Interaction of substituted aromatic compounds with graphene.

We have modeled the adsorption of various substituted derivatives of benzene on a graphene sheet, using a first-principles density functional theory-local density approximation method. The presence of functional groups can significantly alter the overall magnitude of pi-pi interactions between the adsorbed molecules and graphene by giving rise to strong medium-range interactions involving pi-orbitals of the substituents. When the substituents can simultaneously permit the formation of hydrogen bonds between adsorbed molecules, it is possible to evaluate the relative contributions of hydrogen bonding and pi-based interactions to the overall adsorption. Adsorption of individual molecules and hydrogen-bonded aggregates reflects a hierarchical balance of the different interactions that determine the overall energy of adsorption.