4.8 Article

Bifunctional anode catalysts for direct methanol fuel cells

Journal

ENERGY & ENVIRONMENTAL SCIENCE
Volume 5, Issue 8, Pages 8335-8342

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c2ee21455e

Keywords

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Funding

  1. Lundbeck Foundation
  2. US Department of Energy, Basic Energy Sciences, Division of Chemical Sciences
  3. Department of Energy's Office of Biological and Environmental Research located at PNNL
  4. US Department of Energy, Office of Science [DE-AC02-06CH11357, DE-AC05-00OR22725, DE-AC02-05CH11231]
  5. US Department of Energy, Basic Energy Sciences via Stanford Accelerator Laboratory
  6. Center of Excellence (Exzellenzcluster) in Catalysis UNICAT
  7. German National Science Foundation (DFG)
  8. NSF [0955922]
  9. Direct For Mathematical & Physical Scien
  10. Division Of Chemistry [0955922] Funding Source: National Science Foundation

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Using the binding energy of OH* and CO* on close-packed surfaces as reactivity descriptors, we screen bulk and surface alloy catalysts for methanol electro-oxidation activity. Using these two descriptors, we illustrate that a good methanol electro-oxidation catalyst must have three key properties: (1) the ability to activate methanol, (2) the ability to activate water, and (3) the ability to react off surface intermediates (such as CO* and OH*). Based on this analysis, an alloy catalyst made up of Cu and Pt should have a synergistic effect facilitating the activity towards methanol electro-oxidation. Using these two reactivity descriptors, a surface PtCu3 alloy is proposed to have the best catalytic properties of the Pt-Cu model catalysts tested, similar to those of a Pt-Ru bulk alloy. To validate the model, experiments on a Pt(111) surface modified with different amounts of Cu adatoms are performed. Adding Cu to a Pt(111) surface increases the methanol oxidation current by more than a factor of three, supporting our theoretical predictions for improved electrocatalysts.

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