Investigation into the Activity of Heteropolyacids Towards the Oxygen Reduction Reaction on PEMFC Cathodes

Ronald J. Stanis, Mei Chen Kuo, Adam J. Rickett, John A. Turner, Andrew M. Herring

Research output: Contribution to journalArticlepeer-review

52 Scopus Citations

Abstract

A total of 18 heteropolyacids (HPAs) were investigated to determine their activity as non-Pt oxygen reduction reaction (ORR) catalysts in polymer electrolyte membrane fuel cell cathodes (PEMFCs). Polarization curves, cyclic voltammetry and impedance spectroscopy determined that, of the HPAs tested, only molybdenum based HPAs are active for the ORR and that vanadium substitutions improved the activity. The reduction potentials of the HPAs in the fuel cell environment were determined by cyclic voltammetry. This showed that no activity is seen above 0.55 V, as the catalysts must first be reduced in situ by 4e- before the HPA can reduce oxygen. The potential at which the HPA can be reduced has been determined to be the limiting factor when using these catalysts for ORR in PEMFCs. Power densities of 67 mW/cm2 at 0.2 V were obtained using H5PMo10V2O40. Molybdenum based HPAs were covalently bonded to the carbon achieving mass loadings ∼3× that obtained through adsorption. Using this approach catalyst, performance was improved to 86 mW/cm2 at 0.2 V. The increased loadings did not significantly increase the potentials at which the HPA becomes active for the ORR. We were able to show that MEA degradation, as measured by F- emission rates, using these catalysts are reduced during accelerated testing protocols.

Original languageAmerican English
Pages (from-to)8277-8286
Number of pages10
JournalElectrochimica Acta
Volume53
Issue number28
DOIs
StatePublished - 2008

NREL Publication Number

  • NREL/JA-2A0-44841

Keywords

  • Fuel cell cathode catalyst
  • Heteropolyacid
  • Non-precious metal catalyst
  • Oxygen reduction reaction
  • Proton exchange membrane fuel cell

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