Dielectric response and excitations of hydrogenated free-standing graphene

Abstract

The conversion of semimetallic suspended graphene (Gr) to a large-gap semiconducting phase is here realized by controlled adsorption of atomic hydrogen (deuterium) on free-standing nanoporous Gr veils. This approach allows to achieve a very clean and neat adsorption, overcoming any spurious influence associated to the presence of substrates. The effects of local rehybridization from sp2 to sp3 chemical bonding are investigated by combining X-ray photoelectron spectroscopy and high-resolution electron energy-loss spectroscopy (HREELS) with ab-initio based modelling. We find that the hydrogen adatoms on the C sites induce a stretching frequency, clearly identified in the vibrational spectra thanks to the use of the D isotope. Overall, the results are compatible with the predicted fingerprints of adsorption on both sides of Gr corresponding to the graphane configuration. Moreover, HREELS of the deuterated samples shows a sizeable opening of the optical band gap, i.e. 3.25 eV, consistent with the modified spectral density observed in the valence band photoemission. The results are in agreement with ab-initio calculations by GW and Bethe–Salpeter equation approaches, predicting a large quasiparticle gap opening and huge exciton binding energy.

Keywords

• Graphane
• Nanoporous graphene
• Hydrogen functionalization
• Electron energy loss spectroscopy
• Photoelectron spectroscopy
• Density functional theory