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The dynamics of the dissociative adsorption of methane on Pt(533)

The dynamics of the dissociative adsorption of methane on Pt(533)
The dynamics of the dissociative adsorption of methane on Pt(533)
The influence of well-defined steps on the dynamics of the dissociative chemisorption of methane on Pt(533) has been investigated using molecular beam techniques. The initial dissociative chemisorption probability S-0 has been determined as a function of incident energy E-i, angle of incidence theta(i), and surface temperature T-S. For incident kinetic energies in the range 26<Ei(meV)<1450, the initial dissociation probability of CH4 on the Pt(533) surface is higher than on Pt(111), for all surface temperatures investigated. This enhancement in dissociation is associated with the additional direct sticking mediated by the step sites, with no evidence for any additional indirect dynamical channel to dissociation induced by the step sites in the range of energies studied. The E-i dependence can be separated into the contributions of the (111) terraces and the (100) steps. The latter exhibits an effective activation barrier for dissociation approximate to 300 meV lower than the (111) terraces. The angular dependence can also be interpreted as having two contributions, one associated with the (111) terraces, and the second associated with the steps. The angular dependence associated with the step sites is broader than the dependence expected for the (111) terraces, and has a maximum for incident trajectories with an angle between the angles corresponding to the normal directions of the (111) and (100) facets. An enhanced T-S dependence is also observed on the Pt(533) surface over Pt(111). This is also associated with the influence of the step sites, and results either from the lower barrier to dissociation, or more likely a more effective coupling of the energy from the surface into the reaction coordinate.
6-dimensional quantum dynamics, molecular-beam, ch4 dissociation, hydrogen dissociation, chemisorption, activation, pt(111), ru(0001), surface, model
0021-9606
3334-3341
Gee, Adam T.
6f500cc4-366f-401f-aad2-e252e766d688
Hayden, Brian E.
aea74f68-2264-4487-9d84-5b12ddbbb331
Mormiche, Claire
00a2dfb0-7160-453a-9eb1-02808eb60cb4
Kleyn, Aart W.
9b178da3-563e-4faa-99a9-7072f570e9ec
Riedmüller, Bernd
5645d311-82da-4e98-a7cd-efe28c7c12a2
Gee, Adam T.
6f500cc4-366f-401f-aad2-e252e766d688
Hayden, Brian E.
aea74f68-2264-4487-9d84-5b12ddbbb331
Mormiche, Claire
00a2dfb0-7160-453a-9eb1-02808eb60cb4
Kleyn, Aart W.
9b178da3-563e-4faa-99a9-7072f570e9ec
Riedmüller, Bernd
5645d311-82da-4e98-a7cd-efe28c7c12a2

Gee, Adam T., Hayden, Brian E., Mormiche, Claire, Kleyn, Aart W. and Riedmüller, Bernd (2003) The dynamics of the dissociative adsorption of methane on Pt(533). Journal of Chemical Physics, 118 (7), 3334-3341. (doi:10.1063/1.1538184).

Record type: Article

Abstract

The influence of well-defined steps on the dynamics of the dissociative chemisorption of methane on Pt(533) has been investigated using molecular beam techniques. The initial dissociative chemisorption probability S-0 has been determined as a function of incident energy E-i, angle of incidence theta(i), and surface temperature T-S. For incident kinetic energies in the range 26<Ei(meV)<1450, the initial dissociation probability of CH4 on the Pt(533) surface is higher than on Pt(111), for all surface temperatures investigated. This enhancement in dissociation is associated with the additional direct sticking mediated by the step sites, with no evidence for any additional indirect dynamical channel to dissociation induced by the step sites in the range of energies studied. The E-i dependence can be separated into the contributions of the (111) terraces and the (100) steps. The latter exhibits an effective activation barrier for dissociation approximate to 300 meV lower than the (111) terraces. The angular dependence can also be interpreted as having two contributions, one associated with the (111) terraces, and the second associated with the steps. The angular dependence associated with the step sites is broader than the dependence expected for the (111) terraces, and has a maximum for incident trajectories with an angle between the angles corresponding to the normal directions of the (111) and (100) facets. An enhanced T-S dependence is also observed on the Pt(533) surface over Pt(111). This is also associated with the influence of the step sites, and results either from the lower barrier to dissociation, or more likely a more effective coupling of the energy from the surface into the reaction coordinate.

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More information

Published date: 15 February 2003
Keywords: 6-dimensional quantum dynamics, molecular-beam, ch4 dissociation, hydrogen dissociation, chemisorption, activation, pt(111), ru(0001), surface, model
Organisations: Chemistry

Identifiers

Local EPrints ID: 19961
URI: http://eprints.soton.ac.uk/id/eprint/19961
ISSN: 0021-9606
PURE UUID: b993c992-ac94-44e4-962b-cdbb3ee306e0
ORCID for Brian E. Hayden: ORCID iD orcid.org/0000-0002-7762-1812

Catalogue record

Date deposited: 24 Feb 2006
Last modified: 16 Mar 2024 02:36

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Contributors

Author: Adam T. Gee
Author: Brian E. Hayden ORCID iD
Author: Claire Mormiche
Author: Aart W. Kleyn
Author: Bernd Riedmüller

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