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Content from this work may be used under the terms of the Creative Commons Attribution 3.0 licence., An acoustic plasmon is predicted to occur, in addition to the conventional two-dimensional (2D) plasmon, as the collective motion of a system of two types of electronic carriers coexisting in the same 2D band of extrinsic (doped or gated) graphene. The origin of this novel mode stems from the anisotropy present in the graphene band structure near the Dirac points K and K'. This anisotropy allows for the coexistence of carriers moving with two distinct Fermi velocities along the γK and γK' directions, which leads to two modes of collective oscillation: one mode in which the two types of carriers oscillate in phase with one another (this is the conventional 2D graphene plasmon, which at long wavelengths (q → 0) has the same dispersion, q1/2, as the conventional 2D plasmon of a 2D free electron gas), and the other mode found here corresponds to a low-frequency acoustic oscillation (whose energy exhibits at long-wavelengths a linear dependence on the 2D wavenumber q) in which the two types of carriers oscillate out of phase. This prediction represents a realization of acoustic plasmons originated in the collective motion of a system of two types of carriers coexisting within the same band. © 2014 IOP Publishing Ltd and Deutsche Physikalische Gesellschaft., MP acknowledges the financial support of MIUR (FIRB-Futuro in Ricerca 2010—Project PLASMOGRAPH grant no. RBFR10M5BT), the European Commission, the European Social Fund and Regione Calabria, (POR) Calabria—FSE 2007/2013. VMS acknowledges financial support from the Spanish MICINN (no. FIS2010-19609-C02-01), the Departamento de Educación del Gobierno Vasco, and the University of the Basque Country (no. GIC07-IT-366-07).

Deposition of Co atoms on Au(111) surfaces leads to the formation of self-organized bilayer Co nanowires at the step edges between adjacent narrow Au(111) terraces. Scanning tunneling microscopy and spectroscopy at low temperatures is used to probe the influence of the finite dimensions on the local density of states for both the Co wires and the narrow Au terraces. Confinement of Au surface state electrons to narrow Au terraces causes a shift of the Au surface state onset energy to higher energies. For the Co nanowires discrete energy levels are observed. Moreover, standing wave patterns occur at the surface of both the Au and the Co. The patterns increase in complexity with increasing energy. All Co nanowires formed at the edges of narrow Au terraces reveal a characteristic maximum in the local density of states at a significantly different energy when compared to the Co islands that are formed on large Au terraces. The experimental results can be interpreted in terms of a simple particle-in-a-box model. http://iopscience.iop.org/0953-8984/22/25/255504/pdf/0953-8984_22_25_255504.pdf ispartof: Journal of physics-condensed matter vol:22 issue:25 pages:1-6 ispartof: location:England status: published

The electronic structure of highly under-coordinated Rh atoms, namely adatoms and ad-dimers, on homo- metallic surfaces has been probed by combining high-energy resolution core level photoelectron spectroscopy and density functional theory calculations. The Rh3d(5/2) core level shifts are shown to be proportional to the number of Rh nearest-neighbours ( n = 3, 4 and 5). A more refined analysis shows that the energy position of the different core level components is correlated with the calculated changes of the individual inter-atomic bond length and to the energy changes of the d-band centre, which is known to be a reliable descriptor of local chemical reactivity.