碳化
阳极
硫化钴
硫黄
碳纤维
金属有机骨架
硫化物
材料科学
电导率
复合数
化学工程
钴
金属
电极
钠
无机化学
化学
复合材料
冶金
有机化学
电化学
扫描电子显微镜
吸附
物理化学
工程类
作者
Yanchao Wu,Shuming Zhuo,Mi Tang,Yuan Chen,Bo Wang,Shaolong Zhu,Kun Fan,Cheng Jiang,Chengliang Wang
标识
DOI:10.1016/j.jpowsour.2020.228778
摘要
Metal sulfides are one of the most promising anode materials for sodium-ion batteries (SIBs) due to their high theoretical capacity and appropriate electrode potential. However, these materials are still suffering from the low conductivity, large volume change during the charge-discharge process, sluggish reaction kinetics and poor cycle stability. Herein, we report a new strategy to synthesize CoSx-carbon composite (CoSx@C) from a sulfur-rich metal-organic framework for SIBs. The synchronous sulfurization and carbonization facilitated the formation of homogenous composites and the small amount of carbon in the composites significantly enhanced the intrinsic conductivity. As a result, the obtained CoSx@C electrodes showed a high specific capacity of 664 mAh g−1 after 400 cycles at 0.5 A g−1. When the current density increased from 0.2 to 5 A g−1, the capacity only decreased slightly from 653 to 601 mAh g−1, with retention as high as 90%. The capacity and the rate performance outperformed most of the reported cobalt sulfide anodes for SIBs.
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