Graphenes

The role of the covalent interaction in the formation of the electronic structure of Au- and Cu-intercalated graphene on Ni(111)

A. A. Popova^a, A. M. Shikin^a, A. G. Rybkin^a, D. E. Marchenko^a, O. Yu. Vilkov^ab, A. A. Makarova^a, A. Yu. Varykhalov^c, O. Rader<sup>c

a</sup> Saint Petersburg State University
^b Technische Universität Dresden, Dresden, 01069, Germany
^c BESSY II, Helmholtz-Zentrum Berlin, Berlin, 12489, Germany

Abstract: A study is reported of the role played by covalent interaction in the coupling of graphene formed on Ni(111) to the Ni substrate and after intercalation of Au and Cu monolayers underneath the graphene. Covalent interaction of the graphene $\pi$ states with $d$ states of the underlying metal (Ni, Au, Cu) has been shown to bring about noticeable distortion of the dispersion relations of the graphene electronic $\pi$ states in the region of crossing with $d$ states, which can be described in terms of avoided-crossing effects and formation of bonding and antibonding $d$–$\pi$ states. The overall graphene coupling to a substrate is mediated by the energy and occupation of the hybridized states involved. Because graphene formed directly on the Ni(111) surface has only bonding-type occupied states, the coupling to the substrate is very strong. Interaction with intercalated Au and Cu layers makes occupation of states of the antibonding and bonding types comparable, which translates into a weak resultant overall coupling of graphene to the substrate. As a result, after intercalation of Au atoms, the electronic structure becomes similar to that of quasi-free-standing graphene, with linear dispersion of $\pi$ states at the K point of the Brillouin zone and the Dirac point localized close to the Fermi level. Intercalation of Cu atoms under the graphene monolayer results, besides generation of covalent interaction, in a slight charge transport, with a partial occupation of the previously unoccupied $\pi^*$ states and the Dirac point shifted by 0.35 eV toward increasing binding energy.

Received: 18.04.2011

 English version: Physics of the Solid State, 2011, 53:12, 2539–2544

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