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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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (2/2 displayed)

  • 2019Understanding Oxygen Activation on Nanoporous Gold32citations
  • 2018Oxygen-Driven Surface Evolution of Nanoporous Gold30citations

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Tomaschun, Gabriele
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Dononelli, Wilke
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Moskaleva, Lyudmila V.
2 / 5 shared
Baeumer, Marcus
1 / 1 shared
Risse, Thomas
1 / 3 shared
Moreira, Raphaell
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Li, Yong
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2019
2018

Co-Authors (by relevance)

  • Tomaschun, Gabriele
  • Dononelli, Wilke
  • Moskaleva, Lyudmila V.
  • Baeumer, Marcus
  • Risse, Thomas
  • Moreira, Raphaell
  • Li, Yong
OrganizationsLocationPeople

article

Understanding Oxygen Activation on Nanoporous Gold

  • Kluener, Thorsten
  • Tomaschun, Gabriele
  • Dononelli, Wilke
  • Moskaleva, Lyudmila V.
Abstract

<p>Nanoporous gold (np-Au) is a catalytically highly active material, prepared by selectively dealloying silver from a gold-silver alloy. It can promote aerobic CO oxidation and a range of other oxidation reactions. It has been debated whether the remarkable catalytic properties of np-Au are mainly due to its structural features or whether the residual Ag remaining in the material after dealloying is decisive for the activity, especially for the activation of O<sub>2</sub>. Recent theoretical studies provided evidence that Ag impurities can facilitate the adsorption and dissociation of O<sub>2</sub> on np-Au. However, these studies predicted quite a high activation barrier for O<sub>2</sub> dissociation on Au-Ag alloy catalysts, whereas experimentally reported activation energies are much lower. In this work we use the stepped Au(321) surface with Ag impurities, which is arguably a realistic model for np-Au material as well as for Au-Ag catalysts in general. We present alternative routes for O<sub>2</sub> activation via its direct reaction with adsorbed CO or H<sub>2</sub>O. In all of the reactions considered, surface atomic O is generated via a sequence of elementary steps with calculated low activation energies of &lt;0.4 eV with respect to coadsorbed reactants. Ag impurities are shown to increase the adsorption energy of O<sub>2</sub> and hence the probability of a surface-mediated reaction versus desorption. We considered four possible mechanisms of CO oxidation in dry and humid environments in a microkinetic modeling study. We show that via the proposed mechanisms water indeed promotes O<sub>2</sub> dissociation; nevertheless, the "dry" mechanism, in which CO directly reacts with O<sub>2</sub>, is by far the fastest route of CO<sub>2</sub> formation on pure Au and on Au with Ag impurities. Ag impurities lead to significantly higher turnover rates; thus, calculations point to the key role of Ag in promoting the catalytic activity of Au-Ag alloy systems.</p>

Topics
  • impedance spectroscopy
  • surface
  • silver
  • Oxygen
  • gold
  • activation
  • silver alloy