The CKM quark-mixing matrix (open access)

The CKM quark-mixing matrix

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Date: April 1, 2006
Creator: Ligeti, Zoltan; Ceccucci, Augusto; Ligeti, Zoltan & Sakai, Yoshihide
System: The UNT Digital Library
THE ROLE OF DIELECTRIC CONTINUUM MODELS IN ELECTRON TRANSFER: THEORETICAL AND COMPUTATIONAL ASPECTS. (open access)

THE ROLE OF DIELECTRIC CONTINUUM MODELS IN ELECTRON TRANSFER: THEORETICAL AND COMPUTATIONAL ASPECTS.

Condensed phase physical and chemical processes generally involve interactions covering a wide range of distance scales, from short-range molecular interactions requiring orbital overlap to long-range coulombic interaction between local sites of excess charge (positive or negative monopoles). Intermediate-range distances pertain to higher-order multipolar as well as inductive and dispersion interactions. Efforts to model such condensed phase phenomena typically involve a multi-tiered strategy in which quantum mechanics is employed for full electronic structural characterization of a site of primary interest (e.g., a molecular solute or cluster), while more remote sites are treated at various classical limits (e.g., a molecular force field for discrete solvent molecules or a dielectric continuum (DC) model, if the solute is charged or has permanent multipole moments). In particular, DC models have been immensely valuable in modeling chemical reactivity and spectroscopy in media of variable polarity. Simple DC models account qualitatively for many important trends in the solvent dependence of reaction free energies, activation free energies, and optical excitation energies, and many results of semiquantitative or fully quantitative significance in comparison with experiment have been obtained, especially when detailed quantum chemical treatment of the solute is combined self consistently with DC treatment of the solvent (e.g., as …
Date: November 1, 2006
Creator: NEWTON, M.D.
System: The UNT Digital Library
SOME RECENT STUDIES IN RUGHENIUM ELECTROCHEMISTRY AND ELECTROCATALYSIS. (open access)

SOME RECENT STUDIES IN RUGHENIUM ELECTROCHEMISTRY AND ELECTROCATALYSIS.

Ruthenium is a metal of a considerable importance in electrochemical science and technology. It is a catalyst or co-catalyst material in Pt-Ru alloys for methanol- and reformate hydrogen-oxidation in fuel cells, while ruthenium oxide, a component in chlorine-evolution catalysts, represents an attractive material for electrochemical supercapacitors. Its facile surface oxidation generates an oxygen-containing species that provides active oxygen in some reactions. Ru sites in Pt-Ru catalysts increase the ''CO tolerance'' of Pt in the catalytic oxidation-reaction in direct methanol fuel cells (DMFC) and in reformate hydrogen-oxidation in proton exchange membrane fuel cells (PEMFC). The mechanism of Ru action is not completely understood, although current consensus revolves around the so-called ''bifunctional mechanism'' wherein Ru provides oxygenated species to oxidize CO that blocks Pt sites, and has an electronic effect on Pt-CO interaction. While various studies of polycrystalline Ru go back several decades those involving single crystal surfaces and the structural sensitivity of reactions on Ru surfaces emerged only recently. Using well-ordered single crystalline surfaces brings useful information as the processes on realistic catalysts are far too complex to allow identification of the microscopic reaction steps. In this article, we focus on progress in model systems and conditions, such as electrochemistry and …
Date: August 1, 2006
Creator: MARINKOVIC, N.S.; VUKMIROVIC, M.B. & ADZIC, R.R.
System: The UNT Digital Library
SPIN POLARIZED PHOTOELECTRON SPECTROSCOPY AS A PROBE OF MAGNETIC SYSTEMS. (open access)

SPIN POLARIZED PHOTOELECTRON SPECTROSCOPY AS A PROBE OF MAGNETIC SYSTEMS.

Spin-polarized photoelectron spectroscopy has developed into a versatile tool for the study of surface and thin film magnetism. In this chapter, we examine the methodology of the technique and its recent application to a number of different problems. We first examine the photoemission process itself followed by a detailed review of spin-polarization measurement techniques and the related experimental requirements. We review studies of spin polarized surface states, interface states and quantum well states followed by studies of the technologically important oxide systems including half-metallic transition metal oxides, ferromagnet/oxide interfaces and the antiferromagnetic cuprates that exhibit high Tc Superconductivity. We also discuss the application of high-resolution photoemission with spin resolving capabilities to the study of spin dependent self energy effects.
Date: November 1, 2006
Creator: Johnson, P. D. & Guntherodt, G.
System: The UNT Digital Library
PHOTOEMISSION AS A PROBE OF THE COLLECTIVE EXCITATIONS IN CONDENSED MATTER SYSTEMS. (open access)

PHOTOEMISSION AS A PROBE OF THE COLLECTIVE EXCITATIONS IN CONDENSED MATTER SYSTEMS.

New developments in instrumentation have recently allowed photoemission measurements to be performed with very high energy and momentum resolution.[1] This has allowed detailed studies of the self-energy corrections to the lifetime and mass renormalization of excitations in the vicinity of the Fermi level. These developments come at an opportune time. Indeed the discovery of high temperature superconductivity in the cuprates and related systems is presenting a range of challenges for condensed matter physics.[2] Does the mechanism of high T{sub c} superconductivity represent new physics? Do we need to go beyond Landau's concept of the Fermi liquid?[3] What, if any, is the evidence for the presence or absence of quasiparticles in the excitation spectra of these complex oxides? The energy resolution of the new instruments is comparable to or better than the energy or temperature scale of superconductivity and the energy of many collective excitations. As such, photoemission has again become recognized as an important probe of condensed matter. Studies of the high T{sub c} superconductors and related materials are aided by the observation that they are two dimensional. To understand this, we note that the photoemission process results in both an excited photoelectron and a photohole in the final state. …
Date: August 1, 2006
Creator: Johnson, Peter D. & Valla, Tonica
System: The UNT Digital Library