MeV ion scattering from thin Si single crystals: A novel approach to interface studies

N/

Oxygen vacancies as active sites for water dissociation on rutile TiO₂(110)

Through an interplay between scanning tunneling microscopy experiments and density functional theory calculations, we determine unambiguously the active surface site responsible for the dissociation of water molecules adsorbed on rutile TiO2(110). Oxygen vacancies in the surface layer are shown to dissociate H2O through the transfer of one proton to a nearby oxygen atom, forming two hydroxyl groups for every vacancy. The amount of water dissociation is limited by the density of oxygen vacancies present on the clean surface exclusively. The dissociation process sets in as soon as molecular water is able to diffuse to the active site

Palladium Nanocrystals on Al₂O₃: Structure and Adhesion Energy

We have investigated the structure and morphology of nanosized palladium clusters supported by a thin Al2O3 film on NiAl(110) using scanning tunneling microscopy. Well-ordered clusters with a diameter above ≈40Å were imaged with atomic resolution, allowing a crystallographic identification of the cluster facets. A new method to obtain quantitative information on the work of adhesion (adhesion energy) of metal clusters deposited on oxides is introduced. For Pd on Al2O3 we obtain a value of Wadh=2.8±0.2J/m2. This result is at variance with values recently derived on the basis of ab initio density-functional theory

Theory of adsorbate induced surface reconstruction on W(100)

We report results of a theoretical study on an adsorbate induced surface reconstruction. Hydrogen adsorption on a W(100) surface causes a switching transition in the symmetry of the displacements of the W atoms within the ordered c(2x2) phase. This transition is modeled by an effective Hamiltonian, where the hydrogen degrees of freedom are integrated out. Based on extensive Monte Carlo renormalisation group calculations we show that the switching transition is of second order at high temperatures and of first order at low temperatures. This behavior is qualitatively explained in terms of an XY model where there is an interplay between four and eight fold anisotropy fields. We also compare the calculated phase diagrams with a simple mean field theory.Comment: CSC Preprint, 31 pages (plain TeX file, no figures

Adsorption configuration effects on the surface diffusion of large organic molecules: The case of Violet Lander

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Violet Lander (C108H104) is a large organic molecule that when deposited on Cu(110) surface exhibits lock-and-key like behavior [Otero et al., Nature Mater. 3, 779 (2004)]. In this work, we report a detailed fully atomistic molecular mechanics and molecular dynamics study of this phenomenon. Our results show that it has its physical basis on the interplay of the molecular hydrogens and the Cu(110) atomic spacing, which is a direct consequence of the matching between molecule and surface dimensions. This information could be used to find new molecules capable of displaying lock-and-key behavior with new potential applications in nanotechnology. (C) 2010 American Institute of Physics. [doi:10.1063/1.3512623]13322Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Fundação de Amparo à Pesquisa do Estado de Minas Gerais (FAPEMIG)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP

High-coverage structures of carbon monoxide adsorbed on Pt(111) studied by high-pressure scanning tunneling microscopy

High-pressure scanning tunneling microscopy was used to study the room-temperature adsorption of CO on a Pt(111) single-crystal surface in equilibrium with the gas phase. The coverage was found to vary continuously, and over the entire range from 10(-6)-760 Torr pressure-dependent moire patterns were observed, characteristic of a hexagonal or nearly hexagonal CO overlayer. Two different pressure ranges can be distinguished: below 10(-2) Tort, the moire lattice vector is oriented along a 30degrees high-symmetry direction of the substrate, corresponding to a pressure-dependent rotation of the CO overlayer with respect to the (1 x 1) Pt surface lattice, while above 10(-2) Torr, the CO layer angle is independent of the pressure. This behavior is analyzed in terms of the interplay of the repulsive CO-CO interaction potential and the substrate potential