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This experimental investigation is the first to generate a surface iron-tantalum (Fe/Ta) alloy as a sublayer-layer using a plasma focus device. Examining how ion beams from a plasma focus device alloy iron and tantalum with varying melting points is one of the key objectives of this study. Fe/Ta thin film nanostructure and surface morphology were also examined. The distance from the tip anode and the varied number of shots are the experimental variables. Although tantalum's melting point (3020 $$^\circ{\rm C}$$ ∘ C ) is generally known to be near to that of iron (2862 $$^\circ{\rm C}$$ ∘ C ), it is possible that iron vaporizes and partial alloying of iron with tantalum occurs before tantalum reaches its melting point. Fe/Ta thin film identification techniques include scanning electron microscopy, mapping of cross-section, energy dispersive X-ray spectroscopy, and X-ray diffraction pattern. Additionally, the composition of multilayer structures is examined using EDS. In conclusion, the results of the X-ray diffraction pattern showed that the number of shots had a significant impact on the residual strain degree of the thin films that were deposited. Furthermore, structures made of FeTa and Fe2Ta were produced. Additionally, photos from scanning electron microscopy and cross-section mapping verify that the sample with five shots at an 8 cm distance from the tip anode formed a uniform Fe/Ta alloy structure. The sample with five shots at a distance of 4 cm from the tip anode formed micro-island structures, as seen by scanning electron microscopy, with decreasing distance. Furthermore, depth elemental distribution revealed that the optimal depth of penetration in a homogenous material to develop alloying is best determined by number of PF shots.
This experimental investigation is the first to generate a surface iron-tantalum (Fe/Ta) alloy as a sublayer-layer using a plasma focus device. Examining how ion beams from a plasma focus device alloy iron and tantalum with varying melting points is one of the key objectives of this study. Fe/Ta thin film nanostructure and surface morphology were also examined. The distance from the tip anode and the varied number of shots are the experimental variables. Although tantalum's melting point (3020 $$^\circ{\rm C}$$ ∘ C ) is generally known to be near to that of iron (2862 $$^\circ{\rm C}$$ ∘ C ), it is possible that iron vaporizes and partial alloying of iron with tantalum occurs before tantalum reaches its melting point. Fe/Ta thin film identification techniques include scanning electron microscopy, mapping of cross-section, energy dispersive X-ray spectroscopy, and X-ray diffraction pattern. Additionally, the composition of multilayer structures is examined using EDS. In conclusion, the results of the X-ray diffraction pattern showed that the number of shots had a significant impact on the residual strain degree of the thin films that were deposited. Furthermore, structures made of FeTa and Fe2Ta were produced. Additionally, photos from scanning electron microscopy and cross-section mapping verify that the sample with five shots at an 8 cm distance from the tip anode formed a uniform Fe/Ta alloy structure. The sample with five shots at a distance of 4 cm from the tip anode formed micro-island structures, as seen by scanning electron microscopy, with decreasing distance. Furthermore, depth elemental distribution revealed that the optimal depth of penetration in a homogenous material to develop alloying is best determined by number of PF shots.
The hydrogenation of carbon monoxide (CO) offers a promising avenue for reducing air pollution and promoting a cleaner environment. Moreover, by using suitable catalysts, CO can be transformed into valuable hydrocarbons. In this study, we elucidate the mechanistic aspects of the catalytic conversion of CO to hydrocarbons on the surface of manganese-doped graphene oxide (Mn-doped GO), where the GO surface includes one OH group next to one Mn adatom. To gain insight into this process, we have employed calculations based on the density functional theory (DFT) to explore both the thermodynamic properties and reaction energy barriers. The Mn adatoms were found to significantly activate the catalyst surface by providing stronger adsorption geometries. Our study concentrated on two mechanisms for CO hydrogenation, resulting in either CH4 production via the reaction sequence CO → HCO → CH2O → CH2OH → CH2 → CH3 → CH4 or CH3OH formation through the CO → HCO → CH2O → CH2OH → CH3OH pathway. The results reveal that both products are likely to be formed on the Mn-doped GO surface on both thermodynamic grounds and considering the reaction energy barriers. Furthermore, the activation energies associated with each stage of the synthesis show that the conversion reactions of CH2 + OH → CH3 + O and CH2O + OH → CH2OH + O with energy barriers of 0.36 and 3.86 eV are the fastest and slowest reactions, respectively. The results also indicate that the reactions: CH2OH + OH → CH2 + O+H2O and CH2OH + OH → CH3OH + O are the most exothermic and endothermic reactions with reaction energies of −0.18 and 1.21 eV, respectively, in the catalytic pathways.
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