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Sample records for pt pgt non-regulated

  1. Inhibition of the Prostaglandin Transporter PGT Lowers Blood Pressure in Hypertensive Rats and Mice.

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    Yuling Chi

    Full Text Available Inhibiting the synthesis of endogenous prostaglandins with nonsteroidal anti-inflammatory drugs exacerbates arterial hypertension. We hypothesized that the converse, i.e., raising the level of endogenous prostaglandins, might have anti-hypertensive effects. To accomplish this, we focused on inhibiting the prostaglandin transporter PGT (SLCO2A1, which is the obligatory first step in the inactivation of several common PGs. We first examined the role of PGT in controlling arterial blood pressure blood pressure using anesthetized rats. The high-affinity PGT inhibitor T26A sensitized the ability of exogenous PGE2 to lower blood pressure, confirming both inhibition of PGT by T26A and the vasodepressor action of PGE2 T26A administered alone to anesthetized rats dose-dependently lowered blood pressure, and did so to a greater degree in spontaneously hypertensive rats than in Wistar-Kyoto control rats. In mice, T26A added chronically to the drinking water increased the urinary excretion and plasma concentration of PGE2 over several days, confirming that T26A is orally active in antagonizing PGT. T26A given orally to hypertensive mice normalized blood pressure. T26A increased urinary sodium excretion in mice and, when added to the medium bathing isolated mouse aortas, T26A increased the net release of PGE2 induced by arachidonic acid, inhibited serotonin-induced vasoconstriction, and potentiated vasodilation induced by exogenous PGE2. We conclude that pharmacologically inhibiting PGT-mediated prostaglandin metabolism lowers blood pressure, probably by prostaglandin-induced natriuresis and vasodilation. PGT is a novel therapeutic target for treating hypertension.

  2. Inhibition of Prostaglandin Transporter (PGT Promotes Perfusion and Vascularization and Accelerates Wound Healing in Non-Diabetic and Diabetic Rats.

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    Zhongbo Liu

    Full Text Available Peripheral ischemia, resulting from diminished arterial flow and defective local vascularization, is one of the main causes of impaired wound healing in diabetes. Vasodilatory prostaglandins (PGs, including PGE2 and PGI2, regulate blood flow in peripheral tissues. PGs also stimulate angiogenesis by inducing vascular endothelial growth factor. However, PG levels are reduced in diabetes mainly due to enhanced degradation. We hypothesized that inhibition of the prostaglandin transporter (PGT (SLCO2A1, which mediates the degradation of PGs, would increase blood flow and stimulate vascularization, thereby mitigating peripheral ischemia and accelerating wound healing in diabetes. Here we report that inhibiting PGT with intravenously injected PGT inhibitor, T26A, increased blood flow in ischemic hind limbs created in non-diabetic rats and streptozotocin induced diabetic rats. Systemic, or combined with topical, T26A accelerated closure of cutaneous wounds. Immunohistochemical examination revealed that inhibition of PGT enhanced vascularization (marked by larger numbers of vessels formed by CD34+ cells, and accelerated re-epithelialization of cutaneous wounds. In cultured primary human bone marrow CD34+ cells and human epidermal keratinocytes (HEKs either inhibiting or silencing PGT increased migration in both cell lines. Thus PGT directly regulates mobilization of endothelial progenitor cells (EPCs and HEKs, which could contribute to PGT-mediated vascularization and re-epithelialization. At the molecular level, systemic inhibition of PGT raised circulating PGE2. Taken together, our data demonstrate that PGT modulates arterial blood flow, mobilization of EPCs and HEKs, and vascularization and epithelialization in wound healing by regulating vasodilatory and pro-angiogenic PGs.

  3. The effects of somatic hypermutation on neutralization and binding in the PGT121 family of broadly neutralizing HIV antibodies.

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    Devin Sok

    Full Text Available Broadly neutralizing HIV antibodies (bnAbs are typically highly somatically mutated, raising doubts as to whether they can be elicited by vaccination. We used 454 sequencing and designed a novel phylogenetic method to model lineage evolution of the bnAbs PGT121-134 and found a positive correlation between the level of somatic hypermutation (SHM and the development of neutralization breadth and potency. Strikingly, putative intermediates were characterized that show approximately half the mutation level of PGT121-134 but were still capable of neutralizing roughly 40-80% of PGT121-134 sensitive viruses in a 74-virus panel at median titers between 15- and 3-fold higher than PGT121-134. Such antibodies with lower levels of SHM may be more amenable to elicitation through vaccination while still providing noteworthy coverage. Binding characterization indicated a preference of inferred intermediates for native Env binding over monomeric gp120, suggesting that the PGT121-134 lineage may have been selected for binding to native Env at some point during maturation. Analysis of glycan-dependent neutralization for inferred intermediates identified additional adjacent glycans that comprise the epitope and suggests changes in glycan dependency or recognition over the course of affinity maturation for this lineage. Finally, patterns of neutralization of inferred bnAb intermediates suggest hypotheses as to how SHM may lead to potent and broad HIV neutralization and provide important clues for immunogen design.

  4. Somatic populations of PGT135-137 HIV-1-neutralizing antibodies identified by 454 pyrosequencing and bioinformatics

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    Jiang eZhu

    2012-09-01

    Full Text Available Select HIV-1-infected individuals develop sera capable of neutralizing diverse viral strains. The molecular basis of this neutralization is currently being deciphered by the isolation of HIV-1-neutralizing antibodies. In one infected donor, three neutralizing antibodies, PGT135-137, were identified by assessment of neutralization from individually sorted B cells and found to recognize an epitope containing an N-linked glycan at residue 332 on HIV-1 gp120. Here we use deep sequencing and bioinformatics methods to interrogate the B cell record of this donor to gain a more complete understanding of the humoral immune response. PGT135-137-gene family-specific primers were used to amplify heavy and light chain-variable domain sequences. 454 pyrosequencing produced 141,298 heavy-chain sequences of IGHV4-39 origin and 87,229 light-chain sequences of IGKV3-15 origin. A number of heavy and light chain sequences of ~90% identity to PGT137, several to PGT136, and none of high identity to PGT135 were identified. After expansion of these sequences to include close phylogenetic relatives, a total of 202 heavy-chain sequences and 72 light-chain sequences were identified. These sequences were clustered into populations of 95% identity comprising 15 for heavy chain and 10 for light chain, and a select sequence from each population was synthesized and reconstituted with a PGT137-partner chain. Reconstituted antibodies showed varied neutralization phenotypes for HIV-1 clade A and D isolates. Sequence diversity of the antibody population represented by these tested sequences was notably higher than observed with a 454 pyrosequencing-control analysis on 10 antibodies of defined sequence, suggesting that this diversity results primarily from somatic maturation. Our results thus provide an example of how pathogens like HIV-1 are opposed by a varied humoral immune response, derived from intrinsic mechanisms of antibody development, and embodied by somatic populations

  5. Broadly neutralizing antibody PGT121 allosterically modulates CD4 binding via recognition of the HIV-1 gp120 V3 base and multiple surrounding glycans.

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    Jean-Philippe Julien

    Full Text Available New broad and potent neutralizing HIV-1 antibodies have recently been described that are largely dependent on the gp120 N332 glycan for Env recognition. Members of the PGT121 family of antibodies, isolated from an African donor, neutralize ∼70% of circulating isolates with a median IC50 less than 0.05 µg ml(-1. Here, we show that three family members, PGT121, PGT122 and PGT123, have very similar crystal structures. A long 24-residue HCDR3 divides the antibody binding site into two functional surfaces, consisting of an open face, formed by the heavy chain CDRs, and an elongated face, formed by LCDR1, LCDR3 and the tip of the HCDR3. Alanine scanning mutagenesis of the antibody paratope reveals a crucial role in neutralization for residues on the elongated face, whereas the open face, which accommodates a complex biantennary glycan in the PGT121 structure, appears to play a more secondary role. Negative-stain EM reconstructions of an engineered recombinant Env gp140 trimer (SOSIP.664 reveal that PGT122 interacts with the gp120 outer domain at a more vertical angle with respect to the top surface of the spike than the previously characterized antibody PGT128, which is also dependent on the N332 glycan. We then used ITC and FACS to demonstrate that the PGT121 antibodies inhibit CD4 binding to gp120 despite the epitope being distal from the CD4 binding site. Together, these structural, functional and biophysical results suggest that the PGT121 antibodies may interfere with Env receptor engagement by an allosteric mechanism in which key structural elements, such as the V3 base, the N332 oligomannose glycan and surrounding glycans, including a putative V1/V2 complex biantennary glycan, are conformationally constrained.

  6. The outer membrane protease PgtE of Salmonella enterica interferes with the alternative complement pathway by cleaving factors B and H

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    Rauna eRiva

    2015-02-01

    Full Text Available The virulence factor PgtE is an outer membrane protease (omptin of the zoonotic pathogen Salmonella enterica that causes diseases ranging from gastroenteritis to severe enteric fever. It is surface exposed in bacteria that have a short-chain, i.e. rough LPS, as observed e.g. in bacteria residing inside macrophages or just emerging from them. We investigated whether PgtE cleaves the complement factors B (B and H (H, key proteins controlling formation and inactivation of the complement protein C3b and thereby the activity of the complement system. S. enterica serovar Typhimurium or omptin-expressing recombinant E. coli bacteria were incubated with purified human complement proteins or recombinant H fragments. PgtE cleaved both B and H, whereas its close homolog Pla of Yersinia pestis cleaved only H. H was cleaved at both N- and C-termini, while the central region resisted proteolysis. Because of multiple effects of PgtE on complement components (cleavage of C3, C3b, B and H we assessed its effect on the opsonophagocytosis of Salmonella. In human serum, C3 cleavage was dependent on proteolytically active PgtE. Human neutrophils interacted less with serum-opsonized FITC-stained S. enterica 14028R than with the isogenic ΔpgtE strain, as analyzed by flow cytometry. In conclusion, cleavage of B and H by PgtE, together with C3 cleavage, affects the C3-mediated recognition of S. enterica by human neutrophils, thus thwarting the immune protection against Salmonella.

  7. The outer membrane protease PgtE of Salmonella enterica interferes with the alternative complement pathway by cleaving factors B and H

    OpenAIRE

    Rauna eRiva; Korhonen, Timo K.; Seppo eMeri

    2015-01-01

    The virulence factor PgtE is an outer membrane protease (omptin) of the zoonotic pathogen Salmonella enterica that causes diseases ranging from gastroenteritis to severe enteric fever. It is surface exposed in bacteria that have a short-chain, i.e., rough LPS, as observed e.g., in bacteria residing inside macrophages or just emerging from them. We investigated whether PgtE cleaves the complement factors B (B) and H (H), key proteins controlling formation and inactivation of the complement pro...

  8. A dynamical model of non regulated markets

    CERN Document Server

    Schaale, A

    1999-01-01

    The main focus of this work is to understand the dynamics of non regulated markets. The present model can describe the dynamics of any market where the pricing is based on supply and demand. It will be applied here, as an example, for the German stock market presented by the Deutscher Aktienindex (DAX), which is a measure for the market status. The duality of the present model consists of the superposition of the two components - the long and the short term behaviour of the market. The long term behaviour is characterised by a stable development which is following a trend for time periods of years or even decades. This long term growth (or decline) is based on the development of fundamental market figures. The short term behaviour is described as a dynamical evaluation (trading) of the market by the participants. The trading process is described as an exchange between supply and demand. In the framework of this model there the trading is modelled by a system of nonlinear differential equations. The model also...

  9. Complete epitopes for vaccine design derived from a crystal structure of the broadly neutralizing antibodies PGT128 and 8ANC195 in complex with an HIV-1 Env trimer.

    Science.gov (United States)

    Kong, Leopold; Torrents de la Peña, Alba; Deller, Marc C; Garces, Fernando; Sliepen, Kwinten; Hua, Yuanzi; Stanfield, Robyn L; Sanders, Rogier W; Wilson, Ian A

    2015-10-01

    The HIV-1 envelope gp160 glycoprotein (Env) is a trimer of gp120 and gp41 heterodimers that mediates cell entry and is the primary target of the humoral immune response. Broadly neutralizing antibodies (bNAbs) to HIV-1 have revealed multiple epitopes or sites of vulnerability, but mapping of most of these sites is incomplete owing to a paucity of structural information on the full epitope in the context of the Env trimer. Here, a crystal structure of the soluble BG505 SOSIP gp140 trimer at 4.6 Å resolution with the bNAbs 8ANC195 and PGT128 reveals additional interactions in comparison to previous antibody-gp120 structures. For 8ANC195, in addition to previously documented interactions with gp120, a substantial interface with gp41 is now elucidated that includes extensive interactions with the N637 glycan. Surprisingly, removal of the N637 glycan did not impact 8ANC195 affinity, suggesting that the antibody has evolved to accommodate this glycan without loss of binding energy. PGT128 indirectly affects the N262 glycan by a domino effect, in which PGT128 binds to the N301 glycan, which in turn interacts with and repositions the N262 glycan, thereby illustrating the important role of neighboring glycans on epitope conformation and stability. Comparisons with other Env trimer and gp120 structures support an induced conformation for glycan N262, suggesting that the glycan shield is allosterically modified upon PGT128 binding. These complete epitopes of two broadly neutralizing antibodies on the Env trimer can now be exploited for HIV-1 vaccine design.

  10. 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 ( ...

  11. Invisibility and PT symmetry

    OpenAIRE

    MOSTAFAZADEH, Ali

    2013-01-01

    PHYSICAL REVIEW A 87, 012103 (2013) Invisibility and PT symmetry Ali Mostafazadeh* Department of Mathematics, Koc¸ University, Sarıyer 34450, Istanbul, Turkey (Received 9 July 2012; published 3 January 2013) For a general complex scattering potential defined on a real line, we show that the equations governing invisibility of the potential are invariant under the combined action of parity and time-reversal (PT ) transformation. We determine the PT -symmetric as well as no...

  12. PT-symmetric strings

    Energy Technology Data Exchange (ETDEWEB)

    Amore, Paolo, E-mail: paolo.amore@gmail.com [Facultad de Ciencias, CUICBAS, Universidad de Colima, Bernal Díaz del Castillo 340, Colima, Colima (Mexico); Fernández, Francisco M., E-mail: fernande@quimica.unlp.edu.ar [INIFTA (UNLP, CCT La Plata-CONICET), División Química Teórica, Diag. 113 y 64 (S/N), Sucursal 4, Casilla de Correo 16, 1900 La Plata (Argentina); Garcia, Javier [INIFTA (UNLP, CCT La Plata-CONICET), División Química Teórica, Diag. 113 y 64 (S/N), Sucursal 4, Casilla de Correo 16, 1900 La Plata (Argentina); Gutierrez, German [Facultad de Ciencias, CUICBAS, Universidad de Colima, Bernal Díaz del Castillo 340, Colima, Colima (Mexico)

    2014-04-15

    We study both analytically and numerically the spectrum of inhomogeneous strings with PT-symmetric density. We discuss an exactly solvable model of PT-symmetric string which is isospectral to the uniform string; for more general strings, we calculate exactly the sum rules Z(p)≡∑{sub n=1}{sup ∞}1/E{sub n}{sup p}, with p=1,2,… and find explicit expressions which can be used to obtain bounds on the lowest eigenvalue. A detailed numerical calculation is carried out for two non-solvable models depending on a parameter, obtaining precise estimates of the critical values where pair of real eigenvalues become complex. -- Highlights: •PT-symmetric Hamiltonians exhibit real eigenvalues when PT symmetry is unbroken. •We study PT-symmetric strings with complex density. •They exhibit regions of unbroken PT symmetry. •We calculate the critical parameters at the boundaries of those regions. •There are exact real sum rules for some particular complex densities.

  13. 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.

  14. PT symmetry and supersymmetry

    CERN Document Server

    Znojil, M

    2002-01-01

    A re-formulated, non-Hermitian version of the Witten's supersymmetric quantum mechanics is presented. Its use of pseudo-Hermitian (so called PT symmetric) Hamiltonians is reviewed and illustrated via several forms of an innovated supersymmetric partnership between strongly singular ("spiked") harmonic oscillators.

  15. Quality assurance and best research practices for non-regulated veterinary clinical studies.

    Science.gov (United States)

    Davies, R; London, C; Lascelles, B; Conzemius, M

    2017-08-16

    Veterinary clinical trials generate data that advance the transfer of knowledge from clinical research to clinical practice in human and veterinary settings. The translational success of non-regulated and regulated veterinary clinical studies is dependent upon the reliability and reproducibility of the data generated. Clinician-scientists that conduct veterinary clinical studies would benefit from a commitment to research quality assurance and best practices throughout all non-regulated and regulated research environments. Good Clinical Practice (GCP) guidance documents from the FDA provides principles and procedures designed to safeguard data integrity, reliability and reproducibility. While these documents maybe excessive for clinical studies not intended for regulatory oversight it is important to remember that research builds on research. Thus, the quality and accuracy of all data and inference generated throughout the research enterprise remains vulnerable to the impact of potentially unreliable data generated by the lowest performing contributors. The purpose of this first of a series of statement papers is to outline and reference specific quality control and quality assurance procedures that should, at least in part, be incorporated into all veterinary clinical studies.

  16. 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.

  17. Identification of {sup 166}Pt and {sup 167}Pt

    Energy Technology Data Exchange (ETDEWEB)

    Bingham, C.R.; Toth, K.S.; Batchelder, J.C.; Blumenthal, D.J.; Brown, L.T.; Busse, B.C.; Conticchio, L.F.; Davids, C.N.; Davinson, T.; Henderson, D.J.; Irvine, R.J.; Seweryniak, D.; Walters, W.B.; Woods, P.J.; Zimmerman, B.E. [The University of Tennessee, Knoxville, Tennessee 37996 (United States)]|[Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831 (United States)]|[Louisiana State University, Baton Rouge, Louisiana 70803 (United States)]|[Argonne National Laboratory, Argonne, Illinois 60439 (United States)]|[Vanderbilt University, Nashville, Tennessee 37235 (United States)]|[Oregon State University, Corvallis, Oregon 97331 (United States)]|[University of Maryland, College Park, Maryland 20742 (United States)]|[Edinburgh University, Edinburgh, EH9 3JZ (United Kingdom)

    1996-07-01

    In a series of {sup 78}Kr bombardments of {sup 92}Mo the new isotopes {sup 166}Pt and {sup 167}Pt were identified via their {alpha}-decay properties. The {alpha}-decay energies and half-lives of these two nuclides are as follows. (1) {sup 166}Pt, {ital E}{sub {alpha}} = 7110(15) keV, {ital T}{sub 1/2} = 0.3(1) ms, and (2) {sup 167}Pt, {ital E}{sub {alpha}} = 6988(10) keV, {ital T}{sub 1/2} = 0.7(2) ms. Also, the half-life of {sup 168}Pt, which was previously unknown, was determined to be 2.0(4) ms. In a separate but concurrent experiment involving {sup 78}Kr + {sup 96}Ru reactions, {sup 170}Pt was made and a half-life of 14.7(5) ms was measured for it; the one published value is 6{sub {minus}2}{sup +5} ms. Results for {sup 162{minus}164}Os contained in the same data sets were also analyzed and by using mother-daughter correlations, the {alpha} branches of {sup 162,163,164}Os were established to be near 100{percent}. {copyright} {ital 1996 The American Physical Society.}

  18. 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...

  19. 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...

  20. Study on the preparation of Pt nanocapsules

    Science.gov (United States)

    Zhang, Yi-fan; Ji, Zhen; Chen, Ke; Liu, Bo-wen; Jia, Cheng-chang; Yang, Shan-wu

    2017-01-01

    Ag@Pt core-shell nanoparticles (Ag@Pt NPs) were prepared by a co-reduction method. Pt nanocapsules with diameters of less than 10 nm were obtained by an electrochemical method. Cyclic voltammetry (CV) scanning was used to cavitate the Ag@Pt NPs, and the morphology, structure, and cavitation conditions were studied. The results indicate that the effective cavitation conditions to obtain Pt nanoparticles from Ag@Pt NPs are a scanning voltage of 0 to 0.8 V and continuous CV scanning over 2 h. This cavitation method is also applicable for the syntheses of Ir, Ru, and Ru-Pt nanocapsules.

  1. Pt···Pt vs Pt···S contacts between Pt-containing heterobimetallic lantern complexes.

    Science.gov (United States)

    Baddour, Frederick G; Fiedler, Stephanie R; Shores, Matthew P; Bacon, Jeffrey W; Golen, James A; Rheingold, Arnold L; Doerrer, Linda H

    2013-12-01

    A trio of Pt-based heterobimetallic lantern complexes of the form [(py)PtM(SAc)4(py)] (M = Co, 1; Ni, 2; Zn, 3) with unusual octahedral coordination of Pt(II) was prepared from a reaction of [PtM(SAc)4] with excess pyridine. These dipyridine lantern complexes could be converted to monopyridine derivatives with gentle heat to give the series [PtM(SAc)4(py)] (M = Co, 4; Ni, 5; Zn, 6). An additional family of the form [PtM(SAc)4(pyNH2)] (M = Co, 7; Ni, 8; Zn, 9) was synthesized from reaction of [PtM(SAc)4(OH2)] or [PtM(SAc)4] with 4-aminopyridine. Dimethylsulfoxide and N,N-dimethylformamide were also determined to react with [PtM(SAc)4] (M = Co, Ni), respectively, to give [PtCo(SAc)4(DMSO)](DMSO), 10, and [PtNi(SAc)4(DMF)](DMF), 11. Structural and magnetic data for these compounds and those for two other previously published families, [PtM(tba)4(OH2)] and [PtM(SAc)4(L)], L = OH2, pyNO2, are used to divide the structures among three distinct categories based on Pt···Pt and Pt···S distances. In general, the weaker donors H2O and pyNO2 seem to favor metallophilicity and antiferromagnetic coupling between 3d metal centers. When Pt···S interactions are favored over Pt···Pt ones, no coupling is observed and the pKa of the pyridine donor correlates with the interlantern S···S distance. UV-vis-NIR electronic and (1)H NMR spectra provide complementary characterization as well.

  2. 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.

  3. Effect of Pt coverage in Pt-deposited Pd nanostructure electrodes on electrochemical properties

    Energy Technology Data Exchange (ETDEWEB)

    Park, Ah-Reum; Lee, Young-Woo; Kwak, Da-Hee; Park, Kyung-Won [Soongsil University, Seoul (Korea, Republic of)

    2015-06-15

    We have fabricated Pt-deposited Pd electrodes via a two-gun sputtering deposition system by separately operating Pd and Pt target as a function of sputtering time of Pt target. For Pt-deposited Pd electrodes (Pd/Pt-X), Pd were first deposited on the substrates at 20 W for 5min, followed by depositing Pt on the Pd-only electrodes as a function of sputtering time (X=1, 3, 5, 7, and 10min) at 20W on the Pt target. As the sputtering time of Pt target increased, the portion of Pt on the Pd electrodes increased, representing an increased coverage of Pt on the Pd electrodes. The Pd/Pt-7 electrode having an optimized Pt coverage exhibits an excellent electrocatalytic activity for methanol oxidation reaction.

  4. Electron transport in a Pt-CO-Pt nanocontact: Density functional theory calculations

    DEFF Research Database (Denmark)

    Strange, Mikkel; Thygesen, Kristian Sommer; Jacobsen, Karsten Wedel

    2006-01-01

    We have performed first-principles calculations for the mechanic and electric properties of pure Pt nanocontacts and a Pt contact with a single CO molecule adsorbed. For the pure Pt contacts we see a clear difference between point contacts and short chains in good agreement with experiments. We i...... of the transmission function for the Pt-CO-Pt contact, and show that the conductance is largely determined by the local d band at the Pt apex atoms....

  5. Electrodeposited CoPt and FePt alloys nanowires

    Energy Technology Data Exchange (ETDEWEB)

    Cagnon, L. [Laboratoire de Cristallographie, CNRS, BP 166, 38042 Grenoble cedex 9 (France)]. E-mail: laurent.cagnon@grenoble.cnrs.fr; Dahmane, Y. [Laboratoire Louis Neel, CNRS, BP 166, 38042 Grenoble cedex 9 (France); Laboratoire de Materiaux, Electrochimie et Corrosion, BP 17, 15000 Tizi-Ouzou (Algeria); Voiron, J. [Laboratoire Louis Neel, CNRS, BP 166, 38042 Grenoble cedex 9 (France); Pairis, S. [Laboratoire de Cristallographie, CNRS, BP 166, 38042 Grenoble cedex 9 (France); Bacia, M. [Laboratoire de Cristallographie, CNRS, BP 166, 38042 Grenoble cedex 9 (France); Ortega, L. [Laboratoire de Cristallographie, CNRS, BP 166, 38042 Grenoble cedex 9 (France); Benbrahim, N. [Laboratoire de Materiaux, Electrochimie et Corrosion, BP 17, 15000 Tizi-Ouzou (Algeria); Kadri, A. [Laboratoire de Materiaux, Electrochimie et Corrosion, BP 17, 15000 Tizi-Ouzou (Algeria)

    2007-03-15

    We have investigated CoPt and FePt alloys with the face centered tetragonal phase L10, which present very large magnetocrystalline anisotropy. Equiatomic CoPt nanowires exhibiting large coercive fields up to 1.1 T have been successfully prepared by electrodeposition into nanopores of commercial and home-made alumina membranes from a very simple electrolyte. The as-deposited material has the FCC structure with soft magnetic properties. An annealing treatment at 700 deg. C is crucial to transform this phase into the L1{sub 0} phase, which presents hard magnetic properties. Nanowires of annealed samples consist of small grains around 20 nm, with their c axes randomly distributed. The coercivity does not depend on the morphology and porosity of the two types of membranes but only on the deposited material elaborated with the appropriate thermal annealing process. Our preliminary results with FePt alloy indicate a more complicated system since the as-deposited material shows no magnetization. Magnetism appears only after annealing at 700-750 deg. C. Coercivity up to 0.85 T has been obtained at room temperature but with inhomogeneous phase composition. To achieve a single hard phase L1{sub 0}, it is essential to get for the as-deposited sample the equiatomic composition and then to employ the suitable annealing parameters (temperature and time) to change the whole FCC phase into the FCT ordered L1{sub 0} phase.

  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. PT-symmetric quantum theory

    Science.gov (United States)

    Bender, Carl M.

    2015-07-01

    The average quantum physicist on the street would say that a quantum-mechanical Hamiltonian must be Dirac Hermitian (invariant under combined matrix transposition and complex conjugation) in order to guarantee that the energy eigenvalues are real and that time evolution is unitary. However, the Hamiltonian H = p2 + ix3, which is obviously not Dirac Hermitian, has a positive real discrete spectrum and generates unitary time evolution, and thus it defines a fully consistent and physical quantum theory. Evidently, the axiom of Dirac Hermiticity is too restrictive. While H = p2 + ix3 is not Dirac Hermitian, it is PT symmetric; that is, invariant under combined parity P (space reflection) and time reversal T. The quantum mechanics defined by a PT-symmetric Hamiltonian is a complex generalization of ordinary quantum mechanics. When quantum mechanics is extended into the complex domain, new kinds of theories having strange and remarkable properties emerge. In the past few years, some of these properties have been verified in laboratory experiments. A particularly interesting PT-symmetric Hamiltonian is H = p2 - x4, which contains an upside-down potential. This potential is discussed in detail, and it is explained in intuitive as well as in rigorous terms why the energy levels of this potential are real, positive, and discrete. Applications of PT-symmetry in quantum field theory are also discussed.

  8. Results of the Proficiency Test, PT1 and PT2, 2012

    DEFF Research Database (Denmark)

    Vendramin, Niccolò; Nicolajsen, Nicole; Christophersen, Maj-Britt

    A comparative test of diagnostic procedures was provided by the European Union Reference Laboratory (EURL) for Fish Diseases. The test was divided into proficiency test 1 (PT1) and proficiency test 2 (PT2). The number of National Reference Laboratories (NRLs) participating in PT1 and PT2 was 43...

  9. 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)

  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. 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.

  12. 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.

  13. Highly active Pt3Pb and core-shell Pt3Pb-Pt electrocatalysts for formic acid oxidation.

    Science.gov (United States)

    Kang, Yijin; Qi, Liang; Li, Meng; Diaz, Rosa E; Su, Dong; Adzic, Radoslav R; Stach, Eric; Li, Ju; Murray, Christopher B

    2012-03-27

    Formic acid is a promising chemical fuel for fuel cell applications. However, due to the dominance of the indirect reaction pathway and strong poisoning effects, the development of direct formic acid fuel cells has been impeded by the low activity of existing electrocatalysts at desirable operating voltage. We report the first synthesis of Pt(3)Pb nanocrystals through solution phase synthesis and show they are highly efficient formic acid oxidation electrocatalysts. The activity can be further improved by manipulating the Pt(3)Pb-Pt core-shell structure. Combined experimental and theoretical studies suggest that the high activity from Pt(3)Pb and the Pt-Pb core-shell nanocrystals results from the elimination of CO poisoning and decreased barriers for the dehydrogenation steps. Therefore, the Pt(3)Pb and Pt-Pb core-shell nanocrystals can improve the performance of direct formic acid fuel cells at desired operating voltage to enable their practical application. © 2012 American Chemical Society

  14. PT Symmetry as a Generalization of Hermiticity

    CERN Document Server

    Wang, Qing-hai; Zhang, Jie-hong

    2010-01-01

    The Hilbert space in PT-symmetric quantum mechanics is formulated as a linear vector space with a dynamic weight function in the inner product. The most general PT-symmetric matrix Hamiltonians are constructed for 2*2 and 3*3 cases. In the former case, the PT-symmetric Hamiltonian represents the most general matrix Hamiltonian with a real spectrum. In both cases, the Hermitian matrix is shown to be a special case of PT-symmetric matrices. This finding confirms and strengthens the early belief that the PT-symmetric quantum mechanics is a generalization of the conventional Hermitian quantum mechanics.

  15. Perpendicular magnetic anisotropy of Co85Cr15/Pt multilayers

    Institute of Scientific and Technical Information of China (English)

    Pol Hwang; Baohe Li; Tao Yang; Zhonghai Zhai; Fengwu Zhu

    2004-01-01

    The CoCr/Pt bilayers and (CoCr/Pt)20 multilayers with Pt underlayer were prepared by DC magnetron sputtering. The effects of prepared condition on perpendicular magnetic anisotropy were investigated. The results show that the thickness of Pt underlayer has a great effect on the microstructure and perpendicular magnetic anisotropy of CoCr/Pt bilayers and (CoCr/Pt)20 multilayers.When the thickness of Pt underlayer increases, Pt(111) and CoCr(002) peaks of both CoCr/Pt bilayers and (CoCr/Pt)20 multilayers increase and the bilayer periodicity of the multilayers is improved. The effective magnetic anisotropy of (CoCr/Pt)20 multilayers with Pt underlayer was much larger than that of CoCr/Pt bilayers. The (CoCr/Pt)20 multilayers has a stronger perpendicular magnetic anisotropy than that of CoCr/Pt bilayers. This is ascribed to the interface magnetic anisotropy of the multilayers.

  16. PT AND PT/NI "NEEDLE" ELETROCATALYSTS ON CARBON NANOTUBES WITH HIGH ACTIVITY FOR THE ORR

    Energy Technology Data Exchange (ETDEWEB)

    Colon-Mercado, H.

    2011-11-10

    Platinum and platinum/nickel alloy electrocatalysts supported on graphitized (gCNT) or nitrogen doped carbon nanotubes (nCNT) are prepared and characterized. Pt deposition onto carbon nanotubes results in Pt 'needle' formations that are 3.5 nm in diameter and {approx}100 nm in length. Subsequent Ni deposition and heat treatment results in PtNi 'needles' with an increased diameter. All Pt and Pt/Ni materials were tested as electrocatalysts for the oxygen reduction reaction (ORR). The Pt and Pt/Ni catalysts showed excellent performance for the ORR, with the heat treated PtNi/gCNT (1.06 mA/cm{sup 2}) and PtNi/nCNT (0.664 mA/cm{sup 2}) showing the highest activity.

  17. 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.

  18. Low Pt content direct methanol fuel cell anode catalyst: nanophase PtRuNiZr

    Science.gov (United States)

    Narayanan, Sekharipuram R. (Inventor); Whitacre, Jay F. (Inventor)

    2010-01-01

    A method for the preparation of a metallic material having catalytic activity that includes synthesizing a material composition comprising a metal content with a lower Pt content than a binary alloy containing Pt but that displays at least a comparable catalytic activity on a per mole Pt basis as the binary alloy containing Pt; and evaluating a representative sample of the material composition to ensure that the material composition displays a property of at least a comparable catalytic activity on a per mole Pt basis as a representative binary alloy containing Pt. Furthermore, metallic compositions are disclosed that possess substantial resistance to corrosive acids.

  19. Direct Determination of the Ionization Energies of PtC, PtO, and PtO2 with VUVRadiation

    Energy Technology Data Exchange (ETDEWEB)

    Citir, Murat; Metz, Ricardo B.; Belau, Leonid; Ahmed, Musahid

    2008-07-21

    Photoionization efficiency curves were measured for gas-phase PtC, PtO, and PtO2 using tunable vacuum ultraviolet (VUV) radiation at the Advanced Light Source. The molecules were prepared by laser ablation of a platinum tube, followed by reaction with CH4 or N2O and supersonic expansion. These measurements providethe first directly measured ionization energy for PtC, IE(PtC) = 9.45 +- 0.05 eV. The direct measurement also gives greatly improved ionization energies for the platinum oxides, IE(PtO) = 10.0 +- 0.1 eV and IE(PtO2) = 11.35 +- 0.05 eV. The ionization energy connects the dissociation energies of the neutral and cation, leading to greatly improved 0 K bond dissociation energies for the neutrals: D0(Pt-C) = 5.95 +- 0.07 eV, D0(Pt-O)= 4.30 +- 0.12 eV, and D0(OPt-O) = 4.41 +- 0.13 eV, as well as enthalpies of formation for the gas-phase molecules Delta H0 f,0(PtC(g)) = 701 +- 7 kJ/mol, Delta H0f,0(PtO(g)) = 396 +- 12 kJ/mol, and Delta H0f,0(PtO2(g)) = 218 +- 11 kJ/mol. Much of the error in previous Knudsen cell measurements of platinum oxide bond dissociation energies is due to the use of thermodynamic second law extrapolations. Third law values calculated using statistical mechanical thermodynamic functions are in much better agreement with values obtained from ionization energies and ion energetics. These experiments demonstrate that laser ablation production with direct VUV ionization measurements is a versatile tool to measure ionization energies and bond dissociation energies for catalytically interesting species such as metal oxides and carbides.

  20. Comparative study of ethanol oxidation at Pt: Based nanoalloys and UPD modified Pt nanoparticles

    Directory of Open Access Journals (Sweden)

    Tripković Amalija V.

    2010-01-01

    Full Text Available The activity of two alloys, Pt3Sn/C and Pt3Ru2/C, was compared with the activity of Pt/C modified with corresponding amounts of SnUPD (≈25 % and RuUPD (≈40 % in oxidation of ethanol. Pt3Sn/C, Pt3Ru2/C and Pt/C catalysts were characterized by XRD. To establish the activity and stability of the catalysts, potentiodynamic, quasi steady-state and chronoamperometric measurements were performed. Both alloys are more active than SnUPD or RuUPD modified Pt/C catalysts. Electronic effect determining dominantly the activity of Pt3Sn/C is the main reason for its higher activity compared to Pt3Ru2/C. Since SnUPD and RuUPD do not provoke any significant modification of electronic environment, both modified Pt/C catalysts are less active than corresponding alloys. More pronounced difference in activity between Pt3Sn/C and SnUPD modified Pt/C than between Pt3Ru2/C and RuUPD modified Pt/C is caused by electronic effect in Pt3Sn/C. High activity of Pt3Sn/C modified with small amount of SnUPD (≈10% can be explained by combining the electronic effect, causing less strongly bonded adsorbate on Pt sites and easier mobility of SnUPD, with enhanced amount of oxygen-containing species on Sn sites resulting finally in reinforcement of bifunctional mechanism.

  1. 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.

  2. Identification of non-regulated aromatic amines of toxicological concern which can be cleaved from azo dyes used in clothing textiles.

    Science.gov (United States)

    Brüschweiler, Beat J; Küng, Simon; Bürgi, Daniel; Muralt, Lorenz; Nyfeler, Erich

    2014-07-01

    Azo dyes in textiles may release aromatic amines after enzymatic cleavage by skin bacteria or after dermal absorption and metabolism in the human body. From the 896 azo dyes with known chemical structure in the available textile dyes database, 426 azo dyes (48%) can generate one or more of the 22 regulated aromatic amines in the European Union in Annex XVII of REACH. Another 470 azo dyes (52%) can be cleaved into exclusively non-regulated aromatic amines. In this study, a search for publicly available toxicity data on non-regulated aromatic amines was performed. For a considerable percentage of non-regulated aromatic amines, the toxicity database was found to be insufficient or non-existent. 62 non-regulated aromatic amines with available toxicity data were prioritized by expert judgment with objective criteria according to their potential for carcinogenicity, genotoxicity, and/or skin sensitization. To investigate the occurrence of azo dye cleavage products, 153 random samples of clothing textiles were taken from Swiss retail outlets and analyzed for 22 high priority non-regulated aromatic amines of toxicological concern. Eight of these 22 non-regulated aromatic amines of concern could be detected in 17% of the textile samples. In 9% of the samples, one or more of the aromatic amines of concern could be detected in concentrations >30 mg/kg, in 8% of the samples between 5 and 30 mg/kg. The highest measured concentration was 622 mg/kg textile. There is an obvious need to assess consumer health risks for these non-regulated aromatic amines and to fill this gap in the regulation of clothing textiles.

  3. High-performance core-shell PdPt@Pt/C catalysts via decorating PdPt alloy cores with Pt

    Science.gov (United States)

    Wu, Yan-Ni; Liao, Shi-Jun; Liang, Zhen-Xing; Yang, Li-Jun; Wang, Rong-Fang

    A core-shell structured low-Pt catalyst, PdPt@Pt/C, with high performance towards both methanol anodic oxidation and oxygen cathodic reduction, as well as in a single hydrogen/air fuel cell, is prepared by a novel two-step colloidal approach. For the anodic oxidation of methanol, the catalyst shows three times higher activity than commercial Tanaka 50 wt% Pt/C catalyst; furthermore, the ratio of forward current I f to backward current I b is high up to 1.04, whereas for general platinum catalysts the ratio is only ca. 0.70, indicating that this PdPt@Pt/C catalyst has high activity towards methanol anodic oxidation and good tolerance to the intermediates of methanol oxidation. The catalyst is characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS). The core-shell structure of the catalyst is revealed by XRD and TEM, and is also supported by underpotential deposition of hydrogen (UPDH). The high performance of the PdPt@Pt/C catalyst may make it a promising and competitive low-Pt catalyst for hydrogen fueled polymer electrolyte membrane fuel cell (PEMFC) or direct methanol fuel cell (DMFC) applications.

  4. $\\mathcal{PT}$-symmetric mode-locking

    CERN Document Server

    Longhi, Stefano

    2016-01-01

    Parity-time ($\\mathcal{PT}$) symmetry is one of the most important accomplishments in optics over the past decade. Here the concept of $\\mathcal{PT}$ mode-locking of a laser is introduced, in which active phase locking of cavity axial modes is realized by asymmetric mode coupling in a complex time crystal. $\\mathcal{PT}$ mode-locking shows a transition from single to double pulse emission as the $\\mathcal{PT}$ symmetry breaking point is crossed. The transition can show a turbulent behavior, depending on a dimensionless modulation parameter that plays the same role as the Reynolds number in hydrodynamic flows.

  5. Remarks on the PT-pseudo-norm in PT-symmetric quantum mechanics

    Energy Technology Data Exchange (ETDEWEB)

    Duc Tai Trinh [Department of Mathematics, Teacher Training College of Dalat, 29 Yersin, Dalat (Viet Nam)]|[Abdus Salam International Centre for Theoretical Physics, Strada Costiera 11, Trieste 34014 (Italy)

    2005-04-22

    This paper presents an underlying analytical relationship between the PT-pseudo-norm associated with the PT-symmetric Hamiltonian H = p{sup 2} + V(q) and the Stokes multiplier of the differential equation corresponding to this Hamiltonian. We show that the sign alternation of the PT-pseudo-norm, which has been observed as a generic feature of the PT-inner product, is essentially controlled by the derivative of a Stokes multiplier with respect to the eigenparameter.

  6. 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.

  7. A comparative study of Pt and Pt-Pd core-shell nanocatalysts

    Energy Technology Data Exchange (ETDEWEB)

    Long, Nguyen Viet, E-mail: nguyenviet_long@yahoo.com [Department of Materials Science and Engineering, Nagoya Institute of Technology, Gokiso-cho, Showa-ku, Nagoya 466-8555 (Japan); Posts and Telecommunications Institute of Technology, km 10 Nguyen Trai, Thanh Xuan, Ha Dong, Hanoi (Viet Nam); Laboratory for Nanotechnology, Vietnam National University, Ho Chi Minh, Linh Trung, Thu Duc, Ho Chi Minh (Viet Nam); Department of Molecular and Material Sciences, Interdisciplinary Graduate School of Engineering Sciences, Kyushu University, 6-1 Kasugakouen, Kasuga, Fukuoka 816-8580 (Japan); Ohtaki, Michitaka [Department of Molecular and Material Sciences, Interdisciplinary Graduate School of Engineering Sciences, Kyushu University, 6-1 Kasugakouen, Kasuga, Fukuoka 816-8580 (Japan); Hien, Tong Duy [Laboratory for Nanotechnology, Vietnam National University, Ho Chi Minh, Linh Trung, Thu Duc, Ho Chi Minh (Viet Nam); Randy, Jalem [Department of Materials Science and Engineering, Nagoya Institute of Technology, Gokiso-cho, Showa-ku, Nagoya 466-8555 (Japan); Nogami, Masayuki, E-mail: nogami@nitech.ac.jp [Department of Materials Science and Engineering, Nagoya Institute of Technology, Gokiso-cho, Showa-ku, Nagoya 466-8555 (Japan)

    2011-10-30

    Highlights: > The syntheses of Pt (4-8 nm) and Pt-Pd core-shell nanoparticles (15-25 nm) are showed. > Pt-Pd core-shell catalysts possess catalytic property much better than Pt catalysts. > Pt-Pd core-shell catalysts exhibit fast and highly stable catalytic activity. > Fascinatingly, size effect is not as really important as nanostructuring effect. > Fast, stable, sensitive hydrogen adsorption is very crucial for fuel cells. - Abstract: This comparative study characterizes two types of metallic and core-shell bimetallic nanoparticles prepared with our modified polyol method. These nanoparticles consist of Pt and Pt-Pd core-shell nanocatalysts exhibiting polyhedral morphologies. The controlled syntheses of Pt metallic nanoparticles in the 10-nm regime (4-8 nm) and Pt-Pd bimetallic core-shell nanoparticles in the 30-nm regime (15-25 nm) are presented. To realize our ultimate research goals for proton exchange membrane fuel cells (PEMFCs) and direct methanol fuel cells (DMFCs), we thoroughly investigate the dependence of the electrocatalytic properties of the nanoparticles on the structure, size and morphology. Significant differences in the electrocatalysis are also explained in experimental evidences of both Pt and Pt-Pd nanocatalysts. We suggested that the core-shell controlled morphologies and nanostructures of the Pd nanoshell as the Pd atomic monolayers will not only play an important role in producing inexpensive, novel Pt- and Pd-based nanocatalysts but also in designing more efficient Pt- and Pd-based nanocatalysts for practical use in DMFC technology. Our comparative results show that Pt-Pd nanocatalysts with Pd nanoshells exhibited much better electrocatalytic activity and stabilization compared to Pt nanocatalysts. Interestingly, we found that the size effect is not as strong as the nanostructuring effect on the catalytic properties of the researched nanoparticles. A nanostructure effect of the core-shell bimetallic nanoparticles was identified.

  8. AN ANIMAL MODEL OF PLATINUM (PT) HYPERSENSITIVITY

    Science.gov (United States)

    Exposure to Pt salts has been associated with occupational asthma. Pt, the most active component and widely used metal in catalytic converters, is released in automobile exhaust and is a proposed diesel fuel additive. Thus, with the potential for widespread environmental distrib...

  9. Metrology with PT-Symmetric Cavities: Enhanced Sensitivity near the PT-Phase Transition.

    Science.gov (United States)

    Liu, Zhong-Peng; Zhang, Jing; Özdemir, Şahin Kaya; Peng, Bo; Jing, Hui; Lü, Xin-You; Li, Chun-Wen; Yang, Lan; Nori, Franco; Liu, Yu-Xi

    2016-09-09

    We propose and analyze a new approach based on parity-time (PT) symmetric microcavities with balanced gain and loss to enhance the performance of cavity-assisted metrology. We identify the conditions under which PT-symmetric microcavities allow us to improve sensitivity beyond what is achievable in loss-only systems. We discuss the application of PT-symmetric microcavities to the detection of mechanical motion, and show that the sensitivity is significantly enhanced near the transition point from unbroken- to broken-PT regimes. Our results open a new direction for PT-symmetric physical systems and it may find use in ultrahigh precision metrology and sensing.

  10. The robust PT-symmetric chain

    CERN Document Server

    Joglekar, Yogesh N

    2010-01-01

    We study the properties of a parity- and time-reversal- (PT) symmetric tight-binding chain of size N with position-dependent hopping amplitude. In contrast to the fragile PT-symmetric phase of a chain with constant hopping and imaginary impurity potentials, we show that, under very general conditions, our model is {\\it always} in the PT-symmetric phase. We numerically obtain the energy spectrum and the density of states of such a chain, and show that they are widely tunable. By studying the size-dependence of inverse participation ratios, we show that although the chain is not translationally invariant, most of its eigenstates are extended. Our results indicate that tight-binding models with non-Hermitian PT-symmetric hopping have a robust PT-symmetric phase and rich dynamics.

  11. Electrochemical study of the Pt and Pt-Ni upon multiwalled carbon nanotubes

    Science.gov (United States)

    Mohammed, Norani Muti; Mumtaz, Asad; Ansari, Muhammad Shahid; Ahmad, Riaz

    2016-11-01

    Direct methanol fuel cells have attracted great interest in the recent development of portable devices. New routes are being developed for synthesizing the catalysts used in the methanol oxidation. In this work, the electrochemical behavior of the Pt and Pt-Ni upon multiwalled carbon nanotubes, synthesized via a new modified route, has been studied. The results showed that Pt-Ni 10% has the comparable current density to the Pt 20%-loading which is nearly 3 times greater than 10% Pt loading. The transfer of the polarization curve of Pt-Ni 10% towards lower polarization region following the catalyst with 20% Pt loading indicates the higher activity of the nano-electro-catalysts in the alkaline media. Also the long term efficiency and activity of the Pt-Ni with 10% loading is nearly reaching the 20% Pt-loading which is almost 10 folds greater than the 10% Pt loading. The study revealed that Ni in Pt-based nanoalloy impart not only an enhanced activity but also better durability of catalyst in direct methanol fuel cell applications.

  12. Magnetic moments in chemically ordered mass-selected CoPt and FePt clusters

    Energy Technology Data Exchange (ETDEWEB)

    Dupuis, V., E-mail: Veronique.Dupuis@univ-lyon1.fr [Institut Lumière Matière, UMR5306 Université Lyon 1-CNRS, Université de Lyon, 69622 Villeurbanne cedex (France); Khadra, G.; Linas, S.; Hillion, A. [Institut Lumière Matière, UMR5306 Université Lyon 1-CNRS, Université de Lyon, 69622 Villeurbanne cedex (France); Gragnaniello, L. [Institute of Condensed Matter Physics, EPFL, CH-1015 Lausanne (Switzerland); Tamion, A.; Tuaillon-Combes, J.; Bardotti, L.; Tournus, F. [Institut Lumière Matière, UMR5306 Université Lyon 1-CNRS, Université de Lyon, 69622 Villeurbanne cedex (France); Otero, E.; Ohresser, P. [Synchrotron SOLEIL, L’Orme des Merisiers, Saint-Aubin BP 48, F-91192 Gif-sur-Yvette Cedex (France); Rogalev, A.; Wilhelm, F. [European Synchrotron Radiation Facility, BP 220, F-38043 Grenoble Cedex (France)

    2015-06-01

    By combining high photon flux and chemical selectivity, X-ray absorption spectroscopy and X-ray magnetic circular dichroism (XMCD) have been used to study the magnetism of CoPt and FePt clusters before and after their transition to the chemically ordered L1{sub 0}-like phase. Compared to the bulk, we find larger magnetic spin and orbital moments of Fe, Co and Pt atoms in nanoalloys. - Highlights: • Study of magnetism on well-defined CoPt and FePt clusters embedded in carbon matrix • X-ray magnetic circular dichroism (XMCD) at each specific Fe, Co and Pt edges, before and after annealing to induce transition to the chemically L1{sub 0}-like phase. • Quantitative values of the spin and orbital magnetic moments of Co (resp. Fe) and Pt after the chemical ordering transition. • Specific nanoalloy effects.

  13. 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.

  14. Tafsir Kritis Privatisasi Berdasarkan Hermeneutika Gadamerian: Kasus Privatisasi PT Telkom dan PT Indosat

    Directory of Open Access Journals (Sweden)

    Ayudia Sokarina

    2011-08-01

    Full Text Available Privatization Under Critical Meaning by Using Gadamerian Hermeneutics: The Case for Privatization of PT. Telkom And PT. Indosat. The objectives of the study are to search critical meanings of privatisation in PT Telkom and PT Indosat. This research is using an interpretive approach and critical analysis by using Gadamerian hermeneutics. The study finds that there is other reality which shows that the Government views privatisation as a tool to achieve economic rents. Privatisation has failed to enable the distribution of ownership. At the same time, there is exploitation of consumers in the form of higher rates (as in the case of PT Telkomsel. As a result of privatisation of PT Telkom and PT Indosat has failed to provide justice and prosperity for the people and state.

  15. 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.

  16. Pt/MOx/SiO2, Pt/MOx/TiO2, and Pt/MOx/Al2O3 Catalysts for CO Oxidation

    OpenAIRE

    Hongmei Qin; Xiaoshuang Qian; Tao Meng; Yi Lin; Zhen Ma

    2015-01-01

    Conventional supported Pt catalysts have often been prepared by loading Pt onto commercial supports, such as SiO2, TiO2, Al2O3, and carbon. These catalysts usually have simple metal-support (i.e., Pt-SiO2) interfaces. To tune the catalytic performance of supported Pt catalysts, it is desirable to modify the metal-support interfaces by incorporating an oxide additive into the catalyst formula. Here we prepared three series of metal oxide-modified Pt catalysts (i.e., Pt/MOx/SiO2, Pt/MOx/TiO2, a...

  17. Engineering the Activity and Stability of Pt-Alloy Cathode Fuel-Cell Electrocatalysts by Tuning the Pt-Pt Distance

    DEFF Research Database (Denmark)

    Escribano, Maria Escudero; Malacrida, Paolo; Vej-Hansen, Ulrik Grønbjerg

    2014-01-01

    with a thickness of few Pt layers is formed. Accordingly, the effect of alloying Pt is to impose strain onto the Pt overlayer [3,4]. It is likely that this strain would be relaxed by defects [6]. Moreover, the activity of the Pt5Ln catalysts vs. the Pt-Pt distance shows a volcano relationship (Fig. A) [5]. Pt5Ln......One of the main obstacles to the commercialisation of low-temperature fuel cells is the slow kinetics of the oxygen reduction reaction (ORR). In order to decrease the ORR overpotential and reduce the Pt loading we need to develop more active and stable electrocatalysts. A fruitful strategy...... for enhancing the cathode activity is to alloy Pt with transition metals [1-2]. However, alloys of Pt and late transition metals are typically unstable under fuel-cell conditions. Herein, we present experimental and theoretical studies showing the trends in activity and stability of novel cathode catalysts...

  18. Engineering the Activity and Stability of Pt-Alloy Cathode Fuel-Cell Electrocatalysts by Tuning the Pt-Pt Distance

    DEFF Research Database (Denmark)

    Escribano, Maria Escudero; Malacrida, Paolo; Vej-Hansen, Ulrik Grønbjerg

    2014-01-01

    based on alloys of Pt and lanthanides. Sputter-cleaned, polycrystalline Pt5Gd shows a five-fold increase in ORR activity [3], relative to Pt at 0.9 V in 0.1 M HClO4. The rest of the Pt5Ln (Ln = lanthanide) tested present at least a 3-fold enhancement in activity [4,5]. In all cases, a Pt overlayer...

  19. Dynamics of the YSZ-Pt Interface

    DEFF Research Database (Denmark)

    Bay, Lasse; Jacobsen, Torben

    1997-01-01

    Yttria stabilized zirconia (YSZ)-Pt point electrodes were examined by linear potential sweep, potential step and impedance measurements at 1000 degrees C in air. Inductive loops and hysteresis phenomena with long relaxation times were found. Atomic force microscopy showed changes of the interface...... between Pt and YSZ induced by the current passage. These changes involve transport of solid and are slow enough to explain the large time constants. The low frequency capacitance and inductive loop forming an entire circle indicate the presence of gas reservoirs at the YSZ-Pt interface....

  20. PT-Symmetric Quantum Electrodynamics

    CERN Document Server

    Bender, C M; Milton, K A; Shajesh, K V; Bender, Carl M.; Cavero-Pelaez, Ines; Milton, Kimball A.

    2005-01-01

    The Hamiltonian for quantum electrodynamics becomes non-Hermitian if the unrenormalized electric charge $e$ is taken to be imaginary. However, if one also specifies that the potential $A^\\mu$ in such a theory transforms as a pseudovector rather than a vector, then the Hamiltonian becomes PT symmetric. The resulting non-Hermitian theory of electrodynamics is the analog of a spinless quantum field theory in which a pseudoscalar field $\\phi$ has a cubic self-interaction of the form $i\\phi^3$. The Hamiltonian for this cubic scalar field theory has a positive spectrum, and it has recently been demonstrated that the time evolution of this theory is unitary. The proof of unitarity requires the construction of a new operator called C, which is then used to define an inner product with respect to which the Hamiltonian is self-adjoint. In this paper the corresponding C operator for non-Hermitian quantum electrodynamics is constructed perturbatively. This construction demonstrates the unitarity of the theory. Non-Hermit...

  1. 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)

  2. PT-Symmetry Quantum Electrodynamics--PTQED

    CERN Document Server

    Milton, Kimball A; Parashar, Prachi; Shajesh, K V; Wagner, Jef

    2007-01-01

    The construction of $\\mathcal{PT}$-symmetric quantum electrodynamics is reviewed. In particular, the massless version of the theory in 1+1 dimensions (the Schwinger model) is solved. Difficulties with unitarity of the $S$-matrix are discussed.

  3. PT-Symmetric Quantum Field Theory

    CERN Document Server

    Milton, K A

    2003-01-01

    In the context of the PT-symmetric version of quantum electrodynamics, it is argued that the C operator introduced in order to define a unitary inner product has nothing to do with charge conjugation.

  4. Golden Gate and Pt. Reyes Acoustic Detections

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — This dataset contains detections of acoustic tagged fish from two general locations: Golden Gate (east and west line) and Pt. Reyes. Several Vemco 69khz acoustic...

  5. PT-Symmetric Optomechanically-Induced Transparency

    CERN Document Server

    Jing, H; Özdemir, S K; Zhang, J; Lü, X -Y; Peng, B; Yang, L; Nori, F

    2014-01-01

    Optomechanically-induced transparency (OMIT) and the associated slow-light propagation provide the basis for storing photons in nanofabricated phononic devices. Here we study OMIT in parity-time (PT)-symmetric microresonators with a tunable gain-to-loss ratio. This system features a reversed, non-amplifying transparency: inverted-OMIT. When the gain-to-loss ratio is steered, the system exhibits a transition from the PT-symmetric phase to the broken-PT-symmetric phase. We show that by tuning the pump power at fixed gain-to-loss ratio or the gain-to-loss ratio at fixed pump power, one can switch from slow to fast light and vice versa. Moreover, the presence of PT-phase transition results in the reversal of the pump and gain dependence of transmission rates. These features provide new tools for controlling light propagation using optomechanical devices.

  6. Calcium platinum aluminium, CaPtAl

    Directory of Open Access Journals (Sweden)

    Charles Fon Abi

    2011-10-01

    Full Text Available A preliminary X-ray study of CaPtAl has been reported previously by Hulliger [J. Alloys Compd (1993, 196, 225–228] based on X-ray powder diffraction data without structure refinement. With the present single-crystal X-ray study, we confirm the assignment of the TiNiSi type for CaPtAl, in a fully ordered inverse structure. All three atoms of the asymmetric unit have .m. site symmetry. The structure features a ∞3[AlPt] open framework with a fourfold coordination of Pt by Al atoms and vice versa. The Ca atoms are located in the large channels of the structure.

  7. Spatio-temporal variability of non-regulated disinfection by-products within a drinking water distribution network.

    Science.gov (United States)

    Mercier Shanks, Catherine; Sérodes, Jean-Baptiste; Rodriguez, Manuel J

    2013-06-01

    The non-regulated disinfection by-products (NrDBP) targeted in this study include four haloacetonitriles (trichloroacetonitrile (TCAN); dichloroacetonitrile (DCAN); bromochloroacetonitrile (BCAN) and dibromoacetonitrile (DBAN)); one halonitromethane (trichloronitromethane, better known under the name chloropicrin (CPK)); and two haloketones (1,1-dichloro-2-propanone (11DCPone) and 1,1,1-trichloro-2-propanone (111TCPone)). This study provides a detailed picture of the spatial and temporal variability of these NrDBP concentrations throughout a drinking water distribution system located in a region with major seasonal climate variations. The results obtained show that the concentrations of the investigated NrDBPs varied significantly according to time and location. The average concentrations of TCAN, DCAN, CKP and 111TCPone were significantly higher in summer. Surprisingly, the average concentrations of 11DCPone were significantly higher in winter. For BCAN and DBAN, the average concentrations observed in winter were higher, but not in a statistically significant way. On the other hand, the four HANs, CPK and 111TCPone generally had spatial profiles involving an increase of the concentrations along the network according to increasing water residence times, whereas 11DCPone overall had a profile where concentrations increased at the beginning of the network, followed by a drop in the concentrations towards the ends of the network. In spite of certain disparities in the individual spatio-temporal variation profiles, strong correlations were generally observed between NrDBPs, and trihalomethanes (THMs) and haloacetic acids (HAAs). Therefore, THMs and HAAs could be good statistical indicators of the presence of NrDBPs in the drinking water of the system under study.

  8. 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.

  9. 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.

  10. The CO/Pt(111) Puzzle

    Energy Technology Data Exchange (ETDEWEB)

    FEIBELMAN,PETER J.; HAMMER,B.; NORSHOV,J.K.; WAGNER,F.; SCHEFFLER,M.; STUMPF,R.; DUMESIC,J.; WATWE,R.

    2000-07-12

    Notwithstanding half a dozen theoretical publications, well-converged density-functional calculations, whether based on a local or generalized-gradient exchange-correlation potential, whether all-electron or employing pseudopotentials underestimate CO's preference for low-coordination binding sites on Pt(111) and vicinals to it. For example, they imply that CO should prefer hollow- to atop-site adsorption on Pt(111), in apparent contradiction to a host of low temperature experimental studies.

  11. Scattering properties of PT-symmetric objects

    CERN Document Server

    Miri, Mohammad-Ali; Facao, Margarida; Abouraddy, Ayman F; Bakry, Ahmed; Razvi, Mir A N; Alshahrie, Ahmed; Alù, Andrea; Christodoulides, Demetrios N

    2016-01-01

    We investigate the scattering response of parity-time (PT) symmetric structures. We show that, due to the local flow of energy between gain and loss regions, such systems can deflect light in unusual ways, as a function of the gain/loss contrast. Such structures are highly anisotropic and their scattering patterns can drastically change as a function of the angle of incidence. In addition, we derive a modified optical theorem for PT-symmetric scattering systems, and discuss its ramifications.

  12. Reduction of Pt Usage in Fuel Cell Electrocatalysts Using Carbon Nanotubes and Non-Pt Metals

    Institute of Scientific and Technical Information of China (English)

    J. Nakamura; Y. Nagashima; T. Yamazaki; T. Matsumoto; E. Yoo

    2005-01-01

    @@ 1Introduction The high-priced and limited Pt constitutes a high barrier to commercialization of fuel cells. Pt is essential for the electrode catalyst of polymer electrolyte fuel cells (PEFCs). A reduction in Pt usage is one of the key requirements for the commercialization of fuel cells for use in everyday life, because of its high price and limited availability, and the difficulty of finding suitable substitutes. Non-Pt fuel cell catalysts will decrease the demand for Pt by PEFCs, enabling more Pt to be available for use in other essential products, and make fuel cells more popular[1]. The cheaper Mo2C is known to possess similar catalytic activities and electronic structures to Pt[2]. Carbon black (CB) is widely used as the support for Pt nanoparticles. However, we found that when carbon nanotubes (CNTs) rather than CB are used as the support, the performance is improved, especially below 600 mA/cm2[3,4]. Here, we show that a combination of Mo2C catalyst and carbon nanotubes in the anode provides performance as high as half that of the current PEFCs with Pt catalysts below 600mA/cm2.

  13. 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.

  14. Dependence of Magnetic Properties of Co/Pt Multilayers on Deposition Temperature of Pt Buffer Layers

    Science.gov (United States)

    Shiomi, Shigeru; Nishimura, Tomotaka; Kobayashi, Tadashi; Masuda, Morio

    1993-04-01

    A 15-nm-thick Pt buffer layer was deposited on a glass slide at temperature Ts(Ptbuf) ranging from 30 to 300°C by e-gun evaporation. Following the cooling in vacuum to ambient temperature, Co and Pt layers have been alternately deposited on it. Very large perpendicular anisotropy and coercivity have been obtained at Ts(Ptbuf) higher than 200°C. The (111) preferred orientation of the Co/Pt multilayer as well as the Pt buffer layer became more pronounced with elevating Ts(Ptbuf), to which the enhancement of perpendicular anisotropy with elevating Ts(Ptbuf) might be ascribable.

  15. Nanoparticulate CoPt Thin Films

    Science.gov (United States)

    Barekatain, Yasaman; Hadjipanayis, George; Magnetics bLab Team

    Equiatomic FePt and CoPt alloys are very attractive for application in high density recording media because of the high magnetocrystalline anisotropy K of their fct(L10) structure with values exceeding 2MJ/m3.The aim of this study is to fabricate a nanoparticulate CoPt film consisting of CoPt nanoparticles embedded in a matrix. To obtain this we have used co-sputtering of CoPt with different materials M = BN,C, Cu and SiO2. Our first experiments were done on CoPt films with thickness of 200 nm. The as-sputtered films had the fcc structure and a coercivity of 150 Oe. Annealing at 700 oC for 30 min led to an increase in coercivity to 4 kOe. Optimization studies are under way to find the optimum sputtering conditions to obtain a fully ordered tetragonal structure with the highest value of coercivity which can then be used in the nanoparticulate composites. Work supported by DOE BES- FG02-04ERU4612 DOE DE-FG02-04ERU4612.

  16. PT -symmetric model of immune response

    Science.gov (United States)

    Bender, Carl M.; Ghatak, Ananya; Gianfreda, Mariagiovanna

    2017-01-01

    The study of PT -symmetric physical systems began in 1998 as a complex generalization of conventional quantum mechanics, but beginning in 2007 experiments began to be published in which the predicted PT phase transition was clearly observed in classical rather than in quantum-mechanical systems. This paper examines the classical PT phase transition in dynamical-system models that are moderately accurate representations of antigen-antibody systems. A surprising conclusion that can be drawn from these models is that it might be possible treat a serious disease in which the antigen concentration grows out of bounds (and the host dies) by injecting a small dose of a second (different) antigen. In this case a PT -symmetric analysis shows there are two possible favorable outcomes. In the unbroken-PT -symmetric phase the disease becomes chronic and is no longer lethal, while in the appropriate broken-PT -symmetric phase the concentration of lethal antigen goes to zero and the disease is completely cured.

  17. PT phase transition in multidimensional quantum systems

    CERN Document Server

    Bender, Carl M

    2012-01-01

    Non-Hermitian PT-symmetric quantum-mechanical Hamiltonians generally exhibit a phase transition that separates two parametric regions, (i) a region of unbroken PT symmetry in which the eigenvalues are all real, and (ii) a region of broken PT symmetry in which some of the eigenvalues are complex. This transition has recently been observed experimentally in a variety of physical systems. Until now, theoretical studies of the PT phase transition have generally been limited to one-dimensional models. Here, four nontrivial coupled PT-symmetric Hamiltonians, $H=p^2/2+x^2/2+q^2/2+y^2/2+igx^2y$, $H=p^2/2+x^2/2+q^2/2+y^2+igx^2y$, $H=p^2/2+x^2/2+q^2/2+y^2/2+r^2/2+z^2/2+igxyz$, and $H=p^2/2+x^2/2+q^2/2+y^2+r^2/2+3z^2/2+igxyz$ are examined. Based on extensive numerical studies, this paper conjectures that all four models exhibit a phase transition. The transitions are found to occur at $g\\approx 0.1$, $g\\approx 0.04$, $g\\approx 0.1$, and $g\\approx 0.05$. These results suggest that the PT phase transition is a robust phen...

  18. High pressure CO hydrogenation over bimetallic Pt-Co catalysts

    DEFF Research Database (Denmark)

    Christensen, Jakob Munkholt; Medford, Andrew James; Studt, Felix

    2014-01-01

    The potential of bimetallic Pt-Co catalysts for production of higher alcohols in high pressure CO hydrogenation has been assessed. Two catalysts (Pt3Co/SiO2 and PtCo/SiO2) were tested, and the existing literature on CO hydrogenation over Pt-Co catalysts was reviewed. It is found that the catalyst...

  19. 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.

  20. Amorphous Pt@PdCu/CNT Catalyst for Methanol Electrooxidation ...

    African Journals Online (AJOL)

    A multi-walled carbon nanotube-supported, Pt decorated nano-sized ... alloy cores (denoted as Pt@PdCu/CNT) catalyst with lower Pt loading is synthesized via a ... The electrochemical activity of the Pt@PdCu/CNT catalyst is tested by cyclic ...

  1. 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

  2. Resistive switching in Pt/TiO{sub 2}/Pt

    Energy Technology Data Exchange (ETDEWEB)

    Jeong, Doo Seok

    2008-08-15

    Recently, the resistive switching behavior in TiO{sub 2} has drawn attention due to its application to resistive random access memory (RRAM) devices. TiO{sub 2} shows characteristic non-volatile resistive switching behavior, i.e. reversible switching between a high resistance state (HRS) and a low resistance state (LRS). Both unipolar resistive switching (URS) and bipolar resistive switching (BRS) are found to be observed in TiO{sub 2} depending on the compliance current for the electroforming. In this thesis the characteristic current-voltage (I-V) hysteresis in three different states of TiO{sub 2}, pristine, URS-activated, and BRS-activated states, was investigated and understood in terms of the migration of oxygen vacancies in TiO{sub 2}. The I-V hysteresis of pristine TiO{sub 2} was found to show volatile behavior. That is, the temporary variation of the resistance took place depending on the applied voltage. However, the I-V hysteresis of URS- and BRS-activated states showed non-volatile resistive switching behavior. Some evidences proving the evolution of oxygen gas during electroforming were obtained from time-of-flight secondary ion mass spectroscopy analysis and the variation of the morphology of switching cells induced by the electroforming. On the assumption that a large number of oxygen vacancies are introduced by the electroforming process, the I-V behavior in electroformed switching cells was simulated with varying the distribution of oxygen vacancies in electroformed TiO{sub x} (x Pt/TiO{sub x} interface. The oxygen-related reactions given as a function of the applied voltage affect the distribution of oxygen vacancies in TiO{sub x}, consequently, the Schottky barrier height at the cathode/TiO{sub x} interface is influenced by the oxygen vacancy distribution. Therefore, the BRS behavior including the

  3. 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.

  4. Microwave sinthesys and characterization of Pt and Pt-Rh-Sn electrocatalysts for ethanol oxidation

    Directory of Open Access Journals (Sweden)

    Jovanović Vladislava M.

    2011-01-01

    Full Text Available Carbon supported Pt and Pt-Rh-Sn catalysts were synthesized by microwave-polyol method in ethylene glycol solution and investigated for the ethanol electro-oxidation reaction. The catalysts were characterized in terms of structure, morphology and composition by employing XRD, STM and EDX techniques. STM analysis indicated rather uniform particles and particle size of below 2 nm for both catalysts. XRD analysis of the Pt/C catalyst revealed two phases, one with the main characteristic peaks of face centered cubic crystal structure (fcc of platinum and another related to graphite like structure of carbon support Vulcan XC-72R. However, in XRD pattern of the Pt-Rh-Sn/C catalyst diffraction peaks for Pt, Rh or Sn cannot be resolved, indicating an extremely low crystallinity. The small particle sizes and homogeneous size distributions of both catalysts should be attributed to the advantages of microwave assisted modified polyol process in ethylene glycol solution. Pt-Rh- Sn/C catalyst is highly active for the ethanol oxidation with the onset potential shifted for more than 150 mV to negative values and with currents nearly 5 times higher in comparison to Pt/C catalyst. The stability tests of the catalysts, as studied by the chronoamperometric experiments, reveal that the Pt-Rh-Sn/C catalyst is evidently less poisoned then Pt/C catalyst. The increased activity of Pt-Rh-Sn/C in comparison to Pt/C catalyst is most probably promoted by bifunctional mechanism and the electronic effect of alloyed metals.

  5. Preparation of PtSn/C, PtRu/C, PtRh/C, PtRuRh/C and PtSnRh/C electrocatalysts using an alcohol-reduction process for methanol and ethanol oxidation; Preparacao e caracterizacao de eletrocatalisadores PtRu, PtSn, PtRh, PtRuRh e PtSnRh para oxidacao direta de alcoois em celulas a combustivel tipo PEM utilizando a metodologia da reducao por alcool

    Energy Technology Data Exchange (ETDEWEB)

    Dias, Ricardo Rodrigues

    2009-07-01

    In this work, Pt/C, PtRh (90:10), PtRh/C (50:50), PtSn/C (50:50), PtRu (50:50)/C, PtRuRh/C (50:40:10) and PtSnRh/C (50:40:10) were prepared by an alcohol-reduction process with metal loading of 20 wt.% using H{sub 2}PtCl{sub 6}.6H{sub 2}O (Aldrich), SnCl{sub 2}.2H{sub 2}O (Aldrich),and RhCl{sub 2}.XH{sub 2}O (Aldrich) as metals sources and Vulcan XC72 as support. The electrocatalysts were characterized by EDX, XRD and cyclic voltammetry (CV). The electro-oxidation of ethanol was studied by CV, chronoamperomety at room temperature in acid medium and tests at 100 deg C on a single cell of a direct methanol or ethanol fuel cell. The EDX analysis showed that the metal atomic ratios of the obtained electrocatalysts were similar to the nominal atomic ratios used in the preparation. The diffractograms of electrocatalysts prepared showed four peaks at approximately 2{theta} =40 deg, 47 deg, 67 deg and 82 deg, which are associated with the (111), (200), (220) and (311) planes, respectively, of a face cubic-centered (fcc) structure characteristic of platinum and platinum alloys. The average crystallite sizes using the Scherrer equation and the calculated values were in the range of 2-3 nm. For Pt Sn/C and PtSnRh/C two additional peaks were observed at 2 = 34 deg and 52 deg that were identified as a SnO{sub 2} phase. Pt Sn/C (50:50) and PtSnRh/C (50:40:10) electro catalyst showed the best performance for ethanol oxidation at room temperature. For methanol oxidation at room temperature Pt Ru/C, Pt Sn/C and PtRuRh/C electrocatalysts showed the best performance. Tests at 100 deg C on a single cell of a direct ethanol fuel cell PtSnRh/C showed the best performance, for methanol oxidation PtRuRh/C showed the best performance. (author)

  6. 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.

  7. Pt and PtRu catalyst bilayers increase efficiencies for ethanol oxidation in proton exchange membrane electrolysis and fuel cells

    Science.gov (United States)

    Altarawneh, Rakan M.; Pickup, Peter G.

    2017-10-01

    Polarization curves, product distributions, and reaction stoichiometries have been measured for the oxidation of ethanol at anodes consisting of Pt and PtRu bilayers and a homogeneous mixture of the two catalysts. These anode structures all show synergies between the two catalysts that can be attributed to the oxidation of acetaldehyde produced at the PtRu catalyst by the Pt catalyst. The use of a PtRu layer over a Pt layer produces the strongest effect, with higher currents than a Pt on PtRu bilayer, mixed layer, or either catalyst alone, except for Pt at high potentials. Reaction stoichiometries (average number of electrons transferred per ethanol molecule) were closer to the values for Pt alone for both of the bilayer configurations but much lower for PtRu and mixed anodes. Although Pt alone would provide the highest overall fuel cell efficiency at low power densities, the PtRu on Pt bilayer would provide higher power densities without a significant loss of efficiency. The origin of the synergy between the Pt and PtRu catalysts was elucidated by separation of the total current into the individual components for generation of carbon dioxide and the acetaldehyde and acetic acid byproducts.

  8. Analysis of non-regulated vehicular emissions by extractive FTIR spectrometry: tests on a hybrid car in Mexico City

    Science.gov (United States)

    Reyes, F.; Grutter, M.; Jazcilevich, A.; González-Oropeza, R.

    2006-07-01

    A methodology to acquire valuable information on the chemical composition and evolution of vehicular emissions is presented. The analysis of the gases is performed by passing a constant flow of a sample gas from the tail-pipe into a 10 L multi-pass cell. The absorption spectra within the cell are obtained using an FTIR spectrometer at 0.5 cm-1 resolution along a 13.1 m optical path. Additionally, the total flow from the exhaust is continuously measured from a differential pressure sensor on a Pitot tube installed at the exit of the exhaust. This configuration aims to obtain a good speciation capability by coadding spectra during 30 s and reporting the emission (in g/km) of key and non-regulated pollutants, such as CO2, CO, NO, SO2, NH3, HCHO, NMHC, during predetermined driving routines. The advantages and disadvantages of increasing the acquisition frequency, as well as the effect of other parameters such as spectral resolution, cell volume and flow rate, are discussed. With the aim of testing and evaluating the proposed technique, experiments were performed on a dynamometer running FTP-75 and typical driving cycles of the Mexico City Metropolitan Area (MCMA) on a Toyota Prius hybrid vehicle. This car is an example of recent automotive technology to reach the market dedicated to reduce emissions and therefore pressing the need of low detection techniques. This study shows the potential of the proposed technique to measure and report in real time the emissions of a large variety of pollutants, even from a super ultra-low emission vehicle (SULEV). The emissions of HC's, NOx, CO and CO2 obtained here are similar to experiments performed in other locations with the same vehicle model. Some differences suggest that an inefficient combustion process and type of gasoline used in the MCMA may be partly responsible for lower CO2 and higher CO and NO emission factors. Also, a fast reduction of NO emission to very low values is observed after cold ignition, giving rise to

  9. EFEKTIVITAS IMPLEMENTASI CORPORATE SOCIAL RESPOSIBILITY PT. ABC

    Directory of Open Access Journals (Sweden)

    Rizkiaji Rikky Djunaedi

    2015-12-01

    Full Text Available The purposes of this study were 1 to analyze public perceptions on the effectiveness of the implementation of CSR of PT. A B C; 2 to analyze the implementation of CSR activities by PT. A B C; 3 to formulate strategies to improve the effectiveness of the implementation of CSR of PT. A B C. The method used in this research was descriptive analysis with a survey approach to measure expectations and performance assessment on the CSR implemented programs by the public, and there were respondents 104 respondents involved in this study. This study used the Importance-Performance Analysis (IPA aiming to determine the effectiveness of the programs that have been implemented and to map the relationship between the expectations and the performance of each variable. Furthermore, using a SWOT analysis of the data processing and of the objectives of the program made by CSR is expected to provide recommendations to develop strategies in order to increase the effectiveness of CSR program of ABC Company.Keywords: corporate social responsibility (CSR, mining industry, implementation analysis, IPA, SWOTAbstrakTujuan dari  penelitian ini adalah 1 menganalisis persepsi masyarakat teradap efektivitas implementasi CSR PT. ABC; 2 menganalisis pelaksanaan  kegiatan CSR oleh PT. ABC; 3 merumuskan strategi untuk meningkatkan efektivitas implementasi CSR PT. ABC. Metode yang digunakan dalam penelitian ini adalah analisis deskriptif dengan pendekatan survey untuk mengukur harapan dan penilaian kinerja oleh masyarakat atas program CSR yang diterapkan. Jumlah responden sebanyak 104 orang.  Dalam penelitian ini digunakan Analisis Importance-Performance Analysis (IPA bertujuan untuk mengetahui efektifitas dari program-program yang telah dijalankan serta  memetakan hubungan antara harapan dengan kinerja dari masing-masing variabel. Selanjutnya menggunakan analisis SWOT dari hasil pengolahan data dan dari tujuan program dibuat oleh CSR sehingga dapat memberikan rekomendasi

  10. 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.

  11. Electrochemical promotion of catalytic reactions with Pt/C (or Pt/Ru/C)//PBI catalysts

    DEFF Research Database (Denmark)

    Petrushina, Irina; Bjerrum, Niels; Bandur, Viktor;

    2007-01-01

    The paper is an overview of the results of the investigation on electrochemical promotion of three catalytic reactions: methane oxidation with oxygen, NO reduction with hydrogen at 135 degrees C and Fischer-Tropsch synthesis (FTS) at 170 degrees C in the [CH4/O-2(or NO/H-2 or CO/H-2)/Ar//Pt(or Pt...

  12. 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...

  13. Copper dusting effects on perpendicular magnetic anisotropy in Pt/Co/Pt tri-layers

    Directory of Open Access Journals (Sweden)

    Vineeth Mohanan Parakkat

    2016-05-01

    Full Text Available The effect of Cu dusting on perpendicular magnetic anisotropy of sputter grown Pt/Co/Pt stack in which the Cu layer is in proximity with that of Co is investigated in this work. We used magneto optic Kerr effect microscopy measurements to study the variation in the reversal mechanisms in films with Co thicknesses below 0.8nm by systematically varying their perpendicular magnetic anisotropy using controlled Cu dusting. Cu dusting was done separately above and below the cobalt layer in order to understand the role of bottom and top Pt layers in magnetization reversal mechanisms of sputtered Pt/Co/Pt stack. The introduction of even 0.3nm thick Cu layer below the cobalt layer drastically affected the perpendicular magnetic anisotropy as evident from the nucleation behavior. On the contrary, even a 4nm thick top Cu layer had little effect on the reversal mechanism. These observations along with magnetization data was used to estimate the role of top and bottom Pt in the origin of perpendicular magnetic anisotropy as well as magnetization switching mechanism in Pt/Co/Pt thin films. Also, with an increase in the bottom Cu dusting from 0.2 to 0.4nm there was an increase in the number of nucleation sites resulting in the transformation of domain wall patterns from a smooth interface type to a finger like one and finally to maze type.

  14. Copper dusting effects on perpendicular magnetic anisotropy in Pt/Co/Pt tri-layers

    Science.gov (United States)

    Parakkat, Vineeth Mohanan; Ganesh, K. R.; Anil Kumar, P. S.

    2016-05-01

    The effect of Cu dusting on perpendicular magnetic anisotropy of sputter grown Pt/Co/Pt stack in which the Cu layer is in proximity with that of Co is investigated in this work. We used magneto optic Kerr effect microscopy measurements to study the variation in the reversal mechanisms in films with Co thicknesses below 0.8nm by systematically varying their perpendicular magnetic anisotropy using controlled Cu dusting. Cu dusting was done separately above and below the cobalt layer in order to understand the role of bottom and top Pt layers in magnetization reversal mechanisms of sputtered Pt/Co/Pt stack. The introduction of even 0.3nm thick Cu layer below the cobalt layer drastically affected the perpendicular magnetic anisotropy as evident from the nucleation behavior. On the contrary, even a 4nm thick top Cu layer had little effect on the reversal mechanism. These observations along with magnetization data was used to estimate the role of top and bottom Pt in the origin of perpendicular magnetic anisotropy as well as magnetization switching mechanism in Pt/Co/Pt thin films. Also, with an increase in the bottom Cu dusting from 0.2 to 0.4nm there was an increase in the number of nucleation sites resulting in the transformation of domain wall patterns from a smooth interface type to a finger like one and finally to maze type.

  15. 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.

  16. Experimental demonstration of PT-symmetric stripe lasers

    CERN Document Server

    Gu, Zhiyuan; Lyu, Quan; Li, Meng; Xiao, Shumin; Song, Qinghai

    2015-01-01

    Recently, the coexistence of parity-time (PT) symmetric laser and absorber has gained tremendous research attention. While the PT symmetric absorber has been observed in microwave metamaterials, the experimental demonstration of PT symmetric laser is still absent. Here we experimentally study PT-symmetric laser absorber in stripe waveguide. Using the concept of PT symmetry to exploit the light amplification and absorption, PT-symmetric laser absorbers have been successfully obtained. Different from the single-mode PT symmetric lasers, the PT-symmetric stripe lasers have been experimentally confirmed by comparing the relative wavelength positions and mode spacing under different pumping conditions. When the waveguide is half pumped, the mode spacing is doubled and the lasing wavelengths shift to the center of every two initial lasing modes. All these observations are consistent with the theoretical predictions and confirm the PT-symmetry breaking well.

  17. Electrodeposition and electrocatalytic activity of Pt and Pt-alloy nanoparticles and thin films on highly oriented pyrolytic graphite (HOPG)

    Science.gov (United States)

    Lu, Guojin

    Pt and Pt-based alloy catalysts were synthesized by electrodeposition on HOPG. The nucleation and growth, morphology, composition and crystal structure, and electrocatalytic activity (towards relevant reactions in the frame of PEMFCs and DMFCs) of these model electrodes were systematically investigated. The presence of chlorides inhibits the Pt reduction processes. There is a transition from progressive to instantaneous nucleation with increasing overpotential for the deposition from 1 mM H2PtCl6 electrolytes. The possibility of instantaneous nucleation at large overpotential by using electrolytes with large chloride concentration is advantageous for the growth of small, well dispersed nanoparticles. The electrochemical data were confirmed by AFM and SEM imaging studies. Relatively narrow size distributed nanoparticles can be obtained from the current system. While MOR activity decreases with decreasing particle size, the HER and HOR activity of deposited Pt particles increases with decreasing deposition period. The ORR activity first increases then decreases with increasing deposition time. Interactions between Pt and Ru, or Ni or Co are observed and they form solid solution as verified by XRD. Underpotential deposition occurs for Pt-Ni or Pt-Co co-electrodeposition. Pt-Ru deposition can be described as progressive nucleation at low overpotential and instantaneous nucleation at high overpotentials. Through direct morphological observations, the Pt-Ni or Pt-Co nucleation can be approximately described as progressive. Pt-Ru deposits are superior to Pt towards MOR. The optimum Ru content is about 50 at.%. Pt-Ni and Pt-Co deposits are more active than Pt for ORR. The optimum content is about 30 at.% Ni or 50 at.% Co. Dealloying of Pt-Ru and Pt-Ni or Pt-Co electrodeposit is observed after electrochemical characterization. The extent of dealloying increases with the content of the alloying element.

  18. 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

  19. Relaxor-PT Single Crystal Piezoelectric Sensors

    Directory of Open Access Journals (Sweden)

    Xiaoning Jiang

    2014-07-01

    Full Text Available Relaxor-PbTiO3 piezoelectric single crystals have been widely used in a broad range of electromechanical devices, including piezoelectric sensors, actuators, and transducers. This paper reviews the unique properties of these single crystals for piezoelectric sensors. Design, fabrication and characterization of various relaxor-PT single crystal piezoelectric sensors and their applications are presented and compared with their piezoelectric ceramic counterparts. Newly applicable fields and future trends of relaxor-PT sensors are also suggested in this review paper.

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

    Science.gov (United States)

    Seetala, Naidu V.; Harrell, J. W.; Lawson, Jeremy; Nikles, David E.; Williams, John R.; Isaacs-Smith, Tamara

    2005-12-01

    We have studied the effect of ion-beam irradiation on reducing the ordering temperature of FePt and FePtAu nanoparticles. FePt and FePt(Au14%) 4 nm particles dispersed on a Si-substrate were irradiated by 300 keV Al-ions with a dose of 1 × 1016 ions/cm2 at 43 °C using a water-cooled flange in order to minimize the vacancy migration and voids formation within the collision cascades. Partial chemical ordering has been observed in as-irradiated particles with coercivity of 60-130 Oe. Post-irradiation annealing at 220 °C enhanced chemical ordering in FePt nanoparticles with coercivity of 3500 Oe, magnetic anisotropy of 1.5 × 107 erg/cc, and thermal stability factor of 130. A much higher 375 °C post-irradiation annealing was required in FePtAu, presumably because Au atoms were trapped at Fe/Pt lattice sites at lower temperatures. As the annealing temperature increased, anomalous features in the magnetization reversal curves were observed that disappeared at higher annealing temperatures.

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2005-12-15

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

  2. Discovery of the Pt-Based Superconductor LaPt5As.

    Science.gov (United States)

    Fujioka, Masaya; Ishimaru, Manabu; Shibuya, Taizo; Kamihara, Yoichi; Tabata, Chihiro; Amitsuka, Hiroshi; Miura, Akira; Tanaka, Masashi; Takano, Yoshihiko; Kaiju, Hideo; Nishii, Junji

    2016-08-10

    A novel superconductor, LaPt5As, which exhibits a new crystal structure was discovered by high-pressure synthesis using a Kawai-type apparatus. A superconducting transition temperature was observed at 2.6 K. Depending on the sintering pressure, LaPt5As has superconducting and non-superconducting phases with different crystal structures. A sintering pressure of around 10 GPa is effective to form single-phase superconducting LaPt5As. This material has a very unique crystal structure with an extremely long c lattice parameter of over 60 Å and corner-sharing tetrahedrons composed of network-like Pt layers. Density functional theory calculations have suggested that the superconducting current flows through these Pt layers. Also, this unique layered structure characteristic of LaPt5As is thought to play a key role in the emergence of superconductivity. Furthermore, due to a stacking structure which makes up layers, various structural modifications for the LaPt5As family are conceivable. Since such a high-pressure synthesis using a Kawai-type apparatus is not common in the field of materials science, there is large room for further exploration of unknown phases which are induced by high pressure in various materials.

  3. Tailoring Curie temperature and magnetic anisotropy in ultrathin Pt/Co/Pt films

    Directory of Open Access Journals (Sweden)

    Vineeth Mohanan Parakkat

    2016-05-01

    Full Text Available The dependence of perpendicular magnetization and Curie temperature (Tc of Pt/Co/Pt thin films on the thicknesses of Pt seed (Pts and presence of Ta buffer layer has been investigated in this work. Pt and Co thicknesses were varied between 2 to 8 nm and 0.35 to 1.31 nm (across the spin reorientation transition thickness respectively and the Tc was measured using SQUID magnetometer. We have observed a systematic dependence of Tc on the thickness of Pts. For 8nm thickness of Pts the Co layer of 0.35nm showed ferromagnetism with perpendicular anisotropy at room temperature. As the thickness of the Pts was decreased to 2nm, the Tc went down below 250K. XRD data indicated polycrystalline growth of Pts on SiO2. On the contrary Ta buffer layer promoted the growth of Pt(111. As a consequence Ta(5nm/Pt(3nm/Co(0.35nm/Pt(2nm had much higher Tc (above 300K with perpendicular anisotropy when compared to the same stack without the Ta layer. Thus we could tune the ferromagnetic Tc and anisotropy by varying the Pts thickness and also by introducing Ta buffer layer. We attribute these observations to the micro-structural evolution of Pts layer which hosts the Co layer.

  4. Electrochemical quartz crystal microbalance study of the electrodeposition of Co, Pt and Pt-Co alloy

    Energy Technology Data Exchange (ETDEWEB)

    Martin, A.J.; Chaparro, A.M. [CIEMAT, Avda. Complutense, 22, 28040 Madrid (Spain); Daza, L. [CIEMAT, Avda. Complutense, 22, 28040 Madrid (Spain); Instituto de Catalisis y Petroleoquimica (CSIC), C/Marie Curie 2, Campus Cantoblanco, 28049 Madrid (Spain)

    2007-06-10

    The electrochemical deposition of Co, Pt and Pt-Co alloy are studied with the electrochemical quartz crystal microbalance (EQCM) on a gold substrate. Co is deposited from acidic sulphate bath containing boric acid. Different processes are identified in this bath. Electrodeposition of Co on Au substrate is observed at potentials above redox potential, underpotential deposition, most probably due to formation of a Co-Au alloy. At more cathodic potentials, below -0.5 V, metallic Co is formed. The film is completely dissolved at positive potentials during the anodic scan, probably mediated by Co(OH){sub 2}. The electrodeposition of platinum from acidic PtCl{sub 6}{sup 2-} bath occurs below the thermodynamic potential (0.74 V) with almost 100% efficiency. At potentials negative from 0.0 V the efficiency decreases due to parallel water reduction. The codeposition of Co and Pt is also studied in acidic bath. Here, the decrease of pH due to water reduction on Pt deposits gives rise to precipitation of Co(OH){sub 2}, together with the deposition of metallic Pt and Co. The films contain as major component the Pt{sub 3}Co alloy. (author)

  5. Electrochemical quartz crystal microbalance study of the electrodeposition of Co, Pt and Pt-Co alloy

    Science.gov (United States)

    Martín, A. J.; Chaparro, A. M.; Daza, L.

    The electrochemical deposition of Co, Pt and Pt-Co alloy are studied with the electrochemical quartz crystal microbalance (EQCM) on a gold substrate. Co is deposited from acidic sulphate bath containing boric acid. Different processes are identified in this bath. Electrodeposition of Co on Au substrate is observed at potentials above redox potential, underpotential deposition, most probably due to formation of a Co-Au alloy. At more cathodic potentials, below -0.5 V, metallic Co is formed. The film is completely dissolved at positive potentials during the anodic scan, probably mediated by Co(OH) 2. The electrodeposition of platinum from acidic PtCl 6 2- bath occurs below the thermodynamic potential (0.74 V) with almost 100% efficiency. At potentials negative from 0.0 V the efficiency decreases due to parallel water reduction. The codeposition of Co and Pt is also studied in acidic bath. Here, the decrease of pH due to water reduction on Pt deposits gives rise to precipitation of Co(OH) 2, together with the deposition of metallic Pt and Co. The films contain as major component the Pt 3Co alloy.

  6. Mechanisms of current conduction in Pt/BaTiO{sub 3}/Pt resistive switching cell

    Energy Technology Data Exchange (ETDEWEB)

    Pan, R.K. [School of Materials Science and Engineering, Hubei University, Wuhan 430062 (China); Zhang, T.J., E-mail: tj65zhang@yahoo.com.cn [School of Materials Science and Engineering, Hubei University, Wuhan 430062 (China); Wang, J.Y.; Wang, J.Z. [School of Materials Science and Engineering, Hubei University, Wuhan 430062 (China); Wang, D.F. [School of Materials Science and Engineering, Hubei University, Wuhan 430062 (China); q-Psi and Department of Physics, Hanyang University, Seoul 133-791 (Korea, Republic of); Duan, M.G. [School of Materials Science and Engineering, Hubei University, Wuhan 430062 (China)

    2012-03-30

    The 80-nm-thickness BaTiO{sub 3} (BT) thin film was prepared on the Pt/Ti/SiO{sub 2}/Si substrate by the RF magnetron sputtering technique. The Pt/BT/Pt/Ti/SiO{sub 2}/Si structure was investigated using X-ray diffraction and scanning electron microscopy. The current-voltage characteristic measurements were performed. The bipolar resistive switching behavior was found in the Pt/BT/Pt cell. The current-voltage curves were well fitted in different voltage regions at the high resistance state (HRS) and the low resistance state (LRS), respectively. The conduction mechanisms are concluded to be Ohmic conduction and Schottky emission at the LRS, while space-charge-limited conduction and Poole-Frenkel emission at the HRS. The electroforming and switching processes were explained in terms of the valence change mechanism, in which oxygen vacancies play a key role in forming conducting paths. - Highlights: Black-Right-Pointing-Pointer Pt/BaTiO{sub 3}/Pt cell shows the bipolar resistive switching behavior. Black-Right-Pointing-Pointer The current-voltage curves were well fitted for different conduction mechanisms. Black-Right-Pointing-Pointer The electroforming and switching processes were explained.

  7. Carbon supported nanoparticles Pt Ru (Pt Ru/C electrocatalysts) prepared using electron beam irradiation; Preparacao de nanoparticulas de PtRu suportadas em carbono (eletrocatalisadores PtRu/C) utilizando feixe de eletrons

    Energy Technology Data Exchange (ETDEWEB)

    Silva, Dionisio F. da; Oliveira Neto, Almir; Pino, Eddy S.; Linardi, Marcelo; Spinace, Estevam V. [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil). Programa de Celulas a Combustivel], e-mail: espinace@ipen.br, e-mail: dfsilva@ipen.br

    2006-07-01

    Carbon-supported Pt Ru (electrocatalysts PtRu/C nanoparticles) were prepared submitting a water/ethylene glycol mixture containing Pt(IV) and Ru(III) ions and the carbon support to electron beam irradiation. The PtRu/C electrocatalysts were characterized by EDX, XRD and cyclic voltammetry and tested for methanol electro-oxidation aiming fuel cell application. The obtained PtRu/C electrocatalysts were more active for methanol electro-oxidation than the commercial PtRu/C ETEK electrocatalyst at ambient temperature. (author)

  8. Resistive random access memory utilizing ferritin protein with Pt nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Uenuma, Mutsunori; Kawano, Kentaro; Zheng Bin; Okamoto, Naofumi; Horita, Masahiro; Yoshii, Shigeo; Yamashita, Ichiro; Uraoka, Yukiharu, E-mail: uenuma@ms.naist.jp [Nara Institute of Science and Technology, 8916-5, Takayama, Ikoma, Nara 630-0192 (Japan)

    2011-05-27

    This study reports controlled single conductive paths found in resistive random access memory (ReRAM) formed by embedding Pt nanoparticles (Pt NPs) in NiO film. Homogeneous Pt NPs produced and placed by ferritin protein produce electric field convergence which leads to controlled conductive path formation. The ReRAM with Pt NPs shows stable switching behavior. A Pt NP density decrease results in an increase of OFF state resistance and decrease of forming voltage, whereas ON resistance was independent of the Pt NP density, which indicates that a single metal NP in a memory cell will achieve low power and stable operation.

  9. Carbon supported nanoparticles Pt Ru (Pt Ru/C electrocatalysts) prepared using electron beam irradiation; Preparacao de nanoparticulas de PtRu suportadas em carbono (eletrocatalisadores PtRu/C) utilizando feixe de eletrons

    Energy Technology Data Exchange (ETDEWEB)

    Silva, Dionisio F. da; Oliveira Neto, Almir; Pino, Eddy S.; Linardi, Marcelo; Spinace, Estevam V. [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil). Programa de Celulas a Combustivel], e-mail: espinace@ipen.br, e-mail: dfsilva@ipen.br

    2006-07-01

    Carbon-supported Pt Ru (electrocatalysts PtRu/C nanoparticles) were prepared submitting a water/ethylene glycol mixture containing Pt(IV) and Ru(III) ions and the carbon support to electron beam irradiation. The PtRu/C electrocatalysts were characterized by EDX, XRD and cyclic voltammetry and tested for methanol electro-oxidation aiming fuel cell application. The obtained PtRu/C electrocatalysts were more active for methanol electro-oxidation than the commercial PtRu/C ETEK electrocatalyst at ambient temperature. (author)

  10. Multifunctional Pt(II) Reagents: Covalent Modifications of Pt Complexes Enable Diverse Structural Variation and In-Cell Detection.

    Science.gov (United States)

    White, Jonathan D; Haley, Michael M; DeRose, Victoria J

    2016-01-19

    To enhance the functionality of Pt-based reagents, several strategies have been developed that utilize Pt compounds modified with small, reactive handles. This Account encapsulates work done by us and other groups regarding the use of Pt(II) compounds with reactive handles for subsequent elaboration with fluorophores or other functional moieties. Described strategies include the incorporation of substituents for well-known condensation or nucleophilic displacement-type reactions and their use, for example, to tether spectroscopic handles to Pt reagents for in vivo investigation. Other chief uses of displacement-type reactions have included tethering various small molecules exhibiting pharmacological activity directly to Pt, thus adding synergistic effects. Click chemistry-based ligation techniques have also been applied, primarily with azide- and alkyne-appended Pt complexes. Orthogonally reactive click chemistry reactions have proven invaluable when more traditional nucleophilic displacement reactions induce side-reactivity with the Pt center or when systematic functionalization of a larger number of Pt complexes is desired. Additionally, a diverse assortment of Pt-fluorophore conjugates have been tethered via click chemistry conjugation. In addition to providing a convenient synthetic path for diversifying Pt compounds, the use of click-capable Pt complexes has proved a powerful strategy for postbinding covalent modification and detection with fluorescent probes. This strategy bypasses undesirable influences of the fluorophore camouflaged as reactivity due to Pt that may be present when detecting preattached Pt-fluorophore conjugates. Using postbinding strategies, Pt reagent distributions in HeLa and lung carcinoma (NCI-H460) cell cultures were observed with two different azide-modified Pt compounds, a monofunctional Pt(II)-acridine type and a difunctional Pt(II)-neutral complex. In addition, cellular distribution was observed with an alkyne-appended difunctional

  11. Pt Skin Versus Pt Skeleton Structures of Pt3Sc as Electrocatalysts for Oxygen Reduction

    DEFF Research Database (Denmark)

    Johansson, Tobias Peter; Ulrikkeholm, Elisabeth Therese; Hernandez-Fernandez, Patricia

    2014-01-01

    In order for low temperature polymer electrolyte membrane fuel cells to become economically viable Pt catalyst loading must be significantly reduced. The cathode of the polymer electrolyte membrane fuel cell, where oxygen reduction takes place, is responsible for the main activity loss. The devel...

  12. Pt-Pd nanoelectrocatalyst of ultralow Pt content for the oxidation of formic acid: Towards tuning the reaction pathway

    Indian Academy of Sciences (India)

    Sourov Ghosh; C Retna Raj

    2015-05-01

    Synthesis of highly efficient functional electrocatalyst that favours the electrochemical oxidation of formic acid via CO-free dehydrogenation pathway is required for direct formic acid fuel cells. Traditional catalysts favour the dehydration pathway involving the generation of poisonous CO. Herein we demonstrate the superior electrocatalytic performance of Pt-Pd bimetallic nanoelectrocatalyst of ultralow Pt content and tuning the reaction pathway by controlling the Pt content. Bimetallic nanoparticles of Pt4Pd96, Pt7Pd93 and Pt47Pd53 compositions are synthesized by electrochemical co-deposition method in aqueous solution. The nanoparticles of ultralow Pt content, Pt4Pd96, favour the CO-free dehydrogenation pathway for formic acid oxidation with an onset potential of 0 V (SHE) whereas the Pt47Pd53 nanoparticles favour the dehydration pathway involving the formation of CO at high positive potential. The Pt content of the bimetallic nanoparticles actually controls the oxidation peak potential and catalytic activity. Significant negative shift (∼350 mV) in the oxidation peak potential and remarkable enhancement in the current density (2.6 times) are observed for Pt4Pd96 nanoparticles with respect to Pt47Pd53. The absence of three adjacent Pt and Pd atoms could be the reason for the suppression of CO pathway. The electrochemical impedance measurements indirectly support the CO-free pathway for the formic acid oxidation on Pt4Pd96 nanoparticles.

  13. 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.

  14. Heterobimetallic lantern complexes that couple antiferromagnetically through noncovalent Pt···Pt interactions.

    Science.gov (United States)

    Baddour, Frederick G; Fiedler, Stephanie R; Shores, Matthew P; Golen, James A; Rheingold, Arnold L; Doerrer, Linda H

    2013-05-01

    A series of Pt-based heterobimetallic lantern complexes of the form [PtM(SAc)4(OH2)] (M = Co, 1; Ni, 2; Zn, 3) were prepared using a facile, single-step procedure. These hydrated species were reacted with 3-nitropyridine (3-NO2py) to prepare three additional lantern complexes, [PtM(SAc)4(3-NO2py)] (M = Co, 4; Ni, 5; Zn, 6), or alternatively dried in vacuo to the dehydrated species [PtM(SAc)4] (M = Co, 7; Ni, 8; Zn, 9). The Co- and Ni-containing species exhibit Pt-M bonding in solution and the solid state. In the structurally characterized compounds 1-6, the lantern units form dimers in the solid state via a short Pt···Pt metallophilic interaction. Antiferromagnetic coupling between 3d metal ions in the solid state through noncovalent metallophilic interactions was observed for all the paramagnetic lantern complexes prepared, with J-coupling values of -12.7 cm(-1) (1), -50.8 cm(-1) (2), -6.0 cm(-1) (4), and -12.6 cm(-1) (5). The Zn complexes 3 and 6 also form solid-state dimers, indicating that the formation of short Pt···Pt interactions in these complexes is not predicated on the presence of a paramagnetic 3d metal ion. These contacts and the resultant antiferromagnetic coupling are also not unique to heterobimetallic lantern complexes with axially coordinated H2O or the previously reported thiobenzoate supporting ligand.

  15. Disentangling interface and bulk contributions to the anisotropic magnetoresistance in Pt/Co/Pt sandwiches

    Science.gov (United States)

    Kobs, André; Oepen, Hans Peter

    2016-01-01

    We report on interfacial contributions to the anisotropic magnetoresistance (AMR) in Co layers sandwiched between Pt. Utilizing the Fuchs-Sondheimer formalism interface contributions can be separated from bulklike AMR. We demonstrate that for all-metal systems interfacial AMR is also present when varying the magnetization within the film plane. This interfacial in-plane AMR is two times smaller than the contribution that arises when the magnetization is varied within the plane perpendicular to the current direction. This finding is in contrast to the spin Hall MR found for ferromagnetic insulator/Pt bilayers revealing the existence of different MR effects at the interfaces of Pt with conducting and insulating ferromagnets.

  16. Pt/MOx/SiO2, Pt/MOx/TiO2, and Pt/MOx/Al2O3 Catalysts for CO Oxidation

    Directory of Open Access Journals (Sweden)

    Hongmei Qin

    2015-04-01

    Full Text Available Conventional supported Pt catalysts have often been prepared by loading Pt onto commercial supports, such as SiO2, TiO2, Al2O3, and carbon. These catalysts usually have simple metal-support (i.e., Pt-SiO2 interfaces. To tune the catalytic performance of supported Pt catalysts, it is desirable to modify the metal-support interfaces by incorporating an oxide additive into the catalyst formula. Here we prepared three series of metal oxide-modified Pt catalysts (i.e., Pt/MOx/SiO2, Pt/MOx/TiO2, and Pt/MOx/Al2O3, where M = Al, Fe, Co, Cu, Zn, Ba, La for CO oxidation. Among them, Pt/CoOx/SiO2, Pt/CoOx/TiO2, and Pt/CoOx/Al2O3 showed the highest catalytic activities. Relevant samples were characterized by N2 adsorption-desorption, X-ray diffraction (XRD, transmission electron microscopy (TEM, H2 temperature-programmed reduction (H2-TPR, X-ray photoelectron spectroscopy (XPS, CO temperature-programmed desorption (CO-TPD, O2 temperature-programmed desorption (O2-TPD, and CO2 temperature-programmed desorption (CO2-TPD.

  17. PT L 3 near edge structure of halogen-bridged mixed-valence pt complexes and pd-pt mixed-metal complexes

    Science.gov (United States)

    Tanino, H.; Oyanagi, H.; Yamashita, M.; Kobayashi, K.

    1985-03-01

    X-ray absorption near edge structure (XANES) of halogen-bridged mixed-valence Pt complexes and halogen-bridged Pd-Pt mixed-metal complexes have been measured using synchrotron radiation with a high energy resolution. In Pd-Pt mixed metal complexes, we demonstrate that the degree of the valence is estimated from the intensity of the white line at the Pt L 3 edge. In the mixed-valence complexes, the electron system is proved to be the Peierls insulator with a charge density wave of renormalized d electrons of Pt, where the total valence of Pt IV- and Pt 11 is conserved without excess electrons from ligands or anions.

  18. 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.

  19. 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.

  20. PT-symmetric quantum electrodynamics and unitarity.

    Science.gov (United States)

    Milton, Kimball A; Abalo, E K; Parashar, Prachi; Pourtolami, Nima; Wagner, J

    2013-04-28

    More than 15 years ago, a new approach to quantum mechanics was suggested, in which Hermiticity of the Hamiltonian was to be replaced by invariance under a discrete symmetry, the product of parity and time-reversal symmetry, PT. It was shown that, if PT is unbroken, energies were, in fact, positive, and unitarity was satisfied. Since quantum mechanics is quantum field theory in one dimension--time--it was natural to extend this idea to higher-dimensional field theory, and in fact an apparently viable version of PT-invariant quantum electrodynamics (QED) was proposed. However, it has proved difficult to establish that the unitarity of the scattering matrix, for example, the Källén spectral representation for the photon propagator, can be maintained in this theory. This has led to questions of whether, in fact, even quantum mechanical systems are consistent with probability conservation when Green's functions are examined, since the latter have to possess physical requirements of analyticity. The status of PT QED will be reviewed in this paper, as well as the general issue of unitarity.

  1. 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.

  2. Adhesion and bonding of Pt/Ni and Pt/Co overlayers: Density functional calculations

    Science.gov (United States)

    Cabeza, Gabriela F.; Castellani, Norberto J.; Légaré, Pierre

    2006-04-01

    The electronic and energetic properties of bimetallic surfaces Pt/Ni(111) and Pt/Co(111) are examined using the FP-LAPW (Full-PotentialLinearized Augmented Plane Wave) method by means of spin-polarized and non-polarized calculations. We present both the results of the shifts in the d-band centers when one metal (Pt) is pseudomorfically deposited on another with smaller lattice constant (Ni, Co) and those corresponding to the surface and adhesion energies. The surface is modeled by a seven layer slab separated in z direction by a vacuum region of six substrate layers. The results obtained for pure Ni, Co and Pt surfaces are presented in order to compare with experimental and theoretical data reported in the literature

  3. Domain wall pinning on strain relaxation defects in FePt(001)/Pt thin films

    Energy Technology Data Exchange (ETDEWEB)

    Attane, J. P.; Samson, Y.; Marty, A.; Halley, D.; Beigne, C.

    2001-08-06

    Thin FePt (001) films, grown by molecular-beam epitaxy on Pt(001), exhibit a very large perpendicular magnetic anisotropy (K{sub u}=5 x 10{sup 6}Jm{sup -3}) and a 100% magnetic remanence in perpendicular field. The lattice misfit between FePt and Pt (1.5%) relaxes through the pileup of a/6 <112> partial dislocations along {l_brace}111{r_brace} planes, leading to the formation of microtwins. Atomic force microscopy images demonstrate that this process induces a spontaneous rectangular nanostructuration of the sample, while magnetic force microscopy shows that the microtwins act as pinning sites for the magnetic walls. This leads to square magnetic domains and explains the large coercivity associated with the domain wall propagation. {copyright} 2001 American Institute of Physics.

  4. Domain wall pinning on strain relaxation defects in FePt(001)/Pt thin films

    Science.gov (United States)

    Attané, J. P.; Samson, Y.; Marty, A.; Halley, D.; Beigné, C.

    2001-08-01

    Thin FePt (001) films, grown by molecular-beam epitaxy on Pt(001), exhibit a very large perpendicular magnetic anisotropy (Ku=5×106J m-3) and a 100% magnetic remanence in perpendicular field. The lattice misfit between FePt and Pt (1.5%) relaxes through the pileup of a/6 partial dislocations along {111} planes, leading to the formation of microtwins. Atomic force microscopy images demonstrate that this process induces a spontaneous rectangular nanostructuration of the sample, while magnetic force microscopy shows that the microtwins act as pinning sites for the magnetic walls. This leads to square magnetic domains and explains the large coercivity associated with the domain wall propagation.

  5. Selective oxidation of methylamine over zirconia supported Pt-Ru, Pt and Ru catalysts

    Institute of Scientific and Technical Information of China (English)

    Aiying Song; Gongxuan Lu

    2015-01-01

    Pt–Ru, Pt and Ru catalysts supported on zirconia were prepared by impregnation method and were tested in se-lective oxidation of methylamine (MA) in aqueous media. Among three catalysts, Ru/ZrO2 was more active than Pt/ZrO2 while Pt–Ru/ZrO2 demonstrated the best catalytic activity due to the fact that Pt addition efficiently pro-moted the dispersion of active species in bimetallic catalyst. Therefore, the~100%TOC conversion and N2 selec-tivity were achieved over Pt–Ru/ZrO2, Pt/ZrO2 and Ru/ZrO2 catalysts at 190, 220 and 250 °C, respectively.

  6. Ánodos de Pt-Ru y Pt-Ir para Celdas de Combustible Alimentadas con Metano y Propano Directo Pt-Ru and Pt-Ir Anodes for Direct Methane and Propane Proton Exchange Membrane Fuel Cells

    Directory of Open Access Journals (Sweden)

    Bibian A Hoyos

    2007-01-01

    Full Text Available En este trabajo se evalúa el efecto de la temperatura en el desempeño de celdas de combustible de membrana de intercambio protónico alimentadas con metano y propano, utilizando oxígeno como alimentación en el cátodo. Para la oxidación de los combustibles en los ánodos, se probaron cinco catalizadores soportados en carbón: Pt, Pt85Ru15, Pt50Ru50, Pt90Ir10 y Pt50Ir50. Como catalizador en el cátodo se usó platino puro soportado en carbón. El desempeño de las celdas de combustible fue evaluado mediante curvas de polarización obtenidas a partir de los datos corriente-potencial. Los resultados indican que la oxidación de metano se ve favorecida a altas temperaturas sobre los catalizadores Pt90/Ir10, Pt50/Ir50 y Pt50/Ru50. A bajas temperaturas los mejores catalizadores resultaron ser Pt y Pt85/Ru15. La mezcla bimetálica Pt85/Ru15 fue la que presentó mejor desempeño para llevar a cabo la oxidación de propano a 30 °C.In this paper, the effect of temperature in the performance of proton exchange membrane fuel cells feed with methane and propane, using oxygen as feed to the cathode, is presented. For the fuel oxidation in the anodes, five carbon supported catalysts were tested: Pt, Pt85/Ru15, Pt50/Ru50, Pt90/Ir10, and Pt50/Ir50. Carbon-supported pure platinum was used as catalysts in the cathode side. The performance of the fuel cells was evaluated by polarization curves obtained from the current-potential data. Results indicate that methane oxidation is favoured at high temperatures on the Pt90/Ir10, Pt50/Ir50 and Pt50/Ru50 catalysts. At low temperatures the best catalysts were Pt and Pt85/Ru15. The Pt85/Ru15 bimetallic mixture showed the best performance to carry out propane oxidation at 30 °C.

  7. Rapid thermal annealing of FePt and FePt/Cu thin films

    Energy Technology Data Exchange (ETDEWEB)

    Brombacher, Christoph

    2011-01-10

    Chemically ordered FePt is one of the most promising materials to reach the ultimate limitations in storage density of future magnetic recording devices due to its high uniaxial magnetocrystalline anisotropy and a corrosion resistance superior to rare-earth based magnets. In this study, FePt and FePt/Cu bilayers have been sputter deposited at room temperature onto thermally oxidized silicon wafers, glass substrates and self-assembled arrays of spherical SiO{sub 2} particles with diameters down to 10 nm. Millisecond flash lamp annealing, as well as conventional rapid thermal annealing was employed to induce the phase transformation from the chemically disordered A1 phase into the chemically ordered L1{sub 0} phase. The influence of the annealing temperature, annealing time and the film thickness on the ordering transformation and (001) texture evolution of FePt films with near equiatomic composition was studied. Whereas flash lamp annealed FePt films exhibit a polycrystalline morphology with high chemical L1{sub 0} order, rapid thermal annealing can lead to the formation of chemically ordered FePt films with (001) texture on amorphous SiO{sub 2}/Si substrates. The resultant high perpendicular magnetic anisotropy and large coercivities up to 40 kOe are demonstrated. Simultaneously to the ordering transformation, rapid thermal annealing to temperatures exceeding 600 C leads to a break up of the continuous FePt film into separated islands. This dewetting behavior was utilized to create regular arrays of FePt nanostructures on SiO{sub 2} particle templates with periods down to 50 nm. The addition of Cu improves the (001) texture formation and chemical ordering for annealing temperatures T{sub a} {<=}600 C. In addition, the magnetic anisotropy and the coercivity of the ternary FePtCu alloy can be effectively tailored by adjusting the Cu content. The prospects of FePtCu based exchange spring media, as well as the magnetic properties of FePtCu nanostructures fabricated

  8. Irreversible modification of magnetic properties of Pt/Co/Pt ultrathin films by femtosecond laser pulses

    Energy Technology Data Exchange (ETDEWEB)

    Kisielewski, J., E-mail: jankis@uwb.edu.pl [Institute for Molecules and Materials, Radboud University Nijmegen, Heyendaalseweg 135, 6525AJ Nijmegen (Netherlands); Laboratory of Magnetism, University of Białystok, Lipowa 41, 15-424 Białystok (Poland); Dobrogowski, W.; Kurant, Z.; Stupakiewicz, A.; Tekielak, M.; Maziewski, A. [Laboratory of Magnetism, University of Białystok, Lipowa 41, 15-424 Białystok (Poland); Kirilyuk, A.; Kimel, A.; Rasing, Th. [Institute for Molecules and Materials, Radboud University Nijmegen, Heyendaalseweg 135, 6525AJ Nijmegen (Netherlands); Baczewski, L. T.; Wawro, A. [Institute of Physics, Polish Academy of Sciences, al. Lotników 32/46, 02-668 Warsaw (Poland); Balin, K.; Szade, J. [A. Chełkowski Institute of Physics, University of Silesia, Uniwersytecka 4, 40-007 Katowice (Poland)

    2014-02-07

    Annealing ultrathin Pt/Co/Pt films with single femtosecond laser pulses leads to irreversible spin-reorientation transitions and an amplification of the magneto-optical Kerr rotation. The effect was studied as a function of the Co thickness and the pulse fluence, revealing two-dimensional diagrams of magnetic properties. While increasing the fluence, the creation of two branches of the out-of-plane magnetization state was found.

  9. Atomic Aggregation Processes in the Early Stages of Pt/Pt(111) Growth

    Institute of Scientific and Technical Information of China (English)

    ZHUANG Guo-Ce; ZHU Xiao-Bin; WANG Wei

    2000-01-01

    The atomic aggregation processes in the early stages of Pt/Pt(111) growth are studied by using kinetic Monte Carlo simulations. Our results show that the average neighbor coordination number of the atoms in a cluster is a function of temperature, agreeing well with the experiment observations of scanning tunneling microscopy. The influence of diffusion barriers of various atomic processes on the morphology of islands is also studied. Different morphologies of the islands (dendritic, fractal, or compact islands) are found.

  10. SELECTIVE HYDROGENATION OF CINNAMALDEHYDE WITH Pt AND Pt-Fe CATALYSTS: EFFECTS OF THE SUPPORT

    Directory of Open Access Journals (Sweden)

    A.B. da Silva

    1998-06-01

    Full Text Available Low-temperature reduced TiO2-supported Pt and Pt-Fe catalysts are much more active and selective for the liquid–phase hydrogenation of cinnamaldehyde to unsaturated cinnamyl alcohol than the corresponding carbon-supported catalysts. High-temperature reduced catalysts, where the SMSI effect should be present, are almost inactive for this reaction. There is at present no definitive explanation for this effect but an electronic metal-support interaction is most probably involved.

  11. Dry etching of single crystal PMN-PT piezoelectric material.

    OpenAIRE

    Agnus, Joël; Alexandru Ivan, Ioan; Queste, Samuel

    2011-01-01

    International audience; During the last decade, the applications of PMN-PT spread significantly. Unlike PZT, the appropriate microtechnologies for PMN-PT Piezo-MEMS aren't fully documented in the literature. This paper deals with the PMN-PT etching by inductively coupled plasma (ICP) technique, also known as DRIE. The paper quantitatively presents the etching parameters of PMN-PT by the Ar/C4F8 gas combination and reports some related useful experience.

  12. Nonlinear waves in $\\cal PT$-symmetric systems

    OpenAIRE

    Konotop, Vladimir V.; Yang, Jianke; Zezyulin, Dmitry A.

    2016-01-01

    Recent progress on nonlinear properties of parity-time ($\\cal PT$-) symmetric systems is comprehensively reviewed in this article. $\\cal PT$ symmetry started out in non-Hermitian quantum mechanics, where complex potentials obeying $\\cal PT$ symmetry could exhibit all-real spectra. This concept later spread out to optics, Bose-Einstein condensates, electronic circuits, and many other physical fields, where a judicious balancing of gain and loss constitutes a $\\cal PT$-symmetric system. The nat...

  13. Modification of Pt/Co/Pt film properties by ion irradiation

    Science.gov (United States)

    Avchaciov, K. A.; Ren, W.; Djurabekova, F.; Nordlund, K.; Sveklo, I.; Maziewski, A.

    2015-09-01

    We studied the structural modifications of a Pt/Co/Pt trilayer epitaxial film under Ga+ 30-keV ion irradiation by means of classical molecular dynamics and Monte Carlo simulations. The semiclassical tight-binding second-moment approximation potential was adjusted to reproduce the enthalpies of formation, the lattice constants, and the order-disorder transition temperatures for Co-Pt alloys. We found that during irradiation, the sandwich-type Pt(fcc)/Co(hcp)/Pt(fcc) film structure underwent a transition to the new solid solution α -Co /Pt (fcc ) phase. Our analysis of the short-range order indicates the formation, within a nanosecond time scale, of a homogeneous chemically disordered solution. The longer time-scale simulations employing a Monte Carlo algorithm demonstrated that the transition from the disordered phase to the ordered L 10 and L 12 phases was also possible but not significant for the changes in perpendicular magnetic anisotropy (PMA) observed experimentally. The strain analysis showed that the Co layer was under tensile strain in the lateral direction at the fluences of 1.5 ×1014-3.5 ×1014ionscm -2 ; this range of fluences corresponds to the appearance of PMA. This strain was induced in the initially relaxed hcp Co layer due to its partial transformation to the fcc phase and to the influence of atomic layers with larger lattice constants at upper/lower interfaces.

  14. Alternative alloys for platinum jewelry? New structures in Pt-Hf and Pt-Mo

    Science.gov (United States)

    Gilmartin, Erin; Corbitt, Jacqueline; Hart, Gus

    2008-10-01

    The only known intermetallic structure with an 8:1 stoichiometry is that of Pt8Ti. It is intriguing that an ordered compound would occur at such low concentrations of the minority atom. But this structure occurs in about a dozen binary intermetallic systems. The formation of an ordered structure can significantly enhance the performance of the material, particularly the hardness. Pt- and Pd-rich ordered structures have been experimentally studied in the systems Pt/Pd-X where X is Ti, V, Cr, Zr, Nb, M, Hf, Ta, and W. We took a broader look at 80 Pt/Pd rich alloys to find new candidates for the 8:1 structure and have found about 20. In order to verify our predictions, we used the cluster expansion to find the stable structures. We first applied the cluster expansion to Pt-Hf and Pt-Mo because these two candidates are the most likely to form the 8:1 structure. These new candidates can have applications in the jewelry and catalysis industries.

  15. The Mechanism of Direct Formic Acid Fuel Cell Using Pd, Pt and Pt-Ru

    Science.gov (United States)

    Kamiya, Nobuyuki; Liu, Yan; Mitsushima, Shigenori; Ota, Ken-Ichiro; Tsutsumi, Yasuyuki; Ogawa, Naoya; Kon, Norihiro; Eguchi, Mika

    The electro-oxidation of formic acid, 2-propanol and methanol on Pd black, Pd/C, Pt-Ru/C and Pt/C has been investigated to clear the reaction mechanism. It was suggested that the formic acid is dehydrogenated on Pd surface and the hydrogen is occluded in the Pd lattice. Thus obtained hydrogen acts like pure hydrogen supplied from the outside and the cell performance of the direct formic acid fuel cell showed as high as that of a hydrogen-oxygen fuel cell. 2-propanol did not show such dehydrogenation reaction on Pd catalyst. Platinum and Pt-Ru accelerated the oxidation of C-OH of 2-propanol and methanol. Slow scan voltammogram (SSV) and chronoamperometry measurements showed that the activity of formic acid oxidation increased in the following order: Pd black > Pd 30wt.%/C > Pt50wt.%/C > 27wt.%Pt-13wt.%Ru/C. A large oxidation current for formic acid was found at a low overpotential on the palladium electrocatalysts. These results indicate that formic acid is mainly oxidized through a dehydrogenation reaction. For the oxidation of 2-propanol and methanol, palladium was not effective, and 27wt.%Pt-13wt.%Ru/C showed the best oxidation activity.

  16. An evaluation of Pt sulfite acid (PSA) as precursor for supported Pt catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Regalbuto, J.R.; Ansel, O.; Miller, J.T. (BP Res. Cntr.); (UIC)

    2010-11-12

    As a catalyst precursor, platinum sulfite acid (PSA) is easy to use and not relatively expensive, and is a potentially attractive precursor for many types of supported catalysts. The ultimate usefulness for many catalyst applications will depend on the extent that Pt can be dispersed and sulfur eliminated. To our knowledge, there exists no detailed characterization in the catalysis literature of PSA and the nanoparticulate Pt phases derived from it during catalyst pretreatment. To this end a series of supports including alumina, silica, magnesia, niobia, titania, magnesia and carbon were contacted with PSA solutions and subsequently analyzed with extended x-ray absorption fine structure (EXAFS) and x-ray absorption near edge structure (XANES) analysis, and x-ray photoelectron spectroscopy (XPS) to characterize the Pt species formed upon impregnation, calcination, and reduction. While all catalysts show retention of some S, reasonably small particle sizes with relatively little Pt-S can in some instances be produced using PSA. The amount of retained sulfur appears to decrease with decreasing surface acidity, although even the most acidic supports (niobia and silica) display some storage of S even while only Pt-O bands are observed after calcination or reoxidation. More sulfur was eliminated by high temperature calcinations followed by reduction in hydrogen, at the expense of increasing Pt particle size.

  17. Germanene termination of Ge2Pt crystals on Ge(110)

    NARCIS (Netherlands)

    Bampoulis, Pantelis; Zhang, Lijie; Safaei, A.; van Gastel, Raoul; Poelsema, Bene; Zandvliet, Henricus J.W.

    2014-01-01

    We have investigated the growth of Pt on Ge(1 1 0) using scanning tunneling microscopy and spectroscopy. The deposition of several monolayers of Pt on Ge(1 1 0) followed by annealing at 1100 K results in the formation of 3D metallic Pt-Ge nanocrystals. The outermost layer of these crystals exhibits

  18. 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.

  19. 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.

  20. Magnetic Properties and Nanostructures of FePtCu:C Thin Films with FePt Underlayers

    Institute of Scientific and Technical Information of China (English)

    JIN Ling-Fang; YAN Ming-Lang

    2007-01-01

    Magnetic properties and nanostructures of FePtCu:C thin films with FePt underlayers (ULs) are studied. The effect of FePt ULs on the orientation and magnetic properties of the thin films are investigated by adjusting FePt UL thicknesses from 2nm to 14nm. X-ray diffraction (XRD) scans reveal that the orientation of the films is dependent on FePt UL thickness. For a 5-nm FePtCu:C nanocomposite thin film with a 2-nm FePt UL, the coercivity is 6.5 KOe, the correlation length is 59nm, the desired face-centred-tetragonal (fct) ordered structure [L10 phase] is formed and the c axis normal to the film plane [(001) texture] is obtained. These results indicate that the better orientation and magnetic properties of the films can be tuned by decreasing the thickness of the FePt UL.

  1. Concave Pd-Pt Core-Shell Nanocrystals with Ultrathin Pt Shell Feature and Enhanced Catalytic Performance.

    Science.gov (United States)

    Zhang, Ying; Bu, Lingzheng; Jiang, Kezhu; Guo, Shaojun; Huang, Xiaoqing

    2016-02-10

    One-pot creation of unique concave Pd-Pt core-shell polyhedra has been developed for the first time using an efficient approach. Due to the concave feature and ultrathin Pt shell, the created Pd-Pt core-shell polyhedra exhibit enhanced catalytic performance in both the electrooxidation of methanol and hydrogenation of nitrobenzene, as compared with commercial Pt black and Pd black catalysts. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  2. 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

  3. 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.

  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. Asymmetric magnetic bubble expansion under in-plane field in Pt/Co/Pt : Effect of interface engineering

    NARCIS (Netherlands)

    Lavrijsen, R.; Hartmann, D. M. F.; van den Brink, Ton; Yin, Y.; Barcones, B.; Duine, R. A.|info:eu-repo/dai/nl/304830127; Verheijen, M. A.; Swagten, H. J. M.; Koopmans, B.

    2015-01-01

    We analyze the impact of growth conditions on the asymmetric magnetic bubble expansion under an in-plane field in ultrathin Pt/Co/Pt films. Specifically, using sputter deposition, we vary the Ar pressure during the growth of the top Pt layer. This induces a large change in the interfacial structure

  6. Asymmetric magnetic bubble expansion under in-plane field in Pt/Co/Pt : Effect of interface engineering

    NARCIS (Netherlands)

    Lavrijsen, R.; Hartmann, D. M. F.; van den Brink, Ton; Yin, Y.; Barcones, B.; Duine, R. A.; Verheijen, M. A.; Swagten, H. J. M.; Koopmans, B.

    2015-01-01

    We analyze the impact of growth conditions on the asymmetric magnetic bubble expansion under an in-plane field in ultrathin Pt/Co/Pt films. Specifically, using sputter deposition, we vary the Ar pressure during the growth of the top Pt layer. This induces a large change in the interfacial structure

  7. Pt Ru/C electrocatalysts prepared using electron beam irradiation

    Energy Technology Data Exchange (ETDEWEB)

    Silva, Dionisio Furtunato da; Oliveira Neto, Almir; Pino, Eddy Segura; Brandalise, Michele; Linardi, Marcelo; Spinace, Estevam Vitorio [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil)]. E-mail: espinace@ipen.br

    2007-10-15

    Pt Ru/C electrocatalysts (carbon-supported Pt Ru nanoparticles) were prepared submitting water/ethylene glycol mixtures containing Pt(IV) and Ru(III) ions and the carbon support to electron beam irradiation. The electrocatalysts were characterized by energy dispersive X ray analysis (EDX), X ray diffraction (XRD) and cyclic voltammetry and tested for methanol electro-oxidation aiming fuel cell application. The obtained Pt Ru/C electrocatalysts showed superior performance for methanol electro-oxidation at room temperature compared to commercial Pt Ru/C electrocatalyst. (author)

  8. Half-Lantern Pt(II and Pt(III Complexes. New Cyclometalated Platinum Derivatives

    Directory of Open Access Journals (Sweden)

    Violeta Sicilia

    2014-08-01

    Full Text Available The divalent complex [{Pt(bzq(μ-L}2] (1 [Hbzq = benzo[h]quinolone, HL = CF3C4H2N2SH: 4-(trifluoromethylpyrimidine-2-thiol] was obtained from equimolar amounts of [Pt(bzq(NCMe2]ClO4 and 4-(trifluoromethylpyrimidine-2-thiol with an excess of NEt3. The presence of a low intensity absorption band at 486 nm (CH2Cl2, assignable to a metal-metal-to-ligand charge transfer transition (1MMLCT [dσ*(Pt2→π*(bzq], is indicative of the existence of two platinum centers located in close proximity because the rigidity of the half-lantern structure allows the preservation of these interactions in solution. Compound 1 undergoes two-electron oxidation upon treatment with halogens X2 (X2: Cl2, Br2 or I2 to give the corresponding dihalodiplatinum (III complexes [{Pt(bzq(μ-LX}2] (L = CF3C4H2N2S-κN,S; X: Cl 2, Br 3, I 4. Complexes 2–4 were also obtained by reaction of 1 with HX (molar ratio 1:2, 10% excess of HX in THF with yields of about 80% and compound 2 was also obtained by reaction of [{Pt(bzq(μ-Cl}2] with HL (4-(trifluoromethylpyrimidine-2-thiol in molar ratio 1:2 in THF, although in small yield. The X-ray structures of 2 and 3 confirmed the half-lantern structure and the anti configuration of the molecules. Both of them show Pt–Pt distances (2.61188(15 Å 2, 2.61767(16 Å 3 in the low range of those observed in Pt2(III,IIIX2 half-lantern complexes.

  9. Direct determination of the ionization energies of PtC, PtO, and PtO2 with VUV radiation.

    Science.gov (United States)

    Citir, Murat; Metz, Ricardo B; Belau, Leonid; Ahmed, Musahid

    2008-10-02

    Photoionization efficiency curves were measured for gas-phase PtC, PtO, and PtO2 using tunable vacuum ultraviolet (VUV) radiation at the Advanced Light Source. The molecules were prepared by laser ablation of a platinum tube, followed by reaction with CH4 or N2O and supersonic expansion. These measurements provide the first directly measured ionization energy for PtC, IE(PtC) = 9.45 +/- 0.05 eV. The direct measurement also gives greatly improved ionization energies for the platinum oxides, IE(PtO) = 10.0 +/- 0.1 eV and IE(PtO2) = 11.35 +/- 0.05 eV. The ionization energy connects the dissociation energies of the neutral and cation, leading to greatly improved 0 K bond dissociation energies for the neutrals: D0(Pt-C) = 5.95 +/- 0.07 eV, D0(Pt-O) = 4.30 +/- 0.12 eV, and D0(OPt-O) = 4.41 +/- 0.13 eV, as well as enthalpies of formation for the gas-phase molecules DeltaH(0)(f,0)(PtC(g)) = 701 +/- 7 kJ/mol, DeltaH(0)(f,0)(PtO(g)) = 396 +/- 12 kJ/mol, and DeltaH(0)(f,0)(PtO2(g)) = 218 +/- 11 kJ/mol. Much of the error in previous Knudsen cell measurements of platinum oxide bond dissociation energies is due to the use of thermodynamic second law extrapolations. Third law values calculated using statistical mechanical thermodynamic functions are in much better agreement with values obtained from ionization energies and ion energetics. These experiments demonstrate that laser ablation production with direct VUV ionization measurements is a versatile tool to measure ionization energies and bond dissociation energies for catalytically interesting species such as metal oxides and carbides.

  10. Evaluasi Sistem Informasi Penjualan PT SPNS

    Directory of Open Access Journals (Sweden)

    Anderes Gui

    2010-06-01

    Full Text Available The purpose of this paper is to identify and analyze problems that occur in information systems sales PT SPNS. It also serves to control the management and control of applications running well so it can produce accurate information for decision making. The method used is book study method and field study. Study was done by reading library books, scientific papers and other sources, while the field study was done by observation, interviews, and questionnaires. The result of the evaluation is derived from the respective strengths and weaknesses - each control. Weaknesses are found, the findings presented in the form of a matrix that contains the findings and recommendations as a matter of risk remedial action. Conclusions obtained from the audit for security control, operations, limitations, input and output is good enough because it can satisfy and support the sales activities of PT SPNS.

  11. Revisiting the Optical PT-Symmetric Dimer

    Directory of Open Access Journals (Sweden)

    José Delfino Huerta Morales

    2016-08-01

    Full Text Available Optics has proved a fertile ground for the experimental simulation of quantum mechanics. Most recently, optical realizations of PT -symmetric quantum mechanics have been shown, both theoretically and experimentally, opening the door to international efforts aiming at the design of practical optical devices exploiting this symmetry. Here, we focus on the optical PT -symmetric dimer, a two-waveguide coupler where the materials show symmetric effective gain and loss, and provide a review of the linear and nonlinear optical realizations from a symmetry-based point of view. We go beyond a simple review of the literature and show that the dimer is just the smallest of a class of planar N-waveguide couplers that are the optical realization of the Lorentz group in 2 + 1 dimensions. Furthermore, we provide a formulation to describe light propagation through waveguide couplers described by non-Hermitian mode coupling matrices based on a non-Hermitian generalization of the Ehrenfest theorem.

  12. Revisiting the optical $PT$-symmetric dimer

    CERN Document Server

    Morales, J D Huerta; López-Aguayo, S; Rodríguez-Lara, B M

    2016-01-01

    Optics has proved a fertile ground for the experimental simulation of quantum mechanics. Most recently, optical realizations of $\\mathcal{PT}$-symmetric quantum mechanics have been shown, both theoretically and experimentally, opening the door to international efforts aiming at the design of practical optical devices exploiting this symmetry. Here, we focus on the optical $\\mathcal{PT}$-symmetric dimer, a two-waveguide coupler were the materials show symmetric effective gain and loss, and provide a review of the linear and nonlinear optical realizations from a symmetry based point of view. We go beyond a simple review of the literature and show that the dimer is just the smallest of a class of planar $N$-waveguide couplers that are the optical realization of Lorentz group in 2+1 dimensions. Furthermore, we provide a formulation to describe light propagation through waveguide couplers described by non-Hermitian mode coupling matrices based on a non-Hermitian generalization of Ehrenfest theorem.

  13. MANFAAT DATA WAREHOUSE PADA PT ABC

    Directory of Open Access Journals (Sweden)

    Evaristus Didik Madyatmadja

    2013-11-01

    Full Text Available The purpose of this paper is to analyze the current system to find out problems faced by the company and propose alternative solutions and generate information needed by management by designing a data warehouse according to the information needs of PT ABC. This research implements analysis and design of data warehouse by Ralph Kimball and Ross cited by Connolly and Begg, known as Nine-Step Methodology. The result obtained is a data warehouse application that may present a multidimensional historical data that can assist the management in decisions. Designing data warehouse at PT ABC makes concise the enterprise data and can be viewed from several dimensions. It helps users analyze data for strategic decision quickly and accurately.

  14. High Activity of Hexagonal Ag/Pt Nanoshell Catalyst for Oxygen Electroreduction

    Directory of Open Access Journals (Sweden)

    Lee Chien-Liang

    2008-01-01

    Full Text Available Abstract Hexagonal Ag/Pt nanoshells were prepared by using a hexagonal Ag nanoplate as the displacement template and by introducing Pt ions. The prepared Ag/Pt nanoshells played the role of an electrocatalyst in an oxygen reduction process. Compared to spherical Pt and Ag/Pt nanoparticles, the hexagonal Ag/Pt nanoshells showed higher activity for oxygen electroreduction.

  15. Relaxor-PT Single Crystal Piezoelectric Sensors

    OpenAIRE

    Xiaoning Jiang; Jinwook Kim; Kyugrim Kim

    2014-01-01

    Relaxor-PbTiO3 piezoelectric single crystals have been widely used in a broad range of electromechanical devices, including piezoelectric sensors, actuators, and transducers. This paper reviews the unique properties of these single crystals for piezoelectric sensors. Design, fabrication and characterization of various relaxor-PT single crystal piezoelectric sensors and their applications are presented and compared with their piezoelectric ceramic counterparts. Newly applicable fields and futu...

  16. 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.

  17. Spin Hall effects in mesoscopic Pt films with high resistivity

    Science.gov (United States)

    Qin, Chuan; Luo, Yongming; Zhou, Chao; Cai, Yunjiao; Jia, Mengwen; Chen, Shuhan; Wu, Yizheng; Ji, Yi

    2016-10-01

    The energy efficiency of the spin Hall effects (SHE) can be enhanced if the electrical conductivity is decreased without sacrificing the spin Hall conductivity. The resistivity of Pt films can be increased to 150-300 µΩ · cm by mesoscopic lateral confinement, thereby decreasing the conductivity. The SHE and inverse spin Hall effects (ISHE) in these mesoscopic Pt films are explored at 10 K by using the nonlocal spin injection/detection method. All relevant physical quantities are determined in situ on the same substrate, and a quantitative approach is developed to characterize all processes effectively. Extensive measurements with various Pt thickness values reveal an upper limit for the Pt spin diffusion length: {λ\\text{pt}}   ⩽  0.8 nm. The average product of {λ\\text{pt}} and the Pt spin Hall angle {α\\text{H}} is substantial: {α\\text{H}}{λ\\text{pt}}   =  (0.142  ±  0.040) nm for 4 nm thick Pt, though a gradual decrease is observed at larger Pt thickness. The results suggest enhanced spin Hall effects in resistive mesoscopic Pt films.

  18. Fabrication of monometallic (Co, Pd, Pt, Au) and bimetallic (Pt/Au, Au/Pt) thin films with hierarchical architectures as electrocatalysts

    Science.gov (United States)

    Qiu, Cuicui; Zhang, Jintao; Ma, Houyi

    2010-05-01

    Co thin films with novel hierarchical structures were controllably fabricated by simple electrochemical deposition in the absence of hard and soft templates, which were used as sacrificial templates to further prepare noble metal (Pd, Pt, Au) hierarchical micro/nanostructures via metal exchange reactions. SEM characterization demonstrated that the resulting noble metal thin films displayed hierarchical architectures. The as-prepared noble metal thin films could be directly used as the anode catalysts for the electro-oxidation of formic acid. Moreover, bimetallic catalysts (Pt/Au, Au/Pt) fabricated based on the monometallic Au, Pt micro/nanostructures exhibited the higher catalytic activity compared to the previous monometallic catalysts.

  19. XAS and XMCD studies of magnetic properties modifications of Pt/Co/Au and Pt/Co/Pt trilayers induced by Ga⁺ ions irradiation.

    Science.gov (United States)

    Mazalski, Piotr; Sveklo, Iosif; Kurant, Zbigniew; Ollefs, Katharina; Rogalev, Andrei; Wilhelm, Fabrice; Fassbender, Juergen; Baczewski, Lech Tomasz; Wawro, Andrzej; Maziewski, Andrzej

    2015-05-01

    Magnetic and magneto-optical properties of Pt/Co/Au and Pt/Co/Pt trilayers subjected to 30 keV Ga(+) ion irradiation are compared. In two-dimensional maps of these properties as a function of cobalt thickness and ion fluence, two branches with perpendicular magnetic anisotropy (PMA) for Pt/Co/Pt trilayers are well distinguished. The replacement of the Pt capping layer with Au results in the two branches still being visible but the in-plane anisotropy for the low-fluence branch is suppressed whereas the high-fluence branch displays PMA. The X-ray absorption spectra and X-ray magnetic circular dichroism (XMCD) spectra are discussed and compared with non-irradiated reference samples. The changes of their shapes and peak amplitude, particularly for the high-fluence branch, are related to the modifications of the local environment of Co(Pt) atoms and the etching effects induced by ion irradiation. Additionally, in irradiated trilayers the XMCD measurements at the Pt L2,3-edge reveal an increase of the magnetic moment induced in Pt atoms.

  20. Nonlinear waves in $\\cal PT$-symmetric systems

    CERN Document Server

    Konotop, Vladimir V; Zezyulin, Dmitry A

    2016-01-01

    Recent progress on nonlinear properties of parity-time ($\\cal PT$-) symmetric systems is comprehensively reviewed in this article. $\\cal PT$ symmetry started out in non-Hermitian quantum mechanics, where complex potentials obeying $\\cal PT$ symmetry could exhibit all-real spectra. This concept later spread out to optics, Bose-Einstein condensates, electronic circuits, and many other physical fields, where a judicious balancing of gain and loss constitutes a $\\cal PT$-symmetric system. The natural inclusion of nonlinearity into these $\\cal PT$ systems then gave rise to a wide array of new phenomena which have no counterparts in traditional dissipative systems. Examples include the existence of continuous families of nonlinear modes and integrals of motion, stabilization of nonlinear modes above $\\cal PT$-symmetry phase transition, symmetry breaking of nonlinear modes, distinctive soliton dynamics, and many others. In this article, nonlinear $\\cal PT$-symmetric systems arising from various physical disciplines ...

  1. 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.

  2. Highly durable graphene nanoplatelets supported Pt nanocatalysts for oxygen reduction

    Energy Technology Data Exchange (ETDEWEB)

    Shao, Yuyan; Zhang, Sheng; Wang, Chongmin; Nie, Zimin; Liu, Jun; Lin, Yuehe [Pacific Northwest National Laboratory, Richland, WA 99352 (United States); Wang, Yong [Pacific Northwest National Laboratory, Richland, WA 99352 (United States); The Gene and Linda Voiland School of Chemical Engineering and Bioengineering, Washington State University, Pullman, WA 99164 (United States)

    2010-08-01

    We report graphene nanoplatelets (GNPs), which exhibit the advantages of both single-layer graphene and highly graphitic carbon, as a durable alternative support material for Pt nanoparticles for oxygen reduction in fuel cells. Pt nanoparticles are deposited on poly(diallyldimethylammonium chloride) (PDDA)-coated GNP, and characterized with transmission electron microscopy, X-ray diffraction, Raman spectra, and electrochemical tests. Pt/GNP exhibits greatly enhanced electrochemical durability (2-3 times that of Pt/CNT and commercial Etek Pt/C). These are attributed to the intrinsic high graphitization degree of GNP and the enhanced Pt-carbon interaction in Pt/GNP. If considering that GNP can be easily mass produced from graphite, GNP is a promising, low-cost, and durable electrocatalyst support for oxygen reduction in fuel cells. (author)

  3. Peningkatan Prestasi Belajar CAD Mahasiswa Teknik Otomotif Non-Reguler FT UNY melalui Pembuatan “Pohon Kata” Perintah dalam Program AutoCAD

    Directory of Open Access Journals (Sweden)

    Martubi Martubi

    2010-05-01

    Full Text Available Penelitian ini bertujuan meningkatkan prestasi belajar mata kuliah Computer Aided Design (CAD mahasiswa prodi Teknik Otomotif Non-Reguler yang dinyatakan dalam bentuk rerata nilai akhir semester yang berasal dari komponen nilai tugas harian, nilai ujian tengah semester dan nilai ujian akhir semester. Penelitian quasi-eksperimen ini terdiri dari tahapan penelitian diawali dengan penyusunan materi pembelajaran sejumlah pokok bahasan tertentu dalam satu job sheet (lembar kerja, dilanjutkan dengan pembuatan bantuan “Pohon Kata” perintah dalam Auto CAD kepada kelas eksperimen yang ditentukan secara random dari dua kelas peserta kuliah Auto CAD pada Semester Genap 2008/2009. Kedua kelas diamati prestasinya, baik kecepatan penyelesaiannya maupun kualitas kebenaran gambarnya. Prestasi belajar kedua kelas juga diukur melalui pemberian ujian tengah semester dan ujian akhir semester. Setelah data prestasi kedua kelas terkumpul dilanjutkan dengan analisis statistik melalui uji beda (t-test setelah sebelumnya dilakukan uji persyaratan analisis yang ternyata dapat dipenuhi. Hasil penelitian ini disimpulkan bahwa: prestasi belajar CAD mahasiswa pada kelas yang diberi perlakuan strategi pembelajaran menggunakan “Pohon Kata” perintah dalam Program Auto CAD lebih baik dibanding prestasi belajar CAD mahasiswa pada kelas yang tidak diberi perlakuan (75,41>70,89, dengan demikian pembelajaran CAD menggunakan media “Pohon Kata” perintah dalam Program Auto CAD dapat meningkatkan prestasi belajar mahasiswa Teknik Otomotif Program Non-Reguler.

  4. PT-Symmetric Quantum Electrodynamics and Unitarity

    CERN Document Server

    Milton, Kimball A; Parashar, Prachi; Pourtolami, Nima; Wagner, J

    2012-01-01

    More than 15 years ago, a new approach to quantum mechanics was suggested, in which Hermiticity of the Hamiltonian was to be replaced by invariance under a discrete symmetry, the product of parity and time-reversal symmetry, $\\mathcal{PT}$. It was shown that if $\\mathcal{PT}$ is unbroken, energies were, in fact, positive, and unitarity was satisifed. Since quantum mechanics is quantum field theory in 1 dimension, time, it was natural to extend this idea to higher-dimensional field theory, and in fact an apparently viable version of $\\mathcal{PT}$-invariant quantum electrodynamics was proposed. However, it has proved difficult to establish that the unitarity of the scattering matrix, for example, the K\\"all\\'en spectral representation for the photon propagator, can be maintained in this theory. This has led to questions of whether, in fact, even quantum mechanical systems are consistent with probability conservation when Green's functions are examined, since the latter have to possess physical requirements of ...

  5. Density functional theory studies of the adsorption of ethylene and oxygen on Pt(111) and Pt3Sn(111)

    DEFF Research Database (Denmark)

    Watwe, R.M.; Cortright, R.D.; Mavrikakis, Manos

    2001-01-01

    of pi -bonded ethylene, di-sigma -bonded ethylene, and ethylidyne species are weaker on Pt3Sn(111) than on Pt(111) by 21, 31, and 50 kJ/mol, respectively. Hence, the electronic effect of Sn on the adsorption of ethylene depends on the type of adsorption site, with adsorption on three-fold site weakened......Density functional theory, employing periodic slab calculations, was used to investigate the interactions of ethylene and oxygen with Pt(111) and Pt3Sn(111). The predicted energetics and structures of adsorbed species on Pt(111) are in good agreement with experimental data. The binding energies...

  6. Pt skin on AuCu intermetallic substrate: a strategy to maximize Pt utilization for fuel cells.

    Science.gov (United States)

    Wang, Gongwei; Huang, Bing; Xiao, Li; Ren, Zhandong; Chen, Hao; Wang, Deli; Abruña, Héctor D; Lu, Juntao; Zhuang, Lin

    2014-07-09

    The dependence on Pt catalysts has been a major issue of proton-exchange membrane (PEM) fuel cells. Strategies to maximize the Pt utilization in catalysts include two main approaches: to put Pt atoms only at the catalyst surface and to further enhance the surface-specific catalytic activity (SA) of Pt. Thus far there has been no practical design that combines these two features into one single catalyst. Here we report a combined computational and experimental study on the design and implementation of Pt-skin catalysts with significantly improved SA toward the oxygen reduction reaction (ORR). Through screening, using density functional theory (DFT) calculations, a Pt-skin structure on AuCu(111) substrate, consisting of 1.5 monolayers of Pt, is found to have an appropriately weakened oxygen affinity, in comparison to that on Pt(111), which would be ideal for ORR catalysis. Such a structure is then realized by substituting the Cu atoms in three surface layers of AuCu intermetallic nanoparticles (AuCu iNPs) with Pt. The resulting Pt-skinned catalyst (denoted as Pt(S)AuCu iNPs) has been characterized in depth using synchrotron XRD, XPS, HRTEM, and HAADF-STEM/EDX, such that the Pt-skin structure is unambiguously identified. The thickness of the Pt skin was determined to be less than two atomic layers. Finally the catalytic activity of Pt(S)AuCu iNPs toward the ORR was measured via rotating disk electrode (RDE) voltammetry through which it was established that the SA was more than 2 times that of a commercial Pt/C catalyst. Taking into account the ultralow Pt loading in Pt(S)AuCu iNPs, the mass-specific catalytic activity (MA) was determined to be 0.56 A/mg(Pt)@0.9 V, a value that is well beyond the DOE 2017 target for ORR catalysts (0.44 A/mg(Pt)@0.9 V). These findings provide a strategic design and a realizable approach to high-performance and Pt-efficient catalysts for fuel cells.

  7. Characterization of FePt nanoparticles in FePt/C multilayers

    Energy Technology Data Exchange (ETDEWEB)

    Barradas, N.P. E-mail: nunoni@itn.mces.pt; Alves, E.; Babonneau, D

    2004-06-01

    The areal density growth of recording media is expected to reach 100 Gbit/in.{sup 2} within a few years. Such high densities require magnetic grain sizes of 10 nm or less, which is close to the superparamagnetic limit of current media. Therefore, in order to retain thermal stability, it is essential to use a magnetic material with high anisotropy energy. Ordered metallic phases such as FePt and CoPt, which have very large magnetocrystalline anisotropy, are regarded as attractive candidates. We have deposited at different temperatures by ion beam sputtering C/(FePt/C){sub x20} multilayers, with nominal thickness t{sub C}=4 nm and t{sub FePt}=1 nm. The FePt consists of nanoparticles embedded in the C matrix. Using Rutherford backscattering at grazing angles of incidence, we determined the stoichiometry of the nanoparticles, the multilayer periodicity and the nanoparticle height. We compare the results with X-ray reflectivity, grazing incidence small-angle X-ray scattering, and transmission electron microscopy results.

  8. Pt/Mesoporous Carbon Counter Electrode with a Low Pt Loading for High-Efficient Dye-Sensitized Solar Cells

    Directory of Open Access Journals (Sweden)

    Guiqiang Wang

    2010-01-01

    Full Text Available Pt/Mesoporous carbon counter electrodes with a low Pt loading for dye-sensitized solar cells were fabricated by coating Pt/mesoporous carbon on fluorine-doped tin oxide glass. Pt/mesoporous carbon samples were prepared by reducing H2PtCl6 with NaBH4 in mesoporous carbon and characterized by N2 adsorption analysis, X-ray diffraction, X-ray photoelectron spectroscopy, and transmission electron microscopy. The Pt particles deposited on mesoporous carbon support were found to be in uniform shape and narrow range of particle size. Low-Pt-loading Pt/mesoporous carbon counter electrode showed a high electrocatalytic activity for triiodide reduction. Electrochemical impedance spectroscopy measurement displayed a low charge-transfer resistance of 1.2 Ωcm2 for 1-Pt/mesoporous carbon counter electrode. Dye-sensitized solar cells based on the 1-Pt/mesoporous carbon counter electrode achieved an overall conversion efficiency of 6.62% under one sun illumination, which is higher than that of the cell with the conventional Pt counter electrode.

  9. Property comparison of a CoSiB/Pt multilayer to Co/Pt and CoFe/Pt with perpendicular magnetic anisotropy

    Energy Technology Data Exchange (ETDEWEB)

    Jeong, S.; Yim, H. I. [Sookmyung Women' s University, Seoul (Korea, Republic of)

    2011-07-15

    We have investigated the perpendicular magnetic anisotropy of a [CoSiB t{sub CoSiB}/Pt 14 A]{sub 5} multilayer as a function of the CoSiB thickness. We have studied the perpendicular magnetic anisotropy of [Co t{sub Co}/Pt 15 A]{sub 5} and [CoFe t{sub CoFe}/Pt 10 A]{sub 5} multilayers for various thicknesses of Co and CoFe. Furthermore, we have measured and compared the coercivities and the saturation magnetizations of all samples. In this study, samples were [Co t{sub Co} /Pt 15 A]{sub 5}, [CoFe t{sub CoFe}/Pt 10 A]{sub 5} and [CoSiB t{sub CoSiB} /Pt 14 A]{sub 5} with t = 2, 3, 4, and 5 A. The coercivities and the saturation magnetizations were obtained 223.76 Oe and 341.25 emu/cm{sup 3}, 395.86 Oe and 286.79 emu/cm{sup 3} and 155.13 Oe and 429.98 emu/cm{sup 3} in CoSiB/Pt, Co/Pt and CoFe/Pt mutilayers, respectively. The maximum coercivity was obtained 395.86 Oe in the [Co 3 A /Pt 15 A]{sub 5} multilayer, and the minimum saturation magnetization was 286.79 emu/cm{sup 3} in the [Co 2 A /Pt 15 A]{sub 5} multilayer.

  10. Pt- and FePt- nanoparticles on the basis of emulsion techniques

    Energy Technology Data Exchange (ETDEWEB)

    Manzke, Achim; Wiedemann, Stefan; Enderle, Fabian; Plettl, Alfred; Ziemann, Paul [Institut fuer Festkoerperphysik, Universitaet Ulm (Germany); Schreiber, Eyk; Ziener, Ulrich [Institut fuer Organische Chemie III, Universitaet Ulm (Germany); Vogel, Nicolas; Landfester, Katharina [MPI fuer Polymerforschung, Mainz (Germany); Biskupek, Johannes; Kaiser, Ute [Materialwissenschaftliche Elektronenmikroskopie, Universitaet Ulm (Germany)

    2010-07-01

    Metal-precursor loaded colloidal polystyrene (PS) particles in aqueous solution are produced by an emulsion and miniemulsion technique, respectively. We report on colloids loaded with Pt- as well as with Fe- and Pt-complexes. After deposition of a hexagonally ordered monolayer of PS spheres on top of a silicon substrate, optimized plasma and temper sequences are applied to obtain metallic nanoparticles which still exhibit the original lateral order. The metal content within a colloid defines the size of the final particle, which could be varied between 6 and 14 nm, so far. The interparticle distance is determined by the diameter of the starting PS-particles and was varied between 80 and 250 nm. Different process steps are investigated by HRSEM, HRTEM and XPS giving insight in the plasma- and annealing process and demonstrating e.g. the crystalline structure of the Pt- nanoparticles.

  11. Selective formation of tetrahedral Pt nanocrystals from K2PtCl6/PVP

    Institute of Scientific and Technical Information of China (English)

    YU Yingtao; XU Boqing

    2003-01-01

    Tetrahedral platinum (Pt) nanocrystals (3-8 nm) are synthesized in high selectivity (ca. 80%) from hydrogen reduction of aqueous K2PtCl6 by using polyvinylpyrrolidone (PVP: Mw≈360000) as a protector. Morphology (TEM) measurements of the metal colloids and UV-Vis absorption of the colloidal solution are employed to monitor the tetrahedron formation during the syntheses with varying K2PtCl6/PVP ratios. The results clearly show a two-stage process for the selective formation of tetrahedral nanocrystals. Rapid nucleation and crystal formation at the early stage result in round-like crystallites and the external facet evolution in thereafter slow crystal growth leads selectively to the formation of the tetrahedrons.

  12. Nanospheres caped Pt(II and Pt (IV: synthesis and evaluation as antimicrobial and Antifungal Agent

    Directory of Open Access Journals (Sweden)

    Öğütçü Hatice

    2017-03-01

    Full Text Available Antimicrobial and antifungal polymers are gaining the attention of pharmaceutical makers and industrial design. Nanospheres-Polymers attached Platinum(II / (IV complexes have been synthesized to investigate antimicrobial activities. Firstly, nanospheres involving Schiff bases were synthesized from (aminomethyl polystyrene and four substitute salicylaldehyde (2-hydroxy benzaldehyde, 5-fluoro-2-hydroxy benzaldehyde, 5-kloro-2-hydroxy benzaldehyde, 5-bromo-2-hydroxy benzaldehyde. Secondly, polymers attached Platinum(II / (IV complexes have been prepared by means of template method. The IR spectra show that the ligands act in a monovalent bidentate fashion all nanospheres involving Schiff bases. Square-planar and octahedral structures are proposed for Pt(II and Pt(IV, respectively. All these substances have been examined for antibacterial activity against pathogenic strains, and antifungal activity. In particular, Pt(IV complexes were more potent bactericides than all of the synthesized substances.

  13. Effects of anisotropic diffusion and finite island sizes in homoepitaxial growth Pt on Pt(100)-hex

    DEFF Research Database (Denmark)

    Mortensen, Jens Jørgen; Linderoth, T.R.; Jacobsen, Karsten Wedel

    1998-01-01

    size is i=1 and that the mobility of dimers is negligible. Furthermore, an early onset of island coalescence is revealed. From the scaling of the measured saturation island density, N-x similar to(R/h)(chi), where h = v exp(-E-d/k(B)T) is the adatom hopping rate, an effective barrier for diffusion of E......The diffusion, nucleation, and growth of Pt on the hexagonally reconstructed Pt(100)-hex surface are investigated. By means of Scanning Tunneling Microscopy (STM), the positions, sizes, and number densities of monoatomically high, rectangular. reconstructed Pt islands, formed in the submonolayer...... of the determined island positions, it is revealed that the islands are distributed with long/short correlation lengths along, perpendicular to the reconstruction channels. The autocorrelation analysis allows us to quantify the degree of anisotropy in adatom diffusion. Island size distributions obtained...

  14. Study of Hydrogen Adsorption on Pt/WO3-ZrO2 through Pt Sites

    Institute of Scientific and Technical Information of China (English)

    Sugeng Triwahyono; Aishah Abdul Jalil; Hideshi Hattori

    2007-01-01

    The rate determining step and the energy barrier involved in hydrogen adsorption on Pt/WO3ZrO2 were studied based on the assumption that the hydrogen adsorption occurs only through Pt sites.The rate of hydrogen adsorption on Pt/WO3-ZrO2 Was measured in the adsorption temperature range of 323-573 K and an initial hydrogen pressure of 50 Torr.The rates of hydrogen uptake were very high for the initial few minutes and the adsorption continued for more than 5 h below 523 K.The hydrogen uptake far exceeded the H/Pt ratio of unity for all adsorption temperatures,indicating that the adsorption of hydrogen involved the dissociative adsorption of hydrogen on Pt sites to form hydrogen atoms.the spillover of hydrogen atoms onto the surface of the WO3-ZrO2 catalyst.the diffusion of spiltover hydrogen atom over the surface of the WO3-ZrO2 catalyst,and the formation of protonic acid site originated from hydrogen atom by releasing an electron in which the electron may react with a second hydrogen atom to form a hydride near the Lewis acid site.The rate determining step was the spillover with the activation energy of 12.3 kJ/mol.The rate of hydrogen adsorption cannot be expressed by the rate equation based on the assumption that the rate determining step is the surface diffusion.The activity of Pt/WO3-ZrO2 Was examined on n-heptane isomerization in which the increase of hydrogen partial pressure provided positive-effect on the conversion of n-heptane and negative-effect on the selectivity towards iso-heptane.

  15. The role of the cationic Pt sites in the adsorption properties of water and ethanol on the Pt4/Pt(111) and Pt4/CeO2(111) substrates: A density functional theory investigation

    Science.gov (United States)

    Seminovski, Yohanna; Tereshchuk, Polina; Kiejna, Adam; Da Silva, Juarez L. F.

    2016-09-01

    Finite site platinum particles, Ptn, supported on reduced or unreduced cerium oxide surfaces, i.e., CeO2-x(111) ( 0 CeO2-x has been improved in the last years; however, the identification of the active sites on the Ptn/CeO2-x(111) substrates is still far from complete. In this work, we applied density functional theory based calculations with the addition of the on-site Coulomb interactions (DFT+U) for the investigation of the active sites and the role of the Pt oxidation state on the adsorption properties of water and ethanol (probe molecules) on four selected substrates, namely, Pt(111), Pt4/Pt(111), CeO2(111), and Pt4/CeO2(111). Our results show that water and ethanol preferentially bind in the cationic sites of the base of the tetrahedron Pt4 cluster instead of the anionic lower-coordinated Pt atoms located on the cluster-top or in the surface Ce (cationic) and O (anionic) sites. The presence of the Pt4 cluster contributes to increase the adsorption energy of both molecules on Pt(111) and CeO2(111) surfaces; however, its magnitude increases less for the case of Pt4/CeO2(111). Thus, the cationic Pt sites play a crucial role in the adsorption properties of water and ethanol. Both water and ethanol bind to on-top sites via the O atom and adopt parallel and perpendicular configurations on the Pt(111) and CeO2(111) substrates, respectively, while their orientation is changed once the Pt4 cluster is involved, favoring H binding with the surface sites.

  16. Magnetic field and temperature control over Pt/Co/Ir/Co/Pt multistate magnetic logic device

    Science.gov (United States)

    Morgunov, R.; Hamadeh, A.; Fachec, T.; Lvovaa, G.; Koplak, O.; Talantsev, A.; Mangin, S.

    2017-04-01

    Magnetic configurations in Pt/Co/Ir/Co/Pt synthetic ferrimagnet bilayer of strong perpendicular anisotropy have been systematically studied. Magnetization versus field hysteresis loops have been measured for different temperatures ranging from 5 to 300 K. The applied field - temperature (H-T) magnetization switching diagram has been constructed by extracting the different switching fields as a function of temperature. This switching diagram can be well explained by considering the competition between energy barrier of layer's magnetization reversal, interlayer exchange coupling, and Zeeman energy.

  17. Tunable interface anisotropy in a Pt/CO1-xFex/Pt multilayer

    Institute of Scientific and Technical Information of China (English)

    Chen Yong-Yong; Shi Zhong; Zhou Shi-Ming; Rui Wen-Bin; Du Jun

    2013-01-01

    Interfacial magnetic anisotropy in a Pt/Co1-xFex/Pt multilayer is tuned by doping iron atoms into the cobalt layer.The perpendicular magnetic anisotropy and out-of-plane coercivity are found to decrease with increasing x.For a specific x,the out-of-plane coercivity acquires a maximal value as a function of the thickness of the CoFe layer.At low temperature,the coercivity is enhanced.Small coercivity but reasonably large perpendicular magnetic anisotropy can be obtained by controlling the x and CoFe layer thickness.

  18. Modeling the electro-oxidation of CO and H2/CO on Pt, Ru, PtRu and Pt3Sn

    DEFF Research Database (Denmark)

    Liu, Ping; Logadottir, Ashildur; Nørskov, Jens Kehlet

    2003-01-01

    is developed to describe the electro-oxidation of CO and H-2 at conditions relevant to the anode of a PEM fuel cell. The model is very simple and allows us to express the kinetics of a promoted anode surface relative to the activity of pure Pt directly from the calculated adsorption energy differences...... geometry is the same. This ligand effect is ascribed to changes in the electronic structure of the surface atoms due to interactions with the surroundings, and the physical origin of the effect is discussed. The calculated adsorption energetics is used as input into a simple kinetic model, which....... In agreement with experiments, the model shows Ru, PtRu and Pt3Sn to start oxidizing CO at lower potentials than Pt. In addition, the model shows PtRu to have a considerably lower overpotential for H-2 oxidation in the presence of CO than Pt. Pt3Sn is even better than PtRu, while Ru is found to be considerably...

  19. 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.

  20. Exchange interaction in L10-ordered FePt and CoPt from first-principles

    Science.gov (United States)

    Liu, X. B.; Altounian, Z.

    2011-04-01

    The exchange interactions have been studied from a first-principles density functional calculation in FePt and CoPt with the tetragonal L10-type structure. For FePt, the effective exchange parameters of Fe at the sites 1a and 1c, JFe1a and JFe1c, have the same negative value (-1.40 mRy) while that between Fe (1a) and Fe (1c), JFe1a -1c, have a large positive value (8.29 mRy) and JFe-Pt also has a positive value (1.20 mRy). Similarly, for CoPt, the exchange parameters are JCo1a = JCo1c = -0.86 mRy, JCo1a -1c = 8.47 mRy and JCo-Pt = 1.30 mRy. The estimated mean fields TC are about 802 K and 870 K for FePt and CoPt, respectively, in good agreement with the experiments. TC shows peak value at c/a = 1 in FePt and CoPt, respectively, resulting from the interplay between negative and positive exchange interactions.

  1. Synthesis of Pt and Pt-Fe nanoparticles supported on MWCNTs used as electrocatalysts in the methanol oxidation reaction

    Institute of Scientific and Technical Information of China (English)

    J.R.Rodriguez; R.M.F´elix; E.A.Reynoso; Y.Gochi-Ponce; Y.Verde Gómez; S.Fuentes Moyado; G.Alonso-N ´uñez

    2014-01-01

    This work reports a feasible synthesis of highly-dispersed Pt and Pt-Fe nanoparticles supported on multiwall carbon nanotubes (MWCNTs) without Fe and multiwall carbon nanotubes with iron (MWCNTs-Fe) which applied as electrocatalysts for methanol electrooxidation. A Pt coordination complex salt was synthesized in an aqueous solution and it was used as precursor to prepare Pt/MWCNTs, Pt/MWCNTs-Fe, and Pt-Fe/MWCNTs using FeCl2·4H2O as iron source which were named S1, S2 and S3, respectively. The coordination complex of platinum (TOA)2PtCl6 was obtained by the chemical reaction between (NH4)2PtCl6 with tetraoctylammonium bromide (TOAB) and it was characterized by FT-IR and TGA. The materials were characterized by Raman spectroscopy, SEM, EDS, XRD, TEM and TGA. The electrocatalytic activity of Pt-based supported on MWCNTs in the methanol oxidation was investigated by cyclic voltammetry (CV) and chronoamperometry (CA). Pt-Fe/MWCNTs electrocatalysts showed the highest electrocatalytic activity and stability among the tested electrocatalysts due to that the addition of”Fe”promotes the OH species adsorption on the electrocatalyst surface at low potentials, thus, enhancing the activity toward the methanol oxidation reaction (MOR).

  2. Colloidal Toolbox Synthesis of Pt Nanoalloys

    DEFF Research Database (Denmark)

    Spanos, Ioannis

    and then dealloying them. Even without postheat treatment, the observed catalytic activity enhancement was significant after acid treatment,indicating that dealloying plays a crucial catalytic role, without having a detrimental effect on thestructure of the NPs. Apart from alloying though; changing the interparticle......, here raises the question, if such small NPs have a defined crystalstructure capable to justify such an effect on the catalytic activity of nanoalloys. X-rayPhotoelectron Diffraction (XPD) spectroscopy measurements connect the thermal and staticdisplacement of Pt atoms within the crystal lattice of Ptx...

  3. Carbon supported Pt-Y electrocatalysts for the oxygen reduction reaction

    Energy Technology Data Exchange (ETDEWEB)

    Jeon, Min Ku; McGinn, Paul J. [Department of Chemical and Biomolecular Engineering, University of Notre Dame, Notre Dame, IN 46556 (United States)

    2011-02-01

    Carbon supported Pt{sub 3}Y (Pt{sub 3}Y/C) and PtY (PtY/C) were investigated as oxygen reduction reaction (ORR) catalysts. After synthesis via reduction by NaBH{sub 4}, the alloy catalysts exhibited 10-20% higher mass activity (mA mg{sub Pt}{sup -1}) than comparably synthesized Pt/C catalyst. The specific activity ({mu}A cm{sub Pt}{sup -2}) was 23 and 65% higher for the Pt{sub 3}Y/C and PtY/C catalysts, respectively, compared to Pt/C. After annealing at 900 C under a reducing atmosphere, Pt{sub 3}Y/C-900 and PtY/C-900 catalysts showed improved ORR activity; the Pt/C and Pt/C-900 (Pt/C catalyst annealed at 900 C) catalysts exhibited specific activities of 334 and 393 {mu}A cm{sub Pt}{sup -2}, respectively, while those of the Pt{sub 3}Y/C-900 and PtY/C-900 catalysts were 492 and 1050 {mu}A cm{sub Pt}{sup -2}, respectively. X-ray diffraction results revealed that both the Pt{sub 3}Y/C and PtY/C catalysts have a fcc Pt structure with slight Y doping. After annealing, XRD showed that more Y was incorporated into the Pt structure in the Pt{sub 3}Y/C-900 catalyst, while the PtY/C-900 catalyst remained unchanged. Although these results suggested that the high ORR activity of the PtY/C-900 catalyst did not originate from Pt-Y alloy formation, it is clear that the Pt-Y system is a promising ORR catalyst which merits further investigation. (author)

  4. 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.

  5. Hydrodeoxygenation of Guaiacol Over Pt/Al-SBA-15 Catalysts.

    Science.gov (United States)

    Yu, Mi Jin; Park, Sung Hoon; Jeon, Jong-Ki; Ryu, Changkook; Sohn, Jung Min; Kim, Sang Chai; Park, Young-Kwon

    2015-01-01

    Upgrading of bio-oil through catalytic hydrodeoxygenation (HDO) reaction was investigated for guaiacol as a model compound. A batch reactor was used for the reaction condition of 40 bar and 250 degrees C. The target product was cyclohexane. Pt/Al-SBA-15 with the Si/Al ratios of 20, 40, and 80 and Pt/HZSM-5 were used as the catalyst. The SBA-15 catalysts were characterized by N2 adsorption-desorption, X-ray diffraction analysis, and temperature programmed desorption of ammonia. The order of cyclohexane yield was Pt/Al-SBA-15 (Si/Al = 20) > Pt/Al-SBA-15(40) > Pt/Al-SBA-15 (80), indicating that the quantity of acid sites plays an important role in the HDO reaction. On the other hand, Pt/HZSM-5 led to a very low cyclohexane yield, in spite of its abundant strong acid sites, due to its small pore size.

  6. Spin Waves Excitations of Co/Pt Multilayers

    Directory of Open Access Journals (Sweden)

    W. Zhou

    2012-01-01

    Full Text Available The present work investigated interlayer couplings of [Co(20 Å/Pt(30 Å]5, [Co(4 Å/Pt(7 Å]30, and [Co(4 Å/Pt(9 Å]30 multilayers with strong perpendicular magnetic anisotropy (PMA. Brillouin light scattering measurements were utilized to obtain spin waves of these samples with in-plane external magnetic fields. Interlayer couplings were found to be very sensitive to Pt thickness change from 7 Å to 9 Å, which implies that Pt atoms were more difficult to be polarized to provide interlayer coupling between Co layers than in the perpendicular external magnetic field situation. When Pt layer is 30 Å, the observed single spin wave can confirm the disappearance of interlayer coupling even when Co layer thickness is 20 Å.

  7. Pt Ru/C electrocatalysts prepared using electron beam irradiation

    Energy Technology Data Exchange (ETDEWEB)

    Silva, Dionisio F.; Oliveira Neto, Almir; Pino, Eddy S.; Brandalise, Michele; Linardi, Marcelo; Spinace, Estevam V. [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil)]. E-mails: dfsilva@ipen.br; espinace@ipen.br

    2007-07-01

    Pt Ru/C electrocatalysts (carbon-supported Pt Ru nanoparticles) were prepared submitting water/ethylene glycol solutions containing Pt(IV) and Ru(III) ions and the carbon support to electron beam irradiation. The water/ethylene glycol ratio (v/v) was evaluated as synthesis parameters. The Pt Ru/C electrocatalysts were prepared with a nominal Pt:Ru atomic ratio of 50:50 and were characterized by energy dispersive X-ray analysis (EDX) and X-ray diffraction (XRD) and tested for methanol electro-oxidation using cyclic voltammetry and chronoamperometry. The obtained Pt Ru/C electrocatalysts showed the typical fcc structure of platinum-ruthenium alloys and the electrocatalytic activity depends on the water/ethylene glycol ratio used in the preparation.

  8. Electronic and Magnetic Properties of Ultrathin Au/Pt Nanowires

    Energy Technology Data Exchange (ETDEWEB)

    Teng, X.; Feygenson, M; Wang, Q; He, J; Du, W; Frenkel, A; Han, W; Aronson, M

    2009-01-01

    We have reported the synthesis of Au25Pt75 and Au48Pt52 alloyed ultrathin nanowires with average widths of less than 3 nm via a wet chemistry approach at room temperature. Using a combination of techniques, including scanning transmission electron microscopy equipped with X-ray energy dispersive spectroscopy, ultraviolet-visible spectroscopy, and X-ray absorption near-edge structure and extended X-ray absorption fine structure spectroscopies, we identified the stoichiometry-dependent heterogeneous crystalline structures, as well as electronic structures with respect to the charge transfer between Pt and Au within both nanowires. In particular, we observed d-charge depletion at the Au site and the d-charge gain at the Pt site in Au48Pt52 nanowires, which accounted for its ferromagnetic magnetic behavior, in contrast to the paramagnetism and diamagnetism appearing respectively in bulk Pt and Au.

  9. Electronic and magnetic properties of ultrathin Au/Pt nanowires.

    Science.gov (United States)

    Teng, Xiaowei; Feygenson, Mikhail; Wang, Qi; He, Jiaqing; Du, Wenxin; Frenkel, Anatoly I; Han, Weiqiang; Aronson, Meigan

    2009-09-01

    We have reported the synthesis of Au(25)Pt(75) and Au(48)Pt(52) alloyed ultrathin nanowires with average widths of less than 3 nm via a wet chemistry approach at room temperature. Using a combination of techniques, including scanning transmission electron microscopy equipped with X-ray energy dispersive spectroscopy, ultraviolet-visible spectroscopy, and X-ray absorption near-edge structure and extended X-ray absorption fine structure spectroscopies, we identified the stoichiometry-dependent heterogeneous crystalline structures, as well as electronic structures with respect to the charge transfer between Pt and Au within both nanowires. In particular, we observed d-charge depletion at the Au site and the d-charge gain at the Pt site in Au(48)Pt(52) nanowires, which accounted for its ferromagnetic magnetic behavior, in contrast to the paramagnetism and diamagnetism appearing respectively in bulk Pt and Au.

  10. Catalytic reduction of NO by methane using a Pt/C/polybenzimidazole/Pt/C fuel cell

    DEFF Research Database (Denmark)

    Petrushina, Irina; Cleemann, Lars Nilausen; Refshauge, Rasmus;

    2007-01-01

    The catalytic NO reduction by methane was studied using a (NO,CH4,Ar),Pt|polybenzimidazole(PBI)–H3PO4|Pt,(H2,Ar) fuel cell at 135 and 165°C. It has been found that, without any reducing agent (like CH4), NO can be electrochemically reduced in the (NO, Ar), Pt/C|PBI–H3PO4|Pt/C, (H2,Ar) fuel cell...... with participation of H+ or electrochemically produced hydrogen. When added, methane partially suppresses the electrochemical reduction of NO. Methane outlet concentration monitoring has shown the CH4 participation in the chemical catalytic reduction, i.e., methane co-adsorption with NO inhibited the electrochemical...... NO reduction and introduced a dominant chemical path of the NO reduction. The products of the NO reduction with methane were N2, C2H4, and water. The catalytic NO reduction by methane was promoted when the catalyst was negatively polarized (−0.2 V). Repeated negative polarization of the catalyst increased...

  11. Defect-induced loading of Pt nanoparticles on carbon nanotubes

    Science.gov (United States)

    Kim, Sung Jin; Park, Yong Jin; Ra, Eun Ju; Kim, Ki Kang; An, Kay Hyeok; Lee, Young Hee; Choi, Jae Young; Park, Chan Ho; Doo, Seok Kwang; Park, Min Ho; Yang, Cheol Woong

    2007-01-01

    Carbon nanotubes-supported Pt nanoparticles were loaded using a microwave oven on the defective carbon nanotubes generated by an additional oxidant during acid treatment. The authors' Raman spectra and x-ray diffraction analysis demonstrated that defects created during oxidation and microwave treatment acted as nucleation seeds for Pt adsorption. The generated Pt nanoparticles had the size distributions of 2-3nm and were uniformly distributed on the defects of carbon nanotubes. The authors' density functional calculations showed that the adsorption of Pt atom on the vacancy of nanotube was significantly stronger by s-p hybridization with carbon atoms near the defect site.

  12. Prolate and Oblate Shape Coexistence in 188Pt

    Institute of Scientific and Technical Information of China (English)

    LIU Yuan; A.Osa; Y.Hatsukawa; SUN Yang; ZHOU Xiao-Hong; ZHANG Yu-Hu; ZHENG-Yong; LIU Min-Liang; GUO Ying-Xiang; M.Oshima; Y.Toh; M.Koizumi

    2008-01-01

    A standard in-beam γ-spectroscopy experiment for 188Pt is performed via the 176Yb(18O,6n) reaction at beam energies of 88 and 95 Me V,and the level scheme for 188 Pt is established.Prolate and oblate shape coexistence has been demonstrated to occur in 188Pt by applying the projected shell model.The rotation alignment of i13/2neutrons drives the yrast sequence changing suddenly from prolate to oblate shape at angular momentum 10h,indicating likely a new type of shape phase transition along the yrast fine in 188Pt.

  13. Predictions of the Pt(8)Ti phase in unexpected systems.

    Science.gov (United States)

    Taylor, Richard H; Curtarolo, Stefano; Hart, Gus L W

    2010-05-19

    The binary A(8)B phase (prototype Pt(8)Ti) has been experimentally observed in 11 systems. A high-throughput search over all the binary transition intermetallics, however, reveals 59 occurrences of the A(8)B phase: Au(8)Zn(dagger), Cd(8)Sc(dagger), Cu(8)Ni(dagger), Cu(8)Zn(dagger), Hg(8)La, Ir(8)Os(dagger), Ir(8)Re, Ir(8)Ru(dagger), Ir(8)Tc, Ir(8)W(dagger), Nb(8)Os(dagger), Nb(8)Rh(dagger), Nb(8)Ru(dagger), Nb(8)Ta(dagger), Ni(8)Fe, Ni(8)Mo(dagger)*, Ni(8)Nb(dagger)*, Ni(8)Ta*, Ni(8)V*, Ni(8)W, Pd(8)Al(dagger), Pd(8)Fe, Pd(8)Hf, Pd(8)Mn, Pd(8)Mo*, Pd(8)Nb, Pd(8)Sc, Pd(8)Ta, Pd(8)Ti, Pd(8)V*, Pd(8)W*, Pd(8)Zn, Pd(8)Zr, Pt(8)Al(dagger), Pt(8)Cr*, Pt(8)Hf, Pt(8)Mn, Pt(8)Mo, Pt(8)Nb, Pt(8)Rh(dagger), Pt(8)Sc, Pt(8)Ta, Pt(8)Ti*, Pt(8)V*, Pt(8)W, Pt(8)Zr*, Rh(8)Mo, Rh(8)W, Ta(8)Pd, Ta(8)Pt, Ta(8)Rh, V(8)Cr(dagger), V(8)Fe(dagger), V(8)Ir(dagger), V(8)Ni(dagger), V(8)Pd, V(8)Pt, V(8)Rh, and V(8)Ru(dagger) ((dagger) = metastable, * = experimentally observed). This is surprising for the wealth of new occurrences that are predicted, especially in well-characterized systems (e.g., Cu-Zn). By verifying all experimental results while offering additional predictions, our study serves as a striking demonstration of the power of the high-throughput approach. The practicality of the method is demonstrated in the Rh-W system. A cluster-expansion-based Monte Carlo model reveals a relatively high order-disorder transition temperature.

  14. 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.

  15. Reactivity of hydrogen with uranium in the presence of Pt

    Energy Technology Data Exchange (ETDEWEB)

    Balooch, M.; Siekhaus, W.J.

    1997-07-01

    The surface-reaction of di-hydrogen with uranium in the presence of Pt clusters has been studied using scanning tunneling microscopy (STM). Uranium was deposited on highly oriented pyrolytic graphite (HOPG) and annealed at temperatures up to 1200{degrees}C to obtain atomically pyrolytic flat surfaces. Pt clusters were then formed using evaporation from a Pt source onto the surface and subsequent annealing. Hydrogen mainly attacked uranium in the vicinity of Pt clusters and formed hydride. The hydride formation probability is almost constant at 2.3x10{sup -4} over the range of exposures studied.

  16. A novel method to evaluate spin diffusion length of Pt

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Yan-qing; Sun, Niu-yi; Che, Wen-ru [Shanghai Key Laboratory of Special Artificial Microstructure and Pohl Institute of Solid State Physics and School of Physics Science and Engineering, Tongji University, Shanghai 200092 (China); Shan, Rong, E-mail: shan.rong@hotmail.com [Shanghai Key Laboratory of Special Artificial Microstructure and Pohl Institute of Solid State Physics and School of Physics Science and Engineering, Tongji University, Shanghai 200092 (China); Zhu, Zhen-gang, E-mail: zgzhu@ucas.ac.cn [School of Electronic, Electrical and Communication Engineering, University of Chinese Academy of Sciences, Beijing 100049 (China)

    2016-05-01

    Spin diffusion length of Pt is evaluated via proximity effect of spin orbit coupling (SOC) and anomalous Hall effect (AHE) in Pt/Co{sub 2}FeAl bilayers. By varying the thicknesses of Pt and Co{sub 2}FeAl layer, the thickness dependences of AHE parameters can be obtained, which are theoretically predicted to be proportional to the square of the SOC strength. According to the physical image of the SOC proximity effect, the spin diffusion length of Pt can easily be identified from these thickness dependences. This work provides a novel method to evaluate spin diffusion length in a material with a small value.

  17. Spin Hall magnetoresistance in Co2FeSi/Pt thin films: dependence on Pt thickness and temperature

    Science.gov (United States)

    Huang, Xiufeng; Dai, Zhiwen; Huang, Lin; Lu, Guangduo; Liu, Min; Piao, Hongguang; Kim, Dong-Hyun; Yu, Seong-cho; Pan, Liqing

    2016-11-01

    We have investigated the temperature and the Pt layer thickness dependence of the magnetoresistances (MRs) in Co2FeSi/Pt thin films. Based on the field dependent measurements, it can be seen that the spin-current-induced spin Hall magnetoresistance (SMR) plays the dominant role in the MRs in the Co2FeSi/Pt bilayers in the whole temperature range. Meanwhile, a quite small part of anisotropic magnetoresistance (AMR) existed in the MRs. It proved to be originated from magnetic proximity effect (MPE) by measuring the Pt thickness and temperature dependence of the AMR. Moreover, the Co2FeSi layer thickness has much weaker effect on the SMR and AMR compared to the Pt layer thickness. These results indicate that the Co2FeSi/Pt interface is beneficial to be used in the spin-current-induced physical phenomena.

  18. 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.

  19. Effect of Pt:Sn atomic ratio on the preparation of PtSn/C electrocatalysts using electron beam irradiation

    Energy Technology Data Exchange (ETDEWEB)

    Silva, Dionisio F.; Oliveira Neto, Almir; Pino, Eddy S.; Linardi, Marcelo; Spinace, Estevam V., E-mail: dfsilva@ipen.b, E-mail: espinace@ipen.b [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil)

    2009-07-01

    PtSn/C electrocatalysts were prepared with Pt:Sn atomic ratios of 3:1, 1:1 and 1:3 in water/2-propanol using electron beam irradiation. The obtained materials were characterized by EDX, XRD and cyclic voltammetry. The ethanol electro-oxidation was studied by chronoamperometry. The XRD diffractograms of the PtSn/C electrocatalysts showed typical face-centered cubic (fcc) structure of platinum and the presence of a SnO{sub 2} phase (cassiterite). The mean crystallite sizes of Pt fcc phase was in the range of 3.0-3.5 nm. The PtSn/C electrocatalysts were active for ethanol electro-oxidation at room temperature and the material prepared with Pt:Sn atomic ratio of 1:1 showed the best activity. (author)

  20. Efektifitas Pelaksanan Program CSR PT Tirta Bahagia

    Directory of Open Access Journals (Sweden)

    Anggara Prihardana

    2015-12-01

    Full Text Available CSR first appeared in official discourse since the presence of academic writings of Howard Bowen, entitled Social Responsibility of Businessmen raised in 1953. CSR in the meaning of Bowen refers to the obligation of business to make and implement policies, decisions, and actions that follow the norms in a society. In the implementation of the program of corporate social responsibility (CSR, PT Tirta Bahagia has a lot of activities in the field of education, the environment or health. In carrying out these activities there are several stages performed i.e. ranging from planning, implementation, and evaluation. In this discussion that became the focus of research is on the development of the well absorption done by the company in the village which is also the location of the factory. PT Tirta Bahagia starting the planning stages are not based on the order in which they should be, i.e. starts with vision and mission would formulate but positioning the provision of funds (budget being the first with reason a very limited source of funding, causing the program to be run CSR activities should be adapted to the existing funds.

  1. PT-symmetric deformations of integrable models.

    Science.gov (United States)

    Fring, Andreas

    2013-04-28

    We review recent results on new physical models constructed as PT-symmetrical deformations or extensions of different types of integrable models. We present non-Hermitian versions of quantum spin chains, multi-particle systems of Calogero-Moser-Sutherland type and nonlinear integrable field equations of Korteweg-de Vries type. The quantum spin chain discussed is related to the first example in the series of the non-unitary models of minimal conformal field theories. For the Calogero-Moser-Sutherland models, we provide three alternative deformations: a complex extension for models related to all types of Coxeter/Weyl groups; models describing the evolution of poles in constrained real-valued field equations of nonlinear integrable systems; and genuine deformations based on antilinearly invariant deformed root systems. Deformations of complex nonlinear integrable field equations of Korteweg-de Vries type are studied with regard to different kinds of PT-symmetrical scenarios. A reduction to simple complex quantum mechanical models currently under discussion is presented.

  2. Gender politics in the PT government

    Directory of Open Access Journals (Sweden)

    Fiona MACAULAY

    2011-01-01

    Full Text Available What difference will a Workers’ Party (Partido dos Trabalhadores-PT govern­ment make to women’s status and rights in Brazil? In order to analyse the Lula government’s approach to gender issues, the article first examines the party’s foundation and development, and relationship to social movements, including the women’s movement. The PT is shown to be a groundbreaker in the Brazilian party system, in terms both of promoting women’s leadership and of its ideological and institutional commitment to gender equity and equality, as illustrated by the party’s state and municipal governments, by its actions in the legislative sphere. The article then analyses the likely direction of the new Special Secretariat for Policies on Women in the light of the previous, uneven trajectory of Brazil’s national machinery for promoting women’s status, and of the kinds of gender policy orientations discernible in the party’s subnational administrations. It concludes by analysing some of the gender policies put forward since the beginning of the Lula government in January 2003.

  3. Strategi Bisnis pada PT Wirapati Garuda Paksi

    Directory of Open Access Journals (Sweden)

    Rina Astini

    2010-03-01

    Full Text Available PT Garuda Wirapati Paksi (WGP is a private corporation engaged in the Security and Rescue Services Business Sector (BUJPP in guarding. Many challenges arise from the external environment such as unstable political and economic conditions, competition among companies and the entry of foreign firms. To face the above phenomenon, the right and effective business strategy is the right tool for avoiding the challenge. Business strategy planning is absolutely necessary for companies that want to survive in the future. The research method is descriptive. Data collection techniques used are questionnaire and interview with relevant parties within the company. The data have been obtained that, in the analysis through three phases, namely input, matching, and decision stage. The final results of this study concluded that the proposed effective business strategy for PT Garuda Wirapati Paksi based on QSPM matrix is Market Penetration Strategy. This strategy is considered to reduce business risk arising as a result of significant changes to the external environment of the company.

  4. 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.

  5. Conserved loci of leaf and stem rust fungi of wheat share synteny interrupted by lineage-specific influx of repeat elements

    Directory of Open Access Journals (Sweden)

    Fellers John P

    2013-01-01

    Full Text Available Abstract Background Wheat leaf rust (Puccinia triticina Eriks; Pt and stem rust fungi (P. graminis f.sp. tritici; Pgt are significant economic pathogens having similar host ranges and life cycles, but different alternate hosts. The Pt genome, currently estimated at 135 Mb, is significantly larger than Pgt, at 88 Mb, but the reason for the expansion is unknown. Three genomic loci of Pt conserved proteins were characterized to gain insight into gene content, genome complexity and expansion. Results A bacterial artificial chromosome (BAC library was made from P. triticina race 1, BBBD and probed with Pt homologs of genes encoding two predicted Pgt secreted effectors and a DNA marker mapping to a region of avirulence. Three BACs, 103 Kb, 112 Kb, and 166 Kb, were sequenced, assembled, and open reading frames were identified. Orthologous genes were identified in Pgt and local conservation of gene order (microsynteny was observed. Pairwise protein identities ranged from 26 to 99%. One Pt BAC, containing a RAD18 ortholog, shares syntenic regions with two Pgt scaffolds, which could represent both haplotypes of Pgt. Gene sequence is diverged between the species as well as within the two haplotypes. In all three BAC clones, gene order is locally conserved, however, gene shuffling has occurred relative to Pgt. These regions are further diverged by differing insertion loci of LTR-retrotransposon, Gypsy, Copia, Mutator, and Harbinger mobile elements. Uncharacterized Pt open reading frames were also found; these proteins are high in lysine and similar to multiple proteins in Pgt. Conclusions The three Pt loci are conserved in gene order, with a range of gene sequence divergence. Conservation of predicted haustoria expressed secreted protein genes between Pt and Pgt is extended to the more distant poplar rust, Melampsora larici-populina. The loci also reveal that genome expansion in Pt is in part due to higher occurrence of repeat-elements in this species.

  6. Magnetic Properties and Microstructure of FeOx/Fe/FePt and FeOx/FePt Films

    Directory of Open Access Journals (Sweden)

    Jai-Lin Tsai

    2013-01-01

    Full Text Available The Fe(6 nm/FePt film with perpendicular magnetization was deposited on the glass substrate. To study the oxygen diffusion effect on the coupling of Fe/FePt bilayer, the plasma oxidation with 0.5~7% oxygen flow ratio was performed during sputtered part of Fe layer and formed the FeOx(3 nm/Fe(3 nm/FePt trilayer. Two-step magnetic hysteresis loops were found in trilayer with oxygen flow ratio above 1%. The magnetization in FeOx and Fe/FePt layers was decoupled. The moments in FeOx layer were first reversed and followed by coupled Fe/FePt bilayer. The trilayer was annealed again at 500°C and 800°C for 3 minutes. When the FeOx(3 nm/Fe(3 nm/FePt trilayer was annealed at 500°C, the layers structure was changed to FeOx(6 nm/FePt bilayer due to oxygen diffusion. The hard-magnetic FeOx(6 nm/FePt film was coupled with single switching field. The FeOx/(disordered FePt layer structure was observed with further annealing at 800°C and presented soft-magnetic loop. In summary, the coupling between soft-magnetic Fe, FeOx layer, and hard-magnetic L10 FePt layer can be controlled by the oxygen diffusion behavior, and the oxidation of Fe layer was tuned by the annealing temperature. The ordered L10 FePt layer was deteriorated by oxygen and became disordered FePt when the annealed temperature was up to 800°C.

  7. 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.

  8. Tetrahexahedral Pt Nanoparticles: Comparing the Oxygen Reduction Reaction under Transient vs Steady-State Conditions

    DEFF Research Database (Denmark)

    Deng, Yu-Jia; Wiberg, Gustav Karl Henrik; Zana, Alessandro

    2017-01-01

    -state conditions. As a benchmark, the ORR activity is compared with those of polycrystalline Pt and a commercial Pt/C catalyst. The results show that, under transient conditions, the catalytic performance of the THH Pt NPs and Pt/C are approximately the same and about 2 times lower than that of polycrystalline Pt....... However, under steady-state conditions the THH Pt NPs perform considerably better than Pt/C. Under steady-state conditions THH Pt NPs are even slightly more active than polycrystalline Pt...

  9. Characterization of Pt catalysts supported in mixed oxides; Caracterizacion de catalizadores de Pt soportado en oxidos mixtos

    Energy Technology Data Exchange (ETDEWEB)

    Perez H, R.; Garcia C, M.A.; Gomez C, A.; Diaz, G. [Instituto Nacional de Investigaciones Nucleares, A.P. 18-1027, 11801 Mexico D.F. (Mexico)

    2000-07-01

    The catalytic supports TiO{sub 2}, ZrO{sub 2} and TiO{sub 2}-ZrO{sub 2} were prepared by the sol-gel technique. The incorporation of Pt to the supports was by the classical impregnation method. The catalytic materials were characterized (Pt/TiO{sub 2}, Pt/ZrO{sub 2} and Pt/TiO{sub 2}-ZrO{sub 2}) by diverse techniques to determine: the texture (BET), evolution of the catalytic materials synthesised after drying and calcination (Infrared spectroscopy) and by Thermogravimetric analysis. (Author)

  10. Effect of the state of distribution of supported Pt nanoparticles on effective Pt utilization in polymer electrolyte fuel cells.

    Science.gov (United States)

    Uchida, Makoto; Park, Young-Chul; Kakinuma, Katsuyoshi; Yano, Hiroshi; Tryk, Donald A; Kamino, Takeo; Uchida, Hiroyuki; Watanabe, Masahiro

    2013-07-21

    In polymer electrolyte fuel cells, it is essential to minimize Pt loading, particularly at the cathode, without serious loss of performance. From this point of view, we will report an advanced concept for the design of high performance catalysts and membrane-electrode assemblies (MEAs): first, the evaluation of Pt particle distributions on both the interior and exterior walls of various types of carbon black (CB) particles used as supports with respect to the "effective surface (ES)"; second, control of both size and location of Pt particles by means of a new preparation method (nanocapsule method); and finally, a new evaluation method for the properties of MEAs based on the Pt utilization (UPt), mass activity (MA), and effectiveness of Pt (EfPt), based on the ES concept. The amounts of Pt catalyst particles located in the CB nanopores were directly evaluated using the transmission electron microscopy, scanning electron microscopy and corresponding three-dimensional images. By use of the nanocapsule method and optimization of the ionomer, increased MA and EfPt values for the MEA were achieved. The improvement in the cathode performance can be attributed to the sharp particle-size distribution for Pt and the highly uniform dispersion on the exterior surface of graphitized carbon black (GCB) supports.

  11. Measurement of the (gamma,n) reaction rates of the nuclides 190Pt, 192Pt, and 198Pt in the astrophysical gamma-process

    CERN Document Server

    Vogt, K; Babilon, M; Enders, J; Hartmann, T; Hutter, C; Rauscher, T; Volz, S; Zilges, A

    2001-01-01

    The nucleosynthesis of heavy neutron-deficient nuclei in a stellar photon bath at the temperatures relevant for the astrophysical gamma process was investigated. In order to derive (gamma,n) cross sections and reaction rates, the stellar photon bath was simulated by the superposition of several bremsstrahlung spectra with different endpoint energies. As a first test for this method, the (gamma,n) reaction rates of the platinum isotopes 190Pt, 192Pt, and 198Pt were derived. The results are compared to other experimental data and theoretical calculations.

  12. 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.

  13. Chemonuclear studies for identification for new production routes for the therapeutically useful radionuclides {sup 140}Nd, {sup 192}Ir, {sup 191}Pt, {sup 193m}Pt, und {sup 195m}Pt; Kernchemische Studien zur Entwicklung neuerer Produktionsverfahren fuer die therapierelevanten Radionuklide {sup 140}Nd, {sup 192}Ir, {sup 191}Pt, {sup 193m}Pt, und {sup 195m}Pt

    Energy Technology Data Exchange (ETDEWEB)

    Hilgers, K.

    2005-12-15

    New production routes for the therapeutically useful radionuclides {sup 140}Nd, {sup 192}Ir, {sup 191}Pt, {sup 193m}Pt and {sup 195m}Pt were investigated. Cross section data were measured using the stacked-foil technique and compared with theoretical calculations. A production method for the platinum nuclides was developed. The {sup 141}Pr(p, 2n){sup 140}Nd and {sup nat}Ce({sup 3}He, xn){sup 140}Nd reactions were investigated for production of {sup 140}Nd. Cross section data of nuclear reactions leading to the side products {sup 141}Nd, {sup 139}Nd and {sup 139}Ce could also be achieved. The experimental data were compared with theoretical calculations using the code ALICE-IPPE. A comparison of the calculated thick target yields showed that the {sup 141}Pr(p, 2n){sup 140}Nd reaction gives a higher yield. The {sup 192}Os(p, n){sup 192}Ir reaction was examined in the context of the production of {sup 192}Ir. Cross section data were determined and compared with theoretical calculations using the codes ALICE-IPPE and EMPIRE II. The yield of this reaction was compared with the yield of the reactor production of this nuclide. The reactor production seems to be more suitable because of a higher purity and yield. Cross section data were measured for the {sup 192}Os({alpha}, n){sup 195m}Pt, {sup 192}Os({alpha}, 3n){sup 193m}Pt and {sup 192}Os({sup 3}He, 4n){sup 191}Pt reactions. The activity of {sup 193m}Pt and {sup 195m}Pt was determined by X-ray spectroscopy after a chemical separation procedure. The ALICE-IPPE code was found to be inappropriate to reproduce the experimental values. The calculated yields were compared with the yields of other reactions, especially the reactor production of {sup 195m}Pt. The yield of the {sup 192}Os({alpha}, n){sup 195m}Pt reaction is lower compared to the yield of the reactor production, but offers lower target costs and higher specific activity. A production method for {sup 193m}Pt and {sup 195m}Pt was developed. Batch yields of 0.9 MBq

  14. Chemonuclear studies for identification for new production routes for the therapeutically useful radionuclides {sup 140}Nd, {sup 192}Ir, {sup 191}Pt, {sup 193m}Pt, und {sup 195m}Pt; Kernchemische Studien zur Entwicklung neuerer Produktionsverfahren fuer die therapierelevanten Radionuklide {sup 140}Nd, {sup 192}Ir, {sup 191}Pt, {sup 193m}Pt, und {sup 195m}Pt

    Energy Technology Data Exchange (ETDEWEB)

    Hilgers, K.

    2005-12-15

    New production routes for the therapeutically useful radionuclides {sup 140}Nd, {sup 192}Ir, {sup 191}Pt, {sup 193m}Pt and {sup 195m}Pt were investigated. Cross section data were measured using the stacked-foil technique and compared with theoretical calculations. A production method for the platinum nuclides was developed. The {sup 141}Pr(p, 2n){sup 140}Nd and {sup nat}Ce({sup 3}He, xn){sup 140}Nd reactions were investigated for production of {sup 140}Nd. Cross section data of nuclear reactions leading to the side products {sup 141}Nd, {sup 139}Nd and {sup 139}Ce could also be achieved. The experimental data were compared with theoretical calculations using the code ALICE-IPPE. A comparison of the calculated thick target yields showed that the {sup 141}Pr(p, 2n){sup 140}Nd reaction gives a higher yield. The {sup 192}Os(p, n){sup 192}Ir reaction was examined in the context of the production of {sup 192}Ir. Cross section data were determined and compared with theoretical calculations using the codes ALICE-IPPE and EMPIRE II. The yield of this reaction was compared with the yield of the reactor production of this nuclide. The reactor production seems to be more suitable because of a higher purity and yield. Cross section data were measured for the {sup 192}Os({alpha}, n){sup 195m}Pt, {sup 192}Os({alpha}, 3n){sup 193m}Pt and {sup 192}Os({sup 3}He, 4n){sup 191}Pt reactions. The activity of {sup 193m}Pt and {sup 195m}Pt was determined by X-ray spectroscopy after a chemical separation procedure. The ALICE-IPPE code was found to be inappropriate to reproduce the experimental values. The calculated yields were compared with the yields of other reactions, especially the reactor production of {sup 195m}Pt. The yield of the {sup 192}Os({alpha}, n){sup 195m}Pt reaction is lower compared to the yield of the reactor production, but offers lower target costs and higher specific activity. A production method for {sup 193m}Pt and {sup 195m}Pt was developed. Batch yields of 0.9 MBq

  15. EMPLOYER BRANDING PT. CITIBANK INDONESIA PADA KALANGAN WORKFORCE DI MAKASSAR

    OpenAIRE

    -, RUZKYHAQ

    2016-01-01

    2016 Employer Branding PT. Citibank Indonesia pada Kalangan Workforce di Makassar Ruzkyhaq Nurdjanah Hamid Shinta Dewi S. Tikson Jurusan Manajemen, Fakultas Ekonomi dan Bisnis, Universitas Hasanuddin JL. Perintis Kemerdekaan Km.10 Makassar, 90245 Sulawesi Selatan, Indonesia Penelitian ini bertujuan untuk mengetahui dan menganalisis pengaruh Employer Branding PT. Citibank Indonesia yang menghasilkan dua Atribut Daya Tarik yang terdiri dari Atribut Instrument...

  16. Charge optimized many body (COMB) potentials for Pt and Au

    Science.gov (United States)

    Antony, A. C.; Akhade, S. A.; Lu, Z.; Liang, T.; Janik, M. J.; Phillpot, S. R.; Sinnott, S. B.

    2017-06-01

    Interatomic potentials for Pt and Au are developed within the third generation charge optimized many-body (COMB3) formalism. The potentials are capable of reproducing phase order, lattice constants, and elastic constants of Pt and Au systems as experimentally measured or calculated by density functional theory. We also fit defect formation energies, surface energies and stacking fault energies for Pt and Au metals. The resulting potentials are used to map a 2D contour of the gamma surface and simulate the tensile test of 16-grain polycrystalline Pt and Au structures at 300 K. The stress-strain behaviour is investigated and the primary slip systems {1 1 1} are identified. In addition, we perform high temperature (1800 K for Au and 2300 K for Pt) molecular dynamics simulations of 30 nm Pt and Au truncated octahedron nanoparticles and examine morphological changes of each particle. We further calculate the activation energy barrier for surface diffusion during simulations of several nanoseconds and report energies of 0.62+/- 0.16 eV for Pt and 1.44+/- 0.06 eV for Au. This initial parameterization and application of the Pt and Au potentials demonstrates a starting point for the extension of these potentials to multicomponent systems within the COMB3 framework.

  17. Thermal memory effects at the Pt vertical bar YSZ interface

    DEFF Research Database (Denmark)

    Jacobsen, Torben; Bay, Lasse

    2002-01-01

    A current induced activation mechanism in the oxygen reaction on the Pt \\ YSZ interface at 1000 degreesC is demonstrated by impedance measurements. It is shown that Pt point electrodes conditioned at high temperature retain their initial reactivity when cooled to 600 degreesC. At this temperature...

  18. Mechanisms of self-diffusion on Pt(110)

    DEFF Research Database (Denmark)

    Lorensen, Henrik Qvist; Nørskov, Jens Kehlet; Jacobsen, Karsten Wedel

    1999-01-01

    The self-diffusion of Pt on the missing row reconstructed Pt(110) surface is discussed based on density functional calculations of activation energy barriers. Different competing diffusion mechanisms are considered and we show that several different diffusion paths along the reconstruction troughs...

  19. Phase transformations during sintering of mechanically alloyed TiPt

    CSIR Research Space (South Africa)

    Nxumalo, S

    2010-10-01

    Full Text Available A TiPt alloy was produced by mechanically alloying the desired quantities of titanium and platinum. The resultant TiPt alloy powder was cold pressed to produce green bodies. Several sintering conditions were used to sinter this alloy...

  20. Thermochemistry of Pt-Fullerene Complexes: Semiempirical Study

    Science.gov (United States)

    Voityuk, Alexander A.

    2009-07-01

    Modified Neglect of Differential Overlap (MNDO) and MNDO/d based semiempirical methods are widely employed to explore structure and thermochemistry of molecular systems. In this work, the AM1/d method has been parametrized for systems containing platinum. The proposed scheme delivers excellent performance for binding energies of Pt complexes with ethylene and large π conjugated hydrocarbons. The estimated bond energies accurately reproduce the results of MP4(SDQ) calculations and show significant improvement over DFT (B3LYP and M05) data. We apply the AM1/d scheme to explore the structure and thermochemistry of several Pt compounds with C60 and C70. The calculated binding energies of bare Pt atoms and [Pt(PH3)2] units to the fullerenes are 75 and 45 kcal/mol, respectively. We find that coordination of a single metal center to C60 activates the fullerene cage making subsequent coordination of Pt more favorable. The bond energy [C60-PtC60] is calculated to be 65 kcal/mol. The estimated reaction enthalpies are useful for exploring the stability of PtxC60 polymer systems and their interaction with phosphines. AM1/d predicts a very low barrier to rotation of the coordinated fullerenes in [Pt(C60)2]. The AM1/d scheme is computationally very efficient and can be employed to obtain fast quantitative estimates for binding energies and structural parameters of Pt complexes with large π conjugated systems like fullerenes and carbon nanotubes.

  1. The Synthesis of Glycosyl Phosphite-Pt(Ⅱ) Complexes

    Institute of Scientific and Technical Information of China (English)

    Ling Hua CAO; Hong Yun GAO; Chuan Jian ZHOU; Yu Ting LIU

    2004-01-01

    Ethylene glycol phosphorochloridite 1 or catechol phosphorochloridite 2 reacted with isopropylidene derivatives of D-glucose, D-galactose, D-mannose and D-fructose, a series of glycosyl phosphites were obtained. These glycosyl phosphites form optically active complexes with simple Pt (Ⅱ) salts. Pt (Ⅱ) is coordinated to the phosphorus atom, most of the metal complexes are quite stable.

  2. PT-symmetry in quasi-integrable models

    CERN Document Server

    Assis, P E G

    2015-01-01

    We reinforce the observations of almost stable scattering in nonintegrable models and show that $\\mathcal{PT}$-symmetry can be used as a guiding principle to select relevant systems also when it comes to integrability properties. We show that the presence of unbroken $\\mathcal{PT}$-symmetry in classical field theories produces quasi-integrable excitations with asymptotically conserved charges.

  3. Recent Advances in FePt Nanoparticles for Biomedicine

    Directory of Open Access Journals (Sweden)

    Yujuan Shi

    2015-01-01

    Full Text Available FePt nanoparticles have great potential for biomedical applications due to their superior characteristics, including superparamagnetism, resistance to oxidation, and high chemical stability. The present paper reviews the methods used to prepare FePt nanoparticles, surface modifications, and their applications in the biomedical field, such as biosensing, magnetic resonance imaging (MRI, targeted drug delivery, and therapy.

  4. Microemulsion prepared Ni88Pt12 for methane cracking

    KAUST Repository

    Zhou, Lu

    2017-01-16

    Monodispersed NiPt nanoparticles of 10 nm were synthesized by water-in-oil microemulsion. The Ni-Pt alloy structure was stable during the thermal treatment between 330 and 1037 °C, whereas the relatively low temperature range of 600-700 °C was favorable for methane cracking to produce hydrogen and carbon nanotubes.

  5. Invisibility in PT-symmetric complex crystals

    Energy Technology Data Exchange (ETDEWEB)

    Longhi, Stefano, E-mail: longhi@fisi.polimi.it [Dipartimento di Fisica, Politecnico di Milano, Piazza L. da Vinci 32, I-20133 Milano (Italy)

    2011-12-02

    Bragg scattering in sinusoidal PT-symmetric complex crystals of finite thickness is theoretically investigated by the derivation of exact analytical expressions for reflection and transmission coefficients in terms of modified Bessel functions of first kind. The analytical results indicate that unidirectional invisibility, recently predicted for such crystals by coupled-mode theory (Z Lin et al 2011 Phys. Rev. Lett. http://dx.doi.org/10.1103/PhysRevLett.106.213901), breaks down for crystals containing a large number of unit cells. In particular, for a given modulation depth in a shallow sinusoidal potential, three regimes are encountered as the crystal thickness is increased. At short lengths the crystal is reflectionless and invisible when probed from one side (unidirectional invisibility), whereas at intermediate lengths the crystal remains reflectionless but not invisible; for longer crystals both unidirectional reflectionless and invisibility properties are broken. (paper)

  6. Perancangan E-Commerce Pada PT DAF

    Directory of Open Access Journals (Sweden)

    Rudy Rudy

    2010-06-01

    Full Text Available The purpose of this study is to analyze and design e-commerce at. DAF to help the sales process is then expected to improve service. The methodology used is the method of analysis, where the review is held directly to the field, observing and analyzing the data obtained, and using the design method, which includes design of business models, screen designs and database design. Results to be achieved is the application of e-commerce web-based, whereby the system can enable customers to obtain the desired information is complete, make transactions easier and faster. Conclusions obtained are PT DAF can take advantage of e-commerce to support their business today and an appropriate business model is the highest-quality models.

  7. Corporate Governance in PT Lippo Karawaci Tbk

    Directory of Open Access Journals (Sweden)

    Retno Kusumastuti

    2012-06-01

    Full Text Available When mismanagement and misuse run rampant in giant corporations, as in the case of Enron in 2001, good corporate governance becomes mandatory. From the perspective of the agency theory, the separation of capital owners and management must lead to strictly applied good corporate governance. The purpose is to eliminate any disadvantages to the corporation's objective, namely providing added values to all relevant parties. The agency theory also covers two aspects: agency issues and agency costs. The research uses the qualitative approach and data is gathered through extensive interview, secondary data, and bibliography study. Key persons among the sources are selected based on specific criteria. Data validity is obtained through the triangulation technique, and the samples used are PT Lippo Karawaci Tbk and subsidiaries. The results show that governance practices are unique in each corporation, in accordance with their characteristics.

  8. APLIKASI PEMASARAN BERBASIS WEB PT XYZ

    Directory of Open Access Journals (Sweden)

    Henny Hendarti

    2013-11-01

    products, service products, and prices. Thus, customers can be sure in choosing and buying of goods and services. For that e-marketing is introduced as an marketing strategy that integrates internet and marketing. A study was conducted to develop e-marketing application for PT XYZ as a company that produces and sells mens apparel and accessories. The methodology used in developing the e-marketing application is library research, field research, and a seven-stage approach to build e-marketing. The e-marketing strategy developed is expected to expand market share and increase sales. Additionally, it is expected to be a powerful strategy to build relationships with customers, providing information of both company and its products.

  9. Ferroelectric Properties of Pt/Pb5Ge3O11/Pt and Pt/Pb5Ge3O11/HfO2/Si Structures

    Science.gov (United States)

    Ohara, Shuichiro; Aizawa, Koji; Ishiwara, Hiroshi

    2005-09-01

    The ferroelectric properties of metal-ferroelectric-metal (MFM) capacitors with a Pt/Pb5Ge3O11(PGO)/Pt structure and metal-ferroelectric-insulator-semiconductor (MFIS) diodes with a Pt/PGO/HfO2/Si structure were investigated. C-axis-oriented PGO thin films were formed on both Pt/SiO2/Si and HfO2 (6 nm)/Si structures by a sol-gel method. Typical values of remanent polarization (2Pr), coercive field (2Ec), and dielectric constant in the MFM capacitors were 5.7 μC/cm2, 63 kV/cm, and 50, respectively, and the remanent polarization gradually increased with the switching pulses for up to 1 × 1010 cycles. It was also found that the memory window in the MFIS diodes with a 340-nm-thick PGO film was as large as 1.3 V.

  10. Fine grains ceramics of PIN-PT, PIN-PMN-PT and PMN-PT systems: drift of the dielectric constant under high electric field.

    Science.gov (United States)

    Pham-Thi, M; Augier, C; Dammak, H; Gaucher, P

    2006-12-22

    Lead-based ferroelectric ceramics with (1-x)Pb(B1 B2)O3-xPbTiO3 formula have emerged as a group of promising materials for various applications like ultrasonic sonars or medical imaging transducers. (1-x)PMN-xPT, (1-x)PIN-xPT and ternary solutions xPIN-yPMN-zPT ceramics are synthesised using the solid state reaction method. Our objective is to achieve higher structural transition temperatures than those of PMN-PT ceramics with as good dielectric, piezoelectric and electromechanical properties. Ceramics capacitance and loss tangent are measured when the ac field of measurement increases up to E=500 V/mm. Behaviours of these materials under ac field are related to their coercive field and Curie temperature.

  11. Topological states in partially-PT-symmetric azimuthal potentials

    CERN Document Server

    Kartashov, Yaroslav V; Torner, Lluis

    2015-01-01

    We introduce partially-parity-time-symmetric (pPT-symmetric) azimuthal potentials composed from individual PT-symmetric cells located on a ring, where two azimuthal directions are nonequivalent in a sense that in such potentials excitations carrying topological dislo-cations exhibit different dynamics for different directions of energy circulation in the initial field distribution. Such non-conservative ratchet-like structures support rich families of stable vortex solitons in cubic nonlinear media, whose properties depend on the sign of the topological charge due to the nonequivalence of azimuthal directions. In contrast, oppositely charged vortex solitons remain equivalent in similar fully PT-symmetric potentials. The vortex solitons in the pPT- and PT-symmetric potentials are shown to feature qualitatively different internal current distributions, which are described by different discrete rotation symmetries of the intensity profiles.

  12. INFORMATION TECHNOLOGY STRATEGIC PLANNING AT PT. VENTURIUM SYSTEM

    Directory of Open Access Journals (Sweden)

    Lola Oktavia

    2013-01-01

    Full Text Available PT. Venturium System Indonesia is a company engaged in IT solutions which serves IT solution for their customers from banking firms in Indonesia. This purpose of this research is to develop a Strategic IT planning for PT. Venturium System Indonesia in accordance with the strategic plan. The applied research method is a framework for IT Strategic Planning of John Ward and Joe Peppard and Enterprise Architecture documentation from Scott A. Bernard. This research uses SWOT analysis and IT Balanced Scorecard to analyze the requirements of IT at PT. Venturium System Indonesia. Results of the analysis are proposed as Information System applications, such as: Knowledge Management System Application, Automatic File Transfer and E-Report which are parts of the IT strategic plan on PT. Venturium System Indonesia. Results of the analysis also generate some policies requirements to be applied by PT. Venturium System Indonesia.

  13. Stability analysis for solitons in PT-symmetric optical lattices

    CERN Document Server

    Nixon, Sean; Yang, Jianke

    2012-01-01

    Stability of solitons in parity-time (PT)-symmetric periodic potentials (optical lattices) is analyzed in both one- and two-dimensional systems. First we show analytically that when the strength of the gain-loss component in the PT lattice rises above a certain threshold (phase-transition point), an infinite number of linear Bloch bands turn complex simultaneously. Second, we show that while stable families of solitons can exist in PT lattices, increasing the gain-loss component has an overall destabilizing effect on soliton propagation. Specifically, when the gain-loss component increases, the parameter range of stable solitons shrinks as new regions of instability appear. Thirdly, we investigate the nonlinear evolution of unstable PT solitons under perturbations, and show that the energy of perturbed solitons can grow unbounded even though the PT lattice is below the phase transition point.

  14. Bifunctional electrocatalysis in pt-ru nanoparticle systems.

    Science.gov (United States)

    Roth, C; Benker, N; Theissmann, R; Nichols, R J; Schiffrin, D J

    2008-03-04

    Pt-Ru alloys are prominent electrocatalysts in fuel cell anodes as they feature a very high activity for the oxidation of reformate and methanol. The improved CO tolerance of these alloys has been discussed in relation to the so-called ligand and bifunctional mechanisms. Although these effects have been known for many years, they are still not completely understood. A new approach that bridges the gap between single crystals and practical catalysts is presented in this paper. Nanoparticulate model systems attached to an oxidized glassy carbon electrode were prepared by combining both ligand-stabilized and spontaneously deposited Pt and Ru nanoparticles. These electrodes showed very different voltammetric responses for CO and methanol oxidation. The cyclic voltammograms were deconvoluted into contributions attributed to Pt, Ru, and Pt-Ru contact regions to quantify the contribution of the latter to the bifunctional mechanism. Scanning transmission electron microscopy confirmed the proximity of Pt and Ru nanoparticles in the different samples.

  15. Nonlinear switching and solitons in PT-symmetric photonic systems

    CERN Document Server

    Suchkov, Sergey V; Huang, Jiahao; Dmitriev, Sergey V; Lee, Chaohong; Kivshar, Yuri S

    2015-01-01

    One of the challenges of the modern photonics is to develop all-optical devices enabling increased speed and energy efficiency for transmitting and processing information on an optical chip. It is believed that the recently suggested Parity-Time (PT) symmetric photonic systems with alternating regions of gain and loss can bring novel functionalities. In such systems, losses are as important as gain and, depending on the structural parameters, gain compensates losses. Generally, PT systems demonstrate nontrivial non-conservative wave interactions and phase transitions, which can be employed for signal filtering and switching, opening new prospects for active control of light. In this review, we discuss a broad range of problems involving nonlinear PT-symmetric photonic systems with an intensity-dependent refractive index. Nonlinearity in such PT symmetric systems provides a basis for many effects such as the formation of localized modes, nonlinearly-induced PT-symmetry breaking, and all-optical switching. Nonl...

  16. PtRu/C electrocatalysts prepared using {gamma}-irradiation

    Energy Technology Data Exchange (ETDEWEB)

    Silva, Dionisio F.; Neto, Almir Oliveira; Pino, Eddy S.; Linardi, Marcelo; Spinace, Estevam V. [Instituto de Pesquisas Energeticas e Nucleares, IPEN/CNEN-SP, Av. Professor Lineu Prestes, 2242, Cidade Universitaria, 05508-000 Sao Paulo, SP (Brazil)

    2007-07-10

    PtRu/C electrocatalysts (carbon-supported PtRu nanoparticles) were prepared submitting water/ethylene glycol solutions containing Pt(IV) and Ru(III) ions and the carbon support to {gamma}-irradiation. The water/ethylene glycol ratio (v/v) and the total dose (kGy) were evaluated as synthesis parameters. The electrocatalysts were characterized by energy dispersive X-ray analysis (EDX), X-ray diffraction (XRD), transmission electron microscopy (TEM) and cyclic voltammetry and tested for methanol electro-oxidation aiming fuel cell application. The obtained PtRu/C electrocatalysts were more active for methanol electro-oxidation than the commercial PtRu/C electrocatalyst at ambient temperature and the electrocatalytic activity depends on the water/ethylene glycol ratio used in the preparation. (author)

  17. Perpendicular Magnetic Anisotropy and Induced Magnetic Structures of Pt Layers in the Fe/Pt Multilayers Investigated by Resonant X-ray Magnetic Scattering

    Science.gov (United States)

    Lee, Mihee; Takechi, Ryota; Hosoito, Nobuyoshi

    2017-02-01

    Depth distribution of the magnetization induced in the paramagnetic Pt layers of Fe/Pt multilayers was investigated by resonant X-ray magnetic scattering (RXMS) near the Pt L3 absorption edge. Two samples with different perpendicular magnetic anisotropy (PMA) were chosen for RXMS measurements. The magnetic depth profile of the Pt layer was determined in the magnetic saturation state of the Fe magnetization with the sample of weak PMA. The magnetization process of the Pt layer was investigated with the sample of moderate PMA. It is found that the Pt atoms near the interface region have a perpendicular component of the induced magnetization even in the saturation state of the Fe magnetization, suggesting that the PMA of Fe/Pt multilayers originates from the Pt atoms near the interface region. Concerning the magnetization process, the induced Pt magnetization is not proportional to the Fe magnetization. This implies a complicated magnetizing mechanism of the Pt layer by the Fe magnetization.

  18. A partial phase diagram of Pt-rich Pt-Mn alloys

    CERN Document Server

    Sembiring, T; Ohshima, K I; Ota, K; Shishido, T

    2002-01-01

    We have performed the X-ray and electron diffraction studies to reconstruct a partial phase diagram of Pt-rich Pt-Mn alloys in the composition range of 10 to 35 at.% Mn. Electrical resistivity measurement was also used for determining the order-disorder transition temperature in Pt-14.2 at.% Mn alloy. The phase boundary between Cu sub 3 Au type and ABC sub 6 type ordered structures is established, in which the latter has been found recently by the present [J.Phys. Soc. Jpn. 71 (2002) 681]. In the ABC sub 6 type ordered phase, superlattice reflections both at 1/2 1/2 1/2 and its equivalent position (L-point) and at 100, 110 and their equivalent positions (X-point) appear in the composition range from 12.5 to 14.4 at.% Mn below 682degC. In the Cu sub 3 Au type ordered phase, diffuse maxima at L-point appear in the composition range from 15.9 to 19.7 at.% Mn in addition to the superlattice reflections at X-point. The Cu sub 3 Au type ordered structure is found to be stable in the composition range from 19.7 to 3...

  19. Investigation of nano Pt and Pt-based alloys electrocatalysts for direct methanol fuel cells and their properties

    Directory of Open Access Journals (Sweden)

    Chunguang Suo

    2014-03-01

    Full Text Available The electrocatalysts used in micro direct methanol fuel cell (μDMFC, such as Pt/C and Pt alloy/C, prepared by liquid-phase NaBH4 reduction method have been investigated. XC-72 (Cobalt corp. Company, U.S.A is chosen as the activated carrier for the electrocatalysts to keep the catalysts powder in the range of several nanometers. The XRD, SEM, EDX analyses indicated that the catalysts had small particle size in several nanometers, in excellent dispersed phase and the molar ratio of the precious metals was found to be optimal. The performances of the DMFCs using cathodic catalyst with Pt percentage of 30wt% and different anodic catalysts (Pt-Ru, Pt-Ru-Mo were tested. The polarization curves and power density curves of the cells were measured to determine the optimal alloy composition and condition for the electrocatalysts. The results showed that the micro direct methanol fuel cell with 30wt% Pt/C as the cathodic catalyst and n(Pt:n(Ru:n(Mo = 3:2:2 PtRuMo/C as the anodic catalyst at room temperature using 2.0mol/L methanol solution has the best performances.

  20. Three-dimensional shapes and spatial distributions of Pt and PtCr catalyst nanoparticles on carbon black

    DEFF Research Database (Denmark)

    Gontard, Lionel Cervera; Dunin-Borkowski, Rafal E.; Ozkaya, D.

    2008-01-01

    High-angle annular dark-field scanning transmission electron microscopy tomography is applied to the study of Pt and PtCr nanoparticles supported on carbon black, which are used as heterogeneous catalysts in the electrodes of proton exchange membrane fuel cells. By using electron tomography, the ...

  1. Stretching dependence of the vibration modes of a single-molecule Pt-H-2-Pt bridge

    DEFF Research Database (Denmark)

    Djukic, D.; Thygesen, Kristian Sommer; Untiedt, C.

    2005-01-01

    isotope substitution is obtained. The stretching dependence for each of the modes allows uniquely classifying them as longitudinal or transversal modes. The interpretation of the experiment in terms of a Pt-H-2-Pt bridge is verified by density-functional theory calculations for the stability, vibrational...

  2. 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.

  3. Impact of buffer layer and Pt thickness on the interface structure and magnetic properties in (Co/Pt) multilayers

    Science.gov (United States)

    Bersweiler, M.; Dumesnil, K.; Lacour, D.; Hehn, M.

    2016-08-01

    The influence of Pt thickness on the interface structure (roughness / intermixing) and magnetic properties has been investigated for (Co / Pt) multilayers sputtered on a Pt or a thin oxide (MgO or AlO x ) buffer layer. When Pt thickness increases from 1.2 nm-2.2 nm, we observe that the effective anisotropy increases with the Pt thickness, simultaneously with the decrease of roughness, i.e. the occurrence of sharper interfaces. Perpendicular magnetic anisotropy (PMA) is still achieved on the oxide buffer layers, but with a lower effective anisotropy correlated to more perturbed interfaces. The detailed analysis of the saturation magnetization shows that: (i) M s is significantly enhanced in the case of rough/intermixed interfaces, which is attributed to and discussed in the framework of Pt induced polarization, (ii) the change in volume dipolar anisotropy is the main factor responsible for the reduction of K eff for systems grown on oxides. Beyond the major role of volume dipolar contribution that reduces PMA, a supplemental positive contribution promoting PMA can be invoked for rough interfaces and large M s (deposit on oxide). This contribution is consistent with a dipolar surface anisotropy term and increases for rough interfaces, in contrast to the Néel surface anisotropy. These opposite variations may interestingly lead to an enhanced anisotropy in (Co / Pt) stackings grown on oxides compared to systems deposited on Pt, i.e. with sharper interfaces.

  4. Unexpected, spontaneous and selective formation of colloidal Pt 3Sn nanoparticles using organometallic Pt and Sn complexes

    KAUST Repository

    Boualleg, Malika

    2010-01-01

    The facile and selective synthesis of small crystalline Pt3Sn alloy nanoparticles was performed at room temperature under H2, using a colloidal approach without the use of extra-stabilizing ligands. The Pt 3Sn alloy was found to be obtained spontaneously as the unique phase regardless of the number of tin equivalents introduced. © 2010 The Royal Society of Chemistry.

  5. Effects of Pt speedlayer and Ar pressure on magnetic and structural properties of sputtered CoNi/Pt multilayers

    NARCIS (Netherlands)

    Meng, Q.; Haan, de P.; Drent, van W.P.; Lodder, J.C.; Popma, Th.J.A.

    1996-01-01

    CoNi/Pt multilayers were prepared by magnetron sputtering using Ar gas. The effects of the Pt seed layer and the Ar sputtering pressure on magnetic and structural properties are investigated. Microstructures of the multilayers were analysed using XRD and TEM. It was found that perpendicular magnetic

  6. The study on carbon nanotubes-supported Pt catalysts for PEMFC

    Institute of Scientific and Technical Information of China (English)

    朱捷; 朱红; 康晓红; 葛奉娟; 杨玉国

    2004-01-01

    Carbon nanotube-supported-platinum (Pt/CNTs) and carbon-supported-platinum (Pt/C) catalysts were prepared by in situ chemical reduction method and analyzed by TEM and XRD. Then the experiments were carried out to test the performance of PEMFCs with the Pt electrodes. The results showed that in both catalyst, Pt was of small particle size (about 4 nm) and Pt/CNTs exhibited higher catalytic activity than Pt/C.

  7. 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.

  8. New evaluation of alpha decay half-life of {sup 190}Pt isotope for the Pt-Os dating system

    Energy Technology Data Exchange (ETDEWEB)

    Tavares, O.A.P.; Medeiros, E.L. [Centro Brasileiro de Pesquisas Fisicas (CBPF), Rio de Janeiro, RJ (Brazil); Terranova, M.L. [Universita degli Studi di Roma Tor Vergata (Italy). Dipt. di Scienze e Tecnologie Chimiche; Istituto Nazionale di Fisica Nucleare (INFN), Rome (Italy)

    2005-08-15

    A semiempirical model based on the quantum mechanical tunnelling mechanism of alpha emission from nuclei has been used to evaluate the half-life of the Pt isotopes. For the important naturally occurring {sup 190}Pt isotope, the radiogenic parent in the {sup 190} Pt {yields} {sup 186}Os dating system, the model yielded a half-life value of (3.7{+-} 0.3) versus 10{sup 11} y. This is comparable to (3.2{+-}0.1) versus 10{sup 11} y which was obtained in the last direct counting experiment to measure the alpha activity of {sup 190}Pt (Tavares and Terranova, Rad. Measurem. 27 (1997) 19). A literature survey of available alpha decay half-life values for {sup 190}Pt isotope is also reported. The significant discrepancies found between data obtained by direct counting, indirect geological methods and different calculation models are analysed and discussed. (author)

  9. 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...

  10. Formation of FePt Nanoparticles Having High Coercivity

    Energy Technology Data Exchange (ETDEWEB)

    Rutledge, R.D. [Vanderbilt University; MorrisIII, William H [Vanderbilt University; Wellons, M.S. [Vanderbilt University; Gai, Zheng [ORNL; Shen, Jian [ORNL; Bentley, James [ORNL; Wittig, J. E. [Vanderbilt University; Lukehart, C.M. [Vanderbilt University

    2006-01-01

    Ultrasonication of toluene solutions of the heteropolynuclear cluster complex, Pt{sub 3}Fe{sub 3}(CO){sub 15}, in the presence of oleic acid and oleylamine affords surface-capped fcc FePt nanoparticles having an average diameter of ca. 2 nm. Self-assembled arrays of these nanoparticles on oxidized Si wafers undergo a fcc-to-fct phase transition at 775 C to form ferromagnetic FePt nanocrystals ca. 5.8 nm in diameter well dispersed on the Si wafer surface. Room-temperature coercivity measurements of these annealed FePt nanoparticles confirm a high coercivity of ca. 22.3 kOe. Such high coercivity for fct FePt nanoparticles might result from use of a heterpolynuclear complex as a single-source precursor of Fe and Pt neutral atoms or from use of ultrasonication to form fcc FePt nanoparticles under conditions of exceptionally rapid heating. Experiments to determine the critical experimental conditions required to achieve such high room-temperature coercivities in ferromagnetic nanoparticles are underway.

  11. Magnetism of FePt Nanoclusters in Polyimide

    Directory of Open Access Journals (Sweden)

    Mircea Chipara

    2015-01-01

    Full Text Available FePt nanoclusters have been implanted onto polyimide films and subjected to thermal annealing in order to obtain a special magnetic phase (L10 dispersed within the polymer. SQUID measurements quantified the magnetic features of the as-prepared and annealed hybrid films. As-implanted FePt nanoparticles in polyimide films exhibited a blocking temperature of 70 ± 5 K. Thermal annealing in zero and 10 kOe applied magnetic field increased the magnetic anisotropy and coercivity of the samples. Wide Angle X-Ray Scattering confirmed the presence of FePt and L10 phase. All samples (as deposited and annealed exhibited electron spin resonance spectra consisting of two overlapping lines. The broad line was a ferromagnetic resonance originating from FePt nanoparticles. Its angular dependence indicated the magnetic anisotropy of FePt nanoparticles. SEM micrographs suggest a negligible coalescence of FePt nanoparticles, supporting that the enhancement of the magnetic properties is a consequence of the improvement of the L10 structure. The narrow ESR line was assigned to nonmagnetic (paramagnetic impurities within the samples consistent with graphite-like structures generated by the local degradation of the polymer during implantation and annealing. Raman spectroscopy confirmed the formation of graphitic structures in annealed KHN and in KHN-FePt.

  12. Design criteria for stable Pt/C fuel cell catalysts.

    Science.gov (United States)

    Meier, Josef C; Galeano, Carolina; Katsounaros, Ioannis; Witte, Jonathon; Bongard, Hans J; Topalov, Angel A; Baldizzone, Claudio; Mezzavilla, Stefano; Schüth, Ferdi; Mayrhofer, Karl J J

    2014-01-01

    Platinum and Pt alloy nanoparticles supported on carbon are the state of the art electrocatalysts in proton exchange membrane fuel cells. To develop a better understanding on how material design can influence the degradation processes on the nanoscale, three specific Pt/C catalysts with different structural characteristics were investigated in depth: a conventional Pt/Vulcan catalyst with a particle size of 3-4 nm and two Pt@HGS catalysts with different particle size, 1-2 nm and 3-4 nm. Specifically, Pt@HGS corresponds to platinum nanoparticles incorporated and confined within the pore structure of the nanostructured carbon support, i.e., hollow graphitic spheres (HGS). All three materials are characterized by the same platinum loading, so that the differences in their performance can be correlated to the structural characteristics of each material. The comparison of the activity and stability behavior of the three catalysts, as obtained from thin film rotating disk electrode measurements and identical location electron microscopy, is also extended to commercial materials and used as a basis for a discussion of general fuel cell catalyst design principles. Namely, the effects of particle size, inter-particle distance, certain support characteristics and thermal treatment on the catalyst performance and in particular the catalyst stability are evaluated. Based on our results, a set of design criteria for more stable and active Pt/C and Pt-alloy/C materials is suggested.

  13. Design criteria for stable Pt/C fuel cell catalysts

    Directory of Open Access Journals (Sweden)

    Josef C. Meier

    2014-01-01

    Full Text Available Platinum and Pt alloy nanoparticles supported on carbon are the state of the art electrocatalysts in proton exchange membrane fuel cells. To develop a better understanding on how material design can influence the degradation processes on the nanoscale, three specific Pt/C catalysts with different structural characteristics were investigated in depth: a conventional Pt/Vulcan catalyst with a particle size of 3–4 nm and two Pt@HGS catalysts with different particle size, 1–2 nm and 3–4 nm. Specifically, Pt@HGS corresponds to platinum nanoparticles incorporated and confined within the pore structure of the nanostructured carbon support, i.e., hollow graphitic spheres (HGS. All three materials are characterized by the same platinum loading, so that the differences in their performance can be correlated to the structural characteristics of each material. The comparison of the activity and stability behavior of the three catalysts, as obtained from thin film rotating disk electrode measurements and identical location electron microscopy, is also extended to commercial materials and used as a basis for a discussion of general fuel cell catalyst design principles. Namely, the effects of particle size, inter-particle distance, certain support characteristics and thermal treatment on the catalyst performance and in particular the catalyst stability are evaluated. Based on our results, a set of design criteria for more stable and active Pt/C and Pt-alloy/C materials is suggested.

  14. Perpendicular magnetic anisotropy of CoSiB/Pt multilayers

    Energy Technology Data Exchange (ETDEWEB)

    Park, J. S.; Yim, H. I. [Sookmyung Women' s University, Seoul (Korea, Republic of); Hwang, J. Y.; Lee, S. B. [Hanyang University, Seoul (Korea, Republic of); Kim, T. W. [Sejong University, Seoul (Korea, Republic of)

    2010-12-15

    We have investigated the perpendicular magnetic anisotropy of [CoSiB t{sub CoSiB}/Pt t{sub Pt}]{sub n} multilayers as a function of the CoSiB and the Pt thicknesses and the number of repetition of the CoSiB/Pt bilayers. The coercivity (H{sub c}) and the saturation magnetization (M{sub s}) of the amorphous ferromagnetic material Co{sub 75}Si{sub 15}B{sub 10} were taken to be 1.6 Oe and 407 emu/cm{sup 3}, respectively. The H{sub c} in [CoSiB t{sub CoSiB}/Pt 14 A]{sub 5} multilayers increases with increasing t{sub CoSiB} to reach a maximum at t{sub CoSiB} = 3 A and then decreases for t{sub CoSiB} > 3 A. The highest H{sub c} of 224 Oe and the highest perpendicular magnetic anisotropy K{sub u} of 2 x 10{sup 6} erg/cm{sup 3} were obtained in the [CoSiB 3 A/Pt 14 A]{sub 5} multilayer. Additional Pt layers do not contribute to the perpendicular magnetic anisotropy. The single-domain structure evolves into a striped multidomain structure as the bilayer repetition number n increases above 6.

  15. STRATEGI PENGEMBANGAN KEMITRAAN TERNAK AYAM BROILER PT. XYZ

    Directory of Open Access Journals (Sweden)

    Latifa Hanum

    2011-11-01

    Full Text Available Normal 0 false false false MicrosoftInternetExplorer4 /* Style Definitions */ table.MsoNormalTable {mso-style-name:"Table Normal"; mso-tstyle-rowband-size:0; mso-tstyle-colband-size:0; mso-style-noshow:yes; mso-style-parent:""; mso-padding-alt:0cm 5.4pt 0cm 5.4pt; mso-para-margin:0cm; mso-para-margin-bottom:.0001pt; mso-pagination:widow-orphan; font-size:10.0pt; font-family:"Times New Roman"; mso-ansi-language:#0400; mso-fareast-language:#0400; mso-bidi-language:#0400;} The objectives of this research are to (1 analyze profit and BEP of plasma farmers (2 analyze internal and external strategic factors that influence development of broiler partnership in PT. XYZ, (3 formulate the alternative strategies of broiler partnership in PT. XYZ, (4 formulate selected priority strategy to develop broiler partnership in PT. XYZ. This research uses descriptive method based on case study on broiler partnership in PT. XYZ. Based on BEP analysis, BEP (production of plasma farmers is in the range 79,91%-86,58% from chick-in capacity, and BEP (price is in the range of Rp 11.684 – Rp 12.191 per chicken on market price. PT. XYZ partnership’s position in IE matric was second quadrant (grow and builds. The results of SWOT analysis are: a vertical integration strategy through feedmill, breeding and chicken slaughterhouse, b improving production capacity through capacity building of plasma farmers, c improvement in bio-security aspects of maintenance, and d improving the quality of technical staff and improving supervision. The priority strategy from QSPM analysis is improving production capacity through capacity building of plasma farmers. The strategy to improve production capacity can be done by maximize or add their capacity, and add the new plasma farmers.   Keywords: Broiler Partnership, Internal Environment, External Environment, Internal-external, Improvement Priority

  16. Pt(IV) complexes as prodrugs for cisplatin.

    Science.gov (United States)

    Shi, Yi; Liu, Shu-An; Kerwood, Deborah J; Goodisman, Jerry; Dabrowiak, James C

    2012-02-01

    The antitumor effects of platinum(IV) complexes, considered prodrugs for cisplatin, are believed to be due to biological reduction of Pt(IV) to Pt(II), with the reduction products binding to DNA and other cellular targets. In this work we used pBR322 DNA to capture the products of reduction of oxoplatin, c,t,c-[PtCl(2)(OH)(2)(NH(3))(2)], 3, and a carboxylate-modified analog, c,t,c-[PtCl(2)(OH)(O(2)CCH(2)CH(2)CO(2)H)(NH(3))(2)], 4, by ascorbic acid (AsA) or glutathione (GSH). Since carbonate plays a significant role in the speciation of platinum complexes in solution, we also investigated the effects of carbonate on the reduction/DNA-binding process. In pH 7.4 buffer in the absence of carbonate, both 3 and 4 are reduced by AsA to cisplatin (confirmed using ((195))Pt NMR), which binds to and unwinds closed circular DNA in a manner consistent with the formation of the well-known 1, 2 intrastrand DNA crosslink. However, when GSH is used as the reducing agent for 3 and 4, ((195))Pt NMR shows that cisplatin is not produced in the reaction medium. Although the Pt(II) products bind to closed circular DNA, their effect on the mobility of Form I DNA is different from that produced by cisplatin. When physiological carbonate is present in the reduction medium, ((13))C NMR shows that Pt(II) carbonato complexes form which block or impede platinum binding to DNA. The results of the study vis-à-vis the ability of the Pt(IV) complexes to act as prodrugs for cisplatin are discussed. Copyright © 2011 Elsevier Inc. All rights reserved.

  17. 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.

  18. DSC study of martensite transformation in TiPt alloys

    CSIR Research Space (South Africa)

    Chikosha, S

    2012-09-01

    Full Text Available .J. Witcomb, L.A. Cornish, Metall. & Mat. Trans. A , 2001, 32A:1881-86 K. Otsuka & X Ren, Prog. Mat. Scie., 2005, 50:511-75 Page 6 Experimental Procedure ? CSIR 2012 www.csir.co.za Ti-50at%Pt BE powder Hot Press SPS Cold...-Press & Sinter SEM/EDS & DSC Page 7 Spark Plasma Sintering 1200?C, 60 MPa ? Incomplete homogenisation of the bulk ? Pt-rich TiPt phase is formed, coexisting with other phases ? DSC shows two overlapping peaks instead of one, possible two-stage Ti...

  19. Nanopatterned CoPt alloys with perpendicular magnetic anisotropy

    Science.gov (United States)

    Makarov, D.; Bermúdez-Ureña, E.; Schmidt, O. G.; Liscio, F.; Maret, M.; Brombacher, C.; Schulze, S.; Hietschold, M.; Albrecht, M.

    2008-10-01

    CoPt alloy films with perpendicular magnetic anisotropy were grown on SiO2 nanoparticle arrays with particle sizes as small as 10 nm. In order to induce perpendicular magnetic anisotropy in the CoPt film, a MgO seed layer was sputter deposited. Despite the fact that neighboring CoPt film caps are interconnected, individual caps appear as single domain and for most of them their magnetization orientation can be reversed individually. This behavior might be caused by domain wall nucleation and pinning preferentially at the rim of each cap. Thus, arrays of magnetic caps with defined pinning sites can be considered as a percolated perpendicular medium.

  20. Electrochemical characters and structure changes of electrochemically treated Pt nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Yuan, Huiping; Qiu, Xinping; Chen, Liquan [Key Laboratory of Organic Optoelectronics and Molecular Engineering, Department of Chemistry, Tsinghua University, Beijing 100084 (China); Lab of Advanced Power Sources, Graduate School at Shenzhen, Tsinghua University, Shenzhen 518055 (China); Song, Huanqiao; Zhu, Wentao [Key Laboratory of Organic Optoelectronics and Molecular Engineering, Department of Chemistry, Tsinghua University, Beijing 100084 (China)

    2010-01-15

    In this paper, the surface and electrochemical characters of the Pt/CNT electrode before and after voltammetric cyclings were studied using high resolution transmission electron microscopy imaging (HRTEM), X-ray photon electron spectroscopy (XPS) and cyclic voltammetry measurements of CO and methanol oxidation. It was found that Pt nanoparticles were not stable and formed the linked and agglomerated structures. The changes of the crystallites led to the peak multiplicity, the negative shift of CO oxidation peaks, and the increase of the current density of methanol oxidation. We considered the specific activities were due to the increases of oxygen species and defect sites on Pt. (author)

  1. Proton microbeam irradiation effects on PtBA polymer

    Indian Academy of Sciences (India)

    J Kamila; S Roy; K Bhattacharjee; B Rout; B N Dev; R Guico; J Wang; A W Haberl; P Ayyub; P V Satyam

    2006-04-01

    Proton beam lithography has made it possible to make various types of 3D-structures in polymers. Usually PMMA, SU-8, PS polymers have been used as resist materials for lithographic purpose. Microbeam irradiation effects on poly-tert-butyl-acrylate (PtBA) polymer using 2.0 MeV proton microbeam are reported. Preliminary results on pattern formation on PtBA are carried out as a function of fluence. After writing the pattern, a thin layer of Ge is deposited. Distribution of Ge in pristine and ion beam patterned surface of PtBA polymer is studied using the optical and secondary electron microscopic experimental methods.

  2. $\\mathcal{PT}$-symmetric microring laser-absorber

    CERN Document Server

    Longhi, Stefano

    2014-01-01

    The lasing and coherent perfect absorption (CPA) properties of $\\mathcal{PT}$-symmetric microrings with mixed index and gain gratings, externally coupled to a bus waveguide, are theoretically investigated. For a complex grating at the $\\mathcal{PT}$ symmetry breaking point, perfect unidirectional (either clockwise or counterclockwise) laser emission can be realized, however the grating does not discriminate longitudinal modes and CPA can not be simultaneously achieved. Above the grating $\\mathcal{PT}$ symmetry breaking point, single mode emission and simultaneous CPA can be obtained, with unbalanced and controllable excitation of clockwise and counterclockwise modes in the ring.

  3. The Pt(111)/Electrolyte Interface under Oxygen Reduction Reaction Conditions

    DEFF Research Database (Denmark)

    Bondarenko, A.S.; Stephens, Ifan; Hansen, Heine Anton;

    2011-01-01

    between the adsorbate and Pt surface atoms (0.45−1.15 V vs RHE). An equivalent electric circuit is proposed to model the Pt(111)/electrolyte interface under ORR conditions within the selected potential window. This equivalent circuit reflects three processes with different time constants, which occur...... simultaneously during the ORR at Pt(111). Density functional theory (DFT) calculations were used to correlate and interpret the results of the measurements. The calculations indicate that the coadsorption of ClO4* and Cl* with OH* is unlikely. Our analysis suggests that the two-dimensional (2D) structures formed...

  4. Giant Goos-Hänchen shift using PT symmetry

    Science.gov (United States)

    Ziauddin; Chuang, You-Lin; Lee, Ray-Kuang

    2015-07-01

    Influence of PT symmetry on the Goos-Hänchen (GH) shift in the reflected light is presented for an ensemble of atomic medium in a cavity, in the configuration of four-level N -type (87Rb atoms) systems driving by two copropagating strong laser fields and a weak probe field. The atom-field interaction follows the realization of PT symmetry by adjusting the coupling field detunings [J. Shenget al., Phys. Rev. A 88, 041803(R) (2013), 10.1103/PhysRevA.88.041803]. A giant enhancement for the GH shift in the reflected light is revealed when the PT -symmetry condition is satisfied.

  5. PT-symmetric $\\varphi^4$ theory in d=0 dimensions

    CERN Document Server

    Bender, Carl M; Messina, Emanuele

    2015-01-01

    A detailed study of a PT-symmetric zero-dimensional quartic theory is presented and a comparison between the properties of this theory and those of a conventional quartic theory is given. It is shown that the PT-symmetric quartic theory evades the consequences of the Mermin-Wagner-Coleman theorem regarding the absence of symmetry breaking in d<2 dimensions. Furthermore, the PT-symmetric theory does not satisfy the usual Bogoliubov limit for the construction of the Green's functions because one obtains different results for the $h\\to0^-$ and the $h\\to0^+$ limits.

  6. Inverse spin Hall effect in Pt/(Ga,Mn)As

    Energy Technology Data Exchange (ETDEWEB)

    Nakayama, H. [Laboratory for Nanoelectronics and Spintronics, Research Institute of Electrical Communication, Tohoku University, 2-1-1 Katahira, Aoba-ku, Sendai 980-8577 (Japan); Chen, L. [WPI-Advanced Institute for Materials Research (WPI-AIMR), Tohoku University, 2-1-1 Katahira, Aoba-ku, Sendai 980-8577 (Japan); Chang, H. W. [Laboratory for Nanoelectronics and Spintronics, Research Institute of Electrical Communication, Tohoku University, 2-1-1 Katahira, Aoba-ku, Sendai 980-8577 (Japan); Department of Physics and Center for Nanoscience and Nanotechnology, National Sun Yat-Sen University, Kaohsiung 804, Taiwan (China); Ohno, H.; Matsukura, F., E-mail: f-matsu@wpi-aimr.tohoku.ac.jp [Laboratory for Nanoelectronics and Spintronics, Research Institute of Electrical Communication, Tohoku University, 2-1-1 Katahira, Aoba-ku, Sendai 980-8577 (Japan); WPI-Advanced Institute for Materials Research (WPI-AIMR), Tohoku University, 2-1-1 Katahira, Aoba-ku, Sendai 980-8577 (Japan); Center for Spintronics Integrated Systems, Tohoku University, 2-1-1 Katahira, Aoba-ku, Sendai 980-8577 (Japan)

    2015-06-01

    We investigate dc voltages under ferromagnetic resonance in a Pt/(Ga,Mn)As bilayer structure. A part of the observed dc voltage is shown to originate from the inverse spin Hall effect. The sign of the inverse spin Hall voltage is the same as that in Py/Pt bilayer structure, even though the stacking order of ferromagnetic and nonmagnetic layers is opposite to each other. The spin mixing conductance at the Pt/(Ga,Mn)As interface is determined to be of the order of 10{sup 19 }m{sup −2}, which is about ten times greater than that of (Ga,Mn)As/p-GaAs.

  7. Pt3 Co Octapods as Superior Catalysts of CO2 Hydrogenation.

    Science.gov (United States)

    Khan, Munir Ullah; Wang, Liangbing; Liu, Zhao; Gao, Zehua; Wang, Shenpeng; Li, Hongliang; Zhang, Wenbo; Wang, Menglin; Wang, Zhengfei; Ma, Chao; Zeng, Jie

    2016-08-08

    As the electron transfer to CO2 is a critical step in the activation of CO2 , it is of significant importance to engineer the electronic properties of CO2 hydrogenation catalysts to enhance their activity. Herein, we prepared Pt3 Co nanocrystals with improved catalytic performance towards CO2 hydrogenation to methanol. Pt3 Co octapods, Pt3 Co nanocubes, Pt octapods, and Pt nanocubes were tested, and the Pt3 Co octapods achieved the best catalytic activity. Both the presence of multiple sharp tips and charge transfer between Pt and Co enabled the accumulation of negative charges on the Pt atoms in the vertices of the Pt3 Co octapods. Moreover, infrared reflection absorption spectroscopy confirmed that the high negative charge density at the Pt atoms in the vertices of the Pt3 Co octapods promotes the activation of CO2 and accordingly enhances the catalytic activity.

  8. Aplikasi Pemasaran Berbasis Web Pt Xyz

    Directory of Open Access Journals (Sweden)

    Henny Hendarti

    2013-12-01

    Full Text Available Marketing plays an important role in determining the success of a company's sales. Marketing of goods or services over the Internet opens an opportunity for a company to expand the business into new markets, and compete with other businesses in the same field. It is because the internet offers wider selection of good products, service products, and prices. Thus, customers can be sure in choosing and buying of goods and services. For that e-marketing is introduced as an marketing strategy that integrates internet and marketing. A study was conducted to develop e-marketing application for PT XYZ as a company that produces and sells men’s apparel and accessories. The methodology used in developing the e-marketing application is library research, field research, and a seven-stage approach to build e-marketing. The e-marketing strategy developed is expected to expand market share and increase sales. Additionally, it is expected to be a powerful strategy to build relationships with customers, providing information of both company and its products.

  9. Porcelain Product Quality Analysis in PT XYZ

    Directory of Open Access Journals (Sweden)

    Ho Hwi Chie

    2015-12-01

    Full Text Available PT. XYZ is a company engaged in manufacturing porcelain dinner ware such as plates, cups, teapot, bowl, etc Porcelain product is safe for use and product defect will only affect the aesthetic not the functional side. The company always maintain the quality of the products produced as by maintaining a good product, in terms of visuals, will keep customers interested in the product. Good quality products characterized by quality A / B and C, and the product defect characterized by the quality of D, Lost, and BU. Concepts and methods used to analyze is a statistical process control (SPC which includes Pareto diagram, fraction nonconformities, flow charts and fishbone diagrams and management tools (fault tree analysis. Statistical Process Control (SPC is one of the methods, which includes Pareto charts, fraction nonconformities, flow chart, and fishbone diagram and also management tools (fault tree analysis. SPC is useful to find the facts from the problems and factors that affect the quality of the products, while fault tree analysis is useful to analyze each of the production process.

  10. Coupled Oscillator Systems Having Partial PT Symmetry

    CERN Document Server

    Beygi, Alireza; Bender, Carl M

    2015-01-01

    This paper examines chains of $N$ coupled harmonic oscillators. In isolation, the $j$th oscillator ($1\\leq j\\leq N$) has the natural frequency $\\omega_j$ and is described by the Hamiltonian $\\frac{1}{2}p_j^2+\\frac{1}{2}\\omega_j^2x_j^2$. The oscillators are coupled adjacently with coupling constants that are purely imaginary; the coupling of the $j$th oscillator to the $(j+1)$st oscillator has the bilinear form $i\\gamma x_jx_{j+1}$ ($\\gamma$ real). The complex Hamiltonians for these systems exhibit {\\it partial} $\\mathcal{PT}$ symmetry; that is, they are invariant under $i\\to-i$ (time reversal), $x_j\\to-x_j$ ($j$ odd), and $x_j\\to x_j$ ($j$ even). [They are also invariant under $i\\to-i$, $x_j\\to x_j$ ($j$ odd), and $x_j\\to- x_j$ ($j$ even).] For all $N$ the quantum energy levels of these systems are calculated exactly and it is shown that the ground-state energy is real. When $\\omega_j=1$ for all $j$, the full spectrum consists of a real energy spectrum embedded in a complex one; the eigenfunctions correspondi...

  11. Porcelain Product Quality Analysis in PT XYZ

    Directory of Open Access Journals (Sweden)

    Ho Hwi Chie

    2015-12-01

    Full Text Available PT. XYZ is a company engaged in manufacturing porcelain dinner ware such as plates, cups, teapot, bowl, etc Porcelain product is safe for use and product defect will only affect the aesthetic not the functional side. The company always maintain the quality of the products produced as by maintaining a good product, in terms of visuals, will keep customers interested in the product. Good quality products characterized by quality A / B and C, and the product defect characterized by the quality of D, Lost, and BU. Concepts and methods used to analyze is a statistical process control (SPC which includes Pareto diagram, fraction nonconformities, flow charts and fishbone diagrams and management tools (fault tree analysis. Statistical Process Control (SPC is one of the methods, which includes Pareto charts, fraction nonconformities, flow chart, and fishbone diagram and also management tools (fault tree analysis. SPC is useful to find the facts from the problems and factors that affect the quality of the products, while fault tree analysis is useful to analyze each of the production process.

  12. Shape resonances and EXAFS scattering in the $Pt L_{2,3}$ XANES from a Pt electrode

    CERN Document Server

    O'Grady, W E

    1999-01-01

    Atomic hydrogen and oxygen adsorption on a platinum electrode in H /sub 2/SO/sub 4/ and HClO/sub 4/ electrolytes were studied by Pt L /sub 23/ XANES. The Pt electrode was formed of highly dispersed 1.5-3.0 nm particles supported on $9 carbon. A difference procedure utilizing the L/sub 2/ and L/sub 3/ spectra at various applied voltages was used to isolate the electronic and geometric effects in the XANES spectra. At 0.54 V (relative to RHE) the Pt electrode in $9 HClO/sub 4/ is assumed to be "clean". By taking the difference between the spectra at 0.0 and 0.54 V, the Pt-H antibonding state (electronic effect) is isolated and found to have a Fano-resonance line shape. In addition, a $9 significant Pt-H EXAFS scattering (geometric effect) was found for photon energies 0 to 20 eV above the edge. The difference between the spectra at 1.14 and 0.54 V allows isolation of the Pt-O antibonding state and the Pt-O EXAFS $9 scattering. (7 refs).

  13. Switching fields of high-resolution magnetic force microscope tips coated with Co, Co75Pt10Cr15, Co75Pt25, and Co50Pt50 films

    Directory of Open Access Journals (Sweden)

    Ishihara Shinji

    2014-07-01

    Full Text Available Magnetic force microscope (MFM tips are prepared by coating Si tips of 4 nm radius with Co, Co75Pt10Cr15, Co75Pt25, and Co50Pt50 (at. % films of 20 nm thickness at 300 °C. The effects of coating film material on the spatial resolution and the switching field are investigated. Higher resolutions are observed in the order of Co75Pt10Cr15 < (Co50Pt50, Co75Pt25 < Co. The Co-coated tip shows the highest resolution of 7.3 nm, which seems to be depending on a high detection sensitivity related with the magnetic moment of Co material. The saturation magnetization increases in the order of Co75Pt10Cr15 < Co50Pt50 < Co75Pt25 < Co. Higher switching fields are observed in the order of Co < Co75Pt10Cr15 < Co75Pt25 < Co50Pt50. The Co50Pt50-coated tip shows the highest switching field of 1.675±0.025 kOe, which is due to a high coercive field of the magnetic film involving L11 ordered phase with high magnetocrystalline anisotropy energy. The coercive field is recognized in the order of Co < Co75Pt10Cr15 < Co75Pt25 < Co50Pt50. A tip prepared by coating Co50Pt50 film which has high resolution and high switching field is useful for MFM observations of high-density recording media and permanent magnets.

  14. Preparation and characterization of Pt-CeO2/C and Pt-TiO2/C electrocatalysts with improved electrocatalytic activity for methanol oxidation

    Science.gov (United States)

    Hameed, R. M. Abdel; Amin, R. S.; El-Khatib, K. M.; Fetohi, Amani E.

    2016-03-01

    Pt-TiO2/C and Pt-CeO2/C electrocatalysts were synthesized by solid state reaction of TiO2/C and CeO2/C powders using intermittent microwave heating, followed by chemical reduction of platinum ions using mixed reducing agents of ethylene glycol and sodium borohydride. The crystal structure, surface morphology and chemical composition of prepared electrocatalysts were investigated using X-ray diffraction (XRD), transmission electron microscopy (TEM) and energy dispersive X-ray analysis (EDX). The phase angle values of different Pt diffraction planes in Pt-TiO2/C and Pt-CeO2/C were shifted in the positive direction relative to those in Pt/C. Pt particles with diameter values of 3.06 and 2.78 nm were formed in Pt-TiO2/C and Pt-CeO2/C, respectively. The electrochemical performance of prepared electrocatalysts was examined using cyclic voltammetry, chronoamperometry and electrochemical impedance spectroscopy. Pt-CeO2/C showed an enhanced oxidation current density when compared to Pt/C. Long time oxidation test at Pt-TiO2/C and Pt-CeO2/C revealed their improved stability. Lower charge transfer resistance values were estimated at Pt-metal oxide/C electrocatalysts.

  15. Tecnical Note: Analysis of non-regulated vehicular emissions by extractive FTIR spectrometry: tests on a hybrid car in Mexico City

    Directory of Open Access Journals (Sweden)

    F. Reyes

    2006-01-01

    Full Text Available A methodology to acquire valuable information on the chemical composition and evolution of vehicular emissions is presented. The analysis of the gases is performed by passing a constant flow of a sample gas from the tail-pipe into a 10 L multi-pass cell. The absorption spectra within the cell are obtained using an FTIR spectrometer at 0.5 cm−1 resolution along a 13.1 m optical path. Additionally, the total flow from the exhaust is continuously measured from a differential pressure sensor on a extit{Pitot} tube installed at the exit of the exhaust. This configuration aims to obtain a good speciation capability by coadding spectra during 30 s and reporting the emission (in g/km of both criteria and non-regulated pollutants, such as CO2, CO, NO, SO2, NH3, HCHO and some NMHC, during predetermined driving cycles. The advantages and disadvantages of increasing the measurement frequency, as well as the effect of other parameters such as spectral resolution, cell volume and flow rate, are discussed. To test and evaluate the proposed technique, experiments were performed on a dynamometer running FTP-75 and typical driving cycles for the Mexico City Metropolitan Area (MCMA on a Toyota Prius hybrid vehicle. This car is an example of recent marketed automotive technology dedicated to reduced emissions, increasing the need for sensitive detection techniques. This study shows the potential of the proposed technique to measure and report in real time the emissions of a large variety of pollutants, even from a super ultra-low emission vehicle (SULEV. The emissions of HC's, NOx, CO and CO2 obtained here were compared to experiments performed in other locations with the same model vehicle. The proposed technique provides a tool for future studies comparing in detail the emissions of vehicles using alternative fuels and emission control systems.

  16. Tecnical Note: Analysis of non-regulated vehicular emissions by extractive FTIR spectrometry: tests on a hybrid car in Mexico City

    Science.gov (United States)

    Reyes, F.; Grutter, M.; Jazcilevich, A.; González-Oropeza, R.

    2006-11-01

    A methodology to acquire valuable information on the chemical composition and evolution of vehicular emissions is presented. The analysis of the gases is performed by passing a constant flow of a sample gas from the tail-pipe into a 10 L multi-pass cell. The absorption spectra within the cell are obtained using an FTIR spectrometer at 0.5 cm-1 resolution along a 13.1 m optical path. Additionally, the total flow from the exhaust is continuously measured from a differential pressure sensor on a textit{Pitot} tube installed at the exit of the exhaust. This configuration aims to obtain a good speciation capability by coadding spectra during 30 s and reporting the emission (in g/km) of both criteria and non-regulated pollutants, such as CO2, CO, NO, SO2, NH3, HCHO and some NMHC, during predetermined driving cycles. The advantages and disadvantages of increasing the measurement frequency, as well as the effect of other parameters such as spectral resolution, cell volume and flow rate, are discussed. To test and evaluate the proposed technique, experiments were performed on a dynamometer running FTP-75 and typical driving cycles for the Mexico City Metropolitan Area (MCMA) on a Toyota Prius hybrid vehicle. This car is an example of recent marketed automotive technology dedicated to reduced emissions, increasing the need for sensitive detection techniques. This study shows the potential of the proposed technique to measure and report in real time the emissions of a large variety of pollutants, even from a super ultra-low emission vehicle (SULEV). The emissions of HC's, NOx, CO and CO2 obtained here were compared to experiments performed in other locations with the same model vehicle. The proposed technique provides a tool for future studies comparing in detail the emissions of vehicles using alternative fuels and emission control systems.

  17. Quantum mechanics of $PT$ and non-$PT$ -symmetric potentials in three dimensions

    Indian Academy of Sciences (India)

    BHARDWAJ S B; SINGH RAM MEHAR; MISHRA S C

    2016-07-01

    With a view of exploring new vistas with regard to the nature of complex eigenspectra of a non-Hermitian Hamiltonian, the quasi-exact solutions of the Schrödinger equation are investigated for a shifted harmonic potential under the framework of extended complex phase-space approach. Analyticity property ofthe eigenfunction alone is found sufficient to throw light on the nature of the eigenvalues and eigenfunctions of a system. Explicit expressions of eigenvalues and eigenfunctions for the ground state as well as excited state including their $PT$-symmetric version are worked out.

  18. Pt metal-CeO2 interaction: direct observation of redox coupling between Pt0/Pt2+/Pt4+ and Ce4+/Ce3+ states in Ce(0.98)Pt(0.02)O2-delta catalyst by a combined electrochemical and x-ray photoelectron spectroscopy study.

    Science.gov (United States)

    Sharma, Sudhanshu; Hegde, M S

    2009-03-21

    Pt ions-CeO(2) interaction in Ce(1-x)Pt(x)O(2-delta) (x=0.02) has been studied for the first time by electrochemical method combined with x-ray diffraction and x-ray photoelectron spectroscopy. Working electrodes made of CeO(2) and Ce(0.98)Pt(0.02)O(2-delta) mixed with 30% carbon are treated electrochemically between 0.0-1.2 V in potentiostatic (chronoamperometry) and potentiodynamic (cyclic voltametry) mode with reference to saturated calomel electrode. Reversible oxidation of Pt(0) to Pt(2+) and Pt(4+) state due to the applied positive potential is coupled to simultaneous reversible reduction of Ce(4+) to Ce(3+) state. CeO(2) reduces to CeO(2-y) (y=0.35) after applying 1.2 V, which is not reversible; Ce(0.98)Pt(0.02)O(2-delta) reaches a steady state with Pt(2+):Pt(4+) in the ratio of 0.60:0.40 and Ce(4+):Ce(3+) in the ratio of 0.55:0.45 giving a composition Ce(0.98)Pt(0.02)O(1.74) at 1.2 V, which is reversible. Composition of Pt ion substituted compound is reversible between Ce(0.98)Pt(0.02)O(1.95) to Ce(0.98)Pt(0.02)O(1.74) within the potential range of 0.0-1.2 V. Thus, Ce(0.98)Pt(0.02)O(2-delta) forms a stable electrode for oxidation of H(2)O to O(2) unlike CeO(2). A linear relation between oxidation of Pt(2+) to Pt(4+) with simultaneous reduction in Ce(4+) to Ce(3+) is observed demonstrating Pt-CeO(2) metal support interaction is due to reversible Pt(0)/Pt(2+)/Pt(4+) interaction with Ce(4+)/Ce(3+) redox couple.

  19. Continuous Catalytic Hydrodeoxygenation of Guaiacol over Pt/SiO2 and Pt/H-MFI-90

    DEFF Research Database (Denmark)

    Hellinger, Melanie; Baier, Sina; Mortensen, Peter Mølgaard

    2015-01-01

    Hydrodeoxygenation of guaiacol in the presence of 1-octanol was studied in a fixed-bed reactor under mild conditions (50–250 °C) over platinum particles supported on silica (Pt/SiO2) and a zeolite with framework type MFI at a Si/Al-ratio of 45 (Pt/H-MFI-90). The deoxygenation selectivity strongly...... than 30 h, probably due to carbon deposition, whereas Pt/SiO2 was more stable. The catalytic activity of the zeolite catalyst could only partly be regained by calcination in air, as some of the acidic sites were lost....

  20. Platinum Migration at the Pt/YSZ Interface

    DEFF Research Database (Denmark)

    Nielsen, Jimmi; Jacobsen, Torben

    2006-01-01

    by potential sweep, step and impedance techniques. As expected, inductive behaviour and activation during step polarization is confirmed, but furthermore, a very accentuated noise pattern is seen during cathodic step polarization. Investigation of the YSZ and Pt surfaces afterwards reveals the growth......Electrode activation, inductive hysteresis and non-linearity are well known phenomena on Pt-YSZ electrodes, and recently also regular fluctuation patterns have been reported. The oxygen electrode on YSZ surfaces is studied at Pt micro-electrodes prepared by electrochemical etching of platinum wire...... of dendrite like Pt structures from the TPB. The formation of these may explain the observed noise and contribute to the explanation of the activation mechanism taking place at the platinum-YSZ interface....

  1. CLOUD COMPUTING ADOPTION STRATEGIES AT PT TASPEN INDONESIA, Tbk

    Directory of Open Access Journals (Sweden)

    Julirzal Sarmedy

    2014-10-01

    Full Text Available PT. Taspen as Indonesian institution, is responsible for managing social insuranceprograms of civil servants. With branch offices and business partners who are geographicallydispersed throughout Indonesia, information technology is very important to support thebusiness processes. Cloud computing is a model of information technology services that couldpotentially increase the effectiveness and efficiency of PT. Taspen information system. Thisstudy examines the phenomenon exists at PT. Taspen in order to adopt cloud computing inthe information system, by using the framework of Technology-Organization-Environment,Diffusion of Innovation theory, and Partial Least Square method. Organizational factor isthe most dominant for PT. Taspen to adopt cloud computing. Referring to these findings,then a SWOT analysis and TOWS matrix are performed, which in this study recommendsthe implementation of a strategy model of cloud computing services that are private andgradually in process.

  2. Synthesis Gas Production from Natural Gas on Supported Pt Catalysts

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    Auto-thermal reforming of methane, combining partial oxidation and reforming of methane with CO2 or steam, was carried out with Pt/Al2O3, Pt/ZrO2 and Pt/CeO2 catalysts, in a temperature range of 300-900 ℃. The auto-thermal reforming occurs in two simultaneous stages, namely, total combustion of methane and reforming of the unconverted methane with steam and CO2, with the O2 conversion of 100% starting from 450 ℃. For combination with CO2 reforming, the Pt/CeO2 catalyst showed the lowest initial activity at 800 ℃, and the highest stability over 40 h on-stream. This catalyst also presented the best performance for the reaction with steam at 800 ℃. The higher resistance to coke formation of the catalyst supported on ceria is due to the metal-support interactions and the higher mobility of oxygen in the oxide lattice.

  3. Why is metallic Pt the best catalyst for methoxy decomposition?

    Institute of Scientific and Technical Information of China (English)

    Ruipeng Ren; Cuiyu Niu; Shaoyue Bu; Yuhua Zhou; Yongkang Lu; Guichang Wang

    2011-01-01

    The decomposition of methoxy on Cu(111),Ag(111),Au(111),Ni(111),Pt(111),Pd(111),and Rh(111)has been studied in detail by the density functional theory calculations.The calculated activation barriers were successfully correlated with the coupling matrix element V2ad and the d-band center(εd)for the group IB metals and group Ⅷ metals,respectively.By comparison of the activation energy barriers of the methoxy decomposition on different metals,it was found that Pt is the best catalyst for methoxy decomposition.The possible reason why the metallic Pt is the best catalyst has been analyzed from both the energetic data and the electronic structure information,that is,methoxy decomposition on Pt(111)has the largest exothermic behavior due to the closest p-band center of the CH3O among all metals after the adsorption.

  4. Anomalous doublets of states in a PT symmetric quantum model

    CERN Document Server

    Znojil, M; Roy, P; Roychoudhury, R; Znojil, Miloslav; Levai, Geza; Roy, Pinaki; Roychoudhury, Rajkumar

    2001-01-01

    A PT symmetric complexification of a conditionally exactly solvable potential in one dimension leads to a paradox. The set of its normalizable solutions proves larger than one would expect on the basis of its point canonical transformation analysis.

  5. Benzaldehyde hydrogenation over titania-covered Pt powder

    Energy Technology Data Exchange (ETDEWEB)

    Vannice, M.A.; Poondi, D. [Pennsylvania State Univ., University Park, PA (United States). Dept. of Chemical Engineering

    1998-08-15

    Titania when used as a support has been found to have a significant effect on the activity and selectivity of Pt during the hydrogenation of aldehydes and ketones. Turnover frequencies based on hydrogen adsorption sites are markedly enhanced, and rates per gram Pt (at similar dispersions) are also often increased. There are several explanations to account for this performance, at least partially. In an effort to determine the validity of these explanations, and hopefully to eliminate them as possibilities, a Pt powder was studied before and after the addition of varying amounts of TiO{sub 2} on its surface, and a physical mixture of this powder plus TiO{sub 2} was also examined and compared both to these catalysts and to Pt dispersed on TiO{sub 2}. The results follow.

  6. 高温热电偶材料PtRh40/PtRh20合金性能研究%Prorerties of PtRh40/PtRh20 High-temperature Thermocouple Wires

    Institute of Scientific and Technical Information of China (English)

    吴保安; 刘庆宾; 陈德茂; 汪建胜; 唐会毅; 陈小军

    2013-01-01

    The long-term using temperature of PtRh40/PtRh20 high-temperature thermocouple wire is 1750℃. PtRh40/PtRh20 is belong to non-standard thermocouple, and mainly applies to measure the aircraft efflux plasma temperature. The influences of annealing temperature on the tensile strength and resistivity of PtRh40 and PtRh20 alloy wires, and the influences of the cold working on tensile strength and vickers hardness of the wires were studied. The results indicated that the tensile strengths increased with the increase of annealing temperature at first, then decreased sharply, finally it is stable forming a platform. The resistivities were increased with the annealing temperature, and the tensile strength and hardness were increased with the cold working. The errors of matching thermoelectric potential of PtRh40- PtRh20 relative to ASTM E1751-2000 standard thermoelectric power is 1℃ at 1200℃, 2℃ at 1500℃, and 1℃ at 1700℃.%  PtRh40/PtRh20高温热电偶长期使用温度为1750℃,主要用于飞机尾焰高温测量,属于非标热电偶,目前国内主要依靠进口。研究了 PtRh40、PtRh20退火温度与合金电阻率、抗拉强度及加工率与抗拉强度、硬度的关系,并测试了PtRh40/PtRh20热电偶热电性能。结果表明:抗拉强度随退火温度的升高先升高再急剧下降,最后稳定在一个平台,两者大约在900℃时抗拉强度降至最低;电阻率均随退火温度升高而升高;抗拉强度与硬度均随加工率的增加而提高;PtRh40/PtRh20配对热电势相对ASTM E1751-2000标准热电势测试结果为在1200℃时误差为1℃,在1500℃时误差2℃,在1700℃时误差1℃。

  7. Strong Spin Hall effect in PtMn

    Science.gov (United States)

    Ou, Yongxi; Shi, Shengjie; Ralph, Daniel; Buhrman, Robert

    Recent reports indicate that certain metallic antiferromagnets (AFM) can exhibit a significant spin Hall effect. Here we report a large damping-like spin torque efficiency (ξDL) in PtMn/ferromagnet(FM) bilayer structures, determined from both FM-thickness-dependent spin-torque ferromagnetic resonance (ST-FMR), and harmonic response (HR) measurements of layers with perpendicular magnetic anisotropy (PMA). We find that ξDL can vary from 0.15, depending on the thickness of PtMn, the stacking order of the samples, and the choice of the FM material. The field-like spin torque efficiency (ξFL) is also quite variable, 0phase diagram. These results indicate that AFM PtMn has significant potential both for advancing the understanding the physics of the spin Hall effect in Pt alloys, and for enabling new spintronics functionality.

  8. PT Symmetry in Classical and Quantum Statistical Mechanics

    CERN Document Server

    Meisinger, Peter N

    2012-01-01

    PT-symmetric Hamiltonians and transfer matrices arise naturally in statistical mechanics. These classical and quantum models often require the use of complex or negative weights and thus fall outside of the conventional equilibrium statistical mechanics of Hermitian systems. PT-symmetric models form a natural class where the partition function is necessarily real, but not necessarily positive. The correlation functions of these models display a much richer set of behaviors than Hermitian systems, displaying sinusoidally-modulated exponential decay, as in a dense fluid, or even sinusoidal modulation without decay. Classical spin models with PT symmetry include Z(N) models with a complex magnetic field, the chiral Potts model and the anisotropic next-nearest-neighbor Ising (ANNNI) model. Quantum many-body problems with a non-zero chemical potential have a natural PT-symmetric representation related to the sign problem. Two-dimensional QCD with heavy quarks at non-zero chemical potential can be solved by diagona...

  9. Diastereoselective Pt catalyzed cycloisomerization of polyenes to polycycles.

    Science.gov (United States)

    Geier, Michael J; Gagné, Michel R

    2014-02-26

    Application of a tridentate NHC containing pincer ligand to Pt catalyzed cascade cyclization reactions has allowed for the catalytic, diastereoselective cycloisomerization of biogenic alkene terminated substrates to the their polycyclic counterparts.

  10. Electronic Properties of Graphene–PtSe2 Contacts

    KAUST Repository

    Sattar, Shahid

    2017-04-26

    In this article, we study the electronic properties of graphene in contact with monolayer and bilayer PtSe2 using first-principles calculations. It turns out that there is no charge transfer between the components because of the weak van der Waals interaction. We calculate the work functions of monolayer and bilayer PtSe2 and analyze the band bending at the contact with graphene. The formation of an n-type Schottky contact with monolayer PtSe2 and a p-type Schottky contact with bilayer PtSe2 is demonstrated. The Schottky barrier height is very low in the bilayer case and can be reduced to zero by 0.8% biaxial tensile strain.

  11. Single Pt nanowire electrode: preparation, electrochemistry, and electrocatalysis.

    Science.gov (United States)

    Li, Yongxin; Wu, Qingqing; Jiao, Shoufeng; Xu, Chaodi; Wang, Lun

    2013-04-16

    A single Pt nanowire electrode (SPNE) was fabricated through HF etching process from Pt disk nanoelectrode and an underpotential deposition (UPD) redox replacement technique. The electrochemical experiments showed that SPNE had steady-state electrochemical responses at redox species solution and the mass transfer rates were affected by the lengths and radii of SPNEs. The prepared SPNEs were utilized to examine the oxygen-reduction reaction in a KOH solution to explore the feasibility of electrocatalytic activity of single Pt nanowire and the results showed that the electrocatalytic activity of SPNE was dependent on the surface position of single Pt nanowire: the tip end position is more active than the sidewall position. Meanwhile, the electrocatalytic activity of SPNE was related to the radius of nanowire. These observations are not only important to understand the structure-function relationship in single nanowire level but have significant implications for the synthesis and selection of novel catalysts with high efficiency used in electrochemistry, energy, bioanalysis, etc.

  12. $\\mathcal{PT}$-Symmetry-Breaking Chaos in Optomechanics

    CERN Document Server

    Lü, Xin-You; Ma, Jin-Yong; Wu, Ying

    2015-01-01

    We demonstrate a $\\mathcal{PT}$-symmetry-breaking chaos in optomechanical system (OMS), which features an ultralow driving threshold. In principle, this chaos will emerge once a driving laser is applied to the cavity mode and lasts for a period of time. The driving strength is inversely proportional to the starting time of chaos. This originally comes from the dynamical enhancement of nonlinearity by field localization in $\\mathcal{PT}$-symmetry-breaking phase ($\\mathcal{PT}$BP). Moreover, this chaos is switchable by tuning the system parameters so that a $\\mathcal{PT}$-symmetry phase transition occurs. This work may fundamentally broaden the regimes of cavity optomechanics and nonlinear optics. It offers the prospect of exploring ultralow-power-laser triggered chaos and its potential applications in secret communication.

  13. Phase characterisation in spark plasma sintered TiPt alloy

    CSIR Research Space (South Africa)

    Chikosha, S

    2011-12-01

    Full Text Available The conclusions drawn from this presentation are that Spark Plasma Sintering (SPS) of equiatomic BE TiPt powder produces fully sintered specimens, with incomplete homogenisation. There is a need for improved furnace atmosphere control so...

  14. Cliffordized NAC supersymmetry and PT-symmetric Hamiltonians

    Energy Technology Data Exchange (ETDEWEB)

    Toppan, Francesco [Centro Brasileiro de Pesquisas Fisicas (CBPF), Rio de Janeiro, RJ (Brazil)]. E-mail: toppan@cbpf.br

    2007-07-01

    It is shown that non-anti commutative supersymmetry can be described through a Cliffordization of the superspace fermionic coordinates. A NAC supersymmetric quantum mechanical model is shown to be a PT-symmetric Hamiltonian. (author)

  15. Nanocrystalline Fe-Pt alloys. Phase transformations, structure and magnetism

    Energy Technology Data Exchange (ETDEWEB)

    Lyubina, J.V.

    2006-12-21

    This work has been devoted to the study of phase transformations involving chemical ordering and magnetic properties evolution in bulk Fe-Pt alloys composed of nanometersized grains. Nanocrystalline Fe{sub 100-x}Pt{sub x} (x=40-60) alloys have been prepared by mechanical ball milling of elemental Fe and Pt powders at liquid nitrogen temperature. The as-milled Fe-Pt alloys consist of {proportional_to} 100 {mu}m sized particles constituted by randomly oriented grains having an average size in the range of 10-40 nm. Depending on the milling time, three major microstructure types have been obtained: samples with a multilayer-type structure of Fe and Pt with a thickness of 20-300 nm and a very thin (several nanometers) A1 layer at their interfaces (2 h milled), an intermediate structure, consisting of finer lamellae of Fe and Pt (below approximately 100 nm) with the A1 layer thickness reaching several tens of nanometers (4 h milled) and alloys containing a homogeneous A1 phase (7 h milled). Subsequent heat treatment at elevated temperatures is required for the formation of the L1{sub 0} FePt phase. The ordering develops via so-called combined solid state reactions. It is accompanied by grain growth and thermally assisted removal of defects introduced by milling and proceeds rapidly at moderate temperatures by nucleation and growth of the ordered phases with a high degree of the long-range order. In a two-particle interaction model elaborated in the present work, the existence of hysteresis in recoil loops has been shown to arise from insufficient coupling between the low- and the high-anisotropy particles. The model reveals the main features of magnetisation reversal processes observed experimentally in exchange-coupled systems. Neutron diffraction has been used for the investigation of the magnetic structure of ordered and partially ordered nanocrystalline Fe-Pt alloys. (orig.)

  16. Anomalies in PT-Symmetric Quantum Field Theory

    CERN Document Server

    Milton, K A

    2004-01-01

    It is shown that a version of PT-symmetric electrodynamics based on an axial-vector current coupling massless fermions to the photon possesses anomalies and so is rendered nonrenormalizable. An alternative theory is proposed based on the conventional vector current constructed from massive Dirac fields, but in which the PT transformation properties of electromagnetic fields are reversed. Such a theory seems to possess many attractive features.

  17. Highly sensitive NIR PtSi/Si-nanostructure detectors

    Science.gov (United States)

    Li, Hua-gao; Guo, Pei; Yuan, An-bo; Long, Fei; Li, Rui-zhi; Li, Ping; Li, Yi

    2016-10-01

    We report a high external quantum efficiency (EQE) photodiode detector with PtSi/Si-nanostructures. Black silicon nanostructures were fabricated by metal-assist chemical etching (MCE), a 2 nm Pt layer was subsequently deposited on black silicon surface by DC magnetron sputtering system, and PtSi/Si-nanostructures were formed in vacuum annealing at 450 oC for 5 min. As the PtSi/Si-nanostructures presented a spiky shape, the absorption of incident light was remarkably enhanced for the repeat reflection and absorption. The breakdown voltage, dark current, threshold voltage and responsivity of the device were investigated to evaluate the performance of the PtSi/Si-nanostructures detector. The threshold voltage and dark currents of the PtSi/Si-nanostructure photodiode tends to be slightly higher than those of the standard diodes. The breakdown voltage remarkably was reduced because of existing avalanche breakdown in PtSi/Si-nanostructures. However, the photodiodes had high response at room temperature in near infrared region. At -5 V reverse bias voltage, the responsivity was 0.72 A/W in 1064 nm wavelength, and the EQE was 83.9%. By increasing the reverse bias voltage, the responsivity increased. At -60 V reverse bias voltage, the responsivity was 3.5 A/W, and the EQE was 407.5%, which means the quantum efficiency of PtSi/Si-nanostructure photodiodes was about 10 times higher than that of a standard diode. Future research includes how to apply this technology to enhance the NIR sensitivity of image sensors, such as Charge Coupled Devices (CCD).

  18. Unidirectional invisibility induced by PT-symmetric periodic structures.

    Science.gov (United States)

    Lin, Zin; Ramezani, Hamidreza; Eichelkraut, Toni; Kottos, Tsampikos; Cao, Hui; Christodoulides, Demetrios N

    2011-05-27

    Parity-time (PT) symmetric periodic structures, near the spontaneous PT-symmetry breaking point, can act as unidirectional invisible media. In this regime, the reflection from one end is diminished while it is enhanced from the other. Furthermore, the transmission coefficient and phase are indistinguishable from those expected in the absence of a grating. The phenomenon is robust even in the presence of Kerr nonlinearities, and it can also effectively suppress optical bistabilities. © 2011 American Physical Society

  19. PT2262/PT2272编解码IC在视频切换矩阵中的应用%The Application of PT2262/PT2272 Coding and Decoding IC in Video Switching Matrix

    Institute of Scientific and Technical Information of China (English)

    吴文佳

    2003-01-01

    提出了一种用PT2262/PT2272编解码IC制作的16×16视频切换矩阵的设计方案,给出了具体的电路图,同时在对其原理进行分析的基础上,指出了用该方案派生其它规格视频切换矩阵的基本思路.

  20. Srategi Pemasaran Jasa Informasi (Studi Kasus di PT.Data Consult, Inc. dan PT.Agranet Multicitra Siberkom) = The Strategy of Information Service's Marketing (Case Study at PT.Data Consult, Inc. and PT.Agranet Multicitra Siberkom)

    OpenAIRE

    Kurniasih, Nuning

    2005-01-01

    The strategy of information service’s marketing (case studies at pt. data consult,inc. and pt. agranet multicitra siberkom). Depok : University of Indonesia - Thesis - Postgraduate (S2) Department of Library Science, Faculty of Cultural Science. This research proposed to analize (1) The role of mission in implementing marketing strategy (2) The role of market analysis in implementing marketing strategy, and (3) The strategy of allocating resource which included strategy of 7 (seven) elements ...

  1. PT-invariant one-dimensional Coulomb problem

    CERN Document Server

    Sinha, A K; Sinha, Anjana; Roychoudhury, Rajkumar

    2002-01-01

    The one-dimensional Coulomb-like potential with a real coupling constant beta, and a centrifugal-like core of strength G = alpha^2 - {1/4}, viz. V(x) = {alpha^2 - (1/4)}/{(x-ic)^2} + beta/|x-ic|, is discussed in the framework of PT-symmetry. The PT-invariant exactly solvable model so formed, is found to admit a double set of real and discrete energies, numbered by a quasi-parity q = +/- 1.

  2. Super Bloch Oscillation in a PT symmetric system

    CERN Document Server

    Turker, Z

    2016-01-01

    Wannier-Stark ladder in a PT symmetric system is generally complex that leads to amplified/damped Bloch oscillation. We show that a non-amplified wave packet oscillation with very large amplitude can be realized in a non-Hermitian tight binding lattice if certain conditions are satisfied. We show that pseudo PT symmetry guarantees the reality of the quasi energy spectrum in our system.

  3. ANALISA DAN PERANCANGAN JARINGAN BERBASIS VPN PADA PT. FINROLL

    Directory of Open Access Journals (Sweden)

    Johan Muliadi Kerta

    2010-11-01

    person. With the Virtual Private Network (VPN, PT Finroll can do business in secure environment to their partners. The methodologies used in this research are data collection that was started by surveying, interviewing, and analyzing the current network topology, performance and design requirements that support network design. From these results, PT Finroll can increase productivity and performance from competition in their business. In addition, with this research company has a better ability to increase their competitiveness in present and the future.

  4. Monodispersive CoPt Nanoparticles Synthesized Using Chemical Reduction Method

    Institute of Scientific and Technical Information of China (English)

    SHEN Cheng-Min; HUI Chao; YANG Tian-Zhong; XIAO Cong-Wen; CHEN Shu-Tang; DING Hao; GAO Hong-Jun

    2008-01-01

    @@ Monodispersive CoPt nanoparticles in sizes of about 2.2 nm are synthesized by superhydride reduction of CoCl2 and PtCl2 in diphenyl ether. The as-prepared nanoparticles show a chemically disordered A1 structure and are superparamagnetic. Thermal annealing transforms the A1 structure into chemically ordered L1o structure and the particles are ferromagnetic at room temperature.

  5. Oxygen reduction on carbon supported Pt-W electrocatalysts

    Energy Technology Data Exchange (ETDEWEB)

    Meza, D.; Morales, U.; Salgado, L. [Departamento de Quimica, Area de Electroquimica, Universidad Autonoma Metropolitana, Unidad Iztapalapa, San Rafael Atlixco 186, Col. Vicentina, 09340 Distrito Federal (Mexico); Roquero, P. [Unidad de Investigacion en Catalisis, Facultad de Quimica, UNAM, Ciudad Universitaria, 04510 Distrito Federal (Mexico)

    2010-11-15

    The catalytic activity of Pt-W electrocatalysts towards oxygen reduction reaction (ORR) was studied. Pt-W/C materials were prepared by thermolysis of tungsten and platinum carbonyl complexes in 1-2 dichloro-benzene during 48 h. The precursors were mixed to obtain relations of Pt:W: 50:50 and 80:20%w, respectively. The Pt carbonyl complex was previously synthesized by bubbling CO in a chloroplatinic acid solution. The synthesized materials were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), cyclic voltammetry (CV) and a rotating disk electrode (RDE). The results show that both materials (Pt{sub 50}W{sub 50}/C and Pt{sub 80}W{sub 20}/C) have a crystalline phase associated with metallic platinum and an amorphous phase related with tungsten and carbon. The particle size of the electrocatalysts depends on the relationship between platinum and tungsten. Finally, both materials exhibit catalytic activity for oxygen reduction. (author)

  6. PMN-PT/PVDF Nanocomposite for High Output Nanogenerator Applications

    Directory of Open Access Journals (Sweden)

    Chuan Li

    2016-04-01

    Full Text Available The 0.7Pb(Mg1/3Nb2/3O3-0.3PbTiO3(0.7PMN-0.3PT nanorods were obtained via hydrothermal method with high yield (over 78%. Then, new piezoelectric nanocomposites based on (1−xPb(Mg1/3Nb2/3O3-xPbTiO3 (PMN-PT nanorods were fabricated by dispersing the 0.7PMN-0.3PT nanorods into piezoelectric poly(vinylidene fluoride (PVDF polymer. The mechanical behaviors of the nanocomposites were investigated. The voltage and current generation of PMN-PT/PVDF nanocomposites were also measured. The results showed that the tensile strength, yield strength, and Young’s modulus of nanocomposites were enhanced as compared to that of the pure PVDF. The largest Young’s modulus of 1.71 GPa was found in the samples with 20 wt % nanorod content. The maximum output voltage of 10.3 V and output current of 46 nA were obtained in the samples with 20 wt % nanorod content, which was able to provide a 13-fold larger output voltage and a 4.5-fold larger output current than that of pure PVDF piezoelectric polymer. The current density of PMN-PT/PVDF nanocomposites is 20 nA/cm2. The PMN-PT/PVDF nanocomposites exhibited great potential for flexible self-powered sensing applications.

  7. PMN-PT/PVDF Nanocomposite for High Output Nanogenerator Applications.

    Science.gov (United States)

    Li, Chuan; Luo, Wenbo; Liu, Xingzhao; Xu, Dong; He, Kai

    2016-04-11

    The 0.7Pb(Mg1/3Nb2/3)O₃-0.3PbTiO₃(0.7PMN-0.3PT) nanorods were obtained via hydrothermal method with high yield (over 78%). Then, new piezoelectric nanocomposites based on (1-x)Pb(Mg1/3Nb2/3)O₃-xPbTiO₃ (PMN-PT) nanorods were fabricated by dispersing the 0.7PMN-0.3PT nanorods into piezoelectric poly(vinylidene fluoride) (PVDF) polymer. The mechanical behaviors of the nanocomposites were investigated. The voltage and current generation of PMN-PT/PVDF nanocomposites were also measured. The results showed that the tensile strength, yield strength, and Young's modulus of nanocomposites were enhanced as compared to that of the pure PVDF. The largest Young's modulus of 1.71 GPa was found in the samples with 20 wt % nanorod content. The maximum output voltage of 10.3 V and output current of 46 nA were obtained in the samples with 20 wt % nanorod content, which was able to provide a 13-fold larger output voltage and a 4.5-fold larger output current than that of pure PVDF piezoelectric polymer. The current density of PMN-PT/PVDF nanocomposites is 20 nA/cm². The PMN-PT/PVDF nanocomposites exhibited great potential for flexible self-powered sensing applications.

  8. 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.

  9. 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.

  10. 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.

  11. Novel Nanohybrids Derived from the Attachment of FePt Nanoparticles on Carbon Nanotubes

    NARCIS (Netherlands)

    Tsoufis, Theodoros; Tomou, Aphrodite; Gournis, Dimitrios; Douvalis, Alexios P.; Panagiotopoulos, Ioannis; Kooi, Bart; Georgakilas, Vasilios; Arfaoui, Imad; Bakas, Thomas

    2008-01-01

    Multiwalled carbon nanotubes (MWCNTs) were used as nanotemplates for the dispersion and stabilization of FePt nanoparticles (NPs). Pre-formed capped FePt NPs were connected to the MWCNTs external surface via covalent binding through organic linkers. Free FePt NPs and MWCNTs-FePt hybrids were anneale

  12. Resistive switching of Pt/TiO x /Pt devices fabricated on flexible Parylene-C substrates

    Science.gov (United States)

    Khiat, Ali; Cortese, Simone; Serb, Alexander; Prodromakis, Themistoklis

    2017-01-01

    Pt/TiO x /Pt resistive switching (RS) devices are considered to be amongst the most promising candidates in memristor family and the technology transfer to flexible substrates could open the way to new opportunities for flexible memory implementations. Hence, an important goal is to achieve a fully flexible RS memory technology. Nonetheless, several fabrication challenges are present and must be solved prior to achieving reliable device fabrication and good electronic performances. Here, we propose a fabrication method for the successful transfer of Pt/TiO x /Pt stack onto flexible Parylene-C substrates. The devices were electrically characterised, exhibiting both digital and analogue memory characteristics, which are obtained by proper adjustment of pulsing schemes during tests. This approach could open new application possibilities of these devices in neuromorphic computing, data processing, implantable sensors and bio-compatible neural interfaces.

  13. Porous AgPt@Pt Nanooctahedra as an Efficient Catalyst toward Formic Acid Oxidation with Predominant Dehydrogenation Pathway.

    Science.gov (United States)

    Jiang, Xian; Yan, Xiaoxiao; Ren, Wangyu; Jia, Yufeng; Chen, Jianian; Sun, Dongmei; Xu, Lin; Tang, Yawen

    2016-11-16

    For direct formic acid fuel cells (DFAFCs), the dehydrogenation pathway is a desired reaction pathway, to boost the overall cell efficiency. Elaborate composition tuning and nanostructure engineering provide two promising strategies to design efficient electrocatalysts for DFAFCs. Herein, we present a facile synthesis of porous AgPt bimetallic nanooctahedra with enriched Pt surface (denoted as AgPt@Pt nanooctahedra) by a selective etching strategy. The smart integration of geometric and electronic effect confers a substantial enhancement of desired dehydrogenation pathway as well as electro-oxidation activity for the formic acid oxidation reaction (FAOR). We anticipate that the obtained nanocatalyst may hold great promises in fuel cell devices, and furthermore, the facile synthetic strategy demonstrated here can be extendable for the fabrication of other multicomponent nanoalloys with desirable morphologies and enhanced electrocatalytic performances.

  14. CaCu3Pt4O12: the first perovskite with the B site fully occupied by Pt(4+).

    Science.gov (United States)

    Yamada, Ikuya; Takahashi, Yuka; Ohgushi, Kenya; Nishiyama, Norimasa; Takahashi, Ryoji; Wada, Kohei; Kunimoto, Takehiro; Ohfuji, Hiroaki; Kojima, Yohei; Inoue, Toru; Irifune, Tetsuo

    2010-08-02

    A novel A-site ordered perovskite CaCu(3)Pt(4)O(12) was synthesized under high pressure and high temperature of 12 GPa and 1250 degrees C. CaCu(3)Pt(4)O(12) is the first perovskite in which the B site is fully occupied by Pt(4+). The crystal structure refinement based on the synchrotron powder X-ray diffraction data shows that CaCu(3)Pt(4)O(12) crystallizes in the space group Im3 (cubic) with a lattice constant of a = 7.48946(10) A. The magnetic susceptibility data show the antiferromagnetic transition at T(N) = 40 K, which is attributed to the magnetic ordering of Cu(2+) spins with S = 1/2.

  15. Interfacial oxygen migration and its effect on the magnetic anisotropy in Pt/Co/MgO/Pt films

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Xi; Feng, Chun, E-mail: fengchun@ustb.edu.cn, E-mail: ghyu@mater.ustb.edu.cn; Liu, Yang; Jiang, Shaolong; Hua Li, Ming; Hua Yu, Guang, E-mail: fengchun@ustb.edu.cn, E-mail: ghyu@mater.ustb.edu.cn [Department of Materials Physics and Chemistry, University of Science and Technology Beijing, Beijing 100083 (China); Long Wu, Zheng [Analytical and Testing Center, Beijing Normal University, Beijing 100875 (China); Yang, Feng [State Key Laboratory of Heavy Oil Processing, China University of Petroleum, Beijing 102249 (China)

    2014-02-03

    This paper reports the interfacial oxygen migration effect and its induced magnetic anisotropy evolution in Pt/Co/MgO/Pt films. During depositing the MgO layer, oxygen atoms from the MgO combine with the neighboring Co atoms, leading to the formation of CoO at the Co/MgO interface. Meanwhile, the films show in-plane magnetic anisotropy (IMA). After annealing, most of the oxygen atoms in CoO migrate back to the MgO layer, resulting in obvious improvement of Co/MgO interface and the enhancement of effective Co-O orbital hybridization. These favor the evolution of magnetic anisotropy from IMA to perpendicular magnetic anisotropy (PMA). The oxygen migration effect is achieved by the redox reaction at the Co/MgO interface. On the contrary, the transfer from IMA to PMA cannot be observed in Pt/Co/Pt films due to the lack of interfacial oxygen migration.

  16. 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.

  17. Molybdenum-Doped PdPt@Pt Core-Shell Octahedra Supported by Ionic Block Copolymer-Functionalized Graphene as a Highly Active and Durable Oxygen Reduction Electrocatalyst.

    Science.gov (United States)

    Cho, Kie Yong; Yeom, Yong Sik; Seo, Heun Young; Kumar, Pradip; Lee, Albert S; Baek, Kyung-Youl; Yoon, Ho Gyu

    2017-01-18

    Development of highly active and durable electrocatalysts that can effectively electrocatalyze oxygen reduction reactions (ORR) still remains one important challenge for high-performance electrochemical conversion and storage applications such as fuel cells and metal-air batteries. Herein, we propose the combination of molybdenum-doped PdPt@Pt core-shell octahedra and the pyrene-functionalized poly(dimethylaminoethyl methacrylate)-b-poly[(ethylene glycol) methyl ether methacrylate] ionic block copolymer-functionalized reduced graphene oxide (Mo-PdPt@Pt/IG) to effectively augment the interfacial cohesion of both components using a tunable ex situ mixing strategy. The rationally designed Mo-PdPt@Pt core-shell octahedra have unique compositional benefits, including segregation of Mo atoms on the vertexes and edges of the octahedron and 2-3 shell layers of Pt atoms on a PdPt alloy core, which can provide highly active sites to the catalyst for ORR along with enhanced electrochemical stability. In addition, the ionic block copolymer functionalized graphene can facilitate intermolecular charge transfer and good stability of metal NPs, which arises from the ionic block copolymer interfacial layer. When the beneficial features of the Mo-PdPt@Pt and IG are combined, the Mo-PdPt@Pt/IG exhibits substantially enhanced activity and durability for ORR relative to those of commercial Pt/C. Notably, the Mo-PdPt@Pt/IG shows mass activity 31-fold higher than that of Pt/C and substantially maintains high activities after 10 000 cycles of intensive durability testing. The current study highlights the crucial strategies in designing the highly active and durable Pt-based octahedra and effective combination with functional graphene supports toward the synergetic effects on ORR.

  18. Syntheses, Structures, and Electrochemistry of the Defective ccp [Pt33(CO)38](2-) and the bcc [Pt40(CO)40](6-) Molecular Nanoclusters.

    Science.gov (United States)

    Cattabriga, Enrico; Ciabatti, Iacopo; Femoni, Cristina; Funaioli, Tiziana; Iapalucci, Maria Carmela; Zacchini, Stefano

    2016-06-20

    The molecular [Pt33(CO)38](2-) nanocluster was obtained from the thermal decomposition of Na2[Pt15(CO)30] in methanol. The reaction of [Pt19(CO)22](4-) with acids (1-2 equiv) affords the unstable [Pt19(CO)22](3-) trianion, which evolves with time leading eventually to the [Pt40(CO)40](6-) hexa-anion. The total structures of both nanoclusters were determined via single-crystal X-ray diffraction. [Pt33(CO)38](2-) displays a defective ccp Pt33 core and shows that localized deformations occur in correspondence of atomic defects to "repair" them. In contrast, [Pt40(CO)40](6-) shows a bcc Pt40 core and represents the largest Pt cluster with a body-centered structure. The rich electrochemistry of the two high-nuclearity platinum carbonyl clusters was studied by cyclic voltammetry and electrochemical in situ Fourier transform infrared spectroscopy. The redox changes of [Pt33(CO)38](2-) show features of chemical reversibility and electrochemical quasi-reversibility, and the vibrational spectra in the CO stretching region of the nine redox forms of the cluster [Pt33(CO)38](n) (n = 0 to -4, -6 to -9) are reported. Almost all the redox processes exhibited by [Pt40(CO)40](6-) are chemically and electrochemically reversible, and the eight oxidation states of [Pt40(CO)40] from -4 to -11 were spectroscopically characterized. The effect of the more regular bcc Pt-carbonyl cluster structure of [Pt40(CO)40](6-) with respect to that of the defective ccp Pt33 core on the redox behavior is discussed.

  19. Use of Hydrogen Chemisorption and Ethylene Hydrogenation as Predictors for Aqueous Phase Reforming of Lactose over Ni@Pt and Co@Pt Bimetallic Overlayer Catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Lai, Qinghua; Skoglund, Michael D.; Zhang, Chen; Morris, Allen R.; Holles, Joseph H.

    2016-10-20

    Overlayer Pt on Ni (Ni@Pt) or Co (Co@Pt) were synthesized and tested for H2 generation from APR of lactose. H2 chemisorption descriptor showed that Ni@Pt and Co@Pt overlayer catalysts had reduced H2 adsorption strength compared to a Pt only catalyst, which agree with computational predictions. The overlayer catalysts also demonstrated lower activity for ethylene hydrogenation than the Pt only catalyst, which likely resulted from decreased H2 binding strength decreasing the surface coverage of H2. XAS results showed that overlayer catalysts exhibited higher white line intensity than the Pt catalyst, which indicates a negative d-band shift for the Pt overlayer, further providing evidence for overlayer formation. Lactose APR studies showed that lactose can be used as feedstock to produce H2 and CO under desirable reaction conditions. The Pt active sites of Ni@Pt and Co@Pt overlayer catalysts showed significantly enhanced H2 production selectivity and activity when compared with that of a Pt only catalyst. The single deposition overlayer with the largest d-band shift showed the highest H2 activity. The results suggest that overlayer formation using directed deposition technique could modify the behavior of the surface metal and ultimately modify the APR activity.

  20. Preparation of Pt Au/C and Pt Au Bi/C electrocatalysts using electron beam irradiation for ethanol electro-oxidation in alkaline medium

    Energy Technology Data Exchange (ETDEWEB)

    Silva, Dionisio F.; Geraldes, Adriana N.; Cardoso, Elisangela S.Z.; Gomes, Thiago B.; Linardi, Marcelo; Oliveira Neto, Almir; Spinace, Estevam V., E-mail: dfsilva@ipen.b [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil)

    2011-07-01

    Pt Au/C (50:50) and PtAuBi/C electrocatalysts with Pt:Au:Bi atomic ratios of 50:40:10, 50:30:20 and 50:10:40 were prepared in water/2-propanol using electron beam irradiation. The materials were characterized by X-ray diffraction (XRD) and the electro-oxidation of ethanol was studied by chronoamperometry at room temperature. The X-ray diffraction measurements for all electrocatalysts prepared showed four peaks, which are associated with the planes of the face-centered cubic (fcc) structure characteristic of Pt and Pt alloys. For PtAuBi/C it was also observed the presence of a mixture of BiPt alloys and bismuth phases. The average crystallite sizes for Pt/C, PtAu/C, PtAuBi/C (50:40:10), PtAuBi/C (50:30:20) and PtAuBi/C (50:10:40) were in the range of 2.0 - 4.0 nm. The activity of the electrocatalysts for ethanol oxidation in alkaline medium showed that PtAuBi/C (50:40:10) had a higher performance for ethanol oxidation compared to others electrocatalysts prepared. (author)

  1. The electrocatalytic properties of carbon supported PtRu/C nanoalloys in oxidation of small organic molecules: Comparison with Pt/C catalyst

    Directory of Open Access Journals (Sweden)

    Lović Jelena D.

    2012-01-01

    Full Text Available The electrocatalytic activity of carbon supported PtRu/C catalysts, with different composition, toward the electrooxidation of methanol, CO and formic acid were examined in acid and alkaline solution at ambient temperature using thin-film rotating disk electrode (RDE method and compared with activity of Pt/C. The catalysts were characterized by XRD, AFM and STM techniques. XRD pattern revealed that PtRu-1/C catalyst is consisted of two structures e.g. Pt-Ru-fcc and Ru-hcp (the solid solution of Ru in Pt and the small amount of Ru or solid solution of Pt in Ru, as opposed to PtRu-2/C catalyst which is consisted of one structure mostly, Pt-Ru-fcc. According to STM images, PtRu as well as Pt, particles size were between 2 and 6 nm, which is in a good agreement with the mean particles size determined by XRD. To establish the activity and stability of the catalysts potentiodynamic and quasi steady-state measurements were performed. It was found that the activity of Pt and PtRu for CO and methanol oxidation is a strong function of pH of solution. The kinetics are much higher in alkaline than in acid solution and the difference between Pt/C and PtRu/C is much less pronounced in alkaline media. Results presented in this work indicate that activity of PtRu catalysts depends on catalyst composition, e.g. on Pt/Ru atomic ratio, as well as on alloying degree of catalysts. Comparison of CO, methanol and formic acid oxidation on PtRu-2/C, PtRu-1/C and Pt/C catalysts revealed that PtRu-2/C is the most active one. It was shown that the PtRu-2/C catalyst, due to fact that it is consisted of only one phase, with high alloying degree, through the bifunctional mechanism improved by electronic effect, achieve the activity two times higher related to PtRu-1/C in the oxidation of all organic molecules investigated, and about three times higher compared to Pt/C in the oxidation of methanol and CO, and five times higher in formic acid oxidation.

  2. Island Shape-Induced Transition from 2D to 3D Growth for Pt/Pt(111)

    DEFF Research Database (Denmark)

    Jacobsen, Joachim; Jacobsen, Karsten Wedel; Stoltze, Per

    1995-01-01

    We present a kinetic Monte Carlo simulation of the growth of Pt on Pt(111) capable of describing the experimentally observed temperature dependence of the island shapes and the growth mode. We show that the transition from a 2D growth mode at low temperatures to a 3D mode at higher temperatures...... is closely related to the disappearance of kink sites and the appearance of the triangular islands observed in the 3D growth regime....

  3. Electric field mediated non-volatile tuning magnetism in CoPt/PMN-PT heterostructure for magnetoelectric memory devices

    Science.gov (United States)

    Yang, Y. T.; Li, J.; Peng, X. L.; Wang, X. Q.; Wang, D. H.; Cao, Q. Q.; Du, Y. W.

    2016-02-01

    We report a power efficient non-volatile magnetoelectric memory in the CoPt/(011)PMN-PT heterostructure. Two reversible and stable electric field induced coercivity states (i.e., high-HC or low-HC) are obtained due to the strain mediated converse magnetoelectric effect. The reading process of the different coercive field information written by electric fields is demonstrated by using a magnetoresistance read head. This result shows good prospects in the application of novel multiferroic devices.

  4. Investigation of the magnetic domain structure of(PtCoPt)/Si multilayers by magnetic force microscopy

    Institute of Scientific and Technical Information of China (English)

    张臻蓉; 刘洪; 韩宝善

    2002-01-01

    The domain structure of (PtCoPt)/Si multilayers in the dc demagnetized state has been investigated by magnetic force microscopy. The domain structure is found to change dramatically as the thickness of the non-magnetic Si sublayer(tsi) increases. Together with the analysis of magnetic properties, the variation of the domain period indicates that the domain wall energy decreases. Using the model developed by Draaisma and de Jonge, the domain wall energy is obtained.

  5. Preparation of carbon supported Pt-P catalysts and its electrocatalytic performance for oxygen reduction

    Energy Technology Data Exchange (ETDEWEB)

    Ma Juan [Institute of Chemical Power Sources, Soochow University, Suzhou 215006 (China); Tang Yawen; Yang Gaixiu; Chen Yu [College of Chemistry and Material Science, Nanjing Normal University, Nanjing 210097 (China); Zhou Qun [Institute of Chemical Power Sources, Soochow University, Suzhou 215006 (China); Lu Tianhong [College of Chemistry and Material Science, Nanjing Normal University, Nanjing 210097 (China); Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022 (China); Zheng Junwei, E-mail: jwzheng@suda.edu.cn [Institute of Chemical Power Sources, Soochow University, Suzhou 215006 (China)

    2011-05-15

    The carbon supported PtP (PtP/C) catalysts were synthesized from Pt(NO{sub 3}){sub 2} and phosphorus yellow at the room temperature. The content of P in the PtP/C catalysts prepared with this method is high and the average size of the PtP particles is decreased with increasing the content of P. The electrocatalytic performances of the PtP/C catalysts prepared with this method for the oxygen reduction reaction (ORR) are better than that of the commercial Pt/C catalyst. The promotion action of P for enhancing the electrocatalytic performance of the PtP/C catalyst for ORR is mainly due to that Pt and P form the alloy and then the electron density of Pt is decreased.

  6. Simple preparation of Pd-Pt nanoalloy catalysts for methanol-tolerant oxygen reduction

    Science.gov (United States)

    He, Wei; Liu, Juanying; Qiao, Yongjin; Zou, Zhiqing; Zhang, Xiaogang; Akins, Daniel L.; Yang, Hui

    Carbon-supported Pd-Pt bimetallic nanoparticles of different atomic ratios (Pd-Pt/C) have been prepared by a simple procedure involving the complexing of Pd and Pt species with sodium citrate followed by ethylene glycol reduction. As-prepared Pd-Pt alloy nanoparticles evidence a single-phase fcc disordered structure, and the degree of alloying is found to increase with Pd content. Both X-ray diffraction and transmission electron microscopy characterizations indicate that all the Pd-Pt/C catalysts possess a similar mean particle size of ca. 2.8 nm. The highest mass and specific activity of the oxygen reduction reaction (ORR) using the Pd-Pt/C catalysts are found with a Pd:Pt atomic ratio of 1:2. Moreover, all Pd-Pt alloy catalysts exhibit significantly enhanced methanol tolerance during the ORR than the Pt/C catalyst, ensuring a higher ORR performance while diminishing Pt utilization.

  7. Site-selective Cu deposition on Pt dendrimer-encapsulated nanoparticles: correlation of theory and experiment.

    Science.gov (United States)

    Carino, Emily V; Kim, Hyun You; Henkelman, Graeme; Crooks, Richard M

    2012-03-07

    The voltammetry of Cu underpotential deposition (UPD) onto Pt dendrimer-encapsulated nanoparticles (DENs) containing an average of 147 Pt atoms (Pt(147)) is correlated to density functional theory (DFT) calculations. Specifically, the voltammetric peak positions are in good agreement with the calculated energies for Cu deposition and stripping on the Pt(100) and Pt(111) facets of the DENs. Partial Cu shells on Pt(147) are more stable on the Pt(100) facets, compared to the Pt(111) facets, and therefore, Cu UPD occurs on the 4-fold hollow sites of Pt(100) first. Finally, the structures of Pt DENs having full and partial monolayers of Cu were characterized in situ by X-ray absorption spectroscopy (XAS). The results of XAS studies are also in good agreement with the DFT-optimized models.

  8. Unusual weak magnetic exchange in two different structure types: YbPt2Sn and YbPt2In.

    Science.gov (United States)

    Gruner, T; Jang, D; Steppke, A; Brando, M; Ritter, F; Krellner, C; Geibel, C

    2014-12-03

    We present the structural, magnetic, thermodynamic and transport properties of the two new compounds YbPt(2)Sn and YbPt(2)In. X-ray powder diffraction shows that they crystallize in different structure types, the hexagonal ZrPt(2)Al and the cubic Heusler type, respectively. Despite quite different lattice types, both compounds present very similar magnetic properties: a stable trivalent Yb(3+), no evidence for a sizeable Kondo interaction and very weak exchange interactions with a strength below 1 K as deduced from specific heat C(T). Broad anomalies in C(T) suggest short range magnetic ordering at about 250 mK and 180 mK for YbPt(2)Sn and YbPt(2)In, respectively. The weak exchange and the low ordering temperature result in a large magnetocaloric effect as deduced from the magnetic field dependence of C(T), making these compounds interesting candidates for magnetic cooling. In addition we found in YbPt(2)In evidences for a charge density wave transition at about 290 K. The occurrence of such transitions within several RET2X compound series (RE = rare earth, T = noble metal, X = In, Sn) is analyzed.

  9. Alternative alloys for catalysts and platinum jewelry? New structures in Pt-Hf and Pt-Mo

    Science.gov (United States)

    Gilmartin, Erin; Corbitt, Jacqueline; Hart, Gus

    2009-03-01

    The only known intermetallic structure with an 8:1 stoichiometry is that of Pt8Ti. It is intriguing that an ordered phase would occur at such low concentrations of the minority atom, but this structure occurs in about a dozen binary intermetallic systems. The formation of an ordered phase in an alloy can significantly enhance the performance of the material, particularly the hardness. We have taken a broad look at possible systems where this phase forms. Using first-principles, we calculated the stability of this structure relative to experimentally known phases for more than 80 Pt/Pd binary systems. We find the Pt8Ti structure is a possible ground state in more than 20 cases. Our experimental collaborators have verified our prediction in Pt-Mo and observed order-hardening in Pt-Hf. We discuss the discovery of new ground states that are likely to be verified experimentally and their impact on materials for Pt- and Pd-based catalysts and jewelry.

  10. New potential structure for jewelry application. Does it exist in Pt-Mo, Pt-Hf, or other systems?

    Science.gov (United States)

    Gilmartin, Erin; Corbitt, Jacqueline; Hart, Gus

    2009-10-01

    The only known intermetallic structure with an 8:1 stoichiometry is that of Pt8Ti. It is intriguing that an ordered phase would occur at such low concentrations of the minority atom, but this structure occurs in about a dozen binary intermetallic systems. The formation of an ordered phase in an alloy can significantly enhance the performance of the material, particularly the hardness. We have taken a broad look at possible systems where this phase forms. Using first-principles, we calculated the stability of this structure relative to experimentally known phases for more than 70 Pt/Pd binary systems. We find the Pt8Ti structure is a possible ground state in more than 20 cases. Our experimental collaborators have verified our prediction in Pt-Mo and observed order-hardening in Pt-Hf. We discuss the discovery of new ground states via the cluster expansion that are likely to be verified experimentally and their impact on Pt- and Pd-based jewelry and catalysts.

  11. Microscopic evidence of strain-mediated magnetoelectric coupling in Co/Pt multilayers/PMN-PT(011) heterostructures

    Science.gov (United States)

    Sun, Ying; Wang, Wenbo; Wu, Weida; Zheng, Xiaoli; Cai, Jianwang; Zhao, Yonggang; Liu, Ming

    A promising way to control magnetization(M) via an electric field(E-field) is using magnetoelectric(ME) effect in FM/FE heterostructures. We use magnetic(electric) force microscopy(M(e)FM) to study the strain-mediated E-field modulation of M in (Co/Pt)n with perpendicular magnetic anisotropy(PMA) or in-plane anisotropy on PMN-PT(011) substrates. MFM were performed on (Co/Pt)n with an DC E-field applied to PMN-PT. In MeFM, we superimpose an AC modulation on a DC one and utilize lock-in technique to detect weak ME effect. For (Co/Pt)n with PMA, MFM images show stripe domains with no obvious changes at varied DC E-fields. However, MeFM shows interesting structures and the image contrast reverses sign at opposite strain slopes of the PMN-PT substrate. For sample with in-plane anisotropy, both MFM and MeFM images show dipole-like domains. Interestingly, the MeFM image contrast reverses sign at opposite strain slopes of the substrate. The sign reversal of MeFM contrast indicates that features revealed by MeFM are intrinsic local ME effect. Our MeFM data are consistent with the ferromagnetic resonance results showing that strain-induced anisotropy change will cause part of M switching to the in-plane direction. Possible scenarios will be discussed.

  12. Combining voltammetry and ion chromatography: application to the selective reduction of nitrate on Pt and PtSn electrodes.

    Science.gov (United States)

    Yang, Jian; Kwon, Youngkook; Duca, Matteo; Koper, Marc T M

    2013-08-20

    To overcome the shortcomings of electroanalytical methods in analyzing the ionic reaction products that are either electrochemically inert or lack distinct electrochemical/spectroscopic fingerprints, we suggest combining voltammetry with ion chromatography by applying online sample collection to the electrochemical cell and offline ion chromatographic analysis. This combination allows a quantitative analysis including the potential dependence of the product distribution in a straightforward way. As a proof-of-concept example, we discuss the formation of ionic reaction products from nitrate reduction on Pt and Sn-modified Pt electrode in acid. On the Pt electrode, ammonia was the only identifiable product. After Sn modification of the Pt electrode, a change in selectivity was observed to hydroxylamine as the dominant product. Moreover, the rate determining step of nitrate reduction (reduction to nitrite) was enhanced by Sn modification of the Pt electrode, and a significant concentration of nitrite was evidenced on a Pt electrode with a high coverage of Sn species. The suggested combination of voltammetry and online ion chromatography hence proves very useful in the quantitative elucidation of electrocatalytic reactions with different ionic products.

  13. Comparison of formic acid oxidation at supported Pt catalyst and at low-index Pt single crystal electrodes in sulfuric acid solution

    Directory of Open Access Journals (Sweden)

    AMALIJA V. TRIPKOVIC

    2003-11-01

    Full Text Available The oxidation of formic acid was studied at supported Pt catalyst (47.5 wt%. Pt and a low-index single crystal electrodes in sulfuric acid. The supported Pt catalyst was characterized by the TEM and HRTEM techniques. The mean Pt particle diameter, calculated from electrochemical measurements, fits well with Pt particle size distribution determined by HRTEM. For the mean particle diameter the surface averaged distribution of low-index single crystal facets was established. Comparison of the activities obtained at Pt supported catalyst and low-index Pt single crystal electrodes revealed that Pt(111 plane is the most active in the potential region relevant for fuel cell applications.

  14. The effect of thermal treatment on the atomic structure of core-shell PtCu nanoparticles in PtCu/C electrocatalysts

    Science.gov (United States)

    Pryadchenko, V. V.; Belenov, S. V.; Shemet, D. B.; Volochaev, V. A.; Srabionyan, V. V.; Avakyan, L. A.; Tabachkova, N. Yu.; Guterman, V. E.; Bugaev, L. A.

    2017-08-01

    PtCu/C electrocatalysts with bimetallic PtCu nanoparticles were synthesized by successive chemical reduction of Cu2+ and Pt(IV) in a carbon suspension prepared based on an aqueous ethylene glycol solution. The atomic structure of as-prepared PtCu nanoparticles and nanoparticles subjected to thermal treatment at 350°C was examined using Pt L 3 and Cu K EXAFS spectra, transmission electron microscopy (TEM), and X-ray powder diffraction (XRD). The results of joint analysis of TEM microphotographs, XRD profiles, and EXAFS spectra suggest that the synthesized electrocatalysts contain PtCu nanoparticles with a Cu core-Pt shell structure and copper oxides Cu2O and CuO. Thermal treatment of electrocatalysts at 350°C results in partial reduction of copper oxides and fusion of bimetallic nanoparticles with the formation of both homogeneous and ordered PtCu solid solutions.

  15. 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\

  16. The activity of ALD-prepared PtCo catalysts for ethanol oxidation in alkaline media

    OpenAIRE

    Santasalo-Aarnio, Annukka; Sairanen, Emma; Arán-Ais, Rosa M.; Figueiredo, Marta C.; Hua, Jiang; Feliu, Juan M.; Lehtonen, Juha; Karinen, Reetta; Kallio, Tanja

    2014-01-01

    Controlled bimetallic catalyst materials can be obtained using atomic layer deposition (ALD) method. In this paper, this method was applied to prepare Pt, PtCo, and PtCoPt nanoparticle catalysts on carbon support. Their activity for ethanol oxidation was studied by various electrochemical methods and the dependency of the reaction on temperature and mass transfer was evaluated. In addition, FTIR analysis was performed to confirm the reaction products. The results showed that bimetallic PtCo e...

  17. Pt, PtCo and PtNi electrocatalysts prepared with mechanical alloying for oxygen reduction reaction in alkaline medium; Electrocatalizadores de Pt, PtCo y PtNi preparados por aleado mecanico para la reaccion de reduccion de oxigeno en medio alcalino

    Energy Technology Data Exchange (ETDEWEB)

    Garcia-Contreras, M.A.; Fernandez-Valverde, S.M. [Instituto Nacional de Investigaciones Nucleares, Ocoyoacac, Estado de Mexico (Mexico)]. E-mail: miguel.garcia@inin.gob.mx; Vargas-Garcia, J.R. [ESIQIE-IPN, Mexico D.F. (Mexico

    2009-09-15

    Pt, PtCo and PtNi electrocatalysts were prepared using mechanical alloying and their electrocatalytic activity was investigated for oxygen reduction reaction (ORR) in KOH 0.5 M using cyclic voltametry and rotary disc electrode (RDE) techniques. The electrocatalysts were characterized using x-ray diffraction, sweep electron microscopy, dispersive x-ray transmission and chemical analysis. The physical characterization indicated that all the electrocatalysts are alloys formed by agglomerated particles composed of nanocrystals. The chemical analysis showed the presence of iron in the alloys. For the electrocatalytic evaluation, polarization curves and Koutecky-Levich and Tafel graphs were obtained to determine the kinetic parameters of the electrocatalysts in the study. With the same experimental conditions, the PtCo presented better electrocatalytic performance with a higher exchange current density. [Spanish] Se prepararon electrocatalizadores de Pt, PtCo y PtNi por aleado mecanico y se investigo su actividad electrocatalitica para la reaccion de reduccion de oxigeno (RRO) en KOH 0.5 M utilizando las tecnicas de Voltametria ciclica y Electrodo de Disco Rotatorio. Los electrocatalizadores se caracterizaron por difraccion de rayos X, Microscopia electronica de Barrido, de Transmision y analisis quimico por dispersion de rayos X. La caracterizacion fisica indico que todos los electrocatalizadores son aleaciones formadas de particulas aglomeradas, compuestas de nanocristales. El analisis quimico mostro la presencia de hierro en las aleaciones. Para la evaluacion electrocatalitica se obtuvieron curvas de polarizacion, graficas de Koutecky-Levich y de Tafel para determinar los parametros cineticos de los electrocatalizadores en estudio. En las mismas condiciones experimentales, el PtCo presento el mejor desempeno electrocatalitico con la densidad de corriente de intercambio mas alta.

  18. Microemulsion Preparation and Electrochemical Characterization of Pt/C,PtIr/C Electrocatalysts%微乳法合成Pt/C、PtIr/C催化剂及其电化学性能表征

    Institute of Scientific and Technical Information of China (English)

    曾亚平; 隋升

    2011-01-01

    以碳纳米粉(XC-72R)作为载体,以3种不同方法合成Pt/C负载型催化剂.并由X射线衍射(XRD)、透射电镜(TEM)、循环伏安法(CV)、恒电位测试(Potentiostatic)以及线性极化分析(Potentiodynamic polarization)等方法表征该催化剂.结果表明,由微乳法制得的负载型催化剂Pt/C,活性组分的颗粒尺寸为5~10 nm,均匀地分散在载体表面,电化学性能良好.而以同一微乳法由异辛烷/Triton X100/正己醇/水体系合成的含有不同Pt、Ir比例的负载型的Pt100-xIrx/C催化剂,则其中以Pt85Ir15表现出更为良好的电化学综合性能.%The Pt/C electrocatalysts were prepared by three different systems and the PtIr/C electrocatalysts were prepared with four different Ir contents.The samples were characterized by X-ray diffraction(XRD),transmission electron microscope(TEM),cyclic voltammetry(CV),potentiostatic and potentiodynamic polarizations measurements.The experimental results confirmed that the electrocatalyst particles prepared by the microemulsion method were well distributed on XC-72R supports with the active particle sizes of 5~10 nm and good electrocatalysts activity.The Pt85Ir15/C electrocatalysts showed the highest overall electrochemical activity in unitized regenerative fuel cell.

  19. Oxidation of Half-Lantern Pt2(II,II) Compounds by Halocarbons. Evidence of Dioxygen Insertion into a Pt(III)-CH3 Bond.

    Science.gov (United States)

    Sicilia, V; Baya, M; Borja, P; Martín, A

    2015-08-01

    The half-lantern compound [{Pt(bzq)(μ-N^S)}2] (1) [bzq = benzo[h]quinoline, HN^S = 2-mercaptopyrimidine (C4H3N2HS)] reacts with CH3I and haloforms CHX3 (X = Cl, Br, I) to give the corresponding oxidized diplatinum(III) derivatives [{Pt(bzq)(μ-N^S)X}2] (X = Cl 2a, Br 2b, I 2c). These compounds exhibit half-lantern structures with short intermetallic distances (∼2.6 Å) due to Pt-Pt bond formation. The halogen abstraction mechanisms from the halocarbon molecules by the Pt2(II,II) compound 1 were investigated. NMR spectroscopic evidence using labeled reagents support that in the case of (13)CH3I the reaction initiates with an oxidative addition through an SN2 mechanism giving rise to the intermediate species [I(bzq)Pt(μ-N^S)2Pt(bzq)((13)CH3)}]. However, with haloforms the reactions proceed through a radical-like mechanism, thermally (CHBr3, CHI3) or photochemically (CHCl3) activated, giving rise to mixtures of species [X(bzq)Pt(μ-N^S)2Pt(bzq)R] (3a-c) and [X(bzq)Pt(μ-N^S)2Pt(bzq)X] (2a-c). In these cases the presence of O2 favors the formation of species 2 over 3. Transformation of 3 into 2 was possible upon irradiation with UV light. In the case of [I(bzq)Pt(μ-N^S)2Pt(bzq)((13)CH3)}] (3d), in the presence of O2 the formation of the unusual methylperoxo derivative [I(bzq)Pt(μ-N^S)2Pt(bzq)(O-O(13)CH3)}] (4d) was detected, which in the presence of (13)CH3I rendered the final product [{Pt(bzq)(μ-N^S)I}2] (2c) and (13)CH3OH.

  20. PENGARUH PENGALAMAN AUDITOR DAN ETIKA PROFESIONAL TERHADAP PERILAKU AUDITOR INTERNAL DALAM SITUASI KONFLIK AUDIT (STUDI EMPIRIS PT. PLN SATUAN PENGAWASAN INTERN REGIONAL X DAN PT. KALLA GROUP)

    OpenAIRE

    NADIAH ILYAS, FARAH

    2014-01-01

    2014 ABSTRAK Pengaruh Pengalaman Auditor dan Etika Profesional Terhadap Perilaku Auditor Internal dalam Situasi Konflik Audit (Studi Empiris PT. PLN Satuan Pengawasan Intern Regional X dan PT. Kalla Group) Farah Nadiah Ilyas Kartini Nurleni Penelitian ini bertujuan untuk mengetahui apakah pengalaman auditor, etika profesional berpengaruh terhadap perilaku auditor internal dalam situasi konflik audit pada PT. PLN Satuan Pengawasan Intern Regional X dan PT. Kalla Grou...

  1. Anti-prothrombin (aPT) and anti-phosphatidylserine/prothrombin (aPS/PT) antibodies and the risk of thrombosis in the antiphospholipid syndrome. A systematic review.

    Science.gov (United States)

    Sciascia, Savino; Sanna, Giovanni; Murru, Veronica; Roccatello, Dario; Khamashta, Munther A; Bertolaccini, Maria Laura

    2014-02-01

    Antibodies to prothrombin are detected by directly coating prothrombin on irradiated ELISA plates (aPT) or by using the phosphatidylserine/prothrombin complex as antigen (aPS/PT). Although these antibodies have both been associated with antiphospholipid syndrome (APS) and a correlation between the two assays have been reported, it seems that aPT and aPS/PT belong to different populations of autoantibodies. It was our objective to systematically review the available evidence on aPT and aPS/PT antibodies and the risk of thrombosis in APS. Medline-reports published between 1988 and 2013 investigating aPT and aPS/PT as a risk factor for thrombosis were included. Whenever possible, antibody isotype(s) and site of thrombosis were analysed. This systematic review is based on available data from more than 7,000 patients and controls from 38 studies analysing aPT and 10 aPS/PT. Antibodies to prothrombin (both aPT and aPS/PT) increased the risk of thrombosis (odds ratio [OR] 2.3; 95% confidence interval [CI] 1.72-3.5). aPS/PT seemed to represent a stronger risk factor for thrombosis, both arterial and/or venous than aPT (OR 5.11; 95%CI 4.2-6.3 and OR 1.82; 95%CI 1.44-2.75, respectively). In conclusion, routine measurement of aPS/PT (but not aPT) might be useful in establishing the thrombotic risk of patients with previous thrombosis and/or systemic lupus erythematosus. Their inclusion as laboratory criteria for the APS should be indisputably further explored.

  2. 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.

  3. First principles study of (Cd, Hg, In, Tl, Sn, Pb, As, Sb, Bi, Se) modified Pt(111), Pt(100) and Pt(211) electrodes as CO oxidation catalysts

    DEFF Research Database (Denmark)

    Tripkovic, Vladimir

    2015-01-01

    CO oxidation is a prototype reaction for studying oxidation of small organic molecules. Certain adatom modified Pt electrodes have a large promotional effect on CO oxidation. However, the effect is often coverage dependent, and has a limited effect due to short lifetimes of the adatoms. The cover...

  4. Spectroelectrochemical Study of Carbon Monoxide and Ethanol Oxidation on Pt/C, PtSn(3:1/C and PtSn(1:1/C Catalysts

    Directory of Open Access Journals (Sweden)

    Rubén Rizo

    2016-09-01

    Full Text Available PtSn-based catalysts are one of the most active materials toward that contribute ethanol oxidation reaction (EOR. In order to gain a better understanding of the Sn influence on the carbon monoxide (principal catalyst poison and ethanol oxidation reactions in acidic media, a systematic spectroelectrochemical study was carried out. With this end, carbon-supported PtSnx (x = 0, 1/3 and 1 materials were synthesized and employed as anodic catalysts for both reactions. In situ Fourier transform infrared spectroscopy (FTIRS and differential electrochemical mass spectrometry (DEMS indicate that Sn diminishes the amount of bridge bonded CO (COB and greatly improves the CO tolerance of Pt-based catalysts. Regarding the effect of Sn loading on the EOR, it enhances the catalytic activity and decreases the onset potential. FTIRS and DEMS analysis indicate that the C-C bond scission occurs at low overpotentials and at the same potential values regardless of the Sn loading, although the amount of C-C bond breaking decreases with the rise of Sn in the catalytic material. Therefore, the elevated catalytic activity toward the EOR at PtSn-based electrodes is mainly associated with the improved CO tolerance and the incomplete oxidation of ethanol to form acetic acid and acetaldehyde species, causing the formation of a higher amount of both C2 products with the rise of Sn loading.

  5. 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.

  6. The effect of reducing agents on the electronic, magnetic and electrocatalytic properties of thiol-capped Pt/Co and Pt/Ni nanoparticles

    CSIR Research Space (South Africa)

    Mathe, NR

    2015-05-01

    Full Text Available The electronic, magnetic and electrocatalytic properties of bimetallic thiol-capped Pt/Co and Pt/Ni nanoparticles were synthesised using two reducing agents, NaBH(sub4) and N(sub2)H(sub4). X-ray diffraction analysis of the nanoparticles showed Pt...

  7. Methanol oxidation reaction activity of microwave irradiated and heat-treated Pt/Co and Pt/Ni nano-electrocatalysts

    CSIR Research Space (South Africa)

    Mathe, NR

    2014-11-01

    Full Text Available Bimetallic Pt nanoparticles were prepared by alloying Pt with the non-noble transition metals, Co and Ni, using a conventional heat-treatment (HT) method and microwaveirradiation (MW). The resulting samples were PteCo-Ht, PteNi-HT, PteCo, MW and Pt...

  8. High perpendicular hard magnetic properties of nanocomposite Co-rich Co-Pt/Pt double-layered films by epitaxial deposition without capped layer

    Energy Technology Data Exchange (ETDEWEB)

    Chen, S.C., E-mail: chensc@mail.mcut.edu.t [Department of Materials Engineering, MingChi University of Technology, Taipei 243, Taiwan (China); Kuo, P.C.; Shen, C.L.; Hsu, S.L.; Fang, Y.H.; Lin, G.P.; Huang, K.T. [Institute of Materials Science and Engineering, National Taiwan University, Taipei 106, Taiwan (China)

    2009-07-01

    The HRTEM cross-sectional lattice image shows that a well epitaxial growth of hcp Co-rich Co-Pt (002) on Pt (111) underlayer leads to good perpendicular magnetic anisotropy of Co-rich Co-Pt film. It is found that both the perpendicular coercivity (Hc{sub perpendicular}) and perpendicular squareness (S{sub perpendicular}) of Co-rich Co-Pt films without Pt capped layer are larger than that of Co-rich Co-Pt films with Pt capped layer. The cross-sectional TEM-EDS and AES analysis confirm that the oxygen atoms will diffuse from film surface into the Co-rich Co-Pt film without adding Pt capped layer, and it react with cobalt atoms to form CoO, which is detected by XPS analysis. The increase in perpendicular hard magnetic properties of Co-rich Co-Pt film without Pt capped layer is mainly due to form CoO in the Co-rich Co-Pt film.

  9. Pt, PtCo and PtNi electrocatalysts prepared by mechanical alloying for the oxygen reduction reaction in 0.5 M H{sub 2}SO{sub 4}

    Energy Technology Data Exchange (ETDEWEB)

    Garcia-Contreras, M.A. [Instituto Nacional de Investigaciones Nucleares, Depto. de Quimica, Apdo. Postal 18-1027 Col. Escandon, C.P.11801 Mexico D.F. (Mexico); Instituto Politecnico Nacional, Depto. de Ing. Metalurgica, 07300 Mexico D.F. (Mexico); Fernandez-Valverde, S.M. [Instituto Nacional de Investigaciones Nucleares, Depto. de Quimica, Apdo. Postal 18-1027 Col. Escandon, C.P.11801 Mexico D.F. (Mexico); Vargas-Garcia, J.R. [Instituto Politecnico Nacional, Depto. de Ing. Metalurgica, 07300 Mexico D.F. (Mexico); Cortes-Jacome, M.A.; Toledo-Antonio, J.A.; Angeles-Chavez, C. [Instituto Mexicano del Petroleo, Programa de Ingenieria Molecular, Eje Central Lazaro Cardenas 152, Mexico, D.F.,0 7730 (Mexico)

    2008-11-15

    Electrocatalysts of Pt, PtCo and PtNi powders for the oxygen reduction reaction (ORR) were processed by Mechanical Alloying. Physical characterization was made by X-ray diffraction, scanning electron microscopy and scanning transmission electron microscopy. It was found that milled powders formed agglomerates in the range of 0.2-20 {mu}m formed by nanometric size crystallites. The synthesized powders were alloys of PtFe, PtCoFe and PtNiFe due to iron incorporation during the milling process. The binding energies of Pt in the alloys were determined by XPS. Polarization curves were obtained by Rotating Disk Electrode technique in 0.5 M H{sub 2}SO{sub 4} to determine the electrocatalytic activity of the mechanically alloyed powders. Tafel curves were plotted and kinetic parameters for the ORR were calculated. The PtFe alloy showed the highest electrocatalytic activity for the ORR. However, the lowest overpotential was found for the PtCoFe alloy and it also showed a higher current exchange density. A linear relationship was found between the Pt-binding energy in the alloys and the overpotential at the same current density independent of the Pt alloy composition. (author)

  10. Tailoring the morphology of Pt3Cu1 nanocrystals supported on graphene nanoplates for ethanol oxidation

    Science.gov (United States)

    Zhang, Genlei; Yang, Zhenzhen; Zhang, Wen; Hu, Hongwei; Wang, Chunzhen; Huang, Chengde; Wang, Yuxin

    2016-01-01

    In the search for alternatives to conventional Pt electrocatalysts, we synthesized a series of graphene nanoplate (GNP)-supported Pt3Cu1 nanocrystals (NCs), possessing almost the same composition but different morphologies to probe their electrochemical properties as a function of morphology for the ethanol oxidation reaction. The morphology of the Pt3Cu1 catalysts could be systematically evolved from dendritic (D-Pt3Cu1/GNPs) to wire-like (W-Pt3Cu1/GNPs) and spherical (Pt3Cu1/GNPs) by only varying pH of the reaction solution. The as-prepared Pt3Cu1 catalysts were subsequently characterized using a suite of techniques including transmission electron microscopy (TEM), selected area electron diffraction (SAED), X-ray diffraction (XRD), inductively coupled plasma mass spectrometry (ICP-MS) and X-ray photoelectron spectroscopy (XPS) to verify not only their morphologies and chemical compositions but also the incorporation of Cu into the Pt lattice, as well as physical structure and integrity. Gratifyingly, the three Pt3Cu1 catalysts exhibited superior electrocatalytic properties for the ethanol oxidation compared to the monometallic Pt/GNPs and Pt/C-JM (Johnson Matthey), with the activities, durabilities and anti-poisonous abilities following the order Pt3Cu1/GNPs chemical compositions but also the incorporation of Cu into the Pt lattice, as well as physical structure and integrity. Gratifyingly, the three Pt3Cu1 catalysts exhibited superior electrocatalytic properties for the ethanol oxidation compared to the monometallic Pt/GNPs and Pt/C-JM (Johnson Matthey), with the activities, durabilities and anti-poisonous abilities following the order Pt3Cu1/GNPs < W-Pt3Cu1/GNPs < D-Pt3Cu1/GNPs. Electronic supplementary information (ESI) available. See DOI: 10.1039/c5nr08013d

  11. Tuning the Photoelectrocatalytic Hydrogen Evolution of Pt-Decorated Silicon Photocathodes by the Temperature and Time of Electroless Pt Deposition.

    Science.gov (United States)

    Fabre, Bruno; Li, Gaozeng; Gouttefangeas, Francis; Joanny, Loic; Loget, Gabriel

    2016-11-15

    The electroless deposition of Pt nanoparticles (NPs) on hydrogen-terminated silicon (H-Si) surfaces is studied as a function of the temperature and the immersion time. It is demonstrated that isolated Pt structures can be produced at all investigated temperatures (between 22 and 75 °C) for short deposition times, typically within 1-10 min if the temperature is 45 °C or less than 5 min at 75 °C. For longer times, dendritic metal structures start to grow, ultimately leading to highly rough interconnected Pt networks. Upon increasing the temperature from 22 to 75 °C and for an immersion time of 5 min, the average size of the observed Pt NPs monotonously increases from 120 to 250 nm, and their number density calculated using scanning electron microscopy decreases from (4.5 ± 1.0) × 10(8) to (2.0 ± 0.5) × 10(8) Pt NPs cm(-2). The impact of both the morphology and the distribution of the Pt NPs on the photoelectrocatalytic activity of the resulting metallized photocathodes is then analyzed. Pt deposited at 45 °C for 5 min yields photocathodes with the best electrocatalytic activity for the hydrogen evolution reaction. Under illumination at 33 mW cm(-2), this optimized photoelectrode shows a fill factor of 45%, an efficiency (η) of 9.7%, and a short-circuit current density (|Jsc|) at 0 V versus a reversible hydrogen electrode of 15.5 mA cm(-2).

  12. Insight into the Reaction Mechanisms of Methanol on PtRu/Pt(111): A Density Functional Study

    Science.gov (United States)

    Ding, Qiuyue; Xu, Wenbin; Sang, Pengpeng; Xu, Jing; Zhao, Lianming; He, Xiaoli; Guo, Wenyue

    2016-04-01

    Periodic DFT calculations have been performed to systematically investigate the mechanisms of methanol decomposition and oxidation on the PtRu/Pt(111) surface. Geometries and energies for the primary species involved are analyzed and the reaction network has been mapped out. The calculation shows that among three initial Csbnd H, Osbnd H, and Csbnd O bond scissions of methanol, the Osbnd H bond scission is found to be the most favorable and bears a lower energy barrier than the desorption of methanol. The decomposition of CH3O occurs via the path CH3O → CH2O → CHO → CO with the limiting step of the first dehydrogenation. Although the oxidation of CO is hindered by a high barrier, the CHO oxidation to CHOOH could occur facilely. Further decomposition of formic acid to CO2 and/or CO could occur via four possible pathways, that is, initial Csbnd H, Osbnd H, and Csbnd O bond activations as well as simultaneous activation of Csbnd H and Csbnd O bonds, where the first pathway, HCOOH → COOH → CO2, is the most favorable from a kinetic point of view. Compared to that on Pt(111), methanol on PtRu/Pt(111) prefers to decomposition rather than desorption and then oxidation via the favorable non-CO path with a lower rate-determining energy barrier of CH3O → CH2O for the whole reaction, which indicates that PtRu alloy can improved tolerance toward CO poisoning compared with pure Pt.

  13. PT Symmetry and QCD: Finite Temperature and Density

    Directory of Open Access Journals (Sweden)

    Michael C. Ogilvie

    2009-04-01

    Full Text Available The relevance of PT symmetry to quantum chromodynamics (QCD, the gauge theory of the strong interactions, is explored in the context of finite temperature and density. Two significant problems in QCD are studied: the sign problem of finite-density QCD, and the problem of confinement. It is proven that the effective action for heavy quarks at finite density is PT-symmetric. For the case of 1+1 dimensions, the PT-symmetric Hamiltonian, although not Hermitian, has real eigenvalues for a range of values of the chemical potential μ, solving the sign problem for this model. The effective action for heavy quarks is part of a potentially large class of generalized sine-Gordon models which are non-Hermitian but are PT-symmetric. Generalized sine-Gordon models also occur naturally in gauge theories in which magnetic monopoles lead to confinement. We explore gauge theories where monopoles cause confinement at arbitrarily high temperatures. Several different classes of monopole gases exist, with each class leading to different string tension scaling laws. For one class of monopole gas models, the PT-symmetric affine Toda field theory emerges naturally as the effective theory. This in turn leads to sine-law scaling for string tensions, a behavior consistent with lattice simulations.

  14. Gamma Radiolytic Formation of Alloyed Ag-Pt Nanocolloids

    Directory of Open Access Journals (Sweden)

    M. K. Temgire

    2011-01-01

    Full Text Available Colloidal dispersions of Ag-Pt composite nanoparticles were prepared by gamma radiolysis technique in the presence of nonionic surfactant Brij'97. Simultaneous as well as sequential reduction methods were employed in order to study the structural formation of Ag-Pt bimetallic clusters. Similar shape and trend was observed in optical spectra for both methods. Radiolysis yielded nearly spherical Ag-Pt bimetallic clusters by use of AgNO3 instead of AgClO4. The disappearance of the silver resonance and the simultaneous growth of the 260 nm resonance are independent of cluster structure and degree of alloying. To understand formation of Ag-Pt aggregate, the optical studies were also done as a function of amount of dose absorbed, concentration of surfactant, that is, Brij'97. The shape of the absorption spectrum did not change with increase in gamma radiation dose. TEM analysis exhibited fine dispersions of Ag-Pt clusters surrounded by a mantle when capped with Brij'97. The particle size obtained was in the range of 5–9 nm. On the basis of optical, XRD, and TEM analysis, alloy formation is discussed.

  15. Surfactant-Assisted Hydrothermal Synthesis of PMN-PT Nanorods

    Science.gov (United States)

    Li, Chuan; Liu, Xingzhao; Luo, Wenbo; Xu, Dong; He, Kai

    2016-02-01

    The effects of surfactant polyacrylate acid (PAA) on shape evolution of 0.7Pb(Mg1/3Nb2/3)O3-0.3PbTiO3 (0.7PMN-0.3PT) nanorods were studied. The results revealed that the polyacrylic acid content had great influence on the morphology of 0.7PMN-0.3PT. With increasing PAA concentration from 0.45 to 0.82 g/ml, the ratio of perovskite phase (PMN-PT nanorod) increased, while the ratio of pyrochlore phase decreased. When the PAA concentration was 0.82 g/ml, pure 0.7PMN-0.3PT nanorods were obtained. However, when PAA concentration was higher than 0.82 g/ml, the excess of PAA would hindered their [100] orientation growth. The piezoelectric coefficient d 33 of 0.7PMN-0.3PT nanorod was obtained by linear fitting, and the d 33 value was 409 pm/V.

  16. PT symmetry in classical and quantum statistical mechanics.

    Science.gov (United States)

    Meisinger, Peter N; Ogilvie, Michael C

    2013-04-28

    PT-symmetric Hamiltonians and transfer matrices arise naturally in statistical mechanics. These classical and quantum models often require the use of complex or negative weights and thus fall outside the conventional equilibrium statistical mechanics of Hermitian systems. PT-symmetric models form a natural class where the partition function is necessarily real, but not necessarily positive. The correlation functions of these models display a much richer set of behaviours than Hermitian systems, displaying sinusoidally modulated exponential decay, as in a dense fluid, or even sinusoidal modulation without decay. Classical spin models with PT-symmetry include Z(N) models with a complex magnetic field, the chiral Potts model and the anisotropic next-nearest-neighbour Ising model. Quantum many-body problems with a non-zero chemical potential have a natural PT-symmetric representation related to the sign problem. Two-dimensional quantum chromodynamics with heavy quarks at non-zero chemical potential can be solved by diagonalizing an appropriate PT-symmetric Hamiltonian.

  17. Dissipation-Induced Super Scattering and Lasing PT-Spaser

    CERN Document Server

    Feng, Simin

    2015-01-01

    Giant transmission and reflection of a finite bandwidth are shown to occur at the same wavelength when the electromagnetic wave is incident on a periodic array of PT-symmetric dimers embedded in a metallic film. Remarkably, we found that this phenomenon vanishes if the metallic substrate is lossless while keeping other parameters unchanged. When the metafilm is adjusted to the vicinity of a spectral singularity, tuning substrate dissipation to a critical value can lead to supper scattering in stark contrast to what would be expected in conventional systems. The PT-synthetic plasmonic metafilm acts as a lasing PT-spaser, a planar source of coherent radiation. The metallic dissipation provides a mean to couple light out of the dark modes of the PT- spaser. Above a critical gain-loss coupling, the metafilm behaves as a meta-gain medium with the meta-gain atoms made from the PT-plasmonic dimers. This phenomenon implies that super radiation is possible from a cavity having gain elements by tuning the cavity dissip...

  18. Metal Phosphate-Supported Pt Catalysts for CO Oxidation

    Directory of Open Access Journals (Sweden)

    Xiaoshuang Qian

    2014-12-01

    Full Text Available Oxides (such as SiO2, TiO2, ZrO2, Al2O3, Fe2O3, CeO2 have often been used to prepare supported Pt catalysts for CO oxidation and other reactions, whereas metal phosphate-supported Pt catalysts for CO oxidation were rarely reported. Metal phosphates are a family of metal salts with high thermal stability and acid-base properties. Hydroxyapatite (Ca10(PO46(OH2, denoted as Ca-P-O here also has rich hydroxyls. Here we report a series of metal phosphate-supported Pt (Pt/M-P-O, M = Mg, Al, Ca, Fe, Co, Zn, La catalysts for CO oxidation. Pt/Ca-P-O shows the highest activity. Relevant characterization was conducted using N2 adsorption-desorption, inductively coupled plasma (ICP atomic emission spectroscopy, X-ray diffraction (XRD, transmission electron microscopy (TEM, CO2 temperature-programmed desorption (CO2-TPD, X-ray photoelectron spectroscopy (XPS, and H2 temperature-programmed reduction (H2-TPR. This work furnishes a new catalyst system for CO oxidation and other possible reactions.

  19. Development of an Astronomical Infrared PtSi Camera

    Science.gov (United States)

    Hong, S. S.; Ueno, M.; Koo, B. C.; Kim, K.-T.; Kim, C. Y.; Oh, K. S.; Lee, M. G.; Lee, H. M.; Kang, Y. W.; Park, W.-K.

    1996-12-01

    We have built a near-infrared imaging camera with a PtSi array detector manufactured the Mitsubishi Company. The PtSi detector is sensitive in the wavelength range 1 to 5micrometer. Quantum efficiency of PtSi is much lower than that of InSb and HgCdTe types. However, the PtSi array has advantages over the latter ones:(i)The read-out noise is very low;(ii)the characteristics of the array elements are uniform and stable; (iii)it is not difficult to make a large PtSi array; and (iv)consequently the price is affordably low. The array used consists of 512 x 512 pixels and its size is 10.2 mm x 13.3 mm. The filter wheel of the camera is equipped with J, H, K filters, and an aluminum plate for measuring the dark noise. The dewar is cooled with liquid nitrogen. We have adopted a method of installing the clock pattern and the observing softwares in the RAM, which can be easily used for other systems. We have developed a software with a pull-down menu for operating the camera and data acquisition. The camera has been tested by observing Orionis.

  20. EXAFS Peaks and TPR Characterizing Bimetallic Interactions: Effects of Impregnation Methods on the Structure of Pt-Ru/C Catalysts

    Directory of Open Access Journals (Sweden)

    Nan-Yu Chen

    2014-01-01

    Full Text Available To investigate bimetallic interactions, Pt-Ru/C catalysts were prepared by coimpregnation (Pt-Ruco/C and successive impregnation (Ru-Ptse/C, while Pt/C, Ru/C, and reduced Pt-Rublack were used as reference. Those samples were characterized by XAS and TPR. When Pt(absorber-Ru(backscatter phase-and-amplitude correction is applied to Fourier transformed (FT EXAFS of Pt-Rublack at Pt edge, the characteristic peak of Pt-Ru interactions appears at 2.70 Å´, whereas, when Pt-Pt correction is applied, the peak appears at about 2.5 Å´. Detailed EXAFS analysis for Pt-Ruco/C and Pt-Ruse/C confirms the nature of the characteristic peak and further indicates that the interactions can semiquantitatively be determined by the relative intensity between Pt-Ru and Pt-Pt characteristic peaks. This simple method in determining bimetallic interaction can be extended to characterize Pt-Pd/γ-Al2O3. However, for Pt-Re/γ-Al2O3, Pt-Re interactions cannot be determined by the method because of the overlap of Pt-Pt and Pt-Re characteristic peaks due to similar phase functions.

  1. Removal of Formaldehyde Using Highly Active Pt/TiO2 Catalysts without Irradiation

    Directory of Open Access Journals (Sweden)

    Haibao Huang

    2013-01-01

    Full Text Available Formaldehyde (HCHO is one of the major indoor air pollutants. TiO2 supported Pt catalysts were prepared by sol-gel method and used to eliminate HCHO at room temperature without irradiation. The reduced Pt/TiO2 catalyst (denoted as Pt/TiO2-H2 showed much higher activity than that calcined in air (denoted as Pt/TiO2-air. More than 96% of the conversion of HCHO was obtained over 0.5 wt% Pt/TiO2-H2, on which highly dispersed metallic Pt nanoparticles with very small size (~2 nm were identified. Metallic Pt rather than cationic Pt nanoparticles provide the active sites for HCHO oxidation. Negatively charged metallic Pt nanoparticles facilitate the transfer of charge and oxygen species and the activation of oxygen.

  2. 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.

  3. Networks of connected Pt nanoparticles supported on carbon nanotubes as superior catalysts for methanol electrooxidation

    Science.gov (United States)

    Huang, Meihua; Zhang, Jianshuo; Wu, Chuxin; Guan, Lunhui

    2017-02-01

    The high cost and short lifetime of the Pt-based anode catalyst for methanol oxidation reaction (MOR) hamper the widespread commercialization of direct methanol fuel cell (DMFC). Therefore, improving the activity of Pt-based catalysts is necessary for their practical application. For the first time, we prepared networks of connected Pt nanoparticles supported on multi-walled carbon nanotubes with loading ratio as high as 91 wt% (Pt/MWCNTs). Thanks for the unique connected structure, the Pt mass activity of Pt/MWCNTs for methanol oxidation reaction is 4.4 times as active as that of the commercial Pt/C (20 wt%). When carbon support is considered, the total mass activity of Pt/MWCNTs is 20 times as active as that of the commercial Pt/C. The durability and anti-poisoning ability are also improved greatly.

  4. Facile Synthesis of Nanoporous Pt-Y alloy with Enhanced Electrocatalytic Activity and Durability

    Science.gov (United States)

    Cui, Rongjing; Mei, Ling; Han, Guangjie; Chen, Jiyun; Zhang, Genhua; Quan, Ying; Gu, Ning; Zhang, Lei; Fang, Yong; Qian, Bin; Jiang, Xuefan; Han, Zhida

    2017-02-01

    Recently, Pt-Y alloy has displayed an excellent electrocatalytic activity for oxygen reduction reaction (ORR), and is regarded as a promising cathode catalyst for fuel cells. However, the bulk production of nanoscaled Pt-Y alloy with outstanding catalytic performance remains a great challenge. Here, we address the challenge through a simple dealloying method to synthesize nanoporous Pt-Y alloy (NP-PtY) with a typical ligament size of ~5 nm. By combining the intrinsic superior electrocatalytic activity of Pt-Y alloy with the special nanoporous structure, the NP-PtY bimetallic catalyst presents higher activity for ORR and ethanol oxidation reaction, and better electrocatalytic stability than the commercial Pt/C catalyst and nanoporous Pt alloy. The as-made NP-PtY holds great application potential as a promising electrocatalyst in proton exchange membrane fuel cells due to the advantages of facile preparation and excellent catalytic performance.

  5. Methods to synthesize NiPt bimetallic nanoparticles by a reversed-phase microemulsion, deposition of NiPt bimetallic nanoparticles on a support, and application of the supported catalyst for CO2 reforming of methane

    KAUST Repository

    Biausque, Gregory

    2015-09-24

    Embodiments of the present disclosure provide for NiPt nanoparticles, compositions and supports including NiPt nanoparticles, methods of making NiPt nanoparticles, methods of supporting NiPt nanoparticles, methods of using NiPt nanoparticles, and the like.

  6. 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.

  7. Designed nanostructured pt film for electrocatalytic activities by underpotential deposition combined chemical replacement techniques.

    Science.gov (United States)

    Huang, Minghua; Jin, Yongdong; Jiang, Heqing; Sun, Xuping; Chen, Hongjun; Liu, Baifeng; Wang, Erkang; Dong, Shaojun

    2005-08-18

    Multiple-deposited Pt overlayer modified Pt nanoparticle (MD-Pt overlayer/PtNPs) films were deliberately constructed on glassy carbon electrodes through alternately multiple underpotential deposition (UPD) of Ag followed redox replacement reaction by Pt (II) cations. The linear and regular growth of the films characterized by cyclic voltammetry was observed. Atomic force spectroscopy (AFM) provides the surface morphology of the nanostructured Pt films. Rotating disk electrode (RDE) voltammetry and rotating ring-disk electrode (RRDE) voltammetry demonstrate that the MD-Pt overlayer/PtNPs films can catalyze an almost four-electron reduction of O(2) to H(2)O in air-saturated 0.1 M H(2)SO(4). Thus-prepared Pt films behave as novel nanostructured electrocatalysts for dioxygen reduction and hydrogen evolution reaction (HER) with enhanced electrocatalytic activities, in terms of both reduction peak potential and peak current, when compared to that of the bulk polycrystalline Pt electrode. Additionally, it is noted that after multiple replacement cycles, the electrocatalytic activities improved remarkably, although the increased amount of Pt is very low in comparison to that of pre-modified PtNPs due to the intrinsic feature of the UPD-redox replacement technique. In other words, the electrocatalytic activities could be improved markedly without using very much Pt by the technique of tailoring the catalytic surface. These features may provide an interesting way to produce Pt catalysts with a reliable catalytic performance as well as a reduction in cost.

  8. Pt-Ni and Pt-M-Ni (M = Ru, Sn Anode Catalysts for Low-Temperature Acidic Direct Alcohol Fuel Cells: A Review

    Directory of Open Access Journals (Sweden)

    Ermete Antolini

    2017-01-01

    Full Text Available In view of a possible use as anode materials in acidic direct alcohol fuel cells, the electro-catalytic activity of Pt-Ni and Pt-M-Ni (M = Ru, Sn catalysts for methanol and ethanol oxidation has been widely investigated. An overview of literature data regarding the effect of the addition of Ni to Pt and Pt-M on the methanol and ethanol oxidation activity in acid environment of the resulting binary and ternary Ni-containing Pt-based catalysts is presented, highlighting the effect of alloyed and non-alloyed nickel on the catalytic activity of these materials.

  9. Pengukuran Resiko Manajemen Proyek Teknologi Informasi pada PT MSI

    Directory of Open Access Journals (Sweden)

    Henny Hendarti

    2011-12-01

    Full Text Available Pengukuran resiko manajemen proyek teknologi informasi ini bertujuan untuk mengetahui bagaimana penerapan manajemen proyek teknologi informasi (TI berjalan pada PT MSI agar penerapannya dapat sesuai dengan tujuan bisnis yang diharapkan oleh perusahaan dan memperkirakan resiko-resiko apa yang mungkin terjadi. Metode penelitian yang digunakan adalah studi kasus di mana teknik pengumpulan data meliputi studi kepustakaan serta studi lapangan yang meliputi wawancara, kuesioner, dan studi dokumentasi. Pendekatan untuk melakukan pengukuran resiko teknologi informasi pada PT MSI adalah PMBOK (Project Management Body Of Knowledge. Hasil yang dicapai adalah ditemukannya resiko-resiko yang mungkin terjadi pada proyek. Simpulan dari penelitian ini adalah PT MSI sudah menerapkan manajemen proyek teknologi informasi dengan cukup baik melalui proses inisiasi, perencanaan, pelaksanaan dan pengendalian, evaluasi proyek dan penutupan proyek. Hal ini dilihat resiko yang ditemukan tidak banyak dan hanya dibutuhkan sedikit perbaikan dalam mengelola resiko pada proyek tersebut. Namun perusahaan belum melakukan pengukuran terhadap resiko manajemen proyek TI. 

  10. Zero index metamaterials with PT symmetry in a waveguide system.

    Science.gov (United States)

    Fu, Yangyang; Xu, Yadong; Chen, Huanyang

    2016-01-25

    Inspired by the concept of parity-time symmetry, we propose a new waveguide system consisting of zero index metamaterials with an air gap. Based on analytical calculations and numerical simulations, we demonstrate that there are two exceptional points in such a system, which can induce unidirectional transparency. However, the introduced air gap could effectively manipulate the property of the waveguide system with PT symmetry. In particular, coherent perfect absorber-laser modes could be excited in PT broken phase, if a specific phase difference in the air gap is obtained. More interestingly, when Fabry-Pérot resonances take place in the air gap, the PT symmetry property will be suppressed, i.e., the value of loss/gain could not affect transmission and reflection of the waveguide. As a result, perfect bidirectional transmission without reflection can occur in the waveguide system.

  11. Audit Sistem Informasi Akuntansi Siklus Pengeluaran tada PT. Lagio Furniture

    Directory of Open Access Journals (Sweden)

    Aries Wicaksono

    2014-11-01

    Full Text Available Rapid technological developments make the whole thing easier. Many companies also take advantage of these technological developments. Similarly, the corporate accounting system that uses the benefits of information technology in the form of Accounting Information Systems (AIS. PT. Lagio Furniture is a manufacturing company that produces furniture for the premium class. Information system is an important part that helps the company's operations become more effective and efficient, therefore it is important for information systems running properly.This research aimed to audit the general control and applications control on the expenditure cycle accounting information system at PT. Lagio Furniture. This type of audit is audit around the computer. And then also collecting data through observation and interviews with relevant parties. Results of the reserarch is the expenditure cycle accounting information system at PT. Lagio Furniture was good. But there is still need to be improved in the control plan security, operational management control, and control inputs

  12. Audit Sistem Informasi Akuntansi Siklus Pengeluaran pada PT. Lagio Furniture

    Directory of Open Access Journals (Sweden)

    Aries Wicaksono

    2014-11-01

    Full Text Available Rapid technological developments make the whole thing easier. Many companies also take advantage of these technological developments. Similarly, the corporate accounting system that uses the benefits of information technology in the form of Accounting Information Systems (AIS. PT. Lagio Furniture is amanufacturing company that produces furniture for the premium class. Information system is an important part that helps the company's operations become more effective and efficient, therefore it is important for information systems running properly.This research aimed to audit the general control and applications control on the expenditure cycle accounting information system at PT. Lagio Furniture. This type of audit is audit around the computer. And then also collecting data through observation and interviews with relevant parties. Results of thereserarch is the expenditure cycle accounting information system at PT. Lagio Furniture was good. But there is still need to be improved in the control plan security, operational management control, and control inputs.

  13. High $p_{T}$ physics in the heavy ion era

    CERN Document Server

    Rak, Jan

    2013-01-01

    Aimed at graduate students and researchers in the field of high-energy nuclear physics, this book provides an overview of the basic concepts of large transverse momentum particle physics, with a focus on pQCD phenomena. It examines high $p_{T}$ probes of relativistic heavy-ion collisions and will serve as a handbook for those working on RHIC and LHC data analyses. Starting with an introduction and review of the field, the authors look at basic observables and experimental techniques, concentrating on relativistic particle kinematics, before moving onto a discussion about the origins of high $p_{T}$ physics. The main features of high $p_{T}$ physics are placed within a historical context and the authors adopt an experimental outlook, highlighting the most important discoveries leading up to the foundation of modern QCD theory. Advanced methods are described in detail, making this book especially useful for newcomers to the field.

  14. The high-pressure phase of CePtAl

    Energy Technology Data Exchange (ETDEWEB)

    Heymann, Gunter [Univ. Innsbruck (Austria). Inst. fuer Allgemeine, Anorganische und Theoretische Chemie; Heying, Birgit; Rodewald, Ute C. [Univ. Muenster (Germany). Inst. fuer Anorganische und Analytische Chemie; Janka, Oliver [Univ. Muenster (Germany). Inst. fuer Anorganische und Analytische Chemie; Univ. Oldenburg (Germany). Inst. fuer Chemie

    2017-03-01

    The intermetallic aluminum compound HP-CePtAl was synthesized by arc melting of the elements with subsequent high-pressure/high-temperature treatment at 1620 K and 10.5 GPa in a multianvil press. The compound crystallizes in the hexagonal MgZn{sub 2}-type structure (P6{sub 3}/mmc) with lattice parameters of a=552.7(1) and c=898.8(2) pm refined from powder X-ray diffraction data. With the help of single crystal investigations (wR=0.0527, 187 F{sup 2} values, 13 variables), the proposed structure type was confirmed and the mixed Pt/Al site occupations could be refined. Magnetic susceptibility measurements showed a disappearance of the complex magnetic ordering phenomena, which are observed in NP-CePtAl.

  15. STRATEGI PENINGKATAN DAYA SAING RUMAH POTONG AYAM PT XYZ

    Directory of Open Access Journals (Sweden)

    Arli Arli

    2012-07-01

    Full Text Available ABSTRACTThe objectives of this study were (1 analyzing the role of parties in the value chain that affect PT XYZ competitiveness, (2 identifying the RPA PT XYZ  stakeholders’ key players, (3 analyzing internal and external (IE factors that affects the competitiveness of RPA PT XYZ , (4 formulating strategic long term objectives and goals to increase the competitiveness of RPA PT XYZ , (5 analyzing strategies’ priorities and alternatives to improve the competitiveness of RPA PT XYZ . The method used in this study was descriptive analysis. The analysis tools used in this study were global value chain, stakeholders’ analysis, internal factor evaluation, external factor evaluation, IE Matrix, SWOT, and quantitative strategic planning matrix. Based on the results of global value chain analysis, stakeholders analysis, internal and external analysis, and the company’s visions and missions, the long term objectives are (a to provide value added for customers, (b to maximize business operation’s profit, (c to increase stakeholders’ welfare, (d to operate a sustainable business operation. Results on the IE Matrix and the SWOT analysis, the strategies that can be used to achieve the strategic long term objectives and goals are (a to increase the effectiveness and the efficiencies of the supply chain management; (b to implement performance evaluation on employees and business partners; (c to strengthen the company’s image as a high quality domestic chicken-based food producer in Indonesia; (d to enhance researches and developments; (e to build strategic alliances with external live chicken suppliers; (f promote the importance of animal protein consumption to Indonesian society. Three priority strategies resulted from QSPM analysis are create enhancing the effectiveness and efficiency of the supply chain, implementing performance evaluation on employees and business partners, and strengthen the company’s image as a high quality domestic

  16. 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.

  17. Misfit strain phase diagrams of epitaxial PMN–PT films

    Energy Technology Data Exchange (ETDEWEB)

    Khakpash, N.; Khassaf, H.; Rossetti, G. A. [Department of Materials Science and Engineering and Institute of Materials Science, University of Connecticut, Storrs, Connecticut 06269 (United States); Alpay, S. P., E-mail: p.alpay@ims.uconn.edu [Department of Materials Science and Engineering and Institute of Materials Science, University of Connecticut, Storrs, Connecticut 06269 (United States); Department of Physics, University of Connecticut, Storrs, Connecticut 06269 (United States)

    2015-02-23

    Misfit strain–temperature phase diagrams of three compositions of (001) pseudocubic (1 − x)·Pb (Mg{sub l/3}Nb{sub 2/3})O{sub 3} − x·PbTiO{sub 3} (PMN–PT) thin films are computed using a phenomenological model. Two (x = 0.30, 0.42) are located near the morphotropic phase boundary (MPB) of bulk PMN–PT at room temperature (RT) and one (x = 0.70) is located far from the MPB. The results show that it is possible to stabilize an adaptive monoclinic phase over a wide range of misfit strains. At RT, the stability region of this phase is much larger for PMN–PT compared to barium strontium titanate and lead zirconate titanate films.

  18. PMN-PT nanowires with a very high piezoelectric constant.

    Science.gov (United States)

    Xu, Shiyou; Poirier, Gerald; Yao, Nan

    2012-05-09

    A profound way to increase the output voltage (or power) of the piezoelectric nanogenerators is to utilize a material with higher piezoelectric constants. Here we report the synthesis of novel piezoelectric 0.72Pb(Mg(1/3)Nb(2/3))O(3)-0.28PbTiO(3) (PMN-PT) nanowires using a hydrothermal process. The unpoled single-crystal PMN-PT nanowires show a piezoelectric constant (d(33)) up to 381 pm/V, with an average value of 373 ± 5 pm/V. This is about 15 times higher than the maximum reported value of 1-D ZnO nanostructures and 3 times higher than the largest reported value of 1-D PZT nanostructures. These PMN-PT nanostructures are of good potential being used as the fundamental building block for higher power nanogenerators, high sensitivity nanosensors, and large strain nanoactuators.

  19. Misfit strain phase diagrams of epitaxial PMN-PT films

    Science.gov (United States)

    Khakpash, N.; Khassaf, H.; Rossetti, G. A.; Alpay, S. P.

    2015-02-01

    Misfit strain-temperature phase diagrams of three compositions of (001) pseudocubic (1 - x).Pb (Mgl/3Nb2/3)O3 - x.PbTiO3 (PMN-PT) thin films are computed using a phenomenological model. Two (x = 0.30, 0.42) are located near the morphotropic phase boundary (MPB) of bulk PMN-PT at room temperature (RT) and one (x = 0.70) is located far from the MPB. The results show that it is possible to stabilize an adaptive monoclinic phase over a wide range of misfit strains. At RT, the stability region of this phase is much larger for PMN-PT compared to barium strontium titanate and lead zirconate titanate films.

  20. Electrical behaviour of PMN-PT-PVDF nanocomposite

    Energy Technology Data Exchange (ETDEWEB)

    Sen, Shrabanee; Mishra, S K [MST Division, National Metallurgical Laboratory, Jamshedpur 834007 (India)], E-mail: shrabaneesen@yahoo.co.in

    2008-08-21

    Nanocomposites of polyvinyldene fluoride (PVDF) and a solid solution of lead magnesium niobate and lead titanate (0.65PMN-0.35PT) with varying composition ratios were prepared by the hot-press technique. The phase structure and morphology were studied by thermal analysis (DTA), x-ray diffraction and scanning electron microscopy. The PVDF sample showed an exothermic peak due to the crystallization of the PVDF phase, but with the addition of PMN-PT powders an extra peak appeared due to the crystallization of the pyrochlore phase present in the PMN-PT powder. The crystallite size of the prepared samples was found to be between 40 and 60 nm. The value of the relative permittivity increased with the increase in the ceramic concentration. The presence of a single semicircle confirmed the presence of the bulk effect only. The bulk conductivity indicated an Arrhenius type thermally activated process. The ac conductivity spectrum obeyed the Jonscher power law.

  1. PtSi Clustering in Silicon Probed by Transport Spectroscopy

    Directory of Open Access Journals (Sweden)

    Massimo Mongillo

    2013-12-01

    Full Text Available Metal silicides formed by means of thermal annealing processes are employed as contact materials in microelectronics. Control of the structure of silicide/silicon interfaces becomes a critical issue when the characteristic size of the device is reduced below a few tens of nanometers. Here, we report on silicide clustering occurring within the channel of PtSi/Si/PtSi Schottky-barrier transistors. This phenomenon is investigated through atomistic simulations and low-temperature resonant-tunneling spectroscopy. Our results provide evidence for the segregation of a PtSi cluster with a diameter of a few nanometers from the silicide contact. The cluster acts as a metallic quantum dot giving rise to distinct signatures of quantum transport through its discrete energy states.

  2. Electrochemical oxidation of methanol on Pt3Co bulk alloy

    Directory of Open Access Journals (Sweden)

    S. LJ. GOJKOVIC

    2003-11-01

    Full Text Available The electrochemical oxidation of methanol was investigated on a Pt3Co bulk alloy in acid solutions. Kinetic parameters such as transfer coefficient, reaction orders with respect to methanol and H+ ions and energy of activation were determined. It was found that the rate of methanol oxidation is significantly diminished by rotation of the electrode. This effect was attributed to the diffusion of formaldehyde and formic acid from the electrode surface. Stirring of the electrolyte also influenced the kinetic parameters of the reaction. It was speculated that the predominant reaction pathway and rate determining step are different in the quiescent and in the stirred electrolyte. Cobalt did not show a promoting effect on the rate of methanol oxidation on the Pt3Co bulk alloy with respect to a pure Pt surface.

  3. EXCEPTIONAL POINTS IN OPEN AND PT-SYMMETRIC SYSTEMS

    Directory of Open Access Journals (Sweden)

    Hichem Eleuch

    2014-04-01

    Full Text Available Exceptional points (EPs determine the dynamics of open quantum systems and cause also PT symmetry breaking in PT symmetric systems. From a mathematical point of view, this is caused by the fact that the phases of the wavefunctions (eigenfunctions of a non-Hermitian Hamiltonian relative to one another are not rigid when an EP is approached. The system is therefore able to align with the environment to which it is coupled and, consequently, rigorous changes of the system properties may occur. We compare analytically as well as numerically the eigenvalues and eigenfunctions of a 2 × 2 matrix that is characteristic either of open quantum systems at high level density or of PT symmetric optical lattices. In both cases, the results show clearly the influence of the environment on the system in the neighborhood of EPs. Although the systems are very different from one another, the eigenvalues and eigenfunctions indicate the same characteristic features.

  4. Pt-Co multilayers: Interface effects at the monolayer limit

    Energy Technology Data Exchange (ETDEWEB)

    Angelakeris, M.; Natsiopoulos, G.; Flevaris, N.K. [Department of Physics, Aristotle University, 54124 Thessaloniki (Greece); Papaioannou, E.T. [Institut fuer Experimentalphysik, Freie Universitaet, 14195 Berlin-Dahlem (Germany); Poulopoulos, P.; Vlachos, A. [Materials Science Department, University of Patras, 26504 Patras (Greece); Wilhelm, F.; Rogalev, A. [European Synchrotron Radiation Facility, ESRF, B.P. 220, 38043 Grenoble (France)

    2008-10-15

    This work focuses on the structural and magnetic features of Pt-Co multilayers prepared by e-beam evaporation. In order to examine interface and induced magnetism effects, the layer thickness was always kept under 4 monolayers. X-ray diffraction spectra revealed the multilayer nature of the samples while magnetometry measurements recorded tuneable perpendicular magnetic anisotropy and enhanced magnetization values due to the high degree of Pt-polarization in a ferromagnetic environment. The experimental technique that allows one to study induced magnetism is the X-ray magnetic circular dichroism, which provides quantitative information on spin and orbital magnetic moments. Enhanced Pt contribution on the perpendicular anisotropy was evidenced, while the induced (spin, orbital and total) magnetic moments, and the ratio orbital-to-spin magnetic moments were derived by application of the sum rules. (copyright 2008 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  5. PT -symmetric spectral singularity and negative-frequency resonance

    Science.gov (United States)

    Pendharker, Sarang; Guo, Yu; Khosravi, Farhad; Jacob, Zubin

    2017-03-01

    Vacuum consists of a bath of balanced and symmetric positive- and negative-frequency fluctuations. Media in relative motion or accelerated observers can break this symmetry and preferentially amplify negative-frequency modes as in quantum Cherenkov radiation and Unruh radiation. Here, we show the existence of a universal negative-frequency-momentum mirror symmetry in the relativistic Lorentzian transformation for electromagnetic waves. We show the connection of our discovered symmetry to parity-time (PT ) symmetry in moving media and the resulting spectral singularity in vacuum fluctuation-related effects. We prove that this spectral singularity can occur in the case of two metallic plates in relative motion interacting through positive- and negative-frequency plasmonic fluctuations (negative-frequency resonance). Our work paves the way for understanding the role of PT -symmetric spectral singularities in amplifying fluctuations and motivates the search for PT symmetry in novel photonic systems.

  6. Thermodynamic properties of stable and metastable phases of Pt metal

    Institute of Scientific and Technical Information of China (English)

    PENG Hong-jian; XIE You-qing; NIE Yao-zhuang

    2009-01-01

    Isometric heat capacity cv and isobaric heat capacity cp of Pt with stable and metastable phases were calculated by using pure element systematic theory. These results are in excellent agreement with of SGTE (Scientific Group Thermodata Europe) database and JANAF (Joint Army-Navy-Air Force) experimental values. The calculation results of cv and cp of Pt metal in natural state are in good agreement with those calculated by FP(first-principles) method. It is found that the electron devotion to heat capacity is important to adjust in OA(one-atom) method while calculating heat capacity. The full information about thermodynamic properties of Pt metal with stable and metastable phases, such as entropy(S), enthalpy(H) and Gibbs energy(G) were calculated from 0 K to random temperature. The results are in good agreement with JANAF experimental value. In contrast to SGTE database, the thermodynamic properties from 0 K to 298.15 K are implemented.

  7. Differential electrochemical mass spectrometry study of Pt and PtSn nanocatalysts for direct ethanol fuel cells

    Energy Technology Data Exchange (ETDEWEB)

    Saidani, F.; Bommersbach, P.; Guay, D.; Mohamedi, M. [Quebec Univ., Institut National de la Recherche Scientifique, Varennes, PQ (Canada). Centre de l' Energie, Materiaux et Telecommunications; Rochefort, D. [Montreal Univ., PQ (Canada). Dept. of Chemistry

    2008-07-01

    This paper reported on a study that investigated Platinum (Pt) and Pt with tin (Sn) nanoparticles prepared under vacuum and under 2 Torr of He by pulsed laser ablation. This method was chosen because it is possible to control size of nanoparticles, structure and morphology of films by varying deposition conditions. The influence of deposition conditions on the electrocatalytic behaviour was determined. In particular, the objective of the study was to better understand the reaction mechanism involved during ethanol oxidation at Pt and PtSn catalysts by means of cyclic voltammetry combined with Differential Electrochemical Mass Spectrometry (DEMS), a powerful technique to elucidate the Ethanol Oxidation Reaction (EOR) mechanism. Ethanol was shown to be a very attractive liquid biofuel for direct-fuelled systems, since its partial oxidation products are less toxic than other alcohols. During pulsed laser ablation, the interaction between an intense laser and a target material resulted in the creation of plasma. This plasma enabled the transfer of matter from the target to the substrate. Highly nanocrystalline films can be prepared when deposition is performed into a moderate pressure gas. The electrochemical investigations showed that Pt deposited under 2 torr have a beneficial effect on the electrocatalytic activity towards ethanol oxidation. 5 refs., 1 fig.

  8. Spontaneous deposition of Ru on Pt (100: morphological and electrochemical studies. Preliminary results of ethanol oxidation at Pt(100/Ru

    Directory of Open Access Journals (Sweden)

    Colle Vinicius D.

    2003-01-01

    Full Text Available In the present work ruthenium was deposited in submonolayer amounts on Pt(100 by spontaneous deposition at several deposition times. The Pt (100/Ru surfaces were analyzed using ex-situ STM to image the deposits characteristic of ruthenium on Pt (100. It was observed the formation of ruthenium islands with diameters between 1.0 and 4.5 nm with bi-atomic thickness in the center of the islands. A homogeneous distribution of the ruthenium islands on the platinum terraces was found, with no preferential deposition on steps or surface defect sites. The ruthenium coverage degree had been calculated by the decrease of charge of the hydrogen adsorption-desorption peaks in the cyclic voltammograms of the Pt(100/Ru electrodes. The Pt(100/Ru electrodes with a ruthenium coverage degree of ca. 0.3 showed a high activity for the ethanol electrooxidation. The electrochemical experimental results support strongly the bifunctional mechanism for the enhanced ethanol oxidation.

  9. Evaluation of Pt{sub 40}Pd{sub 60}/MWCNT electrocatalyst as ethylene glycol-tolerant oxygen reduction cathodes

    Energy Technology Data Exchange (ETDEWEB)

    Morales-Acosta, D.; Arriaga, L.G. [Centro de Investigacion y Desarrollo Tecnologico en Electroquimica, Parque Tecnologico Queretaro, Sanfandila, Pedro Escobedo, C.P. 76703 Queretaro (Mexico); Alvarez-Contreras, L. [Centro de Investigacion en Materiales Avanzados S.C., Complejo Industrial Chihuahua, C. P. 31109, Chihuahua, Chih. (Mexico); Luna, S. Fraire; Varela, F.J. Rodriguez [Cinvestav Unidad Saltillo, Carr. Saltillo-Monterrey Km. 13.5, Ramos Arizpe, Coahuila, C.P. 25900 (Mexico)

    2009-07-15

    Pt-Pd/MWCNT with Pt:Pd atomic ratio 40:60 and Pt/MWCNT electrocatalyst were synthesized and evaluated as oxygen reduction reaction (ORR) cathodes for Direct Ethylene Glycol Fuel Cells (DEGFC) applications. As reference, a commercial Pt/C material was also tested. We found that Pt-Pd/MWCNT has high tolerance capability to EG and higher selectivity for the ORR compared to the Pt-alone materials. As a result, the shift in onset potential for the ORR, E{sub onset}, at Pt-Pd/MWCNT was considerably smaller than the shift at Pt/MWCNT or Pt/C. The average particle size (from XRD) was 3.5 and 4 nm for Pt/MWCNT and Pt-Pd/MWCNT, respectively. A moderate degree of alloying was determined for the Pt-Pd material. An advantageous application of Pt-Pd electrocatalysts should be in DEGFCs. (author)

  10. Supported bimetallic Pt-Au nanoparticles: Structural features predicted by molecular dynamics simulations

    Science.gov (United States)

    Morrow, Brian H.; Striolo, Alberto

    2010-04-01

    We have utilized all-atom molecular dynamics simulations to study bimetallic Pt-Au nanoparticles supported by carbonaceous materials at 700 K. Nanoparticles containing 250 atoms with 25%, 50%, and 75% Pt ( Pt62Au188 , Pt125Au125 , and Pt188Au62 , respectively) were considered. A single graphite sheet and bundles of seven (10,10), (13,13), and (20,20) single-walled carbon nanotubes were used as supports. It was found that Pt125Au125 forms a well-defined Pt core covered by an Au shell, regardless of the support. Pt62Au188 exhibits a mixed Pt-Au core with an Au shell. Pt188Au62 has a Pt core with a mixed Pt-Au shell. The support affects the atomic distribution. We investigated the percentage of nanoparticle surface atoms that are Pt. Our results show that for Pt62Au188 and Pt125Pt125 , this percentage is lowest when there is no support and highest when carbon nanotubes are supports. We studied the size of clusters of Pt atoms on the nanoparticle surface, finding that the geometry of the support influences the distribution of cluster sizes. Finally, we found that the coordination states of the atoms on the nanoparticle surface are affected by the support structure. These results suggest that it is possible to tailor the distribution of atoms in Pt-Au nanoparticles by controlling the nanoparticle composition and the support geometry. Such level of control is desirable for improving selectivity of catalysts.

  11. Monte carlo simulations of segregation in Pt-Re catalyst nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

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

    2004-04-01

    We have investigated the segregation of Pt atoms to the surfaces of Pt-Re nanoparticles using the Monte Carlo method and Modified Embedded Atom Method potentials that we have developed for Pt-Re alloys. The Pt75Re25 nanoparticles (containing from 586 to 4033 atoms) are assumed to have disordered fcc configurations and cubo-octahedral shapes (terminated by {l_brace}111{r_brace} and {l_brace}100{r_brace} facets), while the Pt50Re50 and Pt25Re75 nanoparticles (containing from 587 to 4061 atoms) are assumed to have disordered hcp configurations and truncated hexagonal bipyramidal shapes (terminated by {l_brace}0001{r_brace} and {l_brace}101 {bar 1}{r_brace} facets). We predict that due to the segregation process the equilibrium Pt-Re nanoparticles would achieve a core-shell structure, with a Pt-enriched shell surrounding a Pt-deficient core. For fcc cubo-octahedral Pt75Re25 nanoparticles, the shells consist of almost 100 at. percent of Pt atoms. Even in the shells of hcp truncated hexagonal bipyramidal Pt50Re50 nanoparticles, the concentrations of Pt atoms exceed 85 at. percent (35 at. percent higher than the overall concentration of Pt atoms in these nanoparticles). Most prominently, all Pt atoms will segregate to the surfaces in the hcp truncated hexagonal bipyramidal Pt25Re75 nanoparticles containing less than 1000 atoms. We also find that the Pt atoms segregate preferentially to the vertex sites, less to edge sites, and least to facet sites on the shell of Pt-Re nanoparticles.

  12. Ternary Pt-Ru-Ni catalytic layers for methanol electrooxidation prepared by electrodeposition and galvanic replacement

    Directory of Open Access Journals (Sweden)

    Athanasios ePapaderakis

    2014-06-01

    Full Text Available Ternary Pt-Ru-Ni deposits on glassy carbon substrates, Pt-Ru(Ni/GC, have been formed by initial electrodeposition of Ni layers onto glassy carbon electrodes, followed by their partial exchange for Pt and Ru, upon their immersion into equimolar solutions containing complex ions of the precious metals. The overall morphology and composition of the deposits has been studied by SEM microscopy and EDS spectroscopy. Continuous but nodular films have been confirmed, with a Pt÷Ru÷Ni % bulk atomic composition ratio of 37÷12÷51 (and for binary Pt-Ni control systems of 47÷53. Fine topographical details as well as film thickness have been directly recorded using AFM microscopy. The composition of the outer layers as well as the interactions of the three metals present have been studied by XPS spectroscopy and a Pt÷Ru÷Ni % surface atomic composition ratio of 61÷12÷27 (and for binary Pt-Ni control systems of 85÷15 has been found, indicating the enrichment of the outer layers in Pt; a shift of the Pt binding energy peaks to higher values was only observed in the presence of Ru and points to an electronic effect of Ru on Pt. The surface electrochemistry of the thus prepared Pt-Ru(Ni/GC and Pt(Ni/GC electrodes in deaerated acid solutions (studied by cyclic voltammetry proves the existence of a shell consisting exclusively of Pt-Ru or Pt. The activity of the Pt-Ru(Ni deposits towards methanol oxidation (studied by slow potential sweep voltammetry is higher from that of the Pt(Ni deposit and of pure Pt; this enhancement is attributed both to the well-known Ru synergistic effect due to the presence of its oxides but also (based on the XPS findings to a modification effect of Pt electronic properties.

  13. Exchange-Coupled FePt Nanoparticle Assembly

    Science.gov (United States)

    Zeng, Hao; Vedantam, T.; Dai, Z. R.; Wang, Z. L.; Liu, J. P.; Sun, Shouheng

    2002-03-01

    High-performance permanent magnetic materials for energy-related applications need large energy-products. A permanent magnet with large (BH) products should exhibit both a high saturation magnetization , M_s, and a large coercive field, H_c. L10 ordered FePt has high Ms ( ~ 1100 emu/cm^3) and large magnetocrystalline anisotropy constant Ku (> 5e10^7 erg/cm^3), therefore may be a suitable candidates for permanent magnetic materials. We report synthesis of exchange-coupled FePt nanoparticle assemblies via solution phase deposition and controlled thermal annealing. FePt nanoparticles are prepared by high temperature solution phase decomposition of Fe(CO)_5and reduction of Pt(acac)2 in the presence of oleic acid and oleyl amine. The Fe and Pt composition of the nanoparticles is tuned by adjusting the molar ratio of Fe(CO)5 to Pt(acac)_2. The nanoparticles are easily dispersed into alkane solvent. Depositing particle dispersion on a solid substrate and controlling solvent evaporation yield self-organized magnetic nanoparticle assemblies. Magnetic hysteresis loops, remanence curves, and δM measurements show that annealing for short time under nitrogen yields isolated particle assemblies with random crystalline orientations. Prolonged annealing under reducing atmosphere leads to the evaporation of the organic surfactants, and results in grain agglomeration and inter grain exchange coupling. The degree of coupling can be readily controlled by annealing conditions. Changes in the magnetization reversal behavior have also been observed.This work is supported by DARPA No. DAAD 19-01-1-0546.

  14. Metallization of cyanide-modified Pt(111) electrodes with copper

    DEFF Research Database (Denmark)

    Escribano, Maria Escudero; Wildi, Christopher; Mwanda, Jonathan A.

    2016-01-01

    The reduction of Cu2+ ions irreversibly attached to the surface of a cyanide-modified Pt(111) electrode via non-covalent or weakly covalent interactions with the N atom of adsorbed cyanide was studied using cyclic voltammetry (CV) and in situ scanning tunneling microscopy (STM). Both CV and STM...... provide evidence that the reduction of irreversibly adsorbed Cu2+ to Cu in Cu2+-free sulfuric acid solutions does not result in the stripping of the cyanide adlayer. This strongly suggests that the reduction process results in the metallization of the cyanide adlayer on Pt(111), yielding a platinum-cyanide...

  15. Bounded dynamics in finite PT-symmetric magnetic metamaterials.

    Science.gov (United States)

    Molina, Mario I

    2014-03-01

    We examine the PT-symmetry-breaking transition for a magnetic metamaterial of a finite extent, modeled as an array of coupled split-ring resonators in the equivalent circuit model approximation. Small-size arrays are solved completely in closed form, while for arrays larger than N=5 results were computed numerically for several gain and loss spatial distributions. In all cases, it is found that the parameter stability window decreases rapidly with the size of the array, until at N=20 approximately it is not possible to support a stable PT-symmetric phase.

  16. Achieving methodological alignment when combining QCA and PT in practice

    DEFF Research Database (Denmark)

    Beach, Derek

    2016-01-01

    negotiations, part of the broader phenomenon of the representation of voter views in public policies. The section develops a range of potential causes for congruence from the existing literature. Second, using a QCA-first design I undertake a fsQCA analysis of sufficiency. Utilized in a theory-building fashion......This article explores the practical challenges one faces when combining Qualitative Comparative Analysis (QCA) and Process-tracing (PT) in a manner that is consistent with their underlying assumptions about the nature of causal relationships. While PT builds on a mechanism-based understanding...

  17. IS PT -SYMMETRIC QUANTUM THEORY FALSE AS A FUNDAMENTAL THEORY?

    Directory of Open Access Journals (Sweden)

    Miloslav Znojil

    2016-06-01

    Full Text Available Yi-Chan Lee et al. claim (cf. Phys. Rev. Lett. 112, 130404 (2014 that the “recent extension of quantum theory to non-Hermitian Hamiltonians” (which is widely known under the nickname of “PT-symmetric quantum theory” is “likely false as a fundamental theory”. By their opinion their results “essentially kill any hope of PT-symmetric quantum theory as a fundamental theory of nature”. In our present text we explain that their toy-model-based considerations are misleading and that they do not imply any similar conclusions.

  18. Nonreciprocal Scattering by PT-symmetric stack of the layers

    CERN Document Server

    Shramkova, Oksana

    2015-01-01

    The nonreciprocal wave propagation in PT-symmetric periodic stack of binary dielectric layers characterised by balances loss and gain is analysed. The main mechanisms and resonant properties of the scattered plane waves are illustrated by the simulation results, and the effects of the periodicity and individual layer parameters on the stack nonreciprocal response are discussed. Gaussian beam dynamics in this type of structure is examined. The beam splitting in PT-symmetric periodic structure is observed. It is demonstrated that for slant beam incidence the break of the symmetry of field distribution takes place.

  19. Low $p_T$ Hadronic Physics with CMS

    CERN Document Server

    AUTHOR|(CDS)2072044

    2007-01-01

    The pixel detector of CMS can be used to reconstruct very low pT charged particles down to about 0.1 GeV/c. This can be achieved with good efficiency, resolution and negligible fake rate for elementary collisions. In case of central PbPb the fake rate can be kept low for pT>0.4 GeV/c. In addition, the detector can be employed for identification of neutral hadrons (V0s) and converted photons.

  20. PT-symmetric quantum oscillator in an optical cavity

    CERN Document Server

    Longhi, Stefano

    2016-01-01

    The quantum harmonic oscillator with parity-time ($\\mathcal{PT}$) symmetry, obtained from the ordinary (Hermitian) quantum harmonic oscillator by an imaginary displacement of the spatial coordinate, provides an important and exactly-solvable model to investigate non-Hermitian extension of the Ehrenfest theorem. Here it is shown that transverse light dynamics in an optical resonator with off-axis longitudinal pumping can emulate a $\\mathcal{PT}$-symmetric quantum harmonic oscillator, providing an experimentally accessible system to investigate non-Hermitian coherent state propagation.

  1. Atomic states and properties of Pt-electrocatalyst

    Institute of Scientific and Technical Information of China (English)

    PENG; Hongjian

    2006-01-01

    Using the one-atom theory (OA), the atomic state of Pt-electrocatalyst with fcc structure was determined as follows: [Xe] (5dn)6.48 (5dc)2.02 (6Sc)1.48(6sf)0.02. The atomic states of this metal with hcp and bcc structures of primary characteristic crystals and liquid state was also studied. According to its atomic states, the relationship between the atomic states and crystalline structure, catalytic performance and conductivity was explained qualitatively. The potential curve, the temperature dependence of bulk modulus and linear thermal expansion coefficient of fcc-Pt were calculated quantitatively.

  2. Stability of solitons in PT-symmetric couplers

    CERN Document Server

    Driben, Rodislav

    2011-01-01

    Families of analytical solutions are found for symmetric and antisymmetric solitons in the dual-core system with the Kerr nonlinearity and PT-balanced gain and loss. The crucial issue is stability of the solitons. A stability region is obtained in an analytical form, and verified by simulations, for the PT-symmetric solitons. For the antisymmetric ones, the stability border is found in a numerical form. Moving solitons of both types collide elastically. The two soliton species merge into one in the "supersymmetric" case, with equal coefficients of the gain, loss and inter-core coupling. These solitons feature a subexponential instability, which may be suppressed by periodic switching ("management").

  3. PENGUKURAN RESIKO MANAJEMEN PROYEK TEKNOLOGI INFORMASI PADA PT MSI

    Directory of Open Access Journals (Sweden)

    Henny Hendarti

    2011-11-01

    kepustakaan serta studi lapangan yang meliputi wawancara, kuesioner, dan studi dokumentasi. Pendekatan untuk melakukan pengukuran resiko teknologi informasi pada PT MSI adalah PMBOK (Project Management Body Of Knowledge. Hasil yang dicapai adalah ditemukannya resiko-resiko yang mungkin terjadi pada proyek. Simpulan dari penelitian ini adalah PT MSI sudah menerapkan manajemen proyek teknologi informasi dengan cukup baik melalui proses inisiasi, perencanaan, pelaksanaan dan pengendalian, evaluasi proyek dan penutupan proyek. Hal ini dilihat resiko yang ditemukan tidak banyak dan hanya dibutuhkan sedikit perbaikan dalam mengelola resiko pada proyek tersebut. Namun perusahaan belum melakukan pengukuran terhadap resiko manajemen proyek TI.

  4. QCD factorization for high $p_T$ heavy quarkonium production

    CERN Document Server

    Ma, Yan-Qing; Sterman, George; Zhang, Hong

    2015-01-01

    In this talk, we present the QCD factorization formula for heavy quarkonium production at large $p_T$ with factorized leading-power and next-to-leading power contributions in the $1/p_T$ expansion. We show that the leading order analytical calculations in this QCD factorization approach can reproduce effectively the full next-to-leading order numerical results derived using non-relativistic QCD (NRQCD) factorization formalism. We demonstrate that the next-to-leading power contributions are crucial to the description of the channels that are the most relevant for the rate as well as polarization of $J/\\psi$ production at current collider energies.

  5. Subcooled boiling of nano-particle suspensions on Pt wires

    Institute of Scientific and Technical Information of China (English)

    LI Chunhui; WANG Buxuan; PENG Xiaofeng

    2004-01-01

    An experimental investigation is conducted to explore the subcooled boiling characteristics of nano-particle suspensions on Pt wires. Some phenomena are observed for the boiling of water-SiO2 nano-particle suspensions on Pt wires. The experiments show that there exist not any evident differences for boiling of pure water and of nano-particle suspensions at high heat fluxes. However, bubble overlap phenomenon can be easily found for nano-particle suspensions at low heat fluxes, which probably results from the increase of the attracter force between bubbles and of the bubble mass.

  6. Light propagation through a PT-symmetric photonic-crystal.

    Science.gov (United States)

    Konotop, Vladimir V; Mantsyzov, Boris I

    2016-11-14

    Light propagation through a finite-width periodically modulated layer obeying parity-time (PT) symmetry is considered. We consider the configuration when the resonant conditions of mode coupling by the grating are satisfied. It is shown that the dependence of the transmission and reflection coefficients on the slab width has resonant character featuring strong amplification of reflected and transmitted waves with negative angles. The dependence of the scattering data on the gain-and-loss intensity also feature strong resonances near the PT-symmetry breaking point, when the slab strongly amplifies waves reflected and transmitted with negative angles, provided the incident wave has a positive angle of incidence.

  7. Exponential growth of colored HOMFLY-PT homology

    CERN Document Server

    Wedrich, Paul

    2016-01-01

    We define reduced colored sl(N) link homologies and use deformation spectral sequences to characterize their dependence on color and rank. We then define reduced colored HOMFLY-PT homologies and prove that they arise as large N limits of sl(N) homologies. Together, these results allow proofs of many aspects of the physically conjectured structure of the family of type A link homologies. In particular, we verify a conjecture of Gorsky, Gukov and Sto\\v{s}i\\'c about the growth of colored HOMFLY-PT homologies.

  8. On the integrability of PT-symmetric dimers

    CERN Document Server

    Pickton, J

    2013-01-01

    The coupled discrete linear and Kerr nonlinear Schrodinger equations with gain and loss describing transport on dimers with parity-time (PT) symmetric potentials are considered. The model is relevant among others to experiments in optical couplers and proposals on Bose-Einstein condensates in PT symmetric double-well potentials. It is shown that the models are integrable. A pendulum equation with a linear potential and a constant force for the phase-difference between the fields is obtained, which explains the presence of unbounded solutions above a critical threshold parameter.

  9. Sources of PT: ideology versus personalism in its electoral support

    Directory of Open Access Journals (Sweden)

    David SAMUELS

    2011-01-01

    Full Text Available This article explores data from the Estudo Eleitoral Brasileiro in order to research the bases of support to the Partido dos Trabalhadores (PT, who reached the Presidency of Brazil in 2002. The results show that PT’s voters are more identified with the leadership of Luiz Inácio Lula da Silva, the current president and the historical leader of the party, than with the PT’s ideology. Nevertheless, the ideological linkages between PT and its voters are still more important that the ideological linkages between the other brazilian parties and theirs respective voters.

  10. Oxygen reduction reaction on a highly-alloyed Pt-Ni supported carbon electrocatalyst in acid solution

    CSIR Research Space (South Africa)

    Zheng, H

    2010-08-31

    Full Text Available Alloyed electrocatalysts such as PtNi/C[1-2], PtCo/C[3], PtCr/C[4], PtFe/C [5-6], and non-alloyed Pt-TiO2/C were reportedly investigated for methanol tolerance during Oxygen reduction reaction (ORR). The high methanol tolerance...

  11. Binuclear Pt-Tl bonded complex with square pyramidal coordination around Pt: a combined multinuclear NMR, EXAFS, UV-Vis, and DFT/TDDFT study in dimethylsulfoxide solution.

    Science.gov (United States)

    Purgel, Mihály; Maliarik, Mikhail; Glaser, Julius; Platas-Iglesias, Carlos; Persson, Ingmar; Tóth, Imre

    2011-07-04

    The structure and bonding of a new Pt-Tl bonded complex formed in dimethylsulfoxide (dmso), (CN)(4)Pt-Tl(dmso)(5)(+), have been studied by multinuclear NMR and UV-vis spectroscopies, and EXAFS measurements in combination with density functional theory (DFT) and time dependent density functional theory (TDDFT) calculations. This complex is formed following the equilibrium reaction Pt(CN)(4)(2-) + Tl(dmso)(6)(3+) ⇆ (CN)(4)Pt-Tl(dmso)(5)(+) + dmso. The stability constant of the Pt-Tl bonded species, as determined using (13)C NMR spectroscopy, amounts to log K = 2.9 ± 0.2. The (NC)(4)Pt-Tl(dmso)(5)(+) species constitutes the first example of a Pt-Tl bonded cyanide complex in which the sixth coordination position around Pt (in trans with respect to the Tl atom) is not occupied. The spectral parameters confirm the formation of the metal-metal bond, but differ substantially from those measured earlier in aqueous solution for complexes (CN)(5)Pt-Tl(CN)(n)(H(2)O)(x)(n-) (n = 0-3). The (205) Tl NMR chemical shift, δ = 75 ppm, is at extraordinary high field, while spin-spin coupling constant, (1)J(Pt-Tl) = 93 kHz, is the largest measured to date for a Pt-Tl bond in the absence of supporting bridging ligands. The absorption spectrum is dominated by two strong absorption bands in the UV region that are assigned to MMCT (Pt → Tl) and LMCT (dmso → Tl) bands, respectively, on the basis of MO and TDDFT calculations. The solution of the complex has a bright yellow color as a result of a shoulder present on the low energy side of the band at 355 nm. The geometry of the (CN)(4)Pt-Tl core can be elucidated from NMR data, but the particular stoichiometry and structure involving the dmso ligands are established by using Tl and Pt L(III)-edge EXAFS measurements. The Pt-Tl bond distance is 2.67(1) Å, the Tl-O bond distance is 2.282(6) Å, and the Pt-C-N entity is linear with Pt-C and Pt···N distances amounting to 1.969(6) and 3.096(6) Å, respectively. Geometry optimizations on

  12. Thermal stability dependence on the stacking order and thickness ratio of the CoPt -TiO2/CoCrPt-SiO2 stacked media

    Science.gov (United States)

    Park, S. H.; Lee, T. D.; Kong, S. H.; Yoon, S. Y.; Lee, H. S.; Kim, H. J.; Oh, H. S.

    2008-04-01

    Thermal stability of the present CoCrPt -SiO2 media becomes a more critical issue as recording density steadily increases. In the present study, thermal stability of the stacked media composed of high Ku CoPt -TiO2 and normal Ku CoCrPt -SiO2 was studied by changing stacking order and thickness of each layer while keeping a constant total thickness. When the CoPt -TiO2 layer was placed under the CoCrPt -SiO2 layer, negative nucleation field and coercivity increased much more than those of the reverse stacking case. Thermal stability of the CoPt -TiO2 bottom group was superior to that of the CoCrPt -SiO2 bottom group when measured by a spin stand.

  13. Design and fabrication of PIN-PMN-PT single-crystal high-frequency ultrasound transducers.

    Science.gov (United States)

    Sun, Ping; Zhou, Qifa; Zhu, Benpeng; Wu, Dawei; Hu, Changhong; Cannata, Jonathan M; Tian, Jin; Han, Pengdi; Wang, Gaofeng; Shung, K Kirk

    2009-12-01

    High-frequency PIN-PMN-PT single crystal ultrasound transducers at center frequencies of 35 MHz and 60 MHz were successfully fabricated using lead indium niobate-lead magnesium niobate-lead titanate (0.23PIN- 0.5PMN-0.27PT) single crystal. The new PIN-PMN-PT single crystal has higher coercivity (6.0 kV/cm) and higher Curie temperature (160 degrees C) than PMN-PT crystal. Experimental results showed that the PIN-PMN-PT transducers have similar performance but better thermal stability compared with the PMN-PT transducers.

  14. Functionalized graphene-Pt composites for fuel cells and photoelectrochemical cells

    Energy Technology Data Exchange (ETDEWEB)

    Diankov, Georgi; An, Jihwan; Park, Joonsuk; Goldhaber, David J. K.; Prinz, Friedrich B.

    2017-08-29

    A method of growing crystals on two-dimensional layered material is provided that includes reversibly hydrogenating a two-dimensional layered material, using a controlled radio-frequency hydrogen plasma, depositing Pt atoms on the reversibly hydrogenated two-dimensional layered material, using Atomic Layer Deposition (ALD), where the reversibly hydrogenated two-dimensional layered material promotes loss of methyl groups in an ALD Pt precursor, and forming Pt-O on the reversibly hydrogenated two-dimensional layered material, using combustion by O.sub.2, where the Pt-O is used for subsequent Pt half-cycles of the ALD process, where growth of Pt crystals occurs.

  15. Study of coordination environments around Pd and Pt in a Pd-core Pt-shell nanoparticle during heating

    Science.gov (United States)

    Nishimura, Y. F.; Hamaguchi, T.; Yamaguchi, S.; Takagi, H.; Dohmae, K.; Nonaka, T.; Nagai, Y.

    2016-05-01

    Local coordination environments around Pd and Pt in a Pd-core Pt-shell nanoparticle (NP) at temperatures ranging from 473 to 873 K was evaluated by utilizing in situ XAFS measurement technique to investigate the temperature range in which a core-shell structure is preserved. The core-shell structure was considered to be kept up to 673 K and start to change at about 773 K. Heating to 873 K accelerated atomic mixing in the core-shell NPs. Catalytic properties of the present Pd-core Pt-shell NP are available in the stoichiometric C3H6-O2 atmosphere at temperatures less than 773 K at most.

  16. 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)

  17. Direct observations of ferromagnetic and antiferromagnetic domains in Pt/Co/Cr2O3/Pt perpendicular exchange biased film

    Directory of Open Access Journals (Sweden)

    Yu Shiratsuchi

    2015-11-01

    Full Text Available By using focused soft X-rays, magnetic domain imaging based on X-ray magnetic circular dichroism (XMCD measurements was performed on a Pt/Co/Cr2O3/Pt film that exhibits both perpendicular magnetic anisotropy and perpendicular exchange anisotropy. In the AC-demagnetized state, spatial distributions of the XMCD corresponding to the magnetic domains were clearly observed. In particular, ferromagnetic and antiferromagnetic magnetic domains were separately observed by tuning the photon energy to either the ferromagnetic Co L3 edge or the antiferromagnetic Cr L3 edge. The ferromagnetic domain pattern is similar to the ones previously reported for Co/Pt multilayers, and the ferromagnetic and antiferromagnetic domains are spatially coupled. The magnetization curve measured after cooling the sample, while maintaining the demagnetized state, exhibited positive and negative exchange biases simultaneously, which suggests that the exchange bias is determined on a domain-by-domain basis.

  18. From Co/Pt multilayered nanowires to Co-Pt alloy nanowires: structural and magnetic evolutions with annealing temperatures

    Energy Technology Data Exchange (ETDEWEB)

    Liu Lifeng; Xie Sishen; Zhou Weiya, E-mail: liulif@mpi-halle.mpg.d [Beijing National Laboratory for Condensed Matter Physics and Institute of Physics, Chinese Academy of Sciences, Beijing 100190 (China)

    2009-10-21

    Co/Pt multilayered (ML) nanowires were prepared by template-assisted pulsed electrodeposition. Structural and magnetic evolutions of the deposited ML nanowires upon annealing in a hydrogen atmosphere were studied by transmission electron microscopy, x-ray diffractometry and magnetometry. It was found that the deposited nanowires undergo a morphological change from multilayers to continuous and dense alloy wires with increasing annealing temperature. The fraction and the grain size of the f.c.t. Co-Pt ordered phase were also found to increase with annealing temperature, giving rise to a markedly enhanced magnetic performance of the annealed nanowires. Our study provides an alternative approach, apart from direct template-based electrodeposition, to the fabrication of Co-Pt alloy nanowires with tunable structures and magnetic properties.

  19. High pressure infrared spectroscopy of Pt(II) complex cis-PtCl2(PEt3)2

    Science.gov (United States)

    Bajaj, Naini; Bhatt, Himal; Garg, Nandini; Deo, M. N.

    2017-05-01

    We report here the high pressure infrared spectroscopy of the Pt(II) complex cis- PtCl2(P(C2H5)3)2 up to 12 GPa. We have analyzed the various ligand related vibrational modes of the complex under pressure. It has been observed that the cis- isomer, which preserved its structure on lowering the temperature, shows change in the rate of variation in vibrational frequencies at 1 GPa. However, no new modes appeared upon compression, unlike in the trans isomer, up to the highest pressure. These observations indicate subtle pressure induced structural changes taking place in cis- PtCl2(P(C2H5)3)2. The highly complex C-H stretching spectral region has also been analyzed and the frequency variation of various modes has been described.

  20. Pt、Rh及Pt-Rh合金电极上氢的吸附%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 (wRh = 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 alloys.

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

    Science.gov (United States)

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

    2006-05-21

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

  2. Wet-chemical synthesis and properties of CoPt and CoPt3 alloy nanoparticles.

    Science.gov (United States)

    Frommen, Christoph; Rösner, Harald; Fenske, Dieter

    2002-10-01

    Surface-protected, air-stable nanoparticles of CoPt and CoPt3 were prepared by thermal decomposition/reduction of organometallic precursors with a long-chain aliphatic diol, also known as the polyol process. Particles 3 nm in diameter showed ferromagnetic behavior up to 350 K (Hc = 65 Oe at T = 300 K; Hc = 410 Oe at T = 5K) and underwent a disordering-ordering phase transformation after annealing that resulted in an increase in coercivity (Hc = 170 Oe at T = 300 K; Hc = 2000 Oe at T = 5 K).

  3. The origin of polarity dependent switching type in solution processed Pt/TiO2/Pt memory devices

    Science.gov (United States)

    Biju, K. P.

    2015-06-01

    Resistive switching characteristics of sol-gel processed TiO2 thin films are investigated. The influence of polarity of the forming voltage on switching type in Pt/TiO2/Pt stack is investigated. Reliability and stability of the device is significantly improved by choosing a proper voltage polarity on electroforming. The device shows excellent switching properties such as high on/off ratio (> 20), good cycling endurance and long retention (> 104 s) and possible to use multi bit storage has been demonstrated. The switching mechanism is explained by a physical model based on localized generation/recovery of oxygen vacancy defects.

  4. Synthesis of Pt, Pd, Pt/Ag and Pd/Ag nanoparticles by microwave-polyol method

    Indian Academy of Sciences (India)

    Kirti Patel; Sudhir Kapoor; Devilal Purshottam Dave; Tulsi Mukherjee

    2005-07-01

    Pt, Pd, Pt-Ag and Pd-Ag bimetallic nanoparticles were synthesized in ethylene glycol and glycerol using the microwave technique in the presence of a stabilizer poly(N-vinylpyrrolidone) (PVP). It has been observed that PVP is capable of complexing and stabilizing nanoparticles. Mixed clusters were formed by simultaneous reduction of the metal ions. The clusters were characterized using UV-Vis spectra, XRD and dynamic light scattering. To understand the mechanism of formation of mixed nanoparticles, several experimental parameters such as in situ irradiation of mixed metal salts and mixing of individual sols were attempted.

  5. 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.

  6. Ethanol Oxidation Reaction on Tandem Pt/Rh/SnOx Catalyst

    Directory of Open Access Journals (Sweden)

    Phuong Tu Mai

    2017-08-01

    Full Text Available To elucidate the atomic arrangement of a Pt-Rh-Sn ternary catalyst with a high catalytic activity for ethanol oxidation reaction (EOR and high CO2 selectivity, we prepared a tandem Pt/Rh/SnOx, in which a Rh adlayer was deposited on a Pt substrate (Rh coverage: 0.28, followed by depositing several layers of SnOx only on the Rh surface (Sn coverage: 0.07. For reference, Sn was randomly deposited on the Rh-modified Pt (Pt/Rh electrode whose Rh and Sn coverages were 0.22 and 0.36 (random Pt/Rh/SnOx. X-ray photoelectron spectroscopy demonstrated that Pt and Rh were metallic, and Sn was largely oxidized. Both Pt/Rh/SnOx electrodes were less positive in onset potential of EOR current density and higher in EOR current density than Pt and Rh/Pt electrodes. In situ infrared reflection-absorption spectroscopy demonstrated that the tandem Pt/Rh/SnOx electrode did not produce acetic acid, but produced CO2 in contrast to the random Pt/Rh/SnOx, suggesting that a tandem arrangement of Pt, Rh and SnOx, in which the Pt and SnOx sites were separated by the Rh sites, was effective for selective CO2 production. In the electrostatic electrolysis at 0.5 V vs. RHE, the tandem Pt/Rh/SnOx electrode exhibited higher EOR current density than the Pt and Pt/Rh electrodes after 1.5 h.

  7. Synergistically Enhanced Optical Limiting Property of Graphene Oxide Hybrid Materials Functionalized with Pt Complexes.

    Science.gov (United States)

    Liu, Rui; Hu, Jinyang; Zhu, Senqiang; Lu, Jiapeng; Zhu, Hongjun

    2017-09-12

    Recently, graphene-based materials have become well-known nonlinear optical materials for the potential application of laser protection. Two new graphene oxide-platinum  complex (GO-Pt) hybrid materials (GO-Pt-1, GO-Pt-2) have been fabricated through covalent modification and electrostatic adsorption of different Pt complexes with GO. The structural and photophysical properties of the resultant hybrid materials were studied. The nonlinear optical properties and optical power limiting (OPL) performance of Pt complexes, GO, and GO-Pt hybrid materials were investigated by using Z-scan measurements at 532 nm. At the same transmittance, the results illustrate that functionalization of GO makes GO-Pt hybrid materials possess better nonlinear optical properties and OPL performance than individual Pt complexes and GO due to a combination of nonlinear scattering, nonlinear absorption, and photoinduced electron and energy transfer between GO and Pt complex moieties. Furthermore, the nonlinear optics and OPL performance of GO-Pt-2 are better than those of GO-Pt-1, due to not only the excellent optical limiting of Pt-2 and more molecules per area of GO but also the way of combination of Pt-2 and GO.

  8. 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.

  9. Synthesis and Characterization of Pt-loaded carbon nanostructures derived from polyaniline nanotubes

    Energy Technology Data Exchange (ETDEWEB)

    Xu, Gong Da; Kim, Pil; Lee, Youn Sik [Div. of Chemical Engineering, Nanomaterials Processing Research Center, Chonbuk NationalUniversity, Jeonju (Korea, Republic of)

    2017-03-15

    Proton exchange membrane fuel cells (PEMFC) are one of the most advanced fuel cells for future energy, owing to their high conversion efficiency, quick start-up, rapid response to variable loading, and relatively low operating temperature, compared with of her conventional energy conversion devices. PANTs were synthesized to have various aspect ratios and inner diameters. As the aniline concentration increased, the PANTs’ inner diameter greatly decreased, but their outer diameters only slightly increased, leading to a decrease in their aspect ratios. Carbonization of PANTs resulted in the formation of corresponding CNSs. Pt nanoparticles were successfully formed on the CNSs under N{sub 2} or N{sub 2}/NH{sub 3} flow. The Pt nanoparticles of the Pt- CNS-N{sub 2} /NH{sub 3} catalysts were smaller in size, less aggregated, and more uniformly dispersed than those of the Pt- CNS-N{sub 2} catalysts. The ECSA values of Pt-CNS-N{sub 2} /NH{sub 3} were larger than those of Pt-CNS-N{sub 2} and Pt/C. The half wave potentials of the Pt-CNS-N{sub 2} catalysts were lower than those of the Pt-CNS-N{sub 2} /NH{sub 3} , and close to those of the Pt/C. The Pt-CNS-N{sub 2} /NH{sub 3} catalysts exhibited better kinetic performance than the Pt-CNS -N{sub 2} catalysts and Pt/C.

  10. X-ray irradiation induced reversible resistance change in Pt/TiO2/Pt cells.

    Science.gov (United States)

    Chang, Seo Hyoung; Kim, Jungho; Phatak, Charudatta; D'Aquila, Kenneth; Kim, Seong Keun; Kim, Jiyoon; Song, Seul Ji; Hwang, Cheol Seong; Eastman, Jeffrey A; Freeland, John W; Hong, Seungbum

    2014-02-25

    The interaction between X-rays and matter is an intriguing topic for both fundamental science and possible applications. In particular, synchrotron-based brilliant X-ray beams have been used as a powerful diagnostic tool to unveil nanoscale phenomena in functional materials. However, it has not been widely investigated how functional materials respond to the brilliant X-rays. Here, we report the X-ray-induced reversible resistance change in 40-nm-thick TiO2 films sandwiched by Pt top and bottom electrodes, and propose the physical mechanism behind the emergent phenomenon. Our findings indicate that there exists a photovoltaic-like effect, which modulates the resistance reversibly by a few orders of magnitude, depending on the intensity of impinging X-rays. We found that this effect, combined with the X-ray irradiation induced phase transition confirmed by transmission electron microscopy, triggers a nonvolatile reversible resistance change. Understanding X-ray-controlled reversible resistance changes can provide possibilities to control initial resistance states of functional materials, which could be useful for future information and energy storage devices.

  11. Transverse Spin Seebeck Effect on YIG/Pt

    Science.gov (United States)

    Prakash, Arati; Boona, Stephen; Jin, Hyungyu; Heremans, Joseph

    2015-03-01

    The existence of the longitudinal spin-Seebeck effect (LSSE) is well established and supported by theory. Much more controversial is the nature of the signals observed in the transverse spin-Seebeck (TSSE) geometry, where the heat current (x) is orthogonal to the direction of spin current propagation (y). TSSE has been described as simply non-local thermal spin-injection, but questions remain about the fact that the effect is observed at macroscopic length scales. To explore possible explanations for the observed TSSE signals, we report data from new TSSE measurements on the YIG/Pt system. The system studied has multiple Pt strips deposited in series upon bulk single crystals of YIG. We investigate the TSSE coefficient as a function of four variables: (1) sample temperature; (2) magnitude of the temperature gradient; (3) position of Pt strips along x; and (4) width of Pt strips along x. We consider nonlinear effects and the role of magnon density in the interpretation of our results. Work supported by the ARO- MURI Grant W911NF-14-1-0016 and NSF MRSEC program, Grant No. DMR 1420451.

  12. An Efficient Passerini Tetrazole Reaction (PT-3CR)

    NARCIS (Netherlands)

    Chandgude, Ajay L; Dömling, Alexander

    2016-01-01

    A sonication accelerated, catalyst free, simple, high yielding and efficient method for the Passerini-type three component reaction (PT-3CR) has been developed. It comprises reaction of an aldehyde/ketone, a isocyanide and a TMS-azide in methanol:water (1:1) as the solvent system. Use of sonication

  13. Lifetime measurements in shape transition nucleus {sup 188}Pt

    Energy Technology Data Exchange (ETDEWEB)

    Rohilla, Aman; Gupta, C.K.; Chamoli, S.K. [University of Delhi, Department of Physics and Astrophysics, New Delhi (India); Singh, R.P.; Muralithar, S. [Inter University Accelerator Centre, New Delhi (India); Chakraborty, S.; Sharma, H.P. [Banaras Hindu University, Department of Physics, Varanasi (India); Kumar, A.; Govil, I.M. [Panjab University, Department of Physics, Chandigarh (India); Biswas, D.C. [Bhabha Atomic Research Center, Nuclear Physics Division, Trombay, Mumbai (India)

    2017-04-15

    Nuclear level lifetimes of high spin states in yrast and non-yrast bands of {sup 188}Pt nucleus have been measured using recoil distance plunger setup present at IUAC, Delhi. In the experiment nuclear states of interest were populated via {sup 174}Yb({sup 18}O,4n){sup 188}Pt reaction at a beam energy of 79MeV provided by 15 UD Pelletron accelerator. The extracted B(E2 ↓) values show an initial rise up to 4{sup +} state and then a nearly constant behavior with spin along yrast band, indicating change of nuclear structure in {sup 188}Pt at low spins. The good agreement between experimental and TPSM model B(E2 ↓) values up to 4{sup +} state suggests an increase in axial deformation of the nucleus. The average absolute β{sub 2} = 0.20 (3) obtained from measured B(E2 ↓) values matches well the values predicted by CHFB and IBM calculations for oblate (β{sub 2} ∝ -0.19) and prolate (β{sub 2} ∝ 0.22) shapes. As the lifetime measurements do not yield the sign of β{sub 2}, no definite conclusion can be drawn on the prolate or oblate collectivity of {sup 188}Pt on the basis of present measurements. (orig.)

  14. Self-suspended permanent magnetic FePt ferrofluids

    KAUST Repository

    Dallas, Panagiotis

    2013-10-01

    We present the synthesis and characterization of a new class of self-suspended ferrofluids that exhibit remanent magnetization at room temperature. Our system relies on the chemisorption of a thiol-terminated ionic liquid with very low melting point on the surface of L10 FePt nanoparticles. In contrast, all types of ferrofluids previously reported employ either volatile solvents as the suspending media or superparamagnetic iron oxide nanoparticles (that lacks permanent magnetization) as the inorganic component. The ferrofluids do not show any sign of flocculation or phase separation, despite the strong interactions between the magnetic nanoparticles due to the strong chemisorption of the ionic liquid as evidenced by Raman spectroscopy and thermal analysis. Composites with high FePt loading (40 and 70. wt%) exhibit a pseudo solid-like rheological behavior and high remanent magnetization values (10.1 and 12.8. emu/g respectively). At lower FePt loading (12. wt%) a liquid like behavior is observed and the remanent and saturation magnetization values are 3.5 and 6.2. emu/g, respectively. The magnetic and flow properties of the materials can be easily fine tuned by controlling the type and amount of FePt nanoparticles used. © 2013 Elsevier Inc.

  15. Adsorption, mobility, and dimerization of benzaldehyde on Pt(111)

    DEFF Research Database (Denmark)

    Rasmussen, Anton Michael Havelund; Hammer, Bjørk

    2012-01-01

    Building on results for the adsorption of benzene on Pt(111), the adsorption of benzaldehyde is investigated using density functional theory. Benzaldehyde is found to chemisorb preferentially with its aromatic ring in the flat-lying bridge geometry that is also preferred for benzene. Across the i...

  16. Study of the Pt/Ru(0001) Interface

    DEFF Research Database (Denmark)

    Godowski, Jan P; Li, Zhe Shen; Bork, Jakob

    2007-01-01

    The growth process of platinum on Ru(0001) near room temperature was characterized using photoelectron spectroscopy of high resolution. The binding energy position and intensity of the Pt 4f7/2 and Ru 3d5/2 core levels as well as the shape and structure of the valence band spectra corresponding t...

  17. Growth and Characterization on PMN-PT-Based Single Crystals

    Directory of Open Access Journals (Sweden)

    Jian Tian

    2014-07-01

    Full Text Available Lead magnesium niobate—lead titanate (PMN-PT single crystals have been successfully commercialized in medical ultrasound imaging. The superior properties of PMN-PT crystals over the legacy piezoelectric ceramics lead zirconate titanate (PZT enabled ultrasound transducers with enhanced imaging (broad bandwidth and improved sensitivity. To obtain high quality and relatively low cost single crystals for commercial production, PMN-PT single crystals were grown with modified Bridgman method, by which crystals were grown directly from stoichiometric melt without flux. For ultrasound imaging application, [001] crystal growth is essential to provide uniform composition and property within a crystal plate, which is critical for transducer performance. In addition, improvement in crystal growth technique is under development with the goals of improving the composition homogeneity along crystal growth direction and reducing unit cost of crystals. In recent years, PIN-PMN-PT single crystals have been developed with higher de-poling temperature and coercive field to provide improved thermal and electrical stability for transducer application.

  18. Nonlinearity-induced PT-symmetry without material gain

    Science.gov (United States)

    Miri, Mohammad-Ali; Alù, Andrea

    2016-06-01

    Parity-time symmetry has raised a great deal of attention in optics in recent years, yet its application has been so far hindered by the stringent requirements on coherent gain balanced with loss. In this paper, we show that the conditions to enable parity and time symmetry can be simultaneously satisfied for a pair of modes with mixed frequencies interacting in a nonlinear medium, without requiring the presence of material gain. First, we consider a guided wave structure with second order nonlinearity and we derive the PT-symmetric Hamiltonian that governs the interaction of two waves of mixed frequencies when accompanied by a high intensity pump beam at the sum frequency. We also extend the results to an array of coupled nonlinear waveguide channels. It is shown that the evolution dynamics of the low-frequency waves is associated with a periodic PT-symmetric lattice while the phase of the pump beams can be utilized as a control parameter to modify the gain and loss distribution, thus realizing different PT lattices by design. Our results suggest that nonlinear wave mixing processes can form a rich platform to realize PT-symmetric Hamiltonians of arbitrary dimensions in optical systems, without requiring material gain.

  19. Prosedur Check In Pada Perusahaan Penerbangan Internasional PT. Malaysia Airlines

    OpenAIRE

    Siregar, Siti Kholilah

    2015-01-01

    Pariwisata adalah kegiatan dinamis yang melibatkan banyak manusia serta menghidupkan berbagai bidang usaha. Transportasi memiliki posisi yang penting dan strategis dalam pembangunan bangsa untuk mencapai tujuan pembangunan nasional. Transportasi udara merupakan moda transportasi yang paling inovatif dibandingkan dengan moda transportasi lain. Jenis transportasi ini membuat waktu tempuh menjadi singkat dan permintaan perjalanan dengan menggunakan transportasi melonjak secara tajam. PT. Malaysi...

  20. Selective laser extraction of the Pt group metals

    Energy Technology Data Exchange (ETDEWEB)

    Fadeeva, S.; Krynetsky, B.; Prokhorov, A.; Zhidkov, A. [General Physics Institute, Russian Academy of Science, Moscow (Russian Federation)

    1995-11-15

    The interest to the platinum-group metals extraction from solutions, especially industry waste, is stimulated by their extraordinary chemical inert. The traditional chemical methods of the extraction are uneffective. Have been investigated process of the extraction of metal Pt-group from acid solutions. Discussed processes reduction of noble metals by resonance laser action.

  1. Bloch oscillations in complex crystals with PT symmetry.

    Science.gov (United States)

    Longhi, S

    2009-09-18

    Bloch oscillations in complex lattices with PT symmetry are theoretically investigated with specific reference to optical Bloch oscillations in photonic lattices with gain or loss regions. Novel dynamical phenomena with no counterpart in ordinary lattices, such as nonreciprocal Bloch oscillations related to violation of the Friedel's law of Bragg scattering in complex potentials, are highlighted.

  2. Ultralow Pt-loading bimetallic nanoflowers: fabrication and sensing applications

    Science.gov (United States)

    Wu, Qingqing; Li, Yongxin; Xian, Hongying; Xu, Chaodi; Wang, Lun; Chen, Zhibing

    2013-01-01

    Ultralow Pt-loading Au nanoflowers (AuNFs) were synthesized on a glassy carbon electrode surface by the underpotential deposition (UPD) monolayer redox replacement technique, which involves redox replacement of a copper UPD monolayer by PtCl42- that can be reduced and deposited simultaneously. Field-emission scanning electron microscopy, energy dispersive spectroscopy, x-ray photoelectron spectroscopy and the electrochemical method were utilized to characterize the ultralow Pt-loading AuNFs. Cyclic voltammogram results showed that the ultralow Pt-loading AuNFs exhibited excellent electrocatalytic activity towards the reduction of hydrogen peroxide and the oxidation of glucose in neutral media, and the reaction pathway of glucose oxidation was changed from an intermediate process based on the electrosorption of glucose to a direct oxidation process. From chronoamperometric results, it could be obtained that this prepared biosensor had wide linear ranges and very low detection limits (DLs) for H2O2 (0.025-94.3 μM DL = 0.006 μM) and glucose (0.0028-8.0 mM DL = 0.8 μM), which were much better than previous results.

  3. 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.

  4. Scattering off PT-symmetric upside-down potentials

    CERN Document Server

    Bender, Carl M

    2016-01-01

    The upside-down $-x^4$, $-x^6$, and $-x^8$ potentials with appropriate PT-symmetric boundary conditions have real, positive, and discrete quantum-mechanical spectra. This paper proposes a straightforward macroscopic quantum-mechanical scattering experiment in which one can observe and measure these bound-state energies directly.

  5. PT-Symmetric Nonlinear Metamaterials and Zero-Dimensional Systems

    CERN Document Server

    Tsironis, G P

    2013-01-01

    A one dimensional, parity-time (${\\cal PT}$)-symmetric magnetic metamaterial comprising split-ring resonators having both gain and loss is investigated. In the linear regime, the transition from the exact to the broken ${\\cal PT}$-phase is determined through the calculation of the eigenfrequency spectrum for two different configurations; the one with equidistant split-rings and the other with the split-rings forming a binary pattern (${\\cal PT}$ dimer chain). The latter system features a two-band, gapped spectrum with its shape determined by the gain/loss coefficient as well as the inter-element coupling. In the presense of nonlinearity, the ${\\cal PT}$ dimer chain with balanced gain and loss supports nonlinear localized modes in the form of novel discrete breathers below the lower branch of the linear spectrum. These breathers, that can be excited from a weak applied magnetic field by frequency chirping, can be subsequently driven solely by the gain for very long times. The effect of a small imbalance betwee...

  6. Sistem Informasi Akuntansi Penjualan Tunai PT. Madjin Crumb Rubber Factory

    OpenAIRE

    Dian Permata Sayang

    2009-01-01

    PT. Madjin Crumb Rubber Factory adalah perusahaan yang bergerak dalam bidang export karet menjadi SIR-20. Dalam penelitian ini penulis menggunakan metode deskriptif. Jenis data yang digunakan adalah data primer dan data sekunder. Adapun teknik pengumpulan data yang digunakan adalah wawancara dan observasi. Metode penganalisaan data adalah metode deskriptif, dimana data dikumpulkan, disusun, diikhtisarkan, dianalisis, dan interpretasikan sehingga menghasilkan keterangan dan jawaban yang jelas ...

  7. Reversal mechanism of submicron patterned CoNi/Pt multilayers

    NARCIS (Netherlands)

    Haast, M.A.M.; Schuurhuis, J.R.; Abelmann, L.; Lodder, J.C.; Popma, Th.J.A.

    1998-01-01

    With laser interference lithography Co50Ni50/Pt multilayers with perpendicular magnetic anisotropy have been patterned into regular matrices of submicron sized dots. Their magnetic properties have been studied with Vibrating Sample Magnetometry. Compared to continuous multilayers (Hc=15 kA/m) the co

  8. On Pták functions for bounded operators

    Directory of Open Access Journals (Sweden)

    Abdellah El Kinani

    2014-10-01

    Full Text Available The purpose of this paper is to prove that if the Pták function p is an operator norm, on \\mathcal{B}(E, associated to a norm | . |, then (E, | . | is a pseudo-Hilbert space. As a consequence, we obtain that if \\mathcal{B}(E  is a C*-algebra, then E is a Hilbert space.

  9. A comparative study of CO adsorption on tetrahexahedral Pt nanocrystals and interrelated Pt single crystal electrodes by using cyclic voltammetry and in situ FTIR spectroscopy.

    Science.gov (United States)

    Liu, Hai-Xia; Tian, Na; Ye, Jin-Yu; Lu, Bang-An; Ren, Jie; Huangfu, Zhi-Chao; Zhou, Zhi-You; Sun, Shi-Gang

    2014-01-01

    This study focuses on CO adsorption at tetrahexahedral Pt nanocrystals (THH Pt NCs) by using cyclic voltammetry and in situ FTIR spectroscopy. Since the electrochemically prepared THH Pt NCs in this study are enclosed by {730} facets which could be considered by a subfacet configuration of 2{210} + {310}, we have also studied CO adsorption on the interrelated Pt(310) and Pt(210) single crystal electrodes as a comparison. Cyclic voltammetry results demonstrated that CO adsorbs dominantly on the (100) sites of THH Pt NCs at low CO coverage (θ(CO)≤ 0.135), while on both (100) and (110) sites at higher CO coverage. On ordered Pt(310) and Pt(210), i.e. they were flame annealed and then cooled in H(2) + Ar, CO adsorption also illustrates relative priority on (100) sites at low CO coverage; while at high CO coverage or on oxygen-disordered Pt(310) and Pt(210) when they were cooled in air after flame annealing, the adsorption of CO presents a weak preference on (100) sites of Pt(310) and even no preference at all on (100) sites of Pt(210). In situ FTIR spectroscopic studies illustrated that CO adsorption on THH Pt NCs yields anomalous infrared effects (AIREs), which are depicted by the Fano-like IR feature on a dense distribution (60 μm(-2)) and the enhancement of abnormal IR absorption on a sparse distribution (22 μm(-2)) of THH Pt NCs on glassy carbon substrate. Systematic investigation of CO coverage dependence of IR features revealed that, on THH Pt NCs, the IR band center (ν(COL)) of linearly bonded CO (COL) is rapidly shifted to higher wavenumbers along with the increase of CO coverage to 0.184, yielding a fast linear increase rate with a high slope (dν(COL)/dθ(IR)(CO) = 219 cm(-1)); when θ > 0.184, the increase of ν(COL) with θCO slows down and deviates drastically from linearity. In contrast, the ν(COL) on the ordered Pt(310) electrode maintains a linear increase with θ(IR)(CO) for the whole range of θ(IR)(CO) variation, and gives a much smaller

  10. The molecular, electronic, bonding, and photophysical features of the [(c-Pt3)Tl(c-Pt3)]+ inorganic metallocenes.

    Science.gov (United States)

    Tsipis, Athanassios C; Gkekas, George N

    2013-06-21

    The molecular, electronic, bonding and photophysical properties of a series of inorganic metallocenes with the general formula {[Pt3(μ2-L)3(L')3]2(μ6-Tl)}(+) (L = CO, CH3CN, PH2, C6F5, or SO2 and L' = CO, PH3, CH3CN, C6F5) have been studied by means of DFT electronic structure calculations. The estimated Tl-cd distances between Tl(+) cations and the centroids (cd) of the trimetallic Pt3(μ2-L)3(L')3 {3 : 3 : 3} decks were found in the range 2.932-3.397 Å. The predicted bond dissociation energy, D0, of the (c-Pt3)···Tl(+) bonds was found to lie within the range -31.5 up to -77.5 kcal mol(-1) at the B3LYP/LANL2TZ(f)(Pt) ∪ 6-31G(d,p)(E) ∪ SRLC(Tl) level of theory. Most of the [(c-Pt3)Tl(c-Pt3)](+) inorganic metallocenes adopt a bend titanocene-like structure. The Localized Orbital Locator (LOL) contour maps along with the 3D contour plots of the Reduced Gradient Density (RDG) mirror the composite nature of the interaction of Tl(+) with the triangular Pt3 metallic ring cores consisting of electrostatic, covalent and dispersion interaction components. The Pt3···Tl(+)···Pt3 bonding mode was further validated by Energy Decomposition Analysis (EDA) calculations which demonstrated that the electrostatic and covalent components of the interaction contribute almost equally to the bonding interactions. Furthermore, Charge Decomposition Analysis (CDA) and Natural Bond Orbital Analysis (NBO) calculations indicated that charge transfer from the Tl(+) cation to the Pt3(0) {3 : 3 : 3} decks also occurs. The {[Pt3(μ2-L)3(L')3]2(μ6-Tl)}(+) sandwiches absorb in the UV-Vis region (300-500 nm) and emit in the visible-near IR region (600-1000 nm). The absorption bands are mainly of MLCT/MC character while phosphorescence is predicted to occur via the first triplet excited state, T1, since the spin density of this excited state could be described as a SOMO - 1/SOMO combination. Generally, no significant distortions occur upon excitation of these systems

  11. B3LYP study of water adsorption on cluster models of Pt(1 1 1), Pt(1 0 0) and Pt(1 1 0): Effect of applied electric field

    Energy Technology Data Exchange (ETDEWEB)

    Blanco, Raquel; Orts, Jose Manuel [Departamento de Quimica Fisica e Instituto Universitario de Electroquimica, Universidad de Alicante, Apartado 99, E-03080 Alicante (Spain)

    2008-11-01

    A density functional theory (DFT) study of the adsorption of a water molecule on Pt(1 1 1), Pt(1 0 0) and Pt(1 1 0) surfaces has been carried out using cluster models, at the B3LYP/LANL2DZ,6-311++G(d,p) level. The water molecule binds preferentially at the top site on Pt(1 1 1) and Pt(1 0 0) with adsorption energy around -27 kJ mol{sup -1}, and is oriented with the molecular plane nearly parallel to the metal surface and the H atoms pointing away from it. On Pt(1 1 0) a hollow site is preferred, with adsorption energy of -32 kJ mol{sup -1}. Potential energy barriers for the rotation around an axis normal to the surface have been estimated to be below 1 kJ mol{sup -1} for Pt(1 1 1) and Pt(1 0 0) when water is adsorbed on top. Upon application of an external electric field (inducing positive charge density on the metal) adsorbed water is additionally stabilized on the three surfaces, especially at the top adsorption site, and adsorption on Pt(1 1 1) and Pt(1 0 0) becomes more favoured than on Pt(1 1 0). Good agreement has been found between harmonic vibrational frequencies calculated at the B3LYP/LANL2DZ,6-311++G(d,p) level and experimental frequencies for adsorbed water monomers on Pt(h k l) surfaces. (author)

  12. Konstruksi Berita Pengerusakan Lingkungan Kawasan Danau Toba Oleh Perusahaan Di Media Cetak (Analisis Framing Berita Pengerusakan Lingkungan Kawasan Danau Toba Oleh PT Gorga Duma Sari, PT Aqua Farm dan PT Allegrindo Nusantara di Harian Sinar Indonesia Baru).

    OpenAIRE

    Sinambela, Debora Blandina

    2015-01-01

    This research aim to know how the group, cultural claim, also media activities that Sinar Indonesia Baru Newspaper use to construct destroyed Toba Lake enviroment news by PT Gorga Duma Sari, PT Aqua Farm, and PT Allegrindo Nusantara. Subject of this research are collections of published news SIB newspaper related to destroyed activities since 2012 until 2013. Then news analysis will be done using Gamson and Mondigliani as analysis knife. Gamson see the media discourse (especially news) arr...

  13. Electrochemical Oxidation of the Carbon Support to Synthesize Pt(Cu and Pt-Ru(Cu Core-Shell Electrocatalysts for Low-Temperature Fuel Cells

    Directory of Open Access Journals (Sweden)

    Griselda Caballero-Manrique

    2015-04-01

    Full Text Available The synthesis of core-shell Pt(Cu and Pt-Ru(Cu electrocatalysts allows for a reduction in the amount of precious metal and, as was previously shown, a better CO oxidation performance can be achieved when compared to the nanoparticulated Pt and Pt-Ru ones. In this paper, the carbon black used as the support was previously submitted to electrochemical oxidation and characterized by XPS. The new catalysts thus prepared were characterized by HRTEM, FFT, EDX, and electrochemical techniques. Cu nanoparticles were generated by electrodeposition and were further transformed into Pt(Cu and Pt-Ru(Cu core-shell nanoparticles by successive galvanic exchange with Pt and spontaneous deposition of Ru species, the smallest ones being 3.3 nm in mean size. The onset potential for CO oxidation was as good as that obtained for the untreated carbon, with CO stripping peak potentials about 0.1 and 0.2 V more negative than those corresponding to Pt/C and Ru-decorated Pt/C, respectively. Carbon oxidation yielded an additional improvement in the catalyst performance, because the ECSA values for hydrogen adsorption/desorption were much higher than those obtained for the non-oxidized carbon. This suggested a higher accessibility of the Pt sites in spite of having the same nanoparticle structure and mean size.

  14. Characterization of Phosphate Transporters BdPT4 and BdPT8 in Mycorrhizal and Non-Mychorrhizal Brachypodium distachyon

    DEFF Research Database (Denmark)

    Clausen, Signe Sandbech

    was observed in non-arbusculated cells of AM plants. In arbusculated cells, BdPT8 was detected in the ER while BdPT4 was localized to the plasma membrane and the periarbuscular membrane (PAM) surrounding the arbuscular trunk and thick branches, which further supported a role of both BdPTs in direct Pi uptake......PT proteins were expressed in cells where direct PTs are believed to perform their function, as well as in the vascular tissue. In NM plants, BdPT4 was localized to the plasma membrane whereas BdPT8 accumulated in the endoplasmic reticulum (ER) in the secretory pathway. A similar expression pattern......, and for BdPT4 in AM-mediated Pi uptake as well. In conclusion, the studies suggest that BdPT4 and possibly also BdPT8 are involved in direct uptake as well as in translocation of Pi in B. distachyon. Interestingly, as BdPT4 was additionally localised to the PAM of arbusculated cells, BdPT4 may also...

  15. Structure of Pt/C and PtRu/C catalytic layers prepared by plasma sputtering and electric performance in direct methanol fuel cells (DMFC)

    Energy Technology Data Exchange (ETDEWEB)

    Caillard, A.; Brault, P.; Mathias, J. [Groupe de Recherche sur l' Energetique des Milieux Ionises, UMR6606 Universite d' Orleans, CNRS, Polytech' Orleans BP6744, F-45067 Orleans Cedex 2 (France); Coutanceau, C.; Leger, J.-M. [Laboratoire de Catalyse en Chimie Organique, UMR6503 Universite de Poitiers, CNRS, F-86022 Poitiers (France)

    2006-11-08

    Plasma sputtering process was used to deposit Pt and PtRu on conductive carbon diffusion layer. Low metal loading catalysts for methanol electrooxidation were prepared and characterized by TEM and XRD. The main result is that codeposition of Pt and Ru leads to alloy phase, whereas multi-layers deposition leads to no-alloyed structure. The electrochemical performance of sputtered Pt/C electrodes was compared with that of standard electrodes, and was found lower. However, the specific activity was much higher, indicating that the catalyst utilization efficiency was higher than that obtained with a standard electrode. Then, different bimetallic PtRu/C electrodes were prepared by plasma sputtering, leading to different catalyst structures (Pt and Ru multilayer deposition or simultaneous deposition of Pt and Ru) and composition (from 100:0 to 50:50 Pt/Ru atomic ratios). At last, the different PtRu electrodes were compared in term of DMFC electrical performance. The best efficiency of the DMFC was reached when both metals Pt and Ru are simultaneously deposited (alloyed) with a ruthenium atomic ratio of 30% or 40 % Ru depending of the working potentials of the cell. (author)

  16. Development of a ReaxFF potential for Pt-O systems describing the energetics and dynamics of Pt-oxide formation.

    Science.gov (United States)

    Fantauzzi, Donato; Bandlow, Jochen; Sabo, Lehel; Mueller, Jonathan E; van Duin, Adri C T; Jacob, Timo

    2014-11-14

    ReaxFF force field parameters describing Pt-Pt and Pt-O interactions have been developed and tested. The Pt-Pt parameters are shown to accurately account for the chemical nature, atomic structures and other materials properties of bulk platinum phases, low and high-index platinum surfaces and nanoclusters. The Pt-O parameters reliably describe bulk platinum oxides, as well as oxygen adsorption and oxide formation on Pt(111) terraces and the {111} and {100} steps connecting them. Good agreement between the force field and both density functional theory (DFT) calculations and experimental observations is demonstrated in the relative surface free energies of high symmetry Pt-O surface phases as a function of the oxygen chemical potential, making ReaxFF an ideal tool for more detailed investigations of more complex Pt-O surface structures. Validation for its application to studies of the kinetics and dynamics of surface oxide formation in the context of either molecular dynamics (MD) or Monte Carlo simulations are provided in part by a two-part investigation of oxygen diffusion on Pt(111), in which nudged elastic band (NEB) calculations and MD simulations are used to characterize diffusion processes and to determine the relevant diffusion coefficients and barriers. Finally, the power of the ReaxFF reactive force field approach in addressing surface structures well beyond the reach of routine DFT calculations is exhibited in a brief proof-of-concept study of oxygen adsorbate displacement within ordered overlayers.

  17. Screening of electrocatalysts for direct ammonia fuel cell: Ammonia oxidation on PtMe (Me: Ir, Rh, Pd, Ru) and preferentially oriented Pt(1 0 0) nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Vidal-Iglesias, F.J.; Solla-Gullon, J.; Montiel, V.; Feliu, J.M.; Aldaz, A. [Instituto de Electroquimica, Universidad de Alicante, Apartado 99, 03080 Alicante (Spain)

    2007-09-27

    Ammonia has attracted attention as a possible fuel for direct fuel cells since it is easy to handle and to transport as liquid or as concentrated aqueous solution. However, on noble metal electrodes ammonia oxidation is a sluggish reaction and the electrocatalyst needs to be improved for developing efficient ammonia fuel cells. In this work, ammonia electrooxidation reaction on 3-4-nm bimetallic PtMe (Ir, Rh, Pd, Ru) and on preferentially oriented Pt(1 0 0) nanoparticles is reported. PtMe nanoparticles have been prepared by using water-in-oil microemulsions to obtain a narrow size distribution whereas preferentially oriented Pt nanoparticles have been prepared through colloidal routes. Among all the bimetallic samples tested, only Pt{sub 75}Ir{sub 25} and Pt{sub 75}Rh{sub 25} nanoparticles show, at the low potential range, an enhancement of the oxidation density current with respect to the behaviour found for pure platinum nanoparticles prepared by the same method. In addition, two Pt(1 0 0) preferentially oriented nanoparticles of different particle size (4 and 9 nm) have been also studied. These oriented nanoparticles show higher current densities than polycrystalline Pt nanoparticles due to the sensitivity of ammonia oxidation toward the presence of surface sites with square symmetry. The reactivity of the different 4-nm nanoparticles parallels well with that expected from bulk PtMe alloys and Pt single crystal electrodes. (author)

  18. Observation of inverse spin Hall effect in ferromagnetic FePt alloys using spin Seebeck effect

    Energy Technology Data Exchange (ETDEWEB)

    Seki, Takeshi, E-mail: go-sai@imr.tohoku.ac.jp; Takanashi, Koki [Institute for Materials Research, Tohoku University, Sendai 980-8577 (Japan); Uchida, Ken-ichi [Institute for Materials Research, Tohoku University, Sendai 980-8577 (Japan); PRESTO, Japan Science and Technology Agency, Saitama 332-0012 (Japan); Kikkawa, Takashi [Institute for Materials Research, Tohoku University, Sendai 980-8577 (Japan); WPI Advanced Institute for Materials Research, Tohoku University, Sendai 980-8577 (Japan); Qiu, Zhiyong [WPI Advanced Institute for Materials Research, Tohoku University, Sendai 980-8577 (Japan); Spin Quantum Rectification Project, ERATO, Japan Science and Technology Agency, Sendai 980-8577 (Japan); Saitoh, Eiji [Institute for Materials Research, Tohoku University, Sendai 980-8577 (Japan); WPI Advanced Institute for Materials Research, Tohoku University, Sendai 980-8577 (Japan); Spin Quantum Rectification Project, ERATO, Japan Science and Technology Agency, Sendai 980-8577 (Japan); Advanced Science Research Center, Japan Atomic Energy Agency, Tokai 319-1195 (Japan)

    2015-08-31

    We experimentally observed the inverse spin Hall effect (ISHE) of ferromagnetic FePt alloys. Spin Seebeck effect due to the temperature gradient generated the spin current (J{sub s}) in the FePt|Y{sub 3}Fe{sub 5}O{sub 12} (YIG) structure, and J{sub s} was injected from YIG to FePt and converted to the charge current through ISHE of FePt. The significant difference in magnetization switching fields for FePt and YIG led to the clear separation of the voltage of ISHE from that of anomalous Nernst effect in FePt. We also investigated the effect of ordering of FePt crystal structure on the magnitude of ISHE voltage in FePt.

  19. Observation of inverse spin Hall effect in ferromagnetic FePt alloys using spin Seebeck effect

    Science.gov (United States)

    Seki, Takeshi; Uchida, Ken-ichi; Kikkawa, Takashi; Qiu, Zhiyong; Saitoh, Eiji; Takanashi, Koki

    2015-08-01

    We experimentally observed the inverse spin Hall effect (ISHE) of ferromagnetic FePt alloys. Spin Seebeck effect due to the temperature gradient generated the spin current (Js) in the FePt|Y3Fe5O12 (YIG) structure, and Js was injected from YIG to FePt and converted to the charge current through ISHE of FePt. The significant difference in magnetization switching fields for FePt and YIG led to the clear separation of the voltage of ISHE from that of anomalous Nernst effect in FePt. We also investigated the effect of ordering of FePt crystal structure on the magnitude of ISHE voltage in FePt.

  20. Influence of bi modification of pt anode catalyst in direct formic acid fuel cells.

    Science.gov (United States)

    Kang, Sungjin; Lee, Jaeyoung; Lee, Jae Kwang; Chung, Seung-Young; Tak, Yongsug

    2006-04-13

    The influence of Bi modification of Pt anode catalyst on the performance of direct formic acid fuel cells was investigated. Compared with the unmodified Pt anode, the Bi modified Pt (PtBi(m)) electrode prepared by under-potential deposition (UPD) caused faster electrocatalytic oxidation of formic acid at the same value of the overpotential, and thus, PtBi(m) resulted in an increase in the power performance of direct formic acid fuel cells. Electrochemical impedance spectra helped to explain the difference of performance between the unmodified Pt and Bi modified Pt electrodes. Solution conductivity and dehydration phenomena occurring in highly concentrated formic acid solutions can also explain the higher power performance of PtBi(m).

  1. 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.

  2. 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 %.

  3. Influence of Pt atoms on the low temperature formation of epitaxial Pd monosilicide

    Science.gov (United States)

    Kawarada, H.; Mizugaki, K.; Ohdomari, I.

    1985-01-01

    The effect of Pt concentration in Pd thin films on the nucleation and growth of PdSi and PdxPt1-xSi (ternary monosilicide) has been investigated by transmission electron microscopy (TEM). Low concentration of Pt (10 at. %) in Pd film enhances PdSi formation at lower temperature than previously reported. It has been proposed that PdSi formation is governed by its slow nucleation. However, in our studies, the nucleation of PtSi, which is substituted for that of PdSi, triggers the subsequent PdSi growth at low temperatures. High concentration of Pt (55 at. %) in Pd-Pt alloy film lowers the temperature of the phase transformation from metal-rich silicide to monosilicide (PdxPt1-xSi). The temperature is the same as that of PtSi formation. In both cases, the monosilicide layers (about 20 nm) have an epitaxial relationship with (111) Si substrates.

  4. TINJAUAN HUKUM ISLAM TERHADAP PEMBIAYAAN HAJI DAN UMRAH MELALUI SISTEM MARKETING DI PT. ARMINAREKA PERDANA YOGYAKARTA

    National Research Council Canada - National Science Library

    Indah Fitriana Sari

    2015-01-01

    ... untuk bergabung dan mendaftarkan diri dengan menjadi jamaah haji dan umroh di PT.Arminareka Perdana. Program solusi yang ditawarkan PT Arminareka Perdana terdapat penilaian dari sebagian masyarakat sebagai bisnis Multi level marketing...

  5. The system Fe-Pt-S at 1100°C

    DEFF Research Database (Denmark)

    Makovicky, Milota; Makovicky, Emil; Rose-Hansen, John

    2002-01-01

    geology, system Fe-Pt-S, iron-platinum alloys, isoferroplatinum, monosulfide solid-solution, cooperite......geology, system Fe-Pt-S, iron-platinum alloys, isoferroplatinum, monosulfide solid-solution, cooperite...

  6. Silicon Nanowires with MoSx and Pt as Electrocatalysts for Hydrogen Evolution Reaction

    Directory of Open Access Journals (Sweden)

    S. H. Hsieh

    2016-01-01

    Full Text Available A convenient method was used for synthesizing Pt-nanoparticle/MoSx/silicon nanowires nanocomposites. Obtained Pt-MoSx/silicon nanowires electrocatalysts were characterized by transmission electron microscopy (TEM. The hydrogen evolution reaction efficiency of the Pt-MoSx/silicon nanowire nanocomposite catalysts was assessed by examining polarization and electrolysis measurements under solar light irradiations. The electrochemical characterizations demonstrate that Pt-MoSx/silicon nanowire electrodes exhibited an excellent catalytic activity for hydrogen evolution reaction in an acidic electrolyte. The hydrogen production capability of Pt-MoSx/silicon nanowires is also comparable to MoSx/silicon nanowires and Pt/silicon nanowires. Electrochemical impedance spectroscopy experiments suggest that the enhanced performance of Pt-MoSx/silicon nanowires can be attributed to the fast electron transfer between Pt-MoSx/silicon nanowire electrodes and electrolyte interfaces.

  7. Direct ethanol fuel cell, CO and ethanol oxidation on core-shell C/Ni-Au-[Pt and (Pt- Ir)] catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Rodrigues, C.A.D.; Tremiliosi-Filho, G. [Universidade de Sao Paulo (IQSC/USP), Sao Carlos, SP (Brazil). Inst. de Quimica], Email: cesaraug@sc.usp.br; Kokoh, K.B.; Coutanceau, C.; Baranton, S. [Universite de Poitiers (France). Lab. de Catalyse en Chimie Organique (LACCO). Equipe Electrocatalyse

    2010-07-01

    In this paper presents to study of the Pt and Pt-Ir monolayer that were deposited on core-shell Ni-Au nanoparticles supported on carbon. Catalysts with the following molar ratios were prepared: Pt and Pt{sub 65}Ir{sub 35}, Pt{sub 75}Ir{sub 2}5, Pt{sub 80}Ir{sub 20} and Pt{sub 85}Ir{sub 15}. The means particle sizes were in the range of 2 - 6 nm for all catalysts. The electrochemical properties examined in the ethanol and CO oxidation by cyclic voltammetry, and In situ IR spectroscopy measurements (SPAIRS) enabled to determine intermediates and reaction products as a function of the metallic compositions of catalysts. All of the catalysts were tested as anodes of a single direct ethanol fuel cell (DEFC) tests in 1.0 M ethanol solution. As a result, higher power densities were obtained with the core-shell particles in comparison to those issued from the commercial catalyst (Pt-ETEK). Thus, the maximum power densities at 90 deg C for the different systems are: (i) commercial C/Pt catalyst (E-TEK): ca. 0.010 W cm{sup -2}, C/Ni-Au-(Pt{sub 85}Ir{sub 15}): ca. 0.013 W cm{sup -2} and C/Ni-Au-Pt: ca. 0.018 W cm{sup -2} (all core-shell systems were normalization by Pt load). As a result, the performance of the core-shell nanoparticles is much better than that produced for the commercial catalyst and the C/Ni-Au-Pt system showed the best performance. (author)

  8. STRATEGI KONVERSI ENERGI DI PT. LION METAL WORKS Tbk.

    Directory of Open Access Journals (Sweden)

    Daud Sudradjad

    2011-08-01

    Full Text Available Normal 0 false false false MicrosoftInternetExplorer4 /* Style Definitions */ table.MsoNormalTable {mso-style-name:"Table Normal"; mso-tstyle-rowband-size:0; mso-tstyle-colband-size:0; mso-style-noshow:yes; mso-style-parent:""; mso-padding-alt:0cm 5.4pt 0cm 5.4pt; mso-para-margin:0cm; mso-para-margin-bottom:.0001pt; mso-pagination:widow-orphan; font-size:10.0pt; font-family:"Times New Roman"; mso-ansi-language:#0400; mso-fareast-language:#0400; mso-bidi-language:#0400;} PT Lion Metal Works is a company producing office equipment, racking system, building material, security and fireproof safe, and cold forming. The production activity has high dependence on the usage of diesel, which influences the quality of the product and the cost of total business. The price fluctuation is one of the reasons for the company to convert the usage of diesel to some energy alternatives. Gas is the best alternative to replace diesel due to some advantages such as price, installation cost, distribution issue, calorie level, and environmental issue. There are some resistances from internal organization emerge in the implementation of the conversion. The alternatives strategy has been explored to reduce the resistances considering the goal of the organization, the actors (department in the company, and the type of resistance using analytical hierarchy process method. The priority strategy is establishing a new division for handling the conversion program and installing the gas facility gradually.

  9. RANCANG SISTEM INFORMASI PERSEDIAAN BAHAN BAKU TERKOMPUTERISASI PT. KPL

    Directory of Open Access Journals (Sweden)

    Oviliani Yenty Yuliana

    2001-01-01

    Full Text Available This study was done at PT. KPL which produces plastic goods. In order to compete with other plastic goods manufacturers during the economic crisis, PT. KPL must be able to minimize production costs. One of the ways is to reduce raw materials cost. The results were obtained with production demand forecasting, using the Holt-Winter method; the Moving Average with Index Seasonal method; the Single Exponential Smoothing Method; the Double Exponential Smoothing method; and the Multiplicative Winter method. Based on economic order quantity, the minimum total inventory cost was obtained. Economic order quantity was entered into Material Requirement Planning (MRP. Relevant, accurate, and timely information is needed for planning and controlling raw material inventory. For that purpuse, a computerized conceptual information system for raw material inventory was designed. Abstract in Bahasa Indonesia : Studi Kasus dilakukan pada PT. KPL yang bergerak dibidang pembuatan barang-barang plastik. Agar PT. KPL dapat bersaing dengan perusahaan sejenis dimasa krisis ekonomi. PT. KPL harus mampu menekan biaya produksi seminimal mungkin. Salah satu cara dengan menekan biaya persediaan bahan baku. Dari hasil penelitian diperoleh ramalan kebutuhan produk, yang diolah menggunakan metode: Holt Winter, Moving Average With Index Seasonal, Single Exponential Smoothing, Double Exponential Smoothing, Multiplicative Winter. Berdasarkan Economic Order Quantity dihasilkan total biaya persediaan yang minimum. Jumlah pemesanan yang ekonomis dimasukkan kedalam Material Requirement Planning (MRP. Informasi yang cepat, tepat, dan akurat diperlukan dalam merencanakan dan mengendalikan persediaan bahan baku. Untuk itu dirancang sistem informasi tersediaan bahan baku terkomputerisasi secara konsep. Kata kunci: ramalan kebutuhan produk, EOQ, MRP, sistem informasi

  10. Synoptic forcing of wind relaxations at Pt. Conception, California

    Science.gov (United States)

    Fewings, Melanie R.; Washburn, Libe; Dorman, Clive E.; Gotschalk, Christopher; Lombardo, Kelly

    2016-08-01

    Over the California Current upwelling system in summer, the prevailing upwelling-favorable winds episodically weaken (relax) or reverse direction for a few days. Near Pt. Conception, California, the wind usually does not reverse, but wind relaxation allows poleward oceanic coastal flow with ecological consequences. To determine the offshore extent and synoptic forcing of these wind relaxations, we formed composite averages of wind stress from the QuikSCAT satellite and atmospheric pressure from the North American Regional Reanalysis (NARR) using 67 wind relaxations during summer 2000-2009. Wind relaxations at Pt. Conception are the third stage of an event sequence that repeatedly affects the west coast of North America in summer. First, 5-7 days before the wind weakens near Pt. Conception, the wind weakens or reverses off Oregon and northern California. Second, the upwelling-favorable wind intensifies along central California. Third, the wind relaxes at Pt. Conception, and the area of weakened winds extends poleward to northern California over 3-5 days. The NARR underestimates the wind stress within ˜200 km of coastal capes by a factor of 2. Wind relaxations at Pt. Conception are caused by offshore extension of the desert heat low. This synoptic forcing is related to event cycles that cause wind reversal as in Halliwell and Allen (1987) and Mass and Bond (1996), but includes weaker events. The wind relaxations extend ˜600 km offshore, similarly to the California-scale hydraulic expansion fan shaping the prevailing winds, and ˜1000 km alongshore, limited by an opposing pressure gradient force at Cape Mendocino.

  11. Rotational Bands of Some Neutron Deficient Odd-A Pt Isotopes in Particle-Triaxial-Rotor Model

    Institute of Scientific and Technical Information of China (English)

    WU Xian-Ming; LIU Yu-Xin

    2008-01-01

    Theoretical calculations are performed for neutron deficient Pt isotopes 177pt and 175,173,171pt in the particle-triaxial-rotor model with variable moment of inertia. The obtained energy spectra agree with experimental data quite well. The calculated results indicate that all these nuclei are in triaxial rotation with 177pt being in prolate and 175,173,171pt in oblate. Several levels are predicted for the 13/2+ band in 169pt.

  12. Self-supported interconnected Pt nanoassemblies as highly stable electrocatalysts for low-temperature fuel cells.

    Science.gov (United States)

    Xia, Bao Yu; Ng, Wan Theng; Wu, Hao Bin; Wang, Xin; Lou, Xiong Wen David

    2012-07-16

    In it for the long haul: Clusters of Pt nanowires (3D Pt nanoassemblies, Pt NA) serve as an electrocatalyst for low-temperature fuel cells. These Pt nanoassemblies exhibit remarkably high stability following thousands of voltage cycles and good catalytic activity, when compared with a commercial Pt catalyst and 20 % wt Pt catalyst supported on carbon black (20 % Pt/CB).

  13. Electrochemical Sensor for Oxidation of NO Based on Au-Pt Nanoparticles Self-assembly Film

    Institute of Scientific and Technical Information of China (English)

    XIE,Jia; YU,Zhihui; XIA,Dingguo

    2009-01-01

    Au-Pt bimetallic nanoparticles film used as an efficient electrochemical sensor was prepared by self-assembled Au-Pt bimetallic nanoparticles on a glassy carbon (GC) substrate using thioglycolic acid as a linker. Atomic force microscopy (AFM) and scanning electron microscopy (SEM) showed that the Au-Pt nanoparticles self-assembly film was dense and uniform. Electrochemical experiments revealed that Au-Pt bimetallic nanoparticles film/GC electrode showed high electrocatalytic activity to the oxidation of nitric oxide.

  14. Ternary Pt-Ru-Ni catalytic layers for methanol electrooxidation prepared by electrodeposition and galvanic replacement

    OpenAIRE

    Athanasios ePapaderakis; Nikolaos ePliatsikas; Chara eProchaska; Kalliopi M. Papazisi; Balomenou, Stella P.; Dimitrios eTsiplakides; Panagiotis ePatsalas; Sotiris eSotiropoulos

    2014-01-01

    Ternary Pt-Ru-Ni deposits on glassy carbon substrates, Pt-Ru(Ni)/GC, have been formed by initial electrodeposition of Ni layers onto glassy carbon electrodes, followed by their partial exchange for Pt and Ru, upon their immersion into equimolar solutions containing complex ions of the precious metals. The overall morphology and composition of the deposits has been studied by SEM microscopy and EDS spectroscopy. Continuous but nodular films have been confirmed, with a Pt ÷ Ru ÷ Ni % bulk atomi...

  15. 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.

  16. Biogenic Pt uptake and nanoparticle formation in Medicago sativa and Brassica juncea

    Science.gov (United States)

    Bali, Roza; Siegele, Rainer; Harris, Andrew T.

    2010-10-01

    The ability of the facultative metallophyte plants, Medicago sativa ( M. sativa) and Brassica juncea ( B. juncea) to accumulate and translocate platinum (Pt) from aqueous substrates is reported. The influence of Pt concentration in the substrate (5, 10, 20, 40 and 80 ppm), exposure time (24, 48 and 72 h) and substrate pH (2, 3, 5, 7 and 9) was determined. In both plants the concentration of Pt increased with substrate concentration and exposure time. Greater accumulation was detected in the roots of M. sativa than B. juncea, up to a maximum of 94.19 mg Pt g-1 (dry biomass) compared with 38.5 mg Pt g-1 (dry biomass) following exposure to 80 ppm Pt after 72 h exposure, respectively. However, at lower substrate concentrations (5 and 20 ppm) greater quantities of Pt were detected in the shoots of B. juncea, ranging between 0.02 and 0.32 mg Pt g-1 (dry biomass) at 5 ppm across the different time intervals studied, compared with 0.02-0.14 mg Pt g-1 (dry biomass) for M. sativa, suggesting B. juncea to be a better translocator of Pt under idealised conditions at low concentrations. Higher Pt uptake was also observed in acidic media, with a maximum at pH 2 for M. sativa and pH 3 for B. juncea, indicating the role of net surface charge on the bioaccumulation of Pt. Once sequestered Pt(II) was reduced to Pt(0) due to the action of local metabolites. TEM images of M. sativa root samples showed the in vivo formation of Pt nanoparticles between 3 and 100 nm in size and of varying morphologies in the epidermal root cells. In vivo Pt distribution profiles were assessed using proton induced X-ray emission (μ-PIXE) spectroscopy, which showed even distribution across all tissue systems (epidermal, cortical and vascular) within the roots of both M. sativa and B. juncea.

  17. Preparation of PtRu/C and PtSn/C electrocatalysts using electron beam irradiation for direct and ethanol fuel cell; Preparacao de eletrocatalisadores PtRu/C e PtSn/C utilizando feixe de eletrons para aplicacao como anodo na oxidacao direta de metanol e etanol em celulas a combustivel de baixa temperatura

    Energy Technology Data Exchange (ETDEWEB)

    Silva, Dionisio Furtunato da

    2009-07-01

    PtRu/C and PtSn/C electrocatalysts were prepared using electron beam irradiation. The metal ions were dissolved in water/2-propanol and water/ethylene glycol solutions and the carbon support was added. The resulting mixtures were irradiated under stirring. The effect of water/ethylene glycol and water/2-propanol (v/v) ratio, Pt:Ru and Pt:Sn atomic ratios, the irradiation time and dose rate were studied. The obtained materials were characterized by Energy dispersive analysis of X-rays (EDX), X-ray diffraction (XRD), cyclic voltammetry (CV) and Moessbauer spectroscopy. The electro-oxidation of methanol and ethanol were studied by cyclic voltammetry and chronoamperometry using the thin porous coating technique. The electrocatalysts were also tested on the Direct Methanol and Ethanol Fuel Cells. PtRu/C electrocatalysts prepared in water/ethylene glycol showed Pt:Ru atomic ratios different from the nominal ones. The results suggested that part of the Ru(III) ions were not reduced. The obtained materials showed the face-centered cubic (fcc) structure of Pt and Pt alloys with crystallite sizes of 2-3 nm. PtRu/C electrocatalysts prepared in water/2-propanol showed Pt:Ru atomic ratios similar to the nominal ones. The obtained materials also showed the fcc structure of platinum and platinum alloys with crystallite sizes of 3-4 nm. PtSn/C electrocatalysts prepared in water/ethylene glycol and water/2-propanol showed Pt:Sn atomic ratios similar to the nominal ones. The obtained materials showed the platinum (fcc) phase with crystallite sizes in the range of 2 - 4 nm and a SnO{sub 2} (cassiterite) phase. The obtained PtRu/C and PtSn/C electrocatalysts showed similar or superior performance for methanol and ethanol electro-oxidation compared to commercial PtRu/C (E-TEK) and PtSn/C (BASF) electrocatalysts. (author)

  18. Preparation of Pt/C Catalyst with Solid Phase Reaction Method

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    The Pt/C catalyst was prepared with solid phase reaction method (Pt/C(S)) for the first time. Its performances were compared with that prepared by the traditional liquid phase reaction method. The results demonstrate that the electrocatalytic activity of Pt/C catalyst with solid phase reaction method for methanol oxidation is higher than that with liquid phase reaction method. XRD and TEM measurements indicate that the Pt/C(S) possesses low crystalline extent and small particle size.

  19. Epitaxial Fe3Pt/FePt nanocomposites on MgO and SrTiO3

    Science.gov (United States)

    Casoli, F.; Lupo, P.; Nasi, L.; Cabassi, R.; Fabbrici, S.; Bolzoni, F.; Ranzieri, P.; Albertini, F.

    2015-02-01

    We have exploited the pseudomorphic growth of the magnetically soft Fe3Pt phase on top of L10-FePt to obtain fully epitaxial soft/hard nanocomposites on both MgO(100) and SrTiO3(100). The magnetic properties of this new nanocomposite system, driven by the soft/hard exchange-coupling, can be tailored by varying soft phase thickness, soft phase magnetic anisotropy and substrate. Coercivity is strongly reduced by the addition of the soft phase, a reduction which is definitely affected by the nominal composition of the soft phase and by the substrate choice; similarly is the magnetic phase diagram of the composite system. Coercive field decreases down to 21% of the hard layer value for Fe3Pt(5 nm)/FePt(3.55 nm) nanocomposites on SrTiO3; this maximum coercivity reduction was obtained with a nominal atomic content of Fe in the soft phase of 80%.

  20. Energy barrier versus switching field for patterned Co80Pt20 alloy and Co/Pt multilayer films

    NARCIS (Netherlands)

    de Vries, Jeroen; Bolhuis, Thijs; Abelmann, Leon

    2013-01-01

    Two Co/Pt multilayer samples have been fabricated with a difference in the number of bilayers, leading to a total magnetic layer thickness of 3nm and 20nm. From these films, large arrays of magnetic islands have been patterned using laser interference lithography and ion beam etching. We have

  1. Correlating Structure and Oxygen Reduction Activity on Y/Pt(111) and Gd/Pt(111) Single Crystals

    DEFF Research Database (Denmark)

    Ulrikkeholm, Elisabeth Therese; Pedersen, Anders Filsøe; Johansson, Tobias Peter

    2015-01-01

    Polymer Electrolyte Membrane Fuel Cells (PEMFC) hold promise as a zero-emission source of power, particularly suitable for automotive vehicles. However, the high loading of Pt required to catalyse the Oxygen Reduction Reaction (ORR) at the PEMFC cathode prevents the commercialisation of this tech...

  2. Magnetic and structural properties of electrodeposited CoPt and FePt nanowires in nanoporous alumina templates

    Energy Technology Data Exchange (ETDEWEB)

    Dahmane, Y [Laboratoire Louis Neel, CNRS, BP 166, 38042 Grenoble cedex 9 (France); Cagnon, L [Laboratoire de Cristallographie, CNRS, BP 166, 38042 Grenoble cedex 9 (France); Voiron, J [Laboratoire Louis Neel, CNRS, BP 166, 38042 Grenoble cedex 9 (France); Pairis, S [Laboratoire de Cristallographie, CNRS, BP 166, 38042 Grenoble cedex 9 (France); Bacia, M [Laboratoire de Cristallographie, CNRS, BP 166, 38042 Grenoble cedex 9 (France); Ortega, L [Laboratoire de Cristallographie, CNRS, BP 166, 38042 Grenoble cedex 9 (France); Benbrahim, N [Laboratoire de Materiaux, Electrochimie et Corrosion, BP 17, 15000 Tizi-Ouzou (Algeria); Kadri, A [Laboratoire de Materiaux, Electrochimie et Corrosion, BP 17, 15000 Tizi-Ouzou (Algeria)

    2006-11-07

    CoPt and FePt nanowire arrays were successfully prepared by electrodeposition into nanochannels of porous alumina membranes. The as-deposited CoPt alloy has a face centred cubic structure and displays soft magnetic properties. Heat treatment at 700 {sup 0}C for different durations, under vacuum condition was carried out in order to obtain the ordered face centred tetragonal phase L1{sub 0}, exhibiting hard magnetic properties. After annealing, arrays of nanowires actually show hard magnetic properties with coercive fields up to 1.1 T at room temperature. Phase transformation, structural and magnetic properties were analysed and necessary conditions to obtain optimum magnetic properties are concluded. The first results obtained with FePt nanowires denote a more complicated system since the as-deposited material shows no magnetization. Magnetism appears only after annealing at 700 {sup 0}C minimum. Coercivity up to 1.1 T has been obtained at room temperature but with inhomogeneous phase composition.

  3. Development of Nanostructured Stress Free Pt-Rich FePt Films for Micro Electro Mechanical System Applications

    Directory of Open Access Journals (Sweden)

    T. M. Selvakumari

    2009-01-01

    Full Text Available Problem statement: The electroplating technique is especially interesting due to its low cost, high throughput and high quality of deposit. Magnetic thin films are extensively used in various electronic devices including high density recording media and Micro Electro Mechanical (MEMS devices. So we examined FePt films and give good magnetic properties. Approach: The Pt-rich FePt alloys were electrodeposited galvanostatically by various temperature baths. Results: The elemental percentage of Pt in the film was very high determined by X-ray spectroscopy. Surface characterization was carried out by using X-Ray Diffractometer (XRD and Scanning Electron Microscope (SEM.The magnetic properties determined by Vibrating sample magnetometer. Hardness and adhesion of the films were also discussed. Conclusion/Recommendation: The films were soft magnetic character of lower temperature bath and become a hard magnetic character of higher temperature bath. Therefore this magnetic films could be an important material for incorporate in Micro electro mechanical devices.

  4. Partial Thermodynamic Properties of gamma-(Ni,Pt)3Al in the Ni-Al-Pt System (Preprint)

    Science.gov (United States)

    2006-02-01

    phases belonging to the Cu family, Journal of Alloys and Compounds , 353, 2003, 207. 4. J. Kamm, W. Milligan, Phase stability in (Ni, Pt)3Al alloys...in the Al-Ni-Ru system by direct reaction synthesis calorimetry, Journal of Alloys and Compounds , 403(1-2), 2005, 217-222. 15 Tables Table 1

  5. Methanol electro-oxidation on Pt-Ru-P/C and Pt-Ru-P/MWCNT in acidic medium

    CSIR Research Space (South Africa)

    Modibedi, M

    2009-06-01

    Full Text Available Pt-Ru-P was prepared by the chemical reduction method using sodium hypophoshite as a reducing agent on Vulcan XC 72 and multi-walled carbon nano-tubes (MWCNTs). Sodium citrate was added as the stabilizer during electro-catalyst preparation...

  6. Verifying predictions of the L13 crystal structure in Cd-Pt and Pd-Pt by exhaustive enumeration

    Science.gov (United States)

    Hart, Gus L. W.

    2009-07-01

    In 2001, S. Müller and A. Zunger [Phys. Rev. Lett. 87, 165502 (2001)] predicted a never-before-observed crystal structure in Ag-Pd. Recently, Curtarolo predicted the same structure to be stable in Pt-Cd and Pt-Pd [S. Curtarolo , CALPHAD: Comput. Coupling Phase Diagrams Thermochem. 29, 163 (2005)]. The predicted structure is unique in several ways. Though never seen in any other face-centered-cubic-based intermetallic binary compound or ordered alloy, it is relatively simple—it contains only four atoms per unit cell. Furthermore, the structure is the only one of this small size, except the L12 structure, that cannot be characterized as a simple stacking of layers where each layer contains only one kind of atom. We construct a first-principles-based Hamiltonian and search it for the thermodynamically stable (lowest energy) structures. Using a (practically) exhaustive enumeration of about three million of the most likely candidate structures, we find that this new structure, designated L13 , is indeed a ground state in both Cd-Pt and Pd-Pt. Experimental efforts to validate the predictions are underway.

  7. Electrolysis of ammonia for hydrogen production catalyzed by Pt and Pt-Ir deposited on nickel foam

    Institute of Scientific and Technical Information of China (English)

    Min; Jiang; Dandan; Zhu; Xuebo; Zhao

    2014-01-01

    Electrolysis of ammonia in alkaline electrolyte solution was applied for the production of hydrogen. Both Pt-loaded Ni foam and Pt-Ir loaded Ni foam electrodes were prepared by electrodeposition and served as anode and cathode in ammonia electrolytic cell, respectively. The electrochemical behaviors of ammonia in KOH solution were individually investigated via cyclic voltammetry on three electrodes, i.e. bare Ni foam electrode, Pt-loaded Ni foam electrode and Pt-Ir loaded Ni foam electrode. The morphology and composition of the prepared Ni foam electrode were analyzed by scanning electron microscopy(SEM) and X-ray diffraction(XRD). Effects of the concentration of electrolyte solution and temperature of electrolytic cell on the electrolysis reaction were examined in order to enhance the efficiency of ammonia electrolysis. The competition of ammonia electrolysis and water electrolysis in the same alkaline solution was firstly proposed to explain the changes of cell voltage with the electrolysis proceeding. At varying current densities, different cell voltages could be obtained from galvanostatic curves.The low cell voltage of 0.58 V, which is less than the practical electrolysis voltage of water(1.6 V), can be obtained at a current density of2.5 mA/cm2. Based on some experimental parameters, such as the applied current, the resulting cell voltage and output of hydrogen gas, the power consumption per gram of H2produced can be estimated.

  8. Thermoelectric and Magnetic Properties of Pt-Substituted {BaFe_{4-{x}}Pt_{{x}}Sb_{12}} Compounds

    Science.gov (United States)

    Sertkol, Murat; Ballıkaya, Sedat; Aydoğdu, Fatih; Güler, Adil; Özdemir, Mustafa; Öner, Yıldırhan

    2017-01-01

    {BaFe_{4-{x}}Pt_{{x}}Sb_{12}} ( x = 0, 0.1, 0.2) compounds were prepared by melting and annealing, followed by a spark plasma sintering method. Low-temperature thermoelectric and magnetic properties were investigated based on Seebeck coefficient, electrical and thermal conductivity and magnetization measurements. The structural properties of {BaFe_{4-{x}}Pt_{{x}}Sb_{12}} ( x = 0, 0.1, 0.2) compounds were ascertained by powder x-ray diffraction analysis, confirming that all samples have a main phase of a skutterudite structure with the space group Im{bar{3}}. The lattice parameters obtained, 9.202(5), 9.199(5) and 9.202(1) Å for x = 0, 0.1 and 0.2, respectively, were found consistent with literature. The Seebeck coefficient sign shows that holes are dominant carriers in all compounds. The local maximum Seebeck coefficient was observed around 50 K which may be a trace of paramagnon-drag effect of charge carriers. Thermal conductivity and electrical resistivity measurements were carried out between 4.2 and 300 K. Temperature dependence of electrical resistivity reflects that all samples show semi-metallic behavior in our temperature range of 4.2-300 K. Samples for x = 0.1 and x = 0.2 show Kondo-like behavior. In magnetization measurement, we observe that there are two successive magnetic transitions in Pt-substituted compounds; however, there is only one (transition from a paramagnetic state to long-range magnetic ordering) in Pt-free compounds. In Pt-substituted compounds, the first transition appears at T _{ c} = 48 K. In addition, the second transition is observed at T _{ irr} = 30 K where an intermediate state is observed before the magnetic ordering transforms to an irreversible ferromagnetic state. We concluded that Pt substitution on the Fe side effectual on the thermoelectric and magnetic properties of {BaFe_{4-{x}}Pt_{{x}}Sb_{12}} ( x = 0, 0.1, 0.2) compounds.

  9. Oxygen Reduction Reaction on Pt Overlayers Deposited onto a Gold Film: Ligand, Strain, and Ensemble Effect

    DEFF Research Database (Denmark)

    Deng, Yu-Jia; Tripkovic, Vladimir; Rossmeisl, Jan;

    2016-01-01

    We study the oxygen reduction reaction (ORR), the catalytic process occurring at the cathode in fuel cells, on Pt layers prepared by electrodeposition onto an Au substrate. Using a nominal Pt layer by layer deposition method previously proposed, imperfect layers of Pt on Au are obtained. The ORR ...

  10. Pd-Pt random alloy nanocubes with tunable compositions and their enhanced electrocatalytic activities.

    Science.gov (United States)

    Yuan, Qiang; Zhou, Zhiyou; Zhuang, Jing; Wang, Xun

    2010-03-07

    Monodisperse, highly-selective sub-10 nm Pd-Pt random alloy nanocubes have been successfully synthesized in aqueous solution, and the electrocatalytic activity of these Pd-Pt alloys towards formic acid oxidation was investigated and compared with the activity of Pd sub-10 nm nanocubes, and the commercial Pd and Pt black.

  11. Localized Pd overgrowth on cubic Pt nanocrystals for enhanced electrocatalytic oxidation of formic acid.

    Science.gov (United States)

    Lee, Hyunjoo; Habas, Susan E; Somorjai, Gabor A; Yang, Peidong

    2008-04-23

    Binary Pt/Pd nanoparticles were synthesized by localized overgrowth of Pd on cubic Pt seeds for the investigation of electrocatalytic formic acid oxidation. The binary particles exhibited much less self-poisoning and a lower activation energy relative to Pt nanocubes, consistent with the single crystal study.

  12. Selective hydrothermal method to create patterned and photoelectrochemically effective Pt/WO3 Interfaces

    NARCIS (Netherlands)

    Zoontjes, Michel G.C.; Huijben, Mark; Baltrusaitis, Jonas; Wiel, van der Wilfred G.; Mul, Guido

    2013-01-01

    A hydrothermal method based on the use of hydrogen peroxide is described to grow a homogeneous layer of tungsten oxide (WO3) on a platinum (Pt) film supported on a silicon wafer. WO3 growth is highly selective for Pt when present on silicon in a patterned arrangement, demonstrating that Pt catalyzes

  13. HUBUNGAN ANTARA IKLIM KOMUNIKASI DAN MOTIVASI KERJA KARYAWAN PT. MARUKI INTERNATIONAL INDONESIA

    OpenAIRE

    SURYANINGSIH, DEWI

    2012-01-01

    Tujuan penelitian ini adalah untuk mengetahui: (1.) Untuk mengetahui keadaan iklim komunikasi yang terbentuk di dalam PT. Maruki International Indonesia. (2.) Untuk mengetahui motivasi kerja karyawan PT. Maruki International Indonesia. (3.) Untuk mengetahui adanya hubungan antara iklim komunikasi dan motivasi kerja karyawan PT. Maruki International Indonesia. Penelitian ini dilaksanakan di Kota Makassar. Penelitian ini dilaksanakan di Kota Makassar. Adapun populasi penelitian ini adalah se...

  14. WC@meso-Pt core-shell nanostructures for fuel cells.

    Science.gov (United States)

    Chen, Zhao-Yang; Ma, Chun-An; Chu, You-Qun; Jin, Jia-Mei; Lin, Xiao; Hardacre, Christopher; Lin, Wen-Feng

    2013-12-25

    We developed a facile method to synthesize core-shell WC@meso-Pt nanocatalysts by carburizing ammonium tungstate and copper nitrate via gas-solid reactions, followed by a Pt replacement reaction. The mesoporous nanocomposite displays higher activity and stability towards methanol electrooxidation than commercial Pt/C catalysts.

  15. Photocatalysis and photoinduced hydrophilicity of WO3 thin films with underlying Pt nanoparticles.

    Science.gov (United States)

    Miyauchi, Masahiro

    2008-11-07

    The photocatalytic oxidation and photoinduced hydrophilicity of thin tungsten trioxide (WO(3)) films coupled with platinum (Pt) nanoparticles were investigated. WO(3) films with underlying Pt nanoparticles (WO(3)/Pt/substrate) and those with overlying Pt nanoparticles (Pt/WO(3)/substrate) were synthesized by sputtering and sol-gel methods. Between these films, underlying Pt nanoparticles greatly enhanced the photocatalytic oxidation activity of WO(3) without decreasing the photoinduced hydrophilic conversion. However, overlying Pt nanoparticles deteriorated the hydrophilicity of WO(3) because the Pt nanoparticle surface was hydrophobic. The enhanced photocatalytic reaction by the Pt nanoparticles was attributed to the multi-electron reduction in Pt, which is caused by the injected electrons from the conduction band of WO(3). The relationship between photocatalytic activity and thin film structure, including the size of Pt nanoparticles, the thickness and porosity of the WO(3) layer, were investigated. Consequently, the optimum structure for high performance in both photocatalysis and photoinduced hydrophilicity was WO(3) (50 nm)/Pt(1.5 nm)/substrate, and this film exhibited a significant self-cleaning property even under visible light irradiation.

  16. Enhanced magnetic properties of FePt nanoparticles codeposited on Ag nanoislands

    Science.gov (United States)

    Castaldi, L.; Giannakopoulos, K.; Travlos, A.; Boukos, N.; Niarchos, D.; Boukari, S.; Beaurepaire, E.

    2009-05-01

    Ag nanoislands have been used as nucleation sites for FePt nanoparticles when deposited on SiO2 surfaces by electron beam evaporation. We demonstrate that it is possible to nucleate FePt nanoparticles on predeposited Ag clusters and that this results in a significant improvement of the hard magnetic Ag/FePt nanoparticles' properties. We find that, besides the usual annealing treatments, a simple predeposition of Ag nanoclusters promotes the formation of the FePt L10 phase at larger FePt nominal thicknesses (fFePt). All the nanoparticles studied are ferromagnetic, except for those FePt samples deposited with lower nominal thicknesses (fFePt˜1.8 nm), which are superparamagnetic. The presence of Ag seeds promotes the A1/L10 transition, which results in a remarkable enhancement of the coercivity (Hc) for both the as-deposited and the annealed samples. Maximum Hc of 8.9 and 9.4 kOe are obtained for the Ag/FePt nanoparticles with fFePt˜1.8 and 3.5 nm, respectively. Our results are a strong indication that the nucleation of the FePt nanoparticles on Ag nanoclusters can promote significant magnetic hardening of the FePt nanoparticles by easing the transition from the disordered to the ordered phase.

  17. 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 *...

  18. Oxygen Reduction Reaction Activity and Durability of Pt Catalysts Supported on Titanium Carbide

    Directory of Open Access Journals (Sweden)

    Morio Chiwata

    2015-06-01

    Full Text Available We have prepared Pt nanoparticles supported on titanium carbide (TiC (Pt/TiC as an alternative cathode catalyst with high durability at high potentials for polymer electrolyte fuel cells. The Pt/TiC catalysts with and without heat treatment were characterized by X-ray diffraction (XRD, X-ray photoelectron spectroscopy (XPS, and transmission electron microscopy (TEM. Hemispherical Pt nanocrystals were found to be dispersed uniformly on the TiC support after heat treatment at 600 °C in 1% H2/N2 (Pt/TiC-600 °C. The electrochemical properties (cyclic voltammetry, electrochemically active area (ECA, and oxygen reduction reaction (ORR activity of Pt/TiC-600 °C and a commercial Pt/carbon black (c-Pt/CB were evaluated by the rotating disk electrode (RDE technique in 0.1 M HClO4 solution at 25 °C. It was found that the kinetically controlled mass activity for the ORR on Pt/TiC-600 °C at 0.85 V (507 A g−1 was comparable to that of c-Pt/CB (527 A g−1. Moreover, the durability of Pt/TiC-600 °C examined by a standard potential step protocol (E = 0.9 V↔1.3 V vs. RHE, holding 30 s at each E was much higher than that for c-Pt/CB.

  19. Electrocatalytic activity of porous nanostructured Fe/Pt-Fe electrode for methanol electrooxidation in alkaline media

    Institute of Scientific and Technical Information of China (English)

    Javad Hosseini; Mehdi Abdolmaleki; Hamid Reza Pouretedal; Mohammad Hossein Keshavarz

    2015-01-01

    An electrochemical approach to fabricate a nanostructured Fe/Pt-Fe catalyst through electrodepo-sition followed by galvanic replacement is presented. An Fe/Pt-Fe nanostructured electrode was prepared by deposition of Fe-Zn onto a Fe electrode surface, followed by replacement of the Zn by Pt at open-circuit potential in a Pt-containing alkaline solution. Scanning electron microscopy and energy-dispersive X-ray techniques reveal that the Fe/Pt-Fe electrode is porous and contains Pt. The electrocatalytic activity of the Fe/Pt-Fe electrode for oxidation of methanol was examined by cyclic voltammetry and chronoamperometry. The electrooxidation current on the Fe/Pt-Fe catalyst is much higher than that on flat Pt and smooth Fe catalysts. The onset potential and peak potential on the Fe/Pt-Fe catalyst are more negative than those on flat Pt and smooth Fe electrodes for methanol electrooxidation. All results show that this nanostructured Fe/Pt-Fe electrode is very attractive for integrated fuel cell applications in alkaline media.

  20. Tuning the activity of Pt alloy electrocatalysts by means of the lanthanide contraction

    DEFF Research Database (Denmark)

    Escribano, Maria Escudero; Malacrida, Paolo; Hansen, Martin Hangaard

    2016-01-01

    The high platinum loadings required to compensate for the slow kinetics of the oxygen reduction reaction (ORR) impede the widespread uptake of low-temperature fuel cells in automotive vehicles. We have studied the ORR on eight platinum (Pt)–lanthanide and Pt-alkaline earth electrodes, Pt5M, where...