Binder-free hybrid cobalt-based sulfide/oxide nanoarrays toward enhanced energy storage performance for hybrid supercapacitors
Cobalt-based materials have excellent electrochemical properties in theory and show great potential for improving the energy density of supercapacitors. The facile synthesis strategy and enhanced energy storage performance of self-supported cobalt-based sulfide/oxide nanoarrays (Co-S/Co-O) are demon...
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Veröffentlicht in: | Journal of energy storage 2023-07, Vol.63, p.106979, Article 106979 |
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Sprache: | eng |
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Zusammenfassung: | Cobalt-based materials have excellent electrochemical properties in theory and show great potential for improving the energy density of supercapacitors. The facile synthesis strategy and enhanced energy storage performance of self-supported cobalt-based sulfide/oxide nanoarrays (Co-S/Co-O) are demonstrated for hybrid supercapacitors in this work. In the Co-S/Co-O nanoarrays, the CoS sulfide and CoO oxide are intertwined with each other to form a whole, bringing positive synergistic effect for Faraday reaction and rapid electrons/ions transfer. As expected, Co-S/Co-O has higher specific capacity (1065 C g−1 at 1 A g−1) than CoS (176 C g−1) and CoO (702.5 C g−1). Furthermore, the Co-S/Co-O hybrid supercapacitor assembled with nitrogen-doped graphene as negative electrode shows higher specific capacitance (110 F g−1 at 1 A g−1) and specific energy (39.38 Wh kg−1 at a specific power of 800 W kg−1). The results show that Co-S/Co-O hybrid materials have great potential for energy storage applications. This work also provides a good strategy for improving the charge storage capacity of cobalt-based materials.
•The nanoarrays integrate the advantages of CoS and CoO.•The combination of Co-S/Co-O brings synergistic effect for Faraday reaction.•High capacity of 1065 C g−1 and good rate capability are demonstrated.•Co-S/Co-O hybrid supercapacitor shows a high specific energy of 39.38 Wh kg−1.•It provides a strategy for enhancing the energy storage of Co-based materials. |
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ISSN: | 2352-152X 2352-1538 |
DOI: | 10.1016/j.est.2023.106979 |