4.8 Article

Sulfur-Doped Nickel Phosphide Nanoplates Arrays: A Monolithic Electrocatalyst for Efficient Hydrogen Evolution Reactions

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 10, 期 31, 页码 26303-26311

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.8b08068

关键词

hydrogen evolution reaction; electrocatalysis; sulfur-doping; nickle phosphosulfides; density functional theory

资金

  1. National Natural Science Foundation of China [21633008, 21733004]
  2. CAS [XDA09030104]
  3. Jilin Province Science and Technology Development Program [20140203012SF, 20160622037JC, 20170520150JH]
  4. Recruitment Program of Foreign Experts [WQ20122200077]
  5. Hundred Talents Program of Chinese Academy of Sciences

向作者/读者索取更多资源

Searching for cost-efficient electrocatalysts with high catalytic activity and stability for hydrogen generation by means of water electrolysis would make a great improvement on energy technologies field. Herein, we report high-performance hydrogen evolution reaction (HER) electrocatalysts based on sulfur-doped Ni5P4 nanoplate arrays grown on carbon paper (S-Ni5P4 NPA/CP). This ternary, robust, monolithic S-Ni5P4 NPA/CP exhibits remarkable performance for the HER compared to nickel phosphide and nickel sulfide catalysts. The S-Ni5P4 NPA/CP with similar to 6% S presents the most promising behavior for water electrolysis applications. Specifically, it shows an onset potential of 6 mV, needing overpotentials (eta) of 56 and 104 mV to attain current densities of 10 and 100 mA cm(-2) with a Tafel slope of 43.6 mV dec(-)1. The turnover frequency of 6% S-Ni5P4 NPA/CP is about 0.11 at overpotential of 100 mV, which is ca. 10 and 40 times that of Ni5P4 NPA/CP and NiS2 NPA/CP, respectively. It also shows remarkable stability and durability in 0.5 M H2SO4 solution. The results indicate that S and P tune the electronic properties mutually and produce an active catalyst phase for the HER Furthermore, the density functional theory calculations show that S-Ni5P4 NPA/CP exhibits only 0.04 eV of hydrogen adsorption free energy(Delta G*(H)), which is more suitable than Pt (similar to-0.09 eV). We propose that the S doping not only restrains the surface oxidation and dissolution of S-Ni5P4 NPA/CP in acid solution but also reduces the Delta G*(H). We believe that our work will provide a new strategy to design transition metal phosphide composite materials for practical applications in catalysis and energy fields.

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