@article{Lin2015, 
author = {Yu-Pu Lin and Younal Ksari and Jean-Marc Themlin},
title = {Hydrogenation of the buffer-layer graphene on 6H-SiC (0001): A possible route for the engineering of graphene-based devices},
year = {2015},
journal = {Nano Research},
volume = {8},
number = {3},
pages = {839-850},
keywords = {graphene, hydrogenation, photoemission spectroscopy, electronic structure},
url = {https://www.sciopen.com/article/10.1007/s12274-014-0566-0},
doi = {10.1007/s12274-014-0566-0},
abstract = {The hydrogenation at various temperatures of the (6√3 × 6√3)R30° reconstruction of SiC(0001), the so-called buffer layer graphene (BLG), is investigated. For the BLG, a significant concentration of remaining dangling bonds related to unsaturated Si atoms of the outermost SiC bilayer is evidenced in the inverse photoemission spectra. These dangling bonds give rise to a peak around 1 eV above the Fermi level, associated with the upper single-electron states of a Mott-Hubbard insulator, which vanishes upon hydrogenation. Hydrogen atoms adsorbed at ambient temperature remain covalently bound to BLG (H-BLG) up to temperatures of ~500 ℃. They induce additional C-Si bonds at the BLG/SiC interface that saturate the remaining Si dangling bonds, as evidenced in both IPES and Auger electron spectra. The H-BLG further shows a large energy gap and an excess n-type doping in comparison to the pristine BLG. Upon hydrogen exposure at higher temperature (> 700 ℃), hydrogen atoms intercalate at the BLG/SiC interface, inducing the formation of a single layer of quasi-free-standing graphene (QFSG) lying on top of a hydrogenated (√3 × √3)R30° reconstruction as supported by IPES. We suggest that the high-stability and the distinct electronic structure of both BLG-derived structures, H-BLG and QFSG, may open a route for the engineering of graphene-based devices.}
}