4.8 Article

Cobalt and nitrogen codoped ultrathin porous carbon nanosheets as bifunctional electrocatalysts for oxygen reduction and evolution

Journal

CARBON
Volume 141, Issue -, Pages 704-711

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.carbon.2018.09.080

Keywords

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Funding

  1. National Natural Science Foundation of China [U1601206, 51872336, 51702370, 51673219, 51422307]
  2. Leading Scientific, Technical and Innovation Talents of Guangdong Special Support Program [2017TX04C248]
  3. National Program for Support of Top-notch Young Professionals
  4. Fundamental Research Funds for the Central Universities [18lgzd10]
  5. National Key Basic Research Program of China [2014CB932402]
  6. Tip-top Scientific and Technical Innovative Youth Talents of Guangdong Special Support Program [2014TQ01C337]
  7. Science and Technology Program of Guangdong [2017A010103008]

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Development of efficient, low-cost, and durable electrocatalysts for the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) is scientifically and technologically important for the conversion and storage of renewable energy. Herein, cobalt and nitrogen codoped ultrathin porous carbon nanosheet (Co-N-PCN) is developed by directly carbonizing the graphene oxide sandwiched cobalt ion adsorbed polyaniline-co-polypyrrole (PACP) precursors. The nitrogen-rich PACP favors the formation of abundant Co-N-x-C active species, while the 2D ultrathin nanosheet structure ensures the high exposure of the generated Co-N-x-C active sites to the electrolyte. In addition, the sandwiched graphene acts as the conductive backbone to facilitate fast charge transfer and enhance the electrode conductivity. Benefiting from the synergistic effect, the Co-N-PCN presents superior electrocatalytic properties with low overpotentials and favorable kinetics to Pt and RuO2 as a bifunctional electrocatalyst for ORR and OER. Remarkably, the potential difference of OER and ORR (Delta E= E-j=10 - E-1/2) is as low as 0.81 V in 0.1 M KOH, indicating the Co-N-PCN outperforms most of the previously reported bifunctional electrocatalysts. (C) 2018 Elsevier Ltd. All rights reserved.

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