Tuning of the electronic properties of H-passivated armchair graphene nanoribbons by mild border oxidation: Theoretical study on periodic models

Abstract

We report the results of a DFT study of the electronic properties, intended as highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) energies, of periodic models of H-passivated armchair graphene nanoribbons (a-GNRs) as that synthetized by bottom-up technique, functionalized by vicinal dialdehydic groups. This material can be obtained by border oxidation in mild and easy to control conditions with 1 D g O 2 as we reported in our previous paper (Ghigo et al., ChemPhysChem 2015, 16, 3030). The calculations show that the two models of border oxidized a-GNRs (model A, 0.98 nm and model B, 1.35 nm wide) present LUMO and HOMO energies lowered by an extend roughly linearly dependent on the amount of oxygen chemically bound. The frontier orbital energy variations dependence on the % wt of oxygen bound are, for model A: 20.

Fundamental properties of alkali-intercalated bilayer graphene nanoribbons

“…Consequently, the largest bandgap could be found in the 3N structure. 7 Generally, GNRs have been successfully synthesized under the top-down and bottom-up schemes including the oxidation reaction, 8,9 chemical vapor deposition, [10][11][12] and unzipping carbon nanotubes. 13,14 However, roughness occurring at the ribbon edges during the synthesis process can reduce the mobility of GNRs because of the edge-scattering effects.…”