4.6 Article

Enhanced Catalytic Performance of FeCoNi/N-Doped Carbon Nanospheres as Bifunctional Oxygen Catalysts

Journal

JOURNAL OF THE ELECTROCHEMICAL SOCIETY
Volume 169, Issue 4, Pages -

Publisher

ELECTROCHEMICAL SOC INC
DOI: 10.1149/1945-7111/ac638e

Keywords

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Funding

  1. National Natural Science Foundation of China [52002198, 21776147, 21905153, 61604086]
  2. Chemcloudcomputing of National Supercomputing Center in Shenzhen (Shenzhen Cloud Computing Center)
  3. Malmstrom Endowed Fund at Hamline University

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In this study, iron, cobalt, nickel, and nitrogen doped-carbon nanospheres were synthesized using a microemulsion method. The content and ratio of different metals in the doped carbon material can be adjusted by adding different amounts of metal ions. The multi-doped carbon nanospheres showed improved conductivity, enhanced catalytic properties, and superior performance in oxygen reduction reaction and oxygen evolution reaction compared to singly doped carbon nanospheres. The co-doping of iron, cobalt, nickel, and nitrogen facilitated the combination of metal and nitrogen and improved the conductivity and bifunctional activities of the carbon material.
Iron, cobalt, nickel, and nitrogen doped-carbon nanospheres (FeCoNi/N-C) are synthesized by the pyrolysis of globular Fe/Co/Ni-polypyrrole formed through a microemulsion method. The content and ratio of Fe/Co/Ni in N-C can be adjusted by adding different quantities of metal ions in microemulsion. Compared to Fe/N-C, FeCoNi/N-C demonstrates high conductivity, fast mass transport, superior catalytic properties of the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER). The results showed multi-doping can facilitate the combination of metal and nitrogen and sustain their contents in pyrolysis process to improve conductivity and enhance bifunctional activities. According to the density functional theory calculations, co-doping of Co or/and Ni with Fe element on N-C material can help the desorption of *OH into water in ORR and accelerate the transformation of *O to *OOH in OER. Besides, FeCoNiN4 is a dominant contributor to bifunctional activities. (C) 2022 The Electrochemical Society (ECS). Published on behalf of ECS by IOP Publishing Limited.

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