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Using the in situ generated H2O2 approach, a similar catalytic productivity was observed but with much higher methanol selectivity (70 80 %).
More interestingly, the AgNi/PtAgNiNPs/C catalyst displays much higher methanol tolerance than the commercial Pt/C catalyst in 0.1 M KOH solution in the presence of 0.5 M methanol.
Moreover, the PdCo/C catalyst exhibited much higher methanol tolerance during the ORR than the Pt/C catalyst, assessing that it may function as a methanol-tolerant cathode catalyst in a direct methanol fuel cell (DMFC).
As expected, the Vo-PO4-BWO layers with the simultaneously efficient light absorption and charge transport properties achieve much higher methanol formation rate of 157 μmol g-1 h-1, over 2 and 262 times larger than that of BWO atomic layers and bulk BWO.
Moreover, the Pt Sn/C catalyst exhibited much higher methanol tolerance during the oxygen reduction reaction than the Pt/C catalyst, assessing that the present Pt Sn/C bimetallic catalyst may function as a methanol-tolerant cathode catalyst in a direct methanol fuel cell.
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The prepared catalyst showed a much higher activity for methanol electro-oxidation than a catalyst prepared by the conventional impregnation method, even higher than that of current commercially available, state-of-the-art catalysts.
Gold modified titania exhibited much higher photocatalytic activity during methanol dehydrogenation under UV irradiation than titania modified with monometallic silver and bimetallic Au Ag NPs.
The peak current density in cyclic voltammetry (CV) curves reaches 360 mA cm−2 in the solution with 0.5 mol L−1 methanol, much higher than that of Ni B/Ti electrode.
The efficiency of formic acid fuel cells can be engineered to a much higher level than that of methanol in addressing the crossover issue with the polymer membrane [8].
Compared with other nickel electrodes, this electrode exhibited much higher electrocatalytic properties toward the methanol electrooxidation, the peak current density reached 510 mA cm−2 and the peak potential shifted negatively.
Though the activity for carbon monoxide hydrogenation was little lower than that of CuZnO catalyst, ZrO2-doped CuZnO catalyst showed much higher activity and selectivity towards methanol synthesis from carbon dioxide hydrogenation.
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