Controllable Electrochemical Synthesis of Copper Sulfides as Sodium-Ion Battery Anodes with Superior Rate Capability and Ultralong Cycle Life

被引:80
作者
Li, Haomiao [1 ,2 ]
Wang, Kangli [1 ]
Cheng, Shijie [1 ]
Jiang, Kai [1 ,2 ]
机构
[1] Huazhong Univ Sci & Technol, Sch Elect & Elect Engn, State Key Lab Adv Electromagnet Engn & Technol, Wuhan 430074, Hubei, Peoples R China
[2] Huazhong Univ Sci & Technol, Sch Mat Sci & Engn, State Key Lab Mat Proc & Die & Mould Technol, Wuhan 430074, Hubei, Peoples R China
基金
中国博士后科学基金;
关键词
electrochemical synthesis; copper sulfides; sodium-ion battery anodes; high rate capability; long cycle life; HIGH-PERFORMANCE ANODE; CARBON NANOTUBES; PRUSSIAN BLUE; QUANTUM-DOTS; CATHODE; LITHIUM; MICROSPHERES; NANOSHEETS; COMPOSITE; MECHANISM;
D O I
10.1021/acsami.7b19138
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Sodium-ion batteries (SIBs) are prospective alternative to lithium-ion batteries for large-scale energy storage applications, owing to the abundant resources of sodium. Metal sulfides are deemed to be promising anode materials for SIBs due to their low-cost and eco-friendliness. Herein, for the first time, series of copper sulfides (Cu2S, Cu7S4, and Cu7KS4) are controllably synthesized via a facile electrochemical route in KCl-NaCl-Na2S molten salts. The as-prepared Cu2S with micron-sized flakes structure is first investigated as anode of SIBs, which delivers a capacity of 430 mAh g(-1) with a high initial Coulombic efficiency of 84.9% at a current density of 100 mA g(-1). Moreover, the Cu2S anode demonstrates superior capability (337 mAh g(-1) at 20 A g(-1), corresponding to 50 C) and ultralong cycle performance (88.2% of capacity retention after 5000 cycles at 5 A g(-1), corresponding to 0.0024% of fade rate per cycle). Meanwhile, the pseudocapacitance contribution and robust porous structure in situ formed during cycling endow the Cu2S anodes with outstanding rate capability and enhanced cyclic performance, which are revealed by kinetics analysis and ex situ characterization.
引用
收藏
页码:8016 / 8025
页数:10
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