A molecular beam study of the catalytic oxidation of CO on a Pt(111) surface
J. Chem. Phys. 73, 5862 (1980); doi:10.1063/1.440029
Issue Date: 1 December 1980
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The oxidation of carbon monoxide catalyzed by Pt(111) was studied in ultrahigh vacuum using reactive molecular beam–surface scattering. Under all conditions studied, the reaction follows a Langmuir–Hinshelwood mechanism: the combination of a chemisorbed CO molecule and an oxygen adatom. When both reactants are at low coverage, the reaction proceeds with an activation energy E
=24.1 kcal/mole and a pre-exponential
4 =0.11 cm2 particles−1 sec−1. At very high oxygen coverage, E
decreases to about 11.7 kcal/mole and
4 to about 2×10−6 cm2 particles−1 sec−1. This is largely attributed to the corresponding increase in the energy of the adsorbed reactants. When a CO molecule incident from the gas phase strikes the surface presaturated with oxygen, it enters a weakly held precursor state to chemisorption. Desorption from this state causes a decrease in chemisorption probability with temperature. Once chemisorbed, the CO molecule then has almost unit probability of reacting to produce CO2 below 540 K. The CO2 product angular distribution varies from cos
to cos4
depending sensitively upon the adsorbed reactant concentrations.
The Journal of Chemical Physics is copyrighted by The American Institute of Physics.
4 =0.11 cm2 particles−1 sec−1. At very high oxygen coverage, E
4 to about 2×10−6 cm2 particles−1 sec−1. This is largely attributed to the corresponding increase in the energy of the adsorbed reactants. When a CO molecule incident from the gas phase strikes the surface presaturated with oxygen, it enters a weakly held precursor state to chemisorption. Desorption from this state causes a decrease in chemisorption probability with temperature. Once chemisorbed, the CO molecule then has almost unit probability of reacting to produce CO2 below 540 K. The CO2 product angular distribution varies from cos
to cos4
depending sensitively upon the adsorbed reactant concentrations.
The Journal of Chemical Physics is copyrighted by The American Institute of Physics.
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KEYWORDS and PACS
MOLECULAR BEAMS,
CARBON MONOXIDE,
PLATINUM,
SURFACES,
CATALYSIS,
OXIDATION,
COLLISIONS,
MOLECULE COLLISIONS
- 82.65.Jv
Physical chemistry Surface processes Heterogeneous catalysis at surfaces and other surface reactions - 79.20.Rf
Electron and ion emission by liquids and solids; impact phenomena Impact phenomena, including electron spectra and sputtering Atomic and molecular beam interactions - 34.50.Lf
Atomic and molecular collision processes and interactions Inelastic scattering of atoms and molecules Chemical reactions, energy disposal, and angular distribution, as studied by atomic and molecular beams - YEAR: 1980
PUBLICATION DATA
0021-9606 (print)
1089-7690 (online)
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