4.8 Article

Cobalt/Molybdenum Phosphide and Oxide Heterostructures Encapsulated in N-Doped Carbon Nanocomposite for Overall Water Splitting in Alkaline Media

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 11, 期 7, 页码 6890-6899

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.8b15653

关键词

metal phosphides; overall water splitting; N-doped carbon; nanowires; synergistic effects

资金

  1. NSFC [21576288, 91127040, 21173269, 21573286, U1662104]
  2. Science Foundation of China University of Petroleum, Beijing [2462015YQ0304]
  3. Specialized Research Fund for the Doctoral Program of Higher Education [20130007110003]
  4. Ministry of Science and Technology of China [2011BAK15B05]
  5. Open Fund of the State Key Laboratory of Chemical Resource Engineering, Beijing

向作者/读者索取更多资源

The development of designing and searching inexpensive electrocatalysts with high activity for both hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) is significant to enable water splitting as a future renewable energy source. Herein, we synthesize a new CoP(MoP)-CoMoO3 heterostructure coated by a N-doped carbon shell [CoP(MoP)-CoMoO3@CN] via thermal decomposition and phosphatizing of the CoMoO4.0.9H(2)O nanowires encapsulated in N-doped carbon. At 10 mA.cm(-2), this CoP(MoP)-CoMoO3@CN nanocomposite exhibits superior electrocatalytic activity at low overpotentials of 296 mV for OER and 198 mV for HER in alkaline media. More importantly, we achieve a current density of 10 mA.cm(-2) at 1.55 V by using this CoP(MoP)-CoMoO3@CN as both cathode and anode for overall water splitting. This promising performance could be due to the high activity of CoP(MoP)-CoMoO3 and the good conductivity of the external mesoporous N-carbon shell, which makes the CoP(MoP)-CoMoO3@CN nanowires a competitive alternative to noble-metal-based catalysts for water splitting.

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