Theoretical study of graphene doping mechanism by iodine molecules

Damien Tristant (1) , Pascal Puech (2) , I.C. Gerber (1)

1 LPCNO - Laboratoire de physique et chimie des nano-objets
2 CEMES - Centre d'élaboration de matériaux et d'études structurales

The adsorption of iodine atoms and molecules on graphene is studied in detail, using first-principles calculations that include nonlocal correlation effects by means of van der Waals density functional approach. Structural, energetic, and electronic structure properties of these systems are reported. We demonstrate that graphene surface can be doped by atomic and molecular iodine. An upward shift of the Dirac point from the Fermi level with values of 0.45 and 0.08 eV is observed for adsorbed atoms and adsorbed I2, respectively. It corresponds to graphene hole densities to be around 1.2 × 1013-3.9 × 1011 cm-2. We also show that the iodine molecule does not dissociate in contact with pure graphene monolayer. Calculation of the surface free energy reveals that the orientation of the adsorbed iodine molecules crucially depends on its concentration and the system temperature. The corresponding phase diagram indicates that the in-plan orientation of molecules is more stable when the iodine concentration decreases for temperatures above approximately 200 K; when beyond 500 K, iodine molecules are completely desorbed.

Mots clés: Atoms; Calculations; Electronic structure; Free energy; Graphene; Molecules; Van der Waals forces; Density-functional approach; First-principles calculation; Iodine concentration; Nonlocal correlations; Orientation of molecules; Surface free energy; System temperature; Theoretical study; Iodine

Domaines: Physique [physics]

Damien Tristant, Pascal Puech, I.C. Gerber. Theoretical study of graphene doping mechanism by iodine molecules. Journal of Physical Chemistry C, 2015, 119 (21), pp.12071-12078. ⟨10.1021/acs.jpcc.5b03246⟩. ⟨hal-01756984⟩