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Self-supported Pt-CoO networks combining high specific activity with high surface area for oxygen reduction

  • Gustav W. Sievers*
  • , Anders W. Jensen
  • , Jonathan Quinson
  • , Alessandro Zana
  • , Francesco Bizzotto
  • , Mehtap Oezaslan
  • , Alexandra Dworzak
  • , Jacob J.K. Kirkensgaard
  • , Thomas Erik Lyck Smitshuysen
  • , Shima Kadkhodazadeh
  • , Mikkel Juelsholt
  • , Kirsten M.Ø. Jensen
  • , Kirsten Anklam
  • , Hao Wan
  • , Jan Schäfer
  • , Klára Čépe
  • , Maria Escudero Escribano
  • , Jan Rossmeisl
  • , Antje Quade
  • , Volker Brüser
  • Matthias Arenz*
*Corresponding author for this work
  • University of Copenhagen
  • University of Bern
  • University of Oldenburg
  • Leibniz Institute for Plasma Science and Technology
  • Palacký University Olomouc

Research output: Contribution to journalJournal articleResearchpeer-review

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Abstract

Several concepts for platinum-based catalysts for the oxygen reduction reaction (ORR) are presented that exceed the US Department of Energy targets for Pt-related ORR mass activity. Most concepts achieve their high ORR activity by increasing the Pt specific activity at the expense of a lower electrochemically active surface area (ECSA). In the potential region controlled by kinetics, such a lower ECSA is counterbalanced by the high specific activity. At higher overpotentials, however, which are often applied in real systems, a low ECSA leads to limitations in the reaction rate not by kinetics, but by mass transport. Here we report on self-supported platinum-cobalt oxide networks that combine a high specific activity with a high ECSA. The high ECSA is achieved by a platinum-cobalt oxide bone nanostructure that exhibits unprecedentedly high mass activity for self-supported ORR catalysts. This concept promises a stable fuel-cell operation at high temperature, high current density and low humidification.
Original languageEnglish
JournalNature Materials
Volume20
Pages (from-to)208-213
ISSN1476-1122
DOIs
Publication statusPublished - 2021

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