Suchergebnisse

The deposition of submonolayer amounts of Au onto Cu(111) results in a Au-Cu surface alloy with temperature- and thickness-dependent stoichiometry. Upon alloying, the characteristic Shockley state of Cu(111) is modified, shifting to 0.53 eV binding energy for a particular surface Au2Cu concentration, which is a very high binding energy for a noble-metal surface. Based on a phase accumulation model analysis, we discuss how this unusually large shift is likely reflecting an effective increase in the topmost layer thickness of the order of, but smaller than, the value expected from the moiré undulation. © 2012 American Physical Society. ; This work was supported in part by the Spanish MINECO (Grants No. MAT2010-21156-C03-01 and No. MAT2010-21156-C03-03), and the Basque Government (Grant No. IT-257-07). The SRC is funded by the National Science Foundation (Award No. DMR-0084402). ; Peer Reviewed

5 páginas, 4 figuras.-- PACS numbers: 73.20.At, 73.22.-f, 79.60.Jv ; The two-dimensional, free-electron-like band structure of noble metal surfaces can be radically transformed by appropriate nanostructuration. A case example is the triangular dislocation network that characterizes the epitaxial Ag/Cu(111) system, which exhibits a highly featured band topology with a full band gap above EF and a hole-pocket-like Fermi surface. Here we show that controlled doping of the Ag/Cu(111) interface with Au allows one to observe a complete Lifshitz transition at 300 K; i.e., the hole pockets fill up, the band gap entirely shifts across EF, and the Fermi surface becomes electron-pocket-like. ; This work was supported by the Spanish MICINN (MAT2010-21156-C03-01 and -C03-03) and the Basque Government (IT-257-07). ; Peer reviewed

7 páginas, 5 figuras, 3 tablas.-- El pdf del artículo es la versión pre-print. ; A novel approach of identifying metal atoms within a metal–organic surface coordination network using scanning tunnelling microscopy (STM) is presented. The Cu adatoms coordinated in the porous surface network of 1,3,8,10-tetraazaperopyrene (TAPP) molecules on a Cu(111) surface give rise to a characteristic electronic resonance in STM experiments. Using density functional theory calculations, we provide strong evidence that this resonance is a fingerprint of the interaction between the molecules and the Cu adatoms. We also show that the bonding of the Cu adatoms to the organic exodentate ligands is characterised by both the mixing of the nitrogen lone-pair orbitals of TAPP with states on the Cu adatoms and the partial filling of the lowest unoccupied molecular orbital (LUMO) of the TAPP molecule. Furthermore, the key interactions determining the surface unit cell of the network are discussed. ; This work was financially supported by the European Union through the Marie Curie Research Training Network PRAIRIES (MRTN-CT-2006-035810). Support from the Swiss National Science Foundation, the National Center of Competence in Research (NCCR) ''Nanoscale Science'' and the Wolfermann Naegeli Stiftung is also acknowledged. MP is also grateful for support from the Swedish Research Council (VR). ; Peer reviewed

Under the terms of the Creative Commons Attribution License 3.0 (CC-BY).-- et al. ; We present a comprehensive study of the magnetism and morphology of an ultrahigh density array of Co nanoclusters self-assembled on the single atomic layer GdAu2 on Au(111) template surface. Combining scanning tunneling microscopy, x-ray magnetic circular dichroism, and magneto-optical Kerr effect measurements, we reveal a significant enhancement of the perpendicular magnetic anisotropy energy for noncoalesced single atomic layer nanoclusters compared to Co/Au(111). For coverages well beyond the onset of coalescence, we observe room-temperature in-plane magnetic remanence. ; We acknowledge funding from the Swiss National Science Foundation, from the Sino-Swiss Science and Technology Cooperation Project No. IZLCZ2 123892, from the Spanish Ministerio de Ciencia e Innovacion (MAT2010-21156-C03-03), from the Gipuzkoako Foru Aldundia, from the European Social Fund within the program JAE-Doc, the Basque Government (IT-621-13 and IT-627-13) and SAIOTEK (S-PE12UN095), as well as from the EU Calipso program for synchrotron access funding. The MBE chamber on DEIMOS was funded by the Agence National de la Recherche with Grant No. ANR-05-NANO-073. ; Peer Reviewed

Under the terms of the Creative Commons Attribution License 3.0 (CC-BY).-- et al. ; Codeposition of two molecular species [copper phtalocyanine (CuPc, donor) and perfluoropentacene (PFP, acceptor)] on noble metal (111) surfaces leads to the self-assembly of an ordered mixed layer with a maximized donor-acceptor contact area. The main driving force behind this arrangement is assumed to be the intermolecular C-Hâ̄F hydrogen-bond interactions. Such interactions would be maximized for a coplanar molecular arrangement. However, precise measurement of molecule-substrate distances in the molecular mixture reveals significantly larger adsorption heights for PFP than for CuPc. Most surprisingly, instead of leveling to increase hydrogen-bond interactions, the height difference is enhanced in the blends as compared to the heights found in single-component CuPc and PFP layers. The increased height of PFP in mixed layers points to an overall reduced interaction with the underlying substrate, and its influence on electronic properties like the interface dipole is investigated through work function measurements. © 2014 American Physical Society. ; This work was supported by the Spanish Grants No. MAT2010-21156-C03-01 and-C03-03, as well as No. PIB2010US-00652, and by the Basque Government (Grant No. IT-621-13). D. G. O. acknowledges support from the European Union under Grant No. FP7-PEOPLE-2010-IOF-271909. We acknowledge funding from the European Community's Seventh Framework Programme (FP7/2007-2013) under Grant No. 226716. ; Peer Reviewed

We investigate the scattering of electrons belonging to Shockley states of (111)-oriented noble metal surfaces using angle-resolved photoemission (ARPES) and scanning tunneling microscopy (STM). Both ARPES and STM indicate that monatomic steps on a noble metal surface may act either as strongly repulsive or highly transmissive barriers for surface electrons, depending on the coherence of the step lattice, and irrespectively of the average step spacing. By measuring curved crystal surfaces with terrace length ranging from 30 to 180 Å, we show that vicinal surfaces of Au and Ag with periodic step arrays exhibit a remarkable wave function coherence beyond 100 Å step spacings, well beyond the Fermi wavelength limit and independently of the projection of the bulk band gap on the vicinal plane. In contrast, the analysis of transmission resonances investigated by STM shows that a pair of isolated parallel steps defining a 58 Å wide terrace confines and decouples the surface state of the small terrace from that of the (111) surface. We conclude that the formation of laterally confined quantum well states in vicinal surfaces as opposed to propagating superlattice states depends on the loss of coherence driven by imperfection in the superlattice order. © 2013 American Physical Society. ; This work was supported in part by the Spanish MICINN (MAT2007-63083 and MAT2010-15659), the Basque Government (IT-257-07), and the Agència de Gestió d'Ajuts Universitaris i de Recerca (2009 SGR 695). The SRC is funded by the National Science Foundation (Award No. DMR-0084402). A.M. and J.L.-C. acknowledge funding from the Ramon y Cajal Fellowship program. ; Peer Reviewed