Charge storage at Pt/YSZ interface as the origin of `permanent' electrochemical promotion of catalysis

Abstract

Tuning of the catalytic reaction rate by electric polarization of the interface between an electron conducting catalyst and an ion conducting support, called electrochemical promotion of catalysis (EPOC), is most often fully reversible. Its stateof-the-art model regards the gas-exposed catalyst surface as the unique location of charge storage via backspillover of electrochemically generated species, responsible for promotion. After long-lasting anodic polarization, a permanent effect (P-EPOC) was observed in ethylene combustion with oxygen over Pt/YSZ catalyst. Double step chronoamperometric and linear sweep voltammetric analysis revealed delayed oxygen storage, located presumably at the vicinity of the catalyst/electrolyte interface. It is proposed that oxygen stored at this location, hence hidden for the reactants and then released during relaxation, was at the origin of the observed P-EPOC. The effect of this 'hidden' promoter on the catalytic reaction rate was found to be highly non Faradaic.

Development and testing of an electrochemical methane sensor

“…The reaction of the PtO 2+ with CH 4 induces electrochemical promotion of catalysis (EPOC). The theory of platinum oxidation and reduction during alternating polarization and EPOC effect is in good agreement with earlier literature studies [23][24][25].…”