Bulk defective graphene produced by thermal exfoliation of graphite oxide was treated under H-2 and investigated with X-ray photoemission spectroscopy, neutron spectroscopy, and solid state nuclear magnetic resonance. Graphene defects appear effective in dissociating H2 molecule and in promoting H covalent absorption on the carbon backbone. Measured generalized phonon density of states shows the presence of localized peaks ascribed to C H bending modes already in pristine graphene, whose intensities enhance when samples are treated under H2 at 1273 K. However, H-1 NMR evidences a thermally activated dynamics with a correlation time of a few microseconds assigned to a part of H atoms bound onto the graphene plane. These findings point toward a diffusive dynamics of the hydrogen chemically e, bound to graphene sheets, already active at room temperature.
Tracking the Hydrogen Motion in Defective Graphene
SANNA, SAMUELE;
2014-01-01
Abstract
Bulk defective graphene produced by thermal exfoliation of graphite oxide was treated under H-2 and investigated with X-ray photoemission spectroscopy, neutron spectroscopy, and solid state nuclear magnetic resonance. Graphene defects appear effective in dissociating H2 molecule and in promoting H covalent absorption on the carbon backbone. Measured generalized phonon density of states shows the presence of localized peaks ascribed to C H bending modes already in pristine graphene, whose intensities enhance when samples are treated under H2 at 1273 K. However, H-1 NMR evidences a thermally activated dynamics with a correlation time of a few microseconds assigned to a part of H atoms bound onto the graphene plane. These findings point toward a diffusive dynamics of the hydrogen chemically e, bound to graphene sheets, already active at room temperature.
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