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rdf:type
lifeskim:mentions
pubmed:issue
10
pubmed:dateCreated
2011-2-23
pubmed:abstractText
We have studied the effect of lattice displacement on the interaction of H(2) with the Cu(111) surface using the Specific Reaction Parameter (SRP) approach to Density Functional Theory (DFT). We have systematically investigated how the motion of the surface atoms affects some features of the Potential Energy Surface (PES), such as the dissociation barrier height and the barrier geometry corresponding to some representative reaction pathways, and the anisotropy of the potential at these geometries. This analysis has allowed us to identify the surface degrees of freedom that are likely to be most relevant for H(2) dissociation. In particular, we have found that the lattice coordinate displacements that have the largest effect on the H(2)/Cu(111) DFT-SRP barrier heights and locations concern the motion of the 1st layer and 2nd layer Cu atoms in the Z direction, and motion of the 1st layer atoms in the directions parallel to the surface. Whereas the first degree of freedom mostly affects the barrier geometry, the second and third motions can lower or raise the barrier height. The latter effect cannot be described with the usual surface oscillator dynamical models employed in the past to include surface motion, and its dynamical influence on the dissociative adsorption needs to be further investigated.
pubmed:language
eng
pubmed:journal
pubmed:status
PubMed-not-MEDLINE
pubmed:month
Mar
pubmed:issn
1463-9084
pubmed:author
pubmed:issnType
Electronic
pubmed:day
14
pubmed:volume
13
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
4552-61
pubmed:year
2011
pubmed:articleTitle
Hydrogen dissociation on Cu(111): the influence of lattice motion. Part I.
pubmed:affiliation
Dipartimento di Chimica Fisica ed Elettrochimica, Università degli Studi di Milano, Milano, Italy. matteo.bonfanti@unimi.it
pubmed:publicationType
Journal Article