Cobalt and oxygen double doping induced C@MoS-CoS-O@C nanocomposites with an improved electronic structure and increased active sites as a high-performance anode for sodium-based dual-ion batteries
A cobalt-doping induced heterogeneous structure of MoS 2 -CoS 2 grown on one-dimensional tubular carbon (ODTC) has been synthesized. The CoS 2 nanoparticles can inhibit the free growth of MoS 2 nanosheets and obtain a MoS 2 -CoS 2 heterostructure with an ultra-small size, which improves the electron...
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Veröffentlicht in: | Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2022-05, Vol.1 (19), p.1651-1661 |
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Zusammenfassung: | A cobalt-doping induced heterogeneous structure of MoS
2
-CoS
2
grown on one-dimensional tubular carbon (ODTC) has been synthesized. The CoS
2
nanoparticles can inhibit the free growth of MoS
2
nanosheets and obtain a MoS
2
-CoS
2
heterostructure with an ultra-small size, which improves the electronic conductivity of the electrode material affected by the internal electric field. Furthermore, oxygen-incorporated C@MoS
2
-CoS
2
accompanied by a double carbon coating process can add active sites, provide a buffer layer and further improve the electronic conductivity of the electrode material, which overcomes the shortcomings of intrinsic low electronic conductivity and structural instability of MoS
2
. Serving as an anode material for sodium ion batteries, the C@MoS
2
-CoS
2
-O@C nanocomposites show superior sodium storage performance with high capacity (466.1 mA h g
−1
at 1 A g
−1
after 200 cycles) and excellent rate capability. And the sodium dual-ion full batteries deliver a reversible discharge capacity of 182.2 mA h g
−1
at 1 A g
−1
over the voltage range of 1.0-4.4 V after 1000 cycles.
Cobalt and oxygen double doping induced C@MoS
2
-CoS
2
-O@C nanocomposites has been synthesized. The special structure improves electronic structure, increases active sites and possesses superior electrochemical performance. |
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ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/d2ta00971d |