Fabrication of CoSe2/CoP with rich selenium- and phosphorus-vacancies and heterogeneous interfaces for asymmetric supercapacitors
[Display omitted] •v-CoSe2/CoP with heterogeneous interfaces and rich anionic vacancies is fabricated.•The v-CoSe2/CoP displays a unique honeycomb-like structure.•The heterostructure and Se- and P-vacancies can boost charge transfer kinetics.•An asymmetric SC is assembled by using v-CoSe2/CoP as cat...
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Veröffentlicht in: | Journal of colloid and interface science 2023-12, Vol.651, p.128-137 |
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Format: | Artikel |
Sprache: | eng |
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•v-CoSe2/CoP with heterogeneous interfaces and rich anionic vacancies is fabricated.•The v-CoSe2/CoP displays a unique honeycomb-like structure.•The heterostructure and Se- and P-vacancies can boost charge transfer kinetics.•An asymmetric SC is assembled by using v-CoSe2/CoP as cathode and AC as anode.•Combination of heterostructure with defect engineering might be a feasible strategy.
CoSe2/CoP with rich Se- and P-vacancies and heterogeneous interfaces (v-CoSe2/CoP) is grown on the surface of nickel foam via a two-step strategy: electrodeposition and NaBH4 reduction, which can be used as the cathode material in asymmetric supercapacitors. The SEM characterization reveals the honeycomb-like structure of the v-CoSe2/CoP, and the results of EPR, XPS and HRTEM reveal the existence of anionic vacancies and heterogeneous interfaces in the v-CoSe2/CoP. The as-fabricated v-CoSe2/CoP exhibits high specific capacitance (3206 mF cm−2 at 1.0 mA cm−2) and cyclic stability (91 % capacitance retention after 2000 cycles). An asymmetric supercapacitor is assembled by using the v-CoSe2/CoP and activated carbon (AC) as cathode and anode materials, respectively, which displays a high energy density of 40.6 Wh kg−1 at the power density of 211.5 W kg−1. The outstanding electrochemical performances of the v-CoSe2/CoP might be ascribed to the synergistic effects of Se- and P-vacancies and the heterogeneous interfaces in the v-CoSe2/CoP. |
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ISSN: | 0021-9797 1095-7103 |
DOI: | 10.1016/j.jcis.2023.07.191 |