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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Materials Map under construction

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 (4/4 displayed)

  • 2024Pulsed‐Laser‐Driven CO<sub>2</sub> Reduction Reaction for the Control of the Photoluminescence Quantum Yield of Organometallic Gold Nanocomposites4citations
  • 2024Stability of binary colloidal mixtures of Au noble metal and ZnS semiconductor nanoparticles4citations
  • 2022Nanocomposite Concept for Electrochemical In Situ Preparation of Pt–Au Alloy Nanoparticles for Formic Acid Oxidation6citations
  • 2022Nanocomposite Concept for Electrochemical in Situ Preparation of Pt-Au Alloy Nanoparticles for Formic Acid Oxidation6citations

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Li, Yao
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Neumann, Stefan
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Anwar, Osama
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Rafaja, David
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Rezvani, Azita
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Segets, Doris
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Schroder, Johanna
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Du, Jia
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Jensen, Kirsten M. Ø.
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Kirkensgaard, Jacob J. K.
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Arenz, Matthias
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Quinson, Jonathan
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Zhang, Damin
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Wang, Baiyu
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Wiberg, Gustav K. H.
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Co-Authors (by relevance)

  • Li, Yao
  • Neumann, Stefan
  • Anwar, Osama
  • Rafaja, David
  • Rezvani, Azita
  • Segets, Doris
  • Schroder, Johanna
  • Du, Jia
  • Jensen, Kirsten M. Ø.
  • Kirkensgaard, Jacob J. K.
  • Arenz, Matthias
  • Barcikowski, Stephan
  • Simonsen, Søren B.
  • Quinson, Jonathan
  • Pittkowski, Rebecca K.
  • Zhang, Damin
  • Wang, Baiyu
  • Wiberg, Gustav K. H.
  • Schröder, Johanna
OrganizationsLocationPeople

article

Nanocomposite Concept for Electrochemical in Situ Preparation of Pt-Au Alloy Nanoparticles for Formic Acid Oxidation

  • Du, Jia
  • Jensen, Kirsten M. Ø.
  • Reichenberger, Sven
  • Kirkensgaard, Jacob J. K.
  • Arenz, Matthias
  • Li, Yao
  • Barcikowski, Stephan
  • Simonsen, Søren B.
  • Quinson, Jonathan
  • Schröder, Johanna
  • Pittkowski, Rebecca K.
  • Zhang, Damin
  • Wang, Baiyu
  • Wiberg, Gustav K. H.
Abstract

Herein, we report a straightforward approach for the in situ preparation of Pt-Au alloy nanoparticles from Pt + xAu/C nanocomposites using monometallic colloidal nanoparticles as starting blocks. Four different compositions with fixed Pt content and varying Pt to Au mass ratios from 1:1 up to 1:7 were prepared as formic acid oxidation reaction (FAOR) catalysts. The study was carried out in a gas diffusion electrode (GDE) setup. It is shown that the presence of Au in the nanocomposites substantially improves the FAOR activity with respect to pure Pt/C, which serves as a reference. The nanocomposite with a mass ratio of 1:5 between Pt and Au displays the best performance during potentiodynamic tests, with the electro-oxidation rates, overpotential, and poisoning resistance being improved simultaneously. By comparison, too low or too high Au contributions in the nanocomposites lead to an unbalanced performance in the FAOR. The combination of operando small-angle X-ray scattering (SAXS), scanning transmission electron microscopy (STEM) elemental mapping, and wide-angle X-ray scattering (WAXS) reveals that for the nanocomposite with a 1:5 mass ratio, a conversion between Pt and Au from separate nanoparticles to alloy nanoparticles occurs during continuous potential cycling in formic acid. By comparison, the nanocomposites with lower Au contents, for example, 1:2, exhibit less in situ alloying, and the concomitant performance improvement is less pronounced. On applying identical location transmission electron microscopy (IL-TEM), it is revealed that the in situ alloying is due to Pt dissolution and re-deposition onto Au as well as Pt migration and coalescence with Au nanoparticles.

Topics
  • nanoparticle
  • Deposition
  • nanocomposite
  • impedance spectroscopy
  • laser emission spectroscopy
  • transmission electron microscopy
  • small angle x-ray scattering
  • wide-angle X-ray scattering