4.6 Article

Atomically dispersed Pt and Fe sites and Pt-Fe nanoparticles for durable proton exchange membrane fuel cells

Journal

NATURE CATALYSIS
Volume 5, Issue 6, Pages 503-512

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41929-022-00796-1

Keywords

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Funding

  1. National Key R&D Program of China [2020YFB1505800]
  2. Shenzhen Science and Technology Innovation Committee [SGDX2019081623340748]
  3. Research Grant Council of the Hong Kong Special Administrative Region [N_HKUST610/17]
  4. Innovation and Technology Commission of the Hong Kong Special Administrative Region [ITC-CNERC14EG03]
  5. Foshan-HKUST Project [FSUST19-FYTRI07]
  6. Southern Marine Science and Engineering Guangdong Laboratory (Guangzhou) [SMSEGL20SC01]
  7. Shenzhen Natural Science Fund [20200925154115001]
  8. US DOE [DE-AC02-06CH11357]
  9. US China Clean Energy Research Center [CERC-CVC2]

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Researchers have designed a hybrid electrocatalyst consisting of atomically dispersed platinum and iron single atoms, as well as platinum-iron alloy nanoparticles. This electrocatalyst exhibits higher activity and durability in proton exchange membrane fuel cells.
Proton exchange membrane fuel cells convert hydrogen and oxygen into electricity without emissions. The high cost and low durability of Pt-based electrocatalysts for the oxygen reduction reaction hinder their wide application, and the development of non-precious metal electrocatalysts is limited by their low performance. Here we design a hybrid electrocatalyst that consists of atomically dispersed Pt and Fe single atoms and Pt-Fe alloy nanoparticles. Its Pt mass activity is 3.7 times higher than that of commercial Pt/C in a fuel cell. More importantly, the fuel cell with a low Pt loading in the cathode (0.015 mg(P)(t) cm(-2)) shows an excellent durability, with a 97% activity retention after 100,000 cycles and no noticeable current drop at 0.6V for over 200 hours. These results highlight the importance of the synergistic effects among active sites in hybrid electrocatalysts and provide an alternative way to design more active and durable low-Pt electrocatalysts for electrochemical devices.

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