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Sample records for pt surface areas

  1. Improving electromechanical output of IPMC by high surface area Pd-Pt electrodes and tailored ionomer membrane thickness

    Directory of Open Access Journals (Sweden)

    Viljar Palmre

    2014-04-01

    Full Text Available In this study, we attempt to improve the electromechanical performance of ionic polymer–metal composites (IPMCs by developing high surface area Pd-Pt electrodes and tailoring the ionomer membrane thickness. With proper electroless plating techniques, a high dispersion of palladium particles is achieved deep in the ionomer membrane, thereby increasing notably the interfacial surface area of electrodes. The membrane thickness is increased using 0.5 and 1 mm thick ionomer films. For comparison, IPMCs with the same ionomer membranes, but conventional Pt electrodes, are also prepared and studied. The electromechanical, mechanoelectrical, electrochemical and mechanical properties of different IPMCs are characterized and discussed. Scanning electron microscopy-energy dispersive X-ray (SEM-EDS is used to investigate the distribution of deposited electrode metals in the cross section of Pd-Pt IPMCs. Our experiments demonstrate that IPMCs assembled with millimeter thick ionomer membranes and newly developed Pd-Pt electrodes are superior in mechanoelectrical transduction, and show significantly higher blocking force compared to conventional type of IPMCs. The blocking forces of more than 0.3 N were measured at 4V DC input, exceeding the force output of typical Nafion® 117-based Pt IPMCs more than two orders of magnitude. The newly designed Pd-Pt IPMCs can be useful in more demanding applications, e.g., in biomimetic underwater robotics, where high stress and drag forces are encountered.

  2. Surface area loss mechanisms of Pt3Co nanocatalysts in proton exchange membrane fuel cells

    Science.gov (United States)

    Rasouli, S.; Ortiz Godoy, R. A.; Yang, Z.; Gummalla, M.; Ball, S. C.; Myers, D.; Ferreira, P. J.

    2017-03-01

    Pt3Co catalyst nanoparticles of 4.9 nm size present on the cathode side of a PEMFC membrane-electrode assembly (MEA) were analyzed by transmission electron microscopy after 10 K voltage cycles under different operating conditions. The operating conditions include baseline (0.4-0.95 V, 80° C, 100% Relative Humidity (RH)), high potential (0.4-1.05 V, 80° C, 100% RH), high temperature (0.4-0.95 V, 90° C, 100% RH), and low humidity (0.4-0.95 V, 80° C, 30% RH). Particle growth and particle loss to the membrane is more severe in the high potential sample than in the high temperature and baseline MEAs, while no significant particle growth and particle precipitation in the membrane can be observed in the low humidity sample. Particles with different morphologies were seen in the cathode including: 1-Spherical individual particles resulting from modified electro-chemical Ostwald ripening and 2-aggregated and coalesced particles resulting from either necking of two or more particles or preferential deposition of Pt between particles with consequent bridging. The difference in the composition of these morphologies results in composition variations through the cathode from cathode/diffusion media (DM) to the cathode/membrane interface.

  3. The role of surface Pt on the coadsorption of hydrogen and CO on Pt monolayer film modified Ru(0001) surfaces

    Science.gov (United States)

    Diemant, T.; Hartmann, H.; Bansmann, J.; Behm, R. J.

    2016-10-01

    We have investigated the impact and role of the Pt surface modification on the coadsorption of hydrogen and CO on structurally well defined bimetallic Pt monolayer island/film modified Ru(0001) surfaces with Pt contents up to a complete Pt layer, employing temperature programmed desorption (TPD) and infrared reflection absorption spectroscopy (IRRAS). Kinetic limitations in the surface diffusion are shown to play an important role for adsorption at 90 K, and lead to profound effects of the dosing sequence on the adsorption and desorption characteristics. Furthermore, they are responsible for spill-over effects during the TPD measurements, where COad becomes mobile and can spill-over from weakly bonding Pt monolayer areas to strongly bonding Pt-free Ru(0001) areas, which displaces Dad from these surface areas. The present findings are discussed in comparison with previous results on related metallic and bimetallic adsorption and coadsorption systems.

  4. Pt nanoparticle modified single walled carbon nanotube network electrodes for electrocatalysis: control of the specific surface area over three orders of magnitude

    NARCIS (Netherlands)

    Miller, T.S.; Sansuk, S.; Lai, S.C.S.; Macpherson, J.V.; Unwin, P.R.

    2015-01-01

    The electrodeposition of Pt nanoparticles (NPs) on two-dimensional single walled carbon nanotube (SWNT) network electrodes is investigated as a means of tailoring electrode surfaces with a well-defined amount of electrocatalytic material. Both Pt NP deposition and electrocatalytic studies are undert

  5. Surface termination of CePt5/Pt (111 ): The key to chemical inertness

    Science.gov (United States)

    Praetorius, C.; Zinner, M.; Held, G.; Fauth, K.

    2015-11-01

    The surface termination of CePt5/Pt (111 ) is determined experimentally by LEED-IV. In accordance with recent theoretical predictions, a dense Pt terminated surface is being found. Whereas the CePt5 volume lattice comprises Pt kagome layers, additional Pt atoms occupy the associated hole positions at the surface. This finding provides a natural explanation for the remarkable inertness of the CePt5 intermetallic. Implications of the structural relaxations determined by LEED-IV analysis are discussed with regard to observations by scanning tunneling microscopy and electron spectroscopies.

  6. Ab-initio study of the coadsorption of Li and H on Pt(001), Pt(110) and Pt(111) surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Saad, Farida [Laboratoire de Physique et Chimie Quantique, Faculte des Sciences, Universite Mouloud Mammeri, 15000 Tizi-Ouzou (Algeria); Zemirli, Mourad, E-mail: zemirlimourad@mail.ummto.dz [Laboratoire de Physique et Chimie Quantique, Faculte des Sciences, Universite Mouloud Mammeri, 15000 Tizi-Ouzou (Algeria); Benakki, Mouloud; Bouarab, Said [Laboratoire de Physique et Chimie Quantique, Faculte des Sciences, Universite Mouloud Mammeri, 15000 Tizi-Ouzou (Algeria)

    2012-02-15

    The coadsorption of Li and H atoms on Pt(001), Pt(110) and Pt(111) surfaces is studied using density functional theory with generalised gradient approximation. In all calculations Li, H and the two topmost layers of the metal were allowed to relax. At coverage of 0.25 mono-layer in a p(2 Multiplication-Sign 2) unit cell, lithium adsorption at the hollow site for the three surfaces is favoured over top and bridge sites. The most favoured adsorption sites for H atom on the Pt(001) and Pt(110) surfaces are the top and bridge sites, while on Pt(111) surface the fcc site appears to be slightly favoured over the hcp site. The coadsorption of Li and atomic hydrogen shows that the interaction between the two adsorbates is stabilising when they are far from each other. The analysis of Li, H and Pt local density of states shows that Li strongly interacts with the Pt surfaces.

  7. Surface Segregation in Supported Pd-Pt Nanoclusters and Alloys

    NARCIS (Netherlands)

    van den Oetelaar, L.C.A.; Nooij, O.W.; Oerlemans, S.; Denier van der Gon, A.W.; Brongersma, H.H.; Lefferts, Leonardus; Roosenbrand, A.G.; van Veen, J.A.R.

    1998-01-01

    Surface segregation processes in Pd-Pt alloys and bimetallic Pd-Pt nanoclusters on alumina and carbon supports (technical catalysts) have been investigated by determining the metal surface composition of these systems by low-energy ion scattering (LEIS). Both Pd-rich (Pd80Pt20) and Pt-rich

  8. Studies of surface processes of electrocatalytic reduction of CO2 on Pt(210), Pt(310) and Pt(510)

    Institute of Scientific and Technical Information of China (English)

    FAN; ChunJie; FAN; YouJun; ZHEN; ChunHua; ZHENG; QingWei; SUN; ShiGang

    2007-01-01

    Surface processes of CO2 reduction on Pt(210), Pt(310), and Pt(510) electrodes were studied by cyclic voltammetry. Different surface structures of these platinum single crystal electrodes were obtained by various treatment conditions. The experimental results illustrated that the electrocatalytic activity of Pt single crystal electrodes towards CO2 reduction is decreased in an order of Pt(210)>Pt(310)>Pt(510), i.e., with the decrease of (110) step density on well-defined surfaces. When the surfaces were reconstructed due to oxygen adsorption, the catalytic activity of all the three electrodes has been enhanced to a certain extent. Although the activity order remains unchanged, the electrocatalytic activity has been enhanced more significantly as the density of (110) step sites is more intensive on the Pt single crystal surface. It has revealed that the more open the surface structure is, the more active the Pt single crystal electrode will be, and the easier for the electrode to be transformed into a surface structure that exhibits higher activity under external inductions. However, the relatively ordered surfaces of Pt single crystal electrode are comparatively stable under the same external inductions. The present study has gained knowledge on the interaction between CO2 and Pt single crystal electrode surfaces at a microscopic level, and thrown new insight into understanding the surface processes of electrocatalytic reduction of CO2.

  9. Structure dependence of Pt surface activated ammonia oxidation

    Energy Technology Data Exchange (ETDEWEB)

    Santen, R A van; Offermans, W K [Schuit Institute of Catalysis, Laboratory of Inorganic Chemistry and Catalysis, Department of Chemical Engineering and Chemistry, Eindhoven University of Technology, PO Box 513, 5600 MB Eindhoven (Netherlands); Ricart, J M; Novell-Leruth, G [Department of Chemical Physics and Inorganic Chemistry, University Rovira I Virgili, C/ Marcel.lI Domingo s/n, 43007 Tarragona (Spain); Perez-RamIrez, J [Institute of Chemical Research of Catalonia (ICIQ) and Catalan, Institution for Research and Advanced Studies (ICREA), Avinguda Paisos Catalans 16, 43007, Tarragona (Spain)], E-mail: r.a.v.santen@tue.nl

    2008-06-01

    Computational advances that enable the prediction of the structures and the energies of surface reaction intermediates are providing essential information to the formulation of theories of surface chemical reactivity. In this contribution this is illustrated for the activation of ammonia by coadsorbed oxygen and hydroxyl on the Pt(111), Pt(100), and Pt(211) surfaces.

  10. Surface reconstruction of Pt(001) quantitatively revisited

    Science.gov (United States)

    Hammer, R.; Meinel, K.; Krahn, O.; Widdra, W.

    2016-11-01

    The complex hexagonal reconstructions of the (001) surfaces of platinum and gold have been under debate for decades. Here, the structural details of the Pt(001) reconstruction have been quantitatively reinvestigated by combining the high resolving power of scanning tunneling microscopy (STM) and spot profile analysis low energy electron diffraction (SPA-LEED). In addition, LEED simulations based on a Moiré approach have been applied. Annealing temperatures around 850 °C yield a superstructure that approaches a commensurable c (26.6 ×118 ) substrate registry. It evolves from a Moiré-like buckling of a compressed hexagonal top layer (hex) where atomic rows of the hex run parallel to atomic rows of the square substrate. Annealing at 920 °C stimulates a continuous rotation of the hex where all angles between ±0.7° are simultaneously realized. At temperatures around 1080 °C, the nonrotated hex coexists with a hex that is rotated by about 0.75°. Annealing at temperatures around 1120 °C yield a locking of the hex in fixed rotation angles of 0.77°, 0.88°, and 0.94°. At temperatures around 1170 °C, the Pt(001)-hex-R 0.94° prevails as the energetically most favored form of the rotated hex.

  11. Kinetic limitations in surface alloy formation: PtCu/Ru(0001)

    Science.gov (United States)

    Engstfeld, A. K.; Jung, C. K.; Behm, R. J.

    2016-01-01

    We have systematically investigated the structure and structure formation of two-dimensional PtCu monolayer surface alloys on Ru(0001) as model systems for bimetallic PtCu catalysts and surfaces by scanning tunneling microscopy (STM). The surface alloys were prepared by deposition of Pt and Cu on Ru(0001) and thermal intermixing; different procedures were developed and tested to produce bimetallic surfaces with homogeneous structure, including also a homogeneous distribution of the different surface species, while at the same time intermixing with the Ru(0001) substrate should be inhibited. STM imaging revealed that for Pt concentrations below 65% surface alloys with homogeneous distribution could be formed, while at higher concentrations in the mixed phase, up to 82%, pure Pt or Pt-rich surface areas were formed as well. At Pt contents of 0.20 0.65 line structures were observed, but of different nature. The distribution of surface atoms in the mixed phase was evaluated from STM images with chemical contrast, the related short-range order parameters were determined. The resulting structures and their energetics, the influence of different deposition and annealing procedures and the suitability of these surfaces as model systems for studies of the surface chemistry of bimetallic PtCu surfaces are discussed.

  12. Surface Chemistry of Aromatic Reactants on Pt- and Mo-Modified Pt Catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Robinson, Allison M.; Mark, Lesli; Rasmussen, Mathew J.; Hensley, Jesse E.; Medlin, J. Will

    2016-11-01

    Supported catalysts containing an oxophilic metal such as Mo and a noble metal such as Pt have shown promising activity and selectivity for deoxygenation of biomass-derived compounds. Here, we report that PtMo catalysts also promote hydrogenolysis of the model compound benzyl alcohol, while decarbonylation is most prevalent over unmodified Pt. A combination of single crystal surface science studies, density functional theory (DFT) calculations, and vapor phase upgrading experiments using supported catalysts was carried out to better understand the mechanism by which Mo promotes deoxygenation. Molybdenum was deposited in submonolayer quantities on a Pt(111) surface and reduced at high temperature. Temperature-programmed desorption (TPD) experiments using benzyl alcohol as a reactant showed greatly enhanced yields of the deoxygenation product toluene at moderate Mo coverages. To understand how the interaction of the aromatic group with the surface influenced this reactivity, we investigated the adsorption of toluene as a probe molecule. We found that the addition of Mo to Pt(111) resulted in a significant decrease in toluene decomposition. DFT calculations indicated that this decrease was consistent with decreased aromatic adsorption strengths that accompany incorporation of Mo into the Pt subsurface. The weaker aromatic-surface interaction on Pt/Mo surfaces led to a tilted adsorption geometry for benzyl alcohol, which presumably promotes hydrogenolysis to produce toluene instead of decarbonylation to produce benzene and CO. Alumina-supported Pt and PtMo catalysts were also tested for benzyl alcohol deoxygenation. PtMo catalysts had a higher rate of toluene production and lower rates of benzene and benzaldehyde production. Additionally, when benzaldehyde was used as the reactant to measure decarbonylation activity the mass-normalized rate of benzene production was 2.5 times higher on Pt than PtMo. Overall, the results of TPD, DFT, and supported catalyst experiments

  13. Theoretical Study of CO Adsorption on Ni(111), Pt(111) and Pt/Ni(111) Surfaces

    Science.gov (United States)

    Cabeza, G. F.; Castellani, N. J.; Légaré, P.

    CO adsorption on a pseudomorphic Pt overlayer supported by Ni(111) has been studied with the use of extended Huckel calculations. Experimental information on the pure Pt(111) and Ni(111) single crystals was employed to select a consistent parameter set for our bimetallic system. This gives a good description of the chemisorption bond changes between the various systems considered in our study. The CO chemisorption energy on Pt/Ni(111) was found to be lowered in comparison with Pt(111) and Ni(111), in good agreement with experimental data on Pt-rich Pt-Ni surface alloys. This observation could be justified by the electronic changes of the Pt states (valence band broadening and decreasing density at the Fermi level). Indeed, they induce, in comparison with the pure substrates, a repulsion between Pt and CO although the 2π* population of the chemisorbed molecule increases. This points to the necessity of going beyond arguments based on an analysis of the 5σ donation and 2π* backdonation for a complete description of the chemisorption bond.

  14. Adsorption of formaldehyde and formyl intermediates on Pt, PtRu-, and PtRuMo-alloy surfaces: A density functional study

    Science.gov (United States)

    Cahyanto, Wahyu Tri; Shukri, Ganes; Agusta, Mohammad Kemal; Kasai, Hideaki

    2013-02-01

    Stable binding configuration for formaldehyde (H2CO) and formyl (HCO) adsorption on Pt, PtRu, and PtRuMo are studied within the frame of density functional theory (DFT). We address this study to investigate the role of Ru and Mo on the binding characteristic of formaldehyde and formyl adsorption with respect to interaction strength and charge analysis. Several binding conformation on all possible surface adsorption sites are considered in determining the most stable adsorption geometry on three surfaces. Our results show that the presence of Ru in PtRu and Mo in PtRuMo stabilize the formaldehyde and formyl, which are indicated by stronger bond strength. Further electronic structure analysis shows that the addition of Ru in PtRu and Mo in PtRuMo modifies the electronic structure of Pt's surface significantly. The presence of both impurities shifted the derived anti-bonding state - which is originally located below the fermi level in pure Pt surface - to be above the fermi level in PtRu and PtRuMo systems. This fact explains the stronger adsorption found on PtRu & PtRuMo as compared to pure Pt surface.

  15. SURFACE PROPERTIES AND CATALYTIC PERFORMANCE OF Pt ...

    African Journals Online (AJOL)

    salt (AO) layers, have been examined for their low cost, high catalytic activity and high thermal ... of each peak after subtraction of the S-shaped background and fitting to a curve mixed of ..... In addition, for the 0.3 % Pt/LaSrCoO4 and 0.5.

  16. Adsorption of CO on Co(0001) and Pt Co(0001) surfaces: an experimental and theoretical study

    Science.gov (United States)

    Cabeza, G. F.; Légaré, P.; Castellani, N. J.

    2000-10-01

    CO adsorption on Co(0001) and Pt submonolayer deposits on Co(0001) at room temperature have been investigated by combining the surface techniques of low-energy electron diffraction and X-ray and UV photoelectron spectroscopy. The influence of bimetallic system formation on the CO adsorption was studied. CO is molecularly adsorbed on both surfaces. The saturation coverage under ultrahigh vacuum conditions corresponds to a well-ordered ( 3× 3)R30° structure in the presence of Pt. The CO uptake on Pt-Co(0001) was found to be lowered in comparison with Co(0001) as the platinum coverage increased between 0 to 0.6 ML. However, CO is adsorbed both on the Pt and Co areas. It is shown that CO is located in the top Pt sites, with an adsorption energy reduced by 38% with respect to the pure Pt(111) surface. This result is in good agreement with our theoretical results of CO chemisorption energy on a pseudomorphic Pt overlayer supported by Co(0001). A decreased Pt density of states at the Fermi level and a high binding energy shift of the d-band center in comparison with the pure metal was observed both experimentally and theoretically.

  17. Double stripe reconstruction of the Pt(111) surface

    Indian Academy of Sciences (India)

    Raghani Pushpa; Shobhana Narasimhan

    2003-01-01

    We have studied the reconstruction of the Pt(111) surface theoretically, using a 2D generalization of the Frenkel–Kontorova model. The parameters in the model are obtained by performing ab initio density functional theory calculations. The Pt(111) surface does not reconstruct under normal conditions but experiments have shown that there are two ways to induce the reconstruction: by increasing the temperature, or by depositing adatoms on the surface. The basic motif of this reconstruction is a `double stripe’ with an increased surface density and alternating hcp and fcc domains, arranged to form a honeycomb pattern with a very large repeat distance of 100–300 Å. In this paper, we have studied the `double stripe’ reconstruction of the Pt(111) surface. In agreement with experiment, we find that it is favourable for the surface to reconstruct in the presence of adatoms, but not otherwise.

  18. Characterization of a surface modified carbon cryogel and a carbon supported Pt catalyst

    Directory of Open Access Journals (Sweden)

    BILJANA M. BABIĆ

    2007-08-01

    Full Text Available A carbon cryogel, synthesized by carbonization of a resorcinol/formaldehyde cryogel and oxidized in nitric acid, was used as catalyst support for Pt nano-particles. The Pt/C catalyst was prepared by a modified polyol synthesis method in an ethylene glycol (EG solution. Characterization by nitrogen adsorption showed that the carbon cryogel support and the Pt/C catalyst were mesoporous materials with high specific surface areas (SBET > 400 m2 g-1 and large mesoporous volumes. X-Ray diffraction of the catalyst demonstrated the successful reduction of the Pt precursor to metallic form. TEM Images of the Pt/C catalyst and Pt particle size distribution showed that the mean Pt particle size was about 3.3 nm. Cyclic voltammetry (CV experiments at various scan rates (from 2 to 200 mV s-1 were performed in 0.5 mol dm-3 HClO4 solution. The large capacitance of the oxidized carbon cryogel electrode, which arises from a combination of the double-layer capacitance and pseudocapacitance, associated with the participation of surface redox-type reactions was demonstrated. For the oxidized carbon cryogel, the total specific capacitance determined by 1/C vs. ν0.5 extrapolation method was found to be 386 F g-1. The hydrogen oxidation reaction at the investigated Pt/C catalyst proceeded as an electrochemically reversible, two-electron direct discharge reaction.

  19. Catalytically favorable surface patterns in Pt-Au nanoclusters

    KAUST Repository

    Mokkath, Junais Habeeb

    2013-01-01

    Motivated by recent experimental demonstrations of novel PtAu nanoparticles with highly enhanced catalytic properties, we present a systematic theoretical study that explores principal catalytic indicators as a function of the particle size and composition. We find that Pt electronic states in the vicinity of the Fermi level combined with a modified electron distribution in the nanoparticle due to Pt-to-Au charge transfer are the origin of the outstanding catalytic properties. From our model we deduce the catalytically favorable surface patterns that induce ensemble and ligand effects. © The Royal Society of Chemistry 2013.

  20. Pt-modified molybdenum carbide for the hydrogen evolution reaction: From model surfaces to powder electrocatalysts

    Science.gov (United States)

    Kelly, Thomas G.; Lee, Kevin X.; Chen, Jingguang G.

    2014-12-01

    This work explores the opportunity to substantially reduce the cost of hydrogen evolution reaction (HER) electrocatalysts by supporting one monolayer (ML) of platinum (Pt) on low-cost molybdenum carbide (Mo2C) substrate. These efforts were primarily directed towards scaling a thin-film catalyst to high surface area particles. Electrochemical experiments investigated single-phase Mo2C thin films modified by different coverages of Pt for the HER. The ML Pt-Mo2C thin film showed Pt-like HER activity while displaying excellent stability under HER conditions. The promising results on thin films were then extended to more practical powder catalysts. Samples of various Pt loadings on Mo2C powders were synthesized using the co-impregnation method and were evaluated for HER activity. The ability to successfully link electrochemical activity on thin films and powder catalysts was thus demonstrated.

  1. The interaction of NH 3 with ordered Pt surfaces

    Science.gov (United States)

    Baetzold, R. C.; Apai, G.; Shustorovich, E.

    1984-11-01

    The interaction of ammonia with ordered Pt surface was studies by means of surface core-level photoemission and tight-binding-type calculations. Clean Pt surfaces have distinguishable surface and bulk components of the 4f 7/2 core level. The 4f 7/2 surface component is shifted to lower binding energy (-0.32 eV) than the bulk on the clean (111) surface, but in the presence of ammonia the surface peak is shifted to positive binding energy (0.7 eV). This result is unexpected, since it indicates a depletion of d-electron density on Pt atoms attached to NH 3, in contrast to common assumptions of NH 3 as a net donor. Thin-film calculations show this depletion in the form of rehybridization of sp with d electrons on the Pt atom. The mixing of p z orbitals with the d band leads to a dipole moment perpendicular to the surface, which in addition to the static dipole of ammonia is also a major factor in the decrease in work function upon chemisorption.

  2. 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.

  3. Adsorption of aromatics on the (111) surface of PtM and PtM3 (M = Fe, Ni) alloys

    Energy Technology Data Exchange (ETDEWEB)

    Hensley, Alyssa; Schneider, Sebastian; Wang, Yong; McEwen, Jean-Sabin

    2015-09-18

    The adsorption of benzene and phenol was studied on PtM and PtM3 (111) surfaces, with M being either Ni or Fe. Under vacuum, the most favorable near surface structures showed an enrichment in Pt over the M species. An analysis of the electronic structure of the metal species in the clean surfaces with different near surface structures was done with the d-band model and showed that the Pt's d-states are significantly shifted away from the Fermi level due to the Pt-M interactions while the M species' d-states were less affected, with Ni's d-band shifting closer to the Fermi level and Fe's d-band shifting away from the Fermi level. The adsorption of aromatics, benzene and phenol, on several near surface structures for the PtM and PtM3 (111) surfaces showed that higher surface M concentrations resulted in a stronger adsorption due to the larger amount of charge transferred between the adsorbate and surface. However, compared to the adsorption of benzene and phenol on monometallic surfaces, the adsorption of these species on the PtM and PtM3 (111) surfaces was significantly weakened. Overall, our results show that the observed behavior of these Pt/Fe and Pt/Ni alloys is similar to that seen for the previously studied Pd/Fe surfaces. Furthermore, balancing the weakly adsorbing Pt surface species with the more strongly interacting Fe or Ni species can lead to the tailored adsorption of aromatics with applications in both hydrodeoxygenation and hydrogenation reactions by increasing the desorption rate of wanted aromatic products.

  4. Surface enrichment of Pt in Ga2O3 films grown on liquid Pt/Ga alloys

    Science.gov (United States)

    Grabau, Mathias; Krick Calderón, Sandra; Rietzler, Florian; Niedermaier, Inga; Taccardi, Nicola; Wasserscheid, Peter; Maier, Florian; Steinrück, Hans-Peter; Papp, Christian

    2016-09-01

    The formation of surface Ga2O3 films on liquid samples of Ga, and Pt-Ga alloys with 0.7 and 1.8 at.% Pt was examined using near-ambient pressure (NAP) X-ray photoelectron spectroscopy (XPS). Thickness, composition and growth of the oxide films were deduced as a function of temperature and Pt content of the alloys, in ultra-high vacuum and at oxygen pressures of 3 × 10- 7, 3 × 10- 3 and 1 mbar. We examined oxide layers up to a thickness of 37 Å. Different growth modes were found for oxidation at low and high pressures. The formed Ga2O3 oxide films showed an increased Pt content, while the pristine GaPt alloy showed a surface depletion of Pt at the examined temperatures. Upon growth of Ga2O3 on Pt/Ga alloys a linear increase of Pt content was observed, due to the incorporation of 3.6 at.% Pt in the Ga2O3. The Pt content in Ga2O3, at the examined temperatures and bulk Pt concentrations is found to be independent of pressure, temperature and the nominal Pt content of the metallic alloy.

  5. Electrooxidation of ethanol on Pt and PtRu surfaces investigated by ATR surface-enhanced infrared absorption spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Silva, Marcio F.; Camara, Giuseppe A., E-mail: giuseppe.silva@ufms.br [Departamento de Quimica, Universidade Federal do Mato Grosso do Sul, Campo Grande-MS (Brazil); Batista, Bruno C.; Boscheto, Emerson [Instituto de Quimica de Sao Carlos, Universidade de Sao Paulo, Sao Carlos-SP, (Brazil); Varela, Hamilton, E-mail: varela@iqsc.usp.br [Ertl Center for Electrochemistry and Catalysis, Gwangju Institute of Science and Technology (GIST), Gwangju (Korea, Republic of)

    2012-05-15

    Herein, it was investigated for the first time the electro-oxidation of ethanol on Pt and PtRu electrodeposits in acidic media by using in situ surface enhanced infrared absorption spectroscopy with attenuated total reflection (ATR-SEIRAS). The experimental setup circumvents the weak absorbance signals related to adsorbed species, usually observed for rough, electrodeposited surfaces, and allows a full description of the CO coverage with the potential for both catalysts. The dynamics of adsorption-oxidation of CO was accessed by ATR-SEIRAS experiments (involving four ethanol concentrations) and correlated with expressions derived from a simple kinetic model. Kinetic analysis suggests that the growing of the CO adsorbed layer is nor influenced by the presence of Ru neither by the concentration of ethanol. The results suggest that the C-C scission is not related to the presence of Ru and probably happens at Pt sites. (author)

  6. Surface composition of Pt-Pd alloys treated in hydrogen

    Science.gov (United States)

    Szabo, A.; Paál, Z.; Szász, A.; Kojnok, J.; Fabian, D. J.

    1989-11-01

    Pd enrichment is observed in Pd-Pt alloy sheets when heated in He and in H 2. The surface composition was monitored by soft X-ray emission spectroscopy (SXES) and by work function measurements. A regular solution model is used to calculate the expected composition of the surface atomic layers, with and without adsorbed hydrogen, and the calculated and measured values for Pd-enrichment are compared. The possible effect of subsurface adsorbed hydrogen is discussed.

  7. Surface-Limited Synthesis of Pt Nanocluster Decorated Pd Hierarchical Structures with Enhanced Electrocatalytic Activity toward Oxygen Reduction Reaction.

    Science.gov (United States)

    Yang, Tao; Cao, Guojian; Huang, Qingli; Ma, Yanxia; Wan, Sheng; Zhao, Hong; Li, Na; Sun, Xia; Yin, Fujun

    2015-08-12

    Exploring superior catalysts with high catalytic activity and durability is of significant for the development of an electrochemical device involving the oxygen reduction reaction. This work describes the synthesis of Pt-on-Pd bimetallic heterogeneous nanostructures, and their high electrocatalytic activity toward the oxygen reduction reaction (ORR). Pt nanoclusters with a size of 1-2 nm were generated on Pd nanorods (NRs) through a modified Cu underpotential deposition (UPD) process free of potential control and a subsequent surface-limited redox reaction. The Pt nanocluster decorated Pd nanostructure with a ultralow Pt content of 1.5 wt % exhibited a mass activity of 105.3 mA mg(-1) (Pt-Pd) toward ORR, comparable to that of the commercial Pt/C catalyst but 4 times higher than that of carbon supported Pd NRs. More importantly, the carbon supported Pt-on-Pd catalyst displays relatively small losses of 16% in electrochemical surface area (ECSA) and 32% in mass activity after 10 000 potential sweeps, in contrast to respective losses of 46 and 64% for the commercial Pt/C catalyst counterpart. The results demonstrated that Pt decoration might be an efficient way to improve the electrocatalytic activity of Pd and in turn allow Pd to be a promising substitution for commercial Pt catalyst.

  8. Adsorption and coupling of 4-aminophenol on Pt(111) surfaces

    Science.gov (United States)

    Otero-Irurueta, G.; Martínez, J. I.; Bueno, R. A.; Palomares, F. J.; Salavagione, H. J.; Singh, M. K.; Méndez, J.; Ellis, G. J.; López, M. F.; Martín-Gago, J. A.

    2016-04-01

    We have deposited 4-aminophenol on Pt(111) surfaces in ultra-high vacuum and studied the strength of its adsorption through a combination of STM, LEED, XPS and ab initio calculations. Although an ordered (2√3 × 2√3)R30° phase appears, we have observed that molecule-substrate interaction dominates the adsorption geometry and properties of the system. At RT the high catalytic activity of Pt induces aminophenol to lose the H atom from the hydroxyl group, and a proportion of the molecules lose the complete hydroxyl group. After annealing above 420 K, all deposited aminophenol molecules have lost the OH moiety and some hydrogen atoms from the amino groups. At this temperature, short single-molecule oligomer chains can be observed. These chains are the product of a new reaction that proceeds via the coupling of radical species that is favored by surface diffusion.

  9. Reversible Vertical Manipulations of Single Pt Adatom on Pt(111)Surface with a Triple-Apex Tip

    Institute of Scientific and Technical Information of China (English)

    XIE Yi-Qun; LIU Qing-Wei; ZHANG Peng; LI Yu-Fen; GAN Fu-Xi; ZHUANG Jun

    2008-01-01

    @@ With a triple-apex tip,we investigate theoretically the vertical manipulation of single Pt adatom on the Pt(111)surface.The adatom adsorbed on the fcc site of the flat Pt(111)surface can be transferred vertically to the tip by adjusting the tip height properly.Moreover,based on the strong vertical trapping ability and the relatively weak lateral trapping ability of the tip,we propose a simple method to realize a reversible vertical manipulation of the Pt adatom from the highly coordinated sites,the kink and the step sites,of the stepped Pt(111)surface.All the vertical manjpulations are completed using only the atomic force between the tip and the adatom,without the electric field.

  10. Surface core-level shifts for Pt single-crystal surfaces

    Science.gov (United States)

    Baetzold, R. C.; Apai, G.; Shustorovich, E.; Jaeger, R.

    1982-10-01

    The (111) and (110) surfaces of Pt, clean, oxidized, and covered by CO, have been investigated for surface 4f core-level binding-energy shifts. For the (111) face the surface Pt4f72 core level was shifted by 0.40+/-0.05 eV to lower binding energy relative to the bulk peak. On the (110)-(1×2) reconstructed surface similarly shifted peaks at 0.21+/-0.05 and 0.55+/-0.05 eV were observed. Chemisorbed carbon monoxide shifts the Pt(111) surface-related core level by 1.3 eV to higher binding energy. Formation of subsurface oxygen did not produce changes in the Pt(111)4f72 core-level binding energies. The results obtained are explained and their possible implications are discussed.

  11. Theoretical investigation of water formation on Rh and Pt Surfaces

    Science.gov (United States)

    Wilke, Steffen; Natoli, Vincent; Cohen, Morrel H.

    2000-06-01

    Catalytic water formation from adsorbed H and O adatoms is a fundamental reaction step in a variety of technologically important reactions involving organic molecules. In particular, the water-formation rate determines the selectivity of the catalytic partial oxidation of methane to syngas. In this report we present a theoretical investigation of the potential-energy diagram for water formation from adsorbed O and H species on Rh(111) and Pt(111) surfaces. The study is based on accurate first-principles calculations applying density-functional theory. Our results are compared to the potential-energy diagram for this reaction inferred from experimental data by Hickman and Schmidt [AIChE. J. 39, 1164 (1993)]. The calculations essentially reproduce the scheme of Hickman and Schmidt for water formation on Rh(111) with the important difference that the OH molecule is significantly more stable than assumed by Hickman and Schmidt. On Pt(111) surfaces, however, the calculations predict a barrier to OH formation very similar to that found on Rh(111). In particular, the calculated barrier to OH formation of about 20 kcal/mol seems to contradict the small 2.5 kcal/mol barrier assumed in the Hickman-Schmidt scheme and the observed large rate of water formation on Pt. A possible explanation for the apparent discrepancy between the large calculated barrier for OH formation on Pt and the experimentally observed rapid formation of water even at low temperatures is that the active sites for water formation on Pt are at "defect" sites and not on the ideally flat terraces. A similar conclusion has been reached by Verheij and co-workers [Surf. Sci. 371, 100 (1997); Chem. Phys. Lett. 174, 449 (1990); Surf. Sci. 272, 276 (1991)], who did detailed experimental work on water formation on Pt surfaces. Analyzing our results, we develop an explicit picture of the interaction processes governing the formation of OH groups. This picture rationalizes the calculated weak dependence of OH

  12. Probing adsorption phenomena on a single crystal Pt-alloy surface under oxygen reduction reaction conditions

    DEFF Research Database (Denmark)

    Bondarenko, Alexander S.; Stephens, Ifan E.L.; Bech, Lone;

    2012-01-01

    The adsorption dynamics of *OH and *O species at Pt(111) and Cu/Pt(111) near-surface alloy (NSA) surfaces in oxygen-free and O2-saturated 0.1M HClO4 was investigated. Subsurface Cu modifies the electronic structure at the Pt(111) surface resulting in weaker bonding to adsorbates like *OH, *H or *...

  13. Effect of Annealing Temperature on the Formation of Silicides and the Surface Morphologies of PtSi Films

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    The effect of annealing temperature on the formation of the PtSi phase, distribution of silicides and the surface morphologies of silicides films is investigated by XPS, AFM. It is shown that the phase sequences of the films change from Pt-Pt2Si-PtSi-Si to Pt+Pt2Si+PtSi-PtSi-Si or Pt+Pt2Si+PtSi-PtSi-Si with an increase of annealing temperature and the reason for the formation of mixed layers is discussed.

  14. CO surface electrochemistry on Pt-nanoparticles: A selective review

    Energy Technology Data Exchange (ETDEWEB)

    Mayrhofer, K.J.J. [Materials Science Division, Lawrence Berkeley National Laboratory, University of California, Berkeley, CA 94720 (United States); Arenz, M. [Materials Science Division, Lawrence Berkeley National Laboratory, University of California, Berkeley, CA 94720 (United States); Blizanac, B.B. [Materials Science Division, Lawrence Berkeley National Laboratory, University of California, Berkeley, CA 94720 (United States); Stamenkovic, V. [Materials Science Division, Lawrence Berkeley National Laboratory, University of California, Berkeley, CA 94720 (United States); Ross, P.N. [Materials Science Division, Lawrence Berkeley National Laboratory, University of California, Berkeley, CA 94720 (United States); Markovic, N.M. [Materials Science Division, Lawrence Berkeley National Laboratory, University of California, Berkeley, CA 94720 (United States)]. E-mail: nmmarkovic@lbl.gov

    2005-09-05

    Oxidation of CO on platinum nanoparticles ranging in size from 1 to 30 nm has been studied in acid electrolytes. We found that Pt nanoparticles, characterized by transmission electron microscopy, are not perfect cubo-octahedrons and that large particles have 'rougher' surfaces than small particles. The importance of 'defect' sites for the catalytic properties of nanoparticles was probed by using infrared reflection absorption spectroscopy (IRAS) and rotating disk electrode. From IRAS experiments, by monitoring how the vibrational frequency of a-top CO ({nu} {sub CO}) as well as the concomitant development of dissolved CO{sub 2} are affected by the number of defects on Pt nanoparticles, we suggested that defects play a significant role in CO 'clustering' on nanoparticles, causing CO to decrease/increase in local coverage, which results in anomalous redshift/blueshift {nu} {sub CO} frequency deviations from the normal Stark-tuning behavior. The observed {nu} {sub CO} deviations are accompanied by CO{sub 2} production, which increases by increasing the number of defects on the nanoparticles, i.e., 1 {<=} 2 < 5 << 30 nm. We suggest that the catalytic activity for CO adlayer oxidation (CO stripping) is predominantly influenced by the ability of the surface to dissociate water and to form OH{sub ad} on defect sites. We demonstrate that the catalytic activity of Pt nanoparticles for CO oxidation under the condition of continuous CO supply to the surface depends on the pre-history of the electrode. If the surface is precovered by CO, the particle size has a negligible effect on CO oxidation. However, on an oxide-precovered surface CO bulk oxidation increases with decreasing particle size, i.e., with increasing oxophilicity of the particles. We found, if specific sites on the surface are active for OH adsorption, then the electrocatalytic activity for CO oxidation changes as the concentration of these sites changes with particle size.

  15. Surface structure and relaxation during the oxidation of carbon monoxide on Pt Pd bimetallic surfaces

    Science.gov (United States)

    Lucas, C. A.; Markovic, N. M.; Ball, M.; Stamenkovic, V.; Climent, V.; Ross, P. N.

    2001-05-01

    The atomic structure and surface relaxation of Pd monolayer on Pt(1 1 1) has been studied by surface X-ray scattering, in an aqueous environment under electrostatic potential control, during the adsorption and oxidation of carbon monoxide. The results show that the Pd-Pt layer spacing contracts at the onset of CO oxidation before the Pd adlayer forms an oxide structure that is incommensurate with the Pt lattice. Both the oxide formation and the lattice contraction are fully reversible over many cycles of the applied electrode potential.

  16. Surface Structures of Cubo-octahedral Pt-Mo Catalyst Nanoparticles from Monte Carlo Simulations

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Guofeng; Van Hove, M.A.; Ross, P.N.; Baskes, M.I.

    2005-03-31

    The surface structures of cubo-octahedral Pt-Mo nanoparticles have been investigated using the Monte Carlo method and modified embedded atom method potentials that we developed for Pt-Mo alloys. The cubo-octahedral Pt-Mo nanoparticles are constructed with disordered fcc configurations, with sizes from 2.5 to 5.0 nm, and with Pt concentrations from 60 to 90 at. percent. The equilibrium Pt-Mo nanoparticle configurations were generated through Monte Carlo simulations allowing both atomic displacements and element exchanges at 600 K. We predict that the Pt atoms weakly segregate to the surfaces of such nanoparticles. The Pt concentrations in the surface are calculated to be 5 to 14 at. percent higher than the Pt concentrations of the nanoparticles. Moreover, the Pt atoms preferentially segregate to the facet sites of the surface, while the Pt and Mo atoms tend to alternate along the edges and vertices of these nanoparticles. We found that decreasing the size or increasing the Pt concentration leads to higher Pt concentrations but fewer Pt-Mo pairs in the Pt-Mo nanoparticle surfaces.

  17. In situ scanning FTIR microscopy and IR imaging of Pt electrode surface towards CO adsorption

    Institute of Scientific and Technical Information of China (English)

    孙世刚; 洪双进; 陈声培; 卢国强; 戴鸿平; 肖晓银

    1999-01-01

    In situ scanning FTIR microscopy was built up for the first time in the present work, which consists of an FTIR apparatus, an IR microscope, an X-Y mapping stage, and the specially designed electrochemical IR cell and computer software. It has been demonstrated that this new space-resolvd in situ IR technique can be used to study vibration properties of micro-area, and to perform IR imaging of electrode surface. The chemical image obtained using this technique fur CO adsorption on Pt electrode illustrated, at a space-resolution of 10-2 cm, the inhomogeneity and the distribution of reactivity of micro-area of electrode surface.

  18. A first-principle calculation of sulfur oxidation on metallic Ni(111) and Pt(111), and bimetallic Ni@Pt(111) and Pt@Ni(111) surfaces.

    Science.gov (United States)

    Yeh, Chen-Hao; Ho, Jia-Jen

    2012-09-17

    Sulfur, a pollutant known to poison fuel-cell electrodes, generally comes from S-containing species such as hydrogen sulfide (H(2)S). The S-containing species become adsorbed on a metal electrode and leave atomic S strongly bound to the metal surface. This surface sulfur is completely removed typically by oxidation with O(2) into gaseous SO(2). According to our DFT calculations, the oxidation of sulfur at 0.25 ML surface sulfur coverage on pure Pt(111) and Ni(111) metal surfaces is exothermic. The barriers to the formation of SO(2) are 0.41 and 1.07 eV, respectively. Various metals combined to form bimetallic surfaces are reported to tune the catalytic capabilities toward some reactions. Our results show that it is more difficult to remove surface sulfur from a Ni@Pt(111) surface with reaction barrier 1.86 eV for SO(2) formation than from a Pt@Ni(111) surface (0.13 eV). This result is in good agreement with the statement that bimetallic surfaces could demonstrate more or less activity than to pure metal surfaces by comparing electronic and structural effects. Furthermore, by calculating the reaction free energies we found that the sulfur oxidation reaction on the Pt@Ni(111) surface exhibits the best spontaneity of SO(2) desorption at either room temperature or high temperatures.

  19. Chemical oscillation in electrochemical oxidation of methanol on Pt surface

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    Based on dual path reaction mechanism, a nonlinear dynamics model reflecting the potential oscilla- tion in electrooxidation of methanol on Pt surface was established. The model involves three variables, the electrode potential (e), the surface coverage of carbon monoxide (x), and adsorbed water (y). The chemical reactions and electrode potential were coupled together through the rate constant ki = exp(ai(e ? ei)). The analysis to the established model discloses the following: there are different kinetics be- haviors in different ranges of current densities. The chemical oscillation in methanol electrooxidation is assigned to two aspects, one from poison mediate CO of methanol electrooxidation, which is the in- duced factor of the chemical oscillation, and the other from the oxygen-containing species, such as H2Oa. The formation and disappearance of H2Oa deeply depend on the electrode potential, and directly cause the chemical oscillation. The established model makes clear that the potential oscillation in methanol electrooxidation is the result of the feedback of electrode potential e on the reactions in- volving poison mediates CO and oxygen-containing species H2Oa. The numerical analysis of the estab- lished model successfully explains why the potential oscillation in methanol galvanostatic oxidation on a Pt electrode only happens in a certain range of current densities but not at any current density.

  20. Chemical oscillation in electrochemical oxidation of methanol on Pt surface

    Institute of Scientific and Technical Information of China (English)

    LI LanLan; WEI ZiDong; QI XueQiang; SUN CaiXin; YIN GuangZhi

    2008-01-01

    Based on dual path reaction mechanism, a nonlinear dynamics model reflecting the potential oscilla-tion in electrooxidation of methanol on Pt surface was established. The model involves three variables, the electrode potential (e), the surface coverage of carbon monoxide (x), and adsorbed water (y). The chemical reactions and electrode potential were coupled together through the rate constant k1= exp(a e-e1)). The analysis to the established model discloses the following: there are different kinetics be-haviors in different ranges of current densities. The chemical oscillation in methanol electrooxidation is assigned to two aspects, one from poison mediate CO of methanol electrooxidallon, which is the in-duced factor of the chemical oscillation, and the other from the oxygen-containing species, such as H2Oa. The formation and disappearance of H2Oa deeply depend on the electrode potential, and directly cause the chemical oscillation. The established model makes clear that the potential oscillation in methanol electrooxidation is the result of the feedback of electrode potential e on the reactions in-volving poison mediates CO and oxygen-containing species H2Oa. The numerical analysis of the estab-lished model successfully explains why the potential oscillation in methanol galvanostatic oxidation on a Pt electrode only happens in a certain range of current densities but not at any current density.

  1. Growth of epitaxial Pt1-xPbx alloys by surface limited redox replacement and study of their adsorption properties.

    Science.gov (United States)

    Mercer, M P; Plana, D; Fermίn, D J; Morgan, D; Vasiljevic, N

    2015-10-06

    The surface limited redox replacement (SLRR) method has been used to design two-dimensional Pt-Pb nanoalloys with controlled thickness, composition, and structure. The electrochemical behavior of these alloys has been systematically studied as a function of alloy composition. A single-cell, two-step SLRR protocol based on the galvanic replacement of underpotentially deposited monolayers of Pb with Pt was used to grow epitaxial Pt1-xPbx (x galvanic replacement step, the Pb atomic content can be controlled in the films. Electrochemical analysis of the alloys showed that the adsorption of both H and CO exhibits similar, and systematic, decreases with small increases in the Pb content. These measurements, commonly used in electrocatalysis for the determination of active surface areas of Pt, suggested area values much lower than those expected based on the net Pt composition in the alloy as measured by XPS. These results show that Pb has a strong screening effect on the adsorption of both H and CO. Moreover, changes in alloy composition result in a negative shift in the potential of the peaks of CO oxidation that scales with the increase of Pb content. The results suggest electronic and bifunctional effects of incorporated Pb on the electrochemical behavior of Pt. The study illustrates the potential of the SLRR methodology, which could be employed in the design of 2-dimensional bimetallic Pt nanoalloys for fundamental studies of electrocatalytic behavior in fuel cell reactions dependent on the nature of alloying metal and its composition.

  2. Quantitative Prediction of Surface Segregation in Bimetallic Pt-MAlloy Nanoparticles (M=Ni, Re, Mo)

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Guofeng; Van Hove, Michel A.; Ross, Phil N.; Baskes,Michael I.

    2005-06-20

    This review addresses the issue of surface segregation inbimetallic alloy nanoparticles, which are relevant to heterogeneouscatalysis, in particular for electro-catalysts of fuel cells. We describeand discuss a theoretical approach to predicting surface segregation insuch nanoparticles by using the Modified Embedded Atom Method and MonteCarlo simulations. In this manner it is possible to systematicallyexplore the behavior of such nanoparticles as a function of componentmetals, composition, and particle size, among other variables. We choseto compare Pt75Ni25, Pt75Re25, and Pt80Mo20 alloys as example systems forthis discussion, due to the importance of Pt in catalytic processes andits high-cost. It is assumed that the equilibrium nanoparticles of thesealloys have a cubo-octahedral shape, the face-centered cubic lattice, andsizes ranging from 2.5 nm to 5.0 nm. By investigating the segregation ofPt atoms to the surfaces of the nanoparticles, we draw the followingconclusions from our simulations at T= 600 K. (1) Pt75Ni25 nanoparticlesform a surface-sandwich structure in which the Pt atoms are stronglyenriched in the outermost and third layers while the Ni atoms areenriched in the second layer. In particular, a nearly pure Pt outermostsurface layer can be achieved in those nanoparticles. (2) EquilibriumPt75Re25 nanoparticles adopt a core-shell structure: a nearly pure Ptshell surrounding a more uniform Pt-Re core. (3) In Pt80Mo20nanoparticles, the facets are fully occupied by Pt atoms, the Mo atomsonly appear at the edges and vertices, and the Pt and Mo atoms arrangethemselves in an alternating sequence along the edges and vertices. Oursimulations quantitatively agree with previous experimental andtheoretical results for the extended surfaces of Pt-Ni, Pt-Re, and Pt-Moalloys. We further discuss the reasons for the different types of surfacesegregation found in the different alloys, and some of theirimplications.

  3. Calculated orientation dependence of surface segregations in Pt50Ni50

    DEFF Research Database (Denmark)

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

    1994-01-01

    We present local-density calculations of surface segregation profiles in a random Pt50Ni50 alloy. We find that the concentration profiles of the three low-index surfaces oscillate and that the two most closely packed surfaces, i.e., (111) and (100), are enriched by Pt while Ni is found to segrega...

  4. Rancang Bangun Sistem Informasi Pengelolaan Kendaraan di PT PLN (Persero Area Mojokerto

    Directory of Open Access Journals (Sweden)

    Mukhamad Masrur

    2015-11-01

    Full Text Available PT Perusahaan Listrik Negara (PT PLN (Persero Area Mojokerto merupakan salah satu cabang dari PT PLN (Persero Distribusi Jawa Timur yang bergerak di bidang pelayanan terhadap pelanggan. Pada PT PLN (Persero Area Mojokerto terdapat sebuah bagian yang khusus menangani pengelolaan kendaraan. Proses pengelolaan kendaraan pada PT PLN (Persero Area Mojokerto saat ini masih menggunakan Microsoft Excel, sehingga belum bisa memberikan pelayanan cepat dalam proses peminjaman mobil dan kurang efisien dalam perihal penyimpanan data. Permasalahan yang akan dituntut ada penyelesaiannya agar pegawai mendapat pelayanan secara proporsional akan pelayanan yang tersedia. Solusi dari permasalahan tersebut adalah membuat adanya aplikasi baru. Adapun aplikasi yang dibuat yaitu Aplikasi berbasis Web dengan menggunakan bahasa pemrograman PHP dan database MySQL. Hasil penelitian ini berupa sebuah Aplikasi Pengelolaan Kendaraan. Dengan adanya solusi yang demikian mampu meningkatkan terlaksana proses kerja pada bagian manajemen kendaraan yang lebih maksimal serta mempermudah pelayanan pada proses peminjaman kendaraan

  5. Electrochemical properties of CO{sub x}/Pt(111) model catalyst surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Wadayama, T.; Todoroki, N.; Yoshida, H.; Yamada, Y. [Tohoku Univ., Sendai (Japan). Dept. of Materials Science

    2010-07-01

    Oxygen reduction reaction (ORR) activities for clean Pt(111) and Co-deposited Pt(111) (CO{sub x}/Pt(111)) model catalyst surfaces fabricated by molecular beam epitaxy (MBE) were evaluated. Low-energy electron diffration (LEED) and infrared reflection absorption spectroscopy (IRRAS) was used to investigate the CO{sub x}/Pt(111) surface structures. 1.0-L-carbon monoxide (CO) exposure to the clean Pt(111) at 323 K yielded linear-bonded and bridge-bonded CO-PT bands at 2092 and 1850 cm{sup -1}. 0.3nm-thick-Co deposition onto the clean Pt(111) at 343 K brought about small hexagons of satellites on a LEED pattern and a main IR band ascribable to Co-CO bonds is located at 2000 cm{sup -1}. In contrast, at 823-K-Co deposition, a LEED pattern is almost identical as that for the clean Pt(111): an absorbed CO band at 2080 cm{sup -1} dominated IR spectrum for the 1.0-L-CO exposed surface. The results suggest that the Co deposition at 823 K generates a Pt-enriched outermost surface (Pt-skin) formed through surface segregation of the substrate Pt atoms. A linear-sweep voltammetry (LSV) curve was recorded for the Co/Pt(111)-skin in O{sub 2}-saturated HCIO{sub 4}. Specific ORR activity for the Pt-skin is 10-times higher than that for the clean Pt(111). (orig.)

  6. Controlled FCC/on-top binding of H/Pt(111) using surface stress

    Science.gov (United States)

    Shuttleworth, I. G.

    2016-08-01

    The preferred binding site of H/Pt(111) has been shown to be change from the on-top to FCC as the Pt(111) surface goes approximately from a state of compressive to tensile strain. A chemical analysis of the system has shown that for both FCC and on-top bound cases the H ssbnd Pt s and H ssbnd Pt d interactions have a similar importance in determining the preferred binding position. It has been seen that FCC-bound H forms a distinct state below the Pt d-band, whereas the on-top bound H does not.

  7. Dissociative adsorption of methane on surface oxide structures of Pd-Pt alloys

    CERN Document Server

    Dianat, Arezoo; Ciacchi, Lucio Colombi; Pompe, Wolfgang; Cuniberti, Gianaurelio; Bobeth, Manfred; 10.1021/jp905689t

    2010-01-01

    The dissociative adsorption of methane on variously oxidized Pd, Pt and Pd-Pt surfaces is investigated using density-functional theory, as a step towards understanding the combustion of methane on these materials. For Pd-Pt alloys, models of surface oxide structures are built on the basis of known oxides on Pd and Pt. The methane adsorption energy presents large variations depending on the oxide structure and composition. Adsorption is endothermic on the bare Pd(111) metal surface as well as on stable thin layer oxide structures such as the ($\\sqrt{5}\\times\\sqrt{5}$) surface oxide on Pd(100) and the PtO$_2$-like oxide on Pt(111). Instead, large adsorption energies are obtained for the (100) surface of bulk PdO, for metastable mixed Pd$_{1-x}$Pt$_x$O$_{4/3}$ oxide layers on Pt(100), and for Pd-Pt(111) surfaces covered with one oxygen monolayer. In the latter case, we find a net thermodynamic preference for a direct conversion of methane to methanol, which remains adsorbed on the oxidized metal substrates via w...

  8. Antisite-defect-induced surface segregation in ordered NiPt alloy

    DEFF Research Database (Denmark)

    Pourovskii, L.V.; Ruban, Andrei; Abrikosov, I.A.;

    2003-01-01

    By means of first principles simulations we demonstrate that tiny deviations from stoichiometry in the bulk composition of the NiPt-L1(0) ordered alloy have a great impact on the atomic configuration of the (111) surface. We predict that at T=600 K the (111) surface of the Ni51Pt49 and Ni50Pt50...... alloys corresponds to the (111) truncation of the bulk L1(0) ordered structure. However, the (111) surface of the nickel deficient Ni49Pt51 alloy is strongly enriched by Pt and should exhibit the pattern of the 2x2 structure. Such a drastic change in the segregation behavior is due to the presence...... of different antisite defects in the Ni- and Pt-rich alloys and is a manifestation of the so-called off-stoichiometric effect....

  9. Surface enrichment of Pt in stable Pt-Ir nano-alloy particles on MgAl 2 O 4 spinel in oxidizing atmosphere

    Energy Technology Data Exchange (ETDEWEB)

    Li, Wei-Zhen; Nie, Lei; Cheng, Yingwen; Kovarik, Libor; Liu, Jun; Wang, Yong

    2017-04-01

    With the capability of MgAl2O4 spinel {111} nano-facets in stabilizing small Rh, Ir and Pt particles, bimetallic Ir-Pt catalysts on the same support were investigated, aiming at further lowering the catalyst cost by substituting expensive Pt with cheaper Ir in the bulk. Small Pt-Ir nano-alloy particles (< 2nm) were successfully stabilized on the spinel {111} nano-facets as expected. Interestingly, methanol oxidative dehydrogenation (ODH) rate on the surface Pt atoms increases with oxidizing aging but decreases upon reducing treatment, where Ir is almost inactive under the same reaction conditions. Up to three times enhancement in Pt exposure was achieved when the sample was oxidized at 800 °C in air for 1 week and subsequently reduced by H2 for 2 h, demonstrating successful surface enrichment of Pt on Pt-Ir nano-alloy particles. A dynamic stabilization mechanism involving wetting\

  10. Surface-enhanced Raman scattering characteristics of nanogaps formed by a flat Ag substrate and spherical Pt nanoparticles.

    Science.gov (United States)

    Kim, Kwan; Lee, Hyang Bong; Shin, Kuan Soo

    2013-01-01

    We estimated the apparent size of the 'hot site' for surface-enhanced Raman scattering (SERS) located within the gaps between Pt nanoparticles and a flat Ag substrate. Initially, no Raman peaks were detected for 4-aminobenzenethiol (4-ABT) on a flat Ag substrate. Upon attaching 68 nm-sized Pt nanoparticles onto the amine group of 4-ABT (thus denoted as Pt-4-ABT/Ag(flat)), Raman peaks were distinctly observed, not only with the excitation at 488 nm but also with the excitation at 632.8 nm. This means that electromagnetic 'hot site' had formed at the gaps between Pt nanoparticles and a flat Ag substrate. When 4-ABT molecules were adsorbed additionally onto the vacant sites of Pt nanoparticles in Pt-4-ABT/Ag(flat), the Raman signal did not increase further, suggesting that the SERS 'hot site' was very limited and located mostly at the gaps between Pt nanoparticles and a flat Ag substrate, in agreement with the finite-difference time-domain (FDTD) calculation. To a rough estimate, about 1000 molecules residing only within a ~15 nm diameter area of the center of the gap must have contributed most of the measured Raman signal of 4-ABT.

  11. Formation and sintering of Pt nanopartictes on vicinal rutile TiO2 surfaces

    DEFF Research Database (Denmark)

    Rieboldt, Felix; Helveg, S.; Bechstein, Ralf;

    2014-01-01

    By means of scanning tunnelling microscopy (STM) the nucleation, growth and sintering of platinum nanoparticles (Pt NP's) was studied on vicinal and flat rutile titanium dioxide (TiO2) surfaces. Utilising physical vapour deposition, the nucleation of Pt NP's on TiO2 surfaces at room temperature (RT...

  12. Dynamics of Surface Exchange Reactions Between Au and Pt for HER and HOR

    DEFF Research Database (Denmark)

    Abrams, Billie; Vesborg, Peter Christian Kjærgaard; Bonde, Jacob Lindner;

    2009-01-01

    Cyclic voltammetric analysis of the Pt-on-Au system for hydrogen evolution and oxidation reactions (HER/HOR) indicates that dynamic surface exchange reactions occur between Pt and Au. HER/HOR activities depend on the dominant surface species present, which is controllable by the potential applied...

  13. PENGARUH CORPORATE SOCIAL ESPONSIBILITY (CSR) TERHADAP CITRA PERUSAHAAN PADA PT TELEKOMUNIKASI INDONESIA, TBK AREA MAKASSAR

    OpenAIRE

    ERWIN, MUHAMMAD

    2012-01-01

    Muhammad Erwin, INFLUENCE OF CORPORATE SOCIAL RESPONSIBILITY TO CORPORATE IMAGE IN PT. TELEKOMUNIKASI INDONESIA, TBK AREA MAKASSAR (mentored by Dr. Idayanti, SE.,M.Siand Abdullah Sanusi, SE., MBA). This research aims to determine the influence either together or partially between CSR (Corporate Social Responsibility) to corporate image in PT. Telekomunikasi Indonesia, TbkMakassar area, that being measured from CSR variables which is Profit, People, and Planet. Expectedly the information o...

  14. Surface electrochemistry of CO on Pt(111): Anion Effects

    Energy Technology Data Exchange (ETDEWEB)

    Markovic, N.M.; Lucas, C.A.; Rodes, A.; Stamenkovic, V.; Ross, P.N.

    2001-07-30

    In-situ studies of CO adsorption by surface x-ray scattering (SXS) and Fourier transform infrared (FTIR) spectroscopy techniques are used to create the link between the macroscopic kinetic rates of CO oxidation and the microscopic level of understanding the structure/site occupancy of CO on Pt(111). A remarkable difference in activity was observed between alkaline and acid solutions. In alkaline solution the oxidation of CO proceeds at low overpotential (<0.2 V) by the surface reaction between the adsorbed CO and OH, the latter forming selectively in the hydrogen underpotential potential region at defect sites. In acid solution these sites are blocked by specific adsorption of anions, and consequently in a solution containing Br{sup -} the ignition potential is shifted positively by 0.6 V. Anions of supporting electrolytes also have dramatic effects on both the potential range of stability and the domain size of the p(2x2)-3CO structure which is formed at 0.05 V. The stability/domain size of this structure increases from KOH (ca. 30 {angstrom} between 0.05 < E < 0.3V), to HClO{sub 4} (ca. 140 {angstrom} between 0.05 < E < 0.6V) to HClO{sub 4} + Br{sup -} (ca 350 {angstrom} between 0.05 < E < 0.8V). The larger the ordered domains of the p(2x2)-CO{sub ad} structure are, the less active the surface is towards CO oxidation.

  15. Influence of surface preparation on atomic layer deposition of Pt films

    Institute of Scientific and Technical Information of China (English)

    Ge Liang; Hu Cheng; Zhu Zhiwei; Zhang Wei; Wu Dongping; Zhang Shili

    2012-01-01

    We report Pt deposition on a Si substrate by means of atomic layer deposition (ALD) using (methylcyclopentadienyl) trimethylplatinum (CH3CsH4Pt(CH3)3) and O2.Silicon substrates with both HF-last and oxidelast surface treatments are employed to investigate the influence of surface preparation on Pt-ALD.A significantlylonger incubation time and less homogeneity are observed for Pt growth on the HF-last substrate compared to the oxide-last substrate.An interfacial oxide layer at the Pt-Si interface is found inevitable even with HF treatment of the Si substrate immediately prior to ALD processing.A plausible explanation to the observed difference of Pt-ALD is discussed.

  16. Structural and electronic properties of bulk and low-index surfaces of zincblende PtC

    Science.gov (United States)

    Gokhan Sensoy, Mehmet; Toffoli, Daniele; Ustunel, Hande

    2017-03-01

    Transition metal carbides have been extensively used in diverse applications over the past decade. Their versatility is in part thanks to their unique bonding, which displays a mixture of ionic, metallic and covalent character. While the bulk structure of zincblende (ZB) PtC has been investigated several times, a detailed understanding of the electronic and structural properties of its low-index surfaces is lacking. In this work, we present an ab initio investigation of the properties of five crystallographic ZB PtC surfaces (Pt/C-terminated PtC(1 0 0), PtC(1 1 0) and Pt/C-terminated PtC(1 1 1)). Upon geometry optimization, both polar and nonpolar surfaces undergo a mild interlayer relaxation, without extensive reconstructions. Calculated vacancy formation energies indicate facile C removal on the (1 1 1) surface while Pt-vacancy formation is endothermic. Finally, atomic O adsorption energies on all surfaces reveal a high affinity of the C-terminated surfaces towards this species.

  17. Structure Determination of Au on Pt(111 Surface: LEED, STM and DFT Study

    Directory of Open Access Journals (Sweden)

    Katarzyna Krupski

    2015-05-01

    Full Text Available Low-energy electron diffraction (LEED, scanning tunneling microscopy (STM and density functional theory (DFT calculations have been used to investigate the atomic and electronic structure of gold deposited (between 0.8 and 1.0 monolayer on the Pt(111 face in ultrahigh vacuum at room temperature. The analysis of LEED and STM measurements indicates two-dimensional growth of the first Au monolayer. Change of the measured surface lattice constant equal to 2.80 Å after Au adsorption was not observed. Based on DFT, the distance between the nearest atoms in the case of bare Pt(111 and Au/Pt(111 surface is equal to 2.83 Å, which gives 1% difference in comparison with STM values. The first and second interlayer spacing of the clean Pt(111 surface are expanded by +0.87% and contracted by −0.43%, respectively. The adsorption energy of the Au atom on the Pt(111 surface is dependent on the adsorption position, and there is a preference for a hollow fcc site. For the Au/Pt(111 surface, the top interlayer spacing is expanded by +2.16% with respect to the ideal bulk value. Changes in the electronic properties of the Au/Pt(111 system below the Fermi level connected to the interaction of Au atoms with Pt(111 surface are observed.

  18. Structural and electronic properties of bulk and low-index surfaces of zincblende PtC.

    Science.gov (United States)

    Sensoy, Mehmet Gokhan; Toffoli, Daniele; Ustunel, Hande

    2017-03-29

    Transition metal carbides have been extensively used in diverse applications over the past decade. Their versatility is in part thanks to their unique bonding, which displays a mixture of ionic, metallic and covalent character. While the bulk structure of zincblende (ZB) PtC has been investigated several times, a detailed understanding of the electronic and structural properties of its low-index surfaces is lacking. In this work, we present an ab initio investigation of the properties of five crystallographic ZB PtC surfaces (Pt/C-terminated PtC(1 0 0), PtC(1 1 0) and Pt/C-terminated PtC(1 1 1)). Upon geometry optimization, both polar and nonpolar surfaces undergo a mild interlayer relaxation, without extensive reconstructions. Calculated vacancy formation energies indicate facile C removal on the (1 1 1) surface while Pt-vacancy formation is endothermic. Finally, atomic O adsorption energies on all surfaces reveal a high affinity of the C-terminated surfaces towards this species.

  19. Role of perfluorosulfonic ionomer as protective agent against strong adsorption of (bi)sulfate anions. Relevance in the determination of the area of Pt/C electrocatalysts

    Energy Technology Data Exchange (ETDEWEB)

    Garcia-Rodriguez, S.; Rojas, S.; Pena, M.A.; Fierro, J.L.G. [Grupo de Quimica y Energia Sostenibles, Instituto de Catalisis y Petroleoquimica, CSIC C/Marie Curie 2, 28049 Madrid (Spain); Vellosillo, M.; Ocon, P. [Departamento de Quimica-Fisica, Facultad de Ciencias, Universidad Autonoma de Madrid, Campus de Cantoblanco, 28049 Madrid (Spain)

    2010-10-15

    This work aims to shed light on the wide dispersion of the values of the area of Pt/C electrodes reported when evaluated by means of the thin-film electrode approach. The effect of the Perfluorosulfonic Ionomer (PFSI) content of the electrodes and the nature of the electrolyte are discussed. The results disclose that the area of the Pt electrodes evaluated by electrochemical techniques is related to the actual PFSI content on the electrode and to the nature of the electrolyte. Using HClO{sub 4} as electrolyte, electrode area values are independent of the PFSI content. On the contrary, if experiments are recorded in H{sub 2}SO{sub 4}, the electrode area value increases with the increasing PFSI content, irrespectively of the Pt loading. Such effect is ascribed to the interaction of the sulfonic groups from the PFSI with the surface of the Pt nanoparticles, avoiding the strong adsorption of the bisulfate anions. (author)

  20. Site preference of NH3-adsorption on Co, Pt and CoPt surfaces: the role of charge transfer, magnetism and strain.

    Science.gov (United States)

    Bhattacharjee, S; Gupta, K; Jung, N; Yoo, S J; Waghmare, U V; Lee, S C

    2015-04-14

    Oxidation of Co at the surface poses a major problem in the cyclable use of CoPt, a cost-effective catalyst for proton exchange membrane fuel cells. This can be alleviated by attaching a ligand selectively to Co-sites to stop its oxidation without compromising the catalytic activity. Here, we present a comparative analysis of adsorption of NH3 on the (0001) surface of Co in the HCP structure and (111) surfaces of Pt and CoPt alloy in the FCC structure, using first-principles density functional theoretical calculations. While NH3 binds more strongly with the Pt surface than with the Co surface, we find that its binding with the Co atom is stronger than that with the Pt atom on the surface of the CoPt alloy. Our analysis of the charge density and electronic structure shows how this originates from (a) the electron transfer from the minority spin d-band of Co to Pt, and (b) shift in the energy of d-bands and the magnetic moments of Co atoms on the surface of the CoPt alloy relative to those on the (0001) surface of Co. Hybridization of the d-states of Co in CoPt with pz states of N in NH3 used to stop Co oxidation also results in improving the charge transfer from Co to Pt that is relevant to the catalytic activity of CoPt. We finally present the analysis of how the interaction of NH3 with the CoPt surface can be tuned with strain.

  1. Design of Low Pt Concentration Electrocatalyst Surfaces with High Oxygen Reduction Reaction Activity Promoted by Formation of a Heterogeneous Interface between Pt and CeO(x) Nanowire.

    Science.gov (United States)

    Chauhan, Shipra; Mori, Toshiyuki; Masuda, Takuya; Ueda, Shigenori; Richards, Gary J; Hill, Jonathan P; Ariga, Katsuhiko; Isaka, Noriko; Auchterlonie, Graeme; Drennan, John

    2016-04-13

    Pt-CeO(x) nanowire (NW)/C electrocatalysts for the improvement of oxygen reduction reaction (ORR) activity on Pt were prepared by a combined process involving precipitation and coimpregnation. A low, 5 wt % Pt-loaded CeO(x) NW/C electrocatalyst, pretreated by an optimized electrochemical conditioning process, exhibited high ORR activity over a commercially available 20 wt % Pt/C electrocatalyst although the ORR activity observed for a 5 wt % Pt-loaded CeO(x) nanoparticle (NP)/C was similar to that of 20 wt % Pt/C. To investigate the role of a CeO(x) NW promotor on the enhancement of ORR activity on Pt, the Pt-CeO(x) NW interface was characterized by using hard X-ray photoelectron spectroscopy (HXPS), transmission electron microscopy (TEM), and electron energy loss spectroscopy (EELS). Microanalytical data obtained by these methods were discussed in relation to atomistic simulation performed on the interface structures. The combined techniques of HXPS, TEM-EELS, and atomistic simulation indicate that the Pt-CeO(x) NW interface in the electrocatalyst contains two different defect clusters: Frenkel defect clusters (i.e., 2Pt(i)(••) - 4O(i)″ - 4V(o)(••) - V(Ce)″″) formed in the surface around the Pt-CeO(x) NW interface and Schottky defect clusters (i.e., (Pt(Ce)″ - 2V(O)(••) - 2Ce(Ce)') and (Pt(Ce)″ - V(O)(••))) which appear in the bulk of the Pt-CeO(x) NW interface similarly to Pt-CeO(x) NP/C. It is concluded that the formation of both Frenkel defect clusters and Schottky defect clusters at the Pt-CeO(x) NW heterointerface contributes to the promotion of ORR activity and permits the use of lower Pt-loadings in these electrocatalysts.

  2. A DFT Structural Investigation of New Bimetallic PtSnx Surface Alloys Formed on the Pt(110) Surface and Their Interaction with Carbon Monoxide

    DEFF Research Database (Denmark)

    Zheng, Jian; Busch, Michael; Artiglia, Luca

    2016-01-01

    Two surface alloys with p(3 x 1) and p(6 x 1) periodicity have been identified after the deposition of metallic Sn on the (1 x 2)-Pt(110) surface. These two structures have been characterized by low energy electron diffraction (LEED), scanning tunneling microscopy (STM), and photoemission spectro...

  3. Tuning the surface electronic structure of a Pt3Ti(111) electro catalyst

    Science.gov (United States)

    Paßens, M.; Caciuc, V.; Atodiresei, N.; Moors, M.; Blügel, S.; Waser, R.; Karthäuser, S.

    2016-07-01

    Increasing the efficiency and stability of bimetallic electro catalysts is particularly important for future clean energy technologies. However, the relationship between the surface termination of these alloys and their catalytic activity is poorly understood. Therefore, we report on fundamental UHV-SPM, LEED, and DFT calculations of the Pt3Ti(111) single crystal surface. Using voltage dependent imaging the surface termination of Pt3Ti(111) was studied with atomic resolution. Combining these images with simulated STM maps based on ab initio DFT calculations allowed us to identify the three upper layers of the Pt3Ti(111) single crystal and their influence upon the surface electronic structure. Our results show that small changes in the composition of the second and third atomic layer are of significant influence upon the surface electronic structure of the Pt3Ti electro catalyst. Furthermore, we provide relevant insights into the dependence of the surface termination on the preparation conditions.Increasing the efficiency and stability of bimetallic electro catalysts is particularly important for future clean energy technologies. However, the relationship between the surface termination of these alloys and their catalytic activity is poorly understood. Therefore, we report on fundamental UHV-SPM, LEED, and DFT calculations of the Pt3Ti(111) single crystal surface. Using voltage dependent imaging the surface termination of Pt3Ti(111) was studied with atomic resolution. Combining these images with simulated STM maps based on ab initio DFT calculations allowed us to identify the three upper layers of the Pt3Ti(111) single crystal and their influence upon the surface electronic structure. Our results show that small changes in the composition of the second and third atomic layer are of significant influence upon the surface electronic structure of the Pt3Ti electro catalyst. Furthermore, we provide relevant insights into the dependence of the surface termination on the

  4. Pt/C Fuel Cell Catalyst Degradation

    DEFF Research Database (Denmark)

    Zana, Alessandro

    This thesis investigates the degradation behavior of Pt/C catalysts under simulated automotive conditions. By using the “tool box” synthesis method the Pt loading has been changed from low to high Pt loadings, therefore permitting to study the role of Pt on the degradation of high surface area (H...

  5. Pt/C Fuel Cell Catalyst Degradation

    DEFF Research Database (Denmark)

    Zana, Alessandro

    This thesis investigates the degradation behavior of Pt/C catalysts under simulated automotive conditions. By using the “tool box” synthesis method the Pt loading has been changed from low to high Pt loadings, therefore permitting to study the role of Pt on the degradation of high surface area (H...

  6. Reforming of oxygenates for H2 production: correlating reactivity of ethylene glycol and ethanol on Pt(111) and Ni/Pt(111) with surface d-band center.

    Science.gov (United States)

    Skoplyak, Orest; Barteau, Mark A; Chen, Jingguang G

    2006-02-02

    The dehydrogenation and decarbonylation of ethylene glycol and ethanol were studied using temperature programmed desorption (TPD) on Pt(111) and Ni/Pt(111) bimetallic surfaces, as probe reactions for the reforming of oxygenates for the production of H2 for fuel cells. Ethylene glycol reacted via dehydrogenation to form CO and H2, corresponding to the desired reforming reaction, and via total decomposition to produce C(ad), O(ad), and H2. Ethanol reacted by three reaction pathways, dehydrogenation, decarbonylation, and total decomposition, producing CO, H2, CH4, C(ad), and O(ad). Surfaces prepared by deposition of a monolayer of Ni on Pt(111) at 300 K, designated Ni-Pt-Pt(111), displayed increased reforming activity compared to Pt(111), subsurface monolayer Pt-Ni-Pt(111), and thick Ni/Pt(111). Reforming activity was correlated with the d-band center of the surfaces and displayed a linear trend for both ethylene glycol and ethanol, with activity increasing as the surface d-band center moved closer to the Fermi level. This trend was opposite to that previously observed for hydrogenation reactions, where increased activity occurred on subsurface monolayers as the d-band center shifted away from the Fermi level. Extrapolation of the correlation between activity and the surface d-band center of bimetallic systems may provide useful predictions for the selection and rational design of bimetallic catalysts for the reforming of oxygenates.

  7. CO-Induced Restructuring on Stepped Pt Surfaces: A Molecular Dynamics Study

    CERN Document Server

    Michalka, Joseph R; Gezelter, J Daniel

    2016-01-01

    The effects of plateau width and step edge kinking on carbon monoxide (CO)-induced restructuring of platinum surfaces were explored using molecular dynamics (MD) simulations. Platinum crystals displaying four different vicinal surfaces [(321), (765), (112), and (557)] were constructed and exposed to partial coverages of carbon monoxide. Platinum-CO interactions were fit to recent experimental data and density functional theory (DFT) calculations, providing a classical interaction model that captures the atop binding preference on Pt. The differences in Pt-Pt binding strength between edge atoms on the various facets were found to play a significant role in step edge wandering and reconstruction events. Because the mechanism for step doubling relies on a stochastic meeting of two wandering edges, the widths of the plateaus on the original surfaces was also found to play a role in these reconstructions. On the Pt(321) surfaces, the CO adsorbate was found to assist in reordering the kinked step edges into straigh...

  8. On the role of reactant transport and (surface) alloy formation for the CO tolerance of carbon supported PtRu polymer electrolyte fuel cell catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Kaiser, J.; Colmenares, L.; Jusys, Z.; Behm, R.J. [Abt. Oberflaechenchemie und Katalyse, Universitaet Ulm (Germany); Moertel, R.; Boennemann, H. [Max-Planck-Institut fuer Kohlenforschung, Muelheim a.d. Ruhr (Germany); Koehl, G.; Modrow, H.; Hormes, J. [Physikalisches Institut, Universitaet Bonn (Germany)

    2006-07-15

    The role of atomic scale intermixing for the electrocatalytic activity of bimetallic PtRu anode catalysts in reformate operated polymer electrolyte fuel cells (PEFC) was investigated, exploiting the specific properties of colloid based catalyst synthesis for the selective preparation of alloyed and non-alloyed bimetallic catalysts. Three different carbon supported PtRu catalysts with different degrees of Pt and Ru intermixing, consisting of (i) carbon supported PtRu alloy particles (PtRu/C), (ii) Pt and Ru particles co-deposited on the same carbon support (Pt+Ru/C), and (iii) a mixture of carbon supported Pt and carbon supported Ru (Pt/C+Ru/C) as well as the respective monometallic Pt/C and Ru/C catalysts were prepared and characterized by electron microscopy (TEM), X-ray absorption spectroscopy, and CO stripping. Their performance as PEFC anode catalysts was evaluated by oxidation of a H{sub 2}/2%CO gas mixture (simulated reformate) under fuel cell relevant conditions (elevated temperature, continuous reaction and controlled reactant transport) in a rotating disk electrode (RDE) set-up. The CO tolerance and H{sub 2} oxidation activity of the three catalysts is comparable and distinctly different from that of the monometallic catalysts. The results indicate significant transport of the reactants, CO{sub ad} and/or OH{sub ad}, between Pt and Ru surface areas and particles for all three catalysts, with only subtle differences from the alloy catalyst to the physical mixture. The high activity and CO tolerance of the bimetallic catalysts, through the formation of bimetallic surfaces, is explained, e.g., by contact formation in nanoparticle agglomerates or by material transport and subsequent surface decoration/surface alloy formation during catalyst preparation, conditioning, and operation. The instability and mobility of the catalysts under these conditions closely resembles concepts in gas phase catalysis. (Abstract Copyright [2006], Wiley Periodicals, Inc.)

  9. Growth of Pt thin films on Cu(111) and formation of Pt/Cu surface alloys: growth mechanism and diffusion barrier

    CERN Document Server

    Boo, J H; Lee, S B; Kwak, H T; Schröder, U; Linke, R; Wandelt, K

    1999-01-01

    Ultra-thin-platinum films evaporated on Cu(111) at 100 K and at room temperature were investigated by using in situ Auger electron spectroscopy (AES) and low energy electron diffraction (LEED). A growth mechanism of the layer-by layer type was evidenced up to at least 5-ML of Pt. Over the first Pt monolayer, the Pt-Pt bond distances were strained about 7 % beyond the equilibrium bond distances found for bulk platinum. Surface alloys were formed by diffusing the Pt adatoms into the Cu(111) substrate at temperatures above 500 K with a diffusion barrier of 0.85 eV. For higher annealing temperatures, the Pt concentration got smaller. From an Auger depth profile, the diffusion barrier for surface alloy formation was estimated using Fick's second law.

  10. Molecular Precursors-Induced Surface Reconstruction at Graphene/Pt(111) Interfaces

    CERN Document Server

    Wang, Qian; Shi, Xingqiang

    2015-01-01

    Inspired by experimental observations of Pt(111) surfaces reconstruction at the Pt/graphene (Gr) interfaces with ordered vacancy networks in the outermost Pt layer, the mechanism of the surface reconstruction is investigated by van-der-Waals-corrected density functional theory in combination with particle-swarm optimization algorithm and ab initio atomistic thermodynamics. Our global structural search finds a more stable reconstructed (Rec) structure than that was reported before. With correction for vacancy formation energy, we demonstrate that the experimental observed surface reconstruction occurred at the earlier stages of graphene formation: 1) reconstruction occurred when C60 adsorption (before decomposition to form graphene) for C60 as a molecular precursor, or 2) reconstruction occurred when there were (partial) hydrogens retain in the adsorbed carbon structures for C2H4 and C60H30 as precursors. The reason can be attributed to that the energy gain, from the strengthened Pt-C bonding for C of C60 or f...

  11. The synthesis of PdPt/carbon paper via surface limited redox replacement reactions for oxygen reduction reaction

    CSIR Research Space (South Africa)

    Motsoeneng, RG

    2015-09-01

    Full Text Available Surface-limited redox replacement reactions using the electrochemical atomic layer deposition (EC-ALD) technique were used to synthesize PdPt bimetallic electrocatalysts on carbon paper substrate. Electrocatalysts having different Pd:Pt ratio were...

  12. Surface composition tuning of Au-Pt bimetallic nanoparticles for enhanced carbon monoxide and methanol electro-oxidation.

    Science.gov (United States)

    Suntivich, Jin; Xu, Zhichuan; Carlton, Christopher E; Kim, Junhyung; Han, Binghong; Lee, Seung Woo; Bonnet, Nicéphore; Marzari, Nicola; Allard, Lawrence F; Gasteiger, Hubert A; Hamad-Schifferli, Kimberly; Shao-Horn, Yang

    2013-05-29

    The ability to direct bimetallic nanoparticles to express desirable surface composition is a crucial step toward effective heterogeneous catalysis, sensing, and bionanotechnology applications. Here we report surface composition tuning of bimetallic Au-Pt electrocatalysts for carbon monoxide and methanol oxidation reactions. We establish a direct correlation between the surface composition of Au-Pt nanoparticles and their catalytic activities. We find that the intrinsic activities of Au-Pt nanoparticles with the same bulk composition of Au0.5Pt0.5 can be enhanced by orders of magnitude by simply controlling the surface composition. We attribute this enhancement to the weakened CO binding on Pt in discrete Pt or Pt-rich clusters surrounded by surface Au atoms. Our finding demonstrates the importance of surface composition control at the nanoscale in harnessing the true electrocatalytic potential of bimetallic nanoparticles and opens up strategies for the development of highly active bimetallic nanoparticles for electrochemical energy conversion.

  13. Oxidation of CO and surface properties of well characterized Pt{sub 3}Sn bimetallic alloy surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Stamenkovic, V.; Arenz, M.; Blizanac, B. B.; Ross, P. N.; Markovic, N. M. [University of California-Berkeley, Materials Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA (United States)

    2004-04-01

    The Pt{sub 3}Sn alloy is known to be one of the most active systems for carbon monoxide oxidation. This paper continues the effort begun earlier to explore the link between macroscopic level properties of the Pt{sub 3}Sn(hkl) surfaces in an electrochemical environment and in-situ atomic level characterization. Specifically, the work reported here entails a further examination of the Pt{sub 3}Sn(110) interface in an electrochemical environment as part of a detailed study of structural effects on electrocatalysis. Alloy surfaces have been characterized in ultra-high vacuum (UHV) by Auger electron microscopy, low energy ion scattering spectroscopy (LEISS) and low energy electron diffraction (LEED). Surface electrochemistry of carbon monoxide was studied in-situ by Fourier transform infrared (FTIR) spectroscopy. Result showed that in contrast to the Pt{sub 3}Sn(111) surface, changes in band morphology and vibrational properties are clearly absent on the Pt{sub 3}Sn(110) surface. In the case of the Pt{sub 3}Sn(hkl)-CO interaction, not only electronic effects, but also other factors, such as surface structure and intermolecular repulsion between adsorbed CO species were found to be responsible for high catalytic activity. 40 refs., 6 figs.

  14. Determination of retinal surface area.

    Science.gov (United States)

    Nagra, Manbir; Gilmartin, Bernard; Thai, Ngoc Jade; Logan, Nicola S

    2017-09-01

    Previous attempts at determining retinal surface area and surface area of the whole eye have been based upon mathematical calculations derived from retinal photographs, schematic eyes and retinal biopsies of donor eyes. 3-dimensional (3-D) ocular magnetic resonance imaging (MRI) allows a more direct measurement, it can be used to image the eye in vivo, and there is no risk of tissue shrinkage. The primary purpose of this study is to compare, using T2-weighted 3D MRI, retinal surface areas for superior-temporal (ST), inferior-temporal (IT), superior-nasal (SN) and inferior-nasal (IN) retinal quadrants. An ancillary aim is to examine whether inter-quadrant variations in area are concordant with reported inter-quadrant patterns of susceptibility to retinal breaks associated with posterior vitreous detachment (PVD). Seventy-three adult participants presenting without retinal pathology (mean age 26.25 ± 6.06 years) were scanned using a Siemens 3-Tesla MRI scanner to provide T2-weighted MR images that demarcate fluid-filled internal structures for the whole eye and provide high-contrast delineation of the vitreous-retina interface. Integrated MRI software generated total internal ocular surface area (TSA). The second nodal point was used to demarcate the origin of the peripheral retina in order to calculate total retinal surface area (RSA) and quadrant retinal surface areas (QRSA) for ST, IT, SN, and IN quadrants. Mean spherical error (MSE) was -2.50 ± 4.03D and mean axial length (AL) 24.51 ± 1.57 mm. Mean TSA and RSA for the RE were 2058 ± 189 and 1363 ± 160 mm(2) , respectively. Repeated measures anova for QRSA data indicated a significant difference within-quadrants (P area/mm increase in AL. Although the differences between QRSAs are relatively small, there was evidence of concordance with reported inter-quadrant patterns of susceptibility to retinal breaks associated with PVD. The data allow AL to be converted to QRSAs, which will assist further

  15. Magnetism of Fe clusters and islands on Pt surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Repetto, D.; Honolka, J.; Enders, A.; Kern, K. [MPI fuer Festkoerperforschung, Stuttgart (Germany); Rusponi, S.; Brune, H. [Institut de Physique des Nanostructures, EPFL, Lausanne (Switzerland)

    2006-01-01

    Clusters and islands of Fe atoms have been prepared by noble gas buffer layer assisted growth as well as by standard molecular beam epitaxy on Pt substrates. Xe buffer layers have been utilized to promote the formation of compact, relaxed Fe clusters with narrow size distribution. Without the Xe buffer, strained Fe islands with a characteristic misfit dislocation network are formed. Magnetization loops obtained by magneto-optical Kerr effect measurements reveal that in-plane easy magnetization axis is only found for the relaxed clusters, pointing out the important role of epitaxial lattice deformations for the magnetic anisotropy. (orig.)

  16. Vibrational properties of the Pt(111)- p(2 × 2)-K surface superstructure

    Science.gov (United States)

    Rusina, G. G.; Eremeev, S. V.; Borisova, S. D.; Chulkov, E. V.

    2008-08-01

    The vibrational spectra of the Pt(111)- p(2 × 2)-K ordered surface superstructure formed on the platinum surface upon adsorption of 0.25 potassium monolayer are calculated using the interatomic interaction potentials obtained within the tight-binding approximation. The surface relaxation, the dispersion of surface phonons, the local density of surface vibrational states, and the polarization of vibrational modes of adatoms and substrate atoms are discussed. The theoretical results are in good agreement with the recently obtained experimental data.

  17. ANALISIS POTENSI SIMPANAN KARBON HUTAN MANGROVE DI AREA PT. INDOCEMENT TUNGGAL PRAKARSA, TBK P 12 TARJUN

    Directory of Open Access Journals (Sweden)

    Eva Ariani

    2016-12-01

    Full Text Available This study aims to analyze the structure of the mangrove forest stands in a conservation area PT. Indocement P12 Tarjun, South Kalimantan. To determine the potential amount of carbon stored in vegetation and soils di area mangrove forests. Merumuskah form of management in accordance with mangrove forests owned by PT Indocement Tunggal Tbk P 12 Tarjun. The results of this study show the type of vegetation that are within the plot observation is Aegicera corniculatum, Acivennia alba, Avicennia lanata, Avicennia Marina, Bruguera gymnorrhiza, Bruguiera parviflora, Ceriops decandra, Lumnitzera, Rhizophora apiculate, Rhizophora mucronata, Scyphiphora hydrophyllacea, Sonneratia alba, Xylocarpus granatum, Acanthus ebracteatus, Hibiscus tiliaceus, Nypa fruticans, Terminalia catappa and type of vegetation present in the area of research, but is not included in the observation plot is Acrostichum aureum Linn, Pandanus odoratissima. Importance Value Index (IVI lenata kind Avicennia highest growth rate of the tree that is 80,2%, Rhizophora apiculata at the level of the pole that is 57%, and Nypa fruticans at the seedling stage is 20,8%. To Nypa fruticans, though IVIs largest/highest species of plants in the seedling stage but this type is only found on two research plots only. Total carbon content was found at the study site was at 714,77 per hectare. The study was conducted on biomass carbon on the surface, lower plants, nekromassa (dead trees, and mangrove sediments (ground. Carbon sequestration at a site can be seen from the height and diameter of trees while a vegetation type had no significant effect on the absorption of carbon. Environmental management in the form of replanting are research needs to be done to avoid more severe harm than good because of logging by humans atupun affected by coastal erosion. Type Lumnitzera, Scyphiphora hydrophyllacea, Ceriops decandra should get more attention because it has a very low INP hat is necessary to manage

  18. Effect of metal support interaction on surface segregation in Pd Pt nanoparticles

    Science.gov (United States)

    De Sarkar, A.; Menon, Mahesh; Khanra, Badal C.

    2001-10-01

    In this work, we present the results of our Monte Carlo (MC) simulation studies for the segregation behavior of supported, clean and gas-covered Pd-Pt nanoparticles as a function of the metal-support interaction. For preferential Pd-support interaction, the base of the nanoparticle is found to get enriched with Pd atoms; while for preferential interaction of Pt atoms with the support the base gets enriched in Pt. The composition of the rest of the particle changes slightly with the metal-support interaction. The presence of oxygen and hydrogen atoms does not influence the role of the metal-support interaction on the surface composition of Pd-Pt nanoparticles. The simulation results are found to be in total agreement with the known experimental results.

  19. Pt-Si Bifunctional Surfaces for CO and Methanol Electro-Oxidation

    DEFF Research Database (Denmark)

    Permyakova, Anastasia A.; Han, Binghong; Jensen, Jens Oluf

    2015-01-01

    Bimetallic surfaces offer activity benefits derived from synergistic effects among active sites with uniquely different functions, which is particularly important for the development of highly effective heterogeneous catalysts for specific technological applications, such as energy conversion...... and storage. Here we report on Pt-Si bulk samples prepared by arc-melting, for the first time, with high activities toward the electro-oxidation of CO and methanol. Increasing the Si concentration on the surface was correlated with the shifts of onset oxidation potentials to lower values and higher activities...... for CO and methanol electro-oxidation. It is proposed that the reaction on the Pt-Si catalyst could follow a Langmuir-Hinshelwood type of mechanism, where substantially enhanced catalytic activity is attributed to the fine-tuning of the surface Pt-Si atomic structure....

  20. Break-up of Pt catalyst surfaces by high CO coverage

    Energy Technology Data Exchange (ETDEWEB)

    Tao, Feng; Dag, Sefa; Wang, Lin-Wang; Liu, Zhi; Butcher, Derek; Bluhm, Henrik; Salmeron, Miquel; Somorjai, Gabor

    2009-09-16

    Stepped Platinum surfaces were found to undergo extensive and reversible restructuring when exposed to CO at pressures above 0.1 Torr. This radically new and previously unknown restructuring phenomenon, has important implications for Pt based catalytic reactions. Novel Scanning Tunneling Microscopy and Photoelectron Spectroscopy techniques operating under gaseous environments near ambient pressure and temperature revealed that as the CO surface coverage approaches 100percent, the originally flat terraces of stepped Pt crystals break up into nanometer size clusters. At room temperature the crystal surface reverts to its initial flat morphology after pumping away the gas phase CO. Density Functional Theory energy calculations provide a rationale for the observations whereby the creation of increased concentrations of low coordination Pt sites at the edges of the formed nanoclusters relieves the strong CO-CO repulsion in the highly compressed adsorbate film.

  1. Structural and Magnetic Properties of Ultrathin Fe Films on Pt(001) Surface

    Institute of Scientific and Technical Information of China (English)

    ZHANG Li-Juan; HE Ke; JIA Jin-Feng; XUE Qi-Kun

    2005-01-01

    @@ Magnetic anisotropy evolution of ultrathin Fe films grown on Pt(001) single-crystal surface is investigated by UHVin situ surface magneto-optical Kerr effect (SMOKE) measurement. After annealing at ~ 600 K, the magnetic anisotropy of Fe film switches from in-plane to perpendicular at low coverage, leading to a spin reorientationtransition (SRT). Meanwhile, in the range of 3-4 monolayer (ML) thickness, the coercivity of the Fe polar hysteresis loop decreases dramatically. Further scanning tunnelling microscopy (STM) and low energy electron diffraction (LEED) investigation correlates the magnetic properties with the film structures. We attribute this SRT to the formation of Fe-Pt ordered alloy.

  2. Laser spectroscopy and photochemistry on metal surfaces, pt.1

    CERN Document Server

    Dai, HL

    1995-01-01

    Using lasers to induce and probe surface processes has the advantages of quantum state specificity, species selectivity, surface sensitivity, fast time-resolution, high frequency resolution, and accessibility to full pressure ranges. These advantages make it highly desirable to use light to induce, control, or monitor surface chemical and physical processes. Recent applications of laser based techniques in studying surface processes have stimulated new developments and enabled the understanding of fundamental problems in energy transfer and reactions. This volume will include discussions on sp

  3. Laser spectroscopy and photochemistry on metal surfaces, pt.2

    CERN Document Server

    Dai, HL

    1995-01-01

    Using lasers to induce and probe surface processes has the advantages of quantum state specificity, species selectivity, surface sensitivity, fast time-resolution, high frequency resolution, and accessibility to full pressure ranges. These advantages make it highly desirable to use light to induce, control, or monitor surface chemical and physical processes. Recent applications of laser based techniques in studying surface processes have stimulated new developments and enabled the understanding of fundamental problems in energy transfer and reactions. This volume will include discussions on sp

  4. Oxidation of formic acid on the Pt(111) surface in the gas phase.

    Science.gov (United States)

    Gao, Wang; Keith, John A; Anton, Josef; Jacob, Timo

    2010-09-28

    Formic acid (HCOOH) oxidation on Pt(111) under gas-phase conditions is a benchmark heterogeneous catalysis reaction used to probe electro-catalytic HCOOH conversion in fuel cells, itself an important reaction in energy conversion. We used density functional theory (DFT) calculations to elucidate the fundamental oxidation mechanisms of HCOOH in the gas phase, determining the relative strengths of chemical interactions between HCOOH oxidation intermediates and the Pt(111) surface. We focused on investigating how water and adsorption coverage affects reaction intermediate structures and transition states. Our results show that adsorbed HCOO is a reactive intermediate in gas phase, and co-adsorbed water plays a key role in HCOOH oxidation influencing the structure of reaction intermediates and reaction barriers on Pt(111). The simulations show the preferred catalytic pathway is qualitatively dependent on surface coverage. These results provide a conceptual basis to better interpret its complicated experimental reaction kinetics.

  5. Perancangan dan Pembuatan Sistem Informasi Gudang (Studi Kasus : PT. PLN (Persero Area Surabaya Barat

    Directory of Open Access Journals (Sweden)

    Budi Prasetyo

    2015-12-01

    Full Text Available Sistem informasi berbasis komputerisasi merupakan salah satu faktor penting bagi perusahaan - perusahaan dalam mengelola segala aktifitas perusahaan. Bahkan penggunaan teknologi komputer tersebut akan menjadi syarat utama untuk menunjukkan kualitas suatu bidang dan menjadi modal terpenting dalam memenangkan persaingan. Sistem Informasi Gudang di PT. PLN (Persero Area Surabaya Utara dibangun karena masih menggunakan cara manual untuk melakukan penerimaan barang datang, permintaan barang, dan pemberian barang, sehingga mempengaruhi dalam pelaksanaan operasional kerja, baik dalam segi kecepatan, pelayanan, dari segi informasi yang dihasilkan. Untuk itu diperlukan suatu sistem yang dapat memudahkan manajemen dalam mengelola seluruh aktifitas yang ada di gudang. Sistem Informasi Gudang PT.PLN (Persero Area Surabaya Utara adalah suatu sistem yang mengelola data barang, data rayon, dan transaksi yang ada di gudang. Sistem ini menggambarkan rangkaian kegiatan dari mulai mengelola barang datang, permintaan barang, barang keluar hingga pelaporannya. Setelah melalui tahapan analisis dan implementasi, kemudian dilakukan tahapan selanjutnya yaitu tahap pengujian sistem dimana pengujian ini menggunakan metode pengujian white box yang berfokus pada pengujian perangkat lunak. Dari hasil pengujian, dapat ditarik kesimpulan bahwa Sistem Informasi Gudang di PT.PLN (Pesero Area Surabaya dibangun untuk mempermudah manajemen dalam melakukan pengawasan dan pengendalian di gudang.

  6. PEMANFAATAN PENGINDERAAN JAUH UNTUK ESTIMASI STOK KARBON DI AREA REKLAMASI PT. ANTAM UBPE PONGKOR, KABUPATEN BOGOR

    Directory of Open Access Journals (Sweden)

    Andini Tribuana Tunggadewi

    2014-07-01

    Full Text Available Mining is an environment-altering activity especially on land by reducing landcover and stored carbon. PT ANTAM, a prominent mining company in an industrial scale, is doing reclamation in order to restore the ability of the land to its optimum function. Reclamation in the relation with global warming, is an efforts to mitigate climate change by increasing the ability of land to absorb carbon (revegetation. Therefore land cover monitoring at reclamation area becomes an important thing to do, one way to do it is by using remote sensing. Not only for land cover, remote sensing also can be used to estimate carbon stocks. Based on visual interpretation of google earth image data in 2007, there were five classes of secondary forest at reclamation area of PT ANTAM UBPE Pongkor : class A (tight forest covering 8,65 ha; class B (medium forest covering 0,88 ha; class C (sparse forest covering 1,57 ha; and class D (shrubs covering 0,92 ha. Meanwhile, the calculation of carbon stocks based on three sampling locations that representing secondary forest classes A, B, and C, resulting estimated average carbon stock in the whole reclamation area of PT ANTAM UBPE Pongkor is 113,79 tons/ha. Keywords: mining, reclamation, google earth image data, carbon stock

  7. Electronic effects of surface oxygen on the bonding of NO to Pt(111)

    Energy Technology Data Exchange (ETDEWEB)

    Bartram, M.E.; Koel, B.E. (Univ. of Colorado, Boulder (United States)); Carter, E.A. (Univ. of California, Los Angeles (United States))

    1989-01-01

    Changes in the bonding of NO on Pt(111) induced by the coadsorption of high coverages of oxygen atoms have been studied with temperature programmed desorption (TPD), vibrational spectroscopy using high resolution electron energy loss spectroscopy (HREELS), and ultraviolet photoelectron spectroscopy (UPS). Modification of the electronic structure of surface Pt atoms by the strongly electron-withdrawing adsorbed oxygen atoms alters the relative stabilities of NO adsorption sites and the nature of the Pt-NO bond. Coadsorption of 0.25 ML (monolayers) of O{sub (a)} destabilizes the two-fold bridge site for NO adsorption that is energetically preferred on clean Pt(111) and causes preferential NO adsorption in the atop site initially. For this oxygen coverage, some population of the bridge site occurs at the highest NO coverages, but occupation of this site can be eliminated completely by preadsorption of 0.75 ML of oxygen. This high coverage of coadsorbed oxygen now induces a further change in the nature of the NO chemisorption bond for NO adsorbed in atop sties, forming bent NO rather than the linear NO species formed on clean Pt(111). The saturation coverage of bent NO is 0.15 ML on this 0.75 ML oxygen-precovered surface and the heat of adsorption is only 1-2 kcal/mol less than linear NO adsorbed in atop sites on clean Pt(111). By using the HREELS and UPS data to identify these three chemically distinct forms of NO{sub (a)}, the authors are able rationalize their formation (and subsequent properties) in different electron environments by correlating bonding configurations with the charge-transfer capabilities of the Pt substrate. Finally, they note that despite the presence of large excesses of O{sub (a)}, NO is never oxidized to form NO{sub 2}.

  8. Chemically Synthesised Pt Particles on Surface Oxidized Carbon Nanotubes as an Effective Catalyst for Direct Methanol Fuel Cell

    Institute of Scientific and Technical Information of China (English)

    Mohammad; yari; Sajjad; Sadaghat; Sharehjini

    2007-01-01

    1 Results The synthesis, physical characterization and electrochemical analysis of Pt particles prepared using the surface oxidized carbon nanotubes prepared by chemically anchoring Pt onto the surface of the CNTs with 2.0 mol/L HNO3 by refluxing for 10 h to introduce surface functional groups.The particles of Pt are synthesized by reduction with sodium borohydride of H2PtCl6. The electro-oxidation of liquid methanol of this catalyst as a thin layer on glassy carbon electrode is investigated at room te...

  9. Fabrication and Surface Properties of Composite Films of SAM/Pt/ZnO/SiO 2

    KAUST Repository

    Yao, Ke Xin

    2008-12-16

    Through synthetic architecture and functionalization with self-assembled monolayers (SAMs), complex nanocomposite films of SAM/Pt/ZnO/SiO2 have been facilely prepared in this work. The nanostructured films are highly uniform and porous, showing a wide range of tunable wettabilities from superhydrophilicity to superhydrophobicity (water contact angles: 0° to 170°). Our approach offers synthetic flexibility in controlling film architecture, surface topography, coating texture, crystallite size, and chemical composition of modifiers (e.g., SAMs derived from alkanethiols). For example, wettability properties of the nanocomposite films can be finely tuned with both inorganic phase (i.e., ZnO/SiO2 and Pt/ZnO/SiO2) and organic phase (i.e., SAMs on Pt/ZnO/SiO2). Due to the presence of catalytic components Pt/ZnO within the nanocomposites, surface reactions of the organic modifiers can further take place at room temperature and elevated temperatures, which provides a means for SAM formation and elimination. Because the Pt/ZnO forms an excellent pair of metal-semiconductors for photocatalysis, the anchored SAMs can also be modified or depleted by UV irradiation (i.e., the films possess self-cleaning ability). Potential applications of these nanocomposite films have been addressed. Our durability tests also confirm that the films are thermally stable and structurally robust in modification- regeneration cycles. © 2008 American Chemical Society.

  10. Molecular N-2 chemisorption-specific adsorption on step defect sites on Pt surfaces

    DEFF Research Database (Denmark)

    Tripa, C. Emil; Zubkov, T.S.; Yates, John T.

    1999-01-01

    Infrared reflection-absorption spectroscopy and density functional theory, within the generalized gradient approximation, were used to investigate both experimentally and theoretically N-2 chemisorption on stepped and smooth Pt surfaces. N-2 chemisorption was observed to occur only on the edge...

  11. Temperature dependent surface electrochemistry on Pt singlecrystals in alkaline electrolyte: Part 3: The oxygen reductionreaction

    Energy Technology Data Exchange (ETDEWEB)

    tom.schmidt@psi.ch

    2002-08-01

    The kinetics of the oxygen reduction reaction (ORR) was studied in alkaline electrolyte at 293-333K on Pt(hkl) surfaces by means of the rotating ring-disk electrode technique with solution phase peroxide detected at the ring electrode. The ORR on Pt(hkl) was found to be highly structure sensitive with activities increasing in the sequence (111) > (100) > (110)(1x2). Very similar apparent activation energies (37-45 {+-} 5 kJmol-1, {eta} = 0.35 V) were found on all three surfaces. Furthermore, at elevated temperature, significantly smaller amounts of peroxide are formed in agreement with enhanced peroxide reduction rates by increasing temperature. We found that the Tafel slopes on all three single crystal surfaces decrease with increasing temperature, indicating that the logi-E relationship is not represented by a classical Butler-Volmer expression. Based on the kinetic analysis of the polarization curves and from simulations of logi-E curves, we propose that the rate of the ORR on Pt(hkl) in alkaline solution is mainly determined by the potential/temperature dependent surface coverage by OH{sub ad}. We propose two modes of action of the OH{sub ad}: (i) OH{sub ad} blocks the adsorption of O{sub 2} on active platinum sites; and (ii) OH{sub ad} alters the adsorption energy of intermediates which are formed during the ORR on Pt sites.

  12. Relativistic tight-binding model: Application to Pt surfaces

    Science.gov (United States)

    Tchernatinsky, A.; Halley, J. W.

    2011-05-01

    We report a parametrization of a previous self-consistent tight-binding model, suitable for metals with a high atomic number in which nonscalar-relativistic effects are significant in the electron physics of condensed phases. The method is applied to platinum. The model is fitted to density functional theory band structures and cohesive energies and spectroscopic data on platinum atoms in five oxidation states, and is then shown without further parametrization to correctly reproduce several low index surface structures. We also predict reconstructions of some vicinal surfaces.

  13. Alloy formation and chemisorption at Zn/Pt(111) bimetallic surfaces using alkali ISS, XPD, and TPD.

    Science.gov (United States)

    Ho, Chih-Sung; Martono, Eddie; Banerjee, Santanu; Roszell, John; Vohs, John; Koel, Bruce E

    2013-11-21

    Alloy formation and chemisorption at bimetallic surfaces formed by vapor-depositing Zn on a Pt(111) single crystal were investigated primarily by using X-ray photoelectron diffraction (XPD), X-ray photoelectron spectroscopy (XPS), low-energy alkali ion scattering spectroscopy (ALISS), low electron energy diffraction (LEED), and temperature programmed desorption (TPD). A wide range of conditions were investigated to explore whether deposition and annealing of Zn films could produce well-defined, ordered alloy surfaces, similar to those encountered for Sn/Pt(111) surface alloys. These attempts were unsuccessful, although weak, diffuse (2 × 2) spots were observed under special conditions. The particular PtZn bimetallic alloy created by annealing one monolayer of Zn on Pt(111) at 600 K, which has a Zn composition in the surface layer of about 5 at. %, was investigated in detail by using XPD and ALISS. Only a diffuse (1 × 1) pattern was observed from this surface by LEED, suggesting that no long-range, ordered alloy structure was formed. Zn atoms were substitutionally incorporated into the Pt(111) crystal to form a near-surface alloy in which Zn atoms were found to reside primarily in the topmost and second layers. The alloyed Zn atoms in the topmost layer are coplanar with the Pt atoms in the surface layer, without any "buckling" of Zn, that is, displacement in the vertical direction. This result is expected because of the similar size of Pt and Zn, based on previous studies of bimetallic Pt alloys. Zn atoms desorb upon heating rather than diffusing deep into the bulk of the Pt crystal. Temperature programmed desorption (TPD) measurements show that both CO and NO have lower desorption energies on the PtZn alloy surface compared to that on the clean Pt(111) surface.

  14. Sn surface-enriched Pt-Sn bimetallic nanoparticles as a selective and stable catalyst for propane dehydrogenation

    KAUST Repository

    Zhu, Haibo

    2014-12-01

    A new one pot, surfactant-free, synthetic route based on the surface organometallic chemistry (SOMC) concept has been developed for the synthesis of Sn surface-enriched Pt-Sn nanoparticles. Bu3SnH selectively reacts with [Pt]-H formed in situ at the surface of Pt nanoparticles, Pt NPs, obtained by reduction of K2PtCl4 by LiB(C2H5)3H. Chemical analysis, 1H MAS and 13C CP/MAS solid-state NMR as well as two-dimensional double-quantum (DQ) and triple-quantum (TQ) experiments show that organo-tin moieties Sn(n-C4H9) are chemically linked to the surface of Pt NPs to produce, in fine, after removal of most of the n-butyl fragment, bimetallic Pt-Sn nanoparticles. The Sn(n-CH2CH2CH2CH3) groups remaining at the surface are believed to stabilize the as-synthesized Pt-Sn NPs, enabling the bimetallic NPs to be well dispersed in THF. Additionally, the Pt-Sn nanoparticles can be supported on MgAl2O4 during the synthesis of the nanoparticles. Some of the Pt-Sn/MgAl2O4 catalyst thus prepared exhibits high activity in PROX of CO and an extremely high selectivity and stability in propane dehydrogenation to propylene. The enhanced activity in propane dehydrogenation is associated with the high concentration of inactive Sn at the surface of Pt nanoparticles which ”isolates” the active Pt atoms. This conclusion is confirmed by XRD, NMR, TEM, and XPS analysis.

  15. Cu-capped surface alloys of Pt/Cu left brace 100 right brace

    CERN Document Server

    Alshamaileh, E; Wander, A

    2003-01-01

    The room-temperature deposition of 0.5 monolayer (ML) Pt on Cu left brace 100 right brace followed by annealing to 525 K results in a sharp c(2 x 2) low-energy electron diffraction (LEED) pattern. The structure of this surface alloy is investigated by means of symmetrized automated tensor low-energy electron diffraction (SATLEED) analysis and ab initio plane wave density functional calculations. The results are then compared with those for the similar system 0.5 ML Pd/Cu left brace 100 right brace. SATLEED results for the Pt/Cu left brace 100 right brace show that it consists of an ordered c(2 x 2) Cu-Pt second layer alloy capped with a pure Cu first layer. The first and second interlayer spacings are found to be expanded by +5.1 +- 1.7 and +3.5 +- 1.7% respectively (relative to the bulk Cu interlayer spacing of 1.807 A) due to the insertion of the 8% larger Pt atoms into the second layer. The ordered mixed layer is found to be rippled by 0.08 +- 0.06 A with Pt atoms rippled outwards towards the solid-vacuum ...

  16. Interactions between interfacial water and CO adsorbed on Pt and Pt-Ru alloy surfaces under electrochemical conditions: Density-functional theory study

    Energy Technology Data Exchange (ETDEWEB)

    Santana, Juan A. [Department of Chemistry, University of Puerto Rico, San Juan, PR 00931-3346 (Puerto Rico); Ishikawa, Yasuyuki, E-mail: yishikawa@uprrp.ed [Department of Chemistry, University of Puerto Rico, San Juan, PR 00931-3346 (Puerto Rico)

    2010-12-30

    The structural and electronic properties of interfacial water and adsorbed CO on platinum and platinum/ruthenium alloy have been studied via density-functional theory calculations to gain insight into the water-adsorbate interaction under electrochemical conditions. The computational simulations reveal a new interpretation for the interaction of adsorbed CO and water at the electrochemical interfaces. The new interaction model rationalizes the observed quantitative relationship between infrared intensities for adsorbed bridging CO and water molecules that impart a high-frequency O-H stretch, ca. 3630-3660 cm{sup -1} on pure Pt and 3600-3620 cm{sup -1} on PtRu alloy. The theoretical modeling indicates that the observed feature common to both pure Pt and PtRu alloy surfaces is due to interfacial water molecules firmly hydrogen-bonded to bridging CO.

  17. In Vivo Neural Recording and Electrochemical Performance of Microelectrode Arrays Modified by Rough-Surfaced AuPt Alloy Nanoparticles with Nanoporosity

    Directory of Open Access Journals (Sweden)

    Zongya Zhao

    2016-11-01

    Full Text Available In order to reduce the impedance and improve in vivo neural recording performance of our developed Michigan type silicon electrodes, rough-surfaced AuPt alloy nanoparticles with nanoporosity were deposited on gold microelectrode sites through electro-co-deposition of Au-Pt-Cu alloy nanoparticles, followed by chemical dealloying Cu. The AuPt alloy nanoparticles modified gold microelectrode sites were characterized by scanning electron microscopy (SEM, electrochemical impedance spectroscopy (EIS, cyclic voltammetry (CV and in vivo neural recording experiment. The SEM images showed that the prepared AuPt alloy nanoparticles exhibited cauliflower-like shapes and possessed very rough surfaces with many different sizes of pores. Average impedance of rough-surfaced AuPt alloy nanoparticles modified sites was 0.23 MΩ at 1 kHz, which was only 4.7% of that of bare gold microelectrode sites (4.9 MΩ, and corresponding in vitro background noise in the range of 1 Hz to 7500 Hz decreased to 7.5 μ V rms from 34.1 μ V rms at bare gold microelectrode sites. Spontaneous spike signal recording was used to evaluate in vivo neural recording performance of modified microelectrode sites, and results showed that rough-surfaced AuPt alloy nanoparticles modified microelectrode sites exhibited higher average spike signal-to-noise ratio (SNR of 4.8 in lateral globus pallidus (GPe due to lower background noise compared to control microelectrodes. Electro-co-deposition of Au-Pt-Cu alloy nanoparticles combined with chemical dealloying Cu was a convenient way for increasing the effective surface area of microelectrode sites, which could reduce electrode impedance and improve the quality of in vivo spike signal recording.

  18. Easy synthesis approach of Pt-nanoparticles on polyaniline surface: an efficient electro-catalyst for methanol oxidation reaction

    Science.gov (United States)

    Mondal, Sanjoy; Malik, Sudip

    2016-10-01

    A facile room temperature and surfactant free synthesis of platinum nanoparticles (Pt-NPs) on benzene tetra-carboxylic acid doped polyaniline (BDP) tube has been successfully demonstrated by solution dipping method. Preparation of Pt-NPs has been done through a red-ox reaction between BDP tubes and Pt-salt, as BDP itself acts as nontoxic reducing agent as well as template cum stabilizer for Pt-NPs. In BDP@Pt composites, ∼2.5 ± 0.5 nm spherical shaped Pt-NPs as observed from TEM studies are nicely decorated on the surface of BDP. The population or the loading density of Pt-NPs on BDP tube is greatly controlled by changing the w/w ratio of BDP to H2PtCl6. Synthesized BDP@Pt composites are subsequently employed as an efficient electro-catalyst for methanol oxidation reaction (MOR) in acidic medium. Furthermore, the observed catalytic activity is consequently ∼12 times higher than that of commercially available Pt/C catalyst. Depending on the loading density of Pt-NPs on BDP tubes, the efficiency and carbon monoxide (CO) tolerance ability of composites have been explored.

  19. SISGR: Theoretically relating the surface composition of Pt alloys to their performance as the electrocatalysts of low-temperature fuel cells

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Guofeng

    2010-12-31

    The main goal of this project is to gain fundamental knowledge about the relation between surface composition and catalytic performance of Pt alloy catalysts for oxygen reduction reaction (ORR). Specific objectives are: to develop and improve a first-principles based multiscale computation approach to simulating surface segregation phenomena in Pt alloy surfaces; to evaluate the surface electronic structure and catalytic activity of Pt alloy catalysts and; to relate the surface composition to the catalytic performance of Pt alloy catalysts.

  20. Finite electric field effects in the large perpendicular magnetic anisotropy surface Pt/Fe/Pt(001): a first-principles study.

    Science.gov (United States)

    Tsujikawa, Masahito; Oda, Tatsuki

    2009-06-19

    We investigate crystalline magnetic anisotropy in the electric field (EF) for the FePt surface which has a large perpendicular anisotropy, by means of the first-principles approach. Anisotropy is reduced linearly with respect to the inward EF, associated with the induced spin density around the Fe layer. Although the magnetic anisotropy energy (MAE) density reveals large variation around the atoms, the intrinsic contribution to the MAE is found to mainly come from the Fe layer. The surface without the capping Pt layer also shows similar linear dependence.

  1. A room temperature surface acoustic wave hydrogen sensor with Pt coated ZnO nanorods.

    Science.gov (United States)

    Huang, Fu-Chun; Chen, Yung-Yu; Wu, Tsung-Tsong

    2009-02-11

    A surface acoustic wave (SAW) sensor with Pt coated ZnO nanorods as the selective layer has been investigated for hydrogen detection. The SAW sensor was fabricated based on a 128 degrees YX-LiNbO(3) substrate with a operating frequency of 145 MHz. A dual delay line configuration was adopted to eliminate external environmental fluctuations. The Pt coated ZnO nanorods were chosen as a selective layer due to their high surface-to-volume ratio, large penetration depth, and fast charge diffusion rate. The ZnO nanorods were synthesized by an aqueous solution method and coated with the noble metal Pt as a catalyst. Finally, the SAW sensor responses to humidity and hydrogen were tested. Results show that the sensor is not sensitive to humidity; moreover, the frequency shift for a hydrogen concentration variation of 6000 ppm is 26 kHz while operating at room temperature. It can be concluded that the Pt coated ZnO nanorod based SAW hydrogen sensor exhibits fast response, good sensitivity and short-term repeatability. It is worth noting that not only is the sensor sensitive enough to operate at room temperature, but also it can avoid the influence of humidity.

  2. Electron Induced Surface Reactions of cis-Pt(CO)2Cl2: A Route to Focused Electron Beam Induced Deposition of Pure Pt Nanostructures.

    Science.gov (United States)

    Spencer, Julie A; Wu, Yung-Chien; McElwee-White, Lisa; Fairbrother, D Howard

    2016-07-27

    Using mechanistic data from surface science studies on electron-induced reactions of organometallic precursors, cis-Pt(CO)2Cl2 (1) was designed specifically for use in focused electron beam induced deposition (FEBID) of Pt nanostructures. Electron induced decomposition of adsorbed 1 under ultrahigh vacuum (UHV) conditions proceeds through initial CO loss as determined by in situ X-ray photoelectron spectroscopy and mass spectrometry. Although the Pt-Cl bonds remain intact during the initial decomposition step, larger electron doses induce removal of the residual chloride through an electron-stimulated desorption process. FEBID structures created from cis-Pt(CO)2Cl2 under steady state deposition conditions in an Auger spectrometer were determined to be PtCl2, free of carbon and oxygen. Coupled with the electron stimulated removal of chlorine demonstrated in the UHV experiments, the Auger deposition data establish a route to FEBID of pure Pt. Results from this study demonstrate that structure-activity relationships can be used to design new precursors specifically for FEBID.

  3. Surface sensitivity of the spin Seebeck effect in the Pt/YIG system

    Science.gov (United States)

    Aqeel, Aisha; Vera-Marun, Ivan J.; van Wees, Bart J.; Palstra, Thomas T. M.

    2015-03-01

    It is well-known that the surface plays an important role in the spin Seebeck effect (SSE). However the effect of mechanical treatment on the SSE has not been systematically studied yet. Here, we have investigated the influence of the interface quality on the SSE in a bilayer system of platinum and yttrium iron garnet (Pt/YIG). The surfaces of the YIG crystals are modified by different types of mechanical polishing before Pt deposition for different samples. We observed that the magnitude and magnetic field dependence of the SSE is strongly influenced by mechanical treatment of the YIG surface. No definite relation has been found between the SSE response and the sample roughness. However, we observe a direct correlation between the saturation magnetic field (Hsat) of the SSE and the roughness of sample, as the former increases by moving from soft toward coarse particle polishing. The change in the magnitude of Hsat can be attributed to the presence of a perpendicular magnetic anisotropy due to the treatment induced surface strain or shape anisotropy in the Pt/YIG system.

  4. Functional link between surface low-coordination sites and the electrochemical durability of Pt nanoparticles

    Science.gov (United States)

    Chung, Dong Young; Shin, Heejong; Yoo, Ji Mun; Lee, Kug-Seung; Lee, Nam-Suk; Kang, Kisuk; Sung, Yung-Eun

    2016-12-01

    A promising strategy for achieving enhanced catalytic activity involves the use of nanoscale electrocatalysts; however, their low stability remains a major challenge. Among the various performance-degradation mechanisms, atomic dissolution is known to cause severe nanoparticle deactivation. To date, the factors influencing these catalysts' durability are not understood. Herein, we assess the role of low-coordination surface sites, focusing on the atomic dissolution of Pt nanoparticles. The density of low-coordination sites was finely controlled, and no significant size change occurred. Based on our findings, we suggest that the initial low-coordination sites trigger metal dissolution, which subsequently accelerates Pt dissolution. We believe that controlling the surface coordination number can open new routes for the design of highly durable nanoscale electrocatalysts.

  5. Preservation of the Pt(100) surface reconstruction after growth of a continuous layer of graphene

    DEFF Research Database (Denmark)

    Nilsson, Louis; Andersen, Mie; Bjerre, Jacob;

    2012-01-01

    Scanning tunneling microscopy shows that a layer of graphene can be grown on the hex-reconstructed Pt(100) surface and that the reconstruction is preserved after growth. A continuous sheet of graphene can be grown across domain boundaries and step edges without loss of periodicity or change...... to accommodation of edge dislocations. The defect formation energy and the induced buckling of the graphene have been characterized by DFT calculations....... in direction. Density functional theory calculations on a simple model system support the observation that the graphene can have different rotation angles relative to the hex-reconstructed Pt surface. The graphene sheet direction can be changed by incorporating pentagon-heptagon defects giving rise...

  6. HUBUNGAN ANTARA PSYCHOLOGICAL CAPITAL DENGAN WORK ENGAGEMENT PADA KARYAWAN PT. BANK MEGA REGIONAL AREA SEMARANG

    Directory of Open Access Journals (Sweden)

    Dwi Ari Setyo Nugroho

    2015-07-01

    Full Text Available This study aimed to assess the relationship between psychological capital with work engagement employees of PT. Bank Mega Regional Area Semarang. Psychological capital is an individual’s positive psychological state of development and is characterized by self- efficacy, optimism, hope and resiliency. Then, work engagement is defined as a positive, fulfilling, work-related state of mind that is characterized by vigor, dedication, and absorption. This study used proportional sampling technique. The subjects were all employees of PT. Bank Mega Regional Area Semarang which have staff levels (N=73. The research instrument was psychological capital scales with 28 items (α = 0.953 and work engagement scales with 29 items (α = 0.938. The results by simple regression analysis obtained rxy = 0.716, with p value = 0.000 (p <0.05. The results indicated that there was a positive correlation between psychological capital and work engagement. The higher psychological capital was higher work engagement. Coefficient of determination by 51,3, it meaning that psychological capital effectively contributed for 51,3 % of work engagement. The remaining 48,7 % determined by other factors that are not revealed in this study, for example: job resources and job demands. Keywords: Psychological capital, work engagement, employee

  7. Surface Plasmon Enhanced Photocatalysis of Au/Pt-decorated TiO2 Nanopillar Arrays

    Science.gov (United States)

    Shuang, Shuang; Lv, Ruitao; Xie, Zheng; Zhang, Zhengjun

    2016-05-01

    The low quantum yields and lack of visible light utilization hinder the practical application of TiO2 in high-performance photocatalysis. Herein, we present a design of TiO2 nanopillar arrays (NPAs) decorated with both Au and Pt nanoparticles (NPs) directly synthesized through successive ion layer adsorption and reaction (SILAR) at room temperature. Au/Pt NPs with sizes of ~4 nm are well-dispersed on the TiO2 NPAs as evidenced by electron microscopic analyses. The present design of Au/Pt co-decoration on the TiO2 NPAs shows much higher visible and ultraviolet (UV) light absorption response, which leads to remarkably enhanced photocatalytic activities on both the dye degradation and photoelectrochemical (PEC) performance. Its photocatalytic reaction efficiency is 21 and 13 times higher than that of pure TiO2 sample under UV-vis and visible light, respectively. This great enhancement can be attributed to the synergy of electron-sink function of Pt and surface plasmon resonance (SPR) of Au NPs, which significantly improves charge separation of photoexcited TiO2. Our studies demonstrate that through rational design of composite nanostructures one can harvest visible light through the SPR effect to enhance the photocatalytic activities initiated by UV-light, and thus realize more effectively utilization of the whole solar spectrum for energy conversion.

  8. Surface Plasmon Enhanced Photocatalysis of Au/Pt-decorated TiO2 Nanopillar Arrays.

    Science.gov (United States)

    Shuang, Shuang; Lv, Ruitao; Xie, Zheng; Zhang, Zhengjun

    2016-05-24

    The low quantum yields and lack of visible light utilization hinder the practical application of TiO2 in high-performance photocatalysis. Herein, we present a design of TiO2 nanopillar arrays (NPAs) decorated with both Au and Pt nanoparticles (NPs) directly synthesized through successive ion layer adsorption and reaction (SILAR) at room temperature. Au/Pt NPs with sizes of ~4 nm are well-dispersed on the TiO2 NPAs as evidenced by electron microscopic analyses. The present design of Au/Pt co-decoration on the TiO2 NPAs shows much higher visible and ultraviolet (UV) light absorption response, which leads to remarkably enhanced photocatalytic activities on both the dye degradation and photoelectrochemical (PEC) performance. Its photocatalytic reaction efficiency is 21 and 13 times higher than that of pure TiO2 sample under UV-vis and visible light, respectively. This great enhancement can be attributed to the synergy of electron-sink function of Pt and surface plasmon resonance (SPR) of Au NPs, which significantly improves charge separation of photoexcited TiO2. Our studies demonstrate that through rational design of composite nanostructures one can harvest visible light through the SPR effect to enhance the photocatalytic activities initiated by UV-light, and thus realize more effectively utilization of the whole solar spectrum for energy conversion.

  9. Size dependence of thermoelectric power of Au, Pd, Pt nanoclusters deposited onto HOPG surface

    OpenAIRE

    Borisyuk, P. V.; V. I. Troyan; Lebedinskii, Yu Yu; Vasilyev, O S

    2016-01-01

    The paper presents the study of tunnel current-voltage characteristics of Au, Pd and Pt nanoclusters deposited onto the highly oriented pyrolytic graphite (HOPG) surface by pulsed laser deposition. The analysis of tunnel current-voltage characteristics obtained by scanning tunneling spectroscopy (STS) allowed to recover the thermoelectric power value of nanoclusters. It was found that the value of thermoelectric power of pulsed laser deposited nanoclusters depends on nanocluster material and ...

  10. Surface Pourbaix diagrams and oxygen reduction activity of Pt, Ag and Ni(111) surfaces studied by DFT

    DEFF Research Database (Denmark)

    Hansen, Heine Anton; Rossmeisl, Jan; Nørskov, Jens Kehlet

    2008-01-01

    (ORR) on the different surface structures and calculate the free energy of the intermediates. We estimate their catalytic activity for ORR by determining the highest potential at which all ORR reaction steps reduce the free energy. We obtain self-consistency in the sense that the surface is stable...... but not in acidic PEM fuel cells. Based on density functional theory calculations we investigate the electrochemically most stable surface structures as a function of pH and electrostatic potential for Pt(111), Ag(111) and Ni(111), and we construct surface Pourbaix diagrams. We study the oxygen reduction reaction...... of the reactive surface. Oxygen absorbed on the surface shifts the reactivity towards the weak binding region, which in turn increases the activity. The oxidation state of the surface and the ORR potential are constant versus the reversible hydrogen electrode (RHE). The dissolution potential in acidic solution...

  11. Tungsten carbide modified high surface area carbon as fuel cell catalyst support

    Science.gov (United States)

    Shao, Minhua; Merzougui, Belabbes; Shoemaker, Krista; Stolar, Laura; Protsailo, Lesia; Mellinger, Zachary J.; Hsu, Irene J.; Chen, Jingguang G.

    Phase pure WC nanoparticles were synthesized on high surface area carbon black (800 m 2 g -1) by a temperature programmed reaction (TPR) method. The particle size of WC can be controlled under 30 nm with a relatively high coverage on the carbon surface. The electrochemical testing results demonstrated that the corrosion resistance of carbon black was improved by 2-fold with a surface modification by phase pure WC particles. However, the WC itself showed some dissolution under potential cycling. Based on the X-ray diffraction (XRD) and inductively coupled plasma (ICP) analysis, most of the WC on the surface was lost or transformed to oxides after 5000 potential cycles in the potential range of 0.65-1.2 V. The Pt catalyst supported on WC/C showed a slightly better ORR activity than that of Pt/C, with the Pt activity loss rate for Pt/WC/C being slightly slower compared to that of Pt/C. The performance and decay rate of Pt/WC/C were also evaluated in a fuel cell.

  12. One pot aqueous synthesis of nanoporous Au85Pt15 material with surface bound Pt islands: an efficient methanol tolerant ORR catalyst

    Science.gov (United States)

    Anandha Ganesh, P.; Jeyakumar, D.

    2014-10-01

    For the first time, we are reporting the synthesis of Au100-xPtx nanoporous materials in the size range of 7-10 nm through the galvanic replacement of Ag by Pt from Au100-xAg2x spherical nano-alloys (x = 20, 15, 10 and 5) in an aqueous medium. The galvanic replacement reaction follows the `Volmer-Weber' growth mode, resulting in the formation of surface bound platinum islands on a nanoporous gold surface. The high angle annular dark field image and low angle X-ray diffraction studies confirm the presence of nanoporous Au100-xPtx NPs. The electrochemical studies using the Au85Pt15/C catalyst show excellent methanol tolerance behaviour and better performance towards oxygen reduction reaction (ORR) in terms of high mass activity, mass-specific activity and figure of merit (FOM) when compared to HiSPEC Pt/C commercial catalyst. Preliminary studies on a full cell using nanoporous Au85Pt15/C (loading 1.0 mg cm-2) as the cathode material and Pt-Ru/C (loading: 0.5 mg cm-2) as the anode material performed better (38 mW cm-2) than the HiSPEC Pt/C cathode material (16 mW cm-2).For the first time, we are reporting the synthesis of Au100-xPtx nanoporous materials in the size range of 7-10 nm through the galvanic replacement of Ag by Pt from Au100-xAg2x spherical nano-alloys (x = 20, 15, 10 and 5) in an aqueous medium. The galvanic replacement reaction follows the `Volmer-Weber' growth mode, resulting in the formation of surface bound platinum islands on a nanoporous gold surface. The high angle annular dark field image and low angle X-ray diffraction studies confirm the presence of nanoporous Au100-xPtx NPs. The electrochemical studies using the Au85Pt15/C catalyst show excellent methanol tolerance behaviour and better performance towards oxygen reduction reaction (ORR) in terms of high mass activity, mass-specific activity and figure of merit (FOM) when compared to HiSPEC Pt/C commercial catalyst. Preliminary studies on a full cell using nanoporous Au85Pt15/C (loading 1.0 mg

  13. Body Surface Area Prediction in Odorrana grahami

    Institute of Scientific and Technical Information of China (English)

    Guiying CHEN; Jiongyu LIU; Qiang DAI; Jianping JIANG

    2014-01-01

    Body surface area (BSA) was regarded as a more readily quantiifable parameter relative to body mass in the normalization of comparative biochemistry and physiology. The BSA prediction has attracted unceasing research back more than a century on animals, especially on humans and rats. Few studies in this area for anurans were reported, and the equation for body surface area (S) and body mass (W):S=9.9 W 0.56, which was concluded from toads of four species in 1969, was generally adopted to estimate the body surface areas for anurans until recent years. However, this equation was not applicable to Odorrana grahami. The relationship between body surface area and body mass for this species was established as:S=15.4 W 0.579. Our current results suggest estimation equations should be used cautiously across different species and body surface area predictions on more species need to be conducted.

  14. Penyajian Data Pelanggan pada Lima Area PT. Telekomunikasi Indonesia, Tbk. Kandatel Pekalongan Menggunakan Google Earth

    Directory of Open Access Journals (Sweden)

    Much Aziz Muslim

    2015-10-01

    Full Text Available Prosedur sistem penyajian data pelanggan di PT. Telekomunikasi Indonesia, Tbk. Kandatel Pekalongan khususnya bidang Divisi Business Services masih menggunakan cara manual, hanya menggunakan media Micorsoft Excel. Dalam hal ini peneliti ingin menerapkannya dalam bentuk aplikasi Google Earth untuk membuat penyajian data pelanggan, karena Google Earth dapat memetakan bumi dari superimposisi gambar yang dikumpulkan dari pemetaan satelit, fotografi udara dan globe GIS tiga dimensi sehingga akan menghasilkan data yang akurat. Penyajian data dengan menggunakan Google Earth dilakukan dengan memanfaatkan bahasa markup HTML. Dengan cara ini, Divisi Business Service akan menjadi lebih mudah ketika menyajikan data-data para pelanggan Telkom yang mencakup lima area yaitu Batang, Pekalongan, Pemalang, Tegal dan Brebes. 

  15. Penyajian Data Pelanggan pada Lima Area PT. Telekomunikasi Indonesia, Tbk. Kandatel Pekalongan Menggunakan Google Earth

    Directory of Open Access Journals (Sweden)

    Much Aziz Muslim

    2015-10-01

    Full Text Available Prosedur sistem penyajian data pelanggan di PT. Telekomunikasi Indonesia, Tbk. Kandatel Pekalongan khususnya bidang Divisi Business Services masih menggunakan cara manual, hanya menggunakan media Micorsoft Excel. Dalam hal ini peneliti ingin menerapkannya dalam bentuk aplikasi Google Earth untuk membuat penyajian data pelanggan, karena Google Earth dapat memetakan bumi dari superimposisi gambar yang dikumpulkan dari pemetaan satelit, fotografi udara dan globe GIS tiga dimensi sehingga akan menghasilkan data yang akurat. Penyajian data dengan menggunakan Google Earth dilakukan dengan memanfaatkan bahasa markup HTML. Dengan cara ini, Divisi Business Service akan menjadi lebih mudah ketika menyajikan data-data para pelanggan Telkom yang mencakup lima area yaitu Batang, Pekalongan, Pemalang, Tegal dan Brebes. 

  16. 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

    Further advances in fuel cell technologies are hampered by kinetic limitations associated with the sluggish cathodic oxygen reduction reaction. We have investigated a range of different formulations of binary and ternary Pt, Pd and Au thin films as electrocatalysts for oxygen reduction. The most...... active binary thin films are near-surface alloys of Pt with subsurface Pd and certain PdAu and PtAu thin films with surface and/or subsurface Au. The most active ternary thin films are with pure metal Pt or Pd skins with some degree of Au in the surface and/or subsurface layer and the near-surface alloys....... 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...

  17. 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

    active binary thin films are near-surface alloys of Pt with subsurface Pd and certain PdAu and PtAu thin films with surface and/or subsurface Au. The most active ternary thin films are with pure metal Pt or Pd skins with some degree of Au in the surface and/or subsurface layer and the near-surface alloys...... of Au with mixed Pt/Pd skins. The activity of the binary and ternary catalysts is explained through weakening of the OH binding energy caused by solute elements. However, given the low alloy formation energies it may be difficult to tune and retain the composition under operating conditions....... 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...

  18. Estimation of surface area and surface area measure of three-dimensional sets from digitizations

    DEFF Research Database (Denmark)

    Ziegel, Johanna; Kiderlen, Markus

    2010-01-01

    A local method for estimating surface area and surface area measure of three-dimensional objects from discrete binary images is presented. A weight is assigned to each 2 × 2 × 2 configuration of voxels and the total surface area of an object is given by summation of the local area contributions. ...

  19. Surface enhanced vibrational spectroscopy and first-principles study of L-cysteine adsorption on noble trimetallic Au/Pt@Rh clusters.

    Science.gov (United States)

    Loganathan, B; Chandraboss, V L; Senthilvelan, S; Karthikeyan, B

    2015-09-07

    The Rh shell of the Au/Pt/Rh trimetallic nanoparticles induces a wide variety of interesting surface reactions by allowing the adsorption of amino acids like L-cysteine (L-Cys). We present a snapshot of theoretical and experimental investigation of L-Cys adsorption on the surface of noble trimetallic Au/Pt@Rh colloidal nanocomposites. Density functional theoretical (DFT) investigations of L-Cys interaction with the Rhodium (Rh) shell of a trimetallic Au/Pt@Rh cluster in terms of geometry, binding energy (E(B)), binding site, energy gap (E(g)), electronic and spectral properties have been performed. L-Cys establishes a strong interaction with the Rh shell. It binds to Rh by the S1-site, which makes a stable L-Cys-Rh surface complex. DFT can be taken as a valuable tool to assign the vibrational spectra of the adsorption of L-Cys on trimetallic Au/Pt@Rh colloidal nanocomposites and mono-metallic Rh nanoparticles. Surface-enhanced infrared spectroscopy (SEIRS) with L-Cys on a Rh6 cluster surface has been simulated for the first time. Experimental information on the L-Cys-Rh surface complex is included to examine the interaction. The experimental spectral observations are in good agreement with the simulated DFT results. Characterization of the synthesized trimetallic Au/Pt@Rh colloidal nanocomposites has been done by high-resolution transmission electron microscopy (HR-TEM) with selected area electron diffraction (SAED) pattern, energy dispersive X-ray (EDX) spectroscopy, dynamic light scattering (DLS) measurements, zeta potential, zeta deviation analysis and UV-visible (UV-Vis) spectroscopic studies.

  20. RKKY-like contributions to the magnetic anisotropy energy: 3 d adatoms on Pt(111) surface

    Science.gov (United States)

    Bouhassoune, Mohammmed; Dias, Manuel dos Santos; Zimmermann, Bernd; Dederichs, Peter H.; Lounis, Samir

    2016-09-01

    The magnetic anisotropy energy defines the energy barrier that stabilizes a magnetic moment. Utilizing density-functional-theory-based simulations and analytical formulations, we establish that this barrier is strongly modified by long-range contributions very similar to Friedel oscillations and Rudermann-Kittel-Kasuya-Yosida interactions. Thus, oscillations are expected and observed, with different decaying factors and highly anisotropic in realistic materials, which can switch nontrivially the sign of the magnetic anisotropy energy. This behavior is general, and for illustration we address the transition-metal adatoms, Cr, Mn, Fe, and Co deposited on a Pt(111) surface. We explain, in particular, the mechanisms leading to the strong site dependence of the magnetic anisotropy energy observed for Fe adatoms on a Pt(111) surface as revealed previously via first-principles-based simulations and inelastic scanning tunneling spectroscopy [A. A. Khajetoorians et al., Phys. Rev. Lett. 111, 157204 (2013), 10.1103/PhysRevLett.111.157204]. The same mechanisms are probably active for the site dependence of the magnetic anisotropy energy obtained for Fe adatoms on Pd or Rh(111) surfaces and for Co adatoms on a Rh(111) surface [P. Blonski et al., Phys. Rev. B 81, 104426 (2010), 10.1103/PhysRevB.81.104426].

  1. Lignin-derived oxygenate reforming on a bimetallic surface: The reaction of benzaldehyde on Zn/Pt(111)

    Science.gov (United States)

    Shi, Daming; Vohs, John M.

    2016-08-01

    Temperature programmed desorption (TPD) and high-resolution electron energy loss spectroscopy (HREELS) were used to characterize the adsorption and reaction of benzaldehyde (C6H5CHO) on hydrogen-covered Pt(111) and Zn-modified Pt(111) surfaces. Benzaldehyde was found to interact with Pt(111) via both the phenyl ring and carbonyl of the aldehyde group. This bonding configuration facilitates unselective decomposition of the benzaldehyde to produce CO, H2, and small hydrocarbon fragments at relatively low temperatures. On the other hand, benzaldehyde was found to bond to Zn-decorated Pt(111) surface exclusively via the carbonyl group in an η2(C, O) configuration, with the phenyl ring tilted away from the surface. This configuration weakens Csbnd O bond in the carbonyl facilitating its cleavage and helps prevent hydrogenation of the phenyl ring.

  2. Surface self-diffusion of adatom on Pt cluster with truncated octahedron structure

    Energy Technology Data Exchange (ETDEWEB)

    Yang Jianyu, E-mail: wuliyangjianyu@yahoo.com.c [Department of Maths and Physics, Hunan Institute of Engineering, Xiangtan 411104 (China); Hu Wangyu, E-mail: wangyuhu2001@yahoo.com.c [Department of Applied Physics, Hunan University, Changsha 410082 (China); Chen Shuguang [Department of Applied Physics, Hunan University, Changsha 410082 (China)

    2010-05-03

    Surface diffusion of single Pt adatom on Pt cluster with truncated octahedron structure is investigated through a combination of molecular dynamics and nudged elastic band method. Using an embedded atom method to describe the atomic interactions, the minimum energy paths are determined and the energy barriers for adatom diffusion across and along step are evaluated. The diffusion of adatom crossing step edge between {l_brace}111{r_brace} and {l_brace}100{r_brace} facets has a surprisingly low barrier of 0.03 eV, which is 0.12 eV lower than the barrier for adatom diffusion from {l_brace}111{r_brace} to neighboring {l_brace}111{r_brace} facet. Owing to the small barrier of adatom diffusion across the step edge between {l_brace}111{r_brace} and {l_brace}100{r_brace} facets, the diffusion of adatom along the step edge cannot occur. The molecular dynamics simulations at low temperatures also support these results. Our results show that mass transport will prefer step with {l_brace}100{r_brace} microfacet and the Pt clusters can have only {l_brace}111{r_brace} facets in epitaxial growth.

  3. Atomically thin Pt shells on Au nanoparticle cores: facile synthesis and efficient synergetic catalysis

    DEFF Research Database (Denmark)

    Engelbrekt, Christian; Seselj, Nedjeljko; Poreddy, Raju

    2016-01-01

    We present a facile synthesis protocol for atomically thin platinum (Pt) shells on top of gold (Au) nanoparticles (NPs) (Au@PtNPs) in one pot under mild conditions. The Au@PtNPs exhibited remarkable stability (> 2 years) at room temperature. The synthesis, bimetallic nanostructures and catalytic...... clearly show that the active surface is dominated by Pt with a specific surface area above 45 m2 per gram of Pt. Interactions with the Au core increase the activity of the Pt shell by up to 55% and improve catalytic selectivity compared to pure Pt. The Au@Pt NPs show exciting catalytic activity...

  4. Current-induced spin polarization on a Pt surface: A new approach using spin-polarized positron annihilation spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Kawasuso, A., E-mail: kawasuso.atsuo@jaea.go.jp [Advanced Science Research Center, Japan Atomic Energy Agency, 1233 Watanuki, Takasaki, Gunma 370-1292 (Japan); Fukaya, Y.; Maekawa, M.; Zhang, H. [Advanced Science Research Center, Japan Atomic Energy Agency, 1233 Watanuki, Takasaki, Gunma 370-1292 (Japan); Seki, T.; Yoshino, T.; Saitoh, E.; Takanashi, K. [Institute for Materials Research, Tohoku University, 2-1-1 Katahira, Aoba-ku, Sendai 980-8577 (Japan)

    2013-09-15

    Transversely spin-polarized positrons were injected near Pt and Au surfaces under an applied electric current. The three-photon annihilation of spin-triplet positronium, which was emitted from the surfaces into vacuum, was observed. When the positron spin polarization was perpendicular to the current direction, the maximum asymmetry of the three-photon annihilation intensity was observed upon current reversal for the Pt surfaces, whereas it was significantly reduced for the Au surface. The experimental results suggest that electrons near the Pt surfaces were in-plane and transversely spin-polarized with respect to the direction of the electric current. The maximum electron spin polarization was estimated to be more than 0.01 (1%). - Highlights: • Annihilation probability of positronium emitted from the Pt surface into the vacuum under direct current exhibited asymmetry upon current reversal. • The maximum asymmetry appeared when positron spin polarization and the direct current were perpendicular to each other. • Electrons near the Pt surfaces were in-plane and transversely spin-polarized with respect to the direction of the electric current. • Spin-polarized positronium annihilation provides a unique tool for investigating spin polarization on metal surfaces.

  5. Influences of surface coatings and components of FePt nanoparticles on the suppression of glioma cell proliferation

    Directory of Open Access Journals (Sweden)

    Sun H

    2012-07-01

    Full Text Available Haiming Sun,1,* Xiaohui Chen,2,* Dan Chen,1 Mingyan Dong,1 Xinning Fu,1 Qian Li,1 Xi Liu,1 Qingzhi Wu,1 Tong Qiu,1 Tao Wan,1 Shipu Li11State Key Laboratory of Advanced Technology for Materials Synthesis and Processing and Biomedical Materials and Engineering Center, Wuhan University of Technology, Wuhan, China; 2Department of Prosthetics, School of Stomatology, Wuhan University, Wuhan, China*Both authors contributed equally to this workAbstract: Malignant gliomas are primary brain tumors with high rates of morbidity and mortality; they are the fourth most common cause of cancer death. Novel diagnostic and therapeutic techniques based on nanomaterials provide promising options in the treatment of malignant gliomas. In order to evaluate the potential of FePt nanoparticles (NPs for malignant glioma therapy, FePt NPs with different surface coatings and components were tunably synthesized using oleic acid/oleylamine (OA/OA and cysteines (Cys as the capping agents, respectively. The samples were characterized using X-ray diffraction, transmission electron microscopy (TEM, X-ray photon spectroscopy, Fourier transform infrared spectroscopy, atomic absorption spectrum, and zeta potential. The influence of the surface coatings and components of the FePt NPs on the proliferation of glioma cells was assessed through MTT assay and TEM observation using three typical glioma cell lines (glioma U251 cells, astrocytoma U87 cells, and neuroglioma H4 cells as in vitro models. The results showed that the proliferation of glioma cells was significantly suppressed by lipophilic FePt-OA/OA NPs in a time- and/or dose-dependent manner, while no or low cytotoxic effects were detected in the case of hydrophilic FePt-Cys NPs. The IC50 value of FePt-OA/OA NPs on the three glioma cell lines was approximately 5–10 µg mL-1 after 24 hours’ incubation. Although the cellular uptake of FePt NPs was confirmed regardless of the surface coatings and components of the FePt NPs

  6. Microcanonical unimolecular rate theory at surfaces. I. Dissociative chemisorption of methane on Pt(111)

    Science.gov (United States)

    Bukoski, A.; Blumling, D.; Harrison, I.

    2003-01-01

    A model of gas-surface reactivity is developed based on the ideas that (a) adsorbate chemistry is a local phenomenon, (b) the active system energy of an adsorbed molecule and a few immediately adjacent surface atoms suffices to fix microcanonical rate constants for surface kinetic processes such as desorption and dissociation, and (c) energy exchange between the local adsorbate-surface complexes and the surrounding substrate can be modeled via a Master equation to describe the system/heat reservoir coupling. The resulting microcanonical unimolecular rate theory (MURT) for analyzing and predicting both thermal equilibrium and nonequilibrium kinetics for surface reactions is applied to the dissociative chemisorption of methane on Pt(111). Energy exchange due to phonon-mediated energy transfer between the local adsorbate-surface complexes and the surface is explored and estimated to be insignificant for the reactive experimental conditions investigated here. Simulations of experimental molecular beam data indicate that the apparent threshold energy for CH4 dissociative chemisorption on Pt(111) is E0=0.61 eV (over a C-H stretch reaction coordinate), the local adsorbate-surface complex includes three surface oscillators, and the pooled energy from 16 active degrees of freedom is available to help surmount the dissociation barrier. For nonequilibrium molecular beam experiments, predictions are made for the initial methane dissociative sticking coefficient as a function of isotope, normal translational energy, molecular beam nozzle temperature, and surface temperature. MURT analysis of the thermal programmed desorption of CH4 physisorbed on Pt(111) finds the physisorption well depth is 0.16 eV. Thermal equilibrium dissociative sticking coefficients for methane on Pt(111) are predicted for the temperature range from 250-2000 K. Tolman relations for the activation energy under thermal equilibrium conditions and for a variety of "effective activation energies" under

  7. Density functional theory study of the adsorption of MeOH and EtOH on the surface of Pt-decorated graphene

    Science.gov (United States)

    Rad, Ali Shokuhi

    2016-09-01

    The adsorption energies and orientation of single alcohol molecule (methanol and ethanol) on the surface of Pt-decorated graphene (PtG) were determined from first-principles density functional (DFT) calculations. We found the same adsorption energies as well as connecting distances upon adsorption of MeOH and EtOH on PtG surface, in which at their relaxed structures, the O atom of alcohol is closed to the Pt of PtG surface. We found high adsorption energies, low connecting distances, and high orbital hybridizing upon adsorption of EtOH and MeOH molecules on PtG surface. There are significant shifts in the location of both the HOMO and LUMO, in addition to variation in the charge transfer when the MeOH and EtOH are adsorbed on PtG surface.

  8. Synthesis of Supported NiPt Bimetallic Nanoparticles, Methods for Controlling the Surface Coverage of Ni Nanoparticles With Pt, Methods Of Making NiPt Multilayer Core-Shell Structures and Application of the Supported Catalysts for CO2 Reforming

    KAUST Repository

    Li, Lidong

    2015-06-25

    Embodiments of the present disclosure provide for supported Ni/Pt bimetallic nanoparticles, compositions including supported NiPt nanoparticles, methods of making supported NiPt nanoparticles, methods of using supported NiPt nanoparticles, and the like.

  9. One-Step Synthesis of Pt/Graphene Composites from Pt Acid Dissolved Ethanol via Microwave Plasma Spray Pyrolysis

    Science.gov (United States)

    Jo, Eun Hee; Chang, Hankwon; Kim, Sun Kyung; Choi, Ji-Hyuk; Park, Su-Ryeon; Lee, Chong Min; Jang, Hee Dong

    2016-09-01

    Pt nanoparticles-laden graphene (Pt/GR) composites were synthesized in the gas phase from a mixture of ethanol and Pt precursor by microwave plasma spray pyrolysis. The morphology of Pt/GR composites has the shape of wrinkled sheets of paper, while Pt nanoparticles (Pt NPs) that are less than 2.6 nm in the mean diameter are uniformly well deposited on the surface of GR sheets stacked in only three layers. The Pt/GR composite prepared with 20 wt% of Pt had the highest specific surface area and electrochemical surface area of up to 402 m2 g-1 and 77 m2 g-1 (Pt), respectively. In addition, the composite showed superior electrocatalytic activity compared with commercial Pt-carbon black. The excellent electrocatalytic activity was attributed to the high specific surface area and electrochemical surface area of the Pt/GR composite directly produced by microwave plasma spray pyrolysis. Thus, it is clearly expected that the Pt/GR composite is a promising material for DMFC catalysts.

  10. Interaction of CO with PtxAg1-x/Pt(111) surface alloys: More than dilution by Ag atoms

    Science.gov (United States)

    Schüttler, K. M.; Mancera, L. A.; Diemant, T.; Groß, A.; Behm, R. J.

    2016-08-01

    We have investigated CO adsorption on structurally well-defined PtxAg1-x/Pt(111) surface alloys, combining temperature-programmed desorption (TPD) and infrared reflection absorption spectroscopy (IRRAS) as well as density functional theory (DFT) based calculations. This is part of a systematic approach including previous studies of CO adsorption on closely related Pt(111)- and Pd(111)-based surface alloys. Following changes in the adsorption properties with increasing Ag content and correlating them with structural changes allow us to assign desorption features to specific adsorption sites/ensembles identified in previous scanning tunneling microscopy (STM) measurements, and thus to identify and separate contributions from different effects such as geometric ensemble effects and electronic ligand/strain effects. DFT calculations give further insight into the nature of the metal-CO bond on these bimetallic sites. Most prominently, the growth of a new CO desorption feature at higher temperature (~ 550 K) in the TPD spectra of Ag-rich surface alloys, which is unique for the group of Pt(111)- and Pd(111)-based surface alloys, is attributed to CO adsorption on Pt atoms surrounded by a Ag-rich neighborhood. Adsorption on these sites manifests in an IR band down-shifted to significantly lower wave number. Systematic comparison of the present results with previous findings for CO adsorption on the related Pt(111)- and Pd(111)-based surface alloys gains a detailed insight into general trends in the adsorption behavior of bimetallic surfaces.

  11. Insight into the Role of Surface Wettability in Electrocatalytic Hydrogen Evolution Reactions Using Light-Sensitive Nanotubular TiO2 Supported Pt Electrodes.

    Science.gov (United States)

    Meng, Chenhui; Wang, Bing; Gao, Ziyue; Liu, Zhaoyue; Zhang, Qianqian; Zhai, Jin

    2017-02-06

    Surface wettability is of importance for electrochemical reactions. Herein, its role in electrochemical hydrogen evolution reactions is investigated using light-sensitive nanotubular TiO2 supported Pt as hydrogen evolution electrodes (HEEs). The HEEs are fabricated by photocatalytic deposition of Pt particles on TiO2 nanotubes followed by hydrophobization with vaporized octadecyltrimethoxysilane (OTS) molecules. The surface wettability of HEEs is subsequently regulated in situ from hydrophobicity to hydrophilicity by photocatalytic decomposition of OTS molecules using ultraviolet light. It is found that hydrophilic HEEs demonstrate a larger electrochemical active area of Pt and a lower adhesion force to a gas bubble when compared with hydrophobic ones. The former allows more protons to react on the electrode surface at small overpotential so that a larger current is produced. The latter leads to a quick release of hydrogen gas bubbles from the electrode surface at large overpotential, which ensures the contact between catalysts and electrolyte. These two characteristics make hydrophilic HEEs generate a much high current density for HERs. Our results imply that the optimization of surface wettability is of significance for improving the electrocatalytic activity of HEEs.

  12. Insight into the Role of Surface Wettability in Electrocatalytic Hydrogen Evolution Reactions Using Light-Sensitive Nanotubular TiO2 Supported Pt Electrodes

    Science.gov (United States)

    Meng, Chenhui; Wang, Bing; Gao, Ziyue; Liu, Zhaoyue; Zhang, Qianqian; Zhai, Jin

    2017-01-01

    Surface wettability is of importance for electrochemical reactions. Herein, its role in electrochemical hydrogen evolution reactions is investigated using light-sensitive nanotubular TiO2 supported Pt as hydrogen evolution electrodes (HEEs). The HEEs are fabricated by photocatalytic deposition of Pt particles on TiO2 nanotubes followed by hydrophobization with vaporized octadecyltrimethoxysilane (OTS) molecules. The surface wettability of HEEs is subsequently regulated in situ from hydrophobicity to hydrophilicity by photocatalytic decomposition of OTS molecules using ultraviolet light. It is found that hydrophilic HEEs demonstrate a larger electrochemical active area of Pt and a lower adhesion force to a gas bubble when compared with hydrophobic ones. The former allows more protons to react on the electrode surface at small overpotential so that a larger current is produced. The latter leads to a quick release of hydrogen gas bubbles from the electrode surface at large overpotential, which ensures the contact between catalysts and electrolyte. These two characteristics make hydrophilic HEEs generate a much high current density for HERs. Our results imply that the optimization of surface wettability is of significance for improving the electrocatalytic activity of HEEs. PMID:28165487

  13. On the vibrational behaviour of cyanide adsorbed at Pt(1 1 1) and Pt(1 0 0) surfaces in alkaline solutions

    Science.gov (United States)

    Huerta, F.; Montilla, F.; Morallón, E.; Vázquez, J. L.

    2006-03-01

    This communication deals with the vibrational behaviour of cyanide adlayers formed on Pt(1 1 1) and Pt(1 0 0) surfaces in the electrochemical environment. In situ FTIR spectroscopy can be employed to follow the potential dependence of the C-N stretching frequency in acidic electrolytes with quite a low uncertainty. Owing to the stability of the cyanide adlayer in alkaline solutions, experiments performed in NaOH medium are usually perturbed by the significant overlapping of the reference and the sample FTIR spectra. Deconvolution of the spectra was carried out assuming a Lorentz oscillator. The procedure allowed to confirm that two potential regions with different band centre frequency tuning coexist for Pt(1 1 1)-CN in perchloric acid medium. Conversely, in the alkaline electrolyte a single tuning rate for the band position was found for both surfaces studied. The lack of reorientation of the C-N molecular axis together with the occurrence of a certain screening effect of negatively charged hydroxyl anions on the electric field at the interface could be at the origin of the different behaviour displayed in both electrolytic media.

  14. Modification of the surface electronic and chemical properties of Pt(111) by subsurface 3d transition metals

    DEFF Research Database (Denmark)

    Kitchin, J. R.; Nørskov, Jens Kehlet; Barteau, M. A.;

    2004-01-01

    The modification of the electronic and chemical properties of Pt(111) surfaces by subsurface 3d transition metals was studied using density-functional theory. In each case investigated, the Pt surface d-band was broadened and lowered in energy by interactions with the subsurface 3d metals......, resulting in weaker dissociative adsorption energies of hydrogen and oxygen on these surfaces. The magnitude of the decrease in adsorption energy was largest for the early 3d transition metals and smallest for the late 3d transition metals. In some cases, dissociative adsorption was calculated...

  15. Direct evidence for active site-dependent formic acid electro-oxidation by topmost-surface atomic redistribution in a ternary PtPdCu electrocatalyst.

    Science.gov (United States)

    Cui, Chun-Hua; Li, Hui-Hui; Cong, Huai-Ping; Yu, Shu-Hong; Tao, Franklin Feng

    2012-12-25

    The active site-dependent electrochemical formic acid oxidation was evidenced by the increased coverage of Pt in the topmost mixed PtPd alloy layer of ternary PtPdCu upon potential cycling, which demonstrated two catalytic pathways only in one catalyst owing to surface atomic redistribution in an acidic electrolyte environment.

  16. Surface sites on Pt-CeO2 mixed oxide catalysts probed by CO adsorption: a synchrotron radiation photoelectron spectroscopy study.

    Science.gov (United States)

    Neitzel, Armin; Lykhach, Yaroslava; Skála, Tomáš; Tsud, Nataliya; Vorokhta, Mykhailo; Mazur, Daniel; Prince, Kevin C; Matolín, Vladimír; Libuda, Jörg

    2014-12-07

    By means of synchrotron radiation photoemission spectroscopy, we have investigated Pt-CeO2 mixed oxide films prepared on CeO2(111)/Cu(111). Using CO molecules as a probe, we associate the corresponding surface species with specific surface sites. This allows us to identify the changes in the composition and morphology of Pt-CeO2 mixed oxide films caused by annealing in an ultrahigh vacuum. Specifically, two peaks in C 1s spectra at 289.4 and 291.2 eV, associated with tridentate and bidentate carbonate species, are formed on the nanostructured stoichiometric CeO2 film. The peak at 290.5-291.0 eV in the C 1s spectra indicates the onset of restructuring, i.e. coarsening, of the Pt-CeO2 film. This peak is associated with a carbonate species formed near an oxygen vacancy. The onset of cerium oxide reduction is indicated by the peak at 287.8-288.0 eV associated with carbonite species formed near Ce(3+) cations. The development of surface species on the Pt-CeO2 mixed oxides suggests that restructuring of the films occurs above 300 K irrespective of Pt loadings. We do not find any adsorbed CO species associated with Pt(4+) or Pt(2+). The onset of Pt(2+) reduction is indicated by the peak at 286.9 eV in the C 1s spectra due to CO adsorption on metallic Pt particles. The thermal stability of Pt(2+) in Pt-CeO2 mixed oxide depends on Pt loading. We find excellent stability of Pt(2+) for 12% Pt content in the CeO2 film, whereas at a Pt concentration of 25% in the CeO2 film, a large fraction of the Pt(2+) is converted into metallic Pt particles above 300 K.

  17. On the stability of the CO adsorption-induced and self-organized CuPt surface alloy

    DEFF Research Database (Denmark)

    Andersson, Klas Jerker; Chorkendorff, Ib

    2010-01-01

    ) from room temperature to 673 K. No indications of substantial changes in surface structure were observed under the latter conditions compared to CO alone whereas the O-2 oxidation resulted in CO removal and the build-up of an ultrathin CuOx-film. However, the oxidized CO/CuPt surface alloy could...

  18. Surface moisture estimation in urban areas

    Science.gov (United States)

    Jiang, Yitong

    Surface moisture is an important parameter because it modifies urban microclimate and surface layer meteorology. The primary objectives of this paper are: 1) to analyze the impact of surface roughness from buildings on surface moisture in urban areas; and 2) to quantify the impact of surface roughness resulting from urban trees on surface moisture. To achieve the objectives, two hypotheses were tested: 1) the distribution of surface moisture is associated with the structural complexity of buildings in urban areas; and 2) The distribution and change of surface moisture is associated with the distribution and vigor of urban trees. The study area is Indianapolis, Indiana, USA. In the part of the morphology of urban trees, Warren Township was selected due to the limitation of tree inventory data. To test the hypotheses, the research design was made to extract the aerodynamic parameters, such as frontal areas, roughness length and displacement height of buildings and trees from Terrestrial and Airborne LiDAR data, then to input the aerodynamic parameters into the urban surface energy balance model. The methodology was developed for comparing the impact of aerodynamic parameters from LiDAR data with the parameters that were derived empirically from land use and land cover data. The analytical procedures are discussed below: 1) to capture the spatial and temporal variation of surface moisture, daily and hourly Land Surface Temperature (LST) were downscaled from 4 km to 1 km, and 960 m to 30 m, respectively, by regression between LST and various components that impact LST; 2) to estimate surface moisture, namely soil moisture and evapotranspiration (ET), land surfaces were classified into soil, vegetation, and impervious surfaces, using Linear Spectral Mixture Analysis (LSMA); 3) aerodynamic parameters of buildings and trees were extracted from Airborne and Terrestrial LiDAR data; 4) the Temperature-Vegetation-Index (TVX) method, and the Two-Source-Energy-Balance (TSEB

  19. Nanoscale compositional changes and modification of the surface reactivity of Pt{sub 3}Co/C nanoparticles during proton-exchange membrane fuel cell operation

    Energy Technology Data Exchange (ETDEWEB)

    Dubau, L. [Laboratoire d' Electrochimie et de Physico-chimie des Materiaux et des Interfaces, UMR 5631 CNRS/Grenoble Universite, 1130 rue de la piscine, BP75, 38402 Saint Martin d' Heres Cedex (France); Maillard, F., E-mail: frederic.maillard@lepmi.grenoble-inp.f [Laboratoire d' Electrochimie et de Physico-chimie des Materiaux et des Interfaces, UMR 5631 CNRS/Grenoble Universite, 1130 rue de la piscine, BP75, 38402 Saint Martin d' Heres Cedex (France); Chatenet, M. [Laboratoire d' Electrochimie et de Physico-chimie des Materiaux et des Interfaces, UMR 5631 CNRS/Grenoble Universite, 1130 rue de la piscine, BP75, 38402 Saint Martin d' Heres Cedex (France); Andre, J.; Rossinot, E. [Axane, 2 rue de Clemenciere, BP 15, 38360 Sassenage (France)

    2010-12-30

    This study bridges the structure/composition of Pt-Co/C nanoparticles with their surface reactivity and their electrocatalytic activity. We show that Pt{sub 3}Co/C nanoparticles are not stable during PEMFC operation (H{sub 2}/air; j = 0.6 A cm{sup -2}, T = 70 {sup o}C) but suffer compositional changes at the nanoscale. In the first hours of operation, the dissolution of Co atoms at their surface yields to the formation of a Pt-enriched shell covering a Pt-Co alloy core ('Pt-skeleton') and increases the affinity of the surface to oxygenated and hydrogenated species. This structure does not ensure stability in PEMFC conditions but is rather a first step towards the formation of 'Pt-shell/Pt-Co alloy core' structures with depleted Co content. In these operating conditions, the Pt-Co/C specific activity for the ORR varies linearly with the fraction of Co alloyed to Pt present in the core and is severely depreciated (ca. -50%) after 1124 h of operation. This is attributed to: (i) the decrease of both the strain and the ligand effect of Co atoms contained in the core (ii) the changes in the surface structure of the electrocatalyst (formation of a multilayer-thick Pt shell) and (iii) the relaxation of the Pt surface atoms.

  20. Thermodynamic studies of phosphate adsorption on Pt(1 1 1) electrode surfaces in perchloric acid solutions

    Energy Technology Data Exchange (ETDEWEB)

    Mostany, Jorge [Instituto de Electroquimica, Universidad de Alicante, Apdo. 99, E-03080 Alicante (Spain); Departamento de Quimica, Universidad Simon Bolivar, Apdo. 89000, Caracas 1080A (Venezuela, Bolivarian Republic of)], E-mail: jmosta@usb.ve; Martinez, Pedro; Climent, Victor; Herrero, Enrique; Feliu, Juan M. [Instituto de Electroquimica, Universidad de Alicante, Apdo. 99, E-03080 Alicante (Spain)

    2009-10-01

    The thermodynamics of the so-called perfectly polarizable electrode was employed to analyze the total charge densities for a nearly defect-free Pt(1 1 1) electrode in a series of NaH{sub 2}PO{sub 4} solutions with an excess of inert electrolyte (0.1 M HClO{sub 4}) at constant ionic strength and pH. Thermodynamic analysis using both electrode potential and charge density as independent electrical variables is described. The Gibbs excess, Gibbs energy of adsorption and charge numbers both at constant electrode potential and constant chemical potential for anion adsorption at the Pt(1 1 1) surface have been determined. The calculated electrosorption valencies and charge numbers at constant chemical potential are close to two electrons per adsorbed anion, suggesting that in the absence of co-adsorbed species, HPO{sub 4}{sup 2-} is the predominant adsorbed species. The maximum Gibbs excess of adsorbed hydrogenphosphate attains a value of {approx}3.2 x 10{sup 14} ions cm{sup -2} which corresponds to a coverage of {approx}0.22 ML.

  1. The Role of OOH Binding Site and Pt Surface Structure on ORR Activities

    Science.gov (United States)

    Jia, Qingying; Caldwell, Keegan; Ziegelbauer, Joseph M.; Kongkanand, Anusorn; Wagner, Frederick T.; Mukerjee, Sanjeev; Ramaker, David E.

    2015-01-01

    We present experimentally observed molecular adsorbate coverages (e.g., O(H), OOH and HOOH) on real operating dealloyed bimetallic PtMx (M = Ni or Co) catalysts under oxygen reduction reaction (ORR) conditions obtained using X-ray absorption near edge spectroscopy (XANES). The results reveal a complex Sabatier catalysis behavior and indicate the active ORR mechanism changes with Pt–O bond weakening from the O2 dissociative mechanism, to the peroxyl mechanism, and finally to the hydrogen peroxide mechanism. An important rearrangement of the OOH binding site, an intermediate in the ORR, enables facile H addition to OOH and faster O–O bond breaking on 111 faces at optimal Pt–O bonding strength, such as that occurring in dealloyed PtM core-shell nanoparticles. This rearrangement is identified by previous DFT calculations and confirmed from in situ measured OOH adsorption coverages during the ORR. The importance of surface structural effects and 111 ordered faces is confirmed by the higher specific ORR rates on solid core vs porous multi-core nanoparticles. PMID:26190857

  2. Flower like Bi structures on Pt surface facilitating effective cholesterol biosensing.

    Science.gov (United States)

    V C, Soorya; Berchmans, Sheela

    2016-07-01

    This work demonstrates effective biosensing of cholesterol with the help of an efficient inorganic H2O2 transducer based on Pt-Bi combined with the organic enzyme platform. It could be shown that the Bi (bismuth) adatoms modified Pt (platinum) surface displays enhanced catalytic oxidation of H2O2 at neutral pH and the catalytic oxidation of H2O2 occurs at a lower potential of 0.25V vs NCE (normal calomel electrode). The sensing platform is highly sensitive and shows linear response towards [H2O2] in the absence of any redox mediator or enzyme. The H2O2 sensing platform, further modified with cholesterol oxidase led to cholesterol biosensing with a sensitivity of 3.41μAmM(-1)cm(-2). The apparent Michaelis-Menten constant (Km(app)) was calculated to be 0.43mM which indicates high binding affinity with the substrate. The cholesterol biosensor does not suffer from the interferences due to other common electroactive species and is highly stable.

  3. Lifting of the Au(100) surface reconstruction by Pt, Cr, Fe, and Cu adsorption

    Science.gov (United States)

    Tempas, Christopher D.; Skomski, Daniel; Tait, Steven L.

    2016-12-01

    The adsorption and growth of metals on the surfaces of other metals is an important topic for studies of heterogeneous catalysis and bimetallic nanoparticles. The surface structure of these systems impacts nanoparticle growth, catalytic activity, and reaction selectivity. In these experiments, platinum, chromium, iron, or copper were vapor deposited on the reconstructed Au(100) surface. The initial growth of each metal was studied by scanning tunneling microscopy (STM) and X-ray photoelectron spectroscopy (XPS). Each of the four metals forms anisotropic rectangular islands oriented in the direction of the gold reconstruction rows. The gradual lifting of the surface reconstruction by increased metal coverage is observed, and the reconstruction is fully lifted after 0.5 ML of Pt, Cr, or Fe, or by 3.3 ML of Cu. After the reconstruction is lifted, the island shape changes from rectangular to square, illustrating the effect of surface structure on growth. Second layer islands begin to form before the completion of the first full layer.

  4. Correlação entre a estrutura atômica superficial e o processo de adsorção-dessorção reversível de hidrogênio em eletrodos monocristalinos Pt(111, Pt(100 e Pt(110 The correlation between the atomic surface structure and the reversible adsorption-desorption of hydrogen on single crystal Pt (111, Pt (100 and Pt (110 electrodes

    Directory of Open Access Journals (Sweden)

    Valderi Pacheco dos Santos

    2001-12-01

    Full Text Available Platinum is widely used as electrode in electrocatalytic processes, however the use of polycrystalline electrodes introduces a series of variables in the electrochemical system due to the aleatory contribution of all the crystallographic orientations with different surface packing of atoms. Single crystal platinum electrodes of low Miller index present surface structure of high regularity and serve as model to establish a correlation among the macroscopic and microscopic properties of the electrochemical interface. Therefore, the main aim of this work is the study of the voltammetric profiles of the reversible adsorption-desorption of hydrogen on Pt(100, Pt(110 and Pt(111, in order to correlate the electrochemical properties of each different orientation with the surface atomic structure.

  5. Adsorption and decomposition of cyclohexanone (C6H10O) on Pt(111) and the (2 × 2) and (√3 × √3)r30°-Sn/Pt(111) surface alloys.

    Science.gov (United States)

    Kim, Jooho; Welch, Lindsey A; Olivas, Amelia; Podkolzin, Simon G; Koel, Bruce E

    2010-11-02

    Adsorption and decomposition of cyclohexanone (C(6)H(10)O) on Pt(111) and on two ordered Pt-Sn surface alloys, (2 × 2)-Sn/Pt(111) and (√3 × √3)R30°-Sn/Pt(111), formed by vapor deposition of Sn on the Pt(111) single crystal surface were studied with TPD, HREELS, AES, LEED, and DFT calculations with vibrational analyses. Saturation coverage of C(6)H(10)O was found to be 0.25 ML, independent of the Sn surface concentration. The Pt(111) surface was reactive toward cyclohexanone, with the adsorption in the monolayer being about 70% irreversible. C(6)H(10)O decomposed to yield CO, H(2)O, H(2), and CH(4). Some C-O bond breaking occurred, yielding H(2)O and leaving some carbon on the surface after TPD. HREELS data showed that cyclohexanone decomposition in the monolayer began by 200 K. Intermediates from cyclohexanone decomposition were also relatively unstable on Pt(111), since coadsorbed CO and H were formed below 250 K. Surface Sn allowed for some cyclohexanone to adsorb reversibly. C(6)H(10)O dissociated on the (2 × 2) surface to form CO and H(2)O at low coverages, and methane and H(2) in smaller amounts than on Pt(111). Adsorption of cyclohexanone on (√3 × √3)R30°-Sn/Pt(111) at 90 K was mostly reversible. DFT calculations suggest that C(6)H(10)O adsorbs on Pt(111) in two configurations: by bonding weakly through oxygen to an atop Pt site and more strongly through simultaneously oxygen and carbon of the carbonyl to a bridged Pt-Pt site. In contrast, on alloy surfaces, C(6)H(10)O bonds preferentially to Sn. The presence of Sn, furthermore, is predicted to make the formation of the strongly bound C(6)H(10)O species bonding through O and C, which is a likely decomposition precursor, thermodynamically unfavorable. Alloying with Sn, thus, is shown to moderate adsorptive and reactive activity of Pt(111).

  6. Modeling of PEM fuel cell Pt/C catalyst degradation

    Science.gov (United States)

    Bi, Wu; Fuller, Thomas F.

    Pt/C catalyst degradation remains as one of the primary limitations for practical applications of proton exchange membrane (PEM) fuel cells. Pt catalyst degradation mechanisms with the typically observed Pt nanoparticle growth behaviors have not been completely understood and predicted. In this work, a physics-based Pt/C catalyst degradation model is proposed with a simplified bi-modal particle size distribution. The following catalyst degradation processes were considered: (1) dissolution of Pt and subsequent electrochemical deposition on Pt nanoparticles in cathode; (2) diffusion of Pt ions in the membrane electrode assembly (MEA); and (3) Pt ion chemical reduction in membrane by hydrogen permeating through the membrane from the negative electrode. Catalyst coarsening with Pt nanoparticle growth was clearly demonstrated by Pt mass exchange between small and large particles through Pt dissolution and Pt ion deposition. However, the model is not adequate to predict well the catalyst degradation rates including Pt nanoparticle growth, catalyst surface area loss and cathode Pt mass loss. Additional catalyst degradation processes such as new Pt cluster formation on carbon support and neighboring Pt clusters coarsening was proposed for further simulative investigation.

  7. The structure of the chiral Pt531 surface: a combined LEED and DFT study.

    Science.gov (United States)

    Puisto, S R; Held, G; Ranea, V; Jenkins, S J; Mola, E E; King, D A

    2005-12-01

    The structure of the chiral kinked Pt531 surface has been determined by low-energy electron diffraction intensity-versus-energy (LEED-IV) analysis and density functional theory (DFT). Large contractions and expansions of the vertical interlayer distances with respect to the bulk-terminated surface geometry were found for the first six layers (LEED: d12 = 0.44 A, d23 = 0.69 A, d34 = 0.49 A, d45 = 0.95 A, d56 = 0.56 A; DFT: d12 = 0.51 A, d23 = 0.55 A, d34 = 0.74 A, d45 = 0.78 A, d56 = 0.63 A; dbulk = 0.66 A). Energy-dependent cancellations of LEED spots over unusually large energy ranges, up to 100 eV, can be explained by surface roughness and reproduced by applying a model involving 0.25 ML of vacancies and adatoms in the scattering calculations. The agreement between the results from LEED and DFT is not as good as in other cases, which could be due to this roughness of the real surface.

  8. DFT study of hydrogen fluoride and sulfur trioxide interactions on the surface of Pt-decorated graphene

    Science.gov (United States)

    Rad, Ali Shokuhi

    2016-08-01

    In this study, we investigate the adsorption properties of hydrogen florid (HF) and sulfur trioxide (SO3) on the surface of platinum decorated graphene (PtG) using density functional theory. We found one optimized configuration for HF and two ones for SO3 upon adsorption on the surface of PtG. Our result show significant adsorption on PtG with calculated energy adsorption of -73.6 (-54.2 BSSE) kJ/mol for HF at its only position and -172.4 (-144.8 BSSE) and -62.7 (-53.7 BSSE) kJ/mol for SO3 at its two positions; P1 and P2, respectively), whereas there is weak physisorption of these analytes on pristine graphene (PG). Results of charge analyses reveled interesting net charge transfer; while the direction of charge is from HF to PtG, reverse direction is found for SO3 for its two configurations. To deep understand the concept of adsorption properties, we used orbital analyses including density of states for interaction of mentioned analytes on the surface of PtG.

  9. Effects of Nanowire Length and Surface Roughness on the Electrochemical Sensor Properties of Nafion-Free, Vertically Aligned Pt Nanowire Array Electrodes

    Directory of Open Access Journals (Sweden)

    Zhiyang Li

    2015-09-01

    Full Text Available In this paper, vertically aligned Pt nanowire arrays (PtNWA with different lengths and surface roughnesses were fabricated and their electrochemical performance toward hydrogen peroxide (H2O2 detection was studied. The nanowire arrays were synthesized by electroplating Pt in nanopores of anodic aluminum oxide (AAO template. Different parameters, such as current density and deposition time, were precisely controlled to synthesize nanowires with different surface roughnesses and various lengths from 3 μm to 12 μm. The PtNWA electrodes showed better performance than the conventional electrodes modified by Pt nanowires randomly dispersed on the electrode surface. The results indicate that both the length and surface roughness can affect the sensing performance of vertically aligned Pt nanowire array electrodes. Generally, longer nanowires with rougher surfaces showed better electrochemical sensing performance. The 12 μm rough surface PtNWA presented the largest sensitivity (654 μA·mM−1·cm−2 among all the nanowires studied, and showed a limit of detection of 2.4 μM. The 12 μm rough surface PtNWA electrode also showed good anti-interference property from chemicals that are typically present in the biological samples such as ascorbic, uric acid, citric acid, and glucose. The sensing performance in real samples (river water was tested and good recovery was observed. These Nafion-free, vertically aligned Pt nanowires with surface roughness control show great promise as versatile electrochemical sensors and biosensors.

  10. Area inequalities for stable marginally trapped surfaces

    CERN Document Server

    Jaramillo, José Luis

    2012-01-01

    We discuss a family of inequalities involving the area, angular momentum and charges of stably outermost marginally trapped surfaces in generic non-vacuum dynamical spacetimes, with non-negative cosmological constant and matter sources satisfying the dominant energy condition. These inequalities provide lower bounds for the area of spatial sections of dynamical trapping horizons, namely hypersurfaces offering quasi-local models of black hole horizons. In particular, these inequalities represent particular examples of the extension to a Lorentzian setting of tools employed in the discussion of minimal surfaces in Riemannian contexts.

  11. Monitoring System for ALICE Surface Areas

    CERN Document Server

    Demirbasci, Oguz

    2016-01-01

    I have been at CERN for 12 weeks within the scope of Summer Student Programme working on a monitoring system project for surface areas of the ALICE experiment during this period of time. The development and implementation of a monitoring system for environmental parameters in the accessible areas where a cheap hardware setup can be deployed were aim of this project. This report explains how it was developed by using Arduino, Raspberry PI, WinCC OA and DIM protocol.

  12. Insights on the SO2 Poisoning of Pt3Co/VC and Pt/VC Fuel Cell Catalysts

    Science.gov (United States)

    2010-01-01

    stripping voltammetry and underpotential deposition (upd) of copper adatoms. Then the performance of PEMFC cathodes employing 30wt.% Pt3Co/VC and 50wt.% Pt/VC...atoms (Pt and Cu atomic radii are 0.139 and 0.128nm, respectively [15]) makes copper underpotential deposition a perfect tool for evaluating the plat...the surface area of Pt3Co/VC catalyst is rigorously characterized by hydrogen adsorption,CO stripping voltammetry and under potential deposition (upd

  13. A Nanostructured Bifunctional platform for Sensing of Glucose Biomarker in Artificial Saliva: Synergy in hybrid Pt/Au surfaces.

    Science.gov (United States)

    Raymundo-Pereira, Paulo A; Shimizu, Flávio M; Coelho, Dyovani; Piazzeta, Maria H O; Gobbi, Angelo L; Machado, Sergio A S; Oliveira, Osvaldo N

    2016-12-15

    We report on a bimetallic, bifunctional electrode where a platinum (Pt) surface was patterned with nanostructured gold (Au) fingers with different film thicknesses, which was functionalized with glucose oxidase (GOx) to yield a highly sensitive glucose biosensor. This was achieved by using selective adsorption of a self-assembled monolayer (SAM) onto Au fingers, which allowed GOx immobilization only onto the Au-SAM surface. This modified electrode was termed bifunctional because it allowed to simultaneously immobilize the biomolecule (GOx) on gold to catalyze glucose, and detect hydrogen peroxide on Pt sites. Optimized electrocatalytic activity was reached for the architecture Pt/Au-SAM/GOx with 50nm thickness of Au, where synergy between Pt and Au allowed for detection of hydrogen peroxide (H2O2) at a low applied potential (0V vs. Ag/AgCl). Detection was performed for H2O2 in the range between 4.7 and 102.7 nmol L(-1), with detection limit of 3.4×10(-9) mol L(-1) (3.4 nmol L(-1)) and an apparent Michaelis-Menten rate constant of 3.2×10(-6)molL(-1), which is considerably smaller than similar devices with monometallic electrodes. The methodology was validated by measuring glucose in artificial saliva, including in the presence of interferents. The synergy between Pt and Au was confirmed in electrochemical impedance spectroscopy measurements with an increased electron transfer, compared to bare Pt and Au electrodes. The approach for fabricating the reproducible bimetallic Pt/Au electrodes is entirely generic and may be explored for other types of biosensors and biodevices where advantage can be taken of the combination of the two metals.

  14. New Synthesis of Pt-Ru Nanoparticles on Surface Modified Carbon Vulcane XC-72 as an Effective Catalyst for Direct Methanol Fuel Cell

    Institute of Scientific and Technical Information of China (English)

    Ahmad; Nozad; Golikand; Sajjad; Sadaghat; Sharehjini; Mohammad; Yari

    2007-01-01

    1 Results Pt-Ru nanoparticles are synthesised on the surface oxidized carbon Vulcane XC-72 as catalyst support by chemically anchoring Pt and Ru onto the surface of modified carbon vulcane XC-72 (by refluxing in 70% HNO3 at 120 ℃ for 12 h to introduce surface functional groups) .The nanoparticles of Pt and Ru are synthesized by reduction of H2PtCl6 and K4Ru(CN)6 with sodium borohydride in a 5.5 buffer solution of sodium citrate,the complexation of citrate with metal ions is beneficial to the formati...

  15. Correlation of Pt-Re Surface Properties with Reaction Pathways for the Aqueous-Phase Reforming of Glycerol

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Liang; Karim, Ayman M.; Engelhard, Mark H.; Wei, Zhehao; King, D. L.; Wang, Yong

    2012-01-17

    The surface properties of Pt-Re catalytic nano-particles supported on carbon following exposure to a hydrogen reducing environment and subsequent hydrothermal conditions have been studied using in-situ X-ray photoelectron spectroscopy (XPS) and ammonia temperature programmed desorption (TPD). These properties have been correlated with the catalyst selectivity for the aqueous phase reforming of glycerol. We show that Pt in reduced Pt-Re/C becomes electron deficient, and a fraction of the Re becomes oxidized when the catalyst is subsequently exposed to hydrothermal reaction conditions. Oxidation of Pt-Re generates surface acidity, which drastically affects the reaction pathways. The acid site concentration, but not acid site strength, increases with Re loading. This acidity increase with Re addition favors C-O over C-C cleavage, which results in higher selectivity to liquid products and alkanes at the expense of hydrogen production. We propose a model for the Pt-Re active site and the origin of acidity enhanced by the addition of Re.

  16. Osmosis and Surface Area to Volume Ratio.

    Science.gov (United States)

    Barrett, D. R. B.

    1984-01-01

    Describes an experiment designed to help students understand the concepts of osmosis and surface area to volume ratio (SA:VOL). The task for students is to compare water uptake in different sizes of potato cubes and relate differences to their SA:VOL ratios. (JN)

  17. Volumes and surface areas of pendular rings

    Science.gov (United States)

    Rose, W.

    1958-01-01

    A packing of spheres is taken as a suitable model of porous media. The packing may be regular and the sphere size may be uniform, but in general, both should be random. Approximations are developed to give the volumes and surface areas of pendular rings that exist at points of sphere contact. From these, the total free volume and interfacial specific surface area are derived as expressive of the textural character of the packing. It was found that the log-log plot of volumes and surface areas of pendular rings vary linearly with the angle made by the line joining the sphere centers and the line from the center of the largest sphere to the closest edge of the pendular ring. The relationship, moreover, was found not to be very sensitive to variation in the size ratio of the spheres in contact. It also was found that the addition of pendular ring material to various sphere packings results in an unexpected decrease in the surface area of the boundaries that confine the resulting pore space. ?? 1958 The American Institute of Physics.

  18. Study of high coverages of atomic oxygen on the Pt(111) surface

    Energy Technology Data Exchange (ETDEWEB)

    Parker, D.H.; Bartram, M.E.; Koel, B.E. (Univ. of Colorado, Boulder (United States))

    1989-01-01

    Atomic oxygen coverages of up to 0.75 monolayer (ML) may be adsorbed cleanly on Pt(111) surfaces under UHV conditions by exposure to NO{sub 2} at 400 K. The authors have studied this adsorbed oxygen layer by using AES, LEED, UPS, HREELS, TPD, and work function ({Delta}{phi}) measurements. The (2{times}2)-O structure formed at {theta}{sub o} = 0.25 ML is still apparent at {theta}{sub o} = 0.60 ML and a faint (2{times}2) pattern persists even up to {theta}{sub o} = 0.75 ML.AES and {Delta}{phi} measurements show no evidence for chemically distinct species in the adlayer as a function of oxygen coverage. HREELS spectra clearly rule out the presence of molecular oxygen and oxide species over the range of oxygen coverage studied. UPS also shows no shift in binding energy of the oxygen-derived peak as the coverage is increased. These spectroscopic probes indicate that all oxygen is present as atomic oxygen with no indication of oxide formation or molecular oxygen at any coverage. Multiple O{sub 2} desorption peaks observed in TPD are interpreted as arising largely from kinetic effects rather than a result of multiple, distinctly different chemical species, even though large changes in the Pt-O bond energy are determined from the TPD data. The activation energy for O{sub 2} desorption reflects the sum of the heat of dissociative adsorption of O{sub 2} and the activation energy for O{sub 2} desorption reflects the sum of the heat of dissociative adsorption of O{sub 2} and the activation energy for O{sub 2} dissociation. The structure in the O{sub 2} TPD spectrum is due to large changes in the activation energy for O{sub 2} desorption resulting from increases in the barrier to dissociative O{sub 2} chemisorption and decreases in the Pt-O bond energy.

  19. Electronic stopping of keV nitrogen ions interacting with a Pt(110) (1 x 2) surface - a tool to characterize electronic surfaces

    NARCIS (Netherlands)

    Robin, A; Postnikov, AV; Heiland, W

    2005-01-01

    Ion channeling is used to investigate the electronic density corrugation at surfaces by analysing the electronic stopping behaviour of ions scattering grazingly off a clean single crystalline Pt(110)(1 x 2) surface. We use the fact that under these conditions the elastic contribution can be separate

  20. Surface-induced clustering in vapor deposited Co{sub 1{minus}x}Pt{sub x} and Ni{sub 1{minus}x}Pt{sub x} films (abstract)

    Energy Technology Data Exchange (ETDEWEB)

    Shapiro, A.L.; Rooney, P.W.; Tran, M.Q.; Hellman, F. [Department of Physics, University of California--San Diego, La Jolla, California 92093-0350 (United States)

    1997-04-01

    We have depostied (100), (110), and (111) oriented single-crystal and polycrystalline Co{sub 1{minus}x}Pt{sub x} (x=0.65, 0.75, 0.80) and polycrystalline Ni{sub 1{minus}x}Pt{sub x} (x=0.25, 0.50) films over a range of growth temperatures from {minus}50 to 800{degree}C. Previous work on CoPt{sub 3} films had demonstrated the correlation between Co clustering and perpendicular magnetic anisotropy. These observations motivated a model in which Co atoms cluster on the growing surface; this clustering is trapped by succeeding layers for growth temperatures below 400{degree}C, the lower limit of bulk atomic mobility. The (110) oriented samples show clustering and anisotropy identical to the (100) and (11) oriented samples despite the sign change of the surface segregation in the (110) orientation. The Ni{endash}Pt alloy system is similar to Co{endash}Pt in structure, lattice constant, and the polarizability of Pt. We have deposited Ni{sub 3}Pt films; these films have significant clustering of the magnetic species which drops off rapidly after the onset of bulk mobility at 400{degree}C. No perpendicular magnetic anisotropy is found in these films, even though interface magnetic anisotropy values in Ni/Pt multilayers have been reported as having up to 1/4 the value of Co/Pt interfaces. Finally, in order to explore whether surface clustering is a kinetic or equilibrium effect, we have varied the deposition rate of CoPt{sub 3} over three orders of magnitude at temperatures below 400{degree}C. We found no dependence of clustering or anisotropy on the deposition rate, suggesting that the clustering is not kinetically limited but is a surface equilibrium effect. {copyright} {ital 1997 American Institute of Physics.}

  1. Structural and chemical characteristics of atomically smooth GaN surfaces prepared by abrasive-free polishing with Pt catalyst

    Science.gov (United States)

    Murata, Junji; Sadakuni, Shun; Okamoto, Takeshi; Hattori, Azusa N.; Yagi, Keita; Sano, Yasuhisa; Arima, Kenta; Yamauchi, Kazuto

    2012-06-01

    This paper reports the structural and chemical characteristics of atomically flat gallium nitride (GaN) surfaces prepared by abrasive-free polishing with platinum (Pt) catalyst. Atomic force microscopy revealed regularly alternating wide and narrow terraces with a step height equivalent to that of a single bilayer on the flattened GaN surfaces, which originate from the differences in etching rate of two neighboring terraces. The material removal characteristics of the method for GaN surfaces were investigated in detail. We confirmed that an atomically smooth GaN surface with an extremely small number of surface defects, including pits and scratches, can be achieved, regardless of the growth method, surface polarity, and doping concentration. X-ray photoelectron spectroscopy showed that the flattening method produces clean GaN surfaces with only trace impurities such as Ga oxide and metallic Ga. Contamination with the Pt catalyst was also evaluated using total-reflection X-ray fluorescence analysis. A wet cleaning method with aqua regia is proposed, which markedly eliminates this Pt contamination without affecting the surface morphology.

  2. Energy loss and charge state dependency of swift Nq+ ions scattered off a Pt(110)(1 x 2) surface

    NARCIS (Netherlands)

    Robin, A; Hatke, N; Jensen, J; Plachke, D; Carstanjen, HD; Heiland, W

    2003-01-01

    We present new surface scattering results combining measurements of energy loss and charge state distributions of 0.7-1.4 MeV Nq+ (q = 1, 2) ions. The energy range is still below the bulk stopping power maximum and charge exchange occurs. The projectiles scatter from a Pt(110)(1 x 2) single crystal

  3. A Compendium of Scale Surface Microstructures: Ni(pt)al Coatings Oxidized at 1150 C for 2000 1-h Cycles

    Science.gov (United States)

    Smialek, James L.; Garg, Anita

    2010-01-01

    The surface structure of scales formed on Ni(Pt)Al coatings was characterized by SEM/EDS/BSE in plan view. Two nominally identical {100} samples of aluminide coated CMSX4 single crystal were oxidized at 1150 C for 2000 1-h cycles and were found to produce somewhat disparate behavior. One sample, with less propensity for coating grain boundary ridge deformation, presented primarily alpha-Al2O3 scale structures, with minimal weight loss and spallation. The original scale structure, still retained over most of the sample, consisted of the classic theta-alpha transformation-induced ridge network structure, with approx. 25 nm crystallographic steps and terraces indicative of surface rearrangement to low energy alumina planes. The scale grain boundary ridges were often decorated with a fine, uniform distribution of (Hf,Ti)O2 particles. Another sample, producing steady state weight losses, exhibited much interfacial spallation and a complex assortment of different structures. Broad areas of interfacial spalling, crystallographically-faceted (Ni,Co)(Al,Cr)2O4 spinel, with an alpha-Al2O3 base scale, were the dominant features. Other regions exhibited nodular spinel grains, with fine or (Ta,Ti)-rich (rutile) particles decorating or interspersed with the spinel. While these features were consistent with a coating that presented more deformation at extruded grain boundaries, the root cause of the different behavior between the duplicate samples could not be conclusively identified.

  4. Fundamental Mechanistic Understanding of Electrocatalysis of Oxygen Reduction on Pt and Non-Pt Surfaces: Acid versus Alkaline Media

    Directory of Open Access Journals (Sweden)

    Nagappan Ramaswamy

    2012-01-01

    Full Text Available Complex electrochemical reactions such as Oxygen Reduction Reaction (ORR involving multi-electron transfer is an electrocatalytic inner-sphere electron transfer process that exhibit strong dependence on the nature of the electrode surface. This criterion (along with required stability in acidic electrolytes has largely limited ORR catalysts to the platinum-based surfaces. New evidence in alkaline media, discussed here, throws light on the involvement of surface-independent outer-sphere electron transfer component in the overall electrocatalytic process. This surface non-specificity gives rise to the possibility of using a wide-range of non-noble metal surfaces as electrode materials for ORR in alkaline media. However, this outer-sphere process predominantly leads only to peroxide intermediate as the final product. The importance of promoting the electrocatalytic inner-sphere electron transfer by facilitation of direct adsorption of molecular oxygen on the active site is emphasized by using pyrolyzed metal porphyrins as electrocatalysts. A comparison of ORR reaction mechanisms between acidic and alkaline conditions is elucidated here. The primary advantage of performing ORR in alkaline media is found to be the enhanced activation of the peroxide intermediate on the active site that enables the complete four-electron transfer. ORR reaction schemes involving both outer- and inner-sphere electron transfer mechanisms are proposed.

  5. Kinetics and thermodynamics of H2O dissociation and CO oxidation on the Pt/WC (0001) surface: A density functional theory study

    Science.gov (United States)

    Liang, Yuanyuan; Chen, Litao; Ma, Chun'an

    2017-02-01

    Adsorptions of H2O and CO on the Pt/WC(0001) [pseudomorphic platinum monolayer on WC(0001)] surface have been studied with periodical slab model by PW91 approach of GGA within the framework of density functional theory (DFT). The reaction pathways and mechanisms of H2O dissociation and CO oxidation are also investigated. For a comparison, similar calculation scheme are performed on the Pt (111) surface as well. The adsorption energies of H2O and CO on both concerned surfaces suggest that H2O binds preferentially on the Pt/WC (0001) surface, while CO prefers the metal surface Pt (111), agreeing well with the experimental observation that the tungsten carbides based material is less susceptible to CO poisoning than platinum. The activation energies for the stepwise H2O dehydrogenation reaction show that the progress of H2O dissociation is similar on the two surfaces; and coincidentally the oxidation of CO by surface hydroxyl is much more likely to occur than that by surface oxygen which comes up with the H2O dissociation. Although the activation barrier of H2O dissociation on the Pt/WC (0001) is similar to that on Pt (111), the key oxidant OH specials which play a key role in turning over surface carbon monoxide to carbon dioxide prefer the Pt/WC(0001) surface, and the improved CO oxidation reaction progress confirms that the Pt/WC surface is more CO-tolerant than the pure Pt. According to the electronic structure analysis we find that the increased CO tolerance is ascribed to the downshift of Pt d-band center because of the charge transfer from WC support to the coating surface.

  6. Evidence of a Surface-Mediated Magnetically Induced Miscibility Gap in Co-Pt Alloy Thin Films

    Energy Technology Data Exchange (ETDEWEB)

    Rooney, P.W.; Shapiro, A.L.; Tran, M.Q.; Hellman, F. [Department of Physics, University of California at San Diego, La Jolla, California 92093 (United States)

    1995-08-28

    (100) and (111) oriented single-crystal CoPt{sub 3} films were deposited over a range of growth temperatures from {minus}50 to 800 {degree}C. The Curie temperature is increased by 200 {degree}C over the value expected for the homogeneous alloy in the as-deposited films (of both orientations) grown near 400 {degree}C. We interpret this as evidence for a previously unobserved, surface-mediated, magnetically driven miscibility gap in vapor-deposited CoPt{sub 3} films. Large perpendicular magnetic anisotropy is also observed in the as-deposited films (of both orientations) grown near 400 {degree}C.

  7. Geometric And Electronic Structure of Methane Adsorbed on a Pt Surface

    Energy Technology Data Exchange (ETDEWEB)

    Ostrom, H.; Ogasawara, H.; Naslund, L.A.; Andersson, K.; Pettersson, L.G.M.; Nilsson, A.; /Stockholm U. /SLAC, SSRL

    2007-11-21

    The electronic structure of methane adsorbed on Pt(977) is investigated using angle-resolved x-ray absorption spectroscopy (XAS) in combination with density functional theory spectrum calculations. XAS, which probes the unoccupied states atom specifically, shows the appearance of the symmetry-forbidden gas-phase lowest unoccupied molecular orbital due to s-p rehybridization. In addition new adsorption-induced states appear just above the Fermi level. A systematic investigation, where computed XA spectra are compared with the experiment, indicates elongation of the C-H bond pointing toward the surface to 1.18+/-0.05 Angstroms. The bond elongation arises due to mixing between bonding and antibonding C-H orbitals. Computed charge density difference plots show that no covalent chemical bond is formed between the adsorbate and substrate upon adsorption. The changes in electronic structure arise in order to minimize the Pauli repulsion by polarizing charge away from the surface toward the carbon atom of the methane molecule.

  8. Study of the Material Transfer Characteristics and Surface Morphology Due to Arc Erosion of PtIr Contact Materials

    Institute of Scientific and Technical Information of China (English)

    WANG Saibei; XIE Ming; YANG Youcai; ZHANG Jiming; CHEN Yongtai; LIU Manmen; YANG Yunfeng; HU Jieqiong; CUI Hao

    2012-01-01

    By means of breaking tests on PtIr contact materials via a JF04C contact material testing machine,it was attempted to elucidate the characterstics of the various surface morphology and material transfer after the arc erosion process caused by break arc.The material transfer characteristics appeared in the experiments were concluded and analyzed.Meanwhile,the morphology of the anode and cathode surface were observed and analyzed by SEM.

  9. High surface area fibrous silica nanoparticles

    KAUST Repository

    Polshettiwar, Vivek

    2014-11-11

    Disclosed are high surface area nanoparticles that have a fibrous morphology. The nanoparticles have a plurality of fibers, wherein each fiber is in contact with one other fiber and each fiber has a length of between about 1 nm and about 5000 nm. Also disclosed are applications of the nanoparticles of the present invention, and methods of fabrication of the nanoparticles of the present invention.

  10. Palatal Surface Area of Maxillary Plaster Casts

    DEFF Research Database (Denmark)

    Darvann, Tron Andre; Hermann, Nuno V.; Ersbøll, Bjarne Kjær

    2007-01-01

    Objective: To investigate the relationship between corresponding two-dimensional and three-dimensional measurements on maxillary plaster casts taken from photographs and three-dimensional surface scans, respectively. Materials and Methods: Corresponding two-dimensional and three-dimensional measu......Objective: To investigate the relationship between corresponding two-dimensional and three-dimensional measurements on maxillary plaster casts taken from photographs and three-dimensional surface scans, respectively. Materials and Methods: Corresponding two-dimensional and three......-dimensional measurements of selected linear distances, curve lengths, and (surface) areas were carried out on maxillary plaster casts from individuals with unilateral or bilateral cleft lip and palate. The relationship between two-dimensional and three-dimensional measurements was investigated using linear regression....... Results and Conclusions: Error sources in the measurement of three-dimensional palatal segment surface area from a two-dimensional photograph were identified as photographic distortion (2.7%), interobserver error (3.3%), variability in the orientation of the plaster cast (3.2%), and natural shape...

  11. A rational computational study of surface defect-mediated stabilization of low-dimensional Pt nanostructures on TiN(100).

    Science.gov (United States)

    Tak, Young Joo; Jang, Woosun; Richter, Norina A; Soon, Aloysius

    2015-04-21

    Platinum is known as a catalyst with exceptional reactivity for many important reactions, e.g. the oxygen reduction reaction. To reduce the high cost of pure platinum catalysts, platinum on a carbon support is widely used in industrial fuel cell applications. However, these Pt/C systems suffer from poor stability. As a cost-efficient and more durable alternative, Pt single-atom catalysts on a TiN support have recently been suggested, and it has been shown that the single-atom catalysts are stable when anchored at a nitrogen vacancy site on the TiN surface in a nitrogen-lean environment. To further explore the perspective of Pt/TiN catalytic systems, we provide insights into the stability and morphology of Pt nanostructures at the TiN(100) surface, using a density-functional theory approach in combination with ab initio atomistic thermodynamics. Our results show that the formation of two-dimensional Pt nano-layers is preferred over the formation of three-dimensional Pt nano-clusters on the TiN substrate. Similar to the single-atom catalysts, nano-layers of Pt can be stabilized on the TiN(100) surface by surface nitrogen vacancies under nitrogen-lean conditions. By analyzing the electronic metal-support interaction (EMSI) between the Pt nano-layer and the TiN surface with surface defects, we demonstrate that a strong EMSI between the surrounding Ti and Pt atoms is important for stabilizing the catalyst nano-layer at the TiN surface, and that N vacancies lead to stronger Pt-Ti interaction. This work provides a rational computational platform for the design of new generation high-performance Pt-based fuel cells.

  12. From mixed to three-layer core/shell PtCu nanoparticles: ligand-induced surface segregation to enhance electrocatalytic activity.

    Science.gov (United States)

    Dai, Changqing; Yang, Yang; Zhao, Zheng; Fisher, Adrian; Liu, Zhiping; Cheng, Daojian

    2017-07-06

    Core-shell segregated bimetallic nanoparticles (NPs) exhibit increased enhanced catalytic performance compared to that of mixed bimetallic NPs. Here, we report a simple, yet efficient, one-pot synthetic strategy to synthesize uniform three-layer core/shell PtCu NPs by adding benzyl ether (BE) in the synthesis process of mixed PtCu NPs. In comparison with commercial Pt/C and also mixed PtCu NPs, the three-layer core/shell PtCu NPs exhibit superior activity in catalyzing the oxygen reduction reaction (ORR), formic acid oxidation reaction (FAOR), methanol oxidation reaction (MOR), and ethanol oxidation reaction (EOR), mainly due to the ligand (BE)-induced surface segregation of Pt on the surface of the NPs.

  13. Surface spectroscopy of CO/Pt(111) with high harmonics in the XUV

    Energy Technology Data Exchange (ETDEWEB)

    Haarlammert, Thorben; Wegner, Sebastian; Tsilimis, Grigorius; Zacharias, Helmut [Physikalisches Institut, Westfaelische Wilhelms-Universitaet, Muenster (Germany); Golovin, Alexander [Institute of Physics, St. Petersburg State University (Russian Federation)

    2008-07-01

    We report on the generation of high harmonic radiation in the photon energy range up to 100 eV with up to 10 kHz repetition rate, based on the conversion of femtosecond Ti:sapphire radiation in rare gases. The fundamental laser is based on a single stage, multiple pass ampli-fication of a cavity-dumped oscillator. Output pulse energies of 1 mJ and pulse durations of les than 30 fs at adjustable repetition rates up to 10 kHz are achieved. The generated High Harmonics are separated by a toroidal grating and directed to the surface. A time-of-flight detector with multiple anodes registers the kinetic energies of emitted photoelectrons. The angular distributions of photoelectrons emitted form CO/Pt(111) under s-polarized excitations have been measured for a variety of initial photon energies. Different from gas phase results a significant intensity of photoelectrons are emitted also in the normal direction, i.e., in the direction of the C-O chemical bond. A first theoretical investigation supports qualitatively the observed angular distributions.

  14. Spin Hall Magnetoresistance as a Probe for Surface Magnetization in Pt /Co Fe2O4 Bilayers

    Science.gov (United States)

    Isasa, Miren; Vélez, Saül; Sagasta, Edurne; Bedoya-Pinto, Amilcar; Dix, Nico; Sánchez, Florencio; Hueso, Luis E.; Fontcuberta, Josep; Casanova, Fèlix

    2016-09-01

    We study the spin Hall magnetoresistance (SMR) in Pt grown in situ on CoFe2O4 (CFO) ferrimagnetic insulating films. A careful analysis of the angle-dependent and field-dependent longitudinal magnetoresistance indicates that the SMR contains a contribution that does not follow the bulk magnetization of CFO, but it is a fingerprint of the complex magnetism at the surface of the CFO layer, thus signaling SMR as a tool for mapping surface magnetization. A systematic study of the SMR for different temperatures and CFO thicknesses gives us information impossible to obtain with any standard magnetometry technique. On one hand, the surface magnetization behaves independently of the CFO thickness and does not saturate up to high fields, evidencing that the surface has its own anisotropy. On the other hand, characteristic zero-field magnetization steps are not present at the surface while they are relevant in the bulk, strongly suggesting that antiphase boundaries are responsible for such intriguing features. In addition, a contribution from the ordinary magnetoresistance of Pt is identified, which is distinguishable only due to the low resistivity of the in situ grown Pt.

  15. 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.

  16. Pt-graphene electrodes for dye-sensitized solar cells

    Energy Technology Data Exchange (ETDEWEB)

    Hoshi, Hajime, E-mail: hoshi@ed.tus.ac.jp; Tanaka, Shumpei; Miyoshi, Takashi

    2014-12-15

    Highlights: • Graphene films with Pt nanoparticles were prepared from commercial graphene. • Pt consumption can be reduced by using Pt-graphene films. • The film showed improved catalytic activity for the reaction I{sub 3}{sup −}/I{sup −}. • The film can be used as the counter electrode of dye-sensitized solar cells (DSSCs). • The performance of DSSC was superior to that of the Pt electrode. - Abstract: A simple paste method for fabricating graphene films with Pt nanoparticles was developed. First, graphene pastes with Pt nanoparticles were prepared from commercially available graphene. The resulting films of graphene nanoplatelet aggregates with Pt nanoparticles (Pt-GNA) contained Pt nanoparticles distributed over the entire three-dimensional surface of the GNA. Then, the catalytic activity for the I{sub 3}{sup −}/I{sup −} redox reaction was evaluated by cyclic voltammetry. The GNA electrode exhibited higher activity than a graphene nanoplatelet electrode because of its higher effective surface area. Addition of Pt nanoparticles to the electrodes improved the catalytic activity. In particular, a large Faradaic current for the I{sub 3}{sup −}/I{sup −} reaction was observed for the Pt-GNA electrode. As the counter electrodes of dye-sensitized solar cells (DSSCs), their performance was consistent with the cyclic voltammetry results. In particular, the DSSC performance of the Pt-GNA electrode was superior to that of the Pt electrodes commonly used in DSSCs.

  17. Nondestructive, stereological estimation of canopy surface area

    DEFF Research Database (Denmark)

    Wulfsohn, Dvora-Laio; Sciortino, Marco; Aaslyng, Jesper M.

    2010-01-01

    with sampling fraction equal to 1/9 followed by point counting using a 4.3 cm2/point grid produced a coefficient of error of less than 7%. The smooth fractionator can be used to ensure that the additional contribution to the estimator variance due to between-plant variability is small.......We describe a stereological procedure to estimate the total leaf surface area of a plant canopy in vivo, and address the problem of how to predict the variance of the corresponding estimator. The procedure involves three nested systematic uniform random sampling stages: (i) selection of plants from...

  18. High surface area graphite as alternative support for proton exchange membrane fuel cell catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Ferreira-Aparicio, P.; Folgado, M.A. [Centro de Investigaciones Energeticas, Medioambientales y Tecnologicas (CIEMAT), Avda. Complutense 22, E-28040 Madrid (Spain); Daza, L. [Centro de Investigaciones Energeticas, Medioambientales y Tecnologicas (CIEMAT), Avda. Complutense 22, E-28040 Madrid (Spain); Instituto de Catalisis y Petroleoquimica (CSIC), C/Marie Curie, 2 Campus de Cantoblanco, E-28049 Madrid (Spain)

    2009-07-01

    The suitability of a high surface area graphite (HSAG) as proton exchange membrane fuel cell (PEMFC) catalyst support has been evaluated and compared with that of the most popular carbon black: the Vulcan XC72. It has been observed that Pt is arranged on the graphite surface resulting in different structures which depend on the catalysts synthesis conditions. The influence that the metal particle size and the metal-support interaction exert on the catalysts degradation rate is analyzed. Temperature programmed oxidation (TPO) under oxygen containing streams has been shown to be a useful method to assess the resistance of PEMFC catalysts to carbon corrosion. The synthesized Pt/HSAG catalysts have been evaluated in single cell tests in the cathode catalytic layer. The obtained results show that HSAG can be a promising alternative to the traditionally used Vulcan XC72 carbon black when suitable catalysts synthesis conditions are used. (author)

  19. The structure and reactivity of adsorbates on stepped Rh and Pt surfaces investigated by LEED, HREELS, TPD, XPS and STM

    Energy Technology Data Exchange (ETDEWEB)

    Batteas, J.D. [Univ. of California, Berkeley, CA (United States). Dept. of Chemistry]|[Lawrence Berkeley Lab., CA (United States). Materials Science Div.

    1995-06-01

    Defects on surfaces such as steps play an important role in surface chemistry. In order to obtain an understanding of the influence of steps in surface chemical reactions, the structure and reactivity of small molecules (O{sub 2}, CO, H{sub 2}S, and C{sub 2}H{sub 4}) on atomically stepped surfaces of RH and Pt have been investigated. The detailed structures of CO and oxygen bonded to the Rh(110) surface were determined. The CO molecules bond near the short bridge sites with the CO molecular axis tilted approximately 24{degree} from the surface normal. Oxygen atoms are bound asymmetrically in the 3-fold fcc hollow-sites to the (111) facets of the steps. The interactions of CO and oxygen on the Rh(311) surface were examined. The reaction of CO with the ordered phases of O shows two distinct reaction channels, a low temperature reaction limited channel (200 K) and a high temperature diffusion limited channel (350 K). Models of the reaction geometry and dynamics are proposed. The thermal decomposition of ethylene was examined on the Rh(311) surface. The stable decomposition species (C{sub 2}H, CH and C{sub 2}) are formed near 300 K, approximately 100 K lower on the stepped Rh(311) than on the flatter Rh(111) surface. The formation of these species at lower temperatures is attributed to the stepped nature of the surface. Finally, in situ STM was used to examine surface structural changes of a stepped Pt(111) crystal under coadsorption of sulfur and CO. This is the first direct evidence for a new mechanism by which a surface covered with an unreactive, strongly chemisorbed overlayer can form new sites, for bonding and reactions to occur, by massive surface restructuring at the step edges. This new surface phenomenon answers some of the puzzles of metal surface catalysis and its implications are described. 278 refs.

  20. High surface area, high permeability carbon monoliths

    Energy Technology Data Exchange (ETDEWEB)

    Lagasse, R.R.; Schroeder, J.L. [Sandia National Labs., Albuquerque, NM (United States). Organic Materials Processing Dept.

    1994-12-31

    The goal of this work is to prepare carbon monoliths having precisely tailored pore size distribution. Prior studies have demonstrated that poly(acrylonitrile) can be processed into a precursor having tailored macropore structure. Since the macropores were preserved during pyrolysis, this synthetic process provided a route to porous carbon having macropores with size =0.1 to 10{mu}m. No micropores of size <2 nm could be detected in the carbon, however, by nitrogen adsorption. In the present work, the authors have processed a different polymer, poly(vinylidene chloride) into a macroporous precursor, Pyrolysis produced carbon monoliths having macropores derived from the polymer precursor as well as extensive microporosity produced during the pyrolysis of the polymer. One of these carbons had BET surface area of 1,050 m{sup 2}/g and about 1.2 cc/g total pore volume, with about 1/3 of the total pore volume in micropores and the remainder in 1{mu}m macropores. No mesopores in the intermediate size range could be detected by nitrogen adsorption. Carbon materials having high surface area as well as micron size pores have potential applications as electrodes for double layer supercapacitors containing liquid electrolyte, or as efficient media for performing chemical separations.

  1. Catalytically Triggered Energy Release from Strained Organic Molecules: The Surface Chemistry of Quadricyclane and Norbornadiene on Pt(111).

    Science.gov (United States)

    Bauer, Udo; Mohr, Susanne; Döpper, Tibor; Bachmann, Philipp; Späth, Florian; Düll, Fabian; Schwarz, Matthias; Brummel, Olaf; Fromm, Lukas; Pinkert, Ute; Görling, Andreas; Hirsch, Andreas; Bachmann, Julien; Steinrück, Hans-Peter; Libuda, Jörg; Papp, Christian

    2017-01-31

    We have investigated the surface chemistry of the polycyclic valence-isomer pair norbornadiene (NBD) and quadricyclane (QC) on Pt(111). The NBD/QC system is considered to be a prototype for energy storage in strained organic compounds. By using a multimethod approach, including UV photoelectron, high-resolution X-ray photoelectron, and IR reflection-absorption spectroscopic analysis and DFT calculations, we could unambiguously identify and differentiate between the two molecules in the multilayer phase, which implies that the energy-loaded QC molecule is stable in this state. Upon adsorption in the (sub)monolayer regime, the different spectroscopies yielded identical spectra for NBD and QC at 125 and 160 K, when multilayer desorption takes place. This behavior is explained by a rapid cycloreversion of QC to NBD upon contact with the Pt surface. The NBD adsorbs in a η(2) :η(1) geometry with an agostic Pt-H interaction of the bridgehead CH2 subunit and the surface. Strong spectral changes are observed between 190 and 220 K because the hydrogen atom that forms the agostic bond is broke. This reaction yields a norbornadienyl intermediate species that is stable up to approximately 380 K. At higher temperatures, the molecule dehydrogenates and decomposes into smaller carbonaceous fragments.

  2. Pt promotion and spill-over processes during deposition and desorption of upd-H(ad) and OH(ad) on Pt(x)Ru(1-x)/Ru(0001) surface alloys.

    Science.gov (United States)

    Hoster, Harry E; Janik, Michael J; Neurock, Matthew; Behm, R Jürgen

    2010-09-21

    The electrochemical adsorption of underpotential deposited hydrogen (upd-H(ad)) and OH(ad) on structurally well-defined Pt(x)Ru(1-x)/Ru(0001) surface alloys was investigated by cyclic voltammetry and density functional theory (DFT) calculations. The adsorption energies of both upd-H(ad) and OH(ad) decrease with increasing Pt content in the adsorption ensemble, shifting the onset of upd-H(ad) and OH(ad) formation to increasingly cathodic and anodic potentials, respectively. For bare Ru(0001) and for Ru(3) sites in the surface alloy, the stability regions of these two species overlap or almost overlap, respectively. Similar to previous findings for upd-H(ad) adsorption/desorption on partly Pt monolayer island covered Ru(0001) surfaces (J. Phys. Chem. B 2004, 108, 14780), we find a sharp peak at approximately 100 mV vs. RHE in each scan direction, which is attributed to a Pt catalyzed OH(ad) upd-H(ad) replacement on Ru(3) sites, via adsorption on Pt rich sites and spill-over to Ru(3) sites. The decrease of the integrated charge in these peaks with the third power of the Ru surface concentration, which for a random distribution of surface atoms reflects the availability of Ru(3) sites, supports the above assignment.

  3. Micro-area Chemical Composition and Preserved P-T Evolution Trace of Phengite in Albite Gneiss from the Donghai Ultrahigh-Pressure Metamorphic Area, East China

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    Study of micro-area chemical compositions indicates that phengite in albite gneiss from hole ZK2304 of the Donghai region has evident compositional zoning. SiO2 and tetrahedrally coordinated Si contents decrease, and Al2O3, AlIV and AlVI contents increase gradually from core to rim. However, K2O, MgO and FeO contents basically remain unchanged from core to rim. According to P-T estimates obtained from geothermometers and barometers, combined with previous experimental data, the core belt (micro-area I) of phengite was formed at T=637- 672° C and P=1.55- 1.73 GPa, and the transitional belt (micro-area II) of the phengite were formed at T=594- 654° C and P=1.35- 1.45 GPa. Towards the rim belt (micro-area III), the temperature decreased slightly, but the pressure decreased rapidly with T=542- 630° C and P=1.12- 1.19 GPa. The P-T evolution path recorded by the compositional zoning of phengite is characterized by significant near-isothermal decompression, revealing that the gneiss has undergone high-pressure-ultrahigh-pressure metamorphism. The compositional zoning of the phengite in the albite gneiss may have formed in the geodynamic process of rapid exhumation in the Sulu ultrahigh-pressure metamorphic belt.

  4. Sulfur deactivation mechanism of Pt/MnOx-CeO2 for soot oxidation: Surface property study

    Science.gov (United States)

    Zhang, Hailong; Hou, Zhongyan; Zhu, Yi; Wang, Jianli; Chen, Yaoqiang

    2017-02-01

    In this work, an advanced diffuse reflectance infrared fourier transform spectra (DRIFTS) technology is used to describe the formation of surface sulfates on Pt/MnOx-CeO2 and study the possible deactivation mechanism for soot oxidation reactions in NO + O2. IR spectra of CO adsorption and H2-TPR results reveal the surface coverage of Pt by sulfates and the loss of partial active oxygen species after the sulfation, respectively. More importantly, in situ DRIRT spectra show sulfur poisoning apparently inhibits the formation of surface intermediates such as monodentate/bidentate nitrates and nitro species, which directly limits the production of NO2. Furthermore, the O2-TPD results indicate that the sulfation weakens the desorption of surface active oxygen resulting from the decomposition of surface nitrates. The sulfate formation would affect the production of oxygen vacant sites and thereby the mobility of surface oxygen species in both NO + O2 and O2. These factors above would play an important role on the deactivation mechanism for soot oxidation.

  5. Accessible surface area from NMR chemical shifts

    Energy Technology Data Exchange (ETDEWEB)

    Hafsa, Noor E.; Arndt, David; Wishart, David S., E-mail: david.wishart@ualberta.ca [University of Alberta, Department of Computing Science (Canada)

    2015-07-15

    Accessible surface area (ASA) is the surface area of an atom, amino acid or biomolecule that is exposed to solvent. The calculation of a molecule’s ASA requires three-dimensional coordinate data and the use of a “rolling ball” algorithm to both define and calculate the ASA. For polymers such as proteins, the ASA for individual amino acids is closely related to the hydrophobicity of the amino acid as well as its local secondary and tertiary structure. For proteins, ASA is a structural descriptor that can often be as informative as secondary structure. Consequently there has been considerable effort over the past two decades to try to predict ASA from protein sequence data and to use ASA information (derived from chemical modification studies) as a structure constraint. Recently it has become evident that protein chemical shifts are also sensitive to ASA. Given the potential utility of ASA estimates as structural constraints for NMR we decided to explore this relationship further. Using machine learning techniques (specifically a boosted tree regression model) we developed an algorithm called “ShiftASA” that combines chemical-shift and sequence derived features to accurately estimate per-residue fractional ASA values of water-soluble proteins. This method showed a correlation coefficient between predicted and experimental values of 0.79 when evaluated on a set of 65 independent test proteins, which was an 8.2 % improvement over the next best performing (sequence-only) method. On a separate test set of 92 proteins, ShiftASA reported a mean correlation coefficient of 0.82, which was 12.3 % better than the next best performing method. ShiftASA is available as a web server ( http://shiftasa.wishartlab.com http://shiftasa.wishartlab.com ) for submitting input queries for fractional ASA calculation.

  6. Oxidation mechanism of formic acid on the bismuth adatom-modified Pt(111) surface.

    Science.gov (United States)

    Perales-Rondón, Juan Victor; Ferre-Vilaplana, Adolfo; Feliu, Juan M; Herrero, Enrique

    2014-09-24

    In order to improve catalytic processes, elucidation of reaction mechanisms is essential. Here, supported by a combination of experimental and computational results, the oxidation mechanism of formic acid on Pt(111) electrodes modified by the incorporation of bismuth adatoms is revealed. In the proposed model, formic acid is first physisorbed on bismuth and then deprotonated and chemisorbed in formate form, also on bismuth, from which configuration the C-H bond is cleaved, on a neighbor Pt site, yielding CO2. It was found computationally that the activation energy for the C-H bond cleavage step is negligible, which was also verified experimentally.

  7. CoPt alloy grown on the WSe 2(0 0 0 1) van der Waals surface

    Science.gov (United States)

    Makarov, D.; Liscio, F.; Brombacher, C.; Simon, J. P.; Schatz, G.; Maret, M.; Albrecht, M.

    The structural and magnetic properties of 3-nm-thick CoPt alloys grown on WSe 2(0 0 0 1) at various temperature are investigated. Deposition at room temperature leads to the formation of a chemically disordered fcc CoPt alloy with [1 1 1] orientation. Growth at elevated temperatures induces L1 0 chemical order starting at 470 K accompanied with an increase in grain size and a change in grain morphology. As a consequence of the [1 1 1] growth direction, the CoPt grains can adopt one of the three possible variants of the L1 0 phase with tetragonal c-axis tilted from the normal to the film plane direction at 54°. The average long-range order parameter is found to be 0.35(±0.05) and does not change with the increase in the deposition temperature from 570 to 730 K. This behavior might be related to Se segregation towards the growing facets and surface disorder effects promoted by a high surface-to-volume ratio. Magnetic studies reveal a superparamagnetic behavior for the films grown at 570 and 730 K in agreement with the film morphology and degree of chemical order. The measurements at 10 K reveal the orientation of the easy axis of the magnetization lying basically in the film plane.

  8. CoPt alloy grown on the WSe{sub 2}(0 0 0 1) van der Waals surface

    Energy Technology Data Exchange (ETDEWEB)

    Makarov, D. [Department of Physics, University of Konstanz, D-78457 Konstanz (Germany)], E-mail: denys.makarov@uni-konstanz.de; Liscio, F. [SIMAP, INP Grenoble-CNRS-UJF, 1130 rue de la Piscine, BP 75, 38402 Saint Martin d' Heres (France); Brombacher, C. [Department of Physics, University of Konstanz, D-78457 Konstanz (Germany); Institute of Physics, Chemnitz University of Technology, D-09107 Chemnitz (Germany); Simon, J.P. [SIMAP, INP Grenoble-CNRS-UJF, 1130 rue de la Piscine, BP 75, 38402 Saint Martin d' Heres (France); Schatz, G. [Department of Physics, University of Konstanz, D-78457 Konstanz (Germany); Maret, M. [SIMAP, INP Grenoble-CNRS-UJF, 1130 rue de la Piscine, BP 75, 38402 Saint Martin d' Heres (France); Albrecht, M. [Department of Physics, University of Konstanz, D-78457 Konstanz (Germany); Institute of Physics, Chemnitz University of Technology, D-09107 Chemnitz (Germany)

    2008-06-15

    The structural and magnetic properties of 3-nm-thick CoPt alloys grown on WSe{sub 2}(0 0 0 1) at various temperature are investigated. Deposition at room temperature leads to the formation of a chemically disordered fcc CoPt alloy with [1 1 1] orientation. Growth at elevated temperatures induces L1{sub 0} chemical order starting at 470 K accompanied with an increase in grain size and a change in grain morphology. As a consequence of the [1 1 1] growth direction, the CoPt grains can adopt one of the three possible variants of the L1{sub 0} phase with tetragonal c-axis tilted from the normal to the film plane direction at 54 deg. The average long-range order parameter is found to be 0.35({+-}0.05) and does not change with the increase in the deposition temperature from 570 to 730 K. This behavior might be related to Se segregation towards the growing facets and surface disorder effects promoted by a high surface-to-volume ratio. Magnetic studies reveal a superparamagnetic behavior for the films grown at 570 and 730 K in agreement with the film morphology and degree of chemical order. The measurements at 10 K reveal the orientation of the easy axis of the magnetization lying basically in the film plane.

  9. Observation of unusual topological surface states in half-Heusler compounds LnPtBi (Ln=Lu, Y).

    Science.gov (United States)

    Liu, Z K; Yang, L X; Wu, S-C; Shekhar, C; Jiang, J; Yang, H F; Zhang, Y; Mo, S-K; Hussain, Z; Yan, B; Felser, C; Chen, Y L

    2016-09-27

    Topological quantum materials represent a new class of matter with both exotic physical phenomena and novel application potentials. Many Heusler compounds, which exhibit rich emergent properties such as unusual magnetism, superconductivity and heavy fermion behaviour, have been predicted to host non-trivial topological electronic structures. The coexistence of topological order and other unusual properties makes Heusler materials ideal platform to search for new topological quantum phases (such as quantum anomalous Hall insulator and topological superconductor). By carrying out angle-resolved photoemission spectroscopy and ab initio calculations on rare-earth half-Heusler compounds LnPtBi (Ln=Lu, Y), we directly observe the unusual topological surface states on these materials, establishing them as first members with non-trivial topological electronic structure in this class of materials. Moreover, as LnPtBi compounds are non-centrosymmetric superconductors, our discovery further highlights them as promising candidates of topological superconductors.

  10. Mesoporous Pt and Pt/Ru alloy electrocatalysts for methanol oxidation

    Energy Technology Data Exchange (ETDEWEB)

    Franceschini, Esteban A. [Grupo de Celdas de Combustible, Departamento de Fisica de la Materia Condensada, Centro Atomico Constituyentes, CNEA. Av. General Paz 1499 (1650), San Martin, Buenos Aires (Argentina); Planes, Gabriel A. [Departamento de Quimica, Facultad de Ciencias Exactas, Fisicoquimicas y Naturales, Universidad Nacional de Rio Cuarto, Agencia Postal No 3, 5800, Rio Cuarto (Argentina); Williams, Federico J. [Departamento de Quimica Inorganica, Analitica y Quimica-Fisica, INQUIMAE CONICET, Facultad Ciencias Exactas y Naturales, Pabellon 2, Ciudad Universitaria, Buenos Aires (Argentina); Soler-Illia, Galo J.A.A. [Gerencia de Quimica, Centro Atomico Constituyentes, CNEA. Av. General Paz 1499 (1650), San Martin, Buenos Aires (Argentina); Corti, Horacio R. [Grupo de Celdas de Combustible, Departamento de Fisica de la Materia Condensada, Centro Atomico Constituyentes, CNEA. Av. General Paz 1499 (1650), San Martin, Buenos Aires (Argentina); Departamento de Quimica Inorganica, Analitica y Quimica-Fisica, INQUIMAE CONICET, Facultad Ciencias Exactas y Naturales, Pabellon 2, Ciudad Universitaria, Buenos Aires (Argentina)

    2011-02-15

    Mesoporous Pt and Pt/Ru catalysts with 2D-hexagonal mesostructure were synthesized using a triblock poly(ethylene oxide)-b-poly(propylene oxide)-b-poly(ethylene oxide) copolymer (Pluronic F127 {sup registered}) template, on a gold support. Large electrochemical surface areas were observed for the catalysts prepared at high overpotentials. Compared to the Pt catalyst, the Pt/Ru alloy containing 3 at% of Ru exhibited lower onset potential and more than three times the limit mass activity for methanol oxidation. This behavior is assigned to the larger pore size of the mesoporous Pt and Pt/Ru catalysts obtained with this template that seems to improve the methanol accessibility to the active sites compared to those obtained using lyotropic liquid crystals. (author)

  11. Hawaii ESI: CASS_PT (Coral Areas of Special Significance - Points)

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — This data set contains sensitive biological resource data for Coral Areas of Special Significance in coastal Hawaii. Coral Areas of Special Significance were...

  12. Investigation of the oxygen exchange mechanism on Pt|yttria stabilized zirconia at intermediate temperatures: Surface path versus bulk path

    Science.gov (United States)

    Opitz, Alexander K.; Lutz, Alexander; Kubicek, Markus; Kubel, Frank; Hutter, Herbert; Fleig, Jürgen

    2011-01-01

    The oxygen exchange kinetics of platinum on yttria-stabilized zirconia (YSZ) was investigated by means of geometrically well-defined Pt microelectrodes. By variation of electrode size and temperature it was possible to separate two temperature regimes with different geometry dependencies of the polarization resistance. At higher temperatures (550–700 °C) an elementary step located close to the three phase boundary (TPB) with an activation energy of ∼1.6 eV was identified as rate limiting. At lower temperatures (300–400 °C) the rate limiting elementary step is related to the electrode area and exhibited a very low activation energy in the order of 0.2 eV. From these observations two parallel pathways for electrochemical oxygen exchange are concluded. The nature of these two elementary steps is discussed in terms of equivalent circuits. Two combinations of parallel rate limiting reaction steps are found to explain the observed geometry dependencies: (i) Diffusion through an impurity phase at the TPB in parallel to diffusion of oxygen through platinum – most likely along Pt grain boundaries – as area-related process. (ii) Co-limitation of oxygen diffusion along the Pt|YSZ interface and charge transfer at the interface with a short decay length of the corresponding transmission line (as TPB-related process) in parallel to oxygen diffusion through platinum. PMID:22210951

  13. Investigation of the oxygen exchange mechanism on Pt|yttria stabilized zirconia at intermediate temperatures: Surface path versus bulk path.

    Science.gov (United States)

    Opitz, Alexander K; Lutz, Alexander; Kubicek, Markus; Kubel, Frank; Hutter, Herbert; Fleig, Jürgen

    2011-11-30

    The oxygen exchange kinetics of platinum on yttria-stabilized zirconia (YSZ) was investigated by means of geometrically well-defined Pt microelectrodes. By variation of electrode size and temperature it was possible to separate two temperature regimes with different geometry dependencies of the polarization resistance. At higher temperatures (550-700 °C) an elementary step located close to the three phase boundary (TPB) with an activation energy of ∼1.6 eV was identified as rate limiting. At lower temperatures (300-400 °C) the rate limiting elementary step is related to the electrode area and exhibited a very low activation energy in the order of 0.2 eV. From these observations two parallel pathways for electrochemical oxygen exchange are concluded.The nature of these two elementary steps is discussed in terms of equivalent circuits. Two combinations of parallel rate limiting reaction steps are found to explain the observed geometry dependencies: (i) Diffusion through an impurity phase at the TPB in parallel to diffusion of oxygen through platinum - most likely along Pt grain boundaries - as area-related process. (ii) Co-limitation of oxygen diffusion along the Pt|YSZ interface and charge transfer at the interface with a short decay length of the corresponding transmission line (as TPB-related process) in parallel to oxygen diffusion through platinum.

  14. Mitigation of CO Poisoning on Functionalized Pt/TiN(001) Surface: A Fundamental Study of the Next-Generation Fuel Cell Technologies

    Science.gov (United States)

    2014-05-27

    TiN(100) surface (Pt/TiN) could be a promising catalyst for proton exchange membrane fuel cells (PEM FCs). The adsorption properties of molecules on Pt...theory, proton exchange membrane , proton exchange membrane 16. SECURITY CLASSIFICATION OF: 17. LIMITATION OF ABSTRACT SAR 18. NUMBER OF PAGES 3 19a...system of embedding single Ptatom in the N-vacancy site on TiN(100) surface (Pt/TiN) could be a promising catalyst for proton exchange membrane fuel

  15. CO Adsorption on Co(0001-Supported Pt Overlayers

    Directory of Open Access Journals (Sweden)

    N. J. Castellani

    2001-11-01

    Full Text Available The growth of Pt deposits on Co(0001 was followed by STM and XPS. The chemical reactivity of the resulting surface was checked by CO adsorption. Pt grows as dendritic islands on the Co terraces whereas forming stripes at the Co step edges. Annealing the sample has no apparent effect on the STM pictures. However, XPS suggests that a limited dilution of Pt in Co takes place. The adsorption of CO on the surface is drastically affected by the presence of Pt even for minute traces. The adsorption energy on the Pt areas is decreased by 40 %. The maximum coverage on the Co areas is also decreased. This indicates that Pt impurities diluted in Co have a high passivating power as a consequence of the induced electronic changes.

  16. Alkyl chain length-dependent surface reaction of dodecahydro-N-alkylcarbazoles on Pt model catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Gleichweit, Christoph; Amende, Max; Bauer, Udo; Schernich, Stefan; Höfert, Oliver; Lorenz, Michael P. A.; Zhao, Wei; Bachmann, Philipp; Papp, Christian, E-mail: christian.papp@fau.de [Lehrstuhl für Physikalische Chemie II, Friedrich-Alexander-Universität Erlangen-Nürnberg, Egerlandstrasse 3, 91058 Erlangen (Germany); Müller, Michael; Koch, Marcus [Lehrstuhl für Chemische Reaktionstechnik, Friedrich-Alexander-Universität Erlangen-Nürnberg, Egerlandstrasse 3, 91058 Erlangen (Germany); Wasserscheid, Peter [Lehrstuhl für Chemische Reaktionstechnik, Friedrich-Alexander-Universität Erlangen-Nürnberg, Egerlandstrasse 3, 91058 Erlangen (Germany); Erlangen Catalysis Resource Center, Friedrich-Alexander-Universität Erlangen-Nürnberg, Egerlandstrasse 3, 91058 Erlangen (Germany); Libuda, Jörg; Steinrück, Hans-Peter [Lehrstuhl für Physikalische Chemie II, Friedrich-Alexander-Universität Erlangen-Nürnberg, Egerlandstrasse 3, 91058 Erlangen (Germany); Erlangen Catalysis Resource Center, Friedrich-Alexander-Universität Erlangen-Nürnberg, Egerlandstrasse 3, 91058 Erlangen (Germany)

    2014-05-28

    The concept of liquid organic hydrogen carriers (LOHC) holds the potential for large scale chemical storage of hydrogen at ambient conditions. Herein, we compare the dehydrogenation and decomposition of three alkylated carbazole-based LOHCs, dodecahydro-N-ethylcarbazole (H{sub 12}-NEC), dodecahydro-N-propylcarbazole (H{sub 12}-NPC), and dodecahydro-N-butylcarbazole (H{sub 12}-NBC), on Pt(111) and on Al{sub 2}O{sub 3}-supported Pt nanoparticles. We follow the thermal evolution of these systems quantitatively by in situ high-resolution X-ray photoelectron spectroscopy. We show that on Pt(111) the relevant reaction steps are not affected by the different alkyl substituents: for all LOHCs, stepwise dehydrogenation to NEC, NPC, and NBC is followed by cleavage of the C–N bond of the alkyl chain starting at 380–390 K. On Pt/Al{sub 2}O{sub 3}, we discern dealkylation on defect sites already at 350 K, and on ordered, (111)-like facets at 390 K. The dealkylation process at the defects is most pronounced for NEC and least pronounced for NBC.

  17. Aplikasi Data Pelanggan Berbasis Java dan Mobile pada PT. PLN (Persero Area Semarang

    Directory of Open Access Journals (Sweden)

    Rizaldi Habibie

    2016-01-01

    Full Text Available In modern times, like today, the role of software or applications that run on top of the platform is very important. This is because almost all of the work done by the people, made by the software or application. Applications can be used to assist in the processing of data and upload the final report. Data recorded previously processed by the paper can be recorded and processed by the application so that more efficiently. PT. PLN (Persero Semarang District State electricity company has many customers in the city of Semarang. Customer data belonging to this company has not been processed in digital form. This causes the data of regular visits undertaken are not directly connected with customer data, owned so inefficient and requires a long process in the course of the report. Thus, it takes an application that can help in the treatment of customer data, data of visited consumer, and generate reports . Customer data Java-based and mobile applications for PLN (Persero Semarang District State intended for the treatment of customer data, data of visited connsumer and generate reports. The application consists of two application. The first applications developed using the programming language Java, which can run on the operating system Windows. The second application was designed and implemented using the framework ionic, which can run on the Android operating system. This application uses MySQL as a database management system, which is used for data storage media.

  18. First-principles studies on the adsorption of S on the Pt skin Pt3 Ni(1 1 1)surface%S在Pt皮肤Pt3 Ni(111)面吸附的第一性原理研究

    Institute of Scientific and Technical Information of China (English)

    张喜林; 殷岩; 李沙沙; 张岩星; 路战胜; 杨宗献

    2014-01-01

    The adsorption properties of S on the Pt skin Pt3Ni(111)surface are studied by first-principles calculations.It is found that S prefer to occupy the fcc site of Pt3Ni(111)surface with a very big adsorp-tion energy (5.49 eV).More importantly,the interaction of the sulfur with Pt surface would reduce up-on the alloy of the Pt and Ni,comparing with that of the pure Pt surface.The electronic structure analy-sis showed that the catalytic effect of Pt-based catalysts reduced is caused by 2p electron of S,and it would be shrinked from the Ni doping.The current results provide a basis for further study the active sites of Pt3Ni(111)surface with adsorbed sulfur.%采用基于密度泛函理论的第一性原理方法,计算并分析了 S原子在 Pt皮肤Pt3 Ni(111)面不同位置的吸附特性.结果表明:S原子在Pt皮肤Pt3 Ni的 fcc位吸附最强,吸附能为5.49 eV;与 S原子在纯净的Pt(111)表面吸附相比较,S原子在Pt皮肤Pt3 Ni(111)面相应吸附位置的吸附能变小,与近邻 Pt原子形成的 S-Pt键变长,表明掺杂的 Ni 会减小相应位点 S 原子的吸附能,降低体系对 S 原子的吸附能力,进而减弱S吸附对体系催化能力的影响;态密度分析发现,S原子的吸附使得Pt基催化剂的催化活性降低,主要是 S的2 p电子引起的;这些结果将为后续研究 Pt基合金电极抗 S中毒效果以及探究 S原子吸附后Pt3 Ni的活性位提供依据.

  19. Enhanced Electrocatalytic Activity of Pt/3D Hierarchical Bimodal Macroporous Carbon Nanospheres.

    Science.gov (United States)

    Balgis, Ratna; Widiyastuti, W; Ogi, Takashi; Okuyama, Kikuo

    2017-07-19

    Proton exchange membrane fuel cells require electrocatalysts with a high platinum (Pt) loading, large active surface area, and favorable hydrodynamic profile for practical applications. Here, we report the design of three-dimensional hierarchical bimodal macroporous carbon nanospheres with an interconnected pore system, which are applied as an electrocatalyst support. Carbon-supported Pt (Pt/C) catalysts were prepared by aerosol spray pyrolysis followed by microwave chemical deposition. The hierarchical porous structures not only increased the dispersion of Pt nanoparticles but also improved catalytic performance. A hierarchical bimodal macroporous Pt/C catalyst with a mixture of 30 and 120 nm size pores showed the best performance. The electrochemical surface area and mass activity values of this support were 96 m(2) g(-1)-Pt and 378 mA mg(-1)-Pt, respectively at a Pt loading of 15 wt %.

  20. Surface acoustic load sensing using a face-shear PIN-PMN-PT single-crystal resonator.

    Science.gov (United States)

    Kim, Kyungrim; Zhang, Shujun; Jiang, Xiaoning

    2012-11-01

    Pb(In(0.5)Nb(0.5))O(3)-Pb(Mg(1/3)Nb(2/3))O(3)-PbTiO(3) (PIN-PMN-PT) resonators for surface acoustic load sensing are presented in this paper. Different acoustic loads are applied to thickness mode, thickness-shear mode, and face-shear mode resonators, and the electrical impedances at resonance and anti-resonance frequencies are recorded. More than one order of magnitude higher sensitivity (ratio of electrical impedance change to surface acoustic impedance change) at the resonance is achieved for the face-shear-mode resonator compared with other resonators with the same dimensions. The Krimholtz, Leedom, and Matthaei (KLM) model is used to verify the surface acoustic loading effect on the electrical impedance spectrum of face-shear PIN-PMN-PT single-crystal resonators. The demonstrated high sensitivity of face-shear mode resonators to surface loads is promising for a broad range of applications, including artificial skin, biological and chemical sensors, touch screens, and other touch-based sensors.

  1. Long-lasting oscillations in the electro-oxidation of formic acid on PtSn intermetallic surfaces.

    Science.gov (United States)

    Perini, Nickson; Batista, Bruno C; Angelo, Antonio C D; Epstein, Irving R; Varela, Hamilton

    2014-06-23

    Even when in contact with virtually infinite reservoirs, natural and manmade oscillators typically drift in phase space on a time-scale considerably slower than that of the intrinsic oscillator. A ubiquitous example is the inexorable aging process experienced by all living systems. Typical electrocatalytic reactions under oscillatory conditions oscillate for only a few dozen stable cycles due to slow surface poisoning that ultimately results in destruction of the limit cycle. We report the observation of unprecedented long-lasting temporal oscillations in the electro-oxidation of formic acid on an ordered intermetallic PtSn phase. The introduction of Sn substantially increases the catalytic activity and retards the irreversible surface oxidation, which results in the stabilization of more than 2200 oscillatory cycles in about 40 h; a 30-40-fold stabilization with respect to the behavior of pure Pt surfaces. The dynamics were modeled and numerical simulations point to the surface processes underlying the high stability. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  2. Surface noble metal modified PdM/C (M = Ru, Pt, Au) as anode catalysts for direct ethanol fuel cells

    Energy Technology Data Exchange (ETDEWEB)

    Mao, Han; Huang, Tao, E-mail: huangt@fudan.edu.cn; Yu, Aishui, E-mail: asyu@fudan.edu.cn

    2016-08-15

    In this article, we studied the surface noble metal modification on Pd nanoparticles, other than the homogeneous or core-shell structure. The surface modification will lead to the uneven constitution within the nanoparticles and thus more obvious optimization effect toward the catalyst brought by the lattice deformation. The surface of the as-prepared Pd nanoparticles was modified with Ru, Pt or Au by a moderate and green approach, respectively. XPS results confirm the interactive electron effects between Pd and the modified noble metal. Electrochemical measurements show that the surface noble metal modified catalysts not only show higher catalytic activity, but also better stability and durability. The PdM/C catalysts all exhibit good dispersion and very little agglomeration after long-term potential cycles toward ethanol oxidation. With only 10% metallic atomic ratio of Au, PdAu/C catalyst shows extraordinary catalytic activity and stability, the peak current reaches 1700 mA mg{sup −1} Pd, about 2.5 times that of Pd/C. Moreover, the PdAu/C maintains 40% of the catalytic activity after 4500 potential cycles. - Highlights: • Pd-based catalysts with complicated exposed facets. • Much enhanced electrocatalytic activity and stability with about 10% noble metal M (M = Ru, Pt, Au) on Pd nanoparticles. • The outstanding electrocatalytic performance of PdAu/C towards ethanol oxidation after the Au modification.

  3. Body surface area formulae: an alarming ambiguity.

    Science.gov (United States)

    Redlarski, Grzegorz; Palkowski, Aleksander; Krawczuk, Marek

    2016-06-21

    Body surface area (BSA) plays a key role in several medical fields, including cancer chemotherapy, transplantology, burn treatment and toxicology. BSA is often a major factor in the determination of the course of treatment and drug dosage. A series of formulae to simplify the process have been developed. Because easy-to-identify, yet general, body coefficient results of those formulae vary considerably, the question arises as to whether the choice of a particular formula is valid and safe for patients. Here we show that discrepancies between most of the known BSA formulae can reach 0.5 m(2) for the standard adult physique. Although many previous studies have demonstrated that certain BSA formulae provide an almost exact fit with the patients examined, all of these studies have been performed on a limited and isolated group of people. Our analysis presents a broader perspective, considering 25 BSA formulae. The analysis revealed that the choice of a particular formula is a difficult task. Differences among calculations made by the formulae are so great that, in certain cases, they may considerably affect patients' mortality, especially for people with an abnormal physique or for children.

  4. Casimir effect in dielectrics Surface area contribution

    CERN Document Server

    Molina-Paris, C; Molina-Paris, Carmen; Visser, Matt

    1997-01-01

    In this paper we take a deeper look at the technically elementary but physically robust viewpoint in which the Casimir energy in dielectric media is interpreted as the change in the total zero point energy of the electromagnetic vacuum summed over all states. Extending results presented in previous papers [hep-th/9609195; hep-th/9702007] we approximate the sum over states by an integral over the density of states including finite volume corrections. For an arbitrarily-shaped finite dielectric, the first finite-volume correction to the density of states is shown to be proportional to the surface area of the dielectric interface and is explicitly evaluated as a function of the permeability and permitivity. Since these calculations are founded in an elementary and straightforward way on the underlying physics of the Casimir effect they serve as an important consistency check on field-theoretic calculations. As a concrete example we discuss Schwinger's suggestion that the Casimir effect might be the underlying ph...

  5. Large-area patterning of sub-100 nm epitaxial L10 FePt dots array via nanoimprint lithography

    Directory of Open Access Journals (Sweden)

    Zheng Li

    2015-08-01

    Full Text Available Bit-patterned media, a promising candidate for next generation high density magnetic recording, requires sub-100 nm dots array on a wafer scale, a high degree of patterning control of the size distribution, and a material with high perpendicular anisotropy. In this work, large area (0.75 cm × 0.75 cm dots array was achieved by nanoimprint lithography and ion milling from L10 FePt thin films that are pre-sputtered at 450 °C with both high crystalline quality and good chemical order. The sub-100 nm dots are decoupled from each other and show both narrow size distributions and high coercivity values on the order of 11 kOe. Our work would cast light for the application of bit-patterned media.

  6. Method for treatment of a surface area of steel

    NARCIS (Netherlands)

    Bhowmik, S.; Aaldert, P.J.

    2009-01-01

    The invention relates to a method for treatment of a surface area of steel by polishing said surface area and performing a plasma treatment of said surface area wherein the plasma treatment is performed at at least atmospheric conditions and wherein the plasma treatment is carried out at a power of

  7. In Situ Surface-Enhanced Raman Spectroscopy Study of the Electrocatalytic Effect of PtFe/C Nanocatalyst on Ethanol Electro-Oxidation in Alkaline Medium

    Directory of Open Access Journals (Sweden)

    A. C. Gómez-Monsiváis

    2017-03-01

    Full Text Available Currently, the ethanol electro-oxidation reaction has attracted considerable attention in fuel cells because of new green ethanol synthetic methods based on biomass processes that have emerged. In this study, PtFe/C and Pt/C nanoparticles were synthesized by a chemical reduction method and tested in the ethanol electro-oxidation reaction. Furthermore, the electrocatalytic effect of the PtFe bimetallic catalyst was analyzed by in situ surface-enhanced Raman spectroscopy (SERS coupled to an electrochemical cell. X-ray diffractograms showed typical face-centered cubic structures with crystallite sizes of 3.31 and 3.94 for Pt/C and PtFe/C, respectively. TEM micrographs revealed nanoparticle sizes of 2 ± 0.4 nm and 3 ± 0.6 nm for Pt/C and PtFe/C respectively. PtFe/C exhibited a Pt90Fe10 composition by both X-ray fluorescence and energy-dispersive X-ray spectroscopy. A better electrocatalytic activity as function of concentration was obtained through the incorporation of a small amount of Fe into the Pt lattice and the presence of Fe2+/Fe3+ (observed by X-ray photoelectron spectroscopy. According to SERS experiments, the presence of these iron species promotes the chemisorption of ethanol, the formation of formic acid as main product and renewal of the catalytic sites, resulting in current densities that were at least three fold higher than the values obtained for the Pt/C nanocatalyst.

  8. Atomically flat surface of (0 0 1) textured FePt thin films by residual stress control

    Science.gov (United States)

    Liu, S. H.; Hsiao, S. N.; Chou, C. L.; Chen, S. K.; Lee, H. Y.

    2015-11-01

    Single-layered Fe52Pt48 films with thickness of 10 nm were sputter-deposited on glass substrates. Rapid thermal annealing with different heating rates (10-110 K/s) was applied to transform as-deposited fcc phase into L10 phase and meanwhile to align [0 0 1]-axis of L10 crystal along plane normal direction. Based on X-ray diffractometry using synchrotron radiation source, the texture coefficient of (0 0 1)-plane increases with increasing heating rate from 10 to 40 K/s, which is correlated with perpendicular magnetic anisotropy and in-plane tensile stress analyzed by asymmetric sin2 ψ method. Furthermore, it was revealed by atomic force microscopy that the dewetting process occurred as heating rate was raised up to 80 K/s and higher. The change in the microstructure due to stress relaxation leads to the degradation of (0 0 1) orientation and magnetic properties. Surface roughness is closely related to the in-plane tensile stress. Enhanced perpendicular magnetic anisotropy and atomically flat surface were achieved for the samples annealed at 40 K/s, which may be suitable for further practical applications. This work also suggests a feasible way for surface engineering by controlling internal stress of the FePt without introducing cap layer.

  9. Understanding the growth mechanism of carbon nanotubes via the ``cluster volume to surface area" model

    Science.gov (United States)

    Mandati, Sreekanth; Kunstmann, Jens; Boerrnert, Felix; Schoenfelder, Ronny; Ruemmeli, Mark; Kar, Kamal K.; Cuniberti, Gianaurelio

    2010-03-01

    The influence of mixed catalysts for the high yield production of carbon nanotubes (CNTs) has been studied systematically. Based on extensive experimental data a ``Catalyst Volume to Surface Area'' (CVSA) model was developed to understand the influence of the process parameters on the yield and CNT diameter distribution [1]. In our study, we present a refined version of the CVSA model developed by combining experiments and simulations. We discuss our current understanding of the growth mechanism and how the model might be used to increase CNT yields by using mixed catalysts.[4pt] [1] S. Tetali et al., ACS Nano (2009), DOI: 10.1021/nn9012548.

  10. Electro-oxidation of ethanol on ternary non-alloyed Pt-Sn-Pr/C catalysts

    Science.gov (United States)

    Corradini, Patricia G.; Antolini, Ermete; Perez, Joelma

    2015-02-01

    Ternary Pt-Sn-Pr/C (70:10:20), (70:15:15) and (45:45:10) electro-catalysts were prepared by a modified formic acid method, and their activity for the ethanol oxidation reaction (EOR) was compared with that of Pt-Pr/C catalysts prepared by the same methods and that of commercial Pt-Sn/C (75:25) and Pt/C catalysts. Among all the catalysts, the Pt-Sn-Pr/C (45:45:10) catalyst presented both the highest mass activity and the highest specific activity. The steady state electrochemical stability of ternary Pt-Sn-Pr catalysts increased with the surface Sn/Pt atomic ratio. Following repetitive potential cycling (RPC), the activity for ethanol oxidation of Pt-Sn-Pr/C catalysts with high surface Sn/Pt atomic ratio was considerably higher than that of the corresponding as-prepared catalysts, and increased with increasing the Sn/Pt ratio. The increase of the EOR mass activity following RPC was ascribed to the increase of either the specific activity (for the Pt-Sn-Pr/C (70:15:15) catalyst) or the electrochemically active surface area (for the Pt-Sn-Pr/C (45:45:10) catalyst). Dissolution of Sn and Pr oxides from Pt-Sn-Pr/C catalyst surface was observed following RPC.

  11. Pd-Pt bimetallic nanodendrites with high activity for oxygen reduction.

    Science.gov (United States)

    Lim, Byungkwon; Jiang, Majiong; Camargo, Pedro H C; Cho, Eun Chul; Tao, Jing; Lu, Xianmao; Zhu, Yimei; Xia, Younan

    2009-06-05

    Controlling the morphology of Pt nanostructures can provide a great opportunity to improve their catalytic properties and increase their activity on a mass basis. We synthesized Pd-Pt bimetallic nanodendrites consisting of a dense array of Pt branches on a Pd core by reducing K2PtCl4 with L-ascorbic acid in the presence of uniform Pd nanocrystal seeds in an aqueous solution. The Pt branches supported on faceted Pd nanocrystals exhibited relatively large surface areas and particularly active facets toward the oxygen reduction reaction (ORR), the rate-determining step in a proton-exchange membrane fuel cell. The Pd-Pt nanodendrites were two and a half times more active on the basis of equivalent Pt mass for the ORR than the state-of-the-art Pt/C catalyst and five times more active than the first-generation supportless Pt-black catalyst.

  12. Self-assembling behaviour of Pt nanoparticles onto surface of TiO2 and their resulting photocatalytic activity

    Indian Academy of Sciences (India)

    M Qamar; Ashok K Ganguli

    2013-11-01

    In the present study, self-assembling behaviour of guest nanoparticles (platinum) onto the surface of host support (titanium dioxide) during photodeposition process as a function of solution pH has been explored in detail by means of transmission electron microscope (TEM). The photocatalytic activity of the resulting bimetallic nanoassembly (Pt/TiO2) was evaluated by studying the degradation of two organic pollutants viz. triclopyr and methyl orange. Microscopic studies revealed that the deposition and/or distribution of Pt nanoparticles onto the surface of TiO2 were strongly guided by the ionization state of support which in turn was regulated by the solution pH of photodeposition process. A direct relationship between the solution pH of deposition process and the photocatalytic activity of resulting bimetallic catalyst has been observed. A mechanism based on the interparticle interaction between TiO2 and hydrolytic products of metal ions has been proposed for the differences in the photocatalytic activity of the resulting nanocomposite.

  13. 30 CFR 56.17001 - Illumination of surface working areas.

    Science.gov (United States)

    2010-07-01

    ... 30 Mineral Resources 1 2010-07-01 2010-07-01 false Illumination of surface working areas. 56.17001... NONMETAL MINE SAFETY AND HEALTH SAFETY AND HEALTH STANDARDS-SURFACE METAL AND NONMETAL MINES Illumination § 56.17001 Illumination of surface working areas. Illumination sufficient to provide safe...

  14. PLD prepared nanostructured Pt-CeO2 thin films containing ionic platinum

    Science.gov (United States)

    Vorokhta, M.; Khalakhan, I.; Matolínová, I.; Nováková, J.; Haviar, S.; Lančok, J.; Novotný, M.; Yoshikawa, H.; Matolín, V.

    2017-02-01

    The composition of nanostructured Pt-CeO2 films on graphite substrates prepared by pulsed laser deposition has been investigated by means of hard X-ray photoelectron spectroscopy, scanning electron microscopy, high resolution transmission electron microscopy, and atomic force microscopy. The influence of morphology of the graphite substrates was investigated with respect to the relative concentrations of ionic and metallic Pt species in the films. It was found that the degree of Pt2+ enrichment is directly related to the surface morphology of graphite substrates. In particular, the deposition of Pt-CeO2 films on rough graphite substrate etched in oxygen plasma yielded nanostructured Pt-CeO2 catalyst films with high surface area and high Pt2+/Pt0 ratio. The presented results demonstrate that PLD is a suitable method for the preparation of thin Pt-CeO2 catalyst films for fuel cell applications.

  15. Investigation of oxygen reduction and methanol oxidation reaction activity of PtAu nano-alloy on surface modified porous hybrid nanocarbon supports

    Science.gov (United States)

    Parambath Vinayan, Bhaghavathi; Nagar, Rupali; Ramaprabhu, Sundara

    2016-09-01

    We investigate the electrocatalytic activity of PtAu alloy nanoparticles supported on various chemically modified carbon morphologies towards oxygen reduction reaction (ORR) and methanol oxidation reaction (MOR). The surface-modification of graphene nanosheets (f-G), multi-walled carbon nanotubes (f-MWNTs) and (graphene nanosheets-carbon nanotubes) hybrid support (f-G-MWNTs) were carried out by soft functionalization method using a cationic polyelectrolyte poly-(diallyldimethyl ammonium chloride). The Pt and PtAu alloy nanoparticles were dispersed over chemically modified carbon supports by sodium-borohydride assisted modified polyol reduction method. The electrochemical performance of all electrocatalysts were studied by half- and full-cell proton exchange membrane fuel cell (PEMFC) measurements and PtAu/f-G-MWNTs catalyst comparatively yielded the best catalytic performance. PEMFC full cell measurements of PtAu/f-G-MWNTs cathode electrocatalyst yield a maximum power density of 319 mW cm-2 at 60 °C without any back pressure,which is 2.1 times higher than that of cathode electrocatalyst Pt on graphene support. The high ORR and MOR activity of PtAu/f-G-MWNTs electrocatalyst is due to the alloying effect and inherent beneficial properties of porous hybrid nanocarbon support.

  16. Adsorption and ring-opening of lactide on the chiral metal surface Pt(321){sup S} studied by density functional theory

    Energy Technology Data Exchange (ETDEWEB)

    Franke, J.-H.; Kosov, D. S. [Department of Physics, Campus Plaine - CP 231, Universite Libre de Bruxelles, 1050 Brussels (Belgium)

    2015-01-28

    We study the adsorption and ring-opening of lactide on the naturally chiral metal surface Pt(321){sup S}. Lactide is a precursor for polylactic acid ring-opening polymerization, and Pt is a well known catalyst surface. We study, here, the energetics of the ring-opening of lactide on a surface that has a high density of kink atoms. These sites are expected to be present on a realistic Pt surface and show enhanced catalytic activity. The use of a naturally chiral surface also enables us to study potential chiral selectivity effects of the reaction at the same time. Using density functional theory with a functional that includes the van der Waals forces in a first-principles manner, we find modest adsorption energies of around 1.4 eV for the pristine molecule and different ring-opened states. The energy barrier to be overcome in the ring-opening reaction is found to be very small at 0.32 eV and 0.30 eV for LL- and its chiral partner DD-lactide, respectively. These energies are much smaller than the activation energy for a dehydrogenation reaction of 0.78 eV. Our results thus indicate that (a) ring-opening reactions of lactide on Pt(321) can be expected already at very low temperatures, and Pt might be a very effective catalyst for this reaction; (b) the ring-opening reaction rate shows noticeable enantioselectivity.

  17. CoPt and FePt magnetic alloys grown on van der Waals WSe{sub 2}(0001) surfaces and on arrays of SiO{sub 2} spherical particles

    Energy Technology Data Exchange (ETDEWEB)

    Makarov, Denys

    2008-06-06

    Modern magnetic recording is based on usage of hard magnetic alloys as a recording media. In order to increase the areal storage density (number of stored bits per square inch), materials with a high value of magnetic anisotropy are required to stabilize the direction of the magnetization and thus satisfy the criteria of thermal stability. The magnetic alloy currently used for hard disk drive production is a granular CoCrPt:SiO2 alloy with a grain size of approximately 7 nm and an anisotropy constant of about 0.4 MJ/m{sup 3}. However, the predicted limit of the highest achievable areal density of this type of granular media is 500-600 Gbit/in{sup 2}. To satisfy the demand of higher densities, new magnetic alloys have to be introduced. The most promising candidates for future ultra-high density magnetic recording applications are chemically L10 ordered FePt and CoPt alloys with anisotropy constants of about 10 MJ/m{sup 3} and 3 MJ/m{sup 3}, respectively. In order to obtain a high value of uniaxial magnetic anisotropy, the substrate temperature during molecular beam epitaxy or sputtering deposition has to be higher than 500 C. For practical use in industrial applications the ordering temperature of the FePt and CoPt alloys has to be reduced. One of the promising approaches to reduce the ordering temperature is related to the enhancement of the adatom mobility by growing the alloy on the chemically saturated surface. In this regard an attempt to reduce the ordering temperature of the CoPt alloy with equiatomic composition was performed in the scope of present work by growing the CoPt alloy on van der Waals WSe{sub 2}(0001) substrates. Moreover, an increase in data density can be gained using the concept of patterned media, where an information unit (bit) is stored in a single nanostructure. The most attractive way to produce patterned magnetic media for ultra-high density magnetic recording applications is based on self-assembly of the magnetic nanostructures. In this

  18. SurfaceWater Source Protection Areas (SPAs)

    Data.gov (United States)

    Vermont Center for Geographic Information — Source Protection Area (SPA) boundaries have been located on RF 24000 & RF 25000 scale USGS topographic maps by Water Supply Division (DEC) and VT Dept of Health...

  19. Immobilization of superoxide dismutase on Pt-Pd/MWCNTs hybrid modified electrode surface for superoxide anion detection.

    Science.gov (United States)

    Zhu, Xiang; Niu, Xiangheng; Zhao, Hongli; Tang, Jie; Lan, Minbo

    2015-05-15

    Monitoring of reactive oxygen species like superoxide anion (O2(∙-)) turns to be of increasing significance considering their potential damages to organism. In the present work, we fabricated a novel O2(∙-) electrochemical sensor through immobilizing superoxide dismutase (SOD) onto a Pt-Pd/MWCNTs hybrid modified electrode surface. The Pt-Pd/MWCNTs hybrid was synthesized via a facile one-step alcohol-reduction process, and well characterized by transmission electron microscopy, X-ray photoelectron spectroscopy and X-ray diffraction. The immobilization of SOD was accomplished using a simple drop-casting method, and the performance of the assembled enzyme-based sensor for O2(∙-) detection was systematically investigated by several electrochemcial techniques. Thanks to the specific biocatalysis of SOD towards O2(∙-) and the Pt-Pd/MWCNTs - promoted fast electron transfer at the fabricated interface, the developed biosensor exhibits a fast, selective and linear amperometric response upon O2(∙-) in the concentration scope of 40-1550 μM (R(2)=0.9941), with a sensitivity of 0.601 mA cm(-2) mM(-1) and a detection limit of 0.71 μM (S/N=3). In addition, the favorable biocompatibility of this electrode interface endows the prepared biosensor with excellent long-term stability (a sensitivity loss of only 3% over a period of 30 days). It is promising that the proposed sensor will be utilized as an effective tool to quantitatively monitor the dynamic changes of O2(∙-) in biological systems.

  20. Faraday efficiency and mechanism of electrochemical surface reactions: CO2 reduction and H2 formation on Pt(111).

    Science.gov (United States)

    Hussain, Javed; Jónsson, Hannes; Skúlason, Egill

    2016-12-22

    An atomic scale model of the electrical double layer is used to calculate the mechanism and rate of electrochemical reduction of CO2 as well as H2 formation at a Pt(111) electrode. The water layer contains solvated protons and the electrode has excess electrons at the surface. Density functional theory within the generalized gradient approximation is used to describe the electronic structure while the mechanism and activation energy of the various elementary reactions is obtained by calculating minimum energy paths using the nudged elastic band method. The applied electrical potential is deduced from the calculated work function. The optimal reaction mechanism for CO2 reduction to either methane or methanol is found and the estimated rate compared with that of the competing reaction, H2 formation. When the free energy of only the intermediates and reactants is taken into account, not the activation energy, Pt(111) would seem to be a good electrocatalyst for CO2 reduction, significantly better than Cu(111). This, however, contradicts experimental findings. Detailed calculations reported here show that the activation energy for CO2 reduction is high for both Heyrovsky and Tafel mechanisms on Pt(111) in the relevant range of applied potential. The rate-limiting step of the Heyrovsky mechanism, *COOH + H(+) + e(-) → *CO + H2O, is estimated to have an activation energy of 0.95 eV at -0.9 V vs. standard hydrogen electrode. Under the same conditions, the activation energy for H2 formation is estimated to be only 0.5 eV. This explains why attempts to reduce CO2 using platinum electrodes have produced only H2. A comparison is made with analogous results for Cu(111) [J. Hussain et al., Procedia Comput. Sci., 2015, 51, 1865] where a reaction mechanism with low activation energy for CO2 electroreduction to methane was identified. The difference between the two electrocatalysts is discussed.

  1. Interaction of oxygen and carbon monoxide with Pt(111) at intermediate pressure and temperature : revisiting the fruit fly of surface science

    NARCIS (Netherlands)

    Bashlakov, Dmytro

    2014-01-01

    This thesis uses the surface science approach to address questions regarding the interaction of oxygen with platinum and its subsequent reaction with carbon monoxide. A Pt(111) single crystal surface is used as a model for the catalyst. Chapter 1 provides an overview of the literature on the

  2. Sediment Surface Areas, Organic Content, and Metal Fractionation of Point Mugu Sediments

    Science.gov (United States)

    Becerra, C. A.; Wong, N.; Khachikian, C. S.

    2002-12-01

    Point Mugu contains one of the largest coastal wetlands ecosystems in California, which includes a Naval Air station, several sewage oxidation ponds and a partly dredged lagoon. Remediation efforts include investigating the feasibility of using the present sewage pond sludge to restore a dredged area in the lagoon. A problem with this approach is the potential release and subsequent environmental impact of the toxic substances from the sludge. Contaminants may become unavailable once sorbed onto particles. In general, this process is a direct function of surface area and organic carbon sorbed onto the sediment. The goal of the current investigation is to provide insight into the biological availability of a suite of metal contaminants in Pt. Mugu marsh sediments by studying changes in the physical and chemical properties of the sediments at horizontal and vertical spatial scales. The surface area and organic carbon for eight cores were measured as well as the first three sequential extraction of a host of metals. We have found that a direct correlation exists between surface area and the organic content of sediments as a function of depth. Surface area and the amount of organic carbon decreases with depth, which could result in higher availability of metals with increasing depth into the sediments.

  3. On semiautomatic estimation of surface area

    DEFF Research Database (Denmark)

    Dvorak, J.; Jensen, Eva B. Vedel

    2013-01-01

    . For convex particles, the estimator is equal to four times the area of the support set (flower set) of the particle transect. We study the statistical properties of the flower estimator and compare its performance to that of two discretizations of the flower estimator, namely the pivotal estimator...

  4. The Surface Chemical Properties of Novel High Surface Area Solids ...

    African Journals Online (AJOL)

    and MFA3 are the result of the high chromium content in the original ash (UFA1). ... ties has a significant influence on the crystal form produced during zeolite ... that the surface is enriched in Si compared with the bulk compo- sition. This is ...

  5. Growth and properties of electrodeposited cobalt films on Pt/Si(1 0 0) surface

    Energy Technology Data Exchange (ETDEWEB)

    Azizi, A.; Sahari, A.; Felloussia, M.L.; Schmerber, G.; Meny, C.; Dinia, A

    2004-04-30

    In this paper, the growth, structural and magnetic properties of cobalt (Co) films electrodeposited on a Pt/Si(1 0 0) substrate have been investigated. Co films with metallic appearance were obtained from aqueous solution of 0.1 M CoSO{sub 4}, 10 mM CoCl{sub 2} as the source of metal ions and 1 M Na{sub 2}SO{sub 4} as a supporting electrolyte with 0.5 M H{sub 3}BO{sub 3} at pH 4.2. This electrochemical technique indicated a deposition peak signature of limited diffusion growth with the transition from progressive to instantaneous nucleation mechanism. The atomic force microscopy (AFM) images showed a granular structure of the electrodeposited layers. X-ray measurements (XRD) and nuclear magnetic resonance (NMR) indicate a small grain size with the presence of a mixture of Co hcp and fcc structures. The magnetic properties of the deposited films were investigated with a magnetic field in the parallel and perpendicular direction and showed that the easy magnetization axis is in the plane.

  6. Why Do We Need the Derivative for the Surface Area?

    Science.gov (United States)

    Hristova, Yulia; Zeytuncu, Yunus E.

    2016-01-01

    Surface area and volume computations are the most common applications of integration in calculus books. When computing the surface area of a solid of revolution, students are usually told to use the frustum method instead of the disc method; however, a rigorous explanation is rarely provided. In this note, we provide one by using geometric…

  7. 30 CFR 57.17001 - Illumination of surface working areas.

    Science.gov (United States)

    2010-07-01

    ... 30 Mineral Resources 1 2010-07-01 2010-07-01 false Illumination of surface working areas. 57.17001 Section 57.17001 Mineral Resources MINE SAFETY AND HEALTH ADMINISTRATION, DEPARTMENT OF LABOR METAL AND... Illumination § 57.17001 Illumination of surface working areas. Illumination sufficient to provide safe...

  8. Pt nanoparticles embedded on reduced graphite oxide with excellent electrocatalytic properties

    Energy Technology Data Exchange (ETDEWEB)

    Saravanan, Gengan, E-mail: saravanan3che@gmail.com [Central University of Tamil Nadu, Department of Chemistry, Thiruvarur, 610101 (India); Mohan, Subramanian, E-mail: sanjnamohan@yahoo.com [EMFT Division, CSIR-Central Electrochemical Research Institute, Tamilnadu, Karaikudi 630 006 (India)

    2016-11-15

    Graphical abstract: RGO/Nano Pt: This study explore the electrocatalytic oxidation performance of reduced graphite oxide (RGO) anchored with nano Pt. This graphene composite reveal superior electrooxidation performance that is associated with the flexible RGO matrix and the uniform distribution of Pt particles, which enhances surface area, fast electron transfer, uniform particle size distribution; consequently, the RGO matrix provides more stability to Pt particles during electrooxidation process. Display Omitted - Highlights: • Greener electrochemical method applied to prepare well-dispersed Pt-rGO. • Pt-rGO large surface area excellent charge transfer better catalytic activity. • Low-cost highly efficient carbon-based electrodes for direct formic acid fuel cell. • rGO an excellent support to anchor Pt nanoparticles on its surface. • Pt-rGO distinctly enhanced current density towards formic acid electrooxidation. - Abstract: Economically viable electrochemical approach has been developed for the synthesis of Pt nanoparticles through electrodeposition technique on the surface of Reduced Graphite Oxide (RGO). Pt nanoparticles embedded Reduced Graphite Oxide on Glassy Carbon Electrode are employed (Pt-rGO/GCE) for electrooxidation of formic acid. Scanning Electron Microscopy (SEM) image and Transmission Electron Microscopy (TEM) image shows that reduced graphite oxide act as an excellent support to anchor the Pt nanoparticles. Cyclic voltammetry results confirmed that Pt-rGO/GCE enhanced current density as many folds than that of bare platinum electrode for electrooxidation of formic acid. X-ray diffraction (XRD) patterns for Pt-graphene composites illustrate that peaks at 69.15 and 23° for Pt (220) and graphene carbon (002) respectively. {sup 13}C NMR spectrum of the electrochemically reduced graphite oxide resonance contains only one peak at 133 ppm which retains graphitic sp{sup 2} carbon and does not contain any oxygenated carbon and the carbonyl

  9. 77 FR 50165 - Escape and Evacuation Plans for Surface Coal Mines, Surface Facilities and Surface Work Areas of...

    Science.gov (United States)

    2012-08-20

    ... Administration. Title: Escape and Evacuation Plans for Surface Coal Mines, Surface Facilities ] and Surface Work... Safety and Health Administration Escape and Evacuation Plans for Surface Coal Mines, Surface Facilities and Surface Work Areas of Underground Coal Mines AGENCY: Mine Safety and Health Administration,...

  10. Potential-dependent water orientation on Pt(1 1 1) stepped surfaces from laser-pulsed experiments

    Energy Technology Data Exchange (ETDEWEB)

    Garcia-Araez, Nuria [Instituto de Electroquimica, Universidad de Alicante, Ap. 99, E-03080 Alicante (Spain); Climent, Victor [Instituto de Electroquimica, Universidad de Alicante, Ap. 99, E-03080 Alicante (Spain)], E-mail: victor.climent@ua.es; Feliu, Juan M. [Instituto de Electroquimica, Universidad de Alicante, Ap. 99, E-03080 Alicante (Spain)

    2009-01-01

    Coulostatic potential transients induced by nanosecond pulsed laser irradiation on Pt(1 1 1) stepped surfaces in perchloric acid solutions are analyzed here. The results provide unique information on the effect of the structure of the metal surface on the potential-dependent water reorientation at the electrified interphase. The most significant information is obtained from the sign and shape of the laser-induced transients. The existence of two potentials where the transient is zero can be related to the local properties of the surface, i.e. the existence of two local potentials of zero free charge, corresponding to the step and terrace sites. The dependency of these quantities with the step density is studied in detail. In addition, it is found that the presence of steps significantly slows down the coulostatic response at potentials in the double-layer region, which has been interpreted as a decrease in the velocity of water reorganization. The corresponding relaxation time is estimated and its dependency with the step density is also analyzed.

  11. Pt deposition on carbon paper and Ti mesh substrates by surface limited redox replacement

    CSIR Research Space (South Africa)

    Modibedi, M

    2011-12-01

    Full Text Available paper and Ti mesh substrates by Surface Limited Redox Replacement MMALEWANE MODIBEDI mmodibedi@csir.co.za AFRICA MRS 2011, Victoria Falls Outline ? CSIR 2011 www.csir.co.za ? Rationale ? Electrochemical atomic layer...

  12. Indexing aortic valve area by body surface area increases the prevalence of severe aortic stenosis

    DEFF Research Database (Denmark)

    Jander, Nikolaus; Gohlke-Bärwolf, Christa; Bahlmann, Edda

    2014-01-01

    To account for differences in body size in patients with aortic stenosis, aortic valve area (AVA) is divided by body surface area (BSA) to calculate indexed AVA (AVAindex). Cut-off values for severe stenosis are......To account for differences in body size in patients with aortic stenosis, aortic valve area (AVA) is divided by body surface area (BSA) to calculate indexed AVA (AVAindex). Cut-off values for severe stenosis are...

  13. Electrochemical properties of mixed WC and Pt-black powders

    Directory of Open Access Journals (Sweden)

    MAJA D. OBRADOVIC

    2008-12-01

    Full Text Available The electrochemical characteristics of a mixture of Pt-black and WC powders and its catalytic activity for methanol and formic acid oxidation were investigated in acid solution. XRD and AFM measurements revealed that the WC powder employed for the investigation was a single-phase material consisting of crystallites/spherical particles of average size of about 50 nm, which were agglomerated into much larger particles. Cyclic voltammetry showed that the WC underwent electrochemical oxidation, producing tungstate species. In the case of the mixed Pt + WC powders, the tungstate species were deposited on the Pt as a thin film of hydrous tungsten oxide. Enhanced hydrogen intercalation in the hydrous tungsten oxide was observed and it was proposed to be promoted in mixed powders by the presence of hydrogen adatoms on bare Pt sites. The determination of Pt surface area in the Pt + WC layer by stripping of underpotentially deposited Cu revealed that the entire Pt surface was accessible for underpotential deposition of Cu. Investigation of the electrochemical oxidation of methanol and formic acid on Pt + WC and pure Pt layers did not indicate electrocatalytic promotion due to the presence of WC.

  14. Radiolytic Preparation of Electrocatalysts with Pt-Co and Pt-Sn Nanoparticles for a Proton Exchange Membrane Fuel Cell

    Directory of Open Access Journals (Sweden)

    Sang Kyum Kim

    2014-01-01

    Full Text Available Nanosized Pt-Sn/VC and Pt-Co/VC electrocatalysts were prepared by a one-step radiation-induced reduction (30 kGy process using distilled water as the solvent and Vulcan XC72 as the supporting material. While the Pt-Co/VC electrodes were compared with Pt/VC (40 wt%, HiSpec 4000, in terms of their electrocatalytic activity towards the oxidation of H2, the Pt-Co/VC electrodes were evaluated in terms of their activity towards the hydrogen oxidation reaction (HOR and compared with Pt/VC (40 wt%, HiSpec 4000, Pt-Co/VC, and Pt-Sn/VC in a single cell. Additionally, the prepared electrocatalyst samples (Pt-Co/VC and Pt-Sn/VC were characterized by transmission electron microscopy (TEM, scanning electron microscope (SEM, thermogravimetric analysis (TGA, X-ray diffraction (XRD, X-ray photoelectron spectroscopy (XPS, electrochemical surface area (ECSA, and fuel cell polarization performance.

  15. Tuning Surface Structure and Strain in Pd-Pt Core-Shell Nanocrystals for Enhanced Electrocatalytic Oxygen Reduction.

    Science.gov (United States)

    Xiong, Yalin; Shan, Hao; Zhou, Zhengnan; Yan, Yucong; Chen, Wenlong; Yang, Yaxiong; Liu, Yongfeng; Tian, He; Wu, Jianbo; Zhang, Hui; Yang, Deren

    2017-02-01

    Icosahedral, octahedral, and cubic Pd@Pt core-shell nanocrystals with two atomic Pt layers are epitaxially generated under thermodynamic control. Such icosahedra exhibit remarkably enhanced catalytic properties for oxygen reduction reaction compared to the octahedra and cubes as well as commercial Pt/C, which can be attributed to ligand and geometry effects, especially twin-induced strain effect that is revealed by geometrical phase analysis. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  16. Propane combustion over Pt/Al{sub 2}O{sub 3} catalysts with different crystalline structures of alumina

    Energy Technology Data Exchange (ETDEWEB)

    Park, Jung Eun; Kim, Bo Bae; Park, Eun Duck [Ajou University, Suwon (Korea, Republic of)

    2015-11-15

    The effects of the crystalline phases (α-Al{sub 2}O{sub 3}, κ-Al{sub 2}O{sub 3}, δ-Al{sub 2}O{sub 3}, θ-Al{sub 2}O{sub 3}, η-Al{sub 2}O{sub 3}, and γ-Al{sub 2}O{sub 3}) of the alumina support of Pt/Al{sub 2}O{sub 3} catalysts on the catalyst activity toward propane combustion were examined. The catalysts were characterized by N{sub 2} physisorption, CO chemisorption, temperature-programmed reduction (TPR), temperature programmed oxidation (TPO), transmission electron microscopy (TEM), and infrared spectroscopy (IR) after CO chemisorption. The Pt dispersion of the catalysts (surface Pt atoms/total Pt atoms), measured via CO chemisorption, was more dependent on the crystalline structure of alumina than on the surface area of alumina. The highest catalytic activity for propane combustion was achieved with Pt/α-Al{sub 2}O{sub 3}, which has the lowest Brunauer, Emmett, and Teller (BET) surface area and Pt dispersion. The lowest catalytic activity for propane combustion was exhibited by Pt/γ-Al{sub 2}O{sub 3}, which has the highest BET surface area and Pt dispersion. The catalytic activity was confirmed to increase with increasing Pt particle size in Pt/δ-Al{sub 2}O{sub 3}. The apparent activation energies for propane combustion over Pt/α-Al{sub 2}O{sub 3}, Pt/κ- Al{sub 2}O{sub 3}, Pt/δ-Al{sub 2}O{sub 3}, Pt/θ-Al{sub 2}O{sub 3}, Pt/η-Al{sub 2}O{sub 3}, and Pt/γ-Al{sub 2}O{sub 3} were determined to be 24.7, 21.4, 24.3, 22.1, 24.0, and 19.1 kcal/mol, respectively.

  17. Pengaruh Kompensasi dan Disiplin Kerja Terhadap Semangat Kerja serta Dampaknya Terhadap Kinerja Karyawan Pada PT. Graha Sarana Duta Area I Sumatera

    OpenAIRE

    Okta, Mila Asmawiani

    2013-01-01

    The performance of employees is the main factor for a company to achieve the goal of organization. The many factors influencing the performance of employees, the ones analyzed in this study were compensation, work discipline, and work spirit. The purpose of this empirical study was to test the influence of compensation and work discipline on the performance of the employees of PT. Graha Sarana Duta Area I Sumatera with work spirit as the intervening variable. The theory used in this study ...

  18. EFFECT OF PRETREATMENT ON PT-CO/C CATHODE CATALYSTS FOR THE OXYGEN-REDUCTION REACTION

    Energy Technology Data Exchange (ETDEWEB)

    Fox, E.; Colon-Mercado, H.

    2010-01-19

    Carbon supported Pt and Pt-Co electrocatalysts for the oxygen reduction reaction in low temperature fuel cells were prepared by the reduction of the metal salts with sodium borohydride and sodium formate. The effect of surface treatment with nitric acid on the carbon surface and Co on the surface of carbon prior to the deposition of Pt was studied. The catalysts where Pt was deposited on treated carbon the ORR reaction preceded more through the two electron pathway and favored peroxide production, while the fresh carbon catalysts proceeded more through the four electron pathway to complete the oxygen reduction reaction. NaCOOH reduced Pt/C catalysts showed higher activity that NaBH{sub 4} reduced Pt/C catalysts. It was determined that the Co addition has a higher impact on catalyst activity and active surface area when used with NaBH{sub 4} as reducing agent as compared to NaCOOH.

  19. MOISTURE AND SURFACE AREA MEASUREMENTS OF PLUTONIUM-BEARING OXIDES

    Energy Technology Data Exchange (ETDEWEB)

    Crowder, M.; Duffey, J.; Livingston, R.; Scogin, J.; Kessinger, G.; Almond, P.

    2009-09-28

    To ensure safe storage, plutonium-bearing oxides are stabilized at 950 C for at least two hours in an oxidizing atmosphere. Stabilization conditions are expected to decompose organic impurities, convert metals to oxides, and result in moisture content below 0.5 wt%. During stabilization, the specific surface area is reduced, which minimizes readsorption of water onto the oxide surface. Plutonium oxides stabilized according to these criteria were sampled and analyzed to determine moisture content and surface area. In addition, samples were leached in water to identify water-soluble chloride impurity content. Results of these analyses for seven samples showed that the stabilization process produced low moisture materials (< 0.2 wt %) with low surface area ({le} 1 m{sup 2}/g). For relatively pure materials, the amount of water per unit surface area corresponded to 1.5 to 3.5 molecular layers of water. For materials with chloride content > 360 ppm, the calculated amount of water per unit surface area increased with chloride content, indicating hydration of hygroscopic salts present in the impure PuO{sub 2}-containing materials. The low moisture, low surface area materials in this study did not generate detectable hydrogen during storage of four or more years.

  20. Metal nanostructures with complex surface morphology: The case of supported lumpy Pd and Pt nanoparticles produced by laser processing of metal films

    Science.gov (United States)

    Ruffino, F.; Maugeri, P.; Cacciato, G.; Zimbone, M.; Grimaldi, M. G.

    2016-09-01

    In this work we report on the formation of lumpy Pd and Pt nanoparticles on fluorine-doped tin oxide/glass (FTO/glass) substrate by a laser-based approach. In general, complex-surface morphology metal nanoparticles can be used in several technological applications exploiting the peculiarities of their physical properties as modulated by nanoscale morphology. For example plasmonic metal nanoparticles presenting a lumpy morphology (i.e. larger particles coated on the surface by smaller particles) can be used in plasmonic solar cell devices providing broadband scattering enhancement over the smooth nanoparticles leading, so, to the increase of the device efficiency. However, the use of plasmonic lumpy nanoparticles remains largely unexplored due to the lack of simply, versatile, low-cost and high-throughput methods for the controllable production of such nanostructures. Starting from these considerations, we report on the observation that nanoscale-thick Pd and Pt films (17.6 and 27.9 nm, 12.1 and 19.5 nm, respectively) deposited on FTO/glass surface irradiated by nanosecond pulsed laser at fluences E in the 0.5-1.5 J/cm2 range, produce Pd and Pt lumpy nanoparticles on the FTO surface. In addition, using scanning electron microscopy analyses, we report on the observation that starting from each metal film of fixed thickness h, the fraction F of lumpy nanoparticles increases with the laser fluence E and saturates at the higher fluences. For each fixed fluence, F was found higher starting from the Pt films (at each starting film thickness h) with respect to the Pd films. For each fixed metal and fluence, F was found to be higher decreasing the starting thickness of the deposited film. To explain the formation of the lumpy Pd and Pt nanoparticles and the behavior of F as a function of E and h both for Pd and Pt, the thermodynamic behavior of the Pd and Pt films and nanoparticles due to the interaction with the nanosecond laser is discussed. In particular, the

  1. The surface morphologies of (Pb, Sr) TiO3 thin film fabricated on Si-buffered Pt/Ti/SiO2/Si substrate

    Institute of Scientific and Technical Information of China (English)

    2005-01-01

    (Pb, Sr)TiO3 (PST) thin film are fabricated by RF magnetron sputtering on Si-buffered Pt/Ti/SiO2/Si substrates with different buffer layer deposition time. Surface morphologies of the buffer layer indicate an improving surface roughness and larger grains with the prolongation of sputtering time. Deposition of PST thin films shows excellent surface fluctuation filling ability to improve the surface roughness of substrates. PST surface morphologies exhibit apparently different grain forms according to the preparation time durance of buffer layer.

  2. The Electrochemical Development of Pt(111 Stepped Surfaces and Its Influence on Methanol Electrooxidation

    Directory of Open Access Journals (Sweden)

    E. Teliz

    2011-01-01

    Full Text Available The progress in the preparation of new electrode surfaces by electrochemical treatments exhibiting high faradaic efficiencies towards industrial electrocatalytic processes has gained more attention in today's scientific community. Most of the papers report new catalysts dispersed on different substrates, but some fundamental studies required for electrochemical and physical characterizations are sometimes forgotten. In this paper, we make a full staging of two electrochemical treatments that can be conducted to enhance the electrocatalytic activity of platinum surfaces, such as, electrofacetting through square wave potential programs and constant cathodic polarizations in the net hydrogen evolution region. The cathodic treatment applied at −2 V clearly develops (111 stepped planes similarly to the electrofacetting performed after applying the square wave program between 1.40 V and 0.70 V at 2.5 kHz. The X-ray diffraction patterns of both surfaces as well as on other electrofacetted platinum electrodes are obtained for comparison purposes. Moreover, the electrocatalytic activity towards methanol electrooxidation also exhibits equivalent coulombic efficiencies and 200% higher than on polycrystalline platinum as demonstrated by linear sweep voltammetry and potentiostatic current decays.

  3. High pressure organic colloid method for the preparation of high performance carbon nanotube-supported Pt and PtRu catalysts for fuel cell applications

    Institute of Scientific and Technical Information of China (English)

    WANG; KateNing; Viola; BIRSS

    2010-01-01

    Highly dispersed,high performance Pt and PtRu catalysts,supported on multiwalled carbon nanotubes(CNTs),were prepared by a high pressure organic colloid method.The particle sizes of the active components were as small as 1.2 nm for Pt and 1.1 nm for PtRu,and the active Pt surface areas were 295 and 395 m2/g,respectively.The catalysts showed very high activities toward the anodic oxidation of methanol,evaluated by cyclic voltammetry,being up to 4 times higher than that of commercial Johnson Matthey Hispec 2000 Pt/XC-72R and 5 times better than Hispec 5000 PtRu/XC-72R catalysts.In a full air/hydrogen fuel cell,a membrane-electrode assembly prepared using our Pt/CNT and PtRu/CNT catalysts showed 50% and 100% higher performances than those prepared with commercial Johnson Matthey Pt/XC-72R and PtRu/XC-72R catalysts for the same Pt loading and operating conditions.

  4. Adsorption of halide anions at the Pt(111)-solution interface studied by {bold {ital in situ}} surface x-ray scattering

    Energy Technology Data Exchange (ETDEWEB)

    Lucas, C.A.; Markovic, N.M.; Ross, P.N. [Materials Sciences Division, Lawrence Berkeley National Laboratory, University of California, Berkeley, California 94720 (United States)

    1997-03-01

    In this paper we present x-ray scattering results of iodide, bromide, and chloride adsorption onto the Pt(111) surface in solution. Iodide forms two commensurate adlayer structures, a ({radical}(7){times}{radical}(7))R19.1{degree} phase and a hexagonal (3{times}3) phase, which coexist on the Pt surface. Formation of the (3{times}3) phase appears to be kinetically limited, whereas the {radical}(7) phase shows a hysteretic effect as a function of the electrode potential, associated with an order-disorder transition. Bromide forms a series of high-order commensurate structures on Pt(111) that are poorly ordered unless the size of the unit cell is small. No ordered structures for chloride adsorption are observed and specular x-ray reflectivity results suggest that the chloride coverage at low potential is too small to form a close-packed monolayer on the surface. The differences between the structures formed by the adsorbed anions, and the differences between results for Pt(111) and Au(111), are discussed in terms of the strength of the metal-halide interaction. {copyright} {ital 1997} {ital The American Physical Society}

  5. Some Inequalities for Lp-mixed Affine Surface Area

    Institute of Scientific and Technical Information of China (English)

    ZHU Xian-yang

    2012-01-01

    In this paper,the concepts of the ith Lp-mixed affine surface area and Lp-polar curvature images are introduced,some new inequalities connecting these new notions with Lp-centroid bodies and p-Blaschke bodies are showed.Moreover,a Blaschke-Santaló type inequality for Lp-mixed affine surface area is established.Our results also imply the similar to the inequalities for Marcus-Lopes,Bergstrom and Ky Fan.

  6. High surface area carbon and process for its production

    Science.gov (United States)

    Romanos, Jimmy; Burress, Jacob; Pfeifer, Peter; Rash, Tyler; Shah, Parag; Suppes, Galen

    2016-12-13

    Activated carbon materials and methods of producing and using activated carbon materials are provided. In particular, biomass-derived activated carbon materials and processes of producing the activated carbon materials with prespecified surface areas and pore size distributions are provided. Activated carbon materials with preselected high specific surface areas, porosities, sub-nm (carbon consumption and metallic potassium intercalation into the carbon lattice during the activation process.

  7. Derivation of the liquidus surface projection for the Al-Pt-Ru system from as-cast samples

    CSIR Research Space (South Africa)

    Prins, SN

    2005-11-10

    Full Text Available .% platinum. Most of the other phases showed more limited solubilities for the ternary element: similar to RuAl2, similar to Pt2Al3 and similar to PtAl contained only about 2at.% of the third component similar to Ru 4Al13 has less than 1at.% solubility...

  8. High temperature polymer electrolyte membrane fuel cell performance of Pt xCo y/C cathodes

    Science.gov (United States)

    Rao, Ch. Venkateswara; Parrondo, Javier; Ghatty, Sundara L.; Rambabu, B.

    Carbon-supported Pt-Co alloy nanoparticles of varying Pt:Co atomic ratios of 1:1, 2:1, 3:1 and 4:1 are prepared, characterized and tested in high temperature PEM fuel cell intend to reduce the Pt loading. These electrocatalysts are prepared by borohydride reduction method in the presence of citric acid as stabilizing agent. Face-centered cubic structure of Pt is evident from XRD. The positive shift of Pt diffraction peaks with increasing cobalt content in the Pt xCo y/C catalysts indicated the solubility of Co in Pt lattice. The average crystallite size is found to be 6 nm in all the prepared catalysts. The electrochemical active surface area (EAS) of the catalysts from CO-stripping voltammetry is calculated to be 65.2, 51.4, 47.7, 41.5 and 38.3 m 2 g -1 Pt for Pt/C, Pt-Co(4:1)/C, Pt-Co(3:1)/C, Pt-Co(2:1)/C and Pt-Co(1:1)/C, respectively. These catalysts are used as cathode in the fabrication of polybenzimidazole-based membrane electrode assembly (MEA) and the polarization curves are recorded at 160 and 180 °C. The results indicate the good performance of Pt-Co alloys than that of Pt under the PEM fuel cell conditions. Among the investigated electrocatalysts, Pt-Co(1:1)/C and Pt-Co(2:1)/C exhibited good fuel cell performance. Durability tests also indicated the good stability of Pt-Co(1:1)/C and Pt-Co(2:1)/C compared to Pt/C.

  9. Determination of Reactive Surface Area of Melt Glass

    Energy Technology Data Exchange (ETDEWEB)

    Bourcier,W.L.; Roberts, S.; Smith, D.K.; Hulsey, S.; Newton,L.; Sawvel, A.; Bruton, C.; Papelis, C.; Um, W.; Russell, C. E.; Chapman,J.

    2000-10-01

    A comprehensive investigation of natural and manmade silicate glasses, and nuclear melt glass was undertaken in order to derive an estimate of glass reactive surface area. Reactive surface area is needed to model release rates of radionuclides from nuclear melt glass in the subsurface. Because of the limited availability of nuclear melt glasses, natural volcanic glass samples were collected which had similar textures and compositions as those of melt glass. A flow-through reactor was used to measure the reactive surface area of the analog glasses in the presence of simplified NTS site ground waters. A measure of the physical surface area of these glasses was obtained using the BET gas-adsorption method. The studies on analog glasses were supplemented by measurement of the surface areas of pieces of actual melt glass using the BET method. The variability of the results reflect the sample preparation and measurement techniques used, as well as textural heterogeneity inherent to these samples. Based on measurements of analog and actual samples, it is recommended that the hydraulic source term calculations employ a range of 0.001 to 0.01 m{sup 2}/g for the reactive surface area of nuclear melt glass.

  10. CCD surface photometry of radio galaxies: Pt. 1. FR class I and II sources

    Energy Technology Data Exchange (ETDEWEB)

    Owen, F.N.; Laing, R.A.

    1989-05-01

    CCD surface photometry of 47 radio galaxies in the R-band is reported. The goal of the programme is to study the relationship of the properties of the parent galaxies to the radio structure and, in particular, to look for differences between Fanaroff and Riley (FR) class I and II sources. In order to clarify some ambiguous cases in the FR classification, we define Classical Double, Twin Jet and Fat Double sources. We describe our definitions of these three classes and their relation to the FR classification. (author).

  11. Quantifying object and material surface areas in residences

    Energy Technology Data Exchange (ETDEWEB)

    Hodgson, Alfred T.; Ming, Katherine Y.; Singer, Brett C.

    2005-01-05

    The dynamic behavior of volatile organic compounds (VOCs) in indoor environments depends, in part, on sorptive interactions between VOCs in the gas phase and material surfaces. Since information on the types and quantities of interior material surfaces is not generally available, this pilot-scale study was conducted in occupied residences to develop and demonstrate a method for quantifying surface areas of objects and materials in rooms. Access to 33 rooms in nine residences consisting of bathrooms, bedroom/offices and common areas was solicited from among research group members living in the East San Francisco Bay Area. A systematic approach was implemented for measuring rooms and objects from 300 cm{sup 2} and larger. The ventilated air volumes of the rooms were estimated and surface area-to-volume ratios were calculated for objects and materials, each segregated into 20 or more categories. Total surface area-to-volume ratios also were determined for each room. The bathrooms had the highest total surface area-to-volume ratios. Bedrooms generally had higher ratios than common areas consisting of kitchens, living/dining rooms and transitional rooms. Total surface area-to-volume ratios for the 12 bedrooms ranged between 2.3 and 4.7 m{sup 2} m{sup -3}. The importance of individual objects and materials with respect to sorption will depend upon the sorption coefficients for the various VOC/materials combinations. When combined, the highly permeable material categories, which may contribute to significant interactions, had a median ratio of about 0.5 m{sup 2} m{sup -3} for all three types of rooms.

  12. Vibrational states of the Pt(111)- $ ≤ft( {sqrt {3} × sqrt {3} } right) $ R30°-K surface structure

    Science.gov (United States)

    Rusina, G. G.; Borisov, S. D.; Eremeev, S. V.; Chulkov, E. V.

    2010-09-01

    Vibrational spectrum of the ordered Pt(111)- left( {sqrt {3} × sqrt {3} } right) R30°- K surface superstructure formed on the platinum surface with adsorption of 1/3 ML potassium is calculated with the use of the interatomic interaction potentials obtained in the strong bond approximation. Relaxation of the surface, dispersion of the surface phonons, local density of vibrational states, and polarization of phonon modes of adatoms and atoms of the substrate are discussed in the work. The theoretical results obtained agree well with the available experimental data.

  13. Surface area considerations for corroding N reactor fuel

    Energy Technology Data Exchange (ETDEWEB)

    Johnson, A.B. Jr.; Pitner, A.L.

    1996-06-01

    The N Reactor fuel is corroding at sites where the Zircaloy cladding was damaged when the fuel was discharged from the reactor. Corroding areas are clearly visible on the fuel stored in open cans in the K East Basin. There is a need to estimate the area of the corroding uranium to analyze aspects of fuel behavior as it is transitioned. from current wet storage to dry storage. In this report, the factors that contribute to {open_quotes}true{close_quotes} surface area are analyzed in terms of what is currently known about the N Reactor fuel. Using observations from a visual examinations of the fuel in the K East wet storage facility, a value for the corroding geometric area is estimated. Based on observations of corroding uranium and surface roughness values for other metals, a surface roughness factor is also estimated and applied to the corroding K East fuel to provide an estimated {open_quotes}true{close_quotes} surface area. While the estimated area may be modified as additional data become available from fuel characterization studies, the estimate provides a basis to assess effects of exposed uranium metal surfaces on fuel behavior in operations involved in transitioning from wet to dry storage, during shipment and staging, conditioning, and dry interim storage.

  14. Pt-Ni and Pt-Co Catalyst Synthesis Route for Fuel Cell Applications

    Science.gov (United States)

    Firdosy, Samad A.; Ravi, Vilupanur A.; Valdez, Thomas I.; Kisor, Adam; Narayan, Sri R.

    2013-01-01

    Oxygen reduction reactions (ORRs) at the cathode are the rate-limiting step in fuel cell performance. The ORR is 100 times slower than the corresponding hydrogen oxidation at the anode. Speeding up the reaction at the cathode will improve fuel cell efficiency. The cathode material is generally Pt powder painted onto a substrate (e.g., graphite paper). Recent efforts in the fuel cell area have focused on replacing Pt with Pt-X alloys (where X = Co, Ni, Zr, etc.) in order to (a) reduce cost, and (b) increase ORR rates. One of these strategies is to increase ORR rates by reducing the powder size, which would result in an increase in the surface area, thereby facilitating faster reaction rates. In this work, a process has been developed that creates Pt-Ni or Pt-Co alloys that are finely divided (on the nano scale) and provide equivalent performance at lower Pt loadings. Lower Pt loadings will translate to lower cost. Precursor salts of the metals are dissolved in water and mixed. Next, the salt mixtures are dried on a hot plate. Finally, the dried salt mixture is heattreated in a furnace under flowing reducing gas. The catalyst powder is then used to fabricate a membrane electrode assembly (MEA) for electrochemical performance testing. The Pt- Co catalyst-based MEA showed comparable performance to an MEA fabri cated using a standard Pt black fuel cell catalyst. The main objective of this program has been to increase the overall efficiencies of fuel cell systems to support power for manned lunar bases. This work may also have an impact on terrestrial programs, possibly to support the effort to develop a carbon-free energy source. This catalyst can be used to fabricate high-efficiency fuel cell units that can be used in space as regenerative fuel cell systems, and terrestrially as primary fuel cells. Terrestrially, this technology will become increasingly important when transition to a hydrogen economy occurs.

  15. First principles study on the adsorption of Pt{sub n} (n = 1–4) on γ-Al{sub 2}O{sub 3}(1 1 0) surface

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Yulu [College of Architecture and Environment, Sichuan University, Chengdu 610065 (China); Cen, Wanglai, E-mail: cenwanglai@scu.edu.cn [College of Architecture and Environment, Sichuan University, Chengdu 610065 (China); National Engineering Center of Flue Gas Desulfurization, Chengdu 610065 (China); Feng, Gang, E-mail: fengg.sshy@sinopec.com [Shanghai Research Institute of Petrochemical Technology SINOPEC, Shanghai 201208 (China); Chu, Yinghao [College of Architecture and Environment, Sichuan University, Chengdu 610065 (China); Kong, Dejin [Shanghai Research Institute of Petrochemical Technology SINOPEC, Shanghai 201208 (China); Yin, Huaqiang [College of Architecture and Environment, Sichuan University, Chengdu 610065 (China); National Engineering Center of Flue Gas Desulfurization, Chengdu 610065 (China); Institute of New Energy and Low Carbon Technology, Sichuan University, Chengdu 610065 (China)

    2014-09-15

    Highlights: • The growth ability of the supported Pt{sub n} cluster is weaker than the gas phase Pt{sub n} clusters. • Basin structures on both of the clean and hydrated γ-Al{sub 2}O{sub 3} (1 1 0) surfaces help to stabilize the Pt clusters. • The hydrogen located at the tri-coordinated surface O atoms was the most effective hydrogen supplier. • The Pt{sub n} (n = 3–4) are much more active than Pt{sub n} (n = 1–2) for hydrogen desorption. - Abstract: The density functional theory (DFT) was applied to investigate the adsorption and growth of Pt{sub n} (n = 1–4) clusters and hydrogen spillover on γ-Al{sub 2}O{sub 3} surface, which is of importance for many catalysis reactions. It was found that the growth ability of the supported Pt{sub n} cluster is weaker than the gas phase Pt{sub n} clusters. Basin structures on both of the clean and hydrated surfaces were found to stabilize the Pt clusters. For the hydrated surface, the basin structure, together with the size of Pt{sub n} cluster, was also found to take trivial impacts on the hydrogen spillover. The most feasible supplier of H species on the hydrated γ-Al{sub 2}O{sub 3} surface was identified. Additionally, it was interesting to found that there would be an optimized size of the supported Pt{sub n} cluster at n > 3.

  16. Model electrochemical interfaces in ultra-high vacuum: solvent-induced surface potential profiles on Pt(111) from work-function measurements and infrared Stark effects

    Science.gov (United States)

    Kizhakevariam, Naushad; Villegas, Ignacio; Weaver, Michael J.

    1995-08-01

    The influence of various solvents upon the interfacial-potential profile on Pt(111) has been investigated by means of work-function changes and infrared frequency Stark shifts attending sequential-molecular dosing in ultra-high vacuum (UHV) at a suitably low temperature (ca. 100 K) with the primary objective of assessing the role of surface solvation in related electrochemical systems. The solvents examined — dichloromethane, benzene, acetone, acetonitrile, methanol, and ammonia — span a range of polarity and other solvating properties. These species were dosed onto both clean and CO-saturated Pt(111), the Stark shifts being evaluated for the CO stretching mode of terminally co-ordinated carbon monoxide. Marked decreases (≥ 1 eV) in the work function, Φ, and hence in the surface potential, φ, are observed on the addition of most solvents onto clean Pt(111). Milder yet still substantial Φ decreases are also observed for solvent dosage upon CO-saturated Pt(111). These latter Φ changes correlate approximately with the observed vCO frequency downshifts, suggesting that the latter property is also sensitive to the solvent-induced electrostatic interfacial field. The functional form of both the Φ decreases and the corresponding vCO frequency downshifts induced by solvent dosage provide insight into the dosage-dependent potential profile and its relationship to both the monolayer and multilayer solvent structure. The present findings are also briefly compared with corresponding vtCO - Φ data obtained for potassium atom dosing, where the surface potential is altered instead by varying the surface electronic charge in the presence of a given solvent. The underlying factors responsible for the surprisingly large solvent-induced surface potential shifts are discussed in detail, and the likely importance of the surface electronic charge distribution as well as solvent dipole orientation and adsorbate-metal charge sharing is pointed out.

  17. Structural and surface coverage effects on CO oxidation reaction over carbon-supported Pt nanoparticles studied by quadrupole mass spectrometry and diffuse reflectance FTIR spectroscopy.

    Science.gov (United States)

    Cheah, Seng Kian; Bernardet, Véronique P; Franco, Alejandro A; Lemaire, Olivier; Gelin, Patrick

    2016-06-01

    The CO oxidation reaction on carbon-supported Pt nanoparticles (average size of 2.8 to 7.7 nm) was studied under flowing conditions at atmospheric pressure and temperatures between 300 and 353 K by coupling quadrupole mass spectrometry (QMS) and diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS). The Pt loading was varied between 20 and 60 wt%. Gases diluted in He (0.5 mol%) were used together with Ar as a tracer. Reactions with CO and O2 introduced separately onto the samples were studied by QMS, applying successive step changes of the reaction mixtures. Variations in the rate of the reactions were observed and correlated with changes of the calculated coverage of the Pt surface by CO and/or O adspecies at varying steps of the experiment. The transient reaction of CO(g) with adsorbed O (Oad) was fast and mass transport-limited while that of O2(g) with adsorbed CO (COad) was sluggish. Following the same experimental procedures, FTIR spectra of adsorbed CO after varying steps were recorded, confirming the variations of COad and Oad as determined by QMS and indicating changes in the CO distribution over varying types of Pt surface sites. The influence of the adlayer composition (co-adsorption of COad and Oad), the particle size/structure and some possible surface reconstruction effects on the CO oxidation rate were evidenced and discussed. The structure of the Pt nanoparticles supported on carbon appears as an important factor for the efficiency of the so-called O2 bleeding as a CO mitigation strategy in polymer electrolyte membrane fuel cells.

  18. Assessment of dialyzer surface in online hemodiafiltration; objective choice of dialyzer surface area

    Directory of Open Access Journals (Sweden)

    Francisco Maduell

    2015-05-01

    Conclusion: The increase in 40% and 80% of dialyzer surface area entails an increase in convective volume of 6 and 16% respectively, showing minimal differences both in convective volume and clearance capacity when UFC was greater than 45 mL/h/mmHg. It is advisable to optimise dialyser efficiency to the smallest surface area possible, adjusting treatment prescription.

  19. A framework for predicting surface areas in microporous coordination polymers.

    Science.gov (United States)

    Schnobrich, Jennifer K; Koh, Kyoungmoo; Sura, Kush N; Matzger, Adam J

    2010-04-20

    A predictive tool termed the linker to metal cluster (LiMe) ratio is introduced as a method for understanding surface area in microporous coordination polymers (MCPs). Calibrated with geometric accessible surface area computations, the LiMe ratio uses molecular weight of building block components to indicate the maximum attainable surface area for a given linker and metal cluster combination. MOF-5 and HKUST-1 are used as prototypical structures to analyze MCPs with octahedral M(4)O(CO(2)R)(6) and paddlewheel M(2)(CO(2)R)(4) metal clusters. Insight into the effects of linker size, geometry, number of coordinating groups, and framework interpenetration is revealed through the LiMe ratio analysis of various MCPs. Experimental surface area deviation provides indication that a material may suffer from incomplete guest removal, structural collapse, or interpenetration. Because minimal data input are required, the LiMe ratio surface area analysis is suggested as a quick method for experimental verification as well as a guide for the design of new materials.

  20. Synthesis of PtNi Alloy Nanoparticles on Graphene-Based Polymer Nanohybrids for Electrocatalytic Oxidation of Methanol

    Directory of Open Access Journals (Sweden)

    Tung-Yuan Yung

    2016-12-01

    Full Text Available We have successfully produced bimetallic PtNi alloy nanoparticles on poly(diallyldimethylammonium chloride (PDDA-modified graphene nanosheets (PtNi/PDDA-G by the “one-pot” hydrothermal method. The size of PtNi alloy nanoparticles is approximately 2–5 nm. The PDDA-modified graphene nanosheets (PDDA-G provides an anchored site for metal precursors; hence, the PtNi nanoparticles could be easily bond on the PDDA-G substrate. PtNi alloy nanoparticles (2–5 nm display a homogenous alloy phase embedded on the PDDA-G substrate, evaluated by Raman, X-ray diffractometer (XRD, thermal gravity analysis (TGA, electron surface chemical analysis (ESCA, and electron energy loss spectroscopy (EELS. The Pt/Ni ratio of PtNi alloy nanoparticles is ~1.7, examined by the energy dispersive spectroscopy (EDS spectra of transmitting electron microscopy (EDS/TEM spectra and mapping technique. The methanol electro-oxidation of PtNi/PDDA-G was evaluated by cyclic voltammetry (CV in 0.5 M of H2SO4 and 0.5 M of CH3OH. Compared to Pt on carbon nanoparticles (Pt/C and Pt on Graphene (Pt/G, the PtNi/PDDA-G exhibits the optimal electrochemical surface area (ECSA, methanol oxidation reaction (MOR activity, and durability by chrono amperometry (CA test, which can be a candidate for MOR in the electro-catalysis of direct methanol fuel cells (DMFC.

  1. Can foot anthropometric measurements predict dynamic plantar surface contact area?

    Directory of Open Access Journals (Sweden)

    Collins Natalie

    2009-10-01

    Full Text Available Abstract Background Previous studies have suggested that increased plantar surface area, associated with pes planus, is a risk factor for the development of lower extremity overuse injuries. The intent of this study was to determine if a single or combination of foot anthropometric measures could be used to predict plantar surface area. Methods Six foot measurements were collected on 155 subjects (97 females, 58 males, mean age 24.5 ± 3.5 years. The measurements as well as one ratio were entered into a stepwise regression analysis to determine the optimal set of measurements associated with total plantar contact area either including or excluding the toe region. The predicted values were used to calculate plantar surface area and were compared to the actual values obtained dynamically using a pressure sensor platform. Results A three variable model was found to describe the relationship between the foot measures/ratio and total plantar contact area (R2 = 0.77, p R2 = 0.76, p Conclusion The results of this study indicate that the clinician can use a combination of simple, reliable, and time efficient foot anthropometric measurements to explain over 75% of the plantar surface contact area, either including or excluding the toe region.

  2. [Quantitative surface analysis of Pt-Co, Cu-Au and Cu-Ag alloy films by XPS and AES].

    Science.gov (United States)

    Li, Lian-Zhong; Zhuo, Shang-Jun; Shen, Ru-Xiang; Qian, Rong; Gao, Jie

    2013-11-01

    In order to improve the quantitative analysis accuracy of AES, We associated XPS with AES and studied the method to reduce the error of AES quantitative analysis, selected Pt-Co, Cu-Au and Cu-Ag binary alloy thin-films as the samples, used XPS to correct AES quantitative analysis results by changing the auger sensitivity factors to make their quantitative analysis results more similar. Then we verified the accuracy of the quantitative analysis of AES when using the revised sensitivity factors by other samples with different composition ratio, and the results showed that the corrected relative sensitivity factors can reduce the error in quantitative analysis of AES to less than 10%. Peak defining is difficult in the form of the integral spectrum of AES analysis since choosing the starting point and ending point when determining the characteristic auger peak intensity area with great uncertainty, and to make analysis easier, we also processed data in the form of the differential spectrum, made quantitative analysis on the basis of peak to peak height instead of peak area, corrected the relative sensitivity factors, and verified the accuracy of quantitative analysis by the other samples with different composition ratio. The result showed that the analytical error in quantitative analysis of AES reduced to less than 9%. It showed that the accuracy of AES quantitative analysis can be highly improved by the way of associating XPS with AES to correct the auger sensitivity factors since the matrix effects are taken into account. Good consistency was presented, proving the feasibility of this method.

  3. Improved electrocatalytic ethanol oxidation activity in acidic and alkaline electrolytes using size-controlled Pt-Sn nanoparticles.

    Science.gov (United States)

    St John, Samuel; Boolchand, Punit; Angelopoulos, Anastasios P

    2013-12-31

    The promotion of the electrocatalytic ethanol oxidation reaction (EOR) on extended single-crystal Pt surfaces and dispersed Pt nanoparticles by Sn under acidic conditions is well known. However, the correlation of Sn coverage on Pt nanoparticle electrocatalysts to their size has proven difficult. The reason is that previous investigations have typically relied on commercially difficult to reproduce electrochemical treatments of prepared macroscopic electrodes to adsorb Sn onto exposed Pt surfaces. We demonstrate here how independent control over both Sn coverage and particle size can yield a significant enhancement in EOR activity in an acidic electrolyte relative to previously reported electrocatalysts. Our novel approach uses electroless nanoparticle synthesis where surface-adsorbed Sn is intrinsic to Pt particle formation. Sn serves as both a reducing agent and stabilizing ligand, producing particles with a narrow particle size distribution in a size range where the mass-specific electrocatalytic activity can be maximized (ca. 1-4 nm) as a result of the formation of a fully developed Sn shell. The extent of fractional Sn surface coverage on carbon-supported Pt nanoparticles can be systematically varied through wet-chemical treatment subsequent to nanoparticle formation but prior to incorporation into macroscopic electrodes. EOR activity for Pt nanoparticles is found to be optimum at a fractional Sn surface coverage of ca. 0.6. Furthermore, the EOR activity is shown to increase with Pt particle size and correlate with the active area of available Pt (110) surface sites for the corresponding Sn-free nanoparticles. The maximum area- and mass-specific EOR activities for the most active catalyst investigated were 17.9 μA/cm(2)Pt and 12.5 A/gPt, respectively, after 1 h of use at 0.42 V versus RHE in an acidic electrolyte. Such activity is a substantial improvement over that of commercially available Pt, Pt-Sn, and Pt-Ru alloy catalysts under either acidic or alkaline

  4. STEREOLOGICAL ESTIMATION OF SURFACE AREA FROM DIGITAL IMAGES

    Directory of Open Access Journals (Sweden)

    Johanna Ziegel

    2011-05-01

    Full Text Available A sampling design of local stereology is combined with a method from digital stereology to yield a novel estimator of surface area based on counts of configurations observed in a digitization of an isotropic 2- dimensional slice with thickness s. As a tool, a result of the second author and J. Rataj on infinitesimal increase of volumes of morphological transforms is refined and used. The proposed surface area estimator is asymptotically unbiased in the case of sets contained in the ball centred at the origin with radius s and in the case of balls centred at the origin with unknown radius. For general shapes bounds for the asymptotic expected relative worst case error are given. A simulation example is discussed for surface area estimation based on 2×2×2-configurations.

  5. The "nylon T" intrauterine device: surface area versus copper adjunct.

    Science.gov (United States)

    Kamal, I; Shaaban, H; Ezzat, R; Zaki, S

    1981-04-01

    A study to evaluate the relative effect of copper ions and increased surface area added through the wiring of the stem of the inert "T" device was performed. The experimental design was set up to test a hypothesis that the effectiveness of a copper device is a result of the increase in surface area of the IUD and not a result of the copper itself. Ninety-eight TCu 200 mm2 devices were stripped of their copper wire and rewound with a "nylon" thread of the same length, caliber and surface area. the devices were then repacked and gas sterilized. The 98 "nylon T" devices were fitted early in 1977 and followed up for 2 years. The major finding was that the replacement of copper wire on the "copper T" device by a "nylon" thread, "nylon T", had shown a comparable antifertility effect.

  6. Observed Asteroid Surface Area in the Thermal Infrared

    Science.gov (United States)

    Nugent, C. R.; Mainzer, A.; Masiero, J.; Wright, E. L.; Bauer, J.; Grav, T.; Kramer, E.; Sonnett, S.

    2017-02-01

    The rapid accumulation of thermal infrared observations and shape models of asteroids has led to increased interest in thermophysical modeling. Most of these infrared observations are unresolved. We consider what fraction of an asteroid’s surface area contributes the bulk of the emitted thermal flux for two model asteroids of different shapes over a range of thermal parameters. The resulting observed surface in the infrared is generally more fragmented than the area observed in visible wavelengths, indicating high sensitivity to shape. For objects with low values of the thermal parameter, small fractions of the surface contribute the majority of thermally emitted flux. Calculating observed areas could enable the production of spatially resolved thermal inertia maps from non-resolved observations of asteroids.

  7. DFT study of the formate formation on Ni(111) surface doped by transition metals [Ni(111)-M; M=Cu, Pd, Pt, Rh

    Science.gov (United States)

    Nugraha; Saputro, A. G.; Agusta, M. K.; Rusydi, F.; Maezono, R.; Dipojono, H. K.

    2016-08-01

    We report on a theoretical study of the formation of formate (HCOO) from the reaction of CO2 gas and a pre- adsorbed H atom (CO2 (g) + *H → *HCOO) on Ni(111) surface doped by transition-metals [Ni(111)-M; M= Cu, Pd, Pt, Rh] by means of density functional theory (DFT) calculations. This *HCOO formation reaction is one of the most important rate- limiting steps in the methanol synthesis process. We find that the presence of transition metal doping on the first-layer of Ni(111) surface could reduce the activation barrier of this reaction [up to ~38.4%, compared to clean Ni(111) surface].

  8. Time-resolved measurements of laser-induced diffusion of CO molecules on stepped Pt(111)-surfaces; Zeitaufgeloeste Untersuchung der laser-induzierten Diffusion von CO-Molekuelen auf gestuften Pt(111)-Oberflaechen

    Energy Technology Data Exchange (ETDEWEB)

    Lawrenz, M.

    2007-10-30

    In the present work the dynamics of CO-molecules on a stepped Pt(111)-surface induced by fs-laser pulses at low temperatures was studied by using laser spectroscopy. In the first part of the work, the laser-induced diffusion for the CO/Pt(111)-system could be demonstrated and modelled successfully for step diffusion. At first, the diffusion of CO-molecules from the step sites to the terrace sites on the surface was traced. The experimentally discovered energy transfer time of 500 fs for this process confirms the assumption of an electronically induced process. In the following it was explained how the experimental results were modelled. A friction coefficient which depends on the electron temperature yields a consistent model, whereas for the understanding of the fluence dependence and time-resolved measurements parallel the same set of parameters was used. Furthermore, the analysis was extended to the CO-terrace diffusion. Small coverages of CO were adsorbed to the terraces and the diffusion was detected as the temporal evolution of the occupation of the step sites acting as traps for the diffusing molecules. The additional performed two-pulse correlation measurements also indicate an electronically induced process. At the substrate temperature of 40 K the cross-correlation - where an energy transfer time of 1.8 ps was extracted - suggests also an electronically induced energy transfer mechanism. Diffusion experiments were performed for different substrate temperatures. (orig.)

  9. High surface area carbon and process for its production

    Energy Technology Data Exchange (ETDEWEB)

    Romanos, Jimmy; Burress, Jacob; Pfeifer, Peter; Rash, Tyler; Shah, Parag; Suppes, Galen

    2016-12-13

    Activated carbon materials and methods of producing and using activated carbon materials are provided. In particular, biomass-derived activated carbon materials and processes of producing the activated carbon materials with prespecified surface areas and pore size distributions are provided. Activated carbon materials with preselected high specific surface areas, porosities, sub-nm (<1 nm) pore volumes, and supra-nm (1-5 nm) pore volumes may be achieved by controlling the degree of carbon consumption and metallic potassium intercalation into the carbon lattice during the activation process.

  10. Electrochemically induced sol-gel deposition of ZnO films on Pt-nanoparticle modified FTO surfaces for enhanced photoelectrocatalytic energy conversion.

    Science.gov (United States)

    Gutkowski, Ramona; Schuhmann, Wolfgang

    2016-04-28

    The low conductivity of transparent conductive oxides such as fluorine-doped tin oxides (FTO) has a high impact on the electrochemically induced deposition of semiconductor films for photoelectrocatalytic investigations. Furthermore, the often high recombination rate of photogenerated electron-hole pairs influences the photoelectrochemical performance of semiconductor films. In order to improve the semiconductor deposition process as well as to decrease electron-hole pair recombination, we propose modification of FTO by electrochemically induced deposition of Pt nanoparticles. The deposited Pt nanoparticles improve on the one hand the conductivity of the FTO and on the other hand they create nuclei at which the sol-gel semiconductor deposition starts. We use ZnO as a well-characterised material to evaluate the effect of the influencing parameters during electrochemically induced sol-gel deposition with respect to the incident photon-to-current efficiency (IPCE) derived from wavelength dependent photocurrent spectroscopy. Using optimised deposition parameters a substantially decreased recombination rate of photogenerated charge carriers is demonstrated, if Pt-nanoparticles are first deposited on the FTO surface. By improving the diffusion of photogenerated electrons to the Pt nanoparticles and hence to the back contact the photoelectrochemical performance of the deposited ZnO films is substantially increased.

  11. Si microwire array photoelectrochemical cells: Stabilized and improved performances with surface modification of Pt nanoparticles and TiO2 ultrathin film

    Science.gov (United States)

    Yan, Jimu; Wu, Shaolong; Zhai, Xiongfei; Gao, Xiang; Li, Xiaofeng

    2017-02-01

    To achieve the semiconductor photoelectrochemical (PEC) cells targeting the industry applications with commercial competitiveness, high efficiency and good stability are requisite properties. To improve the PEC response, the vertically-aligned silicon microwire arrays (SiMWAs) modified with isolated Pt nanoparticles (PtNPs) and conformal TiO2 ultrathin film (TiO2/Pt@SiMWAs) are fabricated and examined in this study. The modified system shows the significantly enhanced responses and operation stability, that is, an enhancement of ∼30.0% in saturation photocurrent density (Jsat), a cathodic shift of ∼0.85 V (relative to the bare SiMWAs) in applied potential for Jsat, and an attenuation ratio of the photocurrent <1.5% during 1800-sec-continuous operation in an aqueous electrolyte. The underlying mechanisms are attributed to: (1) PtNPs concentrate the incident photons, promote the photo-carrier separation, and catalyze the chemical reaction at the photoelectrode-electrolyte interfaces; (2) conformal TiO2 ultrathin film protects the SiMWAs from photo-oxidation/corrosion as well as suppresses the surface recombination. Our results indicate a feasible route for the practical applications of oxidizable and corrodible semiconductor micro-/nanostructures in the fields of PEC solar cells, water splitting, photodegradation, and so on.

  12. MEASUREMENT OF APPLICATION OF ISO 27001 OF CUSTOMER CELLULAR CARD CONFIDENTIALITY DATA IN PT. XYZ AREA JAKARTA

    Directory of Open Access Journals (Sweden)

    Krishna Rahadian

    2014-10-01

    Full Text Available The purpose of this study was to evaluate the effects of the process of ISO 27001 with respect to the confidentiality of customer cellular card Jakarta and to improve cellular card customer data confidentiality at PT.XYZ from data leakage of the customer data due to the third party involvement, clean-desk policy, and access right. Recommendation regarding the improvement is provided after reviewing the confidentiality of customer data. The survey in this study is conducted by questionnaire. From the evaluation results of the questionnaire, it is concluded that the larger customer data leaks are mainly caused by the external factors.

  13. Clay mineralogy in different geomorphic surfaces in sugarcane areas

    Science.gov (United States)

    Camargo, L.; Marques, J., Jr.

    2012-04-01

    The crystallization of the oxides and hydroxides of iron and aluminum and kaolinite of clay fraction is the result of pedogenetic processes controlled by the relief. These minerals have influence on the physical and chemical attributes of soil and exhibit spatial dependence. The pattern of spatial distribution is influenced by forms of relief as the geomorphic surfaces. In this sense, the studies aimed at understanding the relationship between relief and the distribution pattern of the clay fraction attributes contribute to the delineation of specific areas of management in the field. The objective of this study was to evaluate the spatial distribution of oxides and hydroxides of iron and aluminum and kaolinite of clay fraction and its relationship with the physical and chemical attributes in different geomorphic surfaces. Soil samples were collected in a transect each 25 m (100 samples) and in the sides of the same (200 samples) as well as an area of 500 ha (1 sample each six hectare). Geomorphic surfaces (GS) in the transect were mapped in detail to support mapping the entire area. The soil samples were taken to the laboratory for chemical, physical, and mineralogical analysis, and the pattern of spatial distribution of soil attributes was obtained by statistics and geostatistics. The GS I is considered the oldest surface of the study area, with depositional character, and a slope ranging from 0 to 4%. GS II and III are considered to be eroded, and the surface II plan a gentle slope that extends from the edge of the surface until the beginning of I and III. The crystallographic characteristics of the oxides and hydroxides of iron and aluminum and kaolinite showed spatial dependence and the distribution pattern corresponding to the limits present of the GS in the field. Surfaces I and II showed the best environments to the degree of crystallinity of hematite and the surface III to the greatest degree of crystallinity of goethite agreeing to the pedoenvironment

  14. Stereological estimation of surface area from digital images

    DEFF Research Database (Denmark)

    Ziegel, Johanna; Kiderlen, Markus

    2010-01-01

    A sampling design of local stereology is combined with a method from digital stereology to yield a novel estimator of surface area based on counts of configurations observed in a digitization of an isotropic 2- dimensional slice with thickness s. As a tool, a result of the second author and J. Ra....... For general shapes bounds for the asymptotic expected relative worst case error are given. A simulation example is discussed for surface area estimation based on 2×2×2-configurations.......A sampling design of local stereology is combined with a method from digital stereology to yield a novel estimator of surface area based on counts of configurations observed in a digitization of an isotropic 2- dimensional slice with thickness s. As a tool, a result of the second author and J....... Rataj on infinitesimal increase of volumes of morphological transforms is refined and used. The proposed surface area estimator is asymptotically unbiased in the case of sets contained in the ball centred at the origin with radius s and in the case of balls centred at the origin with unknown radius...

  15. Evaluation of Five Formulae for Estimating Body Surface Area of ...

    African Journals Online (AJOL)

    in pediatric practice and child health is body surface area (BSA) ... Conclusion: Formulae by Boyd and Mosteller are the best BSA estimate for. Nigerian .... weight: (21.5 [7.6] kg vs. 20.8 [6.7] .... formula best fits with the “gold standard.” However ...

  16. Characterization of large area nanostructured surfaces using AFM measurements

    DEFF Research Database (Denmark)

    Calaon, Matteo; Hansen, Hans Nørgaard; Tosello, Guido;

    2012-01-01

    magnitude of the 3D surface amplitude parameters chosen for the analysis, when increasing the Al purity from 99,5% to 99,999%. AFM was then employed to evaluate the periodical arrangements of the nano structured cells. Image processing was used to estimate the average areas value, the height variation...

  17. Estimation of Specific Surface Area using Langmuir Isotherm ...

    African Journals Online (AJOL)

    Michael Horsfall

    13.884) units in multiple of 10-3km2kg-1. The reliability of the ... In this present study, the linear least- squares method via the correlation coefficient (R2) was used (Yuh,2006). ... specific surface area determination has been adopted widely for ...

  18. Effect of milling temperatures on surface area, surface energy and cohesion of pharmaceutical powders.

    Science.gov (United States)

    Shah, Umang V; Wang, Zihua; Olusanmi, Dolapo; Narang, Ajit S; Hussain, Munir A; Tobyn, Michael J; Heng, Jerry Y Y

    2015-11-10

    Particle bulk and surface properties are influenced by the powder processing routes. This study demonstrates the effect of milling temperatures on the particle surface properties, particularly surface energy and surface area, and ultimately on powder cohesion. An active pharmaceutical ingredient (API) of industrial relevance (brivanib alaninate, BA) was used to demonstrate the effect of two different, but most commonly used milling temperatures (cryogenic vs. ambient). The surface energy of powders milled at both cryogenic and room temperatures increased with increasing milling cycles. The increase in surface energy could be related to the generation of surface amorphous regions. Cohesion for both cryogenic and room temperature milled powders was measured and found to increase with increasing milling cycles. For cryogenic milling, BA had a surface area ∼ 5× higher than the one obtained at room temperature. This was due to the brittle nature of this compound at cryogenic temperature. By decoupling average contributions of surface area and surface energy on cohesion by salinization post-milling, the average contribution of surface energy on cohesion for powders milled at room temperature was 83% and 55% at cryogenic temperature.

  19. Cluster adsorption on amorphous and crystalline surfaces - A molecular dynamics study of model Pt on Cu and model Pd on Pt

    Science.gov (United States)

    Garofalini, S. H.; Halicioglu, T.; Pound, G. M.

    1981-01-01

    Molecular dynamics was used to study the structure, dispersion and short-time behavior of ten-atom clusters adsorbed onto amorphous and crystalline substrates, in which the cluster atoms differed from the substrate atoms. Two adatom-substrate model systems were chosen; one, in which the interaction energy between adatom pairs was greater than that between substrate pairs, and the other, in which the reverse was true. At relatively low temperature ranges, increased dispersion of cluster atoms occurred: (a) on the amorphous substrate as compared to the FCC(100) surface, (b) with increasing reduced temperature, and (c) with adatom-substrate interaction energy stronger than adatom-adatom interaction. Two-dimensional clusters (rafts) on the FCC(100) surface displayed migration of edge atoms only, indicating a mechanism for the cluster rotation and shape changes found in experimental studies.

  20. Energy loss and charge state dependency of swift N q+ ions scattered off a Pt( 1 1 0 )(1×2) surface

    Science.gov (United States)

    Robin, A.; Hatke, N.; Jensen, J.; Plachke, D.; Carstanjen, H. D.; Heiland, W.

    2003-08-01

    We present new surface scattering results combining measurements of energy loss and charge state distributions of 0.7-1.4 MeV N q+ ( q=1,2) ions. The energy range is still below the bulk stopping power maximum and charge exchange occurs. The projectiles scatter from a Pt(1 1 0)(1×2) single crystal surface under grazing incidence in specular reflection geometry. Comparison of the experimental results with two theoretical models are discussed and the influence of the trajectories on the charge state and the energy loss is investigated.

  1. Energy loss and charge state dependency of swift N{sup q+} ions scattered off a Pt(1 1 0)(1x2) surface

    Energy Technology Data Exchange (ETDEWEB)

    Robin, A. E-mail: robin@kvi.nlarobin@uos.de; Hatke, N.; Jensen, J.; Plachke, D.; Carstanjen, H.D.; Heiland, W

    2003-08-01

    We present new surface scattering results combining measurements of energy loss and charge state distributions of 0.7-1.4 MeV N{sup q+} (q=1,2) ions. The energy range is still below the bulk stopping power maximum and charge exchange occurs. The projectiles scatter from a Pt(1 1 0)(1x2) single crystal surface under grazing incidence in specular reflection geometry. Comparison of the experimental results with two theoretical models are discussed and the influence of the trajectories on the charge state and the energy loss is investigated.

  2. Surface area and conductivity of polyaniline synthesized under UV irradiation

    Science.gov (United States)

    Budi, S.; Fitri, E.; Paristiowati, M.; Cahyana, U.; Pusparini, E.; Nasbey, H.; Imaddudin, A.

    2017-02-01

    This paper reports our study on the synthesis of high electrical conductivity and surface area polyaniline using oxidative polymerization under UV light irradiation. The formation of emeraldine structures of polyaniline was revealed by major absorption bands of FTIR (Fourier transform infrared spectroscopy) spectra attributed to C-N stretching, C=C stretching in the benzenoid ring, C=C stretching in the quinoid ring and QNH+B stretching. XRD (X-ray diffractometer) measurements confirmed typical diffraction patterns with a crystallinity of 13% and 16% for polyaniline prepared under non-stirred and stirred reaction, respectively. SEM (Scanning electron microscope) studies showed more uniform morphology of polyaniline was obtained with stirring reaction process compare to those prepared without stirring. Surface analysis using SAA (surface area analyzer) showed that pure polyaniline with the relatively high surface area of ca.28 m2/g was successfully prepared in this work. Based on four point probe measurement, the prepared polyaniline possesses high conductivity which is important in electrode application.

  3. Low Pt-content ternary PdCuPt nanodendrites: an efficient electrocatalyst for oxygen reduction reaction

    Energy Technology Data Exchange (ETDEWEB)

    Fu, Shaofang; Zhu, Chengzhou; Song, Junhua; Zhang, Peina; Engelhard, Mark H.; Xia, Haibing; Du, Dan; Lin, Yuehe

    2017-01-01

    Dendritic nanostructures are capturing increasing attentions in electrocatalysis owing to their unique structural features and low density. Herein, we report for the first time bromide ions mediated synthesis of low-Pt-content PdCuPt ternary nanodendrites via galvanic replacement reaction between Pt precursor and PdCu template in aqueous solution. The experimental results show that the ternary PdCuPt nanodendrites present enhanced electrocatalytic performance for oxygen reduction reaction in acid solution compared with commercial Pt/C as well as some state-of-the-art catalysts. In details, the mass activity of the PdCuPt catalyst with optimized composition is 1.73 A/mgPt at 0.85 V vs RHE, which is 14 times higher than that of commercial Pt/C catalyst. Moreover, the long-term stability test demonstrates its better durability in acid solution. After 5k cycles, there is still 70% electrochemical surface area maintained. This method provides an efficient way to synthesize trimetallic alloys with controllable composition and specific structure for oxygen reduction reaction.

  4. Competition of terrace and step-edge sputtering under oblique-incidence ion impact on a stepped Pt(1 1 1) surface

    Energy Technology Data Exchange (ETDEWEB)

    Rosandi, Yudi [Fachbereich Physik, Technische Universitaet, 67663 Kaiserslautern (Germany); Redinger, Alex; Michely, Thomas [II. Physikalisches Institut, Universitaet zu Koeln, 50937 Koeln (Germany); Urbassek, Herbert M. [Fachbereich Physik, Technische Universitaet, 67663 Kaiserslautern (Germany)], E-mail: urbassek@rhrk.uni-kl.de

    2009-08-15

    Using molecular-dynamics simulation, we study the sputtering of a Pt(1 1 1) surface under oblique and glancing incidence 5 keV Ar ions. For incidence angles larger than a critical angle {theta}{sub c}, the projectile is reflected off the surface and the sputter yield is zero. We discuss the azimuth dependence of the critical angle {theta}{sub c} with the help of the surface corrugation felt by the impinging ion. If a step exists on the surface, sputtering occurs also for glancing incidence {theta}>{theta}{sub c}. We demonstrate that for realistic step densities, the total sputtering of a stepped surface may be sizable even at glancing incidence.

  5. Formation of a Pt-Decorated Au Nanoparticle Monolayer Floating on an Ionic Liquid by the Ionic Liquid/Metal Sputtering Method and Tunable Electrocatalytic Activities of the Resulting Monolayer.

    Science.gov (United States)

    Sugioka, Daisuke; Kameyama, Tatsuya; Kuwabata, Susumu; Yamamoto, Takahisa; Torimoto, Tsukasa

    2016-05-01

    A novel strategy to prepare a bimetallic Au-Pt particle film was developed through sequential sputter deposition of Au and Pt on a room temperature ionic liquid (RTIL). Au sputter deposition onto an RTIL containing hydroxyl-functionalized cations produced a monolayer of Au particles 4.2 nm in size on the liquid surface. Subsequent Pt sputtering onto the original Au particle monolayer floating on the RTIL enabled decoration of individual Au particles with Pt metals, resulting in the formation of a bimetallic Au-Pt particle monolayer with a Pt-enriched particle surface. The particle size slightly increased to 4.8 nm with Pt deposition for 120 min. The shell layer of a bimetallic particle was composed of Au-Pt alloy, the composition of which was tunable by controlling the Pt sputter deposition time. The electrochemical surface area (ECSA) was determined by cyclic voltammetry of bimetallic Au-Pt particle monolayers transferred onto HOPG electrodes by a horizontal liftoff method. The Pt surface coverage, determined by ECSAs of Au and Pt, increased from 0 to 56 mol % with elapse of the Pt sputter deposition time up to 120 min. Thus-obtained Au-Pt particle films exhibited electrocatalytic activity for methanol oxidation reaction (MOR) superior to the activities of pure Au or Pt particles. Volcano-type dependence was observed between the MOR activity and Pt surface coverage on the particles. Maximum activity was obtained for Au-Pt particles with a Pt coverage of 49 mol %, being ca. 120 times higher than that of pure Pt particles. This method enables direct decoration of metal particles with different noble metal atoms, providing a novel strategy to develop highly efficient multinary particle catalysts.

  6. PT quantum mechanics.

    Science.gov (United States)

    Bender, Carl M; DeKieviet, Maarten; Klevansky, S P

    2013-04-28

    PT-symmetric quantum mechanics (PTQM) has become a hot area of research and investigation. Since its beginnings in 1998, there have been over 1000 published papers and more than 15 international conferences entirely devoted to this research topic. Originally, PTQM was studied at a highly mathematical level and the techniques of complex variables, asymptotics, differential equations and perturbation theory were used to understand the subtleties associated with the analytic continuation of eigenvalue problems. However, as experiments on PT-symmetric physical systems have been performed, a simple and beautiful physical picture has emerged, and a PT-symmetric system can be understood as one that has a balanced loss and gain. Furthermore, the PT phase transition can now be understood intuitively without resorting to sophisticated mathematics. Research on PTQM is following two different paths: at a fundamental level, physicists are attempting to understand the underlying mathematical structure of these theories with the long-range objective of applying the techniques of PTQM to understanding some of the outstanding problems in physics today, such as the nature of the Higgs particle, the properties of dark matter, the matter-antimatter asymmetry in the universe, neutrino oscillations and the cosmological constant; at an applied level, new kinds of PT-synthetic materials are being developed, and the PT phase transition is being observed in many physical contexts, such as lasers, optical wave guides, microwave cavities, superconducting wires and electronic circuits. The purpose of this Theme Issue is to acquaint the reader with the latest developments in PTQM. The articles in this volume are written in the style of mini-reviews and address diverse areas of the emerging and exciting new area of PT-symmetric quantum mechanics.

  7. Resonant core spectroscopies of the charge transfer interactions between C60 and the surfaces of Au(111), Ag(111), Cu(111) and Pt(111)

    Science.gov (United States)

    Gibson, Andrew J.; Temperton, Robert H.; Handrup, Karsten; O'Shea, James N.

    2017-03-01

    Charge transfer interactions between C60 and the metal surfaces of Ag(111), Cu(111), Au(111) and Pt(111) have been studied using synchrotron-based photoemission, resonant photoemission and X-ray absorption spectroscopies. By placing the X-ray absorption and valence band spectra on a common binding energy scale, the energetic overlap of the unoccupied molecular orbitals with the density of states of the underlying metal surface have been assessed in the context of possible charge transfer pathways. Resonant photoemission and resonant Auger data, measuring the valence region as a function of photon energy for C60 adsorbed on Au(111) reveals three constant high kinetic energy features associated with Auger-like core-hole decay involving an electron transferred from the surface to the LUMO of the molecule and electrons from the three highest occupied molecular orbitals, respectively and in the presence of ultra-fast charge transfer of the originally photoexcited molecule to the surface. Data for the C60/Ag(111) surface reveals an additional Auger-like feature arising from a core-hole decay process involving more than one electron transferred from the surface into the LUMO. An analysis of the relative abundance of these core-hole decay channels estimates that on average 2.4 ± 0.3 electrons are transferred from the Ag(111) surface into the LUMO. A core-hole clock analysis has also been applied to assess the charge transfer coupling in the other direction, from the molecule to the Au(111) and Ag(111) surfaces. Resonant photoemission and resonant Auger data for C60 molecules adsorbed on the Pt(111) and Cu(111) surfaces are shown to exhibit no super-Auger features, which is attributed to the strong modification of the unoccupied molecular orbitals arising from stronger chemical coupling of the molecule to the surface.

  8. 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

    of Au with mixed Pt/Pd skins. The activity of the binary and ternary catalysts is explained through weakening of the OH binding energy caused by solute elements. However, given the low alloy formation energies it may be difficult to tune and retain the composition under operating conditions...

  9. 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

    Further advances in fuel cell technologies are hampered by kinetic limitations associated with the sluggish cathodic oxygen reduction reaction. We have investigated a range of different formulations of binary and ternary Pt, Pd and Au thin films as electrocatalysts for oxygen reduction. The most...

  10. Error bounds for surface area estimators based on Crofton's formula

    DEFF Research Database (Denmark)

    Kiderlen, Markus; Meschenmoser, Daniel

    2009-01-01

    and the mean is approximated by a finite weighted sum S(A) of the total projections in these directions. The choice of the weights depends on the selected quadrature rule. We define an associated zonotope Z (depending only on the projection directions and the quadrature rule), and show that the relative error...... in the sense that the relative error of the surface area estimator is very close to the minimal error.......According to Crofton’s formula, the surface area S(A) of a sufficiently regular compact set A in R^d is proportional to the mean of all total projections pA (u) on a linear hyperplane with normal u, uniformly averaged over all unit vectors u. In applications, pA (u) is only measured in k directions...

  11. Tokamak dust particle size and surface area measurement

    Energy Technology Data Exchange (ETDEWEB)

    Carmack, W.J.; Smolik, G.R.; Anderl, R.A.; Pawelko, R.J.; Hembree, P.B.

    1998-07-01

    The INEEL has analyzed a variety of dust samples from experimental tokamaks: General Atomics` DII-D, Massachusetts Institute of Technology`s Alcator CMOD, and Princeton`s TFTR. These dust samples were collected and analyzed because of the importance of dust to safety. The dust may contain tritium, be activated, be chemically toxic, and chemically reactive. The INEEL has carried out numerous characterization procedures on the samples yielding information useful both to tokamak designers and to safety researchers. Two different methods were used for particle characterization: optical microscopy (count based) and laser based volumetric diffraction (mass based). Surface area of the dust samples was measured using Brunauer, Emmett, and Teller, BET, a gas adsorption technique. The purpose of this paper is to present the correlation between the particle size measurements and the surface area measurements for tokamak dust.

  12. Human epididymis: structural pattern, total length and inner surface area.

    Science.gov (United States)

    Skandhan, Kalanghot P; Soni, Ashutosh; Joshi, Anantkumar; Avni, Kalanghot P S; Gupta, Bansi Dhar

    2017-05-24

    The organ epididymis is secured the name considering it functioned as an appendix to the testis; earlier testis was called as didymi. Regarding the length of human epididymis, several values are attributed by different authors. The present study was aimed to find out the pattern, total length and inner surface area of human epididymis. The study was conducted by employing microsurgical procedures on five testes from unclaimed human dead bodies. Caput was formed by few tubes interconnecting at three levels. These tubes led to corpus, which in turn was having more number of tubes interconnecting at different levels. Tubules were many looking like a mesh. United tubes of corpus form the single tube to form cauda. Epididymis length was 30.48 cm. Inner surface area was 818.16 mm2. Reported values of others seem to be a modified version from that of animals. Authors believe that organic revolutionary changes in man led to a reduction in the length of epididymis.

  13. Particle surface area and bacterial activity in recirculating aquaculture systems

    DEFF Research Database (Denmark)

    Pedersen, Per Bovbjerg; von Ahnen, Mathis; Fernandes, Paulo

    2017-01-01

    Suspended particles in recirculating aquaculture systems (RAS) provide surface area that can be colonized by bacteria. More particles accumulate as the intensity of recirculation increases thus potentially increasing the bacterial carrying capacity of the systems. Applying a recent, rapid, culture......-independent fluorometric detection method (Bactiquant®) for measuring bacterial activity, the current study explored the relationship between total particle surface area (TSA, derived from the size distribution of particles >5 μm) and bacterial activity in freshwater RAS operated at increasing intensity of recirculation......-up water; corresponding to 0.32 m3 make-up water kg−1 feed). This was likely due to the accumulation of dissolved nutrients sustaining free-living bacterial populations, and/or accumulation of suspended colloids and fine particles less than 5 μm in diameter, which were not characterized in the study...

  14. Fabrication of Highly Stable and Efficient PtCu Alloy Nanoparticles on Highly Porous Carbon for Direct Methanol Fuel Cells.

    Science.gov (United States)

    Khan, Inayat Ali; Qian, Yuhong; Badshah, Amin; Zhao, Dan; Nadeem, Muhammad Arif

    2016-08-17

    Boosting the durability of Pt nanoparticles by controlling the composition and morphology is extremely important for fuel cells commercialization. We deposit the Pt-Cu alloy nanoparticles over high surface area carbon in different metallic molar ratios and optimize the conditions to achieve desired material. The novel bimetallic electro-catalyst {Pt-Cu/PC-950 (15:15%)} offers exceptional electrocatalytic activity when tested for both oxygen reduction reaction and methanol oxidation reactions. A high mass activity of 0.043 mA/μgPt (based on Pt mass) is recorded for ORR. An outstanding longevity of this electro-catalyst is noticed when compared to 20 wt % Pt loaded either on PC-950 or commercial carbon. The high surface area carbon support offers enhanced activity and prevents the nanoparticles from agglomeration, migration, and dissolution as evident by TEM analysis.

  15. DETERMINATION OF GLACIER SURFACE AREA USING SPACEBORNE SAR IMAGERY

    OpenAIRE

    Fang, L.; Maksymiuk, O.; Schmitt, M.; Stilla, U.

    2013-01-01

    Glaciers are very important climate indicators. Although visible remote sensing techniques can be used to extract glacier variations effectively and accurately, the necessary data are depending on good weather conditions. In this paper, a method for determination of glacier surface area using multi-temporal and multi-angle high resolution TerraSAR-X data sets is presented. We reduce the "data holes" in the SAR scenes affected by radar shadowing and specular backscattering of smooth i...

  16. Excess Surface Area in Bioelectrochemical Systems Causes ion Transport Limitations

    Energy Technology Data Exchange (ETDEWEB)

    Harrington, Timothy D.; Babauta, Jerome T.; Davenport, Emily K.; Renslow, Ryan S.; Beyenal, Haluk

    2015-05-01

    We investigated ion transport limitations on 3D graphite felt electrodes by growing Geobacter sulfurreducens biofilms with advection to eliminate external mass transfer limitations. We characterized ion transport limitations by: (i) showing that serially increasing NaCl concentration up to 200mM increased current linearly up to a total of þ273% vs. 0mM NaCl under advective conditions; (ii) growing the biofilm with a starting concentration of 200mM NaCl, which led to a maximum current increase of 400% vs. current generation without NaCl, and (iii) showing that un-colonized surface area remained even after steadystate current was reached. After accounting for iR effects, we confirmed that the excess surface area existed despite a non-zero overpotential. The fact that the biofilm was constrained from colonizing and producing further current under these conditions confirmed the biofilms under study here were ion transport-limited. Our work demonstrates that the use of high surface area electrodes may not increase current density when the system design allows ion transport limitations to become dominant.

  17. Determination of hand and palm area as a ratio of body surface area in Indian population

    Directory of Open Access Journals (Sweden)

    Agarwal Pawan

    2010-01-01

    Full Text Available Background: Accurate estimation of body surface area (BSA burn is important. In small and patchy burns, the patient′s hand is used to estimate percentage of burn which is traditionally considered as 1%. There is discrepancy about what percentage of TBSA is constituted by the palm and hand. Therefore, this study was designed to determine correctly the TBSA represented by the palmar surface of the entire hand and palm in the Indian population. Material and Methods: 300 healthy adult (male and female and 300 healthy children (male and female were included in the study. TBSA was calculated using DuBois formula and hand and palm surface area was calculated using hand tracing on plain paper. The hand/palm percentage of BSA (ratio was determined by dividing hand/palm surface area by total BSA. Results: The mean hand and palm ratio for adults was 0.92% and 0.50%, respectively. The mean hand and palm ratio in children was 1.06% and 0.632%, respectively. Conclusion: The hand area (palm plus digits is more closely represented to 1% of TBSA in Indian population.

  18. High porosity and surface area self-doped carbon derived from polyacrylonitrile as efficient electrocatalyst towards oxygen reduction

    Science.gov (United States)

    You, Chenghang; Zheng, Ruiping; Shu, Ting; Liu, Lina; Liao, Shijun

    2016-08-01

    A highly porous N self-doped carbon catalyst, with three dimensional morphology/structures and high surface area (810.8 m2 g-1), is prepared through a pyrolysis procedure with polyacrylonitrile as the precursor, and zinc oxide (ZnO) as the templates/pore former. The catalyst exhibits excellent activity and stability towards oxygen reduction reaction (ORR) in alkaline medium, as well as outstanding methanol tolerance and stability. For our optimal catalyst PAC/ZnO-900, its half-wave potential is 26 mV more positive (0.859 V, vs. RHE) than that of commercial Pt/C catalyst (0.833 V, vs. RHE), and its current density at 0.88 V (vs. RHE) is almost twice as high as that of Pt/C catalyst (-1.922 and -0.957 mA cm-2, respectively). It is found that the addition of ZnO plays a crucial role for the formation of catalysts' 3D porous structures and high ORR performance. With the addition of ZnO in precursor, the surface area of the catalyst is enhanced by 13 times, and the ORR activity is enhanced by 10 times. Also, pyrolyzing temperature seems to be another important factor significantly affected the structure and performance of the catalyst.

  19. Spectral theory of infinite-area hyperbolic surfaces

    CERN Document Server

    Borthwick, David

    2016-01-01

    This text introduces geometric spectral theory in the context of infinite-area Riemann surfaces, providing a comprehensive account of the most recent developments in the field. For the second edition the context has been extended to general surfaces with hyperbolic ends, which provides a natural setting for development of the spectral theory while still keeping technical difficulties to a minimum. All of the material from the first edition is included and updated, and new sections have been added. Topics covered include an introduction to the geometry of hyperbolic surfaces, analysis of the resolvent of the Laplacian, scattering theory, resonances and scattering poles, the Selberg zeta function, the Poisson formula, distribution of resonances, the inverse scattering problem, Patterson-Sullivan theory, and the dynamical approach to the zeta function. The new sections cover the latest developments in the field, including the spectral gap, resonance asymptotics near the critical line, and sharp geometric constan...

  20. Determination of Glacier Surface Area Using Spaceborne SAR Imagery

    Science.gov (United States)

    Fang, L.; Maksymiuk, O.; Schmitt, M.; Stilla, U.

    2013-04-01

    Glaciers are very important climate indicators. Although visible remote sensing techniques can be used to extract glacier variations effectively and accurately, the necessary data are depending on good weather conditions. In this paper, a method for determination of glacier surface area using multi-temporal and multi-angle high resolution TerraSAR-X data sets is presented. We reduce the "data holes" in the SAR scenes affected by radar shadowing and specular backscattering of smooth ice surfaces by combining the two complementary different imaging geometries (from ascending and descending satellite tracks). Then, a set of suitable features is derived from the intensity image, the texture information generated based on the gray level co-occurrence matrix (GLCM), glacier velocity estimated by speckle tracking, and the interferometric coherence map. Furthermore, the features are selected by 10-foldcross- validation based on the feature relevance importance on classification accuracy using a Random Forests (RF) classifier. With these most relevant features, the glacier surface is discriminated from the background by RF classification in order to calculate the corresponding surface area.

  1. Analisa Pengaruh Modifikasi Mesin Press Body Area 5a Line Terhadap Peningkatan Kapasitas Produksi Di PT. Astra Daihatsu Motor

    Directory of Open Access Journals (Sweden)

    Januar Nasution

    2011-06-01

    Full Text Available Analysis or the analysis is defined as a study conducted on a discussion of the problems studied in depth to find out the real situation. In this study, analysis of the modifications carried out to assess the influence of such modifications in an increase in production capacity of PT. Astra Daihatsu Motor. Taking into account the physical and technical aspects of data in the field, didapatlah data supporting this research, for subsequent use as a reference from the financial aspect to determine the magnitude of the cost involved in this modification. The purpose of this study was to find the value of the initial investment required in the modification, finding the investment payback period, benefit gained as well as determining whether modification is appropriate or not to apply. Data collection conducted broadly divided into two data technical and financial aspects, and then after that the data is processed through the method of calculation of production, Stoke per Hour (SPH, Gross Stroke per Hour (GSPH. This study also provides recommendations to companies to assess whether the modification is feasible or not to do, from the point of view of project feasibility studies. 

  2. Pd/Pt(1 1 1) surface structure and metal epitaxy by time-of-flight impact-collision ion scattering spectroscopy and scanning tunneling microscopy: Does lattice mismatch really determine the growth mode?

    Science.gov (United States)

    Umezawa, K.; Narihiro, E.; Ohta, Y.; Ohira, Y.; Yoshimura, M.

    2008-04-01

    We have investigated the growth of 3 ML of Pd on Pt(1 1 1) at substrate temperature of around 300 K using TOF-ICISS. Also a series of STM topographs were taken as a function of coverage of Pd atoms. The Pd-Pt(1 1 1) combination does not have lattice mismatch (less than 1%); the nearest neighbor distance of bulk Pd(1 1 1) and Pt(1 1 1) are 2.75 Å and 2.77 Å, respectively. Experimental data and computer simulations result clearly show the growth mode of Pd(1 1 1) [ 2 bar 1 1]/Pt(1 1 1) [ 2 bar 1 1] hetero epitaxy at the coverage of the Pd deposition less than 3 ML. The growth mode of Pd(1 1 1) [ 1 bar 1 bar 2 ]/Pt(1 1 1) [ 2 bar 1 1] could not be observed at all. One would expect that the growth mode of Pd atoms on Pt(1 1 1) surfaces is like homo epitaxy (layer-by-layer growth), because of no lattice mismatch (less than 1%). However, it was not. The calculated surface and interface energies and STM results show 2D or 3D dimensional island growth. Pd atoms is mainly form dense islands at the steps on Pt(1 1 1) surfaces at the coverage of 0.13 ML.

  3. Utilization of surface plasmon resonance of Au/Pt nanoparticles for highly photosensitive ZnO nanorods network based plasmon field effect transistor

    Science.gov (United States)

    Kumar, Ashish; Dixit, Tejendra; Palani, I. A.; Nakamura, D.; Higashihata, M.; Singh, Vipul

    2017-09-01

    Hydrothermally processed highly photosensitive ZnO nanorods based plasmon field effect transistors (PFETs) have been demonstrated utilizing the surface plasmon resonance coupling of Au and Pt nanoparticles at Au/Pt and ZnO interface. A significantly enhanced photocurrent was observed due to the plasmonic effect of the metal nanoparticles (NPs). The Pt coated PFETs showed Ion/Ioff ratio more than 3 × 104 under the dark condition, with field-effect mobility of 26 cm2 V-1 s-1 and threshold voltage of -2.7 V. Moreover, under the illumination of UV light (λ = 350 nm) the PFET revealed photocurrent gain of 105 under off-state (-5 V) of operation. Additionally, the electrical performance of PFETs was investigated in detail on the basis of charge transfer at metal/ZnO interface. The ZnO nanorods growth temperature was preserved at 110 °C which allowed a low temperature, economical and simple method to develop highly photosensitive ZnO nanorods network based PFETs for large scale production.

  4. Vibrational Fingerprints of Low-Lying Pt(n)P(2n) (n = 1-5) Cluster Structures from Global Optimization Based on Density Functional Theory Potential Energy Surfaces.

    Science.gov (United States)

    Jedidi, Abdesslem; Li, Rui; Fornasiero, Paolo; Cavallo, Luigi; Carbonniere, Philippe

    2015-12-03

    Vibrational fingerprints of small Pt(n)P(2n) (n = 1-5) clusters were computed from their low-lying structures located from a global exploration of their DFT potential energy surfaces with the GSAM code. Five DFT methods were assessed from the CCSD(T) wavenumbers of PtP2 species and CCSD relative energies of Pt2P4 structures. The eight first Pt(n)P(2n) isomers found are reported. The vibrational computations reveal (i) the absence of clear signatures made by overtone or combination bands due to very weak mechanical and electrical anharmonicities and (ii) some significant and recurrent vibrational fingerprints in correlation with the different PP bonding situations in the Pt(n)P(2n) structures.

  5. Enhanced catalytic properties of Pt-based electrode by doped Cu and Ce

    Science.gov (United States)

    Yue, Dehuai; Yang, Bin

    2017-08-01

    Novel PtCuCeO x composite membrane electrode materials were fabricated on the surface of graphite fibrous cloth by ion beam sputtering (IBS). The cyclic voltammetry (CV) and linear sweep voltammetry (LSV) were used to analyze the influence of doped Cu and Ce on the membrane electrocatalysis performance in a tri-electrode system. The phase composition, surface structure, interfacial structure and catalytic performance of PtCuCeO x membrane were studied by x-ray diffraction (XRD) and high resolution transmission electron microscope (HR-TEM&STEM). The results indicate that surface particles of membrane electrode are made up of PtCu alloy grains and a few CeO x grains, and the interface structure of oxide metal is formed between them. The crystal plane spacing between PtCu alloy grain is reduced by about 1.11% after the corrosion, which helps increase the electron density on Pt atom. As a result, the catalysis capability of PtCu alloy is enhanced. When the content of Ce is less than or equal to 0.28 wt.%, CeO x exists in the form of amorphous. It is exciting to demonstrate that the existence of CeO x enhances the dispersion of PtCuCeO x catalyst particles. The experimental results reveal that the synthesized material possesses the best electrochemical activity surface area (ESA) and exchange current density (i 0). Compared to pure Pt catalyst, this PtCuCeO x catalyst contains much less Pt content (only 42% of Pt catalyst). However, the electrochemical performance is enhanced by 71.8% compared with pure Pt.

  6. Characterization of azo dyes on Pt and Pt/polyaniline/dispersed Pt electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Molina, J.; Fernandez, J.; Rio, A.I. del; Bonastre, J. [Departamento de Ingenieria Textil y Papelera, EPS de Alcoy, Universitat Politecnica de Valencia, Plaza Ferrandiz y Carbonell s/n, 03801 Alcoy (Spain); Cases, F., E-mail: fjcases@txp.upv.es [Departamento de Ingenieria Textil y Papelera, EPS de Alcoy, Universitat Politecnica de Valencia, Plaza Ferrandiz y Carbonell s/n, 03801 Alcoy (Spain)

    2012-06-15

    The electrochemical characterization of two organic dyes (amaranth and procion orange MX-2R) has been performed on Pt electrodes and Pt electrodes coated with polyaniline and dispersed Pt. Electrodes with different Pt loads have been synthesized and characterized obtaining that a load of 300 {mu}g cm{sup -2} was the optimum one. Scanning electron microscopy (SEM) and atomic force microscopy (AFM) was employed to observe the distribution and morphology of the Pt nanoparticles. The electroactivity of the electrodes has also been characterized by means of scanning electrochemical microscopy (SECM). The chemical characterization of Pt dispersed Pani coated Pt electrodes (Pt-Pani-Pt) was performed by means of X-ray photoelectron spectroscopy (XPS). The electrochemical characterization of the dyes has been performed by means of cyclic voltammetry. Voltammograms have shown that the presence of the dyes diminishes characteristic Pt oxidation and reduction peaks. However, redox processes due to the dyes, appeared in the voltammograms. The different species responsible of these redox processes were generated in the vicinity of the electrode and were not adsorbed on the electrode surface since after stirring, the different redox processes disappeared. Characterization with different scan rates showed that redox processes of both dyes were controlled by diffusion.

  7. 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.

  8. Surface passivation and protection of Pt loaded multicrystalline pn+ silicon photocathodes by atmospheric plasma oxidation for improved solar water splitting

    Science.gov (United States)

    Fan, Ronglei; Tang, Chengshuang; Xin, Yu; Su, Xiaodong; Wang, Xiaodong; Shen, Mingrong

    2016-12-01

    In the traditional methods such as atomic layer deposition and sputtering, a thin metal oxide layer was usually deposited before the loading of catalysts to protect Si photoelectrodes from oxidation during solar water splitting, and this often results in the transfer of photogenerated carriers from Si to electrolyte more or less inhibited. We here use an atmospheric plasma oxidation method to improve this. A SiO2 protective layer, also an effective passivation layer of Si to increase the life time of carriers, is fabricated on Pt loaded multicrystalline pn+-Si photocathodes. Compared with the un-protected one, the energy conversion efficiency of the plasma-treated Pt/pn+-Si photocathode increases from 6.2% to 8.9% under 100 mW/cm2 Xe lamp, and its stability improves from less than 1-22 h under continuous H2 production. This research provides a conceptual strategy to ensure the direct contact among the Si/Pt/electrolyte and protect and passivate the other part of Si simultaneously.

  9. Silicide induced surface defects in FePt nanoparticle fcc-to-fct thermally activated phase transition

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Shu; Lee, Stephen L. [School of Physics and Astronomy, SUPA, University of St Andrews, St Andrews KY16 9SS (United Kingdom); André, Pascal, E-mail: pjpandre@riken.jp [School of Physics and Astronomy, SUPA, University of St Andrews, St Andrews KY16 9SS (United Kingdom); RIKEN, Wako 351-0198 (Japan); Department of Physics, CNRS-Ewha International Research Center (CERC), Ewha W. University, Seoul 120-750 (Korea, Republic of)

    2016-11-01

    Magnetic nanoparticles (MnPs) are relevant to a wide range of applications including high density information storage and magnetic resonance imaging to name but a few. Among the materials available to prepare MnPs, FePt is attracting growing attention. However, to harvest the strongest magnetic properties of FePt MnPs, a thermal annealing is often required to convert face-centered cubic as synthesized nPs into its tetragonal phase. Rarely addressed are the potential side effects of such treatments on the magnetic properties. In this study, we focus on the impact of silica shells often used in strategies aiming at overcoming MnP coalescence during the thermal annealing. While we show that this shell does prevent sintering, and that fcc-to-fct conversion does occur, we also reveal the formation of silicide, which can prevent the stronger magnetic properties of fct-FePt MnPs from being fully realised. This report therefore sheds lights on poorly investigated and understood interfacial phenomena occurring during the thermal annealing of MnPs and, by doing so, also highlights the benefits of developing new strategies to avoid silicide formation.

  10. High surface area aerogels for energy storage and efficiency

    Science.gov (United States)

    Maloney, Ryan Patrick

    ADAI are demonstrated in a third-generation prototypical thermoelectric generator for automotive waste heat recovery. The second chapter then details two different aerogel-based materials for electrochemical energy storage. It begins with lithium titanate aerogel, which takes advantage of the high surface area of the aerogel morphology to display a batt-cap behavior. This should allow the lithium titanate aerogel to perform at higher rates than would normally be expected for the bulk oxide material. Additionally, the flexibility of the sol-gel process is demonstrated through the incorporation of electrically conductive high-surface area exfoliated graphite nanoplatelets in the oxide. The last section describes the characterization of a LiMn2O 4 spinel coated carbon nanofoam in a non-aqueous electrolyte. The short diffusion path, high surface area and intimately wired architecture of the nanofoam allows the oxide to retain its capacity at significantly higher rates when compared with literature values for the bulk oxide. Additionally, the nanometric length scale improves cycle life, and the high surface area dramatically increases the insertion capacity by providing a higher concentration of surface defects. Taken together, it is clear that aerogels are an extremely attractive class of material for applications pertaining to energy and efficiency, and further research in this area will provide valuable solutions for pressing societal needs. (Abstract shortened by UMI.).

  11. Electrochemical oxidation of methanol on Pt/(RuxSn1-xO2 nanocatalyst

    Directory of Open Access Journals (Sweden)

    Krstajić Mila N.

    2013-01-01

    Full Text Available The Ru-doped SnO2 powder, (RuxSn1-xO2, with the Sn:Ru atomic ratio of 9:1 was synthesized and used as a support for Pt nanoparticles (30 mass% loading. The (RuxSn1-xO2 support and Pt/(RuxSn1-xO2 catalyst were characterized by X-ray diffraction, energy dispersive X-ray spectroscopy and transmission electron microscopy (TEM. (RuxSn1-xO2 was found to be two-phase material consisting of probably solid solution of RuO2 in SnO2 and pure RuO2. The average Pt particle size determined by TEM was 5.3 nm. Cyclic voltammetry of Pt/(RuxSn1-xO2 indicated good conductivity of the sup-port and displayed usual features of Pt. The results of the electrochemical oxidation of COads and methanol on Pt/(RuxSn1-xO2 were compared with those on commercial Pt/C and PtRu/C catalysts. Oxidation of COads on Pt/(RuxSn1-xO2 starts at less positive potentials than on PtRu/C and Pt/C. Potentiodynamic polarization curves and chronoamperometric curves of methanol oxidation indicated higher initial activity of Pt/(RuxSn1-xO2 catalyst compared to PtRu/C, but also a greater loss in the current density over time. Potentiodynamic stability test of the catalysts revealed that deactivation of the Pt/(RuxSn1-xO2 and Pt/C was primarily caused by the poisoning of Pt surface by the methanol oxidation residues, which mostly occurred during the first potential cycle. In the case of PtRu/C the poisoning of the surface was minor and deactivation was caused by the PtRu surface area loss. [Projekat Ministarstva nauke Republike Srbije, br. ON-172054

  12. Synthesis and Electrocatalytic Performance of Multi-Component Nanoporous PtRuCuW Alloy for Direct Methanol Fuel Cells

    Directory of Open Access Journals (Sweden)

    Xiaoting Chen

    2015-06-01

    Full Text Available We have prepared a multi-component nanoporous PtRuCuW (np-PtRuCuW electrocatalyst via a combined chemical dealloying and mechanical alloying process. The X-ray diffraction (XRD, transmission electron microscopy (TEM and electrochemical measurements have been applied to characterize the microstructure and electrocatalytic activities of the np-PtRuCuW. The np-PtRuCuW catalyst has a unique three-dimensional bi-continuous ligament structure and the length scale is 2.0 ± 0.3 nm. The np-PtRuCuW catalyst shows a relatively high level of activity normalized to mass (467.1 mA mgPt−1 and electrochemically active surface area (1.8 mA cm−2 compared to the state-of-the-art commercial PtC and PtRu catalyst at anode. Although the CO stripping peak of np-PtRuCuW 0.47 V (vs. saturated calomel electrode, SCE is more positive than PtRu, there is a 200 mV negative shift compared to PtC (0.67 V vs. SCE. In addition, the half-wave potential and specific activity towards oxygen reduction of np-PtRuCuW are 0.877 V (vs. reversible hydrogen electrode, RHE and 0.26 mA cm−2, indicating a great enhancement towards oxygen reduction than the commercial PtC.

  13. ANALISIS JALUR PENGARUH KARAKTERISTIK PEKERJAAN, MOTIVASI, KEPUASAN KERJA TERHADAP KINERJA KARYAWAN (Studi di PT. Perusahaan Listrik Negara (Persero Distribusi Jatim Area Pelayanan dan Jaringan Malang

    Directory of Open Access Journals (Sweden)

    Endi Sarwoko

    2005-01-01

    Full Text Available Tujuan penelitian adalah untuk menganalisis pengaruh karakteristik pekerjaan terhadap motivasi kerja karyawan, pengaruh karakteristik pekerjaan dan motivasi terhadap  kepuasan kerja karyawan, pengaruh kepuasan kerja terhadap kinerja karyawan, serta pengaruh langsung dan tidak langsung karakteristik pekerjaan, motivasi, dan kepuasan kerja terhadap kinerja karyawan PT. Perusahaan Listrik Negara (Persero Distribusi Jatim Area Pelayanan dan Jaringan Malang.Hasil penelitian menunjukkan bahwa karakteristik pekerjaan berpengaruh signifikan terhadap kinerja melalui jalur motivasi dan kepuasan kerja. Jalur hubungan kausal antara karakteristik pekerjaan terhadap kinerja diperoleh tiga jalur yaitu:1.   Jalur hubungan kausal antara karakteristik pekerjaan terhadap kinerja melalui motivasi dan kepuasan kerja. 2.   Jalur hubungan kausal antara karakteristik pekerjaan terhadap kinerja melalui motivasi. 3.Jalur hubungan kausal langsung antara karakteristik pekerjaan terhadap kinerja. 4. Ternyata jalur hubungan kausal antara karakteristik pekerjaan terhadap kinerja melalui motivasi dan kepuasan kerja merupakan jalur paling baik yang memberikan pengaruh paling besar terhadap kinerja, dengan demikian hipotesis kedua ditolak. 

  14. Comparative Analysis of Cobalt Oxide Nanoisland Stability and Edge Structures on Three Related Noble Metal Surfaces: Au (111), Pt (111) and Ag (111)

    DEFF Research Database (Denmark)

    Fester, Jakob; Bajdich, Michal; Walton, Alexander

    2017-01-01

    Metal oxide nanostructures and thin films grown on metallic substrates have attracted strong attention as model catalysts and as interesting inverse catalyst systems in their own right. In this study, we investigate the role of metal support in the growth and stabilization of cobalt oxide...... nanostructures on the three related (111) surfaces of Au, Pt and Ag, as investigated by means of high-resolution scanning tunneling microscopy and DFT calculations. All three substrates promote the growth of crystalline CoOx (x = 1−2) islands under oxidative conditions, but we find several noteworthy differences...... for water dissociation....

  15. Vertically aligned carbon nanotubes/carbon fiber paper composite to support Pt nanoparticles for direct methanol fuel cell application

    Science.gov (United States)

    Zhang, Jing; Yi, Xi-bin; Liu, Shuo; Fan, Hui-Li; Ju, Wei; Wang, Qi-Chun; Ma, Jie

    2017-03-01

    Vertically aligned carbon nanotubes (VACNTs) grown on carbon fiber paper (CFP) by plasma enhanced chemical vapor deposition is introduced as a catalyst support material for direct methanol fuel cells (DMFCs). Well dispersed Pt nanoparticles on VACNTs surface are prepared by impregnation-reduction method. The VACNTs on CFP possess well-maintained alignment, large surface area and good electrical conductivity, which leading to the formation of Pt particles with a smaller size and enhance the Pt utilization rate. The structure and nature of resulting Pt/VACNTs/CFP catalysts for methanol oxidation are investigated by transmission electron microscopy (TEM), X-ray diffraction (XRD) and scanning electron microscope (SEM). With the aid of VACNTs, well-dispersed Pt catalysts enable the reversibly rapid redox kinetic since electron transport efficiently passes through a one-dimensional pathway, which leads to enhance the catalytic activity and Pt utilization rate. Compared with the Pt/XC-72/CFP electrode, the electrochemical measurements results display that the Pt/VACNTs/CFP catalyst shows much higher electrocatalytic activity and better stability for methanol oxidation. In addition, the oxidation current from 200 to 1200 s decayed more slowly for the Pt/VACNTs/CFP than that of the Pt/XC-72/CFP catalysts, indicating less accumulation of adsorbed CO species. All those results imply that the Pt/VACNTs/CFP has a great potential for applications in DMFCs.

  16. Manganese Dioxide with High Specific Surface Area for Alkaline Battery

    Institute of Scientific and Technical Information of China (English)

    HUANG You-ju; LIN Yu-li; LI Wei-shan

    2012-01-01

    The authors reported a facile method for the synthesis of manganese dioxide without any template and catalyst at a low-temperature.The prepared sample was characterized with X-ray diffraction(XRD),scanning electron microscopy(SEM),Brunauer-Emmett-Teller(BET) surface analysis,Fourier transform infrared(FTIR) spectrometry,cyclic voltammetry,altemative current(AC) impedance test and battery discharge test.It is found that the prepared sample belongs to α-MnO2 and has a microsphere morphology and a large BET surface area.The electrochemical characterization indicates that the prepared sample displays a larger electrochemical capacitance than the commercial electrolytic manganese dioxides(EMD) in Na2SO4 solution,and exhibits larger discharge capacity than EMD,especially at a high rate discharge condition when it is used as cathode of alkaline Zn/MnO2 battery.

  17. Surface area-dependent second harmonic generation from silver nanorods.

    Science.gov (United States)

    Ngo, Hoang Minh; Luong, Thanh Tuyen; Ledoux-Rak, Isabelle

    2016-08-17

    The nonlinear optical (NLO) properties of metallic nanoparticles strongly depend on their size and shape. Metallic gold nanorods have already been widely investigated, but other noble metals could also be used for nanorod fabrication towards applications in photonics. Here we report on the synthesis and NLO characterization of silver nanorods (AgNRs) with controllable localized surface plasmon resonance. We have implemented an original, one-step and seedless synthesis method, based on a spontaneous particle growth technique in the presence of polyvinylpyrrolidone (PVP) as a capping agent. Colloidal solutions of AgNRs with various aspect ratios (5.0; 6.3; 7.5; 8.2 and 9.7) have been obtained and characterized using Harmonic light scattering (HLS) at 1064 nm, in order to investigate their quadratic NLO properties. From HLS experiments, we demonstrate that hyperpolarizability (β) values of AgNRs display a strong dependence on their surface area.

  18. Ion-scattering study and Monte Carlo simulations of surface segregation in Pd-Pt nanoclusters obtained by laser vaporization of bulk alloys

    Science.gov (United States)

    Rousset, J. L.; Renouprez, A. J.; Cadrot, A. M.

    1998-07-01

    Bimetallic Pd-Pt clusters deposited on amorphous carbon have been produced by laser vaporization of various bulk alloys. Energy dispersive x-ray analysis and transmission electron microscopy show that they have a perfectly well-defined stoichiometry and a narrow range of size. They constitute ideal systems to investigate segregation processes in finite solids. It is shown that low-energy ion scattering allows the determination of surface concentration, which has been found to be different from the overall one. Monte Carlo simulations coupled with a recently developed energetical model, based on a tight-binding scheme that includes bond strength modifications at surfaces, account well for the experimental finding and give information on the surface distribution of the segregating Pd atoms.

  19. Metal-organic framework materials with ultrahigh surface areas

    Energy Technology Data Exchange (ETDEWEB)

    Farha, Omar K.; Hupp, Joseph T.; Wilmer, Christopher E.; Eryazici, Ibrahim; Snurr, Randall Q.; Gomez-Gualdron, Diego A.; Borah, Bhaskarjyoti

    2015-12-22

    A metal organic framework (MOF) material including a Brunauer-Emmett-Teller (BET) surface area greater than 7,010 m.sup.2/g. Also a metal organic framework (MOF) material including hexa-carboxylated linkers including alkyne bond. Also a metal organic framework (MOF) material including three types of cuboctahedron cages fused to provide continuous channels. Also a method of making a metal organic framework (MOF) material including saponifying hexaester precursors having alkyne bonds to form a plurality of hexa-carboxylated linkers including alkyne bonds and performing a solvothermal reaction with the plurality of hexa-carboxylated linkers and one or more metal containing compounds to form the MOF material.

  20. High surface area graphene-supported metal chalcogenide assembly

    Science.gov (United States)

    Worsley, Marcus A.; Kuntz, Joshua; Orme, Christine A.

    2016-04-19

    A composition comprising at least one graphene-supported assembly, which comprises a three-dimensional network of graphene sheets crosslinked by covalent carbon bonds, and at least one metal chalcogenide compound disposed on said graphene sheets, wherein the chalcogen of said metal chalcogenide compound is selected from S, Se and Te. Also disclosed are methods for making and using the graphene-supported assembly, including graphene-supported MoS.sub.2. Monoliths with high surface area and conductivity can be achieved. Lower operating temperatures in some applications can be achieved. Pore size and volume can be tuned.

  1. Asymptotic variance of grey-scale surface area estimators

    DEFF Research Database (Denmark)

    Svane, Anne Marie

    Grey-scale local algorithms have been suggested as a fast way of estimating surface area from grey-scale digital images. Their asymptotic mean has already been described. In this paper, the asymptotic behaviour of the variance is studied in isotropic and sufficiently smooth settings, resulting...... in a general asymptotic bound. For compact convex sets with nowhere vanishing Gaussian curvature, the asymptotics can be described more explicitly. As in the case of volume estimators, the variance is decomposed into a lattice sum and an oscillating term of at most the same magnitude....

  2. Indexing Glomerular Filtration Rate to Body Surface Area

    DEFF Research Database (Denmark)

    Redal-Baigorri, Belén; Rasmussen, Knud; Heaf, James Goya

    2014-01-01

    BACKGROUND: Kidney function is mostly expressed in terms of glomerular filtration rate (GFR). A common feature is the expression as ml/min per 1.73 m(2) , which represents the adjustment of the individual kidney function to a standard body surface area (BSA) to allow comparison between individuals....... We investigated the impact of indexing GFR to BSA in cancer patients, as this BSA indexation might affect the reported individual kidney function. METHODS: Cross-sectional study of 895 adults who had their kidney function measured with (51) chrome ethylene diamine tetraacetic acid. Mean values of BSA...

  3. Three-dimensional PtNi Hollow Nanochains as Enhanced Electrocatalyst for Oxygen Reduction Reaction

    Energy Technology Data Exchange (ETDEWEB)

    Fu, Shaofang; Zhu, Chengzhou; Song, Junhua; Engelhard, Mark H.; He, Yang; Du, Dan; Wang, Chong M.; Lin, Yuehe

    2016-05-05

    Three-dimensional porous PtNi hollow nanochains are successfully synthesized via galvanic replacement method using Ni nanosponges as sacrificial templates in an aqueous solution. It is found that the composition and shell thickness of the 3D PtNi hollow nanochains can be easily controlled by tuning the concentration of Pt precursors. The as-prepared PtNi hollow nanochains with optimized composition present high electrochemical surface area (70.8 m2 g-1), which is close to that of commercial Pt/C (83 m2 g-1). Moreover, the PtNi catalyst with Pt content of ~77% presents superior electrocatalytic performance for oxygen reduction reaction compared to commercial Pt/C. It shows a mass activity of 0.58 A mgPt-1, which is around 3 times higher than that of Pt/C. This strategy may be extended to the preparation of other multimetallic nanocrystals with 3D hollow nanostructures, which are expected to present high catalytic properties.

  4. Nanostructure and Formation Mechanism of PtWO3/C Nanocatalyst by Ethylene Glycol Method

    Institute of Scientific and Technical Information of China (English)

    WU Feng; LIU Yanhong; WU Chuan

    2011-01-01

    Pt-WO3 nanoparticles uniformly dispersed on Vulcan XC-72R carbon black were prepared by an ethylene glycol method. The morphology, composition, nanosturcture, electrochemical characteristics and electrocatalytic activity were characterized, and the formation mechanism was investigated. The average particle size was 2.3 nm, the same as that of Pt/C catalyst. The W/Pt atomic ratio was 1/20, much lower than the design of 1/3. The deposition of WO3·xH2O nanoparticles on Vulcan XC-72R carbon black was found to be very difficult by TEM. From XPS and XRD, the Pt nanoparticles were formed in the colloidal solution of Na2WO4,the EG insoluble Na2WO4 resulted in the decreased relative crystallinity and increased crystalline lattice constant compared with those of Pt/C catalyst and, subsequently, the higher specific electrocatalytic activity as determined by CV. The Pt-mass and Pt-electrochemically-active-specific-surface-area based anodic peak current densities for ethanol oxidation were 422.2 mA·mg-1Pt and 0.43 mA·cm-2Pt, 1.2 and 1.1 times higher than those of Pt/C catalyst, respectively.

  5. Adsorption and activation of methane and methanol on Pt(100) surface: a density functional study; Adsorption et activation du methane et du methanol sur la surface (100) du platine: une etude par la fonctionnelle de la densite

    Energy Technology Data Exchange (ETDEWEB)

    Moussounda, P.S

    2006-11-15

    The activation of methane (CH{sub 4}) and methanol (CH{sub 3}OH) on Pt(100) surface has been investigated using density functional theory calculations based on plane-wave basis and pseudo-potential. We optimised CH{sub 4}/Pt(100) system. The calculated adsorption energies over the top, bridge and hollow sites are small, weakly dependent on the molecular orientation. The nature of the CH{sub 4}-Pt interaction was examined through the electronic structure changes. The adsorption of methyl (CH{sub 3}) and hydrogen (H) and the co-adsorption of CH{sub 3}+H were also calculated. From these results, we examined the dissociation of CH{sub 4} to CH{sub 3}+H, and the activation energies found are in good agreement with the experimental and theoretical values. The activation of CH{sub 3}OH/Pt(100) has been studied. All the sites have almost the same adsorption energy. The adsorption of oxygen (O) and the co-adsorption of CH{sub 4} and O were also examined. In addition, the formation of CH{sub 3}OH assuming a one-step mechanism step via the co-adsorption of CH{sub 4}+O has been studied and the barrier height was found to be high. (authors)

  6. Effectiveness of Vegetation Index Transformation for Land Use Identifying and Mapping in the Area of Oil palm Plantation based on SPOT-6 Imagery (Case Study: PT.Tunggal Perkasa Plantations, Air Molek, Indragiri Hulu)

    Science.gov (United States)

    Setyowati, H. A.; S, S. H. Murti B.; Sukentyas, E. S.

    2016-11-01

    The reflection of land surface, atmosphere and vegetation conditions affect the reflectance value of the object is recorded on remote sensing image so that it can affect the outcome of information extraction from remote sensing imagery one multispectral classification. This study aims to assess the ability of the transformation of generic vegetation index (Wide Dynamic Range Vegetation Index), the vegetation index transformation that is capable reducing the influence of the atmosphere (Atmospherically Resistant Vegetation Index), and the transformation of vegetation index that is capable of reducing the influence of the background soil (Second Modified Soil Adjusted Vegetation Index) for the identification and mapping of land use in the oil palm plantation area based on SPOT-6 archived on June 13, 2013 from LAPAN. The study area selected oil palm plantations PT. Tunggal Perkasa Plantations, Air Molek, Indragiri Hulu, Riau Province. The method is using the transformation of the vegetation index ARVI, MSAVI2, and WDRVI. Sample selection method used was stratified random sampling. The test method used mapping accuracy of the confusion matrix. The results showed that the best transformation of the vegetation index for the identification and mapping of land use in the plantation area is ARVI transformation with a total of accuracy is 96%. Accuracy of mapping land use settlements 100%, replanting 82.35%, 81.25% young oil palm, old oil palm 99.46%, 100% bush, body of water 100%, and 100% bare-soil.

  7. Influence of growth and anneal conditions on the surface roughness of L1{sub 0} Fe{sub 50}Pd{sub x}Pt{sub 50-x} thin films

    Energy Technology Data Exchange (ETDEWEB)

    Jiang Xin, E-mail: xinjiang@us.ibm.com [Almaden Research Center, IBM Research, 650 Harry Road, San Jose, CA 95120 (United States); Liu Ruisheng; Gao Li; Topuria, Teya; Parkin, Stuart [Almaden Research Center, IBM Research, 650 Harry Road, San Jose, CA 95120 (United States)

    2012-09-15

    We deposit Fe{sub 50}Pd{sub x}Pt{sub 50-x} alloy thin films by magnetron sputtering onto a TiN seed layer. Chemically ordered L1{sub 0} films are obtained which display large perpendicular magnetic anisotropy. We find that the surface roughness of the film depends strongly on the growth and anneal conditions as well as the Pd composition of the film. Smooth films are obtained by deposition above the chemical ordering temperature and by removing Pd from the alloy. - Highlights: Black-Right-Pointing-Pointer FePdPt thin films with strong perpendicular magnetic anisotropy. Black-Right-Pointing-Pointer Strong dependence of surface roughness on Pd composition. Black-Right-Pointing-Pointer FePt roughness strongly influenced by the disorder to order transition process. Black-Right-Pointing-Pointer Reduced FePt film roughness by deposition above the ordering temperature.

  8. Platinum in Earth surface environments

    Science.gov (United States)

    Reith, F.; Campbell, S. G.; Ball, A. S.; Pring, A.; Southam, G.

    2014-04-01

    Platinum (Pt) is a rare precious metal that is a strategic commodity for industries in many countries. The demand for Pt has more than doubled in the last 30 years due to its role in the catalytic conversion of CO, hydrocarbons and NOx in modern automobiles. To explore for new Pt deposits, process ores and deal with ecotoxicological effects of Pt mining and usage, the fundamental processes and pathways of Pt dispersion and re-concentration in surface environments need to be understood. Hence, the aim of this review is to develop a synergistic model for the cycling of Pt in Earth surface environments. This is achieved by integrating the geological/(biogeo)chemical literature, which focuses on naturally occurring Pt mobility around ore deposits, with the environmental/ecotoxicological literature dealing with anthropogenic Pt dispersion. In Pt deposits, Pt occurs as sulfide-, telluride- and arsenide, native metal and alloyed to other PGEs and iron (Fe). Increased mining and utilization of Pt combined with the burning of fossil fuels have led to the dispersion of Pt-containing nano- and micro-particles. Hence, soils and sediments in industrialized areas, urban environments and along major roads are now commonly Pt enriched. Platinum minerals, nuggets and anthropogenic particles are transformed by physical and (bio)geochemical processes. Complexation of Pt ions with chloride, thiosulfate, ammonium, cyanide, low- and high molecular weight organic acids (LMWOAs and HMWOAs) and siderophores can facilitate Pt mobilization. Iron-oxides, clays, organic matter and (micro)biota are known to sequester Pt-complexes and -particles. Microbes and plants are capable of bioaccumulating and reductively precipitating mobile Pt complexes. Bioaccumulation can lead to toxic effects on plants and animals, including humans. (Bio)mineralization in organic matter-rich sediments can lead to the formation of secondary Pt particles and -grains. Ultimately, Pt is enriched in oceanic sediments

  9. Room-temperature formation of Pt$_3$Si/Pt$_2$Si films on poly-Si substrates

    CERN Document Server

    Dubkov, V P; Chizh, K V; Yuryev, V A

    2016-01-01

    We propose a way of formation of thin bilayer Pt$_3$Si/Pt$_2$Si films at room temperature on poly-Si substrates by Pt magnetron sputtering and wet etching, obtain such film, investigate its structure and phase composition and estimate the thickness of its layers. We verify by direct x-ray photoelectron-spectroscopic measurements our previous observation of the Pt$_2$Si layer formaton between Pt and poly-Si films as a result of Pt magnetron sputtering at room temperature. This layer likely appears due to high enough temperature of Pt ions in the magnetron plasma sufficient for chemical reaction of the silicide film formation on the Si surface. The Pt$_3$Si layer likely forms from the Pt--Pt$_3$Si layer (Pt$_{95}$Si$_5$), which arises under Pt film during the magnetron sputtering, as a result of Pt removal by wet etching.

  10. Preparation of Pt-GO composites with high-number-density Pt nanoparticles dispersed uniformly on GO nanosheets

    Institute of Scientific and Technical Information of China (English)

    Nanting Li; Shaochun Tang; Xiangkang Meng

    2016-01-01

    Pt–GO composites with high-number-density Pt nanoparticles dispersed uniformly on GO nanosheets were prepared using ethylene glycol as reducer at 180 °C. The nanoparticles had an average size of 12 nm with corners and edges on their surfaces. The composites had electrochemically active surface area of 31.7 m2 g ? 1 with a ratio (If/Ir ¼ 0.96) of the forward anodic peak current (If) to the reverse anodic peak current (Ir) in cyclic voltammetry curves, which is much higher than those of the reported Pt nano-dendrites/reduced graphene oxide composites.

  11. High surface area graphene foams by chemical vapor deposition

    Science.gov (United States)

    Drieschner, Simon; Weber, Michael; Wohlketzetter, Jörg; Vieten, Josua; Makrygiannis, Evangelos; Blaschke, Benno M.; Morandi, Vittorio; Colombo, Luigi; Bonaccorso, Francesco; Garrido, Jose A.

    2016-12-01

    Three-dimensional (3D) graphene-based structures combine the unique physical properties of graphene with the opportunity to get high electrochemically available surface area per unit of geometric surface area. Several preparation techniques have been reported to fabricate 3D graphene-based macroscopic structures for energy storage applications such as supercapacitors. Although reaserch has been focused so far on achieving either high specific capacitance or high volumetric capacitance, much less attention has been dedicated to obtain high specific and high volumetric capacitance simultaneously. Here, we present a facile technique to fabricate graphene foams (GF) of high crystal quality with tunable pore size grown by chemical vapor deposition. We exploited porous sacrificial templates prepared by sintering nickel and copper metal powders. Tuning the particle size of the metal powders and the growth temperature allow fine control of the resulting pore size of the 3D graphene-based structures smaller than 1 μm. The as-produced 3D graphene structures provide a high volumetric electric double layer capacitance (165 mF cm-3). High specific capacitance (100 Fg-1) is obtained by lowering the number of layers down to single layer graphene. Furthermore, the small pore size increases the stability of these GFs in contrast to the ones that have been grown so far on commercial metal foams. Electrodes based on the as-prepared GFs can be a boost for the development of supercapacitors, where both low volume and mass are required.

  12. Unjuk Kerja Jaringan Seluler 2G dan 3G PT. XL Axiata di Area Jawa Tengah Bagian Utara setelah Proyek Swap dan Modernisasi

    Directory of Open Access Journals (Sweden)

    Eva Yovita Dwi Utami

    2015-04-01

    Full Text Available The increasing number of customers and the need for reliable communication require the availability of coverage, sufficient capacity and good quality of mobile communications networks. New BTS implementation is required to cover a wider area with good network quality. However, it often requires high cost and long time to get permission from the government and local residents. Swap and Modernization Project is a project that swap the previous 3G equipment using BTS 3900 Huawei with Ericsson RBS 6000 and modernize the 2G RBS 2000 to RBS 6000 and then carry out parameter settings to optimize the network. In this paper, we report the results of mobile network performance after Swap and Modernization projects had been done in terms of the signal strength improvements, which are showed by Rx Level, RSCP and CDD Dump parameters. The study was conducted in PT XL Axiata Northern Areas of Central Java with D5 cluster as a sample. The results show improvement of Rx Level that increased by 89.93 %, and RSCP value increased by 58.36 %. The swap and modernization of the BTS and parameter settings are able to improve CDD Dump parameters. These improvements are able to expand the coverage area of cluster D5 sites.

  13. Ethylene glycol oxidation on Pt and Pt-Ru nanoparticle decorated polythiophene/multiwalled carbon nanotube composites for fuel cell applications.

    Science.gov (United States)

    Selvaraj, Vaithilingam; Alagar, Muthukaruppan

    2008-01-30

    A novel supporting material containing polythiophene (PTh) and multiwalled carbon nanotubes (MWCNTs) (PTh-CNTs) is prepared by in situ polymerization of thiophene on carbon nanotubes using FeCl(3) as oxidizing agent under sonication. The prepared polythiophene/CNT composites are further decorated with Pt and Pt-Ru nanoparticles by chemical reduction of the corresponding metal salts using HCHO as reducing agent at pH = 11 (Pt/PTh-CNT and Pt-Ru/PTh-CNT). The fabricated composite films decorated with nanoparticles were investigated towards the electrochemical oxidation of ethylene glycol (EG). The presence of carbon nanotubes in conjugation with a conducting polymer produces a good catalytic effect, which might be due to the higher electrochemically accessible surface areas, electronic conductivity and easier charge-transfer at polymer/electrolyte interfaces, which allows higher dispersion of Pt and Pt-Ru nanoparticles. Such nanoparticle modified PTh-CNT electrodes exhibit better catalytic behavior towards ethylene glycol oxidation. Results show that Pt/PTh-CNT and Pt-Ru/PTh-CNT modified electrodes show enhanced electrocatalytic activity and stability towards the electro-oxidation of ethylene glycol than the Pt/PTh electrodes, which shows that the composite film is more promising for applications in fuel cells.

  14. Ethylene glycol oxidation on Pt and Pt-Ru nanoparticle decorated polythiophene/multiwalled carbon nanotube composites for fuel cell applications

    Energy Technology Data Exchange (ETDEWEB)

    Selvaraj, Vaithilingam; Alagar, Muthukaruppan [Department of Chemical Engineering, Alagappa College of Technology, Anna University, Chennai 600025 (India)

    2008-01-30

    A novel supporting material containing polythiophene (PTh) and multiwalled carbon nanotubes (MWCNTs) (PTh-CNTs) is prepared by in situ polymerization of thiophene on carbon nanotubes using FeCl{sub 3} as oxidizing agent under sonication. The prepared polythiophene/CNT composites are further decorated with Pt and Pt-Ru nanoparticles by chemical reduction of the corresponding metal salts using HCHO as reducing agent at pH = 11 (Pt/PTh-CNT and Pt-Ru/PTh-CNT). The fabricated composite films decorated with nanoparticles were investigated towards the electrochemical oxidation of ethylene glycol (EG). The presence of carbon nanotubes in conjugation with a conducting polymer produces a good catalytic effect, which might be due to the higher electrochemically accessible surface areas, electronic conductivity and easier charge-transfer at polymer/electrolyte interfaces, which allows higher dispersion of Pt and Pt-Ru nanoparticles. Such nanoparticle modified PTh-CNT electrodes exhibit better catalytic behavior towards ethylene glycol oxidation. Results show that Pt/PTh-CNT and Pt-Ru/PTh-CNT modified electrodes show enhanced electrocatalytic activity and stability towards the electro-oxidation of ethylene glycol than the Pt/PTh electrodes, which shows that the composite film is more promising for applications in fuel cells.

  15. The screening effects of the screened exchange hybrid functional in surface systems: A case study on the CO/Pt(111) problem

    Science.gov (United States)

    Li, H.; Gillen, R.; Robertson, J.

    2016-06-01

    The screened exchange (sX) hybrid functional has been widely used in computational material science. Although it has widely been studied in bulk systems, less is known about its functional behavior in surface systems which are crucial to many technologies such as materials synthesis and nano-electronic devices. Assessing the screening dependent functional behaviors in the surface systems is therefore important for its application in such systems. In this work, we investigate the screening effects of the sX in CO adsorption on Pt(111) surface. The differences between the sX and Heyd-Scuseria-Ernzerhof (HSE06) hybrid functionals, and the effects of screening parameters are studied. The screening has two effects: first, the HOMO-LUMO gap is screening dependent. This affects the site preference most significantly. In this work, atop adsorption of CO/Pt(111) is predicted by the hybrid functionals with screened exchange potential. The sX(1.44) gives the largest HOMO-LUMO gap for the isolated CO molecule. The adsorption energy difference between the atop and fcc site is also the largest by the sX(1.44) which is explained by the reduced metal d states to the CO 2π* state back-donation, with stronger effect for the fcc adsorption than for the atop adsorption; second, the adsorption energy is screening dependent. This can be seen by comparing the sX(2.38) and HSE06 which have different screening strengths. They show similar surface band structures for the CO adsorption but different adsorption energies, which is explained by the stronger CO 5σ state to the metal d states donation or the effectively screened Pauli repulsion. This work underlines the screening strength as a main difference between sX and HSE06, as well as an important hybrid functional parameter for surface calculation.

  16. Oxygen reduction activity of Pt and Pt-alloys in acid electrolyte

    Energy Technology Data Exchange (ETDEWEB)

    Paulus, Ursula A. [Paul Scherrer Inst., CH-5232 Villigen PSI (Switzerland); Schmidt, Thomas J.; Stamenkovic, Vojislav R.; Markovic, Nenad M.; Ross, Philip N. [Material Science Division, Lawrence Berkeley National Laboratory, University of California, Berkeley, CA 94720 (United States)

    2001-07-01

    The oxygen reduction reaction (ORR) has been studied on polycrystalline (pc) Pt, Pt{sub 3}Ni and Pt{sub 3}Co bulk alloy electrodes and on carbon supported Pt, PtNi and PtCo alloy catalysts. Base voltammetry measurements as well as complementary Auger Electron Spectroscopy (AES) and Low Energy Ion Scattering (LEIS) on bulk electrodes and High Resolution Transmission Electron Microscopy (HRTEM)-analysis on the supported catalysts allow an estimation of the surface composition. By using the rotating ring-disk electrode (RRDE) technique both the kinetic analysis of the ORR and in parallel the detection and quantification of the amount of peroxide produced during the ORR are possible. The activity for the ORR increases in the order Pt < Pt{sub 3}Ni < Pt{sub 3}Co for equally prepared bulk alloys and Pt < Pt{sub 3}Ni {approx} Pt{sub 3}CO < PtCo for the carbon supported catalysts, respectively. It was proposed that the mechanism for the ORR is the same on pure Pt and the PtNi and PtCo alloys. (author)

  17. Investigation of Sea Surface Temperature (SST) anomalies over Cyprus area

    Science.gov (United States)

    Georgiou, Andreas; Akçit, Nuhcan

    2016-08-01

    The temperature of the sea surface has been identified as an important parameter of the natural environment, governing processes that occur in the upper ocean. This paper focuses on the analysis of the Sea Surface Temperature (SST) anomalies at the greater area of Cyprus. For that, SST data derived from MODerate-resolution Imaging Spectroradiometer (MODIS) instrument on board both Aqua and Terra sun synchronous satellites were used. A four year period was chosen as a first approach to address and describe this phenomenon. Geographical Information Systems (GIS) has been used as an integrated platform of analysis and presentation in addition of the support of MATLAB®. The methodology consists of five steps: (i) Collection of MODIS SST imagery, (ii) Development of the digital geo-database; (iii) Model and run the methodology in GIS as a script; (iv) Calculation of SST anomalies; and (v) Visualization of the results. The SST anomaly values have presented a symmetric distribution over the study area with an increase trend through the years of analysis. The calculated monthly and annual average SST anomalies (ASST) make more obvious this trend, with negative and positive SST changes to be distributed over the study area. In terms of seasons, the same increase trend presented during spring, summer, autumn and winter with 2013 to be the year with maximum ASST observed values. Innovative aspects comprise of straightforward integration and modeling of available tools, providing a versatile platform of analysis and semi-automation of the operation. In addition, the fine resolution maps that extracted from the analysis with a wide spatial coverage, allows the detail representation of SST and ASST respectively in the region.

  18. Highly Durable Supportless Pt Hollow Spheres Designed for Enhanced Oxygen Transport in Cathode Catalyst Layers of Proton Exchange Membrane Fuel Cells.

    Science.gov (United States)

    Dogan, Didem C; Cho, Seonghun; Hwang, Sun-Mi; Kim, Young-Min; Guim, Hwanuk; Yang, Tae-Hyun; Park, Seok-Hee; Park, Gu-Gon; Yim, Sung-Dae

    2016-10-10

    Supportless Pt catalysts have several advantages over conventional carbon-supported Pt catalysts in that they are not susceptible to carbon corrosion. However, the need for high Pt loadings in membrane electrode assemblies (MEAs) to achieve state-of-the-art fuel cell performance has limited their application in proton exchange membrane fuel cells. Herein, we report a new approach to the design of a supportless Pt catalyst in terms of catalyst layer architecture, which is crucial for fuel cell performance as it affects water management and oxygen transport in the catalyst layers. Large Pt hollow spheres (PtHSs) 100 nm in size were designed and prepared using a carbon template method. Despite their large size, the unique structure of the PtHSs, which are composed of a thin-layered shell of Pt nanoparticles (ca. 7 nm thick), exhibited a high surface area comparable to that of commercial Pt black (PtB). The PtHS structure also exhibited twice the durability of PtB after 2000 potential cycles (0-1.3 V, 50 mV/s). A MEA fabricated with PtHSs showed significant improvement in fuel cell performance compared to PtB-based MEAs at high current densities (>800 mA/cm(2)). This was mainly due to the 2.7 times lower mass transport resistance in the PtHS-based catalyst layers compared to that in PtB, owing to the formation of macropores between the PtHSs and high porosity (90%) in the PtHS catalyst layers. The present study demonstrates a successful example of catalyst design in terms of catalyst layer architecture, which may be applied to a real fuel cell system.

  19. The effect of growth surface morphology on the crystal structure and magnetic property of L1{sub 0} order PtFe layers deposited by magnetron sputtering

    Energy Technology Data Exchange (ETDEWEB)

    Ding Wanyu, E-mail: dwysd_2000@163.com [Graduate School of Saitama Institute of Technology, Fukaya, Saitama 369-0293 (Japan) and School of Materials Science and Engineering, Dalian Jiaotong University, Dalian 116028 (China); Ishiguro, Satoshi; Ogatsu, Ryo [Graduate School of Saitama Institute of Technology, Fukaya, Saitama 369-0293 (Japan); Ju, Dongying, E-mail: dyju@sit.ac.jp [Graduate School of Saitama Institute of Technology, Fukaya, Saitama 369-0293 (Japan)

    2012-08-01

    The Fe/Pt/Fe/Pt layers (Pt/Fe multilayer) were deposited on general glass substrate at room temperature by magnetron sputtering technique. Varying the deposition and post-annealing treatment parameters, the PtFe alloy (PtFe) layer with different crystal structures and magnetic properties were obtained at the interface between Fe and Pt layer. The characterization by X-ray diffraction (XRD) showed that the as-deposited Pt/Fe multilayer only contained pure Fe and Pt with body-centered and face-centered cubic structures, respectively. As-deposited Pt layer displayed (2 0 0) preferred orientation, and the columnar grains structure could be observed by the scanning electron microscopy. The PtFe layers with L1{sub 0} face-centered cubic structure could be formed at the interface between Pt and Fe layers by post-annealing the multilayers at 500 Degree-Sign C. In case of Pt/Fe multilayer deposited on smooth substrate, the larger columnar grains in Pt layer resulted in L1{sub 0} PtFe layers without any preferred orientation. While in case of Pt/Fe multilayer deposited on the rough substrate, the thinner columnar grains in Pt layer could induce L1{sub 0} PtFe layers with (2 0 0) preferred orientation. In this case, the vibrating sample magnetometer results indicated that, the magnetic coercivity in plane and out-of-plane model could reach 3.72 and 2.32 kOe, respectively. Based on above results, the L1{sub 0} structure Pt/Fe multilayer with satisfied magnetic properties could be prepared at low temperature by our simple route.

  20. A passive wireless hydrogen surface acoustic wave sensor based on Pt-coated ZnO nanorods.

    Science.gov (United States)

    Huang, Ya-Shan; Chen, Yung-Yu; Wu, Tsung-Tsong

    2010-03-05

    Using a passive wireless sensor to detect hydrogen can reach the goals of reducing cost and increasing the lifetime since the sensor can work without batteries. In this paper, a passive wireless hydrogen SAW sensor operating at room temperature has been achieved by combining a SAW tag and a resistive hydrogen sensor. The SAW tag is fabricated on a 128 degrees YX-LiNbO(3) substrate and its central frequency is 433 MHz. The resistive hydrogen sensor with the Pt-coated ZnO nanorods as the sensing film has the advantages of high stability, good repeatability and simple fabrication. The ZnO nanorods are synthesized by using the aqueous solution method and the Pt coating is employed as a catalyst for the hydrogen detection. The property of the resistive hydrogen sensor is examined before combining with the SAW tag. Results show that the resistance changes caused by the variations of relative humidity and temperature are negligible. Finally, the hydrogen SAW sensor is configured and measured wirelessly for various hydrogen concentrations at room temperature. The difference of the relative return loss caused by the hydrogen concentration variation is obvious and recognizable. All responses show that the proposed hydrogen sensor not only has good repeatability and high sensitivity but is capable of passive wireless detection.

  1. The impact of built-up surfaces on land surface temperatures in Italian urban areas.

    Science.gov (United States)

    Morabito, Marco; Crisci, Alfonso; Messeri, Alessandro; Orlandini, Simone; Raschi, Antonio; Maracchi, Giampiero; Munafò, Michele

    2016-05-01

    Urban areas are characterized by the very high degree of soil sealing and continuous built-up areas: Italy is one of the European countries with the highest artificial land cover rate, which causes a substantial spatial variation in the land surface temperature (LST), modifying the urban microclimate and contributing to the urban heat island effect. Nevertheless, quantitative data regarding the contribution of different densities of built-up surfaces in determining urban spatial LST changes is currently lacking in Italy. This study, which aimed to provide clear and quantitative city-specific information on annual and seasonal spatial LST modifications resulting from increased urban built-up coverage, was conducted generally throughout the whole year, and specifically in two different periods (cool/cold and warm/hot periods). Four cities (Milan, Rome, Bologna and Florence) were included in the study. The LST layer and the built-up-surface indicator were obtained via use of MODIS remote sensing data products (1km) and a very high-resolution map (5m) of built-up surfaces recently developed by the Italian National Institute for Environmental Protection and Research. The relationships between the dependent (mean daily, daytime and nighttime LST values) and independent (built-up surfaces) variables were investigated through linear regression analyses, and comprehensive built-up-surface-related LST maps were also developed. Statistically significant linear relationships (pcities studied, with a higher impact during the warm/hot period than in the cool/cold ones. Daytime and nighttime LST slope patterns depend on the city size and relative urban morphology. If implemented in the existing city plan, the urban maps of built-up-surface-related LST developed in this study might be able to support more sustainable urban land management practices by identifying the critical areas (Hot-Spots) that would benefit most from mitigation actions by local authorities, land-use decision

  2. Superior long-term activity for a Pt-Re alloy compared to Pt in methanol oxidation reactions

    Science.gov (United States)

    Duke, Audrey S.; Xie, Kangmin; Monnier, John R.; Chen, Donna A.

    2017-03-01

    Pt-Re bimetallic catalysts have shown enhanced activity compared to pure Pt for reactions involving oxidation, but the origins of this improved activity are not fully understood. Methanol oxidation on a Pt-Re alloy surface and pure Pt foil was studied in a microreactor coupled to an ultrahigh vacuum chamber. For reaction at 60 °C, the Pt-Re alloy surface exhibits superior long-term activity over a 24 h reaction period compared to pure Pt. The initial activity of Pt is 10-15% higher than on Pt-Re; however, the Pt surface gradually loses activity after 10 h online, whereas the activity of Pt-Re does not diminish. Post-reaction XPS shows that more carbon accumulates on the Pt than on Pt-Re, and the improved long-term activity is attributed to a greater ability of Pt-Re to oxidize the carbonaceous intermediates that eventually poison active sites. Both Pt and Pt-Re surfaces have almost no activity for methanol oxidation until a minimum coverage of oxygen is achieved from O2 dissociation. A comparison with methanol oxidation studies on Pt and Pt-Re in a pressure regime that is 150 times lower than in this work demonstrates that more carbon and less oxygen accumulate on the surfaces during reaction at the lower pressures.

  3. The natural history of the growth of the hand: I. Hand area as a percentage of body surface area.

    Science.gov (United States)

    Amirsheybani, H R; Crecelius, G M; Timothy, N H; Pfeiffer, M; Saggers, G C; Manders, E K

    2001-03-01

    The use of a patient's own hand as a tool to estimate the area of burn injury is well documented. The area of the palmar surface of one hand has been estimated to be 1 percent of the body surface area. The area of the palmar surface of the hand was measured to test the accuracy of this estimate and then compared with the body surface area as calculated by formulas in common use. This study also sought to determine the natural history of the growth of the hand to permit development of a readily available, bedside means of estimating hand area and body surface area. Bilateral hand tracings were obtained from 800 volunteers ranging in age from 2 to 89 years. The area of each tracing was determined using an integrating planimeter. The height and weight of each individual were measured, and his/her body surface area was calculated. The palmar hand's percentage of body surface area was determined by calculating the quotient for hand area divided by body surface area. Additionally, the width of the hand was measured from the ulnar aspect at the palmar digital crease of the small finger to the point where the thumb rested against the base of the index finger. The length of the hand was measured from the middle of the interstylon to the tip of the middle finger. These two figures were multiplied together to obtain a product which approximated the area of the hand. Based on the most commonly used DuBois formula for calculating body surface area, the area of palmar surface of the hand corresponds to 0.78 +/- 0.08 percent of the body surface area in adults. The percentage varies somewhat with age and reaches a maximum of 0.87 +/- 0.06 percent in young children. Multiplying the length of the hand by its width overestimates the area of the hand as determined by planimetry by only 2 percent. A patient's own hand may be used as a complementary, readily available template for estimation of burn area or other areas of disease or injury. In adults, the area of tracing of the outline

  4. Study of surface chemistry and microstructure of TiO2 nanostructures on Pt(111)/Si wafer and FTO glass substrates: a comparative approach

    Science.gov (United States)

    Roy Moulik, Samik; Ghatak, Ankita; Ghosh, Barnali

    2016-09-01

    We report, the kinetically controlled growth of the (002)-oriented TiO2 nanorods on fluorine-doped tin oxide (FTO) coated glass substrate via a cost effective hydrothermal synthesis route of binary oxides. In addition to this, the nanoflowered like growth of TiO2 nanorods using cubic structure Pt(111)/SiO2/Si substrate has also been demonstrated. Tuning of shape, crystallographic structure issues has been discussed by controlling the surface chemistry of the substrate on which the nanostructures were grown. The crystallographic structural aspects of the grown nanorods was confirmed both on ensemble and single nanowire level using spatially resolved tools and techniques. Growth mechanism for different shape, size and crystallographic structure depending on the surface chemistry of the substrate has been proposed. Understanding of growth of oriented TiO2 nanorods and interaction mechanism is quite promising and encouraging for designing optoelectronic and photocatalytic devices to enhanced electron transport and lower exciton recombination rates.

  5. Floristic composition and structure of a peat swamp forest in the conservation area of the PT National Sago Prima, Selat Panjang, Riau, Indonesia

    Directory of Open Access Journals (Sweden)

    Yusi Rosalina

    2014-12-01

    Full Text Available We studied the floristic composition and structure of the logged-over peat swamp forest in the  PT National Sago Prima of PT Sampoerna Agro Tbk. group for future management of the conservation area that has been  set aside by the company.  In January - February 2012, 25 quadrats of 20 m × 20 m were laid out systematically along a transect,  thus covering a sampled area of 1-ha.  The results showed that the study site was a regenerating and developing secondary  peat swamp forests having high plant species richness. The total number of species recorded was 73 species of 38 families, consisting of 49 species (30 families of trees (DBH≥ 10 cm , 42     species (24 families of saplings (H > 1.5 m and DBH < 10 cm and 41 species (27 families of seedlings and undergrowth. Tree density was 550 individuals/ha and total tree basal area was 18.32 m2. The Shannon-Wiener’s Diversity Index for trees was high  (3.05  Two tree species with the highest Importance Values (IV were Pandanus atrocarpus (IV = 45.86 % and Blumeodendron subrotundifolium (22.46%. The tree families with the highest IV were Pandanaceae (45.86, Myrtaceae (40.37 and Dipterocarpaceae (39.20.  Forest structure dominated by trees with a diameter below 20 cm amounting to 408 trees/ha (74.05%. D and E strata with height of less than 20 m, and density of 431 trees/ha (78.36%. Jaccard Similarity index among species, showed strong association between Pandanus atrocarpus and Blumeodendron subrotundifolium and based on this association combined with high IVs, the two parameters of species characterized the forest, hence the forest  could be designated as the Pandanus atrocarpus–Blumeodendron   subrotundifolium association. Primary forest species with high economic values were still present in the forest. Eleven species can be included in the IUCN Red List, of which Shorea rugosa is in the category of Critically Endangered,  Shorea teysmanniana Endangered and

  6. Method for producing high surface area chromia materials for catalysis

    Science.gov (United States)

    Gash, Alexander E.; Satcher, Joe; Tillotson, Thomas; Hrubesh, Lawrence; Simpson, Randall

    2007-05-01

    Nanostructured chromium(III)-oxide-based materials using sol-gel processing and a synthetic route for producing such materials are disclosed herein. Monolithic aerogels and xerogels having surface areas between 150 m.sup.2/g and 520 m.sup.2/g have been produced. The synthetic method employs the use of stable and inexpensive hydrated-chromium(III) inorganic salts and common solvents such as water, ethanol, methanol, 1-propanol, t-butanol, 2-ethoxy ethanol, and ethylene glycol, DMSO, and dimethyl formamide. The synthesis involves the dissolution of the metal salt in a solvent followed by an addition of a proton scavenger, such as an epoxide, which induces gel formation in a timely manner. Both critical point (supercritical extraction) and atmospheric (low temperature evaporation) drying may be employed to produce monolithic aerogels and xerogels, respectively.

  7. Fully automated algorithm for wound surface area assessment.

    Science.gov (United States)

    Deana, Alessandro Melo; de Jesus, Sérgio Henrique Costa; Sampaio, Brunna Pileggi Azevedo; Oliveira, Marcelo Tavares; Silva, Daniela Fátima Teixeira; França, Cristiane Miranda

    2013-01-01

    Worldwide, clinicians, dentists, nurses, researchers, and other health professionals need to monitor the wound healing progress and to quantify the rate of wound closure. The aim of this study is to demonstrate, step by step, a fully automated numerical method to estimate the size of the wound and the percentage damaged relative to the body surface area (BSA) in images, without the requirement for human intervention. We included the formula for BSA in rats in the algorithm. The methodology was validated in experimental wounds and human ulcers and was compared with the analysis of an experienced pathologist, with good agreement. Therefore, this algorithm is suitable for experimental wounds and burns and human ulcers, as they have a high contrast with adjacent normal skin.

  8. High surface area ThO/sub 2/ catalyst

    Science.gov (United States)

    Colmenares, C.A.; Somorjai, G.A.; Maj, J.J.

    1983-06-21

    A ThO/sub 2/ catalyst having a high surface area of about 80 to 125m/sup 2//g is synthesized. The compound is synthesized by simultaneously mixing an aqueous solution of ThNO/sub 3/(NO/sub 3/)/sub 4/.4H/sub 2/O with an aqueous solution of Na/sub 2/CO/sub 3/.H/sub 2/O, to produce a solution and solid ThOCO/sub 3/. The solid ThOCO/sub 3/ is separated from the solution, and then calcined at a temperature of about 225 to 300/sup 0/C for about 40 to 55 hours to produce ThO/sub 2/. The ThO/sub 2/ catalyst produced includes Na present as a substitutional cation in an amount equal to about 5 to 10 at. %.

  9. Estimating the surface area of birds: using the homing pigeon (Columba livia as a model

    Directory of Open Access Journals (Sweden)

    Cristina R. Perez

    2014-05-01

    Full Text Available Estimation of the surface area of the avian body is valuable for thermoregulation and metabolism studies as well as for assessing exposure to oil and other surface-active organic pollutants from a spill. The use of frozen carcasses for surface area estimations prevents the ability to modify the posture of the bird. The surface area of six live homing pigeons in the fully extended flight position was estimated using a noninvasive method. An equation was derived to estimate the total surface area of a pigeon based on its body weight. A pigeon's surface area in the fully extended flight position is approximately 4 times larger than the surface area of a pigeon in the perching position. The surface area of a bird is dependent on its physical position, and, therefore, the fully extended flight position exhibits the maximum area of a bird and should be considered the true surface area of a bird.

  10. Estimating the surface area of birds: using the homing pigeon (Columba livia) as a model.

    Science.gov (United States)

    Perez, Cristina R; Moye, John K; Pritsos, Chris A

    2014-05-08

    Estimation of the surface area of the avian body is valuable for thermoregulation and metabolism studies as well as for assessing exposure to oil and other surface-active organic pollutants from a spill. The use of frozen carcasses for surface area estimations prevents the ability to modify the posture of the bird. The surface area of six live homing pigeons in the fully extended flight position was estimated using a noninvasive method. An equation was derived to estimate the total surface area of a pigeon based on its body weight. A pigeon's surface area in the fully extended flight position is approximately 4 times larger than the surface area of a pigeon in the perching position. The surface area of a bird is dependent on its physical position, and, therefore, the fully extended flight position exhibits the maximum area of a bird and should be considered the true surface area of a bird.

  11. Development of inflatable seals for the rotatable plugs of sodium cooled fast breeder reactors. A review. Pt. I. Key areas

    Energy Technology Data Exchange (ETDEWEB)

    Sinha, Nilay K. [Indira Gandhi Centre for Atomic Research (IGCAR), Kalpakkam, Tamilnadu (India). Dept. of Atomic Energy (DAE); Raj, Baldev [P.S. Govindaswamy Naidu (PSG) Institutions, Coimbatore, Tamilnadu (India)

    2013-11-15

    Identification of development areas and their implementation for rotatable plug (RP) inflatable seals of Na cooled, 500 Mw (e) Prototype Fast Breeder Reactor (PFBR) and 40 MW (t) Fast Breeder Test Reactor (FBTR) are described, largely based on a late 1990s survey of cover gas seal development (1950s - early 1990s) which defined a set of shortlisted design options and developmental strategy to minimize effort, cost and time. Comparative studies of top shield sealing and evolving FBR designs suggest suitability of inflatable seal as primary barrier in RPs. International experience identified choice and qualification of seal elastomer under synergistic degrading environment of reactor as the prime element of development. The low pressure, non-reinforced, unbeaded, PFBR inflatable seal (made of 50/50 blend of Viton {sup registered} GBL 200S/600S) developed for 10 y life provides a unification scheme for nuclear elastomeric sealing based on 5 peroxide cured fluoroelastomer blend formulations, 1 finite element analysis approach, 1 Teflon-like plasma coating technique and 2 manufacturing processes promising significant gains in standardization, economy and safety. Uniqueness was ab initio development in the absence of established industry or ready-made supply. Part I addresses key areas of design shortlisting, strategy, development and unification with a backdrop of international evolution. (orig.)

  12. Surface ozone in the urban area of Manaus, Amazonas, Brazil

    Science.gov (United States)

    Souza, R. A. F. D.; Costa, P. S.; Silva, C.; Godoi, R. M.; Martin, S. T.; Tota, J.; Barbosa, H. M.; Pauliquevis, T.; Ferreira De Brito, J.; Artaxo, P.; Manzi, A. O.; Wolf, S. A.; Cirino, G. G.

    2014-12-01

    When nitrogen oxides from vehicle and industrial emissions mix with volatile organic compounds from trees and plants with exposure to sunlight, a chemical reaction occurs contributing to ground-level ozone pollution. The preliminary results of the surface ozone study in urban area of Manaus, Amazonas State, Brazil, are presented for the first intensive operating period (IOP1) of the GoAmazon experiment (February/March 2014). Photochemical ozone production was found to be a regular process, with an afternoon maximum of the ozone mixing ratio of lower than 20 ppbv for cloudy days or clear sky weather. Typical ozone concentrations at mid-day were low (about 10 ppb). On the other hand, several high-value ozone episodes with surface ozone mixing ratios up to three times larger were registered during the dry season of 2013 (September/October). At the beginning of the wet season, the ozone concentration in Manaus decreased significantly, but diurnal variations can be found during the days with rainfall and other fast changes of meteorological conditions. Possible explanations of the nature of pulsations are discussed. Photochemical ozone production by local urban plumes of Manaus is named as a first possible source of the ozone concentration and biomass burning or power plant emissions are suggested as an alternative or an additional source.

  13. Highly active dealloyed Cu@Pt core-shell electrocatalyst towards 2-propanol electrooxidation in acidic solution

    Science.gov (United States)

    Poochai, Chatwarin

    2017-02-01

    Dealloyed Cu@Pt core-shell electrocatalyst was fabricated by cyclic co-electrodeposition and selective Cu dealloying (CCEd-sCuD) on carbon paper (CP), namely Cu@Pt/CP. The Cu@Pt/CP exhibited a core-shell structure comprising with a Cu-rich core and a Pt-rich shell. The crystalline phases of Pt/CP and Cu@Pt/CP were a face-centered cubic (fcc). The compressive lattice strain approximately 0.85% was found in the Cu@Pt/CP owing to a lattice mismatch between a core and a shell region. In the core-region, Cu was formed Pt-Cu alloy as major and copper oxide and also metallic copper as minor. The morphology and grain size of the Cu@Pt/CP displayed a porous spherical shape with 100 nm in diameter, while those of Pt/CP seemed to be a cubic shape with smaller diameter of 40 nm. In electrochemical and catalytic activity, the surface of Cu@Pt/CP had a larger electrochemical active surface area (ECSA) than that of Pt/CP due to a porous formation caused by Cu dealloying. It is not surprising that the Cu@Pt/CP showed higher catalytic activity and greater stability towards 0.5 M 2-propanol electrooxidation in 0.5 M H2SO4 in terms of peak current density (jp), peak potential (Ep), onset potential (Eonset), diffusion coefficient (D), and charge transfer resistance (Rct) which were caused by electronic structure modification, higher compressive lattice strain, and larger ECSA, compared with Pt/CP.

  14. Molecular orientation and lattice ordering of C60 molecules on the polar FeO/Pt(111) surface

    Science.gov (United States)

    Qin, Zhihui; Liu, Cunding; Chen, Jian; Guo, Qinmin; Yu, Yinghui; Cao, Gengyu

    2012-01-01

    C60 molecules assemble into close packing layer under the domination of the intermolecular interaction when deposited onto Pt(111)-supported FeO layer kept at 400 K. From corresponding high resolution scanning tunneling microscopy (STM) image, a kind of C60 molecular orientational ordering stabilized by the intermolecular interaction is revealed as C60/FeO(111)-(√133 × √133) R17.5° structure and determined from the commensurability between the C60 nearest-neighbor distance and the lattice of the underlying oxygen layer. Moreover, due to the inhomogeneously distributed work function of the underlying FeO layer, the C60 molecular electronic state is periodically modulated resulting in a bright-dim STM contrast. In addition, one coincidence lattice ordering is determined as 8 × 8 superstructure with respect to the C60 primitive cell, which overlays a 3 × 3 moiré cell of the underlying FeO layer.

  15. Computing the Surface Area of Three-Dimensional Scanned Human Data

    Directory of Open Access Journals (Sweden)

    Seung-Hyun Yoon

    2016-07-01

    Full Text Available An efficient surface area evaluation method is introduced by using smooth surface reconstruction for three-dimensional scanned human body data. Surface area evaluations for various body parts are compared with the results from the traditional alginate-based method, and quite high similarity between the two results is obtained. We expect that our surface area evaluation method can be an alternative to measuring surface area by the cumbersome alginate method.

  16. Comparative analysis of the electroactive area of Pt/C PEMFC electrodes in liquid and solid polymer contact by underpotential hydrogen adsorption/desorption

    Energy Technology Data Exchange (ETDEWEB)

    Chaparro, A.M.; Martin, A.J.; Folgado, M.A.; Gallardo, B. [Dep. de Energia, CIEMAT, Avda. Complutense, 22, 28040 Madrid (Spain); Daza, L. [Dep. de Energia, CIEMAT, Avda. Complutense, 22, 28040 Madrid (Spain); Instituto de Catalisis y Petroleoquimica (CSIC), Marie Curie 2, Campus Cantoblanco, 28049 Madrid (Spain)

    2009-06-15

    Because of the different experimental conditions found in literature for the measurement of the electroactive area of Pt/C electrodes of proton exchange membrane fuel cells (PEMFC) by means of underpotential hydrogen adsorption (H{sub UPD}) voltammetry, specially concerning sweep rate and temperature, it was found necessary to perform an analysis of these parameters. With this aim, the electroactive area of PEMFC electrodes has been measured by means of H{sub UPD} voltammetry at different sweep rates and temperatures, in liquid electrolyte and solid polymer contact. Both configurations show that H{sub UPD} adsorption and desorption charges are strongly dependent on sweep rate voltage and temperature. The most common behaviour observed is a maximum in H{sub UPD} desorption charge, typically in the 100-10 mV s{sup -1} sweep rate range, whereas H{sub UPD} adsorption charge shows continuous increase with decreasing sweep rate. The decrease of desorption charge at low sweep rates is attributed to adsorbing species related with carbon support reactivity. These processes are also responsible for the increase in desorption H{sub UPD} charge at low sweep rate. At high sweep rate, both adsorption and desorption H{sub UPD} charges decrease due to limiting diffusion of protons through the microporous electrode. As a consequence, it is found that the closest approximation to the real electroactive area (i.e. the area accessible to protons) corresponds to the maximum in the H{sub UPD} desorption charge in the range of 10-100 mV s{sup -1} sweep rate. The influence of measuring temperature is also tested in the range 25 C-80 C. A dependence of the adsorption and desorption hydrogen charges is found, due to thermodynamic and kinetics factors. We observe that the processes competing with hydrogen adsorption, i.e. generation and adsorption of carbon species are enhanced with temperature, so a low measuring temperature is found as most appropriate. (author)

  17. Solar assisted biogas plants: Pt. 4. Optimum area for blackening and double glazing over a fixed-dome biogas plant

    Energy Technology Data Exchange (ETDEWEB)

    Jayashankar, B.C.; Kishor, J.; Goyal, I.C.; Sawhney, R.L.; Sodha, M.S.

    The economic analysis of a fixed-dome biogas plant of rated capacity 8 m/sup 3/, above which a part of the ground is blackened and doubly glazed in the cold climate of Srinagar is presented. Blackening and glazing of the ground cannot alone maintain the slurry temperature at 35/sup 0/C, which is the optimum temperature in the mesophilic range for the anaerobic digestion of cattle dung, and so a part of the biogas must be burnt. The electrical simulation experiments have been performed to determine the loss or gain of heat from the underground biodigestor to the ambient atmosphere through the ground if a part of the ground above is blackened and double glazed. Economic analysis of the system shows that the optimum area to be blackened and glazed would have a radius 1.5 times that of the biodigestor.

  18. Surface plasmon enhanced the responsivity of the ZnO/Pt nanoparticles/ZnO sandwich structured photodetector via optimizing the thickness of the top ZnO layer

    Science.gov (United States)

    Guo, Zexuan; Jiang, Dayong; Zhao, Man; Guo, Fei; Pei, Jianan; Liu, Rusheng; Sun, Long; Hu, Nan; Zhang, Guoyu

    2016-10-01

    Based on the ZnO/Pt nanoparticles/ZnO multilayer films by magnetron sputtering method, we elaborate the ultraviolet (UV) photodetectors and deduce that they provide an ideal platform for highly using efficient surface plasmon (SP) modes. By only adjusting the thickness of the top layer and remaining other conditions unchanged, we draw a conclusion that the responsivity of the sandwich photodetector can be drastically increased from 0.08 to 0.40 A/W. It firmly provides for our findings that the responsivity enhancement factors without Pt nanoparticles (NPs) are apparently smaller than those by means of introducing Pt NPs. This can be ascribed to the SP of Pt NPs. The near-field effect of SP results in the dependence of the responsivity enhancement of ZnO films on the top layer film thickness. Which are in good agreement with theoretical calculations.

  19. A low-temperature synthesis of electrochemical active Pt nanoparticles and thin films by atomic layer deposition on Si(111) and glassy carbon surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Rui [Joint Center for Artificial Photosynthesis, California Institute of Technology, Pasadena, CA 91125 (United States); Han, Lihao [Joint Center for Artificial Photosynthesis, California Institute of Technology, Pasadena, CA 91125 (United States); Photovoltaic Materials and Devices (PVMD) Laboratory, Delft University of Technology, P.O. Box 5031, GA Delft 2600 (Netherlands); Huang, Zhuangqun; Ferrer, Ivonne M. [Joint Center for Artificial Photosynthesis, California Institute of Technology, Pasadena, CA 91125 (United States); Division of Chemistry and Chemical Engineering, California Institute of Technology, 210 Noyes Laboratory 127-72, Pasadena, CA 91125 (United States); Smets, Arno H.M.; Zeman, Miro [Photovoltaic Materials and Devices (PVMD) Laboratory, Delft University of Technology, P.O. Box 5031, GA Delft 2600 (Netherlands); Brunschwig, Bruce S., E-mail: bsb@caltech.edu [Beckman Institute, California Institute of Technology, Pasadena, CA 91125 (United States); Lewis, Nathan S., E-mail: nslewis@caltech.edu [Joint Center for Artificial Photosynthesis, California Institute of Technology, Pasadena, CA 91125 (United States); Beckman Institute, California Institute of Technology, Pasadena, CA 91125 (United States); Division of Chemistry and Chemical Engineering, California Institute of Technology, 210 Noyes Laboratory 127-72, Pasadena, CA 91125 (United States); Kavli Nanoscience Institute, California Institute of Technology, Pasadena, CA 91125 (United States)

    2015-07-01

    Atomic layer deposition (ALD) was used to deposit nanoparticles and thin films of Pt onto etched p-type Si(111) wafers and glassy carbon discs. Using precursors of MeCpPtMe{sub 3} and ozone and a temperature window of 200–300 °C, the growth rate was 80–110 pm/cycle. X-ray photoelectron spectroscopy (XPS), atomic force microscopy (AFM), and scanning electron microscopy (SEM) were used to analyze the composition, structure, morphology, and thickness of the ALD-grown Pt nanoparticle films. The catalytic activity of the ALD-grown Pt for the hydrogen evolution reaction was shown to be equivalent to that of e-beam evaporated Pt on glassy carbon electrode. - Highlights: • Pure Pt films were grown by atomic layer deposition (ALD) using MeCpPtMe3 and ozone. • ALD-grown Pt thin films had high growth rates of 110 pm/cycle. • ALD-grown Pt films were electrocatalytic for hydrogen evolution from water. • Electrocatalytic activity of the ALD Pt films was equivalent to e-beam deposited Pt. • No carbon species were detected in the ALD-grown Pt films.

  20. Effect of resistance to sintering on Pt/PPy-MWCNT catalysts for PEM fuel cells

    Energy Technology Data Exchange (ETDEWEB)

    Kim, K. [Yonsei Univ., Seoul (Korea, Republic of). Specialized Graduate School of Hydrogen and Fuel Cell; Kim, H. [Yonsei Univ., Seoul (Korea, Republic of). Dept. of Chemical and Biomolecular Engineering

    2010-07-01

    Recent studies have suggested that platinum (Pt) growth contributes to the degradation of fuel cell performance, as the electrochemical surface area of Pt is decreased when the particles increase in size. This study investigated the effect of inhibition to the sintering effect and uniform dispersion of Pt in a polypyrrole(Pp) multiwalled carbon nanotube (MWCNT) composite supported Pt catalyst. The sintering effect was investigated under half-cell conditions using a 0.5M sulfuric acid (H{sub 2}SO{sub 4}) electrolyte with cyclic voltammetry ranging from 0 to 1.2 V with a 5 mV per second sweep rate. The hydrogen desorption peak was carried out from the charge under the electrochemically active surface area at 4000 cycle periods. The study showed that coating the MWCNT with Ppy showed higher Pt distribution and a lower Pt sintering effect. The results were attributed to the rough surface characteristics obtained using the Ppy. Results also indicated that the catalytic activity for the oxygen reduction reaction increased by improving the interaction and stability of the Pt. 1 ref.

  1. Human lung volume, alveolar surface area, and capillary length

    DEFF Research Database (Denmark)

    Wiebe, B. M.; Laursen, Henning

    1995-01-01

    Cavalieri's principle, length density, morphometry, stereology, surface density, vertical sections, vertical slices......Cavalieri's principle, length density, morphometry, stereology, surface density, vertical sections, vertical slices...

  2. Gram-Scale-Synthesized Pd2Co-Supported Pt Monolayer Electrocatalysts for Oxygen Reduction Reaction

    Energy Technology Data Exchange (ETDEWEB)

    Zhou, W.; Sasaki, K; Su, D; Zhu, Y; Wang, J; Adzic, R

    2010-01-01

    Gram-scale synthesis of Pt{sub ML} electrocatalysts with a well-defined core-shell structure has been carried out using method involving galvanic displacement of an underpotential deposition Cu layer. The Pt shell thickness can be controlled by stepwise deposition. The Pt{at}Pd{sub 2}Co/C nanoparticles were characterized by X-ray powder diffraction, aberration-corrected scanning transmission electron microscopy, high-resolution energy-loss spectrometry, and in situ X-ray absorption spectroscopy. A complete Pt shell of 0.6 nm on a Pd{sub 2}Co core has been confirmed. The Pt{at}Pd{sub 2}Co/C core-shell electrocatalysts showed a very high activity for the oxygen reduction reaction; the Pt mass and specific activity were 0.72 A mg{sub Pt}{sup -1} and 0.5 mA cm{sup -2}, respectively (3.5 and 2.5 times higher than the corresponding values for commercial Pt catalysts), at 0.9 V in 0.1 M HClO{sub 4} at room temperature. In an accelerated potential cycling test, a loss in active surface area and a decrease in catalytic activity for gram-scale-synthesized Pt{sub ML} catalysts were also determined.

  3. Te/Pt nanonetwork modified carbon fiber microelectrodes for methanol oxidation

    Science.gov (United States)

    Tsai, Hsiang-Yu; Shih, Zih-Yu; Lin, Zong-Hong; Chang, Huan-Tsung

    2013-05-01

    Te/Pt nanonetwork-decorated carbon fiber microelectrodes (CFMEs) have been fabricated and employed as anodic catalysts in a direct methanol fuel cell (DMFC). Te nanowires were prepared from tellurite ions (TeO32-) through a seed-mediated growth process and were deposited onto CFMEs to form three-dimensional Te nanonetworks. The Te nanonetworks then acted as a framework and reducing agent to reduce PtCl62- ions to form Te/Pt through a galvanic replacement reaction, leading to the formation of Te/PtCFMEs. By controlling the reaction time, the amount of Pt and morphology of Te/Pt nanonetworks were controlled, leading to various degrees of electrocatalytic activity. The Te/PtCFMEs provide a high electrochemical active surface area (129.2 m2 g-1), good catalytic activity (1.2 A mg-1), high current density (20.0 mA cm-2), long durability, and tolerance toward the poisoning species for methanol oxidation in 0.5 M sulfuric acid containing 1 M methanol. We have further demonstrated an enhanced current density by separately using 3 and 5 Te/PtCFMEs. Our results show that the low-cost, stable, and effective Te/PtCFMEs have great potential in the fabrication of cost-effective fuel cells.

  4. Synthesis of Cubic-Shaped Pt Particles with (100) Preferential Orientation by a Quick, One-Step and Clean Electrochemical Method.

    Science.gov (United States)

    Liu, Jie; Fan, Xiayue; Liu, Xiaorui; Song, Zhishuang; Deng, Yida; Han, Xiaopeng; Hu, Wenbin; Zhong, Cheng

    2017-06-07

    A new approach has been developed for in situ preparing cubic-shaped Pt particles with (100) preferential orientation on the surface of the conductive support by using a quick, one-step, and clean electrochemical method with periodic square-wave potential. The whole electrochemical deposition process is very quick (only 6 min is required to produce cubic Pt particles), without the use of particular capping agents. The shape and the surface structure of deposited Pt particles can be controlled by the lower and upper potential limits of the square-wave potential. For a frequency of 5 Hz and an upper potential limit of 1.0 V (vs saturated calomel electrode), as the lower potential limit decreases to the H adsorption potential region, the Pt deposits are changed from nearly spherical particles to cubic-shaped (100)-oriented Pt particles. High-resolution transmission electron microscopy and selected-area electron diffraction reveal that the formed cubic Pt particles are single-crystalline and enclosed by (100) facets. Cubic Pt particles exhibit characteristic H adsorption/desorption peaks corresponding to the (100) preferential orientation. Ge irreversible adsorption indicates that the fraction of wide Pt(100) surface domains is 47.8%. The electrocatalytic activities of different Pt particles are investigated by ammonia electro-oxidation, which is particularly sensitive to the amount of Pt(100) sites, especially larger (100) domains. The specific activity of cubic Pt particles is 3.6 times as high as that of polycrystalline spherical Pt particles, again confirming the (100) preferential orientation of Pt cubes. The formation of cubic-shaped Pt particles is related with the preferential electrochemical deposition and dissolution processes of Pt, which are coupled with the periodic desorption and adsorption processes of O-containing species and H adatoms.

  5. Extent of Stream Burial and Relationships to Watershed Area, Topography, and Impervious Surface Area

    Directory of Open Access Journals (Sweden)

    Roy E. Weitzell

    2016-11-01

    Full Text Available Stream burial—the routing of streams through culverts, pipes, and concrete lined channels, or simply paving them over—is common during urbanization, and disproportionately affects small, headwater streams. Burial undermines the physical and chemical processes governing life in streams, with consequences for water quality and quantity that may amplify from headwaters to downstream receiving waters. Knowledge of the extent of stream burial is critical for understanding cumulative impacts to stream networks, and for future decision-making allowing for urban development while protecting ecosystem function. We predicted stream burial across the urbanizing Potomac River Basin (USA for each 10-m stream segment in the basin from medium-resolution impervious cover data and training observations obtained from high-resolution aerial photography in a GIS. Results were analyzed across a range in spatial aggregation, including counties and independent cities, small watersheds, and regular spatial grids. Stream burial was generally correlated with total impervious surface area (ISA, with areas exhibiting ISA above 30% often subject to elevated ratios of stream burial. Recurring patterns in burial predictions related to catchment area and topographic slope were also detected. We discuss these results in the context of physiographic constraints on stream location and urban development, including implications for environmental management of aquatic resources.

  6. Reduction of Pt2+ species in model Pt-CeO2 fuel cell catalysts upon reaction with methanol

    Science.gov (United States)

    Neitzel, Armin; Johánek, Viktor; Lykhach, Yaroslava; Skála, Tomáš; Tsud, Nataliya; Vorokhta, Mykhailo; Matolín, Vladimír; Libuda, Jörg

    2016-11-01

    The stability of atomically dispersed Pt2+ species on the surface of nanostructured CeO2 films during the reaction with methanol has been investigated by means of synchrotron radiation photoelectron spectroscopy and resonant photoemission spectroscopy. The isolated Pt2+ species were prepared at low Pt concentration in Pt-CeO2 film. Additionally, Pt2+ species coexisting with metallic Pt particles were prepared at high Pt concentration. We found that adsorption of methanol yields similar decomposition products regardless of Pt concentration in Pt-CeO2 films. A small number of oxygen vacancies formed during the methanol decomposition can be replenished in the Pt-CeO2 film with low Pt concentration by diffusion of oxygen from the bulk. In the presence of supported Pt particles, a higher number of oxygen vacancies leads to a partial reduction of the Pt2+ species. The isolated Pt2+ species are reduced under rather strongly reducing conditions only, i.e. during annealing under continuous exposure to methanol. Reduction of isolated Pt2+ species results in the formation of ultra-small Pt particles containing around 25 atoms per particle or less. Such ultra-small Pt particles demonstrate excellent stability against sintering during annealing of Pt-CeO2 film with low Pt concentration under reducing conditions.

  7. Structural and electronic properties and the fermi surface of the new non-centrosymmetric superconductors: 3.6 K CaIrSi3 and 2.3 K CaPtSi3

    Science.gov (United States)

    Bannikov, V. V.; Shein, I. R.; Ivanovskii, A. L.

    2010-09-01

    Ab initio FLAPW-GGA calculations have been performed to investigate structural properties, electronic band structure, and Fermi surface topology of the newly discovered non-centrosymmetric superconductors: 3.6 K CaIrSi3 and 2.3 K CaPtSi3. As a result, the peculiarities of the crystal structure, electronic bands, total and site-projected l-decomposed densities of states, and the shape of the Fermi surface for CaIrSi3 and CaPtSi3 were obtained and analyzed.

  8. Self-consistent linear-muffin-tin-orbitals coherent-potential technique for bulk and surface calculations: Cu-Ni, Ag-Pd, and Au-Pt random alloys

    DEFF Research Database (Denmark)

    Abrikosov, I. A.; Skriver, Hans Lomholt

    1993-01-01

    energies and work functions for three fcc-based alloys (Cu-Ni, Ag-Pd, and Au-Pt) over the complete concentration range. The calculated mixing enthalpies for the Ag-Pd and Au-Pt systems agrees with experimental values, and the calculated concentration dependence of the lattice parameters agrees...... with experiment for all three systems. We find that the calculated surface energies and work functions in the unsegregated case exhibit a small positive deviation from a linear concentration dependence. Finally, we performed a segregation analysis based on the calculated surface energies by means of a simple...

  9. Effect of Ce addition on the surface properties and n-dodecane dehydrogenation performance of Pt-Sn/Ce-Al2O3 catalyst

    Science.gov (United States)

    Li, Xianru; He, Songbo; Wei, Huangzhao; Luo, Sha; Gu, Bin; Sun, Chenglin

    2015-08-01

    Ce-modified alumina carriers with different Ce content were prepared by vacuum isovolume impregnation method aiming to improve the n-dodecane catalytic dehydrogenation performance of PtSn/Al2O3 catalyst. The support and catalyst were characterized by XRD, N2 adsorption-desorption, NH3-TPD, H2-TPR, CO-pulse adsorption and TG-DTG. Results showed that Ce addition decreased the surface acid amount significantly and inhibited the reduction of SnO x species. Besides, Ce containing catalyst showed higher n-dodecane dehydrogenation activity and stability and lower coke deposition amount and coke burning temperature. In our study, the optimal Ce addition amount for n-dodecane dehydrogenation was 2%.

  10. Intracellular surface-enhanced Raman scattering (SERS) with thermally stable gold nanoflowers grown from Pt and Pd seeds

    KAUST Repository

    Song, Hyon Min

    2013-01-01

    SERS provides great sensitivity at low concentrations of analytes. SERS combined with near infrared (NIR)-resonant gold nanomaterials are important candidates for theranostic agents due to their combined extinction properties and sensing abilities stemming from the deep penetration of laser light in the NIR region. Here, highly branched gold nanoflowers (GNFs) grown from Pd and Pt seeds are prepared and their SERS properties are studied. The growth was performed at 80°C without stirring, and this high temperature growth method is assumed to provide great shape stability of sharp tips in GNFs. We found that seed size must be large enough (>30 nm in diameter) to induce the growth of those SERS-active and thermally stable GNFs. We also found that the addition of silver nitrate (AgNO3) is important to induce sharp tip growth and shape stability. Incubation with Hela cells indicates that GNFs are taken up and reside in the cytoplasm. SERS was observed in those cells incubated with 1,10-phenanthroline (Phen)-loaded GNFs. This journal is © 2013 The Royal Society of Chemistry.

  11. Surface geometry and strain energy effects in the failure of a (Ni, Pt)Al/EB-PVD thermal barrier coating

    Energy Technology Data Exchange (ETDEWEB)

    Vaidyanathan, Krishnakumar; Jordan, Eric H.; Gell, Maurice

    2004-03-08

    Thermal cycling tests were conducted on a commercial yttria-stabilized zirconia electron beam-physical vapor deposited thermal barrier coating (TBC) on a platinum aluminide ({beta}-(Ni, Pt)Al) bond coat. Surprisingly, the longest life sample lasted 10 times longer than the shortest life sample. Two distinct mechanisms have been found responsible for the observed damage initiation and progression at the thermally grown oxide (TGO)/bond coat interface. The first mechanism leads to localized debonding at the TGO/bond coat interface due to increasing out-of-plane tensile stresses at ridges that form along bond coat grain boundaries. The second mechanism is driven by cyclic plasticity of the bond coat that leads to cavity formation at the TGO/bond coat interface. The primary finding of this work is that the first mechanism, involving tensile stress at ridge tops, is life limiting. Based on this mechanism, it is demonstrated that the variation in bond coat ridge aspect ratio can explain the unusual 10x variation in observed sample life. It is proposed that ridge top spallation leads to debonds of sufficient size to result in unstable fracture driven by the strain energy stored in the TGO. The criticality of the flaw created by local debonding is supported by experimental determination of the strain energy available in the TGO through measurement of TGO stress and thickness combined with published fracture mechanics solutions of the relevant flaw geometry.

  12. X-ray diffraction and surface acoustic wave analysis of BST/Pt/TiO{sub 2}/SiO{sub 2}/Si thin films

    Energy Technology Data Exchange (ETDEWEB)

    Mseddi, Souhir; Hedi Ben Ghozlen, Mohamed [Laboratoire de Physique des Materiaux, Faculte des Sciences de Sfax, Universite de Sfax, 3018 Sfax (Tunisia); Njeh, Anouar [Unite de Physique, Informatique et Matematiques, Faculte des Sciences de Gafsa, Universite de Gafsa, 2112 Gafsa (Tunisia); Schneider, Dieter [Fraunhofer-Institut fuer Material- und Strahltechnologie, Winterbergstrasse 28, 1277 Dresden (Germany); Fuess, Hartmut [Institute of Materials Science, University of Technology, Petersenstr.23, 64287 Darmstadt (Germany)

    2011-11-15

    High dielectric constant and electrostriction property of (Ba, Sr)Ti0{sub 3} (BST) thin films result in an increasing interest for dielectric devices and microwave acoustic resonator. Barium strontium titanate (Ba{sub 0.645}Sr{sub 0.355}TiO{sub 3}) films of about 300 nm thickness are grown on Pt(111)/TiO{sub 2}/SiO{sub 2}/Si(001) substrates by rf magnetron sputtering deposition techniques. X-ray diffraction is applied for the microstructural characterization. The BST films exhibit a cubic perovskite structure with a dense and smooth surface. A laser acoustic waves (LA-waves) technique is used to generate surface acoustic waves (SAW) propagating in the BST films. Young's modulus E and the Poisson ratio {nu} of TiO{sub 2,} Pt and BST films in different propagation directions are derived from the measured dispersion curves. Estimation of BST elastics constants are served in SAW studies. Impact of stratification process on SAW, propagating along [100] and [110] directions of silicon substrate, has been interpreted on the basis of ordinary differential equation (ODE) and stiffness matrix method (SMM). A good agreement is observed between experimental and calculated dispersion curves. The performed calculations are strongly related to the implemented crystallographic data of each layer. Dispersion curves are found to be sensitive to the SAW propagation direction and the stratification process for the explored frequency ranges 50-250 MHz, even though it corresponds to a wave length clearly higher than the whole films thickness.

  13. Adhesion enhancement for liquid silicone rubber and different surface by organosilane and Pt catalyst at room temperature

    Indian Academy of Sciences (India)

    Fang Wang; Yanni Li; Dan Wang

    2013-11-01

    Surface modification of aluminum, glass, epoxy resin, polypropylene and polyethylene via corona discharge pretreatment and platinum catalyst addition to promote their adhesion with liquid silicone rubber is reported. The corona-pretreated substrate surface was silanized with vinyltrimethoxysilane to generate vinyl groups on the surface, which could be initiated by platinum catalyst to form vinyl radicals. Then, the vinyltrimethoxysilane modified substrate was dipped into platinum catalyst solution to introduce platinum on the vinyltrimethoxysilane surface. The modified aluminum surface was characterized by X-ray photoelectron spectroscopy (XPS). The strong adhesion property between liquid silicone rubber and different surface was achieved by introducing a small amount of vinyltrimethoxysilane and platinum catalyst, followed by curing at low temperature. XPS result indicated the formation of vinyltrimethoxysilane coating on aluminum surface. Peel strength for liquid silicone rubber/vinyltrimethoxysilane–platinum surface was over 3.2 kN/m compared to only 1.1 kN/m for liquid silicone rubber/vinyltrimethoxysilane–aluminum. The cohesive failure in the bulk of liquid silicone rubber was observed for liquid silicone rubber/vinyltrimethoxysilane–platinum surface. It is assumed that the cross-linking reactions between vinyl groups in the vinyltrimethoxysilane coating and unsaturated terminal group of liquid silicone rubber occur due to the existence of platinum catalyst.

  14. High Surface Area Ceria Nanoparticles via Hydrothermal Synthesis Experiment Design

    Directory of Open Access Journals (Sweden)

    Stanislav Kurajica

    2016-01-01

    Full Text Available Hydrothermal synthesis of CeO2 was optimized on two reactant concentrations and synthesis temperature and duration, in order to achieve material having the greatest specific surface area (SSA. Taguchi method of experimental design was employed in evaluation of the relative importance of synthesis parameters. CeO2 nanoparticles were characterized using X-ray diffraction, nitrogen adsorption-desorption isotherms, and scanning electron microscopy. Optimum conditions for obtaining particles with greater SSA were calculated according to Taguchi’s model “the-higher-the-better.” Synthesis temperature was found to be the only parameter significant for enabling nanoparticles with greater SSA. Mesoporous nanocrystalline ceria with SSA as great as 226 m2 g−1 was achieved, which is unprecedented for the hydrothermally synthesized ceria. The reason for this achievement was found in temperature dependence of the diffusion coefficient which, when low, favors nucleation yielding with fine particles, while when high it favors crystal growth and formation of one-dimensional structures. The occurrence of 1D-structure in sample exhibiting the smallest SSA was confirmed. Very fine crystallites with crystallite size as low as 5.9 nm have been obtained being roughly inverse proportional to SSA. Selected samples were tested as catalyst for soot oxidation. Catalyst morphology turned out to be decisive factor for catalytic activity.

  15. Facile synthesis of high surface area molybdenum nitride and carbide

    Science.gov (United States)

    Roy, Aaron; Serov, Alexey; Artyushkova, Kateryna; Brosha, Eric L.; Atanassov, Plamen; Ward, Tim L.

    2015-08-01

    The synthesis of high surface area γ-Mo2N and α-Mo2C is reported (116 and 120 m2/g) without the temperature programmed reduction of MoO3. γ-Mo2N was prepared in an NH3-free synthesis using forming gas (7 at% H2, N2-balance) as the reactive atmosphere. Three precursors were studied ((NH4)6Mo7O24·4H2O, (NH4)2 Mg(MoO4)2, and MgMoO4) along with the sacrificial support method (SSM) as a means of reducing the particle size of Mo2N and Mo2C. In situ X-ray diffraction (XRD) studies were carried out to identify reaction intermediates, the temperature at which various intermediates form, and the average domain size of the Mo2N products. Materials were synthesized in bulk and further characterized by XRD, HRTEM, XPS, and BET.

  16. Highly uniform distribution of Pt nanoparticles on N-doped hollow carbon spheres with enhanced durability for oxygen reduction reaction

    Energy Technology Data Exchange (ETDEWEB)

    Shi, Qiurong; Zhu, Chengzhou; Engelhard, Mark H.; Du, Dan; Lin, Yuehe

    2017-01-01

    Carbon-supported Pt nanostructures currently exhibited great potential in polymer electrolyte membrane fuel cells. Nitrogen-doped hollow carbon spheres (NHCSs) with extra low density and high specific surface area are promising carbon support for loading Pt NPs. The doped heteroatom of nitrogen could not only contribute to the active activity for the oxygen reduction reaction (ORR), but also shows a strong interaction with Pt NPs for entrapping them from dissolution/migration. This synergetic effect/interaction resulted in the uniform dispersion and strong combination of the Pt NPs on the carbon support and thus play a significant role in hindering the degradation of the catalytic activities of Pt NPs. As expected, the as-obtained Pt/NHCSs displayed improved catalytic activity and superior durability toward ORR.

  17. V-doped TiO2 supported Pt as a promising oxygen reduction reaction catalyst: Synthesis, characterization and in-situ evaluation in proton exchange membrane fuel cell

    Science.gov (United States)

    Bharti, Abha; Cheruvally, Gouri

    2017-09-01

    This study deals with the synthesis and characterization of V-doped, TiO2 supported Pt catalyst (Pt/V-TiO2) for oxygen reduction reaction (ORR) and its in-situ performance investigation in proton exchange membrane (PEM) fuel cell. Pt/V-TiO2 nanocomposite catalyst is prepared via a facile sol-gel and microwave assisted, modified chemical reduction route and its performance is compared with the undoped TiO2 supported catalyst, Pt/TiO2 prepared in an identical way. The prepared Pt/V-TiO2 and Pt/TiO2 catalysts are employed as cathode catalyst in PEM fuel cell and compared with standard Pt/C catalyst. Their comparative studies are conducted with physical and electrochemical techniques. In-situ electrochemical characterization studies show improved ORR catalytic activity of Pt/V-TiO2 compared to Pt/TiO2. Furthermore, both Pt/TiO2 and Pt/V-TiO2 are more stable than Pt/C when subjected to 6000 voltammetric cycles in the range of 0.2-1.2 V vs. standard hydrogen electrode in operating fuel cell conditions, losing only <20% of its electrochemical surface area as compared to 50% loss exhibited by Pt/C. This study thus demonstrates Pt/V-TiO2 nanocomposite material as a potential cathode catalyst for PEM fuel cell with immense scope for further investigation.

  18. Pt nanostructure electrodes pulse electrodeposited in PVP for electrochemical power sources.

    Science.gov (United States)

    Song, You-Jung; Oh, Jae-Kyung; Park, Kyung-Won

    2008-09-03

    In this work, we demonstrated that Pt nanostructure electrodes could be obtained by the pulse electrodeposition method in polyvinylpyrrolidone (PVP). The nanocrystal particles were confirmed by scanning electron microscopy, transmission electron microscopy and x-ray diffraction methods. The average size of Pt nanoparticles deposited in additive PVP with low and high molecular weight is 3.4 and 2.9 nm, respectively, whereas that of Pt electrodeposited without PVP is 360 nm. This means that the size of Pt nanoparticles can be controlled by PVP, resulting in an increased electrochemical surface area. The resulting Pt nanostructure electrodes showed such an improved performance for both direct methanol fuel cells and dye-sensitized solar cells.

  19. Pt nanostructure electrodes pulse electrodeposited in PVP for electrochemical power sources

    Energy Technology Data Exchange (ETDEWEB)

    Song, You-Jung; Oh, Jae-Kyung; Park, Kyung-Won [Department of Chemical and Environmental Engineering, Soongsil University, Seoul 156-743 (Korea, Republic of)], E-mail: kwpark@ssu.ac.kr

    2008-09-03

    In this work, we demonstrated that Pt nanostructure electrodes could be obtained by the pulse electrodeposition method in polyvinylpyrrolidone (PVP). The nanocrystal particles were confirmed by scanning electron microscopy, transmission electron microscopy and x-ray diffraction methods. The average size of Pt nanoparticles deposited in additive PVP with low and high molecular weight is 3.4 and 2.9 nm, respectively, whereas that of Pt electrodeposited without PVP is 360 nm. This means that the size of Pt nanoparticles can be controlled by PVP, resulting in an increased electrochemical surface area. The resulting Pt nanostructure electrodes showed such an improved performance for both direct methanol fuel cells and dye-sensitized solar cells.

  20. Nanostructured polypyrrole/carbon composite as Pt catalyst support for fuel cell applications

    Science.gov (United States)

    Zhao, Hongbin; Li, Lei; Yang, Jun; Zhang, Yongming

    A novel catalyst support was synthesized by in situ chemical oxidative polymerization of pyrrole on Vulcan XC-72 carbon in naphthalene sulfonic acid (NSA) solution containing ammonium persulfate as oxidant at room temperature. Pt nanoparticles with 3-4 nm size were deposited on the prepared polypyrrole-carbon composites by chemical reduction method. Scanning electron microscopy and transmission electron microscopy measurements showed that Pt particles were homogeneously dispersed in polypyrrole-carbon composites. The Pt nanoparticles-dispersed catalyst composites were used as anodes of fuel cells for hydrogen and methanol oxidation. Cyclic voltammetry measurements of hydrogen and methanol oxidation showed that Pt nanoparticles deposited on polypyrrole-carbon with NSA as dopant exhibit better catalytic activity than those on plain carbon. This result might be due to the higher electrochemically available surface areas, electronic conductivity and easier charge-transfer at polymer/carbon particle interfaces allowing a high dispersion and utilization of deposited Pt nanoparticles.

  1. Nanostructured polypyrrole/carbon composite as Pt catalyst support for fuel cell applications

    Energy Technology Data Exchange (ETDEWEB)

    Zhao, Hongbin; Li, Lei; Yang, Jun; Zhang, Yongming [School of Chemistry and Chemical Technology, Shanghai Jiao Tong University, Shanghai 200240 (China)

    2008-10-01

    A novel catalyst support was synthesized by in situ chemical oxidative polymerization of pyrrole on Vulcan XC-72 carbon in naphthalene sulfonic acid (NSA) solution containing ammonium persulfate as oxidant at room temperature. Pt nanoparticles with 3-4 nm size were deposited on the prepared polypyrrole-carbon composites by chemical reduction method. Scanning electron microscopy and transmission electron microscopy measurements showed that Pt particles were homogeneously dispersed in polypyrrole-carbon composites. The Pt nanoparticles-dispersed catalyst composites were used as anodes of fuel cells for hydrogen and methanol oxidation. Cyclic voltammetry measurements of hydrogen and methanol oxidation showed that Pt nanoparticles deposited on polypyrrole-carbon with NSA as dopant exhibit better catalytic activity than those on plain carbon. This result might be due to the higher electrochemically available surface areas, electronic conductivity and easier charge-transfer at polymer/carbon particle interfaces allowing a high dispersion and utilization of deposited Pt nanoparticles. (author)

  2. Understanding the effects of the impervious surfaces pattern on land surface temperature in an urban area

    Science.gov (United States)

    Nie, Qin; Xu, Jianhua

    2015-06-01

    It is well known that urban impervious surface (IS) has a warming effect on urban land surface temperature (LST). However, the influence of an IS's structure, components, and spatial distribution on LST has rarely been quantitatively studied within strictly urban areas. Using ETM+ remote sensing images from the downtown area of Shanghai, China in 2010, this study characterized and quantified the influence of the IS spatial pattern on LST by selecting the percent cover of each IS cover feature and ten configuration metrics. The IS fraction was estimated by linear spectral mixture analysis (LSMA), and LST was retrieved using a mono-window algorithm. The results indicate that high fraction IS cover features account for the majority of the study area. The high fraction IS cover features are widely distributed and concentrated in groups, which is similar with that of high temperature zones. Both the percent composition and the configuration of IS cover features greatly affect the magnitude of LST, but the percent composition is a more important factor in determining LST than the configuration of those features. The significances and effects of the given configuration variables on LST vary greatly among IS cover features.

  3. Cocatalyzing Pt/PtO Phase-Junction Nanodots on Hierarchically Porous TiO2 for Highly Enhanced Photocatalytic Hydrogen Production.

    Science.gov (United States)

    Ren, Xiao-Ning; Hu, Zhi-Yi; Jin, Jun; Wu, Liang; Wang, Chao; Liu, Jing; Liu, Fu; Wu, Min; Li, Yu; Tendeloo, Gustaaf Van; Su, Bao-Lian

    2017-09-06

    Phase-junctions between a cocatalyst and its semiconductor host are quite effective to enhance the photocatalytic activity and are widely studied, while reports on the phase-juncted cocatalyst are still rare. In this work, we report the deposition of the Pt/PtO phase-juncted nanodots as cocatalyst via NaOH modification of an interconnected meso-macroporous TiO2 network with high surface area and inner-particle mesopores to enhance the performance of photocatalytic H2 production. Our results show that NaOH modification can largely influence Pt/PtO phase-juncted nanodot formation and dispersity. Compared to the TiO2 nanoparticles, the hierarchically meso-macroporous TiO2 network containing 0.18 wt % Pt/PtO phase-juncted cocatalyst demonstrates a highest photocatalytic H2 rate of 13 mmol g(-1) h(-1) under simulated solar light, and possesses a stable cycling activity without obvious decrease after five cycles. Such high H2 production performance can be attributed to both the phase-juncted Pt/PtO providing more active sites while PtO suppresses the undesirable hydrogen back reaction, and the special hierarchically porous TiO2 network with inner-particle mesopores presenting short diffusion path lengths for photogenerated electrons and enhanced light harvesting efficiency. This work suggests that Pt/PtO phase-juncted cocatalyst on hierarchically porous TiO2 nanostructures is a promising strategy for advanced photocatalytic H2 production.

  4. Efficient Aerobic Oxidation of Cyclohexane to KA Oil Catalyzed by Pt-Sn supported on MWCNTs

    Indian Academy of Sciences (India)

    Mohammad Sadiq; Muhammad Ali; Rashid Iqbal; Khalid Saeed; Aimal Khan; Muhammad Naveed Umar; Haroon Ur Rashid

    2015-07-01

    Pt-Sn supported on MWCNTs were synthesized and characterized by SEM, EDX, XRD, XRF and surface area and pore size analyzer. The catalyst was used for the partial oxidation of cyclohexane in a Parr type reactor. It was found that Pt-Sn supported on MWCNTs can act as an efficient catalyst for the partial oxidation of cyclohexane into cyclohexanol and cyclohexanone, generating both in a high yield under mild reaction conditions.

  5. Reactive surface area in geochemical models - Lessons learned from a natural analogue

    NARCIS (Netherlands)

    Koenen, M.; Wasch, L.J.

    2013-01-01

    Many uncertainties exist in geochemical modeling. Mineral reactive surface area is one of the uncertain parameters. QEMSCAN analyses are performed on sandstone samples from a Dutch CO2 natural analogue to determine reactive surface areas. Geochemical modeling is performed using QEMSCAN surface areas

  6. THE SURFACE AREA PRESERVING MEAN CURVATURE FLOW IN QUASI-FUCHSIAN MANIFOLDS

    Institute of Scientific and Technical Information of China (English)

    Tian Daping; Li Guanghan; Wu Chuanxi

    2012-01-01

    In this paper,we consider the surface area preserving mean curvature flow in quasi-Fuchsian 3-manifolds.We show that the flow exists for all times and converges exponentially to a smooth surface of constant mean curvature with the same surface area as the initial surface.

  7. Area-selective atomic layer deposition of platinum using photosensitive polyimide

    Science.gov (United States)

    Vervuurt, René H. J.; Sharma, Akhil; Jiao, Yuqing; Kessels, Wilhelmus (Erwin M. M.; Bol, Ageeth A.

    2016-10-01

    Area-selective atomic layer deposition (AS-ALD) of platinum (Pt) was studied using photosensitive polyimide as a masking layer. The polyimide films were prepared by spin-coating and patterned using photolithography. AS-ALD of Pt using poly(methyl-methacrylate) (PMMA) masking layers was used as a reference. The results show that polyimide has excellent selectivity towards the Pt deposition, after 1000 ALD cycles less than a monolayer of Pt is deposited on the polyimide surface. The polyimide film could easily be removed after ALD using a hydrogen plasma, due to a combination of weakening of the polyimide resist during Pt ALD and the catalytic activity of Pt traces on the polyimide surface. Compared to PMMA for AS-ALD of Pt, polyimide has better temperature stability. This resulted in an improved uniformity of the Pt deposits and superior definition of the Pt patterns. In addition, due to the absence of reflow contamination using polyimide the nucleation phase during Pt ALD is drastically shortened. Pt patterns down to 3.5 μm were created with polyimide, a factor of ten smaller than what is possible using PMMA, at the typical Pt ALD processing temperature of 300 °C. Initial experiments indicate that after further optimization of the polyimide process Pt features down to 100 nm should be possible, which makes AS-ALD of Pt using photosensitive polyimide a promising candidate for patterning at the nanoscale.

  8. Phenomenological study of monomer adsorption on fcc (335) surfaces with application to CO, O, and N(2) adsorption on Pt(335).

    Science.gov (United States)

    Phares, Alain J; Grumbine, David W; Wunderlich, Francis J

    2009-01-20

    We extend our recent study of adsorption on fcc (112) to fcc (335) surfaces, still considering only first- and second-neighbor interactions with repulsive first-neighbors. We consider the adsorbate-substrate interaction on the step sites of one of the two edges of the infinitely long terraces to be different from that on the remaining sites. The adsorption features on fcc (335) surfaces are richer than those on fcc (112), which can be attributed to the fact that the equilateral triangular terraces are now four-atoms wide rather than three. Our approach is independent of the chemical composition of the substrate and adsorbates and consequently may be applied to a variety of adsorption systems on fcc (335) surfaces which satisfy the limitations of our model. The basic question that our phenomenological approach intends to answer is: what are the constraints that can be obtained on the interaction energies from the experimental observation of one or more phases? This question is answered in the cases of CO, O, and N(2) adsorbed on Pt(335).

  9. Characterization of (1 1 1) surface tailored Pt nanoparticles by electrochemistry and X-ray powder diffraction

    Energy Technology Data Exchange (ETDEWEB)

    Beyerlein, K.R., E-mail: ken.beyerlein@mse.gatech.edu [Georgia Institute of Technology, Materials Science and Engineering, Erskine Love Building, 771 Ferst Drive, Atlanta, GA 30332 (United States); University of Trento, Department of Materials Engineering and Industrial Technologies, via Mesiano, 77-38100 Trento (Italy); Solla-Gullon, J.; Herrero, E. [Instituto de Electroquimica, Universidad de Alicante, Apartado 99, 03080 Alicante (Spain); Garnier, E. [Instituto de Electroquimica, Universidad de Alicante, Apartado 99, 03080 Alicante (Spain); LECCO, Equipe Electrocatalyse, UMR CNRS No 6503, 40 Avenue du Recteur Pineau, 86022 Poitiers France (France); Pailloux, F. [LMP, UMR 6630 CNRS, SP2MI, Teleport 2, Boulevard M. et P. Curie, BP 30179, 86962 Futuroscope Chasseneuil (France); Leoni, M.; Scardi, P. [University of Trento, Department of Materials Engineering and Industrial Technologies, via Mesiano, 77-38100 Trento (Italy); Snyder, R.L. [Georgia Institute of Technology, Materials Science and Engineering, Erskine Love Building, 771 Ferst Drive, Atlanta, GA 30332 (United States); Aldaz, A.; Feliu, J.M. [Instituto de Electroquimica, Universidad de Alicante, Apartado 99, 03080 Alicante (Spain)

    2010-11-25

    Platinum nanoparticles with a mean size of 8.7 nm were synthesized by a salt reduction reaction having polyhedron shapes with preferential (1 1 1) surfaces. In situ electrochemical characterization of nanoparticles was performed which confirmed the existence of mostly (1 1 1) surface sites in the sample. The effect of this surface in the electrooxidation of CO was measured. Debye Function Analysis (DFA) and Whole Powder Pattern Modelling (WPPM) of the measured X-ray diffraction pattern were carried out to obtain statistical information on the particle size and shape present in the sample. Both analyses determined that the octahedron particle shape was the most abundant which was also consistent with TEM observations. The existence of a small percentage of single twinned particles was determined by DFA, WPPM, as well as analysis of HRTEM images.

  10. Visible light photoactivity of TiO{sub 2} loaded with monometallic (Au or Pt) and bimetallic (Au/Pt) nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Gołąbiewska, Anna, E-mail: annagolabiewska@o2.pl [Department of Chemical Technology, Gdansk University of Technology, 80-233 Gdańsk (Poland); Lisowski, Wojciech [Mazovia Center for Surface Analysis, Institute of Physical Chemistry, Polish Academy of Sciences, 01-224 Warsaw (Poland); Jarek, Marcin; Nowaczyk, Grzegorz [NanoBioMedical Center, Adam Mickiewicz University, Umultowska 85, 61-614 Poznań (Poland); Zielińska-Jurek, Anna; Zaleska, Adriana [Department of Chemical Technology, Gdansk University of Technology, 80-233 Gdańsk (Poland)

    2014-10-30

    Graphical abstract: - Highlights: • Au/Pt nanoparticles enhanced TiO{sub 2} photocatalytic activity under visible irradiation. • Higher photoactivity of Au/Pt-TiO{sub 2} resulted from smaller Au/Pt particles. • Intermetallic state of AuPt favors charge transfer between the metals. • TiO{sub 2} obtained by TIP hydrolysis seems to be best matrix for Au/Pt-TiO{sub 2}. - Abstract: TiO{sub 2} modified with monometallic (Au or Pt) and bimetallic (Au/Pt) nanoparticles have been prepared using a water-in-oil microemulsion system (water/AOT/cyclohexane) followed by calcination step. The effect of metal ratio, reducing agent type (NaBH{sub 4} or N{sub 2}H{sub 4}), TiO{sub 2} matrix type (P-25, ST-01, TiO-5, TiO{sub 2} nanotubes or TiO{sub 2} obtained by TIP hydrolysis) as well as calcination temperature (from 350 to 650 °C) were systematically investigated. Obtained photocatalysts were characterized by UV–vis diffuse-reflectance spectroscopy (DRS), BET surface area measurements, scanning transmission microscopy (STEM), X-ray diffraction analysis (XRD), and X-ray photoelectron spectroscopy (XPS). Photocatalytic activity under visible light (λ > 420 nm) has been estimated in phenol degradation reaction in aqueous phase. The results showed that phenol degradation rate under visible light in the presence of TiO{sub 2} loaded with Au/Pt nanoparticles differed from 0.7 to 2.2 μmol dm{sup −3} min{sup −1} for samples prepared using different reducing agent. Sodium borohydride (NaBH{sub 4}) favors formation of smaller Au/Pt nanoparticles and higher amount gold in Au/Pt is in the form of electronegative species (Au{sup δ−}) resulted in higher photoactivity. TiO{sub 2} obtained by TIP hydrolysis in microemulsion system seems to be the best support for Au/Pt nanoparticles from all among investigated matrix. It was also observed that enhancement of calcination temperature from 450 to 650 °C resulted in rapid drop of Au/Pt-TiO{sub 2} photoactivity under visible light

  11. Electrodeposited Pt and Pt-Sn nanoparticles on Ti as anodes for direct methanol fuel cells

    Institute of Scientific and Technical Information of China (English)

    Hanaa B HASSAN

    2009-01-01

    Electro-oxidation of methanol was studied on titanium supported nanocrystallite Pt and Ptx-Sny catalysts prepared by electrodeposition techniques. Their electro-catalytic activities were studied in 0.5mol/L H2SO4 and compared to those of a smooth Pt, Pt/Pt and Pt-Sn/Pt electrodes. Platinum was deposited on Ti by galvanostatic and potentiostatic techniques. X-ray diffractometer (XRD) and energy dispersive X-ray (EDX) techniques were applied in order to investigate the chemical composition and the phase structure of the modified electrodes. Scanning electron microscopy (SEM) was used to characterize the surface morphology and to correlate the results obtained from the two electrochemical deposition methods. Results show that modified Pt/Ti electrodes prepared by the two methods have comparable performance and enhanced catalytic activity towards methanol electro-oxidation compared to Pt/Pt and smooth Pt electrodes. Steady state Tafel plots experiments show a higher rate of methanol oxidation on a Pt/Ti catalyst than that on a smooth Pt. Introduction of a small amount of Sn deposited with Pt improves the catalytic activity and the stability of prepared electrode with time as indicated from the cyclic votlammetry and the chronoamperometric experiments. The effect of variations in the composition for binary catalysts of the type Ptx-Sny/Ti towards the methanol oxidation reaction is reported. Consequently, the Ptx-Sny/Ti (x∶y (8∶1), molar ratio) catalyst is a very promising one for methanol oxidation.

  12. Precision nanometrology of a large area microstructured metrology surface

    Institute of Scientific and Technical Information of China (English)

    WEI Gao; TAKESHI Araki; SATOSHI Kiyono

    2003-01-01

    @@ 1 Introduction The authors have been working on a newsurface encoder for detecting multi-degree-of-freedom(MDOF) translational and tilt motionsof precision stages[1]. The surface encoder con-sists of two fundamental elements: a sinusoidalmicrostructured metrology surface, which is re-ferred to as the angle grid, and a two-dimension-al (2D) slope sensor[2-3].

  13. Pt skin coated hollow Ag-Pt bimetallic nanoparticles with high catalytic activity for oxygen reduction reaction

    Science.gov (United States)

    Fu, Tao; Huang, Jianxing; Lai, Shaobo; Zhang, Size; Fang, Jun; Zhao, Jinbao

    2017-10-01

    The catalytic activity and stability of electrocatalyst is critical for the commercialization of fuel cells, and recent reports reveal the great potential of the hollow structures with Pt skin coat for developing high-powered electrocatalysts due to their highly efficient utilization of the Pt atoms. Here, we provide a novel strategy to prepare the Pt skin coated hollow Ag-Pt structure (Ag-Pt@Pt) of ∼8 nm size at room temperature. As loaded on the graphene, the Ag-Pt@Pt exhibits a remarkable mass activity of 0.864 A/mgPt (at 0.9 V, vs. reversible hydrogen electrode (RHE)) towards oxygen reduction reaction (ORR), which is 5.30 times of the commercial Pt/C catalyst, and the Ag-Pt@Pt also shows a better stability during the ORR catalytic process. The mechanism of this significant enhancement can be attributed to the higher Pt utilization and the unique Pt on Ag-Pt surface structure, which is confirmed by the density functional theory (DFT) calculations and other characterization methods. In conclusion, this original work offers a low-cost and environment-friendly method to prepare a high active electrocatalyst with cheaper price, and this work also discloses the correlation between surface structures and ORR catalytic activity for the hollow structures with Pt skin coat, which can be instructive for designing novel advanced electrocatalysts for fuel cells.

  14. Ethylene hydrogenation catalysis on Pt(111) single-crystal surfaces studied by using mass spectrometry and in situ infrared absorption spectroscopy

    Science.gov (United States)

    Tillekaratne, Aashani; Simonovis, Juan Pablo; Zaera, Francisco

    2016-10-01

    The catalytic hydrogenation of ethylene promoted by a Pt(111) single crystal was studied by using a ultrahigh-vacuum surface-science instrument equipped with a so-called high-pressure cell. Kinetic data were acquired continuously during the catalytic conversion of atmospheric-pressure mixtures of ethylene and hydrogen by using mass spectrometry while simultaneously characterizing the surface species in operando mode by reflection-absorption infrared spectroscopy (RAIRS). Many observations reported in previous studies of this system were corroborated, including the presence of adsorbed alkylidyne intermediates during the reaction and the zero-order dependence of the rate of hydrogenation on the pressure of ethylene. In addition, the high quality of the kinetic data, which could be recorded continuously versus time and processed to calculate time-dependent turnover frequencies (TOFs), afforded a more detailed analysis of the mechanism. Specifically, deuterium labeling could be used to estimate the extent of isotope scrambling reached with mixed-isotope-substituted reactants (C2H4 + D2 and C2D4 + H2). Perhaps the most important new observation from this work is that, although extensive H-D exchange takes place on ethylene before being fully converted to ethane, the average stoichiometry of the final product retains the expected stoichiometry of the gas mixture, that is, four regular hydrogen atoms and two deuteriums per ethane molecule in the case of the experiments with C2H4 + D2. This means that no hydrogen atoms are removed from the surface via their inter-recombination to produce X2 (X = H or D). It is concluded that, under catalytic conditions, hydrogen surface recombination is much slower than ethylene hydrogenation and H-D exchange.

  15. Properties that influence the specific surface areas of carbon nanotubes and nanofibers.

    Science.gov (United States)

    Birch, M Eileen; Ruda-Eberenz, Toni A; Chai, Ming; Andrews, Ronnee; Hatfield, Randal L

    2013-11-01

    Commercially available carbon nanotubes and nanofibers were analyzed to examine possible relationships between their Brunauer-Emmett-Teller specific surface areas (SSAs) and their physical and chemical properties. Properties found to influence surface area were number of walls/diameter, impurities, and surface functionalization with hydroxyl and carboxyl groups. Characterization by electron microscopy, energy-dispersive X-ray spectrometry, thermogravimetric analysis, and elemental analysis indicates that SSA can provide insight on carbon nanomaterials properties, which can differ vastly depending on synthesis parameters and post-production treatments. In this study, how different properties may influence surface area is discussed. The materials examined have a wide range of surface areas. The measured surface areas differed from product specifications, to varying degrees, and between similar products. Findings emphasize the multiple factors that influence surface area and mark its utility in carbon nanomaterial characterization, a prerequisite to understanding their potential applications and toxicities. Implications for occupational monitoring are discussed.

  16. Electroreduction of oxygen on Pt nanoparticle/carbon nanotube nanocomposites in acid and alkaline solutions

    Energy Technology Data Exchange (ETDEWEB)

    Alexeyeva, N. [Institute of Chemistry, University of Tartu, Jakobi 2, 51014 Tartu (Estonia); Tammeveski, K., E-mail: kaido@chem.ut.e [Institute of Chemistry, University of Tartu, Jakobi 2, 51014 Tartu (Estonia); Lopez-Cudero, A.; Solla-Gullon, J.; Feliu, J.M. [Instituto de Electroquimica, Universidad de Alicante, Apartado 99, 03080 Alicante (Spain)

    2010-01-01

    The kinetics of O{sub 2} reduction on novel electrocatalyst materials deposited on carbon substrates were studied in 0.5 M H{sub 2}SO{sub 4} and in 0.1 M NaOH solutions using the rotating disk electrode (RDE) technique. Pt nanoparticles (PtNP) supported on single-walled (PtNP/SWCNT) and multi-walled carbon nanotubes (PtNP/MWCNT) were prepared using two different synthetic routes. Before use, the CNTs were cleaned to minimize the presence of metal impurities coming from the catalyst used in the synthesis of this material, which can interfere in the electrochemical response of the supported Pt nanoparticles. The composite catalyst samples were characterised by transmission electron microscopy (TEM) showing a good dispersion of the particles at the surface of the carbon support and an average Pt particle size of 2.4 +- 0.7 nm in the case of Pt/CNTs prepared in the presence of citrate and of 3.8 +- 1.1 nm for Pt/CNTs prepared in microemulsion. The values of specific activity (SA) and other kinetic parameters were determined from the Tafel plots taking into account the real electroactive area of each electrode. The electrodes exhibited a relatively high electrocatalytic activity for the four-electron oxygen reduction reaction to water.

  17. Thermochemical hydrogen sensor based on Pt-coated nanofiber catalyst deposited on pyramidally textured thermoelectric film

    Science.gov (United States)

    Kim, Seil; Song, Yoseb; Lee, Young-In; Choa, Yong-Ho

    2017-09-01

    The hydrogen gas-sensing performance has been systemically investigated of a new type of thermochemical hydrogen (TCH) sensor, composed of pyramidally textured thermoelectric (TE) film and catalytic Pt-coated nanofibers (NFs) deposited over the TE film. The TE film was composed of stoichiometric Bi2Te3, synthesized by means of cost-effective electrochemical deposition onto a textured silicon wafer. The resulting pyramidally textured TE film played a critical role in maximizing hydrogen gas flow around the overlying Pt NFs, which were synthesized by means of electrospinning followed by sputtering and acted as a heating catalyst. The optimal temperature increase of the Pt NFs was determined by means of optimizations of the electrospinning and sputtering durations. The output voltage signal of the optimized TCH sensor based on Pt NFs was 17.5 times higher than that of a Pt thin film coated directly onto the pyramidal TE material by using the same sputtering duration, under the fixed conditions of 3 vol% H2 in air at room temperature. This observation can be explained by the increased surface area of (111) planes accessible on the Pt-coated NFs. The best response time and recovery time observed for the optimized TCH sensor based on Pt-coated NFs were respectively 17 and 2 s under the same conditions. We believe that this type of TCH sensor can be widely used for supersensitive hydrogen gas detection by employing small-size Pt NFs and various chalcogenide thin films with high thermoelectric performance.

  18. Immersion Deposition of Pt Nanoparticles on Porous Silicon for Methanol Oxidation

    Institute of Scientific and Technical Information of China (English)

    SU Xu; LU Kangle; CHANG Yanlong; ZHANG Yan; WANG Chunming

    2009-01-01

    Porous silicon(PS)was chosen as the substrate for supporting the Pt particles because of great surface area,good conductivity and stability.Pt nanoparticles have been successfully prepared on the substrate by immersion deposition,which is convenient.The component and morphological properties of the films have been investigated by means of X-ray diffraction(XRD),energy dispersive X-ray spectroscopy(EDX)and scanning electron microscopy(SEM),which shows that the Pt particles have small size and big specific surface.Cyclic voltammetry(CV)research showed that the Pt nanoparticles had novel catalytic activity for methanol when the immersion deposition time was past 24 min.

  19. Evaporation of water droplets on Pt-surface in presence of external electric field--A molecular dynamics study.

    Science.gov (United States)

    Hens, Abhiram; Biswas, Gautam; De, Sudipta

    2015-09-01

    Evaporation of a sessile droplet on a hot solid substrate is an important problem in fluid mechanics. It is relevant to theoretical issues in heat transfer as well as several practical applications. This study investigates the spreading and evaporation of a nanoscale water droplet on a solid platinum surface. The major objective was to analyze the effect of an external electric field on these phenomena. Varying the intensity and direction of the external electric field, a series of molecular dynamics simulations were carried out to understand these phenomena at a molecular level. The results reveal that a horizontal electric field assists in droplet spreading, whereas a vertical electric field enhances the rate of evaporation for a certain range of field intensities. It also shows that the substrate temperature plays an important role in such processes. It is seen that the effect of an external electric field on droplet evaporation becomes significant at an intermediate range of surface temperatures and this effect is not clearly visible for either very high or very low range of surface temperatures.

  20. High-surface-area silica nanospheres (KCC-1) with a fibrous morphology

    KAUST Repository

    Polshettiwar, Vivek

    2010-08-02

    Fibrous nanosilica: A new family of high-surface-area silica nanospheres (KCC-1) have been prepared (see picture). KCC-1 features excellent physical properties, including high surface area, unprecedented fibrous surface morphology, high thermal (up to 950 °C) and hydrothermal stabilities, and high mechanical stability. Copyright © 2010 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  1. Effect of impervious surface area and vegetation changes on mean ...

    African Journals Online (AJOL)

    adeniyi adeyemi

    1 Department of Geography, Geoinformatics and Meteorology, University of Pretoria, .... temperature image to Land Surface Temperature (LST) using the equation ..... For example, the study presented the extent of formation urban heat island ...

  2. Fabrication of Pt/(Ta2O5+Pt) coated titanium electrodes using combination of partial thermal decomposition and electrolytic reduction of Pt and Ta complex; Tofu-bubun netsubunkai to denkai kangenho wo kumiawaseta hakkin/(sanka tantaru+hakkin) tanji chitan kitai denkyoku no sakusei

    Energy Technology Data Exchange (ETDEWEB)

    Kamegaya, Y. [Ishifuku Metal Industry Co. Ltd., Saitama (Japan); Saito, J.; Kobayashi, H.; Mitamura, T. [Saitama Univ., Saitama (Japan). Faculty of Engineering; Okuyama, M. [Oyama National College of Technology, Tochigi (Japan)

    1996-02-05

    Recently, the authors proposed a new method, a combination of painting/partial thermal decomposition and electrolytic reduction, for the fabrication of Pt coated electrode. When Pt support carbon substrate electrode and Pt support Ti substrate electrode were fabricated using this method, any of these electrode has higher surface area than that of electrode fabricated by conventional painting/partial thermal decomposition method. In this report, in order to make possible to long life for Ti substrate coated electrode, the fabrication of coated electrode structure made of up catalyst layer/interlayer/electrode substrate was carried out using the electrode fabrication method proposed by authors. As a result, the amount of Ta support for including (Ta2O5+Pt) interlayer having sufficient electric conductivity and corrosion resistance into the coated electrode structure was necessary at least 0.4mg.cm{sup -2} if the amount of Pt was 0.4mg.cm{sup -2}. Further, the fabricated Pt/(Ta2O5+Pt)/Ti electrode had higher surface area and electrode life was 2 times longer than that of Pt/Ti electrode and had better stability. 9 refs., 7 figs.

  3. Efficient electrocatalytic performance of thermally exfoliated reduced graphene oxide-Pt hybrid

    Energy Technology Data Exchange (ETDEWEB)

    Antony, Rajini P., E-mail: raji.anna@gmail.com; Preethi, L.K.; Gupta, Bhavana; Mathews, Tom, E-mail: tom@igcar.gov.in; Dash, S.; Tyagi, A.K.

    2015-10-15

    Highlights: • Synthesis of Pt–RGO nanohybrids of very high electrochemically active surface area. • Electrocatalytic activity-cum-stability: ∼10 times that of commercial Pt-C catalyst. • TEM confirms narrow size distribution and excellent dispersion of Pt nanoparticles. • SAED and XRD indicate (1 1 1) orientation of Pt nanoparticles. • Methanol oxidation EIS reveal decrease in charge transfer resistance with potential - Abstract: High quality thermally exfoliated reduced graphene oxide (RGO) nanosheets decorated with platinum nanocrystals have been synthesized using a simple environmentally benign process. The electrocatalytic behaviour of the Pt–RGO nanohybrid for methanol oxidation was studied using cyclic voltammetry, chronoamperometry and electrochemical impedance spectroscopy. High resolution transmission electron microscopy shows uniform dispersion of Pt nanoparticles of ∼2–4 nm size. X-ray diffraction and selected area diffraction studies reveal (1 1 1) orientation of the platinum nanoparticles. The cyclic voltammetry and chronoamperometry results indicate higher catalytic activity and stability for Pt–RGO compared to commercial Pt-C. The electrochemical active surface area of Pt–RGO (52.16 m{sup 2}/g) is found to be 1.5 times that of commercial Pt-C. Impedance spectroscopy shows different impedance behaviour at different potential regions, indicating change in methanol oxidation reaction mechanism with potential. The reversal of impedance pattern to the second quadrant, at potentials higher than ∼0.40 V, indicates change in the rate determining reaction.

  4. Rate of evolution of the specific surface area of surface snow layers.

    Science.gov (United States)

    Cabanes, Axel; Legagneux, Loïc; Dominé, Florent

    2003-02-15

    The snowpack can impact atmospheric chemistry by exchanging adsorbed or dissolved gases with the atmosphere. Modeling this impact requires the knowledge of the specific surface area (SSA) of snow and its variations with time. We have therefore measured the evolution of the SSA of eight recent surface snow layers in the Arctic and the French Alps, using CH4 adsorption at liquid nitrogen temperature (77 K). The SSA of fresh snow layers was found to decrease with time, from initial values in the range 613-1540 cm2/g to values as low as 257 cm2/g after 6 days. This is explained by snow metamorphism, which causes modifications in crystal shapes, here essentially crystal rounding and the disappearance of microstructures. A parametrization of the rate of SSA decrease is proposed. We fit the SSA decrease to an exponential law and find that the time constant alpha(exp) (day(-1)) depends on temperature according to alpha(exp) = 76.6 exp (-1708/7), with Tin kelvin. Our parametrization predicts that the SSA of a snow layer evolving at -40 degrees C will decrease by a factor of 2 after 14 days, while a similar decrease at -1 degrees C will only require 5 days. Wind was found to increase the rate of SSA decrease, but insufficient data did not allow a parametrization of this effect.

  5. Lung deposited surface area concentrations in a street canyon

    Science.gov (United States)

    Kuuluvainen, Heino; Hietikko, Riina; Järvinen, Anssi; Saukko, Erkka; Irjala, Matti; Niemi, Jarkko V.; Timonen, Hilkka; Keskinen, Jorma; Rönkkö, Topi

    2017-04-01

    Street canyons are interesting environments with respect to the dispersion of traffic emissions and human exposure. Pedestrians may be exposed to relatively high concentrations of fine particles and the vertical dispersion affects the human exposure above the ground level in buildings. Previously, particle concentrations have been measured in street canyons at a few different heights (Marini et al., 2015). The information on the lung deposited surface area (LDSA) concentration, which is a relevant metric for the negative health effects, is very limited even at the ground level of street canyons (Kuuluvainen et al., 2016). More information especially on the vertical dispersion and the ground level concentrations is needed, for instance, for the use of urban planning and the design of ventilation systems in buildings. Measurements were carried out in a busy street canyon in Helsinki, Finland, at an urban super-site measurement station (Mäkelänkatu 50). The data included vertical concentration profiles measured in an intensive measurement campaign with a Partector (Naneos GmbH) installed into a drone, long-term measurements with an AQ Urban particle sensor (Pegasor Ltd.), and an extensive comparison measurement in the field with different devices measuring the LDSA. These devices were an AQ Urban, Partector, DiSCmini (Testo AG), NSAM (TSI Inc.), and an ELPI+ (Dekati Ltd.). In addition, continuous measurements of gas phase components, particle size distributions, and meteorology were run at the supersite. The vertical profile measurements were con-ducted in November 2016 during two days. In the measurements, the drone was flown from the ground level to an altitude of 50 or 100 m, which is clearly above the roof level of the buildings. Altogether, 48 up-and-down flights were conducted during the two days. The vertical profiles were supported by continuous measurements at the ground level on both sides of the street canyon. The long-term measurements were conducted

  6. Restoration of eroded surfaces in Serbian ski-areas

    Directory of Open Access Journals (Sweden)

    Ristić Ratko

    2009-01-01

    Full Text Available The environmental impacts in Serbian ski areas are very strong, leading to landscape degradation and functionality losses. Construction or improvement works cause serious destruction of topsoil and native vegetation. Some activities enhance erosion production and sediment yield: clear cuttings; trunk transport down the slope; road construction and large excavations. Also, lack of erosion control works in ski areas, especially between April and October, result in various forms of land degradation such as furrows, gullies, landslides, or debris from rock weathering. The consequences of mismanagement in ski areas are noticeable in downstream sections of river beds, causing floods and bed-load deposition. Planning and designing activities, with the application of technical and biotechnical erosion control structures, through the concept of restoration, are necessary measures in the protection of ski areas.

  7. Large-area fabrication of superhydrophobic surfaces for practical applications: an overview

    Science.gov (United States)

    Xue, Chao-Hua; Jia, Shun-Tian; Zhang, Jing; Ma, Jian-Zhong

    2010-01-01

    This review summarizes the key topics in the field of large-area fabrication of superhydrophobic surfaces, concentrating on substrates that have been used in commercial applications. Practical approaches to superhydrophobic surface construction and hydrophobization are discussed. Applications of superhydrophobic surfaces are described and future trends in superhydrophobic surfaces are predicted. PMID:27877336

  8. Large-area fabrication of superhydrophobic surfaces for practical applications: an overview

    Directory of Open Access Journals (Sweden)

    Chao-Hua Xue, Shun-Tian Jia, Jing Zhang and Jian-Zhong Ma

    2010-01-01

    Full Text Available This review summarizes the key topics in the field of large-area fabrication of superhydrophobic surfaces, concentrating on substrates that have been used in commercial applications. Practical approaches to superhydrophobic surface construction and hydrophobization are discussed. Applications of superhydrophobic surfaces are described and future trends in superhydrophobic surfaces are predicted.

  9. Large-area fabrication of superhydrophobic surfaces for practical applications: an overview

    OpenAIRE

    Xue, Chao-Hua; Jia, Shun-Tian; Zhang, Jing; Ma, Jian-Zhong

    2010-01-01

    This review summarizes the key topics in the field of large-area fabrication of superhydrophobic surfaces, concentrating on substrates that have been used in commercial applications. Practical approaches to superhydrophobic surface construction and hydrophobization are discussed. Applications of superhydrophobic surfaces are described and future trends in superhydrophobic surfaces are predicted.

  10. 离子液体中Au(111)和Pt(111)表面Ge欠电位沉积的现场STM研究%Underpotential Deposition of Germanium on Au(111) and Pt(111) Surfaces in Ionic Liquids

    Institute of Scientific and Technical Information of China (English)

    谢旭芬; 颜佳伟; 梁景洪; 李纪军; 张梦; 毛秉伟

    2014-01-01

    本文研究BMIPF6离子液体中Au(111)和Pt(111)表面Ge的电沉积行为.循环伏安法测试结果表明,在含0.1 mol· LlGeCL的BMIPF6溶液Au(111)和Pt(111)表面均有两个与Ge沉积过程相关的还原峰.第一个还原峰包含了Ge4+还原成Ge2+及Ge的欠电位沉积,第二个还原峰对应Ge的本体沉积.现场扫描隧道显微镜研究结果表明,Ge在Au(111)和Pt(11 1)表面均有两层欠电位沉积.第一层欠电位沉积厚度平均约为0.25 nm、形貌平整、带有缝隙的亚单层结构.第二层欠电位沉积形貌相对粗糙的点状团簇结构.该欠电位沉积过程伴随表面合金化.

  11. Pore-Scale Heterogeneity in the Mineral Distribution and Reactive Surface Area of Porous Rocks

    Science.gov (United States)

    Lai, P. E. P.; Krevor, S. C.

    2015-12-01

    The reactive surface area is an important control on interfacial processes between minerals and aqueous fluids in porous rocks. Spatial heterogeneity in the surface area can lead to complications in modelling reactive transport processes, but quantitative characterisation of this property has been limited. In this paper 3D images obtained using x-ray micro-tomography were used to characterise heterogeneity in surface area in one sandstone and five carbonate rocks. Measurements of average surface area from x-ray imagery were 1-2 orders of magnitude lower than measurements from nitrogen BET. A roughness factor, defined as the ratio of BET surface area to x-ray based surface area, was correlated to the presence of clay or microporosity. Coregistered images of Berea sandstone from x-ray and energy dispersive spectroscopy imagery were used to guide the identification of quartz, K-feldspar, dolomite, calcite and clays in x-ray images. In Berea sandstone, clay and K-feldspar had higher average surface area fractions than their volumetric fractions in the rock. In the Edwards carbonate, however, modal mineral composition correlated with surface area. By sub-sampling digital images, statistical distributions of the surface area were generated at various length scales of subsampling. Comparing these to distributions used in published modelling studies showed that the common practice of leaving surface area and pore volume uncorrelated in a pore leads to unrealistic combinations of surface area and pore volume in the models. We suggest these models adopt a moderate correlation based on observations. In Berea sandstone, constraining ratios of surface area to pore volume to a range of values between that of quartz-lined and five times that of clay-lined spheres appeared sufficient.

  12. Surface albedo measurements in Mexico City metropolitan area

    Energy Technology Data Exchange (ETDEWEB)

    Castro, T; Mar, B; Longoria, R; Ruiz Suarez, L. G [Centro de Ciencias de la Atmosfera, UNAM, Mexico, D.F. (Mexico); Morales, L [Instituto de Geografia, UNAM, Mexico, D.F. (Mexico)

    2001-04-01

    Optical and thermal properties of soils are important input data for the meteorological and photochemical modules of air quality models. As development of these models increase on spatial resolution good albedo data become more important. In this paper measurements of surface albedo of UV (295-385 nm) and visible (450-550 nm) radiation are reported for different urban and rural surfaces in the vicinity of Mexico City. It was found for the downtown zone and average albedo value of 0.05 which is in very good agreement with reported values for urban surfaces. Our albedo values measured in UV region for grey cement and green grass are of 0.10 and 0.009, respectively, and quite similar to those found at the literature of 0.11 and 0.008 for those type of surfaces. [Spanish] Las propiedades opticas y termicas de suelos son datos importantes para los modulos meteorologicos y fotoquimicos de los modelos de calidad del aire. Conforme aumenta la resolucion espacial del modelo se vuelve mas importante contar con buenos datos de albedo. En este articulo se presentan mediciones de albedo superficial de radiacion Ultravioleta (295-385 nm) y visible (450-550 nm) para diferentes superficies urbanas. Los valores medidos de albedo en la region UV para cemento gris y pasto verde son de 0.10 y 0.009, respectivamente, y son muy similares a los reportados en la literatura, 0.11 y 0.008 para este tipo de superficies.

  13. High-surface-area nanomesh graphene with enriched edge sites as efficient metal-free cathodes for dye-sensitized solar cells

    Science.gov (United States)

    Yang, Wang; Xu, Xiuwen; Gao, Yalun; Li, Zhao; Li, Cuiyu; Wang, Wenping; Chen, Yu; Ning, Guoqing; Zhang, Liqiang; Yang, Fan; Chen, Shengli; Wang, Aijun; Kong, Jing; Li, Yongfeng

    2016-06-01

    Exploiting cost-effective and highly efficient counter electrodes (CEs) has been a persistent objective for practical application of dye-sensitized solar cells (DSSCs). Here, we present an efficient CE by using pure three-dimensional (3D) nanomesh graphene frameworks (NGFs) which are synthesized via a template-directed chemical vapor deposition (CVD) approach. The high-surface-area 3D NGFs associated with the enriched surface edge defects make it very efficient towards I3- reduction even without any Pt catalyst. More interestingly, by virtue of the interpenetrating graphene frameworks, the NGFs exhibit excellent electron conductivity, thus leading to facile charge transfer. Consequently, the DSSCs with pure NGFs as CEs display a power conversion efficiency of 7.32%, which is comparable to that of Pt as CEs (7.28%), thereby exhibiting great potential as low-cost and highly efficient CE materials for large-scale deployment of DSSCs.Exploiting cost-effective and highly efficient counter electrodes (CEs) has been a persistent objective for practical application of dye-sensitized solar cells (DSSCs). Here, we present an efficient CE by using pure three-dimensional (3D) nanomesh graphene frameworks (NGFs) which are synthesized via a template-directed chemical vapor deposition (CVD) approach. The high-surface-area 3D NGFs associated with the enriched surface edge defects make it very efficient towards I3- reduction even without any Pt catalyst. More interestingly, by virtue of the interpenetrating graphene frameworks, the NGFs exhibit excellent electron conductivity, thus leading to facile charge transfer. Consequently, the DSSCs with pure NGFs as CEs display a power conversion efficiency of 7.32%, which is comparable to that of Pt as CEs (7.28%), thereby exhibiting great potential as low-cost and highly efficient CE materials for large-scale deployment of DSSCs. Electronic supplementary information (ESI) available: Additional SEM image, SAED image, cross-sectional SEM

  14. Synthesis and Characterization of Large Surface Area Yttrium Oxide by Precipitation Method

    Institute of Scientific and Technical Information of China (English)

    崔大立; 龙志奇; 张顺利; 崔梅生; 黄小卫

    2004-01-01

    The method for preparing yttrium oxide with large specific surface area was introduced. By means of BET, SEM, TG and DTA analysis, the effects of precipitant, stirring velocity, non-RE impurity in solution, calcination temperature, on the surface area were studied respectively. The Y2O3 sample with specific surface area of more than 60 m2*g-1 and L.O.I less than 1% was prepared in the suitable precipitation condition and calcinations temperature when the ammonia used as precipitant. The SEM shows that the Y2O3 prepared with large surface area is the aggregation of about 50 nm particles.

  15. Pyrrole Hydrogenation over Rh(111) and Pt(111) Single-Crystal Surfaces and Hydrogenation Promotion Mediated by 1-Methylpyrrole: A Kinetic and Sum-Frequency Generation Vibrational Spectroscopy Study

    Energy Technology Data Exchange (ETDEWEB)

    Kliewer, Christopher J.; Bieri, Marco; Somorjai, Gabor A.

    2008-03-04

    Sum-frequency generation (SFG) surface vibrational spectroscopy and kinetic measurements using gas chromatography have been used to study the adsorption and hydrogenation of pyrrole over both Pt(111) and Rh(111) single-crystal surfaces at Torr pressures (3 Torr pyrrole, 30 Torr H{sub 2}) to form pyrrolidine and the minor product butylamine. Over Pt(111) at 298 K it was found that pyrrole adsorbs in an upright geometry cleaving the N-H bond to bind through the nitrogen evidenced by SFG data. Over Rh(111) at 298 K pyrrole adsorbs in a tilted geometry relative to the surface through the p-aromatic system. A pyrroline surface reaction intermediate, which was not detected in the gas phase, was seen by SFG during the hydrogenation over both surfaces. Significant enhancement of the reaction rate was achieved over both metal surfaces by adsorbing 1-methylpyrrole before reaction. SFG vibrational spectroscopic results indicate that reaction promotion is achieved by weakening the bonding between the N-containing products and the metal surface because of lateral interactions on the surface between 1-methylpyrrole and the reaction species, reducing the desorption energy of the products. It was found that the ring-opening product butylamine was a reaction poison over both surfaces, but this effect can be minimized by treating the catalyst surfaces with 1-methylpyrrole before reaction. The reaction rate was not enhanced with elevated temperatures, and SFG suggests desorption of pyrrole at elevated temperatures.

  16. Laser weldability of Pt and Ti alloys

    Energy Technology Data Exchange (ETDEWEB)

    Noolu, N.J. [Center for Advanced Materials Joining, University of Waterloo, Waterloo (Canada)]. E-mail: nnoolu@mecheng1.uwaterloo.ca; Kerr, H.W. [Center for Advanced Materials Joining, University of Waterloo, Waterloo (Canada); Zhou, Y. [Center for Advanced Materials Joining, University of Waterloo, Waterloo (Canada); Xie, J. [Cardiac Rhythm Management Division, Street Jude Medical Inc., Sylmar, CA (United States)

    2005-04-25

    Crack susceptibility of laser spot welds between Pt and Ti alloys was studied by characterizing the surface and the cross-sections of the welds produced at different pulse energies. Increase in laser pulse energy increased the dilution by the Ti alloy, giving rise to the evolution of microstructures with varying Ti contents across the entire fusion zone. Hardness results showed that regions with 66-75% Ti, i.e. consisting of primary Ti{sub 3}Pt and/or Ti{sub 3}Pt + TiPt eutectic, have a hardness higher than 700 Vickers hardness numbers (VHN), while regions with 42-66% Ti, i.e. consisting of primary TiPt, possessed hardness between 400 and 700 VHN. The extent of cracking increased with the increase in pulse energy and the cracked regions consisted of Ti contents between 50 and 75%. Brittle cracking in microstructures consisting of Ti{sub 3}Pt and TiPt phases suggested that one or both of the constituent phases are susceptible to cracking. However, crack arrest in microstructures predominantly consisting of TiPt showed that Ti{sub 3}Pt is the most susceptible phase to cracking in Pt-Ti alloy welds.

  17. Gram-Scale Synthesized Pd2Co-Supported PtMonolayers Electrocatalysts for Oxygen Reduction Reaction

    Energy Technology Data Exchange (ETDEWEB)

    Zhou, W.P.; Sasaki, K.; Su, D.; Zhu, Y.; Wang, J.X.; Adzic, R.R.

    2010-04-21

    Gram-scale synthesis of Pt{sub ML} electrocatalysts with a well-defined core-shell structure has been carried out using method involving galvanic displacement of an underpotential deposition Cu layer. The Pt shell thickness can be controlled by stepwise deposition. The Pt{at}Pd{sub 2}Co/C nanoparticles were characterized by X-ray powder diffraction, aberration-corrected scanning transmission electron microscopy, high-resolution energy-loss spectrometry, and in situ X-ray absorption spectroscopy. A complete Pt shell of 0.6 nm on a Pd{sub 2}Co core has been confirmed. The Pt{at}Pd{sub 2}Co/C core-shell electrocatalysts showed a very high activity for the oxygen reduction reaction; the Pt mass and specific activity were 0.72 A mg{sup -1}{sub Pt} and 0.5 mA cm{sup -2}, respectively (3.5 and 2.5 times higher than the corresponding values for commercial Pt catalysts), at 0.9 V in 0.1 M HClO{sub 4} at room temperature. In an accelerated potential cycling test, a loss in active surface area and a decrease in catalytic activity for gram-scale-synthesized Pt{sub ML} catalysts were also determined.

  18. Preparation of aniline from photocatalytic reduction of nitrobenzene using Pt/Nd{sub 2}O{sub 3} nanocomposite

    Energy Technology Data Exchange (ETDEWEB)

    Mohamed, R.M., E-mail: mhmdouf@gmail.com

    2015-11-05

    In this manuscript, a template method was used to synthesis Pt-doped Nd{sub 2}O{sub 3} nanostructures with controlled Pt doping contents. The characterizations illustrated that the obtained samples have ultra high surface area (190 m{sup 2}/g), high crystallinity, small grain size (20 nm) and hollow spherical like morphology. Also, the band gap of the Pt-doped Nd{sub 2}O{sub 3} nanostructures can be controlled by controlling the Pt contents. The photocatalytic activity of the Pt-doped Nd{sub 2}O{sub 3} nanostructures samples was studied by studying the reduction of nitrobenzene into aniline using visible light irradiation. The photocatalytic performance of Nd{sub 2}O{sub 3} was enhanced by Pt doping. This can be attributed to the fact that the trapping effect of the Pt-doped Nd{sub 2}O{sub 3} nanostructures and the red shift of absorption edge. The study result provides an effective method to create different photocatalysts with enhanced visible-light-driven photocatalytic performance. - Highlights: • Pt-doped Nd{sub 2}O{sub 3} hollow sphere was prepared by a template method. • Photocatalytic preparation of aniline under visible light was dependent on wt % of Pt. • Catalyst re-use revealed the present photocatalyst remain effective and active after five cycles.

  19. Effects of CO/sub 2/ enrichment on internal leaf surface area in soybeans

    Energy Technology Data Exchange (ETDEWEB)

    Leadley, P.W.; Reynolds, J.A.; Thomas, J.F.; Reynolds, J.F.

    1987-06-01

    Internal cell surface areas were measured on fully expanded leaves of soybean seedlings that had been continuously exposed to 348 or 645 ppm CO/sub 2/ environments. Plants grown in the high CO/sub 2/ treatment had thicker leaves but less palisade cell surface area per unit of leaf area. Surface area of the mesophyll per unit leaf area was unaffected by CO/sub 2/. The potential ramifications of these CO/sub 2/-induced changes in leaf anatomy on photosynthesis and water-use efficiency are explored.

  20. Control of the composition of Pt-Ni electrocatalysts in surfactant-free synthesis using neat N-formylpiperidine

    Science.gov (United States)

    Zhang, Na; Tsao, Kai-Chieh; Pan, Yung-Tin; Yang, Hong

    2016-01-01

    This paper describes the facile and surfactant-free synthesis of faceted Pt-Ni alloy nanoparticle electrocatalysts using neat N-formylpiperidine as a new type of solvent. Unlike the widely-used colloidal synthesis based on long-carbon chain surfactants, nanoparticles made in neat N-formylpiperidine possess a directly accessible surface for electrocatalytic reactions, making it a very attractive alternative solvent. The area-specific oxygen reduction reaction (ORR) activity is much higher than the commercial Pt/C catalyst reference and reaches a maximum of 1.12 mA cm-2 for the Pt-Ni alloy nanoparticles. We observed that the freshly formed Pt-Ni alloy could have controllable bulk and near surface compositions under the same initial reaction conditions and precursor ratio. The change in the composition could be attributed to the effect of CO on the formation of uniform nuclei at the initial stage, and a different deposition rate between Pt and Ni metals during the growth. The well-defined Pt-Ni nanoparticle catalysts show strong composition-dependent catalytic behavior in ORR, highlighting the important role of controlling the growth kinetics in the preparation of active Pt-Ni ORR catalysts.This paper describes the facile and surfactant-free synthesis of faceted Pt-Ni alloy nanoparticle electrocatalysts using neat N-formylpiperidine as a new type of solvent. Unlike the widely-used colloidal synthesis based on long-carbon chain surfactants, nanoparticles made in neat N-formylpiperidine possess a directly accessible surface for electrocatalytic reactions, making it a very attractive alternative solvent. The area-specific oxygen reduction reaction (ORR) activity is much higher than the commercial Pt/C catalyst reference and reaches a maximum of 1.12 mA cm-2 for the Pt-Ni alloy nanoparticles. We observed that the freshly formed Pt-Ni alloy could have controllable bulk and near surface compositions under the same initial reaction conditions and precursor ratio. The change

  1. Electrocatalysis of fuel cells reaction on Pt and Pt-bimetallic anode catalysts: A selective review

    Directory of Open Access Journals (Sweden)

    Stamenković Vojislav

    2002-01-01

    Full Text Available In this review we selectively summarize recent progress, primarily from our laboratory, in the development of interrelationships between the kinetics of the fuel cells reactions and the structure/composition of anode catalysts. The focus is placed on two types of metallic surfaces: platinum single crystals and bimetallic surfaces based on Pt. In the first part it was illustrated that the hydcogen reaction is structure sensitive process, with Pt(110 being an order of magnitude more active than either of the atomically "flatter" (100 and (111 surfaces. The hydrogen reaction on Pt(hkl modified by pseudomorphic Pd (submonolayers shows the "volcano-like" behavior, having the maximum rate on Pt(111 modified by 1 ML of Pd. The Pt(111-Pd system is used to demonstrate how the energetics of intermediates formed in the hydrogen reaction is affected by interfacial bonding and energetic constraints produced between pseudomorphic Pd films and the Pt(111 substrate. In the second part it was shown that the oxidation of Ha in the presence of CO occurs concurrently with CO oxidation on Pt and Pt bimetallic surfaces. The Pt-Ru system is used to demonstrate that both the bifunctional effect and the ligand effect contribute to the influence of Ru on the CO oxidation rate and for Hz oxidation process in the presence of CO. The knowledge is then used to create the real-life catalyst with the catalytic activities which are, to the greatest extend possible similar to the tailor-made surface.

  2. ELECTROCHEMICAL OXIDATION OF ETHYLENE AT PANI/Pt AND Ag/PANI/Pt MODIFIED ELECTRODES

    Directory of Open Access Journals (Sweden)

    Lenys Fernández

    Full Text Available The electrochemical behavior of ethylene on PANI/Pt and Ag/PANI/Pt modified electrodes was investigated in different media. Morphology of the deposits of PANI were observed by SEM analysis, complemented by the EDX techniques to obtain the Ag composition that shows that Ag is deposited in the polymeric matrix which covered the whole platinum surface. The electrodic system comprising Ag/PANI/ Pt electrode exhibited a more important electrocatalytic response for ethylene oxidation in neutral solutions than the PAN/Pt and Pt electrodes at 20 ºC.The results suggest that the oxidation of ethylene on Ag/PANI/Pt electrode is limited by adsorption-controlled reaction while the oxidation at PANI/Pt is mass transport-limited.

  3. Synthesis of Pt-Sn core-shell nanoparticles deposited on SBA-15 modified

    Energy Technology Data Exchange (ETDEWEB)

    Alvarez-Contreras, L.; Alonso-Lemus, I. [Centro de Investigacion en Materiales Avanzados S.C., Laboratorio Nacional de Nanotecnologia (Mexico); Botte, G. G. [Ohio University, Center for Electrochemical Engineering Research, Department of Chemical and Biomolecular Engineering (United States); Verde-Gomez, Y., E-mail: ysmaelverde@yahoo.com [Instituto Tecnologico de Cancun (Mexico)

    2013-07-15

    A novel one-step synthesis method to prepare Pt-Sn bimetallic nanoparticles supported on mesoporous silica with high surface area (SBA-15, 700 m{sup 2}/g) and narrow pore size distribution (around 9.5 nm) was developed. Tin incorporation plays an important dual role, to create active sites into the silica walls that serve as particles anchors center, and to grow Pt-Sn core-shell nanoparticles. High-resolution transmission and scanning electron microscopy, and X-ray diffraction pattern confirm the formation of the Pt-Sn core-shell type nanoparticles ( Almost-Equal-To 1-10 nm). The metal loading was 2.2 and 2.3 wt% for Pt and Sn, respectively. Electron microscopy results show that the metal nanoparticles were deposited not only on the matrix, but also inside of it. Structural, textural, and morphological features of the SBA-15 were slightly affected after the nanoparticles deposition, maintaining its high surface area. The results obtained suggest that Pt-Sn on SBA-15 could be attractive material for several catalytic applications, due to the narrow particle size distribution achieved (from 1 to 10 nm) the high dispersion on the support, as well as the Pt-Sn alloy developed.Graphical Abstract.

  4. Understanding the Effects of Surface Chemistry and Microstructure on the Activity and Stability of Pt Electrocatalysts on Non-Carbon Supports

    Energy Technology Data Exchange (ETDEWEB)

    Mustain, William [Univ. of Conneticut, Storrs, CT (United States)

    2015-02-12

    The objective of this project is to elucidate the effects of the chemical composition and microstructure of the electrocatalyst support on the activity, stability and utilization of supported Pt clusters.

  5. Ultrasensitive hydrogen sensor based on Pt-decorated WO₃ nanorods prepared by glancing-angle dc magnetron sputtering.

    Science.gov (United States)

    Horprathum, M; Srichaiyaperk, T; Samransuksamer, B; Wisitsoraat, A; Eiamchai, P; Limwichean, S; Chananonnawathorn, C; Aiempanakit, K; Nuntawong, N; Patthanasettakul, V; Oros, C; Porntheeraphat, S; Songsiriritthigul, P; Nakajima, H; Tuantranont, A; Chindaudom, P

    2014-12-24

    In this work, we report an ultrasensitive hydrogen (H2) sensor based on tungsten trioxide (WO3) nanorods decorated with platinum (Pt) nanoparticles. WO3 nanorods were fabricated by dc magnetron sputtering with a glancing angle deposition (GLAD) technique, and decorations of Pt nanoparticles were performed by normal dc sputtering on WO3 nanorods with varying deposition time from 2.5 to 15 s. Crystal structures, morphologies, and chemical information on Pt-decorated WO3 nanorods were characterized by grazing-incident X-ray diffraction, field-emission scanning electron microscopy, energy-dispersive X-ray spectroscopy, and photoelectron spectroscopy, respectively. The effect of the Pt nanoparticles on the H2-sensing performance of WO3 nanorods was investigated over a low concentration range of 150-3000 ppm of H2 at 150-350 °C working temperatures. The results showed that the H2 response greatly increased with increasing Pt-deposition time up to 10 s but then substantially deteriorated as the deposition time increased further. The optimally decorated Pt-WO3 nanorod sensor exhibited an ultrahigh H2 response from 1530 and 214,000 to 150 and 3000 ppm of H2, respectively, at 200 °C. The outstanding gas-sensing properties may be attributed to the excellent dispersion of fine Pt nanoparticles on WO3 nanorods having a very large effective surface area, leading to highly effective spillover of molecular hydrogen through Pt nanoparticles onto the WO3 nanorod surface.

  6. Assessment of the ethanol oxidation activity and durability of Pt catalysts with or without a carbon support using Electrochemical Impedance Spectroscopy

    Science.gov (United States)

    Saleh, Farhana S.; Easton, E. Bradley

    2014-01-01

    We compared the stability and performance of 3 commercially available Johnson Matthey catalysts with various Pt loadings (20, 40 and 100%) using two different accelerated durability testing (ADT) protocols. The various Pt-loaded catalysts were tested by means of a series of intermittent life tests (1, 200, 400, 1000, 2000, 3000 and 4000 cycles). The electrochemical surface area (ECSA) loss of electrode was investigated by electrochemical technique (CV). The use of EIS as an accelerated-testing protocol distinctly elucidates the extent of degradation of Johnson Matthey catalysts with various Pt loading. Using EIS, it was possible to show that Pt-black catalyst layers suffer from increased electronic resistance over the course of ADT which is not observed when a corrosion stable carbon support is present. The effect of Pt loading was further elucidated by comparing the electrocatalytic activity of the catalyst layers towards ethanol oxidation reaction (EOR). The catalyst layer with the lowest Pt loading showed the enhanced EOR performance.

  7. BLM National Surface Management Agency: Area Polygons, Withdrawal Area Polygons, and Special Public Purpose Withdrawal Area Polygons

    Data.gov (United States)

    Federal Geographic Data Committee — The SMA implementation is comprised of one feature dataset, with several polygon feature classes, rather than a single feature class. SurfaceManagementAgency: The...

  8. High sensitivity hydrogen sensing with Pt-decorated porous gallium nitride prepared by metal-assisted electroless etching.

    Science.gov (United States)

    Duan, Barrett K; Bohn, Paul W

    2010-05-01

    A unique hydrogen sensor structure based on Pt-decorated porous gallium nitride (PGaN) was fabricated by a two-step process consisting of metal-assisted electroless etching to produce PGaN with highly anisotropic pores followed by electroless deposition of Pt in the pores from an ammoniacal PtCl(6)(2-) solution. The Pt-decorated PGaN structure contains 50-100 nm diameter nanopores which are 400 nm to 1 microm deep and filled with Pt islands. Both electroless etching and deposition steps are done in solution and allow for large-scale production. An AC four-point probe conductivity measurement was implemented at f = 1 kHz, a frequency where the impedance of Pt-PGaN is nearly entirely resistive, and the change in conductance upon H(2) exposure was measured for three sample types: PGaN with a surface sputtered layer of Pt only; unetched GaN (CGaN) with both sputtered and electrolessly deposited Pt; and PGaN with both sputtered and electrolessly deposited Pt. The hydrogen sensing performance of the Pt-filled PGaN sensor was more than an order of magnitude better than either of the other two sample types under all experimental conditions, an observation attributed to the significant increase in Pt-GaN interfacial area in the electrolessly decorated PGaN samples, exhibiting a response to H2 concentrations as low as 1 ppm. The conductance changes are ascribed to adsorption-induced changes in interfacial polarization that produce changes in band bending and thus to the width of the space charge region near the Pt-GaN interface.

  9. Snow specific surface area simulation using the one-layer snow model in the Canadian LAnd Surface Scheme (CLASS)

    OpenAIRE

    2013-01-01

    Snow grain size is a key parameter for modeling microwave snow emission properties and the surface energy balance because of its influence on the snow albedo, thermal conductivity and diffusivity. A model of the specific surface area (SSA) of snow was implemented in the one-layer snow model in the Canadian LAnd Surface Scheme (CLASS) version 3.4. This offline multilayer model (CLASS-SSA) simulates the decrease of SSA based on snow age, snow temperature and t...

  10. Insights on the SO{sub 2} poisoning of Pt{sub 3}Co/VC and Pt/VC fuel cell catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Baturina, Olga A., E-mail: olga.baturina@nrl.navy.mi [Naval Research Laboratory, Code 6113, Washington, DC 20375 (United States); Gould, Benjamin D. [Naval Research Laboratory, Code 6113, Washington, DC 20375 (United States); Garsany, Yannick [Naval Research Laboratory, Code 6113, Washington, DC 20375 (United States)] [EXCET, Inc., Springfield, VA 22151 (United States); Swider-Lyons, Karen E. [Naval Research Laboratory, Code 6113, Washington, DC 20375 (United States)

    2010-09-01

    SO{sub 2} poisoning of carbon-supported Pt{sub 3}Co (Pt{sub 3}Co/VC) catalyst is performed at the cathode of proton exchange membrane fuel cells (PEMFCs) in order to link previously reported results at the electrode/solution interface to the FC environment. First, the surface area of Pt{sub 3}Co/VC catalyst is rigorously characterized by hydrogen adsorption, CO stripping voltammetry and underpotential deposition (upd) of copper adatoms. Then the performance of PEMFC cathodes employing 30 wt.% Pt{sub 3}Co/VC and 50 wt.% Pt/VC catalysts is compared after exposure to 1 ppm SO{sub 2} in air for 3 h at constant cell voltage of 0.6 V. In agreement with results reported for the electrode/solution interface, the Pt{sub 3}Co/VC is more susceptive to SO{sub 2} poisoning than Pt/VC at a given platinum loading. Both catalysts can be recovered from adsorbed sulfur species by running successive polarization curves in air or cyclic voltammetry (CV) in inert atmosphere. However, the activity of Pt{sub 3}Co/VC having {approx}3 times higher sulfur coverage is recovered more easily than Pt/VC. To understand the difference between the two catalysts in terms of activity recovery, platinum-sulfur interaction is probed by thermal programmed desorption at the catalyst/inert gas interface and CV at the electrode/solution interface and in the FC environment.

  11. The specific surface area of methane hydrate formed in different conditions and manners

    Institute of Scientific and Technical Information of China (English)

    2009-01-01

    The specific surface area of methane hydrates, formed both in the presence and absence of sodium dodecyl sulfate (SDS) and processed in different manners (stirring, compacting, holding the hydrates at the formation conditions for different periods of time, cooling the hydrates for different periods of time before depressurizing them), was measured under atmospheric pressure and temperatures below ice point. It was found that the specific surface area of hydrate increased with the decreasing temperature. The methane hydrate in the presence of SDS was shown to be of bigger specific surface areas than pure methane hydrates. The experimental results further demonstrated that the manners of forming and processing hydrates affected the specific surface area of hydrate samples. Stirring or compacting made the hydrate become finer and led to a bigger specific surface area.

  12. Preparation and Characterization of Porous Yttrium Oxide Powders with High Specific Surface Area

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    The porous cubic yttrium oxides with high specific surface area were prepared by the explosive decomposition of yttrium nitrate and its complex formed with methyl salicylate. The specific surface area and properties of powders synthesized at various temperatures were characterized using BET, X-ray diffraction (XRD), infrared spectra (IR), and scanning electron microscopy (SEM). The results indicate that the highest specific surface area is found to be 65.37 m2*g-1 at the calcination temperature of 600 ℃, and then decreases to 20.33 m2*g-1 with the calcination temperature rising from 600 to 900 ℃. The powders show strong surface activity for adsorping water and carbon dioxide in air, which also decreases with the rising calcination temperature. The drop both on the surface area and surface activity of samples at higher temperatures may be due to pore-narrowing(sintering) effects.

  13. A method for increasing the surface area of perovskite-type oxides

    Indian Academy of Sciences (India)

    S Banerjee; V R Choudhary

    2000-10-01

    A method based on hydrothermal treatments is described for increasing the surface area of sintered ABO3-type perovskite oxides. Influence of hydrothermal treatments, such as water treatment at 125-300°C under autogeneous pressure and steam treatment at 350-800°C, to low surface area (or sintered) LaCoO3 and LaMnO3 perovskite oxides on their surface properties (viz. surface area, crystal size and morphology and surface La/(Co or Mn) ratio) and also catalytic activity in complete combustion of methane at different temperatures (450-600°C) has been thoroughly investigated. The hydrothermal treatments result in the activation of the perovskite oxides by increasing their surface area very markedly.

  14. Surface and subsurface conditions in permafrost areas - a literature review

    Energy Technology Data Exchange (ETDEWEB)

    Vidstrand, Patrik [Bergab, Goeteborg (Sweden)

    2003-02-01

    This report contains a summary of some of the information within existing technical and scientific literature on permafrost. Permafrost is viewed as one of the future climate driven process domains that may exist in Scandinavia, and that may give rise to significantly different surface and subsurface conditions than the present. Except for changes in the biosphere, permafrost may impact hydraulic, mechanical, and chemical subsurface processes and conditions. Permafrost and its influences on the subsurface conditions are thus of interest for the performance and safety assessments of deep geological waste repositories. The definition of permafrost is 'ground that stays at or below 0 deg C for at least two consecutive years'. Permafrost will effect the geological subsurface to some depth. How deep the permafrost may grow is a function of the heat balance, thermal conditions at the surface and within the ground, and the geothermal heat flux from the Earth's inner parts. The main chapters of the report summaries the knowledge on permafrost evolution, occurrence and distribution, and extracts information concerning hydrology and mechanical and chemical impacts due to permafrost related conditions. The results of a literature review are always dependent on the available literature. Concerning permafrost there is some literature available from investigations in the field of long-term repositories and some from mining industries. However, reports of these investigations are few and the bulk of permafrost literature comes from the science departments concerned with surficial processes (e.g. geomorphology, hydrology, agriculture, etc) and from engineering concerns, such as foundation of constructions and pipeline design. This focus within the permafrost research inevitably yields a biased but also an abundant amount of information on localised surficial processes and a limited amount on regional and deep permafrost characteristics. Possible conclusions are that

  15. Pt Monolayer Shell on Nitrided Alloy Core—A Path to Highly Stable Oxygen Reduction Catalyst

    Directory of Open Access Journals (Sweden)

    Jue Hu

    2015-07-01

    Full Text Available The inadequate activity and stability of Pt as a cathode catalyst under the severe operation conditions are the critical problems facing the application of the proton exchange membrane fuel cell (PEMFC. Here we report on a novel route to synthesize highly active and stable oxygen reduction catalysts by depositing Pt monolayer on a nitrided alloy core. The prepared PtMLPdNiN/C catalyst retains 89% of the initial electrochemical surface area after 50,000 cycles between potentials 0.6 and 1.0 V. By correlating electron energy-loss spectroscopy and X-ray absorption spectroscopy analyses with electrochemical measurements, we found that the significant improvement of stability of the PtMLPdNiN/C catalyst is caused by nitrogen doping while reducing the total precious metal loading.

  16. Methanol electrooxidation on Pt particles dispersed into PANI/SWNT composite films

    Energy Technology Data Exchange (ETDEWEB)

    Wu, Gang; Li, Li; Li, Jing-Hong; Xu, Bo-Qing [Innovative Catalysis Program, Key Laboratory of Organic Optoelectronics and Molecular Engineering, Department of Chemistry, Tsinghua University, Beijing 100084 (China)

    2006-04-21

    Conducting polymer composite films comprised of polyaniline (PANI) and single wall carbon nanotubes (SWNT) was prepared by electrochemical codeposition during the electropolymerization in an aniline solution with suspending SWNT. The fabricated composite films are assessed with respect to their potential application as support materials in Pt electrocatalyst for electrochemical oxidation of methanol. The PANI/SWNT composite film incorporated with SWNT has a higher polymeric degree and lower defect density in PANI structure than PANI film. Furthermore, the incorporation of SWNT also leads to higher electrochemically accessible surface areas (S{sub a}), electronic conductivity and easier charge-transfer at polymer/electrolyte interfaces, which make higher dispersion and utilization for deposited Pt. Therefore, the Pt particles electrodeposited on PANI/SWNT composite polymer film exhibits excellent catalytic activity and stability for the electrooxidation of methanol in comparison to Pt supported on PANI film, which reveals that the composite film is more promising for application in electrocatalyst as a support material. (author)

  17. Suppression of oxygen reduction reaction activity on Pt-based electrocatalysts from ionomer incorporation

    Energy Technology Data Exchange (ETDEWEB)

    Shinozaki, Kazuma; Morimoto, Yu; Pivovar, Bryan S.; Kocha, Shyam S.

    2016-09-01

    The impact of Nafion on the oxygen reduction reaction (ORR) activity is studied for Pt/C and Pt-alloy/C catalysts using thin-film rotating disk electrode (TF-RDE) methods in 0.1 M HClO4. Ultrathin uniform catalyst layers and standardized activity measurement protocols are employed to obtain accurate and reproducible ORR activity. Nafion lowers the ORR activity which plateaus with increasing loading on Pt catalysts. Pt particle size is found not to have significant influence on the extent of the SA decrease upon Nafion incorporation. Catalysts using high surface area carbon (HSC) support exhibit attenuated activity loss resulting from lower ionomer coverage on catalyst particles located within the deep pores. The impact of metallic composition on the activity loss due to Nafion incorporation is also discussed.

  18. Three-year changes of surface albedo of degraded grassland and cropland surfaces in a semiarid area

    Institute of Scientific and Technical Information of China (English)

    LIU HuiZhi; TU Gang; DONG WenJie

    2008-01-01

    Diurnal, seasonal and interannual variations of surface albedo of degraded grassland and cropland surfaces at a semiarid area of Tognyu have been investigated based on the continuous three years observational data from 2003 to 2005. The changes of surface albedo with solar elevation angle and soil moisture have been discussed also. It has been found that surface albedo has almost the same diurnal and seasonal variations on degraded grassland and cropland surfaces in the semiarid area, while sur-face albedo is large in winter and small in summer. The diurnal variation of the surface albedo has re-lationship with the weather condition. The diurnal cycle of the surface albedo likes the "U" shape curve in sunny day, while it is low-high after the rain, and high-low after the snow. The surface albedo has large variation in cloudy day, while it has no any variation in overcast day. The large difference of the surface albedo can be 0.04 in winter between two land surfaces, because the snow has large effects on the surface albedo in winter. The rainfall is an important factor in summer on the surface albedo, while the difference of the surface albedo is 0.01 only between two land surfaces. The differences of the surface aibedo can also be 0.04 in autumn due to vegetation growing. The seasonal-average surface albeo from 2003-2005 is 0.25, 0.22, 0.24, 0.32 respectively in spring, summer, autumn and winter on the degraded grassland surface, while it is 0.25, 0.21,0.22, 0.33 respectively in spring, summer, autumn and winter on the cropland surface. The surface albedo becomes smaller with the increase of solar elevation angle. When the solar elevation angle is greater than 40°, the surface albedo changes very little and tends to be a constant. The surface albedo has negative exponent functions with soil moisture in the growing season.

  19. Long-term studies on the effects of nonvolatile organic compounds on porous media surface areas.

    Science.gov (United States)

    Khachikian, Crist S; Harmon, Thomas C

    2002-01-01

    This paper investigates the long-term behavior of porous media contaminated by nonvolatile organic compounds (NVOC) in terms of specific interfacial surface area. Specifically, a natural sand, Moffett sand (MS), was contaminated with naphthalene and the surface area was measured repeatedly over time using nitrogen adsorption-desorption techniques. A field-contaminated sand affected by lamp-black material (LB) from former manufactured gas plant operations was also studied. Lampblack is a carbonaceous skeleton containing polycyclic aromatic hydrocarbons (PAHs) and other hydrocarbons. It is hypothesized that soils contaminated by these types of chemicals will exhibit significantly less surface area than their clean counterparts. The surface areas for the contaminated MS samples increased toward their clean-MS values during the 700-h aging period, but achieved the clean values only after pentane extraction or heating at 60 degrees C. Heating at 50 degrees C failed to achieve a similar recovery of the clean-MS surface area value. Nonspecific mass loss tracked the increase in surface area as indirect evidence that naphthalene loss was the cause of the surface area increase. For the LB samples, aging at 100 degrees C produced a slight decrease in surface area and mass while aging at 250 degrees C caused the surface area to increase roughly threefold while the mass decreased by approximately 1%. These results suggest that, under moderate heating and over the time scale of this investigation, there is a redistribution of the complex contaminant mixture on the solid matrix. Greater temperatures remove mass more efficiently and therefore exhibited the surface area increase expected in this experiment.

  20. Catalytic oxidation of cyclohexane to cyclohexanone and cyclohexanol by tert-butyl hydroperoxide over Pt/oxide catalysts

    Indian Academy of Sciences (India)

    I Rekkab-Hammoumraoui; A Choukchou-Braham; L Pirault-Roy; C Kappenstein

    2011-08-01

    Heterogeneous oxidation of cyclohexane with tertiobutyl hydroperoxide was carried out on Pt/oxide (Al2O3, TiO2 and ZrO2) catalysts in the presence of different solvents (acetic acid and acetonitrile). The catalysts were prepared using Pt(NH3)2(NO2)2 as a precursor and characterized by chemical analysis using the ICP–AES method, XRD, TEM, FTIR and BET surface area determination. The oxidation reaction was carried out at 70°C under atmospheric pressure. The results showed the catalytic performance of Pt/Al2O3 as being very high in terms of turnover frequency.

  1. Preparation of high dispersion and high performance PtRu/CNTs catalyst by an organic colloid method

    Institute of Scientific and Technical Information of China (English)

    王宁卡特; 刘军民; 廖世军; V.Birss

    2006-01-01

    A high dispersion and high performance PtRu catalyst supported on carbon nanotubes was prepared by an organic colloid method. The particle size of the active components could be as small as 1.0 nm,the active surface area was about 466 m2/g(Pt). The catalytic activity toward anodic oxidation of methanol was about 3 ~ 4 times higher than that of Johnson Matthey PtRu/XC-72R catalyst. The single testing showed that the performance of the prepared catalyst was higher than that of the commercial one.

  2. The domain structure and polarization retention properties of PT/PZT/PT ferroelectric thin film

    Institute of Scientific and Technical Information of China (English)

    WANG LongHai; Yu Jun; ZHAO SuLing; ZHENG ChaoDuan; WANG YunBo; GAO JunXiong

    2007-01-01

    3The Research & Test Center of Materials, Wuhan University of Technology, Wuhan 430070, ChinaThe highly oriented perovskite-phase PT/PZT/PT ferroelectric thin film was prepared by sol-gel method. The domain structures and polarization retention properties were investigated by scanning force microscopy. The amplitude and phase images of piezoresponse show complex various contrasts of dark, bright and gray.The complex variation of contrast in piezoresponse images results from the perplexing orientation of grains and arrangement of domains in the ferroelectric films.The bright and dark areas in phase images correspond to top-to-bottom and bottom-to-top polarization oriented c-domain, respectively. The gray areas are c-domains with the polarization vector deviating from the direction normal to the film plane. The surface potential images of EFM are bright contrast, which is due to positive charges trapped on the film surface after being polarized by positive voltage. And the brighter contrast is obtained from the higher electric field. The time-dependent surface potential images and line potential profiles show that the potential decays with time. And the decay in the region polarized by higher electric field is faster, especially at 15 min. This indicates that the polarization retention is related to the polarized electric field. Better retention properties may be obtained from a proper polarized electric field.

  3. The domain structure and polarization retention properties of PT/PZT/PT ferroelectric thin film

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    The highly oriented perovskite-phase PT/PZT/PT ferroelectric thin film was pre- pared by sol-gel method. The domain structures and polarization retention proper- ties were investigated by scanning force microscopy. The amplitude and phase images of piezoresponse show complex various contrasts of dark, bright and gray. The complex variation of contrast in piezoresponse images results from the per- plexing orientation of grains and arrangement of domains in the ferroelectric films. The bright and dark areas in phase images correspond to top-to-bottom and bot- tom-to-top polarization oriented c-domain, respectively. The gray areas are c-domains with the polarization vector deviating from the direction normal to the film plane. The surface potential images of EFM are bright contrast, which is due to positive charges trapped on the film surface after being polarized by positive volt- age. And the brighter contrast is obtained from the higher electric field. The time-dependent surface potential images and line potential profiles show that the potential decays with time. And the decay in the region polarized by higher electric field is faster, especially at 15 min. This indicates that the polarization retention is related to the polarized electric field. Better retention properties may be obtained from a proper polarized electric field.

  4. Antiproliferative Pt(IV) complexes: synthesis, biological activity, and quantitative structure-activity relationship modeling.

    Science.gov (United States)

    Gramatica, Paola; Papa, Ester; Luini, Mara; Monti, Elena; Gariboldi, Marzia B; Ravera, Mauro; Gabano, Elisabetta; Gaviglio, Luca; Osella, Domenico

    2010-09-01

    Several Pt(IV) complexes of the general formula [Pt(L)2(L')2(L'')2] [axial ligands L are Cl-, RCOO-, or OH-; equatorial ligands L' are two am(m)ine or one diamine; and equatorial ligands L'' are Cl- or glycolato] were rationally designed and synthesized in the attempt to develop a predictive quantitative structure-activity relationship (QSAR) model. Numerous theoretical molecular descriptors were used alongside physicochemical data (i.e., reduction peak potential, Ep, and partition coefficient, log Po/w) to obtain a validated QSAR between in vitro cytotoxicity (half maximal inhibitory concentrations, IC50, on A2780 ovarian and HCT116 colon carcinoma cell lines) and some features of Pt(IV) complexes. In the resulting best models, a lipophilic descriptor (log Po/w or the number of secondary sp3 carbon atoms) plus an electronic descriptor (Ep, the number of oxygen atoms, or the topological polar surface area expressed as the N,O polar contribution) is necessary for modeling, supporting the general finding that the biological behavior of Pt(IV) complexes can be rationalized on the basis of their cellular uptake, the Pt(IV)-->Pt(II) reduction, and the structure of the corresponding Pt(II) metabolites. Novel compounds were synthesized on the basis of their predicted cytotoxicity in the preliminary QSAR model, and were experimentally tested. A final QSAR model, based solely on theoretical molecular descriptors to ensure its general applicability, is proposed.

  5. Influence of surface morphology and surface area on release behavior of hydrogen isotopes in LiNbO{sub 3}

    Energy Technology Data Exchange (ETDEWEB)

    Zhu, Deqiong, E-mail: zhudeqiong@snu.ac.kr [Department of Nuclear Engineering, Seoul National University, 1 Gwanak-ro, Gwanak-gu, Seoul 151-744 (Korea, Republic of); Oda, Takuji [Department of Nuclear Engineering, Seoul National University, 1 Gwanak-ro, Gwanak-gu, Seoul 151-744 (Korea, Republic of); Tanaka, Satoru [Department of Nuclear Engineering and Management, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8656 Japan (Japan)

    2014-11-15

    Surface processes have profound influence on tritium release behavior in ceramic breeder materials. In this paper, the release behavior of hydrogen isotopes in LiNbO{sub 3} is studied by thermal desorption spectroscopy (TDS) with focusing on the influence of the surface morphology and surface area. It is found that the amount of surface hydroxyl groups is proportional to the specific surface area and can be decreased by smoothing the surface roughness through heating pretreatment at high temperatures. The isotope exchange reaction between the surface hydroxyl groups and water molecules residue in the system is discussed and turns out to proceed fast. The release behavior of hydrogen isotopes in LiNbO{sub 3} is compared with that in Li{sub 2}TiO{sub 3} studied in our previous work. It reveals that LiNbO{sub 3} and Li{sub 2}TiO{sub 3} have similar surface environment and similar concentration of surface hydroxyl groups with the level of 10{sup 20} m{sup −2}. The formation mechanism of hydroxyl groups on the surface is discussed and a model to explain the experimental observations is proposed.

  6. Environmental and geochemical assessment of surface sediments on irshansk ilmenite deposit area

    Directory of Open Access Journals (Sweden)

    Наталия Олеговна Крюченко

    2015-03-01

    Full Text Available It is revealed the problem of pollution of surface sediments of Irshansk ilmenite deposit area of various chemical elements hazard class (Mn, V, Ba, Ni, Co, Cr, Mo, Cu, Pb, Zn. It is determined its average content in surface sediments of various functional areas (forest and agricultural land, flood deposits, reclaimed land, calculated geochemical criteria, so given ecological and geochemical assessment of area

  7. 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.

  8. Prothrombin time (PT)

    Science.gov (United States)

    PT; Pro-time; Anticoagulant-prothrombin time; Clotting time: protime; INR; International normalized ratio ... PT is measured in seconds. Most of the time, results are given as what is called INR ( ...

  9. Plasma nitriding induced growth of Pt-nanowire arrays as high performance electrocatalysts for fuel cells

    NARCIS (Netherlands)

    Du, S.; Lin, K.; Malladi, S.R.K.; Lu, Y.; Sun, S.; Xu, Q.; Steinberger-Wilckens, R.; Dong, H.

    2014-01-01

    In this work, we demonstrate an innovative approach, combing a novel active screen plasma (ASP) technique with green chemical synthesis, for a direct fabrication of uniform Pt nanowire arrays on large-area supports. The ASP treatment enables in-situ N-doping and surface modification to the support

  10. Hydrogen Adsorption on Pt, Rh and Pt-Rh Electrodes

    Institute of Scientific and Technical Information of China (English)

    贾梦秋; A.M.Meretskyi

    2005-01-01

    The hydrogen adsorption on Pt-Rh alloys in sulfuric acid aqueous solutions was studied by the method of cathode pulses. Hydrogen adsorption on the electrode with all ratio of alloy components (ωRh = 0-100%) is well described by the Temkin logarithmic isotherm. The surface coverage by adsorbed hydrogen at the same potential is decreased with increasing content of rhodium in the system. A linear dependence of adsorption peak potential on the alloy compositions in the case of weakly bonded adsorbed hydrogen is established. Hydrogen adsorption heat as a function of surface coverage for Pt-Rh-electrodes was obtained. The shape of the current-potential curve and position of the weakly bonded hydrogen adsorption on the potential scale are all related to alloy compositions, thus can serve as the basis for the determination surface composition of allovs.

  11. Premature temporal theta (PT theta).

    Science.gov (United States)

    Hughes, J R; Fino, J J; Hart, L A

    1987-07-01

    A distinctive pattern called premature temporal theta (PT theta) was studied in 436 infants, ranging in age from 24 to 46 weeks. The pattern is seen in early prematurity, maximizes at 29-31 weeks and then diminishes and disappears near term. Usually the pattern is found independently on both temporal areas, but with a right-sided preference. Patients without PT theta or with a significantly low amount had either neurological or non-neurological (medical) conditions. With age there is a tendency for an increase in frequency and a decrease in amplitude. Five different peaks in the amount of this pattern are seen at approximately every month. Unilateral PT theta tends to be seen in older babies, more often on the right side and with an abnormal EEG. An abnormal EEG is usually associated with a delay in both the appearance and disappearance of this wave form. PT theta is also associated mainly with REM or active sleep. A polynomial rather than an exponential or power function best describes these data with changes of age. PT theta may arise from the inferior temporal gyrus and/or especially the transverse gyrus.

  12. Synthesis and alignment of silver nanorods and nanowires and the formation of Pt, Pd, and core/shell structures by galvanic exchange directly on surfaces.

    Science.gov (United States)

    Sławiński, Grzegorz W; Zamborini, Francis P

    2007-09-25

    Here we describe the synthesis of Ag nanorods (NRs) (aspect ratio or =20) directly on surfaces by seed-mediated growth. The procedure involves attaching gold seed nanoparticles (Au NPs) to 3-mercaptopropyltrimethoxysilane (MPTMS)-functionalized silicon or glass surfaces and growing them into NRs/NWs by placing the substrates into a solution containing cetyltrimethylammonium bromide (CTAB), silver nitrate, and ascorbic acid with the pH ranging from 7 to 12. Under our conditions, Ag NRs/NWs grow optimally at pH 10.6 with a 3% yield, where spherical, triangular, and hexagonal nanostructures represent the other byproducts. The length of Ag NRs/NWs ranges from 50 nm to more than 10 microm, the aspect ratio (AR) ranges from 1.4 to >300, and the average diameter is approximately 35 nm. Approximately 40% of the 1D structures are NRs, and 60% are NWs as defined by their ARs. We also report the alignment of Ag NRs/NWs directly on surfaces by growing the structures on amine-functionalized Si(100) surfaces after an amidation reaction with acetic acid and a method to improve the percentage of Ag NRs/NWs on the surface by removing structures of other shapes with adhesive tape. Surface-grown Ag NRs/NWs also react with salts of palladium, platinum, and gold via galvanic exchange reactions to form high-surface-area 1D structures of the corresponding metal. The combination of the seed-mediated growth of Ag on Au NRs followed by the galvanic exchange of Ag with Pd leads to interesting core/shell NRs grown directly on surfaces. We used scanning electron microscopy, UV-vis spectroscopy, and X-ray photoelectron spectroscopy to characterize the surface-grown nanostructures.

  13. Changes in the Surface Area of Glaciers in Northern Eurasia

    Science.gov (United States)

    Khromova, T.; Nosenko, G.

    2012-12-01

    Glaciers are widely recognized as key indicators of climate change. Recent evidence suggests an acceleration of glacier mass loss in several key mountain regions. Glacier recession implies the landscape changes in the glacial zone, origin of new lakes and activation of natural disaster processes, catastrophic mudflows, ice avalanches, outburst floods, and etc. The presence of glaciers in itself threats to human life, economic activity and growing infrastructure. Economical and recreational human activity in mountain regions requires relevant information on snow and ice objects. Absence or inadequacy of such information results in financial and human losses. A more comprehensive evaluation of glacier changes is imperative to assess ice contributions to global sea level rise and the future of water resources from glacial basins. One of the urgent steps is a full inventory of all ice bodies, their volume and changes The first estimation of glaciers state and glaciers distribution in the big part of Northern Eurasia has been done in the USSR Glacier Inventory published in 1966 -1980 as a part of IHD activity. The Inventory is based on topographic maps and air photos and reflects the status of the glaciers in 1957-1970y. There is information about 23796 glaciers with area of 78222.3 km2 in the Inventory. It covers 23 glacier systems on Northern Eurasia. In the 80th the USSR Glacier Inventory has been transformed in the digital form as a part of the World Glacier Inventory. Recent satellite data provide a unique opportunity to look again at these glaciers and to evaluate changes in glacier extent for the second part of XX century. In the paper we report about 15 000 glaciers outlines for Caucasus, Pamir, Tien-Shan, Altai, Syntar-Khayata, Cherskogo Range, Kamchatka and Russian Arctic which have been derived from ASTER and Landsat imagery and could be used for glacier changes evaluation. The results show that glaciers are retreating in all these regions. There is, however

  14. Co@Pt Core@Shell nanoparticles encapsulated in porous carbon derived from zeolitic imidazolate framework 67 for oxygen electroreduction in alkaline media

    Science.gov (United States)

    Wang, Likai; Tang, Zhenghua; Yan, Wei; Wang, Qiannan; Yang, Hongyu; Chen, Shaowei

    2017-03-01

    Nanocomposites based on Co@Pt core@shell nanoparticles encapsulated in nitrogen-doped porous carbons were prepared as a new type of high-performance electrocatalysts for oxygen reduction reaction (ORR). Controlled pyrolysis of zeolitic imidazolate framework 67 (ZIF-67) led to the formation of Co nanoparticles encapsulated in nitrogen-doped porous carbon (Co-NC), which underwent galvanic replacement reactions with K2PtCl4 forming Co@Pt core@shell nanoparticles. The surface microstructure and composition of the resulting Co@Pt-NC nanocomposite were examined by electron microscopic as well as X-ray photoelectron spectroscopic (XPS) measurements. With the Co@Pt particles encapsulated in nitrogen-doped porous carbon, the hybrids exhibited a high specific surface area and abundant catalytically active sites for ORR. Electrochemically, the specific activity and mass activity of the Co@Pt-NC composite at +0.85 V (0.145 mA cm-2 and 71.9 A g-1) were superior to those of commercial Pt/C (0.123 mA cm-2 and 38.4 A g-1). Furthermore, the Co@Pt-NC composite also exhibited remarkably higher durability and more robust tolerance against methanol crossover than commercial Pt/C.

  15. Controllable Deposition of Alloy Clusters or Nanoparticles Catalysts on Carbon Surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Sasaki, K.; Ando, Y.; Su, D.; Adzic, R.

    2011-08-15

    We describe a simple method for controllably depositing Pt-Ru alloy nanoparticles on carbon surfaces that is mediated by Pb or Cu adlayers undergoing underpotential deposition and stripping during Pt and Ru codeposition at diffusion-limiting currents. The amount of surface Pt atoms deposited largely reflects the number of potential cycles causing the deposition and stripping of the metal adlayer at underpotentials, the metal species used as a mediator, and the scan rate of the potential cycles. We employed electrochemical methanol oxidation to gain information on the catalyst's activities. The catalysts with large amounts of surface Pt atoms have relatively high methanol-oxidation activity. Catalysts prepared using this method enhance methanol-oxidation activity per electrode surface area, while maintaining catalytic activity per surface Pt atom; thus, the amount of Pt is reduced in comparison with conventional methanol-oxidation catalysts. The method is suitable for efficient synthesizing various bimetallic catalysts.

  16. Synthesis and composition evolution of bimetallic Pd Pt alloy nanoparticles

    Science.gov (United States)

    Ren, Guoqiang; Shi, Honglan; Xing, Yangchuan

    2007-09-01

    This paper reports a study on the synthesis of Pd-Pt alloy nanoparticles and composition evolution of the alloys. The synthesis involves Pd and Pt acetylacetonate as the metal precursors and trioctylphosphine (TOP) as the solvent. Thermal decomposition of the Pd-TOP complex resulted in Pd nanoparticles, while substitution of Pt in the Pt-TOP complex by Pd allowed formation of the Pd-Pt alloys. It was observed that the Pd-Pt nanoparticles formed at the very beginning in the synthesis process are Pd rich with various nanoparticle sizes ranging from 1.5 to 25 nm in diameter. These nanoparticles averaged out through a digestive ripening process and reached a final size of 3.5 nm in about 10 min. The alloy compositions evolved throughout the synthesis process and only reached the preset Pd to Pt ratio of the precursors in 120 min. It was found that Pt acetylacetonate alone in TOP cannot produce Pt nanoparticles, which was attributed to the formation of a Pt-TOP complex and a strong coordination of Pt to the phosphine. This observation led us to propose an atomic exchange process between the Pt-TOP complex and the Pd atoms at the nanoparticle surface. As a result, the alloy formation process is limited by a substitution and diffusion rate of the Pt atoms at the surface of the alloy nanoparticles.

  17. Surface chemical properties of novel high surface area solids synthesized from coal fly ash

    CSIR Research Space (South Africa)

    Pretorius, PJ

    2003-07-23

    Full Text Available to the presence of =AlOH- and =SiOH-type surface groups. Surface protonation constants for the various solids (unmodified ash, base-modified ash, and acid-etched zeolitic product) are reported. Metal sorption studies were performed for cadmium and copper...

  18. Plasma nitriding induced growth of Pt-nanowire arrays as high performance electrocatalysts for fuel cells.

    Science.gov (United States)

    Du, Shangfeng; Lin, Kaijie; Malladi, Sairam K; Lu, Yaxiang; Sun, Shuhui; Xu, Qiang; Steinberger-Wilckens, Robert; Dong, Hanshan

    2014-09-22

    In this work, we demonstrate an innovative approach, combing a novel active screen plasma (ASP) technique with green chemical synthesis, for a direct fabrication of uniform Pt nanowire arrays on large-area supports. The ASP treatment enables in-situ N-doping and surface modification to the support surface, significantly promoting the uniform growth of tiny Pt nuclei which directs the growth of ultrathin single-crystal Pt nanowire (2.5-3 nm in diameter) arrays, forming a three-dimensional (3D) nano-architecture. Pt nanowire arrays in-situ grown on the large-area gas diffusion layer (GDL) (5 cm(2)) can be directly used as the catalyst electrode in fuel cells. The unique design brings in an extremely thin electrocatalyst layer, facilitating the charge transfer and mass transfer properties, leading to over two times higher power density than the conventional Pt nanoparticle catalyst electrode in real fuel cell environment. Due to the similar challenges faced with other nanostructures and the high availability of ASP for other material surfaces, this work will provide valuable insights and guidance towards the development of other new nano-architectures for various practical applications.

  19. Estimating the surface area of non-convex particles from central planar sections

    DEFF Research Database (Denmark)

    Thórisdóttir, Ólöf; H.Rafati, Ali; Kiderlen, Markus

    . In this section plane a modification of the area tangent count method is used. The Morse type estimator generalizes Cruz-Orive's pivotal estimator for convex objects to non-convex objects. The advantages of the Morse type estimator over existing local surface area estimators are illustrated in a simulation study......In this paper, we present a new surface area estimator in local stereology. This new estimator is called the 'Morse type surface area estimator' and is obtained using a two-stage sampling procedure. First a plane section through a fixed reference point of a three-dimensional structure is taken....... The Morse type estimator is well suited for computer assisted confocal microscopy and we demonstrate its practicability in a biological application: the surface area estimation of the nuclei of giant-cell glioblastoma from microscopy images. We also present an interactive software that allows the user...

  20. Enhanced methanol electro-oxidation reaction on Pt-CoO{sub x}/MWCNTs hybrid electro-catalyst

    Energy Technology Data Exchange (ETDEWEB)

    Nouralishahi, Amideddin, E-mail: Nouralishahi@ut.ac.ir [Catalysis and Nanostructured Materials Research Laboratory, School of Chemical Engineering, University of Tehran, P.O. Box 11155/4563, Tehran (Iran, Islamic Republic of); Caspian Faculty of Engineering, University of Tehran, P.O. Box 43841-119, Rezvanshahr (Iran, Islamic Republic of); Catalysis and Nanotechnology Research Division, Research Institute of Petroleum Industry (RIPI), P.O. Box 14665-1998, Tehran (Iran, Islamic Republic of); Rashidi, Ali Morad, E-mail: Rashidiam@ripi.ir [Catalysis and Nanotechnology Research Division, Research Institute of Petroleum Industry (RIPI), P.O. Box 14665-1998, Tehran (Iran, Islamic Republic of); Mortazavi, Yadollah, E-mail: Mortazav@ut.ac.ir [Catalysis and Nanostructured Materials Research Laboratory, School of Chemical Engineering, University of Tehran, P.O. Box 11155/4563, Tehran (Iran, Islamic Republic of); Khodadadi, Abbas Ali, E-mail: Khodadad@ut.ac.ir [Catalysis and Nanostructured Materials Research Laboratory, School of Chemical Engineering, University of Tehran, P.O. Box 11155/4563, Tehran (Iran, Islamic Republic of); Choolaei, Mohammadmehdi, E-mail: Choolaeimm@ripi.ir [Catalysis and Nanotechnology Research Division, Research Institute of Petroleum Industry (RIPI), P.O. Box 14665-1998, Tehran (Iran, Islamic Republic of)

    2015-04-30

    Highlights: • Promoting effects of Cobalt oxide on methanol electro-oxidation over Pt/MWCNTs are investigated. • Higher activity, about 2.9 times, and enhanced stability are observed on Pt-CoO{sub x}/MWCNTs. • Electrochemical active surface area of Pt nanoparticles is significantly improved upon CoO{sub x} addition. • Bi-functional mechanism is facilitated in presence of CoO{sub x}. - Abstract: The electro-catalytic behavior of Pt-CoO{sub x}/MWCNTs in methanol electro-oxidation reaction (MOR) is investigated and compared to that of Pt/MWCNTs. The electro-catalysts were synthesized by an impregnation method using NaBH{sub 4} as the reducing agent. The morphological and physical characteristics of samples are examined by XRD, TEM, ICP and EDS techniques. In the presence of CoO{sub x}, Pt nanoparticles were highly distributed on the support with an average particle size of 2 nm, an obvious decrease from 5.1 nm for Pt/MWCNTs. Cyclic voltammetry, CO-stripping, Chronoamperometry, and electrochemical impedance spectroscopy (EIS) measurements are used to study the electrochemical behavior of the electro-catalysts. The results revealed a considerable enhancement in the oxidation kinetics of CO{sub ads} on Pt active sites by the participation of CoO{sub x}. Compared to Pt/MWCNTs, Pt-CoO{sub x}/MWCNTs sample has a larger electrochemical active surface area (ECSA) and higher electro-catalytic activity and stability toward methanol electro-oxidation. According to the results of cyclic voltammetry, the forward anodic peak current density enhances more than 89% at the optimum atomic ratio of Pt:Co = 2:1. Furthermore, inclusion of cobalt oxide species causes the onset potential of methanol electro-oxidation reaction to shift 84 mV to negative values compared to that on Pt/MWCNTs. Based on EIS data, dehydrogenation of methanol is the rate-determining step of MOR on both Pt/MWCNTs and Pt-CoO{sub x}/MWCNTs, at small overpotentials. However, at higher overpotentials, the

  1. Assessment of heavy metal levels in surface sediments of estuaries and adjacent coastal areas in China

    Science.gov (United States)

    Liu, Xianbin; Li, Deliang; Song, Guisheng

    2017-03-01

    This article investigates the variations of contamination levels of heavy metals such as copper, lead, chromium, cadmium, zinc, arsenic, and mercury over time in surface sediments of the Changjiang River Estuary (CRE), Yellow River Estuary (YRE), Pearl River Estuary (PRE), and their adjacent coastal areas in China. The contamination factor (CF), pollution load index (PLI), and geoaccumulation index ( I geo) are used to evaluate the quality of the surface sediments in the study areas. The results showed that the CRE, YRE, and their adjacent coastal areas were at a low risk of contamination in terms of heavy metals, while the PRE and its adjacent coastal area were at a moderate level. By comparison, the concentrations of heavy metals in the surface sediments of the YRE and its adjacent coastal area were relatively lower than those in the CRE, PRE, and their adjacent coastal areas.

  2. Synthesis of Pd-Pt bimetallic nanocrystals with a concave structure through a bromide-induced galvanic replacement reaction.

    Science.gov (United States)

    Zhang, Hui; Jin, Mingshang; Wang, Jinguo; Li, Weiyang; Camargo, Pedro H C; Kim, Moon J; Yang, Deren; Xie, Zhaoxiong; Xia, Younan

    2011-04-20

    This article describes a systematic study of the galvanic replacement reaction between PtCl(6)(2-) ions and Pd nanocrystals with different shapes, including cubes, cuboctahedrons, and octahedrons. It was found that Br(-) ions played an important role in initiating, facilitating, and directing the replacement reaction. The presence of Br(-) ions led to the selective initiation of galvanic replacement from the {100} facets of Pd nanocrystals, likely due to the preferential adsorption of Br(-) ions on this crystallographic plane. The site-selective galvanic replacement resulted in the formation of Pd-Pt bimetallic nanocrystals with a concave structure owing to simultaneous dissolution of Pd atoms from the {100} facets and deposition of the resultant Pt atoms on the {111} facets. The Pd-Pt concave nanocubes with different weight percentages of Pt at 3.4, 10.4, 19.9, and 34.4 were also evaluated as electrocatalysts for the oxygen reduction reaction (ORR). Significantly, the sample with a 3.4 wt.% of Pt exhibited the largest specific electrochemical surface area and was found to be four times as active as the commercial Pt/C catalyst for the ORR in terms of equivalent Pt mass.

  3. Relationship between Mineral Soil Surface Area and the Biological Degradation of Biosolids Added to Soil

    Directory of Open Access Journals (Sweden)

    Dongqi Wen

    2015-12-01

    Full Text Available Geochemical and biological processes that operate in the soil matrix and on the soil surface are important to the degradation of biosolids in soil. Due to the large surface area of soils it is assumed that the microbial ecology is associated with mineral soil surface area. The total mineral surface areas were determined for soils from eight different fields selected from a long term study (1972–2006 of annual biosolids application to 41 fields in central Illinois varying in size from 3.6 to 66 ha. The surface areas for the soils varied from 1 to 9 m2/g of soil. The biological degradation rates for the eight soils were determined using a biological degradation rate model (DRM and varied from 0.02 to 0.20/year−1. Regression analysis revealed that the degradation rate was positively associated with mineral soil surface area (1 m2/g produces 0.018 year−1 increase in the degradation rate. The annual soil sequestration rate was calculated to increase from 1% to 6% when the soil total surface area increased from 1 to 9 m2/g of soil. Therefore, land application of biosolids is an effective way to enhance carbon sequestration in soils and reduce greenhouse gas emissions.

  4. Cyclic voltammograms for H on Pt(111) and Pt(100) from first principles

    DEFF Research Database (Denmark)

    Karlberg, Gustav; Jaramillo, Thomas; Skulason, Egill;

    2007-01-01

    Cyclic voltammetry is a fundamental experimental method for characterizing electrochemical surfaces. Despite its wide use, a way to quantitatively and directly relate cyclic voltammetry to ab initio calculations has been lacking. We derive the cyclic voltammogram for H on Pt(111) and Pt(100), based...

  5. Pore Scale Heterogeneity in the Mineral Distribution and Surface Area of Porous Rocks

    Science.gov (United States)

    Lai, Peter; Krevor, Sam

    2015-04-01

    An important control on rate of interfacial processes between minerals and aqueous solutions such as nucleation of solids, and mineral dissolution and growth is reactive surface area. In geochemical modelling, the continuum hypothesis is based on the assumption that the system can be represented by a sufficiently large number of representative elemental volumes. There has been recent interest in studying the impact of this assumption on reaction-transport coupled systems. In this study, the impact of pore-scale heterogeneity on the distribution of reactive surface area is discussed. 3D images obtained using x-ray micro-tomography were used to characterise the distribution of reactive surface area. The results were compared to independent observations. Mineral identification using x- ray diffraction and fluorescence suggested general agreement with CT analysis. Nitrogen BET surface areas were one to two orders of magnitude higher than measurements from x-ray imagery. Co- registered images of Berea sandstone from x-ray and energy dispersive spectroscopy imagery suggested that quartz, K-feldspar and most clays could be identified. However, minor minerals such as albite and illite did not exhibit enough contrast. In Berea sandstone, mineral surface area fraction was poorly correlated to the mineral volumetric fraction. Clay and feldspar minerals exhibited higher surface area fractions than bulk mineralogy suggested. In contrast, in the Edwards carbonate samples, modal mineral composition correlated with mineral-specific surface area. Berea sandstone revealed a characteristic pore size at which a surface area distribution may be used to quantify heterogeneity. Conversely, the carbonate samples suggested a continuous range of pore sizes across length scales. A comparison with pore network model simulations from the literature was made. First order estimates of mineral specific correlations between geometric area measured in the x-ray images were used to convert the CT

  6. Enhanced methanol electro-oxidation activity of PtRu catalysts supported on heteroatom-doped carbon

    Energy Technology Data Exchange (ETDEWEB)

    Wu Gang [Department of Applied Chemistry, Harbin Institute of Technology, Harbin 150001 (China)], E-mail: wugang@lanl.gov; Swaidan, Raja [Department of Chemical Engineering, Cooper Union, New York, NY 10003 (United States); Li Deyu; Li Ning [Department of Applied Chemistry, Harbin Institute of Technology, Harbin 150001 (China)

    2008-11-01

    A typical heteroatom (nitrogen)-doped carbon materials were successfully synthesized through the carbonization of a hybrid containing traditional carbon black covered by in situ polymerized polyaniline. The nitrogen content onto carbon can be adjusted up to 5.1 at.% by changing the coverage of polyaniline. The effects of nitrogen doping on the surface physical and electrochemical properties of carbon were studied using XPS, XRD and HRTEM, as well as CV and EIS techniques. With increasing nitrogen doping, the carbon structure became more compact, showing curvatures and dislocations in the graphene stacking. The nitrogen-doped carbon also exhibited a higher accessible surface area in electrochemical reactions, and a lower charge transfer resistance at the carbon/electrolyte interface. Moreover, to investigate the influence of nitrogen doping on the electrocatalytic activity of the PtRu/C catalyst, comparisons in CO stripping and methanol oxidation were carried out on PtRu catalysts supported by non-doped and nitrogen-doped carbon. Since the promotional roles of nitrogen doping, including the high electrochemically accessible surface area, the richness of the disordered nanostructures and defects, and the high electron density on N-doped carbon supports, contribute to the synthesis of well-dispersed PtRu particles with high Pt utilization and stronger metal-support interactions, an enhanced catalytic activity for methanol oxidation was obtained in the case of the PtRu/N-C catalyst in comparison with the traditional PtRu/C catalyst.

  7. Enhanced methanol electro-oxidation activity of PtRu catalysts supported on heteroatom-doped carbon

    Energy Technology Data Exchange (ETDEWEB)

    Wu, Gang; Li, Deyu; Li, Ning [Department of Applied Chemistry, Harbin Institute of Technology, Harbin 150001 (China); Swaidan, Raja [Department of Chemical Engineering, Cooper Union, New York, NY 10003 (United States)

    2008-11-01

    A typical heteroatom (nitrogen)-doped carbon materials were successfully synthesized through the carbonization of a hybrid containing traditional carbon black covered by in situ polymerized polyaniline. The nitrogen content onto carbon can be adjusted up to 5.1 at.% by changing the coverage of polyaniline. The effects of nitrogen doping on the surface physical and electrochemical properties of carbon were studied using XPS, XRD and HRTEM, as well as CV and EIS techniques. With increasing nitrogen doping, the carbon structure became more compact, showing curvatures and dislocations in the graphene stacking. The nitrogen-doped carbon also exhibited a higher accessible surface area in electrochemical reactions, and a lower charge transfer resistance at the carbon/electrolyte interface. Moreover, to investigate the influence of nitrogen doping on the electrocatalytic activity of the PtRu/C catalyst, comparisons in CO stripping and methanol oxidation were carried out on PtRu catalysts supported by non-doped and nitrogen-doped carbon. Since the promotional roles of nitrogen doping, including the high electrochemically accessible surface area, the richness of the disordered nanostructures and defects, and the high electron density on N-doped carbon supports, contribute to the synthesis of well-dispersed PtRu particles with high Pt utilization and stronger metal-support interactions, an enhanced catalytic activity for methanol oxidation was obtained in the case of the PtRu/N-C catalyst in comparison with the traditional PtRu/C catalyst. (author)

  8. Oriented-assembly of hollow FePt nanochains with tunable catalytic and magnetic properties

    Science.gov (United States)

    Liu, Jialong; Xia, Tianyu; Wang, Shouguo; Yang, Guang; Dong, Bowen; Wang, Chao; Ma, Qidi; Sun, Young; Wang, Rongming

    2016-06-01

    Hollow nanoparticles with large surface areas exhibit a lot of advantages for applications such as catalysis and energy storage. Furthermore, their performance can be manipulated by their deliberate assemblies. Dispersive hollow FePt nanospheres have been assembled into one-dimensional hollow FePt nanochains under the magnetic fields at room temperature. Based on the activation of galvanic replacement at different reaction stages, the size of hollow FePt nanochains can be deliberately manipulated varying from 20 nm to 300 nm, together with the length changing from 200 nm to 10 μm. The competition between movement of paramagnetic Fe3+ ions and shape recovering due to thermal fluctuations plays a critical effect on the structure of contact area between hollow nanospheres, leading to perforative structures. Compared with commercial Pt/C, well aligned hollow FePt nanochains show greatly enhanced catalytic activities in the methanol oxidation reaction (MOR) due to more favorable mass flow. Magnetic measurements indicate that the magnetic properties including Curie temperature and saturation magnetization can be tuned by the control of the size and shape of hollow nanochains.Hollow nanoparticles with large surface areas exhibit a lot of advantages for applications such as catalysis and energy storage. Furthermore, their performance can be manipulated by their deliberate assemblies. Dispersive hollow FePt nanospheres have been assembled into one-dimensional hollow FePt nanochains under the magnetic fields at room temperature. Based on the activation of galvanic replacement at different reaction stages, the size of hollow FePt nanochains can be deliberately manipulated varying from 20 nm to 300 nm, together with the length changing from 200 nm to 10 μm. The competition between movement of paramagnetic Fe3+ ions and shape recovering due to thermal fluctuations plays a critical effect on the structure of contact area between hollow nanospheres, leading to perforative

  9. Analysis of particle size reduction on overall surface area and enzymatic hydrolysis yield of corn stover.

    Science.gov (United States)

    Li, Hanjie; Ye, Chenlin; Liu, Ke; Gu, Hanqi; Du, Weitao; Bao, Jie

    2015-01-01

    Particle size of lignocellulose materials is an important factor for enzymatic hydrolysis efficiency. In this study, corn stover was milled and sieved into different size fractions from 1.42, 0.69, 0.34, to 0.21 mm, and the corresponding enzymatic hydrolysis yields were 24.69, 23.96, 25.34, and 26.97 %, respectively. The results indicate that the hydrolysis yield is approximately constant with changing corn stover particle sizes in the experimental range. The overall surface area and the inner pore size measurement show that the overall specific surface area was less than 2 % with the half reduction of particle size due to the greater inner pore surface area. The scanning electron microscope photographs gave direct evidence of the much greater inner pore surface area of corn stover particles. This result provided a reference when a proper size reduction of lignocellulose materials is considered in biorefining operations.

  10. Modelling skin surface areas involved in water transfer in the Palmate Newt (Lissotriton helveticus)

    National Research Council Canada - National Science Library

    Wardziak, Thomas; Oxarango, Laurent; Valette, Sebastien; Mahieu-Williame, Laurent; Joly, Pierre

    2014-01-01

    Magnetic resonance imaging (MRI) based 3D reconstructions were used to derive accurate quantitative data on body volume and functional skin surface areas involved in water transfer in the Palmate Newt...

  11. Synthesis and characterization of large specific surface area nanostructured amorphous silica materials.

    Science.gov (United States)

    Marquez-Linares, Francisco; Roque-Malherbe, Rolando M A

    2006-04-01

    Large specific surface area materials attract wide attention because of their applications in adsorption, catalysis, and nanotechnology. In the present study, we describe the synthesis and characterization of nanostructured amorphous silica materials. These materials were obtained by means of a modification of the Stobe-Fink-Bohn (SFB) method. The morphology and essential features of the synthesized materials have been studied using an automated surface area and pore size analyzer and scanning electron microscopy. The existence of a micro/mesoporous structure in the obtained materials has been established. It was also found that the obtained particle packing materials show large specific surface area up to 1,600 m2/g. (To our best knowledge, there is no any reported amorphous silica material with such a higher specific surface area.) The obtained materials could be useful in the manufacture of adsorbents, catalyst supports, and other nanotechnological applications.

  12. Evolution of Specific Surface Area Inside Glass Immersed in Beishan Groundwater

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    <正>The surface area of the fissure inside the glass block is an important parameter influencing the long term behavior of high-level radioactive waste glass in the aqueous media during the deep geological

  13. Catalytic Properties of AgPt Nanoshells as a Function of Size: Larger Outer Diameters Lead to Improved Performances.

    Science.gov (United States)

    Rodrigues, Thenner S; da Silva, Anderson G M; Gonçalves, Mariana C; Fajardo, Humberto V; Balzer, Rosana; Probst, Luiz F D; da Silva, Alisson H M; Assaf, Jose M; Camargo, Pedro H C

    2016-09-13

    We report herein a systematic investigation on the effect of the size of silver (Ag) nanoparticles employed as starting materials over the morphological features and catalytic performances of AgPt nanoshells produced by a combination of galvanic replacement between Ag and PtCl6(2-) and PtCl6(2-) reduction by hydroquinone. More specifically, we focused on Ag nanoparticles of four different sizes as starting materials, and found that the outer diameter, shell thickness, and the number of Pt surface atoms of the produced nanoshells increased with the size of the starting Ag nanoparticles. The produced AgPt nanoshells were supported into SiO2, and the catalytic performances of the AgPt/SiO2 nanocatalysts toward the gas-phase oxidation of benzene, toluene, and o-xylene (BTX oxidation) followed the order: AgPt 163 nm/SiO2 > AgPt 133 nm/SiO2 > AgPt 105 nm/SiO2 > AgPt 95 nm/SiO2. Interestingly, bigger AgPt nanoshell sizes lead to better catalytic performances in contrast to the intuitive prediction that particles having larger outer diameters tend to present poorer catalytic activities due to their lower surface to volume ratios as compared to smaller particles. This is in agreement with the H2 chemisorption results, and can be assigned to the increase in the Pt surface area with size due to the presence of smaller NPs islands at the surface of the nanoshells having larger outer diameters. This result indicates that, in addition to the overall diameters, the optimization of the surface morphology may play an important role over the optimization of catalytic activities in metal-based nanocatalysts, which can be even more pronounced that the size effect. Our data demonstrate that the control over surface morphology play a very important role relative to the effect of size to the optimization of catalytic performances in catalysts based on noble-metal nanostructures.

  14. Low content of Pt supported on Ni-MoCx/carbon black as a highly durable and active electrocatalyst for methanol oxidation, oxygen reduction and hydrogen evolution reactions in acidic condition

    Science.gov (United States)

    Zhang, Yan; Zang, Jianbing; Jia, Shaopei; Tian, Pengfei; Han, Chan; Wang, Yanhui

    2017-08-01

    Nickel and molybdenum carbide modified carbon black (Ni-MoCx/C) was synthesized by a two-step microwave-assisted deposition/carbonthermal reduction method and characterized by X-ray diffraction, transmission electron microscopy, energy dispersive spectroscopy and X-ray photoelectron spectroscopy. The as-prepared Ni-MoCx/C supported Pt (10 wt%) electrocatalyst (10Pt/Ni-MoCx/C) was synthesized through a microwave-assisted reduction method and 10Pt/Ni-MoCx/C exhibited high electrocatalytic activity for methanol oxidation, oxygen reduction and hydrogen evolution reactions. Results showed that 10Pt/Ni-MoCx/C electrocatalyst had better electrocatalytic activity and stability performance than 20 wt% Pt/C (20Pt/C) electrocatalyst. Among them, the electrochemical surface area of 10Pt/Ni-MoCx/C reached 68.4 m2 g-1, which was higher than that of 20Pt/C (63.2 m2 g-1). The enhanced stability and activity of 10Pt/Ni-MoCx/C electrocatalyst were attributed to: (1) an anchoring effect of Ni and MoCx formed during carbonthermal reduction process; (2) a synergistic effect among Pt, Ni, MoOx and MoCx. These findings indicated that 10Pt/Ni-MoCx/C was a promising electrocatalyst for direct methanol fuel cells.

  15. The surface area of human V1 predicts the subjective experience of object size

    OpenAIRE

    Schwarzkopf, Dietrich Samuel; Song, Chen; Rees, Geraint

    2010-01-01

    Abstract The surface area of human primary visual cortex (V1) varies substantially between individuals for unknown reasons. Here, we show that this variability is strongly and negatively correlated with the magnitude of two common visual illusions, where two physically identical objects appear different in size due to their context. Because such illusions dissociate conscious perception from physical stimulation, our findings indicate that the surface area of V1 predicts variabilit...

  16. Interdependence between body surface area and ultraviolet B dose in vitamin D production

    DEFF Research Database (Denmark)

    Bogh, M K B; Schmedes, Anne; Philipsen, P A;

    2011-01-01

    Ultraviolet (UV) B radiation increases serum vitamin D level expressed as 25-hydroxyvitamin-D(3) [25(OH)D], but the relationship to body surface area and UVB dose needs investigation.......Ultraviolet (UV) B radiation increases serum vitamin D level expressed as 25-hydroxyvitamin-D(3) [25(OH)D], but the relationship to body surface area and UVB dose needs investigation....

  17. Method of forming macro-structured high surface area transparent conductive oxide electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Forman, Arnold J.; Chen, Zhebo; Jaramillo, Thomas F.

    2016-01-05

    A method of forming a high surface area transparent conducting electrode is provided that includes depositing a transparent conducting thin film on a conductive substrate, where the transparent conducting thin film includes transparent conductive particles and a solution-based transparent conducting adhesive layer which serves to coat and bind together the transparent conducting particles, and heat treating the transparent conducting adhesion layer on the conductive substrate, where an increased surface area transparent conducting electrode is formed.

  18. High-surface-area, dual-function oxygen electrocatalysts for space power applications

    Science.gov (United States)

    Ham, David O.; Moniz, Gary; Taylor, E. Jennings

    1987-01-01

    The processes of hydration/dehydration and carbonation/decarbonation are investigated as an approach to provide higher surface area mixed metal oxides that are more active electrochemically. These materials are candidates for use as electrocatalysts and electrocatalyst supports for alkaline electrolyzers and fuel cells. For the case of the perovskite, LaCoO3 , higher surface areas were achieved with no change in structure and a more active oxygen electrocatalyst.

  19. Estimation of surface area concentration of workplace incidental nanoparticles based on number and mass concentrations

    Science.gov (United States)

    Park, J. Y.; Ramachandran, G.; Raynor, P. C.; Kim, S. W.

    2011-10-01

    Surface area was estimated by three different methods using number and/or mass concentrations obtained from either two or three instruments that are commonly used in the field. The estimated surface area concentrations were compared with reference surface area concentrations (SAREF) calculated from the particle size distributions obtained from a scanning mobility particle sizer and an optical particle counter (OPC). The first estimation method (SAPSD) used particle size distribution measured by a condensation particle counter (CPC) and an OPC. The second method (SAINV1) used an inversion routine based on PM1.0, PM2.5, and number concentrations to reconstruct assumed lognormal size distributions by minimizing the difference between measurements and calculated values. The third method (SAINV2) utilized a simpler inversion method that used PM1.0 and number concentrations to construct a lognormal size distribution with an assumed value of geometric standard deviation. All estimated surface area concentrations were calculated from the reconstructed size distributions. These methods were evaluated using particle measurements obtained in a restaurant, an aluminum die-casting factory, and a diesel engine laboratory. SAPSD was 0.7-1.8 times higher and SAINV1 and SAINV2 were 2.2-8 times higher than SAREF in the restaurant and diesel engine laboratory. In the die casting facility, all estimated surface area concentrations were lower than SAREF. However, the estimated surface area concentration using all three methods had qualitatively similar exposure trends and rankings to those using SAREF within a workplace. This study suggests that surface area concentration estimation based on particle size distribution (SAPSD) is a more accurate and convenient method to estimate surface area concentrations than estimation methods using inversion routines and may be feasible to use for classifying exposure groups and identifying exposure trends.

  20. Probing large area surface plasmon interference in thin metal films using photon scanning tunneling microscopy

    Energy Technology Data Exchange (ETDEWEB)

    Passian, A.; Wig, A.; Lereu, A.L.; Evans, P.G.; Meriaudeau, F.; Thundat, T.; Ferrell, T.L

    2004-08-15

    The interference of surface plasmons can provide important information regarding the surface features of the hosting thin metal film. We present an investigation of the interference of optically excited surface plasmons in the Kretschmann configuration in the visible spectrum. Large area surface plasmon interference regions are generated at several wavelengths and imaged with the photon scanning tunneling microscope. Furthermore, we discuss the non-retarded dispersion relations for the surface plasmons in the probe-metal system modeled as confocal hyperboloids of revolution in the spheroidal coordinate systems.

  1. In situ construction of Ir@Pt/C nanoparticles in the cathode layer of membrane electrode assemblies with ultra-low Pt loading and high Pt exposure

    Science.gov (United States)

    Dang, Dai; Zhang, Lei; Zeng, Xiaoyuan; Tian, Xinlong; Qu, Chong; Nan, Haoxiong; Shu, Ting; Hou, Sanying; Yang, Lijun; Zeng, Jianhuang; Liao, Shijun

    2017-07-01

    A novel membrane electrode assemblies (MEAs) with ultra-low Pt loadings and high Pt exposure in the cathode layer is prepared by spraying Ir/C catalyst ink on the membrane surface to form a substrate layer, followed by in situ pulse electrochemical deposition of a Pt shell layer on the Ir core nanoparticles in the substrate layer. It makes the Pt loadings on cathode lower to 0.044 mg/cm2. In our system, the MEA with our novel cathode exhibits excellent performance in a H2/air single fuel cell, which is comparable to that of the MEA prepared with commercial Pt/C catalyst (Johnson Matthey 40% Pt) with Pt loadings of 0.1 mg/cm2. The electrode with core-shell structured catalysts is characterized by X-ray diffraction, X-ray photoelectron spectroscopy, EDS line-scan, and scanning transmission electron microscopy. Based on the characterization results, it is found that the Pt is highly dispersed on the Ir NPs, and the electronic feature of Pt at shell layer can be tuned by the Ir core particle. Furthermore, the DFT calculation results also reveal the interaction between Pt at shell layer and Ir core. This work may provide a novel pathway to realize low Pt and high Pt utilization in low temperature fuel cells.

  2. Impact of IrRu oxygen evolution reaction catalysts on Pt nanostructured thin films under start-up/shutdown cycling

    Science.gov (United States)

    Cullen, David A.; More, Karren L.; Atanasoska, Ljiljana L.; Atanasoski, Radoslav T.

    2014-12-01

    Electron microscopy and X-ray photoelectron spectroscopy (XPS) were utilized to study the role of oxygen evolution reaction (OER) catalysts in mitigating degradation arising from start-up/shutdown events. Pt nanostructured thin films (NSTF) were coated with a Ru0.1Ir0.9 OER catalyst at loadings ranging from 1 to 10 μg cm-2 and submitted to 5000 potential cycles within a membrane electrode assembly. Analysis of the as-deposited catalyst showed that the Ir and Ru coating is primarily metallic, and further evidence is provided to support the previously reported interaction between Ru and the perylene-red support. Aberration-corrected scanning transmission electron microscopy and energy dispersive X-ray spectroscopy were used to observe the impact of the OER catalysts on Pt dissolution and migration into the membrane. Elemental mapping showed a high percentage of the Ir catalyst was maintained on the NSTF whisker surfaces following testing. The presence of the OER catalysts greatly reduced the smoothing of the Pt NSTF whiskers, which has been correlated with Pt dissolution and losses in electrochemically active surface area. The dissolution of both Ir and Pt led to the formation of IrPt nanoparticle clusters in the membrane close to the cathode, as well as the formation of a Pt band deeper in the membrane.

  3. Ultrasonically treated multi-walled carbon nanotubes (MWCNTs) as PtRu catalyst supports for methanol electrooxidation

    Energy Technology Data Exchange (ETDEWEB)

    Yang, Chunwei; Hu, Xinguo; Wang, Dianlong; Dai, Changsong [Department of Applied Chemistry, Harbin Institute of Technology, Harbin 150001 (China); Zhang, Liang; Jin, Haibo [School of Materials Science and Engineering, Beijing Institute of Technology, Beijing 100081 (China); Agathopoulos, Simeon [Department of Materials Science and Engineering, University of Ioannina, GR-451 10 Ioannina (Greece)

    2006-09-29

    In the quest of fabricating supported catalysts, experimental results of transmission electron microscopy, Raman and infrared spectroscopy indicate that ultrasonic treatment effectively functionalizes multi-walled carbon nanotubes (MWCNTs), endowing them with groups that can act as nucleation sites which can favor well-dispersed depositions of PtRu clusters on their surface. Ultrasonic treatment seems to be superior than functionalization via regular refluxing. This is confirmed by the determination of the electrochemistry active surface area (ECA) and the CO-tolerance performance of the PtRu catalysts, measured by adsorbed CO-stripping voltammetry in 0.5M sulfuric acid solution, and the real surface area of the PtRu catalysts, evaluated by Brunauer-Emmett-Teller (BET) measurements. Finally, the effectiveness for methanol oxidation is assessed by cyclic voltammetry (CV) in a sulfuric acid and methanol electrolyte. (author)

  4. Features of wind field over the sea surface in the coastal area

    Science.gov (United States)

    Monzikova, A. K.; Kudryavtsev, V. N.; Myasoedov, A. G.; Chapron, B.; Zilitinkevich, S. S.

    2017-01-01

    In this paper we analyze SAR wind field features, in particular the effects of wind shadowing. These effects represent the dynamics of the internal atmospheric boundary layer, which is formed due to the transition of the air flow arriving from the rough land surface to the "smooth" water surface. In the wind-shadowed area, the flow accelerates, and a surface wind stress increases with fetch. The width of the shadow depends not only on the wind speed and atmospheric boundary layer stratification, but also on geographic features such as windflow multiple transformations over the complex surface land-Lake Chudskoe-land-Gulf of Finland. Measurements showed that, in the area of wind acceleration, the surface stress normalized by an equilibrium value (far from the coast) is a universal function of dimensionless fetch Xf/G. Surface wind stress reaches an equilibrium value at Xf/G ≈ 0.4, which is the scale of the planetary-boundary-layer relaxation.

  5. Greenland surface mass-balance observations from the ice-sheet ablation area and local glaciers

    NARCIS (Netherlands)

    Machguth, Horst; Thomsen, Henrik H.; Weidick, Anker; Ahlstrøm, Andreas P.; Abermann, Jakob; Andersen, Morten L.; Andersen, Signe B.; Bjørk, Anders A.; Box, Jason E.; Braithwaite, Roger J.; Bøggild, Carl E.; Citterio, Michele; Clement, Poul; Colgan, William; Fausto, Robert S.; Gleie, Karin; Gubler, Stefanie; Hasholt, Bent; Hynek, Bernhard; Knudsen, Niels T.; Larsen, Signe H.; Mernild, Sebastian H.; Oerlemans, Johannes; Oerter, Hans; Olesen, Ole B.; Smeets, C. J P Paul; Steffen, Konrad; Stober, Manfred; Sugiyama, Shin; Van As, Dirk; Van Den Broeke, Michiel R.; Van De Wal, Roderik S W

    2016-01-01

    Glacier surface mass-balance measurements on Greenland started more than a century ago, but no compilation exists of the observations from the ablation area of the ice sheet and local glaciers. Such data could be used in the evaluation of modelled surface mass balance, or to document changes in glac

  6. Greenland surface mass-balance observations from the ice-sheet ablation area and local glaciers

    DEFF Research Database (Denmark)

    Machguth, Horst; Thomsen, Henrik; Weidick, Anker;

    2016-01-01

    Glacier surface mass-balance measurements on Greenland started more than a century ago, but no compilation exists of the observations from the ablation area of the ice sheet and local glaciers. Such data could be used in the evaluation of modelled surface mass balance, or to document changes in g...

  7. Models of bedrock surface and overburden thickness over Olkiluoto island and nearby sea area

    Energy Technology Data Exchange (ETDEWEB)

    Moenkkoenen, H. [WSP Finland Oy, Helsinki (Finland)

    2012-04-15

    In this report, a model of bedrock surface and a model of overburden thickness over the Olkiluoto Island and the nearby sea area are presented. Also in purpose to produce material for biosphere and radionuclide transport modelling, stratigraphy models of different sediment layers were created at two priority areas north and south of the Olkiluoto Island. The work concentrated on the collection and description of available data of bedrock surface and overburden thickness. Because the information on the bedrock surface and overburden is collected from different sources and is based on a number of types of data the quality and applicability of data sets varies. Consequently also the reliability in different parts of the models varies. Input data for the bedrock surface and overburden thickness models include 2928 single points and additional outcrops observations (611 polygons) in the modelled area. In addition, the input data include 173 seismic refraction lines (6534 points) and acousticseismic sounding lines (26655 points from which 13721 points are located in model area) in the Olkiluoto offshore area. The average elevation of bedrock surface in area is 2.1 metres above the sea level. The average thickness of overburden is 2.5 metres varying typically between 2 - 4 metres. Thickest overburden covers (approximately 16 metres) of terrestrial area are located at the western end of the Olkiluoto Island and in sea basin south of the island. (orig.)

  8. A program to compute the area of an irregular polygon on a spheroidal surface

    Digital Repository Service at National Institute of Oceanography (India)

    Sivakholundu, K.M.; Prabaharan, N.

    ) INTRODUCTION A number of oC128shore activities area such as exploration for polymetallic nodules, demarcation of EEZ, etc. necessitates the definition of large boundaries on a geographical surface. The area de- marcated by these boundaries have to be calculated...

  9. Application of stereological methods to estimate post-mortem brain surface area using 3T MRI

    DEFF Research Database (Denmark)

    Furlong, Carolyn; García-Fiñana, Marta; Puddephat, Michael

    2013-01-01

    The Cavalieri and Vertical Sections methods of design based stereology were applied in combination with 3 tesla (i.e. 3T) Magnetic Resonance Imaging (MRI) to estimate cortical and subcortical volume, area of the pial surface, area of the grey-white matter boundary, and thickness of the cerebral...

  10. Remote Sensing Parameterization of Land Surface Heat Fluxes over Arid and Semi-arid Areas

    Institute of Scientific and Technical Information of China (English)

    马耀明; 王介民; 黄荣辉; 卫国安; MassimoMENENTI; 苏中波; 胡泽勇; 高峰; 文军

    2003-01-01

    Dealing with the regional land surfaces heat fluxes over inhomogeneous land surfaces in arid and semi-arid areas is an important but not an easy issue. In this study, one parameterization method based on satellite remote sensing and field observations is proposed and tested for deriving the regional land surface heat fluxes over inhomogeneous landscapes. As a case study, the method is applied to the Dunhuang experimental area and the HEIFE (Heihe River Field Experiment, 1988-1994) area. The Dunhuang area is selected as a basic experimental area for the Chinese National Key Programme for Developing Basic Sciences: Research on the Formation Mecbanism and Prediction Theory of Severe Climate Disaster in China (G1998040900, 1999-2003). The four scenes of Landsat TM data used in this study are 3 June 2000,22 August 2000, and 29 January 2001 for the Dunhuang area and 9 July 1991 for the HEIFE area. The regional distributions of land surface variables, vegetation variables, and heat fluxes over inhomogeneous landscapes in arid and semi-arid areas are obtained in this study.

  11. Soft Landing of Bare PtRu Nanoparticles for Electrochemical Reduction of Oxygen

    Energy Technology Data Exchange (ETDEWEB)

    Johnson, Grant E.; Colby, Robert J.; Engelhard, Mark H.; Moon, DaeWon; Laskin, Julia

    2015-08-07

    Magnetron sputtering of two independent Pt and Ru targets coupled with inert gas aggregation in a modified commercial source has been combined with soft landing of mass-selected ions to prepare bare 4.5 nm diameter PtRu alloy nanoparticles on glassy carbon electrodes with controlled size and morphology for electrochemical reduction of oxygen in solution. Employing atomic force microscopy (AFM) it is shown that the nanoparticles bind randomly to the glassy carbon electrode at a relatively low coverage of 7 x 104 ions µm-2 and that their average height is centered at 4 nm. Scanning transmission electron microscopy images obtained in the high-angle annular dark field mode (STEM-HAADF) further confirm that the soft-landed PtRu alloy nanoparticles are uniform in size and have a Ru core decorated with small regions of Pt on the surface. Wide-area scans of the electrodes using X-ray photoelectron spectroscopy (XPS) reveal the presence of both Pt and Ru in relative atomic concentrations of ~9% and ~33%, respectively. Deconvolution of the high energy resolution XPS spectra in the Pt4f and Ru3d regions indicates the presence of both oxidized Pt and Ru. The substantially higher loading of Ru compared to Pt and enrichment of Pt at the surface of the alloy nanoparticles is confirmed by wide-area analysis of the electrodes using time-of-flight medium energy ion scattering (TOF-MEIS) employing both 80 keV He+ and O+ ions. The activity of electrodes containing 7 x 104 ions µm-2 of bare 4.5 nm PtRu nanoparticles toward the electrochemical reduction of oxygen was evaluated employing cyclic voltammetry (CV) in 0.1 M HClO4 and 0.5 M H2SO4 solutions. In both electrolytes a pronounced reduction peak was observed during O2 purging of the solution that was not evident during purging with Ar. Repeated electrochemical cycling of the electrodes revealed little evolution in the shape or position of the voltammograms indicating high stability of the alloy nanoparticles supported on glassy

  12. Greenland surface mass-balance observations from the ice-sheet ablation area and local glaciers

    DEFF Research Database (Denmark)

    Machguth, Horst; Thomsen, Henrik H.; Weidick, Anker

    2016-01-01

    in glacier melt independently from model output. Here, we present a comprehensive database of Greenland glacier surface mass-balance observations from the ablation area of the ice sheet and local glaciers. The database spans the 123 a from 1892 to 2015, contains a total of similar to 3000 measurements from......Glacier surface mass-balance measurements on Greenland started more than a century ago, but no compilation exists of the observations from the ablation area of the ice sheet and local glaciers. Such data could be used in the evaluation of modelled surface mass balance, or to document changes...

  13. Greenland surface mass-balance observations from the ice-sheet ablation area and local glaciers

    DEFF Research Database (Denmark)

    Machguth, Horst; Thomsen, Henrik H.; Weidick, Anker;

    2016-01-01

    Glacier surface mass-balance measurements on Greenland started more than a century ago, but no compilation exists of the observations from the ablation area of the ice sheet and local glaciers. Such data could be used in the evaluation of modelled surface mass balance, or to document changes...... in glacier melt independently from model output. Here, we present a comprehensive database of Greenland glacier surface mass-balance observations from the ablation area of the ice sheet and local glaciers. The database spans the 123 a from 1892 to 2015, contains a total of similar to 3000 measurements from...

  14. Tunable Architecture of Rhombic Dodecahedral Pt-Ni Nanoframe Electrocatalysts.

    Energy Technology Data Exchange (ETDEWEB)

    Becknell, Nigel; Son, Yoonkook; Kim, Dohyung; Li, Dongguo; Yu, Yi; Niu, Zhiqiang; Lei, Teng; Sneed, Brian T.; More, Karren L.; Markovic, Nenad M.; Stamenkovic, Vojislav R.; Yang, Peidong

    2017-08-30

    Platinum-based alloys are known to demonstrate advanced properties in electrochemical reactions that are relevant for proton exchange membrane fuel cells and electrolyzers. Further development of Pt alloy electrocatalysts relies on the design of architectures with highly active surfaces and optimized utilization of the expensive elpment, Pt. Here, we show that the three-dimensional Pt anisotropy of Pt-Ni rhombic dodecahedra can be tuned by controlling the ratio between Pt and Ni precursors such that either a completely hollow nanoframe or a new architecture, the excavated nanoframe, can be obtained. The excavated nanoframe showed similar to 10 times higher specific and similar to 6 times higher mass activity for the oxygen reduction reaction than Pt/C, and twice the mass activity of the hollow nanoframe. The high activity is attributed to enhanced Ni content in the near-surface region and the extended two-dimensional sheet structure within the nanoframe that minimizes the number of buried Pt sites.

  15. Adhesion of metal on metal. The Pt on Co case

    Science.gov (United States)

    Légaré, P.; Castellani, N. J.; Cabeza, G. F.

    2002-01-01

    The adhesion of Pt overlayers in pseudomorphic epitaxy on hcp Co(0 0 0 1) and fcc Co(1 0 0) was investigated with first-principles calculations. This was compared to the adhesion of the Pt surface layers on Pt(1 1 1) and Pt(1 0 0). We show that adhesion can be analyzed by taking into account the interplay between the chemical and structural properties at the interface. The free Pt planes with the bulk Pt-Pt distance are submitted to tensile stress which can be relaxed by 6.6% and 9.1% contraction for the (1 1 1) and (1 0 0) symmetries respectively. This results in equilibrium interatomic distances which are not far from that of the Co substrate. Consequently the stress energy in a pseudomorphic Pt monolayer on a Co substrate is lower than the stress energy of pure Pt(1 1 1) or Pt(1 0 0) surfaces. However, this is at the expense of the Pt chemical reactivity towards the Co substrate. This is in agreement with the general dependence between chemical reactivity and stress of a metal surface.

  16. N- and S-doped high surface area carbon derived from soya chunks as scalable and efficient electrocatalysts for oxygen reduction

    Science.gov (United States)

    Rana, Moumita; Arora, Gunjan; Gautam, Ujjal K.

    2015-02-01

    Highly stable, cost-effective electrocatalysts facilitating oxygen reduction are crucial for the commercialization of membrane-based fuel cell and battery technologies. Herein, we demonstrate that protein-rich soya chunks with a high content of N, S and P atoms are an excellent precursor for heteroatom-doped highly graphitized carbon materials. The materials are nanoporous, with a surface area exceeding 1000 m2 g-1, and they are tunable in doping quantities. These materials exhibit highly efficie