阳极
重量分析
材料科学
多孔性
无定形固体
沉积(地质)
制作
化学气相沉积
锂(药物)
化学工程
结晶
电流密度
分析化学(期刊)
矿物学
电极
复合材料
纳米技术
化学
结晶学
替代医学
物理化学
内分泌学
病理
工程类
生物
古生物学
色谱法
医学
有机化学
沉积物
量子力学
物理
作者
Jung‐Ho Lee,Kei Hasegawa,Toshiyuki Momma,Tetsuya Ōsaka,Suguru Noda
标识
DOI:10.1016/j.jpowsour.2015.04.024
摘要
We report micrometre-thick porous Si–Cu anodes that are rapidly co-deposited on Cu current collectors in 1 min. This rapid deposition is realized by heating Si and Cu powders to ∼2000 °C and elevating their vapour pressures, while the porous and amorphous anode structure is realized by keeping the substrates at 100 °C. The films spontaneously form a 2–4.5-μm-thick composition gradient that changes from a Cu-rich region at the bottom to a Si-rich region at the top of the film, because of the higher vapour pressure for Cu than Si. A small addition of 5 wt% Cu to the Si source enhances the cycle performance of the film remarkably in a half-cell test, yielding a gravimetric capacity of 1250 mAh gfilm−1, a volumetric capacity of 1956 mAh cmfilm−3, and an areal capacity of 0.96 mAh cmanode−2 at the 100th cycle. However, excess addition of Cu causes partial Si crystallization in the films, which results in poorer cycle performance. While further improvement is needed, this rapid vapour deposition method yields Si–Cu films with compositional gradients on Cu current collectors in 1 min using inexpensive and safe Si and Cu powder sources, and is attractive for practical Si-based anode fabrication.
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