Abstract
The anodic oxidation of CO on nominal Pt(111) and Pt(997) electrodes in a CO-saturated 0.1 M HClO4 electrolyte is studied by optical second harmonic generation (SHG) at a wavelength of 280 nm to monitor the CO adlayer under steady-state reaction conditions in the potential range between 50 mV and 1030 mV vs. RHE. Regarding the catalytic activity of the electrodes, two potential regimes are distinguishable: in the low potential regime, characterized by the presence of a dense CO overlayer, the reaction yield is higher on Pt(997) than on Pt(111). Positive of the overlayer stripping potential [880 mV for Pt(111) and 780 mV for Pt(997)] the Pt(997) electrode exhibits an inferior reactivity. The results confirm the structure sensitivity of anodic CO oxidation on Pt electrode surfaces.
| Original language | English |
|---|---|
| Pages (from-to) | 571-575 |
| Number of pages | 5 |
| Journal | Surface Science |
| Volume | 402-404 |
| DOIs | |
| State | Published - 15 May 1998 |
Keywords
- Carbon monoxide
- Electrochemical methods
- Molecule-solid reactions
- Oxidation
- Platinum
- Second harmonic generation
- Single crystal surfaces
- Solid-liquid interfaces
- Surface chemical reaction
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