摘要
Copper sulfide has received widespread attention for application as anode materials in sodium-ion batteries due to their potent capabilitiess and eco-friendly properties. However, it is a challenge to achieve a high rate capability and long cycle stability owing to the heterogeneous transfer of sodium ions during charge-discharge, the interior poor electron conductivity and repeated volumetric expansion of copper sulfide. In this study, Sb-doped copper sulfide hollow nanocubes coated with carbon shells (Sb-CuS@C) was designed and constructed as anode nanomaterials in sodium-ion batteries. Thanks to the intrinsic good electron conductivity and chemical stability of carbon shells, Sb-CuS@C possesses a higher overall electron transfer as anode material, avoids agglomeration and structural destruction during the cycling. As a result, the synthesized Sb-CuS@C achieved an excellent reversible capacity of 595 mA h g−1 after 100 cycles at 0.5 A g−1 and a good rate capability of 340 mA h g−1 at a higher 10 A g−1. DFT calculations clarify that the uniformly doped Sb would act as active sodiophilic nucleation sites to help adsorbing sodium-ion during discharging and leading uniform sodium deposition. This work provides a new insight into the structural and componential modification for common transition-metal sulfides towards application as anode materials in sodium-ion battery.
| 源语言 | 英语 |
|---|---|
| 文章编号 | e202401271 |
| 期刊 | ChemSusChem |
| 卷 | 18 |
| 期 | 2 |
| DOI | |
| 出版状态 | 已出版 - 14 1月 2025 |
指纹
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