Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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Murphy, Shane

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Science Foundation Ireland

in Cooperation with on an Cooperation-Score of 37%

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Publications (10/10 displayed)

  • 2024Fiber optic sensing for volcano monitoring and imaging volcanic processes1citations
  • 2020Surface rupture in stochastic slip models2citations
  • 2012H2 splitting on Pt, Ru and Rh nanoparticles supported on sputtered HOPG17citations
  • 2008Microtexture of magnetite thin films of (001) and (111) orientations on MgO substrates studied by electron-backscatter diffraction4citations
  • 2004Study of in-plane magnetic anisotropy of ultrathin epitaxial Fe films grown on vicinal Mo(110) surface12citations
  • 2003Formation of the strain-induced electronic superstructure on the magnetite (111) surfacecitations
  • 2003Scanning tunneling microscopy studies of the Fe3O4(001) surface using antiferromagnetic probes7citations
  • 2002Morphology and strain-induced defect structure of ultrathin epitaxial Fe films on Mo(110)32citations
  • 2002Charge ordering on the surface of Fe3O4(001)80citations
  • 2001Surface studies of the Fe/Mo(110) and Fe/W(100) epitaxial systemscitations

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Fichtner, Andreas
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Jousset, Philippe
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Eibl, Eva
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Wollin, Christopher
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Retailleau, Lise
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Currenti, Gilda
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Klaasen, Sara
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Caudron, Corentin
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Krawczyk, Charlotte
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Spica, Zack
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Nishimura, Takeshi
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Le Marchand, Arnaud
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Herrero, A.
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Nielsen, R. M.
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Chorkendorff, Ib
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Fiordaliso, Elisabetta Maria
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Dahl, Søren
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Arora, Sunil Kumar
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Shvets, Igor
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Usov, Victor
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Mariotto, Guido
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Co-Authors (by relevance)

  • Fichtner, Andreas
  • Jousset, Philippe
  • Eibl, Eva
  • Wollin, Christopher
  • Retailleau, Lise
  • Currenti, Gilda
  • Klaasen, Sara
  • Caudron, Corentin
  • Krawczyk, Charlotte
  • Spica, Zack
  • Nishimura, Takeshi
  • Le Marchand, Arnaud
  • Herrero, A.
  • Nielsen, R. M.
  • Chorkendorff, Ib
  • Fiordaliso, Elisabetta Maria
  • Dahl, Søren
  • Arora, Sunil Kumar
  • Shvets, Igor
  • Usov, Victor
  • Mariotto, Guido
OrganizationsLocationPeople

article

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

  • Nielsen, R. M.
  • Chorkendorff, Ib
  • Murphy, Shane
  • Fiordaliso, Elisabetta Maria
  • Dahl, Søren
Abstract

The equilibrium hydrogen exchange rate between adsorbed and gas phase hydrogen at 1bar is measured for Pt, Ru and Rh nanoparticles supported on a sputtered HOPG substrate. The particles are prepared by Electron Beam Physical Vapor Deposition and the diameter of the particles varies between 2 and 5nm. 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 of Pt, the equilibrium dissociative sticking probability, S, is found to be nearly independent of particle diameter. For Ru and Rh, S is found to depend strongly on particle diameter, with the larger particles being more active. The apparent energy of desorption at equilibrium, Eapp, shows a dramatic increase with decreasing particle diameter for diameters below 5nm for Ru and Rh, whereas Eapp is only weakly dependent on particle diameter for Pt. We suggest that the strong variation in the apparent desorption energy with particle diameter for Ru and Rh is due to the formation of compressed hydrogen 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.

Topics
  • nanoparticle
  • impedance spectroscopy
  • experiment
  • physical vapor deposition
  • Hydrogen
  • gas phase