) are investigated. The addition of Ni (3.0 wt.%) resulted in a decrease in the specific surface area and pore volume in the case of the WI method, possibly due to a blockage of mesopores. A minimal addition of In (0.25 wt.%) caused a further decrease in the surface area in both cases. XRD analysis showed that Ni deposited on CeO₂ by DP resulted in some lattice incorporation, affecting the crystallinity of the support. The H₂-TPR profiles altered depending on the different ways of Ni and In introduction. STEM-EDS-derived elemental maps indicated that the Ni and NiIn particles deposited on CeO₂ using the DP method were somewhat smaller than in the WI synthesis. A comprehensive CO-DRIFTS analysis proved a direct Ni-In interaction in bimetallic samples, leading to the formation of a surface NiIn alloy. Ni/CeO₂ catalysts showed a higher activity in the process of dry reforming of methane (DRM) than the bimetallic counterparts at 650 °C, with the Ni_DP sample performing slightly better. However, the Ni_DP catalyst showed significant coking, which was drastically reduced by the addition of In. The agglomeration of Ni and/or NiIn particles during the 6 h DRM reaction somewhat impaired the catalyst performance. Overall, this study highlights the intricate relationship between the catalyst preparation, surface properties and catalytic performance in the DRM reaction and emphasizes the beneficial role of In addition in reducing the coking of the monometallic catalyst and the critical location and surface morphology of nickel nanoparticles decorated with indium and in contact with ceria.

Tribology tests were conducted on silicon nitride-based nanocomposites with various carbon additions to explore the effects of microstructure, the type and quantity of carbon additives and the preparation routes on the behavior. The nanocomposites consisted of Si3N4 and C in the proportions of 1 – 10 wt % carbon nanotube (CNT), or carbon black (CB), or graphite, or graphene. Specimens were produced by hot isostatic pressing. X-ray diffraction and scanning electron microscopy were used to reveal phase composition and microstructure. Unlubricated ball-on-disk tribology tests with silicon nitride counter face were carried out at room temperature in ambient atmosphere. Contact profilometer was used to profile the wear tracks. The friction coefficients of the pure Si3N4 and Si3N4 samples with 3% CNT varied between 0,77-0,81. Addition of 10% graphite and 3% CB to Si3N4 resulted in friction coefficients of 0,83 and 0,72 respectively. Si3N4 samples with 3% graphene showed distinctly lower friction levels of 0,52 and smaller scatter of the measured values. The wear track study revealed that high graphene content in the Si3N4 matrix caused relatively big wear particles and an uneven wear track.