WorldWideScience

Sample records for appliquees au site

  1. Strontium and caesium transport in unsaturated soil from Chernobyl Pilot Site under steady flow conditions; Transfert de radioelements en zone non saturee. Etude experimentale et modelisation appliquees au Site Pilote de Tchernobyl

    Energy Technology Data Exchange (ETDEWEB)

    Szenknect, St

    2003-10-15

    This work is devoted to the quantification and the identification of the predominant processes involved in strontium and caesium transport in unsaturated soil from Chernobyl Pilot Site under steady flow conditions. The transport and fate of radionuclides in the subsurface is affected by various physical and chemical processes including advective and diffusive transport as well as chemical and biological transformations. Laboratory experiments and the use of a multiple tracer approach allow to isolate the contributions of each elementary process and to control the physico-chemical conditions in the system. To be more representative of the field conditions, we decided to perform column miscible displacement experiments. We perform batch and flow-through reactor experiments to characterize the radionuclides sorption mechanisms. Miscible displacement experiments within homogeneous columns and modeling allow to characterize the hydrodynamic properties of the soil and to describe the radionuclides behaviour under dynamic conditions at different water contents. We show that the water content of porous media affect the transport behaviour of inert and strongly sorbing radionuclides. Our results demonstrate that a parametrized transport model that was calibrated under completely saturated conditions was not able to describe the advective-dispersive transport of reactive solutes under unsaturated steady state conditions. Under our experimental conditions, there is no effect of a decrease of the mean water content on the sorption model parameters, but the transport parameters are modified. We established for the studied soil the relation between hydrodynamic dispersion and water content and the relation between pore water velocity and water content. (author)

  2. Site characterization and site response in Port-au-Prince, Haiti

    Science.gov (United States)

    Hough, Susan E.; Yong, Alan K.; Altidor, Jean Robert; Anglade, Dieuseul; Given, Douglas D.; Mildor, Saint-Louis

    2011-01-01

    Waveform analysis of aftershocks of the Mw7.0 Haiti earthquake of 12 January 2010 reveals amplification of ground motions at sites within the Cul de Sac valley in which Port-au-Prince is situated. Relative to ground motions recorded at a hard-rock reference site, peak acceleration values are amplified by a factor of approximately 1.8 at sites on low-lying Mio-Pliocene deposits in central Port-au-Prince and by a factor of approximately 2.5–3 on a steep foothill ridge in the southern Port-au-Prince metropolitan region. The observed amplitude, predominant periods, variability, and polarization of amplification are consistent with predicted topographic amplification by a steep, narrow ridge. A swath of unusually high damage in this region corresponds with the extent of the ridge where high weak-motion amplifications are observed. We use ASTER (Advanced Spaceborne Thermal Emission and Reflection Radiometer) imagery to map local geomorphology, including characterization of both near-surface and of small-scale topographic structures that correspond to zones of inferred amplification.

  3. Site-specific growth of Au particles on ZnO nanopyramids under ultraviolet illumination

    KAUST Repository

    Yao, Kexin

    2011-01-01

    In this work, wurtzite ZnO nanocrystals with unique "pyramid" morphology were firstly prepared via solvothermal synthesis. It was determined that the ZnO nanopyramids are grown along the polar c-axis with the vertexes pointing to the [001] direction. When the mixture of ZnO nanopyramids and Au precursor (HAuCl4) was exposed to ultraviolet (UV) illumination, Au particles were site-specifically formed on the vertexes of ZnO nanopyramids. The obtained Au/ZnO nanocomposite showed significantly enhanced photocatalytic activity as compared to the bare ZnO nanopyramids. First-principles based calculations well explained the formation of ZnO nanopyramids as well as the site-specific growth of Au, and revealed that during the photocatalysis process the Au particles can accommodate photoelectrons and thus facilitate the charge separation. © 2011 The Royal Society of Chemistry.

  4. Site-specific growth of Au particles on ZnO nanopyramids under ultraviolet illumination

    Science.gov (United States)

    Yao, Ke Xin; Liu, Xin; Zhao, Lan; Zeng, Hua Chun; Han, Yu

    2011-10-01

    In this work, wurtzite ZnO nanocrystals with unique ``pyramid'' morphology were firstly prepared via solvothermal synthesis. It was determined that the ZnO nanopyramids are grown along the polar c-axis with the vertexes pointing to the [001] direction. When the mixture of ZnO nanopyramids and Au precursor (HAuCl4) was exposed to ultraviolet (UV) illumination, Au particles were site-specifically formed on the vertexes of ZnO nanopyramids. The obtained Au/ZnO nanocomposite showed significantly enhanced photocatalytic activity as compared to the bare ZnO nanopyramids. First-principles based calculations well explained the formation of ZnO nanopyramids as well as the site-specific growth of Au, and revealed that during the photocatalysis process the Au particles can accommodate photoelectrons and thus facilitate the charge separation.In this work, wurtzite ZnO nanocrystals with unique ``pyramid'' morphology were firstly prepared via solvothermal synthesis. It was determined that the ZnO nanopyramids are grown along the polar c-axis with the vertexes pointing to the [001] direction. When the mixture of ZnO nanopyramids and Au precursor (HAuCl4) was exposed to ultraviolet (UV) illumination, Au particles were site-specifically formed on the vertexes of ZnO nanopyramids. The obtained Au/ZnO nanocomposite showed significantly enhanced photocatalytic activity as compared to the bare ZnO nanopyramids. First-principles based calculations well explained the formation of ZnO nanopyramids as well as the site-specific growth of Au, and revealed that during the photocatalysis process the Au particles can accommodate photoelectrons and thus facilitate the charge separation. Electronic supplementary information (ESI) available: TEM images of Au/ZnO nanocomposites with Au nanoparticles in different sizes, density of states of Au55 and Au20 deposited on ZnO (001) surface, and the first-principles calculation details. See DOI: 10.1039/c1nr10685f

  5. Site-specific growth of Au-Pd alloy horns on Au nanorods: A platform for highly sensitive monitoring of catalytic reactions by surface enhancement raman spectroscopy

    KAUST Repository

    Huang, Jianfeng

    2013-06-12

    Surface-enhanced Raman scattering (SERS) is a highly sensitive probe for molecular detection. The aim of this study was to develop an efficient platform for investigating the kinetics of catalytic reactions with SERS. To achieve this, we synthesized a novel Au-Pd bimetallic nanostructure (HIF-AuNR@AuPd) through site-specific epitaxial growth of Au-Pd alloy horns as catalytic sites at the ends of Au nanorods. Using high-resolution electron microscopy and tomography, we successfully reconstructed the complex three-dimensional morphology of HIF-AuNR@AuPd and identified that the horns are bound with high-index {11l} (0.25 < l < 0.43) facets. With an electron beam probe, we visualized the distribution of surface plasmon over the HIF-AuNR@AuPd nanorods, finding that strong longitudinal surface plasmon resonance concentrated at the rod ends. This unique crystal morphology led to the coupling of high catalytic activity with a strong SERS effect at the rod ends, making HIF-AuNR@AuPd an excellent bifunctional platform for in situ monitoring of surface catalytic reactions. Using the hydrogenation of 4-nitrothiophenol as a model reaction, we demonstrated that its first-order reaction kinetics could be accurately determined from this platform. Moreover, we clearly identified the superior catalytic activity of the rod ends relative to that of the rod bodies, owing to the different SERS activities at the two positions. In comparison with other reported Au-Pd bimetallic nanostructures, HIF-AuNR@AuPd offered both higher catalytic activity and greater detection sensitivity. © 2013 American Chemical Society.

  6. Construction of the Active Site of Metalloenzyme on Au NC Micelles

    Institute of Scientific and Technical Information of China (English)

    ZHANG, Zhiming; FU, Qiuan; HUANG, Xin; XU, Jiayun; LIU, Junqiu; SHEN, Jiacong

    2009-01-01

    For developing an efficient nanoenzyme system with self-assembly strategy, gold nanocrystal micelles (Au NC micelles) with inserted catalytic Zn(Ⅱ) centers were constructed by self-assembly of a catalytic ligand [N,N-bis(2-aminoethyl)-N'dodecylethylenediamine] Zn(Ⅱ) complexes (Zn(Ⅱ)L) on the surface of Au NC via hy- drophobic interaction. The functionalized Au NC micelles acted as an excellent nanoenzyme model for imitating ribonuclease. The catalytic capability of the Au NC micelles was evaluated by accelerating the cleavage of 2-hydroxypropyl p-nitrophenyl phosphate (HPNP). These functionalized Au NC micelles exhibited considerable ri- bonuclease-like activities by a factor of 4.9×104 (kcat/kuncat) for the cleavage of HPNP in comparison to the sponta- neous cleavage of HPNP at 37℃. The catalytic capability of the functionalized Au NC micelles can be considera- bly compared to other models reported previously as nanoenzymes under the comparable conditions.

  7. Effets de site : évalutation expérimentale et modélisations multidimensionnelles : application au site test EURO-SEISTEST (Grèce)

    OpenAIRE

    Riepl, Judith

    1997-01-01

    L'objectif de cette thèse est, l'étude fine des effets d'amplification suite à la géologie locale, notamment dans des bassins sédimentaires, ainsi que l'évaluation des avantages et Iimites des méthodes d'estimations. La partie expérimentale est basée sur des données acquises au site test EURO-SEISTEST, le premier site-test en Europe occidentale proche de Thessalonique (Grèce). Après une évaluation des effets d'amplification au site même et une étude de leur stabilité en fonction de plusieurs ...

  8. Active site densities, oxygen activation and adsorbed reactive oxygen in alcohol activation on npAu catalysts.

    Science.gov (United States)

    Wang, Lu-Cun; Friend, C M; Fushimi, Rebecca; Madix, Robert J

    2016-07-01

    The activation of molecular O2 as well as the reactivity of adsorbed oxygen species is of central importance in aerobic selective oxidation chemistry on Au-based catalysts. Herein, we address the issue of O2 activation on unsupported nanoporous gold (npAu) catalysts by applying a transient pressure technique, a temporal analysis of products (TAP) reactor, to measure the saturation coverage of atomic oxygen, its collisional dissociation probability, the activation barrier for O2 dissociation, and the facility with which adsorbed O species activate methanol, the initial step in the catalytic cycle of esterification. The results from these experiments indicate that molecular O2 dissociation is associated with surface silver, that the density of reactive sites is quite low, that adsorbed oxygen atoms do not spill over from the sites of activation onto the surrounding surface, and that methanol reacts quite facilely with the adsorbed oxygen atoms. In addition, the O species from O2 dissociation exhibits reactivity for the selective oxidation of methanol but not for CO. The TAP experiments also revealed that the surface of the npAu catalyst is saturated with adsorbed O under steady state reaction conditions, at least for the pulse reaction. PMID:27376884

  9. Awareness of households to the development of wind energy sites - Reporting on a survey; Receptivite des menages au developpement des sites eoliens. Rapport d'enquete

    Energy Technology Data Exchange (ETDEWEB)

    Voisard, M.

    2000-07-01

    This report for the Swiss Federal Office of Energy presents in tables and diagrams the results of a survey involving 421 households in Switzerland, about their awareness to energy issues and, in particular, to all what regards wind energy and wind power plants. Globally, 80% of the persons asked for their opinion believe that electric power demand will continue to increase. 66% of them are in favour of increased use of renewable energy sources and would consequently agree with a 10% more expensive end-user energy price. 89% of the persons taking part to the survey approve the installation of wind energy farms in Switzerland. Moreover, statistics indicates that the households living in regions already equipped with wind farms are significantly more favorable to the creation of new wind energy sites than those not living in these regions. By the end of the day, it turns out that the main reasons for accepting wind energy are environmental concerns as well as the fear of being obliged to use nuclear power. [French] Ce rapport presente par des graphiques et des tableaux le resultat d'un sondage d'opinion aupres de 421 menages en Suisse, sur la sensibilite du public aux problemes de l'energie et plus particulierement sur sa perception de tout ce qui concerne l'energie du vent et son exploitation par l'implantation d'eoliennes. Globalement, 80% des menages pensent que la demande d'energie electrique va poursuivre sa croissance. 66% d'entre eux sont favorables au developpement des energies renouvelables et prets a accepter en consequence une augmentation du prix de l'energie allant jusqu'a 10%. 89% des personnes interrogees sont favorables au developpement des eoliennes en Suisse. De plus, la statistique montre de maniere significative que les menages des regions dans lesquelles sont deja implantes des sites eoliens sont plus favorables au developpement des eoliennes que les autres. Finalement, le respect de l

  10. Catalytic activity of Au nanoparticles

    DEFF Research Database (Denmark)

    Larsen, Britt Hvolbæk; Janssens, Ton V.W.; Clausen, Bjerne;

    2007-01-01

    Au is usually viewed as an inert metal, but surprisingly it has been found that Au nanoparticles less than 3–5 nm in diameter are catalytically active for several chemical reactions. We discuss the origin of this effect, focusing on the way in which the chemical activity of Au may change with par......Au is usually viewed as an inert metal, but surprisingly it has been found that Au nanoparticles less than 3–5 nm in diameter are catalytically active for several chemical reactions. We discuss the origin of this effect, focusing on the way in which the chemical activity of Au may change...... with particle size. We find that the fraction of low-coordinated Au atoms scales approximately with the catalytic activity, suggesting that atoms on the corners and edges of Au nanoparticles are the active sites. This effect is explained using density functional calculations....

  11. Syntheses and structural analyses of variable-stoichiometric Au-Pt-Ni carbonyl/phosphine clusters, Pt3(Pt(1-x)Ni(x))(AuPPh3)2(mu2-CO)4(CO)(PPh3)3 and Pt2(Pt(2-y)Ni(y))(AuPPh3)2(mu2-CO)4(CO)2(PPh3)2, with ligation-induced site-specific Pt/Ni substitutional disorder within butterfly-based Pt3(Pt(1-x)Ni(x))Au2 and Pt2(Pt(2-y)Ni(y))Au2 core-geometries.

    Science.gov (United States)

    de Silva, Namal; Nichiporuk, Rita V; Dahl, Lawrence F

    2006-05-21

    In ongoing attempts of directed synthesis of high-nuclearity Au-Pt carbonyl/phosphine clusters with [Ni6(CO)12]2- used as reducing agent and CO source, we have isolated and characterized two new closely related variable-stoichiometric trimetallic clusters, Pt3(Pt(1-x)Ni(x))(AuPPh3)2(mu2-CO)4(CO)(PPh3)3 (1) and Pt2(Pt(2-y)Ni(y))(AuPPh3)2(mu2-CO)4(CO)2(PPh3)2 (2). Their M4Au2 cores may be envisioned as substitutional disordered butterfly-based M4Au2 frameworks (M = Pt/Ni) formed by connections of the two basal M(B) atoms with both (Au-Au)-linked Au(PPh3) moieties. Based upon low-temperature CCD X-ray diffraction studies of eight crystals obtained from different samples, ligation-induced site-specific Pt/Ni substitutional disorder (involving formal insertion of Ni in place of Pt) in a given crystal was found to occur only at the one OC-attached basal M(B) site in 1 or at both OC-attached basal M(B) sites in 2 corresponding to a crystal composite of the Pt3(Pt(1-x)Ni(x))Au2 core in 1 or of the Pt2(Pt(2-y)Ni(y))Au2 core in 2; the Ph3P-attached M(B) site (M(B) = Pt) in 1 and two wingtip M(w) sites (M(w) = Pt) in 1 and 2 were not substitutionally disordered. The resulting variable stoichiometry of the M4Au2 core in 1 may be viewed as a crystal composite of two superimposed individual stereoisomers, Pt4(AuPPh3)2(mu2-CO)4(CO)(PPh3)3 (1a) and Pt3Ni(AuPPh3)2(mu2-CO)4(CO)(PPh3)3 (1b), in the averaged unit cell of a given crystal. Likewise, 2 represents the crystal-averaged composite of three individual stereoisomers, Pt4(AuPPh3)2(mu2-CO)4(CO)2(PPh3)2 (2a), Pt3Ni(AuPPh3)2(mu2-CO)4(CO)2(PPh3)2 (2b), and Pt2Ni2(AuPPh3)2(mu2-CO)4(CO)2(PPh3)2 (2c). Formal Ni substitution for Pt at only the basal M(B) site(s) in the four crystal composites each of 1 and 2 was found to vary widely from 17% to 79% Ni in 1 and from 21% to 95% Ni in 2. Nevertheless, reasonably close Pt/Ni occupancy factors were found within each of the four pairs of composite crystals selected from samples obtained from

  12. Franco-German cooperation for the physical protection of the EPR reactor; Cooperation franco-allemande dans le domaine de la protection physique, appliquee au projet EPR

    Energy Technology Data Exchange (ETDEWEB)

    Jalouneix, J. [CEA/Fontenay aux Roses, Inst. de Protection et de Surete Nucleaire (IPSN), 92 (France); Hagemann, A. [Gesellschaft fuer Anlagen- und Reaktorsicherheit (GRS) mbH, Garching (Germany)

    2001-02-01

    This article presents the proceeding that has been followed in the EPR (European pressurized water reactor) project concerning physical protection against malevolent actions and robbery of nuclear materials. Before the different options of the nuclear island were definitely set, a task group had been constituted to examine if these options could hamper the setting of physical protection measures that are required by the legislation of the 2 countries. Another group composed of experts from IPSN/GRS (Institut de Protection et de Surete Nucleaire / Gesellschaft fur Anlagen und Reaktorsicherheit) had the task to define common requirements concerning the physical protection of reactors in Germany and in France. In this framework the EPR project team has prepared a technical document reviewing the different dispositions that have been retained to assure the physical protection of the reactor. (A.C.)

  13. Study of different ultrasonic focusing methods applied to non destructive testing; Etude de differentes methodes de focalisation ultrasonore appliquees au controle non destructif

    Energy Technology Data Exchange (ETDEWEB)

    El Amrani, M.

    1995-11-17

    The work presented in this thesis concerns the study of different ultrasonic focusing techniques applied to Nondestructive Testing (mechanical focusing and electronic focusing) and compares their capabilities. We have developed a model to predict the ultrasonic field radiated into a solid by water-coupled transducers. The model is based upon the Rayleigh integral formulation, modified to take account the refraction at the liquid-solid interface. The model has been validated by numerous experiments in various configurations. Running this model and the associated software, we have developed new methods to optimize focused transducers and studied the characteristics of the beam generated by transducers using various focusing techniques. (author). 120 refs., 95 figs., 4 appends.

  14. Launching of the site selection proceeding for new nuclear power plants in United-Kingdom; Lancement de la selection des sites pour les futurs reacteurs au Royaume Uni

    Energy Technology Data Exchange (ETDEWEB)

    Anon

    2009-01-15

    The British government has launched the proceeding for the selection of sites for the construction of new nuclear plants. Those sites have to be located in Wales and in England because of the opposition of the authorities of Scotland and Northern Ireland to the construction of nuclear power plants on their territories, moreover manufacturers favor places close to existing sites. EdF-Energy has proposed 5 sites from which 2 (Sizewell and Hinckley Point) may home 4 EPR while the 3 other sites (Heysham, Hartlepool and Dungeness) will be given to rival groups as EdF agreed to do it when it purchased British Energy. New partnerships have been signed between European energy operators wishing to take part into this program of new nuclear power plants: RWE (Germany) and EON (Germany), IBERDROLA (spain) and Scottish and Southern Energy (Great-Britain), GDF-Suez (France) and IBERDROLA. (A.C.)

  15. Enhanced activity for supported Au clusters: Methanol oxidation on Au/TiO2(110)

    Science.gov (United States)

    Tenney, Samuel A.; Cagg, Brett A.; Levine, Mara S.; He, Wei; Manandhar, Kedar; Chen, Donna A.

    2012-08-01

    Gold clusters supported on TiO2(110) exhibit unusual activity for the oxidation of methanol to formaldehyde. Temperature programmed desorption studies of methanol on Au clusters show that both Au and titania sites are necessary for methanol reaction. Isotopic labeling experiments with CD3OH demonstrate that reaction occurs via Osbnd H bond scission to form a methoxy intermediate. When the TiO2 surface is oxidized with 18O2 before or after Au deposition, methanol reaction produces H218O below 300 K, indicating that oxygen from titania promotes Osbnd H bond scission and is incorporated into desorbing products. XPS experiments provide additional evidence that during methanol reaction on the Au/TiO2 surface, methanol adsorption occurs on TiO2, given that the titania support becomes slightly oxidized after exposure to methanol in the presence of Au clusters. While the role of TiO2 is to dissociate the Osbnd H bond and form the reactive methoxy intermediate, the role of the Au sites is to remove hydrogen from the surface as H2, thus preventing the recombination of methoxy and hydrogen to methanol. The decrease in formaldehyde yield with increasing Au coverage above 0.25 ML suggests that reaction occurs at Au-titania interfacial sites; scanning tunneling microscopy images of various Au coverages confirm that the number of interfacial sites at the perimeter of the Au clusters decreases as the Au coverage is increased between 0.25 and 5 ML.

  16. Etude ergonomique des taches conchylicoles appliquee a la conception des centres de purification-expedition de coquillages

    OpenAIRE

    Loste, C; Payeur, F

    1992-01-01

    Technological modernization of existing shellfish shipping or new depuration facilities require theoretical and ergonomic analysis of plant: site, machinery and equipment, staff stations, product traffic. Layout and equipment are sized in accordance with space and volumes, productions, economics, health and safety constraints.

  17. Advanced and Integrated Petrophysical Characterization for CO2 Storage: Application to the Ketzin Site Caractérisation pétrophysique intégrée pour le stockage de CO2 : application au site de Ketzin

    Directory of Open Access Journals (Sweden)

    Fleury M.

    2013-06-01

    perméabilité. La pression d’entrée a également été évaluée. Les diagraphies RMN et de résistivité ont également été utilisées pour estimer de manière continue la saturation irréductible et juger de la représentativité des échantillons analysés au laboratoire. Pour le site de Ketzin, la zone de stockage est un grès argileux d’origine fluviatile localement très cimenté d’une porosité d’environ 30 % et d’une perméabilité variant de 100 à 300 mD. Deux zones se distinguent par des saturations irréductibles variant de 15 à 35 %. La courbe de perméabilité relative à l’eau présente une forte pente et suggère qu’une saturation inférieure à 50 % n’est pas atteignable en pratique. L’exposant de saturation de l’indice de résistivité est de 1,7, plus faible que la valeur standard de 2. La couverture a une perméabilité de 27 nD, une porosité de 15 % et une diffusivité de 0,8 x 10-9 m2/s.

  18. Le site d’Ajakagytma et le complexe culturel de Kel’teminar au sein des processus de néolithisation en Asie centrale

    OpenAIRE

    Brunet, Frédérique; Hudžanazarov, Muhiddin; Szymczak, Karol

    2014-01-01

    La recherche menée dans le cadre de la MAFANAC s’intéresse au Néolithique et plus largement à la période des processus de néolithisation qui voit à partir de la fin du Pléistocène, en Asie centrale, l’émergence de profondes et multiples modifications dans les domaines culturel, technique, économique, social et symbolique. En Ouzbékistan, l’étude réalisée en partenariat avec l’Institut d’archéologie de l’Académie des sciences de cette République (Samarcande) est focalisée sur le Néolithique de...

  19. Formation, Migration, and Reactivity of Au-CO Complexes on Gold Surfaces.

    Science.gov (United States)

    Wang, Jun; McEntee, Monica; Tang, Wenjie; Neurock, Matthew; Baddorf, Arthur P; Maksymovych, Petro; Yates, John T

    2016-02-10

    We report experimental as well as theoretical evidence that suggests Au-CO complex formation upon the exposure of CO to active sites (step edges and threading dislocations) on a Au(111) surface. Room-temperature scanning tunneling microscopy (STM), X-ray photoelectron spectroscopy, transmission infrared spectroscopy, and density functional theory calculations point to Au-CO complex formation and migration. Room-temperature STM of the Au(111) surface at CO pressures in the range from 10(-8) to 10(-4) Torr (dosage up to 10(6) langmuir) indicates Au atom extraction from dislocation sites of the herringbone reconstruction, mobile Au-CO complex formation and diffusion, and Au adatom cluster formation on both elbows and step edges on the Au surface. The formation and mobility of the Au-CO complex result from the reduced Au-Au bonding at elbows and step edges leading to stronger Au-CO bonding and to the formation of a more positively charged CO (CO(δ+)) on Au. Our studies indicate that the mobile Au-CO complex is involved in the Au nanoparticle formation and reactivity, and that the positive charge on CO increases due to the stronger adsorption of CO at Au sites with lower coordination numbers. PMID:26754257

  20. Demosite - Demonstration of the integration of photovoltaic elements in buildings; DEMOSITE. Site de demonstration d'elements de construction photovoltaiques integres au batiment

    Energy Technology Data Exchange (ETDEWEB)

    Roecker, C.; Affolter, P.; Muller, A.N.; Ould-Yenia, A.

    2003-07-01

    This final report for the Swiss Federal Office of Energy summarises Phase 4 of the DEMOSITE project and concludes 10 years of DEMOSITE activities. The DEMOSITE project, started in 1992, demonstrates various ways of integrating photovoltaic elements in buildings by providing stands, pavilions and monitoring facilities at its site in Lausanne, Switzerland. Here, at the Swiss Federal Institute of Technology, roof-mounted installations can be found as well as mock-ups of buildings and roofing systems that also serve as covered parking facilities. The DEMOSITE web site and graphical presentations are also reviewed. Furthermore, the six newest pavilions are presented in detail. The report also presents several sets of data from measurements made on the installations and discusses the dissemination of information and results obtained from the project. A comprehensive annex provides illustrations of examples of building-integrated photovoltaics from around the world.

  1. Ultra-relativistic Au+Au and d+Au collisions:

    Science.gov (United States)

    Back, B. B.; Baker, M. D.; Ballintijn, M.; Barton, D. S.; Betts, R. R.; Bickley, A. A.; Bindel, R.; Budzanowski, A.; Busza, W.; Carroll, A.; Chai, Z.; Decowski, M. P.; García, E.; Gburek, T.; George, N.; Gulbrandsen, K.; Gushue, S.; Halliwell, C.; Hamblen, J.; Hauer, M.; Heintzelman, G. A.; Henderson, C.; Hofman, D. J.; Hollis, R. S.; Hołyński, R.; Holzman, B.; Iordanova, A.; Johnson, E.; Kane, J. L.; Katzy, J.; Khan, N.; Kucewicz, W.; Kulinich, P.; Kuo, C. M.; Lin, W. T.; Manly, S.; McLeod, D.; Mignerey, A. C.; Nouicer, R.; Olszewski, A.; Pak, R.; Park, I. C.; Pernegger, H.; Reed, C.; Remsberg, L. P.; Reuter, M.; Roland, C.; Roland, G.; Rosenberg, L.; Sagerer, J.; Sarin, P.; Sawicki, P.; Seals, H.; Sedykh, I.; Skulski, W.; Smith, C. E.; Stankiewicz, M. A.; Steinberg, P.; Stephans, G. S. F.; Sukhanov, A.; Tang, J.-L.; Tonjes, M. B.; Trzupek, A.; Vale, C.; van Nieuwenhuizen, G. J.; Vaurynovich, S. S.; Verdier, R.; Veres, G. I.; Wenger, E.; Wolfs, F. L. H.; Wosiek, B.; Woźniak, K.; Wuosmaa, A. H.; Wysłouch, B.

    In this talk I will review PHOBOS data on charged particle multiplicities, obtained in Au+Au and d+Au collisions at RHIC. The general features of the Au+Au pseudorapidity distributions results will be discussed and compared to those of /line{p}p collisions. The total charged particle multiplicity, scaled by the number of participant pairs, is observed to be about 40% higher in Au+Au collisions than in /line{p}p and d+Au systems, but, surprisingly at the same level of e+e- collisions. Limiting fragmentation scaling is seen to be obeyed in Au+Au collisions.

  2. Recommandations essentielles de sécurité relatives au travail du personnel des laboratoires géologiques de chantier Essential Safety Recommendations Concerning Work by Personnel in Well Site Mud Logging Units

    Directory of Open Access Journals (Sweden)

    Chambre Syndicale du Pétrole

    2006-11-01

    Full Text Available Le personnel travaillant dans les cabines géologiques sur chantiers de forage doit respecter des règles de sécurité pour la prévention des accidents et doit connaître nécessairement les consignes à suivre en cas de danger. Ces recommandations sont relatives à l'installation des cabines géologiques et aux problèmes créés par leur équipement très diversifié, comprenant notamment de nombreux capteurs dispersés sur le chantier et leur réseau de câbles de liaison. Huit annexes rappellent les risques inhérents à la présence d'hydrogène sulfuré et les conditions d'utilisation des appareils de protection, les problèmes liés aux fours à micro-ondes éventuellement installés, ceux liés à la présence de sources radioactives. Une large part de ces recommandations est consacrée au stockage, à la manipulation et à l'élimination des produits chimiques couramment présents dans les cabines. Dix-neuf fiches de prévention simplifiées rappellent les risques que ces produits chimiques font courir au personnel et précisent les premiers soins à appliquer. Les deux dernières annexes traitent de la définition des zones classées pour les forages à terre et les forages en mer. The personnel working in mud logging units at well sites must respect safety rules for the prevention of accidents and must know the instructions to be followed in case of danger. These recommendations concern the installation of logging units and the problems created by the highly diversified equipment in such units, including in particular numerous sensors scattered around the site and the network of cables linking the sensors to the unit. Eight appendixes review the risks inherent in the presence of hydrogen sulfide and the conditions for using protective equipment, the problems linked to any microwave ovens that may be installed, and the problems linked to the presence of radioactive sources. A large portion of these recommen-dations is devoted to

  3. Decision support for the definition of wind turbine systems adequacy to site specificities and weak electrical networks; Aide a la decision pour la definition d'un systeme eolien, adequation au site et a un reseau faible

    Energy Technology Data Exchange (ETDEWEB)

    Arbaoui, A

    2006-10-15

    A decision support system for the definition of wind turbine systems is developed by taking into account the wind and site characteristics, the wind turbine components and the electrical network properties close to the site. The approach is based on functional analysis, on the investigation of the functional fluxes and on the definition of a model suitable for supporting decision at the preliminary stages of wind turbine design. The complete set of solutions derived from the model is determined using a Constraint Satisfaction Problem solver. The intrinsic capability of the model to support decision is derived from the investigation of the model parsimony, precision, exactness and specialization. The model takes into account performance criteria resulting from knowledge of manufacturers, distributors and investors. These criteria are used to discriminate design alternatives. Design alternatives correspond to choices of site (wind, electric network) and wind turbine architectures (related to 7 design variables). Performance criteria are the cost of electric kWh, the amount of energy being produced and the discounted total cost of the project. Electric network connection to wind turbines is taken into account through slow variations of the voltage and Flickers phenomenon. First, the maximal rate of penetration of the wind turbine energy production is determined. Next, two design alternatives have been investigated to improve wind turbine system integration in electric distribution networks. These alternatives are a reactive power control system and an inertial energy storage system. Inertial storage systems seem to be more expensive than reactive power control systems for this type of application. The influence of site specificities on decision making process has been established through three different sites (a Mediterranean site and two sites located in northern Europe). Profits relative to the cost of kWh appear to be high for Mediterranean sites. Most of the

  4. Au pair trajectories

    DEFF Research Database (Denmark)

    Dalgas, Karina Märcher

    2015-01-01

    Since 2000, thousands of young Filipino migrants have come to Denmark as au pairs. Officially, they are there to “broaden their cultural horizons” by living temporarily with a Danish host family, but they also conduct domestic labor in exchange for food and money, which allows them to send...... ethnographic component of the dissertation consists of four articles, all emphasizing the au pairs’ agency by viewing their migration as a dynamic personal and social experience. Arguing that Filipina au pairs tend to be understood primarily from the perspective of their precarious situation as domestic...... of their Danish host families. Based on their migratory status as au pairs, these young migrants must therefore negotiate the different moral and contractual rights and obligations that characterize the local and transnational family ties in which they are engaged. This study of Filipina au pair migration through...

  5. First principles investigation of the activity of thin film Pt, Pd and Au surface alloys for oxygen reduction

    DEFF Research Database (Denmark)

    Tripkovic, Vladimir; Hansen, Heine Anton; Rossmeisl, Jan;

    2015-01-01

    . This is particularly challenging for alloys containing Au due to a high propensity of Au to segregate to the surface. We also show that once Au is on the surface it will diffuse to defect sites, explaining why small amounts of Au retard dissolution of Pt nanoparticles. For the PtPd thin films there is no pronounced...

  6. Density Functional Study on Adsorption of NO on AuSe (010) Surface

    Institute of Scientific and Technical Information of China (English)

    XU,Xiang-Lan; CHEN,Wen-Kai; WANG,Xia; SUN,Bao-Zhen; LI,Yi; LU,Chun-Hai

    2008-01-01

    NO molecule adsorption on (010) surface of gold selenide (AuSe) has been studied with a periodic slab model by means of the GGA-PW91 exchange-correlation functional within the framework of density functional theory (DFT). Four different on-top adsorption sites Au(1), Au(2), Se(1) and Se(2) were considered for α-AuSe and three on-top adsorption sites Au(1), Au(2) and Se(1) for β-AuSe. N-end and O-end adsorptions of NO were investigated for the above sites. The results show that N-end adsorptions are preferred for α- and β-AuSe and O-end adsorptions are not feasible and thought as physisorption with the weak adsorption energies from 6.0 to 10.8 kJ/mol. For the N-end adsorptions on α-and β-AuSe (010) surfaces, Au(2) sites are most favorable with the adsorption energies 89.0 and 78.0 kJ/mol for α-and β-AuSe, respectively. However, the adsorptions at Au1 sites are very weak with the adsorption energies of 27.8 and 7.5 kJ/mol, respectively. In case of the adsorption of N-down orientations of NO at Se sites for α-and β-AuSe (010) surfaces, the adsorption activities of Se(1) and Se(2) sites on the α-AuSe (010) surface and Se(1) site on the β-AuSe (010) surface are almost the same with the adsorption energies 51.2, 52.7 and 49.2 kJ/mol. The geometric optimizations for adsorption configurations were calculated along with accounting for stretching frequency and density of states in our work.

  7. Diagnosis methodology applied to the preventive maintenance of power generation units in isolated sites; Methodologie de diagnostic appliquee a la maintenance preventive d'unites de production d'electricite en sites isoles

    Energy Technology Data Exchange (ETDEWEB)

    Marie-Joseph, M.

    2003-04-01

    Todays, overseas territories gather more than 25% of the photovoltaic systems of the French territory. More than 600 kWc of this photovoltaic park is located in French Guiana and 75% in isolated areas. This leads to the problem of implementation of a convenient maintenance policy mainly because of the problem of supply of replacement parts, of the lack of qualified local manpower, and of the complexity of a fast diagnosis of the installations. Therefore, the development of a diagnosis tool for the different kinds of failures and defects that can occur on a photovoltaic power system is of prime importance. Starting from the elements of preventive maintenance philosophy developed in the thesis of S. Salvat, this work describes the development of a functional simulation tool allowing the validation of these first results. Using models for the simulation of each sub-part of the system, involving a statistical modeling of the solar resource and of the connected load, a detailed analysis of the operation defects is presented. This tool, which is a key element of the elaboration of the diagnosis, allows the use of detection methods based on pattern recognition principle. The supervised learning makes a classification using the search for a parametric discriminating function minimizing the quadratic error on the base. The algorithms performing the real-time monitoring of the system in the presence of defects are fitted in an experimental kit representing the production of an individual generator at a reduced scale. The experimental detection procedures are then tested on production and regulation defects and then compared to those obtained from simulations performed in the same operating conditions. (J.S.)

  8. Tuning the chemical activity through PtAu nanoalloying: a first principles study

    KAUST Repository

    Mokkath, Junais Habeeb

    2013-06-21

    The electronic structure and adsorption properties of 1.5 nm sized Pt, Au, and PtAu nanoclusters are studied by density functional theory. We explain the recent experimental finding that 20% Au content in PtAu nanoparticles is optimal to induce a dramatically different catalytic behavior. Our results show that the d-band center together with the density of states at the Fermi energy can be used as an indicator of the chemical activity of PtAu nanoclusters. The most favorable adsorption sites on the cluster surfaces as a function of the Pt/Au ratio are identified using atomic H as a probe.

  9. Study of thick, nuclear-compensated silicon detectors; Etude des detecteurs epais au silicium compense nucleairement

    Energy Technology Data Exchange (ETDEWEB)

    Le Coroller, Y. [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1964-09-01

    A study is made here, from the point of view of the realization and the performance, of thick nuclear-compensated silicon detectors. After recalling the need for compensation and reviewing the existing methods, the author describes in detail the controlled realization of thick detectors by nuclear compensation from the theoretical and experimental points of view. The practical precautions which should be observed are given: control of the homogeneity of the starting material, control of the evolution of the compensation, elimination of parasitic processes. The performances of the detectors obtained are then studied: electrical characteristics (current, life-time) on the one hand, detection and spectrometry of penetrating radiations on the other hand. The results show, that the compensated diodes having an effective thickness of two millimeters operate satisfactorily as detectors for applied voltages of about 500 volts. The resolutions observed are then about 2 per cent for mono-energetic electrons and about 4 per cent for the gamma; they can be improved by the use of a pre-amplifier of very low background noise. (author) [French] Les detecteurs epais au silicium compense nucleairement sont etudies ici du double point de vue realisation et performances. Apres un rappel sur la necessite de la compensation et les procedes existants, la realisation controlee des detecteurs epais par compensation nucleaire est decrite en detail sous l'aspect theorique et l'aspect experimental. On met en evidence les precautions a prendre dans la pratique: controle de l'homogeneite du materiau de base, controle de l'evolution de la compensation, elimination des processus parasites. On etudie ensuite les performances de detecteurs obtenus : caracteristiques electriques (courant, duree de vie) d'une part, d'autre part detection et spectrometrie des rayonnements penetrants. Les resultats montrent que les diodes compensees ayant une epaisseur utile de deux

  10. Structured Pd-Au/Cu-fiber catalyst for gas-phase hydrogenolysis of dimethyl oxalate to ethylene glycol.

    Science.gov (United States)

    Zhang, Li; Han, Lupeng; Zhao, Guofeng; Chai, Ruijuan; Zhang, Qiaofei; Liu, Ye; Lu, Yong

    2015-07-01

    Galvanic co-deposition of 0.5 wt% Au and 0.1 wt% Pd on a microfibrous-structure using 8 μm Cu-fibers delivers a Pd-Au/Cu-fiber catalyst, which is highly active, selective and stable for the hydrogenolysis of dimethyl oxalate to ethylene glycol. Au and Pd synergistically promote the hydrogenolysis activity of Cu(+) sites, while Au also critically stabilizes Cu(+) sites to prevent deep reductive deactivation. PMID:26040855

  11. Magnetic susceptibilities of liquid Cr-Au, Mn-Au and Fe-Au alloys

    Energy Technology Data Exchange (ETDEWEB)

    Ohno, S.; Shimakura, H. [Niigata University of Pharmacy and Applied Life Sciences, Higashijima, Akiha-ku, Niigata 956-8603 (Japan); Tahara, S. [Faculty of Science, University of the Ryukyus, Nishihara-cho, Okinawa 903-0213 (Japan); Okada, T. [Niigata College of Technology, Kamishin’eicho, Nishi-ku, Niigata 950-2076 (Japan)

    2015-08-17

    The magnetic susceptibility of liquid Cr-Au, Mn-Au, Fe-Au and Cu-Au alloys was investigated as a function of temperature and composition. Liquid Cr{sub 1-c}Au{sub c} with 0.5 ≤ c and Mn{sub 1-c}Au{sub c} with 0.3≤c obeyed the Curie-Weiss law with regard to their dependence of χ on temperature. The magnetic susceptibilities of liquid Fe-Au alloys also exhibited Curie-Weiss behavior with a reasonable value for the effective number of Bohr magneton. On the Au-rich side, the composition dependence of χ for liquid TM-Au (TM=Cr, Mn, Fe) alloys increased rapidly with increasing TM content, respectively. Additionally, the composition dependences of χ for liquid Cr-Au, Mn-Au, and Fe-Au alloys had maxima at compositions of 50 at% Cr, 70 at% Mn, and 85 at% Fe, respectively. We compared the composition dependences of χ{sub 3d} due to 3d electrons for liquid binary TM-M (M=Au, Al, Si, Sb), and investigated the relationship between χ{sub 3d} and E{sub F} in liquid binary TM-M alloys at a composition of 50 at% TM.

  12. Atomic and electronic structures of Si(1 1 1)-(√3 x √3)R30°-Au and (6 × 6)-Au surfaces.

    Science.gov (United States)

    Patterson, C H

    2015-12-01

    Si(1 1 1)-Au surfaces with around one monolayer of Au exhibit many ordered structures and structures containing disordered domain walls. Hybrid density functional theory (DFT) calculations presented here reveal the origin of these complex structures and tendency to form domain walls. The conjugate honeycomb chain trimer (CHCT) structure of the [Formula: see text]-Au phase contains Si atoms with non-bonding surface states which can bind Au atoms in pairs in interstices of the CHCT structure and make this surface metallic. Si adatoms adsorbed on the [Formula: see text]-Au surface induce a gapped surface through interaction with the non-bonding states. Adsorption of extra Au atoms in interstitial sites of the [Formula: see text]-Au surface is stabilized by interaction with the non-bonding orbitals and leads to higher coverage ordered structures including the [Formula: see text]-Au phase. Extra Au atoms bound in interstitial sites of the [Formula: see text]-Au surface result in top layer Si atoms with an SiAu4 butterfly wing configuration. The structure of a [Formula: see text]-Au phase, whose in-plane top atomic layer positions were previously determined by an electron holography technique (Grozea et al 1998 Surf. Sci. 418 32), is calculated using total energy minimization. The Patterson function for this structure is calculated and is in good agreement with data from an in-plane x-ray diffraction study (Dornisch et al 1991 Phys. Rev. B 44 11221). Filled and empty state scanning tunneling microscopy (STM) images are calculated for domain walls and the [Formula: see text]-Au structure. The [Formula: see text]-Au phase is 2D chiral and this is evident in computed and actual STM images. [Formula: see text]-Au and domain wall structures contain the SiAu4 motif with a butterfly wing shape. Chemical bonding within the Si-Au top layers of the [Formula: see text]-Au and [Formula: see text]-Au surfaces is analyzed and an explanation for the SiAu4 motif structure is given. PMID

  13. Etre touareg au Mali

    OpenAIRE

    Edmond BERNUS

    1992-01-01

    Après une présentation générale de leur espace, de leur culture commune, des stéréotypes dont ils font l'objet, les Touaregs maliens sont décrits dans leurs diversités régionales. Les révoltes passées, celle de Firhoun, le héros de 1916, puis celle de l'Adrar des Iforas en 1963-64 contre le gouvernement de Modibo Keita, précédent la révolte qui s'étend depuis 1990 au Niger et au Mali avec des guerriers sachant manier armes et voitures. Attaques et répression sauvage se succèdent dans une spir...

  14. Introduction au droit commercial

    OpenAIRE

    Thirion, Nicolas; Delvaux, Thierry; Benoit-Moury, Anne

    2009-01-01

    Le cours d'introduction au droit commercial, destiné à des non-juristes, a pour objet de décrire, dans ses grandes lignes, le régime juridique applicable à l'organisation et au fonctionnement de l'économie. Les liens avec des disciplines autres que le droit, notamment l'économie et l'histoire, seront privilégiés, afin d'adapter la matière aux besoins et centres d'intérêts d'étudiants en sciences humaines. Après une introduction générale, le cours s'articule autour de la trilogie fondamentale ...

  15. Design and Preparation of Supported Au Catalyst with Enhanced Catalytic Activities by Rationally Positioning Au Nanoparticles on Anatase.

    Science.gov (United States)

    Wang, Liang; Wang, Hong; Rice, Andrew E; Zhang, Wei; Li, Xiaokun; Chen, Mingshu; Meng, Xiangju; Lewis, James P; Xiao, Feng-Shou

    2015-06-18

    A synergistic effect between individual components is crucial for increasing the activity of metal/metal oxide catalysts. The greatest challenge is how to control the synergistic effect to obtain enhanced catalytic performance. Through density functional theory calculations of model Au/TiO2 catalysts, it is suggested that there is strong interaction between Au nanoparticles and Ti species at the edge/corner sites of anatase, which is favorable for the formation of stable oxygen vacancies. Motivated by this theoretical analysis, we have rationally prepared Au nanoparticles attached to edge/corner sites of anatase support (Au/TiO2-EC), confirmed by their HR-TEM images. As expected, this strong interaction is well characterized by Raman, UV-visible, and XPS techniques. Very interestingly, compared with conventional Au catalysts, Au/TiO2-EC exhibits superior catalytic activity in the oxidations using O2. Our approach to controlling Au nanoparticle positioning on anatase to obtain enhanced catalytic activity offers an efficient strategy for developing more novel supported metal catalysts. PMID:26266615

  16. Antibacterial Au nanostructured surfaces

    Science.gov (United States)

    Wu, Songmei; Zuber, Flavia; Brugger, Juergen; Maniura-Weber, Katharina; Ren, Qun

    2016-01-01

    We present here a technological platform for engineering Au nanotopographies by templated electrodeposition on antibacterial surfaces. Three different types of nanostructures were fabricated: nanopillars, nanorings and nanonuggets. The nanopillars are the basic structures and are 50 nm in diameter and 100 nm in height. Particular arrangement of the nanopillars in various geometries formed nanorings and nanonuggets. Flat surfaces, rough substrate surfaces, and various nanostructured surfaces were compared for their abilities to attach and kill bacterial cells. Methicillin-resistant Staphylococcus aureus, a Gram-positive bacterial strain responsible for many infections in health care system, was used as the model bacterial strain. It was found that all the Au nanostructures, regardless their shapes, exhibited similar excellent antibacterial properties. A comparison of live cells attached to nanotopographic surfaces showed that the number of live S. aureus cells was technological platform for engineering Au nanotopographies by templated electrodeposition on antibacterial surfaces. Three different types of nanostructures were fabricated: nanopillars, nanorings and nanonuggets. The nanopillars are the basic structures and are 50 nm in diameter and 100 nm in height. Particular arrangement of the nanopillars in various geometries formed nanorings and nanonuggets. Flat surfaces, rough substrate surfaces, and various nanostructured surfaces were compared for their abilities to attach and kill bacterial cells. Methicillin-resistant Staphylococcus aureus, a Gram-positive bacterial strain responsible for many infections in health care system, was used as the model bacterial strain. It was found that all the Au nanostructures, regardless their shapes, exhibited similar excellent antibacterial properties. A comparison of live cells attached to nanotopographic surfaces showed that the number of live S. aureus cells was information (ESI) available. See DOI: 10.1039/c5nr06157a

  17. Density functional theory investigation of benzenethiol adsorption on Au(111)

    DEFF Research Database (Denmark)

    Nara, Jun; Higai, Shin’ichi; Morikawa, Yoshitada;

    2004-01-01

    We have studied the adsorption of benzenethiol molecules on the Au(111) surface by using first principles total energy calculations. A single thiolate molecule is adsorbed at the bridge site slightly shifted toward the fcc-hollow site, and is tilted by 61degrees from the surface normal. As for th...

  18. Potential energies of characteristic atoms on basis of experimental heats of formation of AuCu and AuCu_3 compounds (Ⅰ)

    Institute of Scientific and Technical Information of China (English)

    XIE You-qing; LIU Xin-bi; LI Xiao-bo; PENG Hong-jian; NIE Yao-zhuang

    2009-01-01

    The systematic science of alloys(SSA) is a framework of the total energy and total volume able to be separated. The potential energy sequences of characteristic atoms at the central sites of the basic clusters in the fcc-based lattice Au-Cu system are separated out from smaller experimental heats of formation of L10-AuCu and L1_2-AuCu_3 compounds only, by nine potential energy E-functions and through the use of structural unit inversion method. From these potential energy sequences, the potential energies and heats of formation of the disordered Au1-xCux alloys at 0 K are calculated. The potential energies, heats of formation and Tc-temperatures of order-disorder transitions of the L1_0-AuCu, L1_2-Au_3Cu and L1_2-AuCu_3 compounds, as well as the Au_3Cu-, AuCu- and AuCu_3~- type ordered alloys with maximal ordering degrees are calculated too. The results show that the 5th E-function may be chosen for developing it into the free energy-, enthalpy-, vibrational energy- and vibrational entropy-functions for describing thermodynamic properties of the compounds, ordered and disordered phases and for establishing the phase diagram of the Au-Cu system in the future.

  19. Magnetic susceptibilities of liquid Cr-Au, Mn-Au and Fe-Au alloys

    Science.gov (United States)

    Ohno, S.; Shimakura, H.; Tahara, S.; Okada, T.

    2015-08-01

    The magnetic susceptibility of liquid Cr-Au, Mn-Au, Fe-Au and Cu-Au alloys was investigated as a function of temperature and composition. Liquid Cr1-cAuc with 0.5 ≤ c and Mn1-cAuc with 0.3≤c obeyed the Curie-Weiss law with regard to their dependence of χ on temperature. The magnetic susceptibilities of liquid Fe-Au alloys also exhibited Curie-Weiss behavior with a reasonable value for the effective number of Bohr magneton. On the Au-rich side, the composition dependence of χ for liquid TM-Au (TM=Cr, Mn, Fe) alloys increased rapidly with increasing TM content, respectively. Additionally, the composition dependences of χ for liquid Cr-Au, Mn-Au, and Fe-Au alloys had maxima at compositions of 50 at% Cr, 70 at% Mn, and 85 at% Fe, respectively. We compared the composition dependences of χ3d due to 3d electrons for liquid binary TM-M (M=Au, Al, Si, Sb), and investigated the relationship between χ3d and EF in liquid binary TM-M alloys at a composition of 50 at% TM.

  20. Preparation and characterization of planar Ni–Au bimetallic model catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Yang, Fan, E-mail: fan.yang@chem.tamu.edu; Yao, Yunxi; Yan, Zhen; Min, Hlaing; Goodman, D. Wayne

    2013-10-15

    Ni–Au bimetallic model catalysts were prepared as thin films on Re(0 0 0 1) or Ru(0 0 0 1) single crystal substrates. Surface compositions and electronic structures of the Ni–Au thin films were characterized by low energy ion scattering spectroscopy and X-ray photoelectron spectroscopy, respectively. Surface alloys were prepared by annealing Ni–Au thin films from 500 to 800 K, resulting in substantial surface enrichment of Au. Annealing a Ni–Au thin film with a 1:1 bulk composition ratio at 700 K for 10 min resulted in a surface alloy with 84% (atomic concentration) of Au in the outermost surface layer. The surface atomic structure was investigated using CO as probe molecules, which exclusively adsorbs on the Ni atoms rather than on the Au atoms at room temperature. Polarization modulation infrared reflection absorption spectroscopy of CO adsorption on Ni–Au surface alloys showed that CO adsorption on two-fold bridge sites decreased and finally disappeared with an increase of Au surface concentration. The absence of Ni bridge site CO adsorption indicated that Ni atoms were isolated by Au atoms on Ni–Au alloyed surface.

  1. Gold-tin ordering in SrAu{sub 2}Sn{sub 2}

    Energy Technology Data Exchange (ETDEWEB)

    Schwickert, Christian; Gerke, Birgit; Poettgen, Rainer [Univ. Muenster (Germany). Inst. fuer Anorganische und Analytische Chemie

    2014-07-15

    Samples of the solid solutions SrAu{sub x}Sn{sub 4-x} (1.7 ≤ x ≤ 2.2) were obtained by high-frequency melting of the elements in sealed niobium ampoules. Powder and single-crystal X-ray data confirmed the CaBe{sub 2}Ge{sub 2}-type structure, space group P4/nmm. The structures of SrAu{sub 1.76}Sn{sub 2.24}, SrAu{sub 2}Sn{sub 2}, SrAu{sub 2.16}Sn{sub 1.84} (crystal A), SrAu{sub 2.16}Sn{sub 1.84} (crystal B), and SrAu{sub 2.22}Sn{sub 1.78} were refined from single-crystal diffractometer data. Only the SrAu{sub 2}Sn{sub 2} crystal shows complete Au-Sn ordering while all other crystals show substantial mixed occupancies on the four crystallographically independent sites of the polyanionic networks in which the strontium atoms fill cages of coordination number 16. Temperature-dependent susceptibility measurements have revealed diamagnetism for SrAu{sub 2}Sn{sub 2}. {sup 119}Sn Moessbauer spectroscopic data of a bulk SrAu{sub 2}Sn{sub 2} sample have resolved the tetrahedral and square-pyramidal tin sites but point to substantial Au-Sn disorder.

  2. Unique Bonding Properties of the Au36(SR)24 Nanocluster with FCC-Like Core.

    Science.gov (United States)

    Chevrier, Daniel M; Chatt, Amares; Zhang, Peng; Zeng, Chenjie; Jin, Rongchao

    2013-10-01

    The recent discovery on the total structure of Au36(SR)24, which was converted from biicosahedral Au38(SR)24, represents a surprising finding of a face-centered cubic (FCC)-like core structure in small gold-thiolate nanoclusters. Prior to this finding, the FCC feature was only expected for larger (nano)crystalline gold. Herein, we report results on the unique bonding properties of Au36(SR)24 that are associated with its FCC-like core structure. Temperature-dependent X-ray absorption spectroscopy (XAS) measurements at the Au L3-edge, in association with ab initio calculations, show that the local structure and electronic behavior of Au36(SR)24 are of more molecule-like nature, whereas its icosahedral counterparts such as Au38(SR)24 and Au25(SR)18 are more metal-like. Moreover, site-specific S K-edge XAS studies indicate that the bridging motif for Au36(SR)24 has different bonding behavior from the staple motif from Au38(SR)24. Our findings highlight the important role of "pseudo"-Au4 units within the FCC-like Au28 core in interpreting the bonding properties of Au36(SR)24 and suggest that FCC-like structure in gold thiolate nanoclusters should be treated differently from its bulk counterpart.

  3. The nuclear-cytoplasmic shuttling of virion host shutoff RNase is enabled by pUL47 and an embedded nuclear export signal and defines the sites of degradation of AU-rich and stable cellular mRNAs.

    Science.gov (United States)

    Shu, Minfeng; Taddeo, Brunella; Roizman, Bernard

    2013-12-01

    The herpes simplex virus host shutoff RNase (VHS-RNase) is the major early block of host responses to infection. VHS-RNase is introduced into cells during infection and selectively degrades stable mRNAs made before infection and the normally short-lived AU-rich stress response mRNAs induced by sensors of innate immunity. Through its interactions with pUL47, another tegument protein, it spares from degradation viral mRNAs. Analyses of embedded motifs revealed that VHS-RNase contains a nuclear export signal (NES) but not a nuclear localization signal. To reconcile the potential nuclear localization with earlier studies showing that VHS-RNase degrades mRNAs in polyribosomes, we constructed a mutant in which NES was ablated. Comparison of the mutant and wild-type VHS-RNases revealed the following. (i) On infection, VHS-RNase is transported to the nucleus, but only the wild-type protein shuttles between the nucleus and cytoplasm. (ii) Both VHS-RNases localized in the cytoplasm following transfection. On cotransfection with pUL47, a fraction of VHS-RNase was translocated to the nucleus, suggesting that pUL47 may enable nuclear localization of VHS-RNase. (iii) In infected cells, VHS-RNase lacking NES degraded the short-lived AU-rich mRNAs but not the stable mRNAs. In transfected cells, both wild-type and NES mutant VHS-RNases effectively degraded cellular mRNAs. Our results suggest that the stable mRNAs are degraded in the cytoplasm, whereas the AU-rich mRNAs may be degraded in both cellular compartments. The selective sparing of viral mRNAs may take place during the nuclear phase in the course of interaction of pUL47, VHS-RNase, and nascent viral mRNAs.

  4. Enantiospecific adsorption of cysteine on a chiral Au34 cluster

    Science.gov (United States)

    Pelayo, José de Jesús; Valencia, Israel; Díaz, Gabriela; López-Lozano, Xóchitl; Garzón, Ignacio L.

    2015-12-01

    The interaction of biological molecules like chiral amino acids with chiral metal clusters is becoming an interesting and active field of research because of its potential impact in, for example, chiral molecular recognition phenomena. In particular, the enantiospecific adsorption (EA) of cysteine (Cys) on a chiral Au55 cluster was theoretically predicted a few years ago. In this work, we present theoretical results, based on density functional theory, of the EA of non-zwitterionic cysteine interacting with the C3-Au34 chiral cluster, which has been experimentally detected in gas phase, using trapped ion electron diffraction. Our results show that, indeed, the adsorption energy of the amino acid depends on which enantiomers participate in the formation Cys-Au34 chiral complex. EA was obtained in the adsorption modes where both the thiol, and the thiol-amino functional groups of Cys are adsorbed on low-coordinated sites of the metal cluster surface. Similarly to what was obtained for the Cys-Au55 chiral complex, in the present work, it is found that the EA is originated from the different strength and location of the bond between the COOH functional group and surface Au atoms of the Au34 chiral cluster. Calculations of the vibrational spectrum for the different Cys-Au34 diastereomeric complexes predict the existence of a vibro-enantiospecific effect, indicating that the vibrational frequencies of the adsorbed amino acid depend on its handedness.

  5. Vivre, vivre au Japon

    OpenAIRE

    Tardits, Manuel

    2014-01-01

    Comment faire face au caractère récurrent des catastrophes naturelles et liées à l’homme ? À la prévention, on se doit d’adjoindre une vision écologique plus large et renouvelée. Un débat sur le modèle énergétique du nucléaire et sur nos modèles de développement urbains et sociétaux s’impose.

  6. Des femmes au tribunal

    OpenAIRE

    Le Pape, Marc

    2010-01-01

    Les archives judiciaires constituent une source essentielle pour les études des sociabilités africaines en situation coloniale. Cet article prend appui sur l’analyse des procès tenus, entre 1923 et 1939, au tribunal du premier degré d’Abidjan, il vise à décrire les argumentations contradictoires par lesquelles femmes et hommes expliquent leurs différends dans l’espace du prétoire. Les registres issus des « juridictions indigènes » permettent également d’apprécier sur quels repères se fondent ...

  7. Des ignames au riz

    OpenAIRE

    Ivanoff, Jacques

    2003-01-01

    L'igname a toujours été une nourriture importante pour les populations littorales et nomades du monde insulindien. Cependant, avec l'installation du héros civilisateur Gaman le Malais chez le peuple de la reine Sibian, le riz va devenir la composante essentielle des repas moken. En intégrant Gaman en son sein, la société moken va devoir répondre au double défi posé par la menace de la riziculture et de l'islam. En donnant femme à Gaman, en adoptant le nomadisme pour échapper à l'islam ...

  8. Introduction au titre I

    OpenAIRE

    2015-01-01

    Pline a eu dans sa carrière d’homme public à défendre les intérêts de l’Etat et des particuliers, à épurer des comptes, à juger et arbitrer. Ainsi le voulait l’ordonnancement du cursus honorum du Bas-Empire, héritier sur tous ces points de la tradition des charges publiques de la République. Les premières tâches du petiturus furent essentiellement judiciaires - on songe au vigintivirat - et elles se poursuivirent par des fonctions de moyenne importance (préture consulat) puis de haute adminis...

  9. Photoelectrochemical studies of DNA-tagged biomolecules on Au and Au/Ni/Au multilayer nanowires

    Directory of Open Access Journals (Sweden)

    Swaminathan Viswanathan

    2011-01-01

    Full Text Available Abstract The use of nanowires (NWs for labeling, sensing, and sorting is the basis of detecting biomolecules attached on NWs by optical and magnetic properties. In spite of many advantages, the use of biomolecules-attached NWs sensing by photoelectrochemical (PEC study is almost non-existent. In this article, the PEC study of dye-attached single-stranded DNA on Au NWs and Au-Ni-Au multilayer NWs prepared by pulse electrodeposition are investigated. Owing to quantum-quenching effect, the multilayer Au NWs exhibit low optical absorbance when compared with Au NWs. The tagged Au NWs show good fluorescence (emission at 570 nm, indicating significant improvement in the reflectivity. Optimum results obtained for tagged Au NWs attached on functionalized carbon electrodes and its PEC behavior is also presented. A twofold enhancement in photocurrent is observed with an average dark current of 10 μA for Au NWs coated on functionalized sensing electrode. The importance of these PEC and optical studies provides an inexpensive and facile processing platform for Au NWs that may be suitable for biolabeling applications.

  10. Structure and Mobility of Metal Clusters in MOFs: Au, Pd, and AuPd Clusters in MOF-74

    DEFF Research Database (Denmark)

    Vilhelmsen, Lasse; Walton, Krista S.; Sholl, David S.

    2012-01-01

    Understanding the adsorption and mobility of metal–organic framework (MOF)-supported metal nanoclusters is critical to the development of these catalytic materials. We present the first theoretical investigation of Au-, Pd-, and AuPd-supported clusters in a MOF, namely MOF-74. We combine density...... functional theory (DFT) calculations with a genetic algorithm (GA) to reliably predict the structure of the adsorbed clusters. This approach allows comparison of hundreds of adsorbed configurations for each cluster. From the investigation of Au8, Pd8, and Au4Pd4 we find that the organic part of the MOF...... is just as important for nanocluster adsorption as open Zn or Mg metal sites. Using the large number of clusters generated by the GA, we developed a systematic method for predicting the mobility of adsorbed clusters. Through the investigation of diffusion paths a relationship between the cluster...

  11. Le futur site Web du Centre de Documentation Tiers-Monde de Paris : concevoir un outil convivial, au sens du concept développé par Ivan Illitch dans "Tools for conviviality"

    OpenAIRE

    Cathelineau, Antoine

    2010-01-01

    Les outils de la documentation sont censés être utilisés et élaborés au service des usagers, en répondant à leurs besoins réels en information.Pourtant, le constat est souvent dressé d'outils et de systèmes d'information qui répondent mal à ces besoins : l'orientation système pourtant récusée par les sciences de l'information n'est pas encore partout vaincue par les approches orientées usagers. Les professionnels de la gestion de l'information, les premiers sans doute, ont à se poser la quest...

  12. Le marketing au concret

    OpenAIRE

    Gaglio, Gérald

    2010-01-01

    Le terme “marketing” suscite généralement la méfiance, car il est spontanément associé à l’idée de manipulation. Au-delà, que font, concrètement, les “gens du marketing” ? Afin d’apporter des pistes de réponse à cette question, nous nous penchons dans cet article sur les enjeux relatifs à un matériau censé alimenter les réflexions et décisions des marketeurs : les études qualitatives de marketing research réalisées dans le cadre de réunions de consommateurs. Cette approche nous conduit à expl...

  13. Introduction au titre II

    OpenAIRE

    2015-01-01

    159. L’objet de notre propos est de démontrer que l’Administration dispose, à la suite du juge, d’un véritable pouvoir normatif. L’admettre suppose d’en identifier les différentes manifestations qui s’expriment essentiellement par voie de circulaires administratives, de réponses ministérielles et d’avis administratifs et qui ne sauraient être assimilées au pouvoir réglementaire que l’Administration détient par ailleurs. L’ordre logique de la démonstration sera donc semblable à celui adopté po...

  14. Enhancing the reactivity of gold: Nanostructured Au(111) adsorbs CO

    Science.gov (United States)

    Hoffmann, F. M.; Hrbek, J.; Ma, S.; Park, J. B.; Rodriguez, J. A.; Stacchiola, D. J.; Senanayake, S. D.

    2016-08-01

    Low-coordinated sites are surface defects whose presence can transform a surface of inert or noble metal such as Au into an active catalyst. Starting with a well-ordered Au(111) surface we prepared by ion sputtering gold surfaces modified by pits, used microscopy (STM) for their structural characterization and CO spectroscopy (IRAS and NEXAFS) for probing reactivity of surface defects. In contrast to the Au(111) surface CO adsorbs readily on the pitted surfaces bonding to low-coordinated sites identified as step atoms forming {111} and {100} microfacets. Pitted nanostructured surfaces can serve as interesting and easily prepared models of catalytic surfaces with defined defects that offer an attractive alternative to vicinal surfaces or nanoparticles commonly employed in catalysis science.

  15. Amperometric Immunosensor for Carbofuran Detection Based on MWCNTs/GS-PEI-Au and AuNPs-Antibody Conjugate

    Directory of Open Access Journals (Sweden)

    Xiangyou Wang

    2013-04-01

    Full Text Available In this paper, an amperometric immunosensor for the detection of carbofuran was developed. Firstly, multiwall carbon nanotubes (MWCNTs and graphene sheets-ethyleneimine polymer-Au (GS-PEI-Au nanocomposites were modified onto the surface of a glass carbon electrode (GCE via self-assembly. The nanocomposites can increase the surface area of the GCE to capture a large amount of antibody, as well as produce a synergistic effect in the electrochemical performance. Then the modified electrode was coated with gold nanoparticles-antibody conjugate (AuNPs-Ab and blocked with BSA. The monoclonal antibody against carbofuran was covalently immobilized on the AuNPs with glutathione as a spacer arm. The morphologies of the GS-PEI-Au nanocomposites and the fabrication process of the immunosensor were characterized by X-ray diffraction (XRD, ultraviolet and visible absorption spectroscopy (UV-vis and scanning electron microscopy (SEM, respectively. Under optimal conditions, the immunosensor showed a wide linear range, from 0.5 to 500 ng/mL, with a detection limit of 0.03 ng/mL (S/N = 3. The as-constructed immunosensor exhibited notable performance features such as high specificity, good reproducibility, acceptable stability and regeneration performance. The results are mainly due to the excellent properties of MWCNTs, GS-PEI-Au nanocomposites and the covalent immobilization of Ab with free hapten binding sites for further immunoreaction. It provides a new avenue for amperometric immunosensor fabrication.

  16. Amperometric immunosensor for carbofuran detection based on MWCNTs/GS-PEI-Au and AuNPs-antibody conjugate.

    Science.gov (United States)

    Zhu, Ying; Cao, Yaoyao; Sun, Xia; Wang, Xiangyou

    2013-04-19

    In this paper, an amperometric immunosensor for the detection of carbofuran was developed. Firstly, multiwall carbon nanotubes (MWCNTs) and graphene sheets-ethyleneimine polymer-Au (GS-PEI-Au) nanocomposites were modified onto the surface of a glass carbon electrode (GCE) via self-assembly. The nanocomposites can increase the surface area of the GCE to capture a large amount of antibody, as well as produce a synergistic effect in the electrochemical performance. Then the modified electrode was coated with gold nanoparticles-antibody conjugate (AuNPs-Ab) and blocked with BSA. The monoclonal antibody against carbofuran was covalently immobilized on the AuNPs with glutathione as a spacer arm. The morphologies of the GS-PEI-Au nanocomposites and the fabrication process of the immunosensor were characterized by X-ray diffraction (XRD), ultraviolet and visible absorption spectroscopy (UV-vis) and scanning electron microscopy (SEM), respectively. Under optimal conditions, the immunosensor showed a wide linear range, from 0.5 to 500 ng/mL, with a detection limit of 0.03 ng/mL (S/N = 3). The as-constructed immunosensor exhibited notable performance features such as high specificity, good reproducibility, acceptable stability and regeneration performance. The results are mainly due to the excellent properties of MWCNTs, GS-PEI-Au nanocomposites and the covalent immobilization of Ab with free hapten binding sites for further immunoreaction. It provides a new avenue for amperometric immunosensor fabrication.

  17. Au/ZnO nanocomposites: Facile fabrication and enhanced photocatalytic activity for degradation of benzene

    Energy Technology Data Exchange (ETDEWEB)

    Yu, Hang; Ming, Hai; Zhang, Hengchao; Li, Haitao; Pan, Keming [Institute of Functional Nano and Soft Materials (FUNSOM) and Jiangsu Key Laboratory for Carbon-Based Functional Materials and Devices, Soochow University, Suzhou 215123 (China); Liu, Yang, E-mail: yangl@suda.edu.cn [Institute of Functional Nano and Soft Materials (FUNSOM) and Jiangsu Key Laboratory for Carbon-Based Functional Materials and Devices, Soochow University, Suzhou 215123 (China); Wang, Fang; Gong, Jingjing [Institute of Functional Nano and Soft Materials (FUNSOM) and Jiangsu Key Laboratory for Carbon-Based Functional Materials and Devices, Soochow University, Suzhou 215123 (China); Kang, Zhenhui, E-mail: zhkang@suda.edu.cn [Institute of Functional Nano and Soft Materials (FUNSOM) and Jiangsu Key Laboratory for Carbon-Based Functional Materials and Devices, Soochow University, Suzhou 215123 (China)

    2012-11-15

    Au nanoparticles supported on highly uniform one-dimensional ZnO nanowires (Au/ZnO hybrids) have been successfully fabricated through a simple wet chemical method, which were first used for photodegradation of gas-phase benzene. Compared with bare ZnO nanowires, the as-prepared Au/ZnO hybrids were found to possess higher photocatalytic activity for degradation of benzene under UV and visible light (degradation efficiencies reach about 56.0% and 33.7% after 24 h under UV and visible light irradiation, respectively). Depending on excitation happening on ZnO semiconductor or on the surface plasmon band of Au, the efficiency and operating mechanism are different. Under UV light irradiation, Au nanoparticles serve as an electron buffer and ZnO nanowires act as the reactive sites for benzene degradation. When visible light is used as the light irradiation source, Au nanoparticles act as the light harvesters and photocatalytic sites alongside of charge-transfer process, simultaneously. -- Graphical abstract: Under visible light irradiation, Au nanoparticles, which are supported on ZnO nanowires, dominate their catalytic properties in gas-phase degradation benzene reaction. Highlights: Black-Right-Pointing-Pointer The composites that Au nanoparticles supported on ZnO nanowires were synthesized. Black-Right-Pointing-Pointer Au/ZnO composites were firstly used as effective photocatalysts for benzene degradation. Black-Right-Pointing-Pointer Two operating mechanisms were proposed depending on excitation wavelength.

  18. Photoluminescence enhancement in few-layer WS2 films via Au nanoparticles

    Directory of Open Access Journals (Sweden)

    Sin Yuk Choi

    2015-06-01

    Full Text Available Nano-composites of two-dimensional atomic layered WS2 and Au nanoparticles (AuNPs have been fabricated by sulfurization of sputtered W films followed by immersing into HAuCl4 aqueous solution. The morphology, structure and AuNPs distribution have been characterized by electron microscopy. The decorated AuNPs can be more densely formed on the edge and defective sites of triangle WS2. We have compared the optical absorption and photoluminescence of bare WS2 and Au-decorated WS2 layers. Enhancement in the photoluminescence is observed in the Au-WS2 nano-composites, attributed to localized surface plasmonic effect. This work provides the possibility to develop photonic application in two-dimensional materials.

  19. Face au risque

    CERN Document Server

    Grosse, Christian; November, Valérie

    2007-01-01

    Ce volume collectif sur le risque inaugure la collection L'ÉQUINOXE. Ancré dans l'histoire pour mesurer les continuités et les ruptures, il illustre la manière dont les sciences humaines évaluent et mesurent les enjeux collectifs du risque sur les plans politiques, scientifiques, énergétiques, juridiques et éthiques. Puisse-t-il nourrir la réflexion sur la culture et la prévention du risque. Ses formes épidémiques, écologiques, sociales, terroristes et militaires nourrissent les peurs actuelles, structurent les projets sécuritaires et constituent - sans doute - les défis majeurs à notre modernité. Dans la foulée de la richesse scientifique d'Equinoxe, L'ÉQUINOXE hérite de son esprit en prenant à son tour le pari de contribuer - non sans risque - à enrichir en Suisse romande et ailleurs le champ éditorial des sciences humaines dont notre société a besoin pour forger ses repères. Après Face au risque suivra cet automne Du sens des Lumières. (MICHEL PORRET Professeur Ordinaire à la F...

  20. Thermodynamic assessment of Au-Zr system

    Institute of Scientific and Technical Information of China (English)

    李志华; 金展鹏; 刘华山

    2003-01-01

    Au-Zr binary system was reassessed by using the calculation phase diagram (CALPHAD) technique based on experimental thermodynamic data and newly reported phase diagrams. The excess Gibbs energies of the three terminal solutions and the liquid phases were formulated with Redlich-Kister polynomial. All the intermetallic phases were treated as stoichiometric compounds with the exception of ZrAu which is modeled by a two-sublattice model, (Au,Zr) : (Au, Zr). The results show that there exist seven intermetallics: Zr3Au, Zr2Au, Zr5Au4,Zr7Au10, ZrAu2 , ZrAu3, and ZrAu4 in the system. The eutectoid reaction: β(Zr) →α(Zr)+Zr3Au takes place at 1 048 K and the maximal solubility of Au in α-Zr is 4.7 % (mole fraction). The maximal solubility of Zr in Au is 6.0%(mole fraction) at 1 347 K. The homogeneity range of ZrAu phase is about 44.5%-52.9%(mole fraction) of Au. The present assessment fits experimental data very well.

  1. Enhanced electrocatalytic activity of the Au-electrodeposited Pt nanoparticles-coated conducting oxide for the quantum dot-sensitized solar cells

    Science.gov (United States)

    Yoon, Yeung-Pil; Kim, Jae-Hong; Kang, Soon-Hyung; Kim, Hyunsoo; Choi, Chel-Jong; Kim, Kyong-Kook; Ahn, Kwang-Soon

    2014-08-01

    Au was electrodeposited potentiostatically at 0.3 V for 5 min on nanoporous Pt nanoparticle-coated F-doped SnO2 (FTO/Pt) substrates. For comparison, Au-electrodeposited FTO (FTO/Au) and Au-uncoated FTO/Pt were prepared. FTO/Au showed large-sized Au clusters dispersed sparsely over FTO, which resulted in lower electrocatalytic activity than FTO/Pt. In contrast, FTO/Pt exhibited poor stability unlike FTO/Au due to poisoning by the adsorption of sulfur species. The Au-electrodeposited FTO/Pt (FTO/Pt/Au) consisted of small Au clusters deposited over the entire area of Pt due to the effective Au nucleation provided by nanoporous metallic Pt. FTO/Pt/Au exhibited enhanced electrocatalytic activity and excellent stability because the small Au particles well-dispersed over the nanoporous metallic Pt network provided numerous electrochemical reaction sites, and the Pt surface was not exposed to the electrolyte. When FTO/Pt/Au was used as the counter electrode (CE) of a quantum dot-sensitized solar cell, the significantly enhanced electrocatalytic activity of the FTO/Pt/Au CE facilitated the reduction reaction of Sn2- + 2e- (CE) → Sn-12- + S2- at the CE/electrolyte interface, resulting in a significantly hindered recombination reaction, Sn2- + 2e- (TiO2 in the photoanode) → Sn-12- + S2-, and significantly improved overall energy conversion efficiency.

  2. Organisation and Control of Nanoscale Structures on Au(111)

    DEFF Research Database (Denmark)

    Zhang, Jingdong; Chi, Qijin; Andersen, Jens Enevold Thaulov;

    2001-01-01

    We address the formation and characterisation of three different nanoscale systems on single-crystal Au(lll) electrode surfaces in aqueous electrolyte solutions. The systems are investigated particularly by single-crystal electrochernistry and in situ scanning tunnelling rnicroscopy (STM). The [mt...... constitutes a new case for the lise of in situ STM as a tool for manufacturing nanoscale pit structures on IDe Au(lll) surface at small bias voltage. Individually and in combination these data hold perspectives for preparation of atornically planar electrochernical surfaces willi controlled functionalisation......, orientation of functional biological macromolecules, nanoscale biological sensing, and controlled adsorption sites for enzymes and otter reactive molecules....

  3. 4D Joint Stratigraphic Inversion of Prestack Seismic Data: Application to the CO2 Storage Reservoir (Utsira Sand Formation at Sleipner Site Inversion stratigraphique jointe 4D de données sismiques avant sommation : application au réservoir de stockage de CO2 (Formation Utsira du site de Sleipner

    Directory of Open Access Journals (Sweden)

    Labat K.

    2012-04-01

    éservoirs au cours de leur production. Nous présentons ici une méthodologie d'inversion stratigraphique 4D qui fournit une estimation des variations d'impédances des ondes P et S dans le réservoir, par inversion de données de sismiques répétées avant-sommation. L'inversion 4D est implémentée dans le domaine temps et nécessite une loi de mise à l'échelle des temps de trajets pour chaque jeu de données de sismique répétée (aussi appelé "millésime" afin de mettre en correspondance les temps d'arrivée d'événements homologues observés sur les jeux de données appelés référence et monitors. Cette opération est souvent appelée "warping". L'inversion 4D est une méthodologie qui comporte trois étapes : la première étape consiste à inverser chaque millésime sismique séparément, pour produire autant de distributions en impédances P et S que de jeux de données considérés. La seconde étape utilise l'information des impédances P disponibles pour résoudre le problème du warping, qui est un point clé pour la troisième et dernière étape : l'inversion jointe de tous les millésimes sismiques disponibles. Cette séquence d'inversion 4D a été appliquée aux jeux de données enregistrés sur le réservoir de stockage de CO2 du site norvégien de Sleipner (Mer du Nord. Ce dernier est devenu un site industriel de référence pour le stockage à long terme du dioxyde de carbone (CO2 dans un aquifère salin, la formation des sables de l'Utsira. Nous avons focalisé notre étude sur l'inversion 4D des millésimes 1994 et 2006, acquise respectivement avant et dix ans après le début de l'injection de CO2. Le warping a fourni une loi de mise à l'échelle des temps de propagation avec un retard maximum d'environ 45 ms à la base de l'aquifère Utsira. L'inversion 4D jointe a donné des résultats plus cohérents que les inversions 3D : l'inversion 4D fournit en particulier des impédances P pour les grès saturés en CO2 qui sont très proches des

  4. STM observation of sulfur dimerization in alkanethiol self-assembled monolayers on Au{111}

    OpenAIRE

    O'Dwyer, Colm

    2005-01-01

    We present for the first time, direct microscopical observation by STM of sulfur dimer formation on alkanethiol self-assembled monolayers (SAM) on sputtered Au substrates. The sulfur dimers are observed when imaging at a bias where the tip-molecule interaction occurs, and are formed by displacement of sulfur atoms from their normal three-fold hollow site residence of the (4 × 2) superlattice to nearest-neighbor bridge-site residence between two Au atoms. The displacement is ...

  5. Hydrogen evolution on Au(111) covered with submonolayers of Pd

    DEFF Research Database (Denmark)

    Björketun, Mårten; Karlberg, Gustav; Rossmeisl, Jan;

    2011-01-01

    . The energetics of adsorption and desorption of hydrogen on/from different types of sites on the Pd-Au(111) surface are assessed by means of density functional theory calculations combined with thermodynamic modeling. Based on the density functional and Monte Carlo data, the hydrogen evolution activity......A theoretical investigation of electrochemical hydrogen evolution on Au(111) covered with submonolayers of Pd is presented. The size and shape of monoatomically high Pd islands formed on the Au(111) surface are determined using Monte Carlo simulations, for Pd coverages varying from 0.02 to 0.95 ML...... line defects for Pd island formation and hydrogen evolution are discussed. It is argued, with support from theoretical data, that this kind of defects is likely to be responsible for a dramatic increase in activity observed experimentally [ChemPhysChem 7, 985 (2006); Electrochim. Acta 52, 5548 (2007...

  6. Enantiospecific adsorption of cysteine on a chiral Au34 cluster

    Science.gov (United States)

    de Jesús Pelayo, José; Valencia, Israel; Díaz, Gabriela; López-Lozano, Xóchitl; Garzón, Ignacio L.

    2015-12-01

    The interaction of biological molecules like chiral amino acids with chiral metal clusters is becoming an interesting and active field of research because of its potential impact in, for example, chiral molecular recognition phenomena. In particular, the enantiospecific adsorption (EA) of cysteine (Cys) on a chiral Au55 cluster was theoretically predicted a few years ago. In this work, we present theoretical results, based on density functional theory, of the EA of non-zwitterionic cysteine interacting with the C3-Au34 chiral cluster, which has been experimentally detected in gas phase, using trapped ion electron diffraction. Our results show that, indeed, the adsorption energy of the amino acid depends on which enantiomers participate in the formation Cys-Au34 chiral complex. EA was obtained in the adsorption modes where both the thiol, and the thiol-amino functional groups of Cys are adsorbed on low-coordinated sites of the metal cluster surface. Similarly to what was obtained for the Cys-Au55 chiral complex, in the present work, it is found that the EA is originated from the different strength and location of the bond between the COOH functional group and surface Au atoms of the Au34 chiral cluster. Calculations of the vibrational spectrum for the different Cys-Au34 diastereomeric complexes predict the existence of a vibro-enantiospecific effect, indicating that the vibrational frequencies of the adsorbed amino acid depend on its handedness. Contribution to the Topical Issue "Atomic Cluster Collisions (7th International Symposium)", edited by G. Delgado Barrio, A. Solov'Yov, P. Villarreal, R. Prosmiti.

  7. Bienvenue au CERN !

    CERN Multimedia

    CERN Press Office. Geneva

    1998-01-01

    CERN, the Laboratory which invented the World-Wide Web has re-invented its public Web site. The new face of CERN has gone live at http://www.cern.ch/ Public . CERN's new Web pages have been designed to give visitors an informative introduction to the fascinating world of particle physics. For those whose whirl around the Web only allows a short stop, there's the 'CERN in two minutes' page.

  8. Flow in Au+Au collisions at RHIC

    Science.gov (United States)

    Belt Tonjes, Marguerite; PHOBOS Collaboration; Back, B. B.; Baker, M. D.; Ballintijn, M.; Barton, D. S.; Betts, R. R.; Bickley, A. A.; Bindel, R.; Budzanowski, A.; Busza, W.; Carroll, A.; Decowski, M. P.; García, E.; George, N.; Gulbrandsen, K.; Gushue, S.; Halliwell, C.; Hamblen, J.; Heintzelman, G. A.; Henderson, C.; Hofman, D. J.; Hollis, R. S.; Holynski, R.; Holzman, B.; Iordanova, A.; Johnson, E.; Kane, J. L.; Katzy, J.; Khan, N.; Kucewicz, W.; Kulinich, P.; Kuo, C. M.; Lin, W. T.; Manly, S.; McLeod, D.; Mignerey, A. C.; Nouicer, R.; Olszewski, A.; Pak, R.; Park, I. C.; Pernegger, H.; Reed, C.; Remsberg, L. P.; Reuter, M.; Roland, C.; Roland, G.; Rosenberg, L.; Sagerer, J.; Sarin, P.; Sawicki, P.; Skulski, W.; Steinberg, P.; Stephans, G. S. F.; Sukhanov, A.; Tang, J.-L.; Trzupek, A.; Vale, C.; van Nieuwenhuizen, G. J.; Verdier, R.; Wolfs, F. L. H.; Wosiek, B.; Wozniak, K.; Wuosmaa, A. H.; Wyslouch, B.

    2004-08-01

    The study of flow can provide information on the initial state dynamics and the degree of equilibration attained in heavy-ion collisions. This contribution presents results for both elliptic and directed flow as determined from data recorded by the PHOBOS experiment in Au+Au runs at RHIC at \\sqrt{s_{{\\rm NN}}} = 19.6, 130 and 200 GeV. The PHOBOS detector provides a unique coverage in pseudorapidity for measuring flow at RHIC. The systematic dependence of flow on pseudorapidity, transverse momentum, centrality and energy is discussed.

  9. Exotic high activity surface patterns in PtAu nanoclusters

    KAUST Repository

    Mokkath, Junais Habeeb

    2013-05-09

    The structure and chemical ordering of PtAu nanoclusters of 79, 135, and 201 atoms are studied via a combination of a basin hopping atom-exchange technique (to locate the lowest energy homotops at fixed composition), a symmetry orbit technique (to find the high symmetry isomers), and density functional theory local reoptimization (for determining the most stable homotop). The interatomic interactions between Pt and Au are derived from the empirical Gupta potential. The lowest energy structures show a marked tendency toward PtcoreAushell chemical ordering by enrichment of the more cohesive Pt in the core region and of Au in the shell region. We observe a preferential segregation of Pt atoms to (111) facets and Au atoms to (100) facets of the truncated octahedron cluster motif. Exotic surface patterns are obtained particularly for Pt-rich compositions, where Pt atoms are being surrounded by Au atoms. These surface arrangements boost the catalytic activity by creating a large number of active sites. © 2013 American Chemical Society.

  10. Bimetallic Au-decorated Pd catalyst for the liquid phase hydrodechlorination of 2,4-dichlorophenol

    Science.gov (United States)

    Zhou, Juan; Chen, Huan; Chen, Quanyuan; Huang, Zhaolu

    2016-11-01

    Monometallic and bimetallic Pd-Au catalysts supported on multi-walled carbon nanotubes (CNTs) with varied Au cooperation amounts were prepared using the complexing-reduction method in the presence of tetrahydrofuran (THF). The liquid phase catalytic hydrodechlorination (HDC) of 2,4-dichlorophenol (2,4-DCP) was investigated over these bimetallic catalysts. The catalysts were characterized by N2 adsorption-desorption isotherms, X-ray diffraction, transmission electron microscopy, X-ray photoelectron spectroscopy, and H2 chemisorption. Characterization results showed that the co-reduction of Pd and Au mainly formed alloy-like structure. The bimetallic catalysts had smaller metal particles and larger numbers of exposed active site than that of monometallic catalysts. In addition, compared with Pd(1.7)/CNTs and Au(0.4)/CNTs, the binding energies of Pd 3d5/2 shifted to higher positions while that of Au 4f7/2 had negative shifts in the Pd-Au bimetallic catalysts, which can be ascribed to the electrons transferred from metal Pd to Au and the cationization of Pd particles was enhanced. Accordingly, the bimetallic Pd-Au particles with different Au contents in the catalysts exhibited varied synergistic effects for the catalytic HDC of 2,4-DCP, with Pd(1.8)Au(0.4)/CNTs having the highest catalytic activity. For the bimetallic catalysts, a disproportional increase of turnover frequency (TOF) was observed with increasing Au content due to the enhanced cationization of Pd particles. Moreover, the dechlorination of 2,4-DCP over the supported monometallic and bimetallic catalysts proceeded via both the stepwise and concerted pathway, and the concerted pathway became predominant with Au decoration amount in the catalyst.

  11. Incendie au CERN

    CERN Multimedia

    CERN Press Office. Geneva

    1999-01-01

    At 9.15 a.m. on 26 January a fire broke out when part of a particle detector was being dismantled. This apparatus comprised 80 plates of depleted uranium which is used for its strong particle absorption power. Depleted uranium is only very slightly radioactive. The work was being done by two people from a specialist company inside a sealed tent with an entrance lock. The tent itself was located in the large North Experimental Hall on the Prévessin site.

  12. Multiscale Modeling of Au-Island Ripening on Au(100

    Directory of Open Access Journals (Sweden)

    Karin Kleiner

    2011-01-01

    Full Text Available We describe a multiscale modeling hierarchy for the particular case of Au-island ripening on Au(100. Starting at the microscopic scale, density functional theory was used to investigate a limited number of self-diffusion processes on perfect and imperfect Au(100 surfaces. The obtained structural and energetic information served as basis for optimizing a reactive forcefield (here ReaxFF, which afterwards was used to address the mesoscopic scale. Reactive force field simulations were performed to investigate more diffusion possibilities at a lower computational cost but with similar accuracy. Finally, we reached the macroscale by means of kinetic Monte Carlo (kMC simulations. The reaction rates for the reaction process database used in the kMC simulations were generated using the reactive force field. Using this strategy, we simulated nucleation, aggregation, and fluctuation processes for monoatomic high islands on Au(100 and modeled their equilibrium shape structures. Finally, by calculating the step line tension at different temperatures, we were able to make a direct comparison with available experimental data.

  13. First-principles Study on Adsorption of Au Atom on Hydroxylated SiO2 Surfaee

    Institute of Scientific and Technical Information of China (English)

    WAN Miao; HE Kaihua; CHEN QiH; HONG Hanlie

    2011-01-01

    Adsorption of single gold (Au) atom at three kinds of sites (hollow,bridge and top) on the hydroxylated β-cristobalite SiO2 (111) surface was studied using the first-principles calculations with general gradient approximation (GGA).The results of adsorption energies and density of electronic states (DOS)suggest that the hollow and bridge sites have the basically equal capability of binding Au,while the ability of the Top site is weaker.Two new energy levels emerge after the adsorption at all sites; in DOS of the Hollow configuration,one locates at -0.15 eV,composed of Au 5d and O 2p electronic states,another just crosses through the Fermi level,consisting of Au 6s,H 1s and O 2p.In addition,Mulliken population analyses indicate that electron transfer takes place between the Au atom and the surface H and O atoms in the Hollow and Bridge configurations,which can be used to interpret the adsorption of Au onto the positions.However,neither H nor O chemically bonds with Au atom.

  14. Oxygen reduction reaction activity and structural stability of Pt-Au nanoparticles prepared by arc-plasma deposition.

    Science.gov (United States)

    Takahashi, Shuntaro; Chiba, Hiroshi; Kato, Takashi; Endo, Shota; Hayashi, Takehiro; Todoroki, Naoto; Wadayama, Toshimasa

    2015-07-28

    The oxygen reduction reaction (ORR) activity and durability of various Au(x)/Pt100 nanoparticles (where x is the atomic ratio of Au against Pt) are evaluated herein. The samples were fabricated on a highly-oriented pyrolytic graphite substrate at 773 K through sequential arc-plasma depositions of Pt and Au. The electrochemical hydrogen adsorption charges (electrochemical surface area), particularly the characteristic currents caused by the corner and edge sites of the Pt nanoparticles, decrease with increasing Au atomic ratio (x). In contrast, the specific ORR activities of the Au(x)/Pt100 samples were dependent on the atomic ratios of Pt and Au: the Au28/Pt100 sample showed the highest specific activity among all the investigated samples (x = 0-42). As for ORR durability evaluated by applying potential cycles between 0.6 and 1.0 V in oxygen-saturated 0.1 M HClO4, Au28/Pt100 was the most durable sample against the electrochemical potential cycles. The results clearly showed that the Au atoms located at coordinatively-unsaturated sites, e.g. at the corners or edges of the Pt nanoparticles, can improve the ORR durability by suppressing unsaturated-site-induced degradation of the Pt nanoparticles. PMID:26118789

  15. Infrared studies of propene and propene oxide adsorption on nanoparticulate Au/TiO2

    Science.gov (United States)

    Panayotov, Dimitar; McEntee, Monica; Burrows, Steve; Driscoll, Darren; Tang, Wenjie; Neurock, Matthew; Morris, John

    2016-10-01

    Direct gas-phase epoxidation of propene to propene oxide over a heterogeneous catalyst holds the potential to revolutionize production of one of the world's major commodity chemicals. New research into fundamental aspects of propene chemistry on nanoparticulate catalysts will help guide strategies for materials development. In the current study, Fourier transform infrared (FTIR) spectroscopy and density functional theory (DFT) have been employed to explore the molecular-level details of propene and propene oxide binding at a Au/TiO2 catalyst. Competitive binding studies for propene and carbon monoxide reveal that propene readily displaces CO from: first, interfacial Au ||TiO2 sites, then low coordinated Au sites at particulate corners and edges, and finally terrace regions of the particles. DFT calculations show that the Cdbnd C bond of propene weakens upon coordination to Au, which suggests that these sites may activate the molecule for epoxidation. Like propene, propene oxide adsorbs on both Au sites and Ti sites. In addition, Ti-OH sites also readily bind the oxide. However, competitive binding experiments show that the propene oxide adsorption is favored relative to propene on all sites, which would likely passivate the catalyst at room temperature.

  16. Nanoporous Au-based chronocoulometric aptasensor for amplified detection of Pb(2+) using DNAzyme modified with Au nanoparticles.

    Science.gov (United States)

    Zhang, Chen; Lai, Cui; Zeng, Guangming; Huang, Danlian; Tang, Lin; Yang, Chunping; Zhou, Yaoyu; Qin, Lei; Cheng, Min

    2016-07-15

    The authors herein described an amplified detection strategy employing nanoporous Au (NPG) and gold nanoparticles (AuNPs) to detect Pb(2+) ions in aqueous solution. The thiol modified Pb(2+)-specific DNAzyme was self-assembled onto the surface of the NPG modified electrode for hybridizing with the AuNPs labeled oligonucleotide and for forming the DNA double helix structure. Electrochemical signal, redox charge of hexaammineruthenium(III) chloride (RuHex), was measured by chronocoulometry. Taking advantage of amplification effects of the NPG electrode for increasing the reaction sites of capture probe and DNA-AuNPs complexes for bringing about the adsorption of large numbers of RuHex molecules, this electrochemical sensor could detect Pb(2+) quantitatively, in the range of 0.05-100nM, with a limit of detection as low as 0.012nM. Selectivity measurements revealed that the sensor was specific for Pb(2+) even with interference by high concentrations of other metal ions. This sensor was also used to detect Pb(2+) ions from samples of tap water, river water, and landfill leachate samples spiked with Pb(2+) ions, and the results showed good agreement with the found values determined by an atomic fluorescence spectrometer. This simple aptasensor represented a promising potential for on-site detecting Pb(2+) in drinking water. PMID:26921553

  17. Relative Distribution of Au48+ ~ Au52+ in Au Plasma by Ionization Dynamics

    Institute of Scientific and Technical Information of China (English)

    ZHU Zhi-Yan; ZHU Zheng-He; JIANG Gang

    2003-01-01

    The present work proposes a theoretical method called ionization dynamics to derive the ionic charge state distribution. Using relativistic quantum mechanics to calculate the energy level lifetime and average ionic lifetime of each ion, the first-order ionization rate constant can be obtained. Based on these data, from the solution of differential equations for consecutive-irreversible ionization reactions, one will be able to derive the ionic charge state distribution.The calculated average positive charge 49.24 of Au48+ ~ Au52+ and their relative distribution are in good agreement with the results of Lawrence Livermore National Laboratory.

  18. AU Political Solution in Libya

    Institute of Scientific and Technical Information of China (English)

    2011-01-01

    May 3,2011 The African Union(AU),through its High-Level ad hoc Committee on the Situation in Libya and the Commission, is driven by the conviction that, ultimately,only a political solution will make it possible to promote,in a sustainable way,the legitimate aspira-

  19. Global polarization measurement in Au+Au collisions

    CERN Document Server

    Abelev, B I; Ahammed, Z; Anderson, B D; Arkhipkin, D; Averichev, G S; Bai, Y; Balewski, J; Barannikova, O; Barnby, L S; Baudot, J; Baumgart, S; Belaga, V V; Bellingeri-Laurikainen, A; Bellwied, R; Benedosso, F; Betts, R R; Bhardwaj, S; Bhasin, A; Bhati, A K; Bichsel, H; Bielcik, J; Bielcikova, J; Bland, L C; Blyth, S L; Bombara, M; Bonner, B E; Botje, M; Bouchet, J; Brandin, A V; Bravar, A; Burton, T P; Bystersky, M; Cai, X Z; Caines, H; Calderón de la Barca-Sanchez, M; Callner, J; Catu, O; Cebra, D; Chajecki, Z; Chaloupka, P; Chattopadhyay, S; Chen, H F; Chen, J H; Chen, J Y; Cheng, J; Cherney, M; Chikanian, A; Christie, W; Chung, S U; Coffin, J P; Cormier, T M; Cosentino, M R; Cramer, J G; Crawford, H J; Das, D; Dash, S; Daugherity, M; De Moura, M M; Dedovich, T G; De Phillips, M; Derevshchikov, A A; Didenko, L; Dietel, T; Djawotho, P; Dogra, S M; Dong, X; Drachenberg, J L; Draper, J E; Du, F; Dunin, V B; Dunlop, J C; Dutta-Majumdar, M R; Eckardt, V; Edwards, W R; Efimov, L G; Emelianov, V; Engelage, J; Eppley, G; Erazmus, B; Estienne, M; Fachini, P; Fatemi, R; Fedorisin, J; Feng, A; Filip, P; Finch, E; Fine, V; Fisyak, Yu; Fu, J; Gagliardi, C A; Gaillard, L; Ganti, M S; García-Solis, E; Ghazikhanian, V; Ghosh, P; Gorbunov, Y N; Gos, H; Grebenyuk, O; Grosnick, D; Grube, B; Guertin, S M; Guimaraes, K S F F; Gupta, N; Haag, B; Hallman, T J; Hamed, A; Harris, J W; He, W; Heinz, M; Henry, T W; Heppelmann, S; Hippolyte, B; Hirsch, A; Hjort, E; Hoffman, A M; Hoffmann, G W; Hofman, D J; Hollis, R S; Horner, M J; Huang, H Z; Hughes, E W; Humanic, T J; Igo, G; Iordanova, A; Jacobs, P; Jacobs, W W; Jakl, P; Jia, F; Jones, P G; Judd, E G; Kabana, S; Kang, K; Kapitan, J; Kaplan, M; Keane, D; Kechechyan, A; Kettler, D; Khodyrev, V Yu; Kiryluk, J; Kisiel, A; Kislov, E M; Klein, S R; Knospe, A G; Kocoloski, A; Koetke, D D; Kollegger, T; Kopytine, M; Kotchenda, L; Kouchpil, V; Kowalik, K L; Kravtsov, P; Kravtsov, V I; Krüger, K; Kuhn, C; Kulikov, A I; Kumar, A; Kurnadi, P; Kuznetsov, A A; Lamont, M A C; Landgraf, J M; Lange, S; La Pointe, S; Laue, F; Lauret, J; Lebedev, A; Lednicky, R; Lee, C H; Lehocka, S; Le Vine, M J; Li, C; Li, Q; Li, Y; Lin, G; Lin, X; Lindenbaum, S J; Lisa, M A; Liu, F; Liu, H; Liu, J; Liu, L; Ljubicic, T; Llope, W J; Longacre, R S; Love, W A; Lu, Y; Ludlam, T; Lynn, D; Ma, G L; Ma, J G; Ma, Y G; Mahapatra, D P; Majka, R; Mangotra, L K; Manweiler, R; Margetis, S; Markert, C; Martin, L; Matis, H S; Matulenko, Yu A; McClain, C J; McShane, T S; Melnik, Yu M; Meschanin, A; Millane, J; Miller, M L; Minaev, N G; Mioduszewski, S; Mischke, A; Mitchell, J; Mohanty, B; Morozov, D A; Munhoz, M G; Nandi, B K; Nattrass, C; Nayak, T K; Nelson, J M; Nepali, C; Netrakanti, P K; Nogach, L V; Nurushev, S B; Odyniec, Grazyna Janina; Ogawa, A; Okorokov, V; Oldenburg, M; Olson, D; Pachr, M; Pal, S K; Panebratsev, Yu A; Pavlinov, A I; Pawlak, T; Peitzmann, T; Perevozchikov, V; Perkins, C; Peryt, W; Phatak, S C; Planinic, M; Pluta, J; Poljak, N; Porile, N; Poskanzer, A M; Potekhin, M V; Potrebenikova, E V; Potukuchi, B V K S; Prindle, D; Pruneau, C; Putschke, J; Qattan, I A; Raniwala, R; Raniwala, S; Ray, R L; Relyea, D; Ridiger, A; Ritter, H G; Roberts, J B; Rogachevski, O V; Romero, J L; Rose, A; Roy, C; Ruan, L; Russcher, M J; Sahoo, R; Sakrejda, I; Sakuma, T; Salur, S; Sandweiss, J; Sarsour, M; Sazhin, P S; Schambach, J; Scharenberg, R P; Schmitz, N; Seger, J; Selyuzhenkov, I; Seyboth, P; Shabetai, A; Shahaliev, E; Shao, M; Sharma, M; Shen, W Q; Shimansky, S S; Sichtermann, E P; Simon, F; Singaraju, R N; Smirnov, N; Snellings, R; Sørensen, P; Sowinski, J; Speltz, J; Spinka, H M; Srivastava, B; Stadnik, A; Stanislaus, T D S; Staszak, D; Stock, R; Strikhanov, M N; Stringfellow, B C; Suaide, A A P; Suarez, M C; Subba, N L; Sumbera, M; Sun, X M; Sun, Z; Surrow, B; Symons, T J M; Szanto de Toledo, A; Takahashi, J; Tang, A H; Tarnowsky, T J; Thomas, J H; Timmins, A R; Timoshenko, S; Tokarev, M; Trainor, T A; Trentalange, S; Tribble, R E; Tsai, O D; Ulery, J; Ullrich, T; Underwood, D G; Van Buren, G; Van der Kolk, N; Van Leeuwen, M; Van der Molen, A M; Varma, R; Vasilevski, I M; Vasilev, A N; Vernet, R; Vigdor, S E; Viyogi, Y P; Vokal, S; Voloshin, S A; Wada, M; Waggoner, W T; Wang, F; Wang, G; Wang, J S; Wang, X L; Wang, Y; Webb, J C; Westfall, G D; Whitten, C; Wieman, H; Wissink, S W; Witt, R; Wu, J; Wu, Y; Xu, N; Xu, Q H; Xu, Z; Yepes, P; Yoo, I K; Yue, Q; Yurevich, V I; Zawisza, M; Zhan, W; Zhang, H; Zhang, W M; Zhang, Y; Zhang, Z P; Zhao, Y; Zhong, C; Zhou, J; Zoulkarneev, R; Zoulkarneeva, Y; Zubarev, A N; Zuo, J X

    2007-01-01

    The system created in non-central relativistic nucleus-nucleus collisions possesses large orbital angular momentum. Due to spin-orbit coupling, particles produced in such a system could become globally polarized along the direction of the system angular momentum. We present the results of Lambda and anti-Lambda hyperon global polarization measurements in Au+Au collisions at sqrt{s_NN}=62.4 GeV and 200 GeV performed with the STAR detector at RHIC. The observed global polarization of Lambda and anti-Lambda hyperons in the STAR acceptance is consistent with zero within the precision of the measurements. The obtained upper limit, |P_{Lambda,anti-Lambda}| <= 0.02, is compared to the theoretical values discussed recently in the literature.

  20. Onset of nuclear matter expansion in Au+Au collisions

    CERN Document Server

    Crochet, Philippe; Gobbi, A; Donà, R; Coffin, J P; Fintz, P; Guillaume, G; Jundt, F; Kühn, C E; Roy, C; De Schauenburg, B; Tizniti, L; Wagner, P; Alard, J P; Amouroux, V; Andronic, A; Basrak, Z; Bastid, N; Belyaev, I; Best, D; Biegansky, J; Butà, A; Caplar, R; Cindro, N; Dupieux, P; Dzelalija, M; Fan, Z G; Fodor, Z; Fraysse, L; Freifelder, R P; Herrmann, N; Hildenbrand, K D; Hong, B H; Jeong, S C; Kecskeméti, J; Kirejczyk, M; Koncz, P; Korolija, M; Kotte, R; Lebedev, A; Leifels, Y; Man'ko, V I; Moisa, D; Mösner, J; Neubert, W; Pelte, D; Petrovici, M; Pinkenburg, C H; Pras, P; Ramillien, V; Reisdorf, W; Ritman, J L; Sadchikov, A G; Schüll, D; Seres, Z; Sikora, B; Simion, V; Siwek-Wilczynska, K; Sodan, U; Teh, K M; Trzaska, M; Vasilev, M A; Wang, G S; Wessels, J P; Wienold, T; Wisniewski, K; Wohlfarth, D; Zhilin, A V

    1997-01-01

    Using the FOPI detector at GSI Darmstadt, excitation functions of collective flow components were measured for the Au+Au system, in the reaction plane and out of this plane, at seven incident energies ranging from 100AMeV to 800AMeV. The threshold energies, corresponding to the onset of sideward-flow (balance energy) and squeeze-out effect (transition energy), are extracted from extrapolations of these excitation functions toward lower beam energies for charged products with Z>2. The transition energy is found to be larger than the balance energy. The impact parameter dependence of both balance and transition energies, when extrapolated to central collisions, suggests comparable although slightly higher values than the threshold energy for the radial flow. The relevant parameter seems to be the energy deposited into the system in order to overcome the attractive nuclear forces.

  1. Charge fluctuations in Au+Au collisions at RHIC energy

    Institute of Scientific and Technical Information of China (English)

    CAI; Xu(蔡勖); ZHOU; Daimei(周代梅); SA; Benhao(萨本豪)

    2003-01-01

    A hadron and string cascade model, JPCIAE, together with the corresponding Monte Carlo eventgenerator, has been employed in this paper to investigate further the charge fluctuations in Au+Au collisions at√Snn= 130 GeV. The default JPCIAE calculations are in good agreement with PHENIX and STAR data. Wefound that the thermal predictions for the π gas, the resonance π gas and quark matter deviate, respectively,from the corresponding dynamical simulations from the JPCIAE model. The discrepancies were also foundbetween the π charge fluctuations and the charge fluctuations of all species of hadrons. However the chargefluctuations for "π from ρ and ω decay" and for all the hadrons from resonance decay are close to each other,indicating the correlation between positively and negatively charged hadrons is not sensitive to the species ofhadrons. This work shows further that it is questionable to use the charge fluctuations as a signature of QGP.

  2. Nuclear Modification of Jet Fragmentation in Au+Au Collisions

    Science.gov (United States)

    Rowan, Zachary; Phenix Collaboration

    2015-10-01

    The characterization of energy in the quark gluon plasma is facilitated by measurements of modifications to the observed jet fragmentation. A favorable channel of study relies on direct photons created in the initial parton interactions of heavy ion collisions. Such a photon traverses the created medium unscathed and grants us a proxy for the transverse momentum of an away side jet. PHENIX Au+Au data recorded at √{sNN} = 200 GeV during RHIC run 14 benefit from the background rejection capability of the silicon vertex detector, enabling the extraction of a higher purity hadron signal. This advantage, combined with a larger integrated luminosity, allows previous PHENIX measurements of fragmentation functions to be extended to greater jet energies. In this talk, the status of the analysis of direct photon hadron correlations with the new data set will be discussed.

  3. Structural and morphological peculiarities of hybrid Au/nanodiamond engineered nanostructures

    Science.gov (United States)

    Matassa, Roberto; Orlanducci, Silvia; Reina, Giacomo; Cassani, Maria Cristina; Passeri, Daniele; Terranova, Maria Letizia; Rossi, Marco

    2016-08-01

    Nanostructured Au nano-platelets have been synthesized from an Au(III) complex by growth process triggered by nanodiamond (ND). An electroless synthetic route has been used to obtain 2D Au/ND architectures, where individual nanodiamond particles are intimately embedded into face-centered cubic Au platelets. The combined use of high resolution transmission electron microscopy (HR-TEM) and selected area electron diffraction (SAED), was able to reveal the unusual organization of these hybrid nanoparticles, ascertaining the existence of preferential crystallographic orientations for both nanocrystalline species and highlighting their mutual locations. Detailed information on the sample microstructure have been gathered by fast Fourier transform (FFT) and inverse fast Fourier transform (IFFT) of HR-TEM images, allowing us to figure out the role of Au defects, able to anchor ND crystallites and to provide specific sites for heteroepitaxial Au growth. Aggregates constituted by coupled ND and Au, represent interesting systems conjugating the best optoelectronics and plasmonics properties of the two different materials. In order to promote realistically the applications of such outstanding Au/ND materials, the cooperative mechanisms at the basis of material synthesis and their influence on the details of the hybrid nanostructures have to be deeply understood.

  4. Structural and morphological peculiarities of hybrid Au/nanodiamond engineered nanostructures.

    Science.gov (United States)

    Matassa, Roberto; Orlanducci, Silvia; Reina, Giacomo; Cassani, Maria Cristina; Passeri, Daniele; Terranova, Maria Letizia; Rossi, Marco

    2016-01-01

    Nanostructured Au nano-platelets have been synthesized from an Au(III) complex by growth process triggered by nanodiamond (ND). An electroless synthetic route has been used to obtain 2D Au/ND architectures, where individual nanodiamond particles are intimately embedded into face-centered cubic Au platelets. The combined use of high resolution transmission electron microscopy (HR-TEM) and selected area electron diffraction (SAED), was able to reveal the unusual organization of these hybrid nanoparticles, ascertaining the existence of preferential crystallographic orientations for both nanocrystalline species and highlighting their mutual locations. Detailed information on the sample microstructure have been gathered by fast Fourier transform (FFT) and inverse fast Fourier transform (IFFT) of HR-TEM images, allowing us to figure out the role of Au defects, able to anchor ND crystallites and to provide specific sites for heteroepitaxial Au growth. Aggregates constituted by coupled ND and Au, represent interesting systems conjugating the best optoelectronics and plasmonics properties of the two different materials. In order to promote realistically the applications of such outstanding Au/ND materials, the cooperative mechanisms at the basis of material synthesis and their influence on the details of the hybrid nanostructures have to be deeply understood. PMID:27514638

  5. Structural and morphological peculiarities of hybrid Au/nanodiamond engineered nanostructures

    Science.gov (United States)

    Matassa, Roberto; Orlanducci, Silvia; Reina, Giacomo; Cassani, Maria Cristina; Passeri, Daniele; Terranova, Maria Letizia; Rossi, Marco

    2016-01-01

    Nanostructured Au nano-platelets have been synthesized from an Au(III) complex by growth process triggered by nanodiamond (ND). An electroless synthetic route has been used to obtain 2D Au/ND architectures, where individual nanodiamond particles are intimately embedded into face-centered cubic Au platelets. The combined use of high resolution transmission electron microscopy (HR-TEM) and selected area electron diffraction (SAED), was able to reveal the unusual organization of these hybrid nanoparticles, ascertaining the existence of preferential crystallographic orientations for both nanocrystalline species and highlighting their mutual locations. Detailed information on the sample microstructure have been gathered by fast Fourier transform (FFT) and inverse fast Fourier transform (IFFT) of HR-TEM images, allowing us to figure out the role of Au defects, able to anchor ND crystallites and to provide specific sites for heteroepitaxial Au growth. Aggregates constituted by coupled ND and Au, represent interesting systems conjugating the best optoelectronics and plasmonics properties of the two different materials. In order to promote realistically the applications of such outstanding Au/ND materials, the cooperative mechanisms at the basis of material synthesis and their influence on the details of the hybrid nanostructures have to be deeply understood. PMID:27514638

  6. Tailoring metal-oxide interfaces of inverse catalysts of TiO2/nanoporous-Au under hydrogen oxidation.

    Science.gov (United States)

    Qadir, Kamran; Quynh, Bui Thi Phuong; Lee, Hyosun; Moon, Song Yi; Kim, Sang Hoon; Park, Jeong Young

    2015-06-14

    Engineering metal-oxide interfaces in TiO2/nanoporous (np) Au inverse catalysts results in enhancement of H2 oxidation activity. While the intrinsic activity of the novel np-Au prepared from a Au-Si alloy is low, the activity increased as the weight fraction of the TTIP (amount of TiO2) was increased to 0.5 weight%. We correlate the change in activity with the active sites at the perimeter interface between the TiO2 and np-Au. PMID:25959456

  7. Formic Acid Decomposition on Au catalysts: DFT, Microkinetic Modeling, and Reaction Kinetics Experiments

    Energy Technology Data Exchange (ETDEWEB)

    Singh, Suyash; Li, Sha; Carrasquillo-Flores, Ronald; Alba-Rubio, Ana C.; Dumesic, James A.; Mavrikakis, Manos

    2014-04-01

    A combined theoretical and experimental approach is presented that uses a comprehensive mean-field microkinetic model, reaction kinetics experiments, and scanning transmission electron microscopy imaging to unravel the reaction mechanism and provide insights into the nature of active sites for formic acid (HCOOH) decomposition on Au/SiC catalysts. All input parameters for the microkinetic model are derived from periodic, self-consistent, generalized gradient approximation (GGA-PW91) density functional theory calculations on the Au(111), Au(100), and Au(211) surfaces and are subsequently adjusted to describe the experimental HCOOH decomposition rate and selectivity data. It is shown that the HCOOH decomposition follows the formate (HCOO) mediated path, with 100% selectivity toward the dehydrogenation products (CO21H2) under all reaction conditions. An analysis of the kinetic parameters suggests that an Au surface in which the coordination number of surface Au atoms is 4 may provide a better model for the active site of HCOOH decomposition on these specific supported Au catalysts.

  8. Interaction of carbon monoxide and oxygen at the surface of inverse titania/Au model catalyst

    Science.gov (United States)

    Magkoev, Tamerlan T.

    2007-07-01

    Interaction of carbon monoxide and oxygen on the surface of titania/Au(1 1 1) inverse model catalyst held at 200 K has been studied by reflection absorption infrared spectroscopy. It was found that CO adsorbs on the oxide/Au perimeter interface, whereas no or very weak adsorption was observed on Au(1 1 1) or titania surface, respectively. Exposing of such species to oxygen results in their decay possibly due to carbon dioxide formation. Efficiency of this effect is higher at lower CO initial concentration which points at the importance of free surface sites for the reaction process.

  9. Investigation of the Adsorption and Self Assembly of Isocyanide Derivatives on Au(111) Surface

    Institute of Scientific and Technical Information of China (English)

    ZHOU,Jun-Hong; SHI,Liang-Wei; ZHANG,Tao; CHEN,Min-Bo

    2007-01-01

    The adsorption and self-assembly of isocyanide derivatives on Au(111) surface were investigated by density functional theory (DFT) and molecular dynamics simulation. The calculation for phenyl isocyanide by DFT was based on cluster and slab models. The self-assembled monolayers of 2-isocyanoazulene and 1,3-diethoxycarbonyl2-isocyanoazulene on Au(111) were simulated using Au-C force field parameters developed by us. It was found that the top site was the most preferred position, and the isocyanoazulene and its derivatives could form the ordered face to edge self-assembled monolayer on gold surface indeed, and the molecules stood on the gold surface vertically.

  10. Electrochemically Reduced Graphene Oxide-nafion/Au Nanoparticle Modified Electrode for Hydrogen Peroxide Sensing

    OpenAIRE

    Yajie Lv; Fang Wang; Hui Zhu; Xiaorong Zou; Cheng-an Tao; Jianfang Wang

    2016-01-01

    n this paper, a non-enzymatic hydrogen peroxide (H2O2) sensor, based on Au nanoparticles (AuNPs) electrodepos‐ ited on an electrochemically reduced graphene oxide(ER‐ GO)-Nafion modified glass carbon electrode (GCE), was reported. The graphene oxide-(GO-)Nafion nanocompo‐ sites were first assembled on the GCE surface to produce a GO-Nafion electrode. GO was then electrochemically reduced to produce an ERGO-Nafion modified GCE (to be subsequently denoted as GCE/ERGO-Nafion). Afterwards, AuNPs ...

  11. Impact of temperature-induced coalescence on SERS properties of Au nanoparticles deposited on GaN nano-columns

    Science.gov (United States)

    Dzięcielewski, Igor; Smalc-Koziorowska, Julita; Bańkowska, Małgorzata; Sochacki, Tomasz; Khachapuridze, Alexandr; Weyher, Jan

    2016-08-01

    Nanostructured GaN surfaces sputtered with Au provide very promising and reproducible platforms for surface enhanced Raman scattering (SERS). The enhancement factor (EF) in SERS is expected to depend strongly on the local metal (Au) surface structure (size, distribution and morphology). Herein we show how temperature-induced coalescence followed by recrystallization of Au on GaN nano-columns occurs well below the melting point of gold. This process is reflected in SEM, TEM images and SERS spectra of Au/GaN - bound p-mercaptobenzoic acid (4-MBA), a model Raman scatterer. SERS signals of 4-MBA bound to Au/GaN reach minimum for platforms exposed to t = 350 °C before regaining the intensity when annealed in the range of 450-900 °C. The results have been discussed in the light of the nature of SERS active sites - so called "hot spots" and structure of Au nanoparticles.

  12. Decay spectroscopy of $^{178}$Au

    CERN Document Server

    Whitmore, B

    In this thesis, the neutron-deficient nucleus $^{178}$Au is investigated through decay spectroscopy. Si and HPGe detectors were used to analyse the decay radiation of $^{178}$Au and its daughter nuclei. Previous studies have been unable to distinguish decay radiation from different isomeric states of this nucleus. This thesis represents the first time such isomeric discrimination has been achieved, and presents tentative spin assignments of both the ground state and an isomer. The neutron-deficient gold isotopes are an area of interest for the study of shape coexistence. This is the phenomenon exhibited by nuclei able to exist at a number of close lying energy minima, each reflecting a distinct type of deformation. It is hoped that studies such as this can help identify the evolution of nuclear deformation in this region of the nuclear chart.

  13. Tailoring the electrical properties of MoS2 field effect transistors by depositing Au nanoparticles and alkanethiol molecules

    Science.gov (United States)

    Cho, Kyungjune; Jeong, Hyunhak; Kim, Tae-Young; Pak, Jinsu; Kim, Jae-Keun; Choi, Barbara Yuri; Lee, Takhee

    2016-05-01

    We fabricated and characterized MoS2 field effect transistors. First, we measured the electrical properties of MoS2 field effect transistors (FETs) that were made with mechanically exfoliated MoS2 flakes. Then, we deposited Au nanoparticles on the MoS2 channel and measured the electrical properties. We observed whether the source-drain current increased or decreased after the Au particles were deposited. The deposited Au particles either formed an extra current path and increased the current or behaved as charge-withdrawing sites and decreased the current. Next, we deposited alkanethiol molecules on the Au particles to reduce the work function of the Au. Alkanethiol molecules are known to form a self-assembled monolayer on the Au surface, and the electric dipole moment of the molecules causes the work function of the Au to decrease. Au particles can capture electrons from the MoS2 channel due to their high work function. However, the decreased work function of the Au particles subjected to alkanethiol treatment could cause captured electrons to be released from the Au particles to MoS2. Therefore, the current increased after alkanethiol treatment. This study may provide useful methods to utilize surface treatments with particles and molecules to tailor the electrical properties of MoS2-based FETs.

  14. Tailoring the electrical properties of MoS2 field effect transistors by depositing Au nanoparticles and alkanethiol molecules.

    Science.gov (United States)

    Cho, Kyungjune; Jeong, Hyunhak; Kim, Tae-Young; Pak, Jinsu; Kim, Jae-Keun; Choi, Barbara Yuri; Lee, Takhee

    2016-05-11

    We fabricated and characterized MoS2 field effect transistors. First, we measured the electrical properties of MoS2 field effect transistors (FETs) that were made with mechanically exfoliated MoS2 flakes. Then, we deposited Au nanoparticles on the MoS2 channel and measured the electrical properties. We observed whether the source-drain current increased or decreased after the Au particles were deposited. The deposited Au particles either formed an extra current path and increased the current or behaved as charge-withdrawing sites and decreased the current. Next, we deposited alkanethiol molecules on the Au particles to reduce the work function of the Au. Alkanethiol molecules are known to form a self-assembled monolayer on the Au surface, and the electric dipole moment of the molecules causes the work function of the Au to decrease. Au particles can capture electrons from the MoS2 channel due to their high work function. However, the decreased work function of the Au particles subjected to alkanethiol treatment could cause captured electrons to be released from the Au particles to MoS2. Therefore, the current increased after alkanethiol treatment. This study may provide useful methods to utilize surface treatments with particles and molecules to tailor the electrical properties of MoS2-based FETs.

  15. Introduction au filtre de Kalman

    OpenAIRE

    Alazard, Daniel

    2006-01-01

    Ce document est une introduction au filtre optimal de Kalman appliquée aux systèmes linéaires. On suppose connues la théorie des asservissements linéaires et du filtrage fréquentiel (continu et discret) ainsi que les notions d'états pour représenter les systèmes dynamiques linéaires.

  16. L’apprentissage au CERN

    CERN Multimedia

    Staff Association

    2016-01-01

    En 1961, sur la base du constat que l’évolution du marché du travail nécessitait un besoin croissant de personnel qualifié, le 1er accord entre la République et canton de Genève et le CERN fut signé. Cet accord avait notamment pour objet la formation professionnelle de jeunes électroniciens et techniciens de laboratoires en physique. Le CERN, acteur local économique d’importance, soulignait par cet accord sa volonté de participer au développement économique et social local. Le 1er apprenti arriva au CERN en 1965. En 1971, le centre d’apprentissage fut créé ; il accueille aujourd’hui plus d’une vingtaine d’apprentis au total, à raison d’environ six nouveaux apprentis chaque année. Cet apprentissage est dédié aux jeunes âgés e...

  17. Fabricating a Homogeneously Alloyed AuAg Shell on Au Nanorods to Achieve Strong, Stable, and Tunable Surface Plasmon Resonances

    KAUST Repository

    Huang, Jianfeng

    2015-08-13

    Colloidal metal nanocrystals with strong, stable, and tunable localized surface plasmon resonances (SPRs) can be useful in a corrosive environment for many applications including field-enhanced spectroscopies, plasmon-mediated catalysis, etc. Here, a new synthetic strategy is reported that enables the epitaxial growth of a homogeneously alloyed AuAg shell on Au nanorod seeds, circumventing the phase segregation of Au and Ag encountered in conventional synthesis. The resulting core–shell structured bimetallic nanorods (AuNR@AuAg) have well-mixed Au and Ag atoms in their shell without discernible domains. This degree of mixing allows AuNR@AuAg to combine the high stability of Au with the superior plasmonic activity of Ag, thus outperforming seemingly similar nanostructures with monometallic shells (e.g., Ag-coated Au NRs (AuNR@Ag) and Au-coated Au NRs (AuNR@Au)). AuNR@AuAg is comparable to AuNR@Ag in plasmonic activity, but that it is markedly more stable toward oxidative treatment. Specifically, AuNR@AuAg and AuNR@Ag exhibit similarly strong signals in surface-enhanced Raman spectroscopy that are some 30-fold higher than that of AuNR@Au. When incubated with a H2O2 solution (0.5 m), the plasmonic activity of AuNR@Ag immediately and severely decayed, whereas AuNR@AuAg retained its activity intact. Moreover, the longitudinal SPR frequency of AuNR@AuAg can be tuned throughout the red wavelengths (≈620–690 nm) by controlling the thickness of the AuAg alloy shell. The synthetic strategy is versatile to fabricate AuAg alloyed shells on different shaped Au, with prospects for new possibilities in the synthesis and application of plasmonic nanocrystals.

  18. Active and selective conversion of CO2 to CO on ultrathin Au nanowires.

    Science.gov (United States)

    Zhu, Wenlei; Zhang, Yin-Jia; Zhang, Hongyi; Lv, Haifeng; Li, Qing; Michalsky, Ronald; Peterson, Andrew A; Sun, Shouheng

    2014-11-19

    In this communication, we show that ultrathin Au nanowires (NWs) with dominant edge sites on their surface are active and selective for electrochemical reduction of CO2 to CO. We first develop a facile seed-mediated growth method to synthesize these ultrathin (2 nm wide) Au NWs in high yield (95%) by reducing HAuCl4 in the presence of 2 nm Au nanoparticles (NPs). These NWs catalyze CO2 reduction to CO in aqueous 0.5 M KHCO3 at an onset potential of -0.2 V (vs reversible hydrogen electrode). At -0.35 V, the reduction Faradaic efficiency (FE) reaches 94% (mass activity 1.84 A/g Au) and stays at this level for 6 h without any noticeable activity change. Density functional theory (DFT) calculations suggest that the excellent catalytic performance of these Au NWs is attributed both to their high mass density of reactive edge sites (≥16%) and to the weak CO binding on these sites. These ultrathin Au NWs are the most efficient nanocatalyst ever reported for electrochemical reduction of CO2 to CO.

  19. Monitoring continu de site pollué : mise au point d'une méthodologie de contrôle en continu d'un site pollué en phase de surveillance ou de dé pollution

    OpenAIRE

    Portet, Frédéric

    2004-01-01

    The purpose of the Contaminated Site Monitoring (CSM) is to develop a real time management methodology for PAH (Polycyclic Aromatic Hydrocarbons) contaminated aquifer resulting from the coal activity. For the full-scale experimentation, an old coking plant site has been was instrumented (sensors, analysers, datalogger, programmable logic controller, etc.) in June 2000. Its follow-up currently continues with remote supervision, via telecom connection.It is the first time that a CSM is installe...

  20. Hydrodechlorination Catalysis of Pd-on-Au Nanoparticles Varies with Particle Size

    Energy Technology Data Exchange (ETDEWEB)

    Pretzer, Lori A.; Song, Hyun J.; Fang, Yu-Lun; Zhao, Zhun; Guo, Neng; Wu, Tianpin; Arslan, Ilke; Miller, Jeffrey T.; Wong, Michael S.

    2013-02-01

    The dependence of bimetallic PdAu catalytic activity on the relative ratios of Pd and Au has been theoretically predicted and experimentally observed for a number of reactions. Trichloroethene (TCE), a common carcinogenic solvent that is difficult to remove from contaminated groundwater in many industrialized nations, can be chemically degraded especially rapidly with Au nanoparticles partially coated with Pd ("Pd-on-Au NPs"). These NPs catalyze the room-temperature water-phase TCE hydrodechlorination (HDC) reaction with activities that follow a volcano-shape dependence on Pd surface coverage. The effect of particle size is not known, though. Pd-on-Au NPs synthesized with 3, 7, and 10 nm Au NPs and Pd surface coverages between 0 and 150% were studied in detail. Volcano-shape dependence on Au particle size and Pd surface coverage was observed, with 7 nm Au NPs with a Pd coverage of 60-70% having the highest TCE HDC activity. Extended x-ray absorption fine-structure spectroscopy (EXAFS) revealed the correlation was strongest between catalytic activity and the presence of non-oxidized Pd ensembles of ~2-3 atoms in contact with ~8-10 Au atoms. Isolated Pd atoms and Pd ensembles were visualized for the first time through aberration-corrected scanning transmission electron microscopy (STEM). This study provides the most direct evidence yet for Pd-on-Au NPs containing 2-dimensional Pd ensembles as the active sites for TCE HDC and likely for other chemical reactions. A portion of the research was performed using EMSL, a national scientific user facility sponsored by the Department of Energy's Office of Biological and Environmental Research and located at Pacific Northwest National Laboratory. This research was supported by the Laboratory Directed Research and Development program at Pacific Northwest National Laboratory. The Pacific Northwest National Laboratory is operated by Battelle for the US Department of Energy.

  1. Detection and analysis of neutral and charged particles. Application to the study of hot plasmas; Detection et analyse des particules chargees et neutres appliquees a l'etude des plasmas chauds

    Energy Technology Data Exchange (ETDEWEB)

    Renaud, C. [Commissariat a l' Energie Atomique, Fontenay-aux-Roses (France). Centre d' Etudes Nucleaires. Groupe de recherches de l' association EURATOM-CEA sur la fusion controlee

    1966-12-01

    To measure the energy spectrum of ions in a plasma, one must extract the ions without altering the spectrum. For a dense plasma this presents difficulties, one method is the measurement of the energy spectrum of atoms produced by charge-exchange reactions of ions with residual gas. The measurements of both the energy spectrum and the flux of atoms leaving the magnetic configuration of the device DECA II (Dispositif d'Etude de Compression Adiabatique) are made by: an ion detector which permits the measurement of ion currents {>=} 10{sup -16} A, an electrostatic analyser of energy range 10 eV - 10 keV, a magnetic analyser for ion momentum {<=} 10{sup 5} gauss-cm, and a gas cell to convert fast atoms into ions. (author) [French] Pour mesurer le spectre en energie des ions dans un plasma on doit extraire des ions sans en modifier l'energie. Dans le cas de plasmas denses cela presente certaines difficultes. Une mesure du spectre en energie des ions est alors possible a partir du spectre en energie des atomes produits par collision d'echange de charge entre les ions du plasma et le gaz residuel. Pour effectuer la mesure du spectre en energie et du flux d'atomes s'echappant de la configuration magnetique du Dispositif d'Etude de Compression Adiabatique (DECA II) nous avons mis au point: un detecteur d'ions permettant la mesure de courant {>=} 10{sup -16} A, d'un analyseur electrostatique dont la gamme d'analyse en energie est comprise entre 10 eV et 10 keV, d'un analyseur magnetique capable d'analyser des ions d'une quantite de mouvement {<=} 10{sup 5} gauss cm, ainsi qu'une cellule a gaz permettant l'ionisation des atomes rapides. (auteur)

  2. Detection of {alpha} particles using semiconductors. Application to the control of plutonium extraction; Detection des particules {alpha} par semiconducteurs application au controle de l'extraction du plutonium

    Energy Technology Data Exchange (ETDEWEB)

    Tanguy, J. [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1968-03-01

    A study is made of a particles produced by thick sources, using either diffused junction or surface barrier semiconductor detectors for controlling continuously the plutonium extraction process. For this, a presenting apparatus is described in which the solutions to be analyzed flow in contact with the detector protected by a thin mica membrane. A method is described which gives a precise recording of the spectra and which thus allows the separation of two or more {alpha} emitters present in the same solution. This method has been applied to the measurement of {sup 239}Pu in the the presence of {sup 241}Am with an accuracy of {+-}5 per cent. In the second part of the report is considered the detection of plutonium in solutions of {beta} - {gamma} emitting fission products. Pile-up is reduced by using a fast amplification chain associated to totally depleted thin detectors. Under these conditions a few mg of {sup 239}Pu can be detected in solutions of fission products having an activity of 100 curies/liter. A method is given for discriminating {alpha} and {beta} particles, it is based on the difference in the collection times for the charges liberated by these particles in the detector. (author) [French] On etudie la detection de particules {alpha} issues de sources epaisses par detecteurs semiconducteurs a jonction diffusee ou a barriere de surface pour le controle continu du procede d'extraction du plutonium. A cet effet on decrit un appareil presentateur dans lequel les solutions a analyser circulent au contact du detecteur protege par une membrane mince de mica. On decrit une methode qui permet par le trace precis des spectres de separer deux ou plusieurs emetteurs {alpha} presents dans une meme solution. Cette methode a ete appliquee a la mesure du {sup 239}Pu en presence de {sup 241}Am avec une precision de {+-} 5 pour cent. Dans la deuxieme partie on traite de la detection du plutonium dans des solutions de produits de fission emetteurs {beta} and {gamma

  3. Initial state geometry and fluctuations in Au+Au, Cu+Au and U+U collisions at RHIC

    OpenAIRE

    Schenke, Bjoern; Tribedy, Prithwish; Venugopalan, Raju

    2014-01-01

    We study within the IP-Glasma and two-component MC-Glauber models the effects of initial state geometry and fluctuations on multiplicities and eccentricities for several collision species at the Relativistic Heavy Ion Collider (RHIC). These include copper-gold (Cu+Au), gold-gold (Au+Au), and uranium-uranium (U+U) collisions. The multiplicity densities per participant pair are very similar in all systems studied. Ellipticities vary strongly between collision systems, most significantly for cen...

  4. Kinetics of low-temperature CO oxidation on Au(111)

    Science.gov (United States)

    Thuening, Theodore; Walker, Joshua; Adams, Heather; Furlong, Octavio; Tysoe, Wilfred T.

    2016-06-01

    The oxidation of carbon monoxide on oxygen-modified Au(111) surfaces is studied using a combination of reflection-absorption infrared spectroscopy (RAIRS) and temperature-programmed desorption (TPD). TPD reveals that CO desorbs in two states with the low-temperature state have a peak temperature between ~ 130 and 150 K, and the higher-temperature state having a peak temperature that varies from ~ 175 to ~ 220 K depending on the initial oxygen and CO coverages. Infrared spectroscopy indicates that the low-temperature CO desorption state is predominantly associated with CO adsorbed on Auδ + sites, while the higher-temperature states are due to CO on Au0 sites. No additional vibrational features are detected indicating that CO reacts directly with adsorbed atomic oxygen on gold to form CO2. Estimates of the activation energy for CO2 formation suggest that they are in the same range and found for supported gold catalysts at reaction temperature below ~ 300 K.

  5. Study and analysis of failure modes of the electrolytic capacitors and thyristors, applied to the protection system of the LHC (Large Hadron Collider); Etude et analyse des modes de defaillances des condensateurs electrolytiques a l'aluminium et des thyristors: appliquees au systeme de protection du LHC (Large Hadron Collider)

    Energy Technology Data Exchange (ETDEWEB)

    Perisse, F

    2003-07-15

    The study presented in this thesis is a contribution about the analysis of failures modes of electrolytic capacitors and thyristors. The studied components are main elements of the protection system of the superconductive magnets of the LHC. The study of the ageing of the electrolytic capacitors has shown that their reliability is strongly related to their technological characteristic. Evolution of their principal indicator of ageing (ESR) can be modeled according to different laws chosen according to their running mode. It appears that the prediction of failure of these components other than that due to wear can be only statistical taking into account the many causes of failure involving various modes of failure. In order to be able to evaluate influence of the ageing of the electrolytic capacitors on a system, simple models taking into account this parameters as well as the effective temperature of the component are proposed. An acceptable precision taking into account the simplicity of the models is obtained. The study of the thyristors has shown that these components have little drift of parameters in static ageing, on the other hand of many failures by short-circuit were observed. These failures always have a local origin, and are due to defects of the components. The breakdown voltage strongly depends on the quality of the thyristor as well as the technology employed. (author)

  6. Development of morin-conjugated Au nanoparticles: Exploring the interaction efficiency with BSA using spectroscopic methods

    Science.gov (United States)

    Yue, Hua-Li; Hu, Yan-Jun; Huang, Hong-Gui; Jiang, Shan; Tu, Bao

    2014-09-01

    In order to enhance its interaction efficiency with biomacromolecules for the usage as a therapeutic agent, we have conjugated morin, an antioxidant activity and anti-tumor drug, with citrate-coated Au nanoparticles (M-C-AuNPs). M-C-AuNPs were prepared by reducing chloroauric acid using trisodium citrate in the boiling condition, and the resulted M-C-AuNPs were characterized by UV-vis absorption spectroscopy, Transmission Electron Microscopy (TEM), X-ray diffraction (XRD) and FTIR analysis. In this article, UV-vis absorption spectroscopy in combination with fluorescence spectroscopy, and circular dichroism (CD) spectroscopy were employed to investigate the interactions between M-C-AuNPs and bovine serum albumin (BSA), C-AuNPs and BSA in a phosphate buffer at pH 7.4. By comparing the quenching constant KSV, effective quenching constant Ka, binding constant Kb and the number of binding sites n, it is clearly suggested that M-C-AuNPs could enhance the binding force of morin with BSA, which would pave the way for the design of nanotherapeutic agents with improved functionality.

  7. Hydrogen adsorption on bimetallic PdAu(111) surface alloys

    DEFF Research Database (Denmark)

    Takehiro, Naoki; Liu, Ping; Bergbreiter, Andreas;

    2014-01-01

    The adsorption of hydrogen on structurally well defined PdAu-Pd(111) monolayer surface alloys was investigated in a combined experimental and theoretical study, aiming at a quantitative understanding of the adsorption and desorption properties of individual PdAu nanostructures. Combining...... the structural information obtained by high resolution scanning tunneling microscopy (STM), in particular on the abundance of specific adsorption ensembles at different Pd surface concentrations, with information on the adsorption properties derived from temperature programmed desorption (TPD) spectroscopy...... and high resolution electron energy loss spectroscopy (HREELS) provides conclusions on the minimum ensemble size for dissociative adsorption of hydrogen and on the adsorption energies on different sites active for adsorption. Density functional theory (DFT) based calculations give detailed insight...

  8. Predicted Habitat Suitability for Leptoseris in the Au'au Channel Region

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — This raster denotes predicted habitat suitability for Leptoseris in the Au'au Channel region. Maximum Entropy (MaxEnt) modeling software was used to create this...

  9. Predicted Habitat Suitability for Montipora Corals in the Au'au Channel Region

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — This raster denotes predicted habitat suitability for Montipora in the Au'au Channel region. Maximum Entropy (MaxEnt) modeling software was used to create this...

  10. Predicted Habitat Suitability for Leptoseris Corals in the Au'au Channel Region

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — This raster denotes predicted habitat suitability for Leptoseris in the Au'au Channel region. Maximum Entropy (MaxEnt) modeling software was used to create this...

  11. Predicted Habitat Suitability for Porites Corals in the Au'au Channel Region

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — This raster denotes predicted habitat suitability for Porites in the Au'au Channel region. Maximum Entropy (MaxEnt) modeling software was used to create this...

  12. Predicted Habitat Suitability for All Mesophotic Corals in the Au'au Channel Region

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — This dataset is located between the islands of Maui, Lanai, Molokai and Kahoolawe, and includes the Au'au Channel as well as parts of the Kealaikahiki, Alalakeiki...

  13. Predicted Habitat Suitability for Porites in the Au'au Channel Region

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — This raster denotes predicted habitat suitability for Porites in the Au'au Channel region. Maximum Entropy (MaxEnt) modeling software was used to create this...

  14. Predicted Habitat Suitability for All Mesophotic Corals in the Au'au Channel Region

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — This raster denotes predicted habitat suitability for all mesophotic corals in the Au'au Channel region. Maximum Entropy (MaxEnt) modeling software was used to...

  15. A Study of Parton Energy Loss in Au+Au Collisions at RHIC using Transport Theory

    OpenAIRE

    Nara, Y.; Vance, S. E.; Csizmadia, P.

    2001-01-01

    Parton energy loss in Au+Au collisions at RHIC energies is studied by numerically solving the relativistic Boltzmann equation for the partons including $2 \\leftrightarrow 2$ and $2 \\to 2 + final state radiation$ collision processes. Final particle spectra are obtained using two hadronization models; the Lund string fragmentation and independent fragmentation models. Recent, preliminary $\\pi^0$ transverse momentum distributions from central Au+Au collisions at RHIC are reproduced using gluon-g...

  16. Synthesis, characterization and photo-epoxidation performance of Au-loaded photocatalysts

    Indian Academy of Sciences (India)

    Van-Huy Nguyen; Hsiang-Yu Chan; Jeffrey C S Wu

    2013-07-01

    Titanium silicalite-1 (TS-1) was synthesized by hydrothermal crystallization. Au-loaded TS-1 (Au/TS-1) was prepared by the photo-deposition method. The prepared photocatalysts have been fully characterized by Raman, Brunauer-Emmett-Teller (BET), transmission electron microscopy, scanning electron microscopy, X-ray diffraction, X-ray photoelectron spectroscopy, and ultraviolet visible light spectroscopy to reveal their structure, surface morphology and chemical composition. Photocatalytic activity of these photocatalysts was ascertained by gas phase photo-epoxidation of propylene-to-propylene oxide in the presence of molecular oxygen only under light irradiation. No sacrificial reductant such as hydrogen was used during the photoreaction. Au/TS-1 photocatalyst remained highly stable under reaction conditions. It is found that the increased Ti3+ sites due to the incorporation of Au will not only enhance the selectivity of the photocatalyst to form epoxide but also its stability during C3H6 conversion.

  17. Le site paléo-indien de Piedra Museo (Patagonie). Sa contribution au débat sur le premier peuplement du continent américainThe palaeo-indian site of Piedra Museo (Patagonia). Its contribution to the debate on the peopling of the Americas.

    Science.gov (United States)

    Ramirez Rozzi, Fernando V.; d'Errico, Francesco; Zarate, Marcelo

    2000-08-01

    The Piedra Museo site (Santa Cruz, Argentina), excavated over the past nine years has yielded a rich archaeological record, which contributes to the discussion on the first peopling of the Americas. We present here a new study of the site, based on an analysis of the stratigraphy, spatial distribution of archaeological remains, bone taphonomy, and discussion of new AMS- 14C dates. We conclude that remains of extinct species with cut-marks from the lower levels are contemporaneous of stone tools and cores from the same levels. This demonstrates that humans were present in the southern part of Patagonia around 10 300 and 11 100 years BP and suggests that hunting of large mammals was a part of their subsistence strategies.

  18. Bright, NIR-emitting Au23 from Au25: characterization and applications including biolabeling.

    Science.gov (United States)

    Muhammed, Madathumpady Abubaker Habeeb; Verma, Pramod Kumar; Pal, Samir Kumar; Kumar, R C Arun; Paul, Soumya; Omkumar, Ramakrishnapillai Vyomakesannair; Pradeep, Thalappil

    2009-10-01

    A novel interfacial route has been developed for the synthesis of a bright-red-emitting new subnanocluster, Au(23), by the core etching of a widely explored and more stable cluster, Au(25)SG(18) (in which SG is glutathione thiolate). A slight modification of this procedure results in the formation of two other known subnanoclusters, Au(22) and Au(33). Whereas Au(22) and Au(23) are water soluble and brightly fluorescent with quantum yields of 2.5 and 1.3 %, respectively, Au(33) is organic soluble and less fluorescent, with a quantum yield of 0.1 %. Au(23) exhibits quenching of fluorescence selectively in the presence of Cu(2+) ions and it can therefore be used as a metal-ion sensor. Aqueous- to organic-phase transfer of Au(23) has been carried out with fluorescence enhancement. Solvent dependency on the fluorescence of Au(23) before and after phase transfer has been studied extensively and the quantum yield of the cluster varies with the solvent used. The temperature response of Au(23) emission has been demonstrated. The inherent fluorescence of Au(23) was used for imaging human hepatoma cells by employing the avidin-biotin interaction. PMID:19711391

  19. Initial state geometry and fluctuations in Au+Au, Cu+Au and U+U collisions at RHIC

    CERN Document Server

    Schenke, Bjoern; Venugopalan, Raju

    2014-01-01

    We study within the IP-Glasma and two-component MC-Glauber models the effects of initial state geometry and fluctuations on multiplicities and eccentricities for several collision species at the Relativistic Heavy Ion Collider (RHIC). These include copper-gold (Cu+Au), gold-gold (Au+Au), and uranium-uranium (U+U) collisions. The multiplicity densities per participant pair are very similar in all systems studied. Ellipticities vary strongly between collision systems, most significantly for central collisions, while fluctuation driven odd moments vary little between systems. Event-by-event distributions of eccentricities in mid-central collisions are wider in Cu+Au relative to Au+Au and U+U systems. An anti-correlation between multiplicity and eccentricity is observed in ultra central U+U collisions which is weaker in the IP-Glasma model than the two-component MC-Glauber model. In ultra central Au+Au collisions the two models predict opposite signs for the slope of this correlation. Measurements of elliptic flo...

  20. Au 6x6 on Si(111): Evidence for a 2D pseudoglass

    DEFF Research Database (Denmark)

    Marks, L.D.; Grozea, D.; Feidenhans'l, R.;

    1998-01-01

    The atomic structure of the Au 6 x 6 on Si(111) phase has been determined using direct methods and surface X-ray diffraction data. This surface structure is very complicated, with 14 independent gold atoms, relaxations in 24 independent silicon sites and three partially occupied gold sites. In one...... sense the structure can be described as microdomains of the parent root 3 x root 3 Au on Si(111) structure. A better description is in terms of a tiling of incomplete pentagonal and trimer units, essentially a pseudopentagonal glass. In terms of these structural units it appears possible to explain all...

  1. Au@Ag/Au nanoparticles assembled with activatable aptamer probes as smart ``nano-doctors'' for image-guided cancer thermotherapy

    Science.gov (United States)

    Shi, Hui; Ye, Xiaosheng; He, Xiaoxiao; Wang, Kemin; Cui, Wensi; He, Dinggeng; Li, Duo; Jia, Xuekun

    2014-07-01

    Although nanomaterial-based theranostics have increased positive expectations from cancer treatment, it remains challenging to develop in vivo ``nano-doctors'' that provide high-contrast image-guided site-specific therapy. Here we designed an activatable theranostic nanoprobe (ATNP) via self-assembly of activatable aptamer probes (AAPs) on Au@Ag/Au nanoparticles (NPs). As both quenchers and heaters, novel Au@Ag/Au NPs were prepared, showing excellent fluorescence quenching and more effective near-infrared photothermal therapy than Au nanorods. The AAP comprised a thiolated aptamer and a fluorophore-labeled complementary DNA; thus, the ATNP with quenched fluorescence in the free state could realize signal activation through target binding-induced conformational change of the AAP, and then achieve on-demand treatment under image-guided irradiation. By using S6 aptamer as the model, in vitro and in vivo studies of A549 lung cancer verified that the ATNP greatly improved imaging contrast and specific destruction, suggesting a robust and versatile theranostic strategy for personalized medicine in future.Although nanomaterial-based theranostics have increased positive expectations from cancer treatment, it remains challenging to develop in vivo ``nano-doctors'' that provide high-contrast image-guided site-specific therapy. Here we designed an activatable theranostic nanoprobe (ATNP) via self-assembly of activatable aptamer probes (AAPs) on Au@Ag/Au nanoparticles (NPs). As both quenchers and heaters, novel Au@Ag/Au NPs were prepared, showing excellent fluorescence quenching and more effective near-infrared photothermal therapy than Au nanorods. The AAP comprised a thiolated aptamer and a fluorophore-labeled complementary DNA; thus, the ATNP with quenched fluorescence in the free state could realize signal activation through target binding-induced conformational change of the AAP, and then achieve on-demand treatment under image-guided irradiation. By using S6 aptamer as

  2. Seismic rupture modelling, strong motion prediction and seismic hazard assessment: fundamental and applied approaches; Modelisation de la rupture sismique, prediction du mouvement fort, et evaluation de l'alea sismique: approches fondamentale et appliquee

    Energy Technology Data Exchange (ETDEWEB)

    Berge-Thierry, C

    2007-05-15

    The defence to obtain the 'Habilitation a Diriger des Recherches' is a synthesis of the research work performed since the end of my Ph D. thesis in 1997. This synthesis covers the two years as post doctoral researcher at the Bureau d'Evaluation des Risques Sismiques at the Institut de Protection (BERSSIN), and the seven consecutive years as seismologist and head of the BERSSIN team. This work and the research project are presented in the framework of the seismic risk topic, and particularly with respect to the seismic hazard assessment. Seismic risk combines seismic hazard and vulnerability. Vulnerability combines the strength of building structures and the human and economical consequences in case of structural failure. Seismic hazard is usually defined in terms of plausible seismic motion (soil acceleration or velocity) in a site for a given time period. Either for the regulatory context or the structural specificity (conventional structure or high risk construction), seismic hazard assessment needs: to identify and locate the seismic sources (zones or faults), to characterize their activity, to evaluate the seismic motion to which the structure has to resist (including the site effects). I specialized in the field of numerical strong-motion prediction using high frequency seismic sources modelling and forming part of the IRSN allowed me to rapidly working on the different tasks of seismic hazard assessment. Thanks to the expertise practice and the participation to the regulation evolution (nuclear power plants, conventional and chemical structures), I have been able to work on empirical strong-motion prediction, including site effects. Specific questions related to the interface between seismologists and structural engineers are also presented, especially the quantification of uncertainties. This is part of the research work initiated to improve the selection of the input ground motion in designing or verifying the stability of structures. (author)

  3. Highly accessible Pt nanodots homogeneously decorated on Au nanorods surface for sensing

    International Nuclear Information System (INIS)

    Highlights: • Seed-growth of highly-dispersed catalytic Pt nanodot on Au nanorod (PtND@AuNR). • Good accessibility of catalytic sites was evidenced by its peroxidase-like activity. • Excellent assay performances of H2O2 at PtND@AuNR-based sensor. - Abstract: Some nanostructures are reported to possess enzyme-mimetic activities similar to those of natural enzymes. Herein, highly-dispersed Pt nanodots on Au nanorods (HD- PtNDs@AuNRs) with mimetic peroxidase activity were designed as an active electrode modifier for fabrication of a hydrogen peroxide (H2O2) electrochemical sensor. The HD-PtNDs@AuNRs were synthesized by a seed-mediated growth approach and confirmed by scanning electron microscopy, transmission electron microscopy, energy dispersive X-ray spectroscopy, and UV–vis spectroscopy. The electrochemical and catalytical performances of HD-PtNDs@AuNRs towards H2O2 reduction were investigated in detail by cyclic voltammetry and amperometry. The HD-PtNDs@AuNRs modified electrode displayed a high catalytic activity to H2O2 at −0.10 V (versus SCE), a rapid response within 5 s, a wide linear range of 2.0–3800.0 μM, a detection limit of 1.2 μM (S/N = 3), and a high sensitivity of 181 μA mM−1 cm−2. These results suggested a promising potential of fabricating H2O2 electrochemical sensor using HD- PtNDs@AuNRs

  4. Highly accessible Pt nanodots homogeneously decorated on Au nanorods surface for sensing

    Energy Technology Data Exchange (ETDEWEB)

    Feng, Xun [College of Chemistry, Jilin University, Changchun 130012 (China); Li, Xin [College of Electronic Science and Engineering, Jilin University, Changchun 130012 (China); Shi, Hongyan; Huang, Hao [College of Chemistry, Jilin University, Changchun 130012 (China); Wu, Xiaochun [CAS Key Laboratory of Standardization and Measurement for Nanotechnology, National Center for Nanoscience and Technology, Beijing 100190 (China); Song, Wenbo, E-mail: wbsong@jlu.edu.cn [College of Chemistry, Jilin University, Changchun 130012 (China)

    2014-12-10

    Highlights: • Seed-growth of highly-dispersed catalytic Pt nanodot on Au nanorod (PtND@AuNR). • Good accessibility of catalytic sites was evidenced by its peroxidase-like activity. • Excellent assay performances of H{sub 2}O{sub 2} at PtND@AuNR-based sensor. - Abstract: Some nanostructures are reported to possess enzyme-mimetic activities similar to those of natural enzymes. Herein, highly-dispersed Pt nanodots on Au nanorods (HD- PtNDs@AuNRs) with mimetic peroxidase activity were designed as an active electrode modifier for fabrication of a hydrogen peroxide (H{sub 2}O{sub 2}) electrochemical sensor. The HD-PtNDs@AuNRs were synthesized by a seed-mediated growth approach and confirmed by scanning electron microscopy, transmission electron microscopy, energy dispersive X-ray spectroscopy, and UV–vis spectroscopy. The electrochemical and catalytical performances of HD-PtNDs@AuNRs towards H{sub 2}O{sub 2} reduction were investigated in detail by cyclic voltammetry and amperometry. The HD-PtNDs@AuNRs modified electrode displayed a high catalytic activity to H{sub 2}O{sub 2} at −0.10 V (versus SCE), a rapid response within 5 s, a wide linear range of 2.0–3800.0 μM, a detection limit of 1.2 μM (S/N = 3), and a high sensitivity of 181 μA mM{sup −1} cm{sup −2}. These results suggested a promising potential of fabricating H{sub 2}O{sub 2} electrochemical sensor using HD- PtNDs@AuNRs.

  5. Enhanced electrocatalytic activity of the Au-electrodeposited Pt nanoparticles-coated conducting oxide for the quantum dot-sensitized solar cells

    Energy Technology Data Exchange (ETDEWEB)

    Yoon, Yeung-Pil; Kim, Jae-Hong; Ahn, Kwang-Soon, E-mail: kstheory@ynu.ac.kr [School of Chemical Engineering, Yeungnam University, Gyeongsan 712-749 (Korea, Republic of); Kang, Soon-Hyung [Department of Chemistry Education, Chonnam National University, Gwangju 500-757 (Korea, Republic of); Kim, Hyunsoo; Choi, Chel-Jong [School of Semiconductor and Chemical Engineering, Chonbuk National University, Jeonju 561-756 (Korea, Republic of); Kim, Kyong-Kook, E-mail: kim.kk@kpu.ac.kr [Department of Nano-Optical Engineering, Korea Polytechnic University, Siheung 429-793 (Korea, Republic of)

    2014-08-25

    Au was electrodeposited potentiostatically at 0.3 V for 5 min on nanoporous Pt nanoparticle-coated F-doped SnO{sub 2} (FTO/Pt) substrates. For comparison, Au-electrodeposited FTO (FTO/Au) and Au-uncoated FTO/Pt were prepared. FTO/Au showed large-sized Au clusters dispersed sparsely over FTO, which resulted in lower electrocatalytic activity than FTO/Pt. In contrast, FTO/Pt exhibited poor stability unlike FTO/Au due to poisoning by the adsorption of sulfur species. The Au-electrodeposited FTO/Pt (FTO/Pt/Au) consisted of small Au clusters deposited over the entire area of Pt due to the effective Au nucleation provided by nanoporous metallic Pt. FTO/Pt/Au exhibited enhanced electrocatalytic activity and excellent stability because the small Au particles well-dispersed over the nanoporous metallic Pt network provided numerous electrochemical reaction sites, and the Pt surface was not exposed to the electrolyte. When FTO/Pt/Au was used as the counter electrode (CE) of a quantum dot-sensitized solar cell, the significantly enhanced electrocatalytic activity of the FTO/Pt/Au CE facilitated the reduction reaction of S{sub n}{sup 2− }+ 2e{sup −} (CE) → S{sub n−1}{sup 2−} + S{sup 2−} at the CE/electrolyte interface, resulting in a significantly hindered recombination reaction, S{sub n}{sup 2− }+ 2e{sup −} (TiO{sub 2} in the photoanode) → S{sub n-1}{sup 2−} + S{sup 2−}, and significantly improved overall energy conversion efficiency.

  6. Enhanced electrocatalytic activity of the Au-electrodeposited Pt nanoparticles-coated conducting oxide for the quantum dot-sensitized solar cells

    International Nuclear Information System (INIS)

    Au was electrodeposited potentiostatically at 0.3 V for 5 min on nanoporous Pt nanoparticle-coated F-doped SnO2 (FTO/Pt) substrates. For comparison, Au-electrodeposited FTO (FTO/Au) and Au-uncoated FTO/Pt were prepared. FTO/Au showed large-sized Au clusters dispersed sparsely over FTO, which resulted in lower electrocatalytic activity than FTO/Pt. In contrast, FTO/Pt exhibited poor stability unlike FTO/Au due to poisoning by the adsorption of sulfur species. The Au-electrodeposited FTO/Pt (FTO/Pt/Au) consisted of small Au clusters deposited over the entire area of Pt due to the effective Au nucleation provided by nanoporous metallic Pt. FTO/Pt/Au exhibited enhanced electrocatalytic activity and excellent stability because the small Au particles well-dispersed over the nanoporous metallic Pt network provided numerous electrochemical reaction sites, and the Pt surface was not exposed to the electrolyte. When FTO/Pt/Au was used as the counter electrode (CE) of a quantum dot-sensitized solar cell, the significantly enhanced electrocatalytic activity of the FTO/Pt/Au CE facilitated the reduction reaction of Sn2− + 2e− (CE) → Sn−12− + S2− at the CE/electrolyte interface, resulting in a significantly hindered recombination reaction, Sn2− + 2e− (TiO2 in the photoanode) → Sn-12− + S2−, and significantly improved overall energy conversion efficiency.

  7. L’olivier au Maroc

    Directory of Open Access Journals (Sweden)

    El Mouhtadi Issam

    2014-03-01

    Full Text Available L’olivier est une culture traditionnelle sur le pourtour de la Méditerranée. Il est donc naturel de trouver cet arbre au Maroc où il est présent depuis des siècles. Cultivé surtout traditionnellement jusqu’à ses dernières années, il fait l’objet maintenant d’un plan de valorisation très ambitieux pour non seulement garder le Royaume à son niveau actuel (2e producteur mondial pour l’olive de conserve et 6e pour l’huile d’olive mais pour conquérir de nouveaux marchés au niveau mondial et profiter ainsi de l’engouement que connaît cette huile reconnue pour ses bienfaits. Le plan national « Maroc Vert » permet ainsi, grâce à des subventions conséquentes, non seulement de renouveler les vergers existant avec la variété traditionnelle picholine du Maroc, mais également la plantation de nouvelles variétés en super-intensif dans le but d’industrialiser au maximum de nouveaux vergers. Il en est de même pour la transformation des olives en huile de bonne qualité avec la mise en place d’unités de trituration modernes qui doivent supplanter à terme la multitude de « maâsra » et réduire ainsi l’impact environnemental dû aux margines. L’olive ne sera plus dans l’avenir que représentée par son huile et ses formes comestibles, mais les résidus de son extraction seront valorisés soit sous forme de combustible élaboré pour le grignon, soit sous forme d’une base de chimie verte pour les sous-produits du raffinage. D’autres applications sont actuellement à l’étude, car le Maroc à compris, comme tous les autres grands pays producteurs, que l’olive était un nouveau gisement de richesses.

  8. Study of Au+Au relativistic collisions with the Fopi-Phase I detector; Etude des collisions relativistes Au+Au avec le detecteur Fopi-Phase I

    Energy Technology Data Exchange (ETDEWEB)

    Dupieux, P.

    1995-01-01

    Au+Au relativistic collisions, in a 100-1000 MeV energy domain per nucleon, are described. Experiments have been carried out with the SIS accelerator at GSI/Darmstadt. Data are analysed with the FOPI-phase I detector. These data are compared with IQMD model (Isospin Quantum Molecular Dynamics) Predictions. (S.G). 80 refs., 77 figs., 5 tabs.

  9. English for au pairs the au pair's guide to learning English

    CERN Document Server

    Curtis, Lucy

    2014-01-01

    English for Au Pairs has interlinked stories about a group of au pairs new to England. Marta, an 18-year-old from Poland arrives in the UK to work as an au pair. Throughout her year-long stay she has many different experiences - some bad, some good - but with the support of her host family she finds new friends and improves her English. English for Au Pairs offers insight into the joys and difficulties of being an au pair while at the same time reinforcing English language learning through grammar explanations and exercises.

  10. Characteristic atom occupation patterns of Au3Cu, AuCu3, AuCuⅠ and AuCuⅡ based on experimental data of disordered alloys%以无序合金的实验数据为基础的Au3Cu,AuCu3,AuCuⅠ和AuCuⅡ的特征原子占据图

    Institute of Scientific and Technical Information of China (English)

    谢佑卿; 李艳芬; 刘心笔; 李晓波; 彭红建; 聂耀庄

    2011-01-01

    根据无序Au1-xCux合金的实验生成热和晶格常数得到只考虑近邻原子组态的特征原子的势能、体积和电子结构,计算L12-Au3Cu,L12-AuCu3和L10-AuCu化合物的特征原子占据(CAO)图、电子结构、能量和体积性质.Johasson-Linde(J-L)模型的CAO图表明,AuCuⅠ-AuCuⅡ转变是一个放热且体积缩小的反应,但正好与实验现象相反.根据Guymont-Feutelais-Legendre(G-F-L)模型的CAO图,AuCuⅡ晶胞由两个周期反相(PAD)的AuCuⅠ区域和两个PAD边界区域组成;从G-F-L模型的CAO图得出的公式可用来计算PAD AuCuⅠ区域和PAD边界区域的能量性质、体积性质和有序度及AuCuⅡ相的平均性质,计算结果与实验现象相吻合.%The potential energies, volumes and electronic structures of characteristic atoms coordinated by neighboring configurations were obtained from the experimental heats of formation and lattice parameters of disordered Au1-xCux alloys. From characteristic atom occupation (CAO) patterns of L12-Au3Cu, L12-AuCu3 and L10-AuCu compounds, their electronic structures, volumetric and energetic properties were calculated. The CAO pattern of Johasson-Linde(J-L) model shows that the transition AuCuⅠ→ AuCuⅡ is an exothermic and volume contraction reaction, which is opposite from experimental phenomena. According to CAO pattern of Guymont-Feutelais-Legendre(G-F-L) model, the AuCuⅡ cell consists of two periodic antidirection (PAD) AuCuⅠ regions and two PAD boundary regions. The equations derived from CAO pattern of G-F-L model can be used to calculate energetic properties, volumetric properties and ordering degrees of the PAD AuCul region and PAD boundary region, as well as corresponding average properties of the AuCuⅡ phase. The results are consistent with experimental phenomena.

  11. AU-EU “Strategic Partnership”

    DEFF Research Database (Denmark)

    Rodt, Annemarie Peen; Okeke, Jide

    2013-01-01

    This article appraises strategic partnership between the African Union (AU) and European Union (EU). It examines the context and nature of AU and EU security relations and explores the conditions under which partnership has a positive impact in this regard. This includes an evaluation of converge......This article appraises strategic partnership between the African Union (AU) and European Union (EU). It examines the context and nature of AU and EU security relations and explores the conditions under which partnership has a positive impact in this regard. This includes an evaluation...... of convergence between the two organizations and its effect or lack thereof on African security. The article concludes that events leading up to and initiatives following the 2007 Joint Africa–European Union Strategy have produced a degree of AU and EU convergence, which has had limited impact on the efficacy...

  12. Le curriculum scolaire au Chili

    OpenAIRE

    Cox, Cristián

    2012-01-01

    L’article examine l’usage historique du terme « curriculum » au Chili. Il aborde la configuration actuelle de la prescription curriculaire nationale : des « objectifs et contenus minimums », des « programmes d’études », et des « cartes de progrès des apprentissages ». On y décrit les institutions et les processus qui rendent compte de la genèse des définitions curriculaires en vigueur en 2010. Elles sont le résultat de deux étapes de réformes caractérisées par des processus consultatifs et pa...

  13. Portraits de femmes au Biafra

    OpenAIRE

    Ugochukwu, Françoise

    2011-01-01

    Cette étude considère l’impact de la guerre civile nigériane sur la vie quotidienne et les relations interpersonnelles des Biafrais telle qu’elle est présentée dans Femmes en guerre et autres nouvelles d’Achebe et Blow the Fire de Leslie Ofoegbu. Ces deux écrivains, dont l’un, déjà traduit dans plusieurs langues, a été le premier à projeter le pays igbo sur la scène internationale, et dont l’autre est une Écossaise mariée à un Nigérian et qui vécut au Biafra pendant les années de guerre, offr...

  14. Strain distributions of confined Au/Ag and Ag/Au nanoparticles

    Institute of Scientific and Technical Information of China (English)

    黄红华; 章英; 刘晓山; 骆兴芳; 袁彩雷; 叶双莉

    2015-01-01

    The strain distributions of Au/Ag and Ag/Au nanoparticles confined in the Al2O3 matrix with different core sizes are investigated by using the finite element method, respectively. The simulation results clearly indicate that the compressive strains exerted on the Au/Ag and Ag/Au nanoparticles can be induced by the Al2O3 matrix. Moreover, it can be found that the strain gradient existing in a Au/Ag nanoparticle is much larger than that in a Ag/Au nanoparticle, which could be due to the larger Young’s modulus of Au than that of Ag. With the core size increasing, the strain gradient existing in the Au/Ag nanoparticle becomes larger, while the strain gradient existing in the Ag/Au nanoparticle keeps constant. These different strain distributions may have significant infl uences on the structures and morphologies of the Au/Ag and Ag/Au nanoparticles, leading to the different physical properties for potential applications.

  15. Au, Ag and Au:Ag colloidal nanoparticles synthesized by pulsed laser ablation as SERS substrates

    Directory of Open Access Journals (Sweden)

    M. Vinod

    2014-12-01

    Full Text Available Chemically pure colloidal suspensions of gold and silver nanoparticles were synthesized using pulsed laser ablation. The dependence of laser fluence on the surface plasmon characteristics of the nanoparticles was investigated. Au:Ag colloidal suspensions were prepared by mixing highly monodisperse Au and Ag nanocolloids. The plasmon band of these mixtures was found to be highly sensitive to Au:Ag concentration ratio and wavelength of the laser beam used in the ablation process. The Au:Ag mixture consists of almost spherical shaped nanostructures with a tendency to join with adjacent ones. The surface enhanced Raman scattering activity of the Au, Ag and Au:Ag colloidal suspensions was tested using crystal violet as probe molecules. Enhancement in Raman signal obtained with Au:Ag substrates was found to be promising and strongly depends on its plasmon characteristics.

  16. Au, Ag and Au:Ag colloidal nanoparticles synthesized by pulsed laser ablation as SERS substrates

    Institute of Scientific and Technical Information of China (English)

    M. Vinod; K.G.Gopchandran

    2014-01-01

    Chemically pure colloidal suspensions of gold and silver nanoparticles were synthesized using pulsed laser ablation. The dependence of laser fluence on the surface plasmon characteristics of the nanoparticles was investigated. Au:Ag colloidal suspensions were prepared by mixing highly monodisperse Au and Ag nanocolloids. The plasmon band of these mixtures was found to be highly sensitive to Au:Ag concentration ratio and wavelength of the laser beam used in the ablation process. The Au:Ag mixture consists of almost spherical shaped nanostructures with a tendency to join with adjacent ones. The surface enhanced Raman scattering activity of the Au, Ag and Au:Ag colloidal suspensions was tested using crystal violet as probe molecules. Enhancement in Raman signal obtained with Au:Ag substrates was found to be promising and strongly depends on its plasmon characteristics.

  17. Low temperature fabrication and doping concentration analysis of Au/Sb ohmic contacts to n-type Si

    International Nuclear Information System (INIS)

    This paper investigates low temperature ohmic contact formation of Au/Sb to n-type Si substrates through AuSb/NiCr/Au metal stacks. Liquid epitaxy growth is utilized to incorporate Sb dopants into Si substrate in AuSi melt. The best specific contact resistivity achieved is 0.003 Ω ⋅ cm2 at 425 oC. Scanning electron microscopy (SEM) reveals inverted pyramidal crater regions at the metal/semiconductor interface, indicating that AuSi alloying efficiently occurs at such sites. Secondary ion mass spectroscopy (SIMS) shows that Sb atoms are successfully incorporated into Si as doping impurities during the anneal process, and the Sb doping concentration at the contact interface is found to be higher than the solid solubility limit in a Si crystal. This ohmic contacts formation method is suitable for semiconductor fabrication processes with limited thermal budget, such as post CMOS integration of MEMS

  18. Gold nanoparticles supported on mesoporous silica: origin of high activity and role of Au NPs in selective oxidation of cyclohexane

    Science.gov (United States)

    Wu, Pingping; Bai, Peng; Yan, Zifeng; Zhao, George X. S.

    2016-01-01

    Homogeneous immobilization of gold nanoparticles (Au NPs) on mesoporous silica has been achieved by using a one-pot synthesis method in the presence of organosilane mercapto-propyl-trimethoxysilane (MPTMS). The resultant Au NPs exhibited an excellent catalytic activity in the solvent-free selective oxidation of cyclohexane using molecular oxygen. By establishing the structure-performance relationship, the origin of the high activity of mesoporous supported Au catalyst was identified to be due to the presence of low-coordinated Au (0) sites with high dispersion. Au NPs were confirmed to play a critical role in the catalytic oxidation of cyclohexane by promoting the activation of O2 molecules and accelerating the formation of surface-active oxygen species.

  19. Low temperature fabrication and doping concentration analysis of Au/Sb ohmic contacts to n-type Si

    Energy Technology Data Exchange (ETDEWEB)

    Liu, J. Q.; Wang, C.; Zhu, T.; Wu, W. J. [MOE Key Laboratory of Fundamental Physical Quantities Measurement, School of Physics, Huazhong University of Science and Technology, Wuhan 430074 (China); Fan, J.; Tu, L. C., E-mail: tlc@hust.edu.cn [MOE Key Laboratory of Fundamental Physical Quantities Measurement, School of Physics, Huazhong University of Science and Technology, Wuhan 430074 (China); Institute of Geophysics, Huazhong University of Science and Technology, Wuhan 430074 (China)

    2015-11-15

    This paper investigates low temperature ohmic contact formation of Au/Sb to n-type Si substrates through AuSb/NiCr/Au metal stacks. Liquid epitaxy growth is utilized to incorporate Sb dopants into Si substrate in AuSi melt. The best specific contact resistivity achieved is 0.003 Ω ⋅ cm{sup 2} at 425 {sup o}C. Scanning electron microscopy (SEM) reveals inverted pyramidal crater regions at the metal/semiconductor interface, indicating that AuSi alloying efficiently occurs at such sites. Secondary ion mass spectroscopy (SIMS) shows that Sb atoms are successfully incorporated into Si as doping impurities during the anneal process, and the Sb doping concentration at the contact interface is found to be higher than the solid solubility limit in a Si crystal. This ohmic contacts formation method is suitable for semiconductor fabrication processes with limited thermal budget, such as post CMOS integration of MEMS.

  20. First-principles Study of the Au surfactant on the growth of Zn vacancies in ZnO nanostructures

    Institute of Scientific and Technical Information of China (English)

    刘亚明

    2007-01-01

    Influence of Au surfactant on the growth of Zn atom vacancies in ZnO nanostructures has been investigated by using first-principles slab calculations based on density functional theory.The adsorption of Au atoms on the Zn -terminated(0001)polar surface with a(2×2)sudace unit cell is studied by using a standard supercell model.It is found that (1)the binding energies of Au atoms on (0001)-Zn increase and the most stable position of the Au atom is invariable;(2)on the (0001)surface,the preferred sites for Zn atom vacancy are on the first layer of Zn atoms;(3)Under the Au surfactant,the Zn atom vacancies become more difficult to form.

  1. Investigation of the Phase Equilibria of Sn-Cu-Au Ternary and Ag-Sn-Cu-Au Quaternary Systems and Interfacial Reactions in Sn-Cu/Au Couples

    Science.gov (United States)

    Yen, Yee-Wen; Jao, Chien-Chung; Hsiao, Hsien-Ming; Lin, Chung-Yung; Lee, Chiapyng

    2007-02-01

    The phase equilibria of the Sn-Cu-Au ternary, Ag-Sn-Cu-Au quaternary systems and interfacial reactions between Sn-Cu alloys and Au were experimentally investigated at specific temperatures in this study. The experimental results indicated that there existed three ternary intermetallic compounds (IMCs) and a complete solid solubility between AuSn and Cu6Sn5 phases in the Sn-Cu-Au ternary system at 200°C. No quaternary IMC was found in the isoplethal section of the Ag-Sn-Cu-Au quaternary system. Three IMCs, AuSn, AuSn2, and AuSn4, were found in all couples. The same three IMCs and (Au,Cu)Sn/(Cu,Au)6Sn5 phases were found in all Sn-Cu/Au couples. The thickness of these reaction layers increased with increasing temperature and time. The mechanism of IMC growth can be described by using the parabolic law. In addition, when the reaction time was extended and the Cu content of the alloy was increased, the AuSn4 phase disappeared gradually. The (Au, Cu)Sn and (Cu,Au)6Sn5 layers played roles as diffusion barriers against Sn in Sn-Cu/Au reaction couple systems.

  2. Fire at a dry material burial site in Pierrefonds : atmospheric emissions of pollutants and health impacts; Incendie au site d'enfouissement de materiaux secs de Pierrefonds : emissions de polluants a l'atmosphere et impacts sur la sante

    Energy Technology Data Exchange (ETDEWEB)

    Beausoleil, M.

    2005-05-01

    The Quebec Health Agency for the City of Montreal was asked to evaluate the health risk associated with the atmospheric emissions associated with a fire that occurred at a dry material burial site in Pierrefonds in December 2004. The fire lasted several weeks, resulting in a release of pollutants into the ambient air of a residential district located near the site. Air emission concentration measurements were taken at 3 intervals in order to evaluate the health risks that the chemical substances posed to the residents in the area. During the few hours when the fire was out of control and while flames were visible, the concentrations of aldehydes, acids, polycyclic aromatic hydrocarbons and particulates in the plume of smoke were very high, causing residents to experience respiratory problems and irritations to eyes, nose and throat. However, as soon as the fire was controlled, the concentrations of these pollutants decreased quickly. Fire extinction efforts continued for several weeks. Although the concentrations of pollutants measured in the ambient air of the residential district were higher than those generally measured in this district and elsewhere on the island of Montreal, they were in the same order of magnitude as those measured occasionally in certain districts under similar circumstances. The fire was extinguished in February 2005 at which time the measured concentrations were very similar to those generally measured in the urban environment. However, the strong and unpleasant odours that persist, particularly in the evening, correspond to the high values of hydrogen sulphide (H{sub 2}S). The Health Agency has reassured the residents that these values do not present long term health risks, but recognizes that the situation constitutes a reduction in the quality of life for the residents that can have psychosocial impacts of which the long-term repercussions are difficult to measure. refs., tabs., figs.

  3. Tuning the spin, chirality, and adsorption site of metal-phthalocyanine on Au(111) surface with hydrogen atoms%氢原子吸附对金表面金属酞菁分子的吸附位置、自旋和手征性的调控

    Institute of Scientific and Technical Information of China (English)

    肖文德; 刘立巍; 杨锴; 张礼智; 宋博群; 杜世萱; 高鸿钧

    2015-01-01

    Metal-phthalocyanines (MPcs) and their derivates have attracted increasing interest in recent years, due to their potential applications in molecular electronics, spintronics, sensors, and so on. To this end, it is essential to tune the structural, electronic and spin properties of MPcs. Using the low-temperature scanning tunneling microscopy (LT-STM), we demonstrate that the spin, chirality and adsorption site of MnPc on Au(111) surface can be tuned by hydrogen atoms. STM experiments and density functional theory (DFT) calculations reveal that the preferential adsorption sites for the MnPc molecules may switch from the fcc regions to the hcp regions on the Au(111) surface after a hydrogen atom is adsorbed on top of the central Mn ion of each MnPc molecule. Moreover, the molecular spin decreases from S=3/2 to S =1 and the molecule-substrate coupling is weakened after the adsorption of a hydrogen atom on a MnPc molecule, leading to the quenching of Kondo effect at 4.2 K. However, the molecular spin and Kondo effect can be recovered by local voltage pulse or sample heating. Adsorption of three hydrogen atoms on a MnPc molecule not merely lowers the molecular symmetry from 4-to 2-fold, but also breaks down the mirror symmetry of the entire adsorbate complex (molecule and surface), thus rendering it to become chiral without any realignment at the surface. Dehydrogenation of the adsorbate by means of inelastic electron tunneling can also restore the mirror symmetry of the adsorbate complex. STM experiments as well as DFT calculations show that the chirality is actually imprinted into the molecular electronic system by the surface, i.e., the lowest unoccupied orbital is devoid of mirror symmetry. Our novel reversible spin and hand control scheme can be easily realized at single-molecule level, thus opening up a new avenue to broader applications based on the molecular electronic and spin states.%实现单个功能有机分子构型、电子结构和自旋态的可逆调

  4. Vibrational properties at the ordered metallic surface alloy system Au(110)-1×2-Pd

    Science.gov (United States)

    Kheffache, Sedik; Chadli, Rabah; Khater, Antoine

    2016-06-01

    We present a calculation for the vibrational properties of the ordered surface alloy Au(110)-1×2-Pd on a crystalline substrate of Au. The surface phonon dispersion curves and the local vibrations densities of states (LDOS) are calculated in the harmonic approximation for the system, using the phase field matching theory (PFMT) method and associated real space Green’s functions. In particular, it is shown that the surface alloy presents optic vibrational modes above the Au bulk bands, along the directions of high-symmetry ΓX¯, XS¯, SY¯ and Y Γ¯ of the corresponding two-dimensional Brillouin zone. Measurements of the surface phonon dispersion branches can hence be made by different techniques such as helium atom scattering (HAS) to compare with. The calculated LDOS for Au and Pd atomic sites in the four top surface atomic layers span a wider range of frequencies than those for the individual Au(110) or Pd(110) metallic surfaces. These LDOS provide a spectral signature for the progressive transition from the surface dynamics to that of the Au crystal bulk. Knowledge of these LDOS for the surface alloy can also serve as an input for modeling the diffusion and reaction rates of chemical species at its surface.

  5. Au nanoparticles on tryptophan-functionalized graphene for sensitive detection of dopamine

    Energy Technology Data Exchange (ETDEWEB)

    Lian, Qianwen; Luo, Ai; An, Zhenzhen; Li, Zhuang; Guo, Yongyang; Zhang, Dongxia [Key Laboratory of Bioelectrochemistry & Environmental Analysis of Gansu Province, College of Geography and Environment Science, Northwest Normal University, 730070, Lanzhou (China); Xue, Zhonghua [College of Chemistry and Chemical Engineering, Northwest Normal University, 730070, Lanzhou (China); Zhou, Xibin, E-mail: zhouxb@nwnu.edu.cn [Key Laboratory of Bioelectrochemistry & Environmental Analysis of Gansu Province, College of Geography and Environment Science, Northwest Normal University, 730070, Lanzhou (China); Lu, Xiaoquan, E-mail: Luxq@nwnu.edu.cn [College of Chemistry and Chemical Engineering, Northwest Normal University, 730070, Lanzhou (China)

    2015-09-15

    Graphical abstract: - Highlights: • A novel AuNPs/Trp-GR composite was fabricated by directly electrochemical deposition. • The composite exhibited excellent electrocatalytic activity towards DA. • The proposed method was applied to real samples. - Abstract: A novel and uniform gold nanoparticles/tryptophan-functionalized graphene nanocomposite (AuNPs/Trp-GR) has been successfully fabricated by directly electrochemical depositing gold onto the surface of tryptophan-functionalized graphene (Trp-GR). The nanostructure of AuNPs/Trp-GR was characterized by using scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDS). It was demonstrated that Au nanoparticles were well dispersed on the surface of Trp-GR which might attribute to the more binding sites provided by Trp-GR for the formation of Au nanoparticles. The electrocatalytic activity of the AuNPs/Trp-GR towards the dopamine (DA) was systematically investigated using cyclic voltammetry (CV) and differential pulse voltammetry (DPV). Under optimum conditions, a wide and valuable linear range (0.5–411 μM), a low detection limit (0.056 μM, S/N = 3), good repeatability and stability were obtained for the determination of DA. Furthermore, the modified electrode was successfully applied to real samples analysis.

  6. Preparation and Catalytic Activity for Aerobic Glucose Oxidation of Crown Jewel Structured Pt/Au Bimetallic Nanoclusters

    Science.gov (United States)

    Zhang, Haijun; Wang, Liqiong; Lu, Lilin; Toshima, Naoki

    2016-08-01

    Understanding of the “structure-activity” relations for catalysts at an atomic level has been regarded as one of the most important objectives in catalysis studies. Bimetallic nanoclusters (NCs) in its many types, such as core/shell, random alloy, cluster-in-cluster, bi-hemisphere, and crown jewel (one kind of atom locating at the top position of another kind of NC), attract significant attention owing to their excellent optical, electronic, and catalytic properties. PVP-protected crown jewel-structured Pt/Au (CJ-Pt/Au) bimetallic nanoclusters (BNCs) with Au atoms located at active top sites were synthesized via a replacement reaction using 1.4-nm Pt NCs as mother clusters even considering the fact that the replacement reaction between Pt and Au3+ ions is difficult to be occurred. The prepared CJ-Pt/Au colloidal catalysts characterized by UV-Vis, TEM, HR-TEM and HAADF-STEM-EELS showed a high catalytic activity for aerobic glucose oxidation, and the top Au atoms decorating the Pt NCs were about 15 times more active than the Au atoms of Au NCs with similar particle size.

  7. Controlled Synthesis of Au@AgAu Yolk-Shell Cuboctahedra with Well-Defined Facets.

    Science.gov (United States)

    Londono-Calderon, Alejandra; Bahena, Daniel; Yacaman, Miguel J

    2016-08-01

    The synthesis of Au@AgAu yolk-shell cuboctahedra nanoparticles formed by galvanic replacement in a seed-mediated method is described. Initially, single-crystal Au seeds are used for the formation of Au@Ag core-shell nanocubes, which serve as the template material for the deposition of an external Au layer. The well-controlled synthesis yields the formation of cuboctahedra nanoparticles with smooth inner and outer Au/Ag surfaces. The deposition/oxidation process is described to understand the formation of cuboctahedra and octahedra nanoparticles. The Au core maintains the initial morphology of the seed and remains static at the center of the yolk-shell because of residual Ag. Structural analysis of the shell indicates intrinsic stacking faults (SFs) near the surface. Energy dispersive X-ray spectroscopy (EDS) and X-ray photoelectron spectroscopy (XPS) compositional analysis show an Au-Ag nonordered alloy forming the shell. The three-dimensional structure of the nanoparticles presented open facets on the [111] as observed by electron tomography SIRT reconstruction over a stack of high-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM) images. The geometrical model was validated by analyzing the direction of streaks in coherent nanobeam diffraction (NBD). The catalytic activity was evaluated using a model reaction based on the reduction of 4-nitrophenol (4-NTP) by NaBH4 in the presence of Au@AgAu yolk-shell nanoparticles. PMID:27385583

  8. Thermodynamic assessment of Au-La and Au-Er binary systems

    Energy Technology Data Exchange (ETDEWEB)

    Dong, H.Q., E-mail: hongqun.dong@aalto.fi [Department of Electronics, Aalto University School of Science and Technology, FIN-02601 Espoo (Finland); Tao, X.M. [Key Laboratory of New Processing Technology for Nonferrous Metals and Materials of Ministry of Education, Department of Physics, Guangxi University, Nanning 530004 (China); Liu, H.S. [Scientific Center of Phase Diagrams and Materials Design, Central South University, Changsha, Hunan 410083 (China); Laurila, T.; Paulastro-Kroeckel, M. [Department of Electronics, Aalto University School of Science and Technology, FIN-02601 Espoo (Finland)

    2011-03-31

    Research highlights: > It's the first time that Au-La and Au-Er binary systems were thermodynamically assessed since 1985. > Besides, in the present work, the ab initio approach has been employed to calculate the formation enthalpies of the IMCs involved in Au-Er and Au-La binary systems, and then, by combining with all of the available experimental information, these two-system were thermodynamically optimized via CALPHAD method. Therefore, a more reliable thermodynamic description has been obtained for these systems. - Abstract: Phase relationships in Au-La and Au-Er binary systems have been thermodynamically assessed by using the CALPHAD technique. The existing thermodynamic descriptions of the systems were improved by incorporating the ab initio calculated enthalpies of formation of the intermetallic compounds, except for the Au{sub 51}La{sub 14} and Au{sub 10}Er{sub 7} phases. All the binary intermetallic compounds were treated as stoichiometric phases, while the solution phases, including liquid, fcc, bcc, and dhcp, were treated as substitutional solution phases and the excess Gibbs energies were formulated with Redlich-Kister polynomial function. As a result, two self-consist thermodynamic data sets for describing the Au-La and Au-Er binary systems were obtained.

  9. Facile synthesis of Au/ZnO nanoparticles and their enhanced photocatalytic activity for hydroxylation of benzene

    Indian Academy of Sciences (India)

    Hang Yu; Hai Ming; Jingjing Gong; Haitao Li; Hui Huang; Keming Pan; Yang Liu; Zhenhui Kang; Jie Wei; Dongtian Wang

    2013-06-01

    Au/ZnO nanocomposites have been prepared by a simple chemical method. For the first time, the nanocomposites were directly used as photocatalysts for hydroxylation of aromatic hydrocarbons under UV and visible light irradiation. The results show that the as-prepared photocatalysts display high photocatalytic activity for UV and visible catalytic hydroxylation of benzene. Without the assistance of any solvent or additive, high selectivity and high conversion efficiency were still obtained. Different photocatalytic mechanisms were proposed depending on whether excitation happens on ZnO semiconductor or on the surface plasmon band of Au. The former is Au nanoparticles act as electron buffer due to irradiation by UV light and ZnO nanoparticles as reactive sites for hydroxylation of benzene, the latter is that Au nanoparticles act as light harvesters and inject electrons into ZnO conduction band and as photocatalytic sites under visible light irradiation.

  10. Innovation et recomposition territoriale au Maroc

    OpenAIRE

    Boujrouf, Saïd

    2013-01-01

    Introduction Les processus de recomposition territoriale au Maroc se caractérisent par une dynamique continue, reflet des grands changements qui ont affecté les différents secteurs du pays au cours du xxe siècle. Le renouvellement territorial au Maroc est un processus de recomposition permanent, depuis les trames traditionnelles (qu’elles soient tribale, confessionnelle liée aux confréries ou encore « seigneuriale » caïdale) jusqu’aux maillages territoriaux les plus récents en communes et rég...

  11. Être notable au Maghreb

    OpenAIRE

    Abouhani, Abdelghani; Amri-Salameh, Nelly; Blili, Leïla; Boubrik, Rahal; Boujarra, Hussein; Cattedra, Raffaele; CATUSSE, Myriam; Cheraï, Ahmed; Ettayeb, Mahmoud; Feneyrol, Olivier; Hénia, Abdelhamid; Jaïdi, Houcine; Kenbib, Mohammed; Khouaja, Ahmed; Lafi, Nora

    2014-01-01

    Le discours dominant dans les pays du Maghreb continue de stigmatiser les figures de notables dits traditionnels au nom de la modernité. L’usage scientifique de la notion de notable n’est pas pour autant disqualifié. Le présent ouvrage s’intéresse au système élitaire au Maghreb sur la longue durée, de l’Antiquité à nos jours. Il en étudie la dynamique en rapport avec les formes historiques du pouvoir et montre comment la notabilité a pris avec le temps des figures changeantes et des nominatio...

  12. Becoming independent through au pair migration

    DEFF Research Database (Denmark)

    Dalgas, Karina Märcher

    2015-01-01

    . This article argues that, despite this critique, au pairing does play an important formative role for young Filipinas because it opens up for experiences abroad that enable them to be recognised as independent adults in Philippine society. Rather than autonomy, however, au pairs define their independence...... in terms of their capacity to assume responsibility for others, thereby achieving a position of social respect. Based on ethnographic fieldwork in Denmark and the Philippines, this article explores how young Filipinas use the social, economic, and cultural resources they gain from their au pair stay abroad...

  13. Clinical evaluation of short-life radioactive source Au-198 grain

    International Nuclear Information System (INIS)

    Au-198 grain has been used as a new source in brachytherapy instead of Rn-seed since September 1975 in Japan. A total of 60 cases with malignant tumors of the oral cavity treated with Au-198 grain during the period of September 1975 to November 1978 were analyzed. Nineteen cases were treated with Au-198 grain alone, twenty-nine were with combined external beam therapy and the other twelve were treated as a boost implant for Radium needles or as a recurrent disease. Two-year local recurrence free rates were 78% (7/9) by Au-198 grain alone and 67% (10/15) by Au-198 grain combined with external beam therapy. The frequency of local necrosis following the combined therapy was inevitably higher than Au-198 grain alone. However, these results were somewhat better than the results obtained from treatment of tongue cancer using Rn seed with or without external beam which reported previously. An analysis was also made of the local condition of the treated area applying with the TDF values. A suitable permanent implant dose of Au-198 grain might be slightly lower than Rn seed considering from the TDF value analysis. The Au-198 grain technique seemed to be an excellent choice of treatment as far as the lesion was small or superficial enough, or the lesion was locating in the sites anatomically to be not able to apply Radium needles. The technique has also an advantage to be applicable without severe discomfort to the patient and less exposure to the operator compared to the Radium needle technique. (author)

  14. Synthesis of vinyl-terminated Au nanoprisms and nanooctahedra mediated by 3-butenoic acid: direct Au@pNIPAM fabrication with improved SERS capabilities.

    Science.gov (United States)

    Casado-Rodriguez, M A; Sanchez-Molina, M; Lucena-Serrano, A; Lucena-Serrano, C; Rodriguez-Gonzalez, B; Algarra, M; Diaz, A; Valpuesta, M; Lopez-Romero, J M; Perez-Juste, J; Contreras-Caceres, R

    2016-02-28

    Here we describe the first seedless synthesis of vinyl-terminated Au nanotriangular prisms (AuNTPs) and nanooctahedra (AuNOC) in aqueous media. This synthesis is performed by chemical reduction of chloroauric acid (HAuCl4) with 3-butenoic acid (3BA) in the presence of benzyldimethylammonium chloride (BDAC). The principal novelties of the presented method are the use of a mixture of 3BA and BDAC, the synthesis of gold prisms and octahedra with controllable size, and the presence of terminal double bonds on the metal surface. Initially this method produces a mixture of triangular gold nanoprisms and octahedra; however, both morphologies are successfully separated by surfactant micelle induced depletion interaction, reaching percentages up to ∼90%. Moreover, the alkene moieties present on the gold surface are exploited for the fabrication of hybrid core@shell particles. Gold octahedra and triangular prisms are easily encapsulated by free radical polymerization of N-isopropylacrylamide (NIPAM). Finally, in order to obtain a gold core with the most number of tips, AuNTP@pNIPAM microgels were subjected to gold core overgrowth, thus resulting in star-shaped nanoparticles (AuSTs@pNIPAM). We use 4-amino-benzenethiol as the model analyte for SERS investigations. As expected, gold cores with tips and high curvature sites produced the highest plasmonic responses.

  15. Synthesis of ultrathin face-centered-cubic Au@Pt and Au@Pd core-shell nanoplates from hexagonal-close-packed Au square sheets

    KAUST Repository

    Fan, Zhanxi

    2015-03-17

    The synthesis of ultrathin face-centered-cubic (fcc) Au@Pt rhombic nanoplates is reported through the epitaxial growth of Pt on hexagonal-close-packed (hcp) Au square sheets (AuSSs). The Pt-layer growth results in a hcp-to-fcc phase transformation of the AuSSs under ambient conditions. Interestingly, the obtained fcc Au@Pt rhombic nanoplates demonstrate a unique (101)f orientation with the same atomic arrangement extending from the Au core to the Pt shell. Importantly, this method can be extended to the epitaxial growth of Pd on hcp AuSSs, resulting in the unprecedented formation of fcc Au@Pd rhombic nanoplates with (101)f orientation. Additionally, a small amount of fcc (100)f-oriented Au@Pt and Au@Pd square nanoplates are obtained with the Au@Pt and Au@Pd rhombic nanoplates, respectively. We believe that these findings will shed new light on the synthesis of novel noble bimetallic nanostructures. Phase change: Ultrathin Au@Pt and Au@Pd core-shell nanoplates were prepared from Au square sheets. A phase transformation from hexagonal close-packed (hcp) to face-centered cubic (fcc) is observed upon coating the hcp Au square sheets with Pt or Pd under ambient conditions. The prepared fcc Au@Pt and Au@Pd rhombic nanoplates demonstrate unique (101)f orientation (picture shows a typical fcc Au@Pt rhombic nanoplate). © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  16. Rapid Processing of Turner Designs Model 10-Au-005 Internally Logged Fluorescence Data

    Science.gov (United States)

    Continuous recording of dye fluorescence using field fluorometers at selected sampling sites facilitates acquisition of real-time dye tracing data. The Turner Designs Model 10-AU-005 field fluorometer allows for frequent fluorescence readings, data logging, and easy downloading t...

  17. Governing the morphology of Pt-Au heteronanocrystals with improved electrocatalytic performance

    Science.gov (United States)

    Mourdikoudis, Stefanos; Chirea, Mariana; Zanaga, Daniele; Altantzis, Thomas; Mitrakas, Manasis; Bals, Sara; Liz-Marzán, Luis M.; Pérez-Juste, Jorge; Pastoriza-Santos, Isabel

    2015-05-01

    Platinum-gold heteronanostructures comprising either dimer (Pt-Au) or core-satellite (Pt@Au) configurations were synthesized by means of a seeded growth procedure using platinum nanodendrites as seeds. Careful control of the reduction kinetics of the gold precursor can be used to direct the nucleation and growth of gold nanoparticles on either one or multiple surface sites simultaneously, leading to the formation of either dimers or core-satellite nanoparticles, respectively, in high yields. Characterization by electron tomography and high resolution electron microscopy provided a better understanding of the actual three-dimensional particle morphology, as well as the Au-Pt interface, revealing quasi-epitaxial growth of Au on Pt. The prepared Pt-Au bimetallic nanostructures are highly efficient catalysts for ethanol oxidation in alkaline solution, showing accurate selectivity, high sensitivity, and improved efficiency by generating higher current densities than their monometallic counterparts.Platinum-gold heteronanostructures comprising either dimer (Pt-Au) or core-satellite (Pt@Au) configurations were synthesized by means of a seeded growth procedure using platinum nanodendrites as seeds. Careful control of the reduction kinetics of the gold precursor can be used to direct the nucleation and growth of gold nanoparticles on either one or multiple surface sites simultaneously, leading to the formation of either dimers or core-satellite nanoparticles, respectively, in high yields. Characterization by electron tomography and high resolution electron microscopy provided a better understanding of the actual three-dimensional particle morphology, as well as the Au-Pt interface, revealing quasi-epitaxial growth of Au on Pt. The prepared Pt-Au bimetallic nanostructures are highly efficient catalysts for ethanol oxidation in alkaline solution, showing accurate selectivity, high sensitivity, and improved efficiency by generating higher current densities than their

  18. Propylene epoxidation over biogenic Au/TS-1 catalysts by Cinnamomum camphora extract in the presence of H2 and O2

    Science.gov (United States)

    Du, Mingming; Huang, Jiale; Sun, Daohua; Li, Qingbiao

    2016-03-01

    The Au/TS-1 catalysts with different Au nanoparticles (NPs) sizes ranging from 3.1 to 8.4 nm but the same Au loading of 0.5 wt% were prepared by Cinnamomum camphora (CC) extract, and were used for propylene epoxidation. The results showed that the interaction between Au and TS-1 support surface is important for propylene epoxidation and much smaller Au NPs (<3 nm) are the dominant active sites. After reaction of 100 h, there is no decreasing in both the activity and the PO selectivity for the Au/TS-1 catalysts, and only 1.8 wt% of the carbonaceous deposits on the surface of the catalyst after reaction, suggesting that the desorption of the product from the modified catalysts surface by residual biomolecules is much easier.

  19. Et pourquoi pas au CERN ?

    CERN Multimedia

    Staff Association

    2015-01-01

    Télétravail ou travail à distance, aménagement des horaires de travail et autres évolutions favorables à un meilleur équilibre vie privée et vie professionnelle sont adoptés par nombre d’entreprises et d’organisations !   Rendu possible grâce au développement de nouvelles technologies dont Internet, le travail à distance séduit de plus en plus de personnels, ainsi que de plus en plus de sociétés qui y trouvent des avantages en matière de gestion de l’espace, de sécurité (moins de trajets domicile-entreprise), de développement durable (moins de pollution), de motivation et de bien-être de leurs personnels. Les horaires aménagés, voire les « core-hours1 », sont également des pratiques de plus e...

  20. Longitudinal scaling of net-protons in AuAu and pp collisions at RHIC energies

    Science.gov (United States)

    Videbaek, Flemming

    2008-10-01

    BRAHMS has studied net-protons distributions in Au+Au and p+p collisions at √sNN=62.4 and 200 GeV. Net-proton distributions reflect the net-baryon yields and can be used to extract the nuclear stopping in the collisions, thus providing information on baryon number transport and energy available for particle production. The talk will present final and preliminary results from the above mentioned systems. It will be shown that in p+p and in Au+Au central collisions that net-proton distributions exhibit longitudinal scaling once the target contribution to the projectile rapidity range is corrected for. The difference between p+p and Au+Au will be discussed. Aspects of future measurements at the LHC of net-baryons at mid-rapidity will be brought forth.

  1. Studying of the photoluminescence characteristics of Au(0)@Au(I)-thiolate core–shell nanoclusters

    International Nuclear Information System (INIS)

    The photoluminescence characteristics of Au(0)@Au(I)-thiolate Core–shell nanoclusters (Au-NCs), whose size is <2 nm, are investigated. We use the time-resolved single-photon counting technique and the transient absorption technique to distinguish the mechanism of the photoluminescence of Au-NCs. The dynamic spectral data show that the photoluminescence mechanism should be composed of the fluorescence and the phosphorescence. Meanwhile, Au-NCs have the aggregation induced photoluminescence enhancement property, which is attributed to the suppression of conversion from the singlet state to triplet state when they aggregated together. In addition, the photoluminescence characteristics of aggregated Au-NCs should be further improved through infiltrating them into photonic crystals

  2. Charged hadron transverse momentum distributions in Au+Au collisions at S=200 GeV

    Science.gov (United States)

    Roland, Christof; PHOBOS Collaboration; Back, B. B.; Baker, M. D.; Barton, D. S.; Betts, R. R.; Ballintijn, M.; Bickley, A. A.; Bindel, R.; Budzanowski, A.; Busza, W.; Carroll, A.; Decowski, M. P.; García, E.; George, N.; Gulbrandsen, K.; Gushue, S.; Halliwell, C.; Hamblen, J.; Heintzelman, G. A.; Henderson, C.; Hofman, D. J.; Hollis, R. S.; Hołyński, R.; Holzman, B.; Iordanova, A.; Johnson, E.; Kane, J. L.; Katzy, J.; Khan, N.; Kucewicz, W.; Kulinich, P.; Kuo, C. M.; Lin, W. T.; Manly, S.; McLeod, D.; Michałowski, J.; Mignerey, A. C.; Nouicer, R.; Olszewski, A.; Pak, R.; Park, I. C.; Pernegger, H.; Reed, C.; Remsberg, L. P.; Reuter, M.; Roland, C.; Roland, G.; Rosenberg, L.; Sagerer, J.; Sarin, P.; Sawicki, P.; Skulski, W.; Steadman, S. G.; Steinberg, P.; Stephans, G. S. F.; Stodulski, M.; Sukhanov, A.; Tang, J.-L.; Teng, R.; Trzupek, A.; Vale, C.; van Nieuwenhuizen, G. J.; Verdier, R.; Wadsworth, B.; Wolfs, F. L. H.; Wosiek, B.; Woźniak, K.; Wuosmaa, A. H.; Wysłouch, B.

    2003-03-01

    We present transverse momentum distributions of charged hadrons produced in Au+Au collisions at sqrt(s_NN) = 200 GeV. The evolution of the spectra for transverse momenta p_T from 0.25 to 5GeV/c is studied as a function of collision centrality over a range from 65 to 344 participating nucleons. We find a significant change of the spectral shape between proton-antiproton and peripheral Au+Au collisions. Comparing peripheral to central Au+Au collisions, we find that the yields at the highest p_T exhibit approximate scaling with the number of participating nucleons, rather than scaling with the number of binary collisions.

  3. Direct methods determination of the Si(111)-(6x6)Au surface structure

    DEFF Research Database (Denmark)

    Grozea, D.; Landree, E.; Marks, L.D.;

    1998-01-01

    The atomic structure of the Au 6 x 6 on Si(111) phase has been determined using direct methods and surface X-ray diffraction data. This surface structure is very complicated, with 14 independent gold atoms, relaxations in 24 independent silicon sites and three partially occupied gold sites. In on...... the gold structures in the coverage range 0.8-1.5 monolayers as pseudo-glasses with strong short-range order but varying degrees of long-range order. (C) 1998 Elsevier Science B.V. All rights reserved.......The atomic structure of the Au 6 x 6 on Si(111) phase has been determined using direct methods and surface X-ray diffraction data. This surface structure is very complicated, with 14 independent gold atoms, relaxations in 24 independent silicon sites and three partially occupied gold sites. In one...

  4. Site-selective nanoscale-polymerization of pyrrole on gold nanoparticles via plasmon induced charge separation.

    Science.gov (United States)

    Takahashi, Y; Furukawa, Y; Ishida, T; Yamada, S

    2016-04-28

    We proposed a nanoscale oxidative polymerization method which enables site-selective deposition on the surface of gold nanoparticles (AuNPs) combined with TiO2 by using plasmon induced charge separation (PICS) under visible-to-near infrared (IR) light irradiation. The method also revealed that the anodic site of PICS was located at the surface of AuNPs.

  5. Electrical conduction through self-assembled monolayers in molecular junctions: Au/molecules/Au versus Au/molecule/PEDOT:PSS/Au

    International Nuclear Information System (INIS)

    We fabricated and characterized a large number of octanedithiol (denoted as DC8) molecular devices as vertical metal-molecule-metal structure with or without using an intermediate conducting polymer layer of poly (3,4-ethylenedioxythiophene) stabilized with poly(4-styenesulfonic acid) (called as PEDOT:PSS). The electronic transport properties of DC8 molecular devices with and without PEDOT:PSS layer were statistically compared in terms of current density and device yield. The yields of the working molecular devices were found to be ∼ 1.75% (84 out of 4800 devices) for Au/DC8/Au junctions and ∼ 58% (74 out of 128 devices) for Au-DC8/PEDOT:PSS/Au junctions. The tunneling decay constants were obtained with the Simmons tunneling model and a multibarrier tunneling model for two kinds of molecular devices with and without PEDOT:PSS layer.

  6. Proton channeling in Au at low energies

    International Nuclear Information System (INIS)

    The electronic energy loss for low velocity protons channeled in the direction single crystal Au is calculated. The spatial distribution of valence electronic density in Au is calculated using Tight Binding Linear Muffin Tin Method. The proton trajectories are determined by numerical integration of the classical motion equation, and the energy loss is evaluated using the calculated valence electronic density in the friction term. The results allow to describe qualitatively the non linear behavior of energy loss with ion velocity observed experimentally. (author)

  7. Surface structures of Au-Pt bimetallic nanoclusters on thin film Al2O3/NiAl(100) probed with CO

    Science.gov (United States)

    Li, Y. D.; Hong, T. C.; Liao, T. W.; Luo, M. F.

    2013-12-01

    With infrared reflection absorption spectra and temperature-programmed desorption of CO as a probe molecule, we investigated the surface structure of Au-Pt bimetallic nanoclusters on thin-film Al2O3/NiAl(100) under ultrahigh vacuum conditions. Vapor Au and Pt (0.0-2.0 ML) were sequentially deposited onto Al2O3/NiAl(100) at 300 K to form bimetallic clusters; under the kinetic constraint, the order of the metal deposition made a variation in the surface structure of the grown clusters. For the deposition of Au onto Pt clusters (first Pt and then Au), the deposited Au decorated preferentially and then aggregated the edge sites of Pt clusters, instead of decorating the rest of Pt surface. For the metal deposition in the reverse order, the deposited Pt covered uniformly the surface of existing Au clusters and no preferential adsorption site was indicated. The infrared absorption for CO on Au sites was significantly enhanced when alloying occurred; this enhancement is primarily a local field effect depending on the coordination of CO-binding Au, and hence provides additional structural characterization of the grown clusters.

  8. Electrochemical Characterization of Protein Adsorption onto YNGRT-Au and VLGXE-Au Surfaces

    OpenAIRE

    Hanna Trzeciakiewicz; Jose Esteves-Villanueva; Rania Soudy; Kamaljit Kaur; Sanela Martic-Milne

    2015-01-01

    The adsorption of the proteins CD13, mucin and bovine serum albumin on VLGXE-Au and YNGRT-Au interfaces was monitored by electrochemical impedance spectroscopy in the presence of [Fe(CN)6]3−/4−. The hydrophobicity of the Au surface was tailored using specific peptides, blocking agents and diluents. The combination of blocking agents (ethanolamine or n-butylamine) and diluents (hexanethiol or 2-mercaptoethanol) was used to prepare various peptide-modified Au surfaces. Protein adsorption onto t...

  9. Unravelling Thiol’s Role in Directing Asymmetric Growth of Au Nanorod–Au Nanoparticle Dimers

    KAUST Repository

    Huang, Jianfeng

    2015-12-15

    Asymmetric nanocrystals have practical significance in nanotechnologies but present fundamental synthetic challenges. Thiol ligands have proven effective in breaking the symmetric growth of metallic nanocrystals but their exact roles in the synthesis remain elusive. Here, we synthesized an unprecedented Au nanorod-Au nanoparticle (AuNR-AuNP) dimer structure with the assistance of a thiol ligand. On the basis of our experimental observations, we unraveled for the first time that the thiol could cause an inhomogeneous distribution of surface strains on the seed crystals as well as a modulated reduction rate of metal precursors, which jointly induced the asymmetric growth of monometallic dimers. © 2015 American Chemical Society.

  10. Apprentissages techniques : L'apprentissage au CERN

    CERN Multimedia

    2004-01-01

    APPRENTISSAGES TECHNIQUES GESTION ET DEVELOPPEMENT DU PERSONNEL HR/PMD L'APPRENTISSAGE AU CERN pour les professions d'électronicien(ne) et de laborantin(e) en physique L'apprentissage au CERN est régi par les lois, règlements et contrats en vigueur dans le Canton de Genève. En cas de réussite à l'examen de fin d'apprentissage, les apprentis obtiennent le Certificat Fédéral de Capacité Suisse (CFC). 7 places au total sont ouvertes au recrutement pour les deux professions. L'apprentissage dure 4 ans. Minima requis pour faire acte de candidature : • avoir au moins 15 ans et moins de 21 ans à la date de début de l'apprentissage • avoir terminé la scolarité obligatoire, au minimum 9ème du Cycle d'orientation genevois (3ème en France) • être ressortissant d'un pays membre du CERN (Allemagne, Autriche, Belgiqu...

  11. Evidence of final-state suppression of high-p{_ T} hadrons in Au + Au collisions using d + Au measurements at RHIC

    Science.gov (United States)

    Back, B. B.; Baker, M. D.; Ballintijn, M.; Barton, D. S.; Becker, B.; Betts, R. R.; Bickley, A. A.; Bindel, R.; Busza, W.; Carroll, A.; Decowski, M. P.; García, E.; Gburek, T.; George, N.; Gulbrandsen, K.; Gushue, S.; Halliwell, C.; Hamblen, J.; Harrington, A. S.; Henderson, C.; Hofman, D. J.; Hollis, R. S.; Hołyński, R.; Holzman, B.; Iordanova, A.; Johnson, E.; Kane, J. L.; Khan, N.; Kulinich, P.; Kuo, C. M.; Lee, J. W.; Lin, W. T.; Manly, S.; Mignerey, A. C.; Nouicer, R.; Olszewski, A.; Pak, R.; Park, I. C.; Pernegger, H.; Reed, C.; Roland, C.; Roland, G.; Sagerer, J.; Sarin, P.; Sedykh, I.; Skulski, W.; Smith, C. E.; Steinberg, P.; Stephans, G. S. F.; Sukhanov, A.; Tonjes, M. B.; Trzupek, A.; Vale, C.; van Nieuwenhuizen, G. J.; Verdier, R.; Veres, G. I.; Wolfs, F. L. H.; Wosiek, B.; Woźniak, K.; Wysłouch, B.; Zhang, J.

    Transverse momentum spectra of charged hadrons with pT 2 GeV/c). In contrast, the d + Au nuclear modification factor exhibits no suppression of the high-pT yields. These measurements suggest a large energy loss of the high-pT particles in the highly interacting medium created in the central Au + Au collisions. The lack of suppression in d + Au collisions suggests that it is unlikely that initial state effects can explain the suppression in the central Au + Au collisions. PACS: 25.75.-q

  12. Systematic Measurements of Identified Particle Spectra in pp, d+Au and Au+Au Collisions from STAR

    Energy Technology Data Exchange (ETDEWEB)

    STAR Coll

    2009-04-11

    Identified charged particle spectra of {pi}{sup {+-}}, K{sup {+-}}, p and {bar p} at mid-rapidity (|y| < 0.1) measured by the dE/dx method in the STAR-TPC are reported for pp and d + Au collisions at {radical}s{sub NN} = 200 GeV and for Au + Au collisions at 62.4 GeV, 130 GeV, and 200 GeV. Average transverse momenta, total particle production, particle yield ratios, strangeness and baryon production rates are investigated as a function of the collision system and centrality. The transverse momentum spectra are found to be flatter for heavy particles than for light particles in all collision systems; the effect is more prominent for more central collisions. The extracted average transverse momentum of each particle species follows a trend determined by the total charged particle multiplicity density. The Bjorken energy density estimate is at least several GeV/fm{sub 3} for a formation time less than 1 fm/c. A significantly larger net-baryon density and a stronger increase of the net-baryon density with centrality are found in Au + Au collisions at 62.4 GeV than at the two higher energies. Antibaryon production relative to total particle multiplicity is found to be constant over centrality, but increases with the collision energy. Strangeness production relative to total particle multiplicity is similar at the three measured RHIC energies. Relative strangeness production increases quickly with centrality in peripheral Au + Au collisions, to a value about 50% above the pp value, and remains rather constant in more central collisions. Bulk freeze-out properties are extracted from thermal equilibrium model and hydrodynamics-motivated blast-wave model fits to the data. Resonance decays are found to have little effect on the extracted kinetic freeze-out parameters due to the transverse momentum range of our measurements. The extracted chemical freeze-out temperature is constant, independent of collision system or centrality; its value is close to the predicted phase

  13. Art rupestre préhistorique au Yémen

    Directory of Open Access Journals (Sweden)

    Michel-Alain Garcia

    1997-08-01

    Full Text Available Afin de compléter notre documentation, nous avions projeté pour cette année une courte mission à Saada sur les sites déjà étudiés les années passées. C'est le récit d'un militaire ayant séjourné dans le wadi Nushur qui nous a décidé à entreprendre une prospection nouvelle dans ce secteur au nord-ouest de la grande zone ornée de Saada, sur la route menant à Kifa. Notre espoir de trouver un nouveau site n'a pas été déçu car dans un affluent du Nushur, le wadi Gulat, nous avons découvert une sér...

  14. Le Mégalithisme au Yémen

    Directory of Open Access Journals (Sweden)

    Tara Steimer-Herbet

    1999-08-01

    Full Text Available Nécropole de Jabal Ruwaik (YémenLes comptes rendus d’explorations, de missions archéologiques, de fouilles, font état de nombreux monuments funéraires mégalithiques dont l’étude reste encore très sommaire. Cette année deux missions françaises au Yémen, l’une dans le cadre d’une prospection systématique des sites de la période islamique sur les côtes du Hadramawt et du Mahra, et l’autre suivant un programme de prospection recherchant principalement des sites de l’âge du Bronze dans les région...

  15. Electrochemical quartz crystal microbalance study on Au-supported Pt adlayers for electrocatalytic oxidation of methanol in alkaline solution

    Institute of Scientific and Technical Information of China (English)

    2010-01-01

    Underpotential deposition(UPD) of Cu on an Au electrode followed by redox replacement reaction(RRR) of CuUPD with a Pt source(H2PtCl6 or K2PtCl4) yielded Au-supported Pt adlayers(for short,Pt(CuUPD-Pt4+)n/Au for H2PtCl6,or Pt(CuUPD-Pt2+)n/Au for K2PtCl4,where n denotes the number of UPD-redox replacement cycles).The electrochemical quartz crystal microbalance(EQCM) technique was used for the first time to quantitatively study the fabricated electrodes and estimate their mass-normalized specific electrocatalytic activity(SECA) for methanol oxidation in alkaline solution.In comparison with Pt(CuUPD-Pt2+)n/Au,Pt(CuUPD-Pt4+)n/Au exhibited a higher electrocatalytic activity,and the maximum SECA was obtained to be as high as 35.7 mA ?g?1 at Pt(CuUPD-Pt4+)3/Au.The layer-by-layer architecture of Pt atoms on Au is briefly discussed based on the EQCM-revealed redox replacement efficiency,and the calculated distribution percentages of bare Au sites agree with the experimental results deduced from the charge under the AuOx-reduction peaks.The EQCM is highly recommended as an efficient technique to quantitatively examine various electrode-supported catalyst adlayers,and the highly efficient catalyst adlayers of noble metals are promising in electrocatalysis relevant to biological,energy and environmental sciences and technologies.

  16. Suppression of ϒ production in d+Au and Au+Au collisions at √(sNN)=200 GeV

    International Nuclear Information System (INIS)

    We report measurements of ϒ meson production in p+p, d+Au, and Au+Au collisions using the STAR detector at RHIC. We compare the ϒ yield to the measured cross section in p+p collisions in order to quantify any modifications of the yield in cold nuclear matter using d+Au data and in hot nuclear matter using Au+Au data separated into three centrality classes. Our p+p measurement is based on three times the statistics of our previous result. We obtain a nuclear modification factor for ϒ(1S+2S+3S) in the rapidity range |y|<1 in d+Au collisions of RdAu=0.79±0.24(stat.)±0.03(syst.)±0.10(p+p syst.). A comparison with models including shadowing and initial state parton energy loss indicates the presence of additional cold-nuclear matter suppression. Similarly, in the top 10% most-central Au+Au collisions, we measure a nuclear modification factor of RAA=0.49±0.1(stat.)±0.02(syst.)±0.06(p+psyst.), which is a larger suppression factor than that seen in cold nuclear matter. Our results are consistent with complete suppression of excited-state ϒ mesons in Au+Au collisions. The additional suppression in Au+Au is consistent with the level expected in model calculations that include the presence of a hot, deconfined Quark–Gluon Plasma. However, understanding the suppression seen in d+Au is still needed before any definitive statements about the nature of the suppression in Au+Au can be made

  17. Monodisperse Au nanoparticles for selective electrocatalytic reduction of CO2 to CO.

    Science.gov (United States)

    Zhu, Wenlei; Michalsky, Ronald; Metin, Önder; Lv, Haifeng; Guo, Shaojun; Wright, Christopher J; Sun, Xiaolian; Peterson, Andrew A; Sun, Shouheng

    2013-11-13

    We report selective electrocatalytic reduction of carbon dioxide to carbon monoxide on gold nanoparticles (NPs) in 0.5 M KHCO3 at 25 °C. Among monodisperse 4, 6, 8, and 10 nm NPs tested, the 8 nm Au NPs show the maximum Faradaic efficiency (FE) (up to 90% at -0.67 V vs reversible hydrogen electrode, RHE). Density functional theory calculations suggest that more edge sites (active for CO evolution) than corner sites (active for the competitive H2 evolution reaction) on the Au NP surface facilitates the stabilization of the reduction intermediates, such as COOH*, and the formation of CO. This mechanism is further supported by the fact that Au NPs embedded in a matrix of butyl-3-methylimidazolium hexafluorophosphate for more efficient COOH* stabilization exhibit even higher reaction activity (3 A/g mass activity) and selectivity (97% FE) at -0.52 V (vs RHE). The work demonstrates the great potentials of using monodisperse Au NPs to optimize the available reaction intermediate binding sites for efficient and selective electrocatalytic reduction of CO2 to CO.

  18. First-principles study toward CO adsorption on Au/Ni surface alloys.

    Science.gov (United States)

    Huang, Yu Cheng; Du, Jin Yan; Zhou, Tao; Wang, Su Fan

    2012-12-01

    The introduction of a second metal, gold, into a nickel matrix can effectively improve the catalytic performance and thermal stability of the catalysts toward steam reforming of methane. To investigate the effect of Au on the adsorption properties and electronic structure of the Ni(111) surface, we chose CO as a probe molecule and examined CO adsorption on various Au/Ni surfaces. It was revealed that Au addition weakened the absorbate-substrate interactions on the Ni(111) surface. With increasing gold concentration, the binding energy declines further. The variation of the binding energies has been interpreted by exploring the electronic structure of surface nickel atoms. The effect of gold can be quantitatively characterized by the slopes of the fitting equations between the binding energy and the number of gold atoms surrounding the adsorption site. Our results show that the binding energy at top sites can be approximately estimated by counting the number of surrounding gold atoms. On one specific surface, the relative magnitude of the binding energy can be simply judged by the distance between gold and the geometrical center of the adsorption site. This empirical rule holds true for C, H, and O adsorption on the Au/Ni surface. It may be applicable to a system in which a doped atom of larger atomic size is incorporated into the host metal surface by forming a surface alloy. PMID:23047643

  19. Electrochemical Characterization of Protein Adsorption onto YNGRT-Au and VLGXE-Au Surfaces

    Directory of Open Access Journals (Sweden)

    Hanna Trzeciakiewicz

    2015-08-01

    Full Text Available The adsorption of the proteins CD13, mucin and bovine serum albumin on VLGXE-Au and YNGRT-Au interfaces was monitored by electrochemical impedance spectroscopy in the presence of [Fe(CN6]3−/4−. The hydrophobicity of the Au surface was tailored using specific peptides, blocking agents and diluents. The combination of blocking agents (ethanolamine or n-butylamine and diluents (hexanethiol or 2-mercaptoethanol was used to prepare various peptide-modified Au surfaces. Protein adsorption onto the peptide-Au surfaces modified with the combination of n-butylamine and hexanethiol produced a dramatic decrease in the charge transfer resistance, Rct, for all three proteins. In contrast, polar peptide-surfaces induced a minimal change in Rct for all three proteins. Furthermore, an increase in Rct was observed with CD13 (an aminopeptidase overexpressed in certain cancers in comparison to the other proteins when the VLGXE-Au surface was modified with n-butylamine as a blocking agent. The electrochemical data indicated that protein adsorption may be modulated by tailoring the peptide sequence on Au surfaces and that blocking agents and diluents play a key role in promoting or preventing protein adsorption. The peptide-Au platform may also be used for targeting cancer biomarkers with designer peptides.

  20. Electrochemical Characterization of Protein Adsorption onto YNGRT-Au and VLGXE-Au Surfaces.

    Science.gov (United States)

    Trzeciakiewicz, Hanna; Esteves-Villanueva, Jose; Soudy, Rania; Kaur, Kamaljit; Martic-Milne, Sanela

    2015-01-01

    The adsorption of the proteins CD13, mucin and bovine serum albumin on VLGXE-Au and YNGRT-Au interfaces was monitored by electrochemical impedance spectroscopy in the presence of [Fe(CN)6](3-/4-). The hydrophobicity of the Au surface was tailored using specific peptides, blocking agents and diluents. The combination of blocking agents (ethanolamine or n-butylamine) and diluents (hexanethiol or 2-mercaptoethanol) was used to prepare various peptide-modified Au surfaces. Protein adsorption onto the peptide-Au surfaces modified with the combination of n-butylamine and hexanethiol produced a dramatic decrease in the charge transfer resistance, Rct, for all three proteins. In contrast, polar peptide-surfaces induced a minimal change in Rct for all three proteins. Furthermore, an increase in Rct was observed with CD13 (an aminopeptidase overexpressed in certain cancers) in comparison to the other proteins when the VLGXE-Au surface was modified with n-butylamine as a blocking agent. The electrochemical data indicated that protein adsorption may be modulated by tailoring the peptide sequence on Au surfaces and that blocking agents and diluents play a key role in promoting or preventing protein adsorption. The peptide-Au platform may also be used for targeting cancer biomarkers with designer peptides. PMID:26262621

  1. Identified particles in Au+Au collisions at S=200 GeV

    Science.gov (United States)

    Phobos Collaboration; Wosiek, Barbara; Back, B. B.; Baker, M. D.; Barton, D. S.; Betts, R. R.; Ballintijn, M.; Bickley, A. A.; Bindel, R.; Budzanowski, A.; Busza, W.; Carroll, A.; Decowski, M. P.; García, E.; George, N.; Gulbrandsen, K.; Gushue, S.; Halliwell, C.; Hamblen, J.; Heintzelman, G. A.; Henderson, C.; Hofman, D. J.; Hollis, R. S.; Hołyński, R.; Holzman, B.; Iordanova, A.; Johnson, E.; Kane, J. L.; Katzy, J.; Khan, N.; Kucewicz, W.; Kulinich, P.; Kuo, C. M.; Manly, S.; McLeod, D.; Michałowski, J.; Mignerey, A. C.; Nouicer, R.; Olszewski, A.; Pak, R.; Park, I. C.; Pernegger, H.; Reed, C.; Remsberg, L. P.; Reuter, M.; Roland, C.; Roland, G.; Rosenberg, L.; Sagerer, J.; Sarin, P.; Sawicki, P.; Skulski, W.; Steadman, S. G.; Steinberg, P.; Stephans, G. S. F.; Stodulski, M.; Sukhanov, A.; Tang, J.-L.; Teng, R.; Trzupek, A.; Vale, C.; van Nieuwenhuizen, G. J.; Verdier, R.; Wadsworth, B.; Wolfs, F. L. H.; Wosiek, B.; Woźniak, K.; Wuosmaa, A. H.; Wysłouch, B.

    2003-03-01

    The yields of identified particles have been measured at RHIC for Au+Au collisions at S=200 GeV using the PHOBOS spectrometer. The ratios of antiparticle to particle yields near mid-rapidity are presented. The first measurements of the invariant yields of charged pions, kaons and protons at very low transverse momenta are also shown.

  2. Strangelet search in Au+Au collisions at VsNN=200 GeV

    NARCIS (Netherlands)

    Bai, Y.; Benedosso, F.; Botje, M.A.J.; Grebenyuk, O.; Mischke, A.; Peitzmann, T.; Russcher, M.J.; Snellings, R.J.M.; van der Kolk, N.

    2007-01-01

    We have searched for strangelets in a triggered sample of 61 million central (top 4%) Au+Au collisions at √sNN=200 GeV near beam rapidities at the STAR solenoidal tracker detector at the BNL Relativistic Heavy Ion Collider. We have sensitivity to metastable strangelets with lifetimes of order ⩾0.1 n

  3. Charged particle density distributions in Au + Au collisions at relativistic heavy-ion collider energies

    Indian Academy of Sciences (India)

    Fauad Rami

    2003-05-01

    Charged particle pseudorapidity distributions have been measured in Au + Au collisions using the BRAHMS detector at RHIC. The results are presented as a function of the collision centrality and the center of mass energy. They are compared to the predictions of different parton scattering models and the important role of hard scattering processes at RHIC energies is discussed.

  4. EVENT STRUCTURE AT RHIC FROM P-P TO AU-AU.

    Energy Technology Data Exchange (ETDEWEB)

    TRAINOR,T.A.; (FOR THE STAR COLLABORATION)

    2004-03-15

    Several correlation analysis techniques are applied to p-p and Au-Au collisions at RHIC. Strong large-momentum-scale correlations are observed which can be related to local charge and momentum conservation during hadronization and to minijet (minimum-bias parton fragment) correlations.

  5. Study of Au+Au relativistic collisions with the Fopi-Phase I detector

    International Nuclear Information System (INIS)

    Au+Au relativistic collisions, in a 100-1000 MeV energy domain per nucleon, are described. Experiments have been carried out with the SIS accelerator at GSI/Darmstadt. Data are analysed with the FOPI-phase I detector. These data are compared with IQMD model (Isospin Quantum Molecular Dynamics) Predictions. (S.G). 80 refs., 77 figs., 5 tabs

  6. Applied mathematics and condensed matter; Mathematiques appliquees et matiere condensee

    Energy Technology Data Exchange (ETDEWEB)

    Bouche, D.; Jollet, F. [CEA Bruyeres-le-Chatel, 91 (France)

    2011-01-15

    Applied mathematics have always been a key tool in computing the structure of condensed matter. In this paper, we present the most widely used methods, and show the importance of mathematics in their genesis and evolution. After a brief survey of quantum Monte Carlo methods, which try to compute the N electrons wave function, the paper describes the theoretical foundations of N independent particle approximations. We mainly focus on density functional theory (DFT). This theory associated with advanced numerical methods, and high performance computing, has produced significant achievements in the field. This paper presents the foundations of the theory, as well as different numerical methods used to solve DFT equations. (authors)

  7. The adsorption and reaction of vinyl acetate on Au/Pd(100) alloy surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Li, Zhenjun [Pacific Northwest National Laboratory (PNNL); Calaza, Florencia C [ORNL; Tysoe, Wilfred [University of Wisconsin, Milwaukee

    2012-01-01

    The surface chemistry of vinyl acetate monomer (VAM) is studied on Au/Pd(100) alloys as a function of alloy composition using temperature-programmed desorption and reflection adsorption infrared spectroscopy. VAM adsorbs weakly on isolated palladium sites on the alloy with a heat of adsorption of ~55 kJ/mol, with the plane of the VAM adsorbed close to parallel to the surface. The majority of the VAM adsorbed on isolated sites desorbs molecularly with only a small portion decomposing. At lower gold coverages (below ~0.5 ML of gold), where palladium palladium bridge sites are present, VAM binds to the surface in a distorted geometry via a rehybridized vinyl group. A larger proportion of this VAM decomposes and this reaction is initiated by C\\O bond scission in the VAM to form adsorbed acetate and vinyl species. The implication of this surface chemistry for VAM synthesis on Au/Pd(100) alloys is discussed.

  8. Jets and dijets in Au+Au and p+p collisions at RHIC

    Energy Technology Data Exchange (ETDEWEB)

    Hardtke, D.; STAR Collaboration

    2002-12-09

    Recent data from RHIC suggest novel nuclear effects in the production of high p{sub T} hadrons. We present results from the STAR detector on high p{sub T} angular correlations in Au+Au and p+p collisions at {radical}S = 200 GeV/c. These two-particle angular correlation measurements verify the presence of a partonic hard scattering and fragmentation component at high p{sub T} in both central and peripheral Au+Au collisions. When triggering on a leading hadron with p{sub T}>4 GeV, we observe a quantitative agreement between the jet cone properties in p+p and all centralities of Au+Au collisions. This quantitative agreement indicates that nearly all hadrons with p{sub T}>4 GeV/c come from jet fragmentation and that jet fragmentation properties are not substantially modified in Au+Au collisions. STAR has also measured the strength of back-to-back high p{sub T} charged hadron correlations, and observes a small suppression of the back-to-back correlation strength in peripheral collisions, and a nearly complete disappearance o f back-to-back correlations in central Au+Au events. These phenomena, together with the observed strong suppression of inclusive yields and large value of elliptic flow at high p{sub T}, are consistent with a model where high p{sub T} hadrons come from partons created near the surface of the collision region, and where partons that originate or propagate towards the center of the collision region are substantially slowed or completely absorbed.

  9. Alkaline earth-gold-aluminides. Synthesis and structure of SrAu{sub 3}Al{sub 2}, SrAu{sub 2.83}Al{sub 2.17}, BaAu{sub 2.89}Al{sub 2.11} and BaAu{sub 7.09}Al{sub 5.91}

    Energy Technology Data Exchange (ETDEWEB)

    Gerke, Birgit; Poettgen, Rainer [Muenster Univ. (Germany). Inst. fuer Anorganische und Analytische Chemie

    2015-07-01

    New alkaline earth-gold-aluminides were synthesized from the elements in sealed tantalum or quartz ampoules in muffle furnaces at maximum annealing temperatures of 1325 K. The structures were refined from single crystal X-ray diffractometer data. SrAu{sub 3}Al{sub 2} crystallizes in an ordered version of the LT-SrZn{sub 5} structure: Pnma, a = 1315.9(3), b = 549.0(1), c = 684.5(3) pm, wR2 = 0.0232, 930 F{sup 2} values, 35 variables. SrAu{sub 2.83}Al{sub 2.17} (a = 1065.0(2), b = 845.0(2), c = 548.1(1) pm, wR2 = 0.0416, 452 F{sup 2} values, 22 variables) and BaAu{sub 2.89}Al{sub 2.11} (a = 1096.1(3), b = 835.7(3), c = 554.0(1) pm, wR2 = 0.0280, 501 F{sup 2} values, 22 variables) both adopt the BaZn{sub 5} type, space group Cmcm with Au/Al mixing on the 4c site. The gold and aluminum atoms in both types form three-dimensional networks of condensed tetrahedra with the strontium and barium atoms in large cavities. BaAu{sub 7.09}Al{sub 5.91} is a new member of the NaZn{sub 13} type: Fm anti 3c, a = 1257.6(2) pm, wR2 = 0.0267, 168 F{sup 2} values, 12 variables. Both the 96i and 8b sites show Au/Al mixing. The crystal chemical details are discussed.

  10. Spectra and ratios of identified particles in Au+Au and d+Au collisions at sqrt(s_NN)=200 GeV

    CERN Document Server

    Adare, A; Aidala, C; Ajitanand, N N; Akiba, Y; Al-Bataineh, H; Alexander, J; Angerami, A; Aoki, K; Apadula, N; Aramaki, Y; Atomssa, E T; Averbeck, R; Awes, T C; Azmoun, B; Babintsev, V; Bai, M; Baksay, G; Baksay, L; Barish, K N; Bassalleck, B; Basye, A T; Bathe, S; Baublis, V; Baumann, C; Bazilevsky, A; Belikov, S; Belmont, R; Bennett, R; Berdnikov, A; Berdnikov, Y; Bhom, J H; Bickley, A A; Blau, D S; Bok, J S; Boyle, K; Brooks, M L; Buesching, H; Bumazhnov, V; Bunce, G; Butsyk, S; Camacho, C M; Campbell, S; Caringi, A; Chen, C -H; Chi, C Y; Chiu, M; Choi, I J; Choi, J B; Choudhury, R K; Christiansen, P; Chujo, T; Chung, P; Chvala, O; Cianciolo, V; Citron, Z; Cole, B A; del Valle, Z Conesa; Connors, M; Constantin, P; Csanád, M; Csörgő, T; Dahms, T; Dairaku, S; Danchev, I; Das, K; Datta, A; David, G; Dayananda, M K; Denisov, A; Deshpande, A; Desmond, E J; Dharmawardane, K V; Dietzsch, O; Dion, A; Donadelli, M; Drapier, O; Drees, A; Drees, K A; Durham, J M; Durum, A; Dutta, D; D'Orazio, L; Edwards, S; Efremenko, Y V; Ellinghaus, F; Engelmore, T; Enokizono, A; En'yo, H; Esumi, S; Fadem, B; Fields, D E; Finger, M; Jr., \\,; Fleuret, F; Fokin, S L; Fraenkel, Z; Frantz, J E; Franz, A; Frawley, A D; Fujiwara, K; Fukao, Y; Fusayasu, T; Garishvili, I; Glenn, A; Gong, H; Gonin, M; Goto, Y; de Cassagnac, R Granier; Grau, N; Greene, S V; Grim, G; Perdekamp, M Grosse; Gunji, T; Gustafsson, H -Å; Haggerty, J S; Hahn, K I; Hamagaki, H; Hamblen, J; Han, R; Hanks, J; Hartouni, E P; Haslum, E; Hayano, R; He, X; Heffner, M; Hemmick, T K; Hester, T; Hill, J C; Hohlmann, M; Holzmann, W; Homma, K; Hong, B; Horaguchi, T; Hornback, D; Huang, S; Ichihara, T; Ichimiya, R; Ide, J; Ikeda, Y; Imai, K; Inaba, M; Isenhower, D; Ishihara, M; Isobe, T; Issah, M; Isupov, A; Ivanischev, D; Iwanaga, Y; Jacak, B V; Jia, J; Jiang, X; Jin, J; Johnson, B M; Jones, T; Joo, K S; Jouan, D; Jumper, D S; Kajihara, F; Kametani, S; Kamihara, N; Kamin, J; Kang, J H; Kapustinsky, J; Karatsu, K; Kasai, M; Kawall, D; Kawashima, M; Kazantsev, A V; Kempel, T; Khanzadeev, A; Kijima, K M; Kikuchi, J; Kim, A; Kim, B I; Kim, D H; Kim, D J; Kim, E; Kim, E -J; Kim, S H; Kim, Y -J; Kim, Y J; Kinney, E; Kiriluk, K; Kiss, Á; Kistenev, E; Kleinjan, D; Kochenda, L; Komkov, B; Konno, M; Koster, J; Kotchetkov, D; Kozlov, A; Král, A; Kravitz, A; Kunde, G J; Kurita, K; Kurosawa, M; Kwon, Y; Kyle, G S; Lacey, R; Lai, Y S; Lajoie, J G; Lebedev, A; Lee, D M; Lee, J; Lee, K; Lee, K B; Lee, K S; Leitch, M J; Leite, M A L; Leitner, E; Lenzi, B; Li, X; Lichtenwalner, P; Liebing, P; Levy, L A Linden; Liška, T; Litvinenko, A; Liu, H; Liu, M X; Love, B; Luechtenborg, R; Lynch, D; Maguire, C F; Makdisi, Y I; Malakhov, A; Malik, M D; Manko, V I; Mannel, E; Mao, Y; Masui, H; Matathias, F; McCumber, M; McGaughey, P L; McGlinchey, D; Means, N; Meredith, B; Miake, Y; Mibe, T; Mignerey, A C; Mikeš, P; Miki, K; Milov, A; Mishra, M; Mitchell, J T; Mohanty, A K; Moon, H J; Morino, Y; Morreale, A; Morrison, D P; Moukhanova, T V; Murakami, T; Murata, J; Nagamiya, S; Nagle, J L; Naglis, M; Nagy, M I; Nakagawa, I; Nakamiya, Y; Nakamura, K R; Nakamura, T; Nakano, K; Nam, S; Newby, J; Nguyen, M; Nihashi, M; Nouicer, R; Nyanin, A S; Oakley, C; O'Brien, E; Oda, S X; Ogilvie, C A; Oka, M; Okada, K; Onuki, Y; Oskarsson, A; Ouchida, M; Ozawa, K; Pak, R; Pantuev, V; Papavassiliou, V; Park, I H; Park, J; Park, S K; Park, W J; Pate, S F; Pei, H; Peng, J -C; Pereira, H; Peresedov, V; Peressounko, D Yu; Petti, R; Pinkenburg, C; Pisani, R P; Proissl, M; Purschke, M L; Purwar, A K; Qu, H; Rak, J; Rakotozafindrabe, A; Ravinovich, I; Read, K F; Rembeczki, S; Reygers, K; Riabov, V; Riabov, Y; Richardson, E; Roach, D; Roche, G; Rolnick, S D; Rosati, M; Rosen, C A; Rosendahl, S S E; Rosnet, P; Rukoyatkin, P; Ružička, P; Sahlmueller, B; Saito, N; Sakaguchi, T; Sakashita, K; Samsonov, V; Sano, S; Sato, T; Sawada, S; Sedgwick, K; Seele, J; Seidl, R; Semenov, A Yu; Seto, R; Sharma, D; Shein, I; Shibata, T -A; Shigaki, K; Shimomura, M; Shoji, K; Shukla, P; Sickles, A; Silva, C L; Silvermyr, D; Silvestre, C; Sim, K S; Singh, B K; Singh, C P; Singh, V; Slunečka, M; Soltz, R A; Sondheim, W E; Sorensen, S P; Sourikova, I V; Sparks, N A; Stankus, P W; Stenlund, E; Stoll, S P; Sugitate, T; Sukhanov, A; Sziklai, J; Takagui, E M; Taketani, A; Tanabe, R; Tanaka, Y; Taneja, S; Tanida, K; Tannenbaum, M J; Tarafdar, S; Taranenko, A; Tarján, P; Themann, H; Thomas, D; Thomas, T L; Togawa, M; Toia, A; Tomášek, L; Torii, H; Towell, R S; Tserruya, I; Tsuchimoto, Y; Vale, C; Valle, H; van Hecke, H W; Vazquez-Zambrano, E; Veicht, A; Velkovska, J; Vértesi, R; Vinogradov, A A; Virius, M; Vrba, V; Vznuzdaev, E; Wang, X R; Watanabe, D; Watanabe, K; Watanabe, Y; Wei, F; Wei, R; Wessels, J; White, S N; Winter, D; Wood, J P; Woody, C L; Wright, R M; Wysocki, M; Xie, W; Yamaguchi, Y L; Yamaura, K; Yang, R; Yanovich, A; Ying, J; Yokkaichi, S

    2013-01-01

    The transverse momentum (p_T) spectra and ratios of identified charged hadrons (\\pi^+/-, K^+/-, p, p^bar) produced in sqrt(s_NN)=200 GeV Au+Au and d+Au collisions are reported in five different centrality classes for each collision species. The measurements of pions and protons are reported up to p_T=6 GeV/c (5 GeV/c), and the measurements of kaons are reported up to p_T=4 GeV/c (3.5 GeV/c) in Au+Au (d+Au) collisions. In the intermediate p_T region, between 2--5 GeV/c, a significant enhancement of baryon to meson ratios compared to those measured in p+p collisions is observed. This enhancement is present in both Au+Au and d+Au collisions, and increases as the collisions become more central. We compare a class of peripheral Au+Au collisions with a class of central d+Au collisions which have a comparable number of participating nucleons and binary nucleon-nucleon collisions. The p_T dependent particle ratios for these classes display a remarkable similarity, which is then discussed.

  11. Open Heavy Flavor Production in p+p, d+Au and Au+Au Collisions at $\\sqrt{s}$= 200$ GeV

    CERN Document Server

    Wang, X

    2006-01-01

    PHENIX results for open charm production from semi-lepton decay in p+p, d+Au and Au+Au collisions in a wide rapidity ranges at $\\sqrt{s}$= 200$ GeV are presented. Keywords: Relativistic Heavy-ion Collision, Open Charm production, Nuclear Medium Effect PACS: 25.75.-q, 25.75 Dw, 13.20.Gd

  12. Spectra and ratios of identified particles in Au+Au and d+Au collisions at sNN=200 GeV

    Science.gov (United States)

    Adare, A.; Afanasiev, S.; Aidala, C.; Ajitanand, N. N.; Akiba, Y.; Al-Bataineh, H.; Alexander, J.; Angerami, A.; Aoki, K.; Apadula, N.; Aramaki, Y.; Atomssa, E. T.; Averbeck, R.; Awes, T. C.; Azmoun, B.; Babintsev, V.; Bai, M.; Baksay, G.; Baksay, L.; Barish, K. N.; Bassalleck, B.; Basye, A. T.; Bathe, S.; Baublis, V.; Baumann, C.; Bazilevsky, A.; Belikov, S.; Belmont, R.; Bennett, R.; Berdnikov, A.; Berdnikov, Y.; Bhom, J. H.; Bickley, A. A.; Blau, D. S.; Bok, J. S.; Boyle, K.; Brooks, M. L.; Buesching, H.; Bumazhnov, V.; Bunce, G.; Butsyk, S.; Camacho, C. M.; Campbell, S.; Caringi, A.; Chen, C.-H.; Chi, C. Y.; Chiu, M.; Choi, I. J.; Choi, J. B.; Choudhury, R. K.; Christiansen, P.; Chujo, T.; Chung, P.; Chvala, O.; Cianciolo, V.; Citron, Z.; Cole, B. A.; Conesa del Valle, Z.; Connors, M.; Constantin, P.; Csanád, M.; Csörgő, T.; Dahms, T.; Dairaku, S.; Danchev, I.; Das, K.; Datta, A.; David, G.; Dayananda, M. K.; Denisov, A.; Deshpande, A.; Desmond, E. J.; Dharmawardane, K. V.; Dietzsch, O.; Dion, A.; Donadelli, M.; Drapier, O.; Drees, A.; Drees, K. A.; Durham, J. M.; Durum, A.; Dutta, D.; D'Orazio, L.; Edwards, S.; Efremenko, Y. V.; Ellinghaus, F.; Engelmore, T.; Enokizono, A.; En'yo, H.; Esumi, S.; Fadem, B.; Fields, D. E.; Finger, M.; Finger, M., Jr.; Fleuret, F.; Fokin, S. L.; Fraenkel, Z.; Frantz, J. E.; Franz, A.; Frawley, A. D.; Fujiwara, K.; Fukao, Y.; Fusayasu, T.; Garishvili, I.; Glenn, A.; Gong, H.; Gonin, M.; Goto, Y.; Granier de Cassagnac, R.; Grau, N.; Greene, S. V.; Grim, G.; Grosse Perdekamp, M.; Gunji, T.; Gustafsson, H.-Å.; Haggerty, J. S.; Hahn, K. I.; Hamagaki, H.; Hamblen, J.; Han, R.; Hanks, J.; Hartouni, E. P.; Haslum, E.; Hayano, R.; He, X.; Heffner, M.; Hemmick, T. K.; Hester, T.; Hill, J. C.; Hohlmann, M.; Holzmann, W.; Homma, K.; Hong, B.; Horaguchi, T.; Hornback, D.; Huang, S.; Ichihara, T.; Ichimiya, R.; Ide, J.; Ikeda, Y.; Imai, K.; Inaba, M.; Isenhower, D.; Ishihara, M.; Isobe, T.; Issah, M.; Isupov, A.; Ivanischev, D.; Iwanaga, Y.; Jacak, B. V.; Jia, J.; Jiang, X.; Jin, J.; Johnson, B. M.; Jones, T.; Joo, K. S.; Jouan, D.; Jumper, D. S.; Kajihara, F.; Kametani, S.; Kamihara, N.; Kamin, J.; Kang, J. H.; Kapustinsky, J.; Karatsu, K.; Kasai, M.; Kawall, D.; Kawashima, M.; Kazantsev, A. V.; Kempel, T.; Khanzadeev, A.; Kijima, K. M.; Kikuchi, J.; Kim, A.; Kim, B. I.; Kim, D. H.; Kim, D. J.; Kim, E.; Kim, E.-J.; Kim, S. H.; Kim, Y.-J.; Kinney, E.; Kiriluk, K.; Kiss, Á.; Kistenev, E.; Kleinjan, D.; Kochenda, L.; Komkov, B.; Konno, M.; Koster, J.; Kotchetkov, D.; Kozlov, A.; Král, A.; Kravitz, A.; Kunde, G. J.; Kurita, K.; Kurosawa, M.; Kwon, Y.; Kyle, G. S.; Lacey, R.; Lai, Y. S.; Lajoie, J. G.; Lebedev, A.; Lee, D. M.; Lee, J.; Lee, K.; Lee, K. B.; Lee, K. S.; Leitch, M. J.; Leite, M. A. L.; Leitner, E.; Lenzi, B.; Li, X.; Lichtenwalner, P.; Liebing, P.; Linden Levy, L. A.; Liška, T.; Litvinenko, A.; Liu, H.; Liu, M. X.; Love, B.; Luechtenborg, R.; Lynch, D.; Maguire, C. F.; Makdisi, Y. I.; Malakhov, A.; Malik, M. D.; Manko, V. I.; Mannel, E.; Mao, Y.; Masui, H.; Matathias, F.; McCumber, M.; McGaughey, P. L.; McGlinchey, D.; Means, N.; Meredith, B.; Miake, Y.; Mibe, T.; Mignerey, A. C.; Mikeš, P.; Miki, K.; Milov, A.; Mishra, M.; Mitchell, J. T.; Mohanty, A. K.; Moon, H. J.; Morino, Y.; Morreale, A.; Morrison, D. P.; Moukhanova, T. V.; Murakami, T.; Murata, J.; Nagamiya, S.; Nagle, J. L.; Naglis, M.; Nagy, M. I.; Nakagawa, I.; Nakamiya, Y.; Nakamura, K. R.; Nakamura, T.; Nakano, K.; Nam, S.; Newby, J.; Nguyen, M.; Nihashi, M.; Nouicer, R.; Nyanin, A. S.; Oakley, C.; O'Brien, E.; Oda, S. X.; Ogilvie, C. A.; Oka, M.; Okada, K.; Onuki, Y.; Oskarsson, A.; Ouchida, M.; Ozawa, K.; Pak, R.; Pantuev, V.; Papavassiliou, V.; Park, I. H.; Park, J.; Park, S. K.; Park, W. J.; Pate, S. F.; Pei, H.; Peng, J.-C.; Pereira, H.; Peresedov, V.; Peressounko, D. Yu.; Petti, R.; Pinkenburg, C.; Pisani, R. P.; Proissl, M.; Purschke, M. L.; Purwar, A. K.; Qu, H.; Rak, J.; Rakotozafindrabe, A.; Ravinovich, I.; Read, K. F.; Rembeczki, S.; Reygers, K.; Riabov, V.; Riabov, Y.; Richardson, E.; Roach, D.; Roche, G.; Rolnick, S. D.; Rosati, M.; Rosen, C. A.; Rosendahl, S. S. E.; Rosnet, P.; Rukoyatkin, P.; Ružička, P.; Sahlmueller, B.; Saito, N.; Sakaguchi, T.; Sakashita, K.; Samsonov, V.; Sano, S.; Sato, T.; Sawada, S.; Sedgwick, K.; Seele, J.; Seidl, R.; Semenov, A. Yu.; Seto, R.; Sharma, D.; Shein, I.; Shibata, T.-A.; Shigaki, K.; Shimomura, M.; Shoji, K.; Shukla, P.; Sickles, A.; Silva, C. L.; Silvermyr, D.; Silvestre, C.; Sim, K. S.; Singh, B. K.; Singh, C. P.; Singh, V.; Slunečka, M.; Soltz, R. A.; Sondheim, W. E.; Sorensen, S. P.; Sourikova, I. V.; Sparks, N. A.; Stankus, P. W.; Stenlund, E.; Stoll, S. P.; Sugitate, T.; Sukhanov, A.; Sziklai, J.; Takagui, E. M.; Taketani, A.; Tanabe, R.; Tanaka, Y.; Taneja, S.; Tanida, K.; Tannenbaum, M. J.; Tarafdar, S.; Taranenko, A.; Tarján, P.; Themann, H.; Thomas, D.; Thomas, T. L.; Togawa, M.; Toia, A.; Tomášek, L.; Torii, H.; Towell, R. S.; Tserruya, I.; Tsuchimoto, Y.; Vale, C.; Valle, H.; van Hecke, H. W.; Vazquez-Zambrano, E.; Veicht, A.; Velkovska, J.; Vértesi, R.; Vinogradov, A. A.; Virius, M.; Vrba, V.; Vznuzdaev, E.; Wang, X. R.; Watanabe, D.; Watanabe, K.; Watanabe, Y.; Wei, F.; Wei, R.; Wessels, J.; White, S. N.; Winter, D.; Wood, J. P.; Woody, C. L.; Wright, R. M.; Wysocki, M.; Xie, W.; Yamaguchi, Y. L.; Yamaura, K.; Yang, R.; Yanovich, A.; Ying, J.; Yokkaichi, S.; You, Z.; Young, G. R.; Younus, I.; Yushmanov, I. E.; Zajc, W. A.; Zhang, C.; Zhou, S.; Zolin, L.

    2013-08-01

    The transverse momentum (pT) spectra and ratios of identified charged hadrons (π±, K±, p, p¯) produced in sNN=200 GeV Au+Au and d+Au collisions are reported in five different centrality classes for each collision species. The measurements of pions and protons are reported up to pT=6 GeV/c (5 GeV/c), and the measurements of kaons are reported up to pT=4 GeV/c (3.5 GeV/c) in Au+Au (d+Au) collisions. In the intermediate pT region, between 2 and 5 GeV/c, a significant enhancement of baryon-to-meson ratios compared to those measured in p+p collisions is observed. This enhancement is present in both Au+Au and d+Au collisions and increases as the collisions become more central. We compare a class of peripheral Au+Au collisions with a class of central d+Au collisions which have a comparable number of participating nucleons and binary nucleon-nucleon collisions. The pT-dependent particle ratios for these classes display a remarkable similarity, which is then discussed.

  13. An intermetallic Au24Ag20 superatom nanocluster stabilized by labile ligands.

    Science.gov (United States)

    Wang, Yu; Su, Haifeng; Xu, Chaofa; Li, Gang; Gell, Lars; Lin, Shuichao; Tang, Zichao; Häkkinen, Hannu; Zheng, Nanfeng

    2015-04-01

    An intermetallic nanocluster containing 44 metal atoms, Au24Ag20(2-SPy)4(PhC≡C)20Cl2, was successfully synthesized and structurally characterized by single-crystal analysis and density funtional theory computations. The 44 metal atoms in the cluster are arranged as a concentric three-shell Au12@Ag20@Au12 Keplerate structure having a high symmetry. For the first time, the co-presence of three different types of anionic ligands (i.e., phenylalkynyl, 2-pyridylthiolate, and chloride) was revealed on the surface of metal nanoclusters. Similar to thiolates, alkynyls bind linearly to surface Au atoms using their σ-bonds, leading to the formation of two types of surface staple units (PhC≡C-Au-L, L = PhC≡C(-) or 2-pyridylthiolate) on the cluster. The co-presence of three different surface ligands allows the site-specific surface and functional modification of the cluster. The lability of PhC≡C(-) ligands on the cluster was demonstrated, making it possible to keep the metal core intact while removing partial surface capping. Moreover, it was found that ligand exchange on the cluster occurs easily to offer various derivatives with the same metal core but different surface functionality and thus different solubility.

  14. Relative Distribution of Au48+~Au52+ in Au Plasma by Ionization Dynamics

    Institute of Scientific and Technical Information of China (English)

    ZHUZhi-Yan; ZHUZheng-He; JIANGGang

    2003-01-01

    The present work proposes a theoretical method called ionization dynamics to derive the ionic charge state distribution. Using relativistic quantum mechanics to calculate the energy level lifetime and average ionic lifetime of each ion, the first-order ionization rate constant can be obtained. Based on these data, from the solution of differential equations for consecutive-irreversible ionization reactions, one will be able to derive the ionic charge state distribution.The calculated average positive charge 49.24 of Au48+ ~ Au52+ and their relative distribution are in good agreement with the results of Lawrence Livermore National Laboratory.

  15. Polymerase chain reaction of Au nanoparticle-bound primers

    Institute of Scientific and Technical Information of China (English)

    SHEN Hebai; HU Min; YANG Zhongnan; WANG Chen; ZHU Longzhang

    2005-01-01

    Polymerase chain reaction (PCR) is a useful technique for in vitro amplification of a DNA fragment. In this paper, a PCR procedure using Au nanoparticle (AuNP) -bound primers was systemically studied. The 5′-SH- (CH2)6-modified primers were covalently attached to the AuNP surface via Au-S bonds, and plasmid pBluescript SK was used as a template. The effects of the concentration of AuNP-bound primers, annealing temperature and PCR cycles were evaluated, respectively. The results indicate that PCR can proceed successfully under optimized condition, with either forward or reverse primers bound to the AuNP surface or with both the two primers bound to the AuNP surface. Development of PCR procedure based on AuNPs not only makes the isolation of PCR products very convenient, but also provides novel methods to prepare AuNP-bound ssDNA and nanostructured material.

  16. Engineering the strain in graphene layers with Au decoration

    Energy Technology Data Exchange (ETDEWEB)

    Pannu, Compesh, E-mail: compesh@gmail.com; Singh, Udai B.; Kumar, Sunil; Tripathi, A.; Kabiraj, D.; Avasthi, D.K., E-mail: dka4444@gmail.com

    2014-07-01

    Graphene sheets decorated with Au nanodots are synthesized by deposition of Au of three different thicknesses and subsequent annealing at 400 °C. Different thicknesses of Au film for the formation of Au nanodots on graphene are measured using Rutherford backscattering spectrometry and morphology is studied using scanning electron microscopy. Raman spectroscopy indicates 3–6-fold increase in I{sub D}/I{sub G} ratio depending on the content of Au deposited on graphene. The increase in disorder in Au decorated graphene layers is explained on the basis of interaction of Au atoms with Π bonds of graphene. The splitting and blueshift in G band signifies compressive strain in Au deposited graphene. X-ray diffraction studies using synchrotron radiation source confirm compressive strain in graphene, which increases with increase of Au film thickness.

  17. Synthesis and characterization in AuCu–Si nanostructures

    Energy Technology Data Exchange (ETDEWEB)

    Novelo, T.E., E-mail: tenovelo@hotmail.com [Centro de Investigación en Materiales Avanzados, S.C., Laboratorio Nacional de Nanotecnología, Av. Miguel de Cervantes 120, Complejo Industrial Chihuahua, 31109 Chihuahua, Chihuahua Mexico (Mexico); Amézaga-Madrid, P. [Centro de Investigación en Materiales Avanzados, S.C., Laboratorio Nacional de Nanotecnología, Av. Miguel de Cervantes 120, Complejo Industrial Chihuahua, 31109 Chihuahua, Chihuahua Mexico (Mexico); Maldonado, R.D. [Universidad Anáhuac-Mayab, Carretera Mérida-Progreso Km. 15.5 A.P. 96-Cordemex, CP. 97310 Mérida, Yucatán Mexico (Mexico); Oliva, A.I. [Centro de Investigación y de Estudios Avanzados el IPN Unidad Mérida, Departamento de Física Aplicada, Km 6 Antigua Carretera a Progreso, A.P. 73-Cordemex, 97310 Mérida, Yucatán Mexico (Mexico); Alonzo-Medina, G.M. [Universidad Anáhuac-Mayab, Carretera Mérida-Progreso Km. 15.5 A.P. 96-Cordemex, CP. 97310 Mérida, Yucatán Mexico (Mexico)

    2015-03-15

    Au/Cu bilayers with different Au:Cu concentrations (25:75, 50:50 and 75:25 at.%) were deposited on Si(100) substrates by thermal evaporation. The thicknesses of all Au/Cu bilayers were 150 nm. The alloys were prepared by thermal diffusion into a vacuum oven with argon atmosphere at 690 K during 1 h. X-ray diffraction analysis revealed different phases of AuCu and CuSi alloys in the samples after annealing process. CuSi alloys were mainly obtained for 25:75 at.% samples, meanwhile the AuCuII phase dominates for samples prepared with 50:50 at.%. Additionally, the Au:Cu alloys with 75:25 at.%, produce Au{sub 2}Cu{sub 3} and Au{sub 3}Cu phases. The formed alloys were characterized by scanning electron microscopy (SEM), atomic force microscopy (AFM), transmission electron microscopy (TEM) and energy dispersive spectroscopy (EDS) to study the morphology and the elemental concentration of the formed alloys. - Highlights: • AuCu/Si alloy thin films were prepared by thermal diffusion. • Alloys prepared with 50 at.% of Au produce the AuCuII phase. • Alloys prepared with 75 at.% of Au produce Au{sub 3}Cu and Au{sub 2}Cu{sub 3} phases. • All alloys present diffusion of Si and Cu through the CuSi alloy formation.

  18. First principle calculations of nitric oxide on metallic Pt (1 1 1) and Pt (1 0 0), and bimetallic Au/Pt (1 1 1) and Au/Pt (1 0 0) surfaces

    International Nuclear Information System (INIS)

    Highlights: • The chemisorption of NO on Pt (1 1 1), Pt (1 0 0), Au/Pt (1 1 1) and Au/Pt (1 0 0) has been investigated. • The adsorptive position of NO on metal surface has been discussed. • The interaction between NO and metal surface is mainly NO 5σ/2π* and metal d-bands. • Different compositions and facets can produce varied catalytic effects. - Abstract: The chemisorption of NO on pure Pt (1 1 1) and Pt (1 0 0), bimetallic Au/Pt (1 1 1) and Au/Pt (1 0 0) surfaces has been investigated using the pseudo-potential plane-wave method within the generalized-gradient approximation density functional theory (GGA + DFT). The results show that different surfaces have various effects on the adsorption of NO. NO tends to be adsorbed on site coordinated with more Pt atoms, and the substitution number of the top-layer Pt by Au atoms affect the d-band center and adsorption energy. The local density of states of various surfaces are calculated. With the increasing atomic number of surface Au, the d-band center moves away from the Fermi level, and the adsorption energies decrease. The further electronic states analysis reveals that the interaction between NO and metal surfaces is mainly via the hybridization of NO 5σ/2π* orbitals and metal d-bands. And when the top-layer concentrations of Au are equal, Au/Pt (1 0 0) exhibits better catalytic toward NO adsorption than Au/Pt (1 1 1). It indicates that different compositions and facets can produce varied catalytic effects

  19. Plasmonic Au islands on polymer nanopillars

    Energy Technology Data Exchange (ETDEWEB)

    Knoben, Wout; Brongersma, Sywert H; Crego-Calama, Mercedes, E-mail: wout.knoben@imec-nl.nl [Holst Centre/IMEC, High Tech Campus 31, 5656 AE Eindhoven (Netherlands)

    2011-07-22

    The refractive index sensitivity of localized surface plasmon resonance sensors can be improved by placing the plasmonic metal particles on pillars instead of on a planar substrate. In this paper, a simple and versatile colloidal lithography method for the fabrication of plasmonic Au islands on top of polymer nanopillars is described. The pillar height is controlled by varying the thickness of the initial polymer film. An increased pillar height results in a blue shift of the absorption spectrum of the Au islands. This is explained by a decreased effective refractive index around the islands. For pillars higher than approximately 40 nm no further blue shift is observed, in agreement with the decay length of the electromagnetic field around the islands. Pillar-supported Au islands were also fabricated on a flexible foil, demonstrating the potential of the method described here for the fabrication of flexible plasmonic substrates. Benefits and limitations of the method and of using polymers as the pillar material are discussed.

  20. Au nanoparticles films used in biological sensing

    International Nuclear Information System (INIS)

    Lactobacillus para paracasei are used commonly as functional food and probiotic substances. In this work Au nanoparticles self-assembled films were used for Lactobacillus para paracasei determination at five different concentrations. Functionalized substrates were immersed in a colloidal solution for one and a half hour at room temperature and dried at room temperature during four hours. After that, drops of Lactobacillus para paracasei in aqueous solution were put into the Au nanoparticles film and let dry at room temperature for another two hours. Infrared spectroscopy in attenuated total reflectance sampling mode was used to observe generation peaks due to substrate silanization, enhancement of Si-O band intensity due to the Au colloids added to silanized substrate and also to observe the enhancement of Lactobacillus para paracasei infrared intensity of the characteristic frequencies at 1650, 1534 and 1450 cm-1 due to surface enhancement infrared absorption.

  1. Au nanoparticles films used in biological sensing

    Science.gov (United States)

    Rosales Pérez, M.; Delgado Macuil, R.; Rojas López, M.; Gayou, V. L.; Sánchez Ramírez, J. F.

    2009-05-01

    Lactobacillus para paracasei are used commonly as functional food and probiotic substances. In this work Au nanoparticles self-assembled films were used for Lactobacillus para paracasei determination at five different concentrations. Functionalized substrates were immersed in a colloidal solution for one and a half hour at room temperature and dried at room temperature during four hours. After that, drops of Lactobacillus para paracasei in aqueous solution were put into the Au nanoparticles film and let dry at room temperature for another two hours. Infrared spectroscopy in attenuated total reflectance sampling mode was used to observe generation peaks due to substrate silanization, enhancement of Si-O band intensity due to the Au colloids added to silanized substrate and also to observe the enhancement of Lactobacillus para paracasei infrared intensity of the characteristic frequencies at 1650, 1534 and 1450 cm-1 due to surface enhancement infrared absorption.

  2. Violence et ordre politique au Nigeria

    OpenAIRE

    Fourchard, Laurent

    2007-01-01

    International audience De nombreuses analyses ont associé le retour d'un régime civil au Nigeria en 1999 au développement d'organisations armées privées et au regain de conflits dits religieux, inter-ethniques ou communautaires. L'application controversée de la charia dans douze Etats du nord et les actions de guérilla dans la région pétrolière du delta ont ainsi largement focalisé l'attention des médias. Le retour de la " démocratie " témoignerait-t-il d'un déclin de l'Etat ? Ces violence...

  3. Au nanoparticles films used in biological sensing

    Energy Technology Data Exchange (ETDEWEB)

    Rosales Perez, M; Delgado Macuil, R; Rojas Lopez, M; Gayou, V L [Centro de Investigacion en BiotecnologIa Aplicada del IPN, Tepetitla Tlaxcala Mexico C.P. 90700 (Mexico); Sanchez Ramirez, J F, E-mail: mrosalespe@ipn.m [CICATA Legaria Instituto Politecnico Nacional, Mexico Distrito Federal (Mexico)

    2009-05-01

    Lactobacillus para paracasei are used commonly as functional food and probiotic substances. In this work Au nanoparticles self-assembled films were used for Lactobacillus para paracasei determination at five different concentrations. Functionalized substrates were immersed in a colloidal solution for one and a half hour at room temperature and dried at room temperature during four hours. After that, drops of Lactobacillus para paracasei in aqueous solution were put into the Au nanoparticles film and let dry at room temperature for another two hours. Infrared spectroscopy in attenuated total reflectance sampling mode was used to observe generation peaks due to substrate silanization, enhancement of Si-O band intensity due to the Au colloids added to silanized substrate and also to observe the enhancement of Lactobacillus para paracasei infrared intensity of the characteristic frequencies at 1650, 1534 and 1450 cm{sup -1} due to surface enhancement infrared absorption.

  4. A velocity map imaging study of gold-rare gas complexes: Au-Ar, Au-Kr, and Au-Xe

    Science.gov (United States)

    Hopkins, W. Scott; Woodham, Alex P.; Plowright, Richard J.; Wright, Timothy G.; Mackenzie, Stuart R.

    2010-06-01

    The ultraviolet photodissociation dynamics of the gold-rare gas atom van der Waals complexes (Au-RG, RG=Ar, Kr, and Xe) have been studied by velocity map imaging. Photofragmentation of Au-Ar and Au-Kr at several wavelengths permits extrapolation to zero of the total kinetic energy release (TKER) spectra as monitored in the Au(P23/2∘[5d106p]) fragment channel, facilitating the determination of ground state dissociation energies of D0″(Au-Ar)=149±13 cm-1 and D0″(Au-Kr)=240±19 cm-1, respectively. In the same spectral region, transitions to vibrational levels of an Ω'=1/2 state of the Au-Xe complex result in predissociation to the lower Au(P21/2∘[5d106p])+Xe(S10[5p6]) fragment channel for which TKER extrapolation yields a value of D0″(Au-Xe)=636±27 cm-1. Asymmetric line shapes for transitions to the v'=14 level of this state indicate coupling to the Au(P23/2∘[5d106p])+Xe(S10[5p6]) continuum, which allows us to refine this value to D0″(Au-Xe)=607±5 cm-1. The dissociation dynamics of this vibrational level have been studied at the level of individual isotopologues by fitting the observed excitation spectra to Fano profiles. These fits reveal a remarkable variation in the predissociation dynamics for different Au-Xe isotopologues. For Au-Ar and Au-Xe, the determined ground state dissociation energies are in good agreement with recent theoretical calculations; the agreement of the Au-Kr value with theory is less satisfactory.

  5. Creation du Centre Sesame un pas en avant pour la cooperation scientifique dans la region du Moyen-Orient

    CERN Multimedia

    2003-01-01

    "Le projet SESAME (Centre international de rayonnement synchrotron pour les sciences experimentales et appliquees au Moyen-Orient) vient de franchir deux etapes importantes: la pose de la premiere pierre et l'acceptation des statuts du projet par sept membres" (1 page).

  6. Plasmonic Fano resonance and dip of Au-SiO2-Au nanomatryoshka.

    Science.gov (United States)

    Liaw, Jiunn-Woei; Chen, Huang-Chih; Kuo, Mao-Kuen

    2013-01-01

    This study theoretically investigates Fano resonances and dips of an Au-SiO2-Au nanomatryoshka that is excited by a nearby electric dipole. An analytical solution of dyadic Green's functions is used to analyze the radiative and nonradiative power spectra of a radial dipole in the proximity of a nanomatryoshka. From these spectra, the plasmon modes and Fano resonances that accompany the Fano dips are identified. In addition, the scattering and absorption spectra of a nanomatryoshka that is illuminated by a plane wave are investigated to confirm these modes and Fano dips. Our results reveal that a Fano dip splits each of the dipole and quadrupole modes into bonding and anti-bonding modes. The Fano dip and resonance result from the destructive interference of the plasmon modes of the Au shell and the Au core. The Fano factors that are obtained from the nonradiative power spectra of the Au shell and the Au core of a nanomatryoshka are in accordance with those obtained from the absorption cross section spectra. Moreover, these Fano factors increase as the plasmonic coupling of the Au shell with the core increases for both dipole and quadrupole modes. PMID:24206789

  7. Ω production in p+p, Au+Au and U+U collisions at STAR

    International Nuclear Information System (INIS)

    We report STAR's high precision measurements on Ω production at mid-rapidity from √(s)=200 GeVp+p, central √(sNN)=200 GeVAu+Au, and central √(sNN)=193 GeVU+U collisions. With the significantly reduced uncertainty in p+p reference, we observe that the Ω enhancement factors at RHIC are in between SPS and LHC, while enhancement factors are systematically larger in central U+U collisions than in central Au+Au collisions. The ΩRAA is much larger than protons and pions for pT up to 4 GeV/c in central Au+Au collisions. The ratio of ΩRAA in central U+U to that in central Au+Au collisions is above unity for pT up to 6 GeV/c, which indicates coalescence/recombination to be the dominant production mechanism for Ω in these collisions for the measured pT range

  8. H2S 为毒物对乙炔氢氯化反应中 AuCl3/AC 催化剂催化活性的影响%Poisoning effect of H2S on catalytic performance of AuCl3/AC in acetylene hydrochlorination

    Institute of Scientific and Technical Information of China (English)

    代斌; 张春丽; 康丽华; 朱明远

    2015-01-01

    A study about poisoning effect of hydrogen sulfide (H2S) on the catalytic performance of AuCl3/AC during acetylene hydrochlorination deactivation is described and discussed. 1% AuCl3/AC catalyst is prepared by an incipient wetness impregnation technique. The activity tests demonstrate that H2S poisoning results in the rapid and irreversible deactivation of AuCl3/AC catalyst in acetylene hydrochlorination. Temperature-programmed reduction (TPR) and X-ray photoelectron spectra (XPS) show that H2S addition can effectively accelerate active Au3+ reduction to metallic Au0. The formation of metal sulfide may also be another reason for catalyst deactivation in the presence of H2S, which is supported by transmission electron microscopy (TEM) and energy dispersion X-ray spectrometer (EDX) techniques. In other words, with the increase of H2S added to the feed gases, the content of Au3+ is greatly reduced to metallic Au0. Moreover, the active sites are covered with Au-S compound. Both of them could reduce the effective active component, leading to the deactivation of the AuCl3/AC catalyst.%采用等体积浸渍法制备了 1% AuCl3/AC 催化剂,探究了硫化氢(H2S)为毒物对乙炔氢氯化反应中催化剂催化活性的影响及失活机理.催化活性测试结果表明,以 H2S 为毒物可导致乙炔氢氯化反应中的 AuCl3/AC 催化剂的失活,且是一个不可逆过程;程序升温还原(TPR)和 X 射线光电子能谱(XPS)分析结果表明,H2S 的加入可有效地加快 Au3+还原为 Au0;透射电镜能谱(TEM-EDX)观测分析形成的 Au-S 化合物也可导致催化剂失活,即随着 H2S 量的增大,更多的 Au3+被还原为 Au0,且形成的 Au-S 化合物覆盖在活性位点,使有效的活性组分降低进而导致 AuCl3/AC 催化剂失活.

  9. Pd-Au bimetallic catalysts: understanding alloy effects from planar models and (supported) nanoparticles.

    Energy Technology Data Exchange (ETDEWEB)

    Gao, Feng; Goodman, Wayne D.

    2012-12-21

    Pd-Au bimetallic catalysts often display enhanced catalytic activities and selectivities compared with Pd-alone catalysts. This enhancement is often caused by two alloy effects, i.e., ensemble and ligand effects. The ensemble effect is dilution of surface Pd by Au. With increasing surface Au coverages, contiguous Pd ensembles disappear and isolated Pd ensembles form. For certain reactions, for example vinyl acetate synthesis, this effect is responsible for reaction rate enhancement via the formation of highly active surface sites, e.g., isolated Pd pairs. The disappearance of contiguous Pd ensembles also switches off side reactions catalyzed by these sites. This explains selectivity increase of certain reactions, for example direct H2O2 synthesis. The ligand effect is electronic perturbation of Au to Pd. By direct charge transfer or affecting bond length, the ligand effect causes the Pd d band to be more filled and the d-band center away from the Fermi level. Both changes make Pd more "atomic like" therefore binding reactants and products weaker. For certain reactions, this eliminates the so-called "self poisoning" and enhances activity/selectivity.

  10. Production of omega mesons in p+p, d+Au, Cu+Cu, and Au+Au collisions at sqrt(s_NN)=200 GeV

    CERN Document Server

    Adare, A; Aidala, C; Ajitanand, N N; Akiba, Y; Al-Bataineh, H; Al-Jamel, A; Alexander, J; Angerami, A; Aoki, K; Apadula, N; Aphecetche, L; Aramaki, Y; Armendariz, R; Aronson, S H; Asai, J; Atomssa, E T; Averbeck, R; Awes, T C; Azmoun, B; Babintsev, V; Bai, M; Baksay, G; Baksay, L; Baldisseri, A; Barish, K N; Barnes, P D; Bassalleck, B; Basye, A T; Bathe, S; Batsouli, S; Baublis, V; Bauer, F; Baumann, C; Bazilevsky, A; Belikov, S; Belmont, R; Bennett, R; Berdnikov, A; Berdnikov, Y; Bhom, J H; Bickley, A A; Bjorndal, M T; Blau, D S; Boissevain, J G; Bok, J S; Borel, H; Boyle, K; Brooks, M L; Brown, D S; Bucher, D; Buesching, H; Bumazhnov, V; Bunce, G; Burward-Hoy, J M; Butsyk, S; Camacho, C M; Campbell, S; Caringi, A; Chai, J -S; Chang, B S; Charvet, J -L; Chen, C -H; Chernichenko, S; Chi, C Y; Chiba, J; Chiu, M; Choi, I J; Choi, J B; Choudhury, R K; Christiansen, P; Chujo, T; Chung, P; Churyn, A; Chvala, O; Cianciolo, V; Citron, Z; Cleven, C R; Cobigo, Y; Cole, B A; Comets, M P; del Valle, Z Conesa; Connors, M; Constantin, P; Csanád, M; Csörgő, T; Dahms, T; Dairaku, S; Danchev, I; Das, K; Datta, A; David, G; Dayananda, M K; Deaton, M B; Dehmelt, K; Delagrange, H; Denisov, A; d'Enterria, D; Deshpande, A; Desmond, E J; Dharmawardane, K V; Dietzsch, O; Dion, A; Donadelli, M; Drachenberg, J L; Drapier, O; Drees, A; Drees, K A; Dubey, A K; Durham, J M; Durum, A; Dutta, D; Dzhordzhadze, V; D'Orazio, L; Edwards, S; Efremenko, Y V; Egdemir, J; Ellinghaus, F; Emam, W S; Engelmore, T; Enokizono, A; En'yo, H; Espagnon, B; Esumi, S; Eyser, K O; Fadem, B; Fields, D E; Finger, M; Finger, M; Fleuret, F; Fokin, S L; Forestier, B; Fraenkel, Z; Frantz, J E; Franz, A; Frawley, A D; Fujiwara, K; Fukao, Y; Fung, S -Y; Fusayasu, T; Gadrat, S; Garishvili, I; Gastineau, F; Germain, M; Glenn, A; Gong, H; Gonin, M; Gosset, J; Goto, Y; de Cassagnac, R Granier; Grau, N; Greene, S V; Grim, G; Perdekamp, M Grosse; Gunji, T; Gustafsson, H -Å; Hachiya, T; Henni, A Hadj; Haegemann, C; Haggerty, J S; Hagiwara, M N; Hahn, K I; Hamagaki, H; Hamblen, J; Han, R; Hanks, J; Harada, H; Hartouni, E P; Haruna, K; Harvey, M; Haslum, E; Hasuko, K; Hayano, R; He, X; Heffner, M; Hemmick, T K; Hester, T; Heuser, J M; Hiejima, H; Hill, J C; Hobbs, R; Hohlmann, M; Holmes, M; Holzmann, W; Homma, K; Hong, B; Horaguchi, T; Hornback, D; Huang, S; Hur, M G; Ichihara, T; Ichimiya, R; Ide, J; Iinuma, H; Ikeda, Y; Imai, K; Inaba, M; Inoue, Y; Isenhower, D; Isenhower, L; Ishihara, M; Isobe, T; Issah, M; Isupov, A; Ivanischev, D; Iwanaga, Y; Jacak, B V; Jia, J; Jiang, X; Jin, J; Jinnouchi, O; Johnson, B M; Jones, T; Joo, K S; Jouan, D; Jumper, D S; Kajihara, F; Kametani, S; Kamihara, N; Kamin, J; Kaneta, M; Kang, J H; Kanou, H; Kapustinsky, J; Karatsu, K; Kasai, M; Kawagishi, T; Kawall, D; Kawashima, M; Kazantsev, A V; Kelly, S; Kempel, T; Khanzadeev, A; Kijima, K M; Kikuchi, J; Kim, A; Kim, B I; Kim, D H; Kim, D J; Kim, E; Kim, E J; Kim, S H; Kim, Y -J; Kim, Y -S; Kim, Y J; Kinney, E; Kiriluk, K; Kiss, Á; Kistenev, E; Kiyomichi, A; Klay, J; Klein-Boesing, C; Kochenda, L; Kochetkov, V; Komkov, B; Konno, M; Koster, J; Kotchetkov, D; Kozlov, A; Král, A; Kravitz, A; Kroon, P J; Kubart, J; Kunde, G J; Kurihara, N; Kurita, K; Kurosawa, M; Kweon, M J; Kwon, Y; Kyle, G S; Lacey, R; Lai, Y S; Lajoie, J G; Lebedev, A; Bornec, Y Le; Leckey, S; Lee, D M; Lee, J; Lee, K; Lee, K B; Lee, K S; Lee, M K; Lee, T; Leitch, M J; Leite, M A L; Leitner, E; Lenzi, B; Li, X; Li, X H; Lichtenwalner, P; Liebing, P; Lim, H; Levy, L A Linden; Liška, T; Litvinenko, A; Liu, H; Liu, M X; Love, B; Luechtenborg, R; Lynch, D; Maguire, C F; Makdisi, Y I; Malakhov, A; Malik, M D; Manko, V I; Mannel, E; Mao, Y; Mašek, L; Masui, H; Matathias, F; McCain, M C; McCumber, M; McGaughey, P L; Means, N; Meredith, B; Miake, Y; Mibe, T; Mignerey, A C; Mikeš, P; Miki, K; Miller, T E; Milov, A; Mioduszewski, S; Mishra, G C; Mishra, M; Mitchell, J T; Mitrovski, M; Mohanty, A K; Moon, H J; Morino, Y; Morreale, A; Morrison, D P; Moss, J M; Moukhanova, T V; Mukhopadhyay, D; Murakami, T; Murata, J; Nagamiya, S; Nagata, Y; Nagle, J L; Naglis, M; Nagy, M I; Nakagawa, I; Nakamiya, Y; Nakamura, K R; Nakamura, T; Nakano, K; Nam, S; Newby, J; Nguyen, M; Nihashi, M; Norman, B E; Nouicer, R; Nyanin, A S; Nystrand, J; Oakley, C; O'Brien, E; Oda, S X; Ogilvie, C A; Ohnishi, H; Ojha, I D; Oka, M; Okada, K; Omiwade, O O; Onuki, Y; Oskarsson, A; Otterlund, I; Ouchida, M; Ozawa, K; Pak, R; Pal, D; Palounek, A P T; Pantuev, V; Papavassiliou, V; Park, I H; Park, J; Park, S K; Park, W J; Pate, S F; Pei, H; Peng, J -C; Pereira, H; Peresedov, V; Peressounko, D Yu; Petti, R; Pinkenburg, C; Pisani, R P; Proissl, M; Purschke, M L; Purwar, A K; Qu, H; Rak, J; Rakotozafindrabe, A; Ravinovich, I; Read, K F; Rembeczki, S; Reuter, M; Reygers, K; Riabov, V; Riabov, Y; Richardson, E; Roach, D; Roche, G; Rolnick, S D; Romana, A; Rosati, M

    2011-01-01

    The PHENIX experiment at the Relativistic Heavy Ion Collider (RHIC) has measured omega meson production via leptonic and hadronic decay channels in p+p, d+Au, Cu+Cu, and Au+Au collisions at sqrt(s_NN) = 200 GeV. The invariant transverse momentum spectra measured in different decay modes give consistent results. Measurements in the hadronic decay channel in Cu+Cu and Au+Au collisions show that omega production has a suppression pattern at high transverse momentum, similar to that of pi^0 and eta in central collisions, but no suppression is observed in peripheral collisions. The nuclear modification factors, R_AA, are consistent in Cu+Cu and Au+Au collisions at similar numbers of participant nucleons.

  11. Production of ω mesons in p + p, d + Au, Cu + Cu, and Au + Au collisions at sNN=200 GeV

    Science.gov (United States)

    Adare, A.; Afanasiev, S.; Aidala, C.; Ajitanand, N. N.; Akiba, Y.; Al-Bataineh, H.; Al-Jamel, A.; Alexander, J.; Angerami, A.; Aoki, K.; Apadula, N.; Aphecetche, L.; Aramaki, Y.; Armendariz, R.; Aronson, S. H.; Asai, J.; Atomssa, E. T.; Averbeck, R.; Awes, T. C.; Azmoun, B.; Babintsev, V.; Bai, M.; Baksay, G.; Baksay, L.; Baldisseri, A.; Barish, K. N.; Barnes, P. D.; Bassalleck, B.; Basye, A. T.; Bathe, S.; Batsouli, S.; Baublis, V.; Bauer, F.; Baumann, C.; Bazilevsky, A.; Belikov, S.; Belmont, R.; Bennett, R.; Berdnikov, A.; Berdnikov, Y.; Bhom, J. H.; Bickley, A. A.; Bjorndal, M. T.; Blau, D. S.; Boissevain, J. G.; Bok, J. S.; Borel, H.; Boyle, K.; Brooks, M. L.; Brown, D. S.; Bucher, D.; Buesching, H.; Bumazhnov, V.; Bunce, G.; Burward-Hoy, J. M.; Butsyk, S.; Camacho, C. M.; Campbell, S.; Caringi, A.; Chai, J.-S.; Chang, B. S.; Charvet, J.-L.; Chen, C.-H.; Chernichenko, S.; Chi, C. Y.; Chiba, J.; Chiu, M.; Choi, I. J.; Choi, J. B.; Choudhury, R. K.; Christiansen, P.; Chujo, T.; Chung, P.; Churyn, A.; Chvala, O.; Cianciolo, V.; Citron, Z.; Cleven, C. R.; Cobigo, Y.; Cole, B. A.; Comets, M. P.; Conesa Del Valle, Z.; Connors, M.; Constantin, P.; Csanád, M.; Csörgő, T.; Dahms, T.; Dairaku, S.; Danchev, I.; Das, K.; Datta, A.; David, G.; Dayananda, M. K.; Deaton, M. B.; Dehmelt, K.; Delagrange, H.; Denisov, A.; D'Enterria, D.; Deshpande, A.; Desmond, E. J.; Dharmawardane, K. V.; Dietzsch, O.; Dion, A.; Donadelli, M.; Drachenberg, J. L.; Drapier, O.; Drees, A.; Drees, K. A.; Dubey, A. K.; Durham, J. M.; Durum, A.; Dutta, D.; Dzhordzhadze, V.; D'Orazio, L.; Edwards, S.; Efremenko, Y. V.; Egdemir, J.; Ellinghaus, F.; Emam, W. S.; Engelmore, T.; Enokizono, A.; En'yo, H.; Espagnon, B.; Esumi, S.; Eyser, K. O.; Fadem, B.; Fields, D. E.; Finger, M.; Finger, M., Jr.; Fleuret, F.; Fokin, S. L.; Forestier, B.; Fraenkel, Z.; Frantz, J. E.; Franz, A.; Frawley, A. D.; Fujiwara, K.; Fukao, Y.; Fung, S.-Y.; Fusayasu, T.; Gadrat, S.; Garishvili, I.; Gastineau, F.; Germain, M.; Glenn, A.; Gong, H.; Gonin, M.; Gosset, J.; Goto, Y.; Granier de Cassagnac, R.; Grau, N.; Greene, S. V.; Grim, G.; Grosse Perdekamp, M.; Gunji, T.; Gustafsson, H.-Å.; Hachiya, T.; Hadj Henni, A.; Haegemann, C.; Haggerty, J. S.; Hagiwara, M. N.; Hahn, K. I.; Hamagaki, H.; Hamblen, J.; Han, R.; Hanks, J.; Harada, H.; Hartouni, E. P.; Haruna, K.; Harvey, M.; Haslum, E.; Hasuko, K.; Hayano, R.; He, X.; Heffner, M.; Hemmick, T. K.; Hester, T.; Heuser, J. M.; Hiejima, H.; Hill, J. C.; Hobbs, R.; Hohlmann, M.; Holmes, M.; Holzmann, W.; Homma, K.; Hong, B.; Horaguchi, T.; Hornback, D.; Huang, S.; Hur, M. G.; Ichihara, T.; Ichimiya, R.; Ide, J.; Iinuma, H.; Ikeda, Y.; Imai, K.; Inaba, M.; Inoue, Y.; Isenhower, D.; Isenhower, L.; Ishihara, M.; Isobe, T.; Issah, M.; Isupov, A.; Ivanischev, D.; Iwanaga, Y.; Jacak, B. V.; Jia, J.; Jiang, X.; Jin, J.; Jinnouchi, O.; Johnson, B. M.; Jones, T.; Joo, K. S.; Jouan, D.; Jumper, D. S.; Kajihara, F.; Kametani, S.; Kamihara, N.; Kamin, J.; Kaneta, M.; Kang, J. H.; Kanou, H.; Kapustinsky, J.; Karatsu, K.; Kasai, M.; Kawagishi, T.; Kawall, D.; Kawashima, M.; Kazantsev, A. V.; Kelly, S.; Kempel, T.; Khanzadeev, A.; Kijima, K. M.; Kikuchi, J.; Kim, A.; Kim, B. I.; Kim, D. H.; Kim, D. J.; Kim, E.; Kim, E. J.; Kim, S. H.; Kim, Y.-J.; Kim, Y.-S.; Kim, Y. J.; Kinney, E.; Kiriluk, K.; Kiss, Á.; Kistenev, E.; Kiyomichi, A.; Klay, J.; Klein-Boesing, C.; Kochenda, L.; Kochetkov, V.; Komkov, B.; Konno, M.; Koster, J.; Kotchetkov, D.; Kozlov, A.; Král, A.; Kravitz, A.; Kroon, P. J.; Kubart, J.; Kunde, G. J.; Kurihara, N.; Kurita, K.; Kurosawa, M.; Kweon, M. J.; Kwon, Y.; Kyle, G. S.; Lacey, R.; Lai, Y. S.; Lajoie, J. G.; Lebedev, A.; Le Bornec, Y.; Leckey, S.; Lee, D. M.; Lee, J.; Lee, K.; Lee, K. B.; Lee, K. S.; Lee, M. K.; Lee, T.; Leitch, M. J.; Leite, M. A. L.; Leitner, E.; Lenzi, B.; Li, X.; Li, X. H.; Lichtenwalner, P.; Liebing, P.; Lim, H.; Linden Levy, L. A.; Liška, T.; Litvinenko, A.; Liu, H.; Liu, M. X.; Love, B.; Luechtenborg, R.; Lynch, D.; Maguire, C. F.; Makdisi, Y. I.; Malakhov, A.; Malik, M. D.; Manko, V. I.; Mannel, E.; Mao, Y.; Mašek, L.; Masui, H.; Matathias, F.; McCain, M. C.; McCumber, M.; McGaughey, P. L.; Means, N.; Meredith, B.; Miake, Y.; Mibe, T.; Mignerey, A. C.; Mikeš, P.; Miki, K.; Miller, T. E.; Milov, A.; Mioduszewski, S.; Mishra, G. C.; Mishra, M.; Mitchell, J. T.; Mitrovski, M.; Mohanty, A. K.; Moon, H. J.; Morino, Y.; Morreale, A.; Morrison, D. P.; Moss, J. M.; Moukhanova, T. V.; Mukhopadhyay, D.; Murakami, T.; Murata, J.; Nagamiya, S.; Nagata, Y.; Nagle, J. L.; Naglis, M.; Nagy, M. I.; Nakagawa, I.; Nakamiya, Y.; Nakamura, K. R.; Nakamura, T.; Nakano, K.; Nam, S.; Newby, J.; Nguyen, M.; Nihashi, M.; Norman, B. E.; Nouicer, R.; Nyanin, A. S.; Nystrand, J.; Oakley, C.; O'Brien, E.; Oda, S. X.; Ogilvie, C. A.; Ohnishi, H.; Ojha, I. D.; Oka, M.; Okada, K.; Omiwade, O. O.; Onuki, Y.; Oskarsson, A.; Otterlund, I.; Ouchida, M.; Ozawa, K.; Pak, R.; Pal, D.; Palounek, A. P. T.; Pantuev, V.; Papavassiliou, V.; Park, I. H.; Park, J.; Park, S. K.; Park, W. J.; Pate, S. F.; Pei, H.; Peng, J.-C.; Pereira, H.; Peresedov, V.; Peressounko, D. Yu.; Petti, R.; Pinkenburg, C.; Pisani, R. P.; Proissl, M.; Purschke, M. L.; Purwar, A. K.; Qu, H.; Rak, J.; Rakotozafindrabe, A.; Ravinovich, I.; Read, K. F.; Rembeczki, S.; Reuter, M.; Reygers, K.; Riabov, V.; Riabov, Y.; Richardson, E.; Roach, D.; Roche, G.; Rolnick, S. D.; Romana, A.; Rosati, M.; Rosen, C. A.; Rosendahl, S. S. E.; Rosnet, P.; Rukoyatkin, P.; Ružička, P.; Rykov, V. L.; Ryu, S. S.; Sahlmueller, B.; Saito, N.; Sakaguchi, T.; Sakai, S.; Sakashita, K.; Sakata, H.; Samsonov, V.; Sano, S.; Sato, H. D.; Sato, S.; Sato, T.; Sawada, S.; Sedgwick, K.; Seele, J.; Seidl, R.; Semenov, A. Yu.; Semenov, V.; Seto, R.; Sharma, D.; Shea, T. K.; Shein, I.; Shevel, A.; Shibata, T.-A.; Shigaki, K.; Shimomura, M.; Shohjoh, T.; Shoji, K.; Shukla, P.; Sickles, A.; Silva, C. L.; Silvermyr, D.; Silvestre, C.; Sim, K. S.; Singh, B. K.; Singh, C. P.; Singh, V.; Skutnik, S.; Slunečka, M.; Smith, W. C.; Soldatov, A.; Soltz, R. A.; Sondheim, W. E.; Sorensen, S. P.; Sourikova, I. V.; Sparks, N. A.; Staley, F.; Stankus, P. W.; Stenlund, E.; Stepanov, M.; Ster, A.; Stoll, S. P.; Sugitate, T.; Suire, C.; Sukhanov, A.; Sullivan, J. P.; Sziklai, J.; Tabaru, T.; Takagi, S.; Takagui, E. M.; Taketani, A.; Tanabe, R.; Tanaka, K. H.; Tanaka, Y.; Taneja, S.; Tanida, K.; Tannenbaum, M. J.; Tarafdar, S.; Taranenko, A.; Tarján, P.; Themann, H.; Thomas, D.; Thomas, T. L.; Togawa, M.; Toia, A.; Tojo, J.; Tomášek, L.; Torii, H.; Towell, R. S.; Tram, V.-N.; Tserruya, I.; Tsuchimoto, Y.; Tuli, S. K.; Tydesjö, H.; Tyurin, N.; Vale, C.; Valle, H.; van Hecke, H. W.; Vazquez-Zambrano, E.; Veicht, A.; Velkovska, J.; Vértesi, R.; Vinogradov, A. A.; Virius, M.; Vrba, V.; Vznuzdaev, E.; Wagner, M.; Walker, D.; Wang, X. R.; Watanabe, D.; Watanabe, K.; Watanabe, Y.; Wei, F.; Wei, R.; Wessels, J.; White, S. N.; Willis, N.; Winter, D.; Wood, J. P.; Woody, C. L.; Wright, R. M.; Wysocki, M.; Xie, W.; Yamaguchi, Y. L.; Yamaura, K.; Yang, R.; Yanovich, A.; Yasin, Z.; Ying, J.; Yokkaichi, S.; You, Z.; Young, G. R.; Younus, I.; Yushmanov, I. E.; Zajc, W. A.; Zaudtke, O.; Zhang, C.; Zhou, S.; Zimányi, J.; Zolin, L.

    2011-10-01

    The PHENIX experiment at the Relativistic Heavy Ion Collider has measured ω meson production via leptonic and hadronic decay channels in p+p, d+Au, Cu+Cu, and Au+Au collisions at sNN = 200 GeV. The invariant transverse momentum spectra measured in different decay modes give consistent results. Measurements in the hadronic decay channel in Cu+Cu and Au+Au collisions show that ω production has a suppression pattern at high transverse momentum, similar to that of π0 and η in central collisions, but no suppression is observed in peripheral collisions. The nuclear modification factors, RAA, are consistent in Cu+Cu and Au+Au collisions at similar numbers of participant nucleons.

  12. Revisiting the S-Au(111) interaction: Static or Dynamic?

    Energy Technology Data Exchange (ETDEWEB)

    Biener, M M; Biener, J; Friend, C M

    2004-08-17

    The chemical inertness typically observed for Au does not imply a general inability to form stable bonds with non-metals but is rather a consequence of high reaction barriers. The Au-S interaction is probably the most intensively studied interaction of Au surfaces with non-metals as, for example, it plays an important role in Au ore formation, and controls the structure and dynamics of thiol-based self-assembled-monolayers (SAMs). In recent years a quite complex picture of the interaction of sulfur with Au(111) surfaces emerged, and a variety of S-induced surface structures was reported under different conditions. The majority of these structures were interpreted in terms of a static Au surface, where the positions of the Au atoms remain essentially unperturbed. Here we demonstrate that the Au(111) surface exhibits a very dynamic character upon interaction with adsorbed sulfur: low sulfur coverages modify the surface stress of the Au surface leading to lateral expansion of the surface layer; large-scale surface restructuring and incorporation of Au atoms into a growing two-dimensional AuS phase were observed with increasing sulfur coverage. These results provide new insight into the Au-S surface chemistry, and reveal the dynamic character of the Au(111) surface.

  13. The effect of CNTs on structures and catalytic properties of AuPd clusters for H2O2 synthesis.

    Science.gov (United States)

    Yang, Hua-feng; Xie, Peng-yang; Yu, Hui-you; Li, Xiao-nian; Wang, Jian-guo

    2012-12-28

    The structures and catalytic properties of AuPd clusters supported on carbon nanotubes (CNTs) for H(2)O(2) synthesis have been investigated by means of density functional theory calculations. Firstly, the structures of AuPd clusters are strongly influenced by CNTs, in which the bottom layers are mainly composed of Pd and the top layers are a mix of Au and Pd due to the stronger binding of Pd than Au on CNTs. Especially, it is found that O(2) adsorption on the Pd/CNTs interfacial sites is much weaker than that on the only Pd sites, which is in contrast to transition metal oxide (for example TiO(2), Al(2)O(3), CeO(2)) supported metal clusters. Furthermore, Pd ensembles on the interfacial sites have far superior catalytic properties for H(2)O(2) formation than those away from CNT supports due to the changes in electronic structures caused by the CNTs. Therefore, our study provides a physical insight into the enhanced role of carbon supports in H(2)O(2) synthesis over supported AuPd catalysts. PMID:23032860

  14. Thermoelectric properties of Au-containing type-I clathrates Ba{sub 8}Au{sub x}Ga{sub 16−3x}Ge{sub 30+2x}

    Energy Technology Data Exchange (ETDEWEB)

    Ye, Zuxin; Cho, Jung Young; Tessema, Misle M. [Optimal Inc., Plymouth, MI 48170 (United States); Salvador, James R., E-mail: james.salvador@gm.com [Chemical and Materials Systems Laboratory, General Motors Global R and D, Warren, MI 48090 (United States); Waldo, Richard A. [Chemical and Materials Systems Laboratory, General Motors Global R and D, Warren, MI 48090 (United States); Yang, Jihui [Department of Materials, University of Washington (United States); Wang, Hsin; Cai, W.; Kirkham, M.J. [Materials Science and Technology Division, Oak Ridge National Laboratory (United States); Yang, Jiong; Zhang, Wenqing [Shanghai Institute of Ceramics, Chinese Academy of Science, Shanghai (China)

    2014-02-25

    Highlights: • Ba{sub 8}Au{sub x}Ga{sub 16−3x}Ge{sub 30+2x} were prepared, and the solubility limit of Au is x = 5.4. • Glass like thermal conduction at low temperature was found for p-type materials. • Higher DOS effective masses carriers were found in higher Au content samples. • Au was found to preferentially substitute at the 6c Wyckoff site. • ZT = 0.6 at 750 K was found for Ba{sub 8}Au{sub x}Ga{sub 16−3x}Ge{sub 30+2x} (x = 1, 5, and 5.33). -- Abstract: Type I clathrates, with compositions based on Ba{sub 8}Ga{sub 16}Ge{sub 30}, are a class of promising thermoelectric materials due to their intrinsically low thermal conductivity. It has been demonstrated previously that the thermoelectric performance can be improved by transition metal substitution of the framework atoms. In this study, the effects of Au substitution for Ga/Ge on thermal and electrical transport properties of type I clathrate compounds have been investigated. Polycrystalline samples with a large range of Au content have been synthesized using conventional solid state techniques with the actual compositions of resulting materials approximately following Zintl-Klemm rules. The charge carrier type changes from electrons (n) to holes (p) as the Au content increases. The Seebeck coefficient (S) and power factor (S{sup 2}/ρ where ρ is the electrical resistivity) were improved by Au substitution and the resulting overall thermoelectric properties were enhanced by Au substitution as compared to polycrystalline Ba{sub 8}Ga{sub 16}Ge{sub 30}. The thermoelectric figure of merit ZT attains a value of 0.63 at 740 K for the composition Ba{sub 8}Au{sub 5.47}Ge{sub 39.96}, a value that is somewhat lower than those reported previously. The results presented herein show that Au-containing type I clathrates are promising p-type thermoelectric materials for high temperature applications.

  15. 2010 Port-au-Prince, Haiti Images

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — According to official estimates, 222,570 people killed, 300,000 injured, 1.3 million displaced, 97,294 houses destroyed and 188,383 damaged in the Port-au-Prince...

  16. Surface structure of AU3Cu(001)

    DEFF Research Database (Denmark)

    Eckstein, G.A.; Maupai, S.; Dakkouri, A.S.;

    1999-01-01

    The surface morphology, composition, and structure of Au3Cu(001) as determined by scanning tunneling microscopy and surface x-ray diffraction are presented. Atomic resolution STM images reveal distinctive geometric features. The analysis of the surface x-ray diffraction data provides clear evidence...... for the surface structure. [S0163-1829(99)04535-X]....

  17. Didaktik des außerschulischen Lernens

    CERN Document Server

    Sauerborn, Petra

    2012-01-01

    Kernprobleme schulischer Bildung sind die zunehmenden Verluste an Realitäts- und Praxisbezug sowie die einseitige Betonung der fachwissenschaftlichen Kenntnisse. In jüngster Zeit werden insbesondere moderne didaktisch-methodische Konzepte näher diskutiert und praktiziert. So finden sich etwa die Stichwörter Handlungsorientierter Unterricht und Offener Unterricht in der fachdidaktischen Diskussion wieder. Eine wesentlich aktuellere Form stellt das außerschulische Lernen dar. Ein modernes pädagogisches Verständnis sieht den Unterricht heute nicht mehr als ausschließliche Tätigkeit des Lehrers an, sondern als Aktivität der Lernenden. Außerschulisches Lernen beschreibt die originale Begegnung im Unterricht außerhalb des Klassenzimmers. An außerschulischen Lernorten findet eine unmittelbare AuseinanderSetzung des Lernenden mit seiner räumlichen Umgebung statt. Charakteristisch sind hierbei vor allem die aktive(Mit-)Gestaltung sowie die eigenständige Wahrnehmung mehrperspektivischer Bildungsinhalte d...

  18. Stability of gold cages (Au16 and Au17) at finite temperature

    Indian Academy of Sciences (India)

    Prachi Chandrachud; Kavita Joshi; Sailaja Krishnamurty; D G Kanhere

    2009-05-01

    We have employed ab initio molecular dynamics to investigate the stability of the smallest gold cages, namely Au16 and Au17, at finite temperatures. First, we obtain the ground state structure along with at least 50 distinct isomers for both the clusters. This is followed by the finite temperature simulations of these clusters. Each cluster is maintained at 12 different temperatures for a time period of at least 150 ps. Thus, the total simulation time is of the order of 2.4 ns for each cluster. We observe that the cages are stable at least up to 850 K. Although both clusters melt around the same temperature, i.e. around 900 K, Au17 shows a peak in the heat capacity curve in contrast to the broad peak seen for Au16.

  19. Dispersion and STM Characterization of Au-CdSe Nanohybrids on Au(111)

    Institute of Scientific and Technical Information of China (English)

    Bo Gao; Yan-min Kuang; Yuan Liao; Zhen-chao Dong

    2012-01-01

    We report the dispersion and scanning tunneling microscopy (STM) characterization of isolated Au-CdSe nanohybrids on atomically flat Au(111) through surface modifications.The top terminal groups of spacer molecules self-assembled on the surface are found critical for locking the nanohybrids into a well-separated state.The STM results indicate that both thiol and carboxylic terminals are effective in this aspect by making strong interaction with the Au portions of the nanohybrids.An argon ion sputtering technique is also proposed to clean up organic contaminants on the surface for improved STM imaging of individual Au-CdSe nanohybrids.These observations help to enrich technical approaches to dispersing individual nanostructures on the surface and provide opportunities to explore their local electroluminescent and energy transfer properties at the nanoscale.

  20. High Resolution Photoelectron Spectroscopy of Au_2^- and Au_4^- by Photoelectron Imaging

    Science.gov (United States)

    Leon, Iker; Yang, Zheng; Wang, Lai-Sheng

    2013-06-01

    We report high resolution photoelectron spectra of Au_2^- and Au_4^- obtained with a newly-built photoelectron imaging apparatus. Gold anions are produced by laser vaporization and the desired specie is mass selected and focused into the collinear velocity-map imaging (VMI) lens assembly. The design of the imaging lens has allowed us to obtain less than 0.9% energy resolution for high kinetic energy electrons ( > 1eV) while maintaining wavenumber resolution for low kinetic energy electrons. Although gold dimer and tetramer have been studied in the past, we present spectroscopic results under high resolution. For Au_2^-, we report high resolution spectra with an accurate determination of the electron affinity together with a complete vibrational assignment, for both the anion and neutral ground states, while for Au_4^-, we are able to resolve a low frequency mode and obtain accurately the adiabatic detachment energy.

  1. Forward-backward multiplicity correlation in Au+Au collisions at RHIC with transport model PACIAE

    CERN Document Server

    Yan, Yu-Liang; Dong, Bao-Guo; Li, Xiao-Mei; Ma, Hai-Liang; Sa, Ben-Hao

    2009-01-01

    We have studied the charged particle forward-backward multiplicity correlation strength in 0-10% most central Au+Au collisions at \\sqrt{s_{NN}}=200 GeV by a parton and hadron cascade model, PACIAE based on PYTHIA. The real (total), statistical, and NBD (Negative Binomial Distribution) correlation strengths are calculated, respectively, with the real events, mixed events, and NBD fitting the charged particle multiplicity distribution. The corresponding STAR data are well reproduced by the real one. If the discrepancy between real and statistical correlation strengths is identified as dynamical correlation strength, the dynamical correlation strength is then just counted few percent of the total correlation strength. In addition, we also calculated the 0-5 and 5% most central Au+Au collisions and turned out that the correlation strength increases monotonously with increasing size of the centrality bin.

  2. Simulation of energy scan of pion interferometry in central Au+Au collisions at relativistic energies

    International Nuclear Information System (INIS)

    We present a systematic analysis of two-pion interferometry for the central Au+Au collisions at √sNN = 3, 5, 7, 11, 17, 27, 39, 62, 130 and 200 GeV/c with the help of a multiphase transport (AMPT) model. Emission source-size radius parameters Rlong, Rout, Rside and the chaotic parameter λ are extracted and compared with the experimental data. Transverse momentum and azimuthal angle dependencies of the HBT radii are also discussed for central Au+Au collisions at 200 GeV/c. The results show that the HBT radii in central collisions do not change much above 7 GeV/c. For central collisions at 200 GeV/c, the radii decrease with the increasing of transverse momentum pT but are not sensitive to the azimuthal angle. These results provide a theoretical reference for the energy scan program of the RHIC-STAR experiment. (authors)

  3. Charged-particle pseudorapidity distributions in Au+Au collisions at RHIC

    Institute of Scientific and Technical Information of China (English)

    WANG Zeng-Wei; JIANG Zhi-Jin

    2009-01-01

    Using the Glauber model, we present the formulas for calculating the numbers of participants,spectators and binary nucleon-nucleon collisions. Based on this work, we get the pseudorapidity distributions of charged particles as the function of the impact parameter in nucleus-nucleus collisions. The theoretical results agree well with the experimental observations made by the BRAHMS Collaboration in Au+Au collisions at √SNN=200 GeV in different centrality bins over the whole pseudorapidity range.

  4. Baryonic Effect on XcJ Suppression in Au+Au Collisions at RHIC Energies

    Institute of Scientific and Technical Information of China (English)

    PENG Ru; XU Xiao-Ming; ZHOU Dai-Cui

    2004-01-01

    @@ We predict that xcJ mesons at low transverse momentum in the central rapidity region are almost dissociated by nucleons and antinucleons in hadronic matter produced in central Au+Au collisions at relativistic high-ion collider (RHIC) energies √SNN = 130 and 200 GeV. In the calculations the nucleon and antinucleon distributions in hadronic matter are results of evolution from their freeze-out distributions which well fit the experimental transverse momentum spectra of proton and antiproton.

  5. Flow and bose-einstein correlations in Au-Au collisions at RHIC

    Science.gov (United States)

    Phobos Collaboration; Manly, Steven; Back, B. B.; Baker, M. D.; Barton, D. S.; Betts, R. R.; Bindel, R.; Budzanowski, A.; Busza, W.; Carroll, A.; Decowski, M. P.; Garcia, E.; George, N.; Gulbrandsen, K.; Gushue, S.; Halliwell, C.; Hamblen, J.; Henderson, C.; Hofman, D.; Hollis, R. S.; Hołyinski, R.; Holzman, B.; Iordanova, A.; Johnson, E.; Kane, J.; Katzy, J.; Khan, N.; Kucewicz, W.; Kulinich, P.; Kuo, C. M.; Lin, W. T.; Manly, S.; McLeod, D.; Michałowski, J.; Mignerey, A.; Nouicer, R.; Olszewski, A.; Pak, R.; Park, I. C.; Pernegger, H.; Reed, C.; Remsberg, L. P.; Reuter, M.; Roland, C.; Roland, G.; Rosenberg, L.; Sagerer, J.; Sarin, P.; Sawicki, P.; Skulski, W.; Steadman, S. G.; Steinberg, P.; Stephans, G. S. F.; Stodulski, M.; Sukhanov, A.; Tang, J.-L.; Teng, R.; Trzupek, A.; Vale, C.; van Nieuwenhuizen, G. J.; Verdier, R.; Wadsworth, B.; Wolfs, F. L. H.; Wosiek, B.; Woźniak, K.; Wuosmaa, A. H.; Wysłouch, B.

    2003-03-01

    Argonne flow and Bose-Einstein correlations have been measured in Au-Au collisions at S=130 and 200 GeV using the PHOBOS detector at RHIC. The systematic dependencies of the flow signal on the transverse momentum, pseudorapidity, and centrality of the collision, as well as the beam energy are shown. In addition, results of a 3-dimensional analysis of two-pion correlations in the 200 GeV data are presented.

  6. Results from experiment E917 for Au + Au collisions at the AGS

    International Nuclear Information System (INIS)

    The effects of baryon stopping and its resulting energy deposition on the dynamics of Au + Au collisions at 6, 8 and 10.8 GeV/nucleon are explored with recent results from the AGS experiment E917. Current analyses of stopping, collective flow signals and HBT parameters are presented. Strangeness and anti-baryon production is examined using the yields of anti-lambdas and anti-protons

  7. Net baryon density in Au+Au collisions at the Relativistic Heavy Ion Collider

    CERN Document Server

    Bass, S A; Srivastava, D K; Bass, Steffen A.; Müller, Berndt; Srivastava, Dinesh K.

    2003-01-01

    We calculate the net baryon rapidity distribution in Au+Au collisions at the Relativistic Heavy Ion Collider (RHIC) in the framework of the Parton Cascade Model (PCM). Parton rescattering and fragmentation leads to a substantial increase in the net baryon density at mid-rapidity over the density produced by initial primary parton-parton scatterings. The PCM is able to describe the measured net baryon density at RHIC.

  8. Some thoughts on di-jet correlation in Au + Au collisions from PHENIX

    CERN Document Server

    Jia, J

    2006-01-01

    PHENIX has measured the two particle azimuth correlation in Au + Au at $\\sqrt{s}$ = 200 GeV. Jet shape and yield at the away side are found to be strongly modified at intermediate and low $p_T$, and the modifications vary dramatically with $p_T$ and centrality. At high $p_T$, away side jet peak reappears but the yield is suppressed. We discuss the possible physics pictures leading to these complicated modifications.

  9. Anti-flow of K$^0_s$ Mesons in 6 AGeV Au + Au Collisions

    CERN Document Server

    Chung, P; Alexander, J M; Anderson, M; Best, D; Brady, F P; Case, T; Caskey, W; Cebra, D; Chance, J L; Cole, B; Crowe, K M; Das, A; Draper, J E; Gilkes, M L; Gushue, S; Heffner, M; Hirsch, A S; Hjort, E L; Huo, L; Justice, M; Kaplan, M; Keane, D; Kintner, J C; Klay, J L; Krofcheck, D; Lacey, R A; Lauret, J; Lisa, M A; Liu, H; Liu, Y M; McGrath, R; Milosevich, Z; Odyniec, Grazyna Janina; Olson, D L; Panitkin, S Y; Pinkenburg, C H; Porile, N T; Rai, G; Ritter, H G; Romero, J L; Scharenberg, R P; Schröder, L; Srivastava, B; BStone, N T; Symons, T J M; Wienold, T; Whitfield, R W J; Wood, L; Zhang Wei Ning

    2000-01-01

    We have measured the sideward flow of neutral strange ($K^0_s$) mesons in 6 AGeV Au + Au collisions. A prominent anti-flow signal is observed for an impact parameter range (b $\\lesssim 7$ fm) which spans central and mid-central events. Since the $K^0_s$ scattering cross section is relatively small in nuclear matter, this observation suggests that the in-medium kaon vector potential plays an important role in high density nuclear matter.

  10. Critical Behavior in Peripheral Au + Au Collisions at 35 MeV/u

    CERN Document Server

    Bruno, M; Belkacem, M; Agostino, M D; Milazzo, P M; Vannini, G; Bowman, D R; Dinius, J D; Ferrero, A; Fiandri, M L; Gelbke, C K; Glasmacher, T; Gramegna, F; Handzy, D O; Horn, D; Hsi, W C; Huang, M; Iori, I; Kunde, G J; Lisa, M A; Lynch, W G; Margagliotti, G V; Montoya, C P; Moroni, A; Peaslee, G F; Rui, R; Schwarz, C; Tsang, M B; Williams, C; Latora, V; Bonasera, A

    1996-01-01

    The signals theoretically predicted for the occurrence of a critical behavior (conditional moments of charge distributions, Campi scatter plot, fluctuations of the size of the largest fragment, power law in the charge distribution, intermittency) have been found for peripheral events in the reaction Au+Au at 35 MeV/u. The same signals have been studied with a dynamical model which foresees phase transition, like the Classical Molecular Dynamics.

  11. Dissociative adsorption of water on Au/MgO/Ag(001) from first principles calculations

    Science.gov (United States)

    Nevalaita, J.; Häkkinen, H.; Honkala, K.

    2015-10-01

    The molecular and dissociative adsorption of water on a Ag-supported 1 ML, 2 ML and 3 ML-a six atomic layer-thick MgO films with a single Au adatom is investigated using density functional theory calculations. The obtained results are compared to a bulk MgO(001) surface with an Au atom. On thin films the negatively charged Au strengthens the binding of the polar water molecule due to the attractive Au-H interaction. The adsorption energy trends of OH and H with respect to the film thickness depend on an adsorption site. In the case OH or H binds atop Au on MgO/Ag(001), the adsorption becomes more exothermic with the increasing film thickness, while the reverse trend is seen when the adsorption takes place on bare MgO/Ag(001). This behavior can be explained by different bonding mechanisms identified with the Bader analysis. Interestingly, we find that the rumpling of the MgO film and the MgO-Ag interface distance correlate with the charge transfer over the thin film and the interface charge, respectively. Moreover, we employ a modified Born-Haber-cycle to analyze the effect of film thickness to the adsorption energy of isolated Au and OH species on MgO/Ag(001). The analysis shows that the attractive Coulomb interaction between the negatively charged adsorbate and the positive MgO-Ag-interface does not completely account for the weaker binding with increasing film thickness. The redox energy associated with the charge transfer from the interface to the adsorbate is more exothermic with the increasing film thickness and partly compensates the decrease in the attractive Coulomb interaction.

  12. Nuclear modification factors of phi mesons in d+Au, Cu+Cu and Au+Au collisions at sqrt(S_NN)=200 GeV

    CERN Document Server

    Adare, A; Aidala, C; Ajitanand, N N; Akiba, Y; Al-Bataineh, H; Alexander, J; Al-Jamel, A; Angerami, A; Aoki, K; Aphecetche, L; Aramaki, Y; Armendariz, R; Aronson, S H; Asai, J; Atomssa, E T; Averbeck, R; Awes, T C; Azmoun, B; Babintsev, V; Bai, M; Baksay, G; Baksay, L; Baldisseri, A; Barish, K N; Barnes, P D; Bassalleck, B; Basye, A T; Bathe, S; Batsouli, S; Baublis, V; Bauer, F; Baumann, C; Bazilevsky, A; Belikov, S; Belmont, R; Bennett, R; Berdnikov, A; Berdnikov, Y; Bhom, J H; Bickley, A A; Bjorndal, M T; Blau, D S; Boissevain, J G; Bok, J S; Borel, H; Borggren, N; Boyle, K; Brooks, M L; Brown, D S; Bucher, D; Buesching, H; Bumazhnov, V; Bunce, G; Burward-Hoy, J M; Butsyk, S; Campbell, S; Caringi, A; Cassano, N; Chai, J -S; Chang, B S; Charvet, J -L; Chen, C -H; Chernichenko, S; Chiba, J; Chi, C Y; Chiu, M; Choi, I J; Choi, J B; Choudhury, R K; Christiansen, P; Chujo, T; Chung, P; Churyn, A; Chvala, O; Cianciolo, V; Citron, Z; Cleven, C R; Cobigo, Y; Cole, B A; Comets, M P; del Valle, Z Conesa; Connors, M; Constantin, P; Csanad, M; Csorgo, T; Dahms, T; Dairaku, S; Danchev, I; Das, K; Datta, A; David, G; Dayananda, M K; Deaton, M B; Dehmelt, K; Delagrange, H; Denisov, A; d'Enterria, D; Deshpande, A; Desmond, E J; Dharmawardane, K V; Dietzsch, O; Dion, A; Donadelli, M; Orazio, L D; Drachenberg, J L; Drapier, O; Drees, A; Drees, K A; Dubey, A K; Durham, J M; Durum, A; Dutta, D; Dzhordzhadze, V; Edwards, S; Efremenko, Y V; Egdemir, J; Ellinghaus, F; Emam, W S; Engelmore, T; Enokizono, A; En'yo, H; Espagnon, B; Esumi, S; Eyser, K O; Fadem, B; Fields, D E; Finger, M; Finger, M; Fleuret, F; Fokin, S L; Forestier, B; Fraenkel, Z; Frantz, J E; Franz, A; Frawley, A D; Fujiwara, K; Fukao, Y; Fung, S -Y; Fusayasu, T; Gadrat, S; Garishvili, I; Gastineau, F; Germain, M; Glenn, A; Gong, H; Gonin, M; Gosset, J; Goto, Y; de Cassagnac, R Granier; Grau, N; Greene, S V; Grim, G; Perdekamp, M Grosse; Gunji, T; Gustafsson, H -A; Hachiya, T; Henni, A Hadj; Haegemann, C; Haggerty, J S; Hagiwara, M N; Hahn, K I; Hamagaki, H; Hamblen, J; Hanks, J; Han, R; Harada, H; Hartouni, E P; Haruna, K; Harvey, M; Haslum, E; Hasuko, K; Hayano, R; Heffner, M; Hemmick, T K; Hester, T; Heuser, J M; He, X; Hiejima, H; Hill, J C; Hobbs, R; Hohlmann, M; Holmes, M; Holzmann, W; Homma, K; Hong, B; Horaguchi, T; Hornback, D; Huang, S; Hur, M G; Ichihara, T; Ichimiya, R; Iinuma, H; Ikeda, Y; Imai, K; Inaba, M; Inoue, Y; Isenhower, D; Isenhower, L; Ishihara, M; Isobe, T; Issah, M; Isupov, A; Ivanischev, D; Iwanaga, Y; Jacak, B V; Jia, J; Jiang, X; Jin, J; Jinnouchi, O; Johnson, B M; Jones, T; Joo, K S; Jouan, D; Jumper, D S; Kajihara, F; Kametani, S; Kamihara, N; Kamin, J; Kaneta, M; Kang, J H; Kanou, H; Kapustinsky, J; Karatsu, K; Kasai, M; Kawagishi, T; Kawall, D; Kawashima, M; Kazantsev, A V; Kelly, S; Kempel, T; Khanzadeev, A; Kijima, K M; Kikuchi, J; Kim, A; Kim, B I; Kim, D H; Kim, D J; Kim, E J; Kim, E; Kim, Y -J; Kim, Y -S; Kinney, E; Kiss, A; Kistenev, E; Kiyomichi, A; Klay, J; Klein-Boesing, C; Kochenda, L; Kochetkov, V; Komkov, B; Konno, M; Koster, J; Kotchetkov, D; Kotov, D; Kozlov, A; Kral, A; Kravitz, A; Kroon, P J; Kubart, J; Kunde, G J; Kurihara, N; Kurita, K; Kurosawa, M; Kweon, M J; Kwon, Y; Kyle, G S; Lacey, R; Lai, Y S; Lajoie, J G; Lebedev, A; Le Bornec, Y; Leckey, S; Lee, D M; Lee, J; Lee, K B; Lee, K S; Lee, M K; Lee, T; Leitch, M J; Leite, M A L; Lenzi, B; Lichtenwalner, P; Liebing, P; Lim, H; Levy, L A Linden; Liska, T; Litvinenko, A; Liu, H; Liu, M X; Li, X; Li, X H; Love, B; Lynch, D; Maguire, C F; Makdisi, Y I; Malakhov, A; Malik, M D; Manko, V I; Mannel, E; Mao, Y; Masek, L; Masui, H; Matathias, F; McCain, M C; McCumber, M; McGaughey, P L; Means, N; Meredith, B; Miake, Y; Mibe, T; Mignerey, A C; Mikes, P; Miki, K; Miller, T E; Milov, A; Mioduszewski, S; Mishra, G C; Mishra, M; Mitchell, J T; Mitrovski, M; Mohanty, A K; Moon, H J; Morino, Y; Morreale, A; Morrison, D P; Moss, J M; Moukhanova, T V; Mukhopadhyay, D; Murakami, T; Murata, J; Nagamiya, S; Nagata, Y; Nagle, J L; Naglis, M; Nagy, M I; Nakagawa, I; Nakamiya, Y; Nakamura, K R; Nakamura, T; Nakano, K; Nam, S; Newby, J; Nguyen, M; Nihashi, M; Norman, B E; Nouicer, R; Nyanin, A S; Nystrand, J; Oakley, C; O'Brien, E; Oda, S X; Ogilvie, C A; Ohnishi, H; Ojha, I D; Okada, K; Oka, M; Omiwade, O O; Onuki, Y; Oskarsson, A; Otterlund, I; Ouchida, M; Ozawa, K; Pak, R; Pal, D; Palounek, A P T; Pantuev, V; Papavassiliou, V; Park, I H; Park, J; Park, S K; Park, W J; Pate, S F; Pei, H; Peng, J -C; Pereira, H; Peresedov, V; Peressounko, D Yu; Petti, R; Pinkenburg, C; Pisani, R P; Proissl, M; Purschke, M L; Purwar, A K; Qu, H; Rak, J; Rakotozafindrabe, A; Ravinovich, I; Read, K F; Rembeczki, S; Reuter, M; Reygers, K; Riabov, V; Riabov, Y; Richardson, E; Roach, D; Roche, G; Rolnick, S D; Romana, A; Rosati, M; Rosen, C A; Rosendahl, S S E; Rosnet, P; Rukoyatkin, P; Ruzicka, P; Rykov, V L

    2010-01-01

    The PHENIX experiment at the Relativistic Heavy Ion Collider (RHIC) has performed systematic measurements of phi meson production in the K+K- decay channel at midrapidity in p+p, d+Au, Cu+Cu and Au+Au collisions at sqrt(S_NN)=200 GeV. Results are presented on the phi invariant yield and the nuclear modification factor R_AA for Au+Au and Cu+Cu, and R_dA for d+Au collisions, studied as a function of transverse momentum (1Au+Au collisions, the R_AA of phi exhibits a suppression relative to expectations from binary scaled p+p results. The amount of suppression is smaller than that of the neutral pion and the eta meson in the intermediate p_T range (2--5 GeV/c); whereas at higher p_T the phi, pi^0, and eta show similar suppression. The baryon (protons and anti-protons) excess observed in central Au+Au collisions at intermediate p_T is not observed for the phi meson despite the similar mass of the proton and the phi. This suggests that the excess is lin...

  13. Suppression of Upsilon Production in d+Au and Au+Au Collisions at sqrt(s_NN) = 200 GeV

    CERN Document Server

    Adamczyk, L; Agakishiev, G; Aggarwal, M M; Ahammed, Z; Alekseev, I; Alford, J; Anson, C D; Aparin, A; Arkhipkin, D; Aschenauer, E C; Averichev, G S; Banerjee, A; Beavis, D R; Bellwied, R; Bhasin, A; Bhati, A K; Bhattarai, P; Bichsel, H; Bielcik, J; Bielcikova, J; Bland, L C; Bordyuzhin, I G; Borowski, W; Bouchet, J; Brandin, A V; Brovko, S G; Bültmann, S; Bunzarov, I; Burton, T P; Butterworth, J; Caines, H; Sánchez, M Calderón de la Barca; Cebra, D; Cendejas, R; Cervantes, M C; Chaloupka, P; Chang, Z; Chattopadhyay, S; Chen, H F; Chen, J H; Chen, L; Cheng, J; Cherney, M; Chikanian, A; Christie, W; Chwastowski, J; Codrington, M J M; Contin, G; Cramer, J G; Crawford, H J; Cui, X; Das, S; Leyva, A Davila; De Silva, L C; Debbe, R R; Dedovich, T G; Deng, J; Derevschikov, A A; de Souza, R Derradi; Dhamija, S; di Ruzza, B; Didenko, L; Dilks, C; Ding, F; Djawotho, P; Dong, X; Drachenberg, J L; Draper, J E; Du, C M; Dunkelberger, L E; Dunlop, J C; Efimov, L G; Engelage, J; Engle, K S; Eppley, G; Eun, L; Evdokimov, O; Fatemi, R; Fazio, S; Fedorisin, J; Filip, P; Finch, E; Fisyak, Y; Flores, C E; Gagliardi, C A; Gangadharan, D R; Garand, D; Geurts, F; Gibson, A; Girard, M; Gliske, S; Greiner, L; Grosnick, D; Guo, Y; Gupta, A; Gupta, S; Guryn, W; Haag, B; Hajkova, O; Hamed, A; Han, L-X; Haque, R; Harris, J W; Heppelmann, S; Hill, K; Hirsch, A; Hoffmann, G W; Hofman, D J; Horvat, S; Huang, B; Huang, H Z; Huang, X; Huck, P; Humanic, T J; Igo, G; Jacobs, W W; Jang, H; Judd, E G; Kabana, S; Kalinkin, D; Kang, K; Kauder, K; Ke, H W; Keane, D; Kechechyan, A; Kesich, A; Khan, Z H; Kikola, D P; Kisel, I; Kisiel, A; Koetke, D D; Kollegger, T; Konzer, J; Koralt, I; Kotchenda, L; Kravtsov, P; Krueger, K; Kulakov, I; Kumar, L; Kycia, R A; Lamont, M A C; Landgraf, J M; Landry, K D; Lauret, J; Lebedev, A; Lednicky, R; Lee, J H; LeVine, M J; Li, C; Li, W; Li, X; Li, Y; Li, Z M; Lima, L M; Lisa, M A; Liu, F; Ljubicic, T; Llope, W J; Lomnitz, M; Longacre, R S; Luo, X; Ma, G L; Ma, Y G; Don, D M M D Madagodagettige; Mahapatra, D P; Majka, R; Margetis, S; Markert, C; Masui, H; Matis, H S; McDonald, D; McShane, T S; Minaev, N G; Mioduszewski, S; Mohanty, B; Mondal, M M; Morozov, D A; Munhoz, M G; Mustafa, M K; Nandi, B K; Nasim, Md; Nayak, T K; Nelson, J M; Nigmatkulov, G; Nogach, L V; Noh, S Y; Novak, J; Nurushev, S B; Odyniec, G; Ogawa, A; Oh, K; Ohlson, A; Okorokov, V; Oldag, E W; Oliveira, R A N; Pachr, M; Page, B S; Pal, S K; Pan, Y X; Pandit, Y; Panebratsev, Y; Pawlak, T; Pawlik, B; Pei, H; Perkins, C; Peryt, W; Peterson, A; Pile, P; Planinic, M; Pluta, J; Poljak, N; Porter, J; Poskanzer, A M; Pruthi, N K; Przybycien, M; Pujahari, P R; Putschke, J; Qiu, H; Quintero, A; Ramachandran, S; Raniwala, R; Raniwala, S; Ray, R L; Riley, C K; Ritter, H G; Roberts, J B; Rogachevskiy, O V; Romero, J L; Ross, J F; Roy, A; Ruan, L; Rusnak, J; Sahoo, N R; Sahu, P K; Sakrejda, I; Salur, S; Sandweiss, J; Sangaline, E; Sarkar, A; Schambach, J; Scharenberg, R P; Schmah, A M; Schmidke, W B; Schmitz, N; Seger, J; Seyboth, P; Shah, N; Shahaliev, E; Shanmuganathan, P V; Shao, M; Sharma, B; Shen, W Q; Shi, S S; Shou, Q Y; Sichtermann, E P; Singaraju, R N; Skoby, M J; Smirnov, D; Smirnov, N; Solanki, D; Sorensen, P; deSouza, U G; Spinka, H M; Srivastava, B; Stanislaus, T D S; Stevens, J R; Stock, R; Strikhanov, M; Stringfellow, B; Suaide, A A P; Sumbera, M; Sun, X; Sun, X M; Sun, Y; Sun, Z; Surrow, B; Svirida, D N; Symons, T J M; de Toledo, A Szanto; Szelezniak, M A; Takahashi, J; Tang, A H; Tang, Z; Tarnowsky, T; Thomas, J H; Timmins, A R; Tlusty, D; Tokarev, M; Trentalange, S; Tribble, R E; Tribedy, P; Trzeciak, B A; Tsai, O D; Turnau, J; Ullrich, T; Underwood, D G; Van Buren, G; van Nieuwenhuizen, G; Vanfossen,, J A; Varma, R; Vasconcelos, G M S; Vasiliev, A N; Vertesi, R; Videbæk, F; Viyogi, Y P; Vokal, S; Vossen, A; Wada, M; Wang, F; Wang, G; Wang, H; Wang, J S; Wang, X L; Wang, Y; Webb, G; Webb, J C; Westfall, G D; Wieman, H; Wimsatt, G; Wissink, S W; Witt, R; Wu, Y F; Xiao, Z; Xie, W; Xin, K; Xu, H; Xu, J; Xu, N; Xu, Q H; Xu, Y; Xu, Z; Yan, W; Yang, C; Yang, Y; Ye, Z; Yepes, P; Yi, L; Yip, K; Yoo, I-K; Yu, N; Zawisza, Y; Zbroszczyk, H; Zha, W; Zhang, J B; Zhang, J L; Zhang, S; Zhang, X P; Zhang, Y; Zhang, Z P; Zhao, F; Zhao, J; Zhong, C; Zhu, X; Zhu, Y H; Zoulkarneeva, Y; Zyzak, M

    2014-01-01

    We report measurements of Upsilon meson production in p+p, d+Au, and Au+Au collisions using the STAR detector at RHIC. We compare the Upsilon yield to the measured cross section in p+p collisions in order to quantify any modifications of the yield in cold nuclear matter using d+Au data and in hot nuclear matter using Au+Au data separated into three centrality classes. Our p+p measurement is based on three times the statistics of our previous result. We obtain a nuclear modification factor for Upsilon(1S+2S+3S) in the rapidity range |y|<1 in d+Au collisions of R_dAu = 0.67 +/- 0.12 (stat.) +/- 0.04 (sys.) +/- 0.08 (pp sys.). A comparison with models including shadowing and initial state parton energy loss indicates the presence of additional cold-nuclear matter suppression. Similarly, in the top 10% most-central Au+Au collisions, we measure a nuclear modification factor of R_AA=0.36 +/- 0.09 (stat.) +/- 0.01 (sys.) +/- 0.04 (pp sys.), which is a larger suppression factor than that seen in cold nuclear matte...

  14. The point-defect of carbon nanotubes anchoring Au nanoparticles

    DEFF Research Database (Denmark)

    Lv, Y. A.; Cui, Y. H.; Li, X. N.;

    2010-01-01

    The understanding of the interaction between Au and carbon nanotubes (CNTs) is very important since Au/CNTs composites have wide applications in many fields. In this study, we investigated the dispersion of Au nanoparticles on the CNTs by transmission electron microscopy and the bonding mechanism...

  15. La situation politique du Jawf au Ier millénaire avant J.-C.

    Directory of Open Access Journals (Sweden)

    Mounir Arbach

    2003-09-01

    Full Text Available La région du Jawf, située à une centaine de kilomètres au nord-est de Sanaa, possède un nombre important de sites archéologiques sudarabiques. Les plus importants sont, du sud-est au nord-ouest : Barâqish, l’antique Yathill, dont l’enceinte est l’ouvrage défensif le mieux conservé parmi les sites préislamiques ; Ma‘în, l’antique Qarnaw, capitale du royaume de Ma‘în ; Kharibat Hamdân, l’antique Haram ; Kamna, l’antique Kaminahû ; al-Sawdâ’, l’antique Nashshân ; et al-Baydâ’, l’antique Nashq. L...

  16. Bonding, Luminescence, Metallophilicity in Linear Au3 and Au2Ag Chains Stabilized by Rigid Diphosphanyl NHC Ligands.

    Science.gov (United States)

    Ai, Pengfei; Mauro, Matteo; Gourlaouen, Christophe; Carrara, Serena; De Cola, Luisa; Tobon, Yeny; Giovanella, Umberto; Botta, Chiara; Danopoulos, Andreas A; Braunstein, Pierre

    2016-09-01

    The heterofunctional and rigid ligand N,N'-diphosphanyl-imidazol-2-ylidene (PCNHCP; P = P(t-Bu)2), through its phosphorus and two N-heterocyclic carbene (NHC) donors, stabilizes trinuclear chain complexes, with either Au3 or AgAu2 cores, and dinuclear Au2 complexes. The two oppositely situated PCNHCP (L) ligands that "sandwich" the metal chain can support linear and rigid structures, as found in the known tricationic Au(I) complex [Au3(μ3-PCNHCP,κP,κCNHC,κP)2](OTf)3 (OTf = CF3SO3; [Au3L2](OTf)3; Chem. Commun. 2014, 50, 103-105) now also obtained by transmetalation from [Ag3(μ3-PCNHCP,κP,κCNHC,κP)2](OTf)3 ([Ag3L2](OTf)3), or in the mixed-metal tricationic [Au2Ag(μ3-PCNHCP,κP,κCNHC,κP)2](OTf)3 ([Au2AgL2](OTf)3). The latter was obtained stepwise by the addition of AgOTf to the digold(I) complex [Au2(μ2-PCNHCP,κP,κCNHC)2](OTf)2 ([Au2L2](OTf)2). The latter contains two dangling P donors and displays fluxional behavior in solution, and the Au···Au separation of 2.8320(6) Å in the solid state is consistent with metallophilic interactions. In the solvento complex [Au3Cl2(tht)(μ3-PCNHCP,κP,κCNHC,κP)](OTf)·MeCN ([Au3Cl2(tht)L](OTf)·MeCN), which contains only one L and one tht ligand (tht = tetrahydrothiophene), the metal chain is bent (148.94(2)°), and the longer Au···Au separation (2.9710(4) Å) is in line with relaxation of the rigidity due to a more "open" structure. Similar features were observed in [Au3Cl2(SMe2)L](OTf)·2MeCN. A detailed study of the emission properties of [Au3L2](OTf)3, [Au3Cl2(tht)L](OTf)·MeCN, [Au2L2](OTf)2, and [Au2AgL2](OTf)3 was performed by means of steady state and time-resolved photophysical techniques. The complex [Au3L2](OTf)3 displays a bright (photoluminescence quantum yield = 80%) and narrow emission band centered at 446 nm with a relatively small Stokes' shift and long-lived excited-state lifetime on the microsecond timescale, both in solution and in the solid state. In line with the very narrow emission

  17. Charged hadron transverse momentum distributions in Au+Au collisions at √sNN=200 GeV

    Science.gov (United States)

    Back, B. B.; Baker, M. D.; Barton, D. S.; Betts, R. R.; Ballintijn, M.; Bickley, A. A.; Bindel, R.; Budzanowski, A.; Busza, W.; Carroll, A.; Decowski, M. P.; García, E.; George, N.; Gulbrandsen, K.; Gushue, S.; Halliwell, C.; Hamblen, J.; Heintzelman, G. A.; Henderson, C.; Hofman, D. J.; Hollis, R. S.; Hołyński, R.; Holzman, B.; Iordanova, A.; Johnson, E.; Kane, J. L.; Katzy, J.; Khan, N.; Kucewicz, W.; Kulinich, P.; Kuo, C. M.; Lin, W. T.; Lee, J. W.; Manly, S.; McLeod, D.; Mignerey, A. C.; Nouicer, R.; Olszewski, A.; Pak, R.; Park, I. C.; Pernegger, H.; Reed, C.; Remsberg, L. P.; Reuter, M.; Roland, C.; Roland, G.; Rosenberg, L.; Sagerer, J.; Sarin, P.; Sawicki, P.; Skulski, W.; Steadman, S. G.; Steinberg, P.; Stephans, G. S. F.; Sukhanov, A.; Tang, J.-L.; Teng, R.; Trzupek, A.; Vale, C.; van Nieuwenhuizen, G. J.; Verdier, R.; Veres, G. I.; Wadsworth, B.; Wolfs, F. L. H.; Wosiek, B.; Woźniak, K.; Wuosmaa, A. H.; Wysłouch, B.

    2004-01-01

    We present transverse momentum distributions of charged hadrons produced in Au+Au collisions at sNN=200 GeV. The spectra were measured for transverse momenta pT from 0.25 to 4.5 GeV/c in a pseudorapidity range of 0.2<η<1.4. The evolution of the spectra is studied as a function of collision centrality, from 65 to 344 participating nucleons. The results are compared to data from proton-antiproton collisions and Au+Au collisions at lower RHIC energies. We find a significant change of the spectral shape between proton-antiproton and semi-peripheral Au+Au collisions. Comparing semi-peripheral to central Au+Au collisions, we find that the yields at high pT exhibit approximate scaling with the number of participating nucleons, rather than scaling with the number of binary collisions.

  18. Enhanced strange baryon production in Au+Au collisions compared to p+p at sqrts = 200 GeV

    CERN Document Server

    Abelev, B I; Ahammed, Z; Anderson, B D; Arkhipkin, D; Averichev, G S; Bai, Y; Balewski, J; Barannikova, O; Barnby, L S; Baudot, J; Baumgart, S; Bekele, S; Belaga, V V; Bellingeri-Laurikainen, A; Bellwied, R; Benedosso, F; Betts, R R; Bhardwaj, S; Bhasin, A; Bhati, A K; Bichsel, H; Bielcik, J; Bielcikova, J; Bland, L C; Blyth, S L; Bombara, M; Bonner, B E; Botje, M; Bouchet, J; Brandin, A V; Bravar, A; Burton, T P; Bystersky, M; Cadman, R V; Cai, X Z; Caines, H; Calderón de la Barca-Sanchez, M; Callner, J; Castillo, J; Catu, O; Cebra, D; Chajecki, Z; Chaloupka, P; Chattopadhyay, S; Chen, H F; Chen, J H; Cheng, J; Cherney, M; Chikanian, A; Christie, W; Chung, S U; Coffin, J P; Cormier, T M; Cosentino, M R; Cramer, J G; Crawford, H J; Das, D; Das, S; Dash, S; Daugherity, M; De Moura, M M; Dedovich, T G; De Phillips, M; Derevshchikov, A A; Didenko, L; Dietel, T; Djawotho, P; Dogra, S M; Dong, X; Drachenberg, J L; Draper, J E; Du, F; Dunin, V B; Dunlop, J C; Dutta-Majumdar, M R; Eckardt, V; Edwards, W R; Efimov, L G; Emelianov, V; Engelage, J; Eppley, G; Erazmus, B; Estienne, M; Fachini, P; Fatemi, R; Fedorisin, J; Filimonov, K; Filip, P; Finch, E; Fine, V; Fisyak, Yu; Fu, J; Gagliardi, C A; Gaillard, L; Ganti, M S; García-Solis, E; Ghazikhanian, V; Ghosh, P; Gorbunov, Y G; Gos, H; Grebenyuk, O; Grosnick, D; Guertin, S M; Guimaraes, K S F F; Gupta, N; Haag, B; Hallman, T J; Hamed, A; Harris, J W; He, W; Heinz, M; Henry, T W; Hepplemann, S; Hippolyte, B; Hirsch, A; Hjort, E; Hoffman, A M; Hoffmann, G W; Hofman, D; Hollis, R; Horner, M J; Huang, H Z; Huang, S L; Hughes, E W; Humanic, T J; Igo, G; Iordanova, A; Jacobs, P; Jacobs, W W; Jakl, P; Jia, F; Jones, P G; Judd, E G; Kabana, S; Kang, K; Kapitan, J; Kaplan, M; Keane, D; Kechechyan, A; Kettler, D; Khodyrev, V Yu; Kim, B C; Kiryluk, J; Kisiel, A; Kislov, E M; Knospe, A G; Kocoloski, A; Koetke, D D; Kollegger, T; Kopytine, M; Kotchenda, L; Kouchpil, V; Kowalik, K L; Kravtsov, P; Kravtsov, V I; Krüger, K; Kuhn, C; Kulikov, A I; Kumar, A; Kurnadi, P; Kuznetsov, A A; Lamont, M A C; Landgraf, J M; Lange, S; La Pointe, S; Laue, F; Lauret, J; Lebedev, A; Lednicky, R; Lee, C H; Lehocka, S; Le Vine, M J; Li, C; Li, Q; Li, Y; Lin, G; Lin, X; Lindenbaum, S J; Lisa, M A; Liu, F; Liu, H; Liu, J; Liu, L; Liu, Z; Ljubicic, T; Llope, W J; Long, H; Longacre, R S; Love, W A; Lu, Y; Ludlam, T; Lynn, D; Ma, G L; Ma, J G; Ma, Y G; Magestro, D; Mahapatra, D P; Majka, R; Mangotra, L K; Manweiler, R; Margetis, S; Markert, C; Martin, L; Matis, H S; Matulenko, Yu A; McClain, C J; McShane, T S; Melnik, Yu M; Meschanin, A; Millane, J; Miller, M L; Minaev, N G; Mioduszewski, S; Mironov, C; Mischke, A; Mishra, D K; Mitchell, J; Mohanty, B; Molnár, L; Moore, C F; Morozov, D A; Munhoz, M G; Nandi, B K; Nattrass, C; Nayak, T K; Nelson, J M; Nepali, N S; Netrakanti, P K; Nogach, L V; Nurushev, S B; Odyniec, Grazyna Janina; Ogawa, A; Okorokov, V; Oldenburg, M; Olson, D; Pachr, M; Pal, S K; Panebratsev, Yu A; Pavlinov, A I; Pawlak, T; Peitzmann, T; Perevozchikov, V; Perkins, C; Peryt, W; Phatak, S C; Planinic, M; Pluta, J; Poljak, N; Porile, N; Porter, J; Poskanzer, A M; Potekhin, M V; Potrebenikova, E V; Potukuchi, B V K S; Prindle, D; Pruneau, C; Putschke, J; Qattan, I A; Rakness, G; Raniwala, R; Raniwala, S; Ray, R L; Razin, S V; Reinnarth, J; Relyea, D; Ridiger, A; Ritter, H G; Roberts, J B; Rogachevski, O V; Romero, J L; Rose, A; Roy, C; Ruan, L; Russcher, M J; Sahoo, R; Sakuma, T; Salur, S; Sandweiss, J; Sarsour, M; Sazhin, P S; Schambach, J; Scharenberg, R P; Schmitz, N; Schweda, K; Seger, J; Selyuzhenkov, I; Seyboth, P; Shabetai, A; Shahaliev, E; Shao, M; Sharma, M; Shen, W Q; Shimansky, S S; Sichtermann, E P; Simon, F; Singaraju, R N; Smirnov, N; Snellings, R; Sørensen, P; Sowinski, J; Speltz, J; Spinka, H M; Srivastava, B; Stadnik, A; Stanislaus, T D S; Staszak, D; Stock, R; Stolpovsky, A; Strikhanov, M N; Stringfellow, B C; Suaide, A A P; Suarez, M C; Subba, N L; Sugarbaker, E R; Sumbera, M; Sun, Z; Surrow, B; Swanger, M; Symons, T J M; Szanto de Toledo, A; Takahashi, J; Tang, A H; Tarnowsky, T J; Thomas, J H; Timmins, A R; Timoshenko, S; Tokarev, M; Trainor, T A; Trentalange, S; Tribble, R E; Tsai, O D; Ulery, J; Ullrich, T; Underwood, D G; Van Buren, G; Van der Kolk, N; Van Leeuwen, M; Van der Molen, A M; Varma, R; Vasilevski, I M; Vasilev, A N; Vernet, R; Vigdor, S E; Viyogi, Y P; Vokal, S; Voloshin, S A; Waggoner, W T; Wang, F; Wang, G; Wang, J S; Wang, X L; Wang, Y; Watson, J W; Webb, J C; Westfall, G D; Wetzler, A; Whitten, C; Wieman, H; Wissink, S W; Witt, R; Wu, J; Xu, N; Xu, Q H; Xu, Z; Yepes, P; Yoo, I K; Yurevich, V I; Zhan, W; Zhang, H; Zhang, W M; Zhang, Y; Zhang, Z P; Zhao, Y; Zhong, C; Zhou, J; Zoulkarneev, R; Zoulkarneeva, Y; Zubarev, A N; Zuo, J X

    2007-01-01

    We report on the observed differences in production rates of strange and multi-strange baryons in Au+Au collisions at sqrts = 200 GeV compared to p+p interactions at the same energy. The yields in Au+Au collisions, when scaled by the number of participants, are larger than those measured in the p+p data. The magnitudes of the differences grow with the strangeness of the baryon and with increasing centrality. The enhancements of the Au+Au yields are close to those measured in sqrts = 17.3 GeV collisions. Further, when the binary scaled p+p pT spectra are compared to those of Au+Au the heavy-ion yields exceed binary scaling in the pT range 1 < pT< 4 GeV/c.

  19. The gold-rich indide Eu{sub 5}Au{sub 17.7}In{sub 4.3} and its relation with the structures of SrAu{sub 4.76}In{sub 1.24} and BaLi{sub 4}

    Energy Technology Data Exchange (ETDEWEB)

    Muts, Ihor [Muenster Univ. (Germany). Inst. fuer Anorganische und Analytische Chemie; Ivan Franko National Univ. of Lviv (Ukraine). Inorganic Chemistry Dept.; Rodewald, Ute C.; Poettgen, Rainer [Muenster Univ. (Germany). Inst. fuer Anorganische und Analytische Chemie; Zaremba, Vasyl' I.; Pavlosyuk, Orest [Ivan Franko National Univ. of Lviv (Ukraine). Inorganic Chemistry Dept.

    2012-02-15

    The gold-rich indide Eu{sub 5}Au{sub 17.7}In{sub 4.3} was synthesized from the elements in a sealed tantalum ampoule that was heated in a high-frequency furnace. Eu{sub 5}Au{sub 17.7}In{sub 4.3} crystallizes with a new monoclinic structure type: C2/m, a = 902.7(2), b = 722.8(3), c = 1734.1(4) pm, {beta} = 94.31(3) , wR2 = 0.0907, 2640 F{sup 2} values and 74 variables. Eu{sub 5}Au{sub 17.7}In{sub 4.3} has a pronounced gold substructure with Au.Au distances ranging from 278 to 300 pm. The striking structural motifs in the gold substructure are networks of Au6 hexagons and discrete units of corner- and edge-sharing Au{sub 4} tetrahedra. Eu{sub 5}Au{sub 17.70}In{sub 4.30} exhibits a small homogeneity range with In/Au mixing on two Wyckoff sites. Geometrically, the Eu{sub 5}Au{sub 17.7}In{sub 4.3} structure can be explained as an intergrowth variant of slightly distorted SrAu{sub 4.76}In{sub 1.24}- and BaLi{sub 4}-related slabs. The europium coordination in the BaLi{sub 4} slabs is similar to binary EuAu{sub 2}. (orig.)

  20. Solvent-induced desorption of alkanethiol ligands from Au nanoparticles.

    Science.gov (United States)

    Huang, Yuanyuan; Liu, Wei; Cheng, Hao; Yao, Tao; Yang, Lina; Bao, Jie; Huang, Ting; Sun, Zhihu; Jiang, Yong; Wei, Shiqiang

    2016-06-21

    Removing surfactants from a colloidal metal nanoparticle surface is necessary for their realistic applications, and how they could be stripped is a subject of active investigation. Here, we report a solvent-induced desorption of dodecanethiol ligands from the gold nanoparticle surface, and traced this desorption process using a combination of in situ X-ray absorption fine structure (XAFS) and Raman spectroscopic techniques. In situ analysis results reveal that the solvent exchange of ethanol with tetrahydrofuran (THF) can effectively remove dodecanethiol ligands while keeping the particle morphology unchanged. Upon increasing the THF/ethanol ratio from 0 : 1 to 5 : 1, the surface coverage of thiol on the Au surface is reduced from 0.47 to 0.07, suggesting the depletion of ligands first from the nanoparticle facet sites, then from the edge sites, while the ligands at the corner sites are intact. This work enriches our knowledge on surfactant removal and may pave the way towards preparing surface-clean nanoparticles for practical applications. PMID:27241025

  1. Centrality dependence of direct photon production in (square root)S(NN) = 200 GeV Au + Au collisions.

    Science.gov (United States)

    Adler, S S; Afanasiev, S; Aidala, C; Ajitanand, N N; Akiba, Y; Alexander, J; Amirikas, R; Aphecetche, L; Aronson, S H; Averbeck, R; Awes, T C; Azmoun, R; Babintsev, V; Baldisseri, A; Barish, K N; Barnes, P D; Bassalleck, B; Bathe, S; Batsouli, S; Baublis, V; Bazilevsky, A; Belikov, S; Berdnikov, Y; Bhagavatula, S; Boissevain, J G; Borel, H; Borenstein, S; Brooks, M L; Brown, D S; Bruner, N; Bucher, D; Buesching, H; Bumazhnov, V; Bunce, G; Burward-Hoy, J M; Butsyk, S; Camard, X; Chai, J-S; Chand, P; Chang, W C; Chernichenko, S; Chi, C Y; Chiba, J; Chiu, M; Choi, I J; Choi, J; Choudhury, R K; Chujo, T; Cianciolo, V; Cobigo, Y; Cole, B A; Constantin, P; d'Enterria, D; David, G; Delagrange, H; Denisov, A; Deshpande, A; Desmond, E J; Devismes, A; Dietzsch, O; Drapier, O; Drees, A; du Rietz, R; Durum, A; Dutta, D; Efremenko, Y V; El Chenawi, K; Enokizono, A; En'yo, H; Esumi, S; Ewell, L; Fields, D E; Fleuret, F; Fokin, S L; Fox, B D; Fraenkel, Z; Frantz, J E; Franz, A; Frawley, A D; Fung, S-Y; Garpman, S; Ghosh, T K; Glenn, A; Gogiberidze, G; Gonin, M; Gosset, J; Goto, Y; Granier de Cassagnac, R; Grau, N; Greene, S V; Perdekamp, M Grosse; Guryn, W; Gustafsson, H-A; Hachiya, T; Haggerty, J S; Hamagaki, H; Hansen, A G; Hartouni, E P; Harvey, M; Hayano, R; Hayashi, N; He, X; Heffner, M; Hemmick, T K; Heuser, J M; Hibino, M; Hill, J C; Holzmann, W; Homma, K; Hong, B; Hoover, A; Ichihara, T; Ikonnikov, V V; Imai, K; Isenhower, D; Ishihara, M; Issah, M; Isupov, A; Jacak, B V; Jang, W Y; Jeong, Y; Jia, J; Jinnouchi, O; Johnson, B M; Johnson, S C; Joo, K S; Jouan, D; Kametani, S; Kamihara, N; Kang, J H; Kapoor, S S; Katou, K; Kelly, S; Khachaturov, B; Khanzadeev, A; Kikuchi, J; Kim, D H; Kim, D J; Kim, D W; Kim, E; Kim, G-B; Kim, H J; Kistenev, E; Kiyomichi, A; Kiyoyama, K; Klein-Boesing, C; Kobayashi, H; Kochenda, L; Kochetkov, V; Koehler, D; Kohama, T; Kopytine, M; Kotchetkov, D; Kozlov, A; Kroon, P J; Kuberg, C H; Kurita, K; Kuroki, Y; Kweon, M J; Kwon, Y; Kyle, G S; Lacey, R; Ladygin, V; Lajoie, J G; Lebedev, A; Leckey, S; Lee, D M; Lee, S; Leitch, M J; Li, X H; Lim, H; Litvinenko, A; Liu, M X; Liu, Y; Maguire, C F; Makdisi, Y I; Malakhov, A; Manko, V I; Mao, Y; Martinez, G; Marx, M D; Masui, H; Matathias, F; Matsumoto, T; McGaughey, P L; Melnikov, E; Messer, F; Miake, Y; Milan, J; Miller, T E; Milov, A; Mioduszewski, S; Mischke, R E; Mishra, G C; Mitchell, J T; Mohanty, A K; Morrison, D P; Moss, J M; Mühlbacher, F; Mukhopadhyay, D; Muniruzzaman, M; Murata, J; Nagamiya, S; Nagle, J L; Nakamura, T; Nandi, B K; Nara, M; Newby, J; Nilsson, P; Nyanin, A S; Nystrand, J; O'Brien, E; Ogilvie, C A; Ohnishi, H; Ojha, I D; Okada, K; Ono, M; Onuchin, V; Oskarsson, A; Otterlund, I; Oyama, K; Ozawa, K; Pal, D; Palounek, A P T; Pantuev, V; Papavassiliou, V; Park, J; Parmar, A; Pate, S F; Peitzmann, T; Peng, J-C; Peresedov, V; Pinkenburg, C; Pisani, R P; Plasil, F; Purschke, M L; Purwar, A K; Rak, J; Ravinovich, I; Read, K F; Reuter, M; Reygers, K; Riabov, V; Riabov, Y; Roche, G; Romana, A; Rosati, M; Rosnet, P; Ryu, S S; Sadler, M E; Saito, N; Sakaguchi, T; Sakai, M; Sakai, S; Samsonov, V; Sanfratello, L; Santo, R; Sato, H D; Sato, S; Sawada, S; Schutz, Y; Semenov, V; Seto, R; Shaw, M R; Shea, T K; Shibata, T-A; Shigaki, K; Shiina, T; Silva, C L; Silvermyr, D; Sim, K S; Singh, C P; Singh, V; Sivertz, M; Soldatov, A; Soltz, R A; Sondheim, W E; Sorensen, S P; Sourikova, I V; Staley, F; Stankus, P W; Stenlund, E; Stepanov, M; Ster, A; Stoll, S P; Sugitate, T; Sullivan, J P; Takagui, E M; Taketani, A; Tamai, M; Tanaka, K H; Tanaka, Y; Tanida, K; Tannenbaum, M J; Tarján, P; Tepe, J D; Thomas, T L; Tojo, J; Torii, H; Towell, R S; Tserruya, I; Tsuruoka, H; Tuli, S K; Tydesjö, H; Tyurin, N; van Hecke, H W; Velkovska, J; Velkovsky, M; Veszprémi, V; Villatte, L; Vinogradov, A A; Volkov, M A; Vznuzdaev, E; Wang, X R; Watanabe, Y; White, S N; Wohn, F K; Woody, C L; Xie, W; Yang, Y; Yanovich, A; Yokkaichi, S; Young, G R; Yushmanov, I E; Zajc, W A; Zhang, C; Zhou, S; Zhou, S J; Zolin, L

    2005-06-17

    The first measurement of direct photons in Au + Au collisions at (square root)S(NN) = 200 GeV is presented. The direct photon signal is extracted as a function of the Au + Au collision centrality and compared to next-to-leading order perturbative quantum chromodynamics calculations. The direct photon yield is shown to scale with the number of nucleon-nucleon collisions for all centralities. PMID:16090462

  2. Centrality Dependence of Direct Photon Production in √(SNN)=200 GeV Au+Au Collisions

    International Nuclear Information System (INIS)

    The first measurement of direct photons in Au+Au collisions at √(sNN)=200 GeV is presented. The direct photon signal is extracted as a function of the Au+Au collision centrality and compared to next-to-leading order perturbative quantum chromodynamics calculations. The direct photon yield is shown to scale with the number of nucleon-nucleon collisions for all centralities

  3. Volcano-like behavior of Au-Pd core-shell nanoparticles in the selective oxidation of alcohols.

    Science.gov (United States)

    Silva, Tiago A G; Teixeira-Neto, Erico; López, Núria; Rossi, Liane M

    2014-01-01

    Gold-palladium (AuPd) nanoparticles have shown significantly enhanced activity relative to monometallic Au and Pd catalysts. Knowledge of composition and metal domain distributions is crucial to understanding activity and selectivity, but these parameters are difficult to ascertain in catalytic experiments that have primarily been devoted to equimolar nanoparticles. Here, we report AuPd nanoparticles of varying Au:Pd molar ratios that were prepared by a seed growth method. The selective oxidation of benzyl alcohol was used as a model reaction to study catalytic activity and selectivity changes that occurred after varying the composition of Pd in bimetallic catalysts. We observed a remarkable increase in catalytic conversion when using a 10:1 Au:Pd molar ratio. This composition corresponds to the amount of Pd necessary to cover the existing Au cores with a monolayer of Pd as a full-shell cluster. The key to increased catalytic activity derives from the balance between the number of active sites and the ease of product desorption. According to density functional theory calculations, both parameters are extremely sensitive to the Pd content resulting in the volcano-like activity observed. PMID:25042537

  4. Chemial Bond and Stability of Adsorption of[Au(AsS3)]2- on the Surface of Kaolinite

    Institute of Scientific and Technical Information of China (English)

    MIN Xin-min; CHEN Yun; HONG Han-lie

    2004-01-01

    Density function theory and discrete variation method (DFT-DVM) were used to study the adsorption of [Au(AsS3 ) ]2- on the surface of kaolinite. The correlation among structure, chemical bond and stability was discussed. Several models were selected with [ Au( AsS3 ) ]2- in different directions and sites. The resultsshow that the models with gold on the edge of kaolinite basal layer contain pincerlike bond among gold and severaloxygen atoms and form strong Au - O covalent bond, so these models are more stable than those with gold aboveor under the layer. The models with gold near to [ AlO2(OH)4 ] octahedra are more stable than those with goldnear to the vacancy without aluminium. These two stable tendencies in kaolinite- [ Au( AsS3 ) ]2- are stronger thanthat in kaolinite-Au systems. The interaction between [ Au( AsS3 ) ]2- and kaolinite is stronger than that betweengold and kaolinite, and this interaction is strong enough to form the surface complexes.

  5. DNA-templated synthesis of PtAu bimetallic nanoparticle/graphene nanocomposites and their application in glucose biosensor

    Science.gov (United States)

    Leng, Jing; Wang, Wen-Min; Lu, Li-Min; Bai, Ling; Qiu, Xin-Lan

    2014-02-01

    In this paper, single-stranded DNA (ss-DNA) is demonstrated to functionalize graphene (GR) and to further guide the growth of PtAu bimetallic nanoparticles (PtAuNPs) on GR with high densities and dispersion. The obtained nanocomposites (PtAuNPs/ss-DNA/GR) were characterized by transmission electron microscopy (TEM), energy-dispersive X-ray spectrometer (EDS), and electrochemical techniques. Then, an enzyme nanoassembly was prepared by self-assembling glucose oxidase (GOD) on PtAuNP/ss-DNA/GR nanocomposites (GOD/PtAuNPs/ss-DNA/GR). The nanocomposites provided a suitable microenvironment for GOD to retain its biological activity. The direct and reversible electron transfer process between the active site of GOD and the modified electrode was realized without any extra electron mediator. Thus, the prepared GOD/PtAuNP/ss-DNA/GR electrode was proposed as a biosensor for the quantification of glucose. The effects of pH, applied potential, and temperature on the performance of the biosensor were discussed in detail and were optimized. Under optimal conditions, the biosensor showed a linearity with glucose concentration in the range of 1.0 to 1,800 μM with a detection limit of 0.3 μM (S/N = 3). The results demonstrate that the developed approach provides a promising strategy to improve the sensitivity and enzyme activity of electrochemical biosensors.

  6. Des atomes d'antihydrogene produits en quantites substantielles au CERN

    CERN Multimedia

    Sevestre, G

    2002-01-01

    "Des quantites relativement substantielles d'atomes d'antihydrogene a basse temperature ont ete produites cet ete au Laboratoire europeen de physique des particules, le CERN a Geneve, ouvrant la voie a une etude approfondie de cette antimatiere qui pourrait remettre en cause les theories actuelles, a annonce mercredi sur le site Internet de la revue Nature une equipe internationale de chercheurs" (1 page).

  7. Mg-AI Mixed Oxides Supported Bimetallic Au-Pd Nanoparticles with Superior Catalytic Properties in Aerobic Oxidation of Benzyl Alcohol and Glycerol

    Institute of Scientific and Technical Information of China (English)

    王亮; 张伟; 曾尚景; 苏党生; 孟祥举; 肖丰收

    2012-01-01

    Nano-sized Au and Pd catalysts are favorable for oxidations with molecular oxygen, and the preparation of this kind of nanoparticles with high catalytic activities is strongly desirable. We report a successful synthesis of bimetal- lic Au-Pd nanoparticles with rich edge and comer sites on unique support of Mg-AI mixed oxides (Au-Pd/MAO), which are favorable for producing metal nanoparticles with high degree of coordinative unsaturation of metal atoms The systematic microscopic characterizations confirm the bimetallic Au-Pd nanoparticles are present as Au-Pd alloy The irregular shape of the bimetallic nanoparticles are directly observed in HRTEM images. As we expected, Au-Pd/MAO gives very excellent catalytic performances in the aerobic oxidation of benzyl alcohol and glycerol. For example, Au-Pd/MAO shows very high TOF of 91000 h i at 433 K with molecular oxygen at air pressure in solvent-free oxidation of benzyl alcohol; this catalyst also shows relatively high selectivity for tartronic acid (TA- RAC, 36.6%) at high conversion (98.5%) in aerobic oxidation of glycerol. The superior catalytic properties of Au-Pd/MAO would be potentially important tbr production of fine chemicals.

  8. In-situ STM study of phosphate adsorption on Cu(111), Au(111) and Cu/Au(111) electrodes

    DEFF Research Database (Denmark)

    Schlaup, Christian; Horch, Sebastian

    2013-01-01

    The interaction of Cu(111), Au(111) and Cu-covered Au(111) electrodes with a neutral phosphate buffer solution has been studied by means of cyclic voltammetry (CV) and in situ electrochemical scanning tunneling microscopy (EC-STM). Under low potential conditions, both the Cu(111) and the Au(111...

  9. Di-hadron correlations with identified leading hadrons in 200 GeV Au+Au and d+Au collisions at STAR

    Directory of Open Access Journals (Sweden)

    L. Adamczyk

    2015-12-01

    Full Text Available The STAR Collaboration presents for the first time two-dimensional di-hadron correlations with identified leading hadrons in 200 GeV central Au+Au and minimum-bias d+Au collisions to explore hadronization mechanisms in the quark gluon plasma. The enhancement of the jet-like yield for leading pions in Au+Au data with respect to the d+Au reference and the absence of such an enhancement for leading non-pions (protons and kaons are discussed within the context of a quark recombination scenario. The correlated yield at large angles, specifically in the ridge region, is found to be significantly higher for leading non-pions than pions. The consistencies of the constituent quark scaling, azimuthal harmonic model and a mini-jet modification model description of the data are tested, providing further constraints on hadronization.

  10. Spectra and ratios of identified particles in Au+Au and d+Au collisions at sqrt(s_NN)=200 GeV

    OpenAIRE

    Adare, A.; Afanasiev, S.; Aidala, C.; Ajitanand, N. N.; Akiba, Y; Al-Bataineh, H.; Alexander, J.; Angerami, A.(Nevis Laboratory, Columbia University, Irvington, NY, U.S.A.); Aoki, K.; Apadula, N.; Aramaki, Y.; Atomssa, E. T.; Averbeck, R.; Awes, T. C.; Azmoun, B.

    2013-01-01

    The transverse momentum (p_T) spectra and ratios of identified charged hadrons (\\pi^+/-, K^+/-, p, p^bar) produced in sqrt(s_NN)=200 GeV Au+Au and d+Au collisions are reported in five different centrality classes for each collision species. The measurements of pions and protons are reported up to p_T=6 GeV/c (5 GeV/c), and the measurements of kaons are reported up to p_T=4 GeV/c (3.5 GeV/c) in Au+Au (d+Au) collisions. In the intermediate p_T region, between 2--5 GeV/c, a significant enhanceme...

  11. Di-Hadron Correlations with Identified Leading Hadrons in 200 GeV Au+Au and d+Au Collisions at STAR

    CERN Document Server

    Abdelwahab, N M; Adkins, J K; Agakishiev, G; Aggarwal, M M; Ahammed, Z; Alekseev, I; Alford, J; Anson, C D; Aparin, A; Arkhipkin, D; Aschenauer, E C; Averichev, G S; Banerjee, A; Beavis, D R; Bellwied, R; Bhasin, A; Bhati, A K; Bhattarai, P; Bielcik, J; Bielcikova, J; Bland, L C; Bordyuzhin, I G; Borowski, W; Bouchet, J; Brandin, A V; Brovko, S G; Bültmann, S; Bunzarov, I; Burton, T P; Butterworth, J; Caines, H; Sánchez, M Calderón de la Barca; Campbell, J M; Cebra, D; Cendejas, R; Cervantes, M C; Chaloupka, P; Chang, Z; Chattopadhyay, S; Chen, H F; Chen, J H; Chen, L; Cheng, J; Cherney, M; Chikanian, A; Christie, W; Chwastowski, J; Codrington, M J M; Contin, G; Cramer, J G; Crawford, H J; Cui, X; Das, S; Leyva, A Davila; De Silva, L C; Debbe, R R; Dedovich, T G; Deng, J; Derevschikov, A A; de Souza, R Derradi; di Ruzza, B; Didenko, L; Dilks, C; Ding, F; Djawotho, P; Dong, X; Drachenberg, J L; Draper, J E; Du, C M; Dunkelberger, L E; Dunlop, J C; Efimov, L G; Engelage, J; Engle, K S; Eppley, G; Esha, R; Eun, L; Evdokimov, O; Eyser, O; Fatemi, R; Fazio, S; Fedorisin, J; Filip, P; Fisyak, Y; Flores, C E; Gagliardi, C A; Gangadharan, D R; Garand, D; Geurts, F; Gibson, A; Girard, M; Gliske, S; Greiner, L; Grosnick, D; Gunarathne, D S; Guo, Y; Gupta, A; Gupta, S; Guryn, W; Haag, B; Hamad, A; Hamed, A; Han, L-X; Haque, R; Harris, J W; Heppelmann, S; Hirsch, A; Hoffmann, G W; Hofman, D J; Horvat, S; Huang, B; Huang, H Z; Huang, X; Huck, P; Humanic, T J; Igo, G; Jacobs, W W; Jang, H; Judd, E G; Kabana, S; Kalinkin, D; Kang, K; Kauder, K; Ke, H W; Keane, D; Kechechyan, A; Kesich, A; Khan, Z H; Kikola, D P; Kisel, I; Kisiel, A; Koetke, D D; Kollegger, T; Konzer, J; Koralt, I; Kosarzewski, L K; Kotchenda, L; Kraishan, A F; Kravtsov, P; Krueger, K; Kulakov, I; Kumar, L; Kycia, R A; Lamont, M A C; Landgraf, J M; Landry, K D; Lauret, J; Lebedev, A; Lednicky, R; Lee, J H; Li, C; Li, W; Li, X; Li, Y; Li, Z M; Lisa, M A; Liu, F; Ljubicic, T; Llope, W J; Lomnitz, M; Longacre, R S; Luo, X; Ma, G L; Ma, Y G; Mahapatra, D P; Majka, R; Margetis, S; Markert, C; Masui, H; Matis, H S; McDonald, D; McShane, T S; Minaev, N G; Mioduszewski, S; Mohanty, B; Mondal, M M; Morozov, D A; Mustafa, M K; Nandi, B K; Nasim, Md; Nayak, T K; Nelson, J M; Nigmatkulov, G; Nogach, L V; Noh, S Y; Novak, J; Nurushev, S B; Odyniec, G; Ogawa, A; Oh, K; Ohlson, A; Okorokov, V; Oldag, E W; Olvitt, D L; Page, B S; Pan, Y X; Pandit, Y; Panebratsev, Y; Pawlak, T; Pawlik, B; Pei, H; Perkins, C; Pile, P; Planinic, M; Pluta, J; Poljak, N; Poniatowska, K; Porter, J; Poskanzer, A M; Pruthi, N K; Przybycien, M; Putschke, J; Qiu, H; Quintero, A; Ramachandran, S; Raniwala, R; Raniwala, S; Ray, R L; Riley, C K; Ritter, H G; Roberts, J B; Rogachevskiy, O V; Romero, J L; Ross, J F; Roy, A; Ruan, L; Rusnak, J; Rusnakova, O; Sahoo, N R; Sahu, P K; Sakrejda, I; Salur, S; Sandacz, A; Sandweiss, J; Sangaline, E; Sarkar, A; Schambach, J; Scharenberg, R P; Schmah, A M; Schmidke, W B; Schmitz, N; Seger, J; Seyboth, P; Shah, N; Shahaliev, E; Shanmuganathan, P V; Shao, M; Sharma, B; Shen, W Q; Shi, S S; Shou, Q Y; Sichtermann, E P; Simko, M; Skoby, M J; Smirnov, D; Smirnov, N; Solanki, D; Sorensen, P; Spinka, H M; Srivastava, B; Stanislaus, T D S; Stevens, J R; Stock, R; Strikhanov, M; Stringfellow, B; Sumbera, M; Sun, X; Sun, X M; Sun, Y; Sun, Z; Surrow, B; Svirida, D N; Symons, T J M; Szelezniak, M A; Takahashi, J; Tang, A H; Tang, Z; Tarnowsky, T; Thomas, J H; Timmins, A R; Tlusty, D; Tokarev, M; Trentalange, S; Tribble, R E; Tribedy, P; Trzeciak, B A; Tsai, O D; Turnau, J; Ullrich, T; Underwood, D G; Van Buren, G; van Nieuwenhuizen, G; Vandenbroucke, M; Vanfossen,, J A; Varma, R; Vasconcelos, G M S; Vasiliev, A N; Vertesi, R; Videbæk, F; Viyogi, Y P; Vokal, S; Vossen, A; Wada, M; Wang, F; Wang, G; Wang, H; Wang, J S; Wang, X L; Wang, Y; Webb, G; Webb, J C; Wen, L; Westfall, G D; Wieman, H; Wissink, S W; Wu, Y F; Xiao, Z; Xie, W; Xin, K; Xu, H; Xu, J; Xu, N; Xu, Q H; Xu, Y; Xu, Z; Yan, W; Yang, C; Yang, Y; Ye, Z; Yepes, P; Yi, L; Yip, K; Yoo, I-K; Yu, N; Zbroszczyk, H; Zha, W; Zhang, J B; Zhang, J L; Zhang, S; Zhang, X P; Zhang, Y; Zhang, Z P; Zhao, F; Zhao, J; Zhong, C; Zhu, X; Zhu, Y H; Zoulkarneeva, Y; Zyzak, M

    2014-01-01

    The STAR collaboration presents new two-dimensional di-hadron correlations with leading hadrons in 200 GeV central Au+Au and minimum bias d+Au collisions to explore hadronization mechanisms in the quark gluon plasma. The enhancement of the jet-like yield for leading pions in Au+Au data with respect to the d+Au reference and the absence of enhancement for leading non-pions (protons and kaons) are discussed within the context of quark recombination. The correlated yield at large angles, specifically in the \\emph{ridge region}, is significantly higher for leading non-pions than pions. The consistencies of the constituent quark scaling, azimuthal harmonic model and a mini-jet modification model description of the data are tested, providing further constraints on hadronization.

  12. LES SCEAUX DE CERTIFICATION DES SITES WEB : UN OUTIL DE CONFIANCE, OUTIL DE CONFUSION

    OpenAIRE

    Martel, Louise; St-Germain, René

    2002-01-01

    Avec l'évolution des technologies, les entreprises doivent s'adapter au nouveau concept de commerce électronique; les clients aussi. Comment garder leur confiance et ce, au bout des doigts. Ce texte présente un cadre conceptuel de la certification de conformité des sites Web ainsi qu'une typologie des sceaux de certification (labels) existants.

  13. "Dealloying" Phase Separation during Growth of Au on Ni(110)

    DEFF Research Database (Denmark)

    Nielsen, L. Pleth; Besenbacher, Flemming; Stensgaard, I.;

    1995-01-01

    Combined scanning tunneling microscopy and ion-scattering studies have revealed a new "dealloying" phase transition during the growth of Au on Ni(110). The Au atoms, which initially alloy into the Ni(110) surface, phase separate into a vacancy-stabilized Au dimer-trimer chain structure at Au...... coverages larger than 0.4 monolayer. Using the effective-medium theory, we show that the resulting structure as well as the physical mechanism responsible for the phase transition are closely related to the surface stress induced by the substituted Au....

  14. First results on d+Au collisions from PHOBOS

    Science.gov (United States)

    Back, B. B.; Baker, M. D.; Ballintijn, M.; Barton, D. S.; Becker, B.; Betts, R. R.; Bickley, A. A.; Bindel, R.; Budzanowski, A.; Busza, W.; Carroll, A.; Decowski, M. P.; García, E.; Gburek, T.; George, N.; Gulbrandsen, K.; Gushue, S.; Halliwell, C.; Hamblen, J.; Harrington, A. S.; Henderson, C.; Hofman, D. J.; Hollis, R. S.; Hołyński, R.; Holzman, B.; Iordanova, A.; Johnson, E.; Kane, J. L.; Khan, N.; Kulinich, P.; Kuo, C. M.; Lee, J. W.; Lin, W. T.; Manly, S.; Mignerey, A. C.; Noell, A.; Nouicer, R.; Olszewski, A.; Pak, R.; Park, I. C.; Pernegger, H.; Reed, C.; Remsberg, L. P.; Roland, C.; Roland, G.; Sagerer, J.; Sarin, P.; Sawicki, P.; Sedykh, I.; Skulski, W.; Smith, C. E.; Steinberg, P.; Stephans, G. S. F.; Sukhanov, A.; Teng, R.; Tonjes, M. B.; Trzupek, A.; Vale, C.; van Nieuwenhuizen, G. J.; Verdier, R.; Veres, G. I.; Wadsworth, B.; Wolfs, F. L. H.; Wosiek, B.; Woźniak, K.; Wuosmaa, A. H.; Wysłouch, B.; Zhang, J.

    2004-02-01

    We have measured transverse momentum distributions of charged hadrons produced in d+Au collisions at √SNN = 200 GeV, in the range 0.25 < pT < 6.0 GeV/c. With increasing collision centrality, the yield at high transverse momenta increases more rapidly than the overall particle density, leading to a strong modification of the spectral shape. This change in spectral shape is qualitatively different from observations in Au+Au collisions at the same energy. The results provide important information for discriminating between different models for the suppression of high-pT hadrons observed in Au+Au collisions.

  15. Thermal desorption of Au from W(001) surface

    CERN Document Server

    Blaszczyszyn, R; Godowski, P J

    2002-01-01

    Adsorption of Au on W(001) at 450 K up to multilayer structures was investigated. Temperature programmed desorption technique was used in determination of coverage dependent desorption energy (region up to one monolayer). Results were discussed in terms of competitive interactions of Au-Au and Au-W atoms. Simple procedure for prediction of faceting behavior on the interface, basing on the desorption data, was postulated. It was deduced that the Au/W(001) interface should not show faceting tendency after thermal treatment. (author)

  16. Thermal Desorption of Au from W(001) Surface

    Science.gov (United States)

    Błaszczyszyn, R.; Chrzanowski, J.; Godowski, P. J.

    2000-12-01

    Adsorption of Au on W(001) at 450 K up to multilayer structures was investigated. Temperature programmed desorption technique was used in determination of coverage dependent desorption energy (region up to one monolayer). Results were discussed in terms of competitive interactions of Au--Au and Au--W atoms. Simple procedure for prediction of faceting behavior on the interface, basing on the desorption data, was postulated. It was deduced that the Au/W(001) interface should not show faceting tendency after thermal treatment.

  17. Ground-state properties of ordered, partially ordered, and random Cu-Au and Ni-Pt alloys

    DEFF Research Database (Denmark)

    Ruban, Andrei; Abrikosov, I. A.; Skriver, Hans Lomholt

    1995-01-01

    We have studied the ground-state properties of ordered, partially ordered, and random Cu-Au and Ni-Pt alloys at the stoichiometric 1/4, 1/2, and 3/4 compositions in the framework of the multisublattice single-site (SS) coherent potential approximation (CPA). Charge-transfer effects in the random ...

  18. Photoswitchable Faraday effect in EuS-Au nanosystems

    Energy Technology Data Exchange (ETDEWEB)

    Kawashima, Akira; Nakanishi, Takayuki; Kitagawa, Yuichi; Fushimi, Koji; Hasegawa, Yasuchika [Division of Applied Chemistry, Faculty of Engineering, Hokkaido University, North-13 West-8, Kita-ku, 060-8628, Sapporo (Japan)

    2016-01-15

    Effective photoswitchable europium sulfide nanocrystals with gold nanoparticles using dithiol (DDT: 1,10-decanedithiol) joint molecules, EuS-Au nanosystems, are demonstrated. The TEM image indicates the formation of EuS-Au nanosystems composed of cube-shaped EuS nanocrystals and spherical Au nanoparticles. Under visible-light irradiation, a drastic change of absorption band of EuS-Au nanosystems at around 600 nm was observed. The Faraday effects of EuS-Au nanosystems were estimated using magnetic circular dichroism (MCD) measurements. The effective change of the MCD spectra of EuS-Au nanosystems under visible-light irradiation was successfully observed at around 670 nm for the first time. The effective reversible changes in MCD spectra with the alternative irradiation cycles of visible light (>440 nm) and dark are also presented. The decrease rate of rotation angle at 670 nm of EuS-Au nanosystems is larger than that of absorbance. These results indicate that the effective change of MCD spectra of EuS-Au nanosystems would be dominated not only by a drastic change of absorption band related to enhanced LSPR of Au nanoparticles but also by specific interaction between EuS and Au in nanosystem under irradiation. Illustration of photoswitch and TEM image of EuS-Au nanosystems. (copyright 2015 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  19. Au-nanoparticles grafted on plasma treated PE

    Energy Technology Data Exchange (ETDEWEB)

    Svorcik, V., E-mail: vaclav.svorcik@vscht.c [Department of Solid State Engineering, Institute of Chemical Technology, 166 28 Prague (Czech Republic); Chaloupka, A. [Department of Solid State Engineering, Institute of Chemical Technology, 166 28 Prague (Czech Republic); Rezanka, P. [Department of Analytical Chemistry, Institute of Chemical Technology, Prague (Czech Republic); Slepicka, P. [Department of Solid State Engineering, Institute of Chemical Technology, 166 28 Prague (Czech Republic); Kolska, Z. [Department of Chemistry, J.E. Purkyne University, 400 96 Usti nad Labem (Czech Republic); Kasalkova, N.; Hubacek, T.; Siegel, J. [Department of Solid State Engineering, Institute of Chemical Technology, 166 28 Prague (Czech Republic)

    2010-03-15

    Polyethylene (PE) surface was treated with Ar plasma. Activated surface was grafted from methanol solution of 1,2-ethanedithiol. Then the sample was immersed into freshly prepared colloid solution of Au-nanoparticles. Finally Au layer was sputtered on the samples. Properties of the modified PE were studied using various methods: AFM, EPR, RBS and nanoindentation. It was shown that the plasma treatment results in degradation of polymer chain (AFM) and creation of free radicals by EPR. After grafting with dithiol, the concentration of free radicals declines. The presence of Au and S in the surface layer after the coating with Au-nanoparticles was proved by RBS. Plasma treatment changes PE surface morphology and increases surface roughness, too. Another significant change in surface morphology and roughness was observed after deposition of Au-nanoparticles. Nanoindentation measurements show that the grafting with Au-nanoparticles increases adhesion of subsequently sputtered Au layer.

  20. Au-nanoparticles grafted on plasma treated PE

    Science.gov (United States)

    Švorčík, V.; Chaloupka, A.; Řezanka, P.; Slepička, P.; Kolská, Z.; Kasálková, N.; Hubáček, T.; Siegel, J.

    2010-03-01

    Polyethylene (PE) surface was treated with Ar plasma. Activated surface was grafted from methanol solution of 1,2-ethanedithiol. Then the sample was immersed into freshly prepared colloid solution of Au-nanoparticles. Finally Au layer was sputtered on the samples. Properties of the modified PE were studied using various methods: AFM, EPR, RBS and nanoindentation. It was shown that the plasma treatment results in degradation of polymer chain (AFM) and creation of free radicals by EPR. After grafting with dithiol, the concentration of free radicals declines. The presence of Au and S in the surface layer after the coating with Au-nanoparticles was proved by RBS. Plasma treatment changes PE surface morphology and increases surface roughness, too. Another significant change in surface morphology and roughness was observed after deposition of Au-nanoparticles. Nanoindentation measurements show that the grafting with Au-nanoparticles increases adhesion of subsequently sputtered Au layer.

  1. 2D chemistry on Au(111) surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Rauls, Eva; Blankenburg, Stephan; Schmidt, Wolf Gero [Theoretische Physik, Universitaet Paderborn (Germany)

    2009-07-01

    The design of functional two-dimensional molecular networks has become an area of intense research. The constraint to 2 in contrast to the availability of 3 dimensions has a large impact on many chemical reactions. Chemical reactions between surface adsorbed molecules may lead to products very different from those obtained in solutions or the gas phase. The imide formation between a diaminoterphenyl (DATP) and a PTCDA molecule is one very interesting example in this respect. In scanning tunneling microscopy (STM) experiments, it has been observed that the Au surface changes both the reaction path and the reaction product compared to 3D. In order to understand these experimental observations, we have studied the chemical reactions both in solution and on the Au(111) surface by density-functional theory calculations in the generalized-gradient approximation.

  2. Tunable VO2/Au hyperbolic metamaterial

    Science.gov (United States)

    Prayakarao, S.; Mendoza, B.; Devine, A.; Kyaw, C.; van Dover, R. B.; Liberman, V.; Noginov, M. A.

    2016-08-01

    Vanadium dioxide (VO2) is known to have a semiconductor-to-metal phase transition at ˜68 °C. Therefore, it can be used as a tunable component of an active metamaterial. The lamellar metamaterial studied in this work is composed of subwavelength VO2 and Au layers and is designed to undergo a temperature controlled transition from the optical hyperbolic phase to the metallic phase. VO2 films and VO2/Au lamellar metamaterial stacks have been fabricated and studied in electrical conductivity and optical (transmission and reflection) experiments. The observed temperature-dependent changes in the reflection and transmission spectra of the metamaterials and VO2 thin films are in a good qualitative agreement with theoretical predictions. The demonstrated optical hyperbolic-to-metallic phase transition is a unique physical phenomenon with the potential to enable advanced control of light-matter interactions.

  3. De l’individu postcommuniste au citoyen

    OpenAIRE

    Anna Krasteva

    2013-01-01

    L’article analyse le paradoxe de la conception communiste du citoyen engagé : au niveau idéologique, citoyenneté et engagement sont intrinsèquement liés, au niveau politique ils sont souvent radicalement dissociés. Le citoyen communiste est plus engagé que citoyen. La citoyenneté était dépourvue de plusieurs de ses attributs : de la jouissance de la loi qui établit « l’égalité arithmétique » et minorise les maîtres ; de la citoyenneté active – civile et politique – pour ne jouir que la protec...

  4. Collision-spike Sputtering of Au Nanoparticles.

    Science.gov (United States)

    Sandoval, Luis; Urbassek, Herbert M

    2015-12-01

    Ion irradiation of nanoparticles leads to enhanced sputter yields if the nanoparticle size is of the order of the ion penetration depth. While this feature is reasonably well understood for collision-cascade sputtering, we explore it in the regime of collision-spike sputtering using molecular-dynamics simulation. For the particular case of 200-keV Xe bombardment of Au particles, we show that collision spikes lead to abundant sputtering with an average yield of 397 ± 121 atoms compared to only 116 ± 48 atoms for a bulk Au target. Only around 31 % of the impact energy remains in the nanoparticles after impact; the remainder is transported away by the transmitted projectile and the ejecta. The sputter yield of supported nanoparticles is estimated to be around 80 % of that of free nanoparticles due to the suppression of forward sputtering.

  5. Transition probability studies in 175Au

    OpenAIRE

    Grahn, Tuomas; Watkins, H.; Joss, David; Page, Robert; Carroll, R. J.; Dewald, A.; Greenlees, Paul; Hackstein, M.; Herzberg, Rolf-Dietmar; Jakobsson, Ulrika; Jones, Peter; Julin, Rauno; Juutinen, Sakari; Ketelhut, Steffen; Kröll, Th

    2013-01-01

    Transition probabilities have been measured between the low-lying yrast states in 175Au by employing the recoil distance Doppler-shift method combined with the selective recoil-decay tagging technique. Reduced transition probabilities and magnitudes of transition quadrupole moments have been extracted from measured lifetimes allowing dramatic changes in nuclear structure within a low excitation-energy range to probed. The transition quadrupole moment data are discussed in terms...

  6. Ion-irradiation induced chemical ordering of FePt and FePtAu nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Seetala, Naidu V. [Department of Physics, Grambling State University, RWE Jones Drive, Carver Hall 81, Grambling, LA 71245 (United States)]. E-mail: naidusv@gram.edu; Harrell, J.W. [MINT Center, University of Alabama, Tuscaloosa, AL 35487 (United States); Lawson, Jeremy [MINT Center, University of Alabama, Tuscaloosa, AL 35487 (United States); Nikles, David E. [MINT Center, University of Alabama, Tuscaloosa, AL 35487 (United States); Williams, John R. [Department of Physics, Auburn University, Auburn, AL 36849 (United States); Isaacs-Smith, Tamara [Department of Physics, Auburn University, Auburn, AL 36849 (United States)

    2005-12-15

    We have studied the effect of ion-beam irradiation on reducing the ordering temperature of FePt and FePtAu nanoparticles. FePt and FePt(Au14%) 4 nm particles dispersed on a Si-substrate were irradiated by 300 keV Al-ions with a dose of 1 x 10{sup 16} ions/cm{sup 2} at 43 {sup o}C using a water-cooled flange in order to minimize the vacancy migration and voids formation within the collision cascades. Partial chemical ordering has been observed in as-irradiated particles with coercivity of 60-130 Oe. Post-irradiation annealing at 220 {sup o}C enhanced chemical ordering in FePt nanoparticles with coercivity of 3500 Oe, magnetic anisotropy of 1.5 x 10{sup 7} erg/cc, and thermal stability factor of 130. A much higher 375 {sup o}C post-irradiation annealing was required in FePtAu, presumably because Au atoms were trapped at Fe/Pt lattice sites at lower temperatures. As the annealing temperature increased, anomalous features in the magnetization reversal curves were observed that disappeared at higher annealing temperatures.

  7. Nanoporous Au-TiMCM-41 - An inorganic hybrid photocatalyst toward visible photooxidation of methyl orange

    Energy Technology Data Exchange (ETDEWEB)

    Sathish Kumar, Panneer Selvam; Ruby Raj, Michael; Anandan, Sambandam [Nanomaterials and Solar Energy Conversion Lab, Department of Chemistry, National Institute of Technology, Trichy 620 015 (India)

    2010-10-15

    Modification of MCM-41 nanopore materials was found to improve the catalyst activity because it would provide an effective environment for increasing the number of active surface sites for molecular interaction. Hence in this article, with an attempt to extend light absorption of TiMCM-41 based photocatalyst toward the visible light range and to eliminate the rapid recombination of excited electrons/holes during photoreaction, a new type of photocatalyst Au/TiMCM-41 was prepared. The crystal phase composition and surface morphology of the Au/TiMCM-41 photocatalyst were comprehensively examined by X-ray differential detection and transmission electron microscopy analysis. The analytical results of UV-visible diffused reflectance spectra indicated that the absorbance in the visible region above 500 nm for Au/TiMCM-41 photocatalyst made it possible to be excited by visible light. The experiment demonstrated that the photocatalytic degradation of methyl orange using Au/TiMCM-41 photocatalyst was significantly higher than that using TiMCM-41 photocatalyst. Possibilities to enhance catalyst performance further by using electron acceptors are also discussed. (author)

  8. Energetics and the magnetic state of Mn2 adsorbed on Au(111): Dimer bond distance dependence

    Science.gov (United States)

    López-Moreno, S.; Mejía-López, J.; Munoz, Francisco; Calles, A.; Morán-López, J. L.

    2016-04-01

    In this work we present a theoretical study of the adsorption Mn2 dimer on the Au(111) surface. Here we use the density functional theory to construct a map of adsorption energies, EA, of Mn2 on a Au(111) surface as a function of interatomic bond distance, dMn-Mn, among Mn atoms. We employed a 4×4 supercell of Au(111) surface which lead us to reach dMn-Mn values in the range from 2.6 to 6.8 Å. To make a full study of the adsorption energies we considered the antiferromagnetic (AFM) and ferromagnetic (FM) states of the Mn2 on the surface. The energy landscape contains local minima when the Mn atoms are adsorbed above triangular sites and barriers that the Mn adatoms have to overcome when they move across the Au(111) surface along various paths. Our results show that the lowest energy state corresponds to the state in which the Mn atoms are next-nearest neighbors and are antiferromagnetically coupled. Furthermore, all the local minima with higher bonding energy are also those in the antiferromagnetic state. Nevertheless we find a short interval in which the FM state has lower energy than the AFM one. Finally, scanning tunneling microscope simulations for various dimer configurations on surface are reported.

  9. Synthesis of TiO2 Nanoparticles on the Au(111) Surface

    Energy Technology Data Exchange (ETDEWEB)

    Biener, J; Farfan-Arribas, E; Biener, M M; Friend, C M; Madix, R J

    2005-01-11

    The growth of titanium oxide nanoparticles on reconstructed Au(111) surfaces was investigated by scanning tunneling microscopy and X-ray photoelectron spectroscopy. Ti was deposited by physical vapor deposition at 300 K. Regular arrays of titanium nanoparticles form by preferential nucleation of Ti at the elbow sites of the herringbone reconstruction. Titanium oxide clusters were synthesized by subsequent exposure to O{sub 2} at 300 K. Two- and three-dimensional titanium oxide nanocrystallites form during annealing in the temperature range from 600 to 900 K. At the same time, the Au(111) surface assumes a serrated, <110> oriented step-edge morphology, suggesting step-edge pinning by titanium oxide nanoparticles. The oxidation state of these titanium oxide nanoparticles varies with annealing temperature. Specifically, annealing to 900 K results in the formation of stoichiometric TiO{sub 2} nanocrystals as judged by the observed XPS binding energies. Nano-dispersed TiO{sub 2} on Au(111) is an ideal system to test the various models explaining the enhanced catalytic reactivity of supported Au nanoparticles.

  10. Jet structure of baryon excess in Au+Au collisions at √(sNN)=200 GeV

    International Nuclear Information System (INIS)

    Two particle correlations between identified meson and baryon trigger particles with 2.5TT charged hadrons have been measured at midrapidity by the PHENIX experiment at RHIC in p+p,d+Au, and Au+Au collisions at √(sNN)=200 GeV. In noncentral Au+Au collisions, the probability of finding a hadron near in azimuthal angle to the trigger particles is almost identical for mesons and baryons and significantly higher than in p+p collisions. The associated yields for trigger baryons decrease in the most central collisions, consistent with some baryon production by thermal recombination in addition to hard scattering

  11. Mammalian sensitivity to elemental gold (Au?)

    Science.gov (United States)

    Eisler, R.

    2004-01-01

    There is increasing documentation of allergic contact dermatitis and other effects from gold jewelry, gold dental restorations, and gold implants. These effects were especially pronounced among females wearing body-piercing gold objects. One estimate of the prevalence of gold allergy worldwide is 13%, as judged by patch tests with monovalent organogold salts. Eczema of the head and neck was the most common response of individuals hypersensitive to gold, and sensitivity can last for at least several years. Ingestion of beverages containing flake gold can result in allergic-type reactions similar to those seen in gold-allergic individuals exposed to gold through dermal contact and other routes. Studies with small laboratory mammals and injected doses of colloidal gold showed increased body temperatures, accumulations in reticular cells, and dose enhancement in tumor therapy; gold implants were associated with tissue injuries. It is proposed that Au? toxicity to mammals is associated, in part, with formation of the more reactive Au+ and Au3+ species.

  12. Electric Field Induced Surface Modification of Au

    Energy Technology Data Exchange (ETDEWEB)

    Erchak, A.A.; Franklin, G.F.; Houston, J.E.; Mayer, T.M.; Michalske, T.A.

    1999-02-15

    We discuss the role of localized high electric fields in the modification of Au surfaces with a W probe using the Interfacial Force Microscope. Upon bringing a probe close to a Au surface, we measure both the interfacial force and the field emission current as a function of separation with a constant potential of 100 V between tip and sample. The current initially increases exponentially as the separation decreases. However, at a distance of less than {approximately} 500{angstrom} the current rises sharply as the surface begins to distort and rapidly close the gap. Retraction of the tip before contact is made reveals the formation of a mound on the surface. We propose a simple model, in which the localized high electric field under the tip assists the production of mobile Au adatoms by detachment from surface steps, and a radial field gradient causes a net flux of atoms toward the tip by surface diffusion. These processes give rise to an unstable surface deformation which, if left unchecked, results in a destructive mechanical contact. We discuss our findings with respect to earlier work using voltage pulses in the STM as a means of nanofabrication.

  13. Suppression of high transverse momentum π0 spectra in Au + Au collisions at RHIC

    Science.gov (United States)

    Kahana, D. E.; Kahana, S. H.

    2008-02-01

    Au + Au, s1/2 = 200 GeV measurements at RHIC, obtained with the PHENIX, STAR, PHOBOS and BRAHMS detectors, have all indicated a suppression of high p⊥ particle production, relative to an appropriately normalized NN level. For central collisions and vanishing pseudo-rapidity these experiments exhibit suppression in charged meson production, especially at medium-to-large transverse momenta. In the PHENIX experiment similar behaviour has been reported for π0 spectra. In a recent work [1] on the simpler D + Au interaction, to be considered perhaps as a tune-up for Au + Au, we reported on a pre-hadronic cascade mechanism which can explain the mixed observation of moderately reduced p⊥ suppression at higher pseudo-rapidity as well as the Cronin enhancement at mid-rapidity. Here, we present the extension of this work to the more massive ion-ion collisions. Our major thesis is that much of the suppression is generated in a late stage cascade of colourless pre-hadrons produced after an initial short-lived coloured phase. We present a pQCD argument to justify this approach and to estimate the time duration τp of this initial phase. Of essential importance is the brevity in time of the coloured phase existence relative to that of the strongly interacting pre-hadron phase, the latter essentially an interactive cascade. These distinctions in phase are of course not strict, but adequate for treating the suppression of moderate and high p⊥ mesons.

  14. Theoretical study of the Au/TiO2(110) interface

    DEFF Research Database (Denmark)

    Lopez, Nuria; Nørskov, Jens Kehlet

    2002-01-01

    Different gold structures have been deposited on the defect-free rutile TiO2(110) surface. Density functional calculations show that bonding at the interface depends strongly on the Au coverage. At low coverages, the most stable site is the adsorption on the protruding O atoms while at medium...... coverages the fivefold coordinated Ti is preferred and at higher coverages several sites at the rutile surface are simultaneously occupied. Calculations indicate that two dimensional (2D) or quasi-2D deposits are metastable with respect to three-dimensional ones. For large coverages, like 1 ML, we show that...

  15. CO adsorption on small Au{sub n} (n = 1–4) structures supported on hematite. II. Adsorption on the O-rich termination of α-Fe{sub 2}O{sub 3}(0001) surface

    Energy Technology Data Exchange (ETDEWEB)

    Pabisiak, Tomasz; Kiejna, Adam, E-mail: kiejna@ifd.uni.wroc.pl [Institute of Experimental Physics, University of Wrocław, Plac M. Borna 9, 50-204 Wrocław (Poland); Winiarski, Maciej J. [Institute of Experimental Physics, University of Wrocław, Plac M. Borna 9, 50-204 Wrocław (Poland); Institute of Low Temperature and Structure Research, Polish Academy of Sciences, ul. Okólna 2, 50-422 Wrocław (Poland)

    2016-01-28

    The adsorption of small Au{sub n} (n = 1–4) nanostructures on oxygen terminated α-Fe{sub 2}O{sub 3}(0001) surface was investigated using density functional theory in the generalized gradient approximation of Perdew-Burke-Ernzerhof (PBE) form with Hubbard correction U, accounting for strong electron correlations (PBE+U). The structural, energetic, and electronic properties were examined for two classes of the adsorbed Au{sub n} nanostructures with vertical and flattened configurations. Similarly to the Fe-terminated α-Fe{sub 2}O{sub 3}(0001) surface considered in Part I, the flattened configurations were found energetically more favored than vertical ones. The binding of Au{sub n} to the O-terminated surface is much stronger than to the Fe-termination. The adsorption bonding energy of Au{sub n} and the work function of the Au{sub n}/α-Fe{sub 2}O{sub 3}(0001) systems decrease with the increased number of Au atoms in a structure. All of the adsorbed Au{sub n} structures are positively charged. The bonding of CO molecules to the Au{sub n} structures is distinctly stronger than on the Fe-terminated surface; however, it is weaker than the binding to the bare O-terminated surface. The CO molecule binds to the Au{sub n}/α-Fe{sub 2}O{sub 3}(0001) system through a peripheral Au atom partly detached from the Au{sub n} structure. The results of this work indicate that the most energetically favored sites for adsorption of a CO molecule on the Au{sub n}/α-Fe{sub 2}O{sub 3}(0001) systems are atoms in the Au{sup 0.5+} oxidation state.

  16. Charge transport through O-deficient Au-MgO-Au junctions

    KAUST Repository

    Fadlallah, M. M.

    2009-12-29

    Metal-oxide heterostructures have been attracting considerable attention in recent years due to various technological applications. We present results of electronic structure and transport calculations for the Au-MgO-Au (metal-insulator-metal) heterostructure based on density-functional theory and the nonequilibrium Green’s functions method. The dependence of the conductance of the heterostructure on the thickness of the MgO interlayer and the interface spacing is studied. In addition, we address the effects of O vacancies. We observe deviations from an exponentially suppressed conductance with growing interlayer thickness caused by Au-O chemical bonds. Electronic states tracing back to O vacancies can increase the conductance. Furthermore, this effect can be enhanced by enlarging the interface spacing as the vacancy induced Mg states are shifted toward the Fermi energy.

  17. Synthesis and characterization of Au@Pt nanoparticles

    Institute of Scientific and Technical Information of China (English)

    ZHAO Dan; WU Gang; XU Boqing

    2005-01-01

    Aucore-Ptshell (Au@Pt) nanoparticles were synthesized at room temperature by reducing K2PtCl6 with hydrogen in the solution containing Au colloids and polyvinylpyrrolidone (PVP). The particles obtained were characterized with UV-Vis, TEM and XPS techniques. UV-Vis spectra show that the surface plasmon absorption feature of Au colloids is significantly reduced with increasing the amount of reduced Pt. TEM images that the metals are found always appear as spherical nanoparticles and their sizes grow apparently due to the reduction of PtCl62- ions, indicating that Pt is deposited from solution onto Au particle surface and forms a Pt-layer with uniform thickness. In the XPS spectra, the signals of Au metal decrease due to the reductive deposition of Pt on the surface of the Au colloids. UV-Vis and XPS data are consistent in showing that when the amount of Pt in the AuPt colloids is increased to reach an overall atomic ratio of Pt/Au=2, the Pt deposits form a shell covering completely the surface of Au particles, demonstrating the core-shell structure of the synthesized AuPt particles.

  18. Enrichment of the Superheavy Element Rg in Natural Au

    CERN Document Server

    Marinov, A; Kolb, D; Halicz, L; Segal, I; Tepliakov, N; Kashiv, Y; Brandt, R

    2010-01-01

    Based on the observation of the long-lived isotopes 261Rg and 265Rg (Z = 111, t(1/2) >= 10^(8) y) in natural Au, an experiment was performed to enrich Rg in 99.999% Au. 16 mg of Au were heated in vacuum for two weeks at a temperature of 1127 deg. C (63 deg. C above the melting point of Au). The content of 197Au and 261Rg in the residue was studied with high resolution inductively coupled plasma-sector field mass spectrometry (ICP-SFMS). The residue of Au was 3x10^(-6) of its original quantity. The recovery of Rg was a few percent. The abundance of Rg compared to Au in the enriched solution was about 2x10^(-6), which is a three to four orders of magnitude enrichment. It is concluded that the evaporation rate of Rg from an Au matrix in vacuum at 63 deg. C above the Au melting point is lower than that of Au. This experiment reinforces our first observation of Rg in a terrestrial material. As before it is concluded that a long-lived isomeric state exists in 261Rg and that it probably belongs to a new class of iso...

  19. Ternary aurides RE{sub 4}Mg{sub 3}Au{sub 10} (RE = Y, Nd, Sm, Gd-Dy) and their silver analogues

    Energy Technology Data Exchange (ETDEWEB)

    Block, Theresa; Johnscher, Michael; Linsinger, Stefan; Rodewald, Ute C.; Poettgen, Rainer [Muenster Univ. (Germany). Inst. fuer Anorganische und Analytische Chemie

    2015-06-01

    The ternary aurides RE{sub 4}Mg{sub 3}Au{sub 10} (RE = Y, Nd, Sm, Gd-Dy) and their silver analogues were synthesized by induction melting of the elements in sealed niobium tubes. These intermetallic phases were characterized by powder X-ray diffraction. They crystallize with the Ca{sub 4}In{sub 3}Au{sub 10}-type structure, which, from a geometrical point of view, is a ternary ordered version of Zr{sub 7}Ni{sub 10} with the rare earth and magnesium atoms ordering on the four crystallographically independent zirconium sites. The structures of crystals from three differently prepared gadolinium samples were refined from single-crystal X-ray diffractometer data: Cmca, a=1366.69(3), b=998.07(4), c=1005.54(3) pm, wR2=0.0332, 1234 F{sup 2} values, 46 variables for Gd{sub 4.43}Mg{sub 2.57}Au{sub 10}, a=1378.7(1), b=1005.3(1), c=1011.2(1) pm, wR2=0.0409, 1255 F{sup 2} values, 48 variables for Gd{sub 5.50}Mg{sub 1.50}Au{sub 10}, and a=1350.2(5), b=995.5(1), c=1009.3(1) pm, wR2=0.0478, 1075 F{sup 2} values, 48 variables for Gd{sub 5.61}Mg{sub 1.39}Au{sub 10}. All crystals show substantial Mg/Gd mixing on two sites. The gold atoms form a pronounced two-dimensional substructure with Au-Au distances of 278 to 297 pm in Gd{sub 4.43}Mg{sub 2.57}Au{sub 10}. These gold blocks are condensed via magnesium atoms (278-315 pm Mg-Au). The gadolinium atoms fill larger cavities within the three-dimensional networks. The magnesium vs. gadolinium site preference is a consequence of the different coordination numbers of the cation sites. All phases show homogeneity ranges RE{sub 4+x}Mg{sub 3-x}Au{sub 10} and RE{sub 4+x}Mg{sub 3-x}Au{sub 10}. The influence of the synthesis conditions is briefly discussed.

  20. Strangelet search in Au+Au collisions at VsNN=200 GeV

    OpenAIRE

    Bai, Y.(Institute of High Energy Physics, Chinese Academy of Sciences, Beijing, China); Benedosso, F.; Botje, M.A.J.; Grebenyuk, O.; Mischke, A.; Peitzmann, T.; Russcher, M.J.; Snellings, R.J.M.; van der Kolk, N.

    2007-01-01

    We have searched for strangelets in a triggered sample of 61 million central (top 4%) Au+Au collisions at √sNN=200 GeV near beam rapidities at the STAR solenoidal tracker detector at the BNL Relativistic Heavy Ion Collider. We have sensitivity to metastable strangelets with lifetimes of order ⩾0.1 ns, in contrast to limits over ten times longer in BNL Alternating Gradient Synchrotron (AGS) studies and longer still at the CERN Super Proton Synchrotron (SPS). Upper limits of a few 10-6 to 10-7 ...

  1. Relativistic multireference many-body perturbation theory calculations on Au64+ - Au69+ ions

    Energy Technology Data Exchange (ETDEWEB)

    Vilkas, M J; Ishikawa, Y; Trabert, E

    2006-03-31

    Many-body perturbation theory (MBPT) calculations are an adequate tool for the description of the structure of highly charged multi-electron ions and for the analysis of their spectra. They demonstrate this by way of a re-investigation of n=3, {Delta}n=0 transitions in the EUV spectra of Na-, Mg-, Al-like, and Si-like ions of Au that have been obtained previously by heavy-ion accelerator based beam-foil spectroscopy. They discuss the evidence and propose several revisions on the basis of the multi-reference many-body perturbation theory calculations of Ne- through P-like ions of Au.

  2. PARTON STRUCTURE THROUGH TWO PARTICLE CORRELATIONS IN AU-AU AT RHIC.

    Energy Technology Data Exchange (ETDEWEB)

    LONGACRE,R.S.

    1999-10-23

    A method for determining the presence of partonic scattering through two-particle correlations is developed and applied to models which have jets and mini-jets in them. We only consider the correlation of mid-rapidity particles because they will be easily measured in large numbers at RHIC. The level of two-particle correlations will be a direct measure of how dense a system is made in Au-Au collisions at RHIC. The STAR TPC will be ideal for making these measurements in the first year of running.

  3. Elliptic flow in Au+Au collisions at $\\sqrt{S_{NN}}$=130 GeV

    CERN Document Server

    Ackermann, K H; Adler, C; Ahammed, Z; Ahmad, S; Allgower, C; Amsbaugh, J; Anderson, M; Anderssen, E; Arnesen, H; Arnold, L; Averichev, G S; Baldwin, A R; Balewski, J T; Barannikova, O Yu; Barnby, L S; Baudot, J; Beddo, M E; Bekele, S; Belaga, V V; Bellwied, R; Bennett, S; Bercovitz, J; Berger, J; Betts, W; Bichsel, H; Bieser, F; Bland, L C; Bloomer, M A; Blyth, C O; Böhm, J; Bonner, B E; Bonnet, D; Bossingham, R R; Botlo, M; Boucham, A; Bouillo, N; Bouvier, S; Bradley, K; Brady, F P; Braithwaite, E S; Braithwaite, W; Brandin, A B; Brown, R L; Brugalette, G; Byrd, C; Caines, H; Calderón de la Barca-Sanchez, M; Cardenas, A; Carr, L; Carroll, J; Castillo, J; Caylor, B; Cebra, D; Chathopadhyay, S; Chen, M L; Chen, W; Chen, Y; Chernenko, S P; Cherney, M; Chikanian, A; Choi, B; Chrin, J; Christie, W; Coffin, J P; Conin, L; Consiglio, C; Cormier, T M; Cramer, J G; Crawford, H J; Danilov, V I; Dayton, D; De Mello, M; Deng, W S; Derevshchikov, A A; Dialinas, M; Díaz, H; De Young, P A; Didenko, L; Dimassimo, D; Dioguardi, J; Dominik, Wojciech; Drancourt, C; Draper, J E; Dunin, V B; Dunlop, J C; Eckardt, V; Edwards, W R; Efimov, L G; Eggert, T; Emelyanov, V I; Engelage, J; Eppley, G; Erazmus, B; Etkin, A; Fachini, P; Feliciano, C; Ferenc, D; Ferguson, M I; Fessler, H; Finch, E; Fine, V; Fisyak, Yu; Flierl, D; Flores, I; Foley, Kenneth J; Fritz, D; Gagunashvili, N D; Gans, J; Gazdzicki, M; Germain, M; Geurts, F J M; Ghazikhanian, V; Gojak, C; Grabski, J; Grachov, O A; Grau, M; Greiner, D E; Greiner, L; Grigoriev, V; Grosnick, D P; Gross, J; Guilloux, G; Gushin, E M; Hall, J; Hallman, T J; Hardtke, D; Harper, G; Harris, J W; He, P; Heffner, M; Heppelmann, S; Herston, T; Hill, D; Hippolyte, B; Hirsch, A; Hjort, E; Hoffmann, G W; Horsley, M; Howe, M; Huang, H Z; Humanic, T J; Hümmler, H; Hunt, W; Hunter, J; Igo, G; Ishihara, A; Ivanshin, Yu I; Jacobs, P; Jacobs, W W; Jacobson, S; Jared, R; Jensen, P; Johnson, I; Jones, P G; Judd, E; Kaneta, M; Kaplan, M; Keane, D; Kenney, V P; Khodinov, A; Klay, J L; Klein, S R; Klyachko, A A; Koehler, G; Konstantinov, A S; Kormilitsyne, V; Kotchenda, L; Kotov, I V; Kovalenko, A D; Krämer, M; Kravtsov, P; Krüger, K; Krupien, T; Kuczewski, P; Kühn, C E; Kunde, G J; Kunz, C L; Kutuev, R K; Kuznetsov, A A; Lakehal-Ayat, L; Lamont, M A C; Landgraf, J M; Lange, S; Lansdell, C P; Lasiuk, B; Laue, F; Lebedev, A; LeCompte, T J; Leonhardt, W; Leontiev, V M; Leszczynski, P; Le Vine, M J; Li, Q; Li, Z; Liaw, C J; Lin, J; Lindenbaum, S J; Lindenstruth, V; Lindstrom, P J; Lisa, M A; Liu, H; Ljubicic, T; Llope, W J; Lo Curto, G; Long, H; Longacre, R S; López-Noriega, M; Lopiano, D; Love, W A; Lutz, Jean Robert; Lynn, D; Madansky, L; Maier, R S; Majka, R; Maliszewski, A; Margetis, S; Marks, K; Marstaller, R; Martin, L; Marx, J; Matis, H S; Matulenko, Yu A; Matyushevsky, E A; McParland, C P; McShane, T S; Meier, J; Melnik, Yu M; Meshchanin, A P; Middlekamp, P; Mikhalin, N; Miller, B; Milosevich, Z; Minaev, N G; Minor, B; Mitchell, J; Mogavero, E; Moiseenko, V A; Moltz, D M; Moore, C F; Morozov, V; Morse, R; De Moura, M M; Munhoz, M G; Mutchler, G S; Nelson, J M; Nevski, P; Ngo, T; Nguyen, M; Nguyen, T; Nikitin, V A; Nogach, L V; Noggle, T; Norman, B; Nurushev, S B; Nussbaum, T; Nystrand, J; Odyniec, Grazyna Janina; Ogawa, A; Ogilvie, C A; Olchanski, K; Oldenburg, M; Olson, D; Ososkov, G A; Ott, G; Padrazo, D; Paic, G; Pandey, S U; Panebratsev, Yu A; Panitkin, S Y; Pavlinov, A I; Pawlak, T; Pentia, M; Perevozchikov, V; Peryt, W; Petrov, V; Pinganaud, W; Pirogov, S; Platner, E D; Pluta, J; Polk, I; Porile, N T; Porter, J; Poskanzer, A M; Potrebenikova, E V; Prindle, D J; Pruneau, C A; Puskar-Pasewicz, J; Rai, G; Rasson, J E; Ravel, O; Ray, R L; Razin, S V; Reichhold, D M; Reid, J; Renfordt, R E; Retière, F; Ridiger, A; Riso, J; Ritter, H G; Roberts, J B; Röhrich, D; Rogachevski, O V; Romero, J L; Roy, C; Russ, D; Rykov, V L; Sakrejda, I; Sánchez, R; Sandler, Z; Sandweiss, J; Sappenfield, P; Saulys, A C; Savin, I A; Schambach, J; Scharenberg, R P; Scheblien, J; Scheetz, R; Schlüter, R; Schmitz, N; Schröder, L S; Schulz, M; Schüttauf, A; Sedlmeir, J; Seger, J E; Seliverstov, D M; Seyboth, J; Seyboth, P; Seymour, R; Shakaliev, E I; Shestermanov, K E; Shi, Y; Shimansky, S S; Shuman, D B; Shvetcov, V S; Skoro, G P; Smirnov, N; Smykov, L P; Snellings, R; Solberg, K; Sowinski, J; Spinka, H M; Srivastava, B; Stephenson, E J; Stock, Reinhard; Stolpovsky, A; Stone, N; Stone, R; Strikhanov, M N; Stringfellow, B C; Ströbele, H; Struck, C; Suaide, A A P; Sugarbaker, E R; Suire, C; Symons, T J M; Takahashi, J; Tang, A H; Tarchini, A; Tarzian, J; Thomas, J H; Tikhomirov, V; Szanto de Toledo, A; Tonse, S R; Trainor, T; Trentalange, S; Tokarev, M; Tonjes, M B; Trofimov, V N; Tsai, O; Turner, K; Ullrich, T S; Underwood, D G; Vakula, I; Van Buren, G; Van der Molen, A; Vanyashin, A V; Vasilevskii, I M; Vasilev, A N; Vigdor, S E; Visser, G; Voloshin, S A; Vu, C; Wang, F; Ward, H; Weerasundara, D D; Weidenbach, R; Wells, R; Wenaus, T J; Westfall, G D; Whitfield, J P; Whitten, C; Wieman, H H; Willson, R; Wilson, K; Wirth, J; Wisdom, J; Wissink, S W; Witt, R; Wolf, J; Wood, L; Xu, N; Xu, Z; Yakutin, A E; Yamamoto, E; Yang, J; Yepes, P; Yokosawa, A; Yurevich, V I; Zanevsky, Yu V; Zhang, J; Zhang, W M; Zhu, J; Zimmerman, D; Zoulkarneev, R; Zubarev, A N

    2001-01-01

    Elliptic flow from nuclear collisions is a hadronic observable sensitive to the early stages of system evolution. We report first results on elliptic flow of charged particles at midrapidity in Au+Au collisions at sqrt(s_NN)=130 GeV using the STAR TPC at RHIC. The elliptic flow signal, v_2, averaged over transverse momentum, reaches values of about 6% for relatively peripheral collisions and decreases for the more central collisions. This can be interpreted as the observation of a higher degree of thermalization than at lower collision energies. Pseudorapidity and transverse momentum dependence of elliptic flow are also presented.

  4. Spectator matter fragmentation in Au+Au reactions: Phase space analysis

    CERN Document Server

    Vermani, Yogesh K

    2011-01-01

    Clusterization in phase space has been analyzed for peripheral Au+Au reactions at 1000 AMeV using simulated annealing clusterization algorithm (SACA). We investigate how these fragments are correlated in phase space and compare our model calculations with minimum spanning tree (MST) method. Our theoretical study highlights the importance of binding energy criterion in recognizing the fragment structure. MST method however, fails to break-up the spectator matter effectively and thus under-estimates the multiplicity of intermediate mass fragments (IMFs).

  5. Energy Dependence of Particle Multiplicities in Central Au+Au Collisions

    Science.gov (United States)

    Back, B. B.; Baker, M. D.; Barton, D. S.; Betts, R. R.; Bindel, R.; Budzanowski, A.; Busza, W.; Carroll, A.; Corbo, J.; Decowski, M. P.; Garcia, E.; George, N.; Gulbrandsen, K.; Gushue, S.; Halliwell, C.; Hamblen, J.; Henderson, C.; Hicks, D.; Hofman, D.; Hollis, R. S.; Hołyński, R.; Holzman, B.; Iordanova, A.; Johnson, E.; Kane, J.; Katzy, J.; Khan, N.; Kucewicz, W.; Kulinich, P.; Kuo, C. M.; Lin, W. T.; Manly, S.; McLeod, D.; Michałowski, J.; Mignerey, A.; Mülmenstädt, J.; Nouicer, R.; Olszewski, A.; Pak, R.; Park, I. C.; Pernegger, H.; Rafelski, M.; Rbeiz, M.; Reed, C.; Remsberg, L. P.; Reuter, M.; Roland, C.; Roland, G.; Rosenberg, L.; Sagerer, J.; Sarin, P.; Sawicki, P.; Skulski, W.; Steadman, S. G.; Steinberg, P.; Stephans, G. S.; Stodulski, M.; Sukhanov, A.; Tang, J.-L.; Teng, R.; Trzupek, A.; Vale, C.; van Nieuwenhuizen, G. J.; Verdier, R.; Wadsworth, B.; Wolfs, F. L.; Wosiek, B.; Woźniak, K.; Wuosmaa, A. H.; Wysłouch, B.

    2002-01-01

    We present the first measurement of the pseudorapidity density of primary charged particles in Au+Au collisions at (sNN) = 200 GeV. For the 6% most central collisions, we obtain dNch/dη\\|\\|η\\|<1 = 650+/-35(syst). Compared to collisions at (sNN) = 130 GeV, the highest energy studied previously, an increase by a factor of 1.14+/-0.05 at 90% confidence level, is found. The energy dependence of the pseudorapidity density is discussed in comparison with data from proton-induced collisions and theoretical predictions.

  6. Gold nanoparticle (AuNPs) and gold nanopore (AuNPore) catalysts in organic synthesis.

    Science.gov (United States)

    Takale, Balaram S; Bao, Ming; Yamamoto, Yoshinori

    2014-04-01

    Organic synthesis using gold has gained tremendous attention in last few years, especially heterogeneous gold catalysis based on gold nanoparticles has made its place in almost all organic reactions, because of the robust and green nature of gold catalysts. In this context, gold nanopore (AuNPore) with a 3D metal framework is giving a new dimension to heterogeneous gold catalysts. Interestingly, AuNPore chemistry is proving better than gold nanoparticles based chemistry. In this review, along with recent advances, major discoveries in heterogeneous gold catalysis are discussed.

  7. Observation of anisotropic event shapes and transverse flow in ultrarelativistic Au+Au collisions

    International Nuclear Information System (INIS)

    Event shapes for Au + Au collisions at 11.4 GeV/c per nucleon were studied over nearly the full solid angle with the E877 apparatus. The analysis was performed by Fourier expansion of azimuthal distributions of the transverse energy (ET) measured in different pseudorapidity intervals. For semicentral collisions a pronounced event anisotropy is identified with a clear forward-backward anticorrelation. In the forward pseudorapidity interval up to 9% of the ET is in a directed component. The signal decreases for peripheral and very central collisions

  8. Net charge fluctuations in Au + Au interactions at sqrt[s(NN)]=130 GeV.

    Science.gov (United States)

    Adcox, K; Adler, S S; Ajitanand, N N; Akiba, Y; Alexander, J; Aphecetche, L; Arai, Y; Aronson, S H; Averbeck, R; Awes, T C; Barish, K N; Barnes, P D; Barrette, J; Bassalleck, B; Bathe, S; Baublis, V; Bazilevsky, A; Belikov, S; Bellaiche, F G; Belyaev, S T; Bennett, M J; Berdnikov, Y; Botelho, S; Brooks, M L; Brown, D S; Bruner, N; Bucher, D; Buesching, H; Bumazhnov, V; Bunce, G; Burward-Hoy, J; Butsyk, S; Carey, T A; Chand, P; Chang, J; Chang, W C; Chavez, L L; Chernichenko, S; Chi, C Y; Chiba, J; Chiu, M; Choudhury, R K; Christ, T; Chujo, T; Chung, M S; Chung, P; Cianciolo, V; Cole, B A; D'Enterria, D G; David, G; Delagrange, H; Denisov, A; Deshpande, A; Desmond, E J; Dietzsch, O; Dinesh, B V; Drees, A; Durum, A; Dutta, D; Ebisu, K; Efremenko, Y V; El Chenawi, K; En'yo, H; Esumi, S; Ewell, L; Ferdousi, T; Fields, D E; Fokin, S L; Fraenkel, Z; Franz, A; Frawley, A D; Fung, S-Y; Garpman, S; Ghosh, T K; Glenn, A; Godoi, A L; Goto, Y; Greene, S V; Grosse Perdekamp, M; Gupta, S K; Guryn, W; Gustafsson, H-A; Haggerty, J S; Hamagaki, H; Hansen, A G; Hara, H; Hartouni, E P; Hayano, R; Hayashi, N; He, X; Hemmick, T K; Heuser, J M; Hibino, M; Hill, J C; Ho, D S; Homma, K; Hong, B; Hoover, A; Ichihara, T; Imai, K; Ippolitov, M S; Ishihara, M; Jacak, B V; Jang, W Y; Jia, J; Johnson, B M; Johnson, S C; Joo, K S; Kametani, S; Kang, J H; Kann, M; Kapoor, S S; Kelly, S; Khachaturov, B; Khanzadeev, A; Kikuchi, J; Kim, D J; Kim, H J; Kim, S Y; Kim, Y G; Kinnison, W W; Kistenev, E; Kiyomichi, A; Klein-Boesing, C; Klinksiek, S; Kochenda, L; Kochetkov, V; Koehler, D; Kohama, T; Kotchetkov, D; Kozlov, A; Kroon, P J; Kurita, K; Kweon, M J; Kwon, Y; Kyle, G S; Lacey, R; Lajoie, J G; Lauret, J; Lebedev, A; Lee, D M; Leitch, M J; Li, X H; Li, Z; Lim, D J; Liu, M X; Liu, X; Liu, Z; Maguire, C F; Mahon, J; Makdisi, Y I; Manko, V I; Mao, Y; Mark, S K; Markacs, S; Martinez, G; Marx, M D; Masaike, A; Matathias, F; Matsumoto, T; McGaughey, P L; Melnikov, E; Merschmeyer, M; Messer, F; Messer, M; Miake, Y; Miller, T E; Milov, A; Mioduszewski, S; Mischke, R E; Mishra, G C; Mitchell, J T; Mohanty, A K; Morrison, D P; Moss, J M; Mühlbacher, F; Muniruzzaman, M; Murata, J; Nagamiya, S; Nagasaka, Y; Nagle, J L; Nakada, Y; Nandi, B K; Newby, J; Nikkinen, L; Nilsson, P; Nishimura, S; Nyanin, A S; Nystrand, J; O'Brien, E; Ogilvie, C A; Ohnishi, H; Ojha, I D; Ono, M; Onuchin, V; Oskarsson, A; Osterman, L; Otterlund, I; Oyama, K; Paffrath, L; Palounek, A P T; Pantuev, V S; Papavassiliou, V; Pate, S F; Peitzmann, T; Petridis, A N; Pinkenburg, C; Pisani, R P; Pitukhin, P; Plasil, F; Pollack, M; Pope, K; Purschke, M L; Ravinovich, I; Read, K F; Reygers, K; Riabov, V; Riabov, Y; Rosati, M; Rose, A A; Ryu, S S; Saito, N; Sakaguchi, A; Sakaguchi, T; Sako, H; Sakuma, T; Samsonov, V; Sangster, T C; Santo, R; Sato, H D; Sato, S; Sawada, S; Schlei, B R; Schutz, Y; Semenov, V; Seto, R; Shea, T K; Shein, I; Shibata, T-A; Shigaki, K; Shiina, T; Shin, Y H; Sibiriak, I G; Silvermyr, D; Sim, K S; Simon-Gillo, J; Singh, C P; Singh, V; Sivertz, M; Soldatov, A; Soltz, R A; Sorensen, S; Stankus, P W; Starinsky, N; Steinberg, P; Stenlund, E; Ster, A; Stoll, S P; Sugioka, M; Sugitate, T; Sullivan, J P; Sumi, Y; Sun, Z; Suzuki, M; Takagui, E M; Taketani, A; Tamai, M; Tanaka, K H; Tanaka, Y; Taniguchi, E; Tannenbaum, M J; Thomas, J; Thomas, J H; Thomas, T L; Tian, W; Tojo, J; Torii, H; Towell, R S; Tserruya, I; Tsuruoka, H; Tsvetkov, A A; Tuli, S K; Tydesjö, H; Tyurin, N; Ushiroda, T; van Hecke, H W; Velissaris, C; Velkovska, J; Velkovsky, M; Vinogradov, A A; Volkov, M A; Vorobyov, A; Vznuzdaev, E; Wang, H; Watanabe, Y; White, S N; Witzig, C; Wohn, F K; Woody, C L; Xie, W; Yagi, K; Yokkaichi, S; Young, G R; Yushmanov, I E; Zajc, W A; Zhang, Z; Zhou, S

    2002-08-19

    Data from Au + Au interactions at sqrt[s(NN)]=130 GeV, obtained with the PHENIX detector at the Relativistic Heavy-Ion Collider, are used to investigate local net charge fluctuations among particles produced near midrapidity. According to recent suggestions, such fluctuations may carry information from the quark-gluon plasma. This analysis shows that the fluctuations are dominated by a stochastic distribution of particles, but are also sensitive to other effects, like global charge conservation and resonance decays. PMID:12190459

  9. Light Fragment Production and Power Law Behavior in Au + Au Collisions

    International Nuclear Information System (INIS)

    Using charged-particle-exclusive measurements of Au+Au collisions in the LBL Bevalac's EOS time projection chamber, we investigate momentum-space densities of fragments up to 4He as a function of fragment transverse momentum, azimuth relative to the reaction plane, rapidity, multiplicity, and beam energy. Most features of these densities above a transverse momentum threshold are consistent with momentum-space coalescence, and, in particular, the increase in sideward flow with fragment mass is generally well described by a momentum-space power law

  10. On direct photon production in Pb+Pb and Au+Au collisions

    CERN Document Server

    Guptaroy, P

    2003-01-01

    Some aspects of the direct photon production phenomenon are discussed, mainly in the Pb+Pb and Au+Au collisions on the basis of a model for production of the same particle species in PP collisions. The results have, thereafter, been converted to those for a few AB/AA interactions through an appropriate mechanism. Comparison of the theoretical results obtained on the basis of model-based calculations with measured data on the relevant observables leads to a fair agreement between them. This reflects modestly the fair achievements attained by the models that are made use of in the present work. (author)

  11. On direct photon production in Pb+Pb and Au+Au collisions

    International Nuclear Information System (INIS)

    Some aspects of the direct photon production phenomenon are discussed, mainly in the Pb+Pb and Au+Au collisions on the basis of a model for production of the same particle species in PP collisions. The results have, thereafter, been converted to those for a few AB/AA interactions through an appropriate mechanism. Comparison of the theoretical results obtained on the basis of model-based calculations with measured data on the relevant observables leads to a fair agreement between them. This reflects modestly the fair achievements attained by the models that are made use of in the present work. (author)

  12. Sideward Flow in Au + Au Collisions Between 2 AGeV and 8 AGeV

    CERN Document Server

    Liu, H; Alexander, J; Anderson, M; Best, D; Brady, F P; Case, T; Caskey, W; Cebra, D; Chance, J; Chung, P; Cole, B; Crowe, K M; Das, A; Draper, J E; Gilkes, M L; Gushue, S; Heffner, M; Hirsch, A; Hjort, E; Huo, L; Justice, M; Kaplan, M; Keane, D; Kintner, J; Klay, J L; Krofcheck, D; Lacey, R A; Lisa, M A; Liu, Y M; McGrath, R; Milosevich, Z; Odyniec, Grazyna Janina; Olson, D; Panitkin, S Y; Pinkenburg, C H; Porile, N T; Rai, G; Ritter, H G; Romero, J; Scharenberg, R P; Schröder, L S; Srivastava, B; Stone, N T B; Symons, T J M; Wang, S; Whitfield, J; Wienold, T; Witt, R; Wood, L; Yang, X; Zhang Wei Ning; Zhang, Y

    2000-01-01

    Using the large acceptance Time Projection Chamber of experiment E895 at Brookhaven, measurements of collective sideward flow in Au + Au collisions at beam energies of 2, 4, 6 and 8A GeV are presented in the form of in-plane transverse momentum and the first Fourier coefficient of azimuthal anisotropy v_1. These measurements indicate a smooth variation of sideward flow as a function of beam energy. The data are compared with four nuclear transport models which have an orientation towards this energy range. All four exhibit some qualitative trends similar to those found in the data, although none shows a consistent pattern of agreement within experimental uncertainties.

  13. Charged Pion Production in 2 to 8 AGeV Central Au+Au Collisions

    CERN Document Server

    Klay, J L; Alexander, J M; Anderson, M G; Best, D; Brady, F P; Case, T; Caskey, W; Cebra, D; Chance, J L; Chung, P; Cole, B; Crowe, K; Das, A C; Draper, J E; Gilkes, M L; Gushue, S; Heffner, M; Hirsch, A S; Hjort, E L; Huo, L; Justice, M; Kaplan, M; Keane, D; Kintner, J C; Krofcheck, D; Lacey, R A; Lauret, J; Law, C; Lisa, M A; Liu, H; Liu, Y M; McGrath, R; Milosevich, Z; Odyniec, Grazyna Janina; Olson, D L; Panitkin, S Y; Pinkenburg, C H; Porile, N T; Rai, G; Ritter, H G; Romero, J L; Scharenberg, R P; Srivastava, B; Stone, N T B; Symons, T J M; Wang, S; Wells, R; Whitfield, J; Wienold, T; Witt, R; Wood, L; Zhang Wei Ning

    2003-01-01

    Momentum spectra of charged pions over nearly full rapidity coverage from target to beam rapidity have been measured in the 0-5% most central Au+Au collisions in the beam energy range from 2 to 8 AGeV by the E895 Experiment. Using a thermal parameterization to fit the transverse mass spectra, rapidity density distributions are extracted. The observed spectra are compared with predictions from the RQMD v2.3 cascade model and also to a thermal model including longitudinal flow. The total 4$pi$ yields of the charged pions are used to infer an initial state entropy produced in the collisions.

  14. Beam-Energy Dependence of Charge Balance Functions from Au+Au Collisions at RHIC

    OpenAIRE

    STAR Collaboration

    2015-01-01

    Balance functions have been measured in terms of relative pseudorapidity ($\\Delta \\eta$) for charged particle pairs at the Relativistic Heavy-Ion Collider (RHIC) from Au+Au collisions at $\\sqrt{s_{\\rm NN}}$ = 7.7 GeV to 200 GeV using the STAR detector. These results are compared with balance functions measured at the Large Hadron Collider (LHC) from Pb+Pb collisions at $\\sqrt{s_{\\rm NN}}$ = 2.76 TeV by the ALICE Collaboration. The width of the balance function decreases as the collisions beco...

  15. Beam Energy Scan a Case for the Chiral Magnetic Effect in Au-Au Collisions

    Energy Technology Data Exchange (ETDEWEB)

    Longacre, R. [Brookhaven National Lab. (BNL), Upton, NY (United States)

    2014-01-05

    The Chiral Magnetic Effect (CME) is predicted for Au-Au collisions at RHIC. However, many backgrounds can give signals that make the measurement hard to interpret. The STAR experiment has made measurements at different collisions energy ranging from √(sNN)=7.7 GeV to 62.4 GeV. In the analysis that is presented we show that the CME turns on with energy and is not present in central collisions where the induced magnetic is small.

  16. Azimuthal Anisotropy of Identified Hadrons in 200 GeV Au+Au Collisions

    CERN Document Server

    Oldenburg, M

    2006-01-01

    The azimuthal anisotropy parameter v2 has been measured with high statistics for identified hadrons in sqrt(s_NN) = 200 GeV Au+Au collisions with the STAR experiment. At high transverse momentum (pT) a strong v2 for pi+ + pi- and p + pbar is observed. In the intermediate pT region, number-of-constituent-quark scaling was tested to high precision. A detailed comparison of v2 for the multi-strange hadrons phi, Xi + anti-Xi, and Omega + anti-Omega with other particle species substantiates the development of collectivity among partons in the early phase of the collisions at RHIC.

  17. Pronounced matrix effect in YbMo{sub 2}Al{sub 4}-type Ca(Au{sub x}Zn{sub 2−x})Au{sub 4} (x=0.09–0.89)

    Energy Technology Data Exchange (ETDEWEB)

    Mishra, Trinath [Department of Chemistry, Iowa State University, Ames, IA 50011 (United States); Lin, Qisheng, E-mail: qslin@ameslab.gov [Division of Materials Sciences and Engineering, Ames Laboratory, U.S. Department of Energy, Ames, IA 50011 (United States); Corbett, John D. [Department of Chemistry, Iowa State University, Ames, IA 50011 (United States); Division of Materials Sciences and Engineering, Ames Laboratory, U.S. Department of Energy, Ames, IA 50011 (United States)

    2014-10-15

    Electron-poor polar intermetallics Ca(Au{sub x}Zn{sub 2−x})Au{sub 4} have been synthesized through fusion of stoichiometric metals in sealed tantalum tubes at 800 °C and annealing at 400 °C for one week. Single crystal X-ray diffraction analyses reveal that this phase belongs to the YbMo{sub 2}Al{sub 4}-type structure (I4/mmm, Pearson symbol tI14), a≈6.943–7.017 Å, c≈5.278–5.286 Å, Z=2, with homogeneous composition range of x=0.09(1)–0.89(1). The structure exhibits a three-dimensional framework of (Au{sub 8}){sub 1/2} featuring square and octagonal channels extending in c, in which Ca and the infinite linear chains of [(Au,Zn){sub 2}]{sub 1/2} are located, respectively. Mulliken population analyses demonstrate that Zn prefers to form the linear chains in the whole homogeneous composition range, consistent with experimental observations. Crystal orbital Hamilton population (COHP) analyses reveal that the channel-to-chain Au–Zn contact has strong bonding interactions regardless of its large interatomic distance (∼2.85 Å), a signature of pronounced matrix effect. The last mentioned effect in YbMo{sub 2}Al{sub 4}-type structures is expected in case the linear chains are defined by small size atoms. - Graphical abstract: Pronounced matrix effect incurred by Au–Au bonding within the gold substructure in Ca(Au{sub x}Zn{sub 2−x})Au{sub 4} results in an elongation of the channel-to-chain Au–Zn interatomic distance without weakening bonding interactions. - Highlights: • The complete solid solution of Ca(Au{sub x}Zn{sub 2−x})Au{sub 4} was accomplished. • Site preference was explained by “coloring” analyses. • Abnormally large Au–Zn distance but with strong bonding was observed. • Pronounced matrix effect incurred by Au–Au bonding in gold substructure was found.

  18. Area monitor for neutrons with thin sheet of Au; Monitor de area para neutrones con laminilla de Au

    Energy Technology Data Exchange (ETDEWEB)

    Valero L, C.; Guzman G, K. A.; Banuelos F, A.; Borja H, C. G.; Hernandez D, V. M.; Vega C, H. R. [Universidad Autonoma de Zacatecas, Unidad Academica de Estudios Nucleares, Calle Cipres No. 10, Fracc. La Penuela, 98068 Zacatecas (Mexico); Gallego, E.; Lorente, A., E-mail: fermineutron@yahoo.com [Universidad Politecnica de Madrid, Departamento de Ingenieria Nuclear, C/ Jose Gutierrez Abascal 2, E-28006 Madrid (Spain)

    2011-11-15

    A passive area monitor for neutrons with an activation detector was designed and constructed to be used in sites where the radiation field is mixed, intense and pulsed, like happens in the radiotherapy rooms that use lineal accelerators of medical use or in enclosures with cyclotrons for PET, or where the field is mixed and intense as in the nuclear power plants. This equipment is useful for the exposition cases of the patients or workers that receive not counted radiation dose, generating harmful effects to the health, for what is necessary to take the pertinent measures for the radiological protection. The design of the area monitor was realized using the MCNP5 code, where was considered an activation detector and therefore thin sheets of Au-197 located in the moderator center were used. The moderator was designed as a polyethylene cylindrical to moderate the neutrons. The gold was used like detector for its high cross section and its physical and chemical characteristics. The response of the monitor is maxim for energies from 1 to 20 MeV, region where the flowing coefficients and dose are majors. Therefore, the designed and constructed monitor can be used in sites with high, mixed and pulsed radiation fields. (Author)

  19. Au/Pd core-shell nanoparticles with varied hollow Au cores for enhanced formic acid oxidation

    Science.gov (United States)

    Hsu, Chiajen; Huang, Chienwen; Hao, Yaowu; Liu, Fuqiang

    2013-03-01

    A facile method has been developed to synthesize Au/Pd core-shell nanoparticles via galvanic replacement of Cu by Pd on hollow Au nanospheres. The unique nanoparticles were characterized by X-ray diffraction, X-ray photoelectron spectroscopy, transmission electron microscopy, ultraviolet-visible spectroscopy, and electrochemical measurements. When the concentration of the Au solution was decreased, grain size of the polycrystalline hollow Au nanospheres was reduced, and the structures became highly porous. After the Pd shell formed on these Au nanospheres, the morphology and structure of the Au/Pd nanoparticles varied and hence significantly affected the catalytic properties. The Au/Pd nanoparticles synthesized with reduced Au concentrations showed higher formic acid oxidation activity (0.93 mA cm-2 at 0.3 V) than the commercial Pd black (0.85 mA cm-2 at 0.3 V), suggesting a promising candidate as fuel cell catalysts. In addition, the Au/Pd nanoparticles displayed lower CO-stripping potential, improved stability, and higher durability compared to the Pd black due to their unique core-shell structures tuned by Au core morphologies.

  20. Thermal stability of Mo/Au bilayers for TES applications

    International Nuclear Information System (INIS)

    Mo/Au bilayers are among the most suitable materials to be used as transition-edge sensors (TES) in cryogenic microcalorimeters and bolometers, developed, among other fields, for space missions. For this purpose the thermal stability of TES at temperatures below 150 °C is a critical issue. We report on the dependence of functional properties (superconducting critical temperature, residual resistance and α) as well as on microstructure, chemical composition and interface quality for optimized high quality Mo/Au bilayers on annealing temperature and time. Data show that the functional properties of the bilayers remain stable at T C at T ≥ 200 °C are mainly due to an increase in the average Au grain size and to Au migration along the Mo grain boundaries at the Au/Mo interface. A way to stabilize the functional properties of the Mo/Au bilayers against temperature enhancements is proposed. (paper)

  1. Anomalous magnetic moment at Ba in Au

    Science.gov (United States)

    Bhati, A. K.; Kaur, J.; Bansal, N.; Negi, D.; Kumar, R.; Bhowmik, R. K.; Kumar, V.; Dey, C. C.

    2015-04-01

    The Time differential perturbed angular distribution (TDPAD) technique is employed to measure the local susceptibility at the recoil implanted Ba ions in Au following the nuclear reaction 120Sn(12C, 3nγ)129Ba. We have observed first time the local paramagnetic susceptibility of 5.26(18) at Ba ions comparable to 4f-ions in any non-ferromagnetic metal at room temperature which seems to be related to the electronic s-d and s-f transfer at positive lattice pressure.

  2. Le risque alimentaire face au consommateur

    OpenAIRE

    Didier Torny

    2005-01-01

    Dans le contexte contemporain de multiplication des crises sanitaires, de nombreux travaux en sciences économiques et sociales ont cherché à décrire et analyser le comportement des consommateurs face au risque alimentaire. Ces travaux partagent globalement deux prémisses : ils considèrent l'acte de consommation comme un comportement individuel et attribuent aux consommateurs des "perceptions du risque" qui orientent leurs choix. Une critique de ces deux axiomes amène à soulever la question de...

  3. Les produits de terroir au Niger

    OpenAIRE

    Luxereau, Anne

    2013-01-01

    Les productions agricoles localisées, bénéficiant de ce fait d’une notoriété particulière, existent depuis longtemps en Afrique. Au Niger, elles sont nombreuses et leur statut est diversifié, entre des produits « patrimoines » et d’autres qui constituent des opportunités économiques récentes. Longtemps ignorés des projets de développement, ils connaissent actuellement des évolutions disparates mais la plupart du temps endogènes, « informelles » et innovantes. Tous commercialisés, ils particip...

  4. Que faisons-nous au CERN ?

    CERN Multimedia

    1999-01-01

    Le CERN a pour vocation la science pure, l'étude des questions les plus fondamentales de la nature:Qu'est-ce que la matière ?D'ou vient-elle ? Comment s'agglomère-t-elle en formes complexes comme les étoiles, les planètes et les êtres humains ? Au CERN, les collisions de particules servent à sonder le coeur de la matière et les chercheurs du Laboratoire étudient ces millions de collisions de particules afin de trouver des réponses à ces questions.

  5. Phase behavior of Au and Pt surfaces

    DEFF Research Database (Denmark)

    Grübel, G.; Gibbs, D.; Zehner, D.M.;

    1993-01-01

    We summarize the results of X-ray scattering studies of the Au(001) and Pt(001) surfaces between 300 K and their respective bulk melting temperatures (T(m)). Both surfaces exhibit three distinct structural phases. At high temperatures (0.88T(m) < T < T(m)) both surfaces are disordered. The Pt(001......) surface is rough. At a temperature of T/T(m) almost-equal-to 0.88 there are reversible phase transformations to incommensurate, corrugated-hexagonal phases. Below T/T(m) almost-equal-to 0.8 hexagonal domains rotate with respect to the substrate orientation. In Pt, the rotational transformation is...

  6. Les frameworks au coeur des applications web

    OpenAIRE

    Moro, Arielle; Daehne, Peter

    2010-01-01

    Depuis quelques années, Internet est vraiment entré dans les mœurs : tant dans les entreprises qu’au sein de chaque foyer. En effet, Internet permet de communiquer à travers le monde en quelques secondes, de vendre toute sorte de produits en déployant des solutions e-commerce facilement et bien d’autres choses. Internet est donc un véritable vecteur de communication, de commerce et à présent, avec le Web 2.0, un vrai berceau d’informations (tant des informations personnelles que des informati...

  7. Transition probability studies in 175Au

    International Nuclear Information System (INIS)

    Transition probabilities have been measured between the low-lying yrast states in 175Au by employing the recoil distance Doppler-shift method combined with the selective recoil-decay tagging technique. Reduced transition probabilities and magnitudes of transition quadrupole moments have been extracted from measured lifetimes allowing dramatic changes in nuclear structure within a low excitation-energy range to probed. The transition quadrupole moment data are discussed in terms of available systematics as a function of atomic number and aligned angular momentum.

  8. Compressive mechanical behavior of Au nanowires

    Energy Technology Data Exchange (ETDEWEB)

    Wen Yuhua, E-mail: yhwen@xmu.edu.c [Department of Physics, and Institute of Theoretical Physics and Astrophysics, Xiamen University, Xiamen 361005 (China); Department of Mechanical and Manufacturing Engineering, University of Manitoba, Winnipeg, Manitoba, R3T 5V6 (Canada); Wang Quan, E-mail: q_wang@umanitoba.c [Department of Mechanical and Manufacturing Engineering, University of Manitoba, Winnipeg, Manitoba, R3T 5V6 (Canada); Liew, Kim Meow [Department of Building and Construction, City University of Hong Kong (Hong Kong); Zhu Zizhong [Department of Physics, and Institute of Theoretical Physics and Astrophysics, Xiamen University, Xiamen 361005 (China)

    2010-06-28

    The structural evolution, deformation mechanism, and failure behavior of Au [001] nanowires with various sizes and slenderness ratios under uniaxial compression have been investigated using molecular dynamics. The results show that the elastic modulus, yield stress, and strain all are dependent on the diameters and slenderness ratios of the nanowires. Buckling behavior is observed in a long nanowire, followed by slips in the {l_brace}111{r_brace} planes. Differences are identified in the failure behavior of a short nanowire and a medium nanowire, although the plastic deformation of both types of nanowire originates from the slips in the {l_brace}111{r_brace} planes.

  9. Compressive mechanical behavior of Au nanowires

    International Nuclear Information System (INIS)

    The structural evolution, deformation mechanism, and failure behavior of Au [001] nanowires with various sizes and slenderness ratios under uniaxial compression have been investigated using molecular dynamics. The results show that the elastic modulus, yield stress, and strain all are dependent on the diameters and slenderness ratios of the nanowires. Buckling behavior is observed in a long nanowire, followed by slips in the {111} planes. Differences are identified in the failure behavior of a short nanowire and a medium nanowire, although the plastic deformation of both types of nanowire originates from the slips in the {111} planes.

  10. Photosynthetic electron transport system promotes synthesis of Au-nanoparticles.

    Science.gov (United States)

    Shabnam, Nisha; Pardha-Saradhi, P

    2013-01-01

    In this communication, a novel, green, efficient and economically viable light mediated protocol for generation of Au-nanoparticles using most vital organelle, chloroplasts, of the plant system is portrayed. Thylakoids/chloroplasts isolated from Potamogeton nodosus (an aquatic plant) and Spinacia oleracea (a terrestrial plant) turned Au³⁺ solutions purple in presence of light of 600 µmol m⁻² s⁻¹ photon flux density (PFD) and the purple coloration intensified with time. UV-Vis spectra of these purple colored solutions showed absorption peak at ∼545 nm which is known to arise due to surface plasmon oscillations specific to Au-nanoparticles. However, thylakoids/chloroplasts did not alter color of Au³⁺ solutions in dark. These results clearly demonstrated that photosynthetic electron transport can reduce Au³⁺ to Au⁰ which nucleate to form Au-nanoparticles in presence of light. Transmission electron microscopic studies revealed that Au-nanoparticles generated by light driven photosynthetic electron transport system of thylakoids/chloroplasts were in range of 5-20 nm. Selected area electron diffraction and powder X-ray diffraction indicated crystalline nature of these nanoparticles. Energy dispersive X-ray confirmed that these nanoparticles were composed of Au. To confirm the potential of light driven photosynthetic electron transport in generation of Au-nanoparticles, thylakoids/chloroplasts were tested for their efficacy to generate Au-nanoparticles in presence of light of PFD ranging from 60 to 600 µmol m⁻² s⁻¹. The capacity of thylakoids/chloroplasts to generate Au-nanoparticles increased remarkably with increase in PFD, which further clearly demonstrated potential of light driven photosynthetic electron transport in reduction of Au³⁺ to Au⁰ to form nanoparticles. The light driven donation of electrons to metal ions by thylakoids/chloroplasts can be exploited for large scale production of nanoparticles. PMID:23976990

  11. Photosynthetic electron transport system promotes synthesis of Au-nanoparticles.

    Directory of Open Access Journals (Sweden)

    Nisha Shabnam

    Full Text Available In this communication, a novel, green, efficient and economically viable light mediated protocol for generation of Au-nanoparticles using most vital organelle, chloroplasts, of the plant system is portrayed. Thylakoids/chloroplasts isolated from Potamogeton nodosus (an aquatic plant and Spinacia oleracea (a terrestrial plant turned Au³⁺ solutions purple in presence of light of 600 µmol m⁻² s⁻¹ photon flux density (PFD and the purple coloration intensified with time. UV-Vis spectra of these purple colored solutions showed absorption peak at ∼545 nm which is known to arise due to surface plasmon oscillations specific to Au-nanoparticles. However, thylakoids/chloroplasts did not alter color of Au³⁺ solutions in dark. These results clearly demonstrated that photosynthetic electron transport can reduce Au³⁺ to Au⁰ which nucleate to form Au-nanoparticles in presence of light. Transmission electron microscopic studies revealed that Au-nanoparticles generated by light driven photosynthetic electron transport system of thylakoids/chloroplasts were in range of 5-20 nm. Selected area electron diffraction and powder X-ray diffraction indicated crystalline nature of these nanoparticles. Energy dispersive X-ray confirmed that these nanoparticles were composed of Au. To confirm the potential of light driven photosynthetic electron transport in generation of Au-nanoparticles, thylakoids/chloroplasts were tested for their efficacy to generate Au-nanoparticles in presence of light of PFD ranging from 60 to 600 µmol m⁻² s⁻¹. The capacity of thylakoids/chloroplasts to generate Au-nanoparticles increased remarkably with increase in PFD, which further clearly demonstrated potential of light driven photosynthetic electron transport in reduction of Au³⁺ to Au⁰ to form nanoparticles. The light driven donation of electrons to metal ions by thylakoids/chloroplasts can be exploited for large scale production of nanoparticles.

  12. Energy level alignment in Au/pentacene/PTCDA trilayer stacks

    OpenAIRE

    Sehati, Parisa; Braun, Slawomir; Fahlman, Mats

    2013-01-01

    Ultraviolet photoelectron spectroscopy is used to investigate the energy level alignment and molecular orientation at the interfaces in Au/pentacene/PTCDA trilayer stacks. We deduced a standing orientation for pentacene grown on Au while we conclude a flat lying geometry for PTCDA grown onto pentacene. We propose that the rough surface of polycrystalline Au induces the standing geometry in pentacene. It is further shown that in situ deposition of PTCDA on pentacene can influence the orientati...

  13. Evaluation of the Olympus AU 400 clinical chemistry analyzer.

    Science.gov (United States)

    Bilić, A; Alpeza, I; Rukavina, A S

    2000-01-01

    The performance of the Olympus AU 400 clinical chemistry analyzer was evaluated according to the guidelines of the European Committee for Clinical Laboratory Standards. The following analytes were tested: glucose, urea, creatinine, calcium, AST, ALT, CK, LDH, ALP and amylase. The Olympus AU 400 was compared with the Olympus AU 800. Coefficients of correlation showed high correlation between the compared analyzers. Other performances (intra- and inter-assay variation, carry-over and interferences) of the analyzer were satisfactory.

  14. Nonlinear optical properties of Au/PVP composite thin films

    Institute of Scientific and Technical Information of China (English)

    Shen Hong; Cheng Bo-Lin; Lu Guo-Wei; Wang Wei-Tian; Guan Dong-Yi; Chen Zheng-Hao; Yang Guo-Zhen

    2005-01-01

    Colloidal Au and poly(vinylpyrrolidone) (PVP) composite thin films are fabricated by spin-coating method. Linear optical absorption measurements of the Au/PVP composite films indicate an absorption peak around 530 nm due to the surface plasmon resonance of gold nanoparticles. Nonlinear optical properties are studied using standard Z-scan technique, and experimental results show large optical nonlinearities of the Au/PVP composite films. A large value of films.

  15. Thermal Dihydrogen Activation by a Closed-Shell AuCeO2(+) Cluster.

    Science.gov (United States)

    Meng, Jing-Heng; He, Sheng-Gui

    2014-11-01

    Laser-ablation-generated AuCeO2(+) and CeO2(+) oxide clusters were mass-selected using a quadrupole mass filter and reacted with H2 in an ion trap reactor at ambient conditions. The reactions were characterized by mass spectrometry and density functional theory calculations. The gold-cerium bimetallic oxide cluster AuCeO2(+) is more reactive in H2 activation than the pure cerium oxide cluster CeO2(+). The gold atom is the active adsorption site and facilitates the heterolytic cleavage of H2 in collaboration with the separated O(2-) ion of the CeO2 support. To the best of our knowledge, this is the first example of thermal H2 activation by a closed-shell atomic cluster, which provides molecular-level insights into the single gold atom catalysis over metal oxide supports. PMID:26278765

  16. Interfacial and intermolecular interactions determining the rotational orientation of C60 adsorbed on Au(111)

    Science.gov (United States)

    Paßens, Michael; Karthäuser, Silvia

    2015-12-01

    Close-packed monolayers of fullerenes on metallic substrates are very rich systems with respect to their rotational degrees of freedom and possible interactions with different adsorption sites or next neighbours. In this connection, we report in detail on the (2√3 × 2√3)R30°-superstructure of C60 with respect to the Au(111)-surface. We use molecular orbital imaging in systematic UHV-STM studies to reveal the delicate balance of interfacial and intermolecular interactions in this system. Thus, bright C60-molecules in 5:6-top and 6:6-top geometries are observed depending on the respective next neighbours. Moreover, tiny changes in the appearance of the unoccupied molecular orbitals of dim C60-molecules in hex-vac positions are identified which are caused by the respective interaction with the facets surrounding the Au-vacancy.

  17. Identifying low-coordinated atoms on oxide-supported Au clusters

    Energy Technology Data Exchange (ETDEWEB)

    Lin, Xiao; Nilius, Niklas; Freund, Hans-Joachim [Fritz-Haber-Institut der MPG, Faradayweg 4-6, D-14195 Berlin (Germany); Koskinen, Pekka; Haekkinen, Hannu [Department of Physics, University of Jyvaeskylae, Finland (Finland)

    2010-07-01

    The outstanding chemical properties of small metal particles are partly governed by the perimeter atoms that are located at the boundary to the oxide support. Those edge and corner sites are unique due to their low coordination, a peculiar electronic structure and charge state. We have employed STM and DFT to characterize the perimeter atoms around planar Au clusters grown on a MgO/Ag(001) thin film. The atoms exhibit an enhanced state density with respect to the island center in conductance spectra taken around the Fermi level. Furthermore, they carry extra electrons resulting from a charge transfer from the MgO-Ag interface into the Au islands. Both effects render the perimeter atoms highly attractive for binding molecules, as demonstrated via CO adsorption experiments on the system.

  18. Charged-particle rapidity density in Au+Au collisions in a quark combination model

    Science.gov (United States)

    Shao, Feng-Lan; Yao, Tao; Xie, Qu-Bing

    2007-03-01

    Rapidity/pseudorapidity densities for charged particles and their centrality, rapidity, and energy dependence in Au+Au collisions at the Relativistic Heavy Ion Collider are studied in a quark combination model. Using a Gaussian-type rapidity distribution for constituent quarks as a result of Landau hydrodynamic evolution, the data at sNN=130,200 GeV at various centralities in full pseudorapidity range are well described, and the charged-particle multiplicities are reproduced as functions of the number of participants. The energy dependence of the shape of the dNch/dη distribution is also described at various collision energies sNN=200,130,62.4 GeV in central collisions with same value of parameters except 19.6 GeV. The calculated rapidity distributions and yields for the charged pions and kaons in central Au+Au collisions at sNN=200 GeV are compared with experimental data of the BRAHMS Collaboration.

  19. Degree of chemical nonequilibrium in central Au-Au collisions at RHIC energies

    Science.gov (United States)

    Tawfik, Abdel Nasser; El-Bakry, M. Y.; Habashy, D. M.; Mohamed, M. T.; Abbas, Ehab

    2015-08-01

    In this paper, we investigate the difference between hadron resonance gas (HRG) calculations for chemical freeze-out parameters at fully and partly chemical equilibria. To this end, the results are compared with the particle ratios measured in central Au-Au collisions at a wide range of nucleon-nucleon center-of-mass energies, √ {s{ NN}} = 7.7 - 200 GeV as offered by the STAR experiment. We restrict the discussion to STAR, because of large statistics and overall homogeneity of STAR measurements (one detector) against previous experiments. We find that the matter produced at these energies is likely in fully chemical equilibria, which is consistent with recent lattice quantum chromodynamics (QCD) results. The possible improvements by partial chemical equilibria (γS ≠ 1) are very limited. We also discuss these results with the ones deduced from ϕ/π- and Ω-/π- ratios. These hadron ratios are sensitive to the degree of chemical equilibrium. Accordingly, the conclusion that the matter produced reaches fully chemical equilibria in central Au-Au at relativistic heavy-ion collider (RHIC) energies is confirmed.

  20. The self assembly of thymine at Au(110)/liquid interfaces

    Energy Technology Data Exchange (ETDEWEB)

    Molina Contreras, J.R. [Departamento de Ingenieria Electrica y Electronica, Instituto Tecnologico de Aguascalientes, Mexico (Mexico); Smith, C.I.; Bowfield, A.; Weightman, P. [Physics Department, University of Liverpool (United Kingdom); Tillner, F. [Fachbereich Physik, Universitaet Konstanz (Germany)

    2012-06-15

    We show that thymine self-assembles into an ordered structure when adsorbed at a Au(110)/liquid interface. Reflection anisotropy spectroscopy (RAS) shows that as found for cytosine and adenine the adsorbed thymine molecules are oriented essentially vertically on the Au(110) surface with the molecule aligned along one of the principal axes of the Au(110) surface. Simulations of the RA spectra to an empirical model indicates that as found for adsorbed cytosine and adenine, thymine is aligned along the [1 anti 10] direction on the Au(110) surface. (Copyright copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  1. Tailoring the FeRh magnetostructural response with Au diffusion

    OpenAIRE

    Loving, Melissa. L.; De Vries, Mark; Gimenez-Villacorta, Felix; Liu, Xuerong; Langridge, Sean; Heiman, Donald; Marrows, Christopher M.; Lewis, Laura

    2012-01-01

    Factors which contribute to magnetostructural transition control have been demonstrated by study of the effects of Au incorporation on the magnetic and structural character of CsCl-structured equiatomic FeRh thin films. Sputtered films were capped with 2 nm of Au deposited at 873 K and at 323 K and subsequently characterized with magnetometry and synchrotron-based structural probes. Diffusion of Au into the FeRh film layer at 873 K is confirmed by a reduction in the Au capping layer thickness...

  2. Preparations for p-Au run in 2015

    Energy Technology Data Exchange (ETDEWEB)

    Liu, C. [Brookhaven National Lab. (BNL), Upton, NY (United States). Collider-Accelerator Dept.

    2014-12-31

    The p-Au particle collision is a unique category of collision runs. This is resulted from the different charge mass ratio of the proton and fully stripped Au ion (1 vs.79/197). The p-Au run requires a special acceleration ramp, and movement of a number of beam components as required by the beam trajectories. The DX magnets will be moved for the first time in the history of RHIC. In this note, the planning and preparations for p-Au run will be presented.

  3. Structural and optical studies of Au doped titanium oxide films

    Energy Technology Data Exchange (ETDEWEB)

    Alves, E., E-mail: ealves@itn.pt [Instituto Tecnologico e Nuclear (ITN), 2686-953 Sacavem (Portugal); Centro de Fisica Nuclear da Universidade de Lisboa, Av. Gama Pinto, 21649-003 Lisboa (Portugal); Franco, N.; Barradas, N.P. [Instituto Tecnologico e Nuclear (ITN), 2686-953 Sacavem (Portugal); Centro de Fisica Nuclear da Universidade de Lisboa, Av. Gama Pinto, 21649-003 Lisboa (Portugal); Nunes, B. [Instituto Tecnologico e Nuclear (ITN), 2686-953 Sacavem (Portugal); Lopes, J. [Instituto Superior de Engenharia de Lisboa (Portugal); Cavaleiro, A. [SEC-CEMUC - Universidade de Coimbra, Dept. Eng. Mecanica, Polo II, 3030-788 Coimbra (Portugal); Torrell, M.; Cunha, L.; Vaz, F. [Centro de Fisica, Universidade do Minho, 4800-058 Guimaraes (Portugal)

    2012-02-01

    Thin films of TiO{sub 2} were doped with Au by ion implantation and in situ during the deposition. The films were grown by reactive magnetron sputtering and deposited in silicon and glass substrates at a temperature around 150 Degree-Sign C. The undoped films were implanted with Au fluences in the range of 5 Multiplication-Sign 10{sup 15} Au/cm{sup 2}-1 Multiplication-Sign 10{sup 17} Au/cm{sup 2} with a energy of 150 keV. At a fluence of 5 Multiplication-Sign 10{sup 16} Au/cm{sup 2} the formation of Au nanoclusters in the films is observed during the implantation at room temperature. The clustering process starts to occur during the implantation where XRD estimates the presence of 3-5 nm precipitates. After annealing in a reducing atmosphere, the small precipitates coalesce into larger ones following an Ostwald ripening mechanism. In situ XRD studies reveal that Au atoms start to coalesce at 350 Degree-Sign C, reaching the precipitates dimensions larger than 40 nm at 600 Degree-Sign C. Annealing above 700 Degree-Sign C promotes drastic changes in the Au profile of in situ doped films with the formation of two Au rich regions at the interface and surface respectively. The optical properties reveal the presence of a broad band centered at 550 nm related to the plasmon resonance of gold particles visible in AFM maps.

  4. Site organization and site arrangement

    International Nuclear Information System (INIS)

    The present paper deals with criteria for the choice of a production unit or power plant site, the organization and development of a site in terms of its particular characteristics and takes into account personnel considerations in site organizations as well as the problem of integrating the architecture into the environment. (RW)

  5. Magnetic holes in the solar wind between 0.3 AU and 17 AU

    Directory of Open Access Journals (Sweden)

    K. Sperveslage

    2000-01-01

    Full Text Available Magnetic holes (MHs are depressions of the magnetic field magnitude. Turner et al. (1977 identified the first MHs in the solar wind and determined an occurrence rate of 1.5 MHs/d. Winterhalter et al. (1994 developed an automatic identification criterion to search for MHs in Ulysses data in the solar wind between 1 AU and 5.4 AU. We adopt their criterion to expand the search to the heliocentric distances down to 0.3 AU using data from Helios 1 and 2 and up to 17 AU using data from Voyager 2. We relate our observations to two theoretical approaches which describe the so-called linear MHs in which the magnetic vector varies in magnitude rather than direction. Therefore we focus on such linear MHs with a directional change less than 10º. With our observations of about 850 MHs we present the following results: Approximately 30% of all the identified MHs are linear. The maximum angle between the initial magnetic field vector and any vector inside the MH is 20º in average and shows a weak relation to the depth of the MHs. The angle between the initial magnetic field and the minimum variance direction of those structures is large and very probably close to 90º. The MHs are placed in a high β environment even though the average solar wind shows a smaller β. The widths decrease from about 50 proton inertial length in a region between 0.3 AU and 0.4 AU heliocentric distance to about 15 proton inertial length at distances larger than 10 AU. This quantity is correlated with the β of the MH environments with respect to the heliocentric distance. There is a clear preference for the occurrence of depressions instead of compressions. We discuss these results with regard to the main theories of MHs, the mirror instability and the alternative soliton approach. Although our observational results are more consistent with the soliton theory we favour a combination of both. MHs might be the remnants of initial mirror mode structures which can be described as

  6. A mild synthetic route to Fe3O4@TiO2-Au composites: preparation, characterization and photocatalytic activity

    Science.gov (United States)

    Ma, Jianqi; Guo, Shaobo; Guo, Xiaohua; Ge, Hongguang

    2015-10-01

    To prevent and avoid magnetic loss caused by magnetite core phase transitions involved in high-temperature crystallization of sol-gel TiO2, a direct and feasible low-temperature crystallization technique was developed to deposit anatase TiO2 nanoparticle shell on Fe3O4 sphere cores. To promote the photocatalytic efficiency of the obtained core-shell Fe3O4@TiO2 magnetic photocatalyst, uniformly distributed Au nanoparticles (NPs) were successfully immobilized on the core-shell Fe3O4@TiO2 spheres via a seed-mediated growth procedure. The 3 nm Au colloid absorbed on Fe3O4@TiO2 served as a nucleation site for the growth of Au NPs overlayer. The morphology, structure, composition and magnetism of the resulting composites were characterized, and their photocatalytic activities were also evaluated. In comparison to Fe3O4@TiO2, Fe3O4@TiO2-Au exhibited higher photocatalytic activity for organic degradation under UV irradiation. This enhanced mechanism may have resulted from efficient charge separation of photogenerated electrons and holes due to the Au NPs attached on the TiO2. In addition, the composites possessed superparamagnetic properties with a high saturation magnetization of 44.6 emu g-1 and could be easily separated and recycled by a magnet.

  7. An ab-initio study of silicon adsorption on metallic surfaces (Au/Ag): Novel perspective to explore chemical bonding

    Science.gov (United States)

    Chakraborty, S.; Ghaisas, S. V.; Majumder, C.

    2012-07-01

    We report a first-principle investigation of the structure and electronic properties of small Sin (n = 1-6,9) clusters deposited on the Au(111) and Ag(111) surfaces. The calculations were performed using a plane wave based pseudopotential method under the framework of density functional theory. The results reveal the preference of Si atom to be adsorbed on the h.c.p. site of the metal (111) surfaces with strong binding energy. We study monolayer (ML) deposition as well as the cluster deposition on both the surfaces. The clusters introduce interlayer forces in the adsorbate. Based on PDOS (projected density of states) analysis it is found that Si atoms acquire charges from the Au/Ag surface. The binding energies are consistent with the known cohesive energy of Ag and Au silicides. The planar Sin cluster deposition on metal surfaces show that Au provides an adjustable surface with relatively strong Au-Si interaction while Ag-Si relatively weak interaction leading to dimerization of Si. The strong bonding with the surface atoms is a result of p-d hybridization. Some of the 3-D clusters show shape distortions after deposition on metal surfaces. This leads to internal stresses after deposition. A statistical parameter is defined over PDOS. It helps to measure the state delocalization in energy. Implications of the Si-Metal interaction on the initial stages of growth are discussed.

  8. Baryon Stopping in Au+Au and p+p collisions at 62 and 200 GeV

    CERN Document Server

    Dalsgaard, Hans Hjersing

    2009-01-01

    BRAHMS has measured rapidity density distributions of protons and antiprotons in both p+p and Au+Au collisions at 62 GeV and 200 GeV. From these distributions the yields of so-called "net-protons", that is the difference between the proton and antiproton yields, can be determined. The rapidity dependence of the net-proton yields from peripheral Au+Au collisions is found to have a similar behaviour to that found for the p+p results, while a quite different rapidity dependence is found for central Au+Au collisions. The net-proton distributions can be used together with model calculations to find the net-baryon yields as a function of rapidity, thus yielding information on the average rapidity loss of beam particles, the baryon transport properties of the medium, and the amount of "stopping" in these collisions.

  9. Baryon Stopping in Au+Au and p+p collisions at 62 and 200 GeV

    Science.gov (United States)

    Brahms Collaboration; Dalsgaard, Hans Hjersing; BRAHMS Collaboration

    2009-11-01

    BRAHMS has measured rapidity density distributions of protons and antiprotons in both p+p and Au+Au collisions at 62 GeV and 200 GeV. From these distributions the yields of so-called ‘net-protons’, that is the difference between the proton and antiproton yields, can be determined. The rapidity dependence of the net-proton yields from peripheral Au+Au collisions is found to have a similar behaviour to that found for the p+p results, while a quite different rapidity dependence is found for central Au+Au collisions. The net-proton distributions can be used together with model calculations to find the net-baryon yields as a function of rapidity, thus yielding information on the average rapidity loss of beam particles, the baryon transport properties of the medium, and the amount of ‘stopping’ in these collisions.

  10. Design of Au/SPIO composite nanoparticle for facile and biocompatible surface functionalization via Au-S bond

    Energy Technology Data Exchange (ETDEWEB)

    Seino, Satoshi, E-mail: seino@mit.eng.osaka-u.ac.jp; Shibata, Yujin; Yamanaka, Masayuki; Nakagawa, Takashi [Osaka University, Graduate School of Engineering (Japan); Mukai, Yohei; Nakagawa, Shinsaku [Osaka University, Graduate School of Pharmaceutical Sciences and Center for Advanced Medical Engineering and Informatics (Japan); Yamamoto, Takao A. [Osaka University, Graduate School of Engineering (Japan)

    2013-01-15

    Immobilization of Au nanoparticles on super-paramagnetic iron-oxide (SPIO) enables facile and biocompatible surface functionalization via Au-S bond. Au/SPIO composite nanoparticle is easily modified by thiol-modified polyethylene glycol (PEG-SH), and they are successfully applied on MR tumor imaging. However, its large hydrodynamic size ({approx}150 nm) still causes the accumulation to liver in vivo. In this study, we controlled the hydrodynamic size of Au/SPIO by testing different raw SPIOs and stabilizing polymers. As the best candidate, Au/Molday-ION which was synthesized from Molday-ION and polyvinyl alcohol comprised the hydrodynamic size of 56 nm. Moreover, PEGylated Au/Molday-ION showed excellent dispersibility in blood serum, with the hydrodynamic size of 65 nm. This surface functionalization strategy is effective for the constructions of magnetic nanocarriers for in vivo applications.

  11. Enhanced production of direct photons in Au+Au collisions at sqrt(s_NN)=200 GeV

    CERN Document Server

    Adare, A; Aidala, C; Ajitanand, N N; Akiba, Y; Al-Bataineh, H; Alexander, J; Al-Jamel, A; Aoki, K; Aphecetche, L; Armendariz, R; Aronson, S H; Asai, J; Atomssa, E T; Averbeck, R; Awes, T C; Azmoun, B; Babintsev, V; Baksay, G; Baksay, L; Baldisseri, Alberto; Barish, K N; Barnes, P D; Bassalleck, B; Bathe, S; Batsouli, S; Baublis, V; Bauer, F; Bazilevsky, A; Belikov, S; Bennett, R; Berdnikov, Y; Bickley, A A; Bjorndal, M T; Boissevain, J G; Borel, H; Boyle, K; Brooks, M L; Brown, D S; Bucher, D; Büsching, H; Bumazhnov, V; Bunce, G; Burward-Hoy, J M; Butsyk, S; Campbell, S; Chai, J S; Chang, B S; Charvet, J L; Chernichenko, S; Chiba, J; Chi, C Y; Chiu, M; Choi, I J; Chujo, T; Chung, P; Churyn, A; Cianciolo, V; Cleven, C R; Cobigo, Y; Cole, B A; Comets, M P; Constantin, P; Csanad, M; Csrgo, T; Dahms, T; Das, K; David, o G; Deaton, M B; Dehmelt, K; Delagrange, H; Denisov, A; d'Enterria, D; Deshpande, A; Desmond, E J; Dietzsch, O; Dion, A; Donadelli, M; Drachenberg, J L; Drapier, O; Drees, A; Dubey, A K; Durum, A; Dzhordzhadze, V; Efremenko, Yu V; Egdemir, J; Ellinghaus, F; Emam, W S; Enokizono, A; Enyo, H; Espagnon, B; Esumi, S; Eyser, K O; Fields, D E; Finger, M; Finger, M; Fleuret, F; Fokin, S L; Forestier, B; Fraenkel, Zeev; Frantz, J E; Franz, A; Frawley, A D; Fujiwara, K; Fukao, Y; Fung, S Y; Fusayasu, T; Gadrat, S; Garishvili, I; Gastineau, F; Germain, M; Glenn, A; Gong, H; Gonin, M; Gosset, J; Goto, Y; Granier de Cassagnac, R; Grau, N; Greene, S V; Grosse-Perdekamp, M; Gunji, T; Gustafsson, H; Hachiya, AT; Hadj Henni, A; Haegemann, C; Haggerty, J S; Hagiwara, M N; Hamagaki, H; Han, R; Harada, H; Hartouni, E P; Haruna, K; Harvey, M; Haslum, E; Hasuko, K; Hayano, R; Heffner, M; Hemmick, T K; Hester, T; Heuser, J M; He, X; Hiejima, H; Hill, J C; Hobbs, R; Hohlmann, M; Holmes, M; Holzmann, W; Homma, K; Hong, B; Horaguchi, T; Hornback, D; Hur, M G; Ichihara, T; Imai, K; Inaba, M; Inoue, Y; Isenhower, D; Isenhower, L; Ishihara, M; Isobe, T; Issah, M; Isupov, A; Jacak, B V; Jia, J; Jin, J; Jinnouchi, O; Johnson, B M; Joo, K S; Jouan, D; Kajihara, F; Kametani, S; Kamihara, N; Kamin, J; Kaneta, M; Kang, J H; Kanou, H; Kawagishi, T; Kawall, D; Kazantsev, A V; Kelly, S; Khanzadeev, A; Kikuchi, J; Kim, D H; Kim, D J; Kim, E; Kim, Y S; Kinney, E; Kiss, A; Kistenev, E; Kiyomichi, A; Klay, J; Klein-Bösing, C; Kochenda, L; Kochetkov, V; Komkov, B; Konno, M; Kotchetkov, D; Kozlov, A; Krl, A; Kravitz, A; Kroon, P J; Kubart, J; Kunde, G J; Kurihara, N; Kurita, K; Kweon, M J; Kwon, Y; Kyle, G S; Lacey, R; Lai, Y S; Lajoie, J G; Lebedev, A; Le Bornec, Y; Leckey, S; Lee, D M; Lee, M K; Lee, T; Leitch, M J; Leite, M A L; Lenzi, B; Lim, H; Lika, T; Litvinenko, A; Liu, M X; Li, X; Li, X H; Love, s B; Lynch, D; Maguire, C F; Makdisi, Y I; Malakhov, A; Malik, M D; Man'ko, V I; Mao, Y; Maek, L; Masui, H; Matathias, F; McCain, M C; McCumber, M; McGaughey, P L; Miake, Y; Mike, s P; Miki, K; Miller, T E; Milov, A; Mioduszewski, S; Mishra, G C; Mishra, M; Mitchell, J T; Mitrovski, s M; Morreale, A; Morrison, D P; Moss, J M; Moukhanova, T V; Mukhopadhyay, D; Murata, J; Nagamiya, S; Nagata, Y; Nagle, J L; Naglis, M; Nakagawa, I; Nakamiya, Y; Nakamura, T; Nakano, K; Newby, J; Nguyen, M; Norman, B E; Nyanin, A S; Nystrand, J; O'Brien, E; Oda, S X; Ogilvie, C A; Ohnishi, H; Ojha, I D; Okada, H; Okada, K; Oka, M; Omiwade, O O; Oskarsson, A; Otterlund, I; Ouchida, M; Ozawa, K; Pak, R; Pal, D; Palounek, A P T; Pantuev, V; Papavassiliou, V; Park, J; Park, W J; Pate, S F; Pei, H; Peng, J C; Pereira, H; Peresedov, V; Peressounko, D Yu; Pinkenburg, C; Pisani, R P; Purschke, M L; Purwar, A K; Qu, H; Rak, J; Rakotozafindrabe, A; Ravinovich, I; Read, K F; Rembeczki, S; Reuter, M; Reygers, K; Riabov, V; Riabov, Y; Roche, G; Romana, A; Rosati, M; Rosendahl, S S E; Rosnet, P; Rukoyatkin, P; Rykov, V L; Ryu, S S; Sahlmueller, B; Saitô, N; Sakaguchi, T; Sakai, S; Sakata, H; Samsonov, V; Sato, H D; Sato, S; Sawada, S; Seele, J; Seidl, R; Semenov, V; Seto, R; Sharma, D; Shea, T K; Shein, I; Shevel, A; Shibata, T A; Shigaki, K; Shimomura, M; Shohjoh, T; Shoji, K; Sickles, A; Silva, C L; Silvermyr, D; Silvestre, C; Sim, K S; Singh, C P; Singh, V; Skutnik, S; Sluneka, M; Smith, W C; Soldatov, A; Soltz, R A; Sondheim, W E; Sorensen, cS P; Sourikova, I V; Staley, F; Stankus, P W; Stenlund, E; Stepanov, M; Ster, A; Stoll, S P; Sugitate, T; Suire, C; Sullivan, J P; Sziklai, J; Tabaru, T; Takagi, S; Takagui, E M; Taketani, A; Tanaka, K H; Tanaka, Y; Tanida, K; Tannenbaum, M J; Taranenko, A; Tarjn, P; Thomas, T L; Togawa, M; Toia, A; Tojo, J; Tomaek, L; Torii, H; Towell, R S; Tram, V-N; Tserruya, Itzhak; Tsuchimoto, Y; Tuli, S K; Tydesj, H; Tyurin, N; Vale, C; Valle, H; van Hecke, H W; Velkovska, o J; Vertesi, R; Vinogradov, A A; Virius, M; Vrba, V; Vznuzdaev, E; Wagner, M; Walker, D; Wang, X R; Watanabe, Y; Wessels, J; White, S N; Willis, N; Winter, D; Woody, C L; Wysocki, M; Xie, W; Yamaguchi, Y L; Yanovich, A; Yasin, Z; Ying, J; Yokkaichi, S; Young, G R; Younus, I; Yushmanov, I E; Zajc, W A; Zaudtke, O; Zhang, C; Zhou, S; Zimányi, J; Zolin, L

    2008-01-01

    The production of low mass e+e- pairs for m_{e+e-} < 300 MeV/c^2 and 1 < p_T <5 GeV/c is measured in p+p and Au+Au collisions at sqrt(s_NN)=200 GeV. Enhanced e+e- pair yield above hadronic sources is observed in Au+Au collisions. Treating the excess as internal conversion of direct photons, the invariant yield of direct photons is deduced. In central Au+Au collisions, the excess over p+p is exponential in p_T}, with inverse slope T = 221 +/- 23 (stat) +/- 18 (syst) MeV. Hydrodynamical models with initial temperatures T_init ~ 300-600 MeV at times of 0.6 - 0.15 fm/c after the collision are in qualitative agreement with the data. Lattice QCD predicts a phase transition at ~ 170 MeV.

  12. The Modification of high-$p_{T}$ hadro-chemistry in Au+Au collisions relative to p+p

    CERN Document Server

    Timmins, Anthony R

    2009-01-01

    We present high transverse momentum, $p_{T}$, pion ($\\pi$), proton ($p$), kaon ($K$), and rho ($\\rho$) spectra measured with the STAR experiment from p+p and Au+Au collisions with \\sNN{200}. We find the $K/\\pi$ ratio to be enhanced in Au+Au \\sNN{200} collisions relative to p+p \\sNN{200} collisions at $p_{T} > 5$ GeV/c. The enhancement persists until $p_{T} \\sim 12$ GeV/c for central Au+Au 200 GeV collisions. We also show the nuclear modification factor, $R_{AA}$, measured at the same center of mass energy, and find $R_{AA}(K)$ and $R_{AA}(p)$ to be higher than $R_{AA}(\\pi)$ at $p_T > 5$ GeV/c. Implications for medium induced modifications of jet chemistry is discussed.

  13. Deux nouvelles lèvres de Cassidae au PPNB

    Directory of Open Access Journals (Sweden)

    Gaëlle Le Dosseur

    2008-03-01

    Full Text Available En 2008, deux nouvelles lèvres de Cassidae ont été mises au jour sur deux sites néolithiques (Néolithique Précéramique B : PPNB du Levant Sud : Beisamoun et Yiftahel. Il s’agit d’objets façonnés sur la lèvre externe de coquillages méditerranéens appelés Phalium granulatum. Des aménagements pour la suspension (perforations aux extrémités laissent penser que ces objets ont été utilisés comme pendentifs ou qu’ils ont été cousus sur des vêtements ou des accessoires. Ces découvertes alimentent la discussion sur l’approvisionnement en matières premières mais aussi sur les parentés culturelles et les singularités de chaque site à cette époque. Si l’usage de lèvres de Cassidae est partagé par de nombreux sites PPNB, les modes de fabrication et de suspension ne sont pas strictement les mêmes sur tous. Ces variations reflètent-elles une évolution des modes de suspension dans le temps (au cours du PPNB moyen/récent ? Ou révèlent-elles des choix « contemporains » distincts, qui contribueraient à définir l’identité propre de chaque site ?   Après le Néolithique, l’usage des lèvres de Cassidae se poursuit aux Âges des métaux. À cette époque plus qu’au Néolithique, ces objets sont retrouvés dans des contextes funéraires. Il est difficile de savoir si cette situation résulte des méthodes de fouilles distinctes adoptées sur les sites néolithiques et sur ceux des Âges des métaux ou si elle est une réalité archéologique. Dans le second cas, on pourrait proposer que le sens donné aux lèvres de Cassidae, en partie reflété par le lieu de dépôt, a pu évoluer avec le temps.Two more cassid lips for the PPNBBeisamoun and Yiftahel In 2008, two new cassid lips have been found on two Neolithic sites (Pre Pottery Neolithic B, in the Southern Levant: Beisamoun and Yiftahel. These objects are shaped on the external lip of shells coming from the Mediterranean Sea and called Phalium

  14. Hollow Au@Pd and Au@Pt core-shell nanoparticles as electrocatalysts for ethanol oxidation reactions

    KAUST Repository

    Song, HyonMin

    2012-09-27

    Hybrid alloys among gold, palladium and platinum become a new category of catalysts primarily due to their enhanced catalytic effects. Enhancement means not only their effectiveness, but also their uniqueness as catalysts for the reactions that individual metals may not catalyze. Here, preparation of hollow Au@Pd and Au@Pt core-shell nanoparticles (NPs) and their use as electrocatalysts are reported. Galvanic displacement with Ag NPs is used to obtain hollow NPs, and higher reduction potential of Au compared to Ag, Pd, and Pt helps to produce hollow Au cores first, followed by Pd or Pt shell growth. Continuous and highly crystalline shell growth was observed in Au@Pd core-shell NPs, but the sporadic and porous-like structure was observed in Au@Pt core-shell NPs. Along with hollow core-shell NPs, hollow porous Pt and hollow Au NPs are also prepared from Ag seed NPs. Twin boundaries which are typically observed in large size (>20 nm) Au NPs were not observed in hollow Au NPs. This absence is believed to be due to the role of the hollows, which significantly reduce the strain energy of edges where the two lattice planes meet. In ethanol oxidation reactions in alkaline medium, hollow Au@Pd core-shell NPs show highest current density in forward scan. Hollow Au@Pt core-shell NPs maintain better catalytic activities than metallic Pt, which is thought to be due to the better crystallinity of Pt shells as well as the alloy effect of Au cores. © 2012 The Royal Society of Chemistry.

  15. Component conversion from pure Au nanorods to multiblock Ag-Au-Ag nanorods assisted by Pt nanoframe templates

    Science.gov (United States)

    Lee, Sangji; Jang, Hee-Jeong; Jang, Ho Young; Kim, Seong Kyu; Park, Sungho

    2016-06-01

    We developed a new method for synthesizing multiblock Ag-Au-Ag nanorods using Pt nanoframes that had been deposited on the edges of Au nanorod seeds. As a function of Au etching time, the length of the Au nanorod decreased symmetrically starting from the two ends, leading to the formation of empty inner space at the ends. Subsequent reduction of Ag ions could be selectively performed in the inner space confined by Pt nanoframes and the resulting Ag-Au-Ag nanorods exhibited characteristic LSPR modes originating from each block component (in a transverse direction) and SPR coupling (in a longitudinal direction). The high quality of the resulting multiblock nanorods enabled observation of the longitudinal quadrupole mode that was induced by Ag-Au SPR coupling in a long axis. The mode exhibited high sensitivity in accordance with the change in the surrounding media, demonstrating great potential for sensor applications.We developed a new method for synthesizing multiblock Ag-Au-Ag nanorods using Pt nanoframes that had been deposited on the edges of Au nanorod seeds. As a function of Au etching time, the length of the Au nanorod decreased symmetrically starting from the two ends, leading to the formation of empty inner space at the ends. Subsequent reduction of Ag ions could be selectively performed in the inner space confined by Pt nanoframes and the resulting Ag-Au-Ag nanorods exhibited characteristic LSPR modes originating from each block component (in a transverse direction) and SPR coupling (in a longitudinal direction). The high quality of the resulting multiblock nanorods enabled observation of the longitudinal quadrupole mode that was induced by Ag-Au SPR coupling in a long axis. The mode exhibited high sensitivity in accordance with the change in the surrounding media, demonstrating great potential for sensor applications. Electronic supplementary information (ESI) available. See DOI: 10.1039/c6nr03484e

  16. Microstructural evolution of Au/TiO{sub 2} nanocomposite films: The influence of Au concentration and thermal annealing

    Energy Technology Data Exchange (ETDEWEB)

    Borges, J., E-mail: joelborges@fisica.uminho.pt [Instituto Pedro Nunes, Laboratório de Ensaios, Desgaste e Materiais, Rua Pedro Nunes, 3030-199 Coimbra (Portugal); SEG-CEMUC, Mechanical Engineering Department, University of Coimbra, 3030-788 Coimbra (Portugal); Centro/Departamento de Física, Universidade do Minho, Campus de Gualtar, 4710-057 Braga (Portugal); Kubart, T.; Kumar, S.; Leifer, K. [Solid-State Electronics, Department of Engineering Sciences, Uppsala University, P.O. Box 534, Uppsala SE-751 21 (Sweden); Rodrigues, M.S. [Instituto Pedro Nunes, Laboratório de Ensaios, Desgaste e Materiais, Rua Pedro Nunes, 3030-199 Coimbra (Portugal); Centro/Departamento de Física, Universidade do Minho, Campus de Gualtar, 4710-057 Braga (Portugal); Duarte, N.; Martins, B.; Dias, J.P. [Instituto Pedro Nunes, Laboratório de Ensaios, Desgaste e Materiais, Rua Pedro Nunes, 3030-199 Coimbra (Portugal); Cavaleiro, A. [SEG-CEMUC, Mechanical Engineering Department, University of Coimbra, 3030-788 Coimbra (Portugal); Vaz, F. [SEG-CEMUC, Mechanical Engineering Department, University of Coimbra, 3030-788 Coimbra (Portugal); Centro/Departamento de Física, Universidade do Minho, Campus de Gualtar, 4710-057 Braga (Portugal)

    2015-04-01

    Nanocomposite thin films consisting of a dielectric matrix, such as titanium oxide (TiO{sub 2}), with embedded gold (Au) nanoparticles were prepared and will be analysed and discussed in detail in the present work. The evolution of morphological and structural features was studied for a wide range of Au concentrations and for annealing treatments in air, for temperatures ranging from 200 to 800 °C. Major findings revealed that for low Au atomic concentrations (at.%), there are only traces of clustering, and just for relatively high annealing temperatures, T ≥ 500 °C. Furthermore, the number of Au nanoparticles is extremely low, even for the highest annealing temperature, T = 800 °C. It is noteworthy that the TiO{sub 2} matrix also crystallizes in the anatase phase for annealing temperatures above 300 °C. For intermediate Au contents (5 at.% ≤ C{sub Au} ≤ 15 at.%), the formation of gold nanoclusters was much more evident, beginning at lower annealing temperatures (T ≥ 200 °C) with sizes ranging from 2 to 25 nm as the temperature increased. A change in the matrix crystallization from anatase to rutile was also observed in this intermediate range of compositions. For the highest Au concentrations (> 20 at.%), the films tended to form relatively larger clusters, with sizes above 20 nm (for T ≥ 400 °C). It is demonstrated that the structural and morphological characteristics of the films are strongly affected by the annealing temperature, as well as by the particular amounts, size and distribution of the Au nanoparticles dispersed in the TiO{sub 2} matrix. - Highlights: • Au:TiO{sub 2} films were produced by magnetron sputtering and post-deposition annealing. • The Au concentration in the films increases with the Au pellet area. • Annealing induced microstructural changes in the films. • The nanoparticle size evolution with temperature depends on the Au concentration.

  17. Facet selective etching of Au microcrystallites

    Institute of Scientific and Technical Information of China (English)

    Gangaiah Mettela and Giridhar U. Kulkarni

    2015-01-01

    High-symmetry crystals exhibit isotropic properties. Inducing anisotropy, e.g., by facet selective etching, is considered implausible in face-centered cubic (FCC) metals, particularly gold, which, in addition to being an FCC, is noble. We report for the first time the facet selective etching of Au microcrystals obtained in the form of cuboctahedra and pentagonal rods from the thermolysis of a gold- organic precursor. The selective etching of {111} and {100} facets was achieved using a capping method in which tetraoctylammonium cations selectively cap the {111} facets while Br- ions protect the {100} facets. The exposed facets are oxidized by O2/C1-, yielding a variety of interesting geometries. The facet selective etching of the Au microcrystallites is governed only by the nature of the facets; the geometry of the microcystallite does not appear to play a significant role. The etched surfaces appear rough, but a closer examination reveals well-defined corrugations that are indexable to high hkl values. Such surfaces exhibit enhanced Raman activity.

  18. Imaging Prominence Eruptions Out to 1 AU

    CERN Document Server

    Wood, Brian E; Linton, Mark G

    2015-01-01

    Views of two bright prominence eruptions trackable all the way to 1AU are here presented, using the heliospheric imagers on the Solar TErrestrial RElations Observatory (STEREO) spacecraft. The two events first erupted from the Sun on 2011 June 7 and 2012 August 31, respectively. Only these two examples of clear prominence eruptions observable this far from the Sun could be found in the STEREO image database, emphasizing the rarity of prominence eruptions this persistently bright. For the 2011 June event, a time-dependent 3-D reconstruction of the prominence structure is made using point-by-point triangulation. This is not possible for the August event due to a poor viewing geometry. Unlike the coronal mass ejection (CME) that accompanies it, the 2011 June prominence exhibits little deceleration from the Sun to 1 AU, as a consequence moving upwards within the CME. This demonstrates that prominences are not necessarily tied to the CME's magnetic structure far from the Sun. A mathematical framework is developed ...

  19. Apprentissage administratif : L'apprentissage au CERN

    CERN Multimedia

    2004-01-01

    APPRENTISSAGE ADMINISTRATIF FORMATION ET DEVELOPPEMENT HR/PMD/RCC L'APPRENTISSAGE AU CERN pour les professions d'employé(e) de commerce et d'assistant(e) en information documentaire L'apprentissage au CERN est régi par les lois, règlements et contrats en vigueur dans le Canton de Genève. En cas de réussite à l'examen de fin d'apprentissage, les apprentis obtiennent le Certificat Fédéral de Capacité Suisse (CFC). 1 place est offerte pour la formation d'employé(e) de commerce 2 places sont offertes pour la formation d'assistant(e) en information documentaire L'apprentissage dure 3 ans. Minima requis pour faire acte de candidature : • avoir terminé la scolarité obligatoire • être ressortissant d'un pays membre du CERN (Allemagne, Autriche, Belgique, Bulgarie, Danemark, Espagne,Finlande, France, Grèce, Hongrie, Italie, Norvège...

  20. Le fonds Gabriel Tarde au CHEVS

    Directory of Open Access Journals (Sweden)

    Louise Salmon

    2005-09-01

    Full Text Available Le fonds d’archives « Gabriel Tarde » déposé au CHEVS nous permet de mieux saisir l’érudit autodidacte que fut Gabriel Tarde. De la genèse de sa pensée à ses réseaux de sociabilité, de l’homme de sciences à l’homme de lettres, ses archives témoignent à la fois des usages et des enjeux des ressources archivistiques en histoire, mais elles permettent surtout un renouvellement du regard sur Gabriel Tarde en l’inscrivant au cœur de son temps que fut la fin du XIXème siècle.At the CHEVS in Paris, Gabriel Tarde’s archives allow us to grasp the self-taught scholar who was Gabriel Tarde. From the genesis of his intellect thought to his circles of sociability, from the scientist to the man of letters, his archives testify to the uses and the stakes of the archivistic resources in history, but they allow especially a renewal of the glance on Gabriel Tarde by inscribing him in his historical time, the end of the XIXth century.

  1. 197Au Moessbauer study of the deactivation and reactivation of a carbon-supported AuCl4- hydrochlorination catalyst

    International Nuclear Information System (INIS)

    Acetylene hydrochlorination catalysts consisting of activated carbon impregnated with a solution of HAuCl4.xH2O in aqua regia have been studied by 197Au Moessbauer spectroscopy. The relative amounts of AuCl4-, of Au(0), and of an Au(I) species formed under certain process conditions were determined quantitatively. Deactivation of the catalyst at low and high temperatures was shown to be due to different mechanisms, and the reactivation of the catalyst by Cl2 gas was studied. (orig.)

  2. Coating of a layer of Au on Al13 : The findings of icosahedral Al@Al12Au20- and Al12Au202- fullerenes using ab initio pseudopotential calculations

    Science.gov (United States)

    Kumar, Vijay

    2009-02-01

    We report results of ab initio pseudopotential calculations on the nanocoating of gold on an icosahedral Al13 cluster and the findings of icosahedrally symmetric endohedral Al@Al12Au20- and empty cage Al12Au202- compound fullerenes formed of metal atoms. Twelve Al atoms cap the pentagonal faces of a dodecahedral Au20 cage in which each Au atom has three Al atoms and three Au atoms as nearest neighbors. Mixing of Al13 and Au20 magic clusters leads to a large heat of formation of 0.55 eV/atom and high stability of the Al@Al12Au20 compound fullerene. The binding energies of Al12Au20 and Al@Al12Au20 are 3.017 and 3.007 eV/atom, respectively, which are much larger than 2.457 eV/atom for Au32 fullerene, leading to the possibility of their high abundance.

  3. Ultrafast charge carrier dynamics in Au/semiconductor nanoheterostructures

    Science.gov (United States)

    Lambright, Scott

    The charge carrier dynamics in several Au/semiconductor core/shell heterostructures were examined. Firstly, Au/CdS core/shell nanocomposites were synthesized in a four step procedure culminating in a cation exchange performed on the shell. Previous studies of the ultrafast carrier dynamics in Au/CdS nanocomposites with epitaxial boundary regions reported the suppression of plasmon character in transient absorption spectra accompanied by broadband photoinduced absorption. The coupling of electron wavefunctions with lattice defects at the boundary of the two domains has been blamed for these phenomena. In the current study, transmission electron micrographs of Au/CdS synthesized using cation exchange showed no evidence of strain on the lattice of either component, while femtosecond transient absorption data show the retention of bleach regions attributed to CdS's 1S(e)-1S3/2(h) transition and Au's plasmon resonance. Accelerated rates of bleach recovery for both excitations ( tauexiton ≈ 300 ps, tauplasmon ≈ .7 ps) indicated that the interaction of Au and CdS domains leads to faster relaxation to their respective photoexcitations when compared to relaxation times in isolated Au and CdS nanoparticles. It was believed that the Au/CdS boundary was non-epitaxial in the presented core/shell nanocomposites. Secondly, these non-epitaxial Au/CdS core/shells were subsequently used to demonstrate near-field energy transfer from 5 nm diameter Au cores to CdS-encapsulated CdSe quantum dots. To this end, Au/CdS and CdSe/CdS nanocrystals were embedded in semiconductor-matrix-encapsulated-nanocrystal-arrays (SMENA) together. The encapsulation of both domains in the high band-gap semiconductor CdS was a means to suppress charge transfer between the two nanoparticles. The fluorescence intensity in these films was enhanced 6-fold in some cases as a result of the presence of Au domains. It was also demonstrated that the fluorescence enhancement was independent of the potential

  4. Resonance production and exotic clusters in Au+Au, d+Au and p+p collisions at √(s) = 200 AGeV

    International Nuclear Information System (INIS)

    The resonance production in Au+Au, d+Au and p+p collisions at √(s) = 200 AGeV are presented. The resonances are used as a sensitive tool to examine the collision dynamics in the hadronic medium through their decay and regeneration. The modification of resonance mass, width, and shape due to phase space and dynamical effects are also discussed. The measurement of resonances provides an important tool for studying the dynamics in relativistic heavy-ion collisions by probing the time evolution of the source from chemical to kinetic freeze-out and the hadronic interactions at later stages

  5. Site investigations

    International Nuclear Information System (INIS)

    For the construction of nuclear power stations, comprehensive site investigations are required to assure the adequacy and suitability of the site under consideration. The site investigations cover mainly the following matters: 1) hydrology; 2) geology; 3) seismology; 4) meteorology. Site investigations for nuclear power stations are carried out in stages in increasing detail and to an appreciable depth in order to assure the soundness of the project, and, in particular, to determine all measures required to assure the safety of the nuclear power station and the protection of the population against radiation exposure. (orig./RW)

  6. X-ray Absorption Spectroscopy Characterization of Zn Underpotential Deposition on Au(111) from Phosphate Supporting Electrolyte

    Energy Technology Data Exchange (ETDEWEB)

    Lee, J R; O' Malley, R L; O' Connell, T J; Vollmer, A; Rayment, T

    2009-12-11

    Zn K-edge X-ray absorption spectroscopy (XAS) has been used to investigate the structure of Zn monolayers prepared on Au(111) electrodes via underpotential deposition (UPD) from phosphate supporting electrolyte. Theoretical modeling of the XAS data indicates that the Zn adatoms adopt a commensurate ({radical}3x{radical}3)R30{sup o} ({mu}{sub sc} = 0.33) adlayer structure and reside within the 3-fold hollow sites of the Au(111) surface. Meanwhile, phosphate counter-ions co-adsorb on the UPD adlayer and bridge between the Zn adatoms in a ({radical}3x{radical}3)R30{sup o} ({mu}{sub sc} = 0.33) configuration, with each phosphorous atom residing above a vacant 3-fold hollow site of the Au(111). Significantly, this surface structure is invariant between the electrochemical potential for UPD adlayer formation and the onset of bulk Zn electrodeposition. Analysis of the Zn K-edge absorption onset also presents the possibility that the Zn adatoms do not fully discharge during the process of UPD, which had been proposed in prior voltammetric studies of the phosphate/Zn(UPD)/Au(111) system.

  7. EFFECT OF LASER INPUT ENERGY ON AuSnx INTERMETALLIC COMPOUNDS FORMATION IN SOLDER JOINTS WITH DIFFERENT THICKNESS OF Au SURFACE FINISH ON PADS

    Institute of Scientific and Technical Information of China (English)

    W.Liu; C.Q.Wang; Y.H.Tian; M.Y.Li

    2008-01-01

    Formation of AuSnx intermetallic compounds (IMCs) in laser reflowed solder joints was investigated. The results showed that few IMCs formed at the solder/0.1 μm Au interface. Needlelike AuSn4 IMCs were observed at the solder/0.5 μm Au interface.In Sn-2.0Ag-0.75Cu-3.0Bi and Sn-3.5Ag-O.75Cu solder joints, when the laser input energy was increased, AuSn4 IMCs changed from a layer to needlelike or dendritic distribution at the solder/0.9 μm Au interface. As for the solder joints with 4.0 μm thickness of Au surface finish on pads, AuSn4 , AuSn2, AuSn IMCs, and Au2 Sn phases formed at the interface. Moreover, the content of AuSnx IMCs, such as, AuSn4 and AuSn2, which contained high Sn concentration, would become larger as the laser input energy increased. In the Sn-37Pb solder joints with 0.9 μm or 4.0 μm thickness of the Au surface finish on pads, AuSn4 IMCs were in netlike distribution. The interspaces between them were filled with Pb-rich phases.

  8. Microstructural evolution of eutectic Au-Sn solder joints

    Energy Technology Data Exchange (ETDEWEB)

    Song, Ho Geon

    2002-05-31

    Current trends toward miniaturization and the use of lead(Pb)-free solder in electronic packaging present new problems in the reliability of solder joints. This study was performed in order to understand the microstructure and microstructural evolution of small volumes of nominally eutectic Au-Sn solder joints (80Au-20Sn by weight), which gives insight into properties and reliability.

  9. Thermodynamic modeling of the Au-Sb-Si ternary system

    Energy Technology Data Exchange (ETDEWEB)

    Wang, J., E-mail: jiang.wang@empa.ch [School of Materials Science and Engineering, Guilin University of Electronic Technology, Guilin, Guangxi 541004 (China); Swiss Federal Laboratories for Materials Science and Technology, Laboratory for Joining and Interface Technology, Uberlandstrasse 129, Duebendorf, Zuerich CH-8600 (Switzerland); Liu, Y.J. [Western Transportation Institute, Montana State University, Bozeman, MT 59715 (United States); Liu, L.B. [School of Materials Science and Engineering, Central South University, Changsha, Hunan 410083 (China); Zhou, H.Y. [School of Materials Science and Engineering, Guilin University of Electronic Technology, Guilin, Guangxi 541004 (China); Jin, Z.P. [School of Materials Science and Engineering, Central South University, Changsha, Hunan 410083 (China)

    2011-02-10

    Research highlights: > Thermodynamic optimization of the Au-Sb binary system was updated. > The Si-Sb binary system was assessed from critical review of experimental information. > Thermodynamic modeling of the Au-Sb-Si ternary system was performed. > The phase relations of this ternary system are useful to design Au-based solders. - Abstract: Thermodynamic optimization of the Au-Sb binary system was updated as well as the Si-Sb binary system was assessed thermodynamically using the CALPHAD method based on the critical review of the available experimental information from the published literature. The solution phases including liquid, fcc{sub A}1(Au), diamond{sub A}4(Si) and rhombohedral{sub A}7(Sb), are modeled as substitutional solutions and their excess Gibbs energies are expressed by a Redlich-Kister polynomial. The solubility of Si in the intermetallic compound AuSb{sub 2} is not taken into account because of the lack of experimental information. Combined with previous assessment of the Au-Si binary system, thermodynamic modeling of the Au-Sb-Si ternary system was performed to reproduce well the measured phase equilibria. The liquidus projection and several vertical sections of this ternary system were calculated, which are in reasonable agreement with the reported experimental data.

  10. Magnetic order of Au nanoparticle with clean surface

    Energy Technology Data Exchange (ETDEWEB)

    Sato, Ryuju; Ishikawa, Soichiro; Sato, Hiroyuki; Sato, Tetsuya, E-mail: satoh@appi.keio.ac.jp

    2015-11-01

    Au nanoparticles, which are kept in vacuum after the preparation by gas evaporation method, show ferromagnetism even in 1.7 nm in diameter. The intrinsic magnetism is examined by detecting the disappearance of spontaneous magnetization in Au bulk prepared by heating the nanoparticles without exposure to the air. The temperature dependence of spontaneous magnetization is not monotonic and the increase in magnetization is observed after Au nanoparticles are exposed to the air. The magnetic behavior can be interpreted by the ferrimagnetic-like core–shell structure with shell thickness of 0.16±0.01 nm and magnetic moment of (1.5±0.1)×10{sup −2} μ{sub B}/Au atom, respectively. - Highlights: • Au nanoparticles with clean surface were prepared by the gas evaporation method. • The spontaneous magnetization was observed in Au nanoparticles. • Temperature dependent spontaneous magnetization of smaller Au particles was not monotonic. • The magnetic behavior was interpreted by the ferrimagnetic-like core–shell model. • The shell thickness and the magnetic moment per Au atom were estimated.

  11. Microstructural evolution of eutectic Au-Sn solder joints

    OpenAIRE

    Song, Ho Geon

    2002-01-01

    Current trends toward miniaturization and the use of lead(Pb)-free solder in electronic packaging present new problems in the reliability of solder joints. This study was performed in order to understand the microstructure and microstructural evolution of small volumes of nominally eutectic Au-Sn solder joints (80Au-20Sn by weight), which gives insight into properties and reliability.

  12. Site assessment

    DEFF Research Database (Denmark)

    Vesth, Allan; Gómez Arranz, Paula

    This report describes the site assessment of given position in a given site, for a wind turbine with a well-defined hub height and rotor diameter. The analysis is carried out in accordance to IEC 61400-12-1 [1], and both an obstacle assessment and a terrain assessment are performed....

  13. Comparison of AuScope VLBI and GPS geodetic data

    Science.gov (United States)

    Plank, Lucia; Santamaría-Gómez, Alvaro; Lovell, James

    2015-04-01

    The AuScope geodetic Very Long Baseline Interferometry (VLBI) array consists of three telescopes on Australian territory, each of them co-located with Global Navigation Satellite Systems (GNSS) tracking stations. The high cadence VLBI observing program gives baselines and station coordinates of good quality, with baseline length repeatabilities (WRMS) of a few millimetres for the Australian baselines. In this contribution we present the latest VLBI results of regional and global experiments and compare them to baselines and site coordinates derived from GNSS data. For a thorough comparison, we use similar models for both, the VLBI and the GNSS data processing. Investigations of common tropospheric parameters and clock terms, as well as validations against the local ties as determined in the 2014 local surveys will supplement this study. Additional insight into the topic of technique specific errors is expected from the analysis of dedicated experiments with the two co-located telescopes at Hobart, the 26m legacy antenna and the new 12m dish.

  14. Growth and structure of Co/Au magnetic thin films; Croissance et structure des couches minces magnetiques Co/Au

    Energy Technology Data Exchange (ETDEWEB)

    Marsot, N

    1999-01-14

    We have studied the growth and the crystallographic structure of magnetic ultra thin cobalt/gold films (Co/Au), in order to investigate the correlations between their magnetic and structural properties. Room temperature (R.T.) Co growth on Au (111) proceeds in three stages. Up to 2 Co monolayers (ML), a bilayer island growth mode is observed. Between 2 and 5 ML, coalescence of the islands occurs, covering the substrate surface and a Co/Au mixing is observed resulting from the de-construction of the Herringbone reconstruction. Finally, beyond 5 ML, the CoAu mixing is buried and the Co growth continues in a 3-D growth. Annealing studies at 600 K on this system show a smoothing effect of the Co film, and at the same time, segregation of Au atoms. The quality of the Co/Au interface (sharpness) is not enhanced by the annealing. The local order was studied by SEXAFS and the long range order by GIXRD showing that the Co film has a hexagonal close packed structure, with an easy magnetization axis perpendicular to the surface. From a local order point of view, the Co grows with an incoherent epitaxy and keeps its own bulk parameters. The GIXRD analysis shows a residual strain in the Co film of 4%. The difference observed between the local order analysis and the long range order results is explained in terms of the low dimensions of the diffracting domains. The evolution of film strains, as a function of the Co coverage, shows a marked deviation from the elastic strain theory. Modification of the strain field in the Co film as a function of the Au coverage is studied by GIXRD analysis. The Au growth study, at R.T., shows no evidence of a Au/Co mixing in the case of the Au/Co interface. The Au overlayer adopts a twinned face centred cubic structure on the rough Co film surface. (author)

  15. Formation of CuxAu1−x phases by cold homogenization of Au/Cu nanocrystalline thin films

    Directory of Open Access Journals (Sweden)

    Alona Tynkova

    2014-09-01

    Full Text Available It is shown, by using depth profiling with a secondary neutral mass spectrometer and structure investigations by XRD and TEM, that at low temperatures, at which the bulk diffusion is frozen, a complete homogenization can take place in the Cu/Au thin film system, which leads to formation of intermetallic phases. Different compounds can be formed depending on the initial thickness ratio. The process starts with grain boundary interdiffusion, which is followed by a formation of reaction layers at the grain boundaries that leads to the motion of the newly formed interfaces perpendicular to the grain boundary plane. Finally, the homogenization finishes when all the pure components have been consumed. The process is asymmetric: It is faster in the Au layer. In Au(25nm/Cu(50nm samples the final state is the ordered AuCu3 phase. Decrease of the film thicknesses, as expected, results in the acceleration of the process. It is also illustrated that changing the thickness ratio either a mixture of Cu-rich AuCu and AuCu3 phases (in Au(25nm/Cu(25nm sample, or a mixture of disordered Cu- as well as Au-rich solid solutions (in Au(25nm/Cu(12nm sample can be produced. By using a simple model the interface velocity in both the Cu and Au layers were estimated from the linear increase of the average composition and its value is about two orders of magnitude larger in Au (ca. 10−11 m/s than in Cu (ca. 10−13 m/s.

  16. Insight into the adsorption and decomposition mechanism of H2S on clean and S-covered Au (1 0 0) surface: A theoretical study

    International Nuclear Information System (INIS)

    Highlights: • Dehydrogenation mechanism of H2S on clean and S-covered Au (1 0 0) was firstly studied using periodic DFT calculations. • The optimized structures and adsorption energies were obtained. • The results give the performance of using atomic sulfur to modified Au (1 0 0) surface. • The energy barriers and reaction energies were calculated. - Abstract: Density functional theory (DFT) was employed to investigate the adsorption and decomposition of H2S on clean and S-covered Au (1 0 0) surface. Different kinds of possible modes of H2S, as well as HS, S and H adsorbed on both surfaces were considered. It was proposed that H2S prefers to adsorb on the top sites, HS and H adsorb preferentially on the bridge sites, while S atom is opt to occupy the hollow site. In addition, the optimum co-adsorption configurations for HS/H, H/S, H2S/S, HS/S, HS/HS and H/S/S were determined. It was revealed that the co-adsorbed species repel each other slightly on Au (1 0 0) surface and that co-adsorption tends to weaken the adsorbate–substrate interaction due to the presence of atomic sulfur. Finally, the pathways and transition states of H2S dissociation were also investigated. Through comparing the activation barrier on different surfaces, it was found that the presence of S atom can facilitate the first H-S bond scission and go against the second dissociation of HS species. The distinct differences between Au (1 0 0) and Au (1 1 1) surface suggest that the decomposition of H2S over Au-based catalyst is a structure-sensitive reaction

  17. Insight into the adsorption and decomposition mechanism of H{sub 2}S on clean and S-covered Au (1 0 0) surface: A theoretical study

    Energy Technology Data Exchange (ETDEWEB)

    Jiang, Zhao; Li, Mengmeng; Qin, Pei; Fang, Tao, E-mail: taofang@mail.xjtu.edu.cn

    2014-08-30

    Highlights: • Dehydrogenation mechanism of H{sub 2}S on clean and S-covered Au (1 0 0) was firstly studied using periodic DFT calculations. • The optimized structures and adsorption energies were obtained. • The results give the performance of using atomic sulfur to modified Au (1 0 0) surface. • The energy barriers and reaction energies were calculated. - Abstract: Density functional theory (DFT) was employed to investigate the adsorption and decomposition of H{sub 2}S on clean and S-covered Au (1 0 0) surface. Different kinds of possible modes of H{sub 2}S, as well as HS, S and H adsorbed on both surfaces were considered. It was proposed that H{sub 2}S prefers to adsorb on the top sites, HS and H adsorb preferentially on the bridge sites, while S atom is opt to occupy the hollow site. In addition, the optimum co-adsorption configurations for HS/H, H/S, H{sub 2}S/S, HS/S, HS/HS and H/S/S were determined. It was revealed that the co-adsorbed species repel each other slightly on Au (1 0 0) surface and that co-adsorption tends to weaken the adsorbate–substrate interaction due to the presence of atomic sulfur. Finally, the pathways and transition states of H{sub 2}S dissociation were also investigated. Through comparing the activation barrier on different surfaces, it was found that the presence of S atom can facilitate the first H-S bond scission and go against the second dissociation of HS species. The distinct differences between Au (1 0 0) and Au (1 1 1) surface suggest that the decomposition of H{sub 2}S over Au-based catalyst is a structure-sensitive reaction.

  18. Viscoelastic nature of Au nanoparticle–PDMS nanocomposite gels

    Indian Academy of Sciences (India)

    Ritu Gupta; Hima K Nagamanasa; Rajesh Ganapathy; Giridhar U Kulkarni

    2015-08-01

    A stable gel of Au nanoparticles in polydimethylsiloxane (PDMS) nanocomposite is prepared by employing the curing agent of PDMS elastomer as a reducing agent for the formation of Au nanoparticles by an in-situ process. The viscoelastic nature of these gels is very sensitive to the Au nanoparticle loading and the synthetic temperature conditions. Even a very low Au content of 0.09 wt% is sufficient enough to bring in the transition from sponge state to gel state at room temperature. Higher synthetic temperature also forms sponge formation. Infrared and ultraviolet–visible spectroscopy measurements have provided insight into PDMS crosslinking and nanoparticle formation, respectively. The optimization of the gel properties can have direct influence on the processability of Au nanoparticle–PDMS nanocomposite gels, with interesting implications in electronic, optical and microfluidic devices.

  19. La Physique au LHC - Partie I

    CERN Document Server

    CERN. Geneva

    2004-01-01

    Le LHC devrait permettre l'observation du boson de Higgs et pouvoir lever le voile sur l'un des scénarios de nouvelle physique présentés dans la cours précédent. Ce cours détaillera les perspectives de physique au LHC (découvertes possibles et mesures de précision) ainsi que les méthodes et difficultés expérimentales. L'accent sera mis sur les problèmes liés à la brisure de la symétrie electrofaible. Les possibilités de développement futur à plus haute luminosité et/ou énergie seront également discutées.

  20. The AuScope Geodetic VLBI Array

    CERN Document Server

    Lovell, J E J; Reid, P B; McCulloch, P M; Baynes, B E; Dickey, J M; Shabala, S S; Watson, C S; Titov, O; Ruddick, R; Twilley, R; Reynolds, C; Tingay, S J; Shield, P; Adada, R; Ellingsen, S P; Morgan, J S; Bignall, H E; 10.1007/s00190-013-0626-3

    2013-01-01

    The AuScope geodetic Very Long Baseline Interferometry array consists of three new 12 m radio telescopes and a correlation facility in Australia. The telescopes at Hobart (Tasmania), Katherine (Northern Territory) and Yarragadee (Western Australia) are co-located with other space geodetic techniques including Global Navigation Satellite Systems (GNSS) and gravity infrastructure, and in the case of Yarragadee, Satellite Laser Ranging (SLR) and Doppler Orbitography and Radiopositioning Integrated by Satellite (DORIS) facilities. The correlation facility is based in Perth (Western Australia). This new facility will make significant contributions to improving the densification of the International Celestial Reference Frame in the Southern Hemisphere, and subsequently enhance the International Terrestrial Reference Frame through the ability to detect and mitigate systematic error. This, combined with the simultaneous densification of the GNSS network across Australia will enable the improved measurement of intrapl...

  1. De l’invisible au visible

    OpenAIRE

    Tellier, Thibault

    2009-01-01

    Si la place qu’occupent les jeunes d’origine immigrée dans le traitement médiatique des violences urbaines dans certaines cités HLM n’est plus à démontrer, on connaît en revanche beaucoup moins bien la prise en compte de la  pratique religieuse des populations d’origine immigrée durant les années 1970-1990. Cette communication a donc pour but de montrer, à partir de l’exemple des grands ensembles, comment s’est effectuée au cours des Trente Glorieuses la prise en compte spécifique de cette pr...

  2. La géographie au sommet

    OpenAIRE

    Denise Pumain

    2002-01-01

    Le Ministre de l’Environnement d’Afrique du sud annonçant le sommet de Johannesburg, saluait l’occasion ainsi donnée à l’humanité de revenir au continent de ses origines pour ouvrir une ère nouvelle de solidarité (CityPress du 11 aôut). Quelques jours avant, les géographes de l’Union Géographique Internationale réunis pour leur « conférence régionale » à Durban sur le thème de « la renaissance de la géographie à l’aube du troisième millénaire » avaient invité Nelson Mandela. A cette occasion,...

  3. Jusqu’au ciel !

    OpenAIRE

    de Coster, Xavier

    2014-01-01

    Le récit biblique de la Tour de Babel (Gn. XI : 1-9) dit que le sommet de celle-ci devait atteindre les cieux. Ce texte a inspiré de nombreux artistes, au premier rang desquels Pieter Bruegel l'Ancien. Cet article s'intéresse à la manière dont parmi eux quelques prédécesseurs de Bruegel, puis lui-même, ont représenté le ciel, lequel joue dans cette histoire un rôle fondamental : non seulement le ciel est le but que se sont assigné les constructeurs de la tour, mais c'est du ciel que vient la ...

  4. Musique ! : du phonographe au MP3

    OpenAIRE

    Tournès, Ludovic

    2011-01-01

    nouvelle édition revue et augmentée de "Du phonographe au MP3. Une histoire de la musique enregistrée, XIXe-XXIe siècle" [2008] Depuis l'invention du phonographe par Thomas Edison en 1877, jusqu'à la révolution Internet, la musique enregistrée a connu une histoire longue et riche en rebondissements que l'on trouvera retracée de manière claire, synthétique et vivante dans ce livre. A l'heure où l'industrie de la musique est engagée depuis le début des années 2000 dans une mutation historiqu...

  5. Contribution au SAR spatial distribué

    OpenAIRE

    Maréchal, Rozenn

    2006-01-01

    L'obtention d’images à partir de l'émission, de la réception et du traitement d'impulsions radar (SAR) est soumise à différentes contraintes qui limitent les performances telles que la résolution en distance, la résolution en azimut ou la largeur de la Zone imagée (fauchée). Ces limites sont en partie liées à la dimension finie de l’antenne, en particulier dans le cas du SAR spatial. Pour cette raison, on a cherché à étudier la possibilité de mettre au point des systèmes SAR spatiaux distribué...

  6. Anisotropy analysis of energy in Au/Si twist interface%Au/Si扭转界面能各向异性研究

    Institute of Scientific and Technical Information of China (English)

    辛红; 张建民

    2007-01-01

    采用改进型嵌入原子法(modified embedded atom method,MEAM),计算了(001)Au/(111)Si、(011)Au/(111)Si、(111)Au/(111)Si、(001)Au/(001)Si、(011)Au/(001)Si、(111)Au/(001)Si六个扭转界面的界面能.结果表明,不论是对于(111)Si还是(001)Si基底,相同基底的界面均按照(111)Au/Si、(001)Au/Si、(011)Au/Si顺序依次增加;从界面能的最小化考虑,Au在(111)Si或(001)Si基底上的外延生长,Au(111)面为择优晶面,择优扭转角分别为θ=2.68°和θ=2.42°.

  7. Strangeness Production in Au+Au Reactions at √ {SNN} = 62.4\\ GeV

    Science.gov (United States)

    Arsene, Ionut-Cristian

    The measurement of strangeness is a valuable tool for understanding the reaction mechanism of nuclear collisions since all the strange particles need to be created during the reaction. Also, strangeness enhancement is one of the predicted signals of the QGP. In the present work we will discuss the behaviour of the strangeness production (i.e. K/π ratio) with rapidity and baryo-chemical potential in Au+Au collisions at 62.4 A GeV. In this particular reaction, BRAHMS is able to identify particles over 3.5 rapidity units and thereby cover a wide range of bar {p}/p ratios, including the fragmentation region. We will show spectra and ratios of identified particles as a function of pT and rapidity.

  8. Degree of Chemical Non-equilibrium in Central Au-Au Collisions at RHIC energies

    CERN Document Server

    Tawfik, Abdel Nasser; Habashy, D M; Mohamed, M T; Abbas, Ehab

    2014-01-01

    We investigate the difference between hadron resonance gas (HRG) calculations for chemical freeze-out parameters at fully and partly chemical equilibria. To this end, the results are compared with the particle ratios measured in central Au-Au collisions at a wide range of nucleon-nucleon center-of-mass energies, \\hbox{$\\sqrt{s_{NN}}=7.7-200 $GeV} as offered by the STAR experiment. We restrict the discussion to STAR, because of large statistics and overall homogeneity of STAR measurements (one detector) against previous experiments. We find that the matter produced at these energies is likely in fully chemical equilibrium, which is consistent with recent lattice QCD results. The possible improvements by partial chemical equilibrium ($\\gamma_S\

  9. Dynamical approach to spectator fragmentation in Au+Au reactions at 35 MeV/A

    CERN Document Server

    Vermani, Yogesh K

    2010-01-01

    The characteristics of fragment emission in peripheral $^{197}$Au+$^{197}$Au collisions 35 MeV/A are studied using the two clusterization approaches within framework of \\emph{quantum molecular dynamics} model. Our model calculations using \\emph{minimum spanning tree} (MST) algorithm and advanced clusterization method namely \\emph{simulated annealing clusterization algorithm} (SACA) showed that fragment structure can be realized at an earlier time when spectators contribute significantly toward the fragment production even at such a low incident energy. Comparison of model predictions with experimental data reveals that SACA method can nicely reproduce the fragment charge yields and mean charge of the heaviest fragment. This reflects suitability of SACA method over conventional clusterization techniques to investigate spectator matter fragmentation in low energy domain.

  10. Azimuthal anisotropy in Au+Au collisions at √sNN = 200 GeV

    International Nuclear Information System (INIS)

    The results from the STAR Collaboration on directed flow (v1), elliptic flow (v2), and the fourth harmonic (v4) in the anisotropic azimuthal distribution of particles from Au+Au collisions at √sNN = 200 GeV are summarized and compared with results from other experiments and theoretical models. Results for identified particles are presented and fit with a Blast Wave model. For v2, scaling with the number of constituent quarks and parton coalescence is discussed. For v4, scaling with v22 and quark coalescence predictions for higher harmonic flow is discussed. The different anisotropic flow analysis methods are compared and nonflow effects are extracted from the data. For v2, scaling with the number of constituent quarks and parton coalescence are discussed. For v22 and quark coalescence are discussed

  11. Nuclear Shadowing Effect on the K Factor in Au-Au Collisions

    Institute of Scientific and Technical Information of China (English)

    侯召宇; 郑乔; 张本爱

    2002-01-01

    We investigate the nuclear shadowing effect on the K factor in the Drell-Yan process by introducing a shadowing factor into the corresponding quantum chromodynamical αs order corrections. K factors for Au-Au collisions are calculated at the centre-of-mass system energies √s = 60, 130 and 200 GeV while the nuclear shadowing factor is taken into account. The numerical results indicate that the nuclear shadowing factor obviously raises the K value in the small x region, and for the same nucleon the K value becomes smaller as the energy increases. The nuclear shadowing effect could be one reason for creating the non-constancy of the K factor.

  12. Musique populaire et musique savante au XIXe siècle. Du "peuple" au "public"

    OpenAIRE

    Leterrier, Sophie-Anne

    2008-01-01

    La production culturelle englobe des formes musicales dont les statuts sont très variés. La chanson du colporteur et la partition symphonique n'appartiennent pas au même "genre" ni par leurs conditions de production, i par leurs formes matérielles, leur circulation, leur public, leur postérité. À ce sujet, l'étude des évolutions en cours au XIXe siècle est intéressante de plusieurs points de vue. D'abord, parce que c'est alors que les institutions destinées à former des "spécialistes" de la m...

  13. Questions croisées au sujet du documentaire Droit au but

    OpenAIRE

    Bromberger, Christian; Costantini, Philippe; Accolas, Sophie

    2015-01-01

    Sophie Accolas – Comment, à votre avis, le cinéma contemporain aborde‑t‑il le sport au regard de la globalisation ? Christian Bromberger – Il y a deux façons d’envisager la question. Soit l’on englobe dans la production cinématographique les matchs filmés et diffusés à la télévision, soit on ne retient que les films documentaires et de fiction. Dans la première hypothèse, on voit bien quel rôle joue l’image sportive dans le monde contemporain et, comme vous dites, « au regard de la globalisa...

  14. DEPENDENCE OF DOMAIN STRUCTURES ON Au THICKNESS IN Co/Au MULTILAYER FILMS

    Institute of Scientific and Technical Information of China (English)

    1998-01-01

    The magnetic force images and surface topography images of sputtered Co/Au multilayer films in remnant state were measured by magnetic force microscopy. From the surface magnetic structures shown in the magnetic force images it can be seen that the domain pattern and size vary with the increase of the thickness t of the non-ferromagnetic Au layer remarkably. With the measurements of the effective perpendicular anisotropy Ku and the domain period d, it was found that there are similar trends of d and Ku as functions of t. The variations of the domain pattern and size were qualitatively interpreted in terms of magnetic domain theory, the theoretical relations of d and the domain wall energy ow vs t were calculated. As t = 8.5 AL(1AL=0.235nm), the largest ow is 11mJ/m2.

  15. Beam Energy Dependence of Dielectron Production in Au+Au Collisions from STAR at RHIC

    CERN Document Server

    Huck, Patrick

    2014-01-01

    We present the energy-dependent study of dielectron production in 0-80% minimum-bias Au+Au collisions at $\\sqrt{s_{NN}}$ energies of 19.6, 27, 39, and 62.4 GeV in STAR. Invariant mass ($M_{ee}$) and transverse momentum ($p_T$) differential measurements of dielectron yields are compared to cocktail simulations of known hadronic sources and semi-leptonic charmed decays. The enhancement (excess yield) prominent in the Low-Mass Region (LMR) over the cocktail at all energies, is further compared to calculations of $\\rho$ in-medium modifications. Within statistical and systematic uncertainties, we find that the model consistently describes this enhancement from SPS up to top RHIC energies in its $M_{ee}$- as well as $p_T$-dependence. Dielectron measurements drive the statistics for the future BES Phase-II program, which promises to improve our understanding of the LMR enhancement's trend with total baryon densities.

  16. Azimuthal anisotropy in Au+Au collisions at sqrtsNN = 200 GeV

    CERN Document Server

    Adams, J; Ahammed, Z; Amonett, J; Anderson, B D; Arkhipkin, D; Averichev, G S; Badyal, S K; Bai, Y; Balewski, J; Barannikova, O; Barnby, L S; Baudot, J; Bekele, S; Belaga, V V; Bellwied, R; Berger, J; Bezverkhny, B I; Bharadwaj, S; Bhasin, A; Bhati, A K; Bhatia, V S; Bichsel, H; Billmeier, A; Bland, L C; Blyth, C O; Bonner, B E; Botje, M; Boucham, A; Brandin, A V; Bravar, A; Bystersky, M; Cadman, R V; Cai, X Z; Caines, H; Calderón de la Barca-Sanchez, M; Carroll, J; Castillo, J; Cebra, D; Chajecki, Z; Chaloupka, P; Chattopadhyay, S; Chen, H F; Chen, Y; Cheng, J; Cherney, M; Chikanian, A; Christie, W; Coffin, J P; Cormier, T M; Cramer, J G; Crawford, H J; Das, D; Das, S; De Moura, M M; Derevshchikov, A A; Didenko, L; Dietel, T; Dogra, S M; Dong, W J; Dong, X; Draper, J E; Du, F; Dubey, A K; Dunin, V B; Dunlop, J C; Dutta-Majumdar, M R; Eckardt, V; Edwards, W R; Efimov, L G; Emelianov, V; Engelage, J; Eppley, G; Erazmus, B; Estienne, M; Fachini, P; Faivre, J; Fatemi, R; Fedorisin, J; Filimonov, K; Filip, P; Finch, E; Fine, V; Fisyak, Yu; Foley, K J; Fomenko, K; Fu, J; Gagliardi, C A; Gans, J; Ganti, M S; Gaudichet, L; Geurts, F J M; Ghazikhanian, V; Ghosh, P; González, J E; Grachov, O; Grebenyuk, O; Grosnick, D P; Guertin, S M; Guo, Y; Sen-Gupta, A; Gutíerrez, T D; Hallman, T J; Hamed, A; Hardtke, D; Harris, J W; Heinz, M; Henry, T W; Hepplemann, S; Hippolyte, B; Hirsch, A; Hjort, E; Hoffmann, G W; Huang, H Z; Huang Sheng Li; Hughes, E W; Humanic, T J; Igo, G; Ishihara, A; Jacobs, P; Jacobs, W W; Janik, M; Jiang, H; Jones, P G; Judd, E G; Kabana, S; Kang, K; Kaplan, M; Keane, D; Khodyrev, V Yu; Kiryluk, J; Kisiel, A; Kislov, E M; Klay, J; Klein, S R; Klyachko, A; Koetke, D D; Kollegger, T; Kopytine, M; Kotchenda, L; Krämer, M; Kravtsov, P; Kravtsov, V I; Krüger, K; Kuhn, C; Kulikov, A I; Kumar, A; Kunz, C L; Kutuev, R K; Kuznetsov, A A; Lamont, M A C; Landgraf, J M; Lange, S; Laue, F; Lauret, J; Lebedev, A; Lednicky, R; Lehocka, S; Le Vine, M J; Li, C; Li, Q; Li, Y; Lindenbaum, S J; Lisa, M A; Liu, F; Liu, L; Liu, Q J; Liu, Z; Ljubicic, T; Llope, W J; Long, H; Longacre, R S; López-Noriega, M; Love, W A; Lu, Y; Ludlam, T; Lynn, D; Ma, G L; Ma, J G; Ma, Y G; Magestro, D; Mahajan, S; Mahapatra, D P; Majka, R; Mangotra, L K; Manweiler, R; Margetis, S; Markert, C; Martin, L; Marx, J N; Matis, H S; Matulenko, Yu A; McClain, C J; McShane, T S; Meissner, F; Melnik, Yu M; Meschanin, A; Miller, M L; Milosevich, Z; Minaev, N G; Mironov, C; Mischke, A; Mishra, D K; Mitchell, J; Mohanty, B; Molnár, L; Moore, C F; Morozov, D A; Munhoz, M G; Nandi, B K; Nayak, S K; Nayak, T K; Nelson, J M; Netrakanti, P K; Nikitin, V A; Nogach, L V; Nurushev, S B; Odyniec, Grazyna Janina; Ogawa, A; Okorokov, V; Oldenburg, M; Olson, D; Pal, S K; Panebratsev, Yu A; Panitkin, S Y; Pavlinov, A I; Pawlak, T; Peitzmann, Thomas; Perevozchikov, V; Perkins, C; Peryt, W; Petrov, V A; Phatak, S C; Picha, R; Planinic, M; Pluta, J; Porile, N; Porter, J; Poskanzer, A M; Potekhin, M V; Potrebenikova, E V; Potukuchi, B V K S; Prindle, D; Pruneau, C A; Putschke, J; Rai, G; Rakness, G; Raniwala, R; Raniwala, S; Ravel, O; Ray, R L; Razin, S V; Reichhold, D M; Reid, J G; Renault, G; Retière, F; Ridiger, A; Ritter, H G; Roberts, J B; Rogachevski, O V; Romero, J L; Rose, A; Roy, C; Ruan, L; Sahoo, R; Sakrejda, I; Salur, S; Sandweiss, J; Savin, I; Sazhin, P S; Schambach, J; Scharenberg, R P; Schmitz, N; Schröder, L S; Schweda, K; Seger, J; Seyboth, P; Shahaliev, E; Shao, M; Shao, W; Sharma, M; Shen, W Q; Shestermanov, K E; Shimansky, S S; Sichtermann, E P; Simon, F; Singaraju, R N; Skoro, G P; Smirnov, N; Snellings, R; Sood, G; Sørensen, P; Sowinski, J; Speltz, J; Spinka, H M; Srivastava, B; Stadnik, A; Stanislaus, T D S; Stock, R; Stolpovsky, A; Strikhanov, M N; Stringfellow, B C; Suaide, A A P; Sugarbaker, E R; Suire, C; Sumbera, M; Surrow, B; Symons, T J M; Szanto de Toledo, A; Szarwas, P; Tai, A; Takahashi, J; Tang, A H; Tarnowsky, T J; Thein, D; Thomas, J H; Timoshenko, S; Tokarev, M; Trainor, T A; Trentalange, S; Tribble, R E; Tsai, O D; Ulery, J; Ullrich, T; Underwood, D G; Urkinbaev, A R; Van Buren, G; Van, M; Leeuwen; Van der Molen, A M; Varma, R; Vasilevski, I M; Vasilev, A N; Vernet, R; Vigdor, S E; Viyogi, V P; Vokal, S; Voloshin, S A; Vznuzdaev, M; Waggoner, W T; Wang, F; Wang, G; Wang, G; Wang, X L; Wang, Y; Wang, Y; Wang, Z M; Ward, H; Watson, J W; Webb, J C; Wells, R; Westfall, G D; Wetzler, A; Whitten, C; Wieman, H; Wissink, S W; Witt, R; Wood, J; Wu, J; Xu, N; Xu, Z; Xu, Z Z; Yamamoto, E; Yepes, P; Yurevich, V I; Zanevsky, Yu V; Zhang, H; Zhang, W M; Zhang, Z P; Zolnierczuk, P A; Zoulkarneev, R; Zoulkarneeva, Y; Zubarev, A N

    2004-01-01

    The results from the STAR Collaboration on directed flow ($v_1$), elliptic flow ($v_2$), and the fourth harmonic ($v_4$) in the anisotropic azimuthal distribution of particles from Au+Au collisions at $\\sqrtsNN = 200$ GeV are summarized and compared with results from other experiments and theoretical models. Results for identified particles are presented and fit with a Blast Wave model. For $v_2$, scaling with the number of constituent quarks and parton coalescence is discussed. For $v_4$, scaling with $v_2^2$ and quark coalescence predictions for higher harmonic flow is discussed. The different anisotropic flow analysis methods are compared and nonflow effects are extracted from the data.

  17. Directed flow in Au+Au collisions at $\\sqrt{s_{_{NN}}}$ =62 GeV

    CERN Document Server

    Keane, D; Aggarwal, M M; Ahammed, Z; Amonett, J; Anderson, B D; Arkhipkin, D; Averichev, G S; Badyal, S K; Bai, Y; Balewski, J; Barannikova, O; Barnby, L S; Baudot, J; Bekele, S; Belaga, V V; Bellingeri-Laurikainen, A; Bellwied, R; Berger, J; Bezverkhny, B I; Bharadwaj, S; Bhasin, A; Bhati, A K; Bhatia, V S; Bichsel, H; Bielcik, J; Bielcikova, J; Billmeier, A; Bland, L C; Blyth, C O; Blyth, S L; Bonner, B E; Botje, M; Boucham, A; Bouchet, J; Brandin, A V; Bravar, A; Bystersky, M; Cadman, R V; Cai, X Z; Caines, H; Calderón de la Barca-Sanchez, M; Castillo, J; Catu, O; Cebra, D; Chajecki, Z; Chaloupka, P; Chattopadhyay, S; Chen, H F; Chen, J H; Chen, Y; Cheng, J; Cherney, M; Chikanian, A; Choi, H A; Christie, W; Coffin, J P; Cormier, T M; Cosentino, M R; Cramer, J G; Crawford, H J; Das, D; Das, S; Daugherity, M; De Moura, M M; De Phillips, M; Dedovich, T G; Derevshchikov, A A; Didenko, L; Dietel, T; Dogra, S M; Dong, W J; Dong, X; Draper, J E; Du, F; Dubey, A K; Dunin, V B; Dunlop, J C; Dutta-Majumdar, M R; Eckardt, V; Edwards, W R; Efimov, L G; Emelianov, V; Engelage, J; Eppley, G; Erazmus, B; Estienne, M; Fachini, P; Faivre, J; Fatemi, R; Fedorisin, J; Filimonov, K; Filip, P; Finch, E; Fine, V; Fisyak, Yu; Fornazier, K S F; Fu, J; Gagliardi, C A; Gaillard, L; Gans, J; Ganti, M S; Geurts, F; Ghazikhanian, V; Ghosh, P; González, J E; Gos, H; Grachov, O; Grebenyuk, O; Grosnick, D P; Guertin, S M; Guo, Y; Gupta, N; Gutíerrez, T D; Hallman, T J; Hamed, A; Hardtke, D; Harris, J W; Heinz, M; Henry, T W; Hepplemann, S; Hippolyte, B; Hirsch, A; Hjort, E; Hoffmann, G W; Horner, M J; Huang, H Z; Huang, S L; Hughes, E W; Humanic, T J; Igo, G; Ishihara, A; Jacobs, P; Jacobs, W W; Jedynak, M; Jiang, H; Jones, P G; Judd, E G; Kabana, S; Kang, K; Kaplan, M; Kechechyan, A; Khodyrev, V Yu; Kim, B C; Kiryluk, J; Kisiel, A; Kislov, E M; Klay, J; Klein, S R; Koetke, D D; Kollegger, T; Kopytine, M; Kotchenda, L; Kowalik, K L; Kravtsov, P; Kravtsov, V I; Krämer, M; Krüger, K; Kuhn, C; Kulikov, A I; Kumar, A; Kutuev, R K; Kuznetsov, A A; Lamont, M A C; Landgraf, J M; Lange, S; Laue, F; Lauret, J; Le Vine, M J; Lebedev, A; Lednicky, R; Lee, C H; Lehocka, S; Li, C; Li, Q; Li, Y; Lin, G; Lindenbaum, S J; Lisa, M A; Liu, F; Liu, H; Liu, J; Liu, L; Liu, Q J; Liu, Z; Ljubicic, T; Llope, W J; Long, H; Longacre, R S; Love, W A; Lu, Y; Ludlam, T; Lynn, D; López-Noriega, M; Ma, G L; Ma, J G; Ma, Y G; Magestro, D; Mahajan, S; Mahapatra, D P; Majka, R; Mangotra, L K; Manweiler, R; Margetis, S; Markert, C; Martin, L; Marx, J N; Matis, H S; Matulenko, Yu A; McClain, C J; McShane, T S; Meissner, F; Melnik, Yu M; Meschanin, A; Miller, M L; Minaev, N G; Mironov, C; Mischke, A; Mishra, D K; Mitchell, J; Mohanty, B; Molnár, L; Moore, C F; Morozov, D A; Munhoz, M G; Nandi, B K; Nayak, S K; Nayak, T K; Nelson, J M; Netrakanti, P K; Nikitin, V A; Nogach, L V; Nurushev, S B; Odyniec, Grazyna Janina; Ogawa, A; Okorokov, V; Oldenburg, M; Olson, D; Pal, S K; Panebratsev, Yu A; Panitkin, S Y; Pavlinov, A I; Pawlak, T; Peitzmann, T; Perevozchikov, V; Perkins, C; Peryt, W; Petrov, V A; Phatak, S C; Picha, R; Planinic, M; Pluta, J; Porile, N; Porter, J; Poskanzer, A M; Potekhin, M V; Potrebenikova, E V; Potukuchi, B V K S; Prindle, D; Pruneau, C A; Putschke, J; Rakness, G; Raniwala, R; Raniwala, S; Ravel, O; Ray, R L; Razin, S V; Reichhold, D M; Reid, J G; Reinnarth, J; Renault, G; Retière, F; Ridiger, A; Ritter, H G; Roberts, J B; Rogachevski, O V; Romero, J L; Rose, A; Roy, C; Ruan, L; Russcher, M J; Sahoo, R; Sakrejda, I; Salur, S; Sandweiss, J; Sarsour, M; Savin, I; Sazhin, P S; Schambach, J; Scharenberg, R P; Schmitz, N; Schweda, K; Seger, J; Selyuzhenkov, I; Sen-Gupta, A; Seyboth, P; Shahaliev, E; Shao, M; Shao, W; Sharma, M; Shen, W Q; Shestermanov, K E; Shimansky, S S; Sichtermann, E P; Simon, F; Singaraju, R N; Smirnov, N; Snellings, R; Sood, G; Sowinski, J; Speltz, J; Spinka, H M; Srivastava, B; Stadnik, A; Stanislaus, T D S; Stock, R; Stolpovsky, A; Strikhanov, M N; Stringfellow, B C; Suaide, A A P; Sugarbaker, E R; Sumbera, M; Surrow, B; Swanger, M; Symons, T J M; Szanto de Toledo, A; Sørensen, P; Tai, A; Takahashi, J; Tang, A H; Tarnowsky, T J; Thein, D; Thomas, J H; Timmins, A R; Timoshenko, S; Tokarev, M; Trentalange, S; Tribble, R E; Tsai, O D; Ulery, J; Ullrich, T; Underwood, D G; Van Buren, G; Van Leeuwen, M; Van der Kolk, N; Van der Molen, A M; Varma, R; Vasilev, A N; Vasilevski, I M; Vernet, R; Vigdor, S E; Viyogi, Y P; Vokal, S; Voloshin, S A; Waggoner, W T; Wang, F; Wang, G; Wang, X L; Wang, Y; Wang, Z M; Ward, H; Watson, J W; Webb, J C; Westfall, G D; Wetzler, A; Whitten, C; Wieman, H; Wissink, S W; Witt, R; Wood, J; Wu, J; Xu, N; Xu, Z; Xu, Z Z; Yamamoto, E; Yepes, P; Yoo, I K; Yurevich, V I; Zborovský, I; Zhang, H; Zhang, W M; Zhang, Y; Zhang, Z P; Zhong, C; Zoulkarneev, R; Zoulkarneeva, Y; Zubarev, A N; Zuo, J X; Wang, Gang

    2006-01-01

    We present the directed flow ($v_1$) measured in Au+Au collisions at $\\sqrt{s_{_{NN}}}$ = 62 GeV in the mid-pseudorapidity region $|\\eta|<1.3$ and in the forward pseudorapidity region $2.5 < |\\eta| < 4.0$. The results are obtained using the three-particle cumulant method, the event plane method with mixed harmonics, and for the first time at the Relativistic Heavy Ion Collider (RHIC), the standard method with the event plane reconstructed from spectator neutrons. Results from all three methods are in good agreement. Over the pseudorapidity range studied, charged particle directed flow is in the direction opposite to that of fragmentation neutrons.

  18. Replacing a piece of loop-structure in the substrate-binding groove of Aspergillus usamii β-mannanase, AuMan5A, to improve its enzymatic properties by rational design.

    Science.gov (United States)

    Dong, Yun Hai; Li, Jian Fang; Hu, Die; Yin, Xin; Wang, Chun Juan; Tang, Shi Han; Wu, Min Chen

    2016-05-01

    To perfect the enzymatic properties of AuMan5A, a mesophilic glycoside hydrolase (GH) family 5 β-mannanase from Aspergillus usamii, its loop-structure substitution was carried out by rational design and followed by megaprimer PCR. Based on the structural analysis and enzymatic property comparison of various β-mannanases, a piece of loop-structure with seven amino acids between two β-strands (βD and βE) in the substrate-binding groove, named "Loop DE," was speculated to be correlative to the thermostability and catalytic efficiency of GH family 5 β-mannanases. Therefore, three AuMan5A's mutants, AuMan5A-Af, AuMan5A-An, and AuMan5A-Th, were designed by substituting a Loop DE sequence ((316)KSPDGGN(322)) of AuMan5A with the corresponding sequences of other three family 5 β-mannanases, respectively. Then, the mutant-encoding genes, Auman5A-Af, Auman5A-An, and Auman5A-Th, were constructed as designed theoretically and then expressed in Pichia pastoris GS115. The expressed recombinant AuMan5A-Af (re-AuMan5A-Af) displayed the temperature optimum (T opt) of 75 °C, T m value of 76.6 °C and half-life (t 1/2) of 480 min at 70 °C, which were 10 and 12.1 °C higher and 48-fold longer than those of re-AuMan5A, respectively. Its catalytic efficiency (k cat/K m) was 12.7-fold that of re-AuMan5A. What is more, the site-directed mutagenesis of D320G in AuMan5A-Af was performed. The T opt and t 1/2 of expressed re-AuMan5A-Af(D320G) decreased to 70 °C and 40 min, respectively, while its k cat/K m was only 35 % of that of re-AuMan5A-Af. These results demonstrated that the mutation of G320 (in AuMan5A) into D320 (in AuMan5A-Af) through Loop DE substitution was mainly responsible for the thermostability and catalytic efficiency improvement of AuMan5A-Af.

  19. Autopistas: AU-1 25 de Mayo y AU-6 Perito Moreno

    Directory of Open Access Journals (Sweden)

    Editorial, Equipo

    1981-02-01

    Full Text Available Highways AU-1 and AU-6, approximately 17 km. long, were constructed for the purpose of solving the serious traffic problems in Buenos Aires, a city of nine million inhabitants and an evergrowing number of cars. A computer program was created for the design based on the geometric shape of the highway and the position of the supports. Using this, all elements composing the structure were calculated and the framework was sized. This programme made it possible to complete a stretch of 150 metres per week. The very rapid construction was carried out through self-supporting arches made of metallic beams held in place by brackets. The brackets were fitted in specially designed grooves in the major supports of the highway.

    Las autopistas AU-1 y AU-6, con una longitud aproximada de 17 km, se realizaron con objeto de resolver el grave problema de infraestructura vial del Municipio de Buenos Aires, ciudad de nueve millones de habitantes y con un parque de vehículos en rápido crecimiento. Para el proyecto se creó un programa de ordenador con el que, partiendo de la definición geométrica de la autopista y de la posición de las pilas, se calculan todos los elementos que componen la estructura y se dimensionan las armaduras. Este programa permitió proyectar un tramo (150 m por semana. La construcción, a un ritmo muy rápido, se llevó a cabo mediante cimbras autoportantes compuestas por vigas metálicas apoyadas sobre ménsulas, las cuales a su vez apoyan en unos nichos dejados en las pilas.

  20. Differential flow of protons in Au+Au collisions at AGS energies

    Energy Technology Data Exchange (ETDEWEB)

    Sahu, P.K. E-mail: pradip@iopb.res.in; Cassing, W

    2002-12-30

    We study the proton sideward and elliptic differential flow for Au+Au collisions at AGS energies (2-8 A GeV) in a microscopic relativistic transport model that includes all baryon resonances up to a mass of 2 GeV as well as string degrees of freedom for the higher hadronic excitations. In order to explore the sensitivity of the various differential flows to the nuclear equation of state (EoS) we use three different parameterizations of the scalar and vector mean-fields, i.e., NL2 (soft), NL23 (medium) and NL3 (hard), with their momentum dependence fitted to the experimental Schroedinger equivalent potential (at normal nuclear matter density {rho}{sub 0}) up to kinetic energies of 1 GeV. We calculate the excitation function of sideward and elliptic flow within these parameter sets for Au+Au collisions and compare with the recent data from the E895 Collaboration as a function of rapidity, impact parameter and transverse momentum, respectively. We find that the best description of the differential data is provided by a rather 'stiff' EoS at 2 A GeV (NL3) while at higher bombarding energies (4-8 A GeV) a 'medium' EoS leads to the lowest {chi}{sup 2} with respect to the data. However, the differences in the transverse and elliptic flows (from the different parameter sets) become of minor significance at 4-8 A GeV. We attribute this insensitivity to a similar reduction of the vector potential in all models and to the dominance of string degrees of freedom at these bombarding energies.

  1. Isolation of atomically precise mixed ligand shell PdAu24 clusters

    Science.gov (United States)

    Sels, Annelies; Barrabés, Noelia; Knoppe, Stefan; Bürgi, Thomas

    2016-05-01

    Exposure of PdAu24(2-PET)18 (2-PET: 2-phenylethylthiolate) to BINAS (1,1-binaphthyl-2,2-dithiol) leads to species of composition PdAu24(2-PET)18-2x(BINAS)x due to ligand exchange reactions. The BINAS adsorbs in a specific mode that bridges the apex and one core site of two adjacent S(R)-Au-S(R)-Au-S(R) units. Species with different compositions of the ligand shell can be separated by HPLC. Furthermore, site isomers can be separated. For the cluster with exactly one BINAS in its ligand shell only one isomer is expected due to the symmetry of the cluster, which is confirmed by High-Performance Liquid Chromatography (HPLC). Addition of a second BINAS to the ligand shell leads to several isomers. In total six distinguishable isomers are possible for PdAu24(2-PET)14(BINAS)2 including two pairs of enantiomers concerning the adsorption pattern. At least four distinctive isomers are separated by HPLC. Calculations indicate that one of the six possibilities is energetically disfavoured. Interestingly, diastereomers, which have an enantiomeric relationship concerning the adsorption pattern of chiral BINAS, have significantly different stabilities. The relative intensity of the observed peaks in the HPLC does not reflect the statistical weight of the different isomers. This shows, as supported by the calculations, that the first adsorbed BINAS molecule influences the adsorption of the second incoming BINAS ligand. In addition, experiments with the corresponding Pt doped gold cluster reveal qualitatively the same behaviour, however with slightly different relative abundances of the corresponding isomers. This finding points towards the influence of electronic effects on the isomer distribution. Even for clusters containing more than two BINAS ligands a limited number of isomers were found, which is in contrast to the corresponding situation for monothiols, where the number of possible isomers is much larger.Exposure of PdAu24(2-PET)18 (2-PET: 2-phenylethylthiolate) to BINAS (1

  2. Controlling the stereochemistry and regularity of butanethiol self-assembled monolayers on au(111).

    Science.gov (United States)

    Yan, Jiawei; Ouyang, Runhai; Jensen, Palle S; Ascic, Erhad; Tanner, David; Mao, Bingwei; Zhang, Jingdong; Tang, Chunguang; Hush, Noel S; Ulstrup, Jens; Reimers, Jeffrey R

    2014-12-10

    The rich stereochemistry of the self-assembled monolayers (SAMs) of four butanethiols on Au(111) is described, the SAMs containing up to 12 individual C, S, or Au chiral centers per surface unit cell. This is facilitated by synthesis of enantiomerically pure 2-butanethiol (the smallest unsubstituted chiral alkanethiol), followed by in situ scanning tunneling microscopy (STM) imaging combined with density functional theory molecular dynamics STM image simulations. Even though butanethiol SAMs manifest strong headgroup interactions, steric interactions are shown to dominate SAM structure and chirality. Indeed, steric interactions are shown to dictate the nature of the headgroup itself, whether it takes on the adatom-bound motif RS(•)Au(0)S(•)R or involves direct binding of RS(•) to face-centered-cubic or hexagonal-close-packed sites. Binding as RS(•) produces large, organizationally chiral domains even when R is achiral, while adatom binding leads to rectangular plane groups that suppress long-range expression of chirality. Binding as RS(•) also inhibits the pitting intrinsically associated with adatom binding, desirably producing more regularly structured SAMs.

  3. The bifurcation point of the oxygen reduction reaction on Au-Pd nanoalloys.

    Science.gov (United States)

    Staszak-Jirkovský, Jakub; Ahlberg, Elisabet; Panas, Itai; Schiffrin, David J

    2016-07-01

    The oxygen reduction reaction is of major importance in energy conversion and storage. Controlling electrocatalytic activity and its selectivity remains a challenge of modern electrochemistry. Here, first principles calculations and analysis of experimental data unravel the mechanism of this reaction on Au-Pd nanoalloys in acid media. A mechanistic model is proposed from comparison of the electrocatalysis of oxygen and hydrogen peroxide reduction on different Au-Pd ensembles. A H2O production channel on contiguous Pd sites proceeding through intermediates different from H2O2 and OOH(σ) adsorbate is identified as the bifurcation point for the two reaction pathway alternatives to yield either H2O or H2O2. H2O2 is a leaving group, albeit reduction of H2O2 to H2O can occur by electrocatalytic HO-OH dissociation that is affected by the presence of adsorbed OOH(σ). Similarities and differences between electrochemical and direct synthesis from H2 + O2 reaction on Au-Pd nanoalloys are discussed. PMID:27089504

  4. Structural and electronic properties of graphene nanoflakes on Au(111) and Ag(111)

    Science.gov (United States)

    Tesch, Julia; Leicht, Philipp; Blumenschein, Felix; Gragnaniello, Luca; Fonin, Mikhail; Marsoner Steinkasserer, Lukas Eugen; Paulus, Beate; Voloshina, Elena; Dedkov, Yuriy

    2016-01-01

    We investigate the electronic properties of graphene nanoflakes on Ag(111) and Au(111) surfaces by means of scanning tunneling microscopy and spectroscopy as well as density functional theory calculations. Quasiparticle interference mapping allows for the clear distinction of substrate-derived contributions in scattering and those originating from graphene nanoflakes. Our analysis shows that the parabolic dispersion of Au(111) and Ag(111) surface states remains unchanged with the band minimum shifted to higher energies for the regions of the metal surface covered by graphene, reflecting a rather weak interaction between graphene and the metal surface. The analysis of graphene-related scattering on single nanoflakes yields a linear dispersion relation E(k), with a slight p-doping for graphene/Au(111) and a larger n-doping for graphene/Ag(111). The obtained experimental data (doping level, band dispersions around EF, and Fermi velocity) are very well reproduced within DFT-D2/D3 approaches, which provide a detailed insight into the site-specific interaction between graphene and the underlying substrate. PMID:27002297

  5. 超声楔键合Au/Al和Al/Au界面IMC演化%Intermetallic Compound Evolution of Ultrasonic Au/Al and Al/Au Wedge Bond

    Institute of Scientific and Technical Information of China (English)

    计红军; 李明雨; 王春青

    2007-01-01

    基于固体相变理论,研究Au丝、Al丝超声楔-楔键合接头的温度长期可靠性.200℃下,存储时间<48 h时,Au/Al接头界面并未发生明显变化;随着接头存储时间增加,界面金属间化合物(IMC)开始由焊盘向引线方向生长(垂直生长);240 h时,Al焊盘完全被消耗,接头连接界面部位生成Au5Al2,周边为Au2Al;继续增加存储时间,IMC向接头水平方向生长(水平生长),Au5Al2向更稳定的Au2Al转变,IMC与引线之间形成严重的Kirkendall孔洞.Al/Au系统相对稳定得多,界面IMC生长缓慢,然而,界面化合物AuAl2导致接头裂纹,而引线内部出现严重的空洞.对比并分析了两种楔焊系统界面演变特点和产生机制.

  6. Inclusive cross section and correlations of fully reconstructed jets in 200 GEV Au+Au and p+p collisions

    OpenAIRE

    Ploskon, Mateusz; Collaboration, for the STAR

    2009-01-01

    We present an experimental study of full jet reconstruction in the high multiplicity environment of heavy ion collisions, utilizing 200 GeV p+p and central Au+Au data measured by STAR. Inclusive differential jet production cross sections and ratios are reported, as well as high-pT hadron-jet coincidences.

  7. Gold surfaces and nanoparticles are protected by Au(0)-thiyl species and are destroyed when Au(I)-thiolates form

    DEFF Research Database (Denmark)

    Reimers, Jeffrey R.; Ford, Michael J.; Halder, Arnab;

    2016-01-01

    The synthetic chemistry and spectroscopy of sulfur-protected gold surfaces and nanoparticles is analyzed, indicating that the electronic structure of the interface is Au(0)-thiyl, with Au(I)-thiolates identified as high-energy excited surface states. Density-functional theory indicates that it is...

  8. Charged particle multiplicity fluctuations in Au+Au collisions at \\sqrt{s_{NN}} = 200\\, {\\rm GeV}

    Science.gov (United States)

    Wozniak, Krzysztof; PHOBOS Collaboration; Back, B. B.; Baker, M. D.; Ballintijn, M.; Barton, D. S.; Betts, R. R.; Bickley, A. A.; Bindel, R.; Budzanowski, A.; Busza, W.; Carroll, A.; Chai, Z.; Decowski, M. P.; García, E.; George, N.; Gulbrandsen, K.; Gushue, S.; Halliwell, C.; Hamblen, J.; Heintzelman, G. A.; Henderson, C.; Hofman, D. J.; Hollis, R. S.; Holynski, R.; Holzman, B.; Iordanova, A.; Johnson, E.; Kane, J. L.; Katzy, J.; Khan, N.; Kucewicz, W.; Kulinich, P.; Kuo, C. M.; Lin, W. T.; Manly, S.; McLeod, D.; Mignerey, A. C.; Nouicer, R.; Olszewski, A.; Pak, R.; Park, I. C.; Pernegger, H.; Reed, C.; Remsberg, L. P.; Reuter, M.; Roland, C.; Roland, G.; Rosenberg, L.; Sagerer, J.; Sarin, P.; Sawicki, P.; Skulski, W.; Steinberg, P.; Stephans, G. S. F.; Sukhanov, A.; Tang, J. L.; Trzupek, A.; Vale, C.; van Nieuwenhuizen, G. J.; Verdier, R.; Wolfs, F. L. H.; Wosiek, B.; Wuosmaa, A. H.; Wyslouch, B.

    2004-08-01

    This paper presents the first PHOBOS results on charged particle multiplicity fluctuations measured for Au+Au collisions at the highest RHIC energy within a wide pseudorapidity range of |eegr| < 3. The dependence on collision geometry is removed in the analysis by using the normalized difference between the number of particles in separate eegr bins. We compare our data to HIJING model predictions.

  9. Effect of Au nano-particle aggregation on the deactivation of the AuCl3/AC catalyst for acetylene hydrochlorination

    OpenAIRE

    Bin Dai; Qinqin Wang; Feng Yu; Mingyuan Zhu

    2015-01-01

    A detailed study of the valence state and distribution of the AuCl3/AC catalyst during the acetylene hydrochlorination deactivation process is described and discussed. Temperature-programmed reduction and X-ray photoelectron spectral analysis indicate that the active Au3+ reduction to metallic Au0 is one reason for the deactivation of AuCl3/AC catalyst. Transmission electron microscopy characterization demonstrated that the particle size of Au nano-particles increases with increasing reaction...

  10. Structure and dynamics of C60 molecules on Au(111)

    Energy Technology Data Exchange (ETDEWEB)

    Shin, Heekeun [Penn State University; Schwarze, A [Penn State University; Diehl, R D [Penn State University; Pussi, K [Lappeenranta University of Technology; Colombier, A [Universite de Lorraine; Gaudry, E. [Universite de Lorraine; Ledieu, J [Universite de Lorraine; McGuirk, G M [Universite de Lorraine; Serkovic Loli, L N [Universite de Lorraine; Fournee, V [Universite de Lorraine; Wang, Lin-Lin [Ames Laboratory; Schull, G [Universite de Strasbourg; Berndt, R [Christian-Albrechts-Universitt zu Kiel

    2014-06-01

    Earlier studies of C60 adsorption on Au(111) reported many interesting and complex features. We have performed coordinated low-energy electron diffraction, scanning tunneling microscopy (STM), and density functional theory studies to elucidate some of the details of the monolayer commensurate (2√3 × 2√3)R30° phase. We have identified the adsorption geometries of the two states that image as dim and bright in STM. These consist of a C60 molecule with a hexagon side down in a vacancy (hex-vac) and a C60 molecule with a carbon-carbon 6:6 bond down on a top site (6:6-top), respectively. We have studied the detailed geometries of these states and find that there is little distortion of the C60 molecules, but there is a rearrangement of the substrate near the C60 molecules. The two types of molecules differ in height, by about 0.7 Å, which accounts for most of the difference in their contrast in the STM images. The monolayer displays dynamical behavior, in which the molecules flip from bright to dim, and vice versa. We interpret this flipping as the result of the diffusion of vacancies in the surface layers of the substrate. Our measurements of the dynamics of this flipping from one state to the other indicate that the activation energy is 0.66 ± 0.03 eV for flips that involve nearest-neighbor C60 molecules, and 0.93 ± 0.03 for more distant flips. Based on calculated activation energies for vacancies diffusing in Au, we interpret these to be a result of surface vacancy diffusion and bulk vacancy diffusion. These results are compared to the similar system of Ag(111)-(2√3 × 2√3)R30°-C60. In both systems, the formation of the commensurate C60 monolayer produces a large number of vacancies in the top substrate layer that are highly mobile, effectively melting the interfacial metal layer at temperatures well below their normal melting temperatures.

  11. From porphyrins to pyrphyrins: adsorption study and metalation of a molecular catalyst on Au(111)

    Science.gov (United States)

    Mette, Gerson; Sutter, Denys; Gurdal, Yeliz; Schnidrig, Stephan; Probst, Benjamin; Iannuzzi, Marcella; Hutter, Jürg; Alberto, Roger; Osterwalder, Jürg

    2016-04-01

    The molecular ligand pyrphyrin, a tetradentate bipyridine based macrocycle, represents an interesting but widely unexplored class of molecules. It resembles the well-known porphyrin, but consists of pyridyl subunits instead of pyrroles. Metal complexes based on pyrphyrin ligands have recently shown promise as water reduction catalysts in homogeneous photochemical water splitting reactions. In this study, the adsorption and metalation of pyrphyrin on a single crystalline Au(111) surface is investigated in an ultrahigh vacuum by means of scanning tunneling microscopy, low-energy electron diffraction, X-ray photoelectron spectroscopy and density functional theory. Pyrphyrin coverages of approximately one monolayer and less are obtained by sublimation of the molecules on the substrate kept at room temperature. The molecules self-assemble in two distinct phases of long-range molecular ordering depending on the surface coverage. The deposition of cobalt metal and subsequent annealing lead to the formation of Co-ligated pyrphyrin molecules accompanied by a pronounced change of the molecular self-assembly. Electronic structure calculations taking the herringbone reconstruction of Au(111) into account show that the molecules are physisorbed, but preferred adsorption sites are identified where Co and the N atoms of the two terminal cyano groups are optimally coordinated to the surface Au atoms. An intermediate state of the metalation reaction is observed and the reaction steps for the Co metalation of pyrphyrin molecules on Au(111) are established in a joint experimental and computational effort.The molecular ligand pyrphyrin, a tetradentate bipyridine based macrocycle, represents an interesting but widely unexplored class of molecules. It resembles the well-known porphyrin, but consists of pyridyl subunits instead of pyrroles. Metal complexes based on pyrphyrin ligands have recently shown promise as water reduction catalysts in homogeneous photochemical water splitting

  12. Electronic and geometric structures of Au30 clusters: a network of 2e-superatom Au cores protected by tridentate protecting motifs with u3-S

    Science.gov (United States)

    Tian, Zhimei; Cheng, Longjiu

    2015-12-01

    Density functional theory calculations have been performed to study the experimentally synthesized Au30S(SR)18 and two related Au30(SR)18 and Au30S2(SR)18 clusters. The patterns of thiolate ligands on the gold cores for the three thiolate-protected Au30 nanoclusters are on the basis of the ``divide and protect'' concept. A novel extended protecting motif with u3-S, S(Au2(SR)2)2AuSR, is discovered, which is termed the tridentate protecting motif. The Au cores of Au30S(SR)18, Au30(SR)18 and Au30S2(SR)18 clusters are Au17, Au20 and Au14, respectively. The superatom-network (SAN) model and the superatom complex (SAC) model are used to explain the chemical bonding patterns, which are verified by chemical bonding analysis based on the adaptive natural density partitioning (AdNDP) method and aromatic analysis on the basis of the nucleus-independent chemical shift (NICS) method. The Au17 core of the Au30S(SR)18 cluster can be viewed as a SAN of one Au6 superatom and four Au4 superatoms. The shape of the Au6 core is identical to that revealed in the recently synthesized Au18(SR)14 cluster. The Au20 core of the Au30(SR)18 cluster can be viewed as a SAN of two Au6 superatoms and four Au4 superatoms. The Au14 core of Au30S2(SR)18 can be regarded as a SAN of two pairs of two vertex-sharing Au4 superatoms. Meanwhile, the Au14 core is an 8e-superatom with 1S21P6 configuration. Our work may aid understanding and give new insights into the chemical synthesis of thiolate-protected Au clusters.Density functional theory calculations have been performed to study the experimentally synthesized Au30S(SR)18 and two related Au30(SR)18 and Au30S2(SR)18 clusters. The patterns of thiolate ligands on the gold cores for the three thiolate-protected Au30 nanoclusters are on the basis of the ``divide and protect'' concept. A novel extended protecting motif with u3-S, S(Au2(SR)2)2AuSR, is discovered, which is termed the tridentate protecting motif. The Au cores of Au30S(SR)18, Au30(SR)18 and Au30S

  13. Site selection

    International Nuclear Information System (INIS)

    The conditions and criteria for selecting a site for a nuclear weapons test at the Nevada Test Site are summarized. Factors considered are: (1) scheduling of drill rigs, (2) scheduling of site preparation (dirt work, auger hole, surface casing, cementing), (3) schedule of event (when are drill hole data needed), (4) depth range of proposed W.P., (5) geologic structure (faults, Pz contact, etc.), (6) stratigraphy (alluvium, location of Grouse Canyon Tuff, etc.), (7) material properties (particularly montmorillonite and CO2 content), (8) water table depth, (9) potential drilling problems (caving), (10) adjacent collapse craters and chimneys, (11) adjacent expended but uncollapsed sites, (12) adjacent post-shot or other small diameter holes, (13) adjacent stockpile emplacement holes, (14) adjacent planned events (including LANL), (15) projected needs of Test Program for various DOB's and operational separations, and (16) optimal use of NTS real estate

  14. 从头计算方法比较研究B2Au4,Al2Au4和BAlAu4的几何和电子结构%A Comparative Ab initio Study of the Geometric and Electronic Structures of B2Au4, Al2Au4 and BAlAu4

    Institute of Scientific and Technical Information of China (English)

    姚文志; 卢章辉; 李思殿

    2014-01-01

    Au/H similarity is a hot topic in chemistry. Here, we report the theoretical prediction of new members of the Au/H analogy family:covalent B2Au4, ionic Al2Au4, and BAlAu4. A comparative study of the geometric and electronic structures of electron-deficient B2Au4, Al2Au4, and BAlAu4 was performed based on density and wave functional theories. Detailed orbital analyses, adaptive natural density partitioning (AdNDP), and electron localization function (ELF) analyses were performed. Ab initio theoretical evidence strongly suggests that the ground state of slightly distorted C2 B2Au4 is a covalent complex containing two B―Au―B three centers-two electrons (3c-2e) bonds. Unexpectedly, C3v Al+(AlAu4)-and C3v Al+(BAu4)-are predicted to have a salt-like composition with three X―Au―Al 3c-2e bonds (X=Al in Al2Au4, X=B in BAlAu4). Al2Au4 and BAlAu4 represent the first examples of bridging gold bonds in ionic-deficient systems. The adiabatic and vertical detachment energies of the anions were calculated to facilitate their future experimental characterization. Bridging gold addressed in this work provides an interesting bonding mode for covalent and ionic-deficient systems, and may aid in designing new materials and catalysts with highly dispersed Au atoms.%Au/H相似性的研究是现代化学中的一个热门话题.我们从理论上报道Au/H相似的新成员:共价化合物B2Au4,离子化合物Al2Au4和BAlAu4.采用密度泛函和波函数理论方法对比研究了缺电子体系B2Au4、Al2Au4和BAlAu4的几何和电子结构.详细讨论了它们基态结构的轨道、适应性自然密度划分(AdNDP)和电子局域函数(ELF)分析.计算结果表明稍微扭曲变形的C2 B2Au4是基态结构,在这个共价化合物中含有两个B―Au―B三中心二电子(3c-2e)键.然而C3v Al+(AlAu4)-和C3v Al+(BAu4)-被研究证明是含有三个X―Au―Al三中心二电子键的类盐化合物(在Al2Au4中X=Al, BAlAu4中X=B). Al2Au4和BAlAu4是至今为止首例

  15. Ge-Au eutectic bonding of Ge {100} single crystals

    Science.gov (United States)

    Knowlton, W. B.; Itoh, K. M.; Beeman, J. W.; Emes, J. H.; Loretto, D.; Haller, E. E.

    1993-11-01

    We present preliminary results on the eutectic bonding between two {100} Ge single crystal surfaces using thin films of Au ranging from 900Å/surface to 300Å/surface and Pd (10% the thickness of Au). Following bonding, plan view optical microscopy (OM) of the cleaved interface of samples with Au thicknesses ≤ 500Å/surface show a eutectic morphology more conducive to phonon transmission through the bond interface. High resolution transmission electron microscopy (HRTEM) cross sectional interface studies of a 300Å/surface Au sample show epitaxial growth of Ge. In sections of the bond, lattice continuity of the Ge is apparent through the interface. TEM studies also reveal heteroepitaxial growth of Au with a Au-Ge lattice mismatch of less than 2%. Eutectic bonds with 200Å/surface Au have been attained with characterization pending. An optical polishing technique for Ge has been optimized to insure intimate contact between the Ge surfaces prior to bonding. Interferometry analysis of the optically polished Ge surface shows that surface height fluctuations lie within ±150Å across an interval of 1mm. Characterization of phonon transmission through the interface is discussed with respect to low temperature detection of ballistic phonons.

  16. Tailoring the FeRh magnetostructural response with Au diffusion

    Science.gov (United States)

    Loving, M.; de Vries, M. A.; Jimenez-Villacorta, F.; Le Graët, C.; Liu, X.; Fan, R.; Langridge, S.; Heiman, D.; Marrows, C. H.; Lewis, L. H.

    2012-08-01

    Factors which contribute to magnetostructural transition control have been demonstrated by study of the effects of Au incorporation on the magnetic and structural character of CsCl-structured equiatomic FeRh thin films. Sputtered films were capped with 2 nm of Au deposited at 873 K and at 323 K and subsequently characterized with magnetometry and synchrotron-based structural probes. Diffusion of Au into the FeRh film layer at 873 K is confirmed by a reduction in the Au capping layer thickness relative to the film capped at 323 K. The impact of Au diffusion on the FeRh magnetostructural character is noted by a decrease in the onset of the transition temperature, a thermally broadened first-order transition and an increased sensitivity of the transition to applied magnetic field. Additionally, magnetization data indicate that Au diffusion causes retention of the ferromagnetic phase well below the normal magnetostructural transition temperature. These results are attributed to a multiphase FeRh film layer created by thermally driven Au diffusion.

  17. Structural, electronic and magnetic properties of Au-based monolayer derivatives in honeycomb structure

    Science.gov (United States)

    Kapoor, Pooja; Sharma, Munish; Kumar, Ashok; Ahluwalia, P. K.

    2016-05-01

    We present electronic properties of atomic layer of Au, Au2-N, Au2-O and Au2-F in graphene-like structure within the framework of density functional theory (DFT). The lattice constant of derived monolayers are found to be higher than the pristine Au monolayer. Au monolayer is metallic in nature with quantum ballistic conductance calculated as 4G0. Similarly, Au2-N and Au2-F monolayers show 4G0 and 2G0 quantum conductance respectively while semiconducting nature with calculated band gap of 0.28 eV has been observed for Au2-O monolayer. Most interestingly, half metalicity has been predicted for Au2-N and Au2-F monolayers. Our findings may have importance for the application of these monolayers in nanoelectronic and spintronics.

  18. Optical Behaviour of ZnO/Au Nanojunctions

    Directory of Open Access Journals (Sweden)

    Shital V. Kahane

    2011-01-01

    Full Text Available ZnO/Au nanojunctions were prepared by electrochemical method at room temperature. Nanojunction formation is vivid from appearance of ZnO and Au features in x-ray diffraction pattern. Optical absorption spectra reveal excitonic as well as surface plasmon resonance (SPR feature in case of nanojunctions. Bleaching of the excitonic feature associated with the blue shift, is a signature of charge transfer from Au to ZnO at the interface of nanojunction. An increase in intensity of band edge luminescence and quenching of green emission indicates the passivation of surface defects due to formation of nanojunctions.

  19. Energy level alignment in Au/pentacene/PTCDA trilayer stacks

    Science.gov (United States)

    Sehati, P.; Braun, S.; Fahlman, M.

    2013-09-01

    Ultraviolet photoelectron spectroscopy is used to investigate the energy level alignment and molecular orientation at the interfaces in Au/pentacene/PTCDA trilayer stacks. We deduced a standing orientation for pentacene grown on Au while we conclude a flat lying geometry for PTCDA grown onto pentacene. We propose that the rough surface of polycrystalline Au induces the standing geometry in pentacene. It is further shown that in situ deposition of PTCDA on pentacene can influence the orientation of the surface pentacene layer, flipping part of the surface pentacene molecules into a flat lying geometry, maximizing the orbital interaction across the pentacene-PTCDA heterojunction.

  20. Thermodynamic description of Au-Ag-Si ternary system

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Based on the available experimental information, the Ag-Si binary system was thermodynamically assessed using the CALPHAD method. The solution phases, including liquid, fcc-Al and diamond-A4, were modeled as substitutional solutions, of which the excess Gibbs energies were expressed by Redlich-Kister polynomial functions. Combined with previous assessment of the Ag-Au and Au-Si binary systems, thermodynamic description of the Au-Ag-Si ternary system was performed to reproduce the reported phase equilibria. Thermodynamic properties of liquid alloys, liquidus projection and several vertical and isothermal sections of this ternary system were calculated, which are in reasonable agreement with the reported experimental data.

  1. Au(111) and Pt(111) surface phase behavior

    DEFF Research Database (Denmark)

    Sandy, A.R.; Mochrie, S.G.J.; Zehner, D.M.;

    1993-01-01

    We describe our recent X-ray scattering studies of the structure and phases of the clean Au(111) and Pt(111) surfaces. Below 0.65 of their respective bulk melting temperatures, the Au(111) surface has a well-ordered chevron reconstruction and the Pt(111) surface is unreconstructed. Above these...... temperatures, both surfaces reconstruct to form layers that are isotropically compresses and have only short-range order. Throughout their reconstructed phases, the densities of the Au and Pt(111) surfaces increase with increasing temperature....

  2. AuScope VLBI Project and Hobart 26-m Antenna

    Science.gov (United States)

    Lovell, Jim; Dickey, John; Reid, Brett; McCallum, Jamie; Shabala, Stas; Watson, Christopher; Ellingsen, Simon; Memin, Anthony

    2013-01-01

    This is a report on the activities carried out at the three AuScope VLBI observatories and the Hobart 26-m antenna. In 2012 the three AuScope 12-m antennas at Hobart (Hb), Katherine (Ke), and Yarragadee (Yg) completed their first full year of operations as an array. The Hobart 26-m antenna (Ho) continued to make a contribution to IVS, providing overlap with the Hb time series. In total the AuScope antennas and the Hobart 26 m observed for 146 antenna days in 2012. In this report we also briefly highlight our research activities during 2012 and our plans for 2013.

  3. Electrochemical Capacitance DNA Sensing at Hairpin-Modified Au Electrodes

    OpenAIRE

    Joel Rivera-Gandía; Maria del Mar Maldonado; Yarimar De La Torre-Meléndez; Edwin O. Ortiz-Quiles; Vargas-Barbosa, Nella M.; Cabrera, Carlos R.

    2011-01-01

    An interfacial capacitance measurement electrochemical technique has been used for the sensing of self-assembled DNA hairpin probes (M. tuberculosis and B. anthracis) attached to Au electrodes. The double-layer capacitance (Cdl) was determined with electrochemical perturbations from 0.2 V to 0.5 V versus Ag/AgCl at a Au/M. tuberculosis DNA hairpin probe at surface coverage Au electrodes. The capacitance study was done at pH 7, which was necessary to maintain the M. tuberculosis and B. anthrac...

  4. d+Au Hadron Correlation Measurements from PHENIX

    OpenAIRE

    Sickles, Anne M.; Collaboration, for the PHENIX

    2013-01-01

    Recent observations of extended pseudorapidity correlations at the LHC in p+p and p+Pb collisions are of great interest. Here we present related re- sults from d+Au collisions at PHENIX. We present the observed v2 and discuss the possible origin in the geometry of the collision region. We also present new measurements of the pseudorapidity dependence of the ridge in d+Au collision. Future plans to clarify the role of geometry in small collision systems using 3He+Au collisions are discussed.

  5. On the electronic, structural, and thermodynamic properties of Au supported on α-Fe2O3 surfaces and their interaction with CO

    International Nuclear Information System (INIS)

    Extensive first principles calculations are carried out to investigate Au monomers and dimers supported on α-Fe2O3(0001) surfaces in terms of structure optimizations, electronic structure analyses, and ab initio thermodynamics calculations of surface phase diagrams. All computations rely on density functional theory in the generalized gradient approximation (Perdew-Burke-Ernzerhof (PBE)) and account for on-site Coulomb interactions via inclusion of a Hubbard correction (PBE+U). The relative stability of Au monomers/dimers on the stoichiometric termination of α-Fe2O3(0001) decorated with various vacancies (multiple oxygen vacancies, iron vacancy, and mixed iron-oxygen vacancies) has been computed as a function of the oxygen chemical potential. The charge rearrangement induced by Au at the oxide contact is analyzed in detail and discussed. On one hand, ab initio thermodynamics predicts that under O-rich conditions, structures obtained by replacing a surface Fe atom with a Au atom are thermodynamically stable over a wide range of temperatures. On the other hand, the complex of a CO molecule on a Au atom substituting surface Fe atoms is thermodynamically stable only in a much more narrow range of values of the O chemical potential under O-rich conditions. In the case of a Au dimer, under O-rich conditions, supported Au atoms at an O-Fe di-vacancy are more stable. However, upon CO adsorption, the complex of a CO molecule and 2 Au atoms located at a single Fe vacancy is more favorable

  6. Au plasmonics in a WS{sub 2}-Au-CuInS{sub 2} photocatalyst for significantly enhanced hydrogen generation

    Energy Technology Data Exchange (ETDEWEB)

    Cheng, Zhongzhou [CAS Key Laboratory of Nanosystem and Hierarchical Fabrication, National Center for Nanoscience and Technology, Beijing 100190 (China); School of Materials Science and Engineering, University of Science and Technology Beijing, Beijing 100083 (China); Wang, Zhenxing, E-mail: wangzx@nanoctr.cn, E-mail: hej@nanoctr.cn; Shifa, Tofik Ahmed; Wang, Fengmei; Zhan, Xueying; Xu, Kai; He, Jun, E-mail: wangzx@nanoctr.cn, E-mail: hej@nanoctr.cn [CAS Key Laboratory of Nanosystem and Hierarchical Fabrication, National Center for Nanoscience and Technology, Beijing 100190 (China); Liu, Quanlin [School of Materials Science and Engineering, University of Science and Technology Beijing, Beijing 100083 (China)

    2015-11-30

    Promoting the activities of photocatalysts is still the critical challenge in H{sub 2} generation area. Here, a Au plasmon enhanced photocatalyst of WS{sub 2}-Au-CuInS{sub 2} is developed by inserting Au nanoparticles between WS{sub 2} nanotubes and CuInS{sub 2} (CIS) nanoparticles. Due to the localized surface plasmonic resonance properties from Au nanoparticles, WS{sub 2}-Au-CIS shows the best performance as compared to Au-CIS, CIS, WS{sub 2}-CIS, CIS-Au, WS{sub 2}-Au, and WS{sub 2}-CIS-Au. The surface plasmonic resonance effects dramatically intensify the absorption of visible light and help to inject hot electrons into the semiconductors. Our findings open up an efficient method to optimize the type-II structures for photocatalytic water splitting.

  7. Gold surfaces and nanoparticles are protected by Au(0)-thiyl species and are destroyed when Au(I)-thiolates form.

    Science.gov (United States)

    Reimers, Jeffrey R; Ford, Michael J; Halder, Arnab; Ulstrup, Jens; Hush, Noel S

    2016-03-15

    The synthetic chemistry and spectroscopy of sulfur-protected gold surfaces and nanoparticles is analyzed, indicating that the electronic structure of the interface is Au(0)-thiyl, with Au(I)-thiolates identified as high-energy excited surface states. Density-functional theory indicates that it is the noble character of gold and nanoparticle surfaces that destabilizes Au(I)-thiolates. Bonding results from large van der Waals forces, influenced by covalent bonding induced through s-d hybridization and charge polarization effects that perturbatively mix in some Au(I)-thiolate character. A simple method for quantifying these contributions is presented, revealing that a driving force for nanoparticle growth is nobleization, minimizing Au(I)-thiolate involvement. Predictions that Brust-Schiffrin reactions involve thiolate anion intermediates are verified spectroscopically, establishing a key feature needed to understand nanoparticle growth. Mixing of preprepared Au(I) and thiolate reactants always produces Au(I)-thiolate thin films or compounds rather than monolayers. Smooth links to O, Se, Te, C, and N linker chemistry are established.

  8. Effect of water on hydrogenation of 1,3-butadiene over Au (1 1 1): A joint theoretical and experimental study

    Energy Technology Data Exchange (ETDEWEB)

    Bu, Weida; Zhao, Liang, E-mail: Liangzhao@cup.edu.cn; Zhang, Zhicheng; Zhang, Xin; Gao, Jinsen; Xu, Chunming

    2014-01-15

    The effect of water on the hydrogenation of 1,3-butadiene over Au (1 1 1) was investigated based on density functional theory calculations and the results were compared with experimental study on the same reaction over Au/γ-Al{sub 2}O{sub 3} catalysts prepared by different methods. All possible adsorption sites and geometry structures of hydrogen, water and 1,3-butadiene on Au (1 1 1) were considered in the adsorption energy calculations to obtain the optimized adsorption modes. The hydrogenation of 1,3-butadiene was found to be only feasible with dissociated H atoms adsorbed over Au (1 1 1). Our adsorption calculations suggest that H{sub 2}O tended to block the active sites and inhibited the adsorption step, fully consistent with the rapid 1,3-butadiene conversion drop from above 40% to below 10% at low water concentration (<1200 ppm) in experiments. The transition state calculations indicate that water had little impact on the reaction step given slight change of energy barrier from 0.62 eV to 0.55 eV for the major route. This result validated the experimental finding that the conversion of 1,3-butadiene on Au/γ-Al{sub 2}O{sub 3} catalysts had only a slight decrease in a high water concentration range.

  9. Thermodynamic assessment of Au-Pt system%Au-Pt二元合金的热力学评估

    Institute of Scientific and Technical Information of China (English)

    徐晓宁; 任玉平; 李长发; 李松; 秦高梧

    2012-01-01

    基于最近实验测得的Au-Pt二元体系相平衡数据,利用Calphad方法重新评估Au-Pt二元体系的热力学参数.采用亚正规溶体模型Redlich-Kister等式描述液相和面心立方相的Gibbs自由能.考虑热力学第三定律的限定,以再现相平衡数据和固相热力学性质,包括活度和混合焓,优化Au-Pt二元系统热力学参数.优化结果表明:Au-Pt合金系统的溶解度间隙边界向富Au侧偏移,其顶点位置在1200 °c,Au-56%Pt.%The thermodynamic re-assessment of Au-Pt binary system was carded out by using the Calphad method and based on the recent experimental data.The Gibbs energies of face-centred cubic and liquid phases were described by a sub-regular solution model with the Redlich-Kister equation.Much effort was taken to reproduce the phase equilibrium results and thermodynamic properties of the solid phase,including the activity and mixing enthalpy.The constraint of the third law of thermodynamics was also considered in the assessment.According to the presently assessed results,the miscibility gap region in the Au-Pt system slightly shifts to the Au-rich side,and the critical point of the miscibility gap is about 1200 °C and Au-56% Pt.

  10. A simple approach for facile synthesis of Ag, anisotropic Au and bimetallic (Ag/Au) nanoparticles using cruciferous vegetable extracts

    Energy Technology Data Exchange (ETDEWEB)

    Jacob, Jasmine; Mukherjee, Tulsi; Kapoor, Sudhir, E-mail: sudhirk@barc.gov.in

    2012-10-01

    We present a simple and straightforward approach for the synthesis and stabilization of relatively monodisperse Ag, Au and bimetallic (Ag/Au) nanoparticles by using cruciferous vegetable (green/red) extracts by simply adjusting the pH environment in the aqueous medium. The vegetable extracts act both as reducing and capping agents. The monometallic and bimetallic nanoparticles of Ag and Au so obtained were characterized by UV-visible spectroscopy, X-ray diffraction (XRD), dynamic light scattering (DLS) and transmission electron microscopy (TEM). It is shown that red cabbage extract can be used for the preparation of anisotropic Au nanoparticles. The formation of Au anisotropic nanoparticles was found to depend on a number of environmental factors, such as the pH of the reaction medium, reaction time, and initial reactant concentrations. Additionally, it is shown that these extract-stabilized Au and Ag nanoparticles can be used as a seed for preparation of bimetallic Au/Ag nanoparticles. For bimetallic alloy nanoparticles the absorption peak was observed between the two maxima of the corresponding metallic particles. The surface plasmon absorption maxima for bimetallic nanoparticles changed linearly with increasing Au mole ratio content in various alloy compositions. It has been shown that the formation of hollow Au spheres depends on the experimental conditions. - Graphical abstract: TEM image of gold nanoparticles at pH 3.27 formed by red cabbage extract. Highlights: Black-Right-Pointing-Pointer First report on the reactivity of the extracts toward metal ions using a spectrophotometric technique. Black-Right-Pointing-Pointer Red cabbage extract has better reducing properties than green cabbage extract. Black-Right-Pointing-Pointer Red cabbage extract can reduce metal ions at any pH. Black-Right-Pointing-Pointer Reduction of metal ions can have important consequences in the study of soil chemistry.

  11. A simple approach for facile synthesis of Ag, anisotropic Au and bimetallic (Ag/Au) nanoparticles using cruciferous vegetable extracts

    International Nuclear Information System (INIS)

    We present a simple and straightforward approach for the synthesis and stabilization of relatively monodisperse Ag, Au and bimetallic (Ag/Au) nanoparticles by using cruciferous vegetable (green/red) extracts by simply adjusting the pH environment in the aqueous medium. The vegetable extracts act both as reducing and capping agents. The monometallic and bimetallic nanoparticles of Ag and Au so obtained were characterized by UV–visible spectroscopy, X-ray diffraction (XRD), dynamic light scattering (DLS) and transmission electron microscopy (TEM). It is shown that red cabbage extract can be used for the preparation of anisotropic Au nanoparticles. The formation of Au anisotropic nanoparticles was found to depend on a number of environmental factors, such as the pH of the reaction medium, reaction time, and initial reactant concentrations. Additionally, it is shown that these extract-stabilized Au and Ag nanoparticles can be used as a seed for preparation of bimetallic Au/Ag nanoparticles. For bimetallic alloy nanoparticles the absorption peak was observed between the two maxima of the corresponding metallic particles. The surface plasmon absorption maxima for bimetallic nanoparticles changed linearly with increasing Au mole ratio content in various alloy compositions. It has been shown that the formation of hollow Au spheres depends on the experimental conditions. - Graphical abstract: TEM image of gold nanoparticles at pH 3.27 formed by red cabbage extract. Highlights: ► First report on the reactivity of the extracts toward metal ions using a spectrophotometric technique. ► Red cabbage extract has better reducing properties than green cabbage extract. ► Red cabbage extract can reduce metal ions at any pH. ► Reduction of metal ions can have important consequences in the study of soil chemistry.

  12. Evaluation of the Olympus AU-510 analyser.

    Science.gov (United States)

    Farré, C; Velasco, J; Ramón, F

    1991-01-01

    The selective multitest Olympus AU-510 analyser was evaluated according to the recommendations of the Comision de Instrumentacion de la Sociedad Española de Quimica Clinica and the European Committee for Clinical Laboratory Standards. The evaluation was carried out in two stages: an examination of the analytical units and then an evaluation in routine work conditions. The operational characteristics of the system were also studied.THE FIRST STAGE INCLUDED A PHOTOMETRIC STUDY: dependent on the absorbance, the inaccuracy varies between +0.5% to -0.6% at 405 nm and from -5.6% to 10.6% at 340 nm; the imprecision ranges between -0.22% and 0.56% at 405 nm and between 0.09% and 2.74% at 340 nm. Linearity was acceptable, apart from a very low absorbance for NADH at 340 nm; and the imprecision of the serum sample pipetter was satisfactory.TWELVE SERUM ANALYTES WERE STUDIED UNDER ROUTINE CONDITIONS: glucose, urea urate, cholesterol, triglycerides, total bilirubin, creatinine, phosphate, iron, aspartate aminotransferase, alanine aminotransferase and gamma-glutamyl transferase.The within-run imprecision (CV%) ranged from 0.67% for phosphate to 2.89% for iron and the between-run imprecision from 0.97% for total bilirubin to 7.06% for iron. There was no carryover in a study of the serum sample pipetter. Carry-over studies with the reagent and sample pipetters shows some cross contamination in the iron assay.

  13. Activated Dissociation of HCl on Au(111).

    Science.gov (United States)

    Shirhatti, Pranav R; Geweke, Jan; Steinsiek, Christoph; Bartels, Christof; Rahinov, Igor; Auerbach, Daniel J; Wodtke, Alec M

    2016-04-01

    We report zero-coverage reaction probabilities (S0) for HCl dissociative adsorption on Au(111) obtained by the seeded molecular beam hot-nozzle method. For measurements at normal incidence with mean translational energies ranging from 0.94 to 2.56 eV (nozzle temperatures 296 to 1060 K), S0 increased from 6 × 10(-6) to 2 × 10(-2). S0 also increased with increasing nozzle temperature for fixed incidence energy associated with the motion normal to the surface. Accounting for the influence of the vibrational state population and translational energy distributions in the incident beam, we are able to compare the experimental results to recent theoretical predictions. These calculations, performed employing 6-D quantum dynamics on an electronically adiabatic potential energy surface obtained using density functional theory at the level of the generalized gradient approximation and the static surface approximation, severely overestimate the reaction probabilities when compared with our experimental results. We discuss some possible reasons for this large disagreement. PMID:26990513

  14. De l’individu postcommuniste au citoyen

    Directory of Open Access Journals (Sweden)

    Anna Krasteva

    2009-11-01

    Full Text Available L’article analyse le paradoxe de la conception communiste du citoyen engagé : au niveau idéologique, citoyenneté et engagement sont intrinsèquement liés, au niveau politique ils sont souvent radicalement dissociés. Le citoyen communiste est plus engagé que citoyen. La citoyenneté était dépourvue de plusieurs de ses attributs : de la jouissance de la loi qui établit « l’égalité arithmétique » et minorise les maîtres ; de la citoyenneté active – civile et politique – pour ne jouir que la protection sociale ; de la participation au profit de l’appartenance. L’individu communiste était engagé, non pas parce qu’il l’avait choisi dans la liberté, mais parce qu’il n’avait pas la liberté de se désengager. L’article compare l’engagement communiste et postcommuniste en analysant le second au croisement de l’individualité et de la citoyenneté et en distinguant trois formes de désengagement – contestataire, « bonapartiste » et individualiste et trois formes d’engagement – mimétique, héroïque, civique.From the postcommunist individual to the citizenThe article analysis the paradox of the communist conception of the engaged citizen: at ideological level, citizenship and participation are closely linked; at political level, they are radically dissociated. The communist citizen is more engaged than citizen. The citizenship is deprived of several of its attributes: of the law which establishes "the arithmetic equality" and minimises the masters; of the active citizenship, civic and political, enjoying just the social one; of the participation for emphasizing on the belonging. The communist individual is engaged not because he has chosen freely to be such, but because he had not the freedom to disengage him/herself. The article compares the communist and the post communist participation analysing the latter at the intersection of individuality and citizenship and distinguishing three forms

  15. Shadowing effects on the nuclear suppression factor, RdAu, in d+Au interactions

    International Nuclear Information System (INIS)

    We explore how nuclear modifications to the nucleon parton distributions affect production of high transverse momentum hadrons in deuteron-nucleus collisions. We calculate the charged hadron spectra to leading order using standard fragmentation functions and shadowing parameterizations. We obtain the d+Au to pp ratio both in minimum bias collisions and as a function of centrality. The minimum bias results agree reasonably well with the BRAHMS data while the calculated centrality dependence underestimates the data and is a stronger function of pT than the data indicate

  16. Distributions of Charged Hadrons Associated with High Transverse Momentum Particles in pp and Au+Au Collisions at sqrt(s_NN)=200 GeV

    CERN Document Server

    Adams, J; Aggarwal, M M; Ahammed, Z; Amonett, J; Anderson, B D; Arkhipkin, D; Averichev, G S; Badyal, S K; Balewski, J; Barannikova, O; Barnby, L S; Baudot, J; Bekele, S; Belaga, V V; Bellwied, R; Berger, J; Bezverkhny, B I; Bhardwaj, S; Bhati, A K; Bichsel, H; Billmeier, A; Bland, L C; Blyth, C O; Bonner, B E; Botje, M; Boucham, A; Brandin, A; Bravar, A; Cadman, R V; Cai, X Z; Caines, H; Calderón de la Barca-Sanchez, M; Carroll, J; Castillo, J; Cebra, D; Chaloupka, P; Chattopadhyay, S; Chen, H F; Chen, Y; Chernenko, S P; Cherney, M; Chikanian, A; Christie, W; Coffin, J P; Cormier, T M; Cramer, J G; Crawford, H J; Das, D; Das, S; Derevshchikov, A A; Didenko, L; Dietel, T; Dong, W J; Dong, X; Draper, J E; Du, F; Dubey, A K; Dunin, V B; Dunlop, J C; Dutta-Majumdar, M R; Eckardt, V; Efimov, L G; Emelianov, V; Engelage, J; Eppley, G; Erazmus, B; Estienne, M; Fachini, P; Faine, V; Faivre, J; Fatemi, R; Filimonov, K; Filip, P; Finch, E; Fisyak, Yu; Flierl, D; Foley, K J; Fu, J; Gagliardi, C A; Gagunashvili, N; Gans, J; Ganti, M S; Gaudichet, L; Geurts, F J M; Ghazikhanian, V; Ghosh, P; González, J E; Grachov, O; Grebenyuk, O; Gronstal, S; Grosnick, D P; Guertin, S M; Sen-Gupta, A; Gutíerrez, T D; Hallman, T J; Hamed, A; Hardtke, D; Harris, J W; Heinz, M; Henry, T W; Heppelmann, S; Herston, T; Hippolyte, B; Hirsch, A; Hjort, E; Hoffmann, G W; Horsley, M; Huang, H Z; Huang Sheng Li; Hughes, E; Humanic, T J; Igo, G; Ishihara, A; Jacobs, P; Jacobs, W W; Janik, M; Jiang, H; Johnson, I; Jones, P G; Judd, E G; Kabana, S; Kaplan, M; Keane, D; Khodyrev, V Yu; Kiryluk, J; Kisiel, A; Klay, J; Klein, S R; Klyachko, A; Koetke, D D; Kollegger, T; Kopytine, M; Kotchenda, L; Kovalenko, A D; Krämer, M; Kravtsov, P; Kravtsov, V I; Krüger, K; Kuhn, C; Kulikov, A I; Kumar, A; Kunde, G J; Kunz, C L; Kutuev, R K; Kuznetsov, A A; Lamont, M A C; Landgraf, J M; Lange, S; Lasiuk, B; Laue, F; Lauret, J; Lebedev, A; Lednicky, R; Le Vine, M J; Li, C; Li, Q; Lindenbaum, S J; Lisa, M A; Liu, F; Liu, L; Liu, Z; Liu, Q J; Ljubicic, T; Llope, W J; Long, H; Longacre, R S; López-Noriega, M; Love, W A; Ludlam, T; Lynn, D; Ma, J; Ma, Y G; Magestro, D; Mahajan, S; Mangotra, L K; Mahapatra, D P; Majka, R; Manweiler, R; Margetis, S; Markert, C; Martin, L; Marx, J; Matis, H S; Matulenko, Yu A; McClain, C J; McShane, T S; Meissner, F; Melnik, Yu M; Meschanin, A; Miller, M L; Milosevich, Z; Minaev, N G; Mironov, C; Mischke, A; Mishra, D; Mitchell, J; Mohanty, B; Molnár, L; Moore, C F; Mora-Corral, M J; Morozov, D A; Morozov, V; De Moura, M M; Munhoz, M G; Nandi, B K; Nayak, S K; Nayak, T K; Nelson, J M; Netrakanti, P K; Nikitin, V A; Nogach, L V; Norman, B; Nurushev, S B; Odyniec, Grazyna Janina; Ogawa, A; Okorokov, V; Oldenburg, M; Olson, D; Paic, G; Pal, S K; Panebratsev, Yu A; Panitkin, S Y; Pavlinov, A I; Pawlak, T; Peitzmann, T; Perevozchikov, V; Perkins, C; Peryt, W; Petrov, V A; Phatak, S C; Picha, R; Planinic, M; Pluta, J; Porile, N; Porter, J; Poskanzer, A M; Potekhin, M V; Potrebenikova, E V; Potukuchi, B V K S; Prindle, D; Pruneau, C A; Putschke, J; Rai, G; Rakness, G; Raniwala, R; Raniwala, S; Ravel, O; Ray, R L; Razin, S V; Reichhold, D M; Reid, J G; Renault, G; Retière, F; Ridiger, A; Ritter, H G; Roberts, J B; Rogachevski, O V; Romero, J L; Rose, A; Roy, C; Ruan, L J; Sahoo, R; Sakrejda, I; Salur, S; Sandweiss, J; Savin, I; Schambach, J; Scharenberg, R P; Schmitz, N; Schröder, L S; Schweda, K; Seger, J; Seyboth, P; Shahaliev, E; Shao, M; Shao, W; Sharma, M; Shestermanov, K E; Shimansky, S S; Singaraju, R N; Simon, F; Skoro, G P; Smirnov, N; Snellings, R; Sood, G; Sørensen, P; Sowinski, J; Speltz, J; Spinka, H M; Srivastava, B; Stanislaus, T D S; Stock, R; Stolpovsky, A; Strikhanov, M N; Stringfellow, B C; Struck, C; Suaide, A A P; Sugarbaker, E R; Suire, C; Sumbera, M; Surrow, B; Symons, T J M; Szanto de Toledo, A; Szarwas, P; Tai, A; Takahashi, J; Tang, A H; Thein, D; Thomas, J H; Timoshenko, S; Tokarev, M; Tonjes, M B; Trainor, T A; Trentalange, S; Tribble, R E; Tsai, O; Ullrich, T; Underwood, D G; Van Buren, G; Van der Molen, A M; Varma, R; Vasilevski, I; Vasilev, A N; Vernet, R; Vigdor, S E; Viyogi, Y P; Voloshin, S A; Vznuzdaev, M; Waggoner, W; Wang, F; Wang, G; Wang, X L; Wang, Y; Wang, Z M; Ward, H; Watson, J W; Webb, J C; Wells, R; Westfall, G D; Whitten, C; Wieman, H; Willson, R; Wissink, S W; Witt, R; Wood, J; Wu, J; Xu, N; Xu, Z; Xu, Z Z; Yamamoto, E; Yepes, P; Yurevich, V I; Yuting, B; Zanevsky, Yu V; Zhang, H; Zhang, W M; Zhang, Z P; Zhaomin, P; Zizong, Z P; Zolnierczuk, P A; Zoulkarneev, R; Zoulkarneeva, J; Zubarev, A N

    2005-01-01

    Charged hadrons in 0.15 4 GeV/c are reconstructed in pp and Au+Au collisions at sqrt(s_NN)=200 GeV. The associated multiplicity and pt magnitude sum are found to increase from pp to central Au+Au collisions. The associated pt distributions, while similar in shape on the near side, are significantly softened on the away side in central Au+Au relative to pp and not much harder than that of inclusive hadrons. The results, consistent with jet quenching, suggest that the away-side fragments approach equilibration with the medium traversed.

  17. Comparison of the space-time extent of the emission source in $d$$+$Au and Au$+$Au collisions at $\\sqrt{s_{{NN}}}=200$ GeV

    CERN Document Server

    Adare, A; Aidala, C; Ajitanand, N N; Akiba, Y; Akimoto, R; Al-Bataineh, H; Alexander, J; Alfred, M; Angerami, A; Aoki, K; Apadula, N; Aramaki, Y; Asano, H; Atomssa, E T; Averbeck, R; Awes, T C; Azmoun, B; Babintsev, V; Bai, M; Baksay, G; Baksay, L; Bandara, N S; Bannier, B; Barish, K N; Bassalleck, B; Basye, A T; Bathe, S; Baublis, V; Baumann, C; Bazilevsky, A; Beaumier, M; Beckman, S; Belikov, S; Belmont, R; Bennett, R; Berdnikov, A; Berdnikov, Y; Bhom, J H; Bickley, A A; Black, D; Blau, D S; Bok, J; Bok, J S; Boyle, K; Brooks, M L; Bryslawskyj, J; Buesching, H; Bumazhnov, V; Bunce, G; Butsyk, S; Camacho, C M; Campbell, S; Caringi, A; Chen, C -H; Chi, C Y; Chiu, M; Choi, I J; Choi, J B; Choudhury, R K; Christiansen, P; Chujo, T; Chung, P; Chvala, O; Cianciolo, V; Citron, Z; Cole, B A; del Valle, Z Conesa; Connors, M; Constantin, P; Csanád, M; Csörgő, T; Dahms, T; Dairaku, S; Danchev, I; Das, K; Datta, A; Daugherity, M S; David, G; Dayananda, M K; DeBlasio, K; Dehmelt, K; Denisov, A; Deshpande, A; Desmond, E J; Dharmawardane, K V; Dietzsch, O; Ding, L; Dion, A; Do, J H; Donadelli, M; Drapier, O; Drees, A; Drees, K A; Durham, J M; Durum, A; Dutta, D; D'Orazio, L; Edwards, S; Efremenko, Y V; Ellinghaus, F; Engelmore, T; Enokizono, A; En'yo, H; Esumi, S; Fadem, B; Feege, N; Fields, D E; Finger, M; Jr., \\,; Fleuret, F; Fokin, S L; Fraenkel, Z; Frantz, J E; Franz, A; Frawley, A D; Fujiwara, K; Fukao, Y; Fusayasu, T; Gal, C; Gallus, P; Garg, P; Garishvili, I; Ge, H; Giordano, F; Glenn, A; Gong, H; Gonin, M; Goto, Y; de Cassagnac, R Granier; Grau, N; Greene, S V; Grim, G; Perdekamp, M Grosse; Gu, Y; Gunji, T; Guragain, H; Gustafsson, H -Å; Hachiya, T; Haggerty, J S; Hahn, K I; Hamagaki, H; Hamblen, J; Han, R; Han, S Y; Hanks, J; Hartouni, E P; Hasegawa, S; Haslum, E; Hayano, R; He, X; Heffner, M; Hemmick, T K; Hester, T; Hill, J C; Hohlmann, M; Hollis, R S; Holzmann, W; Homma, K; Hong, B; Horaguchi, T; Hornback, D; Hoshino, T; Huang, J; Huang, S; Ichihara, T; Ichimiya, R; Ide, J; Ikeda, Y; Imai, K; Imazu, Y; Inaba, M; Iordanova, A; Isenhower, D; Ishihara, M; Isobe, T; Issah, M; Isupov, A; Ivanischev, D; Ivanishchev, D; Iwanaga, Y; Jacak, B V; Jeon, S J; Jezghani, M; Jia, J; Jiang, X; Jin, J; Johnson, B M; Jones, T; Joo, E; Joo, K S; Jouan, D; Jumper, D S; Kajihara, F; Kametani, S; Kamihara, N; Kamin, J; Kang, J H; Kang, J S; Kapustinsky, J; Karatsu, K; Kasai, M; Kawall, D; Kawashima, M; Kazantsev, A V; Kempel, T; Key, J A; Khachatryan, V; Khanzadeev, A; Kihara, K; Kijima, K M; Kikuchi, J; Kim, A; Kim, B I; Kim, C; Kim, D H; Kim, D J; Kim, E; Kim, E -J; Kim, H -J; Kim, M; Kim, S H; Kim, Y -J; Kim, Y K; Kinney, E; Kiriluk, K; Kiss, Á; Kistenev, E; Klatsky, J; Kleinjan, D; Kline, P; Koblesky, T; Kochenda, L; Kofarago, M; Komkov, B; Konno, M; Koster, J; Kotchetkov, D; Kotov, D; Kozlov, A; Král, A; Kravitz, A; Kunde, G J; Kurita, K; Kurosawa, M; Kwon, Y; Kyle, G S; Lacey, R; Lai, Y S; Lajoie, J G; Lebedev, A; Lee, D M; Lee, J; Lee, K; Lee, K B; Lee, K S; Lee, S H; Leitch, M J; Leite, M A L; Leitgab, M; Leitner, E; Lenzi, B; Li, X; Lichtenwalner, P; Liebing, P; Lim, S H; Levy, L A Linden; Liška, T; Litvinenko, A; Liu, H; Liu, M X; Love, B; Luechtenborg, R; Lynch, D; Maguire, C F; Makdisi, Y I; Makek, M; Malakhov, A; Malik, M D; Manion, A; Manko, V I; Mannel, E; Mao, Y; Masui, H; Matathias, F; McCumber, M; McGaughey, P L; McGlinchey, D; McKinney, C; Means, N; Meles, A; Mendoza, M; Meredith, B; Miake, Y; Mibe, T; Mignerey, A C; Mikeš, P; Miki, K; Miller, A J; Milov, A; Mishra, D K; Mishra, M; Mitchell, J T; Miyasaka, S; Mizuno, S; Mohanty, A K; Montuenga, P; Moon, H J; Moon, T; Morino, Y; Morreale, A; Morrison, D P; Moukhanova, T V; Murakami, T; Murata, J; Mwai, A; Nagamiya, S; Nagle, J L; Naglis, M; Nagy, M I; Nakagawa, I; Nakagomi, H; Nakamiya, Y; Nakamura, K R; Nakamura, T; Nakano, K; Nam, S; Nattrass, C; Netrakanti, P K; Newby, J; Nguyen, M; Nihashi, M; Niida, T; Nouicer, R; Novitzky, N; Nyanin, A S; Oakley, C; O'Brien, E; Oda, S X; Ogilvie, C A; Oka, M; Okada, K; Onuki, Y; Koop, J D Orjuela; Oskarsson, A; Ouchida, M; Ozaki, H; Ozawa, K; Pak, R; Pantuev, V; Papavassiliou, V; Park, I H; Park, J; Park, S; Park, S K; Park, W J; Pate, S F; Patel, L; Patel, M; Pei, H; Peng, J -C; Pereira, H; Perepelitsa, D V; Perera, G D N; Peresedov, V; Peressounko, D Yu; Perry, J; Petti, R; Pinkenburg, C; Pinson, R; Pisani, R P; Proissl, M; Purschke, M L; Purwar, A K; Qu, H; Rak, J; Rakotozafindrabe, A; Ravinovich, I; Read, K F; Rembeczki, S; Reygers, K; Reynolds, D; Riabov, V; Riabov, Y; Richardson, E; Riveli, N; Roach, D; Roche, G; Rolnick, S D; Rosati, M; Rosen, C A; Rosendahl, S S E; Rosnet, P; Rowan, Z; Rubin, J G; Rukoyatkin, P; Ružička, P; Sahlmueller, B; Saito, N; Sakaguchi, T; Sakashita, K; Sako, H; Samsonov, V; Sano, S; Sarsour, M; Sato, S; Sato, T; Sawada, S; Schaefer, B; Schmoll, B K; Sedgwick, K; Seele, J; Seidl, R; Semenov, A Yu; Sen, A; Seto, R; Sett, P; Sexton, A; Sharma, D; Shein, I; Shibata, T -A; Shigaki, K; Shimomura, M; Shoji, K; Shukla, P; Sickles, A; Silva, C L; Silvermyr, D; Silvestre, C; Sim, K S; Singh, B K; Singh, C P; Singh, V; Slunečka, M; Soltz, R A; Sondheim, W E; Sorensen, S P; Sourikova, I V; Sparks, N A; Stankus, P W; Stenlund, E; Stepanov, M; Stoll, S P; Sugitate, T; Sukhanov, A; Sumita, T; Sun, J; Sziklai, J; Takagui, E M; Takahara, A; Taketani, A; Tanabe, R; Tanaka, Y; Taneja, S; Tanida, K; Tannenbaum, M J; Tarafdar, S; Taranenko, A; Tarján, P; Themann, H; Thomas, D; Thomas, T L; Timilsina, A; Todoroki, T; Togawa, M; Toia, A; Tomášek, L; Tomášek, M; Torii, H; Towell, M; Towell, R; Towell, R S; Tserruya, I; Tsuchimoto, Y; Vale, C; Valle, H; van Hecke, H W; Vargyas, M; Vazquez-Zambrano, E; Veicht, A; Velkovska, J; Vértesi, R; Vinogradov, A A; Virius, M; Vrba, V; Vznuzdaev, E; Wang, X R; Watanabe, D; Watanabe, K; Watanabe, Y; Watanabe, Y S; Wei, F; Wei, R; Wessels, J; Whitaker, S; White, S N; Winter, D; Wolin, S; Wood, J P; Woody, C L; Wright, R M; Wysocki, M; Xia, B; Xie, W; Xue, L; Yalcin, S; Yamaguchi, Y L; Yamaura, K; Yang, R; Yanovich, A; Ying, J; Yokkaichi, S; Yoon, I; You, Z; Young, G R; Younus, I; Yushmanov, I E; Zajc, W A; Zelenski, A; Zhang, C; Zhou, S; Zolin, L

    2014-01-01

    Two-pion interferometry measurements in $d$$+$Au and Au$+$Au collisions at $\\sqrt{s_{{NN}}}=200$ GeV are used to extract and compare the Gaussian source radii R$_{{\\rm out}}$, R$_{{\\rm side}}$, and R$_{{\\rm long}}$, which characterize the space-time extent of the emission sources. The comparisons, which are performed as a function of collision centrality and the mean transverse momentum for pion pairs, indicate strikingly similar patterns for the $d$$+$Au and Au$+$Au systems. They also indicate a linear dependence of R$_{{\\rm side}}$ on the initial transverse geometric size $\\bar{R}$, as well as a smaller freeze-out size for the $d$$+$Au system. These patterns point to the important role of final-state rescattering effects in the reaction dynamics of $d$$+$Au collisions.

  18. Composition distributions in FePt(Au) nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Srivastava, C. [University of Alabama, Department of Metallurgical and Materials Engineering (United States); Nikles, D. E. [University of Alabama, Department of Chemistry (United States); Harrell, J. W. [University of Alabama, Department of Physics and Astronomy (United States); Thompson, G. B., E-mail: gthompson@eng.ua.ed [University of Alabama, Department of Metallurgical and Materials Engineering (United States)

    2010-08-15

    Ternary alloy FePt(Au) nanoparticles were prepared by the co-reduction of platinum(II) acetylacetonate and gold(III) acetate and the thermal decomposition of iron pentacarbonyl in hot phenyl ether in the presence of oleic acid and oleylamine ligands. This gave spherical particles with an average diameter of 4.4 nm with a range of diameters from approximately 1.6-9 nm. The as-synthesized particles had a solid solution, face-centered-cubic structure. Though the average composition of the particles was Fe{sub 44}Pt{sub 45}Au{sub 11}, individual particle analysis by Scanning Transmission Electron Microscopy-X-ray Energy Dispersive Spectroscopy showed a broad distribution in composition. In general, smaller-sized particles tended to have a lower amount of Au as compared to larger-sized particles. As the Au content increased, the ratio of Fe/Pt widened.

  19. Coexistence of multiple conformations in cysteamine monolayers on Au(111)

    DEFF Research Database (Denmark)

    Zhang, Jingdong; Bilic, A; Reimers, JR;

    2005-01-01

    The structural organization, catalytic function, and electronic properties of cysteamine monolayers on Au(111) have been addressed comprehensively by voltammetry, in situ scanning tunneling microscopy (STM) in anaerobic environment, and a priori molecular dynamics (MD) simulation and STM image si...

  20. Les immigrants dans les regions metropolitaines de recensement au Canada

    OpenAIRE

    Schellenberg, Grant

    2004-01-01

    Dans ce rapport, on examine les facteurs des immigrants dans les regions metropolitaines de recensement (RMR) au Canada, les repercussions sur les services publics offerts dans les regions urbaines et les caracteristiques de l'emploi des immigrants.

  1. EST Table: AU004617 [KAIKOcDNA[Archive

    Lifescience Database Archive (English)

    Full Text Available AU004617 ws20666 10/09/28 54 %/178 aa ref|XP_002430772.1| tyrosine-protein phosphatase corkscrew..., putative [Pediculus humanus corporis] gb|EEB18034.1| tyrosine-protein phosphatase corkscrew,

  2. Assembling Bare Au Nanoparticles at Positively Charged Templates

    Science.gov (United States)

    Wang, Wenjie; Zhang, Honghu; Kuzmenko, Ivan; Mallapragada, Surya; Vaknin, David

    2016-05-01

    In-situ X-ray reflectivity (XRR) and grazing incidence X-ray small-angle scattering (GISAXS) reveal that unfunctionalized (bare) gold nanoparticles (AuNP) spontaneously adsorb to a cationic lipid template formed by a Langmuir monolayer of DPTAP (1,2-dihexadecanoyl-3-trimethylammonium-propane) at vapor/aqueous interfaces. Analysis of the XRR yields the electron density profile across the charged-interfaces along the surface normal showing the AuNPs assemble with vertical thickness comparable to the particle size. The GISAXS analysis indicates that the adsorbed mono-particle layer exhibits short-range in-plane correlations. By contrast, single-stranded DNA-functionalized AuNPs, while attracted to the positively charged surface (more efficiently with the addition of salt to the solution), display less in-plane regular packing compared to bare AuNPs.

  3. Dynamic features of rod-shaped Au nanoclusters

    Science.gov (United States)

    So, Woong Young; Das, Anindita; Wang, Shuxin; Zhao, Shuo; Byun, Hee Young; Lee, Dana; Kumar, Santosh; Jin, Rongchao; Peteanu, Linda A.

    2015-08-01

    Gold nanoclusters hold many potential applications such as biosensing and optics due to their emission characteristics, small size, and non-toxicity. However, their low quantum yields remain problematic for further applications, and their fluorescence mechanism is still unclear. To increase the low quantum yields, various methods have been performed: doping, tuning structures, and changing number of gold atoms. In the past, most characterizations have been performed on spherical shaped nanoclusters; in this paper, several characterizations of various rod-shaped Au nanoclusters specifically on Au25 are shown. It has been determined that the central gold atom in Au25 nano-rod is crucial in fluorescence. Furthermore, single molecule analysis of silver doped Au25 nano-rod revealed that it has more photo-stability than conjugated polymers and quantum dots.

  4. Prolonged reorganization of thiol-capped Au nanoparticles layered structures

    Directory of Open Access Journals (Sweden)

    Sarathi Kundu

    2013-09-01

    Full Text Available Prolonged reorganization behaviour of mono-, di-, tri- and multi-layer films of Au nanoparticles prepared by Langmuir-Blodgett method on hydrophobic Si(001 substrates have been studied by using X-ray scattering techniques. Out-of-plane study shows that although at the initial stage the reorganization occurs through the compaction of the films keeping the layered structure unchanged but finally all layered structures modify to monolayer structure. Due to this reorganization the Au density increases within the nanometer thick films. In-plane study shows that inside the reorganized films Au nanoparticles are distributed randomly and the particle size modifies as the metallic core of Au nanoparticles coalesces.

  5. Ordered Au Nanodisk and Nanohole Arrays: Fabrication and Applications

    KAUST Repository

    Zheng, Yue Bing

    2010-01-01

    We have utilized nanosphere lithography (NSL) to fabricate ordered Au nanodisk and nanohole arrays on substrates and have studied the localized surface plasmon resonance (LSPR) of the arrays. Through these investigations, we demonstrate that the angle- dependent behavior of the LSPR in the Au nanodisk arrays enables real-time observation of exciton-plasmon couplings. In addition, we show that the NSL-fabricated Au nanohole arrays can be applied as templates for patterning micro-/nanoparticles under capillary force. The unique structural and plasmonic characteristics of the Au nanodisk and nano- hole arrays, as well as the low-cost and high-throughput NSL-based nanofabrication technique, render these arrays excellent platforms for numerous engineering applications. © 2010 by ASME.

  6. Ethylene binding to Au/Cu alloy nanoparticles

    Science.gov (United States)

    Gammage, Michael D.; Stauffer, Shannon; Henkelman, Graeme; Becker, Michael F.; Keto, John W.; Kovar, Desiderio

    2016-11-01

    Weak chemisorption of ethylene has been shown to be an important characteristic in the use of metals for the separation of ethylene from ethane. Previously, density functional theory (DFT) has been used to predict the binding energies of various metals and alloys, with Ag having the lowest chemisorption energy amongst the metals and alloys studied. Here Au/Cu alloys are investigated by a combination of DFT calculations and experimental measurements. It is inferred from experiments that the binding energy between a Au/Cu alloy and ethylene is lower than to either of the pure metals, and DFT calculations confirm that this is the case when Au segregates to the particle surface. Implications of this work suggest that it may be possible to further tune the binding energy with ethylene by compositional and morphological control of films produced from Au-surface segregated alloys.

  7. Cent ans d'aller au cinéma

    OpenAIRE

    Arnaud, Pierre,; Augier, Agnès; Augros, Joël; Berthomé, Jean-Pierre; Bertrand, Claude-Jean; Bordat, Francis; Bosséno, Christian-Marc; Dean, John; Etcheverry, Michel; Frey, Nicole Vigouroux; Gomery, Douglas; Masson, Alain; Muraire, André

    2013-01-01

    Aux Etats-Unis plus manifestement encore qu’en Europe, « aller au cinéma » a recouvert des réalités extraordinairement diverses. « Aller au cinéma », en 1902, dans un Hale’s Tours and Scenes of the World n’a rien à voir avec « aller au cinéma » dans un nickelodeon de 1908 ou dans un picture palace de 1925. « Aller au cinéma » dans les années de la Dépression, quand se généralisent les doubles programmes, les primes de fidélité et les loteries, et quand les chômeurs viennent dormir, sinon rêve...

  8. Assembling Bare Au Nanoparticles at Positively Charged Templates

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Wenjie; Zhang, Honghu; Kuzmenko, Ivan; Mallapragada, Surya; Vaknin, David

    2016-05-26

    In-situ X-ray reflectivity (XRR) and grazing incidence X-ray small-angle scattering (GISAXS) reveal that unfunctionalized (bare) gold nanoparticles (AuNP) spontaneously adsorb to a cationic lipid template formed by a Langmuir monolayer of DPTAP (1,2-dihexadecanoyl-3-trimethylammonium-propane) at vapor/aqueous interfaces. Analysis of the XRR yields the electron density profile across the chargedinterfaces along the surface normal showing the AuNPs assemble with vertical thickness comparable to the particle size. The GISAXS analysis indicates that the adsorbed mono-particle layer exhibits shortrange in-plane correlations. By contrast, single-stranded DNA-functionalized AuNPs, while attracted to the positively charged surface (more efficiently with the addition of salt to the solution), display less in-plane regular packing compared to bare AuNPs.

  9. Site Restoration

    Energy Technology Data Exchange (ETDEWEB)

    Noynaert, L.; Bruggeman, A.; Cornelissen, R.; Massaut, V.; Rahier, A

    2001-04-01

    The objectives, the programme, and the achievements of the Site Restoration Department of SCK-CEN in 2000 are summarised. Main activities include the decommissioning of the BR3 PWR-reactor as well as other clean-up activities, projects on waste minimisation and activities related to the management of decommissioning projects. The department provides consultancy and services to external organisations.

  10. Electrochemical Tuning of the Dielectric Function of Au Nanoparticles

    OpenAIRE

    Brown, Ana M.; Sheldon, Matthew T.; Atwater, Harry A.

    2015-01-01

    The tunable dielectric response of Au nanoparticles under electrochemical bias can be interpreted in terms of changes in the surface charge density, surface damping, and the near-surface volume fraction of the nanoparticles that experience a modified dielectric function, as well as changes in the index of refraction of the surrounding electrolyte medium. Using experimental bias-dependent extinction measurements, we derive a potential-dependent dielectric function for Au nanoparticles that acc...

  11. Surface Crystallization in a Liquid AuSi Alloy

    OpenAIRE

    Shpyrko, Oleg G.; Streitel, Reinhard; Balagurusamy, V. S. K.; Grigoriev, Alexei Y.; Deutsch, Moshe; Ocko, Benjamin M; Meron, Mati; Lin, Binhua; Pershan, Peter S.

    2006-01-01

    X-ray measurements reveal a crystalline monolayer at the surface of the eutectic liquid Au_{82}Si_{18}, at temperatures above the alloy's melting point. Surface-induced atomic layering, the hallmark of liquid metals, is also found below the crystalline monolayer. The layering depth, however, is threefold greater than that of all liquid metals studied to date. The crystallinity of the surface monolayer is notable, considering that AuSi does not form stable bulk crystalline phases at any concen...

  12. Wetting of Au and Ag particles on monocrystalline graphite substrates

    Institute of Scientific and Technical Information of China (English)

    Joonho Lee; Toshihiro Tanaka; Kazufumi Seo; Nobumitsu Hirai; Jung-Goo Lee; Hirotaro Mori

    2006-01-01

    The wetting behavior of Au and Ag particles on a monocrystalline graphite substrate was investigated using the microscopic sessile drop method under a purified Ar atmosphere at 1300 K. The measured contact angles of the liquid Au and Ag on monocrystalline graphite substrates of (0001) face were 129° and 124°, respectively. It is believed that the interaction at the interface is dominated by the physical bonding (van der Waal's interaction).

  13. Study on antibacterial activity of chemically synthesized PANI-Ag-Au nanocomposite

    Energy Technology Data Exchange (ETDEWEB)

    Boomi, Pandi [Department of Industrial Chemistry, School of Chemical Sciences, Alagappa University, Karaikudi 630 003, Tamil Nadu (India); Prabu, Halliah Gurumallesh, E-mail: hgprabu2010@gmail.com [Department of Industrial Chemistry, School of Chemical Sciences, Alagappa University, Karaikudi 630 003, Tamil Nadu (India); Manisankar, Paramasivam [Department of Industrial Chemistry, School of Chemical Sciences, Alagappa University, Karaikudi 630 003, Tamil Nadu (India); Ravikumar, Sundaram [Department of Oceanography and Coastal Area Studies, School of Marine Sciences, Alagappa University, Thondi Campus 623 409, Tamil Nadu (India)

    2014-05-01

    Graphical abstract: - Highlights: • New method of synthesizing PANI-Ag-Au nanocomposite. • Surface Plasmon resonance and formation of composite at nano level were analyzed. • HR-TEM study revealed uniform distribution of nanoparticles. • PANI-Ag-Au nanocomposite exhibited good antibacterial activity. - Abstract: Pristine polyaniline (PANI), PANI-Ag, PANI-Au and PANI-Ag-Au nanocomposites have been successfully synthesized by chemical oxidative polymerization method using aniline as monomer, ammonium persulphate as oxidant and metal (Ag, Au and Ag-Au) colloids. UV-Vis analysis exhibited surface Plasmon resonances of Ag, Au, Ag-Au nanoparticles. FT-IR spectra revealed the shift in peak position of N-H stretching. X-ray diffraction (XRD) results confirm the presence of Ag, Au and Au-Ag nanoparticles. HR-TEM images show nanosizes of Ag, Au, Ag-Au and the incorporation of such nanoparticles into the PANI matrix. Pristine PANI, PANI-Ag, PANI-Au and PANI-Ag-Au nanocomposites were tested for antibacterial activity by agar well diffusion method. PANI-Ag-Au nanocomposite exhibited higher antibacterial activity against both gram-positive [Streptococcus sp. (MTCC 890), Staphylococcus sp. (MTCC 96)] and gram-negative bacteria [Escherichia coli (MTCC 1671) and Klebsiella sp. (MTCC 7407)] when compared with PANI-Ag nanocomposite, PANI-Au nanocomposite and pristine PANI. The novelty of this study is the polymer-bimetal synthesis and its antibacterial potential.

  14. Environment-modulated Kondo phenomena in FePc/Au(111) adsorption systems

    Science.gov (United States)

    Wang, Yu; Zheng, Xiao; Yang, Jinlong

    2016-03-01

    Recent scanning tunneling microscopy experiments on electron transport through iron(II) phthalocyanine (FePc) molecules adsorbed on the Au(111) surface have revealed that the measured Kondo conductance signature depends strongly on the specific adsorption site. To understand the physical origin of experimental observations, particularly the variation of Kondo features with the molecular adsorption site, we employ a combined density functional theory (DFT) and hierarchical equations of motion (HEOM) approach to investigate the electronic structure and Kondo correlation in FePc/Au(111) composite systems. The calculation results indicate that, for the on-top adsorption configuration, the two degenerate spin-unpaired dπ orbitals on the Fe center are coupled indirectly through substrate band states, leading to the Fano-like antiresonance line shape in the d I /d V spectra, while for the bridge adsorption configuration, the environment-induced couplings are largely suppressed because of the two different spin-unpaired d orbitals. Therefore, our work suggests that the environment-induced coupling as an essential physical factor could greatly influence the Fano-Kondo features in magnetic molecule/metal composites, and the crucial role of local orbital degeneracy and symmetry is discovered. These findings provide important insights into the electron correlation effects in complex solid-state systems. The usefulness and practicality of the combined DFT+HEOM method is also highlighted.

  15. Structural and dynamical properties of liquid Al-Au alloys

    Science.gov (United States)

    Peng, H. L.; Voigtmann, Th.; Kolland, G.; Kobatake, H.; Brillo, J.

    2015-11-01

    We investigate temperature- and composition-dependent structural and dynamical properties of Al-Au melts. Experiments are performed to obtain accurate density and viscosity data. The system shows a strong negative excess volume, similar to other Al-based binary alloys. We develop a molecular-dynamics (MD) model of the melt based on the embedded-atom method (EAM), gauged against the available experimental liquid-state data. A rescaling of previous EAM potentials for solid-state Au and Al improves the quantitative agreement with experimental data in the melt. In the MD simulation, the admixture of Au to Al can be interpreted as causing a local compression of the less dense Al system, driven by less soft Au-Au interactions. This local compression provides a microscopic mechanism explaining the strong negative excess volume of the melt. We further discuss the concentration dependence of self- and interdiffusion and viscosity in the MD model. Al atoms are more mobile than Au, and their increased mobility is linked to a lower viscosity of the melt.

  16. Surface segregation phenomena in extended and nanoparticle surfaces of Cu-Au alloys

    Science.gov (United States)

    Li, Jonathan; Wang, Guofeng; Zhou, Guangwen

    2016-07-01

    Using density functional theory (DFT) and Monte Carlo (MC) simulations, we studied the surface segregation phenomena of Au atoms in the extended and nanoparticle surfaces of Cu-Au alloys. Our MC simulations predicted significant Au enrichment in the outermost layer of (111) and (100) extended surfaces, and Au enrichment in the two outermost layers of (110) extended surfaces. The equilibrium Cu-Au nanoparticles were predicted to develop into an Au-enriched shell structure, where Au atoms preferably segregate to the (100) facets while Cu atoms are mainly located on the (111) facet of the nanoparticles. Our simulation predictions agree with experimental measurements.

  17. Rapidity dependency of (Anti)-deuteron Coalescence in Au-Au collisions

    Science.gov (United States)

    Murray, Michael

    2009-05-01

    The coalescence of protons and neutrons into deuterons is sensitive to the space-time extent of the baryon freeze-out region. The coalescence parameter and the phase space density recast the information contained in the proton and deuteron spectra into ``chemical" and ``dynamic" terms. The phase space density is sensitive to the chemical potential and the temperature of the system. The coalescence parameter B2 can be interpreted in terms of a ``volume of homogeniety" which depends upon the temperature of the system and the radial flow. The large rapidity and pT coverage with good particle identification of the BRAHMS spectrometers allow us to measure the rapidity dependence of the volume, which is proportional to 1/B2, and the phase space density of the (anti)-proton source for central Au+Au collisions. We find that B2(pT) is almost independent of rapidity and beam energy. Interpreting 1/B2 as a volume gives numbers that are very close to HBT data and a size which steadily drops with pT. We find that B2(pT) is the same for protons and antiprotons. The phase space density has a weak rapidity dependence but varies rapidily with energy. These results in conjunction with other forward rapidity data start to give us a picture of the longitudinal evolution of the source at RHIC energies. Supported by NSF CAREER award 0449913

  18. A first look at Au + Au collisions at RHIC energies using the PHOBOS detector

    Indian Academy of Sciences (India)

    Birger Back; M D Baker; D S Barton; R R Betts; R Bindel; A Budzanowski; W Busza; A Carroll; J Corbo; M P Decowski; E Garcia; N George; K Gulbrandsen; S Gushue; C Halliwell; J Hamblen; G A Heintzelman; C Henderson; D Hicks; D J Hofman; R Hollis; R Holyńiski; B Holzman; A Iordanova; E Johnson; J L Kane; J Katzy; N Khan; W Kucewicz; P Kulinich; C M Kuo; W T Lin; S Manly; D McLeod; J Michalowski; A C Mignerey; J Mülmenstädt; R Nouicer; A Olszewski; R Pak; I C Park; H Pernegger; M Rafelski; M Rbeiz; C Reed; L P Remsberg; M Reuter; C Roland; G Roland; L Rosenberg; J Sagerer; P Sarin; P Sawicki; W Skulski; S G Steadman; P Steinberg; G S F Stephans; M Stodulski; A Sukhanov; J-L Tang; R Teng; A Trzupek; C Vale; G J van Nieuwenhuizen; R Verdier; B Wadsworth; F L H Wolfs; B Wosiek; K Woźniak; A H Wuosmaa; B Wyslouch

    2003-05-01

    The PHOBOS detector has been used to study Au + Au collisions at $\\sqrt{S_{NN}}=56$, 130, and 200 GeV. Several global observables have been measured and the results are compared with theoretical models. These observables include the charged-particle multiplicity measured as a function of beam energy, pseudo-rapidity, and centrality of the collision. A unique feature of the PHOBOS detector is its almost complete angular coverage such that these quantities can be studied over a pseudo-rapidity interval of ||≤ 5.4. This allows for an almost complete integration of the total charged particle yield, which is found to be about $N^{\\text{tot}}_{\\text{ch}}=4500± 470$ at $\\sqrt{S_{NN}}=130$ GeV and $N^{\\text{tot}}_{\\text{ch}}=5300± 530$ at $\\sqrt{S_{NN}}$ GeV. The ratio of anti-particles to particles emitted in the mid-rapidity region has also been measured using the PHOBOS magnetic spectrometer. Of particular interest is the ratio of anti-protons to protons in the mid-rapidity region, which was found to be $\\overline{p}/p= 0.6± 0.04$(stat) ± 0.06(syst) at $\\sqrt{S_{NN}}=130$ GeV. This high value suggests that an almost baryon-free region has been produced in the collisions.

  19. Thermal Description of Particle Production in Au-Au Collisions at STAR Energies

    CERN Document Server

    Tawfik, A

    2013-01-01

    The hadron ratios measured in central Au-Au collisions are analysed by means of Hadron Resonance Gas (HRG) model over a wide range of nucleon-nucleon center-of-mass energies ranging from 7.7 to 200 GeV as offered by the STAR Beam Energy Scan I (BES-I). We restrict the discussion on STAR BES-I, because of large statistics and over all homogeneity of STAR measurements (one detector) against previous experiments. Over the last three decades, various heavy-ion experiments utilizing different detectors (different certainties) have been carried out. Regularities in produced particles at different energies haven been studied. The temperature and baryon chemical potential are deduced from fits of experimental ratios to thermal model calculations assuming chemical equilibrium. We find that the resulting freeze-out parameters using single hard-core value and point-like constituents of HRG are identical. This implies that the excluded-volume comes up with no effect on the extracted parameters. We compare the results wit...

  20. Azimuthal anisotropy in U+U and Au+Au collisions at RHIC

    CERN Document Server

    Adamczyk, L; Agakishiev, G; Aggarwal, M M; Ahammed, Z; Alekseev, I; Alford, J; Aparin, A; Arkhipkin, D; Aschenauer, E C; Averichev, G S; Bairathi, V; Banerjee, A; Bellwied, R; Bhasin, A; Bhati, A K; Bhattarai, P; Bielcik, J; Bielcikova, J; Bland, L C; Bordyuzhin, I G; Bouchet, J; Brandin, A V; Bunzarov, I; Butterworth, J; Caines, H; Sánchez, M Calderón de la Barca; Campbell, J M; Cebra, D; Cervantes, M C; Chakaberia, I; Chaloupka, P; Chang, Z; Chattopadhyay, S; Chen, J H; Chen, X; Cheng, J; Cherney, M; Christie, W; Contin, G; Crawford, H J; Das, S; De Silva, L C; Debbe, R R; Dedovich, T G; Deng, J; Derevschikov, A A; di Ruzza, B; Didenko, L; Dilks, C; Dong, X; Drachenberg, J L; Draper, J E; Du, C M; Dunkelberger, L E; Dunlop, J C; Efimov, L G; Engelage, J; Eppley, G; Esha, R; Evdokimov, O; Eyser, O; Fatemi, R; Fazio, S; Federic, P; Fedorisin, J; Feng, Z; Filip, P; Fisyak, Y; Flores, C E; Fulek, L; Gagliardi, C A; Garand, D; Geurts, F; Gibson, A; Girard, M; Greiner, L; Grosnick, D; Gunarathne, D S; Guo, Y; Gupta, A; Gupta, S; Guryn, W; Hamad, A; Hamed, A; Haque, R; Harris, J W; He, L; Heppelmann, S; Hirsch, A; Hoffmann, G W; Hofman, D J; Horvat, S; Huang, B; Huang, H Z; Huang, X; Huck, P; Humanic, T J; Igo, G; Jacobs, W W; Jang, H; Jiang, K; Judd, E G; Kabana, S; Kalinkin, D; Kang, K; Kauder, K; Ke, H W; Keane, D; Kechechyan, A; Khan, Z H; Kikola, D P; Kisel, I; Kisiel, A; Kochenda, L; Koetke, D D; Kollegger, T; Kosarzewski, L K; Kraishan, A F; Kravtsov, P; Krueger, K; Kulakov, I; Kumar, L; Kycia, R A; Lamont, M A C; Landgraf, J M; Landry, K D; Lauret, J; Lebedev, A; Lednicky, R; Lee, J H; Li, X; Li, Z M; Li, Y; Li, W; Li, C; Lisa, M A; Liu, F; Ljubicic, T; Llope, W J; Lomnitz, M; Longacre, R S; Luo, X; Ma, G L; Ma, R; Ma, Y G; Ma, L; Magdy, N; Majka, R; Manion, A; Margetis, S; Markert, C; Masui, H; Matis, H S; McDonald, D; Meehan, K; Minaev, N G; Mioduszewski, S; Mishra, D; Mohanty, B; Mondal, M M; Morozov, D A; Mustafa, M K; Nandi, B K; Nasim, Md; Nayak, T K; Nigmatkulov, G; Nogach, L V; Noh, S Y; Novak, J; Nurushev, S B; Odyniec, G; Ogawa, A; Oh, K; Okorokov, V; Olvitt, D; Page, B S; Pak, R; Pan, Y X; Pandit, Y; Panebratsev, Y; Pawlik, B; Pei, H; Perkins, C; Peterson, A; Pile, P; Planinic, M; Pluta, J; Poljak, N; Poniatowska, K; Porter, J; Posik, M; Poskanzer, A M; Putschke, J; Qiu, H; Quintero, A; Ramachandran, S; Raniwala, R; Raniwala, S; Ray, R L; Ritter, H G; Roberts, J B; Rogachevskiy, O V; Romero, J L; Roy, A; Ruan, L; Rusnak, J; Rusnakova, O; Sahoo, N R; Sahu, P K; Sakrejda, I; Salur, S; Sandweiss, J; Sarkar, A; Schambach, J; Scharenberg, R P; Schmah, A M; Schmidke, W B; Schmitz, N; Seger, J; Seyboth, P; Shah, N; Shahaliev, E; Shanmuganathan, P V; Shao, M; Sharma, M K; Sharma, B; Shen, W Q; Shi, S S; Shou, Q Y; Sichtermann, E P; Sikora, R; Simko, M; Skoby, M J; Smirnov, N; Smirnov, D; Song, L; Sorensen, P; Spinka, H M; Srivastava, B; Stanislaus, T D S; Stepanov, M; Stock, R; Strikhanov, M; Stringfellow, B; Sumbera, M; Summa, B; Sun, Z; Sun, X M; Sun, Y; Sun, X; Surrow, B; Svirida, N; Szelezniak, M A; Tang, Z; Tang, A H; Tarnowsky, T; Tawfik, A; Thomas, J H; Timmins, A R; Tlusty, D; Tokarev, M; Trentalange, S; Tribble, R E; Tribedy, P; Tripathy, S K; Trzeciak, B A; Tsai, O D; Ullrich, T; Underwood, D G; Upsal, I; Van Buren, G; van Nieuwenhuizen, G; Vandenbroucke, M; Varma, R; Vasiliev, A N; Vertesi, R; Videbæk, F; Viyogi, Y P; Vokal, S; Voloshin, S A; Vossen, A; Wang, G; Wang, H; Wang, J S; Wang, Y; Wang, F; Webb, J C; Webb, G; Wen, L; Westfall, G D; Wieman, H; Wissink, S W; Witt, R; Wu, Y F; Xiao, Z G; Xie, W; Xin, K; Xu, Y F; Xu, Q H; Xu, H; Xu, N; Xu, Z; Yang, Y; Yang, C; Yang, S; Yang, Q; Ye, Z; Yepes, P; Yi, L; Yip, K; Yoo, I -K; Yu, N; Zbroszczyk, H; Zha, W; Zhang, J B; Zhang, Z; Zhang, J; Zhang, S; Zhang, X P; Zhang, Y; Zhao, J; Zhong, C; Zhou, L; Zhu, X; Zoulkarneeva, Y; Zyzak, M

    2015-01-01

    Collisions between prolate uranium nuclei are used to study how particle production and azimuthal anisotropies depend on initial geometry in heavy-ion collisions. We report the two- and four-particle cumulants, $v_2\\{2\\}$ and $v_2\\{4\\}$, for charged hadrons from U+U collisions at $\\sqrt{s_{\\rm NN}}$ = 193 GeV and Au+Au collisions at $\\sqrt{s_{\\rm NN}}$ = 200 GeV. Nearly fully overlapping collisions are selected based on the amount of energy deposited by spectators in the STAR Zero Degree Calorimeters (ZDCs). Within this sample, the observed dependence of $v_2\\{2\\}$ on multiplicity demonstrates that ZDC information combined with multiplicity can preferentially select different overlap configurations in U+U collisions. An initial-state model with gluon saturation describes the slope of $v_2\\{2\\}$ as a function of multiplicity in central collisions better than one based on Glauber with a two-component multiplicity model.

  1. Bimodality in binary Au + Au collisions from 60 to 100 MeV/u

    International Nuclear Information System (INIS)

    The deexcitation of quasi-projectiles (QP) released in binary Au on Au collisions as been studied from 60 to 100 MeV/u. Bimodality between two different decay patterns has been observed for intermediate violence collisions. The main experimental result is that the system jumps from one mode to the other on a narrow range of energy deposit and/or impact parameter. The sorting of the events (according to the violence of the collision) has been provided by the perpendicular energy of the light charged particles emitted on the quasi-target side. Such a sorting prevents spurious autocorrelation effects between the sorting variable and the observed mechanism. The two modes of the QP decay correspond on the one side to residue or fission fragments production, and on the other side to the multifragmentation channel. A detailed study has been performed in order to try to establish the origin of the observed bimodality in disentangling dynamical or geometrical effects from bulk matter properties linked with a liquid-gas type phase transition. The whole set of data is coherent with a dominant role of the deposited excitation energy as it is expected from theoretical arguments.(lattice gas model) in the framework of a liquid-gas phase transition picture. (authors)

  2. Phospholipid Encapsulated AuNR@Ag/Au Nanosphere SERS Tags with Environmental Stimulus Responsive Signal Property.

    Science.gov (United States)

    Su, Xueming; Wang, Yunqing; Wang, Wenhai; Sun, Kaoxiang; Chen, Lingxin

    2016-04-27

    Surface-enhanced Raman scattering (SERS) tags draw much attention due to the ultrasensitivity and multiplex labeling capability. Recently, a new kind of SERS tags was rationally designed by encapsulating metal nanoparticles with phospholipid bilayers, showing great potential in theranostics. The lipid bilayer coating confers biocompatibility and versatility to changing surface chemistry of the tag; however, its "soft" feature may influence SERS signal stability, which is rarely investigated. Herein, we prepared phospholipid-coated AuNR@Ag/Au nanosphere SERS tags by using three different kinds of Raman reporters, i.e., thio-containing 4-nitrothiophenol (NT), nitrogen-containing hydrophobic chromophore cyanine 7 monoacid (Cy7), and alkyl chain-chromophore conjugate 1,1'-dioctadecyl-3,3,3',3'-tetramethylindodicarbocyanine (DiD). It was found that signal responses were different upon additional stimulation which the tags may encounter in theranostic applications including the presence of detergent Triton X-100, lipid membrane, and photothermal treatment. Living-cell imaging also showed signal changing distinction. The different SERS signal performances were attributed to the different Raman reporter releasing behaviors from the tags. This work revealed that Raman reporter structure determined signal stability of lipid-coated SERS tags, providing guidance for the design of stimulus responsive tags. Moreover, it also implied the potential of SERS technique for real time drug release study of lipid based nanomedicine. PMID:27052206

  3. Entropy in central Au+Au reactions between 100 and 400{ital A} MeV

    Energy Technology Data Exchange (ETDEWEB)

    Dzelalija, M.; Cindro, N.; Basrak, Z.; Caplar, R.; Hoelbling, S.; Bini, M.; Maurenzig, P.R.; Olmi, A.; Pasquali, G.; Poggi, G.; Taccetti, N.; Cerruti, C.; Coffin, J.P.; Dona, R.; Fintz, P.; Guillaume, G.; Houari, A.; Jundt, F.; Kuhn, C.; Rami, F.; Tezkratt, R.; Wagner, P.; Biegansky, J.; Kotte, R.; Moesner, J.; Neubert, W.; Wohlfarth, D.; Alard, J.P.; Amouroux, V.; Bastid, N.; Berger, L.; Belayev, I.; Boussange, S.; Buta, A.; Dupieux, P.; Eroe, J.; Fodor, Z.; Fraysse, L.; Gobbi, A.; Herrmann, N.; Hildenbrand, K.D.; Ibnouzahir, M.; Kecskemeti, J.; Koncz, P.; Korchagin, Y.; Kraemer, M.; Lebedev, A.; Legrand, I.; Manko, V.; Mgebrishvili, G.; Moisa, D.; Montarou, G.; Montbel, I.; Pelte, D.; Petrovici, M.; Pras, P.; Ramillien, V.; Reisdorf, W.; Schuell, D.; Seres, Z.; Sikora, B.; Simion, V.; Smolyankin, S.; Sodan, U.; Trzaska, M.; Vasiliev, M.A.; Wessels, J.P.; Wienold, T.; Wilhelmi, Z.; Zhilin, A.V. [Institute for Physics and Nuclear Engineering, Bucharest (Romania)]|[Central Research Institute for Physics, Budapest (Hungary)]|[Laboratoire de Physique Corpusculaire, Clermont-Ferrand (France)]|[Gesellschaft fuer Schwerionenforschung, Darmstadt (Germany)]|[I.N.F.N. and University of Florence, Florence (Italy)]|[Physikalisches Institut der Universitaet Heidelberg, Heidelberg (Germany)]|[Institute for Experimental and Theoretical Physics, Moscow (Russian Federation)]|[Kurchatov Institute for Atomic Energy, Moscow (Russian Federation)]|[Forschungzentrum, Rossendorf (Germany)]|[Department of Physics, University of Split, Split (Croatia)]|[Centre de Recherches Nucleaires, IN2P3-CNRS, Universite Louis Pasteur, Strasbourg (France)]|[Institute of Experimental Physics, Warsaw University, Warsaw (Poland)]|[Rudjer Boskovic Institute, Zagreb (Croatia)

    1995-07-01

    The ratio of the total charge bound in fragments with {ital Z} between 2 and 15 to the hydrogen yield, ({ital tsum}{sub 2}{sup 15}{ital M}{sub {ital i}{ital Z}{ital i}})/{ital M}{sub {ital H}}, has been measured, and the neutron-to-proton ratio {ital n}/{ital p} has been estimated from the data of central Au + Au reactions between 100 and 400{ital A} MeV, measured with the phase I setup of the detector system FOPI and GSI, Darmstadt, in the polar-angle range between 7{degree} and 30{degree}. These two quantities were used to determine the entropy per nucleon {ital S}/{ital A} by comparing them with the predictions of the FREESCO code. The analysis allows the simulataneous extraction of the values of the baryonic entropy, temperature, and collective flow. The extracted values are in good agreement with the values obtained in earlier FOPI studies, and, for the baryonic entropy, with recent hydrodynamic calculations.

  4. Shape of collective flow in highly central Au(150 A MeV)+Au collisions

    Energy Technology Data Exchange (ETDEWEB)

    Roy, C. [Universite Louis Pasteur, Strasbourg (France). Centre de Recherches Nucl.; Kuhn, C. [Universite Louis Pasteur, Strasbourg (France). Centre de Recherches Nucl.; Coffin, J.P. [Universite Louis Pasteur, Strasbourg (France). Centre de Recherches Nucl.; Crochet, P. [Universite Louis Pasteur, Strasbourg (France). Centre de Recherches Nucl.; Fintz, P. [Universite Louis Pasteur, Strasbourg (France). Centre de Recherches Nucl.; Guillaume, G. [Universite Louis Pasteur, Strasbourg (France). Centre de Recherches Nucl.; Jundt, F. [Universite Louis Pasteur, Strasbourg (France). Centre de Recherches Nucl.; Maazouzi, C. [Universite Louis Pasteur, Strasbourg (France). Centre de Recherches Nucl.; Rami, F. [Universite Louis Pasteur, Strasbourg (France). Centre de Recherches Nucl.; Tizniti, L. [Universite Louis Pasteur, Strasbourg (France). Centre de Recherches Nucl.; Wagner, P. [Universite Louis Pasteur, Strasbourg (France). Centre de Recherches Nucl.; Alard, J.P.; Amouroux, V.; Basrak, Z.; Bastid, N.; Belyaev, I.; Best, D.; Biegansky, J.; Buta, A.; Caplar, R.; Cindro, N.; Dona, R.; Dupieux, P.; Dzelalija, M.; Fan, Z.G.; Fodor, Z.; Fraysse, L.; Gobbi, A.; Herrmann, N.; Hildenbrand, K.D.; Hoelbling, S.; Hong, B.; Jeong, S.C.; Kecskemeti, J.; Kirejczyk, M.; Koncz, P.; Korchagin, Y.; Kotte, R.; Lebedev, A.; Legrand, I.; Leifels, Y.; Manko, V.; Mgebrishvili, G.; Moisa, D.; Moesner, J.; Neubert, W.; Pelte, D.; Petrovici, M.; Pinkenburg, C.; Pras, P.; Reisdorf, W.; Ritman, J.L.; Sadchikov, A.G.; Schuell, D.; Seres, Z.; Sikora, B.; Simion, V.; Smolyankin, V.; Sodan, U.; Trzaska, M.; Vasiliev, M.; Wang, G.S.; Wessels, J.P.; Wienold, T.; Wohlfarth, D.; Zhilin, A.; Konopka, J.; Stoecker, H.

    1997-06-01

    Using the FOPI facility at GSI, charged particles (1{<=}Z{<=}6) produced in the Au(150 A MeV)+Au reaction have been measured at laboratory angles 1.2{sup 0}<{Theta}{sub lab}<30{sup 0}. Highly central collisions have been selected with two criteria, both dealing with the longitudinal and transverse degrees of freedom of the reaction. The relevance of this selection method is supported by QMD calculations which indicate that such criteria are able to select mean impact parameters less than 2 fm. Bias effects introduced by the criteria have been evaluated. The centre-of-mass polar angle distributions of low energy clusters emitted in these central collisions, have been extracted: the intensity ratio deduced for a transverse to longitudinal emission is found to be R=1.4{sup +0.2}{sub -0.4}. Model comparisons using QMD are presented. The value of R appears to depend sensitively on the nucleon-nucleon cross section, {sigma}{sub nn}. Within this model, a value of {sigma}{sub nn}=25{+-}5 mb is derived. (orig.). With 2 figs.

  5. Thermal photon production in Au + Au collisions: Viscous corrections in two different hydrodynamic formalisms

    Energy Technology Data Exchange (ETDEWEB)

    Peralta-Ramos, J., E-mail: jperalta@ift.unesp.b [Instituto de Fisica Teorica, Universidade Estadual Paulista, Rua Doutor Bento Teobaldo Ferraz 271, Bloco II, 01140-070 Sao Paulo (Brazil); Nakwacki, M.S., E-mail: sole@iafe.uba.a [Instituto de Astronomia, Geofisica e Ciencias Atmosfericas, Universidade de Sao Paulo, Rua do Matao 1226, Cidade Universitaria, 05508-090 Sao Paulo (Brazil)

    2011-02-01

    We calculate the spectra of produced thermal photons in Au + Au collisions taking into account the nonequilibrium contribution to photon production due to finite shear viscosity. The evolution of the fireball is modeled by second-order as well as by divergence-type 2+1 dissipative hydrodynamics, both with an ideal equation of state and with one based on Lattice QCD that includes an analytical crossover. The spectrum calculated in the divergence-type theory is considerably enhanced with respect to the one calculated in the second-order theory, the difference being entirely due to differences in the viscous corrections to photon production. Our results show that the differences in hydrodynamic formalisms are an important source of uncertainty in the extraction of the value of {eta}/s from measured photon spectra. The uncertainty in the value of {eta}/s associated with different hydrodynamic models used to compute thermal photon spectra is larger than the one occurring in matching hadron elliptic flow to RHIC data.

  6. Bimodality in binary Au + Au collisions from 60 to 100 MeV/u

    Energy Technology Data Exchange (ETDEWEB)

    Pichon, M.; Tamain, B.; Bougault, R. [Caen Univ., Lab. de Physique Corpusculaire, IN2P3-CNRS, ISMRA, 14 (France)] [and others

    2003-03-01

    The deexcitation of quasi-projectiles (QP) released in binary Au on Au collisions as been studied from 60 to 100 MeV/u. Bimodality between two different decay patterns has been observed for intermediate violence collisions. The main experimental result is that the system jumps from one mode to the other on a narrow range of energy deposit and/or impact parameter. The sorting of the events (according to the violence of the collision) has been provided by the perpendicular energy of the light charged particles emitted on the quasi-target side. Such a sorting prevents spurious autocorrelation effects between the sorting variable and the observed mechanism. The two modes of the QP decay correspond on the one side to residue or fission fragments production, and on the other side to the multifragmentation channel. A detailed study has been performed in order to try to establish the origin of the observed bimodality in disentangling dynamical or geometrical effects from bulk matter properties linked with a liquid-gas type phase transition. The whole set of data is coherent with a dominant role of the deposited excitation energy as it is expected from theoretical arguments.(lattice gas model) in the framework of a liquid-gas phase transition picture. (authors)

  7. Dielectron production in Au$+$Au collisions at $\\sqrt{s_{NN}}$=200 GeV

    CERN Document Server

    Adare, A; Ajitanand, N N; Akiba, Y; Akimoto, R; Alexander, J; Alfred, M; Al-Ta'ani, H; Angerami, A; Aoki, K; Apadula, N; Aramaki, Y; Asano, H; Aschenauer, E C; Atomssa, E T; Averbeck, R; Awes, T C; Azmoun, B; Babintsev, V; Bai, M; Bandara, N S; Bannier, B; Barish, K N; Bassalleck, B; Bathe, S; Baublis, V; Baumgart, S; Bazilevsky, A; Beaumier, M; Beckman, S; Belmont, R; Berdnikov, A; Berdnikov, Y; Blau, D S; Bok, J S; Boyle, K; Brooks, M L; Bryslawskyj, J; Buesching, H; Bumazhnov, V; Butsyk, S; Campbell, S; Castera, P; Chen, C -H; Chi, C Y; Chiu, M; Choi, I J; Choi, J B; Choi, S; Choudhury, R K; Christiansen, P; Chujo, T; Chvala, O; Cianciolo, V; Citron, Z; Cole, B A; Connors, M; Csanád, M; Csörgő, T; Dairaku, S; Danley, D; Datta, A; Daugherity, M S; David, G; DeBlasio, K; Dehmelt, K; Denisov, A; Deshpande, A; Desmond, E J; Dharmawardane, K V; Dietzsch, O; Ding, L; Dion, A; Diss, P B; Do, J H; Donadelli, M; D'Orazio, L; Drapier, O; Drees, A; Drees, K A; Durham, J M; Durum, A; Edwards, S; Efremenko, Y V; Engelmore, T; Enokizono, A; Esumi, S; Eyser, K O; Fadem, B; Feege, N; Fields, D E; Finger, M; Jr., \\,; Fleuret, F; Fokin, S L; Frantz, J E; Franz, A; Frawley, A D; Fukao, Y; Fusayasu, T; Gainey, K; Gal, C; Gallus, P; Garg, P; Garishvili, A; Garishvili, I; Ge, H; Giordano, F; Glenn, A; Gong, X; Gonin, M; Goto, Y; de Cassagnac, R Granier; Grau, N; Greene, S V; Perdekamp, M Grosse; Gunji, T; Guo, L; Gustafsson, H -Å; Hachiya, T; Haggerty, J S; Hahn, K I; Hamagaki, H; Hamilton, H F; Han, S Y; Hanks, J; Hasegawa, S; Haseler, T O S; Hashimoto, K; Haslum, E; Hayano, R; He, X; Hemmick, T K; Hester, T; Hill, J C; Hollis, R S; Homma, K; Hong, B; Horaguchi, T; Hori, Y; Hoshino, T; Hotvedt, N; Huang, J; Huang, S; Ichihara, T; Iinuma, H; Ikeda, Y; Imai, K; Imrek, J; Inaba, M; Iordanova, A; Isenhower, D; Issah, M; Ivanishchev, D; Jacak, B V; Javani, M; Jezghani, M; Jia, J; Jiang, X; Johnson, B M; Joo, K S; Jouan, D; Jumper, D S; Kamin, J; Kanda, S; Kaneti, S; Kang, B H; Kang, J H; Kang, J S; Kapustinsky, J; Karatsu, K; Kasai, M; Kawall, D; Kazantsev, A V; Kempel, T; Key, J A; Khachatryan, V; Khanzadeev, A; Kijima, K M; Kim, B I; Kim, C; Kim, D J; Kim, E -J; Kim, G W; Kim, H J; Kim, K -B; Kim, M; Kim, Y -J; Kim, Y K; Kimelman, B; Kinney, E; Kiss, Á; Kistenev, E; Kitamura, R; Klatsky, J; Kleinjan, D; Kline, P; Koblesky, T; Komatsu, Y; Komkov, B; Koster, J; Kotchetkov, D; Kotov, D; Král, A; Krizek, F; Kunde, G J; Kurita, K; Kurosawa, M; Kwon, Y; Kyle, G S; Lacey, R; Lai, Y S; Lajoie, J G; Lebedev, A; Lee, B; Lee, D M; Lee, J; Lee, K B; Lee, K S; Lee, S; Lee, S H; Lee, S R; Leitch, M J; Leite, M A L; Leitgab, M; Lewis, B; Li, X; Lim, S H; Levy, L A Linden; Liu, M X; Love, B; Lynch, D; Maguire, C F; Makdisi, Y I; Makek, M; Manion, A; Manko, V I; Mannel, E; Masumoto, S; McCumber, M; McGaughey, P L; McGlinchey, D; McKinney, C; Meles, A; Mendoza, M; Meredith, B; Miake, Y; Mibe, T; Mignerey, A C; Milov, A; Mishra, D K; Mitchell, J T; Miyachi, Y; Miyasaka, S; Mizuno, S; Mohanty, A K; Mohapatra, S; Montuenga, P; Moon, H J; Moon, T; Morrison, D P; Motschwiller, S; Moukhanova, T V; Murakami, T; Murata, J; Mwai, A; Nagae, T; Nagamiya, S; Nagashima, K; Nagle, J L; Nagy, M I; Nakagawa, I; Nakagomi, H; Nakamiya, Y; Nakamura, K R; Nakamura, T; Nakano, K; Nattrass, C; Nederlof, A; Netrakanti, P K; Nihashi, M; Niida, T; Nishimura, S; Nouicer, R; Novak, T; Novitzky, N; Nyanin, A S; O'Brien, E; Ogilvie, C A; Okada, K; Koop, J D Orjuela; Osborn, J D; Oskarsson, A; Ouchida, M; Ozawa, K; Pak, R; Pantuev, V; Papavassiliou, V; Park, B H; Park, I H; Park, J S; Park, S; Park, S K; Pate, S F; Patel, L; Patel, M; Pei, H; Peng, J -C; Pereira, H; Perepelitsa, D V; Perera, G D N; Peressounko, D Yu; Perry, J; Petti, R; Pinkenburg, C; Pinson, R; Pisani, R P; Proissl, M; Purschke, M L; Qu, H; Rak, J; Ramson, B J; Ravinovich, I; Read, K F; Reynolds, D; Riabov, V; Riabov, Y; Richardson, E; Rinn, T; Roach, D; Roche, G; Rolnick, S D; Rosati, M; Rowan, Z; Rubin, J G; Sahlmueller, B; Saito, N; Sakaguchi, T; Sako, H; Samsonov, V; Sano, M; Sarsour, M; Sato, S; Sawada, S; Schaefer, B; Schmoll, B K; Sedgwick, K; Seidl, R; Sen, A; Seto, R; Sett, P; Sexton, A; Sharma, D; Shein, I; Shibata, T -A; Shigaki, K; Shimomura, M; Shoji, K; Shukla, P; Sickles, A; Silva, C L; Silvermyr, D; Sim, K S; Singh, B K; Singh, C P; Singh, V; Slunečka, M; Snowball, M; Soltz, R A; Sondheim, W E; Sorensen, S P; Sourikova, I V; Stankus, P W; Stenlund, E; Stepanov, M; Ster, A; Stoll, S P; Sugitate, T; Sukhanov, A; Sumita, T; Sun, J; Sziklai, J; Takagui, E M; Takahara, A; Taketani, A; Tanaka, Y; Taneja, S; Tanida, K; Tannenbaum, M J; Tarafdar, S; Taranenko, A; Tennant, E; Themann, H; Tieulent, R; Timilsina, A; Todoroki, T; Tomášek, L; Tomášek, M; Torii, H; Towell, C L; Towell, R; Towell, R S; Tserruya, I; Tsuchimoto, Y; Tsuji, T; Vale, C; van Hecke, H W; Vargyas, M; Vazquez-Zambrano, E; Veicht, A; Velkovska, J; Vértesi, R; Virius, M; Vossen, A; Vrba, V; Vznuzdaev, E; Wang, X R; Watanabe, D; Watanabe, K; Watanabe, Y; Watanabe, Y S; Wei, F; Wei, R; White, A S; White, S N; Winter, D; Wolin, S; Woody, C L; Wysocki, M; Xia, B; Xue, L; Yalcin, S; Yamaguchi, Y L; Yang, R; Yanovich, A; Ying, J; Yokkaichi, S; Yoo, J H; Yoon, I; You, Z; Younus, I; Yu, H; Yushmanov, I E; Zajc, W A; Zelenski, A; Zhou, S; Zou, L

    2015-01-01

    We present measurements of $e^+e^-$ production at midrapidity in Au$+$Au collisions at $\\sqrt{s_{_{NN}}}$ = 200 GeV. The invariant yield is studied within the PHENIX detector acceptance over a wide range of mass ($m_{ee} <$ 5 GeV/$c^2$) and pair transverse momentum ($p_T$ $<$ 5 GeV/$c$), for minimum bias and for five centrality classes. The \\ee yield is compared to the expectations from known sources. In the low-mass region ($m_{ee}=0.30$--0.76 GeV/$c^2$) there is an enhancement that increases with centrality and is distributed over the entire pair \\pt range measured. It is significantly smaller than previously reported by the PHENIX experiment and amounts to $2.3\\pm0.4({\\rm stat})\\pm0.4({\\rm syst})\\pm0.2^{\\rm model}$ or to $1.7\\pm0.3({\\rm stat})\\pm0.3({\\rm syst})\\pm0.2^{\\rm model}$ for minimum bias collisions when the open-heavy-flavor contribution is calculated with {\\sc pythia} or {\\sc mc@nlo}, respectively. The inclusive mass and $p_T$ distributions as well as the centrality dependence are well repr...

  8. QUELS FUTURS TRAITEMENTS POUR LA DEPENDANCE AU TABAC ET AU CANNABIS?

    Science.gov (United States)

    LE FOLL, Bernard; JUSTINOVA, Zuzana; TANDA, Gianlugi; GOLDBERG, Steven R.

    2009-01-01

    RESUME Plus de trois millions de morts sont attribués au tabagisme dans le monde par an, et l’usage de tabac est en progression dans les pays en voie de développement. L’usage de tabac est donc une des rares causes de mortalité qui augmente, avec une prévision de plus de 10 millions de morts par an dans 30–40 ans. Le cannabis ou marijuana est la drogue illicite la plus consommée dans le monde et il n’y a actuellement pas de traitement disponible. Bien que les systèmes dopaminergiques jouent un rôle central dans les effets renforçants des drogues, d’autres systèmes sont impliqués. Nous présentons ici des résultats récents obtenus avec des antagonistes des récepteurs cannabinoides CB1, des récepteurs D3 de la dopamine et des récepteurs opioïdes. Ces antagonistes qui modulent de façon directe ou indirecte la transmission dopaminergique cérébrale représentent des approches prometteuses pour le traitement du tabagisme ou de la dépendance au cannabis. Ces approches sont à valider dans des essais cliniques. PMID:18663981

  9. Controlled building of CdSe@ZnS/Au and CdSe@ZnS/ Au2S/Au nanohybrids

    Institute of Scientific and Technical Information of China (English)

    Raquel E. Galian[1; Pilar Diaz[1; Antonio Ribera[1; Alejandro Rincon-Bertolin[1; Said Agouram[2; Julia Perez-Prieto[1

    2015-01-01

    The addition of Au3. to spherical amine-capped CdSe@ZnS nanoparticles in toluene at room temperature and under darkness can lead to ternary CdSe@ZnS/Au nanohybrids. We demonstrate that this happens only when the nanoparticles possess a relatively thin ZnS shell, thus showing that thickness plays a key role in gold deposition on the CdSe@ZnS nanoparticle surface. Our hypothesis is that the amine ligand acts as the reductant of Au3+ ions into Au+ ions, whose affinity for sulfur would keep them at the CdSe@ZnS surface. This interaction stabilizes the Au+ ion, making it less prone to reduction than a non-coordinated Au+ ion. In CdSe@ZnS with a thin shell, Au+ ions at the surface of, or most probably within, the ZnS shell cause the transfer of Cd2+ ions into the solution. Subsequently, the core Se2- anion, which is a better reductant than the shell S2- reduces Au+ ions to Au(0), and large gold nanoparticles (AuNPs) are quickly deposited on the CdSe@ZnS surface in room temperature process, leading to ternary CdSe@ZnS/Au nanohybrids. In solution, these ternary nanohybrids progressively transform into quaternary CdSe@ZnS/Au2S/Au nanohybrids due to the reaction of the shell S2- anion with the remaining Au+ at the CdSe@ZnS surface, thus leading to the growth of Au2S nanoparticles on the CdSe@ZnS surface while Zn concomitantly leaches from the nanohybrid into the solution. Photoirradiation of the heterostructures with visible light enhances their emission efficiency. Comparatively, irradiation of the precursors, i.e., CdSe@ZnS nanoparticles, causes a drastic decrease in their emission accompanied by a blue shift of their emission maximum. The optical properties of these nanohybrids were analyzed by absorption and fluorescence (steady-state and time-resolved) spectroscopy, and the composition of the samples and the chemical states were determined by energy dispersive X-ray spectroscopy (EDX) and X-ray photoelectron spectroscopy

  10. The adsorption of ethylene on Au/Pd(100) alloy surfaces

    Science.gov (United States)

    Li, Zhenjun; Thuening, Theodore; Tysoe, Wilfred T.

    2016-04-01

    The surface chemistry of ethylene is explored on model Au/Pd(100) alloy surfaces using a combination of temperature-programmed desorption and reflection-absorption infrared spectroscopy. The heat of adsorption of ethylene on the model alloy surface is found to increase monotonically with increasing palladium coverage in the alloy, from ~ 33 kJ/mol for a completely gold-covered surface to ~ 80 kJ/mol as the gold coverage decreases to zero. A large change in heat of adsorption is found for palladium coverages between 0 and ~ 0.35 monolayers, where previous studies have shown that the surface comprises exclusively isolated palladium sites. The heat of adsorption changes more slowly for higher palladium coverages, when palladium-palladium bridge sites appear. Vinyl species are identified for palladium coverages above ~ 0.8 ML from a vibrational mode at ~ 1120 cm- 1, which disappears when the sample is heated to ~ 250 K, due to vinyl decomposition.

  11. Charged-Particle Pseudorapidity Density Distributions from Au+Au Collisions at (sNN) = 130 GeV

    Science.gov (United States)

    Back, B. B.; Baker, M. D.; Barton, D. S.; Betts, R. R.; Bindel, R.; Budzanowski, A.; Busza, W.; Carroll, A.; Decowski, M. P.; Garcia, E.; George, N.; Gulbrandsen, K.; Gushue, S.; Halliwell, C.; Heintzelman, G. A.; Henderson, C.; Hofman, D. J.; Hołyński, R.; Holzman, B.; Johnson, E.; Kane, J. L.; Katzy, J.; Khan, N.; Kucewicz, W.; Kulinich, P.; Lin, W. T.; Manly, S.; McLeod, D.; Michałowski, J.; Mignerey, A. C.; Mülmenstädt, J.; Nouicer, R.; Olszewski, A.; Pak, R.; Park, I. C.; Pernegger, H.; Reed, C.; Remsberg, L. P.; Reuter, M.; Roland, C.; Roland, G.; Rosenberg, L.; Sarin, P.; Sawicki, P.; Skulski, W.; Steadman, S. G.; Steinberg, P.; Stephans, G. S.; Stodulski, M.; Sukhanov, A.; Tang, J.-L.; Teng, R.; Trzupek, A.; Vale, C.; van Nieuwenhuizen, G. J.; Verdier, R.; Wadsworth, B.; Wolfs, F. L.; Wosiek, B.; Woźniak, K.; Wuosmaa, A. H.; Wysłouch, B.

    2001-09-01

    The charged-particle pseudorapidity density dNch/dη has been measured for Au+Au collisions at (sNN) = 130 GeV at RHIC, using the PHOBOS apparatus. The total number of charged particles produced for the 3% most-central Au+Au collisions for \\|η\\|<=5.4 is found to be 4200+/-470. The evolution of dNch/dη with centrality is discussed, and compared to model calculations and to data from proton-induced collisions. The data show an enhancement in charged-particle production at midrapidity, while in the fragmentation regions, the results are consistent with expectations from pp and pA scattering.

  12. Fabrication of Au nanostructures in the process of amalgam formation followed by Au-Hg alloy thermal decomposition

    International Nuclear Information System (INIS)

    Au films deposited under ultra-high vacuum conditions on air-cleaved mica substrates were exposed in situ to Hg vapor (residual gas pressure ∼1x10-7 Pa, with Hg vapor pressure of 0.24 Pa). This led to transformation of continuous gold film into isolated amalgam islands of nanometer scale. The changes of Au thin film surface topography caused by amalgamation carried out within ∼40 h were studied by the atomic force microscopy method, while the phase transition in the bulk of Hg-dosed Au films was monitored by means of X-ray diffraction. The island's morphology varies from irregular, ramified structures on terraces to compact shapes along the steps on the mica substrate. After thermal decomposition of the amalgam, thin gold films consisting of isolated Au nanostructures on mica can be obtained

  13. Strangeness Enhancement in Cu+Cu and Au+Au Collisions at \\sqrt{s_{NN}} = 200 GeV

    CERN Document Server

    Agakishiev, H; Ahammed, Z; Alakhverdyants, A V; Alekseev, I; Alford, J; Anderson, B D; Anson, C D; Arkhipkin, D; Averichev, G S; Balewski, J; Barnby, L S; Beavis, D R; Behera, N K; Bellwied, R; Betancourt, M J; Betts, R R; Bhasin, A; Bhati, A K; Bichsel, H; Bielcik, J; Bielcikova, J; Biritz, B; Bland, L C; Borowski, W; Bouchet, J; Braidot, E; Brandin, A V; Bridgeman, A; Brovko, S G; Bruna, E; Bueltmann, S; Bunzarov, I; Burton, T P; Cai, X Z; Caines, H; Sánchez, M Calderón de la Barca; Cebra, D; Cendejas, R; Cervantes, M C; Chajecki, Z; Chaloupka, P; Chattopadhyay, S; Chen, H F; Chen, J H; Chen, J Y; Chen, L; Cheng, J; Cherney, M; Chikanian, A; Choi, K E; Christie, W; Chung, P; Codrington, M J M; Corliss, R; Cramer, J G; Crawford, H J; Dash, S; Leyva, A Davila; De Silva, L C; Debbe, R R; Dedovich, T G; Derevschikov, A A; de Souza, R Derradi; Didenko, L; Djawotho, P; Dogra, S M; Dong, X; Drachenberg, J L; Draper, J E; Dunlop, J C; Efimov, L G; Elnimr, M; Engelage, J; Eppley, G; Estienne, M; Eun, L; Evdokimov, O; Fatemi, R; Fedorisin, J; Fersch, R G; Filip, P; Finch, E; Fine, V; Fisyak, Y; Gagliardi, C A; Gangadharan, D R; Geromitsos, A; Geurts, F; Ghosh, P; Gorbunov, Y N; Gordon, A; Grebenyuk, O; Grosnick, D; Guertin, S M; Gupta, A; Guryn, W; Haag, B; Hajkova, O; Hamed, A; Han, L-X; Harris, J W; Hays-Wehle, J P; Heinz, M; Heppelmann, S; Hirsch, A; Hjort, E; Hoffmann, G W; Hofman, D J; Huang, B; Huang, H Z; Humanic, T J; Huo, L; Igo, G; Jacobs, P; Jacobs, W W; Jones, P G; Jena, C; Jin, F; Joseph, J; Judd, E G; Kabana, S; Kang, K; Kapitan, J; Kauder, K; Ke, H; Keane, D; Kechechyan, A; Kettler, D; Kikola, D P; Kiryluk, J; Kisiel, A; Kizka, V; Knospe, A G; Koetke, D D; Kollegger, T; Konzer, J; Koralt, I; Koroleva, L; Korsch, W; Kotchenda, L; Kouchpil, V; Kravtsov, P; Krueger, K; Krus, M; Kumar, L; Kurnadi, P; Lamont, M A C; Landgraf, J M; LaPointe, S; Lauret, J; Lebedev, A; Lednicky, R; Lee, J H; Leight, W; LeVine, M J; Li, C; Li, L; Li, N; Li, W; Li, X; Li, X; Li, Y; Li, Z M; Lisa, M A; Liu, F; Liu, H; Liu, J; Ljubicic, T; Llope, W J; Longacre, R S; Love, W A; Lu, Y; Lukashov, E V; Luo, X; Ma, G L; Ma, Y G; Mahapatra, D P; Majka, R; Mall, O I; Mangotra, L K; Manweiler, R; Margetis, S; Markert, C; Masui, H; Matis, H S; Matulenko, Yu A; McDonald, D; McShane, T S; Meschanin, A; Milner, R; Minaev, N G; Mioduszewski, S; Mischke, A; Mitrovski, M K; Mohanty, B; Mondal, M M; Morozov, B; Morozov, D A; Munhoz, M G; Naglis, M; Nandi, B K; Nayak, T K; Netrakanti, P K; Nelson, J M; Nogach, L V; Nurushev, S B; Odyniec, G; Ogawa, A; Oh, K; Ohlson, A; Okorokov, V; Oldag, E W; Olson, D; Pachr, M; Page, B S; Pal, S K; Pandit, Y; Panebratsev, Y; Pawlak, T; Pei, H; Peitzmann, T; Perkins, C; Peryt, W; Phatak, S C; Pile, P; Planinic, M; Ploskon, M A; Pluta, J; Plyku, D; Poljak, N; Poskanzer, A M; Potukuchi, B V K S; Powell, C B; Prindle, D; Pruneau, C; Pruthi, N K; Pujahari, P R; Putschke, J; Qiu, H; Raniwala, R; Raniwala, S; Ray, R L; Redwine, R; Reed, R; Ritter, H G; Roberts, J B; Rogachevskiy, O V; Romero, J L; Rose, A; Ruan, L; Rusnak, J; Sahoo, N R; Sakai, S; Sakrejda, I; Sakuma, T; Salur, S; Sandweiss, J; Sangaline, E; Sarkar, A; Schambach, J; Scharenberg, R P; Schmah, A M; Schuster, T R; Seele, J; Seger, J; Selyuzhenkov, I; Seyboth, P; Shahaliev, E; Shao, M; Sharma, M; Shi, S S; Shou, Q Y; Sichtermann, E P; Simon, F; Singaraju, R N; Skoby, M J; Smirnov, N; Spinka, H M; Srivastava, B; Stanislaus, T D S; Staszak, D; Steadman, S G; Stevens, J R; Stock, R; Strikhanov, M; Stringfellow, B; Suaide, A A P; Suarez, M C; Subba, N L; Sumbera, M; Sun, X M; Sun, Y; Sun, Z; Surrow, B; Svirida, D N; Symons, T J M; de Toledo, A Szanto; Takahashi, J; Tang, A H; Tang, Z; Tarini, L H; Tarnowsky, T; Thein, D; Thomas, J H; Tian, J; Timmins, A R; Tlusty, D; Tokarev, M; Tram, V N; Trentalange, S; Tribble, R E; Tribedy, P; Tsai, O D; Ullrich, T; Underwood, D G; Van Buren, G; van Nieuwenhuizen, G; Vanfossen, J A; Jr.,; Varma, R; Vasconcelos, G M S; Vasiliev, A N; Videbæk, F; Viyogi, Y P; Vokal, S; Wada, M; Walker, M; Wang, F; Wang, G; Wang, H; Wang, J S; Wang, Q; Wang, X L; Wang, Y; Webb, G; Webb, J C; Westfall, G D; Whitten, C; Wieman, H; Wissink, S W; Witt, R; Witzke, W; Wu, Y F; Xiao, Z; Xie, W; Xu, H; Xu, N; Xu, Q H; Xu, W; Xu, Y; Xu, Z; Xue, L; Yang, Y; Yepes, P; Yip, K; Yoo, I-K; Zawisza, M; Zbroszczyk, H; Zhan, W; Zhang, J B; Zhang, S; Zhang, W M; Zhang, X P; Zhang, Y; Zhang, Z P; Zhao, J; Zhong, C; Zhou, W; Zhu, X; Zhu, Y H; Zoulkarneev, R; Zoulkarneeva, Y

    2011-01-01

    We report new STAR measurements of mid-rapidity yields for the $\\Lambda$, $\\bar{\\Lambda}$, $K^{0}_{S}$, $\\Xi^{-}$, $\\bar{\\Xi}^{+}$, $\\Omega^{-}$, $\\bar{\\Omega}^{+}$ particles in Cu+Cu collisions at \\sNN{200}, and mid-rapidity yields for the $\\Lambda$, $\\bar{\\Lambda}$, $K^{0}_{S}$ particles in Au+Au at \\sNN{200}. We show that at a given number of participating nucleons, the production of strange hadrons is higher in Cu+Cu collisions than in Au+Au collisions at the same center-of-mass energy. We find that aspects of the enhancement factors for all particles can be described by a parameterization based on the fraction of participants that undergo multiple collisions. Such a parameterization may be relevant in the core-corona or string excitation/breaking hadron production schemes.

  14. Centrality Dependence of Direct Photons in Au+Au Collisions at sqrt(s_NN) = 200 GeV

    CERN Document Server

    Fries, R J; Srivastava, D K

    2005-01-01

    We calculate the spectra of high energy photons emitted in relativistic Au+Au collisions for various centralities and compare to data recently collected at the Relativistic Heavy Ion Collider by the PHENIX collaboration. Our results for photons from primary hard scatterings and photons from interactions of jets with the medium are consistent with the measurements of neutral pion and direct photon production in p+p collisions and give a good description of direct photon spectra measured in Au+Au collisions. The contribution of photons from jet-to-photon conversion in the medium can be as large as the photon yield from hard scatterings in the momentum range p_T = 2...6 GeV/c. We show that this novel mechanism is not ruled out by any existing data.

  15. Scaling properties of proton and antiproton production in sqrt[s(NN)]=200 GeV Au+Au collisions.

    Science.gov (United States)

    Adler, S S; Afanasiev, S; Aidala, C; Ajitanand, N N; Akiba, Y; Alexander, J; Amirikas, R; Aphecetche, L; Aronson, S H; Averbeck, R; Awes, T C; Azmoun, R; Babintsev, V; Baldisseri, A; Barish, K N; Barnes, P D; Bassalleck, B; Bathe, S; Batsouli, S; Baublis, V; Bazilevsky, A; Belikov, S; Berdnikov, Y; Bhagavatula, S; Boissevain, J G; Borel, H; Borenstein, S; Brooks, M L; Brown, D S; Bruner, N; Bucher, D; Buesching, H; Bumazhnov, V; Bunce, G; Burward-Hoy, J M; Butsyk, S; Camard, X; Chai, J-S; Chand, P; Chang, W C; Chernichenko, S; Chi, C Y; Chiba, J; Chiu, M; Choi, I J; Choi, J; Choudhury, R K; Chujo, T; Cianciolo, V; Cobigo, Y; Cole, B A; Constantin, P; d'Enterria, D G; David, G; Delagrange, H; Denisov, A; Deshpande, A; Desmond, E J; Dietzsch, O; Drapier, O; Drees, A; du Rietz, R; Durum, A; Dutta, D; Efremenko, Y V; El Chenawi, K; Enokizono, A; En'yo, H; Esumi, S; Ewell, L; Fields, D E; Fleuret, F; Fokin, S L; Fox, B D; Fraenkel, Z; Frantz, J E; Franz, A; Frawley, A D; Fung, S-Y; Garpman, S; Ghosh, T K; Glenn, A; Gogiberidze, G; Gonin, M; Gosset, J; Goto, Y; Granier de Cassagnac, R; Grau, N; Greene, S V; Grosse Perdekamp, G; Guryn, W; Gustafsson, H-A; Hachiya, T; Haggerty, J S; Hamagaki, H; Hansen, A G; Hartouni, E P; Harvey, M; Hayano, R; He, X; Heffner, M; Hemmick, T K; Heuser, J M; Hibino, M; Hill, J C; Holzmann, W; Homma, K; Hong, B; Hoover, A; Ichihara, T; Ikonnikov, V V; Imai, K; Isenhower, L D; Ishihara, M; Issah, M; Isupov, A; Jacak, B V; Jang, W Y; Jeong, Y; Jia, J; Jinnouchi, O; Johnson, B M; Johnson, S C; Joo, K S; Jouan, D; Kametani, S; Kamihara, N; Kang, J H; Kapoor, S S; Katou, K; Kelly, S; Khachaturov, B; Khanzadeev, A; Kikuchi, J; Kim, D H; Kim, D J; Kim, D W; Kim, E; Kim, G-B; Kim, H J; Kistenev, E; Kiyomichi, A; Kiyoyama, K; Klein-Boesing, C; Kobayashi, H; Kochenda, L; Kochetkov, V; Koehler, D; Kohama, T; Kopytine, M; Kotchetkov, D; Kozlov, A; Kroon, P J; Kuberg, C H; Kurita, K; Kuroki, Y; Kweon, M J; Kwon, Y; Kyle, G S; Lacey, R; Ladygin, V; Lajoie, J G; Lebedev, A; Leckey, S; Lee, D M; Lee, S; Leitch, M J; Li, X H; Lim, H; Litvinenko, A; Liu, M X; Liu, Y; Maguire, C F; Makdisi, Y I; Malakhov, A; Manko, V I; Mao, Y; Martinez, G; Marx, M D; Masui, H; Matathias, F; Matsumoto, T; McGaughey, P L; Melnikov, E; Messer, F; Miake, Y; Milan, J; Miller, T E; Milov, A; Mioduszewski, S; Mischke, R E; Mishra, G C; Mitchell, J T; Mohanty, A K; Morrison, D P; Moss, J M; Mühlbacher, F; Mukhopadhyay, D; Muniruzzaman, M; Murata, J; Nagamiya, S; Nagle, J L; Nakamura, T; Nandi, B K; Nara, M; Newby, J; Nilsson, P; Nyanin, A S; Nystrand, J; O'Brien, E; Ogilvie, C A; Ohnishi, H; Ojha, I D; Okada, K; Ono, M; Onuchin, V; Oskarsson, A; Otterlund, I; Oyama, K; Ozawa, K; Pal, D; Palounek, A P T; Pantuev, V S; Papavassiliou, V; Park, J; Parmar, A; Pate, S F; Peitzmann, T; Peng, J-C; Peresedov, V; Pinkenburg, C; Pisani, R P; Plasil, F; Purschke, M L; Purwar, A; Rak, J; Ravinovich, I; Read, K F; Reuter, M; Reygers, K; Riabov, V; Riabov, Y; Roche, G; Romana, A; Rosati, M; Rosnet, P; Ryu, S S; Sadler, M E; Saito, N; Sakaguchi, T; Sakai, M; Sakai, S; Samsonov, V; Sanfratello, L; Santo, R; Sato, H D; Sato, S; Sawada, S; Schutz, Y; Semenov, V; Seto, R; Shaw, M R; Shea, T K; Shibata, T-A; Shigaki, K; Shiina, T; Silva, C L; Silvermyr, D; Sim, K S; Singh, C P; Singh, V; Sivertz, M; Soldatov, A; Soltz, R A; Sondheim, W E; Sorensen, S P; Sourikova, I V; Staley, F; Stankus, P W; Stenlund, E; Stepanov, M; Ster, A; Stoll, S P; Sugitate, T; Sullivan, J P; Takagui, E M; Taketani, A; Tamai, M; Tanaka, K H; Tanaka, Y; Tanida, K; Tannenbaum, M J; Tarján, P; Tepe, J D; Thomas, T L; Tojo, J; Torii, H; Towell, R S; Tserruya, I; Tsuruoka, H; Tuli, S K; Tydesjö, H; Tyurin, N; Van Hecke, H W; Velkovska, J; Velkovsky, M; Villatte, L; Vinogradov, A A; Volkov, M A; Vznuzdaev, E; Wang, X R; Watanabe, Y; White, S N; Wohn, F K; Woody, C L; Xie, W; Yang, Y; Yanovich, A; Yokkaichi, S; Young, G R; Yushmanov, I E; Zajc, W A; Zhang, C; Zhou, S; Zolin, L

    2003-10-24

    We report on the yield of protons and antiprotons, as a function of centrality and transverse momentum, in Au+Au collisions at sqrt[s(NN)]=200 GeV measured at midrapidity by the PHENIX experiment at the BNL Relativistic Heavy Ion Collider. In central collisions at intermediate transverse momenta (1.5Au+Au, p+p, and e(+)e(-) collisions. This enhancement is limited to p(T)<5 GeV/c as deduced from the ratio of charged hadrons to pi(0) measured in the range 1.5

  16. Synthesis of Au/C and Au/Pani for anode electrodes in glucose microfluidic fuel cell

    Energy Technology Data Exchange (ETDEWEB)

    Guerra-Balcazar, M.; Morales-Acosta, D.; Castaneda, F.; Arriaga, L.G. [Centro de Investigacion y Desarrollo Tecnologico en Electroquimica, 76703 Queretaro (Mexico); Ledesma-Garcia, J. [Division de Investigacion y Posgrado, Facultad de Ingenieria, Universidad Autonoma de Queretaro, 76010 Queretaro (Mexico)

    2010-06-15

    Gold nanoparticles have been prepared by two methods: chemical (ex-situ, Au/C) by two phase protocol, and electrochemical (in-situ, Au/Pani) by electroreduction of gold ions on a polyaniline film and compared as anode catalysts in a glucose microfluidic fuel cell. In this paper the structural characteristics and electrocatalytic properties were investigated by X-ray diffraction and electrochemical measurements. The catalytic behavior of both anodes was tested in a microfluidic fuel cell with a reference electrode incorporated, by means of linear sweep voltammetry (LSV), showing a cathodic shift in the glucose oxidation peak for Au/Pani. Results show a higher power density (0.5 mW cm{sup -} {sup 2}) for Au/C anode compared with an already reported value, where a glucose microfluidic fuel cell was used in similar conditions. (author)

  17. Excitonic luminescence of ZnSe single crystals doped with Au

    International Nuclear Information System (INIS)

    Photoluminescence spectra of ZnSe single crystals doped with Au during a long high-temperature treatment of as-grown crystals in Zn+Au or Se+Au melts are investigated in the temperature range from 83 to 300 K. The Au-doping from Zn+Au melt leads to the formation of both simple defects (Aui donors and AuZn acceptors) and acceptor associates (AuZn-Aui). The edge luminescence is attributed to radiative annihilation of Aui and VSe donor-bound excitons. The edge spectra of the crystals doped with Au from Se+Au melt contain the band ascribed to radiative annihilation of AuZn acceptor-bound excitons

  18. Pion Interferometry of $\\sqrt{s_{NN}} = 130$ GeV Au+Au Collisions at RHIC

    OpenAIRE

    STAR Collaboration; Adler, C.

    2001-01-01

    Two-pion correlation functions in Au+Au collisions at $\\sqrt{s_{NN}} = 130$ GeV have been measured by the STAR (Solenoidal Tracker at RHIC) detector. The source size extracted by fitting the correlations grows with event multiplicity and decreases with transverse momentum. Anomalously large sizes or emission durations, which have been suggested as signals of quark-gluon plasma formation and rehadronization, are not observed. The HBT parameters display a weak energy dependence over a broad ran...

  19. NUCLEAR AND HEAVY ION PHYSICS: Charged-particle pseudorapidity distributions in Au+Au collisions at RHIC

    Science.gov (United States)

    Wang, Zeng-Wei; Jiang, Zhi-Jin

    2009-04-01

    Using the Glauber model, we present the formulas for calculating the numbers of participants, spectators and binary nucleon-nucleon collisions. Based on this work, we get the pseudorapidity distributions of charged particles as the function of the impact parameter in nucleus-nucleus collisions. The theoretical results agree well with the experimental observations made by the BRAHMS Collaboration in Au + Au collisions at GeV in different centrality bins over the whole pseudorapidity range.

  20. Azimuthally sensitive hanbury brown-twiss interferometry in Au + Au collisions sqrt S sub NN = 200 GeV

    Energy Technology Data Exchange (ETDEWEB)

    Adams, J.; Adler, C.; Aggarwal, M.M.; Ahammed, Z.; Amonett, J.; Anderson, B.D.; Arkhipkin, D.; Averichev, G.S.; Badyal, S.K.; Balewski, J.; Barannikova, O.; Barnby, L.S.; Baudot, J.; Bekele, S.; Belaga, V.V.; Bellwied, R.; Berger, J.; Bezverkhny, B.I.; Bhardwaj, S.; Bhati, A.K.; Bichsel, H.; Billmeier, A.; Bland, L.C.; Blyth, C.O.; Bonner, B.E.; Botje, M.; Boucham, A.; Brandin, A.; Bravar, A.; Cadman, R.V.; Cai, X.Z.; Caines, H.; Calderon de la Barca Sanchez, M.; Carroll, J.; Castillo, J.; Cebra, D.; Chaloupka, P.; Chattopadhyay, S.; Chen, H.F.; Chen, Y.; Chernenko, S.P.; Cherney, M.; Chikanian, A.; Christie, W.; Coffin, J.P.; Cormier, T.M.; Cramer, J.G.; Crawford, H.J.; Das, D.; Das, S.; Derevschikov, A.A.; Didenko, L.; Dietel, T.; Dong, W.J.; Dong, X.; Draper, J.E.; Du, F.; Dubey, A.K.; Dunin, V.B.; Dunlop, J.C.; Dutta Majumdar, M.R.; Eckardt, V.; Efimov, L.G.; Emelianov, V.; Engelage, J.; Eppley, G.; Erazmus, B.; Estienne, M.; Fachini, P.; Faine, V.; Faivre, J.; Fatemi, R.; Filimonov, K.; Filip, P.; Finch, E.; Fisyak, Y.; Flierl, D.; Foley, K.J.; Fu, J.; Gagliardi, C.A.; Gagunashvili, N.; Gans, J.; Gaudichet, L.; Geurts, F.; Ghazikhanian, V.; Ghosh, P.; Gonzalez, J.E.; Grachov, O.; Grebenyuk, O.; Gronstal, S.; Grosnick, D.; Guertin, S.M.; Gupta, A.; Gutierrez, T.D.; Hallman, T.J.; Hamed, A.; Hardtke, D.; Harris, J.W.; Heinz, M.; Henry, T.W.; Heppelmann, S.; Hippolyte, B.; Hirsch, A.; Hjort, E.; Hoffmann, G.W.; Horsley, M.; Huang, H.Z.; Huang, L.S.; Hughes, E.; Humanic, T.J.; Igo, G.; Ishihara, A.; Jacobs, P.; Jacobs, W.W.; Janik, M.; Jiang, H.; Johnson, I.; Jones, P.G.; Judd, E.G.; Kabana, S.; Kaplan, M.; Keane, D.; Khodyrev, V.Yu.; Kiryluk, J.; Kisiel, A.; Klay, J.; Klein, S.R.; Klyachko, A.; Koetke, D.D.; Kollegger, T.; Kopytine, M.; Kotchenda, L.; Kovalenko, A.D.; Kramer, M.; Kravtsov, V.I.; Kravtsov, P.; Krueger, K.; Kuhn, C.; Kulikov, A.I.; Kumar, A.; Kunde, G.J.; Kunz, C.L.; Kutuev, R.Kh.; Kuznetsov, A.A.; Lamont, M.A.C.; et al.

    2004-06-30

    We present the results of a systematic study of the shape of the pion distribution in coordinate space at freeze-out in Au+Au collisions at RHIC using two-pion Hanbury Brown-Twiss (HBT) interferometry. Oscillations of the extracted HBT radii vs. emission angle indicate sources elongated perpendicular to the reaction plane. The results indicate that the pressure and expansion time of the collision system are not sufficient to completely quench its initial shape.

  1. Elliptic flow of identified hadrons in Au+Au collisions at √(sNN)=200 GeV

    International Nuclear Information System (INIS)

    The anisotropy parameter (v2), the second harmonic of the azimuthal particle distribution, has been measured with the PHENIX detector in Au+Au collisions at √(sNN)=200 GeV for identified and inclusive charged particle production at central rapidities (|η|2 of mesons falls below that of (anti)baryons for pT>2 GeV/c, in marked contrast to the predictions of a hydrodynamical model. A quark-coalescence model is also investigated

  2. Elliptic flow of identified hadrons in Au+Au collisions at sqrt sNN =200 GeV.

    Science.gov (United States)

    Adler, S S; Afanasiev, S; Aidala, C; Ajitanand, N N; Akiba, Y; Alexander, J; Amirikas, R; Aphecetche, L; Aronson, S H; Averbeck, R; Awes, T C; Azmoun, R; Babintsev, V; Baldisseri, A; Barish, K N; Barnes, P D; Bassalleck, B; Bathe, S; Batsouli, S; Baublis, V; Bazilevsky, A; Belikov, S; Berdnikov, Y; Bhagavatula, S; Boissevain, J G; Borel, H; Borenstein, S; Brooks, M L; Brown, D S; Bruner, N; Bucher, D; Buesching, H; Bumazhnov, V; Bunce, G; Burward-Hoy, J M; Butsyk, S; Camard, X; Chai, J-S; Chand, P; Chang, W C; Chernichenko, S; Chi, C Y; Chiba, J; Chiu, M; Choi, I J; Choi, J; Choudhury, R K; Chujo, T; Cianciolo, V; Cobigo, Y; Cole, B A; Constantin, P; D'Enterria, D G; David, G; Delagrange, H; Denisov, A; Deshpande, A; Desmond, E J; Dietzsch, O; Drapier, O; Drees, A; du Rietz, R; Durum, A; Dutta, D; Efremenko, Y V; El Chenawi, K; Enokizono, A; En'yo, H; Esumi, S; Ewell, L; Fields, D E; Fleuret, F; Fokin, S L; Fox, B D; Fraenkel, Z; Frantz, J E; Franz, A; Frawley, A D; Fung, S-Y; Garpman, S; Ghosh, T K; Glenn, A; Gogiberidze, G; Gonin, M; Gosset, J; Goto, Y; Granier de Cassagnac, R; Grau, N; Greene, S V; Grosse Perdekamp, M; Guryn, W; Gustafsson, H-A; Hachiya, T; Haggerty, J S; Hamagaki, H; Hansen, A G; Hartouni, E P; Harvey, M; Hayano, R; He, X; Heffner, M; Hemmick, T K; Heuser, J M; Hibino, M; Hill, J C; Holzmann, W; Homma, K; Hong, B; Hoover, A; Ichihara, T; Ikonnikov, V V; Imai, K; Isenhower, L D; Ishihara, M; Issah, M; Isupov, A; Jacak, B V; Jang, W Y; Jeong, Y; Jia, J; Jinnouchi, O; Johnson, B M; Johnson, S C; Joo, K S; Jouan, D; Kametani, S; Kamihara, N; Kang, J H; Kapoor, S S; Katou, K; Kelly, S; Khachaturov, B; Khanzadeev, A; Kikuchi, J; Kim, D H; Kim, D J; Kim, D W; Kim, E; Kim, G-B; Kim, H J; Kistenev, E; Kiyomichi, A; Kiyoyama, K; Klein-Boesing, C; Kobayashi, H; Kochenda, L; Kochetkov, V; Koehler, D; Kohama, T; Kopytine, M; Kotchetkov, D; Kozlov, A; Kroon, P J; Kuberg, C H; Kurita, K; Kuroki, Y; Kweon, M J; Kwon, Y; Kyle, G S; Lacey, R; Ladygin, V; Lajoie, J G; Lebedev, A; Leckey, S; Lee, D M; Lee, S; Leitch, M J; Li, X H; Lim, H; Litvinenko, A; Liu, M X; Liu, Y; Maguire, C F; Makdisi, Y I; Malakhov, A; Manko, V I; Mao, Y; Martinez, G; Marx, M D; Masui, H; Matathias, F; Matsumoto, T; McGaughey, P L; Melnikov, E; Messer, F; Miake, Y; Milan, J; Miller, T E; Milov, A; Mioduszewski, S; Mischke, R E; Mishra, G C; Mitchell, J T; Mohanty, A K; Morrison, D P; Moss, J M; Mühlbacher, F; Mukhopadhyay, D; Muniruzzaman, M; Murata, J; Nagamiya, S; Nagle, J L; Nakamura, T; Nandi, B K; Nara, M; Newby, J; Nilsson, P; Nyanin, A S; Nystrand, J; O'Brien, E; Ogilvie, C A; Ohnishi, H; Ojha, I D; Okada, K; Ono, M; Onuchin, V; Oskarsson, A; Otterlund, I; Oyama, K; Ozawa, K; Pal, D; Palounek, A P T; Pantuev, V S; Papavassiliou, V; Park, J; Parmar, A; Pate, S F; Peitzmann, T; Peng, J-C; Peresedov, V; Pinkenburg, C; Pisani, R P; Plasil, F; Purschke, M L; Purwar, A; Rak, J; Ravinovich, I; Read, K F; Reuter, M; Reygers, K; Riabov, V; Riabov, Y; Roche, G; Romana, A; Rosati, M; Rosnet, P; Ryu, S S; Sadler, M E; Saito, N; Sakaguchi, T; Sakai, M; Sakai, S; Samsonov, V; Sanfratello, L; Santo, R; Sato, H D; Sato, S; Sawada, S; Schutz, Y; Semenov, V; Seto, R; Shaw, M R; Shea, T K; Shibata, T-A; Shigaki, K; Shiina, T; Silva, C L; Silvermyr, D; Sim, K S; Singh, C P; Singh, V; Sivertz, M; Soldatov, A; Soltz, R A; Sondheim, W E; Sorensen, S P; Sourikova, I V; Staley, F; Stankus, P W; Stenlund, E; Stepanov, M; Ster, A; Stoll, S P; Sugitate, T; Sullivan, J P; Takagui, E M; Taketani, A; Tamai, M; Tanaka, K H; Tanaka, Y; Tanida, K; Tannenbaum, M J; Tarján, P; Tepe, J D; Thomas, T L; Tojo, J; Torii, H; Towell, R S; Tserruya, I; Tsuruoka, H; Tuli, S K; Tydesjö, H; Tyurin, N; van Hecke, H W; Velkovska, J; Velkovsky, M; Villatte, L; Vinogradov, A A; Volkov, M A; Vznuzdaev, E; Wang, X R; Watanabe, Y; White, S N; Wohn, F K; Woody, C L; Xie, W; Yang, Y; Yanovich, A; Yokkaichi, S; Young, G R; Yushmanov, I E; Zajc, W A; Zhang, C; Zhou, S; Zolin, L

    2003-10-31

    The anisotropy parameter (v(2)), the second harmonic of the azimuthal particle distribution, has been measured with the PHENIX detector in Au+Au collisions at sqrt[s(NN)]=200 GeV for identified and inclusive charged particle production at central rapidities (|eta|2 GeV/c, in marked contrast to the predictions of a hydrodynamical model. A quark-coalescence model is also investigated. PMID:14611277

  3. Au - Be/Ru/Au multilayer metallization as a stable ohmic contact scheme to p-type InP

    Science.gov (United States)

    Malina, V.; Moro, L.; Micheli, V.; Mojzes, I.

    1996-07-01

    An attempt has been made to improve the electrical and metallurgical stability of Au - Be alloyed contacts to moderately doped p-type InP by minimizing the thickness of the Au - Be contact layer and using an Ru layer as a new, more effective diffusion barrier between the Au - Be and a thick Au top layer. It was found that the Au - Be contact layer only 40 - 50 nm thick is sufficient to give excellent ohmic contacts with specific contact resistance values as low as 0268-1242/11/7/025/img6 and 0268-1242/11/7/025/img7 (for 0268-1242/11/7/025/img8 and 0268-1242/11/7/025/img9 respectively). When subjected to an aging test at 0268-1242/11/7/025/img10 for 50 h in 0268-1242/11/7/025/img11 gas, the 50 nm Au - Be/50 nm Ru/300 nm Au contacts alloyed at an optimum temperature of about 0268-1242/11/7/025/img12 exhibit good thermal stability and no substantial increase in the specific contact resistance. The remarkable metallurgical stability of such contacts was confirmed by secondary neutral mass spectroscopy (SNMS) in-depth profile measurements. A comparison with the previously investigated diffusion barrier metals (such as Cr, Ti, Pt, etc) shows that the Ru layer is a much better barrier against the migration of Au into the InP substrate and, at the same time, it suppresses the out-diffusion of In and P from the semiconductor.

  4. Production and collective behavior of strange particles in Au + Au collisions at 2-8 AGeV

    CERN Document Server

    Pinkenburg, C H; Alexander, J M; Anderson, M; Best, D; Brady, F P; Case, T; Caskey, W; Cebra, D; Chance, J L; Chung, P; Cole, B; Crowe, K M; Das, A C; Draper, J E; Gilkes, M L; Gushue, S; Heffner, M; Hirsch, A S; Hjort, E L; Huo, L; Justice, M; Kaplan, M; Keane, D; Kintner, J C; Klay, J L; Krofcheck, D; Lacey, R A; Law, C; Lauret, J; Lisa, M A; Liu, H; Liu, Y M; McGrath, R L; Milosevich, Z; Odyniec, Grazyna Janina; Olson, D L; Panitkin, S Y; Porile, N T; Rai, G; Ritter, H G; Romero, J L; Scharenberg, R P; Schröder, L S; Srivastava, B; Stone, N T B; Symons, T J M; Wang, S; Whitfield, J; Witt, R; Wood, L; Zhang Wei Ning

    2002-01-01

    The E895 experiment at the AGS measured strange particle production and collective behavior in Au+Au collisions between 2--8 AGeV. The production of $\\Lambda$ Baryons and K$^0$ Mesons as function of energy rises smoothly and exhibits a nonlinear impact parameter dependence. Neutral and positively charged Kaons exhibit a strong anti-flow behavior. $\\Lambda$ Baryons show a smaller flow signal than protons.

  5. Identified hadron transverse momentum spectra in Au+Au collisions at sNN=62.4 GeV

    Science.gov (United States)

    Back, B. B.; Baker, M. D.; Ballintijn, M.; Barton, D. S.; Betts, R. R.; Bickley, A. A.; Bindel, R.; Busza, W.; Carroll, A.; Chai, Z.; Decowski, M. P.; García, E.; Gburek, T.; George, N.; Gulbrandsen, K.; Halliwell, C.; Hamblen, J.; Hauer, M.; Henderson, C.; Hofman, D. J.; Hollis, R. S.; Hołyński, R.; Holzman, B.; Iordanova, A.; Johnson, E.; Kane, J. L.; Khan, N.; Kulinich, P.; Kuo, C. M.; Lin, W. T.; Manly, S.; Mignerey, A. C.; Nouicer, R.; Olszewski, A.; Pak, R.; Reed, C.; Roland, C.; Roland, G.; Sagerer, J.; Seals, H.; Sedykh, I.; Smith, C. E.; Stankiewicz, M. A.; Steinberg, P.; Stephans, G. S. F.; Sukhanov, A.; Tonjes, M. B.; Trzupek, A.; Vale, C.; Nieuwenhuizen, G. J. Van; Vaurynovich, S. S.; Verdier, R.; Veres, G. I.; Wenger, E.; Wolfs, F. L. H.; Wosiek, B.; Woźniak, K.; Wysłouch, B.

    2007-02-01

    Transverse momentum spectra of pions, kaons, protons, and antiprotons from Au+Au collisions at sNN = 62.4 GeV have been measured by the PHOBOS experiment at the Relativistic Heavy Ion Collider at Brookhaven National Laboratory. The identification of particles relies on three different methods: low momentum particles stopping in the first detector layers; the specific energy loss (dE/dx) in the silicon spectrometer, and time-of-flight measurement. These methods cover the transverse momentum ranges 0.03 0.2, 0.2 1.0, and 0.5 3.0 GeV/c, respectively. Baryons are found to have substantially harder transverse momentum spectra than mesons. The pT region in which the proton to pion ratio reaches unity in central Au+Au collisions at sNN = 62.4 GeV fits into a smooth trend as a function of collision energy. At low transverse mass, the spectra of various species exhibit a significant deviation from transverse mass scaling. The observed particle yields at very low pT are comparable to extrapolations from higher pT for kaons, protons and antiprotons. By comparing our results to Au+Au collisions at sNN = 200 GeV, we conclude that the net proton yield at midrapidity is proportional to the number of participant nucleons in the collision.

  6. Heterojunction metal-oxide-metal Au-Fe{sub 3}O{sub 4}-Au single nanowire device for spintronics

    Energy Technology Data Exchange (ETDEWEB)

    Reddy, K. M., E-mail: mrkongara@boisestate.edu; Punnoose, Alex; Hanna, Charles [Department of Physics, Boise State University, Boise, Idaho 83725 (United States); Padture, Nitin P. [School of Engineering, Brown University, Providence, Rhode Island 02912 (United States)

    2015-05-07

    In this report, we present the synthesis of heterojunction magnetite nanowires in alumina template and describe magnetic and electrical properties from a single nanowire device for spintronics applications. Heterojunction Au-Fe-Au nanowire arrays were electrodeposited in porous aluminum oxide templates, and an extensive and controlled heat treatment process converted Fe segment to nanocrystalline cubic magnetite phase with well-defined Au-Fe{sub 3}O{sub 4} interfaces as confirmed by the transmission electron microscopy. Magnetic measurements revealed Verwey transition shoulder around 120 K and a room temperature coercive field of 90 Oe. Current–voltage (I-V) characteristics of a single Au-Fe{sub 3}O{sub 4}-Au nanowire have exhibited Ohmic behavior. Anomalous positive magnetoresistance of about 0.5% is observed on a single nanowire, which is attributed to the high spin polarization in nanowire device with pure Fe{sub 3}O{sub 4} phase and nanocontact barrier. This work demonstrates the ability to preserve the pristine Fe{sub 3}O{sub 4} and well defined electrode contact metal (Au)–magnetite interface, which helps in attaining high spin polarized current.

  7. Effect of Au nano-particle aggregation on the deactivation of the AuCl3/AC catalyst for acetylene hydrochlorination.

    Science.gov (United States)

    Dai, Bin; Wang, Qinqin; Yu, Feng; Zhu, Mingyuan

    2015-01-01

    A detailed study of the valence state and distribution of the AuCl3/AC catalyst during the acetylene hydrochlorination deactivation process is described and discussed. Temperature-programmed reduction and X-ray photoelectron spectral analysis indicate that the active Au(3+) reduction to metallic Au(0) is one reason for the deactivation of AuCl3/AC catalyst. Transmission electron microscopy characterization demonstrated that the particle size of Au nano-particles increases with increasing reaction time. The results indicated that metallic Au(0) exhibits considerable catalytic activity and that Au nano-particle aggregation may be another reason for the AuCl3/AC catalytic activity in acetylene hydrochlorination. PMID:25994222

  8. Jet-Hadron Correlations in sqrt{s_{NN}} = 200 GeV Au+Au and p+p Collisions

    CERN Document Server

    Adamczyk, L; Agakishiev, G; Aggarwal, M M; Ahammed, Z; Alekseev, I; Alford, J; Anson, C D; Aparin, A; Arkhipkin, D; Aschenauer, E; Averichev, G S; Balewski, J; Banerjee, A; Barnovska, Z; Beavis, D R; Bellwied, R; Betancourt, M J; Betts, R R; Bhasin, A; Bhati, A K; Bhattarai,; Bichsel, H; Bielcik, J; Bielcikova, J; Bland, L C; Bordyuzhin, I G; Borowski, W; Bouchet, J; Brandin, A V; Brovko, S G; Bruna, E; Bültmann, S; Bunzarov, I; Burton, T P; Butterworth, J; Caines, H; Sánchez, M Calderón de la Barca; Cebra, D; Cendejas, R; Cervantes, M C; Chaloupka, P; Chang, Z; Chattopadhyay, S; Chen, H F; Chen, J H; Chen, J Y; Chen, L; Cheng, J; Cherney, M; Chikanian, A; Christie, W; Chung, P; Chwastowski, J; Codrington, M J M; Corliss, R; Cramer, J G; Crawford, H J; Cui, X; Das, S; Leyva, A Davila; De Silva, L C; Debbe, R R; Dedovich, T G; Deng, J; de Souza, R Derradi; Dhamija, S; di Ruzza, B; Didenko, L; Dilks,; Ding, F; Dion, A; Djawotho, P; Dong, X; Drachenberg, J L; Draper, J E; Du, C M; Dunkelberger, L E; Dunlop, J C; Efimov, L G; Elnimr, M; Engelage, J; Engle, K S; Eppley, G; Eun, L; Evdokimov, O; Fatemi, R; Fazio, S; Fedorisin, J; Fersch, R G; Filip, P; Finch, E; Fisyak, Y; Flores, C E; Gagliardi, C A; Gangadharan, D R; Garand, D; Geurts, F; Gibson, A; Gliske, S; Grebenyuk, O G; Grosnick, D; Guo, Y; Gupta, A; Gupta, S; Guryn, W; Haag, B; Hajkova, O; Hamed, A; Han, L-X; Haque, R; Harris, J W; Hays-Wehle, J P; Heppelmann, S; Hirsch, A; Hoffmann, G W; Hofman, D J; Horvat, S; Huang, B; Huang, H Z; Huck, P; Humanic, T J; Igo, G; Jacobs, W W; Jena, C; Judd, E G; Kabana, S; Kang, K; Kauder, K; Ke, H W; Keane, D; Kechechyan, A; Kesich, A; Kikola, D P; Kiryluk, J; Kisel, I; Kisiel, A; Koetke, D D; Kollegger, T; Konzer, J; Koralt, I; Korsch, W; Kotchenda, L; Kravtsov, P; Krueger, K; Kulakov, I; Kumar, L; Kycia, R A; Lamont, M A C; Landgraf, J M; Landry, K D; LaPointe, S; Lauret, J; Lebedev, A; Lednicky, R; Lee, J H; Leight, W; LeVine, M J; Li, C; Li, W; Li, X; Li, Y; Li, Z M; Lima, L M; Lisa, M A; Liu, F; Ljubicic, T; Llope, W J; Longacre, R S; Luo, X; Ma, G L; Ma, Y G; Don, D M M D Madagodagettige; Mahapatra, D P; Majka, R; Margetis, S; Markert, C; Masui, H; Matis, H S; McDonald, D; McShane, T S; Mioduszewski, S; Mitrovski, M K; Mohammed, Y; Mohanty, B; Mondal, M M; Munhoz, M G; Mustafa, M K; Naglis, M; Nandi, B K; Nasim, Md; Nayak, T K; Nelson, J M; Nogach, L V; Novak, J; Odyniec, G; Ogawa, A; Oh, K; Ohlson, A; Okorokov, V; Oldag, E W; Oliveira, R A N; Olson, D; Pachr, M; Page, B S; Pal, S K; Pan, Y X; Pandit, Y; Panebratsev, Y; Pawlak, T; Pawlik, B; Pei, H; Perkins, C; Peryt, W; Pile, P; Planinic, M; Pluta, J; Plyku, D; Poljak, N; Porter, J; Poskanzer, A M; Powell, C B; Pruneau, C; Pruthi, N K; Przybycien, M; Pujahari, P R; Putschke, J; Qiu, H; Ramachandran, S; Raniwala, R; Raniwala, S; Ray, R L; Riley, C K; Ritter, H G; Roberts, J B; Rogachevskiy, O V; Romero, J L; Ross, J F; Roy, A; Ruan, L; Rusnak, J; Sahoo, N R; Sahu, P K; Sakrejda, I; Salur, S; Sandacz, A; Sandweiss, J; Sangaline, E; Sarkar, A; Schambach, J; Scharenberg, R P; Schmah, A M; Schmidke, B; Schmitz, N; Schuster, T R; Seger, J; Seyboth, P; Shah, N; Shahaliev, E; Shao, M; Sharma, B; Sharma, M; Shen, W Q; Shi, S S; Shou, Q Y; Sichtermann, E P; Singaraju, R N; Skoby, M J; Smirnov, D; Smirnov, N; Solanki, D; Sorensen, P; deSouza, U G; Spinka, H M; Srivastava, B; Stanislaus, T D S; Stevens, J R; Stock, R; Strikhanov, M; Stringfellow, B; Suaide, A A P; Suarez, M C; Sumbera, M; Sun, X M; Sun, Y; Sun, Z; Surrow, B; Svirida, D N; Symons, T J M; de Toledo, A Szanto; Takahashi, J; Tang, A H; Tang, Z; Tarini, L H; Tarnowsky, T; Thomas, J H; Timmins, A R; Tlusty, D; Tokarev, M; Trentalange, S; Tribble, R E; Tribedy, P; Trzeciak, B A; Tsai, O D; Turnau, J; Ullrich, T; Underwood, D G; Van Buren, G; van Nieuwenhuizen, G; Vanfossen,, J A; Varma, R; Vasconcelos, G M S; Vertesi, R; Videbæk, F; Viyogi, Y P; Vokal, S; Voloshin, S A; Vossen, A; Wada, M; Walker, M; Wang, F; Wang, G; Wang, H; Wang, J S; Wang, Q; Wang, X L; Wang, Y; Webb, G; Webb, J C; Westfall, G D; Wieman, H; Wissink, S W; Witt, R; Wu, Y F; Xiao, Z; Xie, W; Xin, K; Xu, H; Xu, N; Xu, Q H; Xu, W; Xu, Y; Xu, Z; Yan,; Yang, C; Yang, Y; Yepes, P; Yi, L; Yip, K; Yoo, I-K; Zawisza, Y; Zbroszczyk, H; Zha, W; Zhang, J B; Zhang, S; Zhang, X P; Zhang, Y; Zhang, Z P; Zhao, F; Zhao, J; Zhong, C; Zhu, X; Zhu, Y H; Zoulkarneeva, Y; Zyzak, M

    2013-01-01

    Azimuthal angular correlations of charged hadrons with respect to the axis of a reconstructed (trigger) jet in Au+Au and p+p collisions at $\\sqrt{s_{NN}} = 200$ GeV in STAR are presented. The trigger jet population in Au+Au collisions is biased towards jets that have not interacted with the medium, allowing easier matching of jet energies between Au+Au and p+p collisions while enhancing medium effects on the recoil jet. The associated hadron yield of the recoil jet is significantly suppressed at high transverse momentum ($p_{T}^{assoc}$) and enhanced at low $p_{T}^{assoc}$ in Au+Au collisions, which is indicative of medium-induced parton energy loss in ultrarelativistic heavy-ion collisions.

  9. Le CERN ouvre ses entrailles au public

    CERN Multimedia

    2004-01-01

    "Le CERN se lance dans une grande opération de relations publiques pour son cinquantième anniversaire. Le centre de recherche organisera une journée portes ouvertes le 16 octobre. Quelque 50 sites pourrant être visités" (1/2 page)

  10. Decomposition of H2O on clean and oxygen-covered Au (1 0 0) surface: A DFT study

    International Nuclear Information System (INIS)

    Highlights: • Dehydrogenation mechanism of H2O on Au (1 0 0) was studied using periodic DFT calculations. • The optimized structures and adsorption energies were obtained. • The results offered an explanation to use oxygen to modify Au (1 0 0) surface. • The energy barriers and reaction energies were calculated. - Abstract: Employing density functional theory (DFT) together with periodic slab models, the adsorption and dehydrogenation of H2O on clean and oxygen-covered Au (1 0 0) have been investigated systematically. On the basis of the theoretical analysis, the favorable adsorption sites and stable configurations of all species were clarified. H2O was predicted to adsorb weakly on the top, bridge, hollow sites, with the top site preferred. Whereas OH and atomic O prefer to adsorb on the hollow site and H occupies the bridge site. What's more, this work displayed the optimum configurations for the relevant co-adsorption groups. The results elucidated that co-adsorption is apt to impair the interaction of adsorbate-substrate due to the joining of oxygen atom except for H2O molecule. Eventually, the interrelated transition states and activation energies were calculated to explore the dehydrogenation mechanism of H2O. A feasible mechanism on oxygen pre-covered surfaces for complete dehydrogenation of H2O was also presented. It was illuminated that atomic oxygen could diminish the barrier energy substantially of the first dissociation step and play a pivotal role in the decomposition of H2O molecule

  11. Catalytic Conversion of Short-Chain Alcohols on Atomically Dispersed Au and Pd Supported on Nanoscale Metal Oxides

    Science.gov (United States)

    Wang, Chongyang

    With the development of technologies for cellulosic biomass conversion to fuels and chemicals, bio-alcohols are among the main alternative feedstocks to fossil fuels. The research pursued in my thesis was the investigation of gold and palladium as catalysts for the application of short aliphatic alcohols to hydrogen generation and value-added chemicals production. Specifically, selective methanol steam reforming and non-oxidative ethanol dehydrogenation to hydrogen and acetaldehyde were investigated in this thesis work. A major aim of the thesis was to develop atomically efficient catalysts with tuned surface chemistry for the desired reactions, using suitable synthesis methods. Methanol steam reforming (SRM) for hydrogen production has recently been investigated on gold catalysts to overcome the drawbacks of copper catalysts (deactivation, pyrophoricity). Previous work at Tufts University has shown that both CeO2 and ZnO are suitable supports for gold. In this thesis, nanoscale composite oxides ZnZrOx were prepared by a carbon hard-template method, which resulted in homogeneous distribution of Zn species in the matrix of ZrO2. Tunable surface chemistry of ZnZrO x was demonstrated by varying the Zn/Zr ratio to suppress the strong Lewis acidity of ZrO2, which leads to undesired production of CO through methanol decomposition. With atomic dispersion of gold, Au/ZnZrO x catalyzes the SRM reaction exclusively via the methanol self-coupling pathway up to 375°C. The activity of Au/ZnZrOx catalysts was compared to Au/TiO2, which is another catalyst system demonstrating atomic dispersion of gold. Similarity in the apparent activation energy of SRM on all the supported gold catalysts studied in this thesis and in the literature further confirms the same single-site Au-Ox-MO centers as active sites for SRM with indirect effects of the supports exploited. With this fundamental understanding of gold-catalyzed C1 alcohol reforming, the Au/ZnZrOx catalyst was evaluated for the

  12. Transverse-energy distributions at midrapidity in $p$$+$$p$, $d$$+$Au, and Au$+$Au collisions at $\\sqrt{s_{_{NN}}}=62.4$--200~GeV and implications for particle-production models

    OpenAIRE

    Adler, S. S.; Afanasiev, S.; Aidala, C.; Ajitanand, N. N.; Akiba, Y; Al-Jamel, A.; Alexander, J.; Aoki, K.; Aphecetche, L.; Armendariz, R.; Aronson, S. H.; Averbeck, R.; Awes, T. C.; Azmoun, B.; Babintsev, V.

    2013-01-01

    Measurements of the midrapidity transverse energy distribution, $d\\Et/d\\eta$, are presented for $p$$+$$p$, $d$$+$Au, and Au$+$Au collisions at $\\sqrt{s_{_{NN}}}=200$ GeV and additionally for Au$+$Au collisions at $\\sqrt{s_{_{NN}}}=62.4$ and 130 GeV. The $d\\Et/d\\eta$ distributions are first compared with the number of nucleon participants $N_{\\rm part}$, number of binary collisions $N_{\\rm coll}$, and number of constituent-quark participants $N_{qp}$ calculated from a Glauber model based on th...

  13. A simple electrochemical biosensor based on AuNPs/MPS/Au electrode sensing layer for monitoring carbamate pesticides in real samples.

    Science.gov (United States)

    Song, Yonghai; Chen, Jingyi; Sun, Min; Gong, Coucong; Shen, Yuan; Song, Yonggui; Wang, Li

    2016-03-01

    A simple electrochemical biosensor for quantitative determination of carbamate pesticide was developed based on a sensing interface of citrate-capped gold nanoparticles (AuNPs)/(3-mercaptopropyl)-trimethoxysilane (MPS)/gold electrode (Au). The biosensor was fabricated by firstly assembling three-dimensional (3D) MPS networks on Au electrode and subsequently assembling citrate-capped AuNPs on 3D MPS network via AuS bond. The interface of AuNPs/MPS/Au was negatively charged originating from the citrate coated on AuNPs that would repulse the negatively charged ferricyanide ([Fe(CN)6](3-/4-)) to produce a negative response. In the presence of acetylcholinesterase (AChE) and acetylthiocholine (ATCl), the AChE catalyzes the hydrolysis of ATCl into positively charged thiocholine which would replace the citrate on AuNPs through the strong AuS bond and convert the negative charged surface to be positively charged. The resulted positively charged AuNPs/MPS/Au then attracted the [Fe(CN)6](3-/4-) to produce a positive response. Based on the inhibition of carbamate pesticides on the activity of AChE, the pesticide could be quantitatively determined at a very low potential. The linear range was from 0.003 to 2.00 μM. The sensing platform was also proved to be suitable for carbamate pesticides detection in practical sample.

  14. Efficient H2 production over Au/graphene/TiO2 induced by surface plasmon resonance of Au and band-gap excitation of TiO2

    International Nuclear Information System (INIS)

    Highlights: • Both surface plasmon resonance and band-gap excitation were used for H2 production. • Au/Gr/TiO2 composite photocatalyst was synthesized. • Au/Gr/TiO2 exhibited enhancement of light absorption and charge separation. • H2 production rate of Au/Gr/TiO2 was about 2 times as high as that of Au/TiO2. - Abstract: H2 production over Au/Gr/TiO2 composite photocatalyst induced by surface plasmon resonance of Au and band-gap excitation of TiO2 using graphene (Gr) as an electron acceptor has been investigated. Electron paramagnetic resonance study indicated that, in this composite, Gr collected electrons not only from Au with surface plasmon resonance but also from TiO2 with band-gap excitation. Surface photovoltage and UV–vis absorption measurements revealed that compared with Au/TiO2, Au/Gr/TiO2 displayed more effective photogenerated charge separation and higher optical absorption. Benefiting from these advantages, the H2 production rate of Au/Gr/TiO2 composite with Gr content of 1.0 wt% and Au content of 2.0 wt% was about 2 times as high as that of Au/TiO2. This work represents an important step toward the efficient application of both surface plasmon resonance and band-gap excitation on the way to converting solar light into chemical energy

  15. Stimulus Response of Au-NPs@GMP-Tb Core-Shell Nanoparticles: Toward Colorimetric and Fluorescent Dual-Mode Sensing of Alkaline Phosphatase Activity in Algal Blooms of a Freshwater Lake.

    Science.gov (United States)

    Zhang, Xiaolei; Deng, Jingjing; Xue, Yumeng; Shi, Guoyue; Zhou, Tianshu

    2016-01-19

    In this study, we demonstrate a colorimetric and fluorescent dual-mode method for alkaline phosphatase activity (APA) sensing in freshwater lake with stimuli-responsive gold nanoparticles@terbium-guanosine monophosphate (Au-NPs@GMP-Tb) core-shell nanoparticles. Initially, the core-shell nanoparticles were fabricated based on Au-NPs decorated with a fluorescent GMP-Tb shell. Upon being excited at 290 nm, the as-formed Au-NPs@GMP-Tb core-shell nanoparticles emit green fluorescence, and the decorated GMP-Tb shell causes the aggregation of Au-NPs. However, the addition of ALP destroys GMP-Tb shell, resulting in the release of Au-NPs from the shell into the solvent. As a consequence, the aggregated Au-NPs solubilizes with the changes in the UV-vis spectrum of the dispersion, and in the meantime, the fluorescence of GMP-Tb shell turns off, which constitutes a new mechanism for colorimetric and fluorescent dual-mode sensing of APA. With the method developed here, we could monitor the dynamic change of APA during an algal bloom of a freshwater lake, both by the naked eye and further confirmed by fluorometric determination. This study not only offers a new method for on-site visible detection of APA but also provides a strategy for dual-mode sensing mechanisms by the rational design of the excellent optical properties of Au-NPs and the adaptive inclusion properties of the luminescent infinite coordination polymers.

  16. Chapitre 5. Robots au Japon : le futur se conjugue au présent

    OpenAIRE

    Barral, Étienne

    2016-01-01

    2015... Les analystes japonais aiment bien projeter leurs lecteurs dans le futur. En 2015 donc, selon le Rapport intérimaire du comité stratégique en robotique du ministère japonais de l’Économie, du Commerce et de l’Industrie, le marché de la robotique au Japon représentera 1,1 billion de yens (7,8 milliards d’euros). Une somme, déjà astronomique, à rapprocher de la production japonaise des ordinateurs personnels en 2005 : 1,6 billion de yens (10,8 milliards d’euros). Dans moins d’une décenn...

  17. Structure investigation of organic molecules on Au(111) surfaces; Strukturuntersuchung organischer Molekuele auf Au(111)-Oberflaechen

    Energy Technology Data Exchange (ETDEWEB)

    Kazempoor, Michel

    2009-02-02

    The present work covers two topics namely the coadsorption of formic acid and water on Au(111) and the structure of biphenylalkanthiole SAMs on Au(111) surfaces. The coadsorption of formic acid and water on Au(111) surfaces has been investigated by means of vibrational and photoelectron spectroscopy (HREELS, XPS). Formic acid adsorbs at 90 K molecularly with vibrational modes characteristic for flat lying zig-zag chains in the mono- and multilayer regime, like in solid formic acid. The structure of the flat lying formic acid chains was determined by low energy electron diffraction (LEED) as a (2r3 x r19) unit cell. Annealing results in a complete desorption at 190 K. Sequential adsorption of formic acid and water at 90 K shows no significant chemical interaction. Upon annealing the coadsorbed layer to 140 K a hydrogenbonded cyclic complex of formic acid with one water molecule could be identified using isotopically labelled adsorbates. Upon further annealing this complex decomposes leaving molecularly adsorbed formic acid on the surface at 160 K, accompanied by a proton exchange between formic acid and water. The influence of the alkane spacer chain length on the structure of biphenylalkanethiols on Au(111) surfaces was investigated as well. A systematic study was done on BPn-SAMs deposited from the gas phase. For every chain length a structure was found by LEED. Furthermore the influence of temperature on the structure was investigated in the range from room temperature up to about 400 K. To obviate influences from different preparation methods BP3 and BP4 was deposited from gas phase and from solution. No LEED spots were observed on BP4 SAMs deposited from solution. For BP3 an influence of the preparation could be excluded. For all BPn-SAMs a good agreement between LEED and STM data's was found. Nevertheless different unit cells were determined by LEED and STM consistent structures could be suggested considering the unit cell size given by LEED and the

  18. Mechanical and charge transport properties of alkanethiol self-assembled monolayers on Au (111) surface: The Role of Molecular Tilt

    Energy Technology Data Exchange (ETDEWEB)

    Mulleregan, Alice; Qi, Yabing; Ratera, Imma; Park, Jeong Y.; Ashby, Paul D.; Quek, Su Ying; Neaton, J. B.; Salmeron, Miquel

    2007-11-12

    The relationship between charge transport and mechanical properties of alkanethiol self-assembled monolayers (SAM) on Au(111) films has been investigated using an atomic force microscope with a conductive tip. Molecular tilts induced by the pressure applied by the tip cause stepwise increases in film conductivity. A decay constant {beta} = 0.57 {+-} 0.03 {angstrom}{sup -1} was found for the current passing through the film as a function of tip-substrate separation due to this molecular tilt. This is significantly smaller than the value of {approx} 1 {angstrom}{sup -1} found when the separation is changed by changing the length of the alkanethiol molecules. Calculations indicate that for isolated dithiol molecules S-bonded to hollow sites, the junction conductance does not vary significantly as a function of molecular tilt. The impact of S-Au bonding on SAM conductance is discussed.

  19. Massignon face au sionisme Massignon and Zionism

    Directory of Open Access Journals (Sweden)

    Agathe Mayeres

    2010-03-01

    Full Text Available En 1916, Louis Massignon participe aux négociations franco-britanniques qui envisagent, dans la perspective de la capitulation probable des empires centraux, le futur partage de l’Empire ottoman. Dans ce contexte, Massignon cherche à se situer face la question sioniste qui, pour lui, est avant tout un problème de politique orientale.Sous l’influence d'Aaron Aaronsohn, l’islamologue éprouve d’abord pour les pionniers d’Eretz Israel, au regard de leurs réalisations agricoles, une sympathie enthousiaste qui lui fait souhaiter la réussite de l’établissement du Foyer national juif en Palestine. Son engagement l’incite notamment à rédiger, conjointement avec Maritain, un « rapport sur le sionisme », adressé à Pie XI en 1925, dans le but d’obtenir du Saint-Siège un soutien pour les Juifs convertis au catholicisme qui souhaiteraient participer à l’œuvre commune de la résurrection d’Israël. Cependant, les procédés « colonisateurs » et l’athéisme affiché de nombreux dirigeants sionistes, allant à l’encontre des convictions religieuses des Arabes autochtones chrétiens et musulmans, provoquent peu à peu chez Massignon un revirement total qui lui dicte à l’égard des Juifs des « propos excessifs ». Massignon considère qu’en Terre Sainte, il est impossible de séparer le temporel du spirituel et que les faits doivent être lus à la lumière des événements de l’histoire religieuse qui s’y sont déroulés depuis Abraham, « premier héros de l’hospitalité ».La prise de conscience de la pureté de Marie lui paraît la condition nécessaire à une reconnaissance juive dans l’esprit du Patriarche, bien plus, un préalable à toute paix. Massignon voit dans l’Immaculée Conception le « signe marial » de ralliement des diverses confessions de la famille abrahamique.In 1916, facing the probable capitulation of the Central Powers, Louis Massignon participates in French

  20. Relégation au village

    Directory of Open Access Journals (Sweden)

    Nicolas Renahy

    2010-12-01

    Full Text Available Les thèses de l’individualisation des sociétés occidentales, ou de l’exclusion de ceux qui resteraient en marge d’une vaste classe moyenne aux modes de vie homogénéisés, ont sans doute permis de sortir d’une grille de lecture rigide héritée du marxisme. Mais elles résistent aujourd’hui mal aux faits et sont vivement contredites par le renouvellement des études sur les inégalités sociales pensées en termes de stratification. Enquêtant la population ouvrière d’un village industriel de Bourgogne au cours des années 1990, l’auteur a pu mesurer tout autant la force socialisatrice continue du groupe ouvrier sur sa jeunesse que le lent processus de délitement de ses cadres de références, longtemps stabilisés autour d’une mono-industrie métallurgique, provoquant une crise dans la reproduction de ce monde ouvrier. C’est cette crise de reproduction qui est évoquée ici. Dans un premier temps sont explicitées les formes passées de la présence industrielle au village, qui n’a jamais été celle d’un bastion de la grande industrie – la population locale n’est pas structurellement différenciée de celle de son environnement rural immédiat. L’exemple d’une lignée familiale d’artisans montre pour finir l’étroit maillage entre usine et structures sociales plus classiquement rurales, favorisant la constitution d’un capital d’autochtonie, déclinaison populaire du capital social.Relegation to the villageArguments demonstrating the individualisation of western societies, or the exclusion of those who stay on the margins of a vast middle class homogeneous life style, have no doubt allowed the move away from the rigid interpretations inherited from Marxism. However, these arguments resist today in spite of the facts and they are even keenly contradicted by the renewal of stratification studies on social inequalities. Analyzing the working population of an industrial village in Bourgogne during the

  1. Study of electrodepositing Au on hollow polystyrene microspheres

    Energy Technology Data Exchange (ETDEWEB)

    Jin Rong [Research Center of Laser Fusion, China Academy of Engineering Physics, P.O. Box 919-987, Mianyang 621900 (China); School of Material Science and Engineering, Xihua University, Chengdu 610039 (China); Zhang Yunwang [Research Center of Laser Fusion, China Academy of Engineering Physics, P.O. Box 919-987, Mianyang 621900 (China); Zhang Lin, E-mail: zhlmy@sina.com [Research Center of Laser Fusion, China Academy of Engineering Physics, P.O. Box 919-987, Mianyang 621900 (China); Wei Chengfu, E-mail: wcf@mail.xhu.edu.cn [School of Material Science and Engineering, Xihua University, Chengdu 610039 (China); Guo Jianjun [School of Material Science and Engineering, Xihua University, Chengdu 610039 (China)

    2013-01-15

    Highlights: Black-Right-Pointing-Pointer The gold is electrodeposited on hollow polystyrene microspheres by self-designed setup in this paper. Black-Right-Pointing-Pointer The Au electrodeposit is finer and more uniform on account of the microspheres freely move on the cathode. Black-Right-Pointing-Pointer The morphology, thickness and roughness of Au electrodeposits were analyzed using Scanning Electron Microscopy, X-ray diffraction and Atomic Force Microscope, respectively. - Abstract: The electrodeposited Au film on hollow polystyrene microspheres is successfully prepared by a set of self-designed device. The film is more compact and uniform on account of the microspheres freely moving on the cathode. These experiments mainly focus on the analysis of spherical symmetry, thickness and roughness of electrodeposited Au film. Under conditions of current density 1.5-3 mA cm{sup -2}, the temperature 25 Degree-Sign C, and the stirring rate 150 rpm, the electrodeposited microsphere is coated with a considerably orbicular film. The morphology, thickness and roughness of Au electrodeposits are studied by Scanning Electron Microscopy (SEM), X-ray diffraction (XRD) and Atomic Force Microscope (AFM), respectively.

  2. Observations of high spin states in {sup 179}Au

    Energy Technology Data Exchange (ETDEWEB)

    Carpenter, M.P.; Ahmad, I.; Blumenthal, D.J. [and others

    1995-08-01

    As part of a current study on the properties of the {pi} i{sub 13/2} intruder state in the A = 175-190 region, we conducted an experiment at ATLAS to observe high spin states in {sup 179}Au utilizing the reaction {sup 144}Sm({sup 40}Ar,p4n) at beam energies of 207 MeV and 215 MeV. To aid in the identification of {sup 179}Au, and to filter out the large amount of events from fission by-products, the Fragment Mass Analyzer was utilized in conjunction with ten Compton-suppression germanium detectors. In total, 11 x 10{sup 6} {gamma}-{gamma} and 4 x 10{sup 5} {gamma}-recoil events were collected. By comparing {gamma}-rays in coincidence with an A = 179 recoil mass gate and {gamma}-rays in coincidence with Au K{alpha} and K{beta} X-rays, ten {gamma}-rays were identified as belonging to {sup 179}Au. Based on {gamma}-ray coincidence relationships and on comparisons with neighboring odd-A Au nuclei, we constructed a tentative level scheme and assigned a rotational-like sequence to the {pi} i{sub 13/2} proton configuration.

  3. Collisional modelling of the AU Microscopii debris disc

    CERN Document Server

    Schüppler, Ch; Krivov, A V; Ertel, S; Marshall, J P; Wolf, S; Wyatt, M C; Augereau, J -C; Metchev, S A

    2015-01-01

    The spatially resolved AU Mic debris disc is among the most famous and best-studied debris discs. We aim at a comprehensive understanding of the dust production and the dynamics of the disc objects with in depth collisional modelling including stellar radiative and corpuscular forces. Our models are compared to a suite of observational data for thermal and scattered light emission, ranging from the ALMA radial surface brightness profile at 1.3mm to polarisation measurements in the visible. Most of the data can be reproduced with a planetesimal belt having an outer edge at around 40au and subsequent inward transport of dust by stellar winds. A low dynamical excitation of the planetesimals with eccentricities up to 0.03 is preferred. The radial width of the planetesimal belt cannot be constrained tightly. Belts that are 5au and 17au wide, as well as a broad 44au-wide belt are consistent with observations. All models show surface density profiles increasing with distance from the star as inferred from observatio...

  4. L'APPRENTISSAGE AU CERN - French version only

    CERN Multimedia

    2003-01-01

    APPRENTISSAGES TECHNIQUES FORMATION ET DEVELOPPEMENT HR/TD/AP L'APPRENTISSAGE AU CERN pour les professions d'électronicien(ne) et de laborantin(e) en physique L'apprentissage au CERN est régi par les lois, règlements et contrats en vigueur dans le Canton de Genève. En cas de réussite à l'examen de fin d'apprentissage, les apprentis obtiennent le Certificat Fédéral de Capacité Suisse (CFC). 7 places au total sont ouvertes au recrutement pour les deux professions. L'apprentissage dure 4 ans. Minima requis pour faire acte de candidature : - avoir terminé la scolarité obligatoire - être ressortissant d'un pays membre du CERN (Allemagne, Autriche, Belgique, Bulgarie, Danemark, Espagne, Finlande, France, Grèce, Hongrie, Italie, Norvège, Pays-Bas, Pologne, Portugal, République slovaque, République tchèque, Royaume-Uni, Suède, Suisse) - avoir au moins 15 ans et moins de 21 ans à la date de début de l'apprentissage - avoir un niveau scolaire correspondant à la 9ème générale ou moderne...

  5. Disposable all-solid-state pH and glucose sensors based on conductive polymer covered hierarchical AuZn oxide.

    Science.gov (United States)

    Kim, Dong-Min; Cho, Seong Je; Cho, Chul-Ho; Kim, Kwang Bok; Kim, Min-Yeong; Shim, Yoon-Bo

    2016-05-15

    Poly(terthiophene benzoic acid) (pTBA) layered-AuZn alloy oxide (AuZnOx) deposited on the screen printed carbon electrode (pTBA/AuZnOx/SPCE) was prepared to create a disposable all-solid-state pH sensor at first. Further, FAD-glucose oxidase (GOx) was immobilized onto the pTBA/AuZnOx/SPCE to fabricate a glucose sensor. The characterizations of the sensor probe reveal that AuZnOx forms a homogeneous hierarchical structure, and that the polymerized pTBA layer on the alloy oxide surface captures GOx covalently. The benzoic acid group of pTBA coated on the probe layer synergetically improved the pH response of the alloy oxide and provide chemical binding sites to enzyme, which resulted in a Nernstian behavior (59.2 ± 0.5 mV/pH) in the pH range of 2-13. The experimental parameters affecting the glucose analysis were studied in terms of pH, temperature, humidity, and interferences. The sensor exhibited a fast response time <1s and a dynamic range between 30 and 500 mg/dL glucose with a detection limit of 17.23 ± 0.32 mg/dL. The reliabilities of the disposable pH and glucose sensors were examined for biological samples. PMID:26703994

  6. Interaction Kinetics between Sn-Pb Solder Droplet and Au/Ni/Cu Pad

    Institute of Scientific and Technical Information of China (English)

    Fuquan LI; Chunqing WANG; Yanhong TIAN

    2006-01-01

    The interfacial phenomena of the Sn-Pb solder droplet on Au/Ni/Cu pad are investigated. A continuous AuSn2and needle-like AuSn4 are formed at the interface after the liquid state reaction (soldering). The interfacial reaction between the solder and Au layer continues during solid state aging with AuSn4 breaking off from the interface and felling into the solder. The kinetics of Au layer dissolution and diffusion into the solder during soldering and aging is analyzed to elucidate intermetallic formation mechanism at the solder/Au pad interface.The concentration of Au near the solder/pad interface is identified to increase and reach the solubility limit during the period of liquid state reaction. During solid state reaction, the thickening of Au-Sn compound is mainly controlled by element diffusion.

  7. Ordered phase formation and diffusion composition path in Cu3Au/Pd couple

    International Nuclear Information System (INIS)

    EDX-TEM technique, IKL-ALCHEMI and Monte Carlo simulation were employed to reveal the relation between diffusion composition path and the ordered structures in Cu3Au/Pd diffusion couple annealed at 573 K. A Cu3Au layer including Pd, a CuAu layer including Pd, a CuPd layer and a Pd layer including Cu existed in sequence between Cu3Au and Pd. The Au concentration increased by up-hill diffusion from the Cu3Au layer to the CuAu layer, whereas Au scarcely diffused from the CuAu into the CuPd layer. The diffusion composition path deviated from the Cu3Au-Pd line in the Cu-Au-Pd Gibbs triangle and exhibited an 'S-shaped' curve through the CuAu and CuPd existence regions. The atomic configurations in the L10-type phase were highly ordered and consistent with the equilibrium state. In the Monte Carlo simulation, diffusion couples were virtually produced. The diffusion composition paths, Fourier power spectra and Warren-Cowley parameters were estimated in this way. The strong ordering interactions of the Cu-Au pair and Cu-Pd pair in the first nearest neighbor and the high activation barrier for migration of Au reproduced experimental results

  8. Transverse momentum and centrality dependence of high-pt non-photonic electron suppression in Au+Au collisions at $\\sqrt{s_{NN}}$ = 200 GeV

    CERN Document Server

    Abelev, B I; Aggarwal, M M; Ahammed, Z; Amonett, J; Anderson, B D; Anderson, M; Arkhipkin, D; Averichev, G S; Bai, Y; Balewski, J; Barannikova, O; Barnby, L S; Baudot, J; Bekele, S; Belaga, V V; Bellingeri-Laurikainen, A; Bellwied, R; Benedosso, F; Bhardwaj, S; Bhasin, A; Bhati, A K; Bichsel, H; Bielcik, J; Bielcikova, J; Bland, L C; Blyth, S L; Bonner, B E; Botje, M; Bouchet, J; Brandin, A V; Bravar, A; Bystersky, M; Cadman, R V; Cai, X Z; Caines, H; Calderón de la Barca-Sanchez, M; Castillo, J; Catu, O; Cebra, D; Chajecki, Z; Chaloupka, P; Chattopadhyay, S; Chen, H F; Chen, J H; Cheng, J; Cherney, M; Chikanian, A; Christie, W; Coffin, J P; Cormier, T M; Cosentino, M R; Cramer, J G; Crawford, H J; Das, D; Das, S; Daugherity, M; De Moura, M M; Dedovich, T G; De Phillips, M; Derevshchikov, A A; Didenko, L; Dietel, T; Djawotho, P; Dogra, S M; Dong, W J; Dong, X; Draper, J E; Du, F; Dunin, V B; Dunlop, J C; Dutta-Majumdar, M R; Eckardt, V; Edwards, W R; Efimov, L G; Emelianov, V; Engelage, J; Eppley, G; Erazmus, B; Estienne, M; Fachini, P; Fatemi, R; Fedorisin, J; Filimonov, K; Filip, P; Finch, E; Fine, V; Fisyak, Yu; Fu, J; Gagliardi, C A; Gaillard, L; Ganti, M S; Ghazikhanian, V; Ghosh, P; González, J E; Gorbunov, Y G; Gos, H; Grebenyuk, O; Grosnick, D P; Guertin, S M; Guimaraes, K S F F; Guo, Y; Gupta, N; Gutíerrez, T D; Haag, B; Hallman, T J; Hamed, A; Harris, J W; He, W; Heinz, M; Henry, T W; Hepplemann, S; Hippolyte, B; Hirsch, A; Hjort, E; Hoffmann, G W; Horner, M J; Huang, H Z; Huang, S L; Hughes, E W; Humanic, T J; Igo, G; Jacobs, P; Jacobs, W W; Jakl, P; Jia, F; Jiang, H; Jones, P G; Judd, E G; Kabana, S; Kang, K; Kapitan, J; Kaplan, M; Keane, D; Kechechyan, A; Khodyrev, V Yu; Kim, B C; Kiryluk, J; Kisiel, A; Kislov, E M; Klein, S R; Koetke, D D; Kollegger, T; Kopytine, M; Kotchenda, L; Kouchpil, V; Kowalik, K L; Krämer, M; Kravtsov, P; Kravtsov, V I; Krüger, K; Kuhn, C; Kulikov, A I; Kumar, A; Kuznetsov, A A; Lamont, M A C; Landgraf, J M; Lange, S; La Pointe, S; Laue, F; Lauret, J; Lebedev, A; Lednicky, R; Lee, C H; Lehocka, S; Le Vine, M J; Li, C; Li, Q; Li, Y; Lin, G; Lin, X; Lindenbaum, S J; Lisa, M A; Liu, F; Liu, H; Liu, J; Liu, L; Liu, Z; Ljubicic, T; Llope, W J; Long, H; Longacre, R S; López-Noriega, M; Love, W A; Lu, Y; Ludlam, T; Lynn, D; Ma, G L; Ma, J G; Ma, Y G; Magestro, D; Mahapatra, D P; Majka, R; Mangotra, L K; Manweiler, R; Margetis, S; Markert, C; Martin, L; Matis, H S; Matulenko, Yu A; McClain, C J; McShane, T S; Melnik, Yu M; Meschanin, A; Miller, M L; Minaev, N G; Mioduszewski, S; Mironov, C; Mischke, A; Mishra, D K; Mitchell, J; Mohanty, B; Molnár, L; Moore, C F; Morozov, D A; Munhoz, M G; Nandi, B K; Nattrass, C; Nayak, T K; Nelson, J M; Netrakanti, P K; Nikitin, V A; Nogach, L V; Nurushev, S B; Odyniec, Grazyna Janina; Ogawa, A; Okorokov, V; Oldenburg, M; Olson, D; Pachr, M; Pal, S K; Panebratsev, Yu A; Panitkin, S Y; Pavlinov, A I; Pawlak, T; Peitzmann, T; Perevozchikov, V; Perkins, C; Peryt, W; Petrov, V A; Phatak, S C; Picha, R; Planinic, M; Pluta, J; Poljak, N; Porile, N; Porter, J; Poskanzer, A M; Potekhin, M V; Potrebenikova, E V; Potukuchi, B V K S; Prindle, D; Pruneau, C; Putschke, J; Rakness, G; Raniwala, R; Raniwala, S; Ray, R L; Razin, S V; Reinnarth, J; Relyea, D; Retière, F; Ridiger, A; Ritter, H G; Roberts, J B; Rogachevski, O V; Romero, J L; Rose, A; Roy, C; Ruan, L; Russcher, M J; Sahoo, R; Salur, S; Sandweiss, J; Sarsour, M; Sazhin, P S; Schambach, J; Scharenberg, R P; Schmitz, N; Schweda, K; Seger, J; Selyuzhenkov, I; Seyboth, P; Shabetai, A; Shahaliev, E; Shao, M; Sharma, M; Shen, W Q; Shimansky, S S; Sichtermann, E P; Simon, F; Singaraju, R N; Smirnov, N; Snellings, R; Sood, G; Sørensen, P; Sowinski, J; Speltz, J; Spinka, H M; Srivastava, B; Stadnik, A; Stanislaus, T D S; Stock, R; Stolpovsky, A; Strikhanov, M N; Stringfellow, B C; Suaide, A A P; Sugarbaker, E R; Sumbera, M; Sun, Z; Surrow, B; Swanger, M; Symons, T J M; Szanto de Toledo, A; Tai, A; Takahashi, J; Tang, A H; Tarnowsky, T J; Thein, D; Thomas, J H; Timmins, A R; Timoshenko, S; Tokarev, M; Trainor, T A; Trentalange, S; Tribble, R E; Tsai, O D; Ulery, J; Ullrich, T; Underwood, D G; Van Buren, G; Van der Kolk, N; Van Leeuwen, M; Van der Molen, A M; Varma, R; Vasilevski, I M; Vasilev, A N; Vernet, R; Vigdor, S E; Viyogi, Y P; Vokal, S; Voloshin, S A; Waggoner, W T; Wang, F; Wang, G; Wang, J S; Wang, X L; Wang, Y; Watson, J W; Webb, J C; Westfall, G D; Wetzler, A; Whitten, C; Wieman, H; Wissink, S W; Witt, R; Wood, J; Wu, J; Xu, N; Xu, Q H; Xu, Z; Yepes, P; Yoo, I K; Yurevich, V I; Zhan, W; Zhang, H; Zhang, W M; Zhang, Y; Zhang, Z P; Zhao, Y; Zhong, C; Zoulkarneev, R; Zoulkarneeva, Y; Zubarev, A N; Zuo, J X; al, et

    2006-01-01

    The STAR collaboration at RHIC reports measurements of the inclusive yield of non-photonic electrons, which arise dominantly from semi-leptonic decays of heavy flavor mesons, over a broad range of transverse momenta ($1.2 < \\pt < 10$ \\gevc) in \\pp, \\dAu, and \\AuAu collisions at \\sqrtsNN = 200 GeV. The non-photonic electron yield exhibits unexpectedly large suppression in central \\AuAu collisions at high \\pt, suggesting substantial heavy quark energy loss in hot QCD matter. The centrality and \\pt dependences of the suppression provide stringent constraints on theoretical models of suppression.

  9. Site Restoration

    International Nuclear Information System (INIS)

    The objectives, the programme, and the achievements of SCK-CEN's Site Restoration Department for 2001 are described. Main activities include the decommissioning of the BR3 PWR-reactor as well as other clean-up activities, projects on waste minimisation and the management of spent fuel and the flow of dismantled materials and the recycling of materials from decommissioning activities based on the smelting of metallic materials in specialised foundries. The department provides consultancy and services to external organisations and performs R and D on new techniques including processes for the treatment of various waste components including the reprocessing of spent fuel, the treatment of tritium, the treatment of liquid alkali metals into cabonates through oxidation, the treatment of radioactive organic waste and the reconditioning of bituminised waste products

  10. Mochovce site

    International Nuclear Information System (INIS)

    In Mochovce site the construction of four units of WWER 440 NPP with V-213 type of reactor is being carried out. The financing of Mochovce units completion was resolved in April 1996. The completion work commenced at the construction site under leadership of SKODA Prague, the general supplier. The completion work on building part and tests of constructional electric distributions and lightning constructors started. The revisions in technological part were finished, and final protocols from revisions are the basis for starting of completion work. The assembly of transport container anchorage,ventilation system in hermetic areas and hermetic coverage of pools for stored spent nuclear fuel is being carried out. The pre-completion tests of instrumentation and control of ventilation systems, individual dosimetric control in medical station, and tests of nuclear programme according to commissioning and assembling work schedule at the equipment for physical protection of the NPP area started. Inspection activities at Mochovce were performed in accordance with inspection plan for 1996. Evaluation of routine inspections was performed by means of quarterly protocols. Main findings from the inspections performed in Mochovce were in the following areas: (a) deficiencies in the knowledge of the respective regulation and conditions from the Resolution of the state regulatory body, concerning selected employees; (b) training of the selected employees; (c) aim of the measures imposes by inspectors is to eliminate deficiencies in preparation of programmes for pre-completion and completion testing. NRA SR assessment activities at Mochovce NPP were focused mainly on approving and inspecting of design modification to approving programmes for pre-completion and completion testing of system s and equipment and on approving quality assurance programmes. The suggestions of international missions, which reviewed Mochovce safety in the years, were taken into consideration in the programme

  11. Preparation and evaluation of Au nanoparticle–silica aerogel nanocomposite

    Directory of Open Access Journals (Sweden)

    Naruhito Katagiri

    2015-06-01

    Full Text Available A Au nanoparticle–silica aerogel nanocomposite was prepared by the gelling of a tetramethyl orthosilicate (TMOS/ethanol solution together with Au nanoparticles and drying the wet gel in supercritical carbon dioxide. The aerogel nanocomposite contained Au nanoparticles at a concentration of 0.268 ppm. The bulk density, porosity, and specific surface area of the obtained nanocomposite were 0.126 g/cm3, 94%, and 890 m2/g, respectively. The nanocomposite was reddish-violet in color and transparent, and had a relative permittivity of approximately 6 with a dielectric loss of ca. 1 × 10−3 in the range of 10 MHz to 1 GHz.

  12. Neutral atom transport from the termination shock to 1 AU

    CERN Document Server

    Bzowski, M; Bzowski, Maciej; Tarnopolski, Slawomir

    2006-01-01

    Dynamics of H, D, and heavy Energetic Neutral Atoms (ENA) between the termination shock and 1 AU is discussed in the context of the forthcoming NASA SMEX mission IBEX. In particular, effects of the velocity-dependent radiation pressure on atomic trajectories are considered and ionization losses between TS and 1 AU are studied. It is shown, among others, that most of the dynamical effects and ionization losses are induced within a few AU from the Sun, which translates to the time domain into $\\sim 1 - 3$ solar rotations before detection. This loosens considerably time requirements for tracking the ionization and radiation pressure history to just prior 3 months. ENA seem excellent tracers of the processes within the heliospheric interface, with the transport effects between the termination shock and detector relatively mild and easy to account for.

  13. The Adsorption of Nitromethane on the Au (111 Surface

    Directory of Open Access Journals (Sweden)

    F. Illas

    2001-11-01

    Full Text Available The density functional theory (DFT based hybrid-method B3LYP has been used to study the interaction of the nitromethane molecule (CH3NO2 with the Au(111 surface. The perfect Au(111 surface has been represented by a rather large cluster model, Au22, that was in turn used to extract information about the preferred adsorption geometry of the CH3NO2 species. In order to extract energetic information about the stability of adsorbed nitromethane, calculations were also performed for the gas-phase CH3NO2 molecule. The results obtained here are used to interpret experimental data. The computed geometry for adsorbed CH3NO2 agrees with the structure proposed from a previous experimental work.

  14. Controlled electrodeposition of Au monolayer film on ionic liquid

    Science.gov (United States)

    Ma, Qiang; Pang, Liuqing; Li, Man; Zhang, Yunxia; Ren, Xianpei; Liu, Shengzhong Frank

    2016-05-01

    Gold (Au) nanoparticles have been attractive for centuries for their vibrant appearance enhanced by their interaction with sunlight. Nowadays, there have been tremendous research efforts to develop them for high-tech applications including therapeutic agents, sensors, organic photovoltaics, medical applications, electronics and catalysis. However, there remains to be a challenge to fabricate a monolayer Au coating with complete coverage in controlled fashion. Here we present a facile method to deposit a uniform Au monolayer (ML) film on the [BMIM][PF6] ionic liquid substrate using an electrochemical deposition process. It demonstrates that it is feasible to prepare a solid phase coating on the liquid-based substrate. Moreover, the thickness of the monolayer coating can be controlled to a layer-by-layer accuracy.

  15. Fermi surfaces of surface states on Si(111)-Ag, Au

    Science.gov (United States)

    Crain, J. N.; Altmann, K. N.; Bromberger, C.; Himpsel, F. J.

    2002-11-01

    Metallic surface states on semiconducting substrates provide an opportunity to study low-dimensional electrons decoupled from the bulk. Angle resolved photoemission is used to determine the Fermi surface, group velocity, and effective mass for surface states on Si(111)(3)×(3)-Ag, Si(111)(3)×(3)-Au, and Si(111)(21)×(21)-(Ag+Au). For Si(111)(3)×(3)-Ag the Fermi surface consists of small electron pockets populated by electrons from a few % excess Ag. For Si(111)(21)×(21)-(Ag+Au) the pockets increase their size corresponding to a filling by three electrons per unit cell. The (21)×(21) superlattice leads to an intricate surface umklapp pattern and to minigaps of 110 meV, giving an interaction potential of 55 meV for the (21)×(21) superlattice.

  16. Plasmonic Fano resonances in compositional heterogenous Al- Au nanorod dimers

    Science.gov (United States)

    Wu, Botao; Xue, Yingxian; Ma, Qiang; Ding, Chengjie; Rong, Youying; Liu, Yan; Chen, Lingxiao; Wu, E.; Zeng, Heping

    2016-01-01

    We have investigated theoretically the plasmon resonance coupling in compositional heterogenous Al-Au nanorod dimers organized in a close proximity by end-to-end. It has been proved that the destructive interference between the bright dipole mode from Al nanorod and the dark quadrupole mode from Au nanorod nearby results in the appearance of apparent Fano resonance in the extinction spectra. The Fano resonance response on the structural dimension modifications in the proposed nanorod dimers have been estimated and determined. The Al-Au heterogeneous nanorod dimer shows a high sensitivity to the surrounding environment with a local surface plasmon resonance figure of merit of 7.6, which enables its promising applications in plasmonic sensing and detection.

  17. Adsorption sites of single noble metal atoms on the rutile TiO2 (1 1 0) surface influenced by different surface oxygen vacancies

    International Nuclear Information System (INIS)

    Atomic adsorption of Au and Pt on the rutile (1 1 0) surface was investigated by atomic-resolution aberration-corrected scanning transmission electron microscopy (STEM) measurements combined with density functional theory calculations. Au single atoms were deposited on the surface in a vacuum condition, and the observed results were compared with Pt single atoms on the same surface prepared by the same experimental manner. It was found that Au single atoms are stably adsorbed only at the bridging oxygen vacancy sites, which is quite different from Pt single atoms exhibiting the most frequently observed adsorption at the basal oxygen vacancy sites. Such a difference in oxygen-vacancy effect between Au and Pt can be explained by electronic structures of the surface vacancies as well as characters of outermost atomic orbitals of Au and Pt. (paper)

  18. Une nouvelle exposition permanente au CERN

    CERN Multimedia

    CERN Press Office. Geneva

    1997-01-01

    The work of CERN, the European Laboratory for Particle Physics, is to understand how matter behaves. What are the ultimate constituents of the Universe? Where do they come from? How do they all hold together? These exciting questions have been asked by each successive civilisation and it is the responsibility of scientists to communicate clearly the research which is carried out to further our understanding. CERN takes this responsibility seriously and in 1990 opened Microcosm, a permanent exhibition on the CERN site, to explain to the general public CERN's research and to communicate the excitement of science.

  19. Final Technical Report: First Principles Investigations for the Ensemble Effects of PdAu and PtAu Bimetallic Nanocatalysts

    Energy Technology Data Exchange (ETDEWEB)

    Ruqian Wu

    2012-05-18

    Bimetallic surfaces with tunable chemical properties have attracted broad attention in recent years due to their ample potential for heterogeneous catalysis applications. The local chemical properties of constituents are strongly altered from their parent metals by 'ligand effect', a term encompassing the influences of charge transfer, orbital rehybridization and lattice strain. In comparison to the aforementioned, the 'ensemble effect' associated with particular arrangements of the active constituents have received much less attention, despite their notable importance towards the determination of reactivity and selectivity of bimetallic catalysts. We performed theoretical studies for understanding the ensemble effects on bimetallic catalysis: (i) simulations for the formation of different ensembles on PdAu and PtAu nanoclusters; (ii) studies of the size, shape, and substrate dependence of their electronic properties; and (iii) simulations for model reactions such as CO oxidation, methanol, ethylene and water dehydrogenation on PdAu and PtAu nanoclusters. In close collaboration with leading experimental groups, our theoretical research elucidated the fundamentals of Au based bimetallic nanocatalysts.

  20. Measurement of direct photons in Au+Au collisions at √(s(NN))=200 GeV.

    Science.gov (United States)

    Afanasiev, S; Aidala, C; Ajitanand, N N; Akiba, Y; Al-Jamel, A; Alexander, J; Aoki, K; Aphecetche, L; Armendariz, R; Aronson, S H; Averbeck, R; Awes, T C; Azmoun, B; Babintsev, V; Baldisseri, A; Barish, K N; Barnes, P D; Bassalleck, B; Bathe, S; Batsouli, S; Baublis, V; Bauer, F; Bazilevsky, A; Belikov, S; Bennett, R; Berdnikov, Y; Bjorndal, M T; Boissevain, J G; Borel, H; Boyle, K; Brooks, M L; Brown, D S; Bucher, D; Buesching, H; Bumazhnov, V; Bunce, G; Burward-Hoy, J M; Butsyk, S; Campbell, S; Chai, J-S; Chernichenko, S; Chi, C Y; Chiba, J; Chiu, M; Choi, I J; Chujo, T; Cianciolo, V; Cleven, C R; Cobigo, Y; Cole, B A; Comets, M P; Connors, M; Constantin, P; Csanád, M; Csörgő, T; Dahms, T; Das, K; David, G; Delagrange, H; Denisov, A; d'Enterria, D; Deshpande, A; Desmond, E J; Dietzsch, O; Dion, A; Drachenberg, J L; Drapier, O; Drees, A; Dubey, A K; Durum, A; Dzhordzhadze, V; Efremenko, Y V; Egdemir, J; Enokizono, A; En'yo, H; Espagnon, B; Esumi, S; Fields, D E; Fleuret, F; Fokin, S L; Forestier, B; Fraenkel, Z; Frantz, J E; Franz, A; Frawley, A D; Fukao, Y; Fung, S-Y; Gadrat, S; Gastineau, F; Germain, M; Glenn, A; Gonin, M; Gosset, J; Goto, Y; Granier de Cassagnac, R; Grau, N; Greene, S V; Grosse Perdekamp, M; Gunji, T; Gustafsson, H-Å; Hachiya, T; Hadj Henni, A; Haggerty, J S; Hagiwara, M N; Hamagaki, H; Harada, H; Hartouni, E P; Haruna, K; Harvey, M; Haslum, E; Hasuko, K; Hayano, R; He, X; Heffner, M; Hemmick, T K; Heuser, J M; Hiejima, H; Hill, J C; Hobbs, R; Holmes, M; Holzmann, W; Homma, K; Hong, B; Horaguchi, T; Hur, M G; Ichihara, T; Iinuma, H; Imai, K; Imrek, J; Inaba, M; Isenhower, D; Isenhower, L; Ishihara, M; Isobe, T; Issah, M; Isupov, A; Jacak, B V; Jia, J; Jin, J; Jinnouchi, O; Johnson, B M; Joo, K S; Jouan, D; Kajihara, F; Kametani, S; Kamihara, N; Kaneta, M; Kang, J H; Kawagishi, T; Kazantsev, A V; Kelly, S; Khanzadeev, A; Kim, D J; Kim, E; Kim, Y-S; Kinney, E; Kiss, A; Kistenev, E; Kiyomichi, A; Klein-Boesing, C; Kochenda, L; Kochetkov, V; Komkov, B; Konno, M; Kotchetkov, D; Kozlov, A; Kroon, P J; Kunde, G J; Kurihara, N; Kurita, K; Kweon, M J; Kwon, Y; Kyle, G S; Lacey, R; Lajoie, J G; Lebedev, A; Le Bornec, Y; Leckey, S; Lee, D M; Lee, M K; Leitch, M J; Leite, M A L; Li, X H; Lim, H; Litvinenko, A; Liu, M X; Maguire, C F; Makdisi, Y I; Malakhov, A; Malik, M D; Manko, V I; Masui, H; Matathias, F; McCain, M C; McGaughey, P L; Miake, Y; Miller, T E; Milov, A; Mioduszewski, S; Mishra, G C; Mitchell, J T; Morrison, D P; Moss, J M; Moukhanova, T V; Mukhopadhyay, D; Murata, J; Nagamiya, S; Nagata, Y; Nagle, J L; Naglis, M; Nakamura, T; Newby, J; Nguyen, M; Norman, B E; Nyanin, A S; Nystrand, J; O'Brien, E; Ogilvie, C A; Ohnishi, H; Ojha, I D; Okada, K; Omiwade, O O; Oskarsson, A; Otterlund, I; Ozawa, K; Pak, R; Pal, D; Palounek, A P T; Pantuev, V; Papavassiliou, V; Park, J; Park, W J; Pate, S F; Pei, H; Peng, J-C; Pereira, H; Peresedov, V; Peressounko, D Yu; Pinkenburg, C; Pisani, R P; Purschke, M L; Purwar, A K; Qu, H; Rak, J; Ravinovich, I; Read, K F; Reuter, M; Reygers, K; Riabov, V; Riabov, Y; Roche, G; Romana, A; Rosati, M; Rosendahl, S S E; Rosnet, P; Rukoyatkin, P; Rykov, V L; Ryu, S S; Sahlmueller, B; Saito, N; Sakaguchi, T; Sakai, S; Samsonov, V; Sato, H D; Sato, S; Sawada, S; Semenov, V; Seto, R; Sharma, D; Shea, T K; Shein, I; Shibata, T-A; Shigaki, K; Shimomura, M; Shohjoh, T; Shoji, K; Sickles, A; Silva, C L; Silvermyr, D; Sim, K S; Singh, C P; Singh, V; Skutnik, S; Smith, W C; Soldatov, A; Soltz, R A; Sondheim, W E; Sorensen, S P; Sourikova, I V; Staley, F; Stankus, P W; Stenlund, E; Stepanov, M; Ster, A; Stoll, S P; Sugitate, T; Suire, C; Sullivan, J P; Sziklai, J; Tabaru, T; Takagi, S; Takagui, E M; Taketani, A; Tanaka, K H; Tanaka, Y; Tanida, K; Tannenbaum, M J; Taranenko, A; Tarján, P; Thomas, T L; Togawa, M; Tojo, J; Torii, H; Towell, R S; Tram, V-N; Tserruya, I; Tsuchimoto, Y; Tuli, S K; Tydesjö, H; Tyurin, N; Vale, C; Valle, H; van Hecke, H W; Velkovska, J; Vértesi, R; Vinogradov, A A; Vznuzdaev, E; Wagner, M; Wang, X R; Watanabe, Y; Wessels, J; White, S N; Willis, N; Winter, D; Woody, C L; Wysocki, M; Xie, W; Yanovich, A; Yokkaichi, S; Young, G R; Younus, I; Yushmanov, I E; Zajc, W A; Zaudtke, O; Zhang, C; Zimányi, J; Zolin, L

    2012-10-12

    We report the measurement of direct photons at midrapidity in Au+Au collisions at √(s(NN))=200 GeV. The direct photon signal was extracted for the transverse momentum range of 4 GeV/cAu+Au collision centralities using the measured p+p direct photon spectrum and compared to theoretical predictions. R(AA) was found to be consistent with unity for all centralities over the entire measured p(T) range. Theoretical models that account for modifications of initial direct photon production due to modified parton distribution functions in Au and the different isospin composition of the nuclei predict a modest change of R(AA) from unity. They are consistent with the data. Models with compensating effects of the quark-gluon plasma on high-energy photons, such as suppression of jet-fragmentation photons and induced-photon bremsstrahlung from partons traversing the medium, are also consistent with this measurement. PMID:23102300