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CO Oxidation on Pt(110): Scanning Tunneling Microscopy Inside a High-Pressure Flow Reactor

B. L. M. Hendriksen and J. W. M. Frenken
Phys. Rev. Lett. 89, 046101 – Published 9 July 2002
An article within the collection: Scanning Probe Microscopy: From Sublime to Ubiquitous
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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 O2-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 CO2 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.

  • Received 19 March 2002

DOI:https://doi.org/10.1103/PhysRevLett.89.046101

©2002 American Physical Society

Collections

This article appears in the following collection:

Scanning Probe Microscopy: From Sublime to Ubiquitous

This collection marks the 35th anniversary of scanning tunneling microscopy (STM) and the 30th anniversary of atomic force microscopy (AFM). These papers, all published in the Physical Review journals, highlight the positive impact that STM and AFM have had, and continue to have, on physical science research. The papers included in the collection have been made free to read.

Authors & Affiliations

B. L. M. Hendriksen and J. W. M. Frenken*

  • Kamerlingh Onnes Laboratory, Leiden University, P.O. Box 9504, 2300 RA Leiden, The Netherlands

  • *Electronic address: frenken@phys.leidenuniv.nl

References

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Issue

Vol. 89, Iss. 4 — 22 July 2002

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