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

  • Maria Grazia Betti*
  • , Ernesto Placidi
  • , Chiara Izzo
  • , Elena Blundo
  • , Antonio Polimeni
  • , Marco Sbroscia
  • , José Avila
  • , Pavel Dudin
  • , Kailong Hu
  • , Yoshikazu Ito
  • , Deborah Prezzi*
  • , Miki Bonacci
  • , Elisa Molinari
  • , Carlo Mariani
  • *Corresponding author for this work
  • University of Rome La Sapienza
  • Université Paris-Saclay
  • Harbin Institute of Technology
  • University of Tsukuba
  • National Research Council of Italy
  • University of Modena and Reggio Emilia

Research output: Contribution to journalArticlepeer-review

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.

Original languageEnglish
Pages (from-to)2971-2977
Number of pages7
JournalNano Letters
Volume22
Issue number7
DOIs
StatePublished - 13 Apr 2022
Externally publishedYes

Keywords

  • GW calculations
  • density functional theory
  • graphane
  • hydrogen functionalization
  • nanoporous graphene
  • spectromicroscopy

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