Bound by long-range interactions: Molecular crystals and benzene on Cu(111)
This thesis investigates molecular systems bound by long-range interactions. We
study molecular crystals held together by van der Waals forces and the physisorption of benzene (Bz) on Cu(111). We also study the self-organization of benzene
on the Cu(111) surface which is influenced both by the (semi) long-range van der
Waals forces, and the very-long-ranged indirect electronic interactions mediated by
a metallic surface state on the Cu(111) surface.
The van der Waals bound systems are investigated from first-principle principles
using a van der Waals density functional (vdW-DF), [Phys. Rev. Lett. 92, 246401 (2004)]. We examine the character of these interactions, by studying the asymptotic
account of the van der Waals forces, and compare full vdW-DF with an asymptotic atom-based pair potentials extracted from vdW-DF. The results show that the charac-
ter of the binding differs in the two cases, with vdW-DF being significantly enhanced at relevant binding separations. This suggests that the use of asymptotic atom-based pair potentials as an approximation for non-local correlation is not consistent. For
molecular crystals, we study the structure and cohesive energy of hexamine and the platonic hydrocarbons cubane and dodecahedrane. The calculated lattice parame-
ters and cohesion energy agree well with experiments. For adsorption of benzene on Cu(111), we obtain a binding energy in good agreement with experiment. We also
study diffusion barriers and find that the molecules can move almost freely along a honeycomb web of “corridors” passing between fcc and hcp hollow sites via bridge
To account for the surface-state mediated interactions, we use a formal Harris-functional approach to evaluate nonperturbationally the asymptotic form of this in-
direct interaction. This description is based on input from DFT calculations of the metallic surface state on Cu(111), in addition to a parameterization of the benzene-
induced scattering properties. We combine vdW-DF calculations of benzene dimers and diffusion barriers with the estimates of the surface-state mediated interactions
and find that the more compact (hexagonal) Bz-overlayer phase, with lattice constant ̊
a = 6.74 A, is due to direct Bz-Bz vdW attraction, and the stability of the sparser hexagonal Bz phase, a = 10.24 A, is due to surface-state mediated interactions. Thus, we can account well for benzene self-organization on Cu(111).
These results illustrate the current state of development of quantum-physical based approaches to systems bound by long-range interactions.
van der Waals density functional (vdW-DF)
van der Waals forces