4.6 Article

N-Coordinated cobalt single atom-integrated electrospun nanofibers for an efficient oxygen evolution reaction

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NEW JOURNAL OF CHEMISTRY
卷 47, 期 30, 页码 14177-14184

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ROYAL SOC CHEMISTRY
DOI: 10.1039/d3nj02322b

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The fabrication of N-coordinated cobalt single-atom catalysts (NC-Co-SACs) on a carbon matrix derived from a bimetallic Zn/Co zeolitic imidazole framework is reported. The NC-Co-SACs are integrated into highly conductive cellulose acetate-polyaniline (CP) electrospun nanofibers and exhibit excellent oxygen evolution reaction (OER) efficacy in water splitting. These novel NC-Co-SAC@CP electrospun nanofibers demonstrate superior performance compared to commercial catalysts, highlighting their potential for sustainable energy conversion.
The use of metal single-atom catalysts (SACs) has recently received a lot of attention for achieving an efficient oxygen evolution reaction (OER) in water splitting because of their unique catalytic properties due to unsaturated active sites with maximum atom utilization efficacy. However, designing architectural structures with specific coordination sites to avoid metal cluster formation and stabilization of SACs on a conductive support to overcome the inhomogeneous and slow transportation of ions/molecules is quite challenging. Thus, to overcome this challenge, herein, we report the fabrication of a N-coordinated cobalt SAC (NC-Co-SAC) on a carbon matrix derived from a predesigned bimetallic Zn/Co zeolitic imidazole framework (BM-ZIF). The fabricated NC-Co-SAC was then integrated at the surface of highly conductive cellulose acetate-polyaniline (CP) electrospun nanofibers and was evaluated in terms of its OER efficacy in water splitting. Surprisingly, the designed novel NC-Co-SAC@CP electrospun nanofibers offer lowest overpotential of 320 mV at 10 mA cm(-2) in 1 M KOH and a Tafel slope of 59 mV dec(-1) even much better than those of the commercial IrO2 and RuO2 and most reported non-precious metal catalysts. Additionally, the designed electrode demonstrated exceptional chemical stability, thus opening up more avenues for further exploring efficient noble metal free water splitting electrocatalysts for sustainable energy conversion.

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