“…This shortcoming of the empirical method is expected, because using the bulk dielectric function Pt in the local limit is not sufficient to describe the dispersive response of the Pt surface, as can be seen in Figure 4 below. It should be emphasized that the present measurements, as well as other similar measurements of the π plasmon in graphene supported by metallic Pt(111) and Ni(111) surfaces [8,39], systematically find that the π plasmon energy in the optical limit, Q ≈ 0, is more than 1 eV higher than the energy of the π plasmon in unsupported graphene, as predicted by ab initio calculations [34,57]. The reason for this discrepancy may be attributed to the random-phase approximation (RPA), used in these ab initio calculations, which does not include quasi-particle corrections of graphene's π and π * bands and excitonic effects (interaction between excited π * -electron and π-hole).…”