材料科学
阳极
非阻塞I/O
锂(药物)
化学工程
纳米颗粒
纳米技术
锂离子电池
离子
电化学
电池(电)
无机化学
电极
催化作用
化学
物理
工程类
内分泌学
物理化学
医学
功率(物理)
量子力学
有机化学
生物化学
作者
Chanhoon Kim,Ji‐Won Jung,Ki Ro Yoon,Doo-Young Youn,Soojin Park,Il‐Doo Kim
出处
期刊:ACS Nano
[American Chemical Society]
日期:2016-11-15
卷期号:10 (12): 11317-11326
被引量:185
标识
DOI:10.1021/acsnano.6b06512
摘要
The combination of high-capacity and long-term cyclability has always been regarded as the first priority for next generation anode materials in lithium-ion batteries (LIBs). To meet these requirements, the Ag nanoparticle decorated mesoporous SnO2/NiO nanotube (m-SNT) anodes were synthesized via an electrospinning process, followed by fast ramping rate calcination and subsequent chemical reduction in this work. The one-dimensional porous hollow structure effectively alleviates a large volume expansion during cycling as well as provides a short lithium-ion duffusion length. Furthermore, metallic nickel (Ni) nanoparticles converted from the NiO nanograins during the lithiation process reversibly decompose Li2O during delithiation process, which significantly improves the reversible capacity of the m-SNT anodes. In addition, Ag nanoparticles uniformly decorated on the m-SNT via a simple chemical reduction process significantly improve rate capability and also contribute to long-term cyclability. The m-SNT@Ag anodes exhibited excellent cycling stability without obvious capacity fading after 500 cycles with a high capacity of 826 mAh g–1 at a high current density of 1000 mA g–1. Furthermore, even at a very high current density of 5000 mA g–1, the charge-specific capacity remained as high as 721 mAh g–1, corresponding to 60% of its initial capacity at a current density of 100 mA g–1.
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