School of Material Science and Engineering, ‡State Key Laboratory of Luminescent Materials and Devices, and §School of Physics, South China University of Technology , Guangzhou 510640, China.
Langmuir. 2016 Dec 6;32(48):12593-12602. doi: 10.1021/acs.langmuir.6b02870. Epub 2016 Nov 14.
A CoS/C nanocomposite is prepared using a solid-state reaction followed by a facile mechanical ball-milling treatment, with sucrose as the carbon source. The phases, morphologies, and detailed structures of the CoS/C nanocomposite are well-characterized using X-ray diffraction (XRD), X-ray photoelectron spectroscopy, and high-resolution transmission electron microscopy. When evaluated as an anode material for sodium-ion batteries, the CoS/C nanocomposite electrode displays a reversible capacity of ∼567 mA h g in the initial cycle and maintains a reversible capacity of ∼320 mA h g after 30 cycles, indicating a larger capacity and a stable cycling performance. For comparison, the electrochemical performances of CoS and CoS/C samples synthesized using the solid-state reaction are also displayed. The ex situ XRD and transmission electron microscopy tests demonstrate that CoS undergoes a conversion-type sodium storage mechanism.
采用固态反应结合简便的机械球磨处理方法,以蔗糖作为碳源制备了 CoS/C 纳米复合材料。利用 X 射线衍射(XRD)、X 射线光电子能谱和高分辨率透射电子显微镜对 CoS/C 纳米复合材料的物相、形貌和详细结构进行了很好的表征。将 CoS/C 纳米复合材料用作钠离子电池的阳极材料时,其在初始循环中表现出约 567 mA h g 的可逆容量,并且在 30 次循环后保持约 320 mA h g 的可逆容量,表明其具有更大的容量和稳定的循环性能。为了进行比较,还展示了采用固态反应合成的 CoS 和 CoS/C 样品的电化学性能。原位 XRD 和透射电子显微镜测试表明 CoS 经历了转化型钠存储机制。