Journal
CHEMPHYSCHEM
Volume 11, Issue 7, Pages 1452-1459Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/cphc.200900936
Keywords
electrochemical promotion; ethylene oxidation; heterogeneous catalysis; platinum; yttrium-stabilized zirconia
Funding
- Deutsche Forschungsgemeinschaft (DFG)
- Egyptian government (South Valley University, Egypt)
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The electrochemical promotion of the C2H4+O-2 reaction to form CO2 and H2O is studied in the 10(-5) and 10(-4) mbar range with a Pt catalyst interfaced as working electrode to yttrium-stabilized zirconia (YSZ). Photoemission electron microscopy (PEEM) was used as spatially resolving method. Under open-circuit conditions, that is, without an external voltage applied, the CO2 production exhibits a pronounced hysteresis upon cyclic variation of p(C2H4). The hysteresis is attributed to the build-up of a carbonaceous CHx layer inhibiting O-2 adsorption and hence poisoning the reaction. It is shown that the application of a positive potential of 1 V triggers a transition from the unreactive branch of the reaction to an active branch. The large non-Faradayicity reported in the literature for this reaction system is explained as an ignition effect caused by the partial removal of the inhibiting carbonaceaous layer.
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