Ultrathin metal-organic framework nanosheet arrays and derived self-supported electrodes for overall water splitting
The in situ growth of 2D metal-organic framework (MOF) nanosheet arrays on conductive substrates as self-supported electrodes is highly desirable but challenging. Herein, we demonstrate for the first time that the in situ growth of 2D Co-MOF nanosheet arrays on nickel foam can be achieved by a CoO n...
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Veröffentlicht in: | Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2021-10, Vol.9 (39), p.22597-2262 |
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Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The
in situ
growth of 2D metal-organic framework (MOF) nanosheet arrays on conductive substrates as self-supported electrodes is highly desirable but challenging. Herein, we demonstrate for the first time that the
in situ
growth of 2D Co-MOF nanosheet arrays on nickel foam can be achieved by a CoO nanowall template induced strategy ([Co(bimpy) (
p
-bdc) (H
2
O)]
n
, named Co-MOF, bimpy = 2,5-bis(1
H
-imidazol-1-yl)pyridine,
p
-H
2
bdc =
p
-benzene dicarboxylic acid). The subsequent pyrolysis treatment converts the 2D Co-MOF nanosheet arrays into Ni@CoO@Co-MOFC composites, which can be directly applied as a self-supported electrode for electrocatalysis. Remarkably, Ni@CoO@CoMOFC as a promising electrocatalyst exhibits an excellent electrocatalytic performance of 138 and 247 mV for the HER and OER at a current density of 10 mA cm
−2
, which surpasses that of most reported Co/CoO-based electrocatalysts. More importantly, a two-electrode electrolyzer fabricated from Ni@CoO@CoMOFC displays a low overpotential of 1.61 V (
η
10
) toward overall water splitting. This study provides new insights into the development of 2D MOF nanosheet arrays and derived self-supported electrodes with high performance for overall water-splitting.
The
in situ
growth of 2D metal-organic framework (MOF) nanosheet arrays on conductive substrates as self-supported electrodes is highly desirable but challenging. |
---|---|
ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/d1ta06360j |