4.6 Article

An Fe-N-C electrocatalyst with dense active sites synthesized by expeditious pyrolysis of a natural Fe-N4 macrocyclic complex

Journal

JOURNAL OF MATERIALS CHEMISTRY A
Volume 10, Issue 43, Pages 23001-23007

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2ta03409c

Keywords

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Funding

  1. National Natural Science Foundation of China [22171266]
  2. FJIRSM&IUE Joint Research Fund [RHZX-2019-002]
  3. STS Project [KFJ-STS-QYZD-2021-09-002]

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A highly dispersed Fe-N-C catalyst with dense active sites was successfully synthesized using a simple and rapid pyrolysis method. The catalyst exhibited superior ORR activity in alkaline and acidic environments. When applied in zinc-air batteries and proton exchange membrane fuel cells, the catalyst showed high peak power density.
Platinum group metal (PGM)-free ORR catalysts containing highly dispersed metal-nitrogen sites have been demonstrated as the most promising alternatives to Pt-based catalysts. However, it remains a tremendous challenge to synthesize efficient ORR catalysts with dense active sites expeditiously. Herein, a series of highly dispersive Fe-N-C catalysts derived from N-doped Ketjen Black (N-KJB) and hemin were synthesized by a simple rapid pyrolysis method within 1 min. Benefitting from the spatial confinement effect of N-KJB and high-coordination natural iron source, the highly dispersive Fe is higher than 3 wt% without Fe particle agglomeration. The optimized Fe-KJB-3-60A electrocatalyst exhibits a superior ORR activity with a half-wave potential of 0.90 V in 0.1 M KOH and 0.79 V in 0.1 M HClO4. When used as the cathode catalyst in Zn-air batteries and proton exchange membrane fuel cells, Fe-KJB-3-60A exhibits a maximum peak power density of 251 mW cm(-2) and 348 mW cm(-2), respectively.

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