4.7 Article

Interface engineering: PSS-PPy wrapping amorphous Ni-Co-P for enhancing neutral-pH hydrogen evolution reaction performance

期刊

CHEMICAL ENGINEERING JOURNAL
卷 417, 期 -, 页码 -

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2021.129232

关键词

Transition metals phosphides; Electrodeposition; Interface; Conductivity; Electronic structure

资金

  1. National Natural Science Foundation of China [51871078, 52071119]
  2. Heilongjiang Science Foundation [LH2020B006]

向作者/读者索取更多资源

Transition metal phosphides, specifically PSS-PPy/Ni-Co-P, have been shown to exhibit highly efficient hydrogen evolution reaction performance in neutral-pH electrolyte, with remarkable activity and stability achieved through conductivity, hydrophilicity, and electronic structure optimization. This research paves the way for the design of low-cost, high-efficiency, and stable electrocatalysts for HER in neutral-pH electrolyte.
Transition metal phosphides have shown Pt-like hydrogen evolution reaction (HER) activity in acid and alkaline solution, while their HER performance in neutral-pH is really poor owing to the high resistance and inefficient mass transfer in neutral-pH electrolyte. In this work, the well-arranged core/shell PSS-PPy/Ni-Co-P growing on Cu foil, in which Ni-Co-P is the core and the mixed polymer of pyrrole and sodium polystyrene sulfonate is the shell, has been demonstrated to be a highly efficient electrocatalyst for HER in neutral-pH electrolyte. The PSS-PPy/Ni-Co-P/CF self-supporting electrode was easily synthesized by electrodeposition and chemical deposition at room temperature. According to the experiment and DFT calculation results, PSS-PPy not only improves the conductivity and hydrophilicity of Ni-Co-P, but also optimizes the electronic structure of Ni-Co-P. Thus, the PSSPPy/Ni-Co-P shows remarkable HER activity with only overpotential of 106 and 67 mV at the current density of 10 mA cm(-2) in neutral-pH and alkaline electrolytes, respectively. Furthermore, PSS-PPy/Ni-Co-P has excellent stability in neutral-pH, alkaline electrolytes and even seawater. The current surface modification method directs us to design more low-cost, high-efficiency and stable electrocatalysts for HER in neutral-pH electrolyte.

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