Electroreduction of oxygen on carbon-supported gold catalysts

H Erikson, G Jürmann, A Sarapuu, RJ Potter… - Electrochimica …, 2009 - Elsevier
H Erikson, G Jürmann, A Sarapuu, RJ Potter, K Tammeveski
Electrochimica Acta, 2009Elsevier
The electrochemical reduction of oxygen was studied on Au/C catalysts (20 and 30wt%) in
0.5 M H2SO4 and 0.1 M KOH solutions using the rotating disk electrode (RDE) method. The
thickness of the Au/C–Nafion layers was varied between 1.5 and 10μm. The specific activity
of Au was independent of catalyst loading in both solutions, indicating that the transport of
reactants through the catalyst layer does not limit the process of oxygen reduction under
these conditions. The mass activity of 20wt% Au/C catalysts was higher due to smaller …
The electrochemical reduction of oxygen was studied on Au/C catalysts (20 and 30wt%) in 0.5M H2SO4 and 0.1M KOH solutions using the rotating disk electrode (RDE) method. The thickness of the Au/C–Nafion layers was varied between 1.5 and 10μm. The specific activity of Au was independent of catalyst loading in both solutions, indicating that the transport of reactants through the catalyst layer does not limit the process of oxygen reduction under these conditions. The mass activity of 20wt% Au/C catalysts was higher due to smaller particle size. The number of electrons involved in the reaction and the Tafel slopes were found; the values of these parameters are similar to that of bulk polycrystalline gold and indicate that the mechanism of O2 reduction is not affected by carbon support or the catalyst configuration.
Elsevier
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