4.8 Article

Sustainable Hydrothermal Carbonization Synthesis of Iron/Nitrogen-Doped Carbon Nanofiber Aerogels as Electrocatalysts for Oxygen Reduction

Journal

SMALL
Volume 12, Issue 46, Pages 6398-6406

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/smll.201602334

Keywords

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Funding

  1. National Natural Science Foundation of China [21431006, 21671184]
  2. Foundation for Innovative Research Groups of the National Natural Science Foundation of China [21521001]
  3. National Basic Research Program of China [2014CB931800, 2013CB931800]
  4. Users with Excellence and Scientific Research Grant of Hefei Science Center of CAS [2015HSC-UE007, 2015SRG-HSC038]
  5. Chinese Academy of Sciences [KJZD-EW-M01-1]

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It is urgent to develop new kinds of low-cost and high-performance nonprecious metal (NPM) catalysts as alternatives to Pt-based catalysts for oxygen reduction reaction (ORR) in fuel cells and metal-air batteries, which have been proved to be efficient to meet the challenge of increase of global energy demand and CO2 emissions. Here, an economical and sustainable method is developed for the synthesis of Fe, N codoped carbon nanofibers (Fe-N/CNFs) aerogels as efficient NPM catalysts for ORR via a mild template-directed hydrothermal carbonization (HTC) process, where costeffective biomass-derived d(+)-glucosamine hydrochloride and ferrous gluconate are used as precursors and recyclable ultrathin tellurium nanowires are used as templates. The prepared Fe/N-CNFs catalysts display outstanding ORR activity, i.e., onset potential of 0.88 V and half-wave potential of 0.78 V versus reversible hydrogen electrode in an alkaline medium, which is highly comparable to that of commercial Pt/C (20 wt% Pt) catalyst. Furthermore, the Fe/N-CNFs catalysts exhibit superior long-term stability and better tolerance to the methanol crossover effect than the Pt/C catalyst in both alkaline and acidic electrolytes. This work suggests the great promise of developing new families of NPM ORR catalysts by the economical and sustainable HTC process.

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