4.8 Article

Bimetallic Multi-Level Layered Co-NiOOH/Ni3S2@NF Nanosheet for Hydrogen Evolution Reaction in Alkaline Medium

Journal

SMALL
Volume 18, Issue 43, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/smll.202106904

Keywords

bimetallic catalysts; Co-NiOOH; Ni; S-3; (2); electrocatalysis; hydrogen energy; hydrogen evolution reaction

Funding

  1. National Natural Science Foundation of China [52171078, 51971155]

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The development of efficient non-noble metal catalysts for water splitting is challenging due to the sluggish kinetics of the hydrogen evolution reaction (HER) in alkaline medium. This study reports a bimetallic multi-level layered catalytic electrode with excellent HER electrocatalytic performance in alkaline medium. The electrode exhibits high catalytic activity, stability, and abundant active sites, providing support for the design of high-performance bimetallic electrodes for industrial water splitting.
Development of efficient non-noble metal catalysts for water splitting is of great significance but challenging due to the sluggish kinetics of the hydrogen evolution reaction (HER) in alkaline medium. Herein, a bimetallic multi-level layered catalytic electrode composed of Ni3S2 nanosheets with secondary Co-NiOOH layer of 3D porous and free-standing cathode in alkaline medium is reported. This integrated synergistic catalytic electrode exhibits excellent HER electrocatalytic performance. The resultant Ni0.67Co0.33/Ni3S2@NF electrode displays the highest HER activity with only overpotentials of 87 and 203 mV to afford current densities of 10 and 100 mA center dot cm(-2), respectively, and its Tafel slope is 80 mV center dot dec(-1). The chronopotentiometry operated at high current density of 50 mA center dot cm(-2) shows negligible deterioration, indicating better stability of Ni0.67Co0.33/Ni3S2@NF electrode than Pt/C (20 wt.%). Such a desirable catalytic performance is attributed to the modification of physical and electronic structure that exposes abundant active sites and improves the intrinsic catalytic activity toward HER, which is also confirmed by electrochemically active surface area and X-ray photoelectron spectroscopy analysis. This work provides a strong support for the rational design of high-performance bimetallic electrodes for industrial water splitting.

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