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
Hauptverfasser: Wang, Yanru, Wang, Ani, Xue, Zhenzhen, Wang, Lei, Li, Xiaoyu, Wang, Guoming
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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