4.8 Article

Secondary-Atom-Assisted Synthesis of Single Iron Atoms Anchored on N-Doped Carbon Nanowires for Oxygen Reduction Reaction

Journal

ACS CATALYSIS
Volume 9, Issue 7, Pages 5929-5934

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acscatal.9b00869

Keywords

single-atom catalysts; Fe-N; carbon nanowire; density functional theory; oxygen reduction

Funding

  1. National Key R&D Program of China [2017YFB0102900]
  2. Research Grant Council of the Hong Kong Special Administrative Region [N_HKUST610/17]
  3. Guangdong Special Fund for Science and Technology Development (Hong Kong Technology Cooperation Funding Scheme) [201704030019, 201704030065]
  4. Shenzhen Science and Technology Innovation Commission [JCYJ20180507183818040]
  5. U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences [DE-AC02-06CH11357]
  6. NIU start-up fund

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The development of efficient Fe-N-C materials enriched with single-atom Fe sites toward the oxygen reduction reaction (ORR) is still a great challenge because Fe atoms are mobile and easily aggregate into nanoparticles during the high-temperature treatment. Herein, we proposed a facile and universal secondary-atom-assisted strategy to prepare atomic iron sites with high density hosted on porous nitrogen-doped carbon nanowires (Fe-NCNWs). The Fe-NCNWs showed an impressive half-wave potential (E-1/2) of 0.91 V and average kinetic current density (J(K)) of 6.0 mA cm(-2) at 0.9 V in alkaline media. They also held a high ORR activity in acidic solution with the E-1/2 of 0.82 V and average J(K) of 8.0 mA cm(-2) at 0.8 V. Density functional theory calculations demonstrated that the high ORR activity achieved is originated from single-atom iron sites that decrease the energy barrier in the reaction path efficiently.

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