Changes in electronic structure of graphene by adsorption of low melamine coverages

•Properties of melamine adsorption on graphene at low coverage were analyzed.•The charge separation due to melamine adsorption generates an interfacial dipole.•The origin of melamine preference per the defective sites was explained. Using first-principles simulations at Density Functional Theory (DF...

Full description

Saved in:
Bibliographic Details
Published inSurface science Vol. 723; p. 122120
Main Authors Pantano, Fernando R., Leiva, Ezequiel P.M., Rojas, Mariana I.
Format Journal Article
LanguageEnglish
Published Amsterdam Elsevier B.V 01.09.2022
Elsevier BV
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:•Properties of melamine adsorption on graphene at low coverage were analyzed.•The charge separation due to melamine adsorption generates an interfacial dipole.•The origin of melamine preference per the defective sites was explained. Using first-principles simulations at Density Functional Theory (DFT) level, we concluded a comprehensive study of the molecular doping of graphene by melamine adsorption. We characterized the different possible positions achieved by the molecule on a pristine graphene or a Stone-Wales defect (5-7-7-5) were characterized. We also analyzed adsorption energies, deformations experienced by melamine and charge separation involved in the process. The defective graphene sheet turned out to be more flexible than the pristine one, exhibiting greater deformations. Melamine adsorption on Stone-Wales defect is preferred and it can be used as a useful strategy to carry out the molecular doping of graphene. Due to adsorption, a charge separation is generated between melamine and graphene, giving rise to an organic/organic interface with a net interfacial dipole. This change in the electronic structure of graphene favors the dynamics of the excited electronic state, tuning it an interesting material used in optoelectronic devices. [Display omitted]
ISSN:0039-6028
1879-2758
DOI:10.1016/j.susc.2022.122120