Chemical Stability of (3,1)-Chiral Graphene Nanoribbons.
carbon-based nanostructures
graphene nanoribbons
oxidation
scanning probe microscopy
stability
zigzag edges
Journal
ACS nano
ISSN: 1936-086X
Titre abrégé: ACS Nano
Pays: United States
ID NLM: 101313589
Informations de publication
Date de publication:
23 Mar 2021
23 Mar 2021
Historique:
pubmed:
4
3
2021
medline:
4
3
2021
entrez:
3
3
2021
Statut:
ppublish
Résumé
Nanostructured graphene has been widely studied in recent years due to the tunability of its electronic properties and its associated interest for a variety of fields, such as nanoelectronics and spintronics. However, many of the graphene nanostructures of technological interest are synthesized under ultrahigh vacuum, and their limited stability as they are brought out of such an inert environment may compromise their applicability. In this study, a combination of bond-resolving scanning probe microscopy (BR-SPM), along with theoretical calculations, has been employed to study (3,1)-chiral graphene nanoribbons [(3,1)-chGNRs] that were synthesized on a Au(111) surface and then exposed to oxidizing environments. Exposure to the ambient atmosphere, along with the required annealing treatment to desorb a sufficiently large fraction of contaminants to allow for its postexposure analysis by BR-SPM, revealed a significant oxidation of the ribbons, with a dramatically disruptive effect on their electronic properties. More controlled experiments avoiding high temperatures and exposing the ribbons only to low pressures of pure oxygen show that also under these more gentle conditions the ribbons are oxidized. From these results, we obtain additional insights into the preferential reaction sites and the nature of the main defects that are caused by oxygen. We conclude that graphene nanoribbons with zigzag edge segments require forms of protection before they can be used in or transferred through ambient conditions.
Identifiants
pubmed: 33656868
doi: 10.1021/acsnano.1c00695
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM