材料科学
电化学
假电容
法拉第效率
碳纤维
电极
电压
兴奋剂
微球
钠
化学工程
纳米技术
储能
电阻率和电导率
复合材料
超级电容器
光电子学
冶金
化学
电气工程
功率(物理)
物理
物理化学
量子力学
复合数
工程类
作者
Wen Chen,Anqi Wang,Dongping Zhang,De Li,Feng Yu,Yong Chen,Liang Wang
标识
DOI:10.1016/j.jallcom.2023.171328
摘要
Currently, transition metal sulfides (TMSs) have attached great attention of researchers due to their various structural types and outstanding electrochemical activities. As one of typical TMSs, CuxS materials owes advantages of abundant reserves, lower material cost, excellent electronic conductivity when applied for sodium ion batteries (SIBs). However, CuxS materials inevitably suffer from the differentiation and volume expansion caused by the transformation reaction, which leads to poor electrochemical performance (especially the inferior cycling stability) in low voltage charge-discharge process. Herein, we utilized a facile way to synthesize Cu1.96S/C hollow microspheres by using a carbon-doped strategy. The Cu1.96S/C electrode was tested with optimized cut-off voltage range, demonstrating a remarkable reversible capacity of 351 mAh g−1 after 1500 cycles at 20 A g−1 current density, along with an average coulombic efficiency close to 100%. The outstanding rate performance and long-term cyclic performance of Cu1.96S/C electrode can be attributed to its carbon doped structure and pseudocapacitance behavior. These findings suggest that Cu1.96S/C composites exhibit the potential to enhance the high-rate capability of SIBs for industrial applications.
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