4.8 Article

Uniform Fe3O4/Nitrogen-Doped Mesoporous Carbon Spheres Derived from Ferric Citrate-Bonded Melamine Resin as an Efficient Synergistic Catalyst for Oxygen Reduction

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 9, Issue 1, Pages 335-344

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.6b11608

Keywords

ammonium ferric citrate; nitrogen-doped carbon matrices; iron oxides; mesoporous structure; oxygen reduction reaction

Funding

  1. Innovation Foundation of Huazhong University of Science and Technology Innovation Institute [2015ZZGH010, 2015TS150]
  2. National Natural Science Foundation of China [21401060]
  3. Research Fund for the Doctoral Program of Higher Education of China [20130142120024]

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Developing a facile strategy to synthesize an efficient and inexpensive catalyst for the oxygen reduction reaction (ORR) is critical to the commercialization of many sustainable energy storage and conversion techniques. Herein, a novel and convenient strategy was presented to prepare Fe3O4 embedded into nitrogen-doped mesoporous carbon spheres (Fe3O4/N-MCS) by the polycondensation between methylolmelamines and ammonium ferric citrate (AFC) and subsequent pyrolysis process. In particular, the polycondensation reaction was completely finished within a very short time (6.5 min), and the iron, contents can be adjusted and had a:great influence on the-microstructure. Moreover, the Fe3O4/N-MCS can be used as a robust catalyst for the ORR in alkaline media, and the catalyst with the iron content of 3.35 wt % exhibited excellent electrochemical performance in terms of more positive onset potential (E-0 = 1.036 V vs RHE) and half-wave potential (E-1/2 = 0.861 V) and much better methanol tolerance and long-term durability, in comparison with that of 20% Pt/C. The remarkable performance was ascribed to the characteristics of large specific surface area, mesoporous structure, high contents of pyridinic N and graphitic N, as well as strong electronic interaction between Fe3O4 and protective N-doped graphitic layers.

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