4.8 Article

Structurally ordered intermetallic platinum-cobalt core-shell nanoparticles with enhanced activity and stability as oxygen reduction electrocatalysts

Journal

NATURE MATERIALS
Volume 12, Issue 1, Pages 81-87

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/NMAT3458

Keywords

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Funding

  1. Department of Energy [DE-FG02-87ER45298]
  2. Energy Materials Center at Cornell, an Energy Frontier Research Center
  3. US Department of Energy, Office of Science, Office of Basic Energy Sciences [DE-SC0001086]
  4. Cornell Center for Materials Research, an National Science Foundation Materials Research Science and Engineering Center [DMR-1120296]
  5. American Chemical Society (ACS) Division of Analytical Chemistry
  6. Eastman Chemical Company

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To enhance and optimize nanocatalyst performance and durability for the oxygen reduction reaction in fuel-cell applications, we look beyond Pt-metal disordered alloys and describe a new class of Pt-Co nanocatalysts composed of ordered Pt3Co intermetallic cores with a 2-3 atomic-layer-thick platinum shell. These nanocatalysts exhibited over 200% increase in mass activity and over 300% increase in specific activity when compared with the disordered Pt3Co alloy nanoparticles as well as Pt/C. So far, this mass activity for the oxygen reduction reaction is the highest among the Pt-Co systems reported in the literature under similar testing conditions. Stability tests showed a minimal loss of activity after 5,000 potential cycles and the ordered core-shell structure was maintained virtually intact, as established by atomic-scale elemental mapping. The high activity and stability are attributed to the Pt-rich shell and the stable intermetallic Pt3Co core arrangement. These ordered nanoparticles provide a new direction for catalyst performance optimization for next-generation fuel cells.

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