材料科学
阳极
钠
锡
电池(电)
电极
化学工程
离子
钠离子电池
纳米技术
冶金
化学
法拉第效率
物理化学
功率(物理)
有机化学
工程类
物理
量子力学
作者
Yihang Liu,Yunhua Xu,Yujie Zhu,James N. Culver,Cynthia A. Lundgren,Kang Xu,Chunsheng Wang
出处
期刊:ACS Nano
[American Chemical Society]
日期:2013-03-13
卷期号:7 (4): 3627-3634
被引量:297
摘要
Designed as a high-capacity alloy host for Na-ion chemistry, a forest of Sn nanorods with a unique core–shell structure was synthesized on viral scaffolds, which were genetically engineered to ensure a nearly vertical alignment upon self-assembly onto a metal substrate. The interdigital spaces thus formed between individual rods effectively accommodated the volume expansion and contraction of the alloy upon sodiation/desodiation, while additional carbon-coating engineered over these nanorods further suppressed Sn aggregation during extended electrochemical cycling. Due to the unique nanohierarchy of multiple functional layers, the resultant 3D nanoforest of C/Sn/Ni/TMV1cys, binder-free composite electrode already and evenly assembled on a stainless steel current collector, exhibited supreme capacity utilization and cycling stability toward Na-ion storage and release. An initial capacity of 722 mA·h (g Sn)−1 along with 405 mA·h (g Sn)−1 retained after 150 deep cycles demonstrates the longest-cycling nano-Sn anode material for Na-ion batteries reported in the literature to date and marks a significant performance improvement for neat Sn material as alloy host for Na-ion chemistry.
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