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The designed catalytic system exhibited superior activity for direct conversion of CO and H2O to liquid hydrocarbons with high selectivity.
Comparative testing of our catalysts and a commercial Pt Ru/Vulcan reveals markedly superior activity for our catalysts.
The ceramic composite also exhibited superior activity for cathodic oxygen-reduction-reaction (ORR), thus enabled a symmetrical fuel cell.
Moreover, the Cu2O@g-C3N4 compositexhibitbit superior activity for H2 production to pure Cu2O crystals and g-C3N4 nanosheets.
Our experiment results also show that these samples treated by this method exhibit superior activity for CO oxidation compared with original samples.
When the resultant electrodes act as an electrocatalyst for alkaline water splitting, the Co-Pi/CoP/Ti exhibits the superior activity for electrocatalytic oxygen evolution reaction (OER).
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As compared with bare Pd@MIL-100(Fe), bimetallic PdAu@MIL-100(Fe) showed superior activities for the tandem reactions between amines and alcohols to produce N-alkyl amines under visible-light irradiation, ascribed to the promoting effect of metallic Au in the photocatalytic alcohol-to-aldehyde dehydrogenation.
On the other hand, the superior activity of CMS/Ni for HER, in comparison with that of the pure Co9S8/Ni and MnS/Ni, results from the significant increase in electrochemical active surface areas (ECSAs) to expose more accessible catalytic active sites.
The enhancement of the intermediate formation by the basic sites is proposed to be the key reason for the superior activity of the Au/MgO catalyst.
Easy accessibility of the active sites and the three-dimensional mesoporous structure are the possible causes for the superior activity of these titanosilicate catalysts.
Mesoporosity, three-dimensional architecture, surface hydrophobicity and easy access of Lewis acidic, framework-substituted Ti sites are the factors responsible for the superior activity of Ti-SBA-16 compared to Ti-SBA-12 and the hitherto known solid catalysts for this reaction.
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