Exploring Two-Dimensional MOF-Derived Co/Ni Species for Efficient Electrocatalytic Hydrogen Evolution Reaction
Hydrogen evolution reaction (HER) has received a lot of attention due to its promising advantages in producing “green hydrogen” via electrocatalysis with low cost and high efficiency. Until now, developing transition metal-based electrocatalysts for HER has been a great challenge. In this regard, we...
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Veröffentlicht in: | Journal of the Electrochemical Society 2024-11, Vol.171 (11), p.113503 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Hydrogen evolution reaction (HER) has received a lot of attention due to its promising advantages in producing “green hydrogen” via electrocatalysis with low cost and high efficiency. Until now, developing transition metal-based electrocatalysts for HER has been a great challenge. In this regard, we reported a facile strategy to fabricate Co/Ni species encapsulated by carbon structure (CoNi@C) through annealing two-dimensional (2D) metal-organic framework (MOF) nanosheets. The CoNi@C that was prepared under 600 °C achieved the highest catalytic performance in 1.0 M KOH electrolyte with an overpotential of 330 mV to acquire 100 mA cm
−2
. In addition, the effect of KOH concentrations on the HER performance of CoNi@C-600 was explored. In 3.0 M KOH electrolyte, the current density of 100 mA cm
−2
has been attained at a bias potential of 80 mV. The alkaline environment can improve the electrocatalytic performance and further enhance the stability of the as-prepared catalysts. This work would endow promising opportunities for manipulating MOF-based structures through pyrolysis to fabricate highly efficient electrocatalysts.
Fabrication of cobalt and nickel dual-metal catalysts for improved electrocatalytic hydrogen evolution performance.
MOF-derived carbon layers can act as additional charge transfer channels.
The optimal electrocatalytic performance was achieved by CoNi-MOF that annealed at 600 °C.
Developed sensor is validated for practical applications. |
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ISSN: | 0013-4651 1945-7111 |
DOI: | 10.1149/1945-7111/ad8aef |