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• W1980513633 abstract "Understanding the nature of nonbonded interactions on the graphene surface is a problem of outstanding interest. Highly reliable M05-2X/6-311++G**//M05-2X/6-31G* DFT calculations were performed to understand the interaction of small molecules and ionic species with graphenes. Various linear and branched polycyclic aromatic hydrocarbons (PAHs) were taken as models of the graphene surface, and their interaction with small molecules (CO2 and H2O), metal atoms (Li and Mg), and metal ions (Li+ and Mg2+) has been studied. The effect of ring size is found to be profound on the interaction energy values and shows an interesting contrast with various species. Our results indicate that the metal atoms and ions are chemisorbed, while CO2 and H2O are physisorbed on the PAH surface. H2O displays a stronger affinity for complexation compared to CO2. The binding strength of the molecules has been correlated with the nucleus independent chemical shift (NICS), a local aromaticity index, highest occupied molecular orbital (HOMO) energy, and polarizability of PAHs." @default.
• W1980513633 created "2016-06-24" @default.
• W1980513633 creator A5041265819 @default.
• W1980513633 creator A5042534009 @default.
• W1980513633 date "2011-04-28" @default.
• W1980513633 modified "2023-10-18" @default.
• W1980513633 title "Molecular and Ionic Interaction with Graphene Nanoflakes: A Computational Investigation of CO₂, H₂O, Li, Mg, Li⁺, and Mg²⁺ Interaction with Polycyclic Aromatic Hydrocarbons" @default.
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• W1980513633 doi "https://doi.org/10.1021/jp201578p" @default.
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