LAUSR.org creates dashboard-style pages of related content for over 1.5 million academic articles. Sign Up to like articles & get recommendations!

P-doped CNTs encapsulated nickel hybrids with flower-like structure as efficient catalysts for hydrogen evolution reaction

Photo by saffu from unsplash

Abstract Electrochemical water splitting attracted an increasing attention as a promising approach to produce high-purity hydrogen. Both the design and synthesis of low-cost and high-performance catalysts for hydrogen evolution reaction… Click to show full abstract

Abstract Electrochemical water splitting attracted an increasing attention as a promising approach to produce high-purity hydrogen. Both the design and synthesis of low-cost and high-performance catalysts for hydrogen evolution reaction (HER) remain challenging. Herein, an in-situ growth of carbon nanotubes encapsulated Ni particles on nickel foam is described. This catalyst is synthesized via a one-step chemical vapor deposition (CVD) at different temperatures followed by P-doping treatment (P-doped Ni@CNTs/NF). The corresponding physicochemical and electrochemical results illustrate that the P-doped Ni@CNTs/NF prepared at 600 °C with flower-like structure exhibits excellent activity and stability for HER in acidic electrolytes. In 0.5 M H2SO4 aqueous solution, the sample shows a small overpotential value of −135.2 mV to achieve a current density of −10 mA cm−2, which also displays acceptable long-term stability for lasting 20 h. This work provides a facile approach to prepare a cost-effective catalyst with high efficiency and might promote further study of the transition metal catalysts for hydrogen evolution in acid environments.

Keywords: evolution reaction; doped cnts; flower like; hydrogen evolution; catalysts hydrogen

Journal Title: Electrochimica Acta
Year Published: 2019

Link to full text (if available)


Share on Social Media:                               Sign Up to like & get
recommendations!

Related content

More Information              News              Social Media              Video              Recommended



                Click one of the above tabs to view related content.