4.6 Article

The Interactions of Oxygen with Small Gold Clusters on Nitrogen-Doped Graphene

Journal

MOLECULES
Volume 18, Issue 3, Pages 3279-3291

Publisher

MDPI AG
DOI: 10.3390/molecules18033279

Keywords

gold cluster; graphene; oxygen adsorption; density functional theory

Funding

  1. major program of Beijing Municipal Natural Science Foundation [20110001]
  2. National Natural Science Foundation of China [11179001, 51172007]
  3. Doctoral Fund of Innovation of Beijing University of Technology

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By means of density functional theory, the adsorption properties of O-2 molecule on both isolated and N-graphene supported gold clusters have been studied. The N-graphene is modeled by a C65NH22 cluster of finite size. The results indicate that the catalytic activity and the O-2 adsorption energies of odd-numbered Au clusters are larger than those of adjacent even-numbered ones. The O-2 molecule is in favor of bonding to the bridge sites of odd-numbered Au clusters, whereas for odd-numbered ones, the end-on adsorption mode is favored. The perpendicular adsorption orientation on N-graphene is preferred than the parallel one for Au-2, Au-3 and Au-4 clusters, while for Au-5, Au-6 and Au-7, the parallel ones are favored. When O-2 is adsorbed on N-graphene supported Au clusters, the adsorption energies are largely increased compared with those on gas-phase ones. The increased adsorption energies would significantly facilitate the electron transfer from Au d-orbital to pi* orbital of O-2, which would further weakening the O-O bond and therefore enhancing the catalytic activity. The carbon atoms on N-graphene could anchor the clusters, which could make them more difficult to structural distortion, therefore enhance their stability.

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