Abstract
We have used a novel, high-pressure high-temperature scanning tunneling microscope, which is set up as a flow reactor, to determine simultaneously the surface structure and the reactivity of a Pt(110) model catalyst at semirealistic reaction conditions for CO oxidation. By controlled switching from a CO-rich to an [Formula presented]-rich flow and vice versa, we can reversibly oxidize and reduce the platinum surface. The formation of the surface oxide has a dramatic effect on the [Formula presented] production rate. Our results show that there is a strict one-to-one correspondence between the surface structure and the catalytic activity, and suggest a reaction mechanism which is not observed at low pressures.
| Original language | English |
|---|---|
| Article number | 046101 |
| Number of pages | 4 |
| Journal | Physical Review Letters |
| Volume | 89 |
| Issue number | 4 |
| DOIs | |
| Publication status | Published - 2002 |
| Externally published | Yes |
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