Cobalt Sulfide Quantum Dot Embedded N/S-Doped Carbon Nanosheets with Superior Reversibility and Rate Capability for Sodium-Ion Batteries.
basic_science · Level V
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- Record sourced from PubMed, PMID 29149553.
- Also identified by DOI 10.1021/acsnano.7b07132.
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Abstract
Metal sulfides are promising anode materials for sodium-ion batteries due to their large specific capacities. The practical applications of metal sulfides in sodium-ion batteries, however, are still limited due to their large volume expansion, poor cycling stability, and sluggish electrode kinetics. In this work, a two-dimensional heterostructure of CoS<sub>x</sub> (CoS and Co<sub>9</sub>S<sub>8</sub>) quantum dots embedded N/S-doped carbon nanosheets (CoS<sub>x</sub>@NSC) is prepared by a sol-gel method. The CoS<sub>x</sub> quantum dots are in situ formed within ultrafine carbon nanosheets without further sulfidation, thus resulting in ultrafine CoS<sub>x</sub> particle size and embedded heterostructure. Meanwhile, enriched N and S codoping in the carbon nanosheets greatly enhances the electrical conductivity for the conductive matrix and creates more active sites for sodium storage. As a result, the hybrid CoS<sub>x</sub>@NSC electrode shows excellent rate capability (600 mAh g<sup>-1</sup> at 0.2 A g<sup>-1</sup> and 500 mAh g<sup>-1</sup> at 10 A g<sup>-1</sup>) and outstanding cycling stability (87% capacity retention after 200 cycles at 1 A g<sup>-1</sup>), making it promising as an anode material for high-performance sodium-ion batteries. A CoS<sub>x</sub>@NSC//Na<sub>0.44</sub>MnO<sub>2</sub> full cell is demonstrated, and it can deliver a specific capacity of 414 mAh g<sup>-1</sup> (based on the mass of CoS<sub>x</sub>@NSC) at a current density of 0.2 A g<sup>-1</sup>.