4.7 Article

Highly microporous nitrogen doped graphene-like carbon material as an efficient fuel cell catalyst

Journal

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume 42, Issue 31, Pages 19903-19912

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2017.06.017

Keywords

Micropore; Nitrogen doped graphene-like carbon material; Electrocatalyst; Oxygen reduction reaction; Fuel cell; Non-platinum catalyst

Funding

  1. National Natural Science Foundation of China [21476104, 21676135]
  2. Joint Funds of the National Natural Science Foundation and Liaoning of China [U1508202]
  3. Natural Science Foundation for Distinguished Young Scholars of Jiangsu Province [BK20150009]
  4. PAPD of Jiangsu Higher Education Institutions
  5. Qing Lan Project of Jiangsu Province
  6. Six Talent Peaks Program of Jiangsu Province
  7. Fundamental Research Funds for the Central Universities, China

Ask authors/readers for more resources

Nitrogen-doped carbon materials are known to be promising candidates as oxygen reduction reaction electrocatalysts used in fuel cells. However, developing metal-free catalysts with high performance and stability still remains a big challenge. Herein we report a new route by using the Maillard reaction, to caramelize ribose in a dispersing salt matrix, followed by carbonization of this caramel to synthesize metal-free catalysts. This catalytic material has the morphology of microporous nitrogen doped graphene-like carbon, and a highest surface area of 1261 m(2) g(-1) with a large amount of micropores. Such microporous structure offers numerous defects that generate a large number of reactive sites. As a result, when used as the cathode materials in fuel cells, the fuel cell shows a high power density of 547 mW cm(-2) under 1.0 atm back pressure with good stability with only 12.5% loss after 250 h. Such catalyst has good performance in the class of metal-free oxygen reduction reaction catalysts, and is possible for commercial use. (C) 2017 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.

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