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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Hofmann, Jan, P.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (3/3 displayed)

  • 2024Integration of Multijunction Absorbers and Catalysts for Efficient Solar‐Driven Artificial Leaf Structures: A Physical and Materials Science Perspective6citations
  • 2021Twin boundary migration in an individual platinum nanocrystal during catalytic CO oxidation36citations
  • 2021Stabilization Effects in Binary Colloidal Cu and Ag Nanoparticle Electrodes under Electrochemical CO2 Reduction Conditions36citations

Places of action

Chart of shared publication
Texier, Michaël
1 / 1 shared
Carnis, Jérôme
1 / 6 shared
Favre, Luc
1 / 25 shared
Rabkin, Eugen
1 / 28 shared
Almog, Ehud
1 / 4 shared
Oropeza, Freddy, E.
1 / 1 shared
Schülli, Tobias, U.
1 / 3 shared
Campos, Andrea
1 / 8 shared
Micha, Jean-Sébastien
1 / 13 shared
Thomas, Olivier
1 / 26 shared
Gazit, Nimrod
1 / 4 shared
Leake, Steven, J.
1 / 2 shared
Wu, Longfei
2 / 10 shared
Poloni, Roberta
1 / 4 shared
Richard, Marieingrid
1 / 3 shared
Gao, Lu
1 / 4 shared
Hensen, Emiel, J. M.
2 / 11 shared
Labat, Stéphane
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Kshirsagar, Aseem, Rajan
1 / 1 shared
Dupraz, Maxime
1 / 12 shared
Arnouts, Sven
1 / 8 shared
An, Hongyu
1 / 8 shared
Zhang, Yue
1 / 11 shared
Altantzis, Thomas
1 / 16 shared
Weckhuysen, B. M.
1 / 4 shared
Bals, Sara
1 / 93 shared
Kolmeijer, K. E.
1 / 2 shared
Stam, Ward Van Der
1 / 11 shared
Figueiredo, Marta Costa
1 / 14 shared
Chart of publication period
2024
2021

Co-Authors (by relevance)

  • Texier, Michaël
  • Carnis, Jérôme
  • Favre, Luc
  • Rabkin, Eugen
  • Almog, Ehud
  • Oropeza, Freddy, E.
  • Schülli, Tobias, U.
  • Campos, Andrea
  • Micha, Jean-Sébastien
  • Thomas, Olivier
  • Gazit, Nimrod
  • Leake, Steven, J.
  • Wu, Longfei
  • Poloni, Roberta
  • Richard, Marieingrid
  • Gao, Lu
  • Hensen, Emiel, J. M.
  • Labat, Stéphane
  • Kshirsagar, Aseem, Rajan
  • Dupraz, Maxime
  • Arnouts, Sven
  • An, Hongyu
  • Zhang, Yue
  • Altantzis, Thomas
  • Weckhuysen, B. M.
  • Bals, Sara
  • Kolmeijer, K. E.
  • Stam, Ward Van Der
  • Figueiredo, Marta Costa
OrganizationsLocationPeople

article

Stabilization Effects in Binary Colloidal Cu and Ag Nanoparticle Electrodes under Electrochemical CO2 Reduction Conditions

  • Hofmann, Jan, P.
  • Arnouts, Sven
  • Wu, Longfei
  • An, Hongyu
  • Zhang, Yue
  • Altantzis, Thomas
  • Weckhuysen, B. M.
  • Bals, Sara
  • Kolmeijer, K. E.
  • Hensen, Emiel, J. M.
  • Stam, Ward Van Der
  • Figueiredo, Marta Costa
Abstract

<p>Nanoparticle modified electrodes constitute an attractive way to tailor-make efficient carbon dioxide (CO2) reduction catalysts. However, the restructuring and sintering processes of nanoparticles under electrochemical reaction conditions not only impedes the widespread application of nanoparticle catalysts, but also misleads the interpretation of the selectivity of the nanocatalysts. Here, we colloidally synthesized metallic copper (Cu) and silver (Ag) nanoparticles with a narrow size distribution (&lt;10%) and utilized them in electrochemical CO2 reduction reactions. Monometallic Cu and Ag nanoparticle electrodes showed severe nanoparticle sintering already at low overpotential of -0.8 V vs. RHE, as evidenced by ex situ SEM investigations, and potential-dependent variations in product selectivity that resemble bulk Cu (14% for ethylene at -1.3 V vs. RHE) and Ag (69% for carbon monoxide at -1.0 V vs. RHE). However, by co-deposition of Cu and Ag nanoparticles, a nanoparticle stabilization effect was observed between Cu and Ag, and the sintering process was greatly suppressed at CO2 reducing potentials (-0.8 V vs. RHE). Furthermore, by varying the Cu/Ag nanoparticle ratio, the CO2 reduction reaction (CO2RR) selectivity towards methane (maximum of 20.6% for dense Cu2.5-Ag1 electrodes) and C2 products (maximum of 15.7% for dense Cu1-Ag1 electrodes) can be tuned, which is attributed to a synergistic effect between neighbouring Ag and Cu nanoparticles. We attribute the stabilization of the nanoparticles to the positive enthalpies of Cu-Ag solid solutions, which prevents the dissolution-redeposition induced particle growth under CO2RR conditions. The observed nanoparticle stabilization effect enables the design and fabrication of active CO2 reduction nanocatalysts with high durability.</p>

Topics
  • nanoparticle
  • Deposition
  • impedance spectroscopy
  • Carbon
  • silver
  • scanning electron microscopy
  • copper
  • durability
  • sintering