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The chemisorption of hydrogen on Cu(111): A dynamical study

Journal Article · · International Journal of Quantum Chemistry
;  [1]; ;  [2];
  1. Universita` degli Studi di Milano, Via Golgi (Italy)
  2. Universiteit, De Boelelaan, Amsterdam (Netherlands)

Ab initio band-structure calculations within a density function formalism were performed to computer the binding energy curves of atomic hydrogen with the high-symmetry adsorption sites of the (111) surface of copper. For a two-layer slab of Cu atoms and H coverage equal to 0.25, the binding energies are 2.25, 3.12, and 3.24 eV, for on-top bridge, and threefold sites, so that the chemisorption of H{sub 2} on Cu(111) is exothermic for threefold and bridge sites, but endothermic for on-top sites. Starting from these results, an LEPS potential for the interaction of H{sub 2} with the Cu(111) surface was built. In this model potential, the most favored approaches correspond to a H{sub 2} molecule parallel to the Cu surface, and for them, the activation barrier is located at the corner between the entrance and the exit channels of the reaction, and it lowest value is 0.6 eV. The LEPS potential was used in quasi-classical trajectories calculations to simulate the adsorption of a beam of H{sub 2} molecules on Cu(111). The results show that (a) when H{sub 2} is in the ground vibrational state the dissociative adsorption probability P{sub a} increases from 0-90 along a roughly sigmoidal curve by increasing the collision kinetic energy from 0.4 to 1.3 eV, and (b) the vibrational energy can be as effective as the translation one in promoting dissociative chemisorption, in agreement with the experimental results. 39 refs., 8 figs., 1 tab.

Sponsoring Organization:
USDOE
OSTI ID:
457716
Journal Information:
International Journal of Quantum Chemistry, Journal Name: International Journal of Quantum Chemistry Journal Issue: 4 Vol. 52; ISSN IJQCB2; ISSN 0020-7608
Country of Publication:
United States
Language:
English

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