Spectroscopic signatures of an ordered array of independent Ag heptamers.

A periodic network of Ag heptamers forms on the carburized W(1 1 0)-R(15 × 12) surface, upon deposition of sub-monolayer amounts of Ag. We investigate the electronic structure and dimensionality of this system by angle-resolved photoemission spectroscopy. The observation of very well-defined Ag 4d-levels confirms the highly ordered growth of size-selected Ag nano-particles on the W(1 1 0)-R(15 × 12) template. The absence of energy dispersion of these states indicates negligible coupling among the Ag heptamers, and points out the local character of the heptamer-substrate interaction. The system can be described as an array of Ag heptamers with fully confined Ag 4d-levels.

Highly anisotropic Dirac cones in epitaxial graphene modulated by an island superlattice.

We present a new method to engineer the charge carrier mobility and its directional asymmetry in epitaxial graphene by using metal cluster superlattices self-assembled onto the moiré pattern formed by graphene on Ir(111). Angle-resolved photoemission spectroscopy reveals threefold symmetry in the band structure associated with strong renormalization of the electron group velocity close to the Dirac point giving rise to highly anisotropic Dirac cones. We further find that the cluster superlattice also affects the spectral-weight distribution of the carbon bands as well as the electronic gaps between graphene states.

Excitons at the B K edge of boron nitride nanotubes probed by x-ray absorption spectroscopy.

We have performed a near-edge x-ray absorption fine-structure (NEXAFS) investigation of multi-walled boron nitride nanotubes (BNNTs). We show that the one-dimensionality of BNNTs is clearly evident in the B K edge spectrum, while the N K edge spectrum is similar to that of layered hexagonal BN (h-BN). We observe a sharp feature at the σ* onset of the B K edge, which we ascribe to a core exciton state. We also report a comparison with spectra taken after an ammonia plasma treatment, showing that the B K edge becomes indistinguishable from that of h-BN, due to the breaking of the tubular order and the formation of small h-BN clusters.

Near-edge x-ray absorption fine-structure investigation of graphene.

We report the near-edge x-ray absorption fine-structure (NEXAFS) spectrum of a single layer of graphite (graphene) obtained by micromechanical cleavage of highly ordered pyrolytic graphite on a SiO2 substrate. We utilized a photoemission electron microscope to separately study single-, double-, and few-layers graphene samples. In single-layer graphene we observe a splitting of the pi resonance and a clear signature of the predicted interlayer state. The NEXAFS data illustrate the rapid evolution of the electronic structure with the increased number of layers.