Key Laboratory of the Colloid and Interface Chemistry, Ministry of Education, and School of Chemistry and Chemical Engineering, Shandong University, Jinan, 250100, P.R. China.
Nanoscale. 2018 Feb 8;10(6):2804-2811. doi: 10.1039/c7nr07882j.
Cobalt sulfides are attractive as intriguing candidates for anodes in SIBs and LIBs owing to their unique chemical and physical properties. In this study, a precursor of CoS with a uniform and hollow nanospherical architecture is obtained with a high yield via a mild solvothermal method in the presence of 2-methylimidazole at first. Then, CoS, CoS/C (ultrafine CoS nanoparticles embedded in the shells of the nitrogen-doped porous carbon hollow nanosphere), and CoS@C (CoS nanoparticles entirely covered by an external amorphous carbon layer) were selectively fabricated via direct calcination or PPy coating & calcination of the obtained precursor. CoS/C shows best electrochemical performance than the other two materials as anodes for sodium-ion batteries (SIBs). Besides the excellent rate performance, a high reversible discharge capacity of 320 mA g can be retained after 130 cycles at 1 A g. The impressive performance may be attributed to the unique structure, higher conductivity, and more active sites of CoS/C. In addition, 559 mA h g was maintained after 100 cycles at 500 mA g when the CoS/C composite was applied as an anode in lithium-ion batteries (LIBs). The high reversible capacity, excellent cycle stability combined with the facile synthesis procedure render CoS/C a prospective anode material for rechargeable batteries.
硫化钴由于其独特的化学和物理性质,作为 SIBs 和 LIBs 中阳极的有吸引力的候选材料。在本研究中,首次通过在 2-甲基咪唑存在下的温和溶剂热方法,以高产率获得具有均匀和空心纳米球形结构的 CoS 前体。然后,通过直接煅烧或所得前体的 PPy 涂层和煅烧,选择性地制备了 CoS/C(超细微 CoS 纳米颗粒嵌入氮掺杂多孔碳空心纳米球的壳中)和 CoS@C(CoS 纳米颗粒完全被无定形碳层覆盖)。作为钠离子电池(SIBs)的阳极,CoS/C 比其他两种材料表现出最佳的电化学性能。除了出色的倍率性能外,在 1 A g 下 130 个循环后,还可以保持 320 mA g 的高可逆放电容量。令人印象深刻的性能可能归因于 CoS/C 的独特结构、更高的导电性和更多的活性位点。此外,当 CoS/C 复合材料用作锂离子电池(LIBs)的阳极时,在 500 mA g 下 100 个循环后仍保持 559 mA h g 的容量。高可逆容量、优异的循环稳定性以及简便的合成工艺使 CoS/C 成为可充电电池有前途的阳极材料。