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Gap Opening in Double-Sided Highly Hydrogenated Free-Standing Graphene

Articolo
Data di Pubblicazione:
2022
Citazione:
Gap Opening in Double-Sided Highly Hydrogenated Free-Standing Graphene / Betti, M. G.; Placidi, E.; Izzo, C.; Blundo, E.; Polimeni, A.; Sbroscia, M.; Avila, J.; Dudin, P.; Hu, K.; Ito, Y.; Prezzi, D.; Bonacci, M.; Molinari, E.; Mariani, C.. - In: NANO LETTERS. - ISSN 1530-6984. - 22:7(2022), pp. 2971-2977. [10.1021/acs.nanolett.2c00162]
Abstract:
Conversion of free-standing graphene into pure graphane-where each C atom is sp3bound to a hydrogen atom-has not been achieved so far, in spite of numerous experimental attempts. Here, we obtain an unprecedented level of hydrogenation (≈90% of sp3bonds) by exposing fully free-standing nanoporous samples-constituted by a single to a few veils of smoothly rippled graphene-to atomic hydrogen in ultrahigh vacuum. Such a controlled hydrogenation of high-quality and high-specific-area samples converts the original conductive graphene into a wide gap semiconductor, with the valence band maximum (VBM) ∼3.5 eV below the Fermi level, as monitored by photoemission spectromicroscopy and confirmed by theoretical predictions. In fact, the calculated band structure unequivocally identifies the achievement of a stable, double-sided fully hydrogenated configuration, with gap opening and no trace of πstates, in excellent agreement with the experimental results.
Tipologia CRIS:
Articolo su rivista
Keywords:
density functional theory; graphane; GW calculations; hydrogen functionalization; nanoporous graphene; spectromicroscopy
Elenco autori:
Betti, M. G.; Placidi, E.; Izzo, C.; Blundo, E.; Polimeni, A.; Sbroscia, M.; Avila, J.; Dudin, P.; Hu, K.; Ito, Y.; Prezzi, D.; Bonacci, M.; Molinari, E.; Mariani, C.
Autori di Ateneo:
BONACCI MIKI
MOLINARI Elisa
Link alla scheda completa:
https://iris.unimore.it/handle/11380/1279883
Link al Full Text:
https://iris.unimore.it//retrieve/handle/11380/1279883/425564/acs.nanolett.2c00162.pdf
Pubblicato in:
NANO LETTERS
Journal
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