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Strong Activity Changes Observable during the First Pretreatment Cycles of Trimetallic PtNiMo/C Catalysts

  • Bilal Danisman
  • , Gui Rong Zhang
  • , Adrian F. Baumunk
  • , Juntao Yang
  • , Olaf Brummel
  • , Philipp Darge
  • , Karl J.J. Mayrhofer
  • , Jörg Libuda
  • , Marc Ledendecker
  • , Bastian J.M. Etzold
  • Technische Universität Darmstadt
  • Tianjin Polytechnic University
  • Friedrich-Alexander Universitat Erlangen-Nurnberg (FAU)
  • Forschungszentrum Jülich (FZJ)

Research output: Contribution to journalArticlepeer-review

7 Scopus citations

Abstract

Pt-based alloy catalysts supported on carbon are commonly characterized for oxygen reduction reaction (ORR) activity using the rotating disk electrode technique (RDE). Within this study, we show exemplarily for PtNiMo/C catalysts that the applied pretreatment influences strongly the determined activity. The classically employed descriptor of unchanged cyclic voltammetry response is insufficient to portrait completed surface restructuring, and gives an incorrect impression that stable activity can be determined. This might be one of the reasons for the strongly deviating activities reported in literature. Following the changes in activity during pretreatment also with in-situ FTIR and online dissolution measurements gives insights to an up to now largely overseen high activity of the trimetallic catalysts. A maximum activity of 0.57 mA cmPt−2 at 0.95 VRHE is reached quickly during the first six cycles and decreases slowly subsequently. The maximum activity and change of activity over the cycle number is affected by the scan rate and electrolyte refreshing, while the gas atmosphere plays only a minor role. This exemplary study might be important for Pt alloy catalysts in general.

Original languageEnglish
Article numbere202300109
JournalChemElectroChem
Volume10
Issue number16
DOIs
StatePublished - 14 Aug 2023

Keywords

  • Alloyed Catalyst
  • Cyclic voltammetry
  • Electrochemistry
  • Oxygen Reduction
  • Pretreatment
  • Rotating Disk Electrode

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