4.7 Article

Ketjen black carbon supported CoO@Co-N-C nanochains as an efficient electrocatalyst for oxygen evolution

Journal

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume 43, Issue 51, Pages 22942-22948

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2018.10.142

Keywords

CoO@Co-N-C; Ketjen black carbon; Electrocatalyst; Oxygen evolution reaction; Synergistic effect

Funding

  1. National Natural Science Foundation of China [51874359, 21171174, 21505035]
  2. Hunan Provincial Science and Technology Plan Project [2016TP1007, 2017TP1001]

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We demonstrate an extremely facile in-situ pyrolysis followed by the reduction of partial Co2+ route to synthesize novel Ketjen black carbon (KB) supported CoO@Co-N-C (denoted as CoO@Co-NC/KB) nanochains using KB, urea and cobalt (II) acetate as co-precursors. The as-prepared CoO@Co-NC/KB displays higher electrocatalytic activity, smaller Tafel slope and better durability for the oxygen evolution reaction than those of the benchmark commercial RuO2 catalyst in 1.0 M KOH solution, far outperforming the control groups (i.e. CoO@Co-g-C3N4/KB, Co-NC/KB, CoO-NC/KB, CoO@Co/KB, CoO@Co-NC and Co3O4-NC/KB). The remarkable electrocatalytic performance of CoO@Co-NC/KB is primarily credited to the synergistic effect between Co and CoO species with a core-shell structure, increased active sites and considerably enhanced electronic conductivity. (C) 2018 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.

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