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Sample records for pt nanoparticles deposited

  1. 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.

  2. Synthesis of Pt-Sn core-shell nanoparticles deposited on SBA-15 modified

    Energy Technology Data Exchange (ETDEWEB)

    Alvarez-Contreras, L.; Alonso-Lemus, I. [Centro de Investigacion en Materiales Avanzados S.C., Laboratorio Nacional de Nanotecnologia (Mexico); Botte, G. G. [Ohio University, Center for Electrochemical Engineering Research, Department of Chemical and Biomolecular Engineering (United States); Verde-Gomez, Y., E-mail: ysmaelverde@yahoo.com [Instituto Tecnologico de Cancun (Mexico)

    2013-07-15

    A novel one-step synthesis method to prepare Pt-Sn bimetallic nanoparticles supported on mesoporous silica with high surface area (SBA-15, 700 m{sup 2}/g) and narrow pore size distribution (around 9.5 nm) was developed. Tin incorporation plays an important dual role, to create active sites into the silica walls that serve as particles anchors center, and to grow Pt-Sn core-shell nanoparticles. High-resolution transmission and scanning electron microscopy, and X-ray diffraction pattern confirm the formation of the Pt-Sn core-shell type nanoparticles ( Almost-Equal-To 1-10 nm). The metal loading was 2.2 and 2.3 wt% for Pt and Sn, respectively. Electron microscopy results show that the metal nanoparticles were deposited not only on the matrix, but also inside of it. Structural, textural, and morphological features of the SBA-15 were slightly affected after the nanoparticles deposition, maintaining its high surface area. The results obtained suggest that Pt-Sn on SBA-15 could be attractive material for several catalytic applications, due to the narrow particle size distribution achieved (from 1 to 10 nm) the high dispersion on the support, as well as the Pt-Sn alloy developed.Graphical Abstract.

  3. 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 CO.sub.2 reforming of methane

    KAUST Repository

    Biausque, Gregory

    2015-04-28

    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 CO.sub.2 reforming of methane

  4. Immersion Deposition of Pt Nanoparticles on Porous Silicon for Methanol Oxidation

    Institute of Scientific and Technical Information of China (English)

    SU Xu; LU Kangle; CHANG Yanlong; ZHANG Yan; WANG Chunming

    2009-01-01

    Porous silicon(PS)was chosen as the substrate for supporting the Pt particles because of great surface area,good conductivity and stability.Pt nanoparticles have been successfully prepared on the substrate by immersion deposition,which is convenient.The component and morphological properties of the films have been investigated by means of X-ray diffraction(XRD),energy dispersive X-ray spectroscopy(EDX)and scanning electron microscopy(SEM),which shows that the Pt particles have small size and big specific surface.Cyclic voltammetry(CV)research showed that the Pt nanoparticles had novel catalytic activity for methanol when the immersion deposition time was past 24 min.

  5. Atomic Layer Deposition of Pt Nanoparticles for Microengine with Promoted Catalytic Motion.

    Science.gov (United States)

    Jiang, Chi; Huang, Gaoshan; Ding, Shi-Jin; Dong, Hongliang; Men, Chuanling; Mei, Yongfeng

    2016-12-01

    Nanoparticle-decorated tubular microengines were synthesized by a combination of rolled-up nanotechnology and atomic layer deposition. The presence of Pt nanoparticles with different sizes and distributions on the walls of microengines fabricated from bilayer nanomembranes with different materials results in promoted catalytic reaction efficiency, which leads to an ultrafast speed (the highest speed 3200 μm/s). The motion speed of the decorated microengines fits the theoretical model very well, suggesting that the larger surface area is mainly responsible for the acceleration of the motion speed. The high-speed nanoparticle-decorated microengines hold considerable promise for a variety of applications.

  6. A Study on Reactive Spray Deposition Technology Processing Parameters in the Context of Pt Nanoparticle Formation

    Science.gov (United States)

    Roller, Justin M.; Maric, Radenka

    2015-12-01

    Catalytic materials are complex systems in which achieving the desired properties (i.e., activity, selectivity and stability) depends on exploiting the many degrees of freedom in surface and bulk composition, geometry, and defects. Flame aerosol synthesis is a process for producing nanoparticles with ample processing parameter space to tune the desired properties. Flame dynamics inside the reactor are determined by the input process variables such as solubility of precursor in the fuel; solvent boiling point; reactant flow rate and concentration; flow rates of air, fuel and the carrier gas; and the burner geometry. In this study, the processing parameters for reactive spray deposition technology, a flame-based synthesis method, are systematically evaluated to understand the residence times, reactant mixing, and temperature profiles of flames used in the synthesis of Pt nanoparticles. This provides a framework for further study and modeling. The flame temperature and length are also studied as a function of O2 and fuel flow rates.

  7. Synthesis of nanostructured lean-NO x catalysts by direct laser deposition of monometallic Pt-, Rh- and bimetallic PtRh-nanoparticles on SiO2 support

    Science.gov (United States)

    Savastenko, N.; Volpp, H.-R.; Gerlach, O.; Strehlau, W.

    2008-02-01

    Monometallic Pt and Rh and bimetallic PtRh catalysts with a highly dispersed noble metal weight loading of ca. 1 wt% were produced via the direct deposition of nanoparticles on different SiO2 supports by means of pulsed ultra-violet (248 nm) excimer laser ablation of Pt, Rh bulk metal and PtRh alloy targets. Backscattered electron microscopy (BSE), energy dispersive X-ray spectroscopy (EDX), and transmission electron microscopy (TEM) were employed to characterize the deposited nanoparticles, which were found to exhibit narrow size distribution centred around 2.5 nm. The catalytic activities for lean NO x reduction of the monometallic and bimetallic catalyst samples were investigated in a flow reactor setup in the temperature range 100-400°C using a test gas mixture representative of oxygen rich diesel engine exhaust gas. For comparison a Rh/SiO2 reference catalyst prepared by a conventional impregnation method was also tested. Further experiments were performed in which PtRh nanoparticles were deposited on a Rh/SiO2 reference catalyst sample to study the possibility for controlled modification of its activity. The catalytic activity measurements revealed that among the samples solely prepared by laser deposition the PtRh-SiO2 nanoparticle catalyst showed the highest activity for NO x reduction at low temperatures 100-300°C. In addition, it could be demonstrated that the initially low NO x reduction activity and the N2 selectivity of the Rh/SiO2 reference catalyst sample for temperatures below 250°C can be enhanced by post laser deposition of PtRh nanoparticles.

  8. Atomic Layer Deposition of Pt Nanoparticles within the Cages of MIL-101: A Mild and Recyclable Hydrogenation Catalyst

    Directory of Open Access Journals (Sweden)

    Karen Leus

    2016-03-01

    Full Text Available We present the in situ synthesis of Pt nanoparticles within MIL-101-Cr (MIL = Materials Institute Lavoisier by means of atomic layer deposition (ALD. The obtained Pt@MIL-101 materials were characterized by means of N2 adsorption and X-ray powder diffraction (XRPD measurements, showing that the structure of the metal organic framework was well preserved during the ALD deposition. X-ray fluorescence (XRF and transmission electron microscopy (TEM analysis confirmed the deposition of highly dispersed Pt nanoparticles with sizes determined by the MIL-101-Cr pore sizes and with an increased Pt loading for an increasing number of ALD cycles. The Pt@MIL-101 material was examined as catalyst in the hydrogenation of different linear and cyclic olefins at room temperature, showing full conversion for each substrate. Moreover, even under solvent free conditions, full conversion of the substrate was observed. A high concentration test has been performed showing that the Pt@MIL-101 is stable for a long reaction time without loss of activity, crystallinity and with very low Pt leaching.

  9. Characterization of Pt@Cu Core@Shell Dendrimer-Encapsulated Nanoparticles Synthesized by Cu Underpotential Deposition

    Energy Technology Data Exchange (ETDEWEB)

    E Carino; R Crooks

    2011-12-31

    Dendrimer-encapsulated nanoparticles (DENs) containing averages of 55, 147, and 225 Pt atoms immobilized on glassy carbon electrodes served as the electroactive surface for the underpotential deposition (UPD) of a Cu monolayer. This results in formation of core@shell (Pt@Cu) DENs. Evidence for this conclusion comes from cyclic voltammetry, which shows that the Pt core DENs catalyze the hydrogen evolution reaction before Cu UPD, but that after Cu UPD this reaction is inhibited. Results obtained by in situ electrochemical X-ray absorption spectroscopy (XAS) confirm this finding.

  10. Characterization of Pt@Cu core@shell dendrimer-encapsulated nanoparticles synthesized by Cu underpotential deposition.

    Science.gov (United States)

    Carino, Emily V; Crooks, Richard M

    2011-04-05

    Dendrimer-encapsulated nanoparticles (DENs) containing averages of 55, 147, and 225 Pt atoms immobilized on glassy carbon electrodes served as the electroactive surface for the underpotential deposition (UPD) of a Cu monolayer. This results in formation of core@shell (Pt@Cu) DENs. Evidence for this conclusion comes from cyclic voltammetry, which shows that the Pt core DENs catalyze the hydrogen evolution reaction before Cu UPD, but that after Cu UPD this reaction is inhibited. Results obtained by in situ electrochemical X-ray absorption spectroscopy (XAS) confirm this finding.

  11. 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.

  12. A low-temperature synthesis of electrochemical active Pt nanoparticles and thin films by atomic layer deposition on Si(111) and glassy carbon surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Rui [Joint Center for Artificial Photosynthesis, California Institute of Technology, Pasadena, CA 91125 (United States); Han, Lihao [Joint Center for Artificial Photosynthesis, California Institute of Technology, Pasadena, CA 91125 (United States); Photovoltaic Materials and Devices (PVMD) Laboratory, Delft University of Technology, P.O. Box 5031, GA Delft 2600 (Netherlands); Huang, Zhuangqun; Ferrer, Ivonne M. [Joint Center for Artificial Photosynthesis, California Institute of Technology, Pasadena, CA 91125 (United States); Division of Chemistry and Chemical Engineering, California Institute of Technology, 210 Noyes Laboratory 127-72, Pasadena, CA 91125 (United States); Smets, Arno H.M.; Zeman, Miro [Photovoltaic Materials and Devices (PVMD) Laboratory, Delft University of Technology, P.O. Box 5031, GA Delft 2600 (Netherlands); Brunschwig, Bruce S., E-mail: bsb@caltech.edu [Beckman Institute, California Institute of Technology, Pasadena, CA 91125 (United States); Lewis, Nathan S., E-mail: nslewis@caltech.edu [Joint Center for Artificial Photosynthesis, California Institute of Technology, Pasadena, CA 91125 (United States); Beckman Institute, California Institute of Technology, Pasadena, CA 91125 (United States); Division of Chemistry and Chemical Engineering, California Institute of Technology, 210 Noyes Laboratory 127-72, Pasadena, CA 91125 (United States); Kavli Nanoscience Institute, California Institute of Technology, Pasadena, CA 91125 (United States)

    2015-07-01

    Atomic layer deposition (ALD) was used to deposit nanoparticles and thin films of Pt onto etched p-type Si(111) wafers and glassy carbon discs. Using precursors of MeCpPtMe{sub 3} and ozone and a temperature window of 200–300 °C, the growth rate was 80–110 pm/cycle. X-ray photoelectron spectroscopy (XPS), atomic force microscopy (AFM), and scanning electron microscopy (SEM) were used to analyze the composition, structure, morphology, and thickness of the ALD-grown Pt nanoparticle films. The catalytic activity of the ALD-grown Pt for the hydrogen evolution reaction was shown to be equivalent to that of e-beam evaporated Pt on glassy carbon electrode. - Highlights: • Pure Pt films were grown by atomic layer deposition (ALD) using MeCpPtMe3 and ozone. • ALD-grown Pt thin films had high growth rates of 110 pm/cycle. • ALD-grown Pt films were electrocatalytic for hydrogen evolution from water. • Electrocatalytic activity of the ALD Pt films was equivalent to e-beam deposited Pt. • No carbon species were detected in the ALD-grown Pt films.

  13. The Electrochemical Atomic Layer Deposition of Pt and Pd nanoparticles on Ni foam for the electrooxidation of alcohols

    CSIR Research Space (South Africa)

    Modibedi, RM

    2012-10-01

    Full Text Available Electrodeposition of Pt and Pd metal by surface limited redox replacement reactions was performed using the electrochemical atomic layer deposition. Carbon paper and Ni foam were used as substrates for metal deposition. Supported Pt and Pd...

  14. Effect of nanoparticle (Pd, Pd/Pt, Ni deposition on high temperature hydrogenation of Ti-V alloys in gaseous flow containing CO

    Directory of Open Access Journals (Sweden)

    S. Suwarno

    2017-02-01

    Full Text Available The hydrogenation properties of Ti-V hydrides coated with nanoparticles have been studied in gaseous mixtures of argon and hydrogen with and without additions of 1% CO. Nanoparticles of Pd, Ni, and co-deposited Pd/Pt with particle sizes of ~30–60 nm were formed by electroless deposition on the hydride surfaces. The alloy resistance to CO could be significantly improved by particle deposition. Large amounts of hydrogen were absorbed in a CO-containing gas when Ni and Pd/Pt deposition had been applied, while pure Pd deposition had no positive effect. Ni was found to have a stronger effect than those of Pd/Pt and Pd, possibly because of the size effect of Ni nanoparticles.

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

    Science.gov (United States)

    Gutkowski, Ramona; Schuhmann, Wolfgang

    2016-04-28

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

  16. Photocatalytic Properties of TiO2 Thin Films Modified with Ag and Pt Nanoparticles Deposited by Gas Flow Sputtering.

    Science.gov (United States)

    Maicu, M; Glöss, D; Frach, Peter; Hecker, D; Gerlach, G; Córdoba, José M

    2015-09-01

    In this work, a gas flow sputtering (GFS) process which allows the production and deposition of metal nanoparticles (NPs) in a vacuum environment is described. Aim of the study is to prove the potential of this technology for the fabrication of new TiO2 films with enhanced photocatalytic properties. For this purpose, Ag and Pt NPs have been produced and deposited on photocatalytic float glass coated with TiO2 thin films by magnetron sputtering. The influence of the process parameters and of the metal amount on the final properties of the particles (quantity, size, size distribution, oxidation state etc.,) was widely investigated. Moreover, the effect of the NPs on the photocatalytic activity of the resulting materials was evaluated for the case of the decomposition of stearic acid (SA) during UV-A irradiation. The reduction of the water contact angle (WCA) during the irradiation period was measured in order to test the photo-induced super-hydrophilicity (PSH).

  17. Electroless Pt deposition on Mn3O4 nanoparticles via the galvanic replacement process: electrocatalytic nanocomposite with enhanced performance for oxygen reduction reaction.

    Science.gov (United States)

    Kim, Ki Woong; Kim, Soo Min; Choi, Suhee; Kim, Jongwon; Lee, In Su

    2012-06-26

    A novel electroless Pt deposition method was exploited by employing the galvanic replacement process occurring between the Mn(3)O(4) surface and PtCl(4)(2-) complexes. The newly discovered process provides a simple protocol to produce the catalytic nanocomposite, in which a high density of ultrafine Pt nanocrystals is stably immobilized in a homogeneously dispersive state on the surface of Mn(3)O(4) nanoparticles. When the eletrocatalytic activity was tested for the oxygen reduction reaction, which limits the rate of the overall process in proton-exchange membrane fuel cells, the resulting Pt/Mn(3)O(4) nanocomposite showed highly enhanced specific activity and durability, compared with those of the commercial Pt/C catalyst.

  18. Controlled co-deposition of FePt nanoparticles embedded in MgO: a detailed investigation of structure and electronic and magnetic properties

    Science.gov (United States)

    D'Addato, S.; Grillo, V.; di Bona, A.; Luches, P.; Frabboni, S.; Valeri, S.; Lupo, P.; Casoli, F.; Albertini, F.

    2013-12-01

    Films of FePt nanoparticles (NPs) embedded in MgO were obtained by controlled co-deposition of FePt NPs pre-formed by a gas aggregation source and of Mg evaporated in an oxygen atmosphere. Assemblies of core-shell FePt@MgO NPs and films of FePt NPs embedded in MgO matrix could be obtained by varying FePt and Mg deposition rates. Transmission electron microscopy (TEM) and high resolution-TEM revealed the core-shell structure of the NPs, with an FePt core (of average diameter = 4.75 nm) presenting a multitwinned icosahedral structure, and MgO partially in crystalline form. The functional effect of the MgO shell in shielding the FePt core from external oxidation was shown with XPS. Upon controlled annealing, a transition from A1 to L10 ordering could be obtained, with structural and morphological re-arrangement. The magnetic hysteresis loops obtained from alternating gradient field magnetometry at room temperature show a ‘wasp-waist’ shape, with small values of coercive field (Hc = 300-1400 Oe), decreasing at increasing amounts of co-deposited MgO.

  19. Controlled co-deposition of FePt nanoparticles embedded in MgO: a detailed investigation of structure and electronic and magnetic properties.

    Science.gov (United States)

    D'Addato, S; Grillo, V; di Bona, A; Luches, P; Frabboni, S; Valeri, S; Lupo, P; Casoli, F; Albertini, F

    2013-12-13

    Films of FePt nanoparticles (NPs) embedded in MgO were obtained by controlled co-deposition of FePt NPs pre-formed by a gas aggregation source and of Mg evaporated in an oxygen atmosphere. Assemblies of core-shell FePt@MgO NPs and films of FePt NPs embedded in MgO matrix could be obtained by varying FePt and Mg deposition rates. Transmission electron microscopy (TEM) and high resolution-TEM revealed the core-shell structure of the NPs, with an FePt core (of average diameter (d) = 4.75 nm) presenting a multitwinned icosahedral structure, and MgO partially in crystalline form. The functional effect of the MgO shell in shielding the FePt core from external oxidation was shown with XPS. Upon controlled annealing, a transition from A1 to L10 ordering could be obtained, with structural and morphological re-arrangement. The magnetic hysteresis loops obtained from alternating gradient field magnetometry at room temperature show a 'wasp-waist' shape, with small values of coercive field (Hc = 300-1400 Oe), decreasing at increasing amounts of co-deposited MgO.

  20. 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.

  1. Ru-decorated Pt nanoparticles on N-doped multi-walled carbon nanotubes by atomic layer deposition for direct methanol fuel cells

    DEFF Research Database (Denmark)

    Johansson, Anne-Charlotte Elisabeth Birgitta; Yang, R.B.; Haugshøj, K.B.

    2013-01-01

    (methylcyclopentadienyl)platinum MeCpPtMe3, bis(ethylcyclopentadienyl)ruthenium Ru(EtCp)2 and O2 as the precursors. Catalysts with 5, 10 and 20 ALD Ru cycles grown onto the CNT-supported ALD Pt nanoparticles (150 cycles) were prepared and tested towards the electro-oxidation of CO and methanol, using cyclic voltammetry...

  2. 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.

  3. The electrochemical atomic layer deposition of Pt and Pd nanoparticles on Ni foam for the electro oxidation of alcohols

    CSIR Research Space (South Africa)

    Modibedi, RM

    2013-01-01

    Full Text Available of the electrocatalytic activity of the prepared catalysts. TABLE I. Electrochemical Activity of Pt and Pd Towards the Oxidation of Methanol. Catalyst Onset potential (V vs Ag/AgCl) If/Ib Pt/Carbon paper 0.41 4.30 Pt/Ni foam 0.38 2.16 Pd/Carbon paper* Pd.../Ni foam* -0.456 -0.429 2.86 1.30 *: methanol oxidation performed in alkaline medium TABLE II. Electrochemical Activity of Pd Towards the Oxidation of Ethanol in alkaline electrolyte. Catalyst Onset potential (V vs Ag/AgCl) If/Ib Pd...

  4. 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.

  5. 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.

  6. Characterization of Platinum Nanoparticles Deposited on Functionalized Graphene Sheets

    Directory of Open Access Journals (Sweden)

    Yu-Chun Chiang

    2015-09-01

    Full Text Available Due to its special electronic and ballistic transport properties, graphene has attracted much interest from researchers. In this study, platinum (Pt nanoparticles were deposited on oxidized graphene sheets (cG. The graphene sheets were applied to overcome the corrosion problems of carbon black at operating conditions of proton exchange membrane fuel cells. To enhance the interfacial interactions between the graphene sheets and the Pt nanoparticles, the oxygen-containing functional groups were introduced onto the surface of graphene sheets. The results showed the Pt nanoparticles were uniformly dispersed on the surface of graphene sheets with a mean Pt particle size of 2.08 nm. The Pt nanoparticles deposited on graphene sheets exhibited better crystallinity and higher oxygen resistance. The metal Pt was the predominant Pt chemical state on Pt/cG (60.4%. The results from the cyclic voltammetry analysis showed the value of the electrochemical surface area (ECSA was 88 m2/g (Pt/cG, much higher than that of Pt/C (46 m2/g. The long-term test illustrated the degradation in ECSA exhibited the order of Pt/C (33% > Pt/cG (7%. The values of the utilization efficiency were calculated to be 64% for Pt/cG and 32% for Pt/C.

  7. 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.

  8. 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.

  9. Ag/Au/Pt trimetallic nanoparticles with defects: preparation, characterization, and electrocatalytic activity in methanol oxidation

    Science.gov (United States)

    Thongthai, Kontee; Pakawanit, Phakkhananan; Chanlek, Narong; Kim, Jun-Hyun; Ananta, Supon; Srisombat, Laongnuan

    2017-09-01

    Two series of Ag x /Au/Pt y trimetallic nanoparticles (Ag x Au1Pt2 with x ranging from 1-5 and Ag4Au1Pt y with y ranging from 1-3) were prepared by a sequential chemical reduction method that involved the deposition of Pt on preformed Ag/Au core-shell particles by systematically controlling the amount of Ag, Au, and Pt metal precursor solutions. The structural changes (the diameters and increased surface roughness from the defective features) and absorption patterns (the significant reduction of the peak intensities) of the nanoparticles examined with TEM and UV-vis spectroscopy indicated the selective incorporation of Pt on the Ag/Au nanoparticles regardless of their compositions. In addition, a combination of WDX, XRD, and XPS analyses quantitatively and qualitatively confirmed the successful formation of the Ag x Au1Pt2 and Ag4Au1Pt y trimetallic nanoparticles. Subsequently, these series of nanoparticles were deposited on multi-wall carbon nanotubes (MWCNTs) to evaluate their electrocatalytic property in the methanol oxidation reaction (MOR) as a function of their metal compositions. The results showed that the electrocatalytic activities of all Ag4/Au1/Pt y systems were higher than those of typical Pt on the MWCNTs. In particular, the Ag4Au1Pt2 nanoparticles exhibited the highest electrocatalytic property for the MOR, suggesting the importance of the proper combination of metal constituents and structures to regulate the activity in electrocatalytic systems.

  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. 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.

  12. 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.

  13. New methods of controlled monolayer-to-multilayer deposition of Pt for designing electrocatalysts at an atomic level

    Directory of Open Access Journals (Sweden)

    J. X. WANG

    2001-12-01

    Full Text Available Two new methods for monolayer-to-multileyer Pt deposition are presented. One involves Pt deposition by the replacement of an UPD metal monolayer on an electrode surface and the other the spontaneous deposition of Pt on Ru. The first method, exemplified by the replacement of a Cu monolayer on a Au(111 surface, occurs as a spontaneous irreversible redox reaction in which the Cu monolayer is oxidized by Pt cations, which are reduced and simultaneously deposited. The second method is illustrated by the deposition of Pt on a Ru(0001 surface and on carbon-supported Ru nanoparticles. This deposition takes place upon immersion of a UHV-prepared Ru(0001 crystal or Ru nanoparticles, reduced in H2, in a solution containing PtCl62- ions. The oxidation of Ru to RuOH by a local cell mechanism appears to be coupled with Pt deposition. This method facilitates the design of active Pt-Ru catalysts with ultimately low Pt loadings. Only a quarter of a monolayer of Pt on Ru nanoparticles yields an electrocatalyst with higher activity and CO tolerance for H2/CO oxidation than commercial Pt-Ru alloy electrocatalysts with considerably higher Pt loadings.

  14. A novel preparation method of Sn-modified Pt nanoparticles and application for methanol oxidation

    Science.gov (United States)

    Du, Yongling; Su, Biquan; Zhang, Nuo; Wang, Chunming

    2008-12-01

    With polystyrene latex spheres self-assembled on ITO glass as templates, highly ordered two-dimensional (2D) Pt nanoparticles (PtNPs) were prepared by electrochemical deposition. The morphology and element composition of PtNPs were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). The electrocatalytic properties of PtNPs/ITO and Sn underpotential deposition (UPD) modified PtNPs/ITO for methanol oxidation has been investigated by cyclic voltammetry (CV) and chronoamperometry (CA). The excellent electrocatalytic activity can be observed for these catalytic systems.

  15. 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.

  16. Synthesis and composition evolution of bimetallic Pd Pt alloy nanoparticles

    Science.gov (United States)

    Ren, Guoqiang; Shi, Honglan; Xing, Yangchuan

    2007-09-01

    This paper reports a study on the synthesis of Pd-Pt alloy nanoparticles and composition evolution of the alloys. The synthesis involves Pd and Pt acetylacetonate as the metal precursors and trioctylphosphine (TOP) as the solvent. Thermal decomposition of the Pd-TOP complex resulted in Pd nanoparticles, while substitution of Pt in the Pt-TOP complex by Pd allowed formation of the Pd-Pt alloys. It was observed that the Pd-Pt nanoparticles formed at the very beginning in the synthesis process are Pd rich with various nanoparticle sizes ranging from 1.5 to 25 nm in diameter. These nanoparticles averaged out through a digestive ripening process and reached a final size of 3.5 nm in about 10 min. The alloy compositions evolved throughout the synthesis process and only reached the preset Pd to Pt ratio of the precursors in 120 min. It was found that Pt acetylacetonate alone in TOP cannot produce Pt nanoparticles, which was attributed to the formation of a Pt-TOP complex and a strong coordination of Pt to the phosphine. This observation led us to propose an atomic exchange process between the Pt-TOP complex and the Pd atoms at the nanoparticle surface. As a result, the alloy formation process is limited by a substitution and diffusion rate of the Pt atoms at the surface of the alloy nanoparticles.

  17. Suspended Pt nanoparticles over TiO2 nanotubes for enhanced photocatalytic H2 evolution

    CERN Document Server

    Nguyen, Nhat Truong; Altomare, Marco; Schmuki, Patrik

    2016-01-01

    In the present work we introduce a technique to form a photocatalyst, based on Pt nanoparticles suspended over the mouth of TiO2 nanotubes. These structures are obtained by the decoration of the top end of highly ordered TiO2 nanotubes with a web of TiO2 nanofibrils, followed by sputter deposition of a minimum amount of Pt. A subsequent thermal dewetting step forms 3-6 nm-sized Pt nanoparticles along the nanofibrils. These structures, when compared to conventional Pt decoration techniques of TiO2 nanotubes, show a strongly enhanced photocatalytic H2 evolution efficiency.

  18. 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.

  19. Synthesis and deposition of metal nanoparticles by gas condensation process

    Energy Technology Data Exchange (ETDEWEB)

    Maicu, Marina, E-mail: marina.maicu@fep.fraunhofer.de; Glöß, Daniel; Frach, Peter [Fraunhofer Institut für Elektronenstrahl und Plasmatechnik, FEP, Winterbergstraße 28, 01277 Dresden (Germany); Schmittgens, Ralph; Gerlach, Gerald [Institut für Festkörperelektronik, IFE, TU Dresden, Helmholtz Straße 18, 01069 Dresden (Germany); Hecker, Dominic [Fraunhofer Institut für Elektronenstrahl und Plasmatechnik, FEP, Winterbergstraße 28, 01277 Dresden, Germany and Institut für Festkörperelektronik, IFE, TU Dresden, Helmholtz Straße 18, 01069 Dresden (Germany)

    2014-03-15

    In this work, the synthesis of Pt and Ag nanoparticles by means of the inert gas phase condensation of sputtered atomic vapor is presented. The process parameters (power, sputtering time, and gas flow) were varied in order to study the relationship between deposition conditions and properties of the nanoparticles such as their quantity, size, and size distribution. Moreover, the gas phase condensation process can be combined with a plasma enhanced chemical vapor deposition procedure in order to deposit nanocomposite coatings consisting of metallic nanoparticles embedded in a thin film matrix material. Selected examples of application of the generated nanoparticles and nanocomposites are discussed.

  20. Selective deposition of Pt onto supported metal clusters for fuel cell electrocatalysts

    Science.gov (United States)

    Jeon, Tae-Yeol; Pinna, Nicola; Yoo, Sung Jong; Ahn, Docheon; Choi, Sun Hee; Willinger, Marc-Georg; Cho, Yong-Hun; Lee, Kug-Seung; Park, Hee-Young; Yu, Seung-Ho; Sung, Yung-Eun

    2012-09-01

    We report a new method for deposition of Pt on a metal core to develop real electrocatalysts with significantly reduced amounts of expensive Pt as well as enhanced activity for oxygen reduction reaction. Ru and Pd have different crystal structures and modify the electronic structure of Pt to a different extent (shifts in d-band center). They were chosen as core materials to examine whether hydroquinone dissolved in ethanol can be used to deposit additional Pt atoms onto preformed core nanoparticles, and whether the modified d-character of Pt on different host metals can result in the enhanced ORR activity. The physicochemical characteristics of Pd-Pt and Ru-Pt core-shell nanoparticles are investigated. The core-shell structure was identified through a combination of experimental methods, employing electron microscopy, electrochemical measurements, and synchrotron X-ray measurements such as powder X-ray diffraction, X-ray absorption fine structure, and X-ray photoelectron spectroscopy. The hydroquinone reduction method proved to be an excellent route for the epitaxial growth of a Pt shell on the metal cores, leading to enhanced ORR activities.We report a new method for deposition of Pt on a metal core to develop real electrocatalysts with significantly reduced amounts of expensive Pt as well as enhanced activity for oxygen reduction reaction. Ru and Pd have different crystal structures and modify the electronic structure of Pt to a different extent (shifts in d-band center). They were chosen as core materials to examine whether hydroquinone dissolved in ethanol can be used to deposit additional Pt atoms onto preformed core nanoparticles, and whether the modified d-character of Pt on different host metals can result in the enhanced ORR activity. The physicochemical characteristics of Pd-Pt and Ru-Pt core-shell nanoparticles are investigated. The core-shell structure was identified through a combination of experimental methods, employing electron microscopy

  1. Preparation of Dispersed Platinum Nanoparticles on a Carbon Nanostructured Surface Using Supercritical Fluid Chemical Deposition

    Directory of Open Access Journals (Sweden)

    Mineo Hiramatsu

    2010-03-01

    Full Text Available We have developed a method of forming platinum (Pt nanoparticles using a metal organic chemical fluid deposition (MOCFD process employing a supercritical fluid (SCF, and have demonstrated the synthesis of dispersed Pt nanoparticles on the surfaces of carbon nanowalls (CNWs, two-dimensional carbon nanostructures, and carbon nanotubes (CNTs. By using SCF-MOCFD with supercritical carbon dioxide as a solvent of metal-organic compounds, highly dispersed Pt nanoparticles of 2 nm diameter were deposited on the entire surface of CNWs and CNTs. The SCF-MOCFD process proved to be effective for the synthesis of Pt nanoparticles on the entire surface of intricate carbon nanostructures with narrow interspaces.

  2. Electrochemical oxidation of methanol on Pt nanoparticles composited MnO 2 nanowire arrayed electrode

    Science.gov (United States)

    Zhao, Guang-Yu; Li, Hu-Lin

    2008-03-01

    By use of the membrane-template synthesis route, MnO 2 nanowire arrayed electrodes are successfully synthesized by means of the anodic deposition technique. The Pt nanoparticles composited MnO 2 nanowire arrayed electrodes (PME) are obtained through depositing Pt on MnO 2 nanowire arrayed electrode by cathode deposition technique. For comparison of electrochemical performance, Pt nanowire arrayed electrodes which have the same amount of Pt with PME are also prepared. The electro-oxidation of methanol on PME and Pt nanowire arrayed electrodes is investigated at room temperature by cyclic voltammetry, which show that about 110 mV decreased overpotential and 2.1-fold enhanced votammetric current are achieved on PME. The chronoamperometry result demonstrates that the resistance to carbon monoxide for PME is improved.

  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. Magnetic properties of thermally reduced graphene oxide decorated with PtNi nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Huízar-Félix, A.M. [Universidad Autónoma de Nuevo León, UANL, Facultad de Ingeniería Mecánica y Eléctrica, FIME, Ave. Pedro de Alba s/n, Ciudad Universitaria, C.P.66455 San Nicolás de los Garza, N.L. (Mexico); Departamento de Electricidad y Electrónica, Universidad del País Vasco (UPV/EHU), 48940 Leioa (Spain); BC Materials, Basque Centre for Materials, Applications and Nanostructures, 48160 Derio (Spain); Cruz-Silva, R. [Research Center for Exotic NanoCarbon, Shinshu University, 4-17-1 Wakasato, Nagano 380-8553 (Japan); Barandiarán, J.M. [Departamento de Electricidad y Electrónica, Universidad del País Vasco (UPV/EHU), 48940 Leioa (Spain); BC Materials, Basque Centre for Materials, Applications and Nanostructures, 48160 Derio (Spain); García-Gutiérrez, D.I. [Universidad Autónoma de Nuevo León, UANL, Facultad de Ingeniería Mecánica y Eléctrica, FIME, Ave. Pedro de Alba s/n, Ciudad Universitaria, C.P.66455 San Nicolás de los Garza, N.L. (Mexico); Orue, I. [SGIKER Medidas Magnéticas, Facultad de Ciencia y Tecnología, Universidad del País Vasco (UPV/EHU), 48940 Leioa (Spain); and others

    2016-09-05

    Nanocomposites of reduced graphene oxide (RGO) with PtNi nanoparticles were obtained by in situ thermal reduction of a physical mixture of GO and metallic precursors. RGO and PtNiRGO nanocomposites were studied by differential thermal analysis and thermogravimetry, Fourier transform infrared spectroscopy (FTIR), powder X-ray diffraction (XRD), as well as scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The method presented here is a one-step thermal reduction procedure that allows the deposition of bimetallic PtNi nanoparticles with tetragonal crystalline structure and particle size ranging from 3 nm to 30 nm on RGO. The magnetic properties of the RGO and PtNiRGO nanocomposites were measured by vibrating sample magnetometry, which revealed that the RGO exhibited diamagnetism at room temperature and paramagnetism at temperatures below 10 K. PtNiRGO nanocomposites show hysteresis and ferromagnetic ordering at room temperature with a Curie temperature of 658 K. In addition, its magnetic properties at low temperature were strongly influenced by the paramagnetic contribution of RGO and the morphology of the bimetallic nanoparticles. - Highlights: • Simultaneous synthesis method for growth of PtNi nanoparticles on RGO. • Microstructural features of PtNiRGO nanocomposite were studied with extensive characterization. • Diamagnetic behavior of RGO and ferromagnetic ordering for PtNiRGO nanocomposite.

  5. The Underpotential Deposition of Copper on Pt(311): Site Selective Deposition and Anion Effects

    Science.gov (United States)

    1994-03-14

    AD-A278 022 OFFICE OF NAVAL RESEARCH CONTRACT N00014-84-k-0656/PP0002 R & T Code 4133034 Technical Report #36 The Underpotential Deposition of Copper...Include Security Clauffication) The Underpotential Deposition of Copper on Pt(311): Site Selective Deposition and Anion Effects 𔃼 OERSONAL AUTHOR(S...Alacant, Spain ABSTRACT The underpotential deposition of copper on Pt(31 1)=Pt[2(111 )x(100)] stepped surfaces has been studied and the results are compared

  6. 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.

  7. 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.

  8. 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).

  9. 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.

  10. 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.

  11. 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.

  12. Characterization of self-assembled electrodes based on Au-Pt nanoparticles for PEMFC application

    Energy Technology Data Exchange (ETDEWEB)

    Valenzuela, E. [Politecnica Univ. de Chiapas, Tuxtla Gutierrez, Chiapas (Mexico). Energia y Sustentabilidad; Sebastian, P.J. [Politecnica Univ. de Chiapas, Chiapas (Mexico). Energia y Sustentabilidad; Centro de Investigacion en Energia, UNAM, Morelos (Mexico); Gamboa, S.A. [Centro de Investigacion en Energia, UNAM, Morelos (Mexico); Pal, U. [Inst. de Fisica, Universidad Autonoma de Puebla Univ., Puebla (Mexico). Inst. de Fisica; Gonzalez, I. [Autonoma Metropolitana Univ. (Mexico). Dept. de Quimica

    2008-07-01

    This paper reported on a study in which membrane electrode assemblies (MEAs) were fabricated by depositing Au, Pt and AuPt nanoparticles on Nafion 115 membrane for use in a proton exchange membrane fuel cell (PEMFC). A Rotating Disc Electrode (RDE) was used to measure the nanoparticle catalyst activity. After deposition of the nanoparticles on the membrane, the surface was studied by Scanning Electron Microscopy (SEM) and Energy Dispersive Spectroscopy (EDS). The membrane proton conduction process was studied by Electrochemical Impedance Spectroscopy (EIS) with the 4 probe technique. The MEAs fabricated with Nafion/Metal membranes were evaluated in a PEMFC under standard conditions. Colloidal solutions were used to prepare self-assembled electrodes with nanoparticles deposited on Nafion membrane. The particles deposited on Nafion showed good stability and had homogeneous distribution along the membrane surface. The impedance results revealed an increase in the membrane proton resistance of the self-assembled electrodes compared to unmodified Nafion. The Au-Pt nanoparticles were obtained by chemical reduction. The nanoparticle size in the three systems was about 2 nm. The self-assembled electrodes performed well in standard conditions. The optimum colloidal concentration and immersion time must be determined in order to obtain good catalytic activity and high membrane conductance. The self-assembled Nafion/AuPt had the best open circuit potential (887 mV). The Au and Pt self-assemblies showed a similar performance in terms of maximum power and maximum current density. The performance of the Nafion/Au self-assembly was influenced more by ohmic losses, particularly in the membrane. The maximum power generation was obtained at 0.35 V. The mass transport losses increased after this value, thereby affecting the efficiency of the PEMFC. 2 figs.

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

    Science.gov (United States)

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

    2016-08-17

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

  14. 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.

  15. A method for the formation of Pt metal nanoparticle arrays using nanosecond pulsed laser dewetting

    Energy Technology Data Exchange (ETDEWEB)

    Owusu-Ansah, Ebenezer; Horwood, Corie A.; Birss, Viola I.; Shi, Yujun J., E-mail: shiy@ucalgary.ca [Department of Chemistry, University of Calgary, Calgary, Alberta T2N 1N4 (Canada); El-Sayed, Hany A. [Institute for Technical Electrochemistry, Technische Universität München, D-85748 Garching (Germany)

    2015-05-18

    Nanosecond pulsed laser dewetting of Pt thin films, deposited on a dimpled Ta (DT) surface, has been studied here in order to form ordered Pt nanoparticle (NP) arrays. The DT substrate was fabricated via a simple electrochemical anodization process in a highly concentrated H{sub 2}SO{sub 4} and HF solution. Pt thin films (3–5 nm) were sputter coated on DT and then dewetted under vacuum to generate NPs using a 355 nm laser radiation (6–9 ns, 10 Hz). The threshold laser fluence to fully dewet a 3.5 nm thick Pt film was determined to be 300 mJ/cm{sup 2}. Our experiments have shown that shorter irradiation times (≤60 s) produce smaller nanoparticles with more uniform sizes, while longer times (>60 s) give large nanoparticles with wider size distributions. The optimum laser irradiation time of 1 s (10 pulses) has led to the formation of highly ordered Pt nanoparticle arrays with an average nanoparticle size of 26 ± 3 nm with no substrate deformation. At the optimum condition of 1 s and 500 mJ/cm{sup 2}, as many as 85% of the dewetted NPs were found neatly in the well-defined dimples. This work has demonstrated that pulsed laser dewetting of Pt thin films on a pre-patterned dimpled substrate is an efficient and powerful technique to produce highly ordered Pt nanoparticle arrays. This method can thus be used to produce arrays of other high-melting-point metal nanoparticles for a range of applications, including electrocatalysis, functionalized nanomaterials, and analytical purposes.

  16. 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.

  17. Soft Landing of Bare PtRu Nanoparticles for Electrochemical Reduction of Oxygen

    Energy Technology Data Exchange (ETDEWEB)

    Johnson, Grant E.; Colby, Robert J.; Engelhard, Mark H.; Moon, DaeWon; Laskin, Julia

    2015-08-07

    Magnetron sputtering of two independent Pt and Ru targets coupled with inert gas aggregation in a modified commercial source has been combined with soft landing of mass-selected ions to prepare bare 4.5 nm diameter PtRu alloy nanoparticles on glassy carbon electrodes with controlled size and morphology for electrochemical reduction of oxygen in solution. Employing atomic force microscopy (AFM) it is shown that the nanoparticles bind randomly to the glassy carbon electrode at a relatively low coverage of 7 x 104 ions µm-2 and that their average height is centered at 4 nm. Scanning transmission electron microscopy images obtained in the high-angle annular dark field mode (STEM-HAADF) further confirm that the soft-landed PtRu alloy nanoparticles are uniform in size and have a Ru core decorated with small regions of Pt on the surface. Wide-area scans of the electrodes using X-ray photoelectron spectroscopy (XPS) reveal the presence of both Pt and Ru in relative atomic concentrations of ~9% and ~33%, respectively. Deconvolution of the high energy resolution XPS spectra in the Pt4f and Ru3d regions indicates the presence of both oxidized Pt and Ru. The substantially higher loading of Ru compared to Pt and enrichment of Pt at the surface of the alloy nanoparticles is confirmed by wide-area analysis of the electrodes using time-of-flight medium energy ion scattering (TOF-MEIS) employing both 80 keV He+ and O+ ions. The activity of electrodes containing 7 x 104 ions µm-2 of bare 4.5 nm PtRu nanoparticles toward the electrochemical reduction of oxygen was evaluated employing cyclic voltammetry (CV) in 0.1 M HClO4 and 0.5 M H2SO4 solutions. In both electrolytes a pronounced reduction peak was observed during O2 purging of the solution that was not evident during purging with Ar. Repeated electrochemical cycling of the electrodes revealed little evolution in the shape or position of the voltammograms indicating high stability of the alloy nanoparticles supported on glassy

  18. Extremely stable platinum nanoparticles encapsulated in a zirconia nanocage by area-selective atomic layer deposition for the oxygen reduction reaction.

    Science.gov (United States)

    Cheng, Niancai; Banis, Mohammad Norouzi; Liu, Jian; Riese, Adam; Li, Xia; Li, Ruying; Ye, Siyu; Knights, Shanna; Sun, Xueliang

    2015-01-14

    Encapsulation of Pt nanoparticles (NPs) in a zirconia nanocage by area-selective atomic layer deposition (ALD) can significantly enhance both the Pt stability and activity. Such encapsulated Pt NPs show 10 times more stability than commercial Pt/C catalysts and an oxygen reduction reaction (ORR) activity 6.4 times greater than that of Pt/C.

  19. Nanoscaled alloy formation from self-assembled elemental Co nanoparticles on top of Pt films

    Directory of Open Access Journals (Sweden)

    Luyang Han

    2011-08-01

    Full Text Available The thermally activated formation of nanoscale CoPt alloys was investigated, after deposition of self-assembled Co nanoparticles on textured Pt(111 and epitaxial Pt(100 films on MgO(100 and SrTiO3(100 substrates, respectively. For this purpose, metallic Co nanoparticles (diameter 7 nm were prepared with a spacing of 100 nm by deposition of precursor-loaded reverse micelles, subsequent plasma etching and reduction on flat Pt surfaces. The samples were then annealed at successively higher temperatures under a H2 atmosphere, and the resulting variations of their structure, morphology and magnetic properties were characterized. We observed pronounced differences in the diffusion and alloying of Co nanoparticles on Pt films with different orientations and microstructures. On textured Pt(111 films exhibiting grain sizes (20–30 nm smaller than the particle spacing (100 nm, the formation of local nanoalloys at the surface is strongly suppressed and Co incorporation into the film via grain boundaries is favoured. In contrast, due to the absence of grain boundaries on high quality epitaxial Pt(100 films with micron-sized grains, local alloying at the film surface was established. Signatures of alloy formation were evident from magnetic investigations. Upon annealing to temperatures up to 380 °C, we found an increase both of the coercive field and of the Co orbital magnetic moment, indicating the formation of a CoPt phase with strongly increased magnetic anisotropy compared to pure Co. At higher temperatures, however, the Co atoms diffuse into a nearby surface region where Pt-rich compounds are formed, as shown by element-specific microscopy.

  20. Electroreduction of oxygen on Pt nanoparticle/carbon nanotube nanocomposites in acid and alkaline solutions

    Energy Technology Data Exchange (ETDEWEB)

    Alexeyeva, N. [Institute of Chemistry, University of Tartu, Jakobi 2, 51014 Tartu (Estonia); Tammeveski, K., E-mail: kaido@chem.ut.e [Institute of Chemistry, University of Tartu, Jakobi 2, 51014 Tartu (Estonia); Lopez-Cudero, A.; Solla-Gullon, J.; Feliu, J.M. [Instituto de Electroquimica, Universidad de Alicante, Apartado 99, 03080 Alicante (Spain)

    2010-01-01

    The kinetics of O{sub 2} reduction on novel electrocatalyst materials deposited on carbon substrates were studied in 0.5 M H{sub 2}SO{sub 4} and in 0.1 M NaOH solutions using the rotating disk electrode (RDE) technique. Pt nanoparticles (PtNP) supported on single-walled (PtNP/SWCNT) and multi-walled carbon nanotubes (PtNP/MWCNT) were prepared using two different synthetic routes. Before use, the CNTs were cleaned to minimize the presence of metal impurities coming from the catalyst used in the synthesis of this material, which can interfere in the electrochemical response of the supported Pt nanoparticles. The composite catalyst samples were characterised by transmission electron microscopy (TEM) showing a good dispersion of the particles at the surface of the carbon support and an average Pt particle size of 2.4 +- 0.7 nm in the case of Pt/CNTs prepared in the presence of citrate and of 3.8 +- 1.1 nm for Pt/CNTs prepared in microemulsion. The values of specific activity (SA) and other kinetic parameters were determined from the Tafel plots taking into account the real electroactive area of each electrode. The electrodes exhibited a relatively high electrocatalytic activity for the four-electron oxygen reduction reaction to water.

  1. Room temperature sensing of O2 and CO by atomic layer deposition prepared ZnO films coated with Pt nanoparticles

    NARCIS (Netherlands)

    Erkens, I.J.M.; Blauw, M.A.; Verheijen, M.A.; Roozeboom, F.; Kessels, W.M.M.

    2013-01-01

    Ultralow-power gas sensing devices need to operate without an energy consuming heater element. This requires the design of sensing devices that are so efficient that they can operate at room temperature (RT). Here, we report on the RT sensing performance of atomic layer deposition (ALD) prepared i-Z

  2. Synchrotron radiation based multi-scale structural characterization of CoPt{sub 3} colloidal nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Zargham, Ardalan

    2010-08-05

    Bimetallic CoPt{sub 3} nanoparticles represent a category of colloidal nanoparticles with high application potentials in, e.g., heterogeneous catalysis, sensor technology, and magnetic storage media. Deposition of this system on functionalized supports delivers opportunities for controlled immobilization of the nanoparticles. In this work, self-assembled monolayers (SAMs) of n-alkanethiol molecules served as functionalizing material for the Au covered Si substrates. Deposition of the ligand-terminated nanoparticles took place by means of spin and dip coating and has been optimized for each of the mentioned methods so that monolayers of nanoparticles on supports were fabricated with a well-controlled coverage The morphology of the nanoparticle film arranged is addressed by grazing-incidence small angle x-ray scattering (GISAXS). This together with x-ray standing waves in total external reflection (TER-XSW) enables a 3D structural characterization of such nanoparticle films, so that the mean particle size, mean distance of the arranged nanoparticle films to the substrate, as well as the mean particle-particle distance in lateral direction have been determined. TER-XSW, being an element-specific position-sensitive method, also reveals the elemental distribution of the particles which complementary provides a fundamental understanding of their internal structure. The CoPt{sub 3} nanoparticles investigated here exhibit a core-shell-like structure with cores of CoPt{sub 3} and shells mainly comprise Co. The results regarding the internal structure of the nanoparticles were then verified by extended X-ray absorption fine structure (EXAFS) measurements. (orig.)

  3. Controlled deposition and enhanced visible light photocatalytic performance of Pt-modified TiO{sub 2} nanotube arrays

    Energy Technology Data Exchange (ETDEWEB)

    Lv, Jun, E-mail: lvjun117@126.com [Laboratory of Functional Nanomaterials and Devices, School of Materials Science and Engineering, Hefei University of Technology, Hefei 230009 (China); Gao, Huazhen; Wang, Honge; Lu, Xuejun; Xu, Guangqing; Wang, Dongmei [Laboratory of Functional Nanomaterials and Devices, School of Materials Science and Engineering, Hefei University of Technology, Hefei 230009 (China); Chen, Zhong [School of Materials Science and Engineering, Nanyang Technological University (Singapore); Zhang, Xinyi [School of Chemistry, Monash University, Clayton, Vic. 3800 (Australia); Zheng, Zhixiang [Laboratory of Functional Nanomaterials and Devices, School of Materials Science and Engineering, Hefei University of Technology, Hefei 230009 (China); Wu, Yucheng, E-mail: ycwu@hfut.edu.cn [Laboratory of Functional Nanomaterials and Devices, School of Materials Science and Engineering, Hefei University of Technology, Hefei 230009 (China); Key Laboratory of Advanced Functional Materials and Devices of Anhui Province, Hefei 230009 (China)

    2015-10-01

    Graphical abstract: - Highlights: • Pt nanoparticles were deposited onto TiO{sub 2} NTAs by UV light photoreduction method. • Uniform distribution of nanoparticles was achieved by controlling deposition. • 3 Pt/TiO{sub 2} NTAs show 84.27% degradation rate after visible light irradiation. • The kinetic constant of 3 Pt/TiO{sub 2} NTAs is 0.01493 min{sup −1}. - Abstract: Highly ordered TiO{sub 2} nanotube arrays (TiO{sub 2} NTAs) have been fabricated by the potentiostatic anodization method with Ti foils. Pt nanoparticles have been successfully deposited onto TiO{sub 2} NTAs by UV light photoreduction method. In this work, X-ray diffraction, field emission scanning electron microscope, high resolution transmission electron microscopy, X-ray photoelectron spectroscopy, ultraviolet-visible spectroscopy and energy dispersive X-ray spectrometer methods were adopted to characterize the samples. The influence of different concentration of H{sub 2}PtCl{sub 6} precursor solution on the morphology and photocatalytic performances of samples was discussed. The SEM observations showed that Pt nanoparticles distributed on the wall of TiO{sub 2} nanotubes uniformly. UV–vis spectra analysis showed that the light absorption of Pt/TiO{sub 2} NTAs has been extended to the visible light range. When the concentration of H{sub 2}PtCl{sub 6} was 3 mM, the prepared sample showed the highest photodegradation rate. After irradiated under visible light for 2 h, the degradation rate of methyl orange solution reached 84.27%. Under the same condition, no obvious photodegradation of methyl orange was found for TiO{sub 2} NTAs. Kinetic research showed that photodegradation process followed the first-order reaction, the apparent reaction rate constant of 3 Pt/TiO{sub 2} NTAs was 1.493 × 10{sup −2} min{sup −1}.

  4. Green synthesis and characterization of Au@Pt core-shell bimetallic nanoparticles using gallic acid

    Science.gov (United States)

    Zhang, Guojun; Zheng, Hongmei; Shen, Ming; Wang, Lei; Wang, Xiaosan

    2015-06-01

    In this study, we developed a facile and benign green synthesis approach for the successful fabrication of well-dispersed urchin-like Au@Pt core-shell nanoparticles (NPs) using gallic acid (GA) as both a reducing and protecting agent. The proposed one-step synthesis exploits the differences in the reduction potentials of AuCl4- and PtCl62-, where the AuCl4- ions are preferentially reduced to Au cores and the PtCl62- ions are then deposited continuously onto the Au core surface as a Pt shell. The as-prepared Au@Pt NPs were characterized by transmission electron microscope (TEM); high-resolution transmission electron microscope (HR-TEM); scanning electron microscope (SEM); UV-vis absorption spectra (UV-vis); X-ray diffraction (XRD); Fourier transmission infrared spectra (FT-IR). We systematically investigated the effects of some experimental parameters on the formation of the Au@Pt NPs, i.e., the reaction temperature, the molar ratios of HAuCl4/H2PtCl6, and the amount of GA. When polyvinylpyrrolidone K-30 (PVP) was used as a protecting agent, the Au@Pt core-shell NPs obtained using this green synthesis method were better dispersed and smaller in size. The as-prepared Au@Pt NPs exhibited better catalytic activity in the reaction where NaBH4 reduced p-nitrophenol to p-aminophenol. However, the results showed that the Au@Pt bimetallic NPs had a lower catalytic activity than the pure Au NPs obtained by the same method, which confirmed the formation of Au@Pt core-shell nanostructures because the active sites on the surfaces of the Au NPs were covered with a Pt shell.

  5. 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.

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2005-12-15

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

  7. Controllable Deposition of Alloy Clusters or Nanoparticles Catalysts on Carbon Surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Sasaki, K.; Ando, Y.; Su, D.; Adzic, R.

    2011-08-15

    We describe a simple method for controllably depositing Pt-Ru alloy nanoparticles on carbon surfaces that is mediated by Pb or Cu adlayers undergoing underpotential deposition and stripping during Pt and Ru codeposition at diffusion-limiting currents. The amount of surface Pt atoms deposited largely reflects the number of potential cycles causing the deposition and stripping of the metal adlayer at underpotentials, the metal species used as a mediator, and the scan rate of the potential cycles. We employed electrochemical methanol oxidation to gain information on the catalyst's activities. The catalysts with large amounts of surface Pt atoms have relatively high methanol-oxidation activity. Catalysts prepared using this method enhance methanol-oxidation activity per electrode surface area, while maintaining catalytic activity per surface Pt atom; thus, the amount of Pt is reduced in comparison with conventional methanol-oxidation catalysts. The method is suitable for efficient synthesizing various bimetallic catalysts.

  8. 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)

  9. 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.

  10. (001) textured FePt thin films on spherical SiO{sub 2} nanoparticle template

    Energy Technology Data Exchange (ETDEWEB)

    Brombacher, Christoph; Schubert, Christian; Teichgraeber, Andreas; Hietschold, Michael; Albrecht, Manfred [Institute of Physics, TU Chemnitz, Chemnitz (Germany); Romer-Urban, Sara [Nanoscale Materials Science, Empa, Duebendorf (Switzerland); Maret, Mireille [Laboratoire de Thermodynamique et Physico-Chimie Metallurgiques, ENSEEG, Saint Martin d' Heres (France); Makarov, Denys [Department of Physics, University of Konstanz, Konstanz (Germany)

    2009-07-01

    Due to its high magnetocrystalline anisotropy and excellent corrosion resistance, FePt is considered one of the most promising candidates for future magnetic data storage devices. In this study, densely-packed arrays of SiO{sub 2} nanoparticles have been used as a template to create regular FePt nanostructures suitable for application as patterned media. The sputter deposited FePt film displays a chemically disordered fcc phase. Postannealing in a commercial RTA setup yields both a high ordering parameter and the desired (001) texture as shown by XRD and TEM. The heating rate, heating time and heating temperature have been optimized on planar SiO{sub 2} substrates, obtaining perpendicular magnetic anisotropy and coercivities of up to 2 T. Furthermore, the FePt films exhibit a strong dewetting behavior on both planar substrates and spherical nanoparticles. By tuning the thickness of the FePt layer, the characteristic length scales of the dewetting process can be controlled. This was used to create isolated FePt nanostructures on SiO{sub 2} particle arrays with periodicities down to 50 nm.

  11. Synthesis of platinum nanoparticle electrocatalysts by atomic layer deposition

    Science.gov (United States)

    Lubers, Alia Marie

    Demand for energy continues to increase, and without alternatives to fossil fuel combustion the effects on our environment will become increasingly severe. Fuel cells offer a promising improvement on current methods of energy generation; they are able to convert hydrogen fuel into electricity with a theoretical efficiency of up to 83% and interface smoothly with renewable hydrogen production. Fuel cells can replace internal combustion engines in vehicles and are used in stationary applications to power homes and businesses. The efficiency of a fuel cell is maximized by its catalyst, which is often composed of platinum nanoparticles supported on carbon. Economical production of fuel cell catalysts will promote adoption of this technology. Atomic layer deposition (ALD) is a possible method for producing catalysts at a large scale when employed in a fluidized bed. ALD relies on sequential dosing of gas-phase precursors to grow a material layer by layer. We have synthesized platinum nanoparticles on a carbon particle support (Pt/C) by ALD for use in proton exchange membrane fuel cells (PEMFCs) and electrochemical hydrogen pumps. Platinum nanoparticles with different characteristics were deposited by changing two chemistries: the carbon substrate through functionalization; and the deposition process by use of either oxygen or hydrogen as ligand removing reactants. The metal depositing reactant was trimethyl(methylcyclopentadienyl)platinum(IV). Functionalizing the carbon substrate increased nucleation during deposition resulting in smaller and more dispersed nanoparticles. Use of hydrogen produced smaller nanoparticles than oxygen, due to a gentler hydrogenation reaction compared to using oxygen's destructive combustion reaction. Synthesized Pt/C materials were used as catalysts in an electrochemical hydrogen pump, a device used to separate hydrogen fuel from contaminants. Catalysts deposited by ALD on functionalized carbon using a hydrogen chemistry were the most

  12. Electrochemical Detection of Hydroxylamine via Au-Pt Alloy Nanoparticle-modified Single-walled Carbon Nanotube Electrodes.

    Science.gov (United States)

    Geng, Yanfang; Ko, Euna; Tran, Van-Khue; Chung, Woo Sung; Park, Chan Ho; Kim, Min Ki; Jin, Ga Hyun; Seong, Gi Hun

    2017-01-01

    In the present study, we developed an electrochemical sensor for highly sensitive detection of hydroxylamine using Au-Pt alloy nanoparticles. Au-Pt alloy nanoparticles were electrochemically deposited on a working electrode made of single-walled carbon nanotubes. The framework composition in the Au-Pt alloy nanoparticle was easily controlled by adjusting the Au(3+):Pt(4+) composition ratio in the precursor solution. Morphological and chemical characterizations of the resulting Au-Pt alloy nanoparticles were performed using field emission scanning electron microscopy, X-ray diffraction, and energy dispersion X-ray spectroscopy. When the Au(3+):Pt(4+) ratio in the precursor solution was 1:5, the ratio of Au:Pt atom in alloy nanoparticle was about 6:4. Au60Pt40 alloy nanoparticles were found to have the optimum synthetic ratio for hydroxylamine detection. The electrocatalytic performance of Au-Pt alloy nanoparticles in the presence of hydroxylamine was also characterized using cyclic voltammetry, differential pulse voltammetry, and chronoamperometry. In the chronoamperometric detection of hydroxylamine, the sensor exhibited a detection limit of 0.80 μM (S/N = 3) and a high sensitivity of 184 μA mM(-1) cm(-2). Moreover, the amperometric response of the sensor in 1 mM hydroxylamine was stable for a long time (450 s). Long-term stability tests showed that the current responses to hydroxylamine were 96, 91 and 85% of the initial signal value after storage for 5, 10, and 20 days, respectively.

  13. Electrochemical oxidation of ammonia on carbon-supported bi-metallic PtM (M = Ir, Pd, SnO{sub x}) nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Lomocso, Thegy L. [Department of Chemical and Biological Engineering, University of Ottawa, 161 Louis-Pasteur, Ottawa, ON K1N 6N5 (Canada); Baranova, Elena A., E-mail: elena.baranova@uottawa.ca [Department of Chemical and Biological Engineering, University of Ottawa, 161 Louis-Pasteur, Ottawa, ON K1N 6N5 (Canada)

    2011-10-01

    Highlights: > Oxidation of NH{sub 3} is investigated on carbon-supported Pt and PtM (M = Pd, Ir, SnO{sub x}) nanoparticles. > Carbon supported PtPd and PtIr nanoparticles show higher catalytic activity if compared to Pt nanocatalyst. > Pt{sub 7}Ir{sub 3} nanoparticles combine good catalytic activity and enhanced stability for NH{sub 3} oxidation. > Electronic effect between two metals in PtIr is responsible for increase in the catalytic activity. - Abstract: Ammonia electro-oxidation was studied in alkaline solution on carbon-supported Pt and bimetallic Pt{sub y}M{sub 1-y} (M = Pd, Ir, SnO{sub x} and y = 70, 50 at.%) nanoparticles. Catalysts were synthesized using the modified polyol method and deposited on carbon, resulting in 20 wt.% of metal loading. Particle size, structure and surface composition of the particles were investigated using TEM, XRD and XPS. Mean size of PtM bi-metallic nanoparticles varied between 2.0 and 4.7 nm, depending on the second metal (M). XRD revealed the structure of all bi-metallic particles to be face-centered cubic and confirmed alloy formation for Pt{sub y}Pd{sub 1-y} (y = 70, 50 at.%) and Pt{sub 7}Ir{sub 3}nanoparticles, as well as partial alloying between Pt and SnO{sub x}. Electrochemical behaviour of ammonia on Pt and PtM nanoparticles is comparable to that expected for bulk Pt and PtM alloys. Addition of Pd to Pt at the nanoscale decreased the onset potential of ammonia oxidation if compared to pure platinum nanoparticles; however stability of the catalyst was poor. For Pt{sub 7}(SnO{sub x}){sub 3}, current densities were similar to Pt, whereas catalyst stability against deactivation was improved. It is found that carbon supported Pt{sub 7}Ir{sub 3} nanoparticles combine good catalytic activity with enhanced stability for ammonia electro-oxidation. Electronic effect generated between two metals in the bimetallic nanoparticles might be responsible for increase in the catalytic activity of Pd- and Ir-containing catalysts, causing

  14. Atomic layer deposition of platinum clusters on titania nanoparticles at atmospheric pressure

    NARCIS (Netherlands)

    Goulas, A.; Van Ommen, J.R.

    2013-01-01

    We report the fabrication of platinum nanoclusters with a narrow size distribution on TiO2 nanoparticles using atomic layer deposition. With MeCpPtMe3 and ozone as reactants, the deposition can be carried out at a relatively low temperature of 250 degrees C. Our approach of working with suspended na

  15. Explorations on size limit of L10-FePt nanoparticles for practical magnetic storage

    Directory of Open Access Journals (Sweden)

    Tao Huang

    2016-11-01

    Full Text Available With the advance of HAMR technology, the storage potential of L10-FePt nanoparticles with practical considerations are of great significance. We present an L10-FePt nanoparticle model based on atomistic spin model with Langevin thermodynamics to simulate the magnetic behaviors of L10-FePt nanoparticles at Curie temperature and room temperature to explore their practical design margins. Given specific composites, the Curie temperatures of L10-FePt nanoparticles decrease with their volume sizes decrease starting from 8 nm, meaning no more laser power increment needed for smaller L10-FePt nanoparticles. However, L10-FePt nanoparticles get unstable more easily while their volume sizes decrease at room temperature within 10 years. Above all, a reasonable size of L10-FePt nanoparticles for stable information retaining should not be less than 8 nm at a certain aspect ratio.

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

    NARCIS (Netherlands)

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

    2015-01-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2005-09-05

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

  18. Synthesis and characterization of magnetically hard Fe-Pt alloy nanoparticles and nano-islands

    Science.gov (United States)

    Hu, Xiaocao

    In this dissertation, we explored the fabrication of FePt nanoparticles and nano-islands with the face-centered tetragonal (fct, L10) phase prepared by both chemical synthesis routes and physical vapor deposition. Microstructure and magnetic properties characterizations were used to gain a fundamental understanding of the nano-structure formation and atomic ordering behavior and determine the possible applications in the next generation ultra-high density magnetic storage media. FePt nanoparticles prepared by thermal decomposition of iron pentacarbonyl [Fe(CO)5] have been widely investigated and by tuning the processing procedure monodispersed FePt nanoparticles with good assembly can be obtained. The as-made FePt nanoparticles are usually in the magnetically soft face-centered cubic (fcc) phase. To transformation to the fct phase, post-annealing at above 600°C is needed which, however, introduces undesirable agglomeration and sintering. To address this problem, we used three different fabrication processes which are discussed below. In the first fabrication experiment, the FePt nanoparticles were fabricated by a novel environmental friendly method involving crystalline saline complex hexaaquairon (II) hexachloroplatinate ([Fe(H2O)6]PtCl 6) with a special layered structure. Then the precursor was ball milled with NaCl and annealed at temperatures above 400°C under a reducing atmosphere of forming gas (95% Ar and 5% H2) FePt nanoparticles were obtained after washing away NaCl with deionized water. This method avoids the use of the very poisonous Fe(CO)5 and other organic solvents such as oleylamine and oleic acid. Instead, environmentally friendly NaCl and water were used. The size of FePt nanoparticles was controlled by varying the proportion of precursor and NaCl (from 10mg/20g to 50mg/20g). Particles with size in the range of 6.2--13.2 nm were obtained. All the nanoparticles annealed above 400°C are in the highly ordered fct phase with a coercivity range of 4

  19. 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.

  20. Characterization of self-assembled electrodes based on Au-Pt nanoparticles for PEMFC application

    Energy Technology Data Exchange (ETDEWEB)

    Valenzuela, E. [Univ. Politecnica de Chiapas (Mexico). Energia y Sustentabilidad; Sebastian, P.J.; Gamboa, S.A.; Joseph, S. [Univ. Nacional Autonoma de Mexico, Morelos (Mexico). Centrode Investigacion en Energia; Pal, U. [Univ. Autonoma de Puebla, Pue (Mexico). Inst. de Fisica; Gonzalez, I. [Univ. Autonoma Metropolitana, Mexico City (Mexico). Dept. de Quimica

    2010-07-01

    This paper described the synthesis and characterization of gold (Au), platinum (Pt) and Au-Pt nanoparticles impregnated on a Nafion membrane in a proton exchange membrane fuel cell (PEMFC). The aim of the study was to fabricate the membrane electrode assembly (MEA) by depositing the nanoparticles on the membrane using an immersion technique. Scanning electron microscopy (SEM) and energy dispersive spectroscopy (EDS) were used to study the deposition process. Electrochemical impedance spectroscopy (EIS) was used to study the membrane proton conduction process. An elemental mapping analysis was performed in order to study the location of the Au and Pt in the self-assemblies. Results of the study showed that the particles deposited on the Nafion had good stability and a homogenous distribution along the membrane surface. The particles showed a direct relation in size and location with the hydrophilic and hydrophobic distribution phases of the membrane. The main membrane resistance was located between the membrane and the electrolyte. The self-assembled electrodes demonstrated a good performance at standard conditions. 33 refs., 4 tabs., 11 figs.

  1. CoPt alloy films on SiO{sub 2} nanoparticle arrays

    Energy Technology Data Exchange (ETDEWEB)

    Makarov, Denys; Schatz, Guenter [University of Konstanz (Germany). Department of Physics; Bermudez, Esteban; Schmidt, Oliver G. [IFW, Dresden (Germany); Brombacher, Christoph; Albrecht, Manfred [Chemnitz University of Technology (Germany). Institute of Physics; Liscio, Fabiola; Maret, Mireille [ENSEEG, Saint Martin d' Heres (France)

    2008-07-01

    Combining self-assembled SiO{sub 2} nanoparticle arrays with magnetic film deposited onto the particles, enables an elegant possibility to create magnetic nanostructure arrays with defined magnetic properties. In this regard, materials such as CoPt alloy are of particular interest due to their large magnetic anisotropy required for thermal stability in the high density magnetic recording applications. In order to induce high perpendicular magnetic anisotropy in CoPt alloys, the L1{sub 0} phase with (001) texturing is required. For this purpose, a 10 nm thick MgO(001) seed layer was introduced. Results on planar amorphous SiO{sub 2} substrates reveal an uniaxial out-of-plane magnetic anisotropy and saturation magnetization for the CoPt alloy grown at 450 C of about 5x10{sup 5} J/m{sup 3} and 800 kA/m. These properties were transfered to CoPt alloy deposited onto arrays of SiO{sub 2} particles with diameters down to 50 nm. The formed CoPt nanocaps are in a magnetic single domain state with a large out-of-plane coercivity, which increases with decreasing particle size. In this presentation, the structural and magnetic properties are discussed and compared to the planar film.

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

    Science.gov (United States)

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

    2017-03-01

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

  3. Palladium Electrodeposition onto Pt(100): Two-Layer Underpotential Deposition.

    Science.gov (United States)

    Previdello, Bruno A F; Sibert, Eric; Maret, Mireille; Soldo-Olivier, Yvonne

    2017-03-07

    Electrodeposition of the first Pd layers onto Pt(100) was investigated using cyclic voltammetry at a low scan rate (0.1 mV·s(-1)). Ultrathin films were characterized by cyclic voltammetry in 0.1 M H2SO4 solution and with ex situ AFM (atomic force microscopy). For the first time, we evidenced the underpotential character of the deposition of the first two Pd layers, characterized by a two-step mechanism, each step corresponding to the deposition of a complete Pd atomic layer. For thicker deposits, especially above 10 monolayers as equivalent thickness, the electrochemical characterization displays a strong irreversibility and a broadening of the adsorption/desorption peaks, associated with a reduction of long-range ordered flat areas. Ex situ AFM images are in agreement with this description. They show rough thick deposits and the growth of (100)-oriented rectangular shaped islands with their sides aligned with the two [011] and [0-11] perpendicular directions of the (100) Pt surface.

  4. 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.

  5. Electrochemically deposited Pd-Pt and Pd-Au codeposits on graphite electrodes for electrocatalytic H2O2 reduction.

    Science.gov (United States)

    Nagaiah, Tharamani Chikka; Schäfer, Dominik; Schuhmann, Wolfgang; Dimcheva, Nina

    2013-08-20

    Improved electrocatalytic activity and selectivity for the reduction of H2O2 were obtained by electrodepositing Pd-Pt and Pd-Au on spectrographic graphite from solutions containing salts of the two metals at varying ratio. The electrocatalytic activity of the resulting binary codeposits for H2O2 reduction was evaluated by means of the redox-competition mode of scanning electrochemical microscopy (SECM) and voltammetric methods. In a potential range from 0 to -600 mV (vs. Ag/AgCl/3 M KCl) at pH 7.0 in 0.1 M phosphate citrate buffer, the electrocatalytic activity of both Pd-Pt and Pd-Au codeposits was substantially improved as compared with the identically deposited single metals suggesting an electrocatalytic synergy of the codeposits. Pd-Pt and Pd-Au codeposits were characterized by X-ray diffraction (XRD) analysis and scanning electron microscopy (SEM). Codepositing with Au caused a change of hedgehog-like shaped Pd nanoparticles into cauliflower-like nanoparticles with the particle size decreasing with increasing Au concentration. Codepositing Pd with Pt caused the formation of oblong structures with the size initially increasing with increasing Pt content. However, the particle size decreases with further increase in Pt concentration. The improved electrocatalytic capability for H2O2 reduction of the Pd-Pt electrodeposits on graphite was further demonstrated by immobilizing glucose oxidase as a basis for the development of an interference-free amperometric glucose biosensor.

  6. Improving the Ethanol Oxidation Activity of Pt-Mn Alloys through the Use of Additives during Deposition

    Directory of Open Access Journals (Sweden)

    Mohammadreza Zamanzad Ghavidel

    2015-06-01

    Full Text Available In this work, sodium citrate (SC was used as an additive to control the particle size and dispersion of Pt-Mn alloy nanoparticles deposited on a carbon support. SC was chosen, since it was the only additive tested that did not prevent Mn from co-depositing with Pt. The influence of solution pH during deposition and post-deposition heat treatment on the physical and electrochemical properties of the Pt-Mn alloy was examined. It was determined that careful control over pH is required, since above a pH of four, metal deposition was suppressed. Below pH 4, the presence of sodium citrate reduced the particle size and improved the particle dispersion. This also resulted in larger electrochemically-active surface areas and greater activity towards the ethanol oxidation reaction (EOR. Heat treatment of catalysts prepared using the SC additive led to a significant enhancement in EOR activity, eclipsing the highest activity of our best Pt-Mn/C prepared in the absence of SC. XRD studies verified the formation of the Pt-Mn intermetallic phase upon heat treatment. Furthermore, transmission electron microscopy studies revealed that catalysts prepared using the SC additive were more resistant to particle size growth during heat treatment.

  7. CO adsorption on electrode of Pt nanoparticles investigated by cyclic voltammetry and in situ FTIR spectroscopy

    Institute of Scientific and Technical Information of China (English)

    2003-01-01

    Pt nanoparticles were prepared by the chemical reduction method. The average diameter of Pt nanoparticles was determined to be 2.5 nm by TEM. The electrochemical properties of Pt nanoparticles were studied by cyclic voltammetry. In comparison with massive Pt, the oxidation current peak of CO adsorbed on Pt nanoparticles is broader. Twin adsorbates of CO on Pt nanoparticles were determined by in situ FTIRS for the first time. It has revealed that the linear and twin-bonded CO can be converted into bridge-bonded CO with the variation of electrode potential. A series of special properties of Pt nanoparticles, such as enhanced IR absorption of CO adsorbates, were also observed.

  8. 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.

  9. Electroless deposition of platinum nanoparticles in room-temperature ionic liquids.

    Science.gov (United States)

    Zhang, Da; Okajima, Takeyoshi; Lu, Dalin; Ohsaka, Takeo

    2013-09-24

    The electroless deposition of Pt nanoparticles (Pt-NPs) could be carried out by dissolving potassium tetrachloroplatinate(II) (K2[PtCl4]) in 1-ethyl-3-methylimidazolium (EMI(+)) room-temperature ionic liquids (RTILs) containing bis(trifluoromethylsulfonyl) imide (NTf2(-)) or tetrafluoroborate (BF4(-)) anion and small cations, such as H(+), K(+), and Li(+). In this case, no deposition of Pt-NPs occurred in RTILs without such small cations. The formation of Pt-NPs was only observed in RTILs containing trifluoromethanesulfonimide (HNTf2) and protons at high temperature (≥80 °C) when potassium hexachloroplatinate(IV) (K2[PtCl6]) was dissolved in the RTILs. The obtained Pt-NPs gave a characteristic absorption spectrum of ultrasmall Pt-NPs. The ultrasmall and uniform Pt-NPs of ca. 1-4 nm in diameter were produced and the Pt-NPs/EMI(+)NTf2(-) dispersion was kept stably for several months without adding any additional stabilizers or capping molecules. The identified Fourier-transform patterns along the [0 1 1] zone axis were observed for the TEM images of Pt-NPs. On the basis of the results obtained, a probable mechanism of the electroless formation of Pt-NPs is discussed.

  10. Preparation of Size-tunable, Highly Monodisperse PVP-Protected Pt-nanoparticles by Seed-mediated Growth

    Energy Technology Data Exchange (ETDEWEB)

    Koebel, Matthias Michael; Jones, Louis C.; Somorjai, Gabor A.

    2008-04-02

    We demonstrate a preparative method which produces highly-monodisperse Pt-nanoparticles of tunable size without the external addition of seed particles. Hexachloroplatinic acid is dosed slowly to an ethylene glycol solution at 120 C and reduced in the presence of a stabilizing polymer poly-N-vinylpyrollidone (PVP). Slow addition of the Pt-salt first will first lead to the formation of nuclei (seeds) which then grow further to produce larger particles of any desired size between 3 and 8nm. The amount of added hexachloroplatinic acid precursor controls the size of the final nanoparticle product. TEM was used to determine size and morphology and to confirm the crystalline nature of the nanoparticles. Good reproducibility of the technique was demonstrated. Above 7nm, the particle shape and morphology changes suddenly indicating a change in the deposition selectivity of the Pt-precursor from (100) towards (111) crystal faces and breaking up of larger particles into smaller entities.

  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. 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.

  13. Ultrathin Coating of Confined Pt Nanocatalysts by Atomic Layer Deposition for Enhanced Catalytic Performance in Hydrogenation Reactions.

    Science.gov (United States)

    Wang, Meihua; Gao, Zhe; Zhang, Bin; Yang, Huimin; Qiao, Yan; Chen, Shuai; Ge, Huibin; Zhang, Jiankang; Qin, Yong

    2016-06-13

    Metal-support interfaces play a prominent role in heterogeneous catalysis. However, tailoring the metal-support interfaces to realize full utilization remains a major challenge. In this work, we propose a graceful strategy to maximize the metal-oxide interfaces by coating confined nanoparticles with an ultrathin oxide layer. This is achieved by sequential deposition of ultrathin Al2 O3 coats, Pt, and a thick Al2 O3 layer on carbon nanocoils templates by atomic layer deposition (ALD), followed by removal of the templates. Compared with the Pt catalysts confined in Al2 O3 nanotubes without the ultrathin coats, the ultrathin coated samples have larger Pt-Al2 O3 interfaces. The maximized interfaces significantly improve the activity and the protecting Al2 O3 nanotubes retain the stability for hydrogenation reactions of 4-nitrophenol. We believe that applying ALD ultrathin coats on confined catalysts is a promising way to achieve enhanced performance for other catalysts.

  14. 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.

  15. 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...

  16. 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 ...

  17. 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.

  18. Synthesis and magnetic properties of CoPt nanoparticles

    Institute of Scientific and Technical Information of China (English)

    ZHANG Zhongyan; WANG Hao; WANG Hanbin; MO Qi; CHEN Yan; ZHANG Cong

    2006-01-01

    CoPt nanoparticles were prepared by simultaneous thermally reducing Co(CH3COO)2 and Pt(acac)2 in oleylamine with a small quantity of oleic acid. The composition of the particles was controlled by changing the amount of the reactants. Transmission electronic microscopy reveals that Co 48 Pt 52 particles with an average diameter of 8.4 nm are steadily dispersed in octane in the presence of oleylamine and oleic acid. Selected area electron diffraction indicates that the as-prepared particles have a face center cubic structure. Magnetic properties of these particles measured by a vibrate sample magnetometer yield a coercivity of 1.194×104 A·m-1 and a saturation magnetization of 5.3 emu·g-1 . After annealing at 650 ℃ for 2 h under the flowing Ar, the coercivity increases to 9.552×104 A·m-1 according to partly phase transformation from face center cubic structure to face center tetragonal structure for the nanoparticles.

  19. Production of high-performance and improved-durability Pt-catalyst /support for proton-exchange-membrane fuel cells with pulsed laser deposition

    Science.gov (United States)

    Huang, Ting-Wei; Qayyum, Hamza; Lin, Guan-Ren; Chen, Szu-yuan; Tseng, Chung-Jen

    2016-06-01

    Pulsed laser deposition in Ar atmosphere is used to deposit Pt nanoparticles onto gas diffusion layer, and its application to proton-exchange-membrane fuel cell is optimized and characterized. When used at anode side, with a Pt loading of 17 μg cm-2 the fuel-cell current density at 0.6 V reaches 1.08 A cm-2, which is close to that of a cell with the anode made by conventional slurry process using E-TEK Pt /C of 200 μg cm-2 Pt loading. The usage of Pt is decreased by 12 fold. Such a low usage of Pt prepared by pulsed laser deposition can be ascribed to the prevention of forming isolated regions that occurs with Pt /C slurry, good dispersion of Pt particles on support, and small particle sizes of 2-3 nm. Furthermore, using accelerated degradation test, it is found that the pulsed laser deposition sample retains 60% of its initial electrochemical surface area after 5000 potential cycles, much higher than that with E-TEK Pt /C, which retains only 7% of its initial electrochemical surface area. The higher electrochemical durability can be attributed to the higher degree of graphitization in the gas diffusion layer used as compared with the carbon black in E-TEK Pt /C, which leads to stronger binding of the Pt nanoparticles onto the carbon support and stronger corrosion resistance of the carbon support.

  20. Butylphenyl-functionalized Pt nanoparticles as CO-resistant electrocatalysts for formic acid oxidation.

    Science.gov (United States)

    Zhou, Zhi-You; Ren, Jie; Kang, Xiongwu; Song, Yang; Sun, Shi-Gang; Chen, Shaowei

    2012-01-28

    Butylphenyl-functionalized Pt nanoparticles (Pt-BP) with an average core diameter of 2.93 ± 0.49 nm were synthesized by the co-reduction of butylphenyl diazonium salt and H(2)PtCl(4). Cyclic voltammetric studies of the Pt-BP nanoparticles showed a much less pronounced hysteresis between the oxidation currents of formic acid in the forward and reverse scans, as compared to that on naked Pt surfaces. Electrochemical in situ FTIR studies confirmed that no adsorbed CO, a poisoning intermediate, was generated on the Pt-BP nanoparticle surface. These results suggest that functionalization of the Pt nanoparticles by butylphenyl fragments effectively blocked the CO poisoning pathway, most probably through third-body effects, and hence led to an apparent improvement of the electrocatalytic activity in formic acid oxidation.

  1. PEFC catalytic properties of Pt - Ni nanoparticles prepared by a plasma-gas-condensation

    Science.gov (United States)

    Umezawa, Michihisa; Ishikawa, Ryoichi; Miyazaki, Reona; Hihara, Takehiko

    2017-01-01

    Pt - Ni nanoparticles were fabricated via the gas phase method. Their performance as anode catalysts for the proton exchange membrane fuel cell was investigated as a function of Ni concentration. The microscopic configurations of the nanoparticles were rather heterogeneous; Pt-rich alloys existed in the core region of particles while a part of the surface layer was composed of the Ni-rich layer. Despite the Ni-rich layer in the shell region, the anode catalyst performance of the Pt - Ni nanoparticles was never deteriorated compared with that of the Pt ones. When the anode catalyst was composed of the Pt nanoparticles, a maximum power density of 112 mW/cm2 was obtained. However, 90% of the power density was still kept even when 40 at. % of Pt was replaced with Ni. The results suggest that a further decrease of Pt composition with maintaining its catalyst performance can be feasible by effective particle dispersing.

  2. The size effect of titania-supported Pt nanoparticles on the electrocatalytic activity towards methanol oxidation reaction primarily via the bifunctional mechanism

    Science.gov (United States)

    Ting, Chao-Cheng; Liu, Chung-Hsuan; Tai, Chun-Yen; Hsu, Shih-Chieh; Chao, Chih-Shuan; Pan, Fu-Ming

    2015-04-01

    We prepared Pt nanoparticles of different particle sizes by plasma enhanced atomic layer deposition (PEALD) on the native oxide surface layer of Ti thin films, and investigated the Pt particle size effect on the electrocatalytic activity towards methanol oxidation reaction (MOR) in acidic media. The average Pt nanoparticles size ranges from 3 nm to 7 nm depending on the number of the PEALD reaction cycles. The electronic interaction between Pt nanoparticles and the TiO2 support is insignificant according to x-ray photoelectron spectroscopy analyses, suggesting that the influence of the Pt particle size on the electrocatalytic activity can be mainly described by the bifunctional mechanism. From cyclic voltammetry measurements, Pt particles of smaller size have a better CO tolerance in MOR. We proposed the reaction steps for the electrooxidation of CO adspecies on Pt nanoparticles on the basis of the bifunctional mechanism. The electrode with Pt nanoparticles of ∼5 nm in size shows the best electrocatalytic performance in terms of CO tolerance and electrochemical stability.

  3. Study of PtPd Bimetallic Nanoparticles for Fuel Cell Applications

    OpenAIRE

    Esparza, Rodrigo; Santoveña,Alan; Ruíz-Baltazar, Alvaro; Angeles-Pascual,Alvaro; Bahena,Daniel; Maya-Cornejo,Jose; Ledesma-García, Janet; Pérez,Ramiro

    2017-01-01

    Bimetallic nanoparticles are of special interest for their potential applications for fuel cells, mainly for portable power applications. Among the bimetallic systems, Pt-Pd bimetallic nanoparticles have received great interest as they can be widely used as effective catalysts for various electrochemical reactions. In this work, Pt-Pd alloy bimetallic nanoparticles were synthesized through a chemical reduction method. The nanoparticles were characterized using aberration-corrected scanning/tr...

  4. Environmental transmission electron microscopy investigations of Pt-Fe2O3 nanoparticles for nucleating carbon nanotubes

    DEFF Research Database (Denmark)

    He, Maoshuai; Jin, Hua; Zhang, Lili

    2016-01-01

    Elucidating the evolution of bimetallic catalyst for nucleating carbon nanotube has been challenging. In this work, acorn-like Pt-Fe2O3 nanoparticles are developed for the growth of single-walled carbon nanotubes (SWCNTs) by chemical vapor deposition. Using in situ environmental transmission...... electron microscopy, restructuring of the acorn-like Pt-Fe2O3 nanoparticles at reaction conditions is investigated. Upon heating to reaction temperature, ε-Fe2O3 is converted to β-Fe2O3, which can be subsequently reduced to metallic Fe once introducing CO. As Pt promotes the carburization of Fe, part...

  5. 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 ...

  6. 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.

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

    Science.gov (United States)

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

    2014-08-01

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

  8. 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.

  9. High-temperature catalytic reforming of n-hexane over supported and core-shell Pt nanoparticle catalysts: role of oxide-metal interface and thermal stability.

    Science.gov (United States)

    An, Kwangjin; Zhang, Qiao; Alayoglu, Selim; Musselwhite, Nathan; Shin, Jae-Youn; Somorjai, Gabor A

    2014-08-13

    Designing catalysts with high thermal stability and resistance to deactivation while simultaneously maintaining their catalytic activity and selectivity is of key importance in high-temperature reforming reactions. We prepared Pt nanoparticle catalysts supported on either mesoporous SiO2 or TiO2. Sandwich-type Pt core@shell catalysts (SiO2@Pt@SiO2 and SiO2@Pt@TiO2) were also synthesized from Pt nanoparticles deposited on SiO2 spheres, which were encapsulated by either mesoporous SiO2 or TiO2 shells. n-Hexane reforming was carried out over these four catalysts at 240-500 °C with a hexane/H2 ratio of 1:5 to investigate thermal stability and the role of the support. For the production of high-octane gasoline, branched C6 isomers are more highly desired than other cyclic, aromatic, and cracking products. Over Pt/TiO2 catalyst, production of 2-methylpentane and 3-methylpentane via isomerization was increased selectively up to 420 °C by charge transfer at Pt-TiO2 interfaces, as compared to Pt/SiO2. When thermal stability was compared between supported catalysts and sandwich-type core@shell catalysts, the Pt/SiO2 catalyst suffered sintering above 400 °C, whereas the SiO2@Pt@SiO2 catalyst preserved the Pt nanoparticle size and shape up to 500 °C. The SiO2@Pt@TiO2 catalyst led to Pt nanoparticle sintering due to incomplete protection of the TiO2 shells during the reaction at 500 °C. Interestingly, over the Pt/TiO2 catalyst, the average size of Pt nanoparticles was maintained even after 500 °C without sintering. In situ ambient pressure X-ray photoelectron spectroscopy demonstrated that the Pt/TiO2 catalyst did not exhibit TiO2 overgrowth on the Pt surface or deactivation by Pt sintering up to 600 °C. The extraordinarily high stability of the Pt/TiO2 catalyst promoted high reaction rates (2.0 μmol · g(-1) · s(-1)), which was 8 times greater than other catalysts and high isomer selectivity (53.0% of C6 isomers at 440 °C). By the strong metal-support interaction

  10. Perpendicular coercivity enhancement of CoPt/TiN films by nitrogen incorporation during deposition

    Science.gov (United States)

    An, Hongyu; Wang, Jian; Szivos, Janos; Harumoto, Takashi; Sannomiya, Takumi; Muraishi, Shinji; Safran, Gyorgy; Nakamura, Yoshio; Shi, Ji

    2015-11-01

    The effect of N incorporation on the structure and magnetic properties of CoPt thin films deposited on glass substrates with TiN seed layers has been investigated. During the deposition of CoPt, introducing 20% N2 into Ar atmosphere promotes the (001) texture and enhances the perpendicular coercivity of CoPt film compared with the film deposited in pure Ar and post-annealed under the same conditions. From the in situ x-ray diffraction results, it is confirmed that N incorporation expands the lattice parameter of CoPt, which favors the epitaxial growth of CoPt on TiN. During the post-annealing process, N releases from CoPt film and promotes the L10 ordering transformation of CoPt.

  11. Perpendicular coercivity enhancement of CoPt/TiN films by nitrogen incorporation during deposition

    Energy Technology Data Exchange (ETDEWEB)

    An, Hongyu; Harumoto, Takashi; Sannomiya, Takumi; Muraishi, Shinji; Nakamura, Yoshio; Shi, Ji, E-mail: Shi.j.aa@m.titech.ac.jp [Department of Metallurgy and Ceramics Science, Tokyo Institute of Technology, 2-12-1, Ookayama, Meguro-ku, Tokyo 152-8552 (Japan); Wang, Jian [National Institute for Materials Science (NIMS), Sengen 1-2-1, Tsukuba, Ibaraki 305-0047 (Japan); Szivos, Janos; Safran, Gyorgy [Hungarian Academy of Sciences, Research Institute for Technical Physics and Materials Science, H-1121 Budapest, Konkoly-Thege ut 29-33 (Hungary)

    2015-11-28

    The effect of N incorporation on the structure and magnetic properties of CoPt thin films deposited on glass substrates with TiN seed layers has been investigated. During the deposition of CoPt, introducing 20% N{sub 2} into Ar atmosphere promotes the (001) texture and enhances the perpendicular coercivity of CoPt film compared with the film deposited in pure Ar and post-annealed under the same conditions. From the in situ x-ray diffraction results, it is confirmed that N incorporation expands the lattice parameter of CoPt, which favors the epitaxial growth of CoPt on TiN. During the post-annealing process, N releases from CoPt film and promotes the L1{sub 0} ordering transformation of CoPt.

  12. 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...

  13. Monte Carlo Simulations of Segregation in Pt-Ni Catalyst Nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

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

    2004-04-01

    We have investigated the segregation of Pt atoms in the surfaces of Pt-Ni nanoparticles, using Modified Embedded Atom Model potentials and the Monte Carlo method. The nanoparticles are assumed to have disordered fcc configurations at two fixed overall concentrations (50 at. percent Pt and 75 at. percent Pt). We use four kinds of nanoparticle shapes [cube, tetrahedron, octahedron, and cubo-octahedron] terminated by {l_brace}111{r_brace} and {l_brace}100{r_brace} facets to examine the extent of the Pt segregation to the nanoparticle surfaces and determine the equilibrium structures of Pt-Ni nanoparticles at T=600 K. The model particles contain between 560 and 4631 atoms (particle size ranging from 2.5 to 5 nm). Our results imply that a complete (100)-facet reconstruction could make the cubo-octahendral Pt-Ni nanoparticles most energetically favorable, consistent with experimental observations. We predict that at 600 K due to segregation the equilibrium Pt50Ni50 nanoparticles with fewer than 2000 atoms and Pt75Ni25 nano particles with fewer than 4000 atoms would achieve a surface-sandwich structure, in which the Pt atoms are enriched in the outermost and third atomic shells while the Ni atoms are enriched in the second atomic shell. We also find that due to an order-disorder transition the Pt50Ni50 cubo-octahedral nanoparticles containing more than 2000 atoms would form a core-shell structure with a Pt-enriched surface and a Pt-deficient homogeneous core.

  14. Thermally Stable Nanocatalyst for High Temperature Reactions: Pt-Mesoporous Silica Core-Shell Nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Joo, Sang Hoon; Park, J.Y.; Tsung, C.-K.; Yamada, Y.; Yang, P.; Somorjai, G.A.

    2008-10-25

    Recent advances in colloidal synthesis enabled the precise control of size, shape and composition of catalytic metal nanoparticles, allowing their use as model catalysts for systematic investigations of the atomic-scale properties affecting catalytic activity and selectivity. The organic capping agents stabilizing colloidal nanoparticles, however, often limit their application in high-temperature catalytic reactions. Here we report the design of a high-temperature stable model catalytic system that consists of Pt metal core coated with a mesoporous silica shell (Pt{at}mSiO{sub 2}). While inorganic silica shells encaged the Pt cores up to 750 C in air, the mesopores directly accessible to Pt cores made the Pt{at}mSiO{sub 2} nanoparticles as catalytically active as bare Pt metal for ethylene hydrogenation and CO oxidation. The high thermal stability of Pt{at}mSiO{sub 2} nanoparticles permitted high-temperature CO oxidation studies, including ignition behavior, which was not possible for bare Pt nanoparticles because of their deformation or aggregation. The results suggest that the Pt{at}mSiO{sub 2} nanoparticles are excellent nanocatalytic systems for high-temperature catalytic reactions or surface chemical processes, and the design concept employed in the Pt{at}mSiO{sub 2} core-shell catalyst can be extended to other metal-metal oxide compositions.

  15. Structure of carbon-supported Pt-Ru nanoparticles and their electrocatalytic behavior for hydrogen oxidation reaction

    Energy Technology Data Exchange (ETDEWEB)

    Velazquez, Amado; Centellas, Francesc; Garrido, Jose Antonio; Arias, Conchita; Rodriguez, Rosa Maria; Brillas, Enric; Cabot, Pere-Lluis [Laboratori d' Electroquimica dels Materials i del Medi Ambient, Departament de Quimica Fisica, Universitat de Barcelona, Marti i Franques 1-11, 08028 Barcelona (Spain)

    2010-02-01

    The electrochemical activity towards hydrogen oxidation reaction (HOR) of a high performance carbon-supported Pt-Ru electrocatalyst (HP 20 wt.% 1:1 Pt-Ru alloy on Vulcan XC-72 carbon black) has been studied using the thin-film rotating disk electrode (RDE) technique. The physical properties of the Pt-Ru nanoparticles in the electrocatalyst were previously determined by transmission electron microscopy (TEM), high resolution TEM, fast Fourier transform (FFT), electron diffraction and X-ray diffraction (XRD). The corresponding compositional and size-shape analyses indicated that nanoparticles generally presented a 3D cubo-octahedral morphology with about 26 at.% Ru in the lattice positions of the face-centred cubic structure of Pt. The kinetics for HOR was studied in a hydrogen-saturated 0.5 M H{sub 2}SO{sub 4} solution using thin-film electrodes prepared by depositing an ink of the electrocatalyst with different Nafion contents in a one-step process on a glassy carbon electrode. A maximum electrochemically active surface area (ECSA) of 119 m{sup 2} g Pt{sup -1} was found for an optimum Nafion composition of the film of about 35 wt.%. The kinetic current density in the absence of mass transfer effects was 21 mA cm{sup -2}. A Tafel slope of 26 mV dec{sup -1}, independent of the rotation rate and Nafion content, was always obtained, evidencing that HOR behaves reversibly. The exchange current density referred to the ECSA of the Pt-Ru nanoparticles was 0.17 mA cm{sup -2}, a similar value to that previously found for analogous inks containing pure Pt nanoparticles. (author)

  16. 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.

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

    Directory of Open Access Journals (Sweden)

    Zongya Zhao

    2016-11-01

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

  18. Transition from superparamagnetism to correlated ferromagnetism in Pt capped Co nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Ebbing, Astrid; Petracic, Oleg [Institut fuer Experimentalphysik/Festkoerperphysik, Ruhr-Universitaet Bochum, 44780 Bochum (Germany); Agudo, Leonardo; Eggeler, Gunther [Institut fuer Werkstoffe, Ruhr-Universitaet Bochum, 44780 Bochum (Germany)

    2011-07-01

    In this work we show that by capping Co nanoparticles with small amounts of Pt drastic changes of the magnetic properties can be induced. The magnetic properties were investigated using superconducting quantum interference device (SQUID) magnetometry. We find that for zero and for very small amounts of Pt (nominal thickness t(Pt) < 0.7 nm) the nanoparticles behave superparamagnetic. With increasing t(Pt) the blocking temperature is enhanced from 15 K up to 110 K. However, for values t(Pt) > 1 nm a strongly coupled state is encountered resembling a ferromagnet with T{sub c} values > 300 K.

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

    Science.gov (United States)

    Saravanan, Gengan; Mohan, Subramanian

    2016-11-01

    Economically viable electrochemical approach has been developed for the synthesis of Pt nanoparticles through electrodeposition technique on the surface of Reduced Graphite Oxide (RGO). Pt nanoparticles embedded Reduced Graphite Oxide on Glassy Carbon Electrode are employed (Pt-rGO/GCE) for electrooxidation of formic acid. Scanning Electron Microscopy (SEM) image and Transmission Electron Microscopy (TEM) image shows that reduced graphite oxide act as an excellent support to anchor the Pt nanoparticles. Cyclic voltammetry results confirmed that Pt-rGO/GCE enhanced current density as many folds than that of bare platinum electrode for electrooxidation of formic acid. X-ray diffraction (XRD) patterns for Pt-graphene composites illustrate that peaks at 69.15 and 23° for Pt (220) and graphene carbon (002) respectively. 13C NMR spectrum of the electrochemically reduced graphite oxide resonance contains only one peak at 133 ppm which retains graphitic sp2 carbon and does not contain any oxygenated carbon and the carbonyl carbons.

  20. Pt nanoparticles on titania nanotubes prepared by vapor-phase impregnation-decomposition method

    Energy Technology Data Exchange (ETDEWEB)

    Encarnacion Gomez, C. [National Polytechnic Institute, Dept. of Metallurgical Eng., Mexico 07300 DF, AP 75-874 (Mexico); Vargas Garcia, J.R., E-mail: rvargasga@ipn.m [National Polytechnic Institute, Dept. of Metallurgical Eng., Mexico 07300 DF, AP 75-874 (Mexico); Toledo Antonio, J.A.; Cortes Jacome, M.A.; Angeles Chavez, C. [Petroleum Mexican Institute, Eje Central Lazaro Cardenas No. 152, Mexico 07730 DF (Mexico)

    2010-04-16

    Platinum (Pt) nanoparticles were prepared on titania nanotubes (TNTs) by vapor-phase impregnation-decomposition method using platinum acetylacetonate as precursor. TNTs and Pt precursor were mixed in 3:1 weight ratio before vapor-phase impregnation. The mixed powders were heated at 453 K for 10 min to evaporate the precursor in a horizontal tube quartz reactor at a total pressure of 66.6 kPa. Then, the impregnated TNTs were moved to a higher temperature zone (673 K) inside the tube reactor to achieve the precursor decomposition. HAADF-STEM observations, AAS and XPS results revealed that this method allows the formation of uniformly distributed Pt nanoparticles on the surface of TNTs with a narrow distribution of particle size (2.1 nm mean size). Pt nanoparticles remain mainly as Pt{sup 0} oxidation state with a Pt{sup 0}/Pt{sup 2+} atomic ratio of 3.9.

  1. 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)

  2. 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)

  3. Structural and Magnetic model of self-assembled FePt nanoparticle arrays

    Energy Technology Data Exchange (ETDEWEB)

    Thomson, T

    2004-05-13

    Chemically ordered, self-assembled FePt nanoparticle arrays with high magnetic anisotropy are considered a candidate medium for data storage beyond 1 Tbit/in{sup 2}. We report comprehensive structural and magnetic studies on thin (3 layer) assemblies of polyethylenimine (PEI) and 4 nm Fe{sub 58}Pt{sub 42} nanoparticles using X-ray diffraction, small angle neutron scattering and magnetometry. We show that prior to annealing FePt nanoparticles in the PEI-FePt assembly consist of a metallic, magnetic core surrounded by a weakly magnetic or non-magnetic shell. High temperature annealing creates the desired L1{sub 0} chemical ordering and results in high coercivity FePt nanoparticles. However, we find that the high temperatures necessary to establish full chemical ordering leads to particle sintering and agglomeration. Understanding the magnetic and physical properties of these assemblies allows future research directions to be clarified for nanoparticle arrays as data storage media.

  4. 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).

  5. 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)

  6. Synthesis of Platinum Nanoparticles from K2PtCl4 Solution Using Bacterial Cellulose Matrix

    Directory of Open Access Journals (Sweden)

    H. F. Aritonang

    2014-01-01

    Full Text Available Platinum (Pt nanoparticles have been synthesized from a precursor solution of potassium tetrachloroplatinate (K2PtCl4 using a matrix of bacterial cellulose (BC. The formation of Pt nanoparticles occurs at the surface and the inside of the BC membrane by reducing the precursor solution with a hydrogen gas reductant. The Pt nanoparticles obtained from the variations of precursor concentration, between 3 mM and 30 mM, and the formation of Pt nanoparticles have been studied using X-ray diffraction (XRD, scanning electron microscopy-energy dispersive X-ray spectroscopy (SEM-EDS, and thermogravimetry analysis (TGA. Based on X-ray diffraction patterns, Pt particles have sizes between 6.3 nm and 9.3 nm, and the Pt particle size increases with an increase in precursor concentration. The morphology of the Pt nanoparticles was observed by SEM-EDS and the content of Pt particles inside the membrane is higher than that on the surface of BC membranes. This analysis corresponds to the TGA analysis, but the TGA analysis is more representative in how it describes the content of Pt particles in the BC membrane.

  7. Microbial synthesis of bimetallic PdPt nanoparticles for catalytic reduction of 4-nitrophenol.

    Science.gov (United States)

    Tuo, Ya; Liu, Guangfei; Dong, Bin; Yu, Huali; Zhou, Jiti; Wang, Jing; Jin, Ruofei

    2017-02-01

    Bimetallic nanoparticles are generally believed to have improved catalytic activity and stability due to geometric and electronic changes. In this work, biogenic-Pd (bio-Pd), biogenic-Pt (bio-Pt), and biogenic-PdPt (bio-PdPt) nanoparticles were synthesized by Shewanella oneidensis MR-1 in the absence or presence of quinone. Compared with direct microbial reduction process, the addition of anthraquinone-2,6-disulfonate (AQDS) could promote the reduction efficiency of Pd(II) or/and Pt(IV) and result in decrease of particles size. All kinds of nanoparticles could catalyze 4-nitrophenol reduction by NaBH4 and their catalytic activities took the following order: bio-PdPt (AQDS) ∼ bio-PdPt > bio-Pd (AQDS) > bio-Pd > bio-Pt (AQDS) ∼ bio-Pt. Moreover, the bio-PdPt (AQDS) nanoparticles could be reused for 6 cycles. We believe that this simple and efficient biosynthesis approach for synthesizing bimetallic bio-PdPt nanocatalysts is important for preparing active and stable catalysts.

  8. Direct synthesis of water dispersible superparamagnetic TGA capped FePt nanoparticles: One pot, one shot

    Energy Technology Data Exchange (ETDEWEB)

    Jha, Deepak K. [Department of Physics, Tezpur University (Central University), Tezpur 784028 (India); Varadarajan, Komanduri S.; Patel, Anant B. [Center for Cellular and Molecular Biology, Uppal Road, Hyderabad 500007 (India); Deb, Pritam, E-mail: pdeb@tezu.ernet.in [Department of Physics, Tezpur University (Central University), Tezpur 784028 (India)

    2015-04-15

    Thioglycolic acid (TGA) capped hydrophilic fcc-FePt magnetic nanoparticles (MNPs) were directly synthesized by a facile one pot polyol method. Thioglycolic acid (TGA) was used to functionalize the nanoparticles by incorporating thiol group onto the surface. It helped in the preparation of highly stable dispersions of nanoparticles with spherical morphology. A possible formation mechanism for these FePt MNPs, depending on the role of TGA, was proposed. The as-prepared FePt MNPs possessed a face centered cubic structure with an average size of 6 ± 1 nm and superparamagnetic property at room temperature. MRI study showed that these MNPs exhibited a transverse relaxivity of ∼600 mg{sup −1} ml s{sup −1}, superior to that of reported iron oxide nanoparticles. - Highlights: • One pot synthesis of TGA capped hydrophilic FePt superparamagnetic nanoparticles. • Role of TGA molecules in the formation of FePt nanoparticles. • EDX reveals the equiatomic ratio of Fe and Pt atoms in FePt nanoparticles. • The HR-TEM exhibits spherical nanoparticles with a narrow size distribution. • High transverse relaxivity suggesting as potential MRI contrast agent.

  9. Underpotential Deposition of Silver on Pt(111). Part 1. Concentration Dependence

    Science.gov (United States)

    1990-01-01

    AD-A236 692 Underpotential Deposition of Silver on Pt(111): Part I. Concentration Dependence r T ~.J.F. Rodriguez, D.L. Taylor and H.D. Abruhla* EL...dependence of the underpotential deposition of silver on well-defined Pt(111) electrodes. Electrochemical as well as ultra high vacuum surface...silver are deposited at underpotentials but the stability of the second layer is a strong function of the silver ion concentration in solution. When

  10. The Effects of Organic Adsorbates on the Underpotential Deposition of Silver on Pt(111) Electrodes

    Science.gov (United States)

    1993-01-01

    CV) The Effects of Organic Adsorbates on the Underpotential Deposition W.0 of Silver on Pt(111) Electrodes _• D. L. Taylor and H. D. Abruxla* D TIC...to determine the effects of competing organic adsorbates on the underpotential deposition of silver on Pt(111). The adsorbates studied are known to...hcis )n appive tor pubic release and sal Its distribution is unlimited. fu .. 93-12456 INTRODUCTION The process of underpotential deposition (UPD) of

  11. 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.

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2016-11-15

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

  13. Magnetic properties of the alloy system Fe-Pt. Bulk materials and nanoparticles; Magnetische Eigenschaften des Legierungssystems Fe-Pt. Volumenmaterialien und Nanopartikel

    Energy Technology Data Exchange (ETDEWEB)

    Antoniak, C.

    2007-12-14

    Besides the determination of magnetic properties of epitaxial grown Fe{sub x}Pt{sub 1-x} films like e.g. the magnetic anisotropy, effective magnetisation, exchange length and damping as reference data, wet-chemically synthesised spherical Fe{sub x}Pt{sub 1-x} nanoparticles with different sizes, compositions and crystal structures were examined systematically after the reduction of Fe oxides by a hydrogen plasma treatment. Organic ligands surrounding the particles after the synthesis, were removed as well during this procedure. These ligands prevent the agglomeration of the nanoparticles when deposited onto a substrate, but do not have any measurable effect on the oxide formation under air exposure and do not change the magnetic properties of oxidised nanoparticles within experimental error bars. Static and dynamic magnetic properties were determined using the ferromagnetic resonance technique and themeasurement of the x-ray absorption, especially the analysis of the X-ray circular dichroism. The analysis of the element-specific magnetic moments shows that the effective magnetic spin moment ({mu}{sup eff}{sub s}) of the Fe{sub x}Pt{sub 1-x} nanoparticles is reduced by 20.30% with respect to the one of the corresponding Fe{sub x}Pt{sub 1-x} film due to the inhomogeneous composition within the nanoparticles which was found by the analysis of the extended X-ray absorption fine structure. With decreasing particle size, {mu}{sup eff}{sub s} is further decreasing while the ratio of orbital-to-effective-spin magnetic moment ({mu}{sub l}/{mu}{sup eff}{sub s}) increases. Annealing at 600 C of a sample consisting of Fe{sub 0.50}Pt{sub 0.50} nanoparticles with a mean diameter around 6 nm yields a strong increase of the {mu}{sub l}/{mu}{sup eff}{sub s} ratio at the Fe sites: it reaches a value of about 9% and is as large as the value at the Pt sites. This is accompanied by an enhancement of the coercive field from (36{+-}5) mT to (292{+-}8) mT after annealing that can be

  14. Sonochemical deposition of platinum nanoparticles on polymer beads and their transfer on the pore surface of a silica matrix.

    Science.gov (United States)

    Chave, Tony; Grunenwald, Anthony; Ayral, André; Lacroix-Desmazes, Patrick; Nikitenko, Sergey I

    2013-04-01

    This study reported the sonochemical deposition of platinum on the surface of polystyrene beads (PSBs) and the transfer of obtained Pt nanoparticles into a porous silica matrix using the PSB as a sacrificial template. Platinum nanoparticle deposition was ensured by the sonochemical reduction of Pt(IV) at room temperature in latex solutions containing polystyrene beads in the presence of formic acid under Ar or under Ar/CO atmosphere without any additives. After ultrasonic treatments for few hours, well dispersed Pt nanoparticles within the range of 3-5 nm deposited on PSB were obtained in both studied conditions. Samples were then mixed with TEOS, dried, and heated at 450°C to ensure the PSB removal from the silica matrix. TEM and SEM results clearly show that final silica pore size is within the same order of magnitude than initial PSB. Finally, platinum decorated silica matrix with chosen pore sizes was successfully prepared.

  15. 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.

  16. The synthesis of Pt/Ag bimetallic nanoparticles using a successive solution plasma process.

    Science.gov (United States)

    Kim, Sung Min; Lee, Sang Yul; Lee, Min Hyung; Kim, Jung Wan

    2014-12-01

    A successive solution plasma process was developed for the synthesis of Pt/Ag bimetallic nanoparticles. Ag nanoparticles were made first by applying a high voltage of bipolar pulsed DC to anode and cathode electrodes composed of Ag rods. The solution containing Ag nanoparticles was discharged successively using Pt electrodes. The joule heating and electrolysis between electrodes generated vapors, and solution plasma was sustained due to progressive ionization and excitation in the vapor phase. The maximum current and voltage breakdown was observed at approximately 8.9 A and 900 V with an interval of 25 μs, which indicated that an intense solution plasma was sustained continuously. The Pt-on-Ag heterogeneous nanostructures formed, and finally, the Ag nanoparticles were completely covered by Pt nanoparticles after a discharge duration of 1,200 s.

  17. Self-Decoration of PtNi Alloy Nanoparticles on Multiwalled Carbon Nanotubes for Highly Efficient Methanol Electro-Oxidation

    Institute of Scientific and Technical Information of China (English)

    Yu-Yan Zhou; Chang-Hai Liu; Jie Liu; Xin-Lei Cai; Ying Lu; Hui Zhang; Xu-Hui Sun; Sui-Dong Wang

    2016-01-01

    A simple one-pot method was developed to prepare PtNi alloy nanoparticles, which can be self-decorated on multiwalled carbon nanotubes in [BMIm][BF4] ionic liquid. The nanohybrids are targeting stable nanocatalysts for fuel cell applications. The sizes of the supported PtNi nanoparticles are uniform and as small as 1–2 nm. Pt-to-Ni ratio was controllable by simply selecting a PtNi alloy target. The alloy nanoparticles with Pt-to-Ni ratio of 1:1 show high catalytic activity and stability for methanol electro-oxidation. The performance is much higher compared with those of both Pt-only nanoparticles and commercial Pt/C catalyst. The electronic structure characterization on the PtNi nanoparticles demon-strates that the electrons are transferred from Ni to Pt, which can suppress the CO poisoning effect.

  18. Pt-Pd bimetallic nanoparticles on MWCNTs: catalyst for hydrogen peroxide electrosynthesis

    Energy Technology Data Exchange (ETDEWEB)

    Felix-Navarro, R. M., E-mail: moi6salazar@hotmail.com; Beltran-Gastelum, M.; Salazar-Gastelum, M. I.; Silva-Carrillo, C.; Reynoso-Soto, E. A.; Perez-Sicairos, S.; Lin, S. W. [Centro de Graduados e Investigacion, Instituto Tecnologico de Tijuana (Mexico); Paraguay-Delgado, F. [Centro de Investigacion en Materiales Avanzados (Mexico); Alonso-Nunez, G. [Centro de Nanociencias y Nanotecnologia (Mexico)

    2013-08-15

    Bimetallic nanoparticles of Pt-Pd were deposited by the microemulsion method on a multiwall carbon nanotube (MWCNTs) to obtain a Pt-Pd/MWCNTs for electrocatalytic reduction of O{sub 2} to H{sub 2}O{sub 2}. The activity and selectivity of the catalyst was determined qualitatively by the rotating disk electrode method in acidic medium. The catalyst was spray-coated onto a reticulated vitreous carbon substrate and quantitatively was tested in bulk electrolysis for 20 min under potentiostatic conditions (0.5 V vs Ag/AgCl) in a 0.5 M H{sub 2}SO{sub 4} electrolyte using dissolved O{sub 2}. The bulk electrolysis experiments show that the Pt-Pd/MWCNTs catalyst is more efficient for H{sub 2}O{sub 2} electrogeneration than a MWCNTs catalyst. Nitrobenzene degradation by electrogenerated H{sub 2}O{sub 2} alone and Electro-Fenton process were also tested. Our results show that both processes decompose nitrobenzene, but the Electro-Fenton process does it more efficiently. The prepared nanoparticulated catalyst shows a great potential in environmental applications.

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

    Institute of Scientific and Technical Information of China (English)

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

    2012-01-01

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

  20. Synthesis of carbon-supported PtRh random alloy nanoparticles using electron beam irradiation reduction method

    Science.gov (United States)

    Matsuura, Yoshiyuki; Seino, Satoshi; Okazaki, Tomohisa; Akita, Tomoki; Nakagawa, Takashi; Yamamoto, Takao A.

    2016-05-01

    Bimetallic nanoparticle catalysts of PtRh supported on carbon were synthesized using an electron beam irradiation reduction method. The PtRh nanoparticle catalysts were composed of particles 2-3 nm in size, which were well dispersed on the surface of the carbon support nanoparticles. Analyses of X-ray diffraction and scanning transmission electron microscopy-energy-dispersive X-ray spectroscopy revealed that the PtRh nanoparticles have a randomly alloyed structure. The lattice constant of the PtRh nanoparticles showed good correlation with Vegard's law. These results are explained by the radiochemical formation process of the PtRh nanoparticles. Catalytic activities of PtRh/C nanoparticles for ethanol oxidation reaction were found to be higher than those obtained with Pt/C.

  1. Dispersion of Pt Nanoparticle-Doped Reduced Graphene Oxide Using Aniline as a Stabilizer

    Directory of Open Access Journals (Sweden)

    Hyoung-Joon Jin

    2012-12-01

    Full Text Available In this study, a simple one-step method was developed to load small-sized Pt nanoparticles (3.1 ± 0.3 nm in large quantities (50 wt % on aniline-functionalized and reduced graphene oxide (r-fGO. In the process, an ethylene glycol solution and aniline-functionalized moiety play the roles of reducing agent and stabilizer for the Pt nanoparticles, respectively, without damaging the graphite structures of the r-fGO. The Pt nanoparticles loading on the surface of r-fGO with uniform dispersion have a great effect on the electrical conductivity.

  2. The effect of Rhδ+ dopant in SrTiO3 on the active oxidation state of co-catalytic Pt nanoparticles in overall water splitting

    NARCIS (Netherlands)

    Zoontjes, M.G.C.; Han, K.; Huijben, M.; Wiel, van der W.G.; Mul, G.

    2016-01-01

    We report on the oxidation state of Pt nanoparticles when deposited on SrTiO3 or Rh-doped SrTiO3 under realistic solar water-splitting conditions. The oxidation state was investigated using state-of-the-art analysis of the reaction in a continuously stirred tank reactor (CSTR) connected to a micro g

  3. Fabrication of Pt deposited on carbon nanotubes and performance of its polymer electrolyte membrane fuel cells

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    A new method of depositing nano-sized Pt particles on the surface of the carbon nano-tubes was introduced, and the performance of Pt/carbon nanotube compound on polymer electrolyte membrane fuel cells was measured. The experimental results show that the fine platinum particles (about 3 nm) were well dispersed on carbon nanotubes, which demonstrates the excellent catalytic properties of the Pt/CNTs compound in polymer electrolyte membrane fuel cells.

  4. Shear instabilities in metallic nanoparticles: hydrogen-stabilized structure of Pt37 on carbon.

    Science.gov (United States)

    Wang, Lin-Lin; Johnson, D D

    2007-03-28

    Using density functional theory calculations, we have studied the morphology of a Pt37 nanoparticle supported on carbon with and without hydrogen (H) passivation that arises with postprocessing of nanoparticles before characterization. Upon heating in an anneal cycle, we find that without H (e.g., in a helium atmosphere or evacuation at high temperature), the morphology change of a truncated cuboctahedral Pt37 is driven by the shearing of (100) to (111) facets to lower the surface energy, a remnant shear instability that drives surface reconstruction in semi-infinite Pt(100). With H passivation from a postprocessing anneal, we show that the sheared structure automatically reverts to the observed truncated cuboctahedral structure and the average first nearest-neighbor Pt-Pt bond length increases by 3%, agreeing well with experiment. We explain the stabilization of the truncated cuboctahedral structure due to H passivation via adsorption energetics of hydrogen on Pt(100) and (111) facets, specifically, the preference for H adsorption at bridge sites on (100) facets, which should be considered in a realistic model for H adsorption on Pt nanoparticles. We find that dramatic morphological change of a nanoparticle can occur even with small changes to first-shell Pt-Pt coordination number. The implications of our findings when comparing to experimental data are discussed.

  5. The formation mechanism of bimetallic PtRu alloy nanoparticles in solvothermal synthesis.

    Science.gov (United States)

    Mi, Jian-Li; Nørby, Peter; Bremholm, Martin; Becker, Jacob; Iversen, Bo B

    2015-10-21

    An understanding of the nucleation and growth mechanism of bimetallic nanoparticles in solvothermal synthesis is important for further development of nanoparticles with tailored nanostructures and properties. Here the formation of PtRu alloy nanoparticles in a solvothermal synthesis using metal acetylacetonate salts as precursors and ethanol as both the solvent and reducing agent has been studied by in situ synchrotron radiation powder X-ray diffraction (SR-PXRD). Unlike the classical mechanism for the synthesis of monodisperse sols, the nucleation and growth processes of bimetallic PtRu nanoparticles occur simultaneously under solvothermal conditions. In the literature co-reduction of Pt and Ru is often assumed to be required to form PtRu bimetallic nanocrystals, but it is shown that monometallic Pt nanocrystals nucleate first and rapidly grow to an average size of 5 nm. Subsequently, the PtRu bimetallic alloy is formed in the second nucleation stage through a surface nucleation mechanism related to the reduction of Ru. The calculated average crystallite size of the resulting PtRu nanocrystals is smaller than that of the primary Pt nanocrystals due to the large disorder in the PtRu alloyed structure.

  6. Optical properties of PMN-PT thin films prepared using pulsed laser deposition

    Energy Technology Data Exchange (ETDEWEB)

    Tong, X.L., E-mail: tongxinglin@yahoo.com.cn [Key Laboratory of Fiber Optic Sensing Technology and Information Processing, Wuhan University of Technology, Ministry of Education, 122 Luoshi Road, Wuhan 430070 (China); Lin, K.; Lv, D.J.; Yang, M.H.; Liu, Z.X.; Zhang, D.S. [Key Laboratory of Fiber Optic Sensing Technology and Information Processing, Wuhan University of Technology, Ministry of Education, 122 Luoshi Road, Wuhan 430070 (China)

    2009-06-30

    (1 - x)Pb(Mg{sub 1/3}Nb{sub 2/3})O{sub 3}-xPbTiO{sub 3} (PMN-PT) thin films have been deposited on quartz substrates using pulsed laser deposition (PLD). Crystalline microstructure of the deposited PMN-PT thin films has been investigated with X-ray diffraction (XRD). Optical transmission spectroscopy and Raman spectroscopy are used to characterize optical properties of the deposited PMN-PT thin films. The results show that the PMN-PT thin films of perovskite structure have been formed, and the crystalline and optical properties of the PMN-PT thin films can be improved as increasing the annealing temperature to 750 deg. C, but further increasing the annealing temperature to 950 deg. C may lead to a degradation of the crystallinity and the optical properties of the PMN-PT thin films. In addition, a weak second harmonic intensity (SHG) has been observed for the PMN-PT thin film formed at the optimum annealing temperature of 750 deg. C according to Maker fringe method. All these suggest that the annealing temperature has significant effect on the structural and optical properties of the PMN-PT thin films.

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

    Science.gov (United States)

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

    2016-09-01

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

  8. Nanoparticle cluster gas sensor: Pt activated SnO2 nanoparticles for NH3 detection with ultrahigh sensitivity.

    Science.gov (United States)

    Liu, Xu; Chen, Nan; Han, Bingqian; Xiao, Xuechun; Chen, Gang; Djerdj, Igor; Wang, Yude

    2015-09-28

    Pt activated SnO2 nanoparticle clusters were synthesized by a simple solvothermal method. The structure, morphology, chemical state and specific surface area were analyzed by X-ray powder diffraction (XRD), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS) and N2-sorption studies, respectively. The SnO2 nanoparticle cluster matrix consists of tens of thousands of SnO2 nanoparticles with an ultra-small grain size estimated to be 3.0 nm. And there are abundant random-packed wormhole-like pores, caused by the inter-connection of the SnO2 nanoparticles, throughout each cluster. The platinum element is present in two forms including metal (Pt) and tetravalent metal oxide (PtO2) in the Pt activated SnO2 nanoparticle clusters. The as-synthesized pure and Pt activated SnO2 nanoparticle clusters were used to fabricate gas sensor devices. It was found that the gas response toward 500 ppm of ammonia was improved from 6.48 to 203.44 through the activation by Pt. And the results indicate that the sensor based on Pt activated SnO2 not only has ultrahigh sensitivity but also possesses good response-recovery properties, linear dependence, repeatability, selectivity and long-term stability, demonstrating the potential to use Pt activated SnO2 nanoparticle clusters as ammonia gas sensors. At the same time, the formation mechanisms of the unique nanoparticle clusters and highly enhanced sensitivity are also discussed.

  9. Underpotential deposition: From planar surfaces to nanoparticles

    Science.gov (United States)

    Oviedo, O. A.; Vélez, P.; Macagno, V. A.; Leiva, E. P. M.

    2015-01-01

    An overview is given of selected theoretical, experimental and computer simulation research on thermodynamic modeling applied to the metal underpotential deposition. Focus is made mainly on the last 20 years. The upd-theory on planar surfaces is revisited and the thermodynamic framework is extended to consider underpotential deposition on nanoparticles and to include anion coadsorption, solvation and double layer charging. Results from molecular dynamics and Monte Carlo simulations are shown for systems of experimental interest. At the end some perspectives for further advanced modeling of the present problem are given.

  10. Atomistic computer simulations of FePt nanoparticles. Thermodynamic and kinetic properties

    Energy Technology Data Exchange (ETDEWEB)

    Mueller, M.

    2007-12-20

    In the present dissertation, a hierarchical multiscale approach for modeling FePt nanoparticles by atomistic computer simulations is developed. By describing the interatomic interactions on different levels of sophistication, various time and length scales can be accessed. Methods range from static quantum-mechanic total-energy calculations of small periodic systems to simulations of whole particles over an extended time by using simple lattice Hamiltonians. By employing these methods, the energetic and thermodynamic stability of non-crystalline multiply twinned FePt nanoparticles is investigated. Subsequently, the thermodynamics of the order-disorder transition in FePt nanoparticles is analyzed, including the influence of particle size, composition and modified surface energies by different chemical surroundings. In order to identify processes that reduce or enhance the rate of transformation from the disordered to the ordered state, the kinetics of the ordering transition in FePt nanoparticles is finally investigated by assessing the contributions of surface and volume diffusion. (orig.)

  11. Novel route to synthesize Pt-Ws2 nanoparticles for electrochemical applications

    Energy Technology Data Exchange (ETDEWEB)

    Gochi-Ponce, Y. [Inst. Tecnologico de Oaxaca, Oaxaca (Mexico). Dept. of Mechanical Engineering; Research Center on Advanced Materials, Chihuahua, (Mexico). Dept. of Chemical Materials; Morales, D.; Arriaga, L.G. [Centro de Investigacion y Desarrollo Tecnologico en Electroquimica, Queretaro (Mexico); Chinas-Castillo, F. [Inst. Tecnologico de Oaxaca, Oaxaca (Mexico). Dept. of Mechanical Engineering; Alonso-Nunez, G. [Research Center on Advanced Materials, Chihuahua, (Mexico). Dept. of Chemical Materials; Centro de Investigacion y Desarrollo Tecnologico en Electroquimica, Queretaro (Mexico)

    2008-07-01

    This paper reported on a new and easier way to prepare platinum (Pt)-WS2 nanostructures supported on Vulcan carbon and multi-walled carbon nanotubes (MWCNTs). The chemical synthesis included heat treatment. The study focused on the influence of exfoliated sulphide on Pt that modifies the catalytic properties and enhances the activity of pure Pt. The resulting material was characterized by X-ray Diffraction, Scanning Electron Microscopy and High-Resolution Transmission Electron Microscopy. The material was compared to commercial Pt/C. Synthesized Pt-WS2 nanoparticles exhibited high dispersion on both supporting carbon materials. The study showed that the amount of platinum can be optimized to be lower when diluted or coordinated in the chalcogenic environment. This represents a good alternative to tailor new materials based essentially on non-noble metals for electrochemical applications. It was concluded that the WS2 modified Pt nanoparticles are a promising material for electrochemical applications. 7 refs., 4 figs.

  12. Efficient electrocatalytic oxidation of formic acid using Au@Pt dendrimer-encapsulated nanoparticles.

    Science.gov (United States)

    Iyyamperumal, Ravikumar; Zhang, Liang; Henkelman, Graeme; Crooks, Richard M

    2013-04-17

    We report electrocatalytic oxidation of formic acid using monometallic and bimetallic dendrimer-encapsulated nanoparticles (DENs). The results indicate that the Au147@Pt DENs exhibit better electrocatalytic activity and low CO formation. Theoretical calculations attribute the observed activity to the deformation of nanoparticle structure, slow dehydration of formic acid, and weak binding of CO on Au147@Pt surface. Subsequent experiments confirmed the theoretical predictions.

  13. Pure magnetic hard fct FePt nanoparticles: Chemical synthesis, structural and magnetic properties correlations

    Energy Technology Data Exchange (ETDEWEB)

    Suber, L., E-mail: lorenza.suber@ism.cnr.it [ISM-CNR, Area della Ricerca di Roma 1, Via Salaria km 29.300, 00015 Monterotondo Scalo, RM (Italy); Marchegiani, G. [ISM-CNR, Area della Ricerca di Roma 1, Via Salaria km 29.300, 00015 Monterotondo Scalo, RM (Italy); Olivetti, E.S.; Celegato, F.; Coïsson, M.; Tiberto, P. [INRIM, Electromagnetism Division, Strada delle Cacce 91, 10135 Torino (Italy); Allia, P. [DISAT Politecnico di Torino, Corso Duca degli Abruzzi 24, 10129 Torino (Italy); Barrera, G. [Dipartimento di Chimica, Università di Torino, Via Pietro Giuria 7, 10125 Torino (Italy); Pilloni, L. [UTTMAT-CHI, Via Anguillarese 10, 00123 S. Maria di Galeria, Roma (Italy); Barba, L. [IC-CNR, Area Science Park, SS 14 Km 163.5 Basovizza, 34149 Trieste (Italy); Padella, F. [UTTMAT-CHI, Via Anguillarese 10, 00123 S. Maria di Galeria, Roma (Italy); Cossari, P. [IGAG-CNR, Area della Ricerca di Roma 1, Via Salaria km 29.300, 00015 Monterotondo Scalo, RM (Italy); Chiolerio, A. [Istituto Italiano di Tecnologia, Center for Space Human Robotics, Corso Trento 21, 10129 Torino (Italy)

    2014-03-01

    FePt nanoparticles, containing a near-equal atomic percentage of Fe and Pt, with a face centered tetragonal structure (fct), are challenging for potential applications in high performance permanent magnets and high density data storage. In this study, we report on the chemical synthesis, carried out both solvothermally and hydrothermally in autoclave reacting iron (III) acetylacetonate and platinum (II) acetylacetonate with tri- or tetra-ethylene glycol, these employed as solvents, reducers and particle surface protecting agents as well. In both methods, a subsequent thermal treatment at high temperatures is necessary to transform the magnetic soft face centered cubic (fcc) phase to the hard fct one. Organic low-weight molecules, generally used to protect the nanoparticle surface and avoid particle aggregation, are decomposed by the thermal treatment resulting in particle aggregation and coalescence phenomena; on the contrary, in this case, a polymer matrix is formed as particle protecting agent and, by thermally treating the hydrothermally prepared nanoparticles up to 750 °C for 1 h, the pure magnetic hard fct phase is obtained while preserving the nanostructure. A detailed study is carried out on FePt nanoparticle structure (fcc and fct phases) and correlated to the magnetic properties of the system. - Highlights: • fct FePt nanoparticles for hard magnetic nanotechnology applications. • Influence of synthesis parameters on the precursor fcc FePt nanoparticle structure. • Easy hydrothermal method for preparing pure fct FePt nanoparticles. • Monitoring the role of temperature and time on the FePt fcc–fct phase transformation. • Correlation between FePt nanoparticle structural and magnetic properties.

  14. 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.

  15. Direct Synthesis and Size Selection of Ferromagnetic FePt Nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

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

    2007-01-01

    A one-step synthesis of L10 FePt nanoparticles ca. 17.0 nm in diameter by reductive decomposition of the single-source precursor, FePt(CO)4dppmBr2, on a water-soluble support (Na2CO3) is demonstrated. Direct conversion of a FePt(CO)4dppmBr2/Na2CO3 composite to a L10 FePt/Na2CO3 nanocomposite occurs at 600 C under getter gas with metal-ion reduction and minimal nanoparticle coalescence. Triturating the resulting nanocomposite with water simultaneously dissolves the sodium carbonate solid support and precipitates the formed fct FePt nanoparticles. As-prepared FePt nanoparticles are ferromagnetic and exhibit coercivities of 14.5 kOe at 300 K and 21.8 kOe at 5 K. When capped by functionalized methoxypoly(ethylene glycol) surfactant molecules, as-prepared, polydisperse ferromagnetic FePt nanoparticles can be dispersed and size-selected by fractional precipitation.

  16. PtRu colloid nanoparticles for CO oxidation in microfabricated reactors

    DEFF Research Database (Denmark)

    Klerke, Asbjørn; Saadi, Souheil; Toftegaard, Maja Bøg

    2006-01-01

    The catalytic activity of PtRu colloid nanoparticles for CO oxidation is investigated in microfabricated reactors. The measured catalytic performance describes a volcano curve as a function of the Pt/Ru ratio. The apparent activation energies for the different alloy catalysts are between 21 and 117...

  17. Fuel cell electrocatalsis : oxygen reduction on Pt-based nanoparticle catalysts

    NARCIS (Netherlands)

    Vliet, Dennis Franciscus van der

    2010-01-01

    The thesis contains a discussion on the subject of the Oxygen Reduction Reaction (ORR) on Pt-alloy nanoparticle catalysts in the Rotating Disk Electrode (RDE) method. An insight in some of the difficulties of this method is given with proper solutions and compensations for these problems. Pt3Co, Au-

  18. Electro-Deposition Pt Catalysts Supported on Carbon-Nanotubes for Methanol Oxidation

    Institute of Scientific and Technical Information of China (English)

    Hailin Song; Peixia Yang; Xiaoyu Wen; Maozhong An; Jinqiu Zhang

    2015-01-01

    In order to study the properties of supporting Pt catalysts for methanol oxidation, carbon⁃nanotubes are used by electrochemical deposition method. Different deposition turns, different cyclic voltammetry scanning speeds and processing time with ascorbic acid are investigated in this paper. The micrographs of Pt/CNTs catalysts are characterized by scanning electron microscopy, the electro⁃catalytic properties of Pt/CNTs catalysts for methanol oxidation are investigated by cycle voltammetry and chronoamperometry. The results show that the size of platinum will be greater with the faster scanning speed. After dissolution in ascorbic acid, Pt nano⁃particles disperse uniformly. The obtained Pt/CNTs catalysts show a high electro⁃catalytic activity and stability.

  19. Factors influencing the charge distribution on Pd x Pt y bimetallic nanoparticles

    Directory of Open Access Journals (Sweden)

    Carlos M. Celis-Cornejo

    2013-12-01

    Full Text Available We performed quantum mechanics calculations to elucidate the electronic behavior of Pd-Pt bimetallic nanoparticles, using density functional theory, in response to particle size and stoichiometric composition. Using neutrally charged nanoparticles and the Bader charge analysis, we found that external Pd atoms were positively charged, which agrees with previous XPS observations of supported Pd-Pt nanoparticles. From the calculations, unsupported nanoparticles exhibit an electron transfer from Pd to Pt. This result supports the idea that Pd electron-deficient species are possibly responsible of the hydrogenating function of these catalysts, in the hydrodesulfurization of dibenzothiophene. Additionally, it was found that the particle size does not affect the electronic charge distribution and the stoichiometric composition is the factor that greatly influences this property in nanoparticles.

  20. Structural and magnetic properties of FePt nanoparticles from the gas phase; Strukturelle und magnetische Eigenschaften von FePt-Nanopartikeln aus der Gasphase

    Energy Technology Data Exchange (ETDEWEB)

    Dmitrieva, O.

    2007-09-21

    In this work, we present the structural and magnetic characterization of FePt nanoparticles. The nanoparticles with mean size of about 6 nm were prepared by sputtering in the gas and subsequent inert gas condensation. The particles are annealed in the furnace during their flight prior to deposition on a substrate. The aim of this work is to prepare magnetically hard FePt nanoparticles in the L1{sub 0}-ordered phase. The structure of the particles was investigated by high-resolution transmission electron microscopy, and the investigations were supported by contrast simulations. The morphology of the particles varies with the sputter-gas pressure and with the annealing temperature. At a pressure of 0.5 mbar, the FePt-nanoparticles are multiply-twinned with an icosahedral structure and exhibit no formation of the L1{sub 0}-ordered phase. At a higher pressure of 1 mbar and an annealing temperature of 1000 C, the particles are partially single-crystalline. About 36 % of the particles are found to be in the L1{sub 0}-ordered state as was estimated by statistical counting supported by simulations. In order to activate the volume diffusion in the particles and to stabilize the formation of the L1{sub 0}-ordered state, the addition of nitrogen was used during the sputtering phase. In this phase, atomic nitrogen is incorporated interstitially into the structure of the primary particles. After annealing nitrogen effuses out of the particles and, thereby, increases the volume diffusion of the Fe and Pt atoms. The incorporation of nitrogen atoms during nucleation and their effusion at an annealing temperature of 1000 C was verified by electron energy loss spectroscopy (EELS) and X-ray absorption spectroscopy (XAS). Structural investigations on particles prepared in the presence of nitrogen shows that most of the particles are single-crystalline and about 70 % of them are L1{sub 0}-ordered. Detailed structural analysis of the nanoparticles was done by the exit wave

  1. 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).

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

    Directory of Open Access Journals (Sweden)

    Tung-Yuan Yung

    2016-12-01

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

  3. Synthesis of Fe3O4/Pt Nanoparticles Decorated Carbon Nanotubes and Their Use as Magnetically Recyclable Catalysts

    Directory of Open Access Journals (Sweden)

    Hongkun He

    2011-01-01

    Full Text Available We report a facile approach to prepare Fe3O4/Pt nanoparticles decorated carbon nanotubes (CNTs. The superparamagnetic Fe3O4 nanoparticles with average size of 4∼5 nm were loaded on the surfaces of carboxyl groups functionalized CNTs via a high-temperature solution-phase hydrolysis method from the raw material of FeCl3. The synthesis process of magnetic CNTs is green and readily scalable. The loading amounts of Fe3O4 nanopartilces and the magnetizations of the resulting magnetic CNTs show good tunability. The Pt nanopaticles with average size of 2.5 nm were deposited on the magnetic CNTs through a solution-based method. It is demonstrated that the Fe3O4/Pt nanoparticles decorated CNTs have high catalytic activity in the reduction reaction of 4-nitrophenol and can be readily recycled by a magnet and reused in the next reactions with high efficiencies for at least fifteen successive cycles. The novel CNTs-supported magnetically recyclable catalysts are promising in heterogeneous catalysis applications.

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

    Science.gov (United States)

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

    2013-05-29

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

  5. Thermochemical hydrogen sensor based on Pt-coated nanofiber catalyst deposited on pyramidally textured thermoelectric film

    Science.gov (United States)

    Kim, Seil; Song, Yoseb; Lee, Young-In; Choa, Yong-Ho

    2017-09-01

    The hydrogen gas-sensing performance has been systemically investigated of a new type of thermochemical hydrogen (TCH) sensor, composed of pyramidally textured thermoelectric (TE) film and catalytic Pt-coated nanofibers (NFs) deposited over the TE film. The TE film was composed of stoichiometric Bi2Te3, synthesized by means of cost-effective electrochemical deposition onto a textured silicon wafer. The resulting pyramidally textured TE film played a critical role in maximizing hydrogen gas flow around the overlying Pt NFs, which were synthesized by means of electrospinning followed by sputtering and acted as a heating catalyst. The optimal temperature increase of the Pt NFs was determined by means of optimizations of the electrospinning and sputtering durations. The output voltage signal of the optimized TCH sensor based on Pt NFs was 17.5 times higher than that of a Pt thin film coated directly onto the pyramidal TE material by using the same sputtering duration, under the fixed conditions of 3 vol% H2 in air at room temperature. This observation can be explained by the increased surface area of (111) planes accessible on the Pt-coated NFs. The best response time and recovery time observed for the optimized TCH sensor based on Pt-coated NFs were respectively 17 and 2 s under the same conditions. We believe that this type of TCH sensor can be widely used for supersensitive hydrogen gas detection by employing small-size Pt NFs and various chalcogenide thin films with high thermoelectric performance.

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

    Science.gov (United States)

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

    2001-10-01

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

  7. 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.

  8. Co oxidation on spontaneous Pt-Ru deposits on composite polymeric electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Bavio, M.A.; Kessler, T. [Departamento de Ingenieria Quimica, Facultad de Ingenieria, Universidad Nacional del Centro de la Provincia de Buenos Aires, Av. del Valle 5737, B7400JWI, Olavarria (Argentina); Castro Luna, A.M. [Instituto de Investigaciones Fisicoquimicas Teoricas y Aplicadas, INIFTA, Facultad de Ciencias Exactas, Universidad Nacional de La Plata, Diagonal 113 y 64, 1900, La Plata (Argentina)

    2010-06-15

    Composite polyaniline electrodes containing carbon nanotubes incorporated in the film and spontaneous Pt-Ru deposits as catalytic material for CO oxidation are reported. PANI films were electrosynthesized from a monomer acid solution with the addition of carbon nanotubes. Then, Pt-Ru deposits were obtained by immersing the polymeric film in H{sub 2}PtCl{sub 6} and/or RuCl{sub 3} in HCl. Three series of deposits were prepared by either immersion in a solution containing both metallic ions during a fixed time or successive immersion in different solutions containing only one of the metallic ions during half of the established time and varying the sequence as follows: (i) first in H{sub 2}PtCl{sub 6} and then in RuCl{sub 3} or (ii) first in RuCl{sub 3} and then in H{sub 2}PtCl{sub 6}. Adsorbed CO oxidation was studied by cyclic voltammetry in H{sub 2}SO{sub 4} solution. The electrodes were characterized through SEM and EDX. The different ways to obtain spontaneous Pt-Ru deposits are analyzed and their influence on CO oxidation is discussed. (author)

  9. 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.

  10. Nanoparticle cluster gas sensor: Pt activated SnO2 nanoparticles for NH3 detection with ultrahigh sensitivity

    Science.gov (United States)

    Liu, Xu; Chen, Nan; Han, Bingqian; Xiao, Xuechun; Chen, Gang; Djerdj, Igor; Wang, Yude

    2015-09-01

    Pt activated SnO2 nanoparticle clusters were synthesized by a simple solvothermal method. The structure, morphology, chemical state and specific surface area were analyzed by X-ray powder diffraction (XRD), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS) and N2-sorption studies, respectively. The SnO2 nanoparticle cluster matrix consists of tens of thousands of SnO2 nanoparticles with an ultra-small grain size estimated to be 3.0 nm. And there are abundant random-packed wormhole-like pores, caused by the inter-connection of the SnO2 nanoparticles, throughout each cluster. The platinum element is present in two forms including metal (Pt) and tetravalent metal oxide (PtO2) in the Pt activated SnO2 nanoparticle clusters. The as-synthesized pure and Pt activated SnO2 nanoparticle clusters were used to fabricate gas sensor devices. It was found that the gas response toward 500 ppm of ammonia was improved from 6.48 to 203.44 through the activation by Pt. And the results indicate that the sensor based on Pt activated SnO2 not only has ultrahigh sensitivity but also possesses good response-recovery properties, linear dependence, repeatability, selectivity and long-term stability, demonstrating the potential to use Pt activated SnO2 nanoparticle clusters as ammonia gas sensors. At the same time, the formation mechanisms of the unique nanoparticle clusters and highly enhanced sensitivity are also discussed.Pt activated SnO2 nanoparticle clusters were synthesized by a simple solvothermal method. The structure, morphology, chemical state and specific surface area were analyzed by X-ray powder diffraction (XRD), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS) and N2-sorption studies, respectively. The SnO2 nanoparticle cluster matrix consists of tens of thousands of SnO2 nanoparticles with an ultra-small grain size estimated to be 3.0 nm. And there are abundant random-packed wormhole-like pores, caused by the inter

  11. Synthesis of cubic PtPd alloy nanoparticles as anode electrocatalysts for methanol and formic acid oxidation reactions.

    Science.gov (United States)

    Lee, Jin-Yeon; Kwak, Da-Hee; Lee, Young-Woo; Lee, Seul; Park, Kyung-Won

    2015-04-14

    The electrocatalytic properties for electro-oxidation reactions of shape-controlled Pt-based catalysts have been improved by alloying with 2nd elements. In this study, we demonstrate cubic PtPd alloy nanoparticles synthesized using a thermal decomposition method. The cubic PtPd nanoparticles exhibit a homogeneous distribution of alloy nanostructures in the presence of Pt and Pd metallic phases. The improved electrocatalytic activity for the electro-oxidation reactions of methanol and formic acid as chemical fuels might be attributed to the cubic alloy nanostructures. Furthermore, the cubic PtPd alloy nanoparticles as electrocatalysts exhibit excellent stability for electro-oxidation reactions.

  12. In Situ Generation of Two-Dimensional Au–Pt Core–Shell Nanoparticle Assemblies

    Directory of Open Access Journals (Sweden)

    Khalid Madiha

    2009-01-01

    Full Text Available Abstract Two-dimensional assemblies of Au–Pt bimetallic nanoparticles are generated in situ on polyethyleneimmine (PEI silane functionalized silicon and indium tin oxide (ITO coated glass surfaces. Atomic force microscopy (AFM, UV–Visible spectroscopy, and electrochemical measurements reveal the formation of core–shell structure with Au as core and Pt as shell. The core–shell structure is further supported by comparing with the corresponding data of Au nanoparticle assemblies. Static contact angle measurements with water show an increase in hydrophilic character due to bimetallic nanoparticle generation on different surfaces. It is further observed that these Au–Pt core–shell bimetallic nanoparticle assemblies are catalytically active towards methanol electro-oxidation, which is the key reaction for direct methanol fuel cells (DMFCs.

  13. Shape-controlled synthesis of Pt-Pd core-shell nanoparticles exhibiting polyhedral morphologies by modified polyol method

    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, Nguyen Trai, Hanoi (Viet Nam); Asaka, Toru; Matsubara, Takashi [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)

    2011-04-15

    Pt-Pd core-shell nanoparticles were synthesized by a simple synthetic method. First, Pt nanoparticles were synthesized in a controlled manner via the reduction of chloroplantinic acid hexahydrate in ethylene glycol (EG) at 160 deg. C in the presence of silver nitrate and the stabilization of polyvinylpyrrolidon. AgNO{sub 3} used acts as a structure-modifying agent to the morphology of the Pt nanoparticles. These Pt nanoparticles function as the seeds for the successive reduction of sodium tetrachloropalladate (II) hydrate in EG under stirring for 15 min at 160 deg. C in order to synthesize Pt-Pd core-shell nanoparticles. To characterize the as-prepared Pt-Pd nanoparticles, transmission electron microscopy (TEM) and high-resolution TEM are used. The high-resolution elemental mappings were carried out using the combination of scanning TEM and X-ray energy-dispersive spectroscopy. The results also demonstrate the homogeneous nucleation and growth of the Pd metal shell on the definite Pt core. The synthesized Pt-Pd core-shell nanoparticles exhibit a sharp and polyhedral morphology. The epitaxial growth of the controlled Pd shells on the Pt cores via a polyol method was observed. It is suggested that Frank-van der Merwe and Stranski-Krastanov growth modes coexisted in the nucleation and growth of Pt-Pd core-shell nanoparticles.

  14. Plasma-assisted atomic layer deposition of conformal Pt films in high aspect ratio trenches

    Science.gov (United States)

    Erkens, I. J. M.; Verheijen, M. A.; Knoops, H. C. M.; Keuning, W.; Roozeboom, F.; Kessels, W. M. M.

    2017-02-01

    To date, conventional thermal atomic layer deposition (ALD) has been the method of choice to deposit high-quality Pt thin films grown typically from (MeCp)PtMe3 vapor and O2 gas at 300 °C. Plasma-assisted ALD of Pt using O2 plasma can offer several advantages over thermal ALD, such as faster nucleation and deposition at lower temperatures. In this work, it is demonstrated that plasma-assisted ALD at 300 °C also allows for the deposition of highly conformal Pt films in trenches with high aspect ratio ranging from 3 to 34. Scanning electron microscopy inspection revealed that the conformality of the deposited Pt films was 100% in trenches with aspect ratio (AR) up to 34. These results were corroborated by high-precision layer thickness measurements by transmission electron microscopy for trenches with an aspect ratio of 22. The role of the surface recombination of O-radicals and the contribution of thermal ALD reactions is discussed.

  15. Underpotential deposition of Cu on Pt(001): Interface structure and the influence of adsorbed bromide

    Energy Technology Data Exchange (ETDEWEB)

    Lucas, C.A. [Oliver Lodge Laboratory, Department of Physics, University of Liverpool, Liverpool, L697ZE (United Kingdom); Markovic, N.M.; Ross, P.N. [Materials Sciences Division, Lawrence Berkeley National Laboratory, University of California, Berkeley, California 94720 (United States)

    1998-05-01

    Using {ital in situ} x-ray diffraction, we studied the underpotential deposition (UPD) of copper onto a Pt(001) electrode both in pure perchloric acid and in the presence of bromide anions. In pure perchloric acid, the Cu is deposited in pseudomorphic p(1{times}1) islands. In the presence of bromide anions, the strong Pt-Br interaction significantly broadens the potential range of Cu UPD. We propose that Br remains in the interface region throughout the UPD process, at first in a disordered Cu-Br phase and then, at more negative potential, forming a c(2{times}2) closed-packed monolayer on top of the completed p(1{times}1) Cu monolayer. The structures are compared to those found during Cu UPD onto Pt(111), and explained in terms of the metal-halide interactions and the Pt surface atomic geometry. {copyright} {ital 1998} {ital The American Physical Society}

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

    OpenAIRE

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

    2016-01-01

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

  17. Stellated Ag-Pt bimetallic nanoparticles: An effective platform for catalytic activity tuning

    Science.gov (United States)

    Liu, Hui; Ye, Feng; Yao, Qiaofeng; Cao, Hongbin; Xie, Jianping; Lee, Jim Yang; Yang, Jun

    2014-01-01

    The usefulness of Pt-based nanomaterials for catalysis can be greatly enhanced by coupling morphology engineering to the strategic presence of a second or even third metal. Here we demonstrate the design and preparation of stellated Ag-Pt bimetallic nanoparticles where significant activity difference between the methanol oxidation reaction (MOR) and the oxygen reduction reaction (ORR) may be realized by relegating Ag to the core or by hollowing out the core. In particular the stellated Pt surface, with an abundance of steps, edges, corner atoms, and {111} facets, is highly effective for the ORR but is ineffective for MOR. MOR activity is only observed in the presence of a Ag core through electronic coupling to the stellated Pt shell. The bimetallic Ag-Pt stellates therefore demonstrate the feasibility of tuning a Pt surface for two very different structure sensitive catalytic reactions. Stellated bimetallics may therefore be an effective platform for highly tunable catalyst designs. PMID:24495979

  18. Biomimetic Synthesis of FePt Nanoparticles on Multi-Walled Carbon Nanotubes for Functional Nanomaterials

    Science.gov (United States)

    Wang, Li; Wang, Jiku; Li, Zhuang

    2013-02-01

    We present a facile green biomimetic synthesis of FePt nanoparticles (NPs) on the sidewalls of multi-walled carbon nanotubes (CNTs). A core-shell globular protein, ferritin (Fr), was bound onto Z-glycine N-succinimidyl ester (Z-Gly-OSu) modified CNTs and served as precursor to create FePt NPs at the core part of Fr. Biomimetic synthesis of FePt NPs was carried out by chemical reducing of Fe2+ and PtCl_{6}^{2-} ions that transferred into the core part of Fr molecules. The created one-dimensional CNT-FePt nanohybrids were characterized by transmission electron microscopy and X-ray photoelectron spectroscopy. The synthesized CNT-FePt nanohybrids show multi-properties of high water-solubility, ferromagnetism, and electrocatalytic activity.

  19. Colloidal synthesis and structural control of PtSn bimetallic nanoparticles.

    Science.gov (United States)

    Wang, Xiaodong; Stöver, Jörg; Zielasek, Volkmar; Altmann, Lena; Thiel, Karsten; Al-Shamery, Katharina; Bäumer, Marcus; Borchert, Holger; Parisi, Jürgen; Kolny-Olesiak, Joanna

    2011-09-06

    PtSn bimetallic nanoparticles with different particle sizes (1-9 nm), metal compositions (Sn content of 10-80 mol %), and organic capping agents (e.g., amine, thiol, carboxylic acid and polymer) were synthesized by colloidal chemistry methods. Transmission electron microscopy (TEM) measurements show that, depending on the particle size, the as-prepared bimetallic nanocrystals have quasi-spherical or faceted shapes. Energy-dispersive X-ray (EDX) analyses indicate that for all samples the signals of both Pt and Sn can be detected from single nanoparticles, confirming that the products are actually bimetallic but not only a physical mixture of pure Pt and Sn metal nanoparticles. X-ray diffraction (XRD) measurements were also conducted on the bimetallic particle systems. When compared with the diffraction patterns of monometallic Pt nanoparticles, the bimetallic samples show distinct shifts of the Bragg reflections to lower degrees, which gives clear proof of the alloying of Pt with Sn. However, a quantitative analysis of the lattice parameter shifts indicates that only part of the Sn atoms are incorporated into the alloy nanocrystals. This is consistent with X-ray photoelectron spectroscopy (XPS) measurements that reveal the segregation of Sn at the surfaces of the nanocrystals. Moreover, short PtSn bimetallic nanowires were synthesized by a seed-mediated growth method with amine-capped bimetallic particles as precursors. The resulting nanowires have an average width of 2.3 nm and lengths ranging from 5 to 20 nm. © 2011 American Chemical Society

  20. Magnetic Properties of FePt Nanoparticles Prepared by a Micellar Method

    Directory of Open Access Journals (Sweden)

    Gao Y

    2009-01-01

    Full Text Available Abstract FePt nanoparticles with average size of 9 nm were synthesized using a diblock polymer micellar method combined with plasma treatment. To prevent from oxidation under ambient conditions, immediately after plasma treatment, the FePt nanoparticle arrays were in situ transferred into the film-growth chamber where they were covered by an SiO2 overlayer. A nearly complete transformation of L10 FePt was achieved for samples annealed at temperatures above 700 °C. The well control on the FePt stoichiometry and avoidance from surface oxidation largely enhanced the coercivity, and a value as high as 10 kOe was obtained in this study. An evaluation of magnetic interactions was made using the so-called isothermal remanence (IRM and dc-demagnetization (DCD remanence curves and Kelly–Henkel plots (ΔM measurement. The ΔM measurement reveals that the resultant FePt nanoparticles exhibit a rather weak interparticle dipolar coupling, and the absence of interparticle exchange interaction suggests no significant particle agglomeration occurred during the post-annealing. Additionally, a slight parallel magnetic anisotropy was also observed. The results indicate the micellar method has a high potential in preparing FePt nanoparticle arrays used for ultrahigh density recording media.

  1. High-performance energy harvester fabricated with aerosol deposited PMN-PT material

    Science.gov (United States)

    Chen, C. T.; Lin, S. C.; Lin, T. K.; Wu, W. J.

    2016-11-01

    This paper reports a high-performance piezoelectric energy harvester (EH) fabricated with xPb(Mg1/3Nb2/3)-(l-x)PbTiO3 (PMN-PT) by aerosol deposition method. The result indicates that PMN-PT based EH owns 1.8 times output power which is higher than traditional PbZrxTi1- xO3 (PZT) based EH. In order to compare the output performance of EH fabricated with PMN- PT compared with PZT, the similar thickness of PMN-PT and PZT thin film is deposited on stainless steel subtracted. The experimental results show that PZT-based EH had a maximum output power of 4.65 μW with 1.11 Vp-p output voltage excited at 94.4 Hz under 0.5g base excitation, while the PMN-PT based device has a maximum output power of 8.42 μW with 1.49 Vp-p output voltage at a vibration frequency of 94.8 Hz and the same base excitation level. The volumetric power density was 82.95 μW/mm3 and 48.05 μW/mm3 for the device based on PMN- PT and PZT materials, respectively. All the results demonstrate that PMN-PT has better output performance than PZT.

  2. Ethylene glycol oxidation on Pt and Pt-Ru nanoparticle decorated polythiophene/multiwalled carbon nanotube composites for fuel cell applications.

    Science.gov (United States)

    Selvaraj, Vaithilingam; Alagar, Muthukaruppan

    2008-01-30

    A novel supporting material containing polythiophene (PTh) and multiwalled carbon nanotubes (MWCNTs) (PTh-CNTs) is prepared by in situ polymerization of thiophene on carbon nanotubes using FeCl(3) as oxidizing agent under sonication. The prepared polythiophene/CNT composites are further decorated with Pt and Pt-Ru nanoparticles by chemical reduction of the corresponding metal salts using HCHO as reducing agent at pH = 11 (Pt/PTh-CNT and Pt-Ru/PTh-CNT). The fabricated composite films decorated with nanoparticles were investigated towards the electrochemical oxidation of ethylene glycol (EG). The presence of carbon nanotubes in conjugation with a conducting polymer produces a good catalytic effect, which might be due to the higher electrochemically accessible surface areas, electronic conductivity and easier charge-transfer at polymer/electrolyte interfaces, which allows higher dispersion of Pt and Pt-Ru nanoparticles. Such nanoparticle modified PTh-CNT electrodes exhibit better catalytic behavior towards ethylene glycol oxidation. Results show that Pt/PTh-CNT and Pt-Ru/PTh-CNT modified electrodes show enhanced electrocatalytic activity and stability towards the electro-oxidation of ethylene glycol than the Pt/PTh electrodes, which shows that the composite film is more promising for applications in fuel cells.

  3. Ethylene glycol oxidation on Pt and Pt-Ru nanoparticle decorated polythiophene/multiwalled carbon nanotube composites for fuel cell applications

    Energy Technology Data Exchange (ETDEWEB)

    Selvaraj, Vaithilingam; Alagar, Muthukaruppan [Department of Chemical Engineering, Alagappa College of Technology, Anna University, Chennai 600025 (India)

    2008-01-30

    A novel supporting material containing polythiophene (PTh) and multiwalled carbon nanotubes (MWCNTs) (PTh-CNTs) is prepared by in situ polymerization of thiophene on carbon nanotubes using FeCl{sub 3} as oxidizing agent under sonication. The prepared polythiophene/CNT composites are further decorated with Pt and Pt-Ru nanoparticles by chemical reduction of the corresponding metal salts using HCHO as reducing agent at pH = 11 (Pt/PTh-CNT and Pt-Ru/PTh-CNT). The fabricated composite films decorated with nanoparticles were investigated towards the electrochemical oxidation of ethylene glycol (EG). The presence of carbon nanotubes in conjugation with a conducting polymer produces a good catalytic effect, which might be due to the higher electrochemically accessible surface areas, electronic conductivity and easier charge-transfer at polymer/electrolyte interfaces, which allows higher dispersion of Pt and Pt-Ru nanoparticles. Such nanoparticle modified PTh-CNT electrodes exhibit better catalytic behavior towards ethylene glycol oxidation. Results show that Pt/PTh-CNT and Pt-Ru/PTh-CNT modified electrodes show enhanced electrocatalytic activity and stability towards the electro-oxidation of ethylene glycol than the Pt/PTh electrodes, which shows that the composite film is more promising for applications in fuel cells.

  4. Effect of Cu doping on the structure and phase transition of directly synthesized FePt nanoparticles

    Science.gov (United States)

    Wang, Hanbin; Li, Yang; Chen, Xu; Shu, Dan; Liu, Xiang; Wang, Xina; Zhang, Jun; Wang, Hao; Wang, Yi; Ruterana, Pierre

    2017-01-01

    In this work, ternary Cu doped FePt nanoparticles were prepared in hexadecylamine at 320 °C by choosing FeCl2 as the Fe source. The experimental results showed that without Cu doping the as-prepared FePt nanoparticles possessed fcc structure and gradually exhibited typical fct diffraction peaks after increasing the Cu doping concentration. TEM images showed that the FePt nanoparticles had larger size and wider size distribution after introducing Cu additive. Magnetic property measurement showed that a coercivity of 4800 Oe was obtained when the composition of the ternary nanoparticles reached Fe35Pt45Cu20, in which the content of Fe+Cu was higher than Pt. The research indicates that Cu doping promotes the phase transition of FePt nanoparticles at temperature as low as 320 °C.

  5. Laser-induced in situ synthesis of Pd and Pt nanoparticles on polymer films

    Science.gov (United States)

    Mehrabanian, Mehran; Morselli, Davide; Caputo, Gianvito; Scarpellini, Alice; Palazon, Francisco; Athanassiou, Athanassia; Fragouli, Despina

    2016-12-01

    We present the localized in situ formation of Pd and Pt nanoparticles embedded in chitosan solid films. This is achieved by the photo-induced reduction of metallic precursors, previously incorporated in chitosan films, through controlled UV pulsed laser irradiation. Interestingly, at high number of laser pulses, Pd and Pt follow different formation pathways, contrary to their common photoreduction mechanism occurring at low irradiation pulses. Specifically, in the case of the Pd, a photofragmentation process takes place fracturing the previously formed nanoparticles into smaller ones; whereas in the case of Pt, the prolonged irradiation promotes the nanoparticles agglomeration. The combination of both precursors in a binary solid system results in the combined formation of both Pd and Pt nanoparticles in the polymer film upon laser irradiation. The herein reported approach is an efficient and precise tool to generate size- and density-controlled Pd and Pt nanoparticles in desired areas of polymeric films, rendering this method a potential candidate for the fabrication of flexible polymeric devices for gas-sensing or electro-catalysis applications.

  6. Porous Pt Nanoparticles with High Near-Infrared Photothermal Conversion Efficiencies for Photothermal Therapy.

    Science.gov (United States)

    Zhu, Xiao-Ming; Wan, Hong-Ye; Jia, Henglei; Liu, Liang; Wang, Jianfang

    2016-12-01

    Plasmonic nanostructures are of potential in acting as a type of optical agents for cancer photothermal therapy. To effectively function as photothermal therapy agents, plasmonic nanostructures are strongly desired to have good biocompatibility and high photothermal conversion efficiencies. In this study, poly(diallyldimethylammonium chloride)-coated porous Pt nanoparticles are synthesized for photothermal therapy. The Pt nanoparticles possess broadband near-infrared light absorption in the range from 650 to 1200 nm, therefore allowing for selecting different laser wavelengths for photothermal therapy. The as-prepared Pt nanoparticles exhibit remarkable photothermal conversion efficiencies under 809 and 980 nm laser irradiation. In vitro studies indicate that the Pt nanoparticles display good biocompatibility and high cellular uptake efficiencies through an endocytosis pathway. Photothermal heating using 808 nm laser irradiation (>7.0 W cm(-2) , 3 min) leads to notable cytotoxic effect, and more than 70% of cells are photothermally ablated after 3 min irradiation at 8.4 W cm(-2) . Furthermore, simultaneous application of photothermal therapy synergistically enhances the cytotoxicity of an anti-cancer drug doxorubicin. Therefore, the porous Pt nanoparticles have great potential as an attractive photothermal agent for cancer therapy.

  7. FePt nanoparticle formation with lower phase transition temperature by single shot plasma focus ion irradiation

    Science.gov (United States)

    Lin, J. J.; Roshan, M. V.; Pan, Z. Y.; Verma, R.; Lee, P.; Springham, S. V.; Tan, T. L.; Rawat, R. S.

    2008-07-01

    Uniform FePt nanoparticles were synthesized through nanostructuring of pulsed laser deposited FePt thin films by single shot H+ ion irradiation using a plasma focus device. The annealing temperature required for phase transition from low Ku face-centred cubic to high Ku face-centred tetragonal, for ion irradiated samples, is simultaneously lowered down to 400 °C. The energetic H+ ion irradiation significantly reduces the activation energy for atomic ordering by increasing the number of vacancies. The advantage of using a plasma focus device is that it can achieve nanostructuring in much shorter time, in single shot ion exposure with pulse duration of typically about a few hundreds of nanoseconds, as compared with much longer duration required by continuous ion sources.

  8. Methanol Electro-Oxidation on Pt-Ru Alloy Nanoparticles Supported on Carbon Nanotubes

    Directory of Open Access Journals (Sweden)

    Yangchuan Xing

    2009-09-01

    Full Text Available Carbon nanotubes (CNTs have been investigated in recent years as a catalyst support for proton exchange membrane fuel cells. Improved catalyst activities were observed and attributed to metal-support interactions. We report a study on the kinetics of methanol electro-oxidation on CNT supported Pt-Ru alloy nanoparticles. Alloy catalysts with different compositions, Pt53Ru47/CNT, Pt69Ru31/CNT and Pt77Ru23/CNT, were prepared and investigated in detail. Experiments were conducted at various temperatures, electrode potentials, and methanol concentrations. It was found that the reaction order of methanol electro-oxidation on the PtRu/CNT catalysts was consistent with what has been reported for PtRu alloys with a value of 0.5 in methanol concentrations. However, the electro-oxidation reaction on the PtRu/CNT catalysts displayed much lower activation energies than that on the Pt-Ru alloy catalysts unsupported or supported on carbon black (PtRu/CB. This study provides an overall kinetic evaluation of the PtRu/CNT catalysts and further demonstrates the beneficial role of CNTs.

  9. Synergistic Effects in CNTs-PdAu/Pt Trimetallic Nanoparticles with High Electrocatalytic Activity and Stability

    Science.gov (United States)

    Cai, Xin-Lei; Liu, Chang-Hai; Liu, Jie; Lu, Ying; Zhong, Ya-Nan; Nie, Kai-Qi; Xu, Jian-Long; Gao, Xu; Sun, Xu-Hui; Wang, Sui-Dong

    2017-10-01

    We present a straightforward physical approach for synthesizing multiwalled carbon nanotubes (CNTs)-PdAu/Pt trimetallic nanoparticles (NPs), which allows predesign and control of the metal compositional ratio by simply adjusting the sputtering targets and conditions. The small-sized CNTs-PdAu/Pt NPs ( 3 nm, Pd/Au/Pt ratio of 3:1:2) act as nanocatalysts for the methanol oxidation reaction (MOR), showing excellent performance with electrocatalytic peak current of 4.4 A mg Pt -1 and high stability over 7000 s. The electrocatalytic activity and stability of the PdAu/Pt trimetallic NPs are much superior to those of the corresponding Pd/Pt and Au/Pt bimetallic NPs, as well as a commercial Pt/C catalyst. Systematic investigation of the microscopic, crystalline, and electronic structure of the PdAu/Pt NPs reveals alloying and charge redistribution in the PdAu/Pt NPs, which are responsible for the promotion of the electrocatalytic performance.

  10. Large faceted Pd nanocrystals supported small Pt nanoparticles as highly durable electrocatalysts for oxygen reduction

    Science.gov (United States)

    Zhang, Geng; Lu, Wangting; Cao, Longsheng; Qin, Xiaoping; Ding, Fei; Tang, Shun; Shao, Zhi-Gang; Yi, Baolian

    2016-09-01

    The reduction of Pt content together with the improvement of the durability of the catalyst for oxygen reduction reaction (ORR) is required to the large-scale commercialization of proton exchange membrane fuel cells. In this work, a novel ORR catalyst consisting of large Pd nanocrystal as the core with small Pt nanoparticles supported on the Pd core is prepared by a facile one-step synthesis method. The Pd substrate is presented in the form of well-defined cuboctahedrons and icosahedrons. The type of metal precursors and Pt/Pd molar ratio are important factors to obtain this Pd-supporting-Pt structure. The Pd2-s-Pt1 catalyst with a nominal Pt/Pd atomic ratio at 1/2 shows improved ORR activity: its mass specific activity and area specific activity is 2.5 and 3.5 times that of commercial Pt/C, respectively. More importantly, the Pd2-s-Pt1 catalyst demonstrates outstanding durability against potential cycling which can be ascribed to the slow dissolution of Pd core and the structure transformation from Pd@Pt to hollow PdPt alloyed nanocages. This exciting result provides a new pathway to the design of ORR catalyst with excellent durability.

  11. Energetic and structural analysis of 102-atom Pd-Pt nanoparticles

    Science.gov (United States)

    Pacheco-Contreras, Rafael; Arteaga-Guerrero, Alvaro; Borbon-Gonzalez, Dora Julia; Posada-Amarillas, Alvaro; Schoen, J. Christian; Johnston, Roy L.

    2009-03-01

    We present an extensive study of the structural and energetic changes of 102-atom PdmPt102-m nanoparticles as a function of composition m, where the interatomic interactions are modeled with the many-body Gupta potential. The minimum energy structures are obtained through a genetic algorithm. The excess energy is calculated, as well as the pair distribution function g(r). The radial distribution of the atoms is computed for each composition; the result indicates a multi-layer segregation for some compositions, with a shell growth sequence as follows: a core with a small number of Pd atoms is followed by an intermediate shell of Pt atoms and the external shell consists of Pd atoms. A region where Pd and Pt atoms are mixed is observed between the outermost and intermediate shells. Furthermore, the pure Pd102 and Pt102 nanoparticles have the same structure, while a variety of different structures are observed for the bimetallic clusters.

  12. Nano Brazing of Pt-Ag Nanoparticles under Femtosecond Laser Irradiation

    Institute of Scientific and Technical Information of China (English)

    L Liu; H Huang; A Hu; G Zou; L Quintino; Y Zhou

    2013-01-01

    Nano brazing of Pt-Ag nanoparticles with nano Ag filler metal is reported in this letter, which presents an effective way to join nanoobjects by femtosecond laser irradiation. The nano brazed interface between Pt-Ag and Ag showed good lattice matching along (111)Ag//(111)Ag-Pt. Lattice mismatch can hardly be observed at the interface between the filler metal and Pt-Ag nanoparticle, which is important for the joint strength and normally does not occur during joining. The very low mismatch also suggested that melting and solidification occurred during nano brazing by femtosecond laser. The role of Brownian motion on the nano joining process is also discussed in this paper.

  13. Study of carbon-supported bimetallic PtCu nanoparticles by ASAXS

    Science.gov (United States)

    Bulat, N. V.; Avakyan, L. A.; Pryadchenko, V. V.; Srabionyan, V. V.; Belenov, S. V.; Bugaev, L. A.

    2017-05-01

    Bimetallic platinum-copper nanoparticles on carbon support are studied as a perspective electrochemical catalyst by anomalous small-angle X-ray scattering near the Pt absorption L3-edge. The simultaneous fitting of several diffraction patterns measured at different photon energies lead to a satisfactory agreement between experimental and model curves in the assumption of core-shell structure of the particles with Pt-rich shell and Cu-rich core. It is shown that the average size of as prepared nanoparticles is about 6 nm with distribution spread of about ±2 nm and with thickness of Pt-rich shell approximately 1.6 nm. After annealing at 350o C the average size of the particles increased by two times with additional enlargement of the Pt-rich shell thickness.

  14. Electrospray deposition of isolated chemically synthesized magnetic nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Agostini, Pierre; Meffre, Anca; Lacroix, Lise-Marie; Ugnati, Damien [Université de Toulouse (France); INSA, UPS, CNRS, Laboratoire de Physique et Chimie des Nano-objets (LPCNO) (France); Ondarçuhu, Thierry [Centre d’Elaboration de Matériaux et d’Etudes Structurales (CEMES-CNRS) (France); Respaud, Marc; Lassagne, Benjamin, E-mail: lassagne@insa-toulouse.fr [Université de Toulouse (France); INSA, UPS, CNRS, Laboratoire de Physique et Chimie des Nano-objets (LPCNO) (France)

    2016-01-15

    The deposition of isolated magnetic nanoparticles onto a substrate was performed using electrohydrodynamic spraying. Two kinds of nanoparticles were sprayed, 11 nm CoFe carbide nanospheres and 10.5 nm Fe nanocubes. By studying carefully the evolution of the sprayed charged droplets and the mechanism of nanoparticle dispersion in them, we could optimize the nanoparticle concentration within the initial nanoparticle solution (i) to reduce the magnetic interaction and therefore prevent agglomeration and (ii) to obtain in a relatively short period (1 h) a deposit of isolated magnetic nanoparticles with a density of up to 400 nanoparticles per µm{sup 2}. These results open great perspectives for magnetic measurements on single objects using advanced magnetometry techniques as long as spintronics applications based on single chemically synthesized magnetic nanoparticles.

  15. RIR-MAPLE deposition of plasmonic silver nanoparticles

    Science.gov (United States)

    Ge, Wangyao; Hoang, Thang B.; Mikkelsen, Maiken H.; Stiff-Roberts, Adrienne D.

    2016-09-01

    Nanoparticles are being explored in many different applications due to the unique properties offered by quantum effects. To broaden the scope of these applications, the deposition of nanoparticles onto substrates in a simple and controlled way is highly desired. In this study, we use resonant infrared matrix-assisted pulsed laser evaporation (RIR-MAPLE) for the deposition of metallic, silver nanoparticles for plasmonic applications. We find that RIR-MAPLE, a simple and versatile approach, is able to deposit silver nanoparticles as large as 80 nm onto different substrates with good adhesion, regardless of substrate properties. In addition, the nanoparticle surface coverage of the substrates, which result from the random distribution of nanoparticles across the substrate per laser pulse, can be simply and precisely controlled by RIR-MAPLE. Polymer films of poly(3-hexylthiophene-2,5-diyl) (P3HT) are also deposited by RIR-MAPLE on top of the deposited silver nanoparticles in order to demonstrate enhanced absorption due to the localized surface plasmon resonance effect. The reported features of RIR-MAPLE nanoparticle deposition indicate that this tool can enable efficient processing of nanoparticle thin films for applications that require specific substrates or configurations that are not easily achieved using solution-based approaches.

  16. Effects of different additives on bimetallic Au-Pt nanoparticles electrodeposited onto indium tin oxide electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Ballarin, Barbara, E-mail: ballarin@ms.fci.unibo.i [Dipartimento di Chimica Fisica ed Inorganica, Universita di Bologna, V.le Risorgimento, 4, 40136-Bologna (Italy)] [INSTM, UdR Bologna (Italy); Gazzano, Massimo [ISOF-CNR, V. Selmi, 40126-Bologna (Italy); Tonelli, Domenica [Dipartimento di Chimica Fisica ed Inorganica, Universita di Bologna, V.le Risorgimento, 4, 40136-Bologna (Italy)] [INSTM, UdR Bologna (Italy)

    2010-09-01

    Bimetallic Au-Pt nanoparticles (Au-Pt{sub NPs}) have been synthesized using an electrochemical reduction approach. The effects of the addition of different additives in the electrodeposition bath namely KI, 1-nonanesulfonic acid sodium salt and Triton X-100 have been investigated. The structural characterization of the bimetallic nanoparticles has been carried out using scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), UV-vis spectroscopy, X-ray diffraction (XRD) and cyclic voltammetry (CV). The Au-Pt{sub NPs} prepared in the presence of KI and Triton X-100 characterized by a relatively narrow size distribution as well as a higher particle density and surface coverage whereas no changes in the morphology were observed. These results suggest a dependence of the size and distribution of the bimetallic nanoparticles from the type and concentration of the additives employed.

  17. Fabrication of monodisperse FePt rate at Au core-shell nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Wei, D.H. [Institute of Physics, Academia Sinica, Taipei 115 (China); Hung, D.S. [Department of Information and Telecommunications Engineering, Ming Chuan University, Taipei 111 (China); Ho, C.S.; Wang, J.W. [Department of Chemical Engineering, Tunghai University, Taichung 407 (China); Yao, Y.D. [Department of Materials Engineering, Tatung University, Taipei 104 (China)

    2007-12-15

    Hydrophobic FePt rate at Au core-shell nanoparticles were chemically synthesized and with controllable surface-function properties. The enhanced optical property is due to the contribution of Au shell. The surface modification of FePt rate at Au nanoiparticles by using 11-mercaptoundecanoic acid (MUA) was hydrophilic through ligand exchange and with good biocompatibility for future multi-functional applications. (copyright 2008 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

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

    Science.gov (United States)

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

    2013-12-31

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

  19. Formation and Characterization of Pd, Pt and Pd-Pt Alloy Films on Polyimide by Catalyst-Enhanced Chemical Vapor Deposition

    Institute of Scientific and Technical Information of China (English)

    ZHOU Jinlan; CHENG Yinhua; Yousuf Hamadan; YU Kaichao

    2007-01-01

    Platinum, palladium and their alloy films on polyimide were formed by catalyst-enhanced chemical vapor deposition (CVD) in the carrier gas (N2, O2) at 220-300 ℃ under reduced pressure and normal pressure. The deposition of palladium complexes [ Pd((η3-allyl)(hfac) and Pd(hfac)2 ] gives pure palladium film,while the deposition of platinum needs the enhancement of palladium complex by mixing precursor platinum complex Pt(COD)Me2 and palladium complex in the same chamber. The co-deposition of Pd and Pt metals was used for the deposition of alloy films. During the CVD of palladium-platinum alloy, the Pd/Pt atomic ratios vary under different co-deposition conditions. These metal films were characterized by XPS and SEM, and show a good adhesive property.

  20. Activity improvement of Pt/C catalysts by adding CeO2 nanoparticles

    Institute of Scientific and Technical Information of China (English)

    YANG Yuying; ZHANG Ziyu; HU Zhongai

    2011-01-01

    Carbon-supported platinum catalysts were prepared by NaBH4 reduction of metal precursors and the CeO2 nanoparticles were prepared by citric acid sol-gel method. The structure and morphology of two kinds of nanoparticles were characterized by X-ray diffraction (XRD) and transmission electron microscopy (TEM), respectively. The Pt particles were uniformly dispersed on the carbon surface and showed the rod-like morphology. The CeO2 was spherical in shape. The appropriate amount of CeO2 nanoparticles was added into Pt/C systems to improve activity of the catalysts. Several electrochemical techniques such as cyclic voltammogram (CV), chronoamperometry (I-t)and electrochemical impedance spectroscopy (EIS) were used to investigate the properties of CeO2-Pt/C catalysts for methanol electrooxidation in 1 mol/L CH3OH+0.5H2SO4 aqueous solutions. The results revealed that compared with Pt/C catalysts CeO2-pt/C exhibited a higher activity and stability for methanol electro-oxidation. Moreover, the effect of CeO2 content on the activity of Pt/C catalysts was discussed in detail.

  1. Modeling the local potential at Pt nanoparticles in polymer electrolyte membranes.

    Science.gov (United States)

    Eslamibidgoli, Mohammad Javad; Melchy, Pierre-Éric Alix; Eikerling, Michael H

    2015-04-21

    We present a physical-analytical model for the potential distribution at Pt nanodeposits in a polymer electrolyte membrane (PEM). Experimental studies have shown that solid deposits of Pt in PEM play a dual role in radical-initiated membrane degradation. Surface reactions at Pt particles could facilitate the formation as well as the scavenging of ionomer-attacking radical species. The net radical balance depends on local equilibrium conditions at Pt nanodeposits in the PEM, specifically, their equivalent local electrode potential. Our approach utilizes a continuum description of crossover fluxes of reactant gases, coupled with the kinetics of electrochemical surface reactions at Pt nanodeposits to calculate the potential distribution. The local potential is a function of the PEM structure and composition, which is determined by PEM thickness, concentrations of H2 and O2, as well as the size and density distribution of Pt particles. Model results compare well with experimental data for the potential distribution in PEMs.

  2. WO3/Pt nanoparticles promote light-induced lipid peroxidation and lysosomal instability within tumor cells

    Science.gov (United States)

    Clark, Andrea J.; Petty, Howard R.

    2016-02-01

    Although metal-metal oxide nanoparticles have attracted considerable interest as catalysts, they have attracted little interest in nanomedicine. This is likely due to the fact that metal oxide semiconductors generally require biologically harmful ultraviolet excitation. In contrast, this study focuses upon WO3/Pt nanoparticles, which can be excited by visible light. To optimize the nanoparticles’ catalytic performance, platinization was performed at alkaline pH. These nanoparticles destroyed organic dyes, consumed dissolved oxygen and produced hydroxyl radicals. 4T1 breast cancer cells internalized WO3/Pt nanoparticles within the membrane-bound endo-lysosomal compartment as shown by electron and fluorescence microscopy. During visible light exposure, but not in darkness, WO3/Pt nanoparticles manufacture reactive oxygen species, promote lipid peroxidation, and trigger lysosomal membrane disruption. As cells of the immune system degrade organic molecules, produce reactive oxygen species, and activate the lipid peroxidation pathway within target cells, these nanoparticles mimic the chemical attributes of immune effector cells. These biomimetic nanoparticles should become useful in managing certain cancers, especially ocular cancer.

  3. Deposition of copper selenide thin films and nanoparticles

    Science.gov (United States)

    Hu, Yunxiang; Afzaal, Mohammad; Malik, Mohammad A.; O'Brien, Paul

    2006-12-01

    A new method is reported for the growth of copper selenide thin films and nanoparticles using copper acetylacetonate and trioctylphosphine selenide. Aerosol-assisted chemical vapor deposition experiments lead to successful deposition of tetragonal Cu 2Se films. In contrast, hexadecylamine capped nanoparticles are composed of cubic Cu 2-xSe. The deposited materials are optically and structurally characterized. The results of this comprehensive study are described and discussed.

  4. Fabrication of Nonenzymatic Glucose Sensors Based on Multiwalled Carbon Nanotubes with Bimetallic Pt-M (M = Ru and Sn Catalysts by Radiolytic Deposition

    Directory of Open Access Journals (Sweden)

    Sun-Young Kwon

    2012-01-01

    Full Text Available Nonenzymatic glucose sensors employing multiwalled carbon nanotubes (MWNTs with highly dispersed Pt-M (M = Ru and Sn nanoparticles (Pt-M@PVP-MWNTs were fabricated by radiolytic deposition. The Pt-M nanoparticles on the MWNTs were characterized by transmittance electron microscopy, elemental analysis, and X-ray diffraction. They were found to be well dispersed and to exhibit alloy properties on the MWNT support. Electrochemical testing showed that these nonenzymatic sensors had larger currents (mA than that of a bare glassy carbon (GC electrode and one modified with MWNTs. The sensitivity (A mM−1, linear range (mM, and detection limit (mM (S/N = 3 of the glucose sensor with the Pt-Ru catalyst in NaOH electrolyte were determined as 18.0, 1.0–2.5, 0.7, respectively. The corresponding data of the sensor with Pt-Sn catalyst were 889.0, 1.00–3.00, and 0.3, respectively. In addition, these non-enzymatic sensors can effectively avoid interference arising from the oxidation of the common interfering species ascorbic acid and uric acid in NaOH electrolyte. The experimental results show that such sensors can be applied in the detection of glucose in commercial red wine samples.

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

    Indian Academy of Sciences (India)

    M Qamar; Ashok K Ganguli

    2013-11-01

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

  6. Electro-oxidation of methanol at the different carbon materials supported Pt nano-particles

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Yu.; Zhang, Guojie; Zhou, Yiming; Tang, Yawen; Lu, Tianhong [The Laboratory of Electrochemistry, College of Chemistry and Material Science, Nanjing Normal University, 1 Wenyuan Road, Nanjing 210046 (China); Ma, Juan [Institute of Electrochemical Power Sources, Soochow University, Suzhou 215006 (China)

    2010-10-15

    Single-wall carbon nano-tubes (SWNTs), multi-wall carbon nano-tubes (MWNTs) and Vulcan XC-72 carbon (XC-72) are used as supporting carbon materials to prepare Pt/XC-72, Pt/SWNTs and Pt/MWNTs catalysts in tetrahydrofuran/water/ethanol mixture solution. Transmission electron microscope (TEM) and X-ray photoelectron spectroscopy (XPS) measurements demonstrate that the type of supporting carbon material affects significantly the morphology and the electronic structure of supported Pt nano-particles (NPs). Electrochemical measurements indicate that the Pt/SWNTs catalyst exhibited the highest current density, the lowest onset oxidation potential and the best stability for methanol electro-oxidation among the three samples, indicating SWNTs are an ideal anode catalyst supporting material for the practical application of direct methanol fuel cells. (author)

  7. Chemically ordered face-centred tetragonal Fe–Pt nanoparticles embedded SiO2 films

    Indian Academy of Sciences (India)

    Sourav Pramanik; Goutam De

    2012-12-01

    Chemically ordered face-centred tetragonal (fct) Fe–Pt alloy nanoparticles (NPs) embedded SiO2 films were synthesized on glass substrate by in situ hybrid sol–gel approach followed by heating at 450–900 °C in air and reducing (10% H2–90% Ar) atmospheres. Heat treatment of Fe/Pt co-doped films in air caused generation of Pt NPs first. At this stage, Fe remained in ionic state covalently bonded with silica network. Further heat treatment at 800–900 °C in reducing atmosphere facilitated the formation of uniformly dispersed fct Fe–Pt alloy NPs in amorphous SiO2 film matrix. The generated alloy composition was estimated by grazing incidence X-ray diffraction and TEM analysis to be Fe0.42Pt0.58 which is close to the nominal value.

  8. A dispenser-reactor apparatus applied for in situ XAS monitoring of Pt nanoparticle formation.

    Science.gov (United States)

    Boita, Jocenir; Castegnaro, Marcus Vinicius; Alves, Maria do Carmo Martins; Morais, Jonder

    2015-05-01

    In situ time-resolved X-ray absorption spectroscopy (XAS) measurements collected at the Pt L3-edge during the synthesis of Pt nanoparticles (NPs) in aqueous solution are reported. A specially designed dispenser-reactor apparatus allowed for monitoring changes in the XAS spectra from the earliest moments of Pt ions in solution until the formation of metallic nanoparticles with a mean diameter of 4.9 ± 1.1 nm. By monitoring the changes in the local chemical environment of the Pt atoms in real time, it was possible to observe that the NPs formation kinetics involved two stages: a reduction-nucleation burst followed by a slow growth and stabilization of NPs. Subsequently, the synthesized Pt NPs were supported on activated carbon and characterized by synchrotron-radiation-excited X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD) and extended X-ray absorption fine structure (EXAFS). The supported Pt NPs remained in the metallic chemical state and with a reduced size, presenting slight lattice parameter contraction in comparison with the bulk Pt values.

  9. Structural characterization of Pt-Pd core-shell nanoparticles by Cs-corrected STEM

    Energy Technology Data Exchange (ETDEWEB)

    Esparza, R., E-mail: resparza@fata.unam.mx [Universidad Nacional Autonoma de Mexico, Centro de Fisica Aplicada y Tecnologia Avanzada (Mexico); Garcia-Ruiz, Amado F. [UPIICSA-COFAA, Instituto Politecnico Nacional (Mexico); Velazquez Salazar, J. J. [University of Texas at San Antonio, Department of Physics and Astronomy (United States); Perez, R. [Universidad Nacional Autonoma de Mexico, Centro de Fisica Aplicada y Tecnologia Avanzada (Mexico); Jose-Yacaman, M. [The University of Texas at San Antonio, Department of Physics and Astronomy (United States)

    2013-01-15

    Pt-Pd core-shell nanoparticles were synthesized using a modified polyol method. A thermal method under refluxing, carrying on the reaction up to 285 Degree-Sign C, has been performed to reduce metallic salts using ethylene glycol as reducer and poly(N-vinyl-2-pyrrolidone) as protective reagent of the formed bimetallic nanoparticles. According to other works, this type of structure has been studied and utilized to successfully increase the catalytic properties of monometallic nanoparticles Pt or Pd. Core-shell bimetallic nanoparticles were structurally characterized using aberration-corrected scanning transmission electron microscopy (Cs-STEM) equipped with a high-angle annular dark field detector, energy-dispersive X-ray spectrometry (EDS), and electron energy-loss spectroscopy (EELS). The high-resolution elemental line scan and mappings were carried out using a combination of STEM-EDS and STEM-EELS. The obtained results show the growth of the Pd shell on the Pt core with polyhedral morphology. The average size of the bimetallic nanoparticles was 13.5 nm and the average size of the core was 8.5 nm; consequently, the thickness of the shell was around 2.5 nm. The growth of the Pd shell on the Pt core is layer by layer, suggesting a Frank-van der Merwe growth mechanism.

  10. Purity and resistivity improvements for electron-beam-induced deposition of Pt

    Energy Technology Data Exchange (ETDEWEB)

    Mulders, J.J.L. [FEI Company, Eindhoven (Netherlands)

    2014-12-15

    Electron-beam-induced deposition (EBID) of platinum is used by many researchers. Its main application is the formation of a protective layer and the ''welding material'' for making a TEM lamella with a focused ion beam thinning process. For this application, the actual composition of the deposition is less relevant, and in practice, both the mechanical strength and the conductivity are sufficient. Another important application is the creation of an electrical connection to nanoscale structures such as nano-wires and graphene. To serve as an electrical contact, the resistivity of the Pt deposited structure has to be sufficiently low. Using the commonly used precursor MeCpPtMe{sub 3} for deposition, the resistivity as created by the basic process is 10{sup +5}-10{sup +6} higher than the value for bulk Pt, which is 10.6 μΩ cm. The reason for this is the high abundance of carbon in the deposition. To improve the deposition process, much attention has been given by the research community to parameter optimization, to ex situ or in situ removal of carbon by anneal steps, to prevention of carbon deposition by use of a carbon-free precursor, to electron beam irradiation under a high flux of oxygen and to the combination with other techniques such as atomic layer deposition (ALD). In the latter technique, the EBID structures are used as a 1-nm-thick seed layer only, while the ALD is used to selectively add pure Pt. These techniques have resulted in a low resistivity, today approaching the 10-150 μΩ cm, while the size and shape of the structure are preserved. Therefore, now, the technique is ready for application in the field of contacting nano-wires. (orig.)

  11. Synthesis of Pt nanowires with the participation of physical vapour deposition

    Science.gov (United States)

    Dobrzański, Leszek A.; Szindler, Marek; Pawlyta, Mirosława; Szindler, Magdalena M.; Boryło, Paulina; Tomiczek, Błazej

    2016-01-01

    The following paper presents the possibility of formation of Pt nanowires, achieved by a three-step method consisting of conformal deposition of a carbon nanotube and conformal coverage with platinum by physical vapour deposition, followed by removal of the carbonaceous template. The characterization of this new nanostructure was carried out through scanning electron microscopy (SEM), transmission electron microscopy (TEM) and X-ray diffraction (XRD).

  12. Synthesis of Pt nanowires with the participation of physical vapour deposition

    Directory of Open Access Journals (Sweden)

    Dobrzański Leszek A.

    2016-01-01

    Full Text Available The following paper presents the possibility of formation of Pt nanowires, achieved by a three-step method consisting of conformal deposition of a carbon nanotube and conformal coverage with platinum by physical vapour deposition, followed by removal of the carbonaceous template. The characterization of this new nanostructure was carried out through scanning electron microscopy (SEM, transmission electron microscopy (TEM and X-ray diffraction (XRD.

  13. Sintering of oxide-supported Pt and Pd nanoparticles in air studied by in situ TEM

    DEFF Research Database (Denmark)

    Simonsen, Søren Bredmose

    at elevated temperatures. The time-resolved TEM images are presented and these offer direct insight into the fundamental dynamics of the sintering process at the nano-scale. For Pt, Pd and bimetallic Pt-Pd nanoparticles it is shown that the sintering process is governed by the Ostwald ripening mechanism...... correlations between neighbouring nanoparticles in the atom-exchange process. The sintering process was also presented statistically by particle size distributions extracted from the TEM images. The statistical data agreed only partly with the mean-field kinetic models for ripening, but the deviations could......This thesis presents a fundamental study of the sintering of supported nanoparticles in relation to diesel oxidation catalysts. The sintering of supported nanoparticles is an important challenge in relation to this catalyst, as well as many other catalyst systems, and a fundamental understanding...

  14. Tailoring nucleation and growth conditions for narrow compositional distributions in colloidal synthesized FePt nanoparticles

    Science.gov (United States)

    Srivastava, Chandan; Nikles, David E.; Thompson, Gregory B.

    2008-11-01

    To eliminate compositional and size variabilities between individual binary nanoparticles, it is essential to control the mechanistic steps involved in nanoparticle synthesis. A common method for synthesizing FePt nanoparticles involves the simultaneous decomposition and reduction in iron and platinum precursors, respectively. This simultaneous nucleation and growth method yields wide composition and size distributions. This paper describes and experimentally validates a methodology needed to tighten composition and size distributions for this process. By engineering the surfactant chemistry with tertiary phosphines to tightly bind the iron atoms in the iron precursor, uniform platinum rich seeds form during the initial stages of the synthesis. A thermodynamically preferred heterogeneous nucleation of iron atoms into these uniform platinum seeds in the subsequent stages produces a final dispersion with uniform particle-to-particle compositions. The paper addresses the understanding for optimizing the nucleation and growth sequences for compositional control in FePt nanoparticles.

  15. Oxygen-induced shape changes of Pt nanoparticles on MgO(100)

    Energy Technology Data Exchange (ETDEWEB)

    Hejral, Uta; Stierle, Andreas; Vlad, Alina; Delheusy, Melissa; Dosch, Helmut [Max-Planck-Institut fuer Metallforschung, Heisenbergstr. 3, 70569 Stuttgart (Germany)

    2010-07-01

    Platinum nanoparticles on oxide carrier materials are used in heterogenous catalysis and are applied successfully in reactions like the oxidation of hydrocarbons or carbon monoxide. In order to achieve better catalyst efficiency, lifetime and selectivity it is important to comprehend catalytic processes on an atomic basis. Thus, the interplay between particle shape, adsorbed oxygen, bulk oxides and catalytic activity needs to be understood. Therefore Pt nanoparticles have been grown epitaxially on MgO(100) substrates under controlled conditions. It has previously been reported that Rh nanoparticles undergo reversible shape changes induced by surface oxides. We have studied oxygen-induced shape changes of Pt nanoparticles on MgO(100) by means of in situ X-ray diffraction. The experiment was performed at 300 C and oxygen pressures ranging from UHV to 500 mbar. The experimental results are compared to theoretically predicted ones.

  16. Deposition and biokinetics of inhaled nanoparticles

    Directory of Open Access Journals (Sweden)

    Kreyling Wolfgang G

    2010-01-01

    Full Text Available Abstract Particle biokinetics is important in hazard identification and characterization of inhaled particles. Such studies intend to convert external to internal exposure or biologically effective dose, and may help to set limits in that way. Here we focus on the biokinetics of inhaled nanometer sized particles in comparison to micrometer sized ones. The presented approach ranges from inhaled particle deposition probability and retention in the respiratory tract to biokinetics and clearance of particles out of the respiratory tract. Particle transport into the blood circulation (translocation, towards secondary target organs and tissues (accumulation, and out of the body (clearance is considered. The macroscopically assessed amount of particles in the respiratory tract and secondary target organs provides dose estimates for toxicological studies on the level of the whole organism. Complementary, microscopic analyses at the individual particle level provide detailed information about which cells and subcellular components are the target of inhaled particles. These studies contribute to shed light on mechanisms and modes of action eventually leading to adverse health effects by inhaled nanoparticles. We review current methods for macroscopic and microscopic analyses of particle deposition, retention and clearance. Existing macroscopic knowledge on particle biokinetics and microscopic views on particle organ interactions are discussed comparing nanometer and micrometer sized particles. We emphasize the importance for quantitative analyses and the use of particle doses derived from real world exposures.

  17. Deposition and biokinetics of inhaled nanoparticles

    Science.gov (United States)

    2010-01-01

    Particle biokinetics is important in hazard identification and characterization of inhaled particles. Such studies intend to convert external to internal exposure or biologically effective dose, and may help to set limits in that way. Here we focus on the biokinetics of inhaled nanometer sized particles in comparison to micrometer sized ones. The presented approach ranges from inhaled particle deposition probability and retention in the respiratory tract to biokinetics and clearance of particles out of the respiratory tract. Particle transport into the blood circulation (translocation), towards secondary target organs and tissues (accumulation), and out of the body (clearance) is considered. The macroscopically assessed amount of particles in the respiratory tract and secondary target organs provides dose estimates for toxicological studies on the level of the whole organism. Complementary, microscopic analyses at the individual particle level provide detailed information about which cells and subcellular components are the target of inhaled particles. These studies contribute to shed light on mechanisms and modes of action eventually leading to adverse health effects by inhaled nanoparticles. We review current methods for macroscopic and microscopic analyses of particle deposition, retention and clearance. Existing macroscopic knowledge on particle biokinetics and microscopic views on particle organ interactions are discussed comparing nanometer and micrometer sized particles. We emphasize the importance for quantitative analyses and the use of particle doses derived from real world exposures. PMID:20205860

  18. Preparation of Nano-Particles (Pb,La)TiO3 Thin Films by Liquid Source Misted Chemical Deposition

    Institute of Scientific and Technical Information of China (English)

    张之圣; 曾建平; 李小图

    2004-01-01

    Nano-particles lanthanum-modified lead titanate (PLT) thin films are grown on Pt/Ti/SiO2/Si substrate by liquid source misted chemical deposition (LSMCD). PLT films are deposited for 4-8 times, and then annealed at various temperature. XRD and SEM show that the prepared films have good crystallization behavior and perovskite structure. The crystallite is about 60 nm. The deposition speed is 3 nm/min. This deposition method can exactly control stoichiometry ratios, doping concentration ratio and thickness of PLT thin films. The best annealing process is to bake at 300 ℃ for 10 min and anneal at 600 ℃ for 1 h.

  19. TiN@nitrogen-doped carbon supported Pt nanoparticles as high-performance anode catalyst for methanol electrooxidation

    Science.gov (United States)

    Zhang, Jun; Ma, Li; Gan, Mengyu; Fu, Shenna; Zhao, Yi

    2016-08-01

    In this paper, TiN@nitrogen-doped carbons (NDC) composed of a core-shell structure are successfully prepared through self-assembly and pyrolysis treatment using γ-aminopropyltriethoxysilane as coupling agent, polyaniline as carbon and nitrogen source, respectively. Subsequently, TiN@NDC supporting Pt nanoparticles (Pt/TiN@NDC) are obtained by a microwave-assisted polyol process. The nitrogen-containing functional groups and TiN nanoparticles play a critical role in decreasing the average particle size of Pt and improving the electrocatalytic activity of Pt/TiN@NDC. Transmission electron microscope results reveal that Pt nanoparticles are uniformly dispersed in the TiN@NDC surface with a narrow particle size ranging from 1 to 3 nm in diameter. Moreover, the Pt/TiN@NDC catalyst shows significantly improved catalytic activity and high durability for methanol electrooxidation in comparison with Pt/NDC and commercial Pt/C catalysts, revealed by cyclic voltammetry and chronoamperometry. Strikingly, this novel Pt/TiN@NDC catalyst reveals a better CO tolerance related to Pt/NDC and commercial Pt/C catalysts, which due to the bifunctional mechanism and strong metal-support interaction between Pt and TiN@NDC. In addition, the probable reaction steps for the electrooxidation of CO adspecies on Pt NPs on the basis of the bifunctional mechanism are also proposed. These results indicate that the TiN@NDC is a promising catalyst support for methanol electrooxidation.

  20. Magnetoelectric effect in FeCo/PMN-PT/FeCo trilayers prepared by electroless deposition of FeCo on PMN-PT crystals with various orientations

    Energy Technology Data Exchange (ETDEWEB)

    Shen, H.Q.; Wang, Y.G., E-mail: yingang.wang@nuaa.edu.cn; Xie, D.; Cheng, J.H.

    2014-10-15

    Highlights: • The composites FeCo/PMN-PT/FeCo were prepared by electroless deposition. • The influence of the crystal cut of PMN-PT on ME coupling is discussed. • Optimizing the crystal cut of the piezoelectric substrate, proper resonant frequency and ME effect could be obtained. - Abstract: The magnetoelectric (ME) effect was studied in the FeCo/PMN-PT/FeCo trilayer composites prepared by electroless deposition of the FeCo layers on the single crystal PMN-PT substrates with various crystal cuts. X-ray diffraction reveals that the orientation of PMN-PT substrate has no effect on the growth of FeCo layer. The structures with PMN-PT crystals of various orientations have different acoustic resonance frequencies. FeCo/PMN-PT/FeCo composites with PMN-PT of 〈0 0 1〉{sup L} × 〈01{sup ‾}1〉{sup W} × 〈0 1 1〉{sup T} crystal cut shows superior ME performance, which is due to the highest piezoelectric module of PMN-PT.

  1. Microwave-assisted synthesis and characterization of bimetallic PtRu alloy nanoparticles supported on carbon nanotubes

    Energy Technology Data Exchange (ETDEWEB)

    Rahsepar, Mansour, E-mail: rahsepar@shirazu.ac.ir [Department of Materials Science and Engineering, School of Engineering, Shiraz University, Zand Boulevard, Shiraz, 7134851154 (Iran, Islamic Republic of); Kim, Hasuck, E-mail: hasuckim@snu.ac.kr [Department of Chemistry, Seoul National University, 599 Gwanak-ro, Gwanak-gu, Seoul, 151-747 (Korea, Republic of); Department of Energy Systems Engineering, Daegu Gyeongbuk Institute of Science & Technology, Daegu, 711-873 (Korea, Republic of)

    2015-11-15

    Multiwalled carbon nanotube (MWCNT) supported PtRu nanoparticles were synthesized by using a microwave-assisted improved impregnation technique. X-ray diffraction, transmission electron microscopy and X-ray photo electron spectroscopy were used to characterize the prepared PtRu/MWCNT nanoparticles. The PtRu nanoparticles with a satisfactory dispersion were formed on the external surface of MWCNTs. The CO stripping experiment was performed to evaluate the poisoning resistance of the prepared PtRu/MWCNT nanoparticles. Results of electrochemical measurements indicate that the prepared PtRu/MWCNTs shows an enhanced performance toward CO poisoning. The results of characterization revealed that microwave-assisted improved impregnation technique have a high yield of alloy phase formation and could be effectively used as a simple, quick and efficient technique for preparation of bimetallic PtRu/MWCNT nanoparticles. - Highlights: • Highly dispersed PtRu/MWCNTs were formed without use of any stabilizing agent. • Microwave irradiation enhances the uniform dispersion of the PtRu nanoparticles. • Microwave-assisted improved impregnation have a high yield of alloy phase formation. • The prepared PtRu/MWCNTs shows an enhanced performance toward CO poisoning.

  2. PdPt bimetallic nanoparticles enabled by shape control with halide ions and their enhanced catalytic activities.

    Science.gov (United States)

    Zhang, Jinfeng; Wan, Lei; Liu, Lei; Deng, Yida; Zhong, Cheng; Hu, Wenbin

    2016-02-21

    In this study, a new and convenient one step approach is described for synthesizing shape controlled PdPt bimetallic nanoparticles. It is found that the resultant morphologies of these PdPt nanoparticles can be well controlled by simply altering the participation of different halide ions that serve as shape controlling agents in the reaction solution. The dendritic core-shell PdPt bimetallic nanoparticles generated with Pt atoms adopt usual island growth pattern in the presence of Cl(-) ions, whereas the introduction of Br(-) ions with a relatively strong adsorption effect facilitate the formation of a layered core-shell structure due to the layered growth mode of Pt atoms on the exterior surface of the central Pd core. Moreover, the stronger adsorption function of I(-) ions and the resulting fast atomic diffusion promoted the generation of mesoporous core-shell PdPt bimetallic nanoparticles with many pore channels. In addition, the size of these synthesized PdPt nanoparticles exhibited a significant dependence on the concentration of the halide ions involved. Due to their specific structural features and synergistic effects, these PdPt catalysts exhibited shape-dependent catalytic performance and drastically enhanced electrocatalytic activities relative to that of commercial Pt black and Pt/C toward methanol oxidation.

  3. CO oxidation on PtSn nanoparticle catalysts occurs at the interface of Pt and Sn oxide domains formed under reaction conditions

    KAUST Repository

    Michalak, William D.

    2014-04-01

    The barrier to CO oxidation on Pt catalysts is the strongly bound adsorbed CO, which inhibits O2 adsorption and hinders CO2 formation. Using reaction studies and in situ X-ray spectroscopy with colloidally prepared, monodisperse ∼2 nm Pt and PtSn nanoparticle catalysts, we show that the addition of Sn to Pt provides distinctly different reaction sites and a more efficient reaction mechanism for CO oxidation compared to pure Pt catalysts. To probe the influence of Sn, we intentionally poisoned the Pt component of the nanoparticle catalysts using a CO-rich atmosphere. With a reaction environment comprised of 100 Torr CO and 40 Torr O2 and a temperature range between 200 and 300 C, Pt and PtSn catalysts exhibited activation barriers for CO2 formation of 133 kJ/mol and 35 kJ/mol, respectively. While pure Sn is readily oxidized and is not active for CO oxidation, the addition of Sn to Pt provides an active site for O2 adsorption that is important when Pt is covered with CO. Sn oxide was identified as the active Sn species under reaction conditions by in situ ambient pressure X-ray photoelectron spectroscopy measurements. While chemical signatures of Pt and Sn indicated intermixed metallic components under reducing conditions, Pt and Sn were found to reversibly separate into isolated domains of Pt and oxidic Sn on the nanoparticle surface under reaction conditions of 100 mTorr CO and 40 mTorr O2 between temperatures of 200-275 C. Under these conditions, PtSn catalysts exhibited apparent reaction orders in O2 for CO 2 production that were 0.5 and lower with increasing partial pressures. These reaction orders contrast the first-order dependence in O 2 known for pure Pt. The differences in activation barriers, non-first-order dependence in O2, and the presence of a partially oxidized Sn indicate that the enhanced activity is due to a reaction mechanism that occurs at a Pt/Sn oxide interface present at the nanoparticle surface. © 2014 Published by Elsevier Inc.

  4. Carbon-Pt nanoparticles modified TiO2 nanotubes for simultaneous detection of dopamine and uric acid.

    Science.gov (United States)

    Mahshid, Sara; Luo, Shenglian; Yang, Lixia; Mahshid, Sahar Sadat; Askari, Masoud; Dolati, Abolghasem; Cai, Qingyun

    2011-08-01

    The present work describes sensing application of modified TiO2 nanotubes having carbon-Pt nanoparticles for simultaneous detection of dopamine and uric acid. The TiO2 nanotubes electrode was prepared using anodizing method, followed by electrodeposition of Pt nanoparticles onto the tubes. Carbon was deposited by decomposition of polyethylene glycol in a tube furnace to improve the conductivity. The C-Pt-TiO2 nanotubes modified electrode was characterized by cyclic voltammetry and differential pulse voltammetry methods. The modified electrode displayed high sensitivity towards the oxidation of dopamine and uric acid in a phosphate buffer solution (pH 7.00). The electro-oxidation currents of dopamine and uric acid were linearly related to the concentration over a wide range of 3.5 x 10(-8) M to 1 x 10(-5) M and 1 x 10(-7) M to 3 x 10(-5) M respectively. The limit of detection was determined as 2 x 10(-10) M for dopamine at signal-to-noise ratio of 3. The interference of uric acid was also investigated. Electro-oxidation currents of dopamine in the presence of fix amount of uric acid represented a linear behaviour towards successive addition of dopamine in range of 1 x 10(-7) M to 1 x 10(-5) M. Furthermore, in a solution containing dopamine, uric acid and ascorbic acid the overlapped oxidation peaks of dopamine and ascorbic acid could be easily separated by using C-Pt-TiO2 nanotubes modified electrode.

  5. Biogenic Pt uptake and nanoparticle formation in Medicago sativa and Brassica juncea

    Energy Technology Data Exchange (ETDEWEB)

    Bali, Roza [University of Sydney, Laboratory for Sustainable Technology, School of Chemical and Biomolecular Engineering (Australia); Siegele, Rainer [Australian Nuclear Science and Technology Organization, Institute for Environmental Research (Australia); Harris, Andrew T., E-mail: a.harris@usyd.edu.a [University of Sydney, Laboratory for Sustainable Technology, School of Chemical and Biomolecular Engineering (Australia)

    2010-10-15

    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{sup -1} (dry biomass) compared with 38.5 mg Pt g{sup -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{sup -1} (dry biomass) at 5 ppm across the different time intervals studied, compared with 0.02-0.14 mg Pt g{sup -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 ({mu}-PIXE) spectroscopy, which showed even distribution across all tissue systems (epidermal, cortical and vascular) within the roots of both M. sativa and B. juncea.

  6. Visible light photoactivity of TiO{sub 2} loaded with monometallic (Au or Pt) and bimetallic (Au/Pt) nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Gołąbiewska, Anna, E-mail: annagolabiewska@o2.pl [Department of Chemical Technology, Gdansk University of Technology, 80-233 Gdańsk (Poland); Lisowski, Wojciech [Mazovia Center for Surface Analysis, Institute of Physical Chemistry, Polish Academy of Sciences, 01-224 Warsaw (Poland); Jarek, Marcin; Nowaczyk, Grzegorz [NanoBioMedical Center, Adam Mickiewicz University, Umultowska 85, 61-614 Poznań (Poland); Zielińska-Jurek, Anna; Zaleska, Adriana [Department of Chemical Technology, Gdansk University of Technology, 80-233 Gdańsk (Poland)

    2014-10-30

    Graphical abstract: - Highlights: • Au/Pt nanoparticles enhanced TiO{sub 2} photocatalytic activity under visible irradiation. • Higher photoactivity of Au/Pt-TiO{sub 2} resulted from smaller Au/Pt particles. • Intermetallic state of AuPt favors charge transfer between the metals. • TiO{sub 2} obtained by TIP hydrolysis seems to be best matrix for Au/Pt-TiO{sub 2}. - Abstract: TiO{sub 2} modified with monometallic (Au or Pt) and bimetallic (Au/Pt) nanoparticles have been prepared using a water-in-oil microemulsion system (water/AOT/cyclohexane) followed by calcination step. The effect of metal ratio, reducing agent type (NaBH{sub 4} or N{sub 2}H{sub 4}), TiO{sub 2} matrix type (P-25, ST-01, TiO-5, TiO{sub 2} nanotubes or TiO{sub 2} obtained by TIP hydrolysis) as well as calcination temperature (from 350 to 650 °C) were systematically investigated. Obtained photocatalysts were characterized by UV–vis diffuse-reflectance spectroscopy (DRS), BET surface area measurements, scanning transmission microscopy (STEM), X-ray diffraction analysis (XRD), and X-ray photoelectron spectroscopy (XPS). Photocatalytic activity under visible light (λ > 420 nm) has been estimated in phenol degradation reaction in aqueous phase. The results showed that phenol degradation rate under visible light in the presence of TiO{sub 2} loaded with Au/Pt nanoparticles differed from 0.7 to 2.2 μmol dm{sup −3} min{sup −1} for samples prepared using different reducing agent. Sodium borohydride (NaBH{sub 4}) favors formation of smaller Au/Pt nanoparticles and higher amount gold in Au/Pt is in the form of electronegative species (Au{sup δ−}) resulted in higher photoactivity. TiO{sub 2} obtained by TIP hydrolysis in microemulsion system seems to be the best support for Au/Pt nanoparticles from all among investigated matrix. It was also observed that enhancement of calcination temperature from 450 to 650 °C resulted in rapid drop of Au/Pt-TiO{sub 2} photoactivity under visible light

  7. Effect of Particle Morphology on the Ripening of Supported Pt Nanoparticles

    DEFF Research Database (Denmark)

    Simonsen, Søren Bredmose; Chorkendorff, Ib; Dahl, Søren;

    2012-01-01

    To improve the understanding of sintering in diesel and lean-burn engine exhaust after-treatment catalysts, we examined oxygen-induced sintering in a model catalyst consisting of Pt nanoparticles supported on a planar, amorphous Al2O3 substrate. After aging at increasing temperatures, a transmiss...

  8. Monolayer-directed Assembly and Magnetic Properties of FePt Nanoparticles on Patterned Aluminum Oxide

    NARCIS (Netherlands)

    Yildirim, Oktay; Gang, Tian; Kinge, Sachin; Reinhoudt, David N.; Blank, Dave H.; Wiel, van der Wilfred G.; Rijnders, Guus; Huskens, Jurriaan

    2010-01-01

    FePt nanoparticles (NPs) were assembled on aluminum oxide substrates, and their ferromagnetic properties were studied before and after thermal annealing. For the first time, phosph(on)ates were used as an adsorbate to form self-assembled monolayers (SAMs) on alumina to direct the assembly of NPs ont

  9. Effect of Particle Morphology on the Ripening of Supported Pt Nanoparticles

    DEFF Research Database (Denmark)

    Simonsen, Søren Bredmose; Chorkendorff, Ib; Dahl, Søren;

    2012-01-01

    To improve the understanding of sintering in diesel and lean-burn engine exhaust after-treatment catalysts, we examined oxygen-induced sintering in a model catalyst consisting of Pt nanoparticles supported on a planar, amorphous Al2O3 substrate. After aging at increasing temperatures...

  10. Ethanol oxidation reaction activity of highly dispersed Pt/SnO{sub 2} double nanoparticles on carbon black

    Energy Technology Data Exchange (ETDEWEB)

    Higuchi, Eiji; Miyata, Kazumasa; Takase, Tomonori; Inoue, Hiroshi [Department of Applied Chemistry, Graduate School of Engineering, Osaka Prefecture University, Sakai, Osaka 599-8531 (Japan)

    2011-02-15

    Highly dispersed Pt and SnO{sub 2} double nanoparticles containing different Pt/Sn ratios (denoted as Pt/SnO{sub 2}/CB) were prepared on carbon black (CB) by the modified Boennemann method. The average size of Pt and SnO{sub 2} nanoparticles was 3.1 {+-} 0.5 nm and 2.5 {+-} 0.3 nm, respectively, in Pt/SnO{sub 2}(3:1)/CB, 3.0 {+-} 0.5 nm and 2.6 {+-} 0.3 nm, respectively, in Pt/SnO{sub 2}(1:1)/CB, and 2.8 {+-} 0.5 nm and 2.5 {+-} 0.3 nm, respectively, in Pt/SnO{sub 2}(1:3)/CB. The Pt/SnO{sub 2}(3:1)/CB electrode showed the highest specific activity and lowest overpotential for ethanol oxidation reaction (EOR), and was superior to a Pt/CB electrode. Current density for EOR at 0.40 and 0.60 V vs. reversible hydrogen electrode for the Pt/SnO{sub 2}(3:1)/CB electrode decayed more slowly than that for the Pt/CB electrode because of a synergistic effect between Pt and SnO{sub 2} nanoparticles. The predominant reaction product was acetic acid, and its current efficiency was about 70%, while that for CO{sub 2} production was about 30%. (author)

  11. Preparation of birnessite-supported pt nanoparticles and their application in catalytic oxidation of formaldehyde.

    Science.gov (United States)

    Liu, Linlin; Tian, Hua; He, Junhui; Wang, Donghui; Yang, Qiaowen

    2012-01-01

    Flaky and nanospherical birnessite and birnessite-supported Pt catalysts were successfully prepared and characterized by means of Xray diffraction (XRD), transmission electron microscopy (TEM), energy dispersive spectroscopy (EDS) and N2 adsorption-desorption. Effects of the birnessite morphology and Pt reduction method on the catalytic activity for the complete oxidation of formaldehyde (HCHO) were investigated. It was found that flaky birnessite exhibited higher catalytic activity than nanospherical birnessite. The promoting effect of Pt on the birnessite catalyst indicated that the reduction method of the Pt precursor greatly influenced the catalytic performance. Flaky birnessite-supported Pt nanoparticles reduced by KBH4 showed the highest catalytic activity and could completely oxidize HCHO into CO2 and H20 at 50 degreesC, whereas the sample reduced using H2-plasma showed lower activity for HCHO oxidation. The differences in catalytic activity of these materials were jointly attributed to the effects of pore structure, surface active sites exposed to HCHO and the dispersion of Pt nanoparticles.

  12. Nickel-doped ceria nanoparticles for promoting catalytic activity of Pt/C for ethanol electrooxidation

    Science.gov (United States)

    Tan, Qiang; Du, Chunyu; Sun, Yongrong; Du, Lei; Yin, Geping; Gao, Yunzhi

    2014-10-01

    This paper reports the facile synthesis of monodispersed nickel-doped ceria nanoparticles by a thermal decomposition method, which is used to promote catalytic properties of Pt/C. The Pt/Ni-doped CeO2/C catalyst obtained exhibits remarkably high activity and stability towards the ethanol electrooxidation in acidic media. This is attributed to higher oxygen releasing capacity and stronger interaction of Ni-doped CeO2 with Pt than pure CeO2 nanoparticles that contribute positively to the removal of poisoning intermediates. We believe that the design concept and synthetic strategy of metal doped oxides used for fuel cell catalysts can be potentially extended to other catalytic fields.

  13. Fast response and recovery of hydrogen sensing in Pd-Pt nanoparticle-graphene composite layers

    Science.gov (United States)

    Kumar, Rakesh; Varandani, Deepak; Mehta, B. R.; Singh, V. N.; Wen, Zhenhai; Feng, Xinliang; Müllen, Klaus

    2011-07-01

    This study reports the fast response and recovery of hydrogen sensing in nanoparticle-graphene composite layers fabricated using chemical methods and comprising of isolated Pd alloy nanoparticles dispersed onto graphene layers. For 2% hydrogen at 40 °C and 1 atm pressure, a response time of Pd-Pt nanoparticle-graphene composite material are important for understanding the effect of gas adsorption on electronic conduction in graphene layers and for developing a new type of gas sensor based on changes in the electronic properties of the interface.

  14. High methanol oxidation activity of well-dispersed pt nanoparticles on carbon nanotubes using nitrogen doping.

    Science.gov (United States)

    Fang, Wei-Chuan

    2009-10-09

    Pt nanoparticles (NPs) with the average size of 3.14 nm well dispersed on N-doped carbon nanotubes (CNTs) without any pretreatment have been demonstrated. Structural properties show the characteristic N bonding within CNTs, which provide the good support for uniform distribution of Pt NPs. In electrochemical characteristics, N-doped CNTs covered with Pt NPs show superior current density due to the fact that the so-called N incorporation could give rise to the formation of preferential sites within CNTs accompanied by the low interfacial energy for immobilizing Pt NPs. Therefore, the substantially enhanced methanol oxidation activity performed by N-incorporation technique is highly promising in energy-generation applications.

  15. High Methanol Oxidation Activity of Well-Dispersed Pt Nanoparticles on Carbon Nanotubes Using Nitrogen Doping

    Directory of Open Access Journals (Sweden)

    Fang Wei-Chuan

    2009-01-01

    Full Text Available Abstract Pt nanoparticles (NPs with the average size of 3.14 nm well dispersed on N-doped carbon nanotubes (CNTs without any pretreatment have been demonstrated. Structural properties show the characteristic N bonding within CNTs, which provide the good support for uniform distribution of Pt NPs. In electrochemical characteristics, N-doped CNTs covered with Pt NPs show superior current density due to the fact that the so-called N incorporation could give rise to the formation of preferential sites within CNTs accompanied by the low interfacial energy for immobilizing Pt NPs. Therefore, the substantially enhanced methanol oxidation activity performed by N-incorporation technique is highly promising in energy-generation applications.

  16. One-step synthesis of PtPdAu ternary alloy nanoparticles on graphene with superior methanol electrooxidation activity

    Energy Technology Data Exchange (ETDEWEB)

    Zhang Yuzhen; Gu Yonge; Lin Shaoxiong; Wei Jinping; Wang Zaihua [Department of Chemistry, Lanzhou University, Lanzhou 730000 (China); Wang Chunming, E-mail: wangcm@lzu.edu.cn [Department of Chemistry, Lanzhou University, Lanzhou 730000 (China); Du Yongling; Ye Weichun [Department of Chemistry, Lanzhou University, Lanzhou 730000 (China)

    2011-10-01

    Highlights: > PtPdAu nanoparticles were synthesized on graphene sheets via chemical reduction method. > The prepared PtPdAu nanoparticles were ternary alloy with fcc structure. > The catalyst exhibited superior catalytic activity and stability for MOR in alkaline. - Abstract: Well-dispersed PtPdAu ternary alloy nanoparticles were synthesized on graphene sheets via a simple one-step chemical reduction method in ethylene glycol (EG) and water system, in which EG served as both reductive and dispersing agent. The electrocatalytic activity of PtPdAu/G was tested by methanol oxidation reaction (MOR). The catalyst was further characterized by transmission electron microscopy (TEM), energy dispersive X-ray spectroscopy (EDX), X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD), which indicated that the as-synthesized PtPdAu nanoparticles with alloy structures were successfully dispersed on the graphene sheets. Electrocatalytic properties of the catalyst for MOR in alkaline have been investigated by cyclic voltammetry (CV), chronoamperometry and Tafel curves. The electrocatalytic activity and stability of PtPdAu/G were superior to PtPd/G, PtAu/G and Pt/G. In addition, the anodic peak current on PtPdAu/G catalyst was proportional to the concentration of methanol in the range of 0.05-1.00 M. This study implies that the prepared catalyst have great potential applications in fuel cells.

  17. 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.

  18. Flame spray pyrolysis synthesis and aerosol deposition of nanoparticle films

    DEFF Research Database (Denmark)

    Tricoli, Antonio; Elmøe, Tobias Dokkedal

    2012-01-01

    The assembly of nanoparticle films by flame spray pyrolysis (FSP) synthesis and deposition on temperature‐controlled substrates (323–723 K) was investigated for several application‐relevant conditions. An exemplary SnO2 nanoparticle aerosol was generated by FSP and its properties (e.g., particle...

  19. Low-temperature FCC to L10 phase transformation in CoPt(Bi nanoparticles

    Directory of Open Access Journals (Sweden)

    Frank M. Abel

    2016-05-01

    Full Text Available This work is focused on the effects of Bi substitution on the synthesis of CoPt nanoparticles with the L10 structure using a modified organometallic approach. The structural and magnetic properties of the nanoparticles have been studied and compared directly with those of CoPt nanoparticles synthesized by the same technique but in the absence of Bi substitution. The as-synthesized particles at 330 °C have an average size of 11.7 nm and a partially ordered L10 phase with a coercivity of 1 kOe. The coercivity is increased to 9.3 kOe and 12.4 kOe after annealing for 1 hour at 600 and 700 °C. The structural and magnetic properties suggest that Bi promotes the formation of ordered L10 phase at low temperatures leading to the development of high coercivities.

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

    KAUST Repository

    Zhu, Haibo

    2014-12-01

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

  1. Critical Factors Controlling Pd and Pt Potential in Porphyry Cu–Au Deposits: Evidence from the Balkan Peninsula

    Directory of Open Access Journals (Sweden)

    Demetrios G. Eliopoulos

    2014-03-01

    Full Text Available Porphyry Cu–Au–Pd±Pt deposits are significant Au resources, but their Pd and Pt potential is still unknown. Elevated Pd, Pt (hundreds of ppb and Au contents are associated with typical stockwork magnetite-bornite-chalcopyrite assemblages, at the central parts of certain porphyry deposits. Unexpected high grade Cu–(Pd+Pt (up to 6 ppm mineralization with high Pd/Pt ratios at the Elatsite porphyry deposit, which is found in a spatial association with the Chelopech epithermal deposit (Bulgaria and the Skouries porphyry deposit, may have formed during late stages of an evolved hydrothermal system. Estimated Pd, Pt and Au potential for porphyry deposits is consistent with literature model calculations demonstrating the capacity of aqueous vapor and brine to scavenge sufficient quantities of Pt and Pd, and could contribute to the global platinum-group element (PGE production. Critical requirements controlling potential of porphyry deposits may be from the metals contained in magma (metasomatized asthenospheric mantle wedge as indicated by significant Cr, Co, Ni and Re contents. The Cr content may be an indicator for the mantle input.

  2. Catalytic soot oxidation in microscale experiments: Simulation of interactions between co-deposited graphitic nanoparticle agglomerates and platinum nanoparticles

    Science.gov (United States)

    Seipenbusch, Martin; Friedlander, Sheldon K.

    2004-12-01

    Continuously regenerating catalytic soot traps are under development to reduce particulate emissions from diesel exhaust. A good understanding of the processes that take place during soot oxidation is needed to optimize diesel soot trap performance. To gain insight into these processes from the perspective of nanoparticle technology, the effects of catalyst particle size and the interparticle distance between soot and catalyst particles were measured. A model catalyst was prepared by depositing Pt nanoparticles on a SiO/SiO2-coated transmission electron microscope (TEM) grid. A soot surrogate composed of graphitic nanoparticle agglomerates generated by laser ablation was deposited on the same surface. This system simulates, morphologically, catalytic soot traps used in practice. The reaction was carried out in a tubular flow reactor in which the gas phase simulated diesel exhaust gas, composed of a mixture of 10% O2 and 1000 ppm NO with the remainder N2. The progress of the carbon nanoparticle oxidation was monitored off-line by analysis of electron microscopy images of the agglomerates before and after reaction. This experimental method permitted the correlation of reaction rate with particle sizes and separation distances as well as catalyst surface area in the direct environs of the soot particles. The experimental results revealed no effect of Pt catalyst particle size in the range 7-31 nm on the rate of reaction. Also observed were a decrease in the rate of reaction with increasing distance between carbon agglomerates and catalyst particles and a linear dependence of the reaction rate on the fractional catalyst surface area coverage.

  3. Spectroscopic study of tetradecyltrimethylammonium bromide Pt-C14TAB nanoparticles: Structure and Stability

    Energy Technology Data Exchange (ETDEWEB)

    Borodko, Y.; Jones, L.; Frei, H.; Somorjai, G.

    2009-01-09

    The vibrational spectra of platinum nanoparticles (12 nm) capped with tetradecyltrimethylammonium bromide, C{sub 14}TAB, were investigated by Fourier transform infrared (FTIR) spectroscopy. We have shown that the thermal decay of Pt-C{sub 14}TAB nanoparticles in N{sub 2}, H{sub 2} and O{sub 2} atmospheres leads to the release of hydrocarbon chain of surfactant and the formation of strongly bonded layer of ammonium cations on the platinum surface. The platinum atoms accessible to CO chemisorptions were not reducible by hydrogen in the temperature ranging from 30 C to 200 C. A FTIR spectrum of C{sub 14}TAB adsorbed on Pt nanoparticles dramatically perturbed as compared with pure C{sub 14}TAB. New intense and broad bands centered at 1450 cm{sup -1} and 760 cm{sup -1} are making their appearance in Pt-C{sub 14}TAB. It may be speculated, that new bands are result of coupling between conducting electrons of Pt and molecular vibrations of adsorbed C{sub 14}TAB and as a consequence specific vibrational modes of ammonium cation transformed into electron-vibrational modes.

  4. The structural transition from epitaxial Fe/Pt multilayers to an ordered FePt film using low energy ion beam sputtering deposition with no buffer layer

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Chih-Hao, E-mail: chlee@mx.nthu.edu.tw [Department of Engineering and System Science, National Tsing Hua University, Hsinchu 30013, Taiwan (China); Chen, Yu-Sheng [Department of Engineering and System Science, National Tsing Hua University, Hsinchu 30013, Taiwan (China); Electronics and Optoelectronics Research Laboratories, Industrial Technology Research Institute, Hsinchu 31040, Taiwan (China); Liu, Li-Jung [Department of Engineering and System Science, National Tsing Hua University, Hsinchu 30013, Taiwan (China); Huang, J.C.A. [Department of Physics, National Cheng Kung University, Tainan 70101, Taiwan (China)

    2014-11-03

    An epitaxial L1{sub 0} FePt thin film grown from an [Fe(10 Å)/Pt(10 Å)]{sub 15} multilayer with the orientation of (001) was prepared by an ion beam sputtering deposition method without buffer layer. From the measurement data of X-ray diffraction and X-ray reflectivity, the multilayer structure was totally disappeared and a uniform FePt alloy thin film was formed at temperatures higher than 600 °C. For the as-deposited thin film grown at 100 °C, the multilayer already possesses an epitaxial structure. The epitaxial relation is FePt(001)[100]//MgO(001)[100] and this epitaxial relation persists after sequential high temperature annealing. An epitaxial L1{sub 0} ordered FePt(001) film with order parameter of 0.95 was obtained when the annealing temperature reached 650 °C. The ordered FePt(001) thin film has a perpendicular magnetic anisotropy with a squareness of 0.95 ± 0.03 on the magnetic hysteresis loop. This experiment demonstrates that the low energy ion beam sputtering deposition will preserve the epitaxial relation with no buffer layer between multilayer and substrate. - Highlights: • The Fe/Pt films using ion sputtering deposition with no buffer layer is epitaxial. • Multilayer structure was totally disappeared at temperatures higher than 600 °C. • Order parameter reach 0.95 after annealing at 650 °C. • Interfacial epitaxial FePt alloy already formed at 100 °C.

  5. Photosensitive Pt(IV)-azide prodrug-loaded nanoparticles exhibit controlled drug release and enhanced efficacy in vivo.

    Science.gov (United States)

    Xiao, Haihua; Noble, Gavin T; Stefanick, Jared F; Qi, Ruogu; Kiziltepe, Tanyel; Jing, Xiabin; Bilgicer, Basar

    2014-01-10

    Cisplatin has long been the first line of treatment for a variety of solid tumors. However, poor pharmacokinetics and high incidences of resistance in the clinic have motivated the production of numerous alternative Pt-based anticancer species. Recently, photosensitive Pt(IV) complexes have garnered much interest because they offer a method of selective induction of active Pt(II) at the tumor site by UVA irradiation. Here, we report the first synthesis, in vitro and in vivo characterization of a novel series of photosensitive Pt(IV)–azide prodrugs and micellar nanoparticle formulations thereof. Upon mild UVA irradiation, both free Pt(IV) complexes and micellar nanoparticles rapidly released biologically active Pt(II), capable of binding to 5′-GMP,while remaining extremely stable in the dark. In vitro, uptake of photosensitive Pt(IV) prodrugs by ovarian cancer SKOV-3 cells was greatly enhanced with the micellar nanoparticles compared to their free prodrug analogs, as well as cisplatin and oxaliplatin. Increased cytotoxicity was observed upon UVA treatment, with up to a 13-fold enhancement over oxaliplatin for the micellar nanoparticles. In vivo bioavailability of micellar nanoparticles was enhanced ~10 fold over free Pt(IV) prodrugs. Importantly, micellar nanoparticles demonstrated significantly improved efficacy against H22 murine hepatocarcinoma, showing decreased systemic toxicity and increased tumor growth inhibition relative to small molecule drugs. These findings establish that photosensitive Pt(IV) complexes, specifically when formulated into micellar nanoparticles, have the potential to offer a robust platform for the controlled delivery and selective activation of Pt-based anticancer therapeutics.

  6. Construction of an amperometric glycated hemoglobin biosensor based on Au-Pt bimetallic nanoparticles and poly (indole-5-carboxylic acid) modified Au electrode.

    Science.gov (United States)

    Jain, Utkarsh; Gupta, Shaivya; Chauhan, Nidhi

    2017-07-14

    The glucose level measurement in the diabetic patient plays a vital role in identification of the treatments going on and it also provides the control over the diabetics. A new electrochemical sensing device was constructed for determination of glycated hemoglobin (HbA1c) in whole blood samples. Fructosyl amine oxidase (FAO) was bioconjugated onto hybrid nanocomposite i.e., gold nanoparticles-platinum nanoparticles (AuNPs-PtNPs) and poly indole-5-carboxylic acid (PIN5COOH), deposited electrochemically on gold electrode. Bimetallic nanoparticles not only show their individual properties but also provides the synergistic effect between the two noble metal nanoparticles. AuNPs-PtNPs shown as an amplified sensing interface at lower voltage which makes the sensor more sensitive and specific. The FAO/AuNPs-PtNPs onto PIN5COOH/Au electrode shows a promising future in diagnosis of HbA1c and diabetes management. The novel sensor formed has good accuracy, selectivity, sensitivity, precision and reliability. In addition to these, it showed good storage stability and retained 50% of its initial activity within 12 weeks at 4°C. Copyright © 2017 Elsevier B.V. All rights reserved.

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

    Science.gov (United States)

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

    2016-07-27

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

  8. Monolayer-directed Assembly and Magnetic Properties of FePt Nanoparticles on Patterned Aluminum Oxide

    OpenAIRE

    Guus Rijnders; Jurriaan Huskens; van der Wiel, Wilfred G.; Blank, Dave H. A.; Reinhoudt, David N.; Sachin Kinge; Tian Gang; Oktay Yildirim

    2010-01-01

    FePt nanoparticles (NPs) were assembled on aluminum oxide substrates, and their ferromagnetic properties were studied before and after thermal annealing. For the first time, phosph(on)ates were used as an adsorbate to form self-assembled monolayers (SAMs) on alumina to direct the assembly of NPs onto the surface. The Al2O3 substrates were functionalized with aminobutylphosphonic acid (ABP) or phosphonoundecanoic acid (PNDA) SAMs or with poly(ethyleneimine) (PEI) as a reference. FePt NPs assem...

  9. Electrochemical deposition of copper onto Pt(111) in the presence of (bi)sulfate anions

    Energy Technology Data Exchange (ETDEWEB)

    Lucas, C.A. [Materials Sciences Division, Lawrence Berkeley National Laboratory, University of California, Berkeley, California 94720 (United States)]|[Department of Physics, University of Liverpool, Oliver Lodge Laboratory, Liverpool, L69 7ZE (United Kingdom); Markovic, N.M.; Ross, P.N. [Materials Sciences Division, Lawrence Berkeley National Laboratory, University of California, Berkeley, California 94720 (United States)

    1997-08-01

    Using {ital in situ} x-ray diffraction we have studied the underpotential deposition (UPD) of copper onto a Pt(111) electrode in sulfuric acid. Deposition occurs in a two-stage process; close to a full monolayer of Cu being preceded by a ({radical}(3){times}{radical}(3))R30{degree} structure that consists of both Cu and (bi)sulfate anions and is similar to the structure observed on the Au(111) electrode. Utilizing anomalous scattering methods we can accurately determine the Cu coverage during UPD and propose structural models based on crystal truncation rod measurements. {copyright} {ital 1997} {ital The American Physical Society}

  10. Fabrication of Supported AuPt Alloy Nanocrystals with Enhanced Electrocatalytic Activity for Formic Acid Oxidation through Conversion Chemistry of Layer-Deposited Pt(2+) on Au Nanocrystals.

    Science.gov (United States)

    Kim, Seong Hyeon; Jeong, Hwakyeung; Kim, Jongwon; Lee, In Su

    2015-10-07

    The exploitation of nanoconfined conversion of Au- and Pt-containing binary nanocrystals for developing a controllable synthesis of surfactant-free AuPt nanocrystals with enhanced formic acid oxidation (FAO) activity is reported, which can be stably and evenly immobilized on various support materials to diversify and optimize their electrocatalytic performance. In this study, an atomic layer of Pt(2+) species is discovered to be spontaneously deposited in situ on the Au nanocrystal generated from a reverse-microemulsion solution. The resulting Au/Pt(2+) nanocrystal thermally transforms into a reduced AuPt alloy nanocrystal during the subsequent solid-state conversion process within the SiO2 nanosphere. The alloy nanocrystals can be isolated from SiO2 in a surfactant-free form and then dispersedly loaded on the carbon sphere surface, allowing for the production of a supported electrocatalyst that exhibits much higher FAO activity than commercial Pt/C catalysts. Furthermore, by involving Fe3O4 nanocrystals in the conversion process, the AuPt alloy nanocrystals can be grown on the oxide surface, improving the durability of supported metal catalysts, and then uniformly loaded on a reduced graphene oxide (RGO) layer with high electroconductivity. This produces electrocatalytic AuPt/Fe3O4/RGO nanocomposites whose catalyst-oxide-graphene triple-junction structure provides improved electrocatalytic properties in terms of both activity and durability in catalyzing FAO. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  11. Real-time electrochemical detection of hydrogen peroxide secretion in live cells by Pt nanoparticles decorated graphene-carbon nanotube hybrid paper electrode.

    Science.gov (United States)

    Sun, Yimin; He, Kui; Zhang, Zefen; Zhou, Aijun; Duan, Hongwei

    2015-06-15

    In this work, we develop a new type of flexible and lightweight electrode based on highly dense Pt nanoparticles decorated free-standing graphene-carbon nanotube (CNT) hybrid paper (Pt/graphene-CNT paper), and explore its practical application as flexible electrochemical biosensor for the real-time tracking hydrogen peroxide (H2O2) secretion by live cells. For the fabrication of flexible nanohybrid electrode, the incorporation of CNT in graphene paper not only improves the electrical conductivity and the mechanical strength of graphene paper, but also increases its surface roughness and provides more nucleation sites for metal nanoparticles. Ultrafine Pt nanoparticles are further decorated on graphene-CNT paper by well controlled sputter deposition method, which offers several advantages such as defined particle size and dispersion, high loading density and strong adhesion between the nanoparticles and the substrate. Consequently, the resultant flexible Pt/graphene-CNT paper electrode demonstrates a variety of desirable electrochemical properties including large electrochemical active surface area, excellent electrocatalytic activity, high stability and exceptional flexibility. When used for nonenzymatic detection of H2O2, Pt/graphene-CNT paper exhibits outstanding sensing performance such as high sensitivity, selectivity, stability and reproducibility. The sensitivity is 1.41 µA µM(-1) cm(-2) with a linear range up to 25 µM and a low detection limit of 10 nM (S/N=3), which enables the resultant biosensor for the real-time tracking H2O2 secretion by live cells macrophages.

  12. Pt nanoparticles functionalized 3D SnO2 nanoflowers for gas sensor application

    Science.gov (United States)

    Liu, Yinglin; Huang, Jing; Yang, Jiedi; Wang, Shurong

    2017-04-01

    3D SnO2 nanoflowers (NFs) assembled by rod-like nanostructures were synthesized by a facile hydrothermal method only using simple and inexpensive SnCl4·5H2O and NaOH as the starting materials, without using any surfactants or templates. The as-synthesized 3D SnO2 NFs were further functionalized by Pt nanoparticles (NPs) by a simple ammonia precipitate method, and the derived Pt NP-functionalized 3D SnO2 NFs were further investigated for gas sensor application using ethanol as a probe gas. Obtained results showed that the Pt NP-functionalized 3D SnO2 NF sensor exhibited much higher response in comparison with pure SnO2 sensor, altogether with short response/recovery times and good reproducibility. The enhanced gas sensing performances could be attributed to spill-over effect of Pt NPs for promoting gas sensing reactions, the synergic electronic interaction between Pt NPs and SnO2 support, the high surface-to-volume ratio and good electron mobility of the 1D SnO2 nanorod units, and unique 3D hierarchical flower-like nanostructures. It is also expected that the as-prepared 3D SnO2 NFs and Pt NP-functionalized product can be used in other fields such as optoelectronic devices, Li-ion battery and dye sensitized solar cells.

  13. Mixed-PtPd-shell PtPdCu nanoparticle nanotubes templated from copper nanowires as efficient and highly durable electrocatalysts

    Energy Technology Data Exchange (ETDEWEB)

    Li, Hui-Hui; Cui, Chun-Hua; Zhao, Shuo; Yao, Hong-Bin; Gao, Min-Rui; Fan, Feng-Jia; Yu, Shu-Hong [National Synchrotron Radiation Laboratory, University of Science and Technology of China, Hefei, Anhui 230026 (China); Div. of Nanomaterials and Chemistry, Heifei National Lab. for Physical, Sciences at Microscale (China)

    2012-10-15

    The controlled synthesis of mixed-PtPd-shell PtPdCu-alloy nanoparticle nanotubes (ANNTs) is demonstrated by galvanic displacement with partially sacrificial copper-nanowire templates, and following the electrochemical leaching of the non-noble metal Cu in the acidic electrolyte. These core-shell catalysts significantly reduce the amount of expensive Pt and highly improve the electrocatalytic activity and durability through their modified electronic structure, atomic distribution, and 1D structure property. (Copyright copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  14. 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.

  15. Highly dispersed Pt-Ni nanoparticles on nitrogen-doped carbon nanotubes for application in direct methanol fuel cells.

    Science.gov (United States)

    Jiang, Shujuan; Ma, Yanwen; Tao, Haisheng; Jian, Guoqiang; Wang, Xizhang; Fan, Yining; Zhu, Jianmin; Hu, Zheng

    2010-06-01

    Binary Pt-Ni alloyed nanoparticles supported on nitrogen-doped carbon nanotubes (NCNTs) have been facilely constructed without pre-modification by making use of the active sites in NCNTs due to the N-participation. So-obtained binary Pt-Ni alloyed nanoparticles have been highly dispersed on the outer surface of the support with the size of about 3-4 nm. The electrochemical properties of the catalysts for methanol oxidation have been systematically evaluated. Binary Pt-Ni alloyed composites with molar ratio (Pt:Ni) of 3:2 and 3:1 present enhanced electrocatalytic activities and improved tolerance to CO poisoning as well as the similar stability, in comparison with the commercial Pt/C catalyst and the monometallic Pt/NCNTs catalysts. These results imply that so-constructed nanocomposite catalysts have the potential for applications in direct methanol fuel cells.

  16. Electrochemical Deposition of Platinum and Palladium on Gold Nanoparticles Loaded Carbon Nanotube Support for Oxidation Reactions in Fuel Cell

    Directory of Open Access Journals (Sweden)

    Surin Saipanya

    2014-01-01

    Full Text Available Pt and Pd sequentially electrodeposited Au nanoparticles loaded carbon nanotube (Au-CNT was prepared for the electrocatalytic study of methanol, ethanol, and formic acid oxidations. All electrochemical measurements were carried out in a three-electrode cell. A platinum wire and Ag/AgCl were used as auxiliary and reference electrodes, respectively. Suspension of the Au-CNT, phosphate buffer, isopropanol, and Nafion was mixed and dropped on glassy carbon as a working electrode. By sequential deposition method, PdPtPt/Au-CNT, PtPdPd/Au-CNT, and PtPdPt/Au-CNT catalysts were prepared. Cyclic voltammograms (CVs of those catalysts in 1 M H2SO4 solution showed hydrogen adsorption and hydrogen desorption reactions. CV responses for those three catalysts in methanol, ethanol, and formic acid electrooxidations studied in 2 M CH3OH, CH3CH2OH, and HCOOH in 1 M H2SO4 show characteristic oxidation peaks. The oxidation peaks at anodic scan contribute to those organic substance oxidations while the peaks at cathodic scan are related with the reoxidation of the adsorbed carbonaceous species. Comparing all those three catalysts, it can be found that the PdPtPt/Au-CNT catalyst is good at methanol oxidation; the PtPdPt/Au-CNT effectively enhances ethanol oxidation while the PtPdPd/Au-CNT exceptionally catalyzes formic acid oxidation. Therefore, a different stoichiometry affects the electrochemical active surface area of the catalysts to achieve the catalytic oxidation reactions.

  17. Array Formation and Size Effects in Chemically Synthesized FePt Nanoparticles

    Science.gov (United States)

    Colak, Levent; Hadjipanayis, George

    2007-03-01

    FePt nanoparticles with controlled size have been synthesized following a route given by Shukla et. al.[1] The effect of particle size on the magnetic properties has been investigated for nanoparticles with sizes of 3.0 and 6.0 nm. With the addition of the surfactants at a later stage of preparation, a long range self-assembled array of particles was obtained as evidenced by transmission electron microscope (TEM). By comparing bright field images of the samples with projected potential image simulations^ [2], the packing structures and stacking sequences of the arrays were identified. Well-aligned mono and multi layered hcp to bcc nanostructures are formed from 5 nm FePt nanoparticles. Subjecting the NP's to thermal processing at 800 ^oC results in a transformation of the nanoparticles from the disordered fcc phase to the ordered L10 phase. HRTEM studies have been carried out to investigate the development of particle morphology and microstructure during the synthesis and subsequent annealing of nanoparticles. 1. N. Shukla, C. Liu, A. G. Roy, Matt. Lett. 60, 2006, 995-998. 2. S. Yamamuro, D. F. Farrell and S. A. Majetich, Phys. Rev. B 65, 224431 (2002).

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

    Science.gov (United States)

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

    2016-12-01

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

  19. Electrochemical pulsed deposition of platinum nanoparticles on indium tin oxide/polyethylene terephthalate as a flexible counter electrode for dye-sensitized solar cells

    Energy Technology Data Exchange (ETDEWEB)

    Wei, Yu-Hsuan; Chen, Chih-Sheng [Department of Materials Engineering, Ming Chi University of Technology, New Taipei City 24301, Taiwan (China); Ma, Chen-Chi M. [Department of Chemical Engineering, National Tsing Hua University, Hsinchu 30013, Taiwan (China); Tsai, Chuen-Horng [Department of Engineering and System Science, National Tsing Hua University, Hsinchu 30013, Taiwan (China); Hsieh, Chien-Kuo, E-mail: jack_hsieh@mail.mcut.edu.tw [Department of Materials Engineering, Ming Chi University of Technology, New Taipei City 24301, Taiwan (China)

    2014-11-03

    In this study, a pulsed-mode electrochemical deposition (Pulse-ECD) technique was employed to deposit platinum nanoparticles (PtNPs) on the indium tin oxide/polyethylene terephthalate (ITO/PET) substrate as a flexible counter electrode for dye-sensitized solar cells (DSSCs). The characteristic properties of the Pulse-ECD PtNPs were prepared and compared to the traditional (electron beam) Pt film. The surface morphologies of the PtNPs were examined by field emission scanning electron microscopy (FE-SEM) and the atomic force microscope (AFM). The FE-SEM results showed that our PtNPs were deposited uniformly on the ITO/PET flexible substrates via the Pulse-ECD technique. The AFM results indicated that the surface roughness of the pulsed PtNPs influenced the power conversion efficiency (PCE) of DSSCs, due to the high specific surface area of PtNPs which enhanced the catalytic activities for the reduction (I{sub 3}{sup −} to I{sup −}) of redox electrolyte. In combination with a N719 dye-sensitized TiO{sub 2} working electrode and an iodine-based electrolyte, the DSSCs with the PtNPs flexible counter electrode showed a PCE of 4.3% under the illumination of AM 1.5 (100 mW cm{sup −2}). The results demonstrated that the Pulse-ECD PtNPs are good candidate for flexible DSSCs. - Highlights: • We used indium tin oxide/polyethylene terephthalate as a flexible substrate. • We utilized pulse electrochemical deposition to deposit platinum nanoparticles. • We synthesized a flexible counter electrode for dye-sensitized solar cell (DSSC). • The power conversion efficiency of DSSC was measured to be 4.3%.

  20. The Effect of PtRuIr Nanoparticle Crystallinity in Electrocatalytic Methanol Oxidation

    Directory of Open Access Journals (Sweden)

    Vladimir Linkov

    2013-04-01

    Full Text Available Two structural forms of a ternary alloy PtRuIr/C catalyst, one amorphous and one highly crystalline, were synthesized and compared to determine the effect of their respective structures on their activity and stability as anodic catalysts in methanol oxidation. Characterization techniques included TEM, XRD, and EDX. Electrochemical analysis using a glassy carbon disk electrode for cyclic voltammogram and chronoamperometry were tested in a solution of 0.5 mol L−1 CH3OH and 0.5 mol L−1 H2SO4. Amorphous PtRuIr/C catalyst was found to have a larger electrochemical surface area, while the crystalline PtRuIr/C catalyst had both a higher activity in methanol oxidation and increased CO poisoning rate. Crystallinity of the active alloy nanoparticles has a big impact on both methanol oxidation activity and in the CO poisoning rate.

  1. Effect of Pt Nanoparticles on the Photocatalytic Activity of ZnO Nanofibers

    Science.gov (United States)

    Di Mauro, Alessandro; Zimbone, Massimo; Scuderi, Mario; Nicotra, Giuseppe; Fragalà, Maria Elena; Impellizzeri, Giuliana

    2015-12-01

    For this study, we originally realized ZnO nanofibers (˜50 nm in mean radius) mixed with Pt nanoparticles (˜30 nm in mean radius), prepared by pulsed laser ablation in liquid, and investigated their photocatalytic performance. The material was synthesized by the simple electrospinning method coupled with subsequent thermal treatments. Methylene blue was employed as a representative dye pollutant to evaluate the photocatalytic activity of the nanofibers. It was found that the Pt-ZnO fibers exhibit a photodegradation reaction rate that is ˜40 % higher than the one obtained for reference ZnO fibers. These encouraging results demonstrate that Pt-ZnO nanofibers can be fruitfully applied for environmental applications.

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

    Science.gov (United States)

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

    2013-01-01

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

  3. Characterization of Au and Bimetallic PtAu Nanoparticles on PDDA-Graphene Sheets as Electrocatalysts for Formic Acid Oxidation

    Science.gov (United States)

    Yung, Tung-Yuan; Liu, Ting-Yu; Huang, Li-Ying; Wang, Kuan-Syun; Tzou, Huei-Ming; Chen, Po-Tuan; Chao, Chi-Yang; Liu, Ling-Kang

    2015-09-01

    Nanocomposite materials of the Au nanoparticles (Au/PDDA-G) and the bimetallic PtAu nanoparticles on poly-(diallyldimethylammonium chloride) (PDDA)-modified graphene sheets (PtAu/PDDA-G) were prepared with hydrothermal method at 90 °C for 24 h. The composite materials Au/PDDA-G and PtAu/PDDA-G were evaluated by transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and thermogravimetric analysis (TGA) for exploring the structural characterization for the electrochemical catalysis. According to TEM results, the diameter of Au and bimetallic PtAu nanoparticles is about 20-50 and 5-10 nm, respectively. X-ray diffraction (XRD) results indicate that both of PtAu and Au nanoparticles exhibit the crystalline plane of (111), (200), (210), and (311). Furthermore, XRD data also show the 2°-3° difference between pristine graphene sheets and the PDDA-modified graphene sheets. For the catalytic activity tests of Au/PDDA-G and PtAu/PDDA-G, the mixture of 0.5 M aqueous H2SO4 and 0.5 M aqueous formic acid was used as model to evaluate the electrochemical characterizations. The catalytic activities of the novel bimetallic PtAu/graphene electrocatalyst would be anticipated to be superior to the previous electrocatalyst of the cubic Pt/graphene.

  4. Characterization of Au and Bimetallic PtAu Nanoparticles on PDDA-Graphene Sheets as Electrocatalysts for Formic Acid Oxidation.

    Science.gov (United States)

    Yung, Tung-Yuan; Liu, Ting-Yu; Huang, Li-Ying; Wang, Kuan-Syun; Tzou, Huei-Ming; Chen, Po-Tuan; Chao, Chi-Yang; Liu, Ling-Kang

    2015-12-01

    Nanocomposite materials of the Au nanoparticles (Au/PDDA-G) and the bimetallic PtAu nanoparticles on poly-(diallyldimethylammonium chloride) (PDDA)-modified graphene sheets (PtAu/PDDA-G) were prepared with hydrothermal method at 90 °C for 24 h. The composite materials Au/PDDA-G and PtAu/PDDA-G were evaluated by transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and thermogravimetric analysis (TGA) for exploring the structural characterization for the electrochemical catalysis. According to TEM results, the diameter of Au and bimetallic PtAu nanoparticles is about 20-50 and 5-10 nm, respectively. X-ray diffraction (XRD) results indicate that both of PtAu and Au nanoparticles exhibit the crystalline plane of (111), (200), (210), and (311). Furthermore, XRD data also show the 2°-3° difference between pristine graphene sheets and the PDDA-modified graphene sheets. For the catalytic activity tests of Au/PDDA-G and PtAu/PDDA-G, the mixture of 0.5 M aqueous H2SO4 and 0.5 M aqueous formic acid was used as model to evaluate the electrochemical characterizations. The catalytic activities of the novel bimetallic PtAu/graphene electrocatalyst would be anticipated to be superior to the previous electrocatalyst of the cubic Pt/graphene.

  5. Alloy ratio effect of Pd/Pt nanoparticles on carbon nanotubes for catalysing methanol-tolerant oxygen reduction

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Chien-Liang, E-mail: cl_lee@url.com.t [Department of Chemical and Materials Engineering, National Kaohsiung University of Applied Science, Kaohsiung, Taiwan (China); Chiou, Hsueh-Ping; Wu, Shi-Chi; Wu, Chen-Chung [Department of Chemical and Materials Engineering, National Kaohsiung University of Applied Science, Kaohsiung, Taiwan (China)

    2010-12-30

    Pd{sub 1}Pt{sub 3}, Pd{sub 1}Pt{sub 1}, and Pd{sub 3}Pt{sub 1} nanoparticles supported on multi-wall carbon nanotubes (CNTs) were prepared by the self-regulation reduction of sodium n-dodecyl sulphate and used as catalysts in oxygen reduction reactions (ORRs). The crystal properties of these alloy nanoparticles on the CNT were measured by X-ray diffraction spectroscopy (XRD) and high-resolution transmission electron microscopy (HRTEM). The angle shifting of the XRD peak and the lattice spacing of the nanoparticles measured by HRTEM increased with an increase in Pd amount, indicating a regulable Pd-Pt ratio for the alloy nanoparticle composition. Rotating ring-disk electrode (RRDE) measurements indicate that the number of electrons catalysed by the Pd{sub 1}Pt{sub 3}/CNT, Pd{sub 1}Pt{sub 1}/CNT, and Pd{sub 3}Pt{sub 1}/CNT nanocatalysts in the ORRs were 3.98, 3.97, and 3.93, respectively. These results show that these ORRs occur via a 4-electron pathway. Linearly scanned voltammetry in the electrolyte with methanol revealed that Pd{sub 3}Pt{sub 1}/CNT has high methanol tolerance during ORRs.

  6. Pd@Pt Core–Shell Nanoparticles with Branched Dandelion-like Morphology as Highly Efficient Catalysts for Olefin Reduction

    Science.gov (United States)

    A facile synthesis based on the addition of ascorbic acid to a mixture of Na2PdCl4, K2PtCl6, and Pluronic P123 results in highly branched core–shell nanoparticles (NPs) with a micro–mesoporous dandelion-like morphology comprising Pd core and Pt shell. The slow reduction kinetics ...

  7. Pd@Pt Core–Shell Nanoparticles with Branched Dandelion-like Morphology as Highly Efficient Catalysts for Olefin Reduction

    Science.gov (United States)

    A facile synthesis based on the addition of ascorbic acid to a mixture of Na2PdCl4, K2PtCl6, and Pluronic P123 results in highly branched core–shell nanoparticles (NPs) with a micro–mesoporous dandelion-like morphology comprising Pd core and Pt shell. The slow reduction kinetics ...

  8. Magnetron sputtering deposition of [FePt/Ag]n multilayers for perpendicular recording

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    [FePt/Ag]n multilayers were deposited on glass substrates by RF magnetron sputtering and ex situ annealed at 550℃ for 30 min. The effects of inserted Ag layer thickness and the number of bilayer repetitions (n) on the structure and magnetic properties of the multilayers were investigated. It was found that the difference between in-plane and out-of-plane coercivities varied with an increase of inserted Ag layer thickness in the [FePt 2 nm/Ag x nm]10 multilayers. The ratio of out-of-plane coercivity to in-plane coercivity reached the maximum value with the Ag layer thickness of 5 nm, indicating that the Ag layer thickness plays an important role in obtaining perpendicular orientation. For the [FePt 2 nm/Ag 5 nm]n multilayers, perpendicular orientation is also influenced by n. The maximum value of the ratio of out-of-plane coercivity to in-plane coercivity appeared when n was given as 8. It was found that the [FePt 2 nm/Ag 5 nm]8 had a high perpendicular coercivity of 520 kA/m and a low in-plane one of 88 kA/m, which shows a strong perpendicular anisotropy.

  9. A Novel Cholesterol Oxidase Biosensor Based on Pt-nanoparticle /Carbon Nanotube Modified Electrode

    Institute of Scientific and Technical Information of China (English)

    Qiao Cui SHI; Tu Zhi PENG

    2005-01-01

    A Pt-nanoparticle/carbon nanotube modified graphite electrode immobilized with cholesterol oxidase/sol-gel layer was developed for monitoring cholesterol. Using this electrode,cholesterol concentration (4.0×10-6 to 1.0×10 mol/L) could be determined accurately in the presence of ascorbic or uric acid, and the response time was rapid (< 20 s). This biosensor has high sensitivity and selectivity.

  10. XMCD study of CoPt nanoparticles embedded in MgO and amorphous carbon matrices

    Energy Technology Data Exchange (ETDEWEB)

    Tournus, F. [Universite de Lyon, F-69000, France and Univ. Lyon 1, Laboratoire PMCN, CNRS, UMR 5586, F69622 Villeurbanne Cedex (France)], E-mail: ftournus@lpmcn.univ-lyon1.fr; Blanc, N.; Tamion, A. [Universite de Lyon, F-69000, France and Univ. Lyon 1, Laboratoire PMCN, CNRS, UMR 5586, F69622 Villeurbanne Cedex (France); Ohresser, P. [Synchrotron SOLEIL, BP 48, 91192 Gif sur Yvette (France); Perez, A.; Dupuis, V. [Universite de Lyon, F-69000, France and Univ. Lyon 1, Laboratoire PMCN, CNRS, UMR 5586, F69622 Villeurbanne Cedex (France)

    2008-11-15

    We report the synthesis and characterization of CoPt nanoparticles, using X-ray magnetic circular dichroism (XMCD) at the Co L{sub 2,3} edges. Clusters are produced in ultra-high vacuum conditions, following a physical route, and embedded in non-metallic matrices: MgO and amorphous carbon (a-C). In MgO, Co atoms are partially oxidized, which goes with a {mu}{sub L}/{mu}{sub S} enhancement. On the contrary, a-C appears as a very suitable matrix. In particular, annealing of CoPt cluster embedded in a-C is able to promote L 1{sub 0} chemical order, without alteration of the sample. This transformation, which has been directly evidenced by transmission electron microscopy observations, is accompanied by a striking augmentation of {mu}{sub S}, {mu}{sub L} and the {mu}{sub L}/{mu}{sub S} ratio of Co. The presence of Pt leads to an enhanced Co magnetic moment, as compared to Co bulk, even for the chemically disordered alloy. Moreover, the high value of 1.91{mu}{sub B}/at. measured for {mu}{sub S} is unusual for Co and must be a signature of chemical order in CoPt alloy nanoparticles.

  11. Characterization and formic acid oxidation studies of PtAu nanoparticles.

    Science.gov (United States)

    Saipanya, Surin; Srisombat, Laongnuan; Wongtap, Pitak; Sarakonsri, Thapanee

    2014-10-01

    Characterization and electrocatalytic oxidation of formic acid on PtAu nanoparticles supported multiwalled carbon nanotube (MWCNT) were studied. Electrochemical measurements were conducted in a self-made conventional three-electrode glass cell at room temperature. A Pt wire and Ag/AgCl were used as auxiliary and reference electrodes, respectively. The Pt was electrodeposited onto the electrode and their catalytic activities in the electrooxidation of formic acid were examined and compared. The morphology and composition were studied by a combination of transmission electron microscopy (TEM) and energy dispersive X-ray spectroscopy (EDX). Cyclic voltamograms of formic acid electrooxidation show a distinguishing shape with a prominent oxidation peak in the forward scan contributed to the formic acid oxidation whilst the backward scan is associated with the oxidation of exclusion of carbonaceous species. On the basis of the onset potential and current density, the resulting PtAu nanoparticles showed much higher electrocatalytic activity than other counterparts. The results show an excellent sign of applications for fuel cell.

  12. Preparation and characterization of Fe{sub 3}O{sub 4}-Pt nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Andrade, Ângela Leão, E-mail: angelala01@hotmail.com [Federal University of Ouro Preto (UFOP), Department of Chemistry, ICEB (Brazil); Cavalcante, Luis Carlos Duarte [Federal University of Piauí (UFPI), Center of Natural Sciences (Brazil); Fabris, José Domingos [Federal University of Minas Gerais (UFMG), Department of Chemistry, ICEx (Brazil); Pereira, Márcio César [Federal University of the Jequitinhonha and Mucuri Valleys (UFVJM), Institute of Science, Engineering and Technology (Brazil); Ardisson, José Domingos [Center for the Development of the Nuclear Technology (CDTN), Laboratory of Applied Physics (Brazil); Domingues, Rosana Zacarias [Federal University of Minas Gerais (UFMG), Department of Chemistry, ICEx (Brazil)

    2017-11-15

    Pt and Pt-based nanomaterials are active anticancer drugs for their ability to inhibit the division of living cells. Nanoparticles of magnetite containing variable proportions of platinum were prepared in the laboratory. The magnetite nanoparticles with platinum (Pt-Fe{sub 3}O{sub 4}) were obtained by reducing the Fe{sup 3+} of the maghemite (γ Fe{sub 2}O{sub 3}) mixed with platinum (II) acetylacetonate and sucrose in two inversely coupled ceramic crucibles and heated in a furnace at 400 °C for 20 min. The formed carbon during this preparation acts to chemically reduce the ferric iron in maghemite. Moreover, its residual layer on the particle surface prevents the forming magnetite from oxidizing in air and helps retain the platinum in the solid mixture. The produced Pt-magnetite samples were characterized by {sup 57}Fe-Mössbauer spectroscopy, powder X-ray diffraction, scanning electron microscopy, and magnetization measurements. Measurements of AC magnetic-field-induced heating properties of the obtained nanocomposites, in aqueous solution, showed that they are suitable as a hyperthermia agent for biological applications.

  13. WO3/Pt nanoparticles are NADPH oxidase biomimetics that mimic effector cells in vitro and in vivo.

    Science.gov (United States)

    Clark, Andrea J; Coury, Emma L; Meilhac, Alexandra M; Petty, Howard R

    2016-02-12

    To provide a means of delivering an artificial immune effector cell-like attack on tumor cells, we report the tumoricidal ability of inorganic WO3/Pt nanoparticles that mimic a leukocyte's functional abilities. These nanoparticles route electrons from organic structures and electron carriers to form hydroxyl radicals within tumor cells. During visible light exposure, WO3/Pt nanoparticles manufacture hydroxyl radicals, degrade organic compounds, use NADPH, trigger lipid peroxidation, promote lysosomal membrane disruption, promote the loss of reduced glutathione, and activate apoptosis. In a model of advanced breast cancer metastasis to the eye's anterior chamber, we show that WO3/Pt nanoparticles prolong the survival of 4T1 tumor-bearing Balb/c mice. This new generation of inorganic photosensitizers do not photobleach, and therefore should provide an important therapeutic advance in photodynamic therapy. As biomimetic nanoparticles destroy targeted cells, they may be useful in treating ocular and other forms of cancer.

  14. Deposition temperature mediated tunable tilt angle magnetization in Co–Pt/Ni{sub 81}Fe{sub 19} exchange springs

    Energy Technology Data Exchange (ETDEWEB)

    Saravanan, P. [Department of Physics, National Taiwan University, Taipei 106, Taiwan (China); Defence Metallurgical Research Laboratory, Hyderabad 500058 (India); Hsu, Jen-Hwa, E-mail: jhhsu@phys.ntu.edu.tw [Department of Physics, National Taiwan University, Taipei 106, Taiwan (China); Tsai, C.L. [Department of Physics, National Taiwan University, Taipei 106, Taiwan (China); Lee, C.-M. [Graduate School of Materials Science, National Yunlin University of Science and Technology, Douliou 64002, Taiwan (China)

    2015-05-01

    In this study, we investigate the effect of deposition temperature of Co–Pt fixed layer, T{sub d,CoPt} (150, 250 and 350 °C) on the tilt angle magnetization (θ{sub M}) of Ni{sub 81}Fe{sub 19}-layer grown at room temperature (RT) and at different thicknesses (t{sub NiFe}=0, 1.0, 2.5 and 4.0 nm) in Co–Pt(T{sub d,CoPt})/NiFe(t{sub NiFe}) exchange springs. The magnetic studies demonstrated a strong perpendicular magnetic anisotropy (PMA) for the equi-compositional ordered Co–Pt layer grown on glass substrate using the film sequence: Ta(20 nm)/Pt(20 nm)/CoPt(5 nm), regardless of T{sub d,CoPt}. The PMA can be retained with the addition of a 4-nm NiFe layer on the top when T{sub d,CoPt}≥250 °C. In contrast, relatively a thin layer of Ni–Fe (2.5 nm) can destroy the perpendicular exchange-spring behavior if the Co–Pt layer is deposited at RT. Using 3-D micromagnetic simulation, the interfacial exchange coupling strength (A{sub ij}) between the Co–Pt and NiFe-layers was estimated and the A{sub ij} value is found to increase rapidly when T{sub d,CoPt} is increased from RT to 300 °C. Besides, the magnetization tilted angle (θ{sub M}) of NiFe can be easily tuned from completely out-of-plane to almost 60° when t{sub NiFe}=4.0 nm. Through this study, it is demonstrated that the θ{sub M} of NiFe-layer can be tuned by not only altering the t{sub NiFe}; but also by varying the T{sub d,CoPt}. - Highlights: • Equi-compositional ordered 5-nm thick Co–Pt with strong PMA was grown on glass. • The ordered Co–Pt and Ni{sub 81}Fe{sub 19} layers were utilized for OOP and IP-anisotropies. • Tunable tilt angle magnetization was investigated by varying T{sub d,CoPt}. • Using micromagnetic simulation, interfacial exchange coupling strength was deduced. • Deposition temperature mediated θ{sub M} in Co–Pt/NiFe provides a new scope for STO.

  15. FePt and CoPt nanoparticles prepared by micellar method. Effects of A1{yields}L1{sub 0} transition on oxidation resistance and magnetic properties

    Energy Technology Data Exchange (ETDEWEB)

    Han, Luyang

    2011-02-15

    In this thesis FePt and CoPt alloy nanoparticles are prepared with reverse micelles. The metallic nanoparticles with diameters of 2-12 nm and interparticle distances of 20-140 nm are obtained on Si substrates. The magnetic properties of FePt and CoPt nanoparticles as well as oxidation behavior of FePt nanoparticles are investigated. X-ray magnetic circular dichroism (XMCD) measurements on 5.8 nm FePt nanoparticles after hydrogen plasma reduction at 300 C reveals that the magnetic moment per Fe atom and magnetic anisotropy energy match chemically disordered FePt in A1 phase. Annealing at 650 C transform portion of FePt particles to chemically ordered L1{sub 0} phase. The presense of nanoparticles in L1{sub 0} phase is identified by high-resolution transmission electronmicroscopy (HRTEM) investigation, where it is also observed that large fraction of the particles contain defects such as twin boundaries and stacking faults. By increasing the annealing temperature or prolonging annealing time, ratio of transformed particles increases. The average magnetic anisotropy energy of the transformed particles is below 30% of the value of bulk FePt in L1{sub 0} phase. Annealing at above 750 C, however, decreases the average magnetic anisotropy in the sample. Similar A1 {yields} L1{sub 0} transition is observed in FePt nanoparticles with different diameters as well as in CoPt nanoparticles. The spin moment of Fe in FePt nanoparticles decreases with smaller particle diameter, while the orbital moment stays almost constant. Magnetic moments at room temperature are significantly reduced compared to those at low temperature, suggesting the Curie temperatures in FePt and CoPt nanoparticles are significantly lower than in the bulk. The annealing also induces Pt segregation towards the surface in FePt nanoparticles, which is identified by the decreased apparent Fe content measured by X-ray photoelectron spectroscopy (XPS) and X-ray absorption spectroscopy (XAS). The segregation of Pt

  16. Magnetic properties of BaM /Pd-Pt double-layered thin film deposited at various substrate temperatures

    Science.gov (United States)

    Nahar Shams, Nazmun; Liu, Xiaoxi; Matsumoto, Mitsunori; Morisako, Akimitsu

    2005-05-01

    Crystallographic and magnetic properties of barium ferrite (BaM) thin films deposited onto Pt, Pd, and an alloy of Pd-Pt underlayers by sputtering at different substrate temperatures (Ts) from 400to600°C have been studied. It is found that the coercivity values in the perpendicular direction (Hcperp) of the BaM /Pd-Pt films are higher than those of the BaM films deposited on Pd and Pt underlayers. C-axis orientation of BaM /Pd-Pt film can be achieved at very low Ts of 450°C with a Hcperp of 2.1kOe for 30-nm BaM.

  17. Atomic structure and thermal stability of Pt-Fe bimetallic nanoparticles: from alloy to core/shell architectures.

    Science.gov (United States)

    Huang, Rao; Wen, Yu-Hua; Shao, Gui-Fang; Sun, Shi-Gang

    2016-06-22

    Bimetallic nanoparticles comprising noble metal and non-noble metal have attracted intense interest over the past few decades due to their low cost and significantly enhanced catalytic performances. In this article, we have explored the atomic structure and thermal stability of Pt-Fe alloy and core-shell nanoparticles by molecular dynamics simulations. In Fe-core/Pt-shell nanoparticles, Fe with three different structures, i.e., body-centered cubic (bcc), face-centered cubic (fcc), and amorphous phases, has been considered. Our results show that Pt-Fe alloy is the most stable configuration among the four types of bimetallic nanoparticles. It has been discovered that the amorphous Fe cannot stably exist in the core and preferentially transforms into the fcc phase. The phase transition from bcc to hexagonal close packed (hcp) has also been observed in bcc-Fe-core/Pt-shell nanoparticles. In contrast, Fe with the fcc structure is the most preferred as the core component. These findings are helpful for understanding the structure-property relationships of Pt-Fe bimetallic nanoparticles, and are also of significance to the synthesis and application of noble metal based nanoparticle catalysts.

  18. Large coercivity FePt nanoparticles prepared via a one-step method without post-annealing

    Science.gov (United States)

    Zhang, Xinwei; Xiong, Fang; Jiang, Xiaohong; Hua, Zhenghe; Wang, Chunlei; Yang, Shaoguang

    2016-12-01

    L10 FePt nanoparticles were synthesized by a one-step sol-gel autocombustion method, using nontoxic ferric nitrate, hexachloroplatinic acid, and glycine as starting materials. In contrast to common syntheses, high-temperature post-annealing was not required to form the L10 FePt phase. The entire ignition and combustion process lasted no more than one minute. The L10 FePt phase could form in the presence of the high temperature caused by the exothermic combustion reaction. Adjusting the glycine-to-metal ion molar ratio from 0.5 to 6.0 allowed its effects on the phase transformation and magnetic properties of the products to be investigated. X-ray diffraction indicated that pure phase L10 FePt was obtained at a glycine-to-metal ion molar ratio of 1.5. Transmission electron microscopy indicated that the monodisperse L10 FePt nanoparticles had an average particle size of about 20 nm. The reasons why the as-synthesized L10 FePt nanoparticles were not aggregated and sintered could be attributed to the large amount, a gas is being released and the short duration of heat treatment during this combustion. This finding constituted a significant improvement in the synthesis of L10 FePt nanoparticles. Magnetic measurements showed that the L10 FePt nanoparticles had a coercivity of 15.8 kOe at 300 K, and 23.2 kOe at 5 K. Thus, the L10 FePt nanoparticles had a very large coercivity.

  19. Newly developed stepwise electroless deposition enables a remarkably facile synthesis of highly active and stable amorphous Pd nanoparticle electrocatalysts for oxygen reduction reaction.

    Science.gov (United States)

    Poon, Kee Chun; Tan, Desmond C L; Vo, Thang D T; Khezri, Bahareh; Su, Haibin; Webster, Richard D; Sato, Hirotaka

    2014-04-09

    This paper reports on highly active and stable amorphous Pd nanoparticle electrocatalysts for the oxygen reduction reaction. The amorphous catalysts were synthesized by a remarkably facile and quick electroless deposition process newly developed in this study (process time <5 min). An electrode substrate (glassy carbon, carbon cloth) was sequentially dipped for 10 s into two separate solutions of a reducing agent (sodium hypophosphite (NaH2PO2)) and Pd ions to deposit amorphous Pd nanoparticles containing phosphorus (Pd-P). By repeating the deposition cycles, the specific and mass activities of the Pd nanoparticles can be actively tuned. Owing to the nanoscale amorphous nature, the obtained Pd-P nanoparticle electrocatalysts exhibited superior specific and mass activities compared with crystalline Pd nanoparticles synthesized by another reducing agent (N2H4) and commercial Pt-loaded carbon (Pt/C) and Pd-loaded carbon (Pd/C). The specific and mass activities of the amorphous Pd-P nanoparticles were over 4.5 times and 2.6 times higher than previously reported values of Pd and Pt catalysts.

  20. Low-temperature deposition of crystalline silicon nitride nanoparticles by hot-wire chemical vapor deposition

    Science.gov (United States)

    Kim, Chan-Soo; Youn, Woong-Kyu; Lee, Dong-Kwon; Seol, Kwang-Soo; Hwang, Nong-Moon

    2009-07-01

    The nanocrystalline alpha silicon nitride (α-Si 3N 4) was deposited on a silicon substrate by hot-wire chemical vapor deposition at the substrate temperature of 700 °C under 4 and 40 Torr at the wire temperatures of 1430 and 1730 °C, with a gas mixture of SiH 4 and NH 3. The size and density of crystalline nanoparticles on the substrate increased with increasing wire temperature. With increasing reactor pressure, the crystallinity of α-Si 3N 4 nanoparticles increased, but the deposition rate decreased.

  1. Reduced-temperature ordering of FePt nanoparticle assembled films by Fe30Pt70/Fe3O4 core/shell structure

    Institute of Scientific and Technical Information of China (English)

    He Shu-Li; Peng Yin; Liu Li-Li; Jiang Hong-Wei; Liu Li-Feng; Zheng Wu; Wang Ai-Ling

    2007-01-01

    In this paper, Fe3oPt70/Fe3O4 core/shell nanoparticles were synthesized by chemical routine and the layered polycthylenimine (PEI)-Fe30Pt70/Fe3O4 structure was constructed by molecule-mediated self-assembly technique. The dimension of core/shell structured nanoparticles was that of 4nm core and 2 nm shell. After annealing under a flow of forming gas (50%Ar2%%30%H2) for 1h at or above 400℃, the iron oxide shell was reduced to Fe and diffused to Pt-rich core, which leaded to the formation of L10 phase FePt at low temperature. The x-ray diffraction results and magnetic properties measurement showed that the chemical ordering temperature of Fe30Pt70/Fe3O4 core/shell nanoparticles assembly can be reduced to as low as 400℃. The sample annealed at 400℃ showed the coercivity of 4 KOe with the applied field of 1.5T. The core/shell structure was suggested to be an effective way to reduce the ordering temperature obviously.

  2. Monolayer-directed assembly and magnetic properties of FePt nanoparticles on patterned aluminum oxide.

    Science.gov (United States)

    Yildirim, Oktay; Gang, Tian; Kinge, Sachin; Reinhoudt, David N; Blank, Dave H; van der Wiel, Wilfred G; Rijnders, Guus; Huskens, Jurriaan

    2010-03-19

    FePt nanoparticles (NPs) were assembled on aluminum oxide substrates, and their ferromagnetic properties were studied before and after thermal annealing. For the first time, phosph(on)ates were used as an adsorbate to form self-assembled monolayers (SAMs) on alumina to direct the assembly of NPs onto the surface. The Al(2)O(3) substrates were functionalized with aminobutylphosphonic acid (ABP) or phosphonoundecanoic acid (PNDA) SAMs or with poly(ethyleneimine) (PEI) as a reference. FePt NPs assembled on all of these monolayers, but much less on unmodified Al(2)O(3), which shows that ligand exchange at the NPs is the most likely mechanism of attachment. Proper modification of the Al(2)O(3) surface and controlling the immersion time of the modified Al(2)O(3) substrates into the FePt NP solution resulted in FePt NPs assembly with controlled NP density. Alumina substrates were patterned by microcontact printing using aminobutylphosphonic acid as the ink, allowing local NP assembly. Thermal annealing under reducing conditions (96%N(2)/4%H(2)) led to a phase change of the FePt NPs from the disordered FCC phase to the ordered FCT phase. This resulted in ferromagnetic behavior at room temperature. Such a process can potentially be applied in the fabrication of spintronic devices.

  3. Monolayer-directed Assembly and Magnetic Properties of FePt Nanoparticles on Patterned Aluminum Oxide

    Directory of Open Access Journals (Sweden)

    Guus Rijnders

    2010-03-01

    Full Text Available FePt nanoparticles (NPs were assembled on aluminum oxide substrates, and their ferromagnetic properties were studied before and after thermal annealing. For the first time, phosph(onates were used as an adsorbate to form self-assembled monolayers (SAMs on alumina to direct the assembly of NPs onto the surface. The Al2O3 substrates were functionalized with aminobutylphosphonic acid (ABP or phosphonoundecanoic acid (PNDA SAMs or with poly(ethyleneimine (PEI as a reference. FePt NPs assembled on all of these monolayers, but much less on unmodified Al2O3, which shows that ligand exchange at the NPs is the most likely mechanism of attachment. Proper modification of the Al2O3 surface and controlling the immersion time of the modified Al2O3 substrates into the FePt NP solution resulted in FePt NPs assembly with controlled NP density. Alumina substrates were patterned by microcontact printing using aminobutylphosphonic acid as the ink, allowing local NP assembly. Thermal annealing under reducing conditions (96%N2/4%H2 led to a phase change of the FePt NPs from the disordered FCC phase to the ordered FCT phase. This resulted in ferromagnetic behavior at room temperature. Such a process can potentially be applied in the fabrication of spintronic devices.

  4. 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.

  5. Nanoparticle-electrode collision processes: the underpotential deposition of thallium on silver nanoparticles in aqueous solution.

    Science.gov (United States)

    Zhou, Yi-Ge; Rees, Neil V; Compton, Richard G

    2011-08-01

    The electrochemistry of collisions between metal nanoparticles (NPs) and electrode surfaces has been of recent interest with the development of anodic particle coulometry as a characterisation method. For the first time the underpotential deposition of metal ions from solution onto metal nanoparticles during collisions between the NPs and an inert electrode is reported.

  6. Temperature dependence of the kinetics of oxygen reduction on carbon-supported Pt nanoparticles

    Directory of Open Access Journals (Sweden)

    NEVENKA R. ELEZOVIC

    2008-06-01

    Full Text Available The temperature dependence of oxygen reduction reaction (ORR was studied on highly dispersed Pt nanoparticles supported on a carbon cryogel. The specific surface area of the support was 517 m2 g-1, the Pt particles diameter was about 2.7 nm and the loading of the catalyst was 20 wt. %. The kinetics of the ORR at the Pt/C electrode was examined in 0.50 mol dm-3 HClO4 solution in the temperature range from 274 to 318 K. At all temperatures, two distinct E–log j regions were observed; at low current densities with a slope of –2.3RT/F and at high current densities with a slope of –2.3´2RT/F. In order to confirm the mechanism of oxygen reduction previously suggested at a polycrystalline Pt and a Pt/Ebonex nanostructured electrode, the apparent enthalpies of activation at selected potentials vs. the reversible hydrogen electrode were calculated in both current density regions. Although ∆Ha,1≠ > ∆Ha,h≠, it was found that the enthalpies of activation at the zero Galvani potential difference were the same and hence it could be concluded that the rate-determining step of the ORR was the same in both current density regions. The synthesized Pt/C catalyst showed a small enhancement in the catalytic activity for ORR in comparison to the polycrystalline Pt, but no change in the mechanism of the reaction.

  7. Insight into growth of Au-Pt bimetallic nanoparticles: an in situ XAS study.

    Science.gov (United States)

    Nayak, Chandrani; Bhattacharyya, D; Bhattacharyya, K; Tripathi, A K; Bapat, R D; Jha, S N; Sahoo, N K

    2017-07-01

    Au-Pt bimetallic nanoparticles have been synthesized through a one-pot synthesis route from their respective chloride precursors using block copolymer as a stabilizer. Growth of the nanoparticles has been studied by simultaneous in situ measurement of X-ray absorption spectroscopy (XAS) and UV-Vis spectroscopy at the energy-dispersive EXAFS beamline (BL-08) at Indus-2 SRS at RRCAT, Indore, India. In situ XAS spectra, comprising both X-ray near-edge structure (XANES) and extended X-ray absorption fine-structure (EXAFS) parts, have been measured simultaneously at the Au and Pt L3-edges. While the XANES spectra of the precursors provide real-time information on the reduction process, the EXAFS spectra reveal the structure of the clusters formed in the intermediate stages of growth. This insight into the formation process throws light on how the difference in the reduction potential of the two precursors could be used to obtain the core-shell-type configuration of a bimetallic alloy in a one-pot synthesis method. The core-shell-type structure of the nanoparticles has also been confirmed by ex situ energy-dispersive spectroscopy line-scan and X-ray photoelectron spectroscopy measurements with in situ ion etching on fully formed nanoparticles.

  8. Deposition temperature mediated tunable tilt angle magnetization in Co-Pt/Ni81Fe19 exchange springs

    Science.gov (United States)

    Saravanan, P.; Hsu, Jen-Hwa; Tsai, C. L.; Lee, C.-M.

    2015-05-01

    In this study, we investigate the effect of deposition temperature of Co-Pt fixed layer, Td,CoPt (150, 250 and 350 °C) on the tilt angle magnetization (θM) of Ni81Fe19-layer grown at room temperature (RT) and at different thicknesses (tNiFe=0, 1.0, 2.5 and 4.0 nm) in Co-Pt(Td,CoPt)/NiFe(tNiFe) exchange springs. The magnetic studies demonstrated a strong perpendicular magnetic anisotropy (PMA) for the equi-compositional ordered Co-Pt layer grown on glass substrate using the film sequence: Ta(20 nm)/Pt(20 nm)/CoPt(5 nm), regardless of Td,CoPt. The PMA can be retained with the addition of a 4-nm NiFe layer on the top when Td,CoPt≥250 °C. In contrast, relatively a thin layer of Ni-Fe (2.5 nm) can destroy the perpendicular exchange-spring behavior if the Co-Pt layer is deposited at RT. Using 3-D micromagnetic simulation, the interfacial exchange coupling strength (Aij) between the Co-Pt and NiFe-layers was estimated and the Aij value is found to increase rapidly when Td,CoPt is increased from RT to 300 °C. Besides, the magnetization tilted angle (θM) of NiFe can be easily tuned from completely out-of-plane to almost 60° when tNiFe=4.0 nm. Through this study, it is demonstrated that the θM of NiFe-layer can be tuned by not only altering the tNiFe; but also by varying the Td,CoPt.

  9. Beet juice utilization: Expeditious green synthesis of nobel metal nanoparticles (Ag, Au, Pt, and Pd) using microwaves

    Science.gov (United States)

    Metal nanoparticles of Ag, Au, Pt, and Pd were prepared in aqueous solutions via a rapid microwave-assisted green method using beet juice, an abundant sugar-rich agricultural produce, served as both a reducing and a capping reagent. The Ag nanoparticles with capping prepared by b...

  10. Beet juice utilization: Expeditious green synthesis of nobel metal nanoparticles (Ag, Au, Pt, and Pd) using microwaves

    Science.gov (United States)

    Metal nanoparticles of Ag, Au, Pt, and Pd were prepared in aqueous solutions via a rapid microwave-assisted green method using beet juice, an abundant sugar-rich agricultural produce, served as both a reducing and a capping reagent. The Ag nanoparticles with capping prepared by b...

  11. Increasing the Collision Rate of Particle Impact Electroanalysis with Magnetically Guided Pt-Decorated Iron Oxide Nanoparticles.

    Science.gov (United States)

    Robinson, Donald A; Yoo, Jason J; Castañeda, Alma D; Gu, Brett; Dasari, Radhika; Crooks, Richard M; Stevenson, Keith J

    2015-07-28

    An integrated microfluidic/magnetophoretic methodology was developed for improving signal response time and detection limits for the chronoamperometric observation of discrete nanoparticle/electrode interactions by electrocatalytic amplification. The strategy relied on Pt-decorated iron oxide nanoparticles which exhibit both superparamagnetism and electrocatalytic activity for the oxidation of hydrazine. A wet chemical synthetic approach succeeded in the controlled growth of Pt on the surface of FeO/Fe3O4 core/shell nanocubes, resulting in highly uniform Pt-decorated iron oxide hybrid nanoparticles with good dispersibility in water. The unique mechanism of hybrid nanoparticle formation was investigated by electron microscopy and spectroscopic analysis of isolated nanoparticle intermediates and final products. Discrete hybrid nanoparticle collision events were detected in the presence of hydrazine, an electrochemical indicator probe, using a gold microband electrode integrated into a microfluidic channel. In contrast with related systems, the experimental nanoparticle/electrode collision rate correlates more closely with simple theoretical approximations, primarily due to the accuracy of the nanoparticle tracking analysis method used to quantify nanoparticle concentrations and diffusion coefficients. Further modification of the microfluidic device was made by applying a tightly focused magnetic field to the detection volume to attract the magnetic nanoprobes to the microband working electrode, thereby resulting in a 6-fold increase to the relative frequency of chronoamperometric signals corresponding to discrete nanoparticle impact events.

  12. The origin of enhanced L1 0 chemical ordering in Ag-doped FePt nanoparticles

    Science.gov (United States)

    Sung, Yun-Mo; Lee, Myung-Ki; Kim, Ki-Eun; Kim, Tae Geun

    2007-08-01

    FePt and Ag-doped FePt nanoparticles were synthesized by the thermolysis and polyol reductions. The A1-to-L1 0 transformation of the nanoparticles was investigated by differential scanning calorimetry (DSC) at different scanning rates, and the DSC endothermic peak shifts were monitored and used for the Kissinger analyses. The activation energy for the phase transformation was determined to be ˜251 and ˜219 kJ/mol for the pure and doped FePt nanoparticles, respectively. The decrease in the activation energy is the evidence of increased number of vacancies, which turned out to be the origin for the reduced L1 0 chemical ordering temperature in doped FePt.

  13. Electrochemical atomic layer deposition of Pt nanostructures on fuel cell gas diffusion layer

    CSIR Research Space (South Africa)

    Modibedi, M

    2010-12-01

    Full Text Available . Acta 42(10) 1587. 4. Stickney, J.L., et al., (2002) Encyclopedia of Electrochemistry, Wiley-VCH: Weinheim 513 5. Mkwizu T.S., Mathe M.K., Cukrowski I., (2010) Langmuir 26 (1) 570. Electrochemical Atomic Layer Deposition of Pt nanostructures on fuel... cell gas diffusion layer Mmalewane Modibedi1, Tumaini Mkwizu1, 2, Nikiwe Kunjuzwa1,3 , Kenneth Ozoemena1 and Mkhulu Mathe1 1. Energy and Processes, Materials Science and Manufacturing, The Council for Scientific and Industrial Research (CSIR...

  14. Preparation of Ultrafine Fe-Pt Alloy and Au Nanoparticle Colloids by KrF Excimer Laser Solution Photolysis.

    Science.gov (United States)

    Watanabe, Masato; Takamura, Hitoshi; Sugai, Hiroshi

    2009-03-10

    We prepared ultrafine Fe-Pt alloy nanoparticle colloids by UV laser solution photolysis (KrF excimer laser of 248 nm wavelength) using precursors of methanol solutions into which iron and platinum complexes were dissolved together with PVP dispersant to prevent aggregations. From TEM observations, the Fe-Pt nanoparticles were found to be composed of disordered FCC A1 phase with average diameters of 0.5-3 nm regardless of the preparation conditions. Higher iron compositions of nanoparticles require irradiations of higher laser pulse energies typically more than 350 mJ, which is considered to be due to the difficulty in dissociation of Fe(III) acetylacetonate compared with Pt(II) acetylacetonate. Au colloid preparation by the same method was also attempted, resulting in Au nanoparticle colloids with over 10 times larger diameters than the Fe-Pt nanoparticles and UV-visible absorption peaks around 530 nm that originate from the surface plasmon resonance. Differences between the Fe-Pt and Au nanoparticles prepared by the KrF excimer laser solution photolysis are also discussed.

  15. Preparation of Ultrafine Fe–Pt Alloy and Au Nanoparticle Colloids by KrF Excimer Laser Solution Photolysis

    Directory of Open Access Journals (Sweden)

    Sugai Hiroshi

    2009-01-01

    Full Text Available Abstract We prepared ultrafine Fe–Pt alloy nanoparticle colloids by UV laser solution photolysis (KrF excimer laser of 248 nm wavelength using precursors of methanol solutions into which iron and platinum complexes were dissolved together with PVP dispersant to prevent aggregations. From TEM observations, the Fe–Pt nanoparticles were found to be composed of disordered FCC A1 phase with average diameters of 0.5–3 nm regardless of the preparation conditions. Higher iron compositions of nanoparticles require irradiations of higher laser pulse energies typically more than 350 mJ, which is considered to be due to the difficulty in dissociation of Fe(III acetylacetonate compared with Pt(II acetylacetonate. Au colloid preparation by the same method was also attempted, resulting in Au nanoparticle colloids with over 10 times larger diameters than the Fe–Pt nanoparticles and UV–visible absorption peaks around 530 nm that originate from the surface plasmon resonance. Differences between the Fe–Pt and Au nanoparticles prepared by the KrF excimer laser solution photolysis are also discussed.

  16. In situ investigation of ordering phase transformations in FePt magnetic nanoparticles.

    Science.gov (United States)

    Wittig, James E; Bentley, James; Allard, Lawrence F

    2016-12-11

    In situ high-resolution electron microscopy was used to reveal information at the atomic level for the disordered-to-ordered phase transformation of equiatomic FePt nanoparticles that can exhibit outstanding magnetic properties after transforming from disordered face-centered-cubic into the tetragonal L10 ordered structure. High-angle annular dark-field imaging in the scanning transmission electron microscope provided sufficient contrast between the Fe and Pt atoms to readily monitor the ordering of the atoms during in situ heating experiments. However, during continuous high-magnification imaging the electron beam influenced the kinetics of the transformation so annealing had to be performed with the electron beam blanked. At 500°C where the reaction rate was relatively slow, observation of the transformation mechanisms using this sequential imaging protocol revealed that ordering proceeded from (002) surface facets but was incomplete and multiple-domain particles were formed that contained anti-phase domain boundaries and anti-site defects. At 600 and 700°C, the limitations of sequential imaging were revealed as a consequence of increased transformation kinetics. Annealing for only 5min at 700°C produced complete single-domain L10 order; such single-domain particles were more spherical in shape with (002) facets. The in situ experiments also provided information concerning nanoparticle sintering, coalescence, and consolidation. Although there was resistance to complete sintering due to the crystallography of L10 order, the driving force from the large surface-area-to-volume ratio resulted in considerable nanoparticle coalescence, which would render such FePt nanoparticles unsuitable for use as magnetic recording media. Comparison of the in situ data acquired using the protocol described above with parallel ex situ annealing experiments showed that identical behavior resulted in all cases.

  17. The effect of growth surface morphology on the crystal structure and magnetic property of L1{sub 0} order PtFe layers deposited by magnetron sputtering

    Energy Technology Data Exchange (ETDEWEB)

    Ding Wanyu, E-mail: dwysd_2000@163.com [Graduate School of Saitama Institute of Technology, Fukaya, Saitama 369-0293 (Japan) and School of Materials Science and Engineering, Dalian Jiaotong University, Dalian 116028 (China); Ishiguro, Satoshi; Ogatsu, Ryo [Graduate School of Saitama Institute of Technology, Fukaya, Saitama 369-0293 (Japan); Ju, Dongying, E-mail: dyju@sit.ac.jp [Graduate School of Saitama Institute of Technology, Fukaya, Saitama 369-0293 (Japan)

    2012-08-01

    The Fe/Pt/Fe/Pt layers (Pt/Fe multilayer) were deposited on general glass substrate at room temperature by magnetron sputtering technique. Varying the deposition and post-annealing treatment parameters, the PtFe alloy (PtFe) layer with different crystal structures and magnetic properties were obtained at the interface between Fe and Pt layer. The characterization by X-ray diffraction (XRD) showed that the as-deposited Pt/Fe multilayer only contained pure Fe and Pt with body-centered and face-centered cubic structures, respectively. As-deposited Pt layer displayed (2 0 0) preferred orientation, and the columnar grains structure could be observed by the scanning electron microscopy. The PtFe layers with L1{sub 0} face-centered cubic structure could be formed at the interface between Pt and Fe layers by post-annealing the multilayers at 500 Degree-Sign C. In case of Pt/Fe multilayer deposited on smooth substrate, the larger columnar grains in Pt layer resulted in L1{sub 0} PtFe layers without any preferred orientation. While in case of Pt/Fe multilayer deposited on the rough substrate, the thinner columnar grains in Pt layer could induce L1{sub 0} PtFe layers with (2 0 0) preferred orientation. In this case, the vibrating sample magnetometer results indicated that, the magnetic coercivity in plane and out-of-plane model could reach 3.72 and 2.32 kOe, respectively. Based on above results, the L1{sub 0} structure Pt/Fe multilayer with satisfied magnetic properties could be prepared at low temperature by our simple route.

  18. Templated assembly of Co-Pt nanoparticles via thermal and laser-induced dewetting of bilayer metal films.

    Science.gov (United States)

    Oh, Yong-Jun; Kim, Jung-Hwan; Thompson, Carl V; Ross, Caroline A

    2013-01-07

    Templated dewetting of a Co/Pt metal bilayer film on a topographic substrate was used to assemble arrays of Co-Pt alloy nanoparticles, with highly uniform particle size, shape and notably composition compared to nanoparticles formed on an untemplated substrate. Solid-state and liquid-state dewetting processes, using furnace annealing and laser irradiation respectively, were compared. Liquid state dewetting produced more uniform, conformal nanoparticles but they had a polycrystalline disordered fcc structure and relatively low magnetic coercivity. In contrast, solid state dewetting enabled formation of magnetically hard, ordered L1(0) Co-Pt single-crystal particles with coercivity >12 kOe. Furnace annealing converted the nanoparticles formed by liquid state dewetting into the L1(0) phase.

  19. Growth-induced magnetic anisotropy and clustering in vapor-deposited Co-Pt alloy films

    Energy Technology Data Exchange (ETDEWEB)

    Shapiro, A.L.; Rooney, P.W.; Tran, M.Q.; Hellman, F. [Department of Physics, University of California--San Diego, La Jolla, California 92093 (United States); Ring, K.M.; Kavanagh, K.L. [Department of Electrical and Computer Engineering, University of California--San Diego, La Jolla, California 92093 (United States); Rellinghaus, B.; Weller, D. [IBM Almaden Research Center, 650 Harry Road, San Jose, California 95120 (United States)

    1999-11-01

    Polycrystalline and epitaxial (100)-, (110)-, and (111)-oriented CoPt{sub 3} and Co{sub 0.35}Pt{sub 0.65} films were deposited at various growth rates and over a range of growth temperatures from {minus}50 to 800&hthinsp;{degree}C. Films grown at moderate temperatures (200{endash}400&hthinsp;{degree}C) exhibit remarkable growth-induced properties: perpendicular magnetic anisotropy and large coercivity, as well as enhanced Curie temperature and low-temperature saturation magnetization. Magnetic measurements indicate significant Co clustering in these epitaxial fcc films. These properties are independent of crystallographic orientation, increase with increasing growth temperature, and vanish with annealing. We propose that the correlation between magnetic inhomogeneity, magnetic anisotropy, and enhanced moment is explained by clustering of Co into thin platelets in a Pt-rich lattice. This clustering occurs at the growth surface and is trapped into the growing film by low bulk atomic mobility. {copyright} {ital 1999} {ital The American Physical Society}

  20. Plasma-induced synthesis of Pt nanoparticles supported on TiO2 nanotubes for enhanced methanol electro-oxidation

    Science.gov (United States)

    Su, Nan; Hu, Xiulan; Zhang, Jianbo; Huang, Huihong; Cheng, Jiexu; Yu, Jinchen; Ge, Chao

    2017-03-01

    A Pt/C/TiO2 nanotube composite catalyst was successfully prepared for enhanced methanol electro-oxidation. Pt nanoparticles with a particle size of 2 nm were synthesized by plasma sputtering in water, and anatase TiO2 nanotubes with an inner diameter of approximately 100 nm were prepared by a simple two-step anodization method and annealing process. Field-emission scanning electron microscopy images indicated that the different morphologies of TiO2 synthesized on the surface of Ti foils were dependent on the different anodization parameters. The electrochemical performance of Pt/C/TiO2 catalysts for methanol oxidation showed that TiO2 nanotubes were more suitable for use as Pt nanoparticle support materials than irregular TiO2 short nanorods due to their tubular morphology and better electronic conductivity. X-ray photoelectron spectroscopy characterization showed that the binding energies of the Pt 4f of the Pt/C/TiO2 nanotubes exhibited a slightly positive shift caused by the relatively strong interaction between Pt and the TiO2 nanotubes, which could mitigate the poisoning of the Pt catalyst by COads, and further enhance the electrocatalytic performance. Thus, the as-obtained Pt/C/TiO2 nanotubes composites may become a promising catalyst for methanol electro-oxidation.

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

    Science.gov (United States)

    Mondal, Sanjoy; Malik, Sudip

    2016-10-01

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

  2. Electrospun carbon nanofibers decorated with Ag-Pt bimetallic nanoparticles for selective detection of dopamine.

    Science.gov (United States)

    Huang, Yunpeng; Miao, Yue-E; Ji, Shanshan; Tjiu, Weng Weei; Liu, Tianxi

    2014-08-13

    Electrospun nanoporous carbon nanofibers (pCNFs) decorated with Ag-Pt bimetallic nanoparticles have been successfully synthesized by combining template carbonization and seed-growth reduction approach. Porous-structured polyacrylonitrile (PAN) nanofibers (pPAN) were first prepared by electrospinning PAN/polyvinylpyrrolidone (PVP) blend solution, followed by subsequent water extraction and heat treatment to obtain pCNFs. Ag-Pt/pCNFs were then obtained by using pCNFs as support for bimetallic nanoparticle loading. Thus, the obtained Ag-Pt/pCNFs were used to modify glassy carbon electrode (GCE) for selective detection of dopamine (DA) in the presence of uric acid (UA) and ascorbic acid (AA). This novel sensor exhibits fast amperometric response and high sensitivity toward DA with a wide linear concentration range of 10-500 μM and a low detection limit of 0.11 μM (S/N = 3), wherein the interference of UA and AA can be eliminated effectively.

  3. Underpotential deposition of hydrogen on benzene-modified Pt(111) in aqueous H2SO4.

    Science.gov (United States)

    Jerkiewicz, Gregory; DeBlois, Martin; Radovic-Hrapovic, Zorana; Tessier, Jean-Pierre; Perreault, Frédéric; Lessard, Jean

    2005-04-12

    The Pt(111) electrode is modified by an overlayer of C6H6 (ads) upon its cycling in the 0.05-0.80 V range in aq H2SO4 + 1 mM C6H6. The C6H6 (ads) overlayer significantly changes the underpotential-deposited H (H(UPD)) and anion adsorption, and cyclic-voltammetry (CV) profiles show a sharp cathodic peak and an asymmetric anodic one in the 0.05-0.80 V potential range. The C6H6 (ads) layer blocks the (bi)sulfate adsorption but facilitates the adsorption of one monolayer of H(UPD). Cycling of the benzene-modified Pt(111) in benzene-free aq 0.05 H2SO4 from 0.05 to 0.80 V results in a partial desorption of C6H6 (ads) and in a partial recovery of the CV profile characteristic of an unmodified Pt(111). The peak potential of the cathodic and anodic feature is independent of the scan rate, s (10 0 to 0 kJ mol(-1) at theta(H(UPD) --> 1. The nonzero values of delta Delta G degrees testify that the adsorbing and desorbing H(UPD) adatoms interact with an energetically different substrate. The lateral interactions changed from repulsive (omega = 29 kJ mol(-1) at theta(H(UPD) --> 0) to attractive (omega = -28 kJ mol(-1) at theta(H(UPD) --> 1) as the H(UPD) coverage increases. The values of delta S degrees(ads)(H(UPD)) increase from 19 to 56 J K(-1) mol(-1), while those of delta S degrees(des)(H(UPD)) decrease from 45 to -30 J K(-1) mol(-1) with an increase of H(UPD) coverage. The values of delta H degrees(des)(H(UPD)) and delta H degrees(des)(H(UPD)) vary from 0 to 27 kJ mol(-1). The Pt(111)-H(UPD) surface bond energy at the benzene-modified Pt(111) electrode falls in the 191-218 kJ mol(-1) range and is weaker than in the case of the unmodified Pt(111) electrode in the same electrolyte.

  4. Underpotential deposition-induced synthesis of composition-tunable Pt-Cu nanocrystals and their catalytic properties.

    Science.gov (United States)

    Jiang, Yaqi; Jia, Yanyan; Zhang, Jiawei; Zhang, Lei; Huang, Huang; Xie, Zhaoxiong; Zheng, Lansun

    2013-02-25

    Pt-Cu alloy octahedral nanocrystals (NCs) have been synthesized successfully by using N,N-dimethylformamide as both the solvent and the reducing agent in the presence of cetyltrimethylammonium chloride. Cu underpotential deposition (UPD) is found to play a key role in the formation of the Pt-Cu alloy NCs. The composition in the Pt-Cu alloy can be tuned by adjusting the ratio of metal precursors in solution. However, the Cu content in the Pt-Cu alloy NCs cannot exceed 50%. Due to the fact that Cu precursor cannot be reduced to metallic copper and the Cu content cannot exceed 50%, we achieved the formation of the Pt-Cu alloy by using Cu UPD on the Pt surface. In addition, the catalytic activities of Pt-Cu alloy NCs with different composition were investigated in electrocatalytic oxidation of formic acid. The results reveal that the catalytic performance is strongly dependent on Pt-Cu alloy composition. The sample of Pt(50)Cu(50) exhibits excellent activity in electrocatalytic oxidation of formic acid.

  5. Nanoparticle layer deposition for highly controlled multilayer formation based on high-coverage monolayers of nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Yue; Williams, Mackenzie G.; Miller, Timothy J.; Teplyakov, Andrew V., E-mail: andrewt@udel.edu

    2016-01-01

    This paper establishes a strategy for chemical deposition of functionalized nanoparticles onto solid substrates in a layer-by-layer process based on self-limiting surface chemical reactions leading to complete monolayer formation within the multilayer system without any additional intermediate layers — nanoparticle layer deposition (NPLD). This approach is fundamentally different from previously established traditional layer-by-layer deposition techniques and is conceptually more similar to well-known atomic and molecular layer deposition processes. The NPLD approach uses efficient chemical functionalization of the solid substrate material and complementary functionalization of nanoparticles to produce a nearly 100% coverage of these nanoparticles with the use of “click chemistry”. Following this initial deposition, a second complete monolayer of nanoparticles is deposited using a copper-catalyzed “click reaction” with the azide-terminated silica nanoparticles of a different size. This layer-by-layer growth is demonstrated to produce stable covalently-bound multilayers of nearly perfect structure over macroscopic solid substrates. The formation of stable covalent bonds is confirmed spectroscopically and the stability of the multilayers produced is tested by sonication in a variety of common solvents. The 1-, 2- and 3-layer structures are interrogated by electron microscopy and atomic force microscopy and the thickness of the multilayers formed is fully consistent with that expected for highly efficient monolayer formation with each cycle of growth. This approach can be extended to include a variety of materials deposited in a predesigned sequence on different substrates with a highly conformal filling. - Highlights: • We investigate the formation of high-coverage monolayers of nanoparticles. • We use “click chemistry” to form these monolayers. • We form multiple layers based on the same strategy. • We confirm the formation of covalent bonds

  6. Green and Facile Synthesis of Pd-Pt Alloy Nanoparticles by Laser Irradiation of Aqueous Solution.

    Science.gov (United States)

    Nakamura, Takahiro; Sato, Shunichi

    2015-01-01

    Solid-solution palladium-platinum (Pd-Pt) alloy nanoparticles (NPs) with fully tunable compositions were directly fabricated through high-intensity laser irradiation of an aqueous solution of palladium and platinum ions without using any reducing agents or thermal processes. Transmission electron microscopy (TEM) observations showed that nanometer-sized particles were fabricated by laser irradiation of mixed aqueous solutions of palladium and platinum ions with different feeding ratios. The crystalline nature of the NPs was precisely characterized by X-ray diffraction (XRD). Despite the fact that, for the bulk systems, a pair of XRD peak was detected between the palladium and platinum peaks because of the large miscibility gap in the Pd-Pt binary phase diagram, only a single XRD peak was seen for the Pd-Pt NPs fabricated in the present study. Moreover, the peak position shifted from that of pure palladium towards platinum with increasing fraction of platinum ions in solution. Consequently, the interplanar spacings of the alloy NPs agreed well with the estimated values obtained from Vegard's law. These observations strongly indicate the formation of solid-solution Pd-Pt alloy NPs with fully tunable compositions. This technique is not only a "green" (environmentally-friendly) and facile process, but is also widely applicable to other binary and ternary systems.

  7. Structural stability of alloyed and core-shell Cu-Pt bimetallic nanoparticles

    Science.gov (United States)

    Peng, Hongcheng; Qi, Weihong; Ji, Wenhai; Li, Siqi; He, Jieting

    2017-03-01

    Combining the bond-energy model and Debye theory, we generalized the Gibbs free energy model for Cu-Pt nanoparticles (NPs) by introducing a shape factor considering the shape effect. We studied the structural stability of the Cu-Pt NPs and plotted the corresponding composition-, shape- and size-dependent phase diagrams. It is shown that the Cu-Pt NPs can form alloyed structure in a large size range. But when the particle size continues to decrease, the NPs will form the core-shell structure due to surface segregation. Meanwhile, the composition segregation could make the atoms of less-content element to gather in the surface. The predictions from the present calculated phase diagrams are consistent with a series of experimental results in literatures. To further prove the efficiency of the phase diagrams, we synthesized the alloyed Cu-Pt NPs of 4-15 nm by a co-reduction method, which is in agreement with the predictions from the phase diagrams.

  8. Nonlinear optical properties of laser synthesized Pt nanoparticles: saturable and reverse saturable absorption

    Science.gov (United States)

    Chehrghani, A.; Torkamany, M. J.

    2014-01-01

    In this paper, the spectral and nonlinear optical properties of a colloidal solution of platinum nanoparticles (Pt NPs) in water are presented. The Pt NPs were prepared by laser ablation of a Pt metallic target in distilled water using a 1064 nm high frequency Nd:YAG laser. The intensity-dependent nonlinear optical absorption and nonlinear refraction behaviors of the sample exposed to the 532 nm nanosecond laser pulses were investigated by applying the Z-scan technique. The saturated nonlinear absorption coefficient 5.4 × 10-7 cm W-1 was obtained in a saturation intensity of 1.8 × 107 W cm-2. The saturable absorption response of the Pt NPs was switched to the reverse saturable absorption in the higher laser intensities. The nonlinear refractive index that has a negative value was increased from -3.5 × 10-13 cm2 W-1 up to -15 × 10-13 cm2 W-1 by increasing the laser intensity.

  9. Electrophoretic deposition of titania nanoparticles: Wet density of deposits during EPD

    Indian Academy of Sciences (India)

    Morteza Farrokhi-Rad; Taghi Shahrabi; Shirin Khanmohammadi

    2014-08-01

    Electrophoretic deposition (EPD) of titania nanoparticles was performed at different voltages and times. The wet density of deposits was calculated according to the Archimedes’ principle. The wet density as well as the electric field over the deposits increased with time and attained the plateau at longer times. The velocity at which particles attach to the deposit, strongly influences its wet density at initial times. However, the effect of electro-osmotic flow is dominant at longer times. The coating with higher wet density had the higher corrosion resistance in Ringer’s solution at 37.5 °C due to its closely packed and crack free microstructure.

  10. Z-STEM of L1o Ordering in FePt Magnetic Nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Wittig, J. E. [Vanderbilt University; Bentley, James [ORNL; Lupini, Andrew R [ORNL; Lukehart, C.M. [Vanderbilt University

    2007-01-01

    The L1{sub o} (CuAuI) ordered FePt structure exhibits exceptional magnetic properties with uniaxial-magnetocrystalline anisotropy (K{sub u}) greater than 10{sup 6} ergs/cm3. Chemical synthesis methods can produce monodispersed FePt nanoparticles that have diameters ranging from 3 to 10 nm with a standard deviation of less than 5%. As-synthesized, the FePt nanoparticles are face-centered cubic (FCC) and require annealing at temperatures greater than 550 C for chemical ordering into the L1{sub o} structure. X-ray diffraction (XRD) methods typically characterize the ordering phase transformation by measuring the superlattice peaks. However, since the FePt nanoparticles coarsen during annealing, the larger particles may dominate the XRD data while the smallest particles correspondingly may contribute little to the diffracted intensity. Since recent data suggest that the FePt L1{sub o} ordering transformation is particle-size dependent, the current study employs high-angle annular dark-field (HAADF) scanning transmission electron microscopy (STEM), also known as atomic-number contrast or Z-STEM, methods to investigate the presence of L1{sub o} order in individual FePt nanoparticles.

  11. Size effect on order-disorder transition kinetics of FePt nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Shuaidi [School of Materials Science and Engineering, Central South University, Changsha 410083 (China); Qi, Weihong, E-mail: qiwh216@csu.edu.cn [School of Materials Science and Engineering, Central South University, Changsha 410083 (China); State Key Laboratory of Powder Metallurgy, Central South University, Changsha 410083 (China); Key Laboratory of Non-ferrous Materials Science and Engineering, Ministry of Education, Changsha 410083 (China); Huang, Baiyun [State Key Laboratory of Powder Metallurgy, Central South University, Changsha 410083 (China)

    2014-01-28

    The kinetics of order-disorder transition of FePt nanoparticles during high temperature annealing is theoretically investigated. A model is developed to address the influence of large surface to volume ratio of nanoparticles on both the thermodynamic and kinetic aspect of the ordering process; specifically, the nucleation and growth of L1{sub 0} ordered domain within disordered nanoparticles. The size- and shape-dependence of transition kinetics are quantitatively addressed by a revised Johnson-Mehl-Avrami equation that included corrections for deviations caused by the domination of surface nucleation in nanoscale systems and the non-negligible size of the ordered nuclei. Calculation results based on the model suggested that smaller nanoparticles are kinetically more active but thermodynamically less transformable. The major obstacle in obtaining completely ordered nanoparticles is the elimination of antiphase boundaries. The results also quantitatively confirmed the existence of a size-limit in ordering, beyond which, inducing order-disorder transitions through annealing is impossible. A good agreement is observed between theory, experiment, and computer simulation results.

  12. H2 splitting on Pt, Ru and Rh nanoparticles supported on sputtered HOPG

    DEFF Research Database (Denmark)

    Fiordaliso, Elisabetta Maria; Murphy, Shane; Nielsen, R.M.;

    2012-01-01

    nm. The rate of hydrogen exchange is measured in the temperature range 40–200°C at 1bar, by utilization of the H–D exchange reaction. We find that the rate of hydrogen exchange increases with the particle diameter for all the metals, and that the rate for Ru and Rh is higher than for Pt. In the case...... adlayers on the terraces of the larger particles. Experiments are also carried out in the presence of 10ppm CO. Pt is found to be very sensitive to CO poisoning and the H–D exchange rate drops below the detection limit when CO is added to the gas mixture. In the case of Ru and Rh nanoparticles, CO...... decreases the splitting rate significantly, also at 200°C. The variation of the sensitivity to CO poisoning with particle diameter for Ru and Rh is found to be weak....

  13. Comparison of galvanic displacement and electroless methods for deposition of gold nanoparticles on synthetic calcite

    Indian Academy of Sciences (India)

    Chamarthi K Srikanth; P Jeevanandam

    2012-11-01

    Gold nanoparticles have been deposited on synthetic calcite substrate by galvanic displacement reaction and electroless deposition methods. A comparative study has shown that electroless deposition is superior compared to galvanic displacement reaction for uniform deposition of gold nanoparticles on calcite. Characterization of the samples, prepared by two different deposition methods, was carried out by X-ray diffraction, transmission electron microscopy, field emission scanning electron microscopy (FE–SEM) and diffuse reflectance spectroscopy (DRS) measurements. FE–SEM studies prove that smaller nanoparticles of gold are deposited uniformly on calcite if electroless deposition method was employed and DRS measurements show the characteristic surface plasmon resonance of gold nanoparticles.

  14. Thermal Stability of Co-Pt and Co-Au Core-Shell Structured Nanoparticles: Insights from Molecular Dynamics Simulations.

    Science.gov (United States)

    Wen, Yu-Hua; Huang, Rao; Shao, Gui-Fang; Sun, Shi-Gang

    2017-09-07

    Co-Pt and Co-Au core-shell nanoparticles were heated by molecular dynamics simulations to investigate their thermal stability. Two core structures, that is, hcp Co and fcc Co, have been addressed. The results demonstrate that the hcp-fcc phase transition happens in the hcp-Co-core/fcc-Pt-shell nanoparticle, while it is absent in the hcp-Co-core/fcc-Au-shell one. The stacking faults appear in both Pt and Au shells despite different structures of the Co core. The Co core and Pt shell concurrently melt and present an identical melting point in both Co-Pt core-shell nanoparticles. However, typical two-stage melting occurs in both Co-Au core-shell nanoparticles. Furthermore, the Au shell in the hcp-Co-core/fcc-Au-shell nanoparticle exhibits a lower melting point than that in the fcc-Co-core/fcc-Au-shell one, while the melting points are closely equal for both hcp and fcc Co cores. All of these observations suggest that their thermal stability strongly depends on the structure of the core and the element of the shell.

  15. Sub-nanometer dimensions control of core/shell nanoparticles prepared by atomic layer deposition.

    Science.gov (United States)

    Weber, M J; Verheijen, M A; Bol, A A; Kessels, W M M

    2015-03-06

    Bimetallic core/shell nanoparticles (NPs) are the subject of intense research due to their unique electronic, optical and catalytic properties. Accurate and independent control over the dimensions of both core and shell would allow for unprecedented catalytic performance. Here, we demonstrate that both core and shell dimensions of Pd/Pt core/shell nanoparticles (NPs) supported on Al2O3 substrates can be controlled at the sub-nanometer level by using a novel strategy based on atomic layer deposition (ALD). From the results it is derived that the main conditions for accurate dimension control of these core/shell NPs are: (i) a difference in surface energy between the deposited core metal and the substrate to obtain island growth; (ii) a process yielding linear growth of the NP cores with ALD cycles to obtain monodispersed NPs with a narrow size distribution; (iii) a selective ALD process for the shell metal yielding a linearly increasing thickness to obtain controllable shell growth exclusively on the cores. For Pd/Pt core/shell NPs it is found that a minimum core diameter of 1 nm exists above which the NP cores are able to catalytically dissociate the precursor molecules for shell growth. In addition, initial studies on the stability of these core/shell NPs have been carried out, and it has been demonstrated that core/shell NPs can be deposited by ALD on high aspect ratio substrates such as nanowire arrays. These achievements show therefore that ALD has significant potential for the preparation of tuneable heterogeneous catalyst systems.

  16. Research of special carbon nanobeads supported Pt catalyst for fuel cell through high temperature pyrolysis and deposition from novel phthalocyanine

    Institute of Scientific and Technical Information of China (English)

    GUO Yanchuan; YUE Jun; PAN Zhongxiao; XU Haitao; ZHANG Bing; HAN Fengmei; CHEN Lijuan; PENG Bixian; XIE Wenwei; QIAN Haisheng; YAN Tiantang

    2004-01-01

    The carbon nanobeads were prepared through high temperature pyrolysis and deposition from phthaiocyanine. After surface's functionalization treatment of the carbon beads, the carbon nanobeads supported Pt catalyst was produced. The Pt/C catalyst was characterized by SEM,TEM, Raman spectrum, EDS and XRD methods. Combining the carbonaceous paper spreaded up with the catalyst with Nafion membrane, we made MEA electrode. The discharge curves indicated that this carbon nanobeads supported Pt is a good fuel cell catalyst with excellent performance, high activity and sign of a long-time life.

  17. Electrospun Nb-doped TiO2 nanofiber support for Pt nanoparticles with high electrocatalytic activity and durability.

    Science.gov (United States)

    Kim, MinJoong; Kwon, ChoRong; Eom, KwangSup; Kim, JiHyun; Cho, EunAe

    2017-03-14

    This study explores a facile method to prepare an efficient and durable support for Pt catalyst of polymer electrolyte membrane fuel cell (PEMFC). As a candidate, Nb-doped TiO2 (Nb-TiO2) nanofibers are simply fabricated using an electrospinning technique, followed by a heat treatment. Doping Nb into the TiO2 nanofibers leads to a drastic increase in electrical conductivity with doping level of up to 25 at. % (Nb0.25Ti0.75O2). Pt nanoparticles are synthesized on the prepared 25 at. % Nb-doped TiO2-nanofibers (Pt/Nb-TiO2) as well as on a commercial powdered carbon black (Pt/C). The Pt/Nb-TiO2 nanofiber catalyst exhibits similar oxygen reaction reduction (ORR) activity to that of the Pt/C catalyst. However, during an accelerated stress test (AST), the Pt/Nb-TiO2 nanofiber catalyst retained more than 60% of the initial ORR activity while the Pt/C catalyst lost 65% of the initial activity. The excellent durability of the Pt/Nb-TiO2 nanofiber catalyst can be attributed to high corrosion resistance of TiO2 and strong interaction between Pt and TiO2.

  18. Electrospun Nb-doped TiO2 nanofiber support for Pt nanoparticles with high electrocatalytic activity and durability

    Science.gov (United States)

    Kim, Minjoong; Kwon, Chorong; Eom, Kwangsup; Kim, Jihyun; Cho, Eunae

    2017-03-01

    This study explores a facile method to prepare an efficient and durable support for Pt catalyst of polymer electrolyte membrane fuel cell (PEMFC). As a candidate, Nb-doped TiO2 (Nb-TiO2) nanofibers are simply fabricated using an electrospinning technique, followed by a heat treatment. Doping Nb into the TiO2 nanofibers leads to a drastic increase in electrical conductivity with doping level of up to 25 at. % (Nb0.25Ti0.75O2). Pt nanoparticles are synthesized on the prepared 25 at. % Nb-doped TiO2-nanofibers (Pt/Nb-TiO2) as well as on a commercial powdered carbon black (Pt/C). The Pt/Nb-TiO2 nanofiber catalyst exhibits similar oxygen reaction reduction (ORR) activity to that of the Pt/C catalyst. However, during an accelerated stress test (AST), the Pt/Nb-TiO2 nanofiber catalyst retained more than 60% of the initial ORR activity while the Pt/C catalyst lost 65% of the initial activity. The excellent durability of the Pt/Nb-TiO2 nanofiber catalyst can be attributed to high corrosion resistance of TiO2 and strong interaction between Pt and TiO2.

  19. Synthesis of PtRu nanoparticles from the hydrosilylation reaction and application as catalyst for direct methanol fuel cell.

    Science.gov (United States)

    Huang, Junchao; Liu, Zhaolin; He, Chaobin; Gan, Leong Ming

    2005-09-08

    Nanosized Pt, PtRu, and Ru particles were prepared by a novel process, the hydrosilylation reaction. The hydrosilylation reaction is an effective method of preparation not only for Pt particles but also for other metal colloids, such as Ru. Vulcan XC-72 was selected as catalyst support for Pt, PtRu, and Ru colloids, and TEM investigations showed nanoscale particles and narrow size distribution for both supported and unsupported metals. All Pt and Pt-rich catalysts showed the X-ray diffraction pattern of a face-centered cubic (fcc) crystal structure, whereas the Ru and Ru-rich alloys were more typical of a hexagonal close-packed (hcp) structure. As evidenced by XPS, most Pt and Ru atoms in the nanoparticles were zerovalent, except a trace of oxidation-state metals. The electrooxidation of liquid methanol on these catalysts was investigated at room temperature by cyclic voltammetry and chronoamperometry. The results concluded that some alloy catalysts showed higher catalytic activities and better CO tolerance than the Pt-only catalyst; Pt56Ru44/C have displayed the best electrocatalytic performance among all carbon-supported catalysts.

  20. Electrospun Nb-doped TiO2 nanofiber support for Pt nanoparticles with high electrocatalytic activity and durability

    Science.gov (United States)

    Kim, MinJoong; Kwon, ChoRong; Eom, KwangSup; Kim, JiHyun; Cho, EunAe

    2017-01-01

    This study explores a facile method to prepare an efficient and durable support for Pt catalyst of polymer electrolyte membrane fuel cell (PEMFC). As a candidate, Nb-doped TiO2 (Nb-TiO2) nanofibers are simply fabricated using an electrospinning technique, followed by a heat treatment. Doping Nb into the TiO2 nanofibers leads to a drastic increase in electrical conductivity with doping level of up to 25 at. % (Nb0.25Ti0.75O2). Pt nanoparticles are synthesized on the prepared 25 at. % Nb-doped TiO2-nanofibers (Pt/Nb-TiO2) as well as on a commercial powdered carbon black (Pt/C). The Pt/Nb-TiO2 nanofiber catalyst exhibits similar oxygen reaction reduction (ORR) activity to that of the Pt/C catalyst. However, during an accelerated stress test (AST), the Pt/Nb-TiO2 nanofiber catalyst retained more than 60% of the initial ORR activity while the Pt/C catalyst lost 65% of the initial activity. The excellent durability of the Pt/Nb-TiO2 nanofiber catalyst can be attributed to high corrosion resistance of TiO2 and strong interaction between Pt and TiO2. PMID:28290503

  1. Preparation of IrO2 nanoparticles with SBA-15 template and its supported Pt nanocomposite as bifunctional oxygen catalyst

    Science.gov (United States)

    Kong, Fan-Dong; Liu, Jing; Ling, Ai-Xia; Xu, Zhi-Qiang; Wang, Hui-Yun; Kong, Qing-Sheng

    2015-12-01

    In the present work, we report the syntheses of IrO2 nanoparticles with SBA-15 template (s-IrO2), and s-IrO2 supported Pt nanocomposite (Pt/s-IrO2) as bifunctional oxygen catalyst. Physical characterizations including X-ray diffraction and transmission electron microscopy demonstrate that s-IrO2 catalyst has excellent uniformity and regularity in particle shape and much ordered distribution in geometric space, and Pt/s-IrO2 catalyst shows a uniform Pt dispersion on the surface of the s-IrO2 particles. Electrochemical analyses prove that s-IrO2 catalyst possesses superior OER activity at operating potentials; and that Pt/s-IrO2 catalyst, in comparison to Pt/commercial IrO2, has higher ESA value and ORR catalytic performance with a mechanism of four-electron pathway and a high ORR efficiency. And as a bifunctional oxygen catalyst, Pt/s-IrO2 also exhibits more remarkable OER performance than the commercial one. The s-IrO2 nanoparticles will be a promising active component (for OER), and suitable for Pt support (for ORR).

  2. Synthesis and Electrochemical Evaluation of Carbon Supported Pt-Co Bimetallic Catalysts Prepared by Electroless Deposition and Modified Charge Enhanced Dry Impregnation

    Directory of Open Access Journals (Sweden)

    John Meynard M. Tengco

    2016-06-01

    Full Text Available Carbon-supported bimetallic Pt-Co cathode catalysts have been previously identified as higher activity alternatives to conventional Pt/C catalysts for fuel cells. In this work, a series of Pt-Co/C catalysts were synthesized using electroless deposition (ED of Pt on a Co/C catalyst prepared by modified charge enhanced dry impregnation. X-ray diffraction (XRD and scanning transmission electron microscopy (STEM characterization of the base catalyst showed highly dispersed particles. A basic ED bath containing PtCl62− as the Pt precursor, dimethylamine borane as reducing agent, and ethylenediamine as stabilizing agent successfully targeted deposition of Pt on Co particles. Simultaneous action of galvanic displacement and ED resulted in Pt-Co alloy formation observed in XRD and energy dispersive X-ray spectroscopy (XEDS mapping. In addition, fast deposition kinetics resulted in hollow shell Pt-Co alloy particles while particles with Pt-rich shell and Co-rich cores formed with controlled Pt deposition. Electrochemical evaluation of the Pt-Co/C catalysts showed lower active surface but much higher mass and surface activities for oxygen reduction reaction compared to a commercial Pt/C fuel cell catalyst.

  3. Comparing and Optimizing Nitrate Adsorption from Aqueous Solution Using Fe/Pt Bimetallic Nanoparticles and Anion Exchange Resins

    Directory of Open Access Journals (Sweden)

    Muhammad Daud

    2015-01-01

    Full Text Available This research work was carried out for the removal of nitrate from raw water for a drinking water supply. Nitrate is a widespread ground water contaminant. Methodology employed in this study included adsorption on metal based nanoparticles and ion exchange using anionic resins. Fe/Pt bimetallic nanoparticles were prepared in the laboratory, by the reduction of their respective salts using sodium borohydride. Scanning electron microscope, X-ray diffraction, energy dispersive spectrometry, and X-ray florescence techniques were utilized for characterization of bimetallic Fe/Pt nanoparticles. Optimum dose, pH, temperature, and contact time were determined for NO3- removal through batch tests, both for metal based nanoparticles and anionic exchange resin. Adsorption data fitted well the Langmuir isotherm and conformed to the pseudofirst-order kinetic model. Results indicated 97% reduction in nitrate by 0.25 mg/L of Fe/Pt nanoparticles at pH 7 and 83% reduction in nitrate was observed using 0.50 mg/L anionic exchange resins at pH 4 and contact time of one hour. Overall, Fe/Pt bimetallic nanoparticles demonstrated greater NO3- removal efficiency due to the small particle size, extremely large surface area (627 m2/g, and high adsorption capacity.

  4. Structural and magnetic characterization of FePt films deposited onto SiO{sub 2} spherical particle arrays

    Energy Technology Data Exchange (ETDEWEB)

    Brombacher, Christoph; Makarov, Denys; Schatz, Guenter; Albrecht, Manfred [University of Konstanz, Department of Physics, D-78457 Konstanz (Germany); Maret, Mireille; Liscio, Fabiola [Laboratoire de Thermodynamique et Physico-Chimie Metallurgiques, ENSEEG, Saint Martin d' Heres (France)

    2007-07-01

    The growth of FePt films at 450 C on a Pt/Cr buffer layer deposited onto SiO{sub 2} spherical particle arrays and for comparison on flat thermally oxidized Si(001) substrates has been studied. The structural properties of the FePt films, such as the orientation and size of the crystalline grains and the degree of L1{sub 0}-type chemical ordering, were investigated by in-situ RHEED and ex-situ XRD. Magnetic characterization was performed by MFM, polar MOKE and SQUID. Increasing the Cr buffer underlayer thickness favors the formation of the FePt chemically ordered L1{sub 0} phase. An out-of-plane coercivity of the FePt alloy about 4 kOe was thus obtained for a Cr thickness of 50 nm. While the continuous films on oxidized Si(001) substrates show magnetic domain patterns with domain sizes in the range of 50-100 nm, multi-domain states are observed for the FePt alloy grown on the particle arrays. The influence of the Cr underlayer thickness and Pt buffer layer on the magnetic properties of FePt are discussed for various particle arrays and compared to micromagnetic simulations, providing a description of magnetization reversal.

  5. Numerical simulation of nanoparticle pattern fabricated by electrostatic spray deposition

    Institute of Scientific and Technical Information of China (English)

    Wei Wei; Zhaolin Gu; Sheng Wang; Takeshi Fukuda; Kiwamu Kase; Jungmyoung Ju; Yutaka Yamagata

    2013-01-01

    Electrospray deposition (ESD) as a patterning method of nanoparticles deposited on a substrate has attracted much attention due to several advantages over other methods.However,obtaining an optimum ESD processing condition for nanoparticle pattern relies much on trial experiments because of the lack of reliable numerical simulation.In this study,the deposition characteristics of nanoparticle generated by electrospray were investigated by using a three-dimensional Lagrangian model.Three important process parameters,including solution dielectric constant,applied voltage and surface charge density on mask were considered by fixing the geometrical parameters of the ESD device.Simulation result showed that under the condition of without a mask,the spray diameter increases with increasing solvent dielectric constant,and higher applied voltage makes the spray area wider.Controllability of focusing by changing surface charge density on the mask was confirmed:higher surface charge density on the mask results in more focused deposition.Validity of the numerical simulation developed in this study was verified by comparison with experimental data.

  6. Synthesis and structural, magnetic and electrochemical characterization of PtCo nanoparticles prepared by water-in-oil microemulsion

    Energy Technology Data Exchange (ETDEWEB)

    Solla-Gullon, J., E-mail: jose.solla@ua.e [Universidad de Alicante, Instituto de Electroquimica (Spain); Gomez, Elvira; Valles, Elisa [Instituto de Nanociencia y Nanotecnologia de la Universidad de Barcelona (IN2UB), Departamento Quimica Fisica (Spain); Aldaz, Antonio; Feliu, Juan M. [Universidad de Alicante, Instituto de Electroquimica (Spain)

    2010-05-15

    PtCo nanoparticles with homogeneous size (around 3-4 nm) have been synthesized in a water-in-oil microemulsion of water/polyethylenglycol-dodecylether (BRIJ 30)/n-heptane. X-ray diffraction study revealed the formation of a cubic phase with a gradual decrease of the cell parameter with increasing cobalt incorporation in the crystalline lattice of platinum. In relation to their magnetic properties, the PtCo nanoparticles present a superparamagnetic behaviour even after annealing, although higher permeability was induced by the thermal treatment. Finally, the electrocatalytic activity of the particles towards oxalic acid oxidation in H{sub 2}SO{sub 4} was evaluated. The Pt74Co26 nanoparticles showed the highest reactivity for this reaction.

  7. Formation of Pt-Zn Alloy Nanoparticles by Electron-Beam Irradiation of Wurtzite ZnO in the TEM

    Science.gov (United States)

    Lee, Sung Bo; Park, Jucheol; van Aken, Peter A.

    2016-07-01

    As is well documented, platinum nanoparticles, promising for catalysts for fuel cells, exhibit better catalytic activities, when alloyed with Zn. Pre-existing syntheses of Pt-Zn alloy catalysts are composed of a number of complex steps. In this study, we have demonstrated that nanoparticles of Pt-Zn alloys are simply generated by electron-beam irradiation in a transmission electron microscope of a wurtzite ZnO single-crystal specimen. The initial ZnO specimen is considered to have been contaminated by Pt during specimen preparation by focused ion beam milling. The formation of the nanoparticle is explained within the framework of ionization damage (radiolysis) by electron-beam irradiation and accompanying electrostatic charging.

  8. 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.

  9. TER-XSW investigation of CoPt{sub 3} nanoparticle films on Si and sapphire substrates

    Energy Technology Data Exchange (ETDEWEB)

    Zargham, Ardalan; Schmidt, Thomas; Hildebrand, Radowan; Falta, Jens [Institute of Solid State Physics, University of Bremen (Germany); Gehl, Bernhard; Baeumer, Marcus [Institute of Physical Chemistry, University of Bremen (Germany)

    2008-07-01

    CoPt{sub 3} bimetallic colloidal nanoparticle films on Si and sapphire substrates are investigated concerning the real space distribution of Co and Pt in specifically defined layers above the substrates as well as the structural dependancy on plasma treatments. TER-XSW is considered to be a suitable method for these types of investigation because of its ability of material specification in vertical resolution. It is simultaneously possible to understand the surface morphology by means of XRR.

  10. Formate adsorption on Pt nanoparticles during formic acid electro-oxidation: insights from in situ infrared spectroscopy.

    Science.gov (United States)

    McPherson, Ian J; Ash, Philip A; Jacobs, Robert M J; Vincent, Kylie A

    2016-10-18

    Adsorbed formate is observed on a supported Pt nanoparticle for the first time during formic acid electro-oxidation. Bands assigned to OCO stretching and CH bending reveal some OCO but little CH bond weakening on adsorption compared to the free anion. The formate potential dependence is similar to polycrystalline electrodes while adsorbed CO persists up to +1.2 V, 0.5 V higher than on polycrystalline Pt.

  11. Aqueous Phase Glycerol Reforming by PtMo Bimetallic Nano-Particle Catalyst: Product Selectivity and Structural Characterization

    Energy Technology Data Exchange (ETDEWEB)

    Stach E. A.; Dietrich, P.J.; Lobo-Lapidus, R.J.; Wu, T.; Sumer, A.; Akatay, M.C.; Fingland, B.R.; Guo, N.; Dumesic, J.A.; Marshall, C.L.; Jellinek, J.; Delgass, W.N.; Ribeiro, F.H.; Miller, J.T.

    2012-03-01

    A carbon supported PtMo aqueous phase reforming catalyst for producing hydrogen from glycerol was characterized by analysis of the reaction products and pathway, TEM, XPS and XAS spectroscopy. Operando X-ray absorption spectroscopy (XAS) indicates the catalyst consists of bimetallic nano-particles with a Pt rich core and a Mo rich surface. XAS of adsorbed CO indicates that approximately 25% of the surface atoms are Pt. X-ray photoelectron spectroscopy indicates that there is unreduced and partially reduced Mo oxide (MoO{sub 3} and MoO{sub 2}), and Pt-rich PtMo bimetallic nano-particles. The average size measured by transmission electron microscopy of the fresh PtMo nano-particles is about 2 nm, which increases in size to 5 nm after 30 days of glycerol reforming at 31 bar and 503 K. The catalyst structure differs from the most energetically stable structure predicted by density functional theory (DFT) calculations for metallic Pt and Mo atoms. However, DFT indicates that for nano-particles composed of metallic Pt and Mo oxide, the Mo oxide is at the particle surface. Subsequent reduction would lead to the experimentally observed structure. The aqueous phase reforming reaction products and intermediates are consistent with both C-C and C-OH bond cleavage to generate H{sub 2}/CO{sub 2} or the side product CH{sub 4}. While the H{sub 2} selectivity at low conversion is about 75%, cleavage of C-OH bonds leads to liquid products with saturated carbon atoms. At high conversions (to gas), these will produced additional CH{sub 4} reducing the H{sub 2} yield and selectivity.

  12. 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...

  13. Chemical Vapour Deposition of Graphene with Re-useable Pt and Cu substrates for Flexible Electronics

    Science.gov (United States)

    Karamat, Shumaila; Sonusen, Selda; Celik, Umit; Uysalli, Yigit; Oral, Ahmet

    2015-03-01

    Graphene has gained the attention of scientific world due to its outstanding physical properties. The future demand of flexible electronics such as solar cells, light emitting diodes, photo-detectors and touch screen technology requires more exploration of graphene properties on flexible substrates. The most interesting application of graphene is in organic light emitting diodes (OLED) where efforts are in progress to replace brittle indium tin oxide (ITO) electrode with a flexible graphene electrode because ITO raw materials are becoming increasingly expensive, and its brittle nature makes it unsuitable for flexible devices. In this work, we grow graphene on Pt and Cu substrates using chemical vapour deposition (CVD) and transferred it to a polymer material (PVA) using lamination technique. We used hydrogen bubbling method for separating graphene from Pt and Cu catalyst to reuse the substrates many times. After successful transfer of graphene on polymer samples, we checked the resistivity values of the graphene sheet which varies with growth conditions. Furthermore, Raman, atomic force microscopy (AFM), I-V and Force-displacement measurements will be presented for these samples.

  14. In situ spectroscopic ellipsometry during atomic layer deposition of Pt, Ru and Pd

    Science.gov (United States)

    Leick, N.; Weber, J. W.; Mackus, A. J. M.; Weber, M. J.; van de Sanden, M. C. M.; Kessels, W. M. M.

    2016-03-01

    The preparation of ultra-thin platinum-group metal films, such as Pt, Ru and Pd, by atomic layer deposition (ALD) was monitored in situ using spectroscopic ellipsometry in the photon energy range of 0.75-5 eV. The metals’ dielectric function was parametrized using a ‘flexible’ Kramers-Kronig consistent dielectric function because it was able to provide accurate curve shape control over the optical response of the metals. From this dielectric function, it was possible to extract the film thickness values during the ALD process. The important ALD process parameters, such as the nucleation period and growth per cycle of Pt, Ru and Pd could be determined from the thickness evolution. In addition to process parameters, the film resistivity in particular could be extracted from the modeled dielectric function. Spectroscopic ellipsometry thereby revealed itself as a feasible and valuable technique to be used in research and development applications, as well as for process monitoring during ALD.

  15. Growth and microstructure of columnar Y-doped SrZrO{sub 3} films deposited on Pt-coated MgO by pulsed laser deposition

    Energy Technology Data Exchange (ETDEWEB)

    Luo, Sijun, E-mail: sluo1@tulane.edu; Riggs, Brian C.; Shipman, Joshua T.; Adireddy, Shiva; Sklare, Samuel C.; Chrisey, Douglas B., E-mail: dchrisey@tulane.edu [Department of Physics and Engineering Physics, Tulane University, New Orleans, Louisiana 70118 (United States); Zhang, Xiaodong; Koplitz, Brent [Department of Chemistry, Tulane University, New Orleans, Louisiana 70118 (United States)

    2015-07-21

    Direct integration of proton conductor films on Pt-coated substrates opens the way to film-based proton transport devices. Columnar SrZr{sub 0.95}Y{sub 0.05}O{sub 3−δ} (SZY) films with dense microstructure were deposited on Pt-coated MgO(100) substrates at 830 °C by pulsed laser deposition. The optimal window of ambient O{sub 2} pressure for good crystallinity of SZY films is from 400 to 600 mTorr. The ambient O{sub 2} compresses the plasma plume of SZY and increases the deposition rate. The 10 nm thick Ti adhesion layer on MgO(100) greatly affects the orientation of the sputtered Pt layers. Pt deposited directly on MgO shows a highly (111)-preferred orientation and leads to preferentially oriented SZY films while the addition of a Ti adhesion layer makes Pt show a less preferential orientation that leads to randomly oriented SZY films. The RMS surface roughness of preferentially oriented SZY films is larger than that of randomly oriented SZY films deposited under the same ambient O{sub 2} pressure. As the O{sub 2} pressure increased, the RMS surface roughness of preferentially oriented SZY films increased, reaching 45.7 nm (2.61% of film thickness) at 600 mTorr. This study revealed the ambient O{sub 2} pressure and orientation dependent surface roughness of SZY films grown on Pt-coated MgO substrates, which provides the potential to control the surface microstructure of SZY films for electrochemical applications in film-based hydrogen devices.

  16. Electrophoretic deposition of nickel zinc ferrite nanoparticles into microstructured patterns

    Directory of Open Access Journals (Sweden)

    Stefan J. Kelly

    2016-05-01

    Full Text Available Using DC electric fields, nickel-zinc ferrite (Ni0.5Zn0.5Fe2O4 nanoparticles (Dh =16.6 ± 3.6 nm are electrophoretically deposited onto silicon substrates to form dense structures defined by photoresist molds. Parameters such as electric field, bath composition, and deposition time are tuned to produce films ranging in thickness from 177 to 805 nm. The deposited films exhibit soft magnetic properties with a saturation magnetization of 60 emu/g and a coercivity of 2.6 kA/m (33 Oe. Additionally, the influence of the photoresist mold on the deposit profile is studied, and patterned films with different shapes (lines, squares, circles, etc. are demonstrated with feature sizes down to 5 μm.

  17. Preparation of Pt–GO composites with high-number-density Pt nanoparticles dispersed uniformly on GO nanosheets

    Directory of Open Access Journals (Sweden)

    Nanting Li

    2016-04-01

    Full Text Available 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=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 nanodendrites/reduced graphene oxide composites.

  18. 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.

  19. Tuning the composition of AuPt bimetallic nanoparticles for antibacterial application.

    Science.gov (United States)

    Zhao, Yuyun; Ye, Chunjie; Liu, Wenwen; Chen, Rong; Jiang, Xingyu

    2014-07-28

    We show that bimetallic nanoparticles (NPs) of AuPt without any surface modification are potent antibiotic reagents, while pure Au NPs or pure Pt NPs display no antibiotic activities. The most potent antibacterial AuPt NPs happen to be the most effective catalysts for chemical transformations. The mechanism of antibiotic action includes the dissipation of membrane potential and the elevation of adenosine triphosphate (ATP) levels. These bimetallic NPs are unique in that they do not produce reactive oxygen species as most antibiotics do. Being non-toxic to human cells, these bimetallic noble NPs might open an entry to a new class of antibiotics. © 2014 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution Non-Commercial NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.

  20. The Deposition of Gold Nanoparticles Onto Activated Carbon

    Directory of Open Access Journals (Sweden)

    Jaworski W.

    2014-10-01

    Full Text Available This work reports the results of spectrophotometric, dynamic light scattering (DLS and microscopic (SEM studies of the gold nanoparticles (AuNPs deposition on activated carbon (AC surface modified with primary (ethanolamine and secondary (diethylenetriamine and triethylenetetramine amines. It was found that this method is efficient for deposition of AuNPs from aqueous solution. However, nanoparticles change their morphology depending on the kind of amine used in experiments. On the AC surface modified with ethanolamine, the uniform spherical AuNPs were formed. In case of diethylenetriamine and triethylenetetramine application, the agglomerates of AuNPs are present. The diameter of individual AuNPs did not exceed 15 nm and was bigger as compared with the diameter of particles present in precursor solution (ca. 10 nm.

  1. Structural characterization and catalytic activity of Pt dendrimer encapsulated nanoparticles supported over Al2O3 for SCR of NOx.

    Science.gov (United States)

    Bae, HyunSook; Rao, Komateedi N; Ha, HeonPhil

    2011-07-01

    Pt/Al2O3 and Pt-Mg/Al2O3 nano composites were successfully prepared by dendrimer templated synthesis route. The obtained dendritic nanoparticles were dispersed in alumina support and they were evaluated for SCR of NOx using methane as reductant. Thermal analysis results of uncalcined samples revealed that the oxygen can accelerate the rate of dendrimer shell decomposition. X-ray diffractograms of 500 degrees C calcined samples disclosed the amorphous nature of materials, whereas 1000 degrees C air calcined samples showed enhanced crystallinity as well as diffraction pattern corresponding to Pt and PtO. HRTEM images of Pt40-G4OH dendritic nanoparticles showed uniform particulate distribution with average particle size of 2.4 nm. The STEM results of 0.5 Pt/Al2O3 sample calcined at 500 degrees C exhibited a wide range of particles between 2 and 20 nm. This indicates the huge segregation of platinum metal particles during impregnation and subsequent calcination. Among the synthesized materials 0.5 wt% Pt/Al2O3 sample showed excellent conversion and selectivity for SCR of NOx.

  2. Fabrication of single TiO2 nanotube devices with Pt interconnections using electron- and ion-beam-assisted deposition

    Science.gov (United States)

    Lee, Mingun; Cha, Dongkyu; Huang, Jie; Ha, Min-Woo; Kim, Jiyoung

    2016-06-01

    Device fabrication using nanostructured materials, such as nanotubes, requires appropriate metal interconnections between nanotubes and electrical probing pads. Here, electron-beam-assisted deposition (EBAD) and ion-beam-assisted deposition (IBAD) techniques for fabrication of Pt interconnections for single TiO2 nanotube devices are investigated. IBAD conditions were optimized to reduce the leakage current as a result of Pt spreading. The resistivity of the IBAD-Pt was about three orders of magnitude less than that of the EBAD-Pt, due to low carbon concentration and Ga doping, as indicated by X-ray photoelectron spectroscopy analysis. The total resistances of single TiO2 nanotube devices with EBAD- or IBAD-Pt interconnections were 3.82 × 1010 and 4.76 × 108 Ω, respectively. When the resistivity of a single nanotube is low, the high series resistance of EBAD-Pt cannot be ignored. IBAD is a suitable method for nanotechnology applications, such as photocatalysis and biosensors.

  3. 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.

  4. 电沉积铂铋纳米颗粒在甲酸电化学氧化中的催化性能%Electrodeposited PtBi Nanoparticles for Electrocatalytic Oxidation of Formic Acid

    Institute of Scientific and Technical Information of China (English)

    李甜; 杨民力

    2012-01-01

    In the studies of direct formic acid fuel cells, the choice, preparation and performance of catalysts are still at the central position. PtBi alloy was used as the catalyst for formic acid electrooxidation and showed good performance. However, neither physical melting nor chemical reduction was convenient to fabrication and electrochemical characterization because of their fussy and time-consuming operations. It was necessary to explore new and simple preparation methods. In the present work, well-distributed spherical PtBi nanoparticles were deposited on glassy carbon surface by a potentiostatic technique. The average size of PtBi nanoparticles was (63 ± 20 ) nm in diameter. The atomic ratio of Pt to Bi (1.18) was close to the molar ratio of [ PtCl6]2- to Bi3+ ions in electrolyte (1.11). These results proved that potentiostatic electrodeposition could act as a simple and effective method to produce spherical PtBi nanoparticles with uniform size and preset chemical composition. Their catalytic performances toward formic acid electrooxidation were studied with cyclic voltammetry and chronoamperometry. The experimental results showed that, in 0.5 mol·L-1 H2SO4 solution, the onset potential for formic acid electrooxidation at PtBi nanoparticles was more negative than that at PtRu nanoparticles by at least 200 mV. In 1. 0 mol·L-1 NaOH solution, the difference between the onset potentials for formic acid electrooxidation at PtBi nanoparticles and at PtRu nanoparticles was about 400 mV. Besides, either in acid media or in alkaline media, the formic acid electrooxidation had higher current on PtBi nanoparticles than on PtRu nanoparticles. All these results displayed that PtBi nanoparticles had better catalytic activities toward formic acid electrooxidation than PtRu nanoparticles.%在直接甲酸燃料电池的研究中,催化剂的选择、制备和性能研究依然是探索的重点.虽然PtBi合金已被报道用于甲酸的电化学催化氧化且具有良好的

  5. Synthesis and characterization of Pt-Pd nanoparticles with core-shell morphology: Nucleation and overgrowth of the Pd shells on the as-prepared and defined Pt seeds

    Energy Technology Data Exchange (ETDEWEB)

    Long, Nguyen Viet, E-mail: nguyenvietlong@yahoo.com [Department of Materials Scienceand Engineering, Nagoya Institute of Technology, Gokiso-cho, Showa-ku, Nagoya 466-8555 (Japan); Posts and Telecommunications Institute of Technology, km 10 Nguyen Trai, Hanoi (Viet Nam); Laboratory for Nanotechnology, Vietnam National University at Ho Chi Minh, Linh Trung, Thu Duc, Ho Chi Minh (Viet Nam); Department of Molecular and Material Sciences, Interdisciplinary Graduate School of Engineering Sciences, 6-1 Kasugakouen, Kasuga, Fukuoka 861-8580 (Japan); Hien, Tong Duy [Laboratory for Nanotechnology, Vietnam National University at Ho Chi Minh, Linh Trung, Thu Duc, Ho Chi Minh (Viet Nam); Asaka, Toru [Department of Materials Scienceand Engineering, Nagoya Institute of Technology, Gokiso-cho, Showa-ku, Nagoya 466-8555 (Japan); Ohtaki, Michitaka [Department of Molecular and Material Sciences, Interdisciplinary Graduate School of Engineering Sciences, 6-1 Kasugakouen, Kasuga, Fukuoka 861-8580 (Japan); Nogami, Masayuki, E-mail: nogami@nitech.ac.jp [Department of Materials Scienceand Engineering, Nagoya Institute of Technology, Gokiso-cho, Showa-ku, Nagoya 466-8555 (Japan)

    2011-07-21

    Highlights: > The Pt-Pd core-shell nanoparticles based on the as-prepared Pt cores are synthesized. > Not only the Pt-Pd core-shell nanoparticles are formed, but also the separate formation of Pd nanoparticles as well. > The Pt cores without the morphological changes are protected by the Pd-shell overgrowths. > There are the co-existence of the layer-by-layer and island-on-wetting-layer growth modes of the Pd shells and the latter becomes the favorable overgrowth in the formation of core-shell structures. - Abstract: In the present research, Pt-Pd core-shell nanoparticles based on the as-prepared and defined Pt-seed cores with well-controlled size and morphology were synthesized. Their characterizations were investigated by using UV-vis spectroscopy, transmission electron microscopy (TEM), and high resolution (HR)TEM measurements. The high resolution elemental mappings were performed in the operation of high angle annular dark field (HAADF) in conjunction with scanning (S)TEM mode and X-ray energy dispersive spectroscopy (XEDS). It is found that not only the Pt-Pd core-shell nanoparticles were formed, but also the nucleation, growth, and the separate formation of single Pd nanoparticles as well. Interestingly, the as-prepared Pt cores without the morphological changes were protected by the overgrowths of the Pd shells during the successive reduction of sodium tetrachloropalladate (II) hydrate. There were the co-existence of the Frank-van der Merwe (FM) layer-by-layer and Stranski-Krastanov (SK) island-on-wetting-layer growth modes of the Pd shells on the as-prepared Pt cores. It is predicted that the SK growth became the favorable growth mode in the formation of the Pd shells in the formation Pt-Pd core-shell nanoparticles.

  6. Synthesis and Electrochemical Evaluation of Carbon Supported Pt-Co Bimetallic Catalysts Prepared by Electroless Deposition and Modified Charge Enhanced Dry Impregnation

    OpenAIRE

    John Meynard M. Tengco; Bahareh Alsadat Tavakoli Mehrabadi; Yunya Zhang; Akkarat Wongkaew; John R. Regalbuto; Weidner, John W.; John R. Monnier

    2016-01-01

    Carbon-supported bimetallic Pt-Co cathode catalysts have been previously identified as higher activity alternatives to conventional Pt/C catalysts for fuel cells. In this work, a series of Pt-Co/C catalysts were synthesized using electroless deposition (ED) of Pt on a Co/C catalyst prepared by modified charge enhanced dry impregnation. X-ray diffraction (XRD) and scanning transmission electron microscopy (STEM) characterization of the base catalyst showed highly dispersed particles. A basic E...

  7. Self-assembly of mixed Pt and Au nanoparticles on PDDA-functionalized graphene as effective electrocatalysts for formic acid oxidation of fuel cells.

    Science.gov (United States)

    Wang, Shuangyin; Wang, Xin; Jiang, San Ping

    2011-04-21

    Pt and Au nanoparticles with controlled Pt : Au molar ratios and PtAu nanoparticle loadings were successfully self-assembled onto poly(diallyldimethylammonium chloride) (PDDA)-functionalized graphene (PDDA-G) as highly effective electrocatalysts for formic acid oxidation in direct formic acid fuel cells (DFAFCs). The simultaneously assembled Pt and Au nanoparticles on PDDA-G showed superb electrocatalytic activity for HCOOH oxidation, and the current density associated with the preferred dehydrogenation pathway for the direct formation of CO(2) through HCOOH oxidation on a Pt(1)Au(8)/PDDA-G (i.e., a Pt : Au ratio of 1 : 8) is 32 times higher than on monometallic Pt/PDDA-G. The main function of the Au in the mixed Pt and Au nanoparticles on PDDA-G is to facilitate the first electron transfer from HCOOH to HCOO(ads) and the effective spillover of HCOO(ads) from Au to Pt nanoparticles, where HCOO(ads) is further oxidized to CO(2). The Pt : Au molar ratio and PtAu nanoparticle loading on PDDA-G supports are the two critical factors to achieve excellent electrocatalytic activity of PtAu/PDDA-G catalysts for the HCOOH oxidation reactions.

  8. Self-assemble nanoparticles based on polypeptides containing C-terminal luminescent Pt-cysteine complex

    Science.gov (United States)

    Vlakh, E. G.; Grachova, E. V.; Zhukovsky, D. D.; Hubina, A. V.; Mikhailova, A. S.; Shakirova, J. R.; Sharoyko, V. V.; Tunik, S. P.; Tennikova, T. B.

    2017-01-01

    The growing attention to the luminescent nanocarriers is strongly stimulated by their potential application as drug delivery systems and by the necessity to monitor their distribution in cells and tissues. In this communication we report on the synthesis of amphiphilic polypeptides bearing C-terminal phosphorescent label together with preparation of nanoparticles using the polypeptides obtained. The approach suggested is based on a unique and highly technological process where the new phosphorescent Pt-cysteine complex serves as initiator of the ring-opening polymerization of α-amino acid N-carboxyanhydrides to obtain the polypeptides bearing intact the platinum chromophore covalently bound to the polymer chain. It was established that the luminescent label retains unchanged its emission characteristics not only in the polypeptides but also in more complicated nanoaggregates such as the polymer derived amphiphilic block-copolymers and self-assembled nanoparticles. The phosphorescent nanoparticles display no cytotoxicity and hemolytic activity in the tested range of concentrations and easily internalize into living cells that makes possible in vivo cell visualization, including prospective application in time resolved imaging and drug delivery monitoring. PMID:28155880

  9. Self-assemble nanoparticles based on polypeptides containing C-terminal luminescent Pt-cysteine complex

    Science.gov (United States)

    Vlakh, E. G.; Grachova, E. V.; Zhukovsky, D. D.; Hubina, A. V.; Mikhailova, A. S.; Shakirova, J. R.; Sharoyko, V. V.; Tunik, S. P.; Tennikova, T. B.

    2017-02-01

    The growing attention to the luminescent nanocarriers is strongly stimulated by their potential application as drug delivery systems and by the necessity to monitor their distribution in cells and tissues. In this communication we report on the synthesis of amphiphilic polypeptides bearing C-terminal phosphorescent label together with preparation of nanoparticles using the polypeptides obtained. The approach suggested is based on a unique and highly technological process where the new phosphorescent Pt-cysteine complex serves as initiator of the ring-opening polymerization of α-amino acid N-carboxyanhydrides to obtain the polypeptides bearing intact the platinum chromophore covalently bound to the polymer chain. It was established that the luminescent label retains unchanged its emission characteristics not only in the polypeptides but also in more complicated nanoaggregates such as the polymer derived amphiphilic block-copolymers and self-assembled nanoparticles. The phosphorescent nanoparticles display no cytotoxicity and hemolytic activity in the tested range of concentrations and easily internalize into living cells that makes possible in vivo cell visualization, including prospective application in time resolved imaging and drug delivery monitoring.

  10. CO tolerant PtRu-MoO{sub x} nanoparticles supported on carbon nanofibers for direct methanol fuel cells

    Energy Technology Data Exchange (ETDEWEB)

    Tsiouvaras, N.; Pena, M.A.; Fierro, J.L.G. [Instituto de Catalisis y Petroleoquimica, CSIC, Marie Curie 2, 28049 Madrid (Spain); Martinez-Huerta, M.V. [Instituto de Catalisis y Petroleoquimica, CSIC, Marie Curie 2, 28049 Madrid (Spain); Facultad de Quimicas, Universidad de La Laguna, Astrofisico Francisco Sanchez s/n, 38071, La Laguna, Tenerife (Spain); Moliner, R.; Lazaro, M.J. [Instituto de Carboquimica, CSIC, Miguel Luesma Castan 4, 50018 Zaragoza (Spain); Rodriguez, J.L.; Pastor, E. [Facultad de Quimicas, Universidad de La Laguna, Astrofisico Francisco Sanchez s/n, 38071, La Laguna, Tenerife (Spain)

    2009-01-15

    Novel nanostructured catalysts based on PtRu-MoO{sub x} nanoparticles supported on carbon nanofibers have been investigated for CO and methanol electrooxidation. Carbon nanofibers are prepared by thermocatalytic decomposition of methane (NF), and functionalized with HNO{sub 3} (NF.F). Electrocatalysts are obtained using a two-step procedure: (1) Pt and Ru are incorporated on the carbon substrates (Vulcan XC 72R, NF and NF.F), and (2) Mo is loaded on the PtRu/C samples. Differential electrochemical mass spectrometry (DEMS) analyses establish that the incorporation of Mo increases significantly the CO tolerance than respective binary counterparts. The nature of the carbon support affects considerably the stabilization of MoO{sub x} nanoparticles and also the performance in methanol electrooxidation. Accordingly, a significant increase of methanol oxidation is obtained in PtRu-MoO{sub x} nanoparticles supported on non-functionalized carbon nanofiber, in parallel with a large reduction of the Pt amount in comparison with binary counterparts and commercial catalyst. (author)

  11. Deposition of silver nanoparticles on titanium surface for antibacterial effect

    Directory of Open Access Journals (Sweden)

    Liao Juan

    2010-04-01

    Full Text Available Liao Juan1, Zhu Zhimin3, Mo Anchun1,2, Li Lei1, Zhang Jingchao11State Key Laboratory of Oral Diseases, Sichuan University, Chengdu 610041, PR China; 2Department of Dental Implant, West China Stomatology Hospital, Sichuan University, Chengdu 610041, PR China; 3Department of Prosthodontics, West China Stomatology Hospital, Sichuan University, Chengdu 610041, PR ChinaAbstract: Microbial colonization on implanted devices and biofilm formation is a recurrent complication in implant surgery and may result in loss of implants. The aim of this study was to deposit silver nanoparticles on a titanium surface to obtain antibacterial properties. In the present study, we prepared a silver nanoparticle-modified titanium (Ti-nAg surface using silanization method. The morphology and chemical components of the Ti-nAg surface were characterized by scanning electron microscopy (SEM equipped with energy-dispersive spectroscopy (EDS. Two species of bacteria, Staphylococcus aureus and Escherichia coli, were utilized to test the antibacterial effect of the Ti-nAg treated surface. The SEM examination revealed that a small quantity of silver nanoparticles was sparsely deposited on the titanium surface. The diameter of these nanoparticles ranged from ten to several hundred nm. EDS analyses revealed that there was 4.26% of Ag present on the surface. After a 24-hour incubation, 94% of Staphylococcus aureus and over 95% of Escherichia coli had been killed on the Ti-nAg surface, and the SEM examination of anti-adhesive efficacy test showed that there were less bacteria attached to Ti-nAg surface than to a control surface of untreated Titanium. These data suggest that silver nanoparticle-modified titanium is a promising material with an antibacterial property that may be used as an implantable biomaterial.Keywords: nano-silver, titanium, antibacterial activity, silanization method

  12. Broadband infrared absorption enhancement by electroless-deposited silver nanoparticles

    DEFF Research Database (Denmark)

    Gritti, Claudia; Raza, Søren; Kadkhodazadeh, Shima

    2017-01-01

    Decorating semiconductor surfaces with plasmonic nanoparticles (NPs) is considered a viable solution for enhancing the absorptive properties of photovoltaic and photodetecting devices. We propose to deposit silver NPs on top of a semiconductor wafer by a cheap and fast electroless plating technique....... Optical characterization confirms that the random array of electroless-deposited NPs improves absorption by up to 20% in a broadband of nearinfrared frequencies from the bandgap edge to 2000 nm. Due to the small filling fraction of particles, the reflection in the visible range is practically unchanged......, which points to the possible applications of such deposition method for harvesting photons in nanophotonics and photovoltaics. The broadband absorption is a consequence of the resonant behavior of particles with different shapes and sizes, which strongly localize the incident light at the interface...

  13. Structural assembly effects of Pt nanoparticle-carbon nanotube-polyaniline nanocomposites on the enhancement of biohydrogen fuel cell performance

    Energy Technology Data Exchange (ETDEWEB)

    Hoa, Le Quynh, E-mail: hoa@p.eng.osaka-u.ac.jp [Department of Applied Physics, Graduate School of Engineering, Osaka University, 2-1 Yamadaoka, Suita, Osaka 565-0871 (Japan); Sugano, Yasuhito; Yoshikawa, Hiroyuki; Saito, Masato [Department of Applied Physics, Graduate School of Engineering, Osaka University, 2-1 Yamadaoka, Suita, Osaka 565-0871 (Japan); Tamiya, Eiichi, E-mail: tamiya@ap.eng.osaka-u.ac.jp [Department of Applied Physics, Graduate School of Engineering, Osaka University, 2-1 Yamadaoka, Suita, Osaka 565-0871 (Japan)

    2011-11-30

    Graphical abstract: - Abstract: In this work, we designed various polyaniline (PANI) nanocomposites with platinum (Pt) nanoparticle-decorated multi-walled carbon nanotubes (MWCNTs), employed them as anodic catalysts, and studied their structural assembly effects with regard to enhancing biohydrogen fuel cell performance. Of two proposed structures, the PANI/Pt/MWCNTs multilayer nanocomposites showed superior electrocatalytic activities in the hydrogen oxidation reaction and in fuel cell power density relative to the Pt/MWCNTs-PANI core-shell design. These enhancements were attributed to the active interface formed between the Pt nanoparticles and polyaniline nanofibers, where the higher electronic and ionic conductivities of the thin PANI nanofiber layers in contact with Pt active sites were better than with the PANI bound Pt/MWCNTs. We also investigated the change in the electronic state of the composites and the charge-transfer rate caused by varying the structural assembly. Finally, the role of each catalyst component was examined to understand its individual effect on fuel cell performance and to understand its structural assembly effect on enhanced power density.

  14. Ultra-small platinum and gold nanoparticles by arc plasma deposition

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Sang Hoon, E-mail: kim_sh@kist.re.kr [Center for Materials Architecturing, Korea Institute of Science and Technology (KIST), Seoul 136-791 (Korea, Republic of); Jeong, Young Eun; Ha, Heonphil; Byun, Ji Young [Center for Materials Architecturing, Korea Institute of Science and Technology (KIST), Seoul 136-791 (Korea, Republic of); Kim, Young Dok [Department of Chemistry, Sungkyunkwan University, Suwon 440-746 (Korea, Republic of)

    2014-04-01

    Highlights: • Ultra-small (<2 nm) and bigger platinum and gold nanoparticles were produced by arc plasma deposition (APD). • Size and coverage of deposited nanoparticles were easily controlled with APD parameters. • Crystalline structures of deposited nanoparticles emerged only when the particle size was bigger than ∼2 nm. - Abstract: Ultra-small (<2 nm) nanoparticles of platinum and gold were produced by arc plasma deposition (APD) in a systematic way and the deposition behavior was studied. Nanoparticles were deposited on two dimensional amorphous carbon and amorphous titania thin films and characterized by transmission electron microscopy (TEM). Deposition behavior of nanoparticles by APD was studied with discharge voltage (V), discharge condenser capacitance (C), and the number of plasma pulse shots (n) as controllable parameters. The average size of intrinsic nanoparticles generated by APD process was as small as 0.9 nm and deposited nanoparticles began to have crystal structures from the particle size of about 2 nm. V was the most sensitive parameter to control the size and coverage of generated nanoparticles compared to C and n. Size of APD deposited nanoparticles was also influenced by the nature of evaporating materials and substrates.

  15. Electroless deposition of Gold-Platinum Core@Shell Nanoparticles on Glassy Carbon Electrode for Non-Enzymatic Hydrogen Peroxide sensing#

    Indian Academy of Sciences (India)

    Gowthaman N S K; Abraham John S

    2016-03-01

    A non-enzymatic hydrogen peroxide sensor was developed using gold@platinum nanoparticlesz (Au@PtNPs) with core@shell structure fabricated on glassy carbon electrode (GCE) by electroless depositionmethod. Initially, gold nanoparticles (AuNPs) were deposited on GCE by reducing HAuCl4 in the presence of NH2OH and the deposited AuNPs on GCE act as the nucleation centre for the deposition of platinum nanoparticles (PtNPs) in the presence of H2PtCl6 and NH2OH. SEM and AFM studies demonstrated that the electrolessdeposition of Pt on Au was isotropic and uniform. Further, Au@PtNP-modified substrates were characterizedby X-ray photoelectron spectroscopy (XPS), energy dispersive X-ray analysis (EDAX) and cyclic voltammetry (CV). XPS showed characteristic binding energies at 71.2 and 74.4 eV for PtNPs and, 83.6 and 87.3 eV forAuNPs indicating the zero-valent nature in both of them. The electrocatalytic activity of Au@PtNP-modifiedelectrode was investigated towards hydrogen peroxide (HP) reduction. The modified electrode exhibited higherelectrocatalytic activity towards HP by not only shifting its reduction potential by 370 mV towards less positivepotential but also by enhancing the reduction current when compared to bare and AuNP-modified GCE. Thepresent method shows better sensitivity compared to the reported methods in literature and the detection limitwas found to be 60 nM.

  16. 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...

  17. A curious interplay in the films of N-heterocyclic carbene PtII complexes upon deposition of alkali metals

    Science.gov (United States)

    Makarova, Anna A.; Grachova, Elena V.; Niedzialek, Dorota; Solomatina, Anastasia I.; Sonntag, Simon; Fedorov, Alexander V.; Vilkov, Oleg Yu.; Neudachina, Vera S.; Laubschat, Clemens; Tunik, Sergey P.; Vyalikh, Denis V.

    2016-05-01

    The recently synthesized series of PtII complexes containing cyclometallating (phenylpyridine or benzoquinoline) and N-heterocyclic carbene ligands possess intriguing structures, topologies, and light emitting properties. Here, we report curious physicochemical interactions between in situ PVD-grown films of a typical representative of the aforementioned PtII complex compounds and Li, Na, K and Cs atoms. Based on a combination of detailed core-level photoelectron spectroscopy and quantum-chemical calculations at the density functional theory level, we found that the deposition of alkali atoms onto the molecular film leads to unusual redistribution of electron density: essential modification of nitrogen sites, reduction of the coordination PtII centre to Pt0 and decrease of electron density on the bromine atoms. A possible explanation for this is formation of a supramolecular system “Pt complex-alkali metal ion” the latter is supported by restoration of the system to the initial state upon subsequent oxygen treatment. The discovered properties highlight a considerable potential of the PtII complexes for a variety of biomedical, sensing, chemical, and electronic applications.

  18. A curious interplay in the films of N-heterocyclic carbene Pt(II) complexes upon deposition of alkali metals.

    Science.gov (United States)

    Makarova, Anna A; Grachova, Elena V; Niedzialek, Dorota; Solomatina, Anastasia I; Sonntag, Simon; Fedorov, Alexander V; Vilkov, Oleg Yu; Neudachina, Vera S; Laubschat, Clemens; Tunik, Sergey P; Vyalikh, Denis V

    2016-05-06

    The recently synthesized series of Pt(II) complexes containing cyclometallating (phenylpyridine or benzoquinoline) and N-heterocyclic carbene ligands possess intriguing structures, topologies, and light emitting properties. Here, we report curious physicochemical interactions between in situ PVD-grown films of a typical representative of the aforementioned Pt(II) complex compounds and Li, Na, K and Cs atoms. Based on a combination of detailed core-level photoelectron spectroscopy and quantum-chemical calculations at the density functional theory level, we found that the deposition of alkali atoms onto the molecular film leads to unusual redistribution of electron density: essential modification of nitrogen sites, reduction of the coordination Pt(II) centre to Pt(0) and decrease of electron density on the bromine atoms. A possible explanation for this is formation of a supramolecular system "Pt complex-alkali metal ion"; the latter is supported by restoration of the system to the initial state upon subsequent oxygen treatment. The discovered properties highlight a considerable potential of the Pt(II) complexes for a variety of biomedical, sensing, chemical, and electronic applications.

  19. Defect Kinetics and Magnetic Studies of Ion-Irradiated FePt Nanoparticles

    Science.gov (United States)

    Seetala, Naidu V.

    2009-03-01

    We have used 300 keV Al+-irradiation and 1 MeV proton-irradiation to obtain vacancy-migration enhanced phase transformation of FePt nanoparticles at lower temperatures (˜200° C). SRIM-2006 computer code was used to estimate the irradiation parameters and the defect concentrations. Low temperature annealing showed promising results, but further annealing at higher temperatures gave detrimental effects due to lattice strain produced by larger defect clusters. These effects are more prominent in proton-irradiation and the effects of vacancy clusters seem to remain stronger even at higher temperatures. The magnetization results indicate dissociation of vacancy clusters above 600° C. The magnetization studies of 700° C and 800° C annealed particles aged for one year at room temperature showed defect strain release over time.

  20. Interaction of the Mu-cyclohexadienyl radical with metallic (Au, Pt) nanoparticles in mesoporous silica

    Science.gov (United States)

    Xiao, J.; Arseneau, D. J.; Bridges, M. D.; Cortie, D.; Cottrell, S. P.; Dehn, M.; Fleming, D. G.; Kelly, J.; Kiefl, R. F.; MacFarlane, W. A.; MacLachlan, M.; McKenzie, I.

    2014-12-01

    μSR and ALCR techniques have been used to investigate the structure and dynamics of the Mu-cyclohexadienyl radical interacting with Au and Pt metal nanoparticles (MNPs) supported in mesoporous silica (SBA-15). Surprisingly, coherent precession signals are observed and the isotropic hyperfine coupling constants are almost the same in loaded and unloaded samples, implying that the electronic structure of MuC6H6 is only weakly perturbed by the presence of the MNPs. We propose the observed radicals are shielded from the metallic surfaces by a benzene coating on the MNPs. The Δ1 resonance is observable in MNP-loaded samples at higher temperatures than in the unloaded SBA-15. This is attributed to stronger binding of MuC6H6 to the benzene coated MNPs.

  1. Carbon paper supported Pt/Au catalysts prepared via Cu underpotential deposition-redox replacement and investigation of their electrocatalytic activity for methanol oxidation and oxygen reduction reactions

    Energy Technology Data Exchange (ETDEWEB)

    Khosravi, Mohsen; Amini, Mohammad K. [Chemistry Department, University of Isfahan, Isfahan 81744-73441 (Iran)

    2010-10-15

    Through a simple and rapid method, carbon papers (CPs) were coated with Au and the resulting Au/CP substrates were used for the preparation of Pt/Au/CP by Cu underpotential deposition (Cu UPD) and redox replacement technique. A series of Pt{sub n}/Au/CP catalysts (where n = number of UPD-redox replacement cycles) were synthesized and their electrochemical properties for methanol oxidation reaction (MOR), and oxygen reduction reaction (ORR) were investigated by electrochemical measurements. The Pt{sub n}/Au/CP electrodes show higher electrocatalytic activity and enhanced poison tolerance for the MOR as compared to a commercial Pt/C on CP (Pt/C/CP). The highest mass specific activity and Pt utilization efficiency for MOR was observed on Pt{sub 1}/Au/CP with a thickness close to a monatomic Pt layer. Chronoamperometric tests in methanol solution revealed that Pt{sub n}/Au/CPs have much higher CO tolerance compared to Pt/C/CP. Among the Pt{sub n}/Au/CPs, CO tolerance decreases with increasing the amount of deposited Pt, indicating that the exposed Au atoms in close proximity to Pt plays a positive role against CO poisoning. Compared with the Pt/C/CP, all the Pt{sub n}/Au/CP electrodes show more positive onset potentials and lower overpotentials for ORR. For instance, the onset potential of ORR is 150 mV more positive and the overpotential is {proportional_to}140 mV lower on Pt{sub 4}/Au/CP with respect to Pt/C/CP. (author)

  2. 石墨烯负载Pt-Co纳米粒子及其在氧化还原反应中的应用%Preparation of graphene-supported Pt-Co nanoparticles and their use in oxygen reduction reactions

    Institute of Scientific and Technical Information of China (English)

    马延文; 刘忠儒; 王博琳; 朱磊; 杨建平; 李兴鳌

    2012-01-01

    采用微波-乙二醇方法还原氧化石墨烯和Pt(v)、Co(Ⅱ)粒子混合物,再经300℃H2还原,制备了石墨烯负载Pt-Co合金催化剂(Pt-Co/G).利用透射电镜、X-射线能谱、X-射线衍射和光电子能谱对所制催化剂进行表征.Pt-Co合金的粒径为3nm~8 nm,均匀地分散在石墨烯片上.与单金属的Pt/G和商品化的Pt/C催化剂相比,所制合金化的Pt-Co/G催化剂对氧还原反应展现出高的催化活性和可比拟的稳定性,显示了其在燃料电池中的应用潜力.%Electrocatalysts of graphene-supported Pt-Co alloy nanoparticles (Pt-Co/G) were prepared by a simultaneous reduction of mixtures of graphene oxide and Pt(Ⅳ),Co(Ⅱ) ions with ethylene glycol assisted by a microwave and further H2 treatment at 300 ℃.As-prepared Pt-Co/G catalysts were characterized by transmission electron microscopy,energy-dispersive X-ray spectrometry,X-ray diffraction,and X-ray photoelectron spectroscopy.The Pt-Co binary alloy nanoparticles with a size of 3-8 nm were homogeneously dispersed on the graphene.Compared with the monometallic Pt/ G and commercial Pt/C catalysts,the Pt-Co/G catalysts have a high stability and increased electrocatalytic activity that is conducive for the oxygen reduction reaction,suggesting their potential application in fuel cells.

  3. “Single-” and “multi-core” FePt nanoparticles: from controlled synthesis via zwitterionic and silica bio-functionalization to MRI applications

    Energy Technology Data Exchange (ETDEWEB)

    Kostevšek, Nina, E-mail: nina.kostevsek@ijs.si; Šturm, Sašo [Jožef Stefan Institute, Department for Nanostructured Materials (Slovenia); Serša, Igor; Sepe, Ana [Jožef Stefan Institute, Department for Condensed Matter Physics (Slovenia); Bloemen, Maarten; Verbiest, Thierry [KU Leuven, Department of Chemistry (Belgium); Kobe, Spomenka; Žužek Rožman, Kristina [Jožef Stefan Institute, Department for Nanostructured Materials (Slovenia)

    2015-12-15

    The value of the magnetization has a strong influence on the performance of nanoparticles that act as the contrast agent material for MRI. In this article, we describe processing routes for the synthesis of FePt nanoparticles of different sizes, which, as a result, exhibit different magnetization values. “Single-core” FePt nanoparticles of different sizes (3–15 nm) were prepared via one-step or two-step synthesis, with the latter exhibiting twice the magnetization (m{sub (1.5T)} = 14.5 emu/g) of the nanoparticles formed via the one-step synthesis (m{sub (1.5T)} < 8 emu/g). Furthermore, we propose the synthesis of “multi-core” FePt nanoparticles by changing the ratio between the two surfactants (oleylamine and oleic acid). The step from smaller “single-core” FePt nanoparticles towards the larger, “multi-core” FePt nanoparticles (>20 nm) leads to an increase in the magnetization m{sub (1.5T)} from 8 to 19.5 emu/g, without exceeding the superparamagnetic limit. Stable water suspensions were prepared using two different approaches: (a) functionalization with a biocompatible, zwitterionic, catechol ligand, which was used on the FePt nanoparticles for the first time, and (b) coating with SiO{sub 2} shells of various thicknesses. These FePt-based nanostructures, the catechol- and SiO{sub 2}-coated “single-core” and “multi-core” FePt nanoparticles, were investigated in terms of the relaxation rates. The higher r{sub 2} values obtained for the “multi-core” FePt nanoparticles compared to that for the “single-core” ones indicate the superiority of the “multi-core” FePt nanoparticles as T{sub 2} contrast agents. Furthermore, it was shown that the SiO{sub 2} coating reduces the r{sub 1} and r{sub 2} relaxation values for both the “single-core” and “multi-core” FePt nanoparticles. The high r{sub 2}/r{sub 1} ratios obtained in our study put FePt nanoparticles near the top of the list of candidate materials for use in MRI

  4. Low content Pt nanoparticles anchored on N-doped reduced graphene oxide with high and stable electrocatalytic activity for oxygen reduction reaction

    Science.gov (United States)

    Li, Zeyu; Gao, Qiuming; Zhang, Hang; Tian, Weiqian; Tan, Yanli; Qian, Weiwei; Liu, Zhengping

    2017-01-01

    A novel kind of Pt/N-rGO hybrid possessing of low content 5.31 wt.% Pt anchored on the surface of nitrogen doped reduced graphene oxide (N-rGO) evenly was prepared. The Pt has uniformed 2.8 nm diameter and exposed (111) crystal planes; meanwhile, the N works as the bridge between Pt and rGO with the Pt-N and N-C chemical bonds in Pt/N-rGO. The Pt/N-rGO material has a very high electrocatalytic activity in oxygen reduction reaction with the mass catalytic activity more than 1.5 times of the commercial Pt/C due to the synergistic catalytic effect of both N-doped carbon matrix and Pt nanoparticles. Moreover, the Pt/N-rGO exhibits an excellent stability with hardly loss (only 0.4%) after accelerated durability tests of 5000 cycles based on the stable Pt-N-C chemical bonds in Pt/N-rGO, which can prevent the detachment, dissolution, migration and aggregation of Pt nanoparticles on the matrix during the long-term cycling. PMID:28233857

  5. Low content Pt nanoparticles anchored on N-doped reduced graphene oxide with high and stable electrocatalytic activity for oxygen reduction reaction

    Science.gov (United States)

    Li, Zeyu; Gao, Qiuming; Zhang, Hang; Tian, Weiqian; Tan, Yanli; Qian, Weiwei; Liu, Zhengping

    2017-02-01

    A novel kind of Pt/N-rGO hybrid possessing of low content 5.31 wt.% Pt anchored on the surface of nitrogen doped reduced graphene oxide (N-rGO) evenly was prepared. The Pt has uniformed 2.8 nm diameter and exposed (111) crystal planes; meanwhile, the N works as the bridge between Pt and rGO with the Pt-N and N-C chemical bonds in Pt/N-rGO. The Pt/N-rGO material has a very high electrocatalytic activity in oxygen reduction reaction with the mass catalytic activity more than 1.5 times of the commercial Pt/C due to the synergistic catalytic effect of both N-doped carbon matrix and Pt nanoparticles. Moreover, the Pt/N-rGO exhibits an excellent stability with hardly loss (only 0.4%) after accelerated durability tests of 5000 cycles based on the stable Pt-N-C chemical bonds in Pt/N-rGO, which can prevent the detachment, dissolution, migration and aggregation of Pt nanoparticles on the matrix during the long-term cycling.

  6. Aggregation and deposition behavior of boron nanoparticles in porous media.

    Science.gov (United States)

    Liu, Xuyang; Wazne, Mahmoud; Christodoulatos, Christos; Jasinkiewicz, Kristin L

    2009-02-01

    New kinds of solid fuels and propellants comprised of nanomaterials are making their way into civilian and military applications yet the impact of their release on the environment remains largely unknown. One such material is nano boron, a promising solid fuel and propellant. The fate and transport of nano boron under various aquatic systems was investigated in aggregation and deposition experiments. Column experiments were performed to examine the effects of electrolyte concentration and flow velocity on the transport of boron nanoparticles under saturated conditions, whereas aggregation tests were conducted to assess the effects of electrolytes on the aggregation of the boron nanoparticles. Aggregation tests indicated the presence of different reaction-controlled and diffusion-controlled regimes and yielded critical coagulation concentrations (CCC) of 200 mM, 0.7 mM and 1.5 mM for NaCl, CaCl(2), and MgCl(2), respectively. Aggregation and deposition experimental data corresponded with the classic Derjaguin-Landau-Verwey-Overbeek (DLVO) model and the constant attachment efficiency filtration model, respectively. Theoretical calculations indicated that both the primary and secondary energy minima play important roles in the deposition of nano boron in sand columns.

  7. Controlling core/shell Au/FePt nanoparticle electrocatalysis via changing the core size and shell thickness.

    Science.gov (United States)

    Sun, Xiaolian; Li, Dongguo; Guo, Shaojun; Zhu, Wenlei; Sun, Shouheng

    2016-02-01

    Using a modified seed-mediated method, we synthesized core/shell Au/FePt nanoparticles (NPs) with Au sizes of 4, 7, and 9 nm and the FePt shell was controlled to have similar FePt compositions and 0.5, 1, and 2 nm thickness. We studied both core and shell effects on electrochemical and electrocatalytic properties of the Au/FePt NPs, and found that the Au core did change the redox chemistry of the FePt shell and promoted its electrochemical oxidation of methanol. The catalytic activity was dependent on the FePt thicknesses, but not much on the Au core sizes, and the 1 nm FePt shell was found to be the optimal thickness for catalyzing methanol oxidation in 0.1 M HClO4 + 0.1 M methanol, offering not only high activity (1.19 mA cm(-2) at 0.5 V vs. Ag/AgCl), but also enhanced stability. Our studies demonstrate a general approach to the design and tuning of shell catalysis in the core/shell structure to achieve optimal catalysis for important electrochemical reactions.

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

    Institute of Scientific and Technical Information of China (English)

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

    2007-01-01

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

  9. Magnetic heating properties and neutron activation of tungsten-oxide coated biocompatible FePt core-shell nanoparticles.

    Science.gov (United States)

    Seemann, K M; Luysberg, M; Révay, Z; Kudejova, P; Sanz, B; Cassinelli, N; Loidl, A; Ilicic, K; Multhoff, G; Schmid, T E

    2015-01-10

    Magnetic nanoparticles are highly desirable for biomedical research and treatment of cancer especially when combined with hyperthermia. The efficacy of nanoparticle-based therapies could be improved by generating radioactive nanoparticles with a convenient decay time and which simultaneously have the capability to be used for locally confined heating. The core-shell morphology of such novel nanoparticles presented in this work involves a polysilico-tungstate molecule of the polyoxometalate family as a precursor coating material, which transforms into an amorphous tungsten oxide coating upon annealing of the FePt core-shell nanoparticles. The content of tungsten atoms in the nanoparticle shell is neutron activated using cold neutrons at the Heinz Maier-Leibnitz (FRMII) neutron facility and thereby transformed into the radioisotope W-187. The sizeable natural abundance of 28% for the W-186 precursor isotope, a radiopharmaceutically advantageous gamma-beta ratio of γβ≈30% and a range of approximately 1mm in biological tissue for the 1.3MeV β-radiation are promising features of the nanoparticles' potential for cancer therapy. Moreover, a high temperature annealing treatment enhances the magnetic moment of nanoparticles in such a way that a magnetic heating effect of several degrees Celsius in liquid suspension - a prerequisite for hyperthermia treatment of cancer - was observed. A rise in temperature of approximately 3°C in aqueous suspension is shown for a moderate nanoparticle concentration of 0.5mg/ml after 15min in an 831kHz high-frequency alternating magnetic field of 250Gauss field strength (25mT). The biocompatibility based on a low cytotoxicity in the non-neutron-activated state in combination with the hydrophilic nature of the tungsten oxide shell makes the coated magnetic FePt nanoparticles ideal candidates for advanced radiopharmaceutical applications.

  10. Nanostructured polypyrrole/carbon composite as Pt catalyst support for fuel cell applications

    Science.gov (United States)

    Zhao, Hongbin; Li, Lei; Yang, Jun; Zhang, Yongming

    A novel catalyst support was synthesized by in situ chemical oxidative polymerization of pyrrole on Vulcan XC-72 carbon in naphthalene sulfonic acid (NSA) solution containing ammonium persulfate as oxidant at room temperature. Pt nanoparticles with 3-4 nm size were deposited on the prepared polypyrrole-carbon composites by chemical reduction method. Scanning electron microscopy and transmission electron microscopy measurements showed that Pt particles were homogeneously dispersed in polypyrrole-carbon composites. The Pt nanoparticles-dispersed catalyst composites were used as anodes of fuel cells for hydrogen and methanol oxidation. Cyclic voltammetry measurements of hydrogen and methanol oxidation showed that Pt nanoparticles deposited on polypyrrole-carbon with NSA as dopant exhibit better catalytic activity than those on plain carbon. This result might be due to the higher electrochemically available surface areas, electronic conductivity and easier charge-transfer at polymer/carbon particle interfaces allowing a high dispersion and utilization of deposited Pt nanoparticles.

  11. Nanostructured polypyrrole/carbon composite as Pt catalyst support for fuel cell applications

    Energy Technology Data Exchange (ETDEWEB)

    Zhao, Hongbin; Li, Lei; Yang, Jun; Zhang, Yongming [School of Chemistry and Chemical Technology, Shanghai Jiao Tong University, Shanghai 200240 (China)

    2008-10-01

    A novel catalyst support was synthesized by in situ chemical oxidative polymerization of pyrrole on Vulcan XC-72 carbon in naphthalene sulfonic acid (NSA) solution containing ammonium persulfate as oxidant at room temperature. Pt nanoparticles with 3-4 nm size were deposited on the prepared polypyrrole-carbon composites by chemical reduction method. Scanning electron microscopy and transmission electron microscopy measurements showed that Pt particles were homogeneously dispersed in polypyrrole-carbon composites. The Pt nanoparticles-dispersed catalyst composites were used as anodes of fuel cells for hydrogen and methanol oxidation. Cyclic voltammetry measurements of hydrogen and methanol oxidation showed that Pt nanoparticles deposited on polypyrrole-carbon with NSA as dopant exhibit better catalytic activity than those on plain carbon. This result might be due to the higher electrochemically available surface areas, electronic conductivity and easier charge-transfer at polymer/carbon particle interfaces allowing a high dispersion and utilization of deposited Pt nanoparticles. (author)

  12. Computational study of platinum nanoparticle deposition on the surfaces of crevices

    Energy Technology Data Exchange (ETDEWEB)

    Gu, H.F., E-mail: guhaifeng@hrbeu.edu.cn [Laboratory for Thermal-Hydraulics, Nuclear Energy and Safety Research Department, Paul Scherrer Institut, CH-5232 Villigen PSI (Switzerland); College of Nuclear Science and Technology, Harbin Engineering University, 150001 Harbin (China); Niceno, B. [Laboratory for Thermal-Hydraulics, Nuclear Energy and Safety Research Department, Paul Scherrer Institut, CH-5232 Villigen PSI (Switzerland); Grundler, P.V. [Laboratory for Nuclear Materials, Nuclear Energy and Safety Research Department, Paul Scherrer Institut, CH-5232 Villigen PSI (Switzerland); Sharabi, M. [Laboratory for Thermal-Hydraulics, Nuclear Energy and Safety Research Department, Paul Scherrer Institut, CH-5232 Villigen PSI (Switzerland); Mechanical Power Engineering Department, Mansoura University, 35516 Mansoura (Egypt); Veleva, L. [Laboratory for Nuclear Materials, Nuclear Energy and Safety Research Department, Paul Scherrer Institut, CH-5232 Villigen PSI (Switzerland); Hot Laboratory Division, Nuclear Energy and Safety Research Department, Paul Scherrer Institut, CH-5232 Villigen PSI (Switzerland); Ritter, S. [Laboratory for Nuclear Materials, Nuclear Energy and Safety Research Department, Paul Scherrer Institut, CH-5232 Villigen PSI (Switzerland)

    2016-08-01

    Highlights: • Nano-particle deposition on the surface of crevices is studied using RANS simulation. • Model results are validated by comparing with experimental data. • Behaviours and mechanisms of particle deposition in different crevices are analyzed. • RANS models with Lagrangian particle tracking method are evaluated and discussed. - Abstract: A well-known issue in boiling water reactors (BWR), which can threaten their structural integrity, is stress corrosion cracking (SCC) of reactor internals and recirculation pipes due to the accumulation of oxidizing radiolysis products of water. Currently, many operators of BWRs use combined platinum particle and hydrogen injection into the reactor water to mitigate SCC by lowering the electrochemical corrosion potential. It is essential for efficient mitigation that Pt particles reach all water-wetted surfaces, including crevices and cracks, which are also reached by the oxidizing species. In this study, a set of crevices with different widths and orientations with respect to the fluid flow are investigated using numerical simulation tools and compared against experimental findings. The Reynolds-Averaged Navier–Stokes models are used to compute the mean turbulent flow quantities in three-dimensional crevices, and the discrete random walk model is used to evaluate the effect of velocity fluctuations on particle movement. The Lagrangian particle tracking analysis is performed and the average concentration of deposited particles on the surface of crevices is evaluated and compared with experimental results. The results show that Reynolds stress model combined with enhanced wall treatment provides a more accurate prediction of particle concentration and distribution on the surface of crevices than SST k–ω turbulence model, which was expected, owing to the anisotropic nature of the Reynolds stress model. Furthermore, analyses on the particle deposition shows that three different mechanisms play important roles in

  13. Orientation of FePt nanoparticles on top of a-SiO2/Si(001), MgO(001) and sapphire(0001): effect of thermal treatments and influence of substrate and particle size.

    Science.gov (United States)

    Schilling, Martin; Ziemann, Paul; Zhang, Zaoli; Biskupek, Johannes; Kaiser, Ute; Wiedwald, Ulf

    2016-01-01

    Texture formation and epitaxy of thin metal films and oriented growth of nanoparticles (NPs) on single crystal supports are of general interest for improved physical and chemical properties especially of anisotropic materials. In the case of FePt, the main focus lies on its highly anisotropic magnetic behavior and its catalytic activity, both due to the chemically ordered face-centered tetragonal (fct) L10 phase. If the c-axis of the tetragonal system can be aligned normal to the substrate plane, perpendicular magnetic recording could be achieved. Here, we study the orientation of FePt NPs and films on a-SiO2/Si(001), i.e., Si(001) with an amorphous (a-) native oxide layer on top, on MgO(001), and on sapphire(0001) substrates. For the NPs of an approximately equiatomic composition, two different sizes were chosen: "small" NPs with diameters in the range of 2-3 nm and "large" ones in the range of 5-8 nm. The 3 nm thick FePt films, deposited by pulsed laser deposition (PLD), served as reference samples. The structural properties were probed in situ, particularly texture formation and epitaxy of the specimens by reflection high-energy electron diffraction (RHEED) and, in case of 3 nm nanoparticles, additionally by high-resolution transmission electron microscopy (HRTEM) after different annealing steps between 200 and 650 °C. The L10 phase is obtained at annealing temperatures above 550 °C for films and 600 °C for nanoparticles in accordance with previous reports. On the amorphous surface of a-SiO2/Si substrates we find no preferential orientation neither for FePt films nor nanoparticles even after annealing at 630 °C. On sapphire(0001) supports, however, FePt nanoparticles exhibit a clearly preferred (111) orientation even in the as-prepared state, which can be slightly improved by annealing at 600-650 °C. This improvement depends on the size of NPs: Only the smaller NPs approach a fully developed (111) orientation. On top of MgO(001) the effect of annealing on

  14. Porous-Al2O3 thermal barrier coatings with dispersed Pt particles prepared by cathode plasma electrolytic deposition

    Institute of Scientific and Technical Information of China (English)

    Jin Zhang

    2016-01-01

    Porousa-Al2O3 thermal barrier coatings (TBCs) containing dispersed Pt particles were prepared by cathode plasma electrolytic deposition (CPED). The influence of the Pt particles on the microstructure of the coatings and the CPED process were studied. The prepared coatings were mainly composed ofα-Al2O3. The average thickness of the coatings was approximately 100μm. Such single-layer TBCs ex-hibited not only excellent high-temperature cyclic oxidation and spallation resistance, but also good thermal insulation properties. Porousa-Al2O3 TBCs inhibit further oxidation of alloy substrates because of their extremely low oxygen diffusion rate, provide good thermal insu-lation because of their porous structure, and exhibit excellent mechanical properties because of the toughening effect of the Pt particles and because of stress relaxation induced by deformation of the porous structure.

  15. Optimizing coverage of metal oxide nanoparticle prepared by pulsed laser deposition on nonenzymatic glucose detection.

    Science.gov (United States)

    Kaneko, Satoru; Ito, Takeshi; Hirabayashi, Yasuo; Ozawa, Takeshi; Okuda, Tetsuya; Motoizumi, Yu; Hirai, Kiyohito; Naganuma, Yasuhiro; Soga, Masayasu; Yoshimoto, Mamoru; Suzuki, Koji

    2011-04-15

    Metal oxide nanoparticles prepared by pulsed laser deposition (PLD) were applied to nonenzymatic glucose detection. NiO nanoparticles with size of 3 nm were deposited on glassy carbon (GC) and silicon substrates at room temperature in an oxygen atmosphere. Transmission electron microscope (TEM) image showed nanoparticles with the size of 3 nm uniformly scattered on the Si(001) substrate. Unlike co-sputtering nanoparticle and carbon simultaneously, the PLD method can easily control the surface coverage of nanoparticles on the surface of substrate by deposition time. Cyclic voltammetry was performed on the samples deposited on the GC substrates for electrochemical detection of glucose. The differences between peak currents with and without glucose was used to optimize the coverage of nanoparticles on carbon electrode. The results indicated that optimal coverage of nanoparticles on carbon electrode.

  16. STS study of TiO2 film and Pt-deposited TiO2 film in air

    Institute of Scientific and Technical Information of China (English)

    Zhang Min; Jin Zhensheng

    2004-01-01

    Direct investigation of the electronic structure of catalyst surfaces on the near-atomic scale in general has not been impossible in the past. However, with the advent of the scanning tunneling microscope (STM), the opportunity arises for incorporating the scanning tunneling spectroscopy (STS) for correlation in-situ surface electronic structure with topography on a sub-nanometer scale. In this paper, we report the STS results of thin film TiO2 and Pt-deposited TiO2 annealed at 450℃. It was found that the TiO2 semiconductor changes from n-type to p-type after Pt deposition.Fig. 1 shows the surface electronic property (Ⅰ-Ⅴ curve) of thin TiO2 film measured in air by STS. A steep descent of the anodic tunneling current at ca.- 1.0 Ⅴ and a rapid ascent of cathodic tunneling current at ca. +2.0V. The zero bias represents the Fermi level (Ef). Ef is situated at the Ecb side indicating that the thin TiO2 film possesses the same band gap as that of bulk TiO2 phase ( Egs =3.0 to 3.2 eV). For the sample of Pt-deposited TiO2 film, Pt/(Pt+Ti+O) atomic ratio≈0.2, which indicates that the surface of TiO2 film is partly covered by Pt particles, and there are two types of Ⅰ-Ⅴ curves to be detected. One of them (Fig.2a)is attributed to the electronic property of TiO2, which has same Egs as that shown in Fig. 1. However, the Ef is transferred to valence side (△≈1eV). This phenomenon hints that TiO2 is doped by an impurity which can introduce h+ into TiO2 lattice.Such a type of defects may be described by Ti1-xPtxO2(h )2x, here Pt+2 as a substitutional site of Ti+4. Fig.2b is the Ⅰ-Ⅴ curve of a Pt particle situated on a TiO2 particle contained Ti1-xPtxO2(h )2x.

  17. Nanoparticle formation and thin film deposition in aniline containing plasmas

    Science.gov (United States)

    Pattyn, Cedric; Dias, Ana; Hussain, Shahzad; Strunskus, Thomas; Stefanovic, Ilija; Boulmer-Leborgne, Chantal; Lecas, Thomas; Kovacevic, Eva; Berndt, Johannes

    2016-09-01

    This contribution deals with plasma based polymerization processes in mixtures of argon and aniline. The investigations are performed in a capacitively coupled RF discharge (in pulsed and continuous mode) and concern both the observed formation of nanoparticles in the plasma volume and the deposition of films. The latter process was used for the deposition of ultra-thin layers on different kind of nanocarbon materials (nanotubes and free standing graphene). The analysis of the plasma and the plasma chemistry (by means of mass spectroscopy and in-situ FTIR spectroscopy) is accompanied by several ex-situ diagnostics of the obtained materials which include NEXAFS and XPS measurements as well as Raman spectroscopy and electron microscopy. The decisive point of the investigations concern the preservation of the original monomer structure during the plasma polymerization processes and the stability of the thin films on the different substrates.

  18. DETERMINING THE ACUTE TOXIC EFFECTS OF POLY(VINYLFERROCENIUM SUPPORTED PLATINUM NANOPARTICLE (PT/PVF+ NPS ON APIS MELLIFERA

    Directory of Open Access Journals (Sweden)

    Yeşim Dağlıoğlu

    2016-12-01

    Full Text Available The use of engineering nanomaterials on a large scale along with their production, and their potential effects on the environment and on human health as well as their environmental emission have increased these concerns. For this reason, nanoparticles which are released into the environment are necessary determine the toxicity by using indicator organisms. With this study, it was aimed that the acute toxic effects of Polyvinylferrocene (PVF+- supported platinum (Pt nanoparticle (Pt/PVF+ NPs, Poly(vinylferrocenium (PVF+ and K2PtCl4 be evaluted comparatively by using the honey bees (Apis Mellifera. LC50 values for 48 and 96 hours of these substances respectively; 713.290 ve 6.899 mg/l for K2PtCl4; 12458374.000 ve 178.262 mg/l for Pt/PVF+ NPs and 148.153 ve 0.344 mg/l for PVF+. When we look at this value, the toxic effect for all three substance had increased on a serious level, depending on the exposure time.

  19. Pt nanoparticles on graphene – polyelectrolyte nanocomposite: Investigation of H{sub 2}O{sub 2} and methanol electrocatalysis

    Energy Technology Data Exchange (ETDEWEB)

    Bragaru, Adina [National Institute for Research and Development in Microtechnology (IMT-Bucharest), 126A, Erou Iancu Nicolae, 077190 Bucharest (Romania); Vasile, Eugeniu [University Politehnica of Bucharest, Faculty of Applied Chemistry and Material Science, Department of Science and Engineering of Oxidic Materials and Nanomaterials, 011061 Bucharest (Romania); Obreja, Cosmin; Kusko, Mihaela; Danila, Mihai [National Institute for Research and Development in Microtechnology (IMT-Bucharest), 126A, Erou Iancu Nicolae, 077190 Bucharest (Romania); Radoi, Antonio, E-mail: radoiantonio@yahoo.com [National Institute for Research and Development in Microtechnology (IMT-Bucharest), 126A, Erou Iancu Nicolae, 077190 Bucharest (Romania)

    2014-08-01

    Poly (diallyldimethylammonium chloride) (PDDA) functionalized graphene oxide (GO) decorated with Pt nanoparticles (PtNPs) was obtained and investigated. This hybrid nanocomposite material was morphologically characterized by several instrumental techniques like high-resolution transmission electron microscopy (HR-TEM), selected area electron diffraction (SAED) and X-ray diffraction (XRD). Good coverage of crystalline Pt nanoparticles was achieved, the average diameter being 2 nm, meanwhile in the absence of polyelectrolyte the average diameter increased up to 4 nm. The electrocatalytic properties of this hybrid nanocomposite against H{sub 2}O{sub 2} and methanol were ascertained by cyclic voltammetry. A modified glassy carbon electrode (GC) was able to reduce H{sub 2}O{sub 2} at positive potentials (starting from ∼150 mV vs. Ag/AgCl) meanwhile for methanol the ratio of the forward anodic peak current (I{sub f}) to the reverse anodic peak current (I{sub b}) was 1.42, indicating good tolerance of the catalyst towards the intermediate carbonaceous species accumulated on the electrode surface. - Highlights: • Hybrid nanocomposite for H{sub 2}O{sub 2} and methanol electrocatalysis. • A good coverage of PtNPs on graphene polyelectrolyte composite was obtained. • The efficiency for PtNPs-GO-PDDA is similar to commercially available catalysts. • Good tolerance towards carbonaceous species during methanol oxidation.

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

    Directory of Open Access Journals (Sweden)

    Sun H

    2012-07-01

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

  1. Tunable thermodynamic stability of Au-CuPt core-shell trimetallic nanoparticles by controlling the alloy composition: insights from atomistic simulations.

    Science.gov (United States)

    Huang, Rao; Shao, Gui-Fang; Wen, Yu-Hua; Sun, Shi-Gang

    2014-11-07

    A microscopic understanding of the thermal stability of metallic core-shell nanoparticles is of importance for their synthesis and ultimately application in catalysis. In this article, molecular dynamics simulations have been employed to investigate the thermodynamic evolution of Au-CuPt core-shell trimetallic nanoparticles with various Cu/Pt ratios during heating processes. Our results show that the thermodynamic stability of these nanoparticles is remarkably enhanced upon rising Pt compositions in the CuPt shell. The melting of all the nanoparticles initiates at surface and gradually spreads into the core. Due to the lattice mismatch among Au, Cu and Pt, stacking faults have been observed in the shell and their numbers are associated with the Cu/Pt ratios. With the increasing temperature, they have reduced continuously for the Cu-dominated shell while more stacking faults have been produced for the Pt-dominated shell because of the significantly different thermal expansion coefficients of the three metals. Beyond the overall melting, all nanoparticles transform into a trimetallic mixing alloy coated by an Au-dominated surface. This work provides a fundamental perspective on the thermodynamic behaviors of trimetallic, even multimetallic, nanoparticles at the atomistic level, indicating that controlling the alloy composition is an effective strategy to realize tunable thermal stability of metallic nanocatalysts.

  2. Broadband infrared absorption enhancement by electroless-deposited silver nanoparticles

    Science.gov (United States)

    Gritti, Claudia; Raza, Søren; Kadkhodazadeh, Shima; Kardynal, Beata; Malureanu, Radu; Mortensen, N. Asger; Lavrinenko, Andrei V.

    2017-01-01

    Decorating semiconductor surfaces with plasmonic nanoparticles (NPs) is considered a viable solution for enhancing the absorptive properties of photovoltaic and photodetecting devices. We propose to deposit silver NPs on top of a semiconductor wafer by a cheap and fast electroless plating technique. Optical characterization confirms that the random array of electroless-deposited NPs improves absorption by up to 20% in a broadband of near-infrared frequencies from the bandgap edge to 2000 nm. Due to the small filling fraction of particles, the reflection in the visible range is practically unchanged, which points to the possible applications of such deposition method for harvesting photons in nanophotonics and photovoltaics. The broadband absorption is a consequence of the resonant behavior of particles with different shapes and sizes, which strongly localize the incident light at the interface of a high-index semiconductor substrate. Our hypothesis is substantiated by examining the plasmonic response of the electroless-deposited NPs using both electron energy loss spectroscopy and numerical calculations.

  3. Broadband infrared absorption enhancement by electroless-deposited silver nanoparticles

    Directory of Open Access Journals (Sweden)

    Gritti Claudia

    2016-07-01

    Full Text Available Decorating semiconductor surfaces with plasmonic nanoparticles (NPs is considered a viable solution for enhancing the absorptive properties of photovoltaic and photodetecting devices. We propose to deposit silver NPs on top of a semiconductor wafer by a cheap and fast electroless plating technique. Optical characterization confirms that the random array of electroless-deposited NPs improves absorption by up to 20% in a broadband of near-infrared frequencies from the bandgap edge to 2000 nm. Due to the small filling fraction of particles, the reflection in the visible range is practically unchanged, which points to the possible applications of such deposition method for harvesting photons in nanophotonics and photovoltaics. The broadband absorption is a consequence of the resonant behavior of particles with different shapes and sizes, which strongly localize the incident light at the interface of a high-index semiconductor substrate. Our hypothesis is substantiated by examining the plasmonic response of the electroless-deposited NPs using both electron energy loss spectroscopy and numerical calculations.

  4. The effect of nanoparticles size on photocatalytic and antimicrobial properties of Ag-Pt/TiO{sub 2} photocatalysts

    Energy Technology Data Exchange (ETDEWEB)

    Zielińska-Jurek, Anna, E-mail: annjurek@pg.gda.pl [Department of Chemical Technology, Faculty of Chemistry, Gdansk University of Technology, 80-233 Gdansk (Poland); Wei, Zhishun [Catalysis Research Center, Hokkaido University, N21, W10, 001-0021, Sapporo (Japan); Wysocka, Izabela [Department of Chemical Technology, Faculty of Chemistry, Gdansk University of Technology, 80-233 Gdansk (Poland); Szweda, Piotr [Department of Pharmaceutical Technology and Biochemistry, Faculty of Chemistry, Gdansk University of Technology, 80-233 Gdansk (Poland); Kowalska, Ewa [Catalysis Research Center, Hokkaido University, N21, W10, 001-0021, Sapporo (Japan)

    2015-10-30

    Graphical abstract: - Highlights: • Enhanced photocatalytic activity under visible light for bimetallic Ag-Pt/TiO{sub 2} was observed. • Phenol was removed efficiently after 60 min irradiation under Vis. • Most active sample contains fine Pt (1–3 nm) on TiO{sub 2}. • Ag/TiO{sub 2}, Ag-Pt/TiO{sub 2} revealed antimicrobial activity. - Abstract: Ag-Pt-modified TiO{sub 2} nanocomposites were synthesized using the sol–gel method. Bimetallic modified TiO{sub 2} nanoparticles exhibited improved photocatalytic activity under visible-light irradiation, better than monometallic Ag/TiO{sub 2} and Pt/TiO{sub 2} nanoparticles (NPs). All modified powders showed localized surface plasmon resonance (LSPR) in visible region. The photocatalysts’ characteristics by X-ray diffractometry (XRD), scanning transmission electron microscopy (STEM), diffuse reflectance spectroscopy (DRS), X-ray photoelectron spectroscopy (XPS), nitrogen adsorption (BET method for specific surface area) showed that sample with the highest photocatalytic activity had anatase structure, about 93 m{sup 2}/g specific surface area, maximum plasmon absorption at ca. 420 nm and contained small NPs of silver of 6 nm and very fine platinum NPs of 3 nm. The photocatalytic activity was estimated by measuring the decomposition rate of phenol in 0.2 mM aqueous solution under Vis and UV/vis light irradiation. It was found that size of platinum was decisive for the photocatalytic activity under visible light irradiation, i.e., the smaller Pt NPs were, the higher was photocatalytic activity. While, antimicrobial activities, estimated for bacteria Escherichia coli and Staphylococcus aureus, and pathogenic fungi belonging to Candida family, were only observed for photocatalysts containing silver, i.e., Ag/TiO{sub 2} and Ag-Pt/TiO{sub 2} nanocomposites.

  5. Incorporation of precious metal nanoparticles into various aerogels by different supercritical deposition methods

    Science.gov (United States)

    Saquing, Carl D.

    2005-11-01

    One major hurdle in nanoparticle fabrication is the difficulty in controlling size, distribution and concentration. Conventional methods in nanoparticle formation require high temperatures which lead to particle agglomeration and size broadening, or involve substantial amount of organic solvents. A clean route to supported-nanoparticles fabrication was investigated using various supercritical (SC) based deposition methods. The SC deposition involves the organometallic precursor (OP) (dimethyl(1,5-cyclooctadiene)platinum(II)[CODPtMe 2] or bis(2,2,6,6-tetramethyl-3,5-heptanedionato) (1,5-cyclooctadiene) ruthenium(II)) dissolution in SC fluid and contacting this solution with a substrate. The OP is adsorbed and subsequent reduction of the OP-impregnated substrate produces metal/substrate composites. The various methods were: (1) thermal reduction at atmospheric pressure in an inert atmosphere; (2) thermal reduction in SC carbon dioxide (scCO2); (3) chemical reduction in scCO2 with H2; and (4) chemical reduction at atmospheric pressure with H2. The synthesis of resorcinol-formaldehyde aerogels (RFAs) and carbon aerogels (CAs) was also studied and used as substrates (along with commercial silica aerogels (SAs)) in the SC deposition. The surface area, pore properties, and density of these aerogels were evaluated and the effects of reactant concentration, pyrolysis and SC deposition on these properties were determined. Using a static method, the adsorption isotherms of CODPtMe2 in scCO2 on two CAs with different pore sizes were measured at 28 MPa and 80°C to determine the maximum metal loading and the effect of pore properties on adsorption and to examine the interactions between the three components. The isotherms could be represented by the Langmuir model and the adsorption data indicated a strong CODPtMe2-CA interaction and that almost all the preexistent micropore area was covered with CODPtMe 2 molecules even at adsorption lower than the maximum capacity. The

  6. Study of underpotential deposited Cu layers on Pt(111) and their stability against CO and CO2 in perchloric acid

    DEFF Research Database (Denmark)

    Schlaup, Christian Georg; Horch, Sebastian

    2013-01-01

    The underpotential deposition (UPD) of copper on a Pt(111) electrode and the influence of gas coadsorbates, i.e. CO and CO2, on the thus deposited copper layer were studied in a 0.1 M HClO4 electrolyte by means of EC-STM. By UPD, an atomically flat Cu layer is formed, which exhibits a pseudomorphic...... (1 × 1) structure. However, it contains several point defects due to which its total coverage is less than a monolayer, in agreement with the measured charge density in the CV curves. Upon exposure to a CO-saturated solution the pseudomorphic structure collapses to a coalescent structure with many...... vacancy islands. This phase transition is induced by the preferential binding of CO to the Pt(111) surface. In contrast, CO2, which binds stronger to copper, does not affect the pseudomorphic structure of the Cu layer....

  7. 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)

  8. Hexagonal-to-cubic phase transformation in composite thin films induced by FePt nanoparticles located at PS/PEO interfaces.

    Science.gov (United States)

    Aissou, Karim; Fleury, Guillaume; Pecastaings, Gilles; Alnasser, Thomas; Mornet, Stéphane; Goglio, Graziella; Hadziioannou, Georges

    2011-12-06

    The organization process of asymmetric poly(styrene-block-ethylene oxide) (PS-b-PEO) copolymer thin films blended with FePt nanoparticles is studied. In a first step, it is shown that FePt nanoparticles stabilized by oleic acid ligands are distributed within the PS matrix phase, whereas the same particles partially covered with short dopamine-terminated-methoxy poly(ethylene oxide) (mPEO-Dopa) are located at PS/PEO interfaces. The swelling of PS domains, induced by FePt_oleic acid nanoparticles during the solvent annealing process, results in formation of a disordered microstructure in comparison to the well-organized hexagonally close-packed (HCP) cylinder phase formed in the neat PS-b-PEO copolymer. The evolution of the microstructure of PS-b-PEO/FePt_mPEO-Dopa composite has been investigated for different solvent annealing treatments. Under high-humidity conditions during the vapor annealing process, the addition of FePt nanoparticles results in formation of spheres in the film split into terraces. The upper and lower terraces are occupied by spheres organized in an unusual square and HCP phases, respectively. Under low-humidity conditions, undulated PEO cylinders oriented parallel to substrate are formed in the presence of FePt nanoparticles. In this case, we observe that most of the nanoparticles accumulate within the core of topological defects, which induces a low nanoparticle concentration at the PS/PEO interfaces and so stabilizes an intermediate undulated cylinder phase.

  9. Recording-media-related morphology and magnetic properties of crystalline CoPt{sub 3} and CoPt{sub 3}-Au core-shell nanoparticles synthesized via reverse microemulsion

    Energy Technology Data Exchange (ETDEWEB)

    Bahmanrokh, Ghazaleh, E-mail: ghazalehbahmanrokh@yahoo.com; Hashim, Mansor; Matori, Khamirul Amin; Kanagesan, Samikannu; Sabbaghizadeh, Rahim; Ezzad Shafie, Mohd Shamsul [Materials Synthesis and Characterization Laboratory, Institute of Advanced Technology, Universiti Putra Malaysia, 43400 UPM Serdang, Selangor (Malaysia); Navasery, Manizheh; Soltani, Nayereh [Department of Physics, Faculty of Science, Universiti Putra Malaysia, 43400 UPM, Serdang, Selangor (Malaysia); Vaziri, Parisa [Department of Medical Physics and Biomedical Engineering, Shahid Beheshti University of Medical Sciences, Tehran (Iran, Islamic Republic of)

    2014-09-07

    A comparative experimental study of the magnetic properties of CoPt{sub 3} and CoPt{sub 3}/Au nanoparticles as well as a detailed study of the structural properties of the samples by X-ray diffraction, Transmission electron microscopy, and vibrating sample magnetometer is presented in this work. In addition, the effect of particle size on the structure and magnetic properties of nanoparticles prepared by microemulsion is studied. The correlation between particle size, crystallinity, and magnetization was studied as well. CoPt nanoparticles have been studied intensively over the last decade because of their increased magnetic anisotropy in the ordered phase that can be interesting for high density magnetic recording. A significant high coercivity for as-prepared CoPt{sub 3} and CoPt{sub 3}-Au nanoparticles was obtained at room temperature and enhanced after annealing. The focused aim of our study is to obtain high coercivity at room temperature that follows the Curie-Weiss law. This indicates an interacting system in which the nanoparticles behave like single domain ferromagnetic materials in the particle size range of 8 to 35 nm. In addition, the interaction increases by cooling the samples to low temperature around 15 K. Temperature dependence 1/M graph was obtained to investigate the behavior of nanoparticles at low temperature and shows the best fit with Curie-Weis mode.

  10. Electrochemical promotion of propane oxidation on Pt deposited on a dense β"-Al2O3 ceramic Ag+ conductor

    Directory of Open Access Journals (Sweden)

    Michail eTsampas

    2013-08-01

    Full Text Available A new kind of electrochemical catalyst based on a Pt porous catalyst film deposited on a β"-Al2O3 ceramic Ag+ conductor was developed and evaluated during propane oxidation. It was observed that upon anodic polarization, the rate of propane combustion was significantly electropromoted up to 400%. Moreover, for the first time, exponential increase of the catalytic rate was evidenced during galvanostatic transient experiment in excellent agreement with EPOC equation.

  11. Electrochemical promotion of propane oxidation on Pt deposited on a dense β"-Al2O3 ceramic Ag+ conductor

    Science.gov (United States)

    Tsampas, Michail; Kambolis, Anastasios; Obeid, Emil; Lizarraga, Leonardo; Sapountzi, Foteini; Vernoux, Philippe

    2013-08-01

    A new kind of electrochemical catalyst based on a Pt porous catalyst film deposited on a β"-Al2O3 ceramic Ag+ conductor was developed and evaluated during propane oxidation. It was observed that upon anodic polarization, the rate of propane combustion was significantly electropromoted up to 400%. Moreover, for the first time, exponential increase of the catalytic rate was evidenced during galvanostatic transient experiment in excellent agreement with EPOC equation.

  12. An opening route to the design of cathode materials for fuel cells based on PtCo nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Hernandez-Fernandez, Patricia [Departamento de Quimica-Fisica Aplicada, Electroquimica, Universidad Autonoma de Madrid, Campus Cantoblanco (Spain); Rojas, Sergio; De la Fuente, Jose Luis Gomez; Terreros, Pilar; Pena, Miguel Antonio; Garcia-Fierro, Jose Luis [Instituto de Catalisis y Petroleoquimica C.S.I.C., C/Marie Curie 2, 28049 Madrid (Spain); Ocon, Pilar [Departamento de Quimica-Fisica Aplicada, Electroquimica, Universidad Autonoma de Madrid, Campus Cantoblanco (Spain)

    2007-11-30

    The performance of PtCo/C electrocatalysts in the oxygen reduction reaction is enhanced after thermal treatment in hydrogen. In fact, the intrinsic activity (per gram of Pt) of PtCo/C electrocatalyst after the adequate treatment is far superior to that of the commercial sample. The PtCo nanoparticles were prepared from the water-in-oil microemulsion technique. The total metal loading of the catalyst was 30 wt%, and two reduction temperatures, 300 and 875 C, were studied. Electrochemical measurements were carried out using the rotating disk electrode method in 0.5 M H{sub 2}SO{sub 4} at room temperature, while the Pt real surface area was determined by CO stripping voltammetry. Analyses from XPS and TPR revealed that the amount of Co and Pt reduced species as well as the particle size (XRD), increased with the thermal treatment. Results derived from the electrochemical analyses were in agreement with those obtained in a H{sub 2}/O{sub 2} single cell. These results demonstrate the important role of the cobalt as well as the reduction temperature and atmosphere, and open new ways for the design of improved bimetallic catalyst. (author)

  13. Proton conductive Pt-Co nanoparticles anchoring on citric acid functionalized graphene for efficient oxygen reduction reaction

    Science.gov (United States)

    Zhao, Yige; Liu, Jingjun; Wu, Yijun; Wang, Feng

    2017-08-01

    Designing highly efficient electro-catalysts for the oxygen reduction reaction (ORR) has been regarded as a demanding task in the development of renewable energy sources. However, little attention has been paid on improving Pt-based catalysts by promoting proton transfer from the electrolyte solutions to the catalyst layer at the cathode. Herein, we design proton conductive Pt-Co alloy nanoparticles anchoring on citric acid functionalized graphene (Pt-Co/CA-G) catalysts for efficient ORR. The facile modification approach for graphene can introduce oxygenated functional groups on the graphene surface to promote proton transfer as well as keeping the high electron conductivity without destroying the graphene original structure. The electrochemical results show that the Pt-Co/CA-G catalyst exhibits more excellent ORR activity and stability than the commercial Pt/C catalyst, which can be attributed to its improved proton transfer ability. The fast proton transfer comes from the hydrogen-bonding networks formed by the interaction between the oxygenated functional groups and water molecules. This work provides not only a novel and simple approach to modify graphene but also an effective strategy to improve Pt-based catalysts for the ORR.

  14. An investigation of the internal temperature dependence of Pd-Pt cluster beam deposition: A molecular dynamics study

    Science.gov (United States)

    Chen, Cha'o.-Kuang; Chang, Shing-Cheng

    2010-02-01

    We investigated the internal temperature dependence of the Pd 1- aPt a cluster beam deposition in the present study via the molecular dynamics simulations of soft-landing. By analysis of the velocity distribution and diffusion coefficient of the bimetallic cluster, Pd atoms with better mobility improved the diffusibility of Pt atoms. The radial composition distribution showed that a Pt-core/Pd-shell structure of the cluster formed at high internal temperatures through migrations of the Pd atoms from inner to surface shells. In the soft-landing process, the diffusing and epitaxial behaviors of the deposited clusters mainly depended on the internal temperature because the incident energy of the cluster was very small. By depositing clusters at high internal temperatures, we obtained a thin film of good epitaxial growth as the energetic cluster impact. Furthermore, nonepitaxial configurations such as scattered nonepitaxial atoms, misoriented particles, and grain boundaries of (1 1 1) planes were produced in the growth of the cluster-assembled film. As the size of the incident cluster increased, the internal temperature of the cluster needed for better interfacial diffusion and contact epitaxy on the substrate also rose.

  15. Platinum-group minerals from the Jinbaoshan Pd-Pt deposit, SW China: evidence for magmatic origin and hydrothermal alteration

    Science.gov (United States)

    Wang, Christina Yan; Prichard, Hazel M.; Zhou, Mei-Fu; Fisher, Peter C.

    2008-09-01

    The Jinbaoshan Pt-Pd deposit in Yunnan, SW China, is hosted in a wehrlite body, which is a member of the Permian (˜260 Ma) Emeishan Large Igneous Province (ELIP). The deposit is reported to contain one million tonnes of Pt-Pd ore grading 0.21% Ni and 0.16% Cu with 3.0 g/t (Pd + Pt). Platinum-group minerals (PGM) mostly are ˜10 μm in diameter, and are commonly Te-, Sn- and As-bearing, including moncheite (PtTe2), atokite (Pd3Sn), kotulskite (PdTe), sperrylite (PtAs2), irarsite (IrAsS), cooperite (PtS), sudburyite (PdSb), and Pt-Fe alloy. Primary rock-forming minerals are olivine and clinopyroxene, with clinopyroxene forming anhedral poikilitic crystals surrounding olivine. Primary chromite occurs either as euhedral grains enclosed within olivine or as an interstitial phase to the olivine. However, the intrusion has undergone extensive hydrothermal alteration. Most olivine grains have been altered to serpentine, and interstitial clinopyroxene is often altered to actinolite/tremolite and locally biotite. Interstitial chromite grains are either partially or totally replaced by secondary magnetite. Base-metal sulfides (BMS), such as pentlandite and chalcopyrite, are usually interstitial to the altered olivine. PGM are located with the BMS and are therefore also interstitial to the serpentinized olivine grains, occurring within altered interstitial clinopyroxene and chromite, or along the edges of these minerals, which predominantly altered to actinolite/tremolite, serpentine and magnetite. Hydrothermal fluids were responsible for the release of the platinum-group elements (PGE) from the BMS to precipitate the PGM at low temperature during pervasive alteration. A sequence of alteration of the PGM has been recognized. Initially moncheite and atokite have been corroded and recrystallized during the formation of actinolite/tremolite, and then, cooperite and moncheite were altered to Pt-Fe alloy where they are in contact with serpentine. Sudburyite occurs in veins

  16. Dynamics of electrocatalytic oxidation of ethylene glycol, methanol and formic acid at MWCNT platform electrochemically modified with Pt/Ru nanoparticles

    CSIR Research Space (South Africa)

    Maxakato, NW

    2010-03-01

    Full Text Available Comparative electrocatalytic behavior of functionalized multiwalled carbon nanotubes (fMWCNTs) electrodecorated with Pt/Ru nanoparticles towards the oxidation of methanol (MeOH), ethylene glycol (EG) and formic acid (FA) has been investigated...

  17. Electron postgrowth irradiation of platinum-containing nanostructures grown by electron-beam-induced deposition from Pt(PF3)4

    NARCIS (Netherlands)

    Botman, A.; Hagen, C.W.; Li, J.; Thiel, B.L.; Dunn, K.A.; Mulders, J.J.L.; Randolph, S.; Toth, M.

    2009-01-01

    The material grown in a scanning electron microscope by electron beam-induced deposition (EBID) using Pt(PF3)4 precursor is shown to be electron beam sensitive. The effects of deposition time and postgrowth electron irradiation on the microstructure and resistivity of the deposits were assessed by t

  18. Plasmonic nanoparticle films for solar cell applications fabricated by size-selective aerosol deposition

    NARCIS (Netherlands)

    Pfeiffer, T.V.; Ortiz Gonzalez, J.; Santbergen, R.; Tan, H.; Schmidt-Ott, A.; Zeman, M.; Smets, A.H.M.

    2014-01-01

    A soft deposition method for incorporating surface plasmon resonant metal nanoparticles within photovoltaic devices was studied. This self-assembly method provides excellent control over both nanoparticle size and surface coverage. Films of spherical Ag nanoparticles with diameter of ∼100 nm were fa

  19. Highly porous ZnS microspheres for superior photoactivity after Au and Pt deposition and thermal treatment

    Energy Technology Data Exchange (ETDEWEB)

    Singla, Shilpa; Pal, Bonamali, E-mail: bpal@thapar.edu

    2013-11-15

    Graphical abstract: Highly porous ZnS microsphere of size 2–5 μm having large surface area ca. 173.14 m{sup 2} g{sup −1} exhibits superior photocatalytic activity for the oxidation of 4-nitrophenol under UV light irradiation. The rate of photooxidation has been significantly improved by Au and Pt deposition and after sintering, respectively, due to rapid electron acceptance by metal from photoexcited ZnS and growth of crystalline ZnS phase. - Highlights: • Photoactive ZnS microsphere of size 2–5 μm was prepared by hydrothermal route. • Highly porous cubic spherical ZnS crystals possess a large surface area, 173 m{sup 2} g{sup −1}. • 1 wt% Au and Pt photodeposition highly quenched the photoluminescence at 437 nm. • Sintering and metal loading notably improve the photooxidation rate of 4-nitrophenol. • Pt co-catalyst always exhibits superior photoactivity of ZnS microsphere than Au. - Abstract: This work highlights the enhanced photocatalytic activity of porous ZnS microspheres after Au and Pt deposition and heat treatment at 500 °C for 2 h. Microporous ZnS particles of size 2–5 μm with large surface area 173.14 m{sup 2} g{sup −1} and pore volume 0.0212 cm{sup 3} g{sup −1} were prepared by refluxing under an alkaline medium. Photoluminescence of ZnS at 437 nm attributed to sulfur or zinc vacancies were quenched to 30% and 49%, respectively, after 1 wt% Au and Pt loading. SEM images revealed that each ZnS microparticle consist of several smaller ZnS spheres of size 2.13 nm as calculated by Scherrer's equation. The rate of photooxidation of 4-nitrophenol (10 μM) under UV (125 W Hg arc–10.4 mW/cm{sup 2}) irradiation has been significantly improved by Au and Pt deposition followed by sintering due to better electron capturing capacity of deposited metals and growth of crystalline ZnS phase with less surface defects.

  20. Effect of substrate bias on deposition behaviour of charged silicon nanoparticles in ICP-CVD process

    Science.gov (United States)

    Yoo, Seung-Wan; You, Shin-Jae; Kim, Jung-Hyung; Seong, Dae-Jin; Seo, Byong-Hoon; Hwang, Nong-Moon

    2017-01-01

    The effect of a substrate bias on the deposition behaviour of crystalline silicon films during inductively coupled plasma chemical vapour deposition (ICP-CVD) was analysed by consideration of non-classical crystallization, in which the building block is a nanoparticle rather than an individual atom or molecule. The coexistence of positively and negatively charged nanoparticles in the plasma and their role in Si film deposition are confirmed by applying bias voltages to the substrate, which is sufficiently small as not to affect the plasma potential. The sizes of positively and negatively charged nanoparticles captured on a carbon membrane and imaged using TEM are, respectively, 2.7-5.5 nm and 6-13 nm. The film deposited by positively charged nanoparticles has a typical columnar structure. In contrast, the film deposited by negatively charged nanoparticles has a structure like a powdery compact with the deposition rate about three times higher than that for positively charged nanoparticles. All the films exhibit crystallinity even though the substrate is at room temperature, which is attributed to the deposition of crystalline nanoparticles formed in the plasma. The film deposited by negatively charged nanoparticles has the highest crystalline fraction of 0.84.

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2010-12-30

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

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

    KAUST Repository

    Song, Hyon Min

    2012-09-27

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

  3. National implementation of the UNECE convention on long-range transboundary air pollution (effects). Pt. 1. Deposition loads: methods, modelling and mapping results, trends

    Energy Technology Data Exchange (ETDEWEB)

    Gauger, Thomas [Federal Agricultural Research Centre, Braunschweig (DE). Inst. of Agroecology (FAL-AOE); Stuttgart Univ. (Germany). Inst. of Navigation; Haenel, Hans-Dieter; Roesemann, Claus [Federal Agricultural Research Centre, Braunschweig (DE). Inst. of Agroecology (FAL-AOE)] (and others)

    2008-09-15

    The report on the implementation of the UNECE convention on long-range transboundary air pollution Pt.1, deposition loads (methods, modeling and mapping results, trends) includes the following chapters: Introduction, deposition on air pollutants used for the input for critical loads in exceeding calculations, methods applied for mapping total deposition loads, mapping wet deposition, wet deposition mapping results, mapping dry deposition, dry deposition mapping results, cloud and fog mapping results, total deposition mapping results, modeling the air concentration of acidifying components and heavy metals, agricultural emissions of acidifying and eutrophying species.

  4. Formic acid electro-oxidation on carbon supported Pd{sub x}Pt{sub 1-x} (0 {>=} x {>=} 1) nanoparticles synthesized via modified polyol method

    Energy Technology Data Exchange (ETDEWEB)

    Baranova, Elena A., E-mail: elena.baranova@uottawa.c [Department of Chemical and Biological Engineering, University of Ottawa, 161 Louis-Pasteur St., Ottawa, ON, K1N 6N5 (Canada); Miles, Neil [Department of Chemical and Biological Engineering, University of Ottawa, 161 Louis-Pasteur St., Ottawa, ON, K1N 6N5 (Canada); Mercier, Patrick H.J.; Le Page, Yvon; Patarachao, Bussaraporn [Institute for Chemical Process and Environmental Technology, National Research Council Canada, 1200 Montreal Rd., Ottawa, ON, K1A 0R6 (Canada)

    2010-11-30

    Carbon supported nanoparticle catalysts of Pd{sub x}Pt{sub 1-x} (0 {>=} x {>=} 1) were synthesized using a modified polyol method and poly(N-vinyl-2-pyrrolidone) (PVP) as a stabilizer. Resulting nanoparticles were characterized by X-ray photoelectron spectroscopy (XPS), cyclic voltammetry (CV) and chronoamperommetry (CA) study for formic acid electro-oxidation. Surface composition of the synthesized nanoparticles found from XPS revealed the Pt surface segregation even for the Pd-rich compositions. It is suggested that the surface segregation behavior in PdPt nanoparticles supported on carbon may be influenced, in addition to the difference in Pd and Pt surface energies, by particle size and particle interaction with the support. According to CA, the carbon supported Pd nanoparticles show the highest initial activity towards formic acid electro-oxidation at the potential of 0.3 V (RHE), due to the promotion of the direct dehydrogenation mechanism. However its stability is quite poor resulting in the fast deactivation of the Pd surface. Addition of Pt considerably improves the steady-state activity of Pd in 12 h CA experiment. CA measurements show that the most active catalyst is Pd{sub 0.5}Pt{sub 0.5} of 4 nm size, which displays narrow size distribution and Pd to Pt surface atomic ratio of 27-73.

  5. Au-Pt alloy nanoparticles obtained by nanosecond laser irradiation of gold and platinum bulk targets in an ethylene glycol solution

    Science.gov (United States)

    Moniri, Samira; Reza Hantehzadeh, Mohammad; Ghoranneviss, Mahmood; Asadi Asadabad, Mohsen

    2017-07-01

    Au-Pt alloy nanoparticles (NPs) of different compositions ( Au0Pt100 , Au30Pt70 , Au50Pt50 , Au70Pt30 , and Au100Pt0 were obtained using the nanosecond laser ablation of gold and platinum bulk targets in ethylene glycol, followed by mixing highly monodisperse Au and Pt nanocolloids, for the first time. UV-vis absorption spectra of NPs showed that by increasing the Au content in the Au-Pt NPs, the surface plasmon resonance (SPR) peak red-shifted, from 260 to 573nm in a nonlinear way. In addition, the mean crystalline size, crystal structure, d-spacing, and lattice parameters of NPs were estimated from the XRD spectra. Microscopy studies revealed the most NPs have a spherical or near-spherical shape, and the average sizes of Au0Pt100 , Au30Pt70 , Au50Pt50 , Au70Pt30 , and Au100Pt0 NPs were calculated to be 12.50, 14.15, 18.53, 19.29, and 26.38nm, respectively. Also, the chemical identity of the molecules adhering to the NPs surface was considered by Raman and FT-IR spectroscopy techniques. Among different synthesis methods, the demonstrated technique allows easy synthesis of alloy NPs in aqueous media at room temperature with no formation of by-products.

  6. Asymmetric silica encapsulation toward colloidal Janus nanoparticles: a concave nanoreactor for template-synthesis of an electocatalytic hollow Pt nanodendrite

    Science.gov (United States)

    Koo, Jung Hun; Kim, Daun; Kim, Jin Goo; Jeong, Hwakyeung; Kim, Jongwon; Lee, In Su

    2016-07-01

    A novel reverse microemulsion strategy was developed to asymmetrically encapsulate metal-oxide nanoparticles in silica by exploiting the self-catalytic growth of aminosilane-containing silica at a single surface site. This strategy produced various colloidal Janus nanoparticles, including Au/Fe3O4@asy-SiO2, which were converted to an Au-containing silica nanosphere, Au@con-SiO2, by reductive Fe3O4 dissolution. The use of Au@con-SiO2 as a metal-growing nanoreactor allowed the templated synthesis of various noble-metal nanocrystals, including a hollow dendritic Pt nanoshell which exhibits significantly better electrocatalytic activities for the oxygen reduction reaction than commercial Pt/C catalysts.A novel reverse microemulsion strategy was developed to asymmetrically encapsulate metal-oxide nanoparticles in silica by exploiting the self-catalytic growth of aminosilane-containing silica at a single surface site. This strategy produced various colloidal Janus nanoparticles, including Au/Fe3O4@asy-SiO2, which were converted to an Au-containing silica nanosphere, Au@con-SiO2, by reductive Fe3O4 dissolution. The use of Au@con-SiO2 as a metal-growing nanoreactor allowed the templated synthesis of various noble-metal nanocrystals, including a hollow dendritic Pt nanoshell which exhibits significantly better electrocatalytic activities for the oxygen reduction reaction than commercial Pt/C catalysts. Electronic supplementary information (ESI) available. See DOI: 10.1039/c6nr03557d

  7. Structure, growth and magnetic property of hard magnetic CoPtP nanowires synthesized by electrochemical deposition

    Energy Technology Data Exchange (ETDEWEB)

    Ramulu, T.S.; Venu, R.; Anandakumar, S.; Rani, V. Sudha [Department of Materials Science and Engineering, Chungnam National University, Daejeon 305-764 (Korea, Republic of); Yoon, S.S. [Department of Physics, Andong National University, Andong 760-749 (Korea, Republic of); Kim, C.G., E-mail: cgkim@cnu.ac.kr [Department of Materials Science and Engineering, Chungnam National University, Daejeon 305-764 (Korea, Republic of)

    2012-06-30

    This paper reports the electrochemical synthesis and characterization of one dimensional hard magnetic CoPtP nanowires. Three electrode potentiostatic electrochemical technique was used to deposit nanowires into a nanoporous track-etched polycarbonate membrane with a nominal pore diameter 50 nm and thickness around 6-9 {mu}m. The room temperature electrolyte used for the deposition of nanowires consists of 60 g/lt CoSO{sub 4}7H{sub 2}O, 4.1 g/lt H{sub 2}PtCl{sub 6}, 4.5 g/lt NaHPO{sub 2} and 25 g/lt B(OH){sub 3}. The structural morphology was observed by scanning electron microscope and transmission electron microscope. The magnetic property of the nanowires was measured by vibrating sample magnetometer before removing the template. The coercive fields were measured to be 143 kA m{sup -1} and 103 kA m{sup -1} for parallel (H{sub Parallel-To }) and perpendicular to the nanowire axis, respectively. The higher coercivity value for H{sub Parallel-To} indicating nanowires' easy magnetization direction lies along the nanowires' axis. The average composition of the CoPtP nanowires was determined by electron dispersive spectroscopy and the crystallinity was measured by X-ray diffractometer. - Highlights: Black-Right-Pointing-Pointer CoPtP hard magnetic nanowires are synthesized by electrochemical deposition. Black-Right-Pointing-Pointer The synthesized magnetic nanowires are an average of 6 {mu}m in length. Black-Right-Pointing-Pointer Coercivity of nanowires is 143 kA m{sup -1} when the field is parallel to nanowire axis. Black-Right-Pointing-Pointer The magnetization direction of the nanowires lies along the nanowire's axis.

  8. Microstructure and magnetic properties of FePt/MgO multilayers deposited by RF magnetron sputtering

    Institute of Scientific and Technical Information of China (English)

    Xiaoli Li; Fang Wang; Fengxian Jiang; Xiaohong Xu; Haishun Wu

    2008-01-01

    FePt (50 rim) and [FePt(a nm)/MgO(b nm)]5/glass (a=1, 2, 3; b=1, 2, 3)films Were prepared by radio frequency (RF) magnetron sputtering technique, and then were annealed at 600℃ for 30 min. The effect of MgO layer thickness on the structures and magnetic properties of the FePt/MgO multilayers was investigated. The coercivities and inter-grain interactions of the FePt/MgO films were decreased, yet the degree of (001) texturing drastically increased with the increase in MgO layer thickness when the FePt layer thickness was fixed. Thus, the FePt/MgO films with appropriate coercivities, high perpendicular anisotropy, and weak inter- grain interactions were obtained by controlling the MgO layer thickness. Overall, these results indicate that the FePt/MgO nanos- tructured films are promising candidates for future high-density perpendicular recording media. C 2008 University of Science and Technology Beijing. All fights reserved.

  9. Conformal nanocoating of zirconia nanoparticles by atomic layer deposition in a fluidized bed reactor.

    Science.gov (United States)

    Hakim, Luis F; George, Steven M; Weimer, Alan W

    2005-07-01

    Primary zirconia nanoparticles were conformally coated with alumina ultrathin films using atomic layer deposition (ALD) in a fluidized bed reactor. Alternating doses of trimethylaluminium and water vapour were performed to deposit Al(2)O(3) nanolayers on the surface of 26 nm zirconia nanoparticles. Transmission Fourier transform infrared spectroscopy was performed ex situ. Bulk Al(2)O(3) vibrational modes were observed for coated particles after 50 and 70 cycles. Coated nanoparticles were also examined with transmission electron microscopy, high-resolution field emission scanning electron microscopy and energy dispersive spectroscopy. Analysis revealed highly conformal and uniform alumina nanofilms throughout the surface of zirconia nanoparticles. The particle size distribution and surface area of the nanoparticles are not affected by the coating process. Primary nanoparticles are coated individually despite their high aggregation tendency during fluidization. The dynamic aggregation behaviour of zirconia nanoparticles in the fluidized bed plays a key role in the individual coating of nanoparticles.

  10. Electroless Deposited Gold Nanoparticles on Glass Plates as Sensors for Measuring the Dielectric Constant of Solutions

    OpenAIRE

    Kobayashi, Y.; Ishii, Y.

    2013-01-01

    This work describes a method for the deposition of Au nanoparticles on glass plates (Au-glass). An electroless metal plating technique was extended to the Au nanoparticle deposition. The technique consisted of three steps that took place on the glass plate: (1) adsorption of Sn2+ ions, (2) deposition of metallic Ag nuclei generated by reducing Ag+ ions with Sn2+ ions on the Sn-adsorbed sites, and (3) deposition of Au nanoparticles by reducing Au+ ions on the Ag surface. TEM observation reveal...

  11. Facile and Rapid Synthesis of Ultrafine PtPd Bimetallic Nanoparticles and Their High Performance toward Methanol Electrooxidation

    Directory of Open Access Journals (Sweden)

    Tiantian Xia

    2014-01-01

    Full Text Available Uniform and sub-10 nm size bimetallic PtPd nanoparticles (NPs have been synthesized via a simple and facile method without using any surfactants at an ambient temperature. As a green and clean reductive agent, ascorbic acid (AA was employed for the coreduction of K2PtCl4 and K2PdCl4 in aqueous solution. The morphology, composition, and structure of PtPd NPs had been characterized by transmission electron microscopy (TEM, field emission high resolution transmission electron microscopy (FE-HRTEM, energy dispersive spectroscopy (EDS, X-ray diffraction (XRD, and X-ray photoelectron spectroscope (XPS. Comparing with both the monometallic Pt and Pd, the as-prepared alloy nanoparticles show superior electrocatalytic activity and better tolerance against poisoning by intermediates generated during methanol electrooxidation, which makes them a promising electrocatalysts for direct methanol fuel cells (DMFCs. Meanwhile, the green and simple approach could be easily extended to the manufacture of bimetallic or trimetallic alloy nanomaterials.

  12. Direct synthesis of L1{sub 0} FePt nanoparticles within carbon nanotubes by wet chemical procedure

    Energy Technology Data Exchange (ETDEWEB)

    Capobianchi, A; Laureti, S; Fiorani, D [Consiglio Nazionale delle Ricerche (CNR), Istituto di Struttura della Materia (ISM), Rome (Italy); Foglia, S [Consiglio Nazionale delle Ricerche (CNR), Istituto di Fotonica e Nanotecnologie, Rome (Italy); Palange, E, E-mail: aldo.capobianchi@ism.cnr.i [Universita degli Studi dell' Aquila, Dipartimento di Ingegneria Elettrica e dell' Informazione, L' Aquila (Italy)

    2010-12-01

    This paper reports on the low temperature synthesis of L1{sub 0} iron-platinum (FePt) particles within multiwall carbon nanotubes using a novel wet chemical method that allows the filling of the nanotube cavity keeping clean its external wall. In the proposed procedure, nanotubes are filled with a precursor salt of hexaaquairon(II) hexachloroplatinate, ([Fe(H{sub 2}O){sub 6}][PtCl{sub 6}]) and nanoparticles of the magnetically hard phase are directly obtained by heating at 400 {sup 0}C in a reductive atmosphere. The advantage of such a precursor, allowing one to obtain at low temperature the L1{sub 0} phase without passing through the soft fcc phase, is due to its structure, where the Fe and Pt atoms are arranged in alternating planes, as in the fct FePt structure. Morphological, structural and magnetic properties of the filled nanotubes have been investigated by transmission electron microscopy, x-ray diffraction and magnetization measurements. The results show the coexistence of nanoparticles in the superparamagnetic and blocked state, depending on the temperature, due to the particle size distribution.

  13. The effect of nanoparticles size on photocatalytic and antimicrobial properties of Ag-Pt/TiO2 photocatalysts

    Science.gov (United States)

    Zielińska-Jurek, Anna; Wei, Zhishun; Wysocka, Izabela; Szweda, Piotr; Kowalska, Ewa

    2015-10-01

    Ag-Pt-modified TiO2 nanocomposites were synthesized using the sol-gel method. Bimetallic modified TiO2 nanoparticles exhibited improved photocatalytic activity under visible-light irradiation, better than monometallic Ag/TiO2 and Pt/TiO2 nanoparticles (NPs). All modified powders showed localized surface plasmon resonance (LSPR) in visible region. The photocatalysts' characteristics by X-ray diffractometry (XRD), scanning transmission electron microscopy (STEM), diffuse reflectance spectroscopy (DRS), X-ray photoelectron spectroscopy (XPS), nitrogen adsorption (BET method for specific surface area) showed that sample with the highest photocatalytic activity had anatase structure, about 93 m2/g specific surface area, maximum plasmon absorption at ca. 420 nm and contained small NPs of silver of 6 nm and very fine platinum NPs of 3 nm. The photocatalytic activity was estimated by measuring the decomposition rate of phenol in 0.2 mM aqueous solution under Vis and UV/vis light irradiation. It was found that size of platinum was decisive for the photocatalytic activity under visible light irradiation, i.e., the smaller Pt NPs were, the higher was photocatalytic activity. While, antimicrobial activities, estimated for bacteria Escherichia coli and Staphylococcus aureus, and pathogenic fungi belonging to Candida family, were only observed for photocatalysts containing silver, i.e., Ag/TiO2 and Ag-Pt/TiO2 nanocomposites.

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

    Energy Technology Data Exchange (ETDEWEB)

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

    1997-04-01

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

  15. Co@Pt Core@Shell nanoparticles encapsulated in porous carbon derived from zeolitic imidazolate framework 67 for oxygen electroreduction in alkaline media

    Science.gov (United States)

    Wang, Likai; Tang, Zhenghua; Yan, Wei; Wang, Qiannan; Yang, Hongyu; Chen, Shaowei

    2017-03-01

    Nanocomposites based on Co@Pt core@shell nanoparticles encapsulated in nitrogen-doped porous carbons were prepared as a new type of high-performance electrocatalysts for oxygen reduction reaction (ORR). Controlled pyrolysis of zeolitic imidazolate framework 67 (ZIF-67) led to the formation of Co nanoparticles encapsulated in nitrogen-doped porous carbon (Co-NC), which underwent galvanic replacement reactions with K2PtCl4 forming Co@Pt core@shell nanoparticles. The surface microstructure and composition of the resulting Co@Pt-NC nanocomposite were examined by electron microscopic as well as X-ray photoelectron spectroscopic (XPS) measurements. With the Co@Pt particles encapsulated in nitrogen-doped porous carbon, the hybrids exhibited a high specific surface area and abundant catalytically active sites for ORR. Electrochemically, the specific activity and mass activity of the Co@Pt-NC composite at +0.85 V (0.145 mA cm-2 and 71.9 A g-1) were superior to those of commercial Pt/C (0.123 mA cm-2 and 38.4 A g-1). Furthermore, the Co@Pt-NC composite also exhibited remarkably higher durability and more robust tolerance against methanol crossover than commercial Pt/C.

  16. Discrete deposition of hydroxyapatite nanoparticles on a titanium implant with predisposing substrate microtopography accelerated osseointegration

    Energy Technology Data Exchange (ETDEWEB)

    Nishimura, Ichiro [UCLA School of Dentistry, Weintraub Center for Reconstructive Biotechnology and Division of Advanced Prosthodontics, Biomaterials and Hospital Dentistry, Los Angeles, CA (United States); Huang Yuhong [Chemat Technology, Incorporated, Northridge, CA (United States); Butz, Frank [UCLA School of Dentistry, Weintraub Center for Reconstructive Biotechnology and Division of Advanced Prosthodontics, Biomaterials and Hospital Dentistry, Los Angeles, CA (United States); Ogawa, Takahiro [UCLA School of Dentistry, Weintraub Center for Reconstructive Biotechnology and Division of Advanced Prosthodontics, Biomaterials and Hospital Dentistry, Los Angeles, CA (United States); Lin, Audrey [UCLA School of Dentistry, Weintraub Center for Reconstructive Biotechnology and Division of Advanced Prosthodontics, Biomaterials and Hospital Dentistry, Los Angeles, CA (United States); Wang, Chiachien Jake [UCLA School of Dentistry, Weintraub Center for Reconstructive Biotechnology and Division of Advanced Prosthodontics, Biomaterials and Hospital Dentistry, Los Angeles, CA (United States)

    2007-06-20

    We report here a new versatile method to deposit discrete hydroxyapatite (HA) nanoparticles on a titanium (Ti) implant with predisposing substrate microtopography, which exhibited an unexpectedly robust biological effect. Commercially pure Ti substrates were treated with 3-aminopropyltriethoxysilane, on which HA nanoparticles (20 nm) were deposited and chemically bonded to TiO{sub 2}. The HA deposition rate was linearly related to the treatment time and HA nanoparticles were deposited on up to 50% of the substrate surface. As a result, the discrete deposition of HA nanoparticles generated novel 20-40 nm nanotopography on the Ti substrate with microtopography that was smooth (turned) or roughened by double acid etching (DAE). The experimental implants with or without HA nanoparticles were surgically placed in rat femur and an implant push-in test was performed after two weeks of healing. The deposition of HA nanoparticles on the DAE surface increased the mechanical withstanding load by 129% and 782% as compared to the control DAE and turned implants, respectively. Micro-computed tomography-based 3D bone morphometry revealed equivalent bone volumes around the DAE implant with or without HA nanoparticles. These data suggest that the discrete deposition of HA nanoparticles accelerates the early osseointegration process, likely through increased shear bonding strengths.

  17. Electrochemical properties of boron-doped ordered mesoporous carbon as electrocatalyst and Pt catalyst support.

    Science.gov (United States)

    Nsabimana, Anaclet; Bo, Xiangjie; Zhang, Yufan; Li, Mian; Han, Ce; Guo, Liping

    2014-08-15

    The electrochemical properties of boron-doped ordered mesoporous carbon (BOMC) as an electrode material and Pt catalyst support were investigated. The BOMC was synthesized and its structure was examined by transmission electron microscopy (TEM), scanning electron microscopy, nitrogen adsorption-desorption, X-ray diffraction, Raman spectroscopy, and X-ray photoelectron spectroscopy (XPS). More defective sites were introduced into OMC by the doping of boron. Six electroactive compounds were employed to investigate their electrochemical responses on BOMC and OMC modified glassy carbon electrodes. The BOMC, with more defective sites, exhibited high activity toward the electroactive compounds. The property of BOMC of supporting platinum nanoparticle catalyst was examined. Pt nanoparticles were loaded onto BOMC and OMC, and this was confirmed by TEM, XPS and thermogravimetric analysis. Pt nanoparticles with an average diameter of 2.62 nm were deposited on BOMC. The doping of boron into OMC facilitates the dispersion of Pt nanoparticles. Pt nanoparticles supported on BOMC (Pt-BOMC) and Pt nanoparticles supported on OMC (Pt-OMC) were electrochemically characterized. The electrocatalytic activity of Pt-BOMC toward methanol oxidation reaction was compared with that of Pt-OMC and commercial Pt-C catalyst. The results show that the electrocatalytic activity of BOMC is significantly higher than that of other used catalysts. Copyright © 2014 Elsevier Inc. All rights reserved.

  18. Electrical Properties of Sputter-deposited ZrO2-based Pt/ZrO2/Si Capacitors

    Institute of Scientific and Technical Information of China (English)

    Keunbin YIM; Yeonkyu PARK; Anna PARK; Namhee CHO; Chongmu LEE

    2006-01-01

    Pt/ZrO2/Si sandwich structures where ZrO2 is deposited by radio frequency (r.f.) magnetron sputtering using a Zr target in an atmosphere of O2/Ar gas mixture, were fabricated and the effects of the O2/Ar flow ratio in the reactive sputtering process, the annealing temperature, the ZrO2 film thickness on the structure,the surface roughness of ZrO2 films and the electric properties of Pt/ZrO2/Si metal-oxide-semiconductor (MOS) capacitors were investigated. The optimum process parameters of the Pt/ZrO2/Si capacitor based on reactively sputtered-ZrO2 determined in such a way as the capacitance is maximized and the leakage current,the oxide charge, and the interface trap density are minimized that is the O2/Ar flow ratio of 1.5, the annealing temperature of 800℃, and the film thickness of 10 nm. Also the conduction mechanism in the Pt/ZrO2/Si capacitor has been discussed.

  19. Size-Controlled Synthesis of Sub-10 nm PtNi3 Alloy Nanoparticles and their Unusual Volcano-Shaped Size Effect on ORR Electrocatalysis.

    Science.gov (United States)

    Gan, Lin; Rudi, Stefan; Cui, Chunhua; Heggen, Marc; Strasser, Peter

    2016-06-01

    Dealloyed Pt bimetallic core-shell catalysts derived from low-Pt bimetallic alloy nanoparticles (e.g, PtNi3 ) have recently shown unprecedented activity and stability on the cathodic oxygen reduction reaction (ORR) under realistic fuel cell conditions and become today's catalyst of choice for commercialization of automobile fuel cells. A critical step toward this breakthrough is to control their particle size below a critical value (≈10 nm) to suppress nanoporosity formation and hence reduce significant base metal (e.g., Ni) leaching under the corrosive ORR condition. Fine size control of the sub-10 nm PtNi3 nanoparticles and understanding their size dependent ORR electrocatalysis are crucial to further improve their ORR activity and stability yet still remain unexplored. A robust synthetic approach is presented here for size-controlled PtNi3 nanoparticles between 3 and 10 nm while keeping a constant particle composition and their size-selected growth mechanism is studied comprehensively. This enables us to address their size-dependent ORR activities and stabilities for the first time. Contrary to the previously established monotonic increase of ORR specific activity and stability with increasing particle size on Pt and Pt-rich bimetallic nanoparticles, the Pt-poor PtNi3 nanoparticles exhibit an unusual "volcano-shaped" size dependence, showing the highest ORR activity and stability at the particle sizes between 6 and 8 nm due to their highest Ni retention during long-term catalyst aging. The results of this study provide important practical guidelines for the size selection of the low Pt bimetallic ORR electrocatalysts with further improved durably high activity.

  20. The Next Generation of Platinum Drugs: Targeted Pt(II) Agents, Nanoparticle Delivery, and Pt(IV) Prodrugs.

    Science.gov (United States)

    Johnstone, Timothy C; Suntharalingam, Kogularamanan; Lippard, Stephen J

    2016-03-09

    The platinum drugs, cisplatin, carboplatin, and oxaliplatin, prevail in the treatment of cancer, but new platinum agents have been very slow to enter the clinic. Recently, however, there has been a surge of activity, based on a great deal of mechanistic information, aimed at developing nonclassical platinum complexes that operate via mechanisms of action distinct from those of the approved drugs. The use of nanodelivery devices has also grown, and many different strategies have been explored to incorporate platinum warheads into nanomedicine constructs. In this Review, we discuss these efforts to create the next generation of platinum anticancer drugs. The introduction provides the reader with a brief overview of the use, development, and mechanism of action of the approved platinum drugs to provide the context in which more recent research has flourished. We then describe approaches that explore nonclassical platinum(II) complexes with trans geometry or with a monofunctional coordination mode, polynuclear platinum(II) compounds, platinum(IV) prodrugs, dual-threat agents, and photoactivatable platinum(IV) complexes. Nanoparticles designed to deliver platinum(IV) complexes will also be discussed, including carbon nanotubes, carbon nanoparticles, gold nanoparticles, quantum dots, upconversion nanoparticles, and polymeric micelles. Additional nanoformulations, including supramolecular self-assembled structures, proteins, peptides, metal-organic frameworks, and coordination polymers, will then be described. Finally, the significant clinical progress made by nanoparticle formulations of platinum(II) agents will be reviewed. We anticipate that such a synthesis of disparate research efforts will not only help to generate new drug development ideas and strategies, but also will reflect our optimism that the next generation of approved platinum cancer drugs is about to arrive.

  1. Synthesis and characterization of FePt nanoparticles by high energy ball milling with and without surfactant

    Energy Technology Data Exchange (ETDEWEB)

    Velasco, V., E-mail: vvjimeno@fis.ucm.es [Instituto de Magnetismo Aplicado, UCM-ADIF-CSIC, 28230 Las Rozas (Spain); Martinez, A.; Recio, J. [Instituto de Magnetismo Aplicado, UCM-ADIF-CSIC, 28230 Las Rozas (Spain); Hernando, A.; Crespo, P. [Instituto de Magnetismo Aplicado, UCM-ADIF-CSIC, 28230 Las Rozas (Spain); Dpto. de Fisica de Materiales, UCM, 28040 Madrid (Spain)

    2012-09-25

    Highlights: Black-Right-Pointing-Pointer Fe and Pt powders in the presence of surfactants don't alloyed by HEBM technique. Black-Right-Pointing-Pointer FePt alloys obtained by dry milling exhibit particle sizes of around 10 {mu}m. Black-Right-Pointing-Pointer FePt alloys obtained by dry milling exhibit soft magnetic behavior. Black-Right-Pointing-Pointer A thermal treatment induces a phase transformation from FCC to FCT. - Abstract: FePt nanoparticles were prepared by high energy ball milling (HEBM) in two different ways. In the first one, elemental powders were mixed and milled whereas in the second one the milling was performed in the presence of oleyl amine and oleic acid as surfactants and hexane as a solvent. X-ray diffraction shows that when the milling is performed in dry conditions, Fe and Pt are alloyed after 5 h, whereas in the wet milling procedure alloying does not take place. In the first case, the diffraction pattern corresponds to the disordered FCC phase. This behavior is also corroborated by the evolution of the magnetic characteristics. In the case of the alloy obtained in dry conditions, the powder was heat treated in order to induce the transformation to the ordered phase. Coercivities of 2.5 kOe are obtained after 650 Degree-Sign C for 2 h.

  2. Switching-off toluene formation in the solvent-free oxidation of benzyl alcohol using supported trimetallic Au-Pd-Pt nanoparticles.

    Science.gov (United States)

    He, Qian; Miedziak, Peter J; Kesavan, Lokesh; Dimitratos, Nikolaos; Sankar, Meenakshisundaram; Lopez-Sanchez, Jose Antonio; Forde, Michael M; Edwards, Jennifer K; Knight, David W; Taylor, Stuart H; Kiely, Christopher J; Hutchings, Graham J

    2013-01-01

    Trimetallic Au-Pd-Pt nanoparticles have been supported on activated carbon by the sol-immobilisation method. They are found to be highly active and selective catalysts for the solvent-free aerobic oxidation of benzyl alcohol. The addition of Pt promotes the selectivity to the desired product benzaldehyde at the expense of toluene formation. Detailed aberration corrected STEM-XEDS analysis confirmed that the supported particles are indeed Au-Pd-Pt ternary alloys, but also identified composition fluctuations from particle-to-particle which vary systematically with nanoparticle size.

  3. Sub-4 nm PtZn Intermetallic Nanoparticles for Enhanced Mass and Specific Activities in Catalytic Electrooxidation Reaction

    Energy Technology Data Exchange (ETDEWEB)

    Qi, Zhiyuan; Xiao, Chaoxian; Liu, Cong; Goh, Tian Wei; Zhou, Lin; Maligal-Ganesh, Raghu; Pei, Yuchen; Li, Xinle; Curtiss, Larry A.; Huang, Wenyu

    2017-03-22

    Atomically ordered intermetallic nanoparticles (iNPs) have sparked considerable interest in fuel cell applications by virtue of their exceptional electronic and structural properties. However, the synthesis of small iNPs in a controllable manner remains a formidable challenge because of the high temperature generally required in the formation of intermetallic phases. Here we report a general method for the synthesis of PtZn. iNPs (3.2 +/- 0.4 nm) on multiwalled carbon nanotubes (MWNT) via a facile and capping agent free strategy using a sacrificial mesoporous silica (mSiO(2)) shell. The as-prepared PtZn iNPs exhibited ca. 10 times higher mass activity in both acidic and basic solution toward the methanol oxidation reaction (MOR) compared to larger PtZn iNPs synthesized on MWNT without the mSiO2 shell. Density functional theory (DFT) calculations predict that PtZn systems go through a "non-CO" pathway for MOR because of the stabilization of the OH* intermediate by Zn atoms, while a pure Pt system forms highly stable COH* and CO* intermediates, leading to catalyst deactivation. Experimental studies on the origin of the backward oxidation peak of MOR coincide well with DFT predictions. Moreover, the calculations demonstrate that MOR on smaller PtZn iNPs is energetically more favorable than larger iNPs, due to their high density of corner sites and lower-lying energetic pathway. Therefore, smaller PtZn iNPs not only increase the number but also enhance the activity of the active sites in MOR compared with larger ones. This work opens a new avenue for the synthesis of small iNPs with more undercoordinated and enhanced active sites for fuel cell applications.

  4. Electroactivity of high performance unsupported Pt-Ru nanoparticles in the presence of hydrogen and carbon monoxide

    Energy Technology Data Exchange (ETDEWEB)

    Velazquez-Palenzuela, Amado; Cabot, Pere-Lluis; Centellas, Francesc; Garrido, Jose Antonio; Arias, Conchita; Rodriguez, Rosa Maria; Brillas, Enric [Laboratori d' Electroquimica dels Materials i del Medi Ambient, Departament de Quimica Fisica, Universitat de Barcelona, Marti i Franques 1-11, 08028 Barcelona (Spain)

    2010-10-15

    The electrochemical activity of high performance unsupported (1:1) Pt-Ru electrocatalyst in the presence of hydrogen and carbon monoxide has been studied using the thin-film rotating disk electrode (RDE) technique. The kinetic parameters of these reactions were determined in H{sub 2}- and CO-saturated 0.5 M H{sub 2}SO{sub 4} solutions by means of cyclic voltammetry, including CO stripping, and RDE voltammetry. Pt-Ru/Nafion inks were prepared in one step with different Nafion mass fractions, allowing determining the ionomer influence in electrocatalytic response and obtaining the kinetic current density in absence of mass-transfer effects, being 41 and 12 mA cm{sup 2} (geometrical area), for H{sub 2} and CO oxidation, respectively. These values correspond to mass activities of 1.37 and 0.40 A mg{sub Pt}{sup 1} and to specific activities of 1.52 and 0.44 mA cm{sub Pt}{sup 2}. The Tafel analysis confirmed that hydrogen oxidation was a two-electron reversible reaction, while CO oxidation exhibited an irreversible behavior with a charge-transfer coefficient of 0.42. The kinetic results for CO oxidation are in agreement with the bifunctional theory, in which the reaction between Pt-CO and Ru-OH is the rate-determining step. The exchange current density for hydrogen reaction was 0.28 mA cm{sup 2} (active surface area), thus showing similar kinetics to those found for carbon-supported Pt and Pt-Ru electrocatalyst nanoparticles. (author)

  5. A silk derived carbon fiber mat modified with Au@Pt urchilike nanoparticles: A new platform as electrochemical microbial biosensor.

    Science.gov (United States)

    Deng, Liu; Guo, Shaojun; Zhou, Ming; Liu, Ling; Liu, Chang; Dong, Shaojun

    2010-06-15

    We present here a facile and efficient route to prepare silk derived carbon mat modified with Au@Pt urchilike nanoparticles (Au@Pt NPs) and develop an Escherichia coli (E. coli)-based electrochemical sensor using this material. Silk is a natural protein fiber, and it is abundant with kinds of functionalities which are important in the development of the derived material. The S-derived carbon fiber mat have amino, pyridine and carbonyl functional groups, these natural existent functionalities allow the Au@Pt NPs to self-assemble on the carbon fiber surface and provide a biocompatible microenvironment for bacteria. The Au@Pt NPs modified S-derived carbon fiber is sensitive to detect the E. coli activities with a low detection limit, where glucose is used as a prelimiltary substrate to evaluate them. The performance of Au@Pt/carbon fiber mat based biosensor is much better than that of commercial carbon paper based biosensor. The high sensitivity of this biosensor stems from the unique electrocatalytic properties of Au@Pt urchilike NPs and quinone groups presented in S-derived carbon fiber. This biosensor is also tested for detection of organophosphate pesticides, fenamiphos. The relative inhibition of E. coli activity is linear with -log[fenamiphos] at the concentration range from 0.5mg/L to 36.6 mg/L with lowest observable effect concentration (LOEC) of 0.09 mg/L. The Au@Pt NPs modified S-derived carbon fiber mat possesses high conductivity, biocompatibility and high electrocatalytic activity and be can used as advanced electrode materials for microbial biosensor improvement. The microbial biosensor based on this material shows potential applications in environmental monitoring.

  6. Enhancement of R6G fluorescence by N-type porous silicon deposited with gold nanoparticles

    Science.gov (United States)

    Mo, Jia-qing; Jiang, Jing; Zhai, Zhen-gang; Shi, Fu-gui; Jia, Zhen-hong

    2017-01-01

    By the electrochemical anodization method, we achieve the single-layer macroporous silicon on the N-type silicon, and prepare gold nanoparticles with sodium citrate reduction method. Through injecting the gold nanoparticles into the porous silicon by immersion, the fluorescence quenching mechanism of porous silicon influenced by gold nanoparticles is analyzed. Then the macroporous silicon deposited with gold nanoparticles is utilized to enhance the fluorescence of rhodamine 6G (R6G). It is found that when the macroporous silicon is deposited with gold nanoparticles for 6 h, the maximum fluorescence enhancement of R6G (about ten times) can be realized. The N-type porous silicon deposited with gold nanoparticles can be an excellent substrate for fluorescence detection.

  7. Optically sensitive devices based on Pt nano particles fabricated by atomic layer deposition and embedded in a dielectric stack

    Energy Technology Data Exchange (ETDEWEB)

    Mikhelashvili, V.; Padmanabhan, R.; Eisenstein, G. [Electrical Engineering Department, Technion, Haifa 3200 (Israel); Russell Berrie Nanotechnology Institute, Technion, Haifa 3200 (Israel); Meyler, B.; Yofis, S.; Weindling, S.; Salzman, J. [Electrical Engineering Department, Technion, Haifa 3200 (Israel); Atiya, G.; Cohen-Hyams, Z.; Kaplan, W. D. [Department of Material Science and Engineering, Technion, Haifa 3200 (Israel); Russell Berrie Nanotechnology Institute, Technion, Haifa 3200 (Israel); Ankonina, G. [Russell Berrie Nanotechnology Institute, Technion, Haifa 3200 (Israel); Photovoltaic Laboratory, Technion, Haifa 3200 (Israel)

    2015-10-07

    We report a series of metal insulator semiconductor devices with embedded Pt nano particles (NPs) fabricated using a low temperature atomic layer deposition process. Optically sensitive nonvolatile memory cells as well as optical sensors: (i) varactors, whose capacitance-voltage characteristics, nonlinearity, and peak capacitance are strongly dependent on illumination intensity; (ii) highly linear photo detectors whose responsivity is enhanced due to the Pt NPs. Both single devices and back to back pairs of diodes were used. The different configurations enable a variety of functionalities with many potential applications in biomedical sensing, environmental surveying, simple imagers for consumer electronics and military uses. The simplicity and planar configuration of the proposed devices makes them suitable for standard CMOS fabrication technology.

  8. Optically sensitive devices based on Pt nano particles fabricated by atomic layer deposition and embedded in a dielectric stack

    Science.gov (United States)

    Mikhelashvili, V.; Padmanabhan, R.; Meyler, B.; Yofis, S.; Atiya, G.; Cohen-Hyams, Z.; Weindling, S.; Ankonina, G.; Salzman, J.; Kaplan, W. D.; Eisenstein, G.

    2015-10-01

    We report a series of metal insulator semiconductor devices with embedded Pt nano particles (NPs) fabricated using a low temperature atomic layer deposition process. Optically sensitive nonvolatile memory cells as well as optical sensors: (i) varactors, whose capacitance-voltage characteristics, nonlinearity, and peak capacitance are strongly dependent on illumination intensity; (ii) highly linear photo detectors whose responsivity is enhanced due to the Pt NPs. Both single devices and back to back pairs of diodes were used. The different configurations enable a variety of functionalities with many potential applications in biomedical sensing, environmental surveying, simple imagers for consumer electronics and military uses. The simplicity and planar configuration of the proposed devices makes them suitable for standard CMOS fabrication technology.

  9. Palladium nanoparticles deposited on silanized halloysite nanotubes: synthesis, characterization and enhanced catalytic property

    Science.gov (United States)

    Zhang, Yi; He, Xi; Ouyang, Jing; Yang, Huaming

    2013-10-01

    Palladium (Pd) nanoparticles were deposited on the surface of halloysite nanotubes (HNTs) modified with γ-aminopropyltriethoxysilane (APTES) to produce Pd/NH2-HNTs nanocomposites. The results indicated that Pd nanoparticles were densely immobilized onto NH2-HNTs with an average diameter of ~ 3 nm. The Pd distribution on the surface of silanized HNTs showed much more uniform, and the Pd nanoparticle size became smaller compared with those directly deposited onto HNTs without silanization. Systematic characterization demonstrated that APTES were chemically bonded onto HNTs, and further confirmed the bond formation between Pd and -NH2 groups, which could ensure the firm deposit of Pd nanoparticles on the surface of silanized HNTs. The as-synthesized Pd/NH2-HNTs exhibited an excellent catalytic activity in the liquid-phase hydrogenation of styrene to ethylbenzene with full conversion within 30 min. The mechanism of the deposit of Pd nanoparticles on silanized HNTs was also investigated.

  10. Transport and deposition of nanoparticles in bend tube with circular cross-section

    Institute of Scientific and Technical Information of China (English)

    Peifeng Lin; Jianzhong Lin

    2009-01-01

    Transport and deposition of nanoparticles in bend tube with circular cross-section were simulated numerically for different Reynolds numbers and Dean numbers.A finite-volume code and the SIMPLE scheme were used to solve the equations.The results show that the distribution of nanoparticle concentration is symmetrical with respect to the top and bottom sides of the tube.The diameter of the nanoparticles has a weak effect on the distribution of nanoparticle concentration.The maximum and minimum of the deposition enhancement factor occur near the outside and inside walls of the bend tube,respectively.The higher the Reynolds number is,the shorter is the time for nanoparticle deposition.The bend curvature radius has a slight effect on the deposition enhancement factor.

  11. Submesothelial deposition of carbon nanoparticles after toner exposition: Case report

    Directory of Open Access Journals (Sweden)

    Philippou Stathis

    2010-12-01

    Full Text Available Abstract Inhalation of carbon nanoparticles (CNP from toner dust has been shown to have impact on the respiratory health of persons exposed. Office printers are known emitters of CNP. We report about a female open office worker who developed weight loss and diarrhoea. Laparoscopy done for suspected endometriosis surprisingly revealed black spots within the peritoneum. Submesothelial aggregates of CNP with a diameter of 31-67 nm were found by scanning and transmission electron microscopy in these tissue specimens. Colon biopsies showed inflammatory bowel disease with typically signs of Crohn disease, but no dust deposits. Transport of CNP via lymphatic and blood vessels after inhalation in the lungs has to be assumed. In this case respiratory symptoms were not reported, therefore no lung function tests were done. We have shown that workers with toner dust exposure from laser printers can develop submesothelial deposition of CNP in the peritoneum. Impact of toner dust exposure on the respiratory health of office workers, as suspected in other studies, has to be evaluated further.

  12. Deposition of thick Co-rich CoPtP films with high energy product for magnetic microelectromechanical applications

    Energy Technology Data Exchange (ETDEWEB)

    Kulkarni, Santosh [Microsystems Center, Tyndall National Institute, University College Cork, Lee Maltings, Prospect Row, Cork (Ireland); Roy, Saibal, E-mail: saibal.roy@tyndall.i [Microsystems Center, Tyndall National Institute, University College Cork, Lee Maltings, Prospect Row, Cork (Ireland)

    2010-05-15

    We report the development of Co-rich CoPtP films of thicknesses up to 82 mum for use in magnetic MEMS applications. These films have been deposited using a combination of pulse-reverse plating with the addition of stress-relieving additives to the bath. The films were electroplated on sputtered Cu/Ti seed layer on silicon with an optimized thickness of 100/20 nm. The composition, crystalline structure, grain size and magnetic properties of the CoPtP films of varying thickness are compared and analyzed. The 3-mum-thick CoPtP film showed a columnar structure and strong perpendicular anisotropy. This film shows a perpendicular coercivity of 2150 Oe, a remanence of 0.564 T and a maximum energy product of 20 kJ/m{sup 3}. As the thickness of the plated film is increased, there is a gradual decrease in the coercivity and anisotropy. The 82-mum-thick film had a perpendicular coercivity of 1150 Oe and a remanence of 0.35 T. While there is a drop in coercivity and anisotropy, the remanence and maximum energy product remain constant for film thicknesses greater than 13 mum. The reason for the drop in coercivity and the near-constant remanence for thicker CoPtP films is discussed here. The coercivity of the thick Co-rich CoPtP film reported in this work is similar to those reported in the literature; the values of remanence, maximum energy product and saturation magnetization are the highest of all the thick (>50 mum) electroplated films in the literature.

  13. Microstructures and magnetic properties of L1{sub 0} FePt films deposited on NaCl-type films

    Energy Technology Data Exchange (ETDEWEB)

    Sun, T.H., E-mail: s9931829@m99.nthu.edu.tw [Department of Materials Science and Engineering, National Tsing Hua University, Hsinchu 30013, Taiwan (China); Chen, S.C.; Su, W.H. [Department of Materials Engineering and Center for Thin Film Technologies and Applications, Ming Chi University of Technology, Taipei 24301, Taiwan (China); Chen, J.R. [Department of Materials Science and Engineering, National Tsing Hua University, Hsinchu 30013, Taiwan (China)

    2013-10-01

    A single-layered FePt film of 30 nm thickness with perpendicular magnetic anisotropy is achieved by depositing the film onto a heated Si(100) substrate at 620 °C. Its perpendicular coercivity (Hc{sub ⊥}), saturation magnetization (M{sub s}) and perpendicular squareness (S{sub ⊥}) are as high as 1113 kA/m, 0.594 Wb/m{sup 2} and 0.96, respectively. The perpendicular magnetic anisotropy degrades when a 5-nm NiO film is introduced under this single-layered film. Upon further increasing the thickness of the NiO film to 10 nm, the Hc{sub ⊥} of the single-layered film decreases greatly to around 330 kA/m. Compared to a NiO underlayer, the Hc{sub ⊥} of the FePt film remains above 1000 kA/m when a 10-nm MgO underlayer is introduced. Furthermore, when the thickness of the MgO underlayer is decreased to 5 nm, the perpendicular magnetic anisotropy of the single-layered FePt film is further enhanced. Its Hc{sub ⊥} stays high at 1081 kA/m; however, S{sub ⊥} increases significantly to 1. - Highlights: ► A thin MgO underlayer enhances the perpendicular magnetic anisotropy of FePt film. ► A NiO underlayer degrades the perpendicular magnetic anisotropy of the film. ► Ni atoms diffuse from NiO underlayer into FePt layer forming NiFe compounds.

  14. Construction of Au@Pt core—satellite nanoparticles based on in-situ reduction of polymeric ionic liquid protected gold nanoparticles

    Science.gov (United States)

    Wu, Wenlan; Li, Junbo; Zou, Sheng; Guo, Jinwu; Zhou, Huiyun

    2017-01-01

    A method of in-situ reduction to prepare Au@Pt core-satellite nanoparticles (NPs) is described by using Au NPs coating poly[1-methyl 3-(2-methacryloyloxy propylimidazolium bromine)] (PMMPImB-@-Au NPs) as the template. After electrostatic complex chloroplatinic acid with PMMPImB shell, the composite NP was directly reduced with N2H4 to produce Au@Pt core-satellite NPs. The characterization of composite and core-satellite NPs under different amounts of chloroplatinic acid were studied by DLS, UV-vis absorption spectrum and TEM. The satellite Pt NPs with a small size ( 2 nm) dotted around Au core, and the resulting Au@Pt core-satellite NPs showed a red-shift surface plasmon resonance (SPR) and a good dispersion due to effectively electrostatic repulsion providing by the polymeric ionic liquid (PIL) shell. Finally, Au@Pt core-satellite NPs exhibit an enhanced catalytic activity and cycled catalytic capability for the reduction of p-nitrophenol with NaBH4.

  15. Heterostructured Au/Pd-M (M = Au, Pd, Pt) nanoparticles with compartmentalized composition, morphology, and electrocatalytic activity

    Science.gov (United States)

    Lutz, Patrick S.; Bae, In-Tae; Maye, Mathew M.

    2015-09-01

    The synthesis, processing, and galvanic exchange of three heterostructured nanoparticle systems is described. The surface accessibility and redox potential of a Au/Pd-Ag dumbbell nanoparticle, where a Au/Pd core/shell region, and a silver region make up the domains, was used to prepare the new nanostructures with controlled composition, morphology, and microstructure. Results indicate that the silver domain was particularly susceptible to galvanic displacement, and was exchanged to Au/Pd-M (M = Au, Pd, Pt). Interestingly, the dumbbell morphology remained after exchange, and the silver region was transformed to hollow, parachute, or concentric domains respectively. The morphology and microstructure change was visualized via TEM and HRTEM, and the composition changes were probed via STEM-EDS imaging and XPS. The electrocatalytic activity of the Au/Pd-M towards methanol oxidation was studied, with results indicating that the Au/Pd-Pt nanoparticles had high activity attributed to the porous nature of the platinum domains.The synthesis, processing, and galvanic exchange of three heterostructured nanoparticle systems is described. The surface accessibility and redox potential of a Au/Pd-Ag dumbbell nanoparticle, where a Au/Pd core/shell region, and a silver region make up the domains, was used to prepare the new nanostructures with controlled composition, morphology, and microstructure. Results indicate that the silver domain was particularly susceptible to galvanic displacement, and was exchanged to Au/Pd-M (M = Au, Pd, Pt). Interestingly, the dumbbell morphology remained after exchange, and the silver region was transformed to hollow, parachute, or concentric domains respectively. The morphology and microstructure change was visualized via TEM and HRTEM, and the composition changes were probed via STEM-EDS imaging and XPS. The electrocatalytic activity of the Au/Pd-M towards methanol oxidation was studied, with results indicating that the Au/Pd-Pt nanoparticles had

  16. Pt3Ti nanoparticles: fine dispersion on SiO2 supports, enhanced catalytic CO oxidation, and chemical stability at elevated temperatures.

    Science.gov (United States)

    Saravanan, Govindachetty; Abe, Hideki; Xu, Ya; Sekido, Nobuaki; Hirata, Hirohito; Matsumoto, Shin-ichi; Yoshikawa, Hideki; Yamabe-Mitarai, Yoko

    2010-07-06

    A platinum-based intermetallic phase with an early d-metal, Pt(3)Ti, has been synthesized in the form of nanoparticles (NPs) dispersed on silica (SiO(2)) supports. The organometallic Pt and Ti precursors, Pt(1,5-cyclooctadiene)Cl(2) and TiCl(4)(tetrahydrofuran)(2), were mixed with SiO(2) and reduced by sodium naphthalide in tetrahydrofuran. Stoichiometric Pt(3)Ti NPs with an average particle size of 2.5 nm were formed on SiO(2) (particle size: 20-200 nm) with an atomically disordered FCC-type structure (Fm3m; a = 0.39 nm). A high dispersivity of Pt(3)Ti NPs was achieved by adding excessive amounts of SiO(2) relative to the Pt precursor. A 50-fold excess of SiO(2) resulted in finely dispersed, SiO(2)-supported Pt(3)Ti NPs that contained 0.5 wt % Pt. The SiO(2)-supported Pt(3)Ti NPs showed a lower onset temperature of catalysis by 75 degrees C toward the oxidation reaction of CO than did SiO(2)-supported pure Pt NPs with the same particle size and Pt fraction, 0.5 wt %. The SiO(2)-supported Pt(3)Ti NPs also showed higher CO conversion than SiO(2)-supported pure Pt NPs even containing a 2-fold higher weight fraction of Pt. The SiO(2)-supported Pt(3)Ti NPs retained their stoichiometric composition after catalytic oxidation of CO at elevated temperatures, 325 degrees C. Pt(3)Ti NPs show promise as a catalytic center of purification catalysts for automobile exhaust due to their high catalytic activity toward CO oxidation with a low content of precious metals.

  17. High loading of uniformly dispersed Pt nanoparticles on polydopamine coated carbon nanotubes and its application in simultaneous determination of dopamine and uric acid

    Science.gov (United States)

    Lin, Mouhong; Huang, Haoliang; Liu, Yingju; Liang, Canjian; Fei, Shidong; Chen, Xiaofen; Ni, Chunlin

    2013-02-01

    Multiwalled carbon nanotubes (MWCNT) were homogeneously covered with a bio-functional polydopamine (PDOP) by a simple dip-coating approach in mild basic solution. Then, uniformly dispersed and highly loaded platinum nanoparticles (PtNPs) were deposited on MWCNT@PDOP by a mild reductant, and were characterized by transmission electron microscopy and x-ray photoelectron spectroscopy. Afterwards, this nanocomposite was modified on the glass carbon electrode and applied to simultaneously determine dopamine (DA) and uric acid (UA) by differential pulse voltammetry (DPV). Results showed that a linear electro-oxidation response was found for DA and UA in the range of 0.25-20 μM and 0.3-13 μM with the detection limit (S/N = 3) of 0.08 μM and 0.12 μM, respectively. In addition, the detection sensitivities for DA and UA by DPV were 1.03 μA μM-1 and 2.09 μA μM-1, respectively, which were much higher than those from a cyclic voltammogram. Finally, the reproducibility and stability of the nanocomposite were also evaluated, demonstrating that such MWCNT@PDOP@PtNPs can be a promising candidate for advanced electrode material in electrochemical sensing and other electrocatalytic applications.

  18. High loading of uniformly dispersed Pt nanoparticles on polydopamine coated carbon nanotubes and its application in simultaneous determination of dopamine and uric acid.

    Science.gov (United States)

    Lin, Mouhong; Huang, Haoliang; Liu, Yingju; Liang, Canjian; Fei, Shidong; Chen, Xiaofen; Ni, Chunlin

    2013-02-15

    Multiwalled carbon nanotubes (MWCNT) were homogeneously covered with a bio-functional polydopamine (PDOP) by a simple dip-coating approach in mild basic solution. Then, uniformly dispersed and highly loaded platinum nanoparticles (PtNPs) were deposited on MWCNT@PDOP by a mild reductant, and were characterized by transmission electron microscopy and x-ray photoelectron spectroscopy. Afterwards, this nanocomposite was modified on the glass carbon electrode and applied to simultaneously determine dopamine (DA) and uric acid (UA) by differential pulse voltammetry (DPV). Results showed that a linear electro-oxidation response was found for DA and UA in the range of 0.25-20 μM and 0.3-13 μM with the detection limit (S/N = 3) of 0.08 μM and 0.12 μM, respectively. In addition, the detection sensitivities for DA and UA by DPV were 1.03 μA μM(-1) and 2.09 μA μM(-1), respectively, which were much higher than those from a cyclic voltammogram. Finally, the reproducibility and stability of the nanocomposite were also evaluated, demonstrating that such MWCNT@PDOP@PtNPs can be a promising candidate for advanced electrode material in electrochemical sensing and other electrocatalytic applications.

  19. Stability of Y-Ti-O nanoparticles during laser deposition of oxide dispersion strengthened steel powder

    Science.gov (United States)

    Euh, Kwangjun; Arkhurst, Barton; Kim, Il Hyun; Kim, Hyun-Gil; Kim, Jeoung Han

    2017-09-01

    This study investigated the feasibility of a direct energy deposition process for fabrication of oxide dispersion strengthened steel cladding. The effect of the laser working power and scan speed on the microstructural stability of oxide nanoparticles in the deposition layer was examined. Y-Ti-O type oxide nanoparticles with a mean diameter of 45 nm were successfully dispersed by the laser deposition process. The laser working power significantly affected nanoparticle size and number density. A high laser power with a low scan speed seriously induced particle coarsening and agglomeration. Compared with bulk oxide dispersion strengthened steel, the hardness of the laser deposition layer was much lower because of a relatively coarse particle and grain size. Formation mechanism of nanoparticles during laser deposition was discussed.

  20. The Transport and Deposition of Nanoparticles in Respiratory System by Inhalation

    Directory of Open Access Journals (Sweden)

    Huiting Qiao

    2015-01-01

    Full Text Available The inhaled nanoparticles have attracted more and more attention, since they are more easily to enter the deep part of respiratory system. Some nanoparticles were reported to cause pulmonary inflammation. The toxicity of nanoparticles depends not only on its chemical component but also on the quantity and position of the deposition. The deposition of nanoparticles is not uniform and is influenced by airflow transport. The high deposition mainly occurs at the carinal ridges and the inside walls around the carinal ridges. Many factors could affect the transport and deposition of nanoparticles, such as particle size, flow rate, structure of airway, pulmonary function, and age. In this review, we discussed the methods and technique involved in particle transport and deposition studies. The features of particles deposition could be observed in clinic experiments and animal experiments. The mechanism of transport could be studied by numerical simulation. Numerical model and experiment study supplement each other. Some techniques such as medical imaging may support the study of nanoparticles transport and deposition. The knowledge of particles transport and deposition may be helpful both to defend the toxicity of inhaled particles and to direct inhaled drug delivery.

  1. Pt@Ag and Pd@Ag core/shell nanoparticles for catalytic degradation of Congo red in aqueous solution.

    Science.gov (United States)

    Salem, Mohamed A; Bakr, Eman A; El-Attar, Heba G

    2018-01-05

    Platinum/silver (Pt@Ag) and palladium/silver (Pd@Ag) core/shell NPs have been synthesized in two steps reaction using the citrate method. The progress of nanoparticle formation was followed by the UV/Vis spectroscopy. Transmission electron microscopy revealed spherical shaped core/shell nanoparticles with average particle diameter 32.17nm for Pt@Ag and 8.8nm for Pd@Ag. The core/shell NPs were further characterized by FT-IR and XRD. Reductive degradation of the Congo red dye was chosen to demonstrate the excellent catalytic activity of these core/shell nanostructures. The nanocatalysts act as electron mediators for the transfer of electrons from the reducing agent (NaBH4) to the dye molecules. Effect of reaction parameters such as nanocatalyst dose, dye and NaBH4 concentrations on the dye degradation was investigated. A comparison between the catalytic activities of both nanocatalysts was made to realize which of them the best in catalytic performance. Pd@Ag was the higher in catalytic activity over Pt@Ag. Such greater activity is originated from the smaller particle size and larger surface area. Pd@Ag nanocatalyst was catalytically stable through four subsequent reaction runs under the utilized reaction conditions. These findings can thus be considered as possible economical alternative for environmental safety against water pollution by dyes. Copyright © 2017. Published by Elsevier B.V.

  2. Chain Assemblies from Nanoparticles Synthesized by Atmospheric Pressure Plasma Enhanced Chemical Vapor Deposition: The Computational View.

    Science.gov (United States)

    Mishin, Maxim V; Zamotin, Kirill Y; Protopopova, Vera S; Alexandrov, Sergey E

    2015-12-01

    This article refers to the computational study of nanoparticle self-organization on the solid-state substrate surface with consideration of the experimental results, when nanoparticles were synthesised during atmospheric pressure plasma enhanced chemical vapor deposition (AP-PECVD). The experimental study of silicon dioxide nanoparticle synthesis by AP-PECVD demonstrated that all deposit volume consists of tangled chains of nanoparticles. In certain cases, micron-sized fractals are formed from tangled chains due to deposit rearrangement. This work is focused on the study of tangled chain formation only. In order to reveal their formation mechanism, a physico-mathematical model was developed. The suggested model was based on the motion equation solution for charged and neutral nanoparticles in the potential fields with the use of the empirical interaction potentials. In addition, the computational simulation was carried out based on the suggested model. As a result, the influence of such experimental parameters as deposition duration, particle charge, gas flow velocity, and angle of gas flow was found. It was demonstrated that electrical charges carried by nanoparticles from the discharge area are not responsible for the formation of tangled chains from nanoparticles, whereas nanoparticle kinetic energy plays a crucial role in deposit morphology and density. The computational results were consistent with experimental results.

  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. 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.

  5. In Situ Synthesis and Deposition of Gold Nanoparticles with Different Morphologies on Glass and ITO Substrate by Ultrasonic Spray Pyrolysis

    OpenAIRE

    María de la Garza; Israel López; Idalia Gómez

    2013-01-01

    Gold nanoparticles were synthesized and deposited in situ by ultrasonic spray pyrolysis on glass and indium tin oxide (ITO) substrates. This technique led to the formation of gold nanoparticles with different morphologies without the use of any capping agent. The gold nanoparticles deposited on glass substrate were obtained as nanospheres with an average particle size of 30 nm with some agglomerates; however, the nanoparticles deposited on ITO substrate were obtained with different morphologi...

  6. The effect of antimony-tin and indium-tin oxide supports on the catalytic activity of Pt nanoparticles for ammonia electro-oxidation

    Energy Technology Data Exchange (ETDEWEB)

    Silva, Júlio César M. [Department of Chemical & Biological Engineering, Centre for Catalysis Research and Innovation (CCRI), University of Ottawa, 161 Louis-Pasteur, Ottawa, ON K1N 6N5 (Canada); Instituto de Pesquisas Energéticas e Nucleares, IPEN/CNEN-SP, Av. Prof. Lineu Prestes, 2242 Cidade Universitária, CEP 05508-900, São Paulo, SP (Brazil); Piasentin, Ricardo M.; Spinacé, Estevam V.; Neto, Almir O. [Instituto de Pesquisas Energéticas e Nucleares, IPEN/CNEN-SP, Av. Prof. Lineu Prestes, 2242 Cidade Universitária, CEP 05508-900, São Paulo, SP (Brazil); Baranova, Elena A., E-mail: elena.baranova@uottawa.ca [Department of Chemical & Biological Engineering, Centre for Catalysis Research and Innovation (CCRI), University of Ottawa, 161 Louis-Pasteur, Ottawa, ON K1N 6N5 (Canada)

    2016-09-01

    Platinum nanoparticles supported on carbon (Pt/C) and carbon with addition of ITO (Pt/C-ITO (In{sub 2}O{sub 3}){sub 9}·(SnO{sub 2}){sub 1}) and ATO (Pt/C-ATO (SnO{sub 2}){sub 9}·(Sb{sub 2}O{sub 5}){sub 1}) oxides were prepared by sodium borohydride reduction method and used for ammonia electro-oxidation reaction (AmER) in alkaline media. The effect of the supports on the catalytic activity of Pt for AmER was investigated using electrochemical (cyclic voltammetry and chronoamperometry) and direct ammonia fuel cell (DAFC) experiments. X-ray diffraction (XRD) showed Pt peaks attributed to the face-centered cubic (fcc) structure, as well as peaks characteristic of In{sub 2}O{sub 3} in ITO support and cassiterite SnO{sub 2} phase of ATO support. According to transmission electron micrographs the mean particles sizes of Pt over carbon were 5.4, 4.9 and 4.7 nm for Pt/C, Pt/C-ATO and Pt/C-ITO, respectively. Pt/C-ITO catalysts showed the highest catalytic activity for ammonia electrooxidation in both electrochemical and fuel cell experiments. We attributed this to the presence of In{sub 2}O{sub 3} phase in ITO, which provides oxygenated or hydroxide species at lower potentials resulting in the removal of poisonous intermediate, i.e., atomic nitrogen (N{sub ads}) and promotion of ammonia electro-oxidation. - Highlights: • Oxide support effect on the catalytic activity of Pt towards ammonia electro-oxidation. • Direct ammonia fuel cell (DAFC) performance using Pt over different supports as anode. • Pt/C-ITO shows better catalytic activity for ammonia oxidation than Pt/C and Pt/C-ATO.

  7. Layers of Metal Nanoparticles on Semiconductors Deposited by Electrophoresis from Solutions with Reverse Micelles

    Science.gov (United States)

    Zdansky, K.; Kacerovsky, P.; Zavadil, J.; Lorincik, J.; Fojtik, A.

    2007-09-01

    Pd nanoparticles were prepared with reverse micelles of water/AOT/isooctane solution and deposited onto silicon or InP substrates by electrophoresis. A large change of capacitance-voltage characteristics of mercury contacts on a semiconductor was found after Pd deposition. This change could be modified when the Pd deposition is followed by a partial removal of the deposited AOT. The deposited Pd nanoparticles were investigated by optical mictroscopy, SIMS and SEM. Finally, Schottky diodes with barrier height as high as 1.07 eV were prepared by deposition of Pd nanoparticles on n-type InP and by a partial removal of superfluous AOT. These diodes are prospective structures for further testing as hydrogen sensors.

  8. Layers of Metal Nanoparticles on Semiconductors Deposited by Electrophoresis from Solutions with Reverse Micelles

    Directory of Open Access Journals (Sweden)

    Fojtik A

    2007-01-01

    Full Text Available AbstractPd nanoparticles were prepared with reverse micelles of water/AOT/isooctane solution and deposited onto silicon or InP substrates by electrophoresis. A large change of capacitance-voltage characteristics of mercury contacts on a semiconductor was found after Pd deposition. This change could be modified when the Pd deposition is followed by a partial removal of the deposited AOT. The deposited Pd nanoparticles were investigated by optical mictroscopy, SIMS and SEM. Finally, Schottky diodes with barrier height as high as 1.07 eV were prepared by deposition of Pd nanoparticles on n-type InP and by a partial removal of superfluous AOT. These diodes are prospective structures for further testing as hydrogen sensors.

  9. Perpendicular magnetic anisotropy and magneto-optical Kerr effect of vapor-deposited Co/Pt-layered structures

    Science.gov (United States)

    Zeper, W. B.; Greidanus, F. J. A. M.; Carcia, P. F.; Fincher, C. R.

    1989-06-01

    We prepared by vapor deposition at room temperature thin (500 Å) Co/Pt multilayers or layered structures directly onto glass or Si substrates. They show a preferential magnetization perpendicular to the film plane for Co thicknesses below 12 Å and a 100% perpendicular remanence for Co thicknesses below 4.5 Å. The magnetic anisotropy can be explained by an interface contribution to the anisotropy. We also investigated the magneto-optical (MO) polar Kerr effect of these multilayers. Because of their excellent magnetic properties and their potentially high oxidation and corrosion resistance, these Co/Pt-layered structures are very promising candidates for MO recording. The Kerr rotation θk at λ=820 nm for a 35×(4.0 Å Co+12.7 Å Pt)-layered structure, which has 100% magnetic remanence, is modest (-0.12°), but the reflectivity R is high (70%), which results in a respectable figure of merit Rθ2k. Furthermore, the Kerr effect increases towards shorter wavelengths and thus favors future higher-density recording.

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

    Science.gov (United States)

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

    2017-07-06

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

  11. Preparation of the Pt nanoparticles decorated poly(N-acetylaniline)/MWNTs nanocomposite and its electrocatalytic oxidation toward formaldehyde

    Energy Technology Data Exchange (ETDEWEB)

    Jiang Chunming; Chen Hui; Yu Cheng; Zhang Song; Liu Baohong [Department of Chemistry, Fudan University, Shanghai, 200433 (China); Kong Jilie [Department of Chemistry, Fudan University, Shanghai, 200433 (China); Institutes of Biomedical Science, Fudan University, Shanghai, 200433 (China); Research Center for Analysis and Measurement, Fudan University, Shanghai, 200433 (China)], E-mail: jlkong@fudan.edu.cn

    2009-01-01

    In this work, a novel 3D nanocomposite is presented, which is consisted of poly(N-acetylaniline) (PAANI)/multi-walled carbon nanotubes (MWNTs) nanorods (in which the inner layer was comprised of MWNTs and the outer layer was PAANI, forming a core-shell structure) and the decorated Pt nanoparticles. Electrochemical techniques (such as electrochemical impedance spectroscopy (EIS)), X-ray photoelectron spectroscopy (XPS), scanning electron microscope (SEM), X-ray diffraction (XRD) and transmission electron microscopy (TEM) are used to characterize the nanocomposite. The resulting Pt/PAANI/MWNTs nanocomposite can be served as a higher efficient catalyst for the electrochemical oxidation of formaldehyde at 0.41 V with the catalytic current of 0.73 mA, which was accompanied with about 45 mV potential negative shifts and two-fold increase in peak current comparison to the Pt/PAANI. These results reveal that the Pt/PAANI/MWNTs nanocomposite film is quite promising in the fuel cell applications.

  12. Au-Pt bimetallic nanoparticles supported on functionalized nitrogen-doped graphene for sensitive detection of nitrite.

    Science.gov (United States)

    Li, Zhuang; An, Zhenzhen; Guo, Yongyang; Zhang, Kangning; Chen, Xiaoling; Zhang, Dongxia; Xue, Zhonghua; Zhou, Xibin; Lu, Xiaoquan

    2016-12-01

    In this work, we report a novel Au-Pt bimetallic nanoparticles (Au-PtNPs) decorated on the surface of nitrogen-doped graphene (NG) functionalized with 1, 3, 6, 8-pyrene tetra sulfonic acid sodium salt (PyTS) by direct electrodeposition method. The results of scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS) and electrochemical impendence spectrum (EIS) reveal that the Au-PtNPs were successfully anchored on the surface of NG sheets with a diameter of 20-40nm. Further, the prepared Au-PtNPs/PyTS-NG nanocomposite exhibits superior catalytic activity for the oxidation of nitrite. Under optimal experimental conditions, an amperometric sensor with a linear range of 0.5-1621μM and a detection limit of 0.19μM (S/N=3) for the detection of nitrite was set up and applied to real samples. Copyright © 2016 Elsevier B.V. All rights reserved.

  13. Synthesis of Pt nanoparticles and their burrowing into Si due to synergistic effects of ion beam energy losses

    Directory of Open Access Journals (Sweden)

    Pravin Kumar

    2014-10-01

    Full Text Available We report the synthesis of Pt nanoparticles and their burrowing into silicon upon irradiation of a Pt–Si thin film with medium-energy neon ions at constant fluence (1.0 × 1017 ions/cm2. Several values of medium-energy neon ions were chosen in order to vary the ratio of the electronic energy loss to the nuclear energy loss (Se/Sn from 1 to 10. The irradiated films were characterized using Rutherford backscattering spectroscopy (RBS, atomic force microscopy (AFM, scanning electron microscopy (SEM, X-ray diffraction (XRD and high resolution transmission electron microscopy (HRTEM. A TEM image of a cross section of the film irradiated with Se/Sn = 1 shows ≈5 nm Pt NPs were buried up to ≈240 nm into the silicon. No silicide phase was detected in the XRD pattern of the film irradiated at the highest value of Se/Sn. The synergistic effect of the energy losses of the ion beam (molten zones are produced by Se, and sputtering and local defects are produced by Sn leading to the synthesis and burrowing of Pt NPs is evidenced. The Pt NP synthesis mechanism and their burrowing into the silicon is discussed in detail.

  14. Controlled Deposition of Tin Oxide and Silver Nanoparticles Using Microcontact Printing

    Directory of Open Access Journals (Sweden)

    Joo C. Chan

    2015-02-01

    Full Text Available This report describes extensive studies of deposition processes involving tin oxide (SnOx nanoparticles on smooth glass surfaces. We demonstrate the use of smooth films of these nanoparticles as a platform for spatially-selective electroless deposition of silver by soft lithographic stamping. The edge and height roughness of the depositing metallic films are 100 nm and 20 nm, respectively, controlled by the intrinsic size of the nanoparticles. Mixtures of alcohols as capping agents provide further control over the size and shape of nanoparticles clusters. The distribution of cluster heights obtained by atomic force microscopy (AFM is modeled through a modified heterogeneous nucleation theory as well as Oswald ripening. The thermodynamic modeling of the wetting properties of nanoparticles aggregates provides insight into their mechanism of formation and how their properties might be further exploited in wide-ranging applications.

  15. Gyroscopic behavior exhibited by the optical Kerr effect in bimetallic Au-Pt nanoparticles suspended in ethanol

    Science.gov (United States)

    Fernández-Valdés, D.; Torres-Torres, C.; Martínez-González, C. L.; Trejo-Valdez, M.; Hernández-Gómez, L. H.; Torres-Martínez, R.

    2016-07-01

    The modification in the third-order nonlinear optical response exhibited by rotating bimetallic Au-Pt nanoparticles in an ethanol solution was analyzed. The samples were prepared by a sol-gel processing route. The anisotropy associated to the elemental composition of the nanoparticles was confirmed by high-resolution transmission electron microscopy and energy-dispersive X-ray spectroscopy measurements. The size of the nanoparticles varies in the range from 9 to 13 nm, with an average size of 11 nm. Changes in the spatial orientation of the nanomaterials automatically generated a variation in their plasmonic response evaluated by UV-Vis spectroscopy. A two-wave mixing experiment was conducted to explore an induced birefringence at 532 nm wavelength with nanosecond pulses interacting with the samples. A strong optical Kerr effect was identified to be the main responsible effect for the third-order nonlinear optical phenomenon exhibited by the nanoparticles. It was estimated that the rotation of inhomogeneous nanostructures can provide a remarkable change in the participation of different surface plasmon resonances, if they correspond to multimetallic nanoparticles. Potential applications for developing low-dimensional gyroscopic systems can be contemplated.

  16. Confined-space alloying of nanoparticles for the synthesis of efficient PtNi fuel-cell catalysts.

    Science.gov (United States)

    Baldizzone, Claudio; Mezzavilla, Stefano; Carvalho, Hudson W P; Meier, Josef Christian; Schuppert, Anna K; Heggen, Marc; Galeano, Carolina; Grunwaldt, Jan-Dierk; Schüth, Ferdi; Mayrhofer, Karl J J

    2014-12-15

    The efficiency of polymer electrolyte membrane fuel cells is strongly depending on the electrocatalyst performance, that is, its activity and stability. We have designed a catalyst material that combines both, the high activity for the decisive cathodic oxygen reduction reaction associated with nanoscale Pt alloys, and the excellent durability of an advanced nanostructured support. Owing to the high specific activity and large active surface area, the catalyst shows extraordinary mass activity values of 1.0 A mgPt(-1). Moreover, the material retains its initial active surface area and intrinsic activity during an extended accelerated aging test within the typical operation range. This excellent performance is achieved by confined-space alloying of the nanoparticles in a controlled manner in the pores of the support.

  17. Monodisperse Pt Nanoparticles Assembled on Reduced Graphene Oxide: Highly Efficient and Reusable Catalyst for Methanol Oxidation and Dehydrocoupling of Dimethylamine-Borane (DMAB).

    Science.gov (United States)

    Yildiz, Yunus; Erken, Esma; Pamuk, Handan; Sert, Hakan; Sen, Fatih

    2016-06-01

    Herein, monodisperse platinum (0) nanocatalyst assembled on reduced graphene oxide (Pt(0)@RGO) was easily and reproducibly prepared by the double solvent reduction method at room temperature. Pt(0)@RGO was characterized by X-ray diffraction (XRD), X-ray photoelectron microscopy (XPS) and transmission electron microscopy (TEM) measurements that verify the formation of monodisperse Pt (0) nanoparticles on RGO. The catalytic and electrocatalytic performances of Pt(0) @ RGO in terms of activity, isolability and reusability were investigated for both methanol oxidation and the dehydrocoupling of dimethylamine-borane (DMAB) in which Pt(0)@RGO was found to be highly active and reusable heterogeneous catalyst even at room temperature. The prepared nanoparticles can also electrocatalyze methanol oxidation with very high electrochemical activities (5.64 A/cm2 at 0.58 V for methanol). The activation energy (Ea), activation enthalpy (ΔH#), and activation entropy (ΔS#) for DMAB dehydrogenation were calculated to be 59.33 kJ mol(-1), 56.79 kJ mol(-1) and -151.68 J mol(-1) K(-1), respectively. The exceptional stability of new Pt(0) @ RGO nanoparticles towards agglomeration, leaching and CO poisoning allow these particles to be recycled and reused in the catalysis of DMAB dehydrogenation and methanol oxidation. After four subsequent reaction and recovery cycles, Pt(0) @ RGO retained ≥ 75% activity towards the complete dehydrogenation of DMAB.

  18. Electroless deposition of metal nanoparticle clusters: Effect of pattern distance

    KAUST Repository

    Gentile, Francesco

    2014-04-03

    Electroless plating is a deposition technique in which metal ions are reduced as atoms on specific patterned sites of a silicon surface to form metal nanoparticles (NPs) aggregates with the desired characteristics. Those NPs, in turn, can be used as constituents of surface enhanced Raman spectroscopy substrates, which are devices where the electromagnetic field and effects thereof are giantly amplified. Here, the electroless formation of nanostructures was studied as a function of the geometry of the substrate. High resolution, electron beam lithography techniques were used to obtain nonperiodic arrays of circular patterns, in which the spacing of patterns was varied over a significant range. In depositing silver atoms in those circuits, the authors found that the characteristics of the aggregates vary with the pattern distance. When the patterns are in close proximity, the interference of different groups of adjacent aggregates cannot be disregarded and the overall growth is reduced. Differently from this, when the patterns are sufficiently distant, the formation of metal clusters of NPs is independent on the spacing of the patterns. For the particular subset of parameters used here, this critical correlation distance is about three times the pattern diameter. These findings were explained within the framework of a diffusion limited aggregation model, which is a simulation method that can decipher the formation of nanoaggregates at an atomic level. In the discussion, the authors showed how this concept can be used to fabricate ordered arrays of silver nanospheres, where the size of those spheres may be regulated on varying the pattern distance, for applications in biosensing and single molecule detection.

  19. Controlling size, amount, and crystalline structure of nanoparticles deposited on graphenes for highly efficient energy conversion and storage.

    Science.gov (United States)

    Choi, Bong Gill; Park, Ho Seok

    2012-04-01

    A facilitated electrochemical reaction at the surface of electrodes is crucial for highly efficient energy conversion and storage. Herein, various nanoparticles (NPs) including Au, Pt, Pd, Ru, and RuO(2), were synthesized in situ and directly deposited on the ionic liquid (IL)-functionalized reduced graphene oxides (RGOs) in a controlled manner. The size, amount, and crystalline structures of discrete NPs were readily controlled, giving rise to enhanced methanol oxidation and pseudocapacitance. The well-defined nanostructure of decorated NPs and the favorable interaction between ILs and RGOs (or NPs) facilitated the electrochemical reaction, where NPs acted as electrocatalysts for energy conversion and played the role of redox-active electrodes for energy storage.

  20. Anisotropic silver nanoparticles deposited on zeolite a for selective Hg2+ colorimetric sensing and antibacterial studies

    Directory of Open Access Journals (Sweden)

    Khorshidi Alireza

    2015-01-01

    Full Text Available Silver nanoparticles deposited on the surface of zeolite A were prepared via post ion-exchange reduction, and reduction-deposition methods. Formation of the silver nanoparticles on the surface of zeolite A was verified by surface plasmon spectra using diffuse reflectance spectroscopy and ultraviolet-visible spectroscopy. Morphology of the prepared samples was characterized by X-ray diffraction and scanning electron microscopy. Furthermore, silver nanoparticles deposited on the zeolite A, after fixation of Rhodamine B dye molecules over themselves, were successful in detecting Hg2+ ions selectively. After treatment with the so-obtained sensor, color change from colorless to pink was visible to the naked eye for the Hg2+ solution concentrations down to 1.0×10-8 mol.L-1. Antibacterial tests demonstrated the multifunctional application of the silver nanoparticles deposited on zeolite A.

  1. The effect of Pt nanoparticles loading on H{sub 2} sensing properties of flame-spray-made SnO{sub 2} sensing films

    Energy Technology Data Exchange (ETDEWEB)

    Liewhiran, Chaikarn, E-mail: chaikarn_l@yahoo.com [Department of Physics and Materials Science, Faculty of Science, Chiang Mai University, Chiang Mai 50202 (Thailand); Materials Science Research Center, Faculty of Science, Chiang Mai University, Chiang Mai 50202 (Thailand); Tamaekong, Nittaya [Program in Materials Science, Faculty of Science, Maejo University, Chiang Mai 50290 (Thailand); Tuantranont, Adisorn; Wisitsoraat, Anurat [Nanoelectronics and MEMS Laboratory, National Electronics and Computer Technology Center, Klong Luang, Pathumthani 12120 (Thailand); Phanichphant, Sukon [Materials Science Research Center, Faculty of Science, Chiang Mai University, Chiang Mai 50202 (Thailand)

    2014-10-15

    SnO{sub 2} nanoparticles loaded with 0.2–2 wt% Pt have successfully been synthesized in a single step by flame spray pyrolysis (FSP) and investigated for gas sensing towards hydrogen (H{sub 2}). According to characterization results by X-ray diffraction, nitrogen adsorption, scanning/high resolution-transmission electron microscopy and analyses based on Hume-Rothery rules using atomic radii, crystal structure, electronegativities, and valency/oxidation states of Pt and Sn, it is conclusive that Pt is not solute in SnO{sub 2} crystal but forms nanoparticles loaded on SnO{sub 2} surface. H{sub 2} gas sensing was studied at 200–10,000 ppm and 150–350 °C in dry air. It was found that H{sub 2} response was enhanced by more than one order of magnitude with a small Pt loading concentration of 0.2 wt% but further increase of Pt loading amount resulted in deteriorated H{sub 2}-sensing performance. The optimal SnO{sub 2} sensing film (0.2 wt% Pt-loaded SnO{sub 2}, 20 μm in thickness) showed an optimum H{sub 2} response of ∼150.2 at 10,000 ppm and very short response time in a few seconds at a low optimal operating temperature of 200 °C. In addition, the response tended to increase linearly and the response times decreased drastically with increasing H{sub 2} concentration. Moreover, the selectivity against carbon monoxide (CO) and acetylene (C{sub 2}H{sub 2}) gases was also found to be considerably improved with the small amount of Pt loading. The H{sub 2} response dependence on Pt concentration can be explained based on the spillover mechanism, which is highly effective only when Pt catalyst is well-dispersed at the low Pt loading concentration of 0.2 wt%. - Highlights: • Pt/SnO{sub 2} nanoparticles were prepared in a single step by flame spray pyrolysis. • Pt loading on SnO{sub 2} nanoparticles at low level of 0.2 wt% gives optimal H{sub 2} response. • 0.2 wt% Pt/SnO{sub 2} sensor exhibits a low optimum operating temperature of 200 °C. • H

  2. Theoretical studies of preparation of core-shell nanoparticles by electrochemical metal deposition

    Energy Technology Data Exchange (ETDEWEB)

    Oviedo, O.A.; Mariscal, M.M. [INFIQC, Departamento de Matematica y Fisica, Facultad de Ciencias Quimicas, Universidad Nacional de Cordoba, Cordoba (Argentina); Leiva, E.P.M., E-mail: eleiva@fcq.unc.edu.a [INFIQC, Departamento de Matematica y Fisica, Facultad de Ciencias Quimicas, Universidad Nacional de Cordoba, Cordoba (Argentina)

    2010-11-30

    In the present work we discuss the statistical mechanical framework for predicting the decoration of metallic nanoparticles using electrochemical methods, in thermodynamic equilibrium. It is found that depending on the interactions between the two metals, controlled decoration may be achieved for core-shell nanoparticles in undersaturation and oversaturation conditions. The concept of underpotential deposition is discussed for the case of nanoparticles, with the finding that this phenomenon may be size dependent.

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

    DEFF Research Database (Denmark)

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

    2014-01-01

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

  4. Simultaneous electrochemical detection of ascorbic acid, dopamine and uric acid based on graphene anchored with Pd-Pt nanoparticles.

    Science.gov (United States)

    Yan, Jun; Liu, Shi; Zhang, Zhenqin; He, Guangwu; Zhou, Ping; Liang, Haiying; Tian, Lulu; Zhou, Xuemin; Jiang, Huijun

    2013-11-01

    Pd-Pt bimetallic nanoparticles anchored on functionalized reduced graphene oxide (RGO) nanomaterials were synthesized via a one-step in situ reduction process, in which Pt and Pd ions were first attached to poly(diallyldimethylammonium chloride) (PDDA) functionalized graphene oxide (GO) sheets, and then the encased metal ions and GO were subjected to simultaneous reduction by ethylene glycol. The as-prepared Pd3Pt1/PDDA-RGO nanocomposites were characterized by transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), Raman spectroscopy and electrochemical methods. In addition, an electrochemical sensor based on the graphene nanocomposites was fabricated for the simultaneous detection of ascorbic acid (AA), dopamine (DA) and uric acid (UA) in their ternary mixture. Three well-separated voltammetric peaks along with remarkable increasing electro-oxidation currents were obtained in differential pulse voltammetry (DPV) measurements. Under the optimized conditions, there were linear relationships between the peak currents and the concentrations in the range of 40-1200 μM for AA, 4-200 μM for DA and 4-400 μM for UA, with the limit of detection (LOD) (based on S/N=3) of 0.61, 0.04 and 0.10 μM for AA, DA and UA, respectively. This improved electrochemical performance can be attributed to the synergistic effect of metallic nanoparticles and RGO and the combination of the bimetallic nanoparticles. Furthermore, the practical electroanalytical utility of the sensor was demonstrated by the determination of AA, DA and together with UA in human urine and blood serum samples with satisfactory results. Copyright © 2013 Elsevier B.V. All rights reserved.

  5. Functionalization and Area-Selective Deposition of Magnetic Carbon-Coated Iron Nanoparticles from Solution

    Directory of Open Access Journals (Sweden)

    Erika Widenkvist

    2011-01-01

    Full Text Available A route to area-selective deposition of carbon-coated iron nanoparticles, involving chemical modification of the surface of the particles, is described. Partial oxidative etching of the coating introduces carboxylic groups, which then are esterified. The functionalized particles can be selectively deposited on the Si areas of Si/SiO2 substrates by a simple dipping procedure. Nanoparticles and nanoassemblies have been analyzed using SEM, TEM, and XPS.

  6. An Effective Approach towards the Immobilization of PtSn Nanoparticles on Noncovalent Modified Multi-Walled Carbon Nanotubes for Ethanol Electrooxidation

    Directory of Open Access Journals (Sweden)

    Xi Geng

    2016-03-01

    Full Text Available In this article, we describe an effective method to tether Pt and PtSn nanoparticles (NPs on polyelectrolyte modified multi-walled carbon nanotubes (MWCNTs for ethanol electrooxidation. By using a polymer wrapping technique, positively charged polyethyleneimine (PEI was attached onto carbon nanotubes (CNTs to provide preferential linking sites for metal precursors. Well-dispersed Pt and PtSn nanocrystals (2–5 nm were subsequently decorated on PEI-functionalized MWCNTs through the polyol reduction method. The successful non-covalent modification of MWCNTs was confirmed by Fourier transform infrared spectroscopy (FTIR and Zeta potential measurements. Energy dispersive X-ray (EDX spectrum indicates approximately 20 wt % Pt loading and a desirable Pt:Sn atomic ratio of 1:1. Electrochemical analysis demonstrated that the as-synthesized PtSn/PEI-MWCNTs nanocomposite exhibited improved catalytic activity and higher poison tolerance for ethanol oxidation as compared to Pt/PEI-MWCNTs and commercial Pt/XC-72 catalysts. The enhanced electrochemical performance may be attributed to the uniform dispersion of NPs as well as the mitigating of CO self-poisoning effect by the alloying of Sn element. This modification and synthetic strategy will be studied further to develop a diversity of carbon supported Pt-based hybrid nanomaterials for electrocatalysis.

  7. Pt/YSZ electrochemical catalysts prep