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Targeted Assembly of Ultrathin NiO/MoS(2) Electrodes for Electrocatalytic Hydrogen Evolution in Alkaline Electrolyte
The development of non-noble metal catalysts for hydrogen revolution in alkaline media is highly desirable, but remains a great challenge. Herein, synergetic ultrathin NiO/MoS(2) catalysts were prepared to improve the sluggish water dissociation step for HER in alkaline conditions. With traditional...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7466591/ https://www.ncbi.nlm.nih.gov/pubmed/32784567 http://dx.doi.org/10.3390/nano10081547 |
Sumario: | The development of non-noble metal catalysts for hydrogen revolution in alkaline media is highly desirable, but remains a great challenge. Herein, synergetic ultrathin NiO/MoS(2) catalysts were prepared to improve the sluggish water dissociation step for HER in alkaline conditions. With traditional electrode assembly methods, MoS(2):NiO-3:1 exhibited the best catalytic performance; an overpotential of 158 mV was required to achieve a current density of 10 mA/cm(2). Further, a synergetic ultrathin NiO/MoS(2)/nickel foam (NF) electrode was assembled by electrophoretic deposition (EPD) and post-processing reactions. The electrode displayed higher electrocatalytic ability and stability, and an overpotential of only 121 mV was needed to achieve a current density of 10 mA/cm(2). The improvement was ascribed to the better catalytic environment, rather than a larger active surface area, a higher density of exposed active sites or other factors. DFT calculations indicated that the hybrid NiO/MoS(2) heterostuctured interface is advantageous for the enhanced water dissociation step and the corresponding lower kinetic energy barrier—from 1.53 to 0.81 eV. |
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