4.6 Article

Highly active and stable electrocatalyst of Ni2P nanoparticles supported on 3D ordered macro-/mesoporous Co-N-doped carbon for acidic hydrogen evolution reaction

Journal

JOURNAL OF MATERIALS CHEMISTRY A
Volume 6, Issue 26, Pages 12751-12758

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c8ta03672a

Keywords

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Funding

  1. National Natural Science Foundation of China [21676018, 51172014, 21622601]
  2. State Key Laboratory of Organic-Inorganic Composites [oic-201601003]
  3. China Postdoctoral Science Foundation [2017M610864]

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The development of highly efficient and stable non-precious metal electrocatalysts to substitute Pt for the hydrogen evolution reaction (HER) is significant for hydrogen-based energy technologies. Herein, we fabricated Ni2P nanoparticles supported on 3D ordered macro-/mesoporous Co-N-doped carbon (Ni2P/OMM-CoN-C) and applied it as a robust HER electrocatalyst under strong acidic conditions. In the as-prepared Ni2P/OMM-CoN-C, ultrafine Ni2P nanoparticles with size of 3-5 nm are evenly distributed in the mesopore walls of the carbon matrix. The Ni2P/OMM-CoN-C catalyst exhibits excellent HER electrocatalytic performance with distinctly low overpotential of 68 mV at 10 mA cm(-2), small Tafel slope of 37 mV dec(-1), and excellent long-term stability, rendering it as a very promising substitute for the Pt catalyst. The superior catalytic performance of Ni2P/OMM-CoN-C could be ascribed to the synergetic effect of the highly dispersed active Ni2P nanoparticles and the porous Co-N-doped carbon support with 3D hierarchical architecture consisting of ordered interconnected macropores and mesopores, which offers the distinct advantages of highly exposed active sites, high-efficiency mass transport, and great electronic conductivity.

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