Role of silicon dangling bonds in the electronic properties of epitaxial graphene on silicon carbide.

In this paper, we study the electronic properties of epitaxial graphene (EG) on silicon carbide by means of ab initio calculations based on the local spin density approximation + U method taking into account the Coulomb interaction between Si localized electrons. We show that this interaction is not completely suppressed but is screened by carbon layers grown on-top of silicon carbide. This finding leads to a good qualitative understanding of the experimental results reported on EG on silicon carbide. Our results highlight the presence of the Si localized states and might explain the anomalous Hanle curve and the high values of spin relaxation time in EG.

Vacancy formation on C60/Pt (111): unraveling the complex atomistic mechanism.

The interaction of fullerenes with transition metal surfaces leads to the development of an atomic network of ordered vacancies on the metal. However, the structure and formation mechanism of this intricate surface reconstruction is not yet understood at an atomic level. We combine scanning tunneling microscopy, high resolution and temperature programmed-x-ray photoelectrons spectroscopy, and density functional theory calculations to show that the vacancy formation in C60/Pt(111) is a complex process in which fullerenes undergo two significant structural rearrangements upon thermal annealing. At first, the molecules are physisorbed on the surface; next, they chemisorb inducing the formation of an adatom-vacancy pair on the side of the fullerene. Finally, this metastable state relaxes when the adatom migrates away and the vacancy moves under the molecule. The evolution from a weakly-bound fullerene to a chemisorbed state with a vacancy underneath could be triggered by residual H atoms on the surface which prevent a strong surface-adsorbate bonding right after deposition. Upon annealing at about 440 K, when all H has desorbed, the C60 interacts with the Pt surface atoms forming the vacancy-adatom pair. This metastable state induces a small charge transfer and precedes the final adsorption structure.

Atomic force microscopy nanomanipulation of shape persistent, spherical, self-assembled aggregates of gold nanoparticles.

Gold (Au) nanoparticles have been synthesized that are stabilized by an organic ligand bearing a dithiolane functional group for binding to Au, an oligo(p-phenylene vinylene) (OPV) chromophoric group to drive self-assembly via π-π interactions, and a hydroxy functionality for interparticle hydrogen bonding. The OPV-Au particles reversibly self-assemble in n-heptane solution, forming shape persistent, spherical, nanometer-sized aggregates that do not collapse on a substrate. Optical absorption and transmission electron microscopy tomography studies show that the size and shape persistency can be tuned by modification of the ligands, adjustment of the core size, and variation of the concentration. The spherical assemblies can be manipulated with the tip of an atomic force microscope: an aggregate can be pushed over the surface for at least 20 times with nanometer precision and without substantial loss of material.