Abstract

A double chamber SrCe 0.95Yb 0.05O 3 − a proton conducting membrane reactor was used in order to explore N 2O and NO cathodic reduction, over Pd cathodes, by hydrogen generated from steam electrolysis at the anode. Non-Faradaic enhancement of N 2O decomposition was observed at cathodic overpotentials, and |Λ| values above unity were achieved. Electrochemically transferred protons not only liberated the active sites from oxygen ad-atoms but also activated inactive, at open circuit, sites to adsorb and dissociate N 2O. In the NO-containing reactant mixtures the NO reduction rate was always negligible at open circuit since Pd was essentially inactive towards NO dissociation. Nevertheless, Pd became active at cathodic overpotentials, and |Λ| values equal to unity revealed a Faradaic enhancement according to the “decomposition” mechanism. In presence of C 3H 8 and O 2 data suggested a “reduction” type of mechanism.

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