4.6 Article

Interfacial dehalogenation-enabled hollow N-doped carbon network as bifunctional catalysts for rechargeable Zn-air battery

Journal

ELECTROCHIMICA ACTA
Volume 247, Issue -, Pages 1044-1051

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.electacta.2017.07.099

Keywords

Dehalogenation; interfacial reaction; carbon network; Zn-air battery

Funding

  1. Natural Science Foundation of China (NSFC)
  2. PetroChina Innovation Foundation
  3. Beijing Natural Science Foundation [2172042]
  4. Beijing Engineering Center for Hierarchical Catalysts
  5. 973 program [2014CB932104]
  6. National Key Research and Development Project [2016YFF0204402]
  7. Program for Changjiang Scholars and Innovative Research Team in the University
  8. Fundamental Research Funds for the Central Universities
  9. Ministry of Finance of PRC
  10. Ministry of Education of PRC

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Promoting oxygen reduction and evolution reactions using effective catalysts hold broad significance for clean energy utilization. In this work, hollow N-doped carbon networks (N-CNs) were fabricated via interfacial dehalogenation of polyvinyl dichloride (PVDC) on 2D CoAl-layered double hydroxide (LDH) with the presence of N source and used as efficient bifunctional catalysts. BET results revealed that as-made N-CNs had very large specific surface area (SSA, 550.4 m(2) g (1) for 900 degrees C-annealed N-CN (N-CN9)) and abundant pore hierarchy. Additionally, interconnected graphitic carbon walls, forming separated cells, can ensure high electrical conductivity, which were formed after acid-leaching of metallic components. Remarkably, N-CN9 showed excellent bifunctional activities towards oxygen reduction and evolution reactions. Moreover, N-CN9 assembled Zn-air battery (ZAB) exhibited an operating voltage of 1.35 V under applied current density of 1.0 mA cm (2), which is highly comparable to that of PtRu/C catalyst. Moreover, due to the pore hierarchy and large SSA, N-CN9-ZAB possessed much better rate capability and cycling stability than that of PtRu/C-ZAB. (C) 2017 Published by Elsevier Ltd.

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