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We report a novel fabrication of nickel-molybdenum alloy nanorods catalyst for hydrogen evolution reaction (HER), which is prepared by co-deposition of pure nickel and molybdenum in a multisource sputtering system on the surface of Ni foam substrate. The Ni–Mo alloy film exhibits favorable vertical nanorods structure and presents the most efficient activity for HER compared to the film only including one metal element. The remarkably enhanced catalytic activity is attributed to its ordered array geometry as well as the synergistic interaction between Ni and Mo. Meanwhile, the open space within nanorod arrays facilitates the electrolyte penetration and diffusion of ionic species, allowing high utilization efficiency of active species as well as rapidly release of evolved hydrogen gas from the electrode surface. [ABSTRACT FROM AUTHOR]

The (RuTiSnSb)O-TiO nanotubes (TNTs) anode has been prepared via anodization, deposition, and annealing. X-ray diffraction, field-emission scanning electron microscopy, cyclic voltammetry, and linear scanning voltammetry were used to scrutinize the electrodes and the electrochemical activity. The results indicate that highly ordered TNTs with large specific surface area could be implanted with active metal oxides. The catalyst firmly binds with the TNTs and enhances the electrochemical stability of the electrode. It displays high over-potential for oxygen evolution reaction. Accordingly, the constructed (RuTiSnSb)O-TNTs anode exhibits a greater potential difference (Δ E) between the evolutions of oxygen and chlorine than that exhibited by the traditional dimensionally stable anode, which is beneficial for improving the selectivity toward chlorine evolution reaction. This superior performance is explained in terms of the surface properties and geometric structure of coated catalyst, as well as the electrochemical selectivity ascribed by the addition of tin and antimony species. [ABSTRACT FROM AUTHOR]

[Display omitted] • Green Fenton-like selective oxidation of alcohol driven by the active oxygen species from air. • Highly efficient selective oxidation with low-cost and super-facile reaction operation. • Highly efficient MnCoOx catalysts characterized by uniform MnCo 2 O 4 -Co 3 O 4 oxide pair for selective oxidation of alcohol using air as oxidant. • A facile method with an in - situ heating enhancement for the formation of spinel MnCo 2 O 4 mixed oxide. Mn reinforced Co 3 O 4 catalysts (MnCoOx) were prepared by a facile solid phase mixed foaming method with an in-situ heating enhancement for the formation of spinel phase mixed oxide species, and studied in the selective oxidation of benzyl alcohol just the air in reactor as oxygen donor. It was found that the MnCoOx catalysts are composed of relatively minimal spinel MnCo 2 O 4 mixed oxide and massive Co 3 O 4 to form MnCo 2 O 4 -Co 3 O 4 oxide pair. The micro-domains of MnCo 2 O 4 -Co 3 O 4 oxide pair present two redox couples of Mn3+/Mn2+ and Co3+/Co2+ instead of the single one of Co3+/Co2+ in Co 3 O 4 , and then dramatically enhance the formation of superoxide radicals (•O2–) species from the O 2 in air, which can efficiently initiate the conversion of benzyl alcohol to benzaldehyde in a Fenton-like processes. With no oxidant other than air in reactor, the interaction between MnCo 2 O 4 and Co 3 O 4 in MnCoOx catalysts leads to a benzyl alcohol conversion up to 98 % with a 100 % benzaldehyde selectivity at atmospheric pressure while single component Co 3 O 4 can only present a benzyl alcohol conversion at 37 %. This embodiment of highly efficient heterogeneous selective oxidation just with air as oxidant provides a probability for developing a low-cost and super-facile radical-induced selective oxidation process for alcohols. [ABSTRACT FROM AUTHOR]