▎ 摘　　要

We use x-ray spectroscopy and density functional theory to investigate the hydrogenation-induced electronic structure changes in graphene on Pt(111). The atom-specific properties of the spectroscopy allow for a direct projection of the band structure onto the carbon atoms; this was compared with the calculated density of states. Instead of the generally expected band opening behavior, we observe states at the Fermi level in the carbon-projected density of states. Hydrogenation is accompanied by pinning of the graphene to the substrate through the formation of local C-Pt bonds which cause the graphene layer to become metallic upon hydrogenation.