4.8 Article

Scalable preparation of sized-controlled Co-N-C electrocatalyst for efficient oxygen reduction reaction

期刊

JOURNAL OF POWER SOURCES
卷 368, 期 -, 页码 46-56

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.jpowsour.2017.09.067

关键词

Metal-nitrogen-carbon; Catalyst; Nanomaterials; ZIF-67; Oxygen reduction reaction

资金

  1. National Key Research and Development Program of China [2016YFA0200400]
  2. Natural Science Foundation of China [51571100]
  3. Graduate Innovation Fund of Jilin University [2016075]
  4. Specialized Research Fund for the Doctoral Program of Higher Education [20130061110035]

向作者/读者索取更多资源

Heat-treated metal-nitrogen-carbon (M-N-C) materials are emerging as promising non-precious catalysts to replace expensive Pt-based materials for oxygen reduction reaction (ORR) in energy conversion and storage devices. Despite recent progress, their activity and durability are still far from satisfactory. The activity site and particle size are among the most important factors for the ORR activity of M-N-C catalysts. Extensive efforts have been made to reveal the correlation of active site and activity. However, it remains unclear to what extent the particle size will influence the ORR activity of M-N-C materials. Moreover, to the best of our knowledge, controllable synthesis of M-N-C catalysts with high-density activity sites remains elusive. Herein, we develop a straightforward method to produce a mono disperse and size-controlled Co-N-C (Nano-P-ZIF-67) electrocatalyst, and systemically investigate its catalytic mechanisms. Only by optimizing the particle size, Nano-P-ZIF-67 outperforms the commercial 20 wt% Pt/C regarding all evaluating indicators for ORR catalysts in alkaline media including higher catalytic activity, durability, and stronger methanol tolerance. Nano-P-ZIF-67 is assembled into a cell, and the cell shows a power density of 45.5 mW/cm(2), which is the highest value among currently studied cathode catalysts. We expect Nano-P-ZIF-67 to be a highly interesting candidate for the next generation of ORR catalysts. (C) 2017 Elsevier B.V. All rights reserved.

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