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%

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Publications (5/5 displayed)

  • 2023(Keynote) Insight into Carbon Corrosion of Different Carbon Supports for Pt-Based Electrocatalysts for Polymer Electrolyte Fuel Cells from Interfacial Perspectivecitations
  • 2023(Keynote) Insight into Carbon Corrosion of Different Carbon Supports for Pt-Based Electrocatalysts for Polymer Electrolyte Fuel Cells from Interfacial Perspectivecitations
  • 2023The 2022 applied physics by pioneering women: a roadmap3citations
  • 2022(Invited) Impact of Pore Morphology and Surface Hydrophobicity of the Carbon Matrix on the Macrokinetics of the Oxygen Reduction Reaction Performance for Atomically Dispersed Fe-N-C Catalystscitations
  • 2020Evolution of Ionomer Coverage during Accelerated Stress Tests in Polymer Electrolyte Fuel Cellscitations

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Perego, Andrea
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  • Perego, Andrea
  • Asset, Tristan
  • Qi, Yongzhen
  • Avid, Arezoo
  • Odgaard, Madeleine
  • Atanassov, Plamen
  • Saha, Prantik
  • Yildirim, Hakan
  • Gao, Ziliang
  • Chen, Celine H.
  • Huang, Ying
  • Khedekar, Kaustubh
  • Chen, Celine
  • Mamania, Divija Nitin
  • Liu, Yuanchao
  • Jaouen, Frederic
  • Murphy, Eamonn
  • Mamania, Divija N.
  • Schlueter, Debbie
  • Yildrim, Hakan
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document

Evolution of Ionomer Coverage during Accelerated Stress Tests in Polymer Electrolyte Fuel Cells

  • Perego, Andrea
  • Qi, Yongzhen
  • Zenyuk, Iryna
  • Avid, Arezoo
  • Odgaard, Madeleine
  • Mamania, Divija N.
  • Schlueter, Debbie
  • Yildrim, Hakan
Abstract

Despite the current readiness level and the market availability of the polymer electrolyte fuel cells (PEFCs) durability is still a technical challenge that the technology, has to resolve to become competitive with internal combustion engines (ICE). In the automotive sector, the ICE engines typically reach lifetimes of more than a decade. In the nearest future PEFCs can become competitive in the medium to heavy-duty vehicles sector, where the space constraints and the power density requirements are more relaxed, but cell lifetime becomes of critical importance for such vehicles, that drive for up to 100,000 miles per year. Accelerated stress tests (ASTs) are used to assess the lifetime of a PEFC in a limited amount of time. the US Drive Fuel Cell Technical Team of the US DOE adopted several protocols targeting specific components of the cell or ageing phenomena (platinum dissolution or carbon corrosion).</jats:p><jats:p>In the PEFC cathode electrode ionomer is added to enable proton transport to the electrocatalyst. Ionomer forms thin films around Pt/C agglomerates. The SO<jats:sub>3</jats:sub><jats:sup>-</jats:sup> groups (from the side chains of PFSA-based polymer ionomers) adsorb onto the platinum surface and reduce its overall specific activity. Additionally, when Nafion ionomer that has crystalline backbone aligns parallel to the catalyst surface it impedes local oxygen transport<jats:sup>1</jats:sup> . Recent study did not show direct correlation between SO<jats:sub>3</jats:sub><jats:sup>-</jats:sup> group coverage and specific mass activity, when the coverage was varied from 0.16 to 0.26<jats:sup>2</jats:sup> . This may be because even with 0.16 coverage Pt has already been ‘poisoned’ and further addition of ionomer can actually have a positive effect enhancing proton accessibility. Understanding the behavior of the ionomer in the electrode and its evolution during the cell lifetime is of great importance, but at the present the literature does not show durability studies focused on this aspect.</jats:p><jats:p>In this contribution, we aim to investigate and understand the coverage of the ionomer on Pt and carbon and SO3- groups adsorption in a PEFC during ASTs. CO stripping and displacement were used to probe the ionomer coverage as described by Garrick et al.<jats:sup>3</jats:sup> Two types of cells were investigated using carbon corrosion AST: the first one with traditional carbon material and the second one with start/stop tolerant catalyst support. While the tolerant support led to small performance decrease and ECSA loss, the cell without start/stop tolerant support saw a sharp decrease in the ionomer coverage in the electrode between 100 and 500 cycles, that corresponded to a considerable loss in polarization. The ECSA was not changed between 100 to 500 cycles indicating that Pt loss was not a reason for polarization decrease and therefore we attribute the cause of the cell failure mainly to the loss of ionomer.</jats:p><jats:p>Catalyst AST was also investigated, and the ionomer coverage was measured both in dry and wet conditions to separate the contribution of the interfaces between platinum/ionomer and platinum/water as in Iden and Ohma work<jats:sup>4</jats:sup>. By comparing the ECSA in dry and wet conditions, we see that while ECSA in wet condition decreases (that corresponds to the total ECSA reachable by protons) the dry ECSA (that considers only the Pt portion contacted by ionomer) remains constant. This behavior, coupled with an ionomer coverage that remains rather constant during the cycling, suggests that Pt dissolution is accelerated in the regions where Pt is not covered by ionomer. This work highlights the importance of the ionomer coverage and its evolution during aging. It suggests the role of ionomer is critical for catalyst stability in both carbon corrosion and catalyst ASTs.

Topics
  • density
  • impedance spectroscopy
  • surface
  • polymer
  • Carbon
  • corrosion
  • thin film
  • Oxygen
  • Platinum
  • combustion
  • aging
  • aging