First-principles study of the interaction and charge transfer between graphene and metals


Khomyakov, P.A. and Giovannetti, G. and Rusu, P.C. and Brocks, G. and Brink, J. van den and Kelly, P.J. (2009) First-principles study of the interaction and charge transfer between graphene and metals. Physical Review B: Condensed matter and materials physics, 79 (19). p. 195425. ISSN 1098-0121

[img] PDF
Restricted to UT campus only
: Request a copy
Abstract:Measuring the transport of electrons through a graphene sheet necessarily involves contacting it with metal electrodes. We study the adsorption of graphene on metal substrates using first-principles calculations at the level of density-functional theory. The bonding of graphene to Al, Ag, Cu, Au, and Pt (111) surfaces is so weak that its unique “ultrarelativistic” electronic structure is preserved. The interaction does, however, lead to a charge transfer that shifts the Fermi level by up to 0.5 eV with respect to the conical points. The crossover from p-type to n-type doping occurs for a metal with a work function ~5.4 eV, a value much larger than the work function of free-standing graphene, 4.5 eV. We develop a simple analytical model that describes the Fermi-level shift in graphene in terms of the metal substrate work function. Graphene interacts with and binds more strongly to Co, Ni, Pd, and Ti. This chemisorption involves hybridization between graphene pz states and metal d states that opens a band gap in graphene, and reduces its work function considerably. The supported graphene is effectively n-type doped because in a current-in-plane device geometry the work-function lowering will lead to electrons being transferred to the unsupported part of the graphene sheet.
Item Type:Article
Copyright:© 2009 American Physical Society
Science and Technology (TNW)
Research Group:
Link to this item:
Official URL:
Export this item as:BibTeX
HTML Citation
Reference Manager


Repository Staff Only: item control page

Metis ID: 257191