材料科学
电化学
电极
电池(电)
钠离子电池
纳米技术
纳米管
离子
降级(电信)
化学工程
硫化铜
相(物质)
钠
铜
化学
碳纳米管
计算机科学
电信
功率(物理)
物理
有机化学
物理化学
量子力学
法拉第效率
工程类
冶金
作者
Xiangang Zhai,Zicheng Zuo,Zecheng Xiong,Houhe Pan,Xiaoya Gao,Yuliang Li
出处
期刊:2D materials
[IOP Publishing]
日期:2022-03-14
卷期号:9 (2): 025024-025024
被引量:16
标识
DOI:10.1088/2053-1583/ac5d84
摘要
Abstract Copper sulfide (CuS) is emerged as a promising electrode material for Na-ion batteries due to its high theoretical specific capacity, environmental friendliness and abundant resource. However, the conversion type mechanism for storing the Na + causes huge volume variations, irreversible phase changes and disintegration of the structure during charge and discharge processes. These intractable issues lead to the fast capacity degradation, and sluggish reaction kinetics, and performances are hard to fulfill the criteria in practical applications. Herein, the large-scale free-standing CuS nanotube arrays sandwiched by successive graphdiyne (GDY) nanofilm are readily prepared using a simple and efficient strategy. The in-situ protection of GDY nanofilm successfully enhances the structural stability and the network conductivity of the free-standing electrode. The as-obtained CuS electrode protected by GDY exhibits excellent electrochemical sodium storage capability, in the term of long-term reversibility (After 1000 cycles at 2 C, the capacity retention is 78.7%.) and rate performance.
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