材料科学
电解质
钠
电极
原子层沉积
化学工程
离子
接口(物质)
锂离子电池的纳米结构
沉积(地质)
图层(电子)
电化学
无机化学
纳米技术
碳纤维
复合材料
冶金
有机化学
化学
复合数
工程类
沉积物
物理化学
古生物学
毛细管作用
毛细管数
生物
作者
Haiyan Lu,Xiaoyang Chen,Yanlong Jia,Hui Chen,Yunxiao Wang,Xinping Ai,Hanxi Yang,Yuliang Cao
出处
期刊:Nano Energy
[Elsevier BV]
日期:2019-07-15
卷期号:64: 103903-103903
被引量:170
标识
DOI:10.1016/j.nanoen.2019.103903
摘要
Hard carbon has been regarded as one of the most promising anodes for sodium-ion batteries due to its low cost and high reverisble capacity. However, the practical use of hard carbon materials has been hindered by its limited initial Coulombic efficiency (ICE) and cycling stability. Herein, ultrathin Al2O3-coated hard carbon materials are synthesized through direct atomic layer deposition (ALD). When served as an anode in sodium-ion batteries, the optimal Al2O3-coated hard carbon electrode delivers a high reversible capacity (355 mA h g−1), ICE (75%) and superior cycling stability (a capacity retention of 90.7% over 150 cycles) compared with the bare one (260.9 mA h g−1, ICE: 67%, capacity retention: 82.8%). The deposited Al2O3 film as an “artificial solid electrolyte interface (SEI)” on the electrode surface, efficiently suppresses the decomposition of the electrolyte, leading to high ICE and cycling stability. Meanwhile, the Al2O3-coated film reduces interfacial resistance and electrode overpotential, resulting in an increased reversible capacity. A critical thickness (about 2 nm) of Al2O3-artificial SEI is also proposed to meet the requirements to electron and ion transport. Therefore, this work provides a general and straightforward surface modification method to enhance the interface stability of hard carbon anodes for high-performance sodium-ion batteries.
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