Investigation of the "permanent" electrochemical promotion of catalysis (P-EPOC) by electrochemical mass spectrometry (EMS) measurements

The phenomenon of electrochemical promotion of catalysis (EPOC) is most often fully reversible. Subsequent to long-lasting polarization, however, the new steady-state open-circuit catalytic activity after current interruption may remain significantly higher than that before polarization. This phenomenon has been reported as "permanent electrochemical promotion of catalysis" (P-EPOC). The catalytic oxidation Of C2H4 was studied over a Pt/YSZ/Au electrochemical cell under excess O-2 at 375 degrees C, combining cyclic voltammetry and mass spectrometry. it has been found that after positive current interruption, the catalytic rate remains in a highly active P-EPOC steady-state, where it is almost double than the initial open-circuit rate. During this highly active steady-state, the application of a similar negative current for a similar time period has been found to result in the return of the catalytic rate to the initial open-circuit state. Similar reversibility of the rate has been observed after cyclic voltammetry experiments where after a complete potential oscillation the open-circuit rate is almost the same to that before polarization. These establish the reported mechanism for the origin of P-EPOC, on promoting species storage and concomitant migration to the metal/gas interface after positive current interruption, through the three phase boundaries. (C) 2009 Elsevier B.V. All rights reserved.


Published in:
Electrochemistry Communications, 12, 323-326
Year:
2010
Publisher:
Elsevier
ISSN:
1388-2481
Keywords:
Laboratories:




 Record created 2010-05-25, last modified 2018-12-03


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