Theoretical study of NH3, H2S, and HCN adsorption enhancement on defective graphene‐supported Cu19 clusters

Plane-wave DFT study of adsorptions of NH₃, H₂S, and HCN on Cu₁₉ and defective graphene-supported Cu₁₉ clusters reveal that the three gas molecules can be adsorbed on three top sites of copper atoms, respectively. The adsorption energies at the corresponding adsorption sites on defective graphene-supported Cu₁₉ clusters are all enhanced compared with those on Cu₁₉ clusters.

Abstract

Recent studies have shown that graphene-supported metal clusters can enhance catalytic reactivity compared with corresponding metal clusters. In this study, the adsorptions of NH₃, H₂S, and HCN on Cu₁₉ and defective graphene-supported Cu₁₉ clusters are investigated using plane-wave density functional theory. The results reveal the three gas molecules can be adsorbed on three types of top sites of Cu atoms, respectively. The adsorption energies of the corresponding adsorption sites on the defective graphene-supported Cu₁₉ clusters are all increased compared with those on the Cu₁₉ clusters. The orbital-resolved, crystal orbital Hamilton population analysis demonstrates that the larger the integrated crystal orbital Hamilton population, the stronger the adsorption between the gas molecule and the bonded Cu atom. The center of antibonding states on the defective graphene-supported Cu₁₉ is shifted upward relative to Fermi level compared to the corresponding one on pure Cu₁₉, which explains the enhanced adsorption energy on defective graphene-supported Cu_19. In addition, the closer d-band center to the Fermi level on the defective graphene-supported Cu₁₉ indicates a stronger adsorption capacity than on pure Cu₁₉.

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