纳米线
材料科学
氧化钒
电极
钒
纳米技术
锂(药物)
电化学
纳米线电池
电导
光电子学
氧化物
离子
化学
磷酸钒锂电池
凝聚态物理
物理化学
有机化学
冶金
内分泌学
物理
医学
作者
Liqiang Mai,Yajie Dong,Lin Xu,Chunhua Han
出处
期刊:Nano Letters
[American Chemical Society]
日期:2010-09-10
卷期号:10 (10): 4273-4278
被引量:155
摘要
We report the single nanowire electrode devices designed as a unique platform for in situ probing the intrinsic reason for electrode capacity fading in Li ion based energy storage devices. In this device, a single vanadium oxide nanowire or single Si/a-Si core/shell nanowire was used as working electrode, and electrical transport of the single nanowire was recorded in situ to detect the evolution of the nanowire during charging and discharging. Along with lithium ion intercalation by shallow discharge, the vanadium oxide nanowire conductance was decreased over 2 orders. The conductance change can be restored to previous scale upon lithium ion deintercalation with shallow charge. However, when the nanowire was deeply discharged, the conductance dropped over 5 orders, indicating that permanent structure change happens when too many lithium ions were intercalated into the vanadium oxide layered structures. Different from vanadium oxide, the conductance of a single Si/a-Si core/shell nanowire monotonously decreased along with the electrochemical test, which agrees with Raman mapping of single Si/a-Si nanowire at different charge/discharge states, indicating permanent structure change after lithium ion insertion and extraction. Our present work provides the direct relationship between electrical transport, structure, and electrochemical properties of a single nanowire electrode, which will be a promising and straightforward way for nanoscale battery diagnosis.
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