材料科学
原子层沉积
纳米技术
电极
锂(药物)
碳纳米管
纳米管
成核
电池(电)
电化学
图层(电子)
化学工程
化学
功率(物理)
有机化学
物理化学
内分泌学
工程类
物理
医学
量子力学
作者
Keith Gregorczyk,Alexander C. Kozen,Xinyi Chen,Marshall A. Schroeder,Malachi Noked,Anyuan Cao,Liangbing Hu,Gary W. Rubloff
出处
期刊:ACS Nano
[American Chemical Society]
日期:2014-12-17
卷期号:9 (1): 464-473
被引量:63
摘要
Pushing lithium-ion battery (LIB) technology forward to its fundamental scaling limits requires the ability to create designer heterostructured materials and architectures. Atomic layer deposition (ALD) has recently been applied to advanced nanostructured energy storage devices due to the wide range of available materials, angstrom thickness control, and extreme conformality over high aspect ratio nanostructures. A class of materials referred to as conversion electrodes has recently been proposed as high capacity electrodes. RuO2 is considered an ideal conversion material due to its high combined electronic and ionic conductivity and high gravimetric capacity, and as such is an excellent material to explore the behavior of conversion electrodes at nanoscale thicknesses. We report here a fully characterized atomic layer deposition process for RuO2, electrochemical cycling data for ALD RuO2, and the application of the RuO2 to a composite carbon nanotube electrode scaffold with nucleation-controlled RuO2 growth. A growth rate of 0.4 Å/cycle is found between ∼ 210-240 °C. In a planar configuration, the resulting RuO2 films show high first cycle electrochemical capacities of ∼ 1400 mAh/g, but the capacity rapidly degrades with charge/discharge cycling. We also fabricated core/shell MWCNT/RuO2 heterostructured 3D electrodes, which show a 50× increase in the areal capacity over their planar counterparts, with an areal lithium capacity of 1.6 mAh/cm(2).
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