4.8 Article

Mesoporous N-Doped Carbons Prepared with Thermally Removable Nanoparticle Templates: An Efficient Electrocatalyst for Oxygen Reduction Reaction

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 137, Issue 16, Pages 5555-5562

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jacs.5b02027

Keywords

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Funding

  1. National Recruitment Program of Global Experts
  2. Fundamental Research Funds for the Central Universities (SCUT) [2013ZM0019]
  3. National Science Foundation [CHE-1265635, DMR-1409396]
  4. Direct For Mathematical & Physical Scien [1409396] Funding Source: National Science Foundation
  5. Direct For Mathematical & Physical Scien
  6. Division Of Chemistry [1265635] Funding Source: National Science Foundation
  7. Division Of Materials Research [1409396] Funding Source: National Science Foundation

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Thermally removable nanoparticle templates were used for the fabrication of self-supported N-doped mesoporous carbons with a trace amount of Fe (Fe-N/C). Experimentally Fe-N/C was prepared by pyrolysis of poly(2-fluoroaniline) (P2FANI) containing a number of FeO(OH) nanorods that were prepared by a one-pot hydrothermal synthesis and homogeneously distributed within the polymer matrix. The FeO(OH) nanocrystals acted as rigid templates to prevent the collapse of P2FANI during the carbonization process, where a mesoporous skeleton was formed with a medium surface area of about 400 m(2)/g. Subsequent thermal treatments at elevated temperatures led to the decomposition and evaporation of the FeO(OH) nanocrystals and the formation of mesoporous carbons with the surface area markedly enhanced to 934.8 m(2)/g. Electrochemical measurements revealed that the resulting mesoporous carbons exhibited apparent electrocatalytic activity for oxygen reduction reactions (ORR), and the one prepared at 800 degrees C (Fe-N/C-800) was the best among the series, with a more positive onset potential (+0.98 V vs RHE), higher diffusion-limited current, higher selectivity (number of electron transfer n > 3.95 at +0.75 V vs RHE), much higher stability, and stronger tolerance against methanol crossover than commercial Pt/C catalysts in a 0.1 M KOH solution. The remarkable ORR performance was attributed to the high surface area and sufficient exposure of electrocatalytically active sites that arose primarily from N-doped carbons with minor contributions from Fe-containing species.

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