Carbide-Supported PtRu Catalysts for Hydrogen Oxidation Reaction in Alkaline Electrolyte

Eliran R. Hamo, Ramesh K. Singh, John C. Douglin, Sian Chen, Mohamed Ben Hassine, Enrique Carbo-Argibay, Shanfu Lu, Haining Wang, Paulo J. Ferreira, Brian A. Rosen*, Dario R. Dekel*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

68 Scopus citations

Abstract

Owing to the sluggish kinetics of the hydrogen oxidation reaction (HOR) in alkaline electrolyte, it is considered a limiting reaction for the development of anion-exchange membrane fuel cell (AEMFC) technology. Studies of alkaline HOR catalysis mainly focus on carbon-supported nanoparticles, which have weak metal-support interactions. In this contribution, we present a unique support based on transition metal carbides (TMCs = Mo2C, Mo2C-TaC, and Mo2C-W2C) for the HOR. PtRu nanoparticles are deposited onto the TMC supports and are characterized by a variety of analytical techniques. The major findings are (i) experimental and theoretical evidence for strong-metal support interaction by both X-ray absorption near-edge structure and density functional theory, (ii) the kinetic current density (jk,s) @25 mV of PtRu/Mo2C-TaC catalyst are 1.65 and 1.50 times higher than that of PtRu/Mo2C and PtRu/Mo2C-W2C, respectively, and (iii) enhanced "tethering"of PtRu nanoparticles on TMC supports. Furthermore, the AEMFC based on the PtRu/Mo2C-TaC anode exhibited a peak power density of 1.2 W cm-2 @70 °C, opening the doors for the development of advanced catalysts based on engineering support materials.

Original languageEnglish
Pages (from-to)932-947
Number of pages16
JournalACS Catalysis
Volume11
Issue number2
DOIs
StatePublished - 15 Jan 2021

Keywords

  • DFT
  • alkaline electrolyte
  • anion-exchange membrane fuel cell
  • carbide supports
  • hydrogen oxidation reaction

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