Mechanical Properties Estimation of Standard and Advanced Materials using the Nanoindentation technique

info:eu-repo/semantics/nonPublishe

Combination of instrumented nanoindentation and scanning probe microscopy for adequate mechanical surface testing

SCOPUS: ar.jinfo:eu-repo/semantics/publishe

Effect of the target composition on the microstructure and properties of TiAlNSi nanocomposite coatings

info:eu-repo/semantics/nonPublishe

Hexagonal BN- and BNO-supported Au and Pt nanocatalysts in carbon monoxide oxidation and carbon dioxide hydrogenation reactions

Environmental protection requires solving the problem of utilization and reduction of CO and CO2 emissions. Herein, Au/h-BN(O) and Pt/h-BN(O) nanohybrids are thoroughly analyzed in CO oxidation and CO2 hydrogenation reactions. The nanohybrids differ in catalytic particle size and particle distribution. The particles are smaller (1-6 nm) and display a narrower size distribution in the case of Pt-based nanomaterials. The Pt/h-BN(O) nanohybrids exhibit high catalytic activity in CO conversion and carbon dioxide hydrogenation reactions. For both systems, the oxidative state of BN support affects the catalytic activity. The possible catalytic reaction mechanisms are proposed based on DFT calculations. A charge density distribution at the Pt/h-BN interface increases oxygen absorption, thereby accelerating oxygen-associated chemical reactions

Microstructure and catalytic properties of Fe3O4/BN, Fe3O4(Pt)/BN, and FePt/BN heterogeneous nanomaterials in CO2 hydrogenation reaction: Experimental and theoretical insights

Hexagonal boron nitride (h-BN) nanosheets are a promising material for various applications including catalysis. Herein, h-BN-supported Fe-based catalysts are characterised with respect to CO2 hydrogenation reaction. Heterogeneous Fe3O4/BN, Fe3O4(Pt)/BN, and FePt/BN nanostructures are obtained via polyol synthesis in ethylene glycol. The sizes of Fe3O4 nanoparticles and their distributions over h-BN surfaces depend on the amount of H2PtCl6 added to the synthesis media. Bimetallic FePt nanoparticles are formed when Pt content is high enough. In situ TEM analysis shows the formation of core–shell h-BN@FePt nanoparticles during heating that prevents FePt NPs from further sintering during the catalytic process. The mechanism of Fe and Pt interaction is elucidated based on the molecular dynamic simulations. The FePt/BN nanomaterials show significantly higher CO2 conversion rate compared to the Fe3O4/BN and Fe3O4(Pt)/BN heterogeneous nanomaterials and exhibit almost 100% selectivity to carbon monoxide. The Fe3O4/BN and Fe3O4(Pt)/BN nanomaterials show better selectivity to hydrocarbons. The possible reaction pathways are discussed based on the calculated sorption energies of all reactants, intermediate compounds, and reaction products. The study highlights pronounced catalytic properties of the developed system and reveals a unique interaction mechanism between its components increasing their stability.</p