Porous interconnected NiCo2O4 nanosheets and nitrogen- and sulfur-codoped reduced graphene oxides for high-performance hybrid supercapacitors
We demonstrate a facile hydrothermal synthesis of the interconnected porous NiCo2O4 nanosheets for hybrid supercapacitor applications. The as-synthesized NiCo2O4 nanosheets show a high specific capacitance of 3137 F g−1 at a current density of 2 A g−1, which is much greater than 1916 and 1251 F g−1...
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Veröffentlicht in: | Journal of alloys and compounds 2019-04, Vol.781, p.515-523 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | We demonstrate a facile hydrothermal synthesis of the interconnected porous NiCo2O4 nanosheets for hybrid supercapacitor applications. The as-synthesized NiCo2O4 nanosheets show a high specific capacitance of 3137 F g−1 at a current density of 2 A g−1, which is much greater than 1916 and 1251 F g−1 of Co3O4 and NiO, respectively. Interestingly, the total specific capacitance of the NiCo2O4 is almost close to the sum of the specific capacitance of the NiO and Co3O4. Furthermore, a hybrid supercapacitor is configured with the NiCo2O4 nanosheets and the nitrogen- and sulfur-codoped reduced graphene oxide as the positive and negative electrodes, respectively. This hybrid supercapacitor delivers a maximum energy density of 33.64 W h kg−1 at a power density of 1196 W kg−1 and excellent long-term cyclic stability over 12,000 charge/discharge cycles at the enlarged voltage window of 1.5 V. The remarkable supercapacitive performances of the hybrid device are attributed to the interconnected porous structure of NiCo2O4 nanosheets and three-dimensional continuous macropores of codoped reduced graphene oxides.
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•The interconnected porous NiCo2O4 nanosheets are synthesized.•The NiCo2O4 shows high capacitances of 3137 and 2420 F g−1 at 2 and 20 A g−1.•The HSC consists of NiCo2O4 nanosheets and 3D N,S-rGO.•The HSC delivers a maximum energy density of 33.64 W h kg−1.•The HSC exhibits the outstanding cyclic stability and Coulombic efficiency. |
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ISSN: | 0925-8388 1873-4669 |
DOI: | 10.1016/j.jallcom.2018.12.013 |