原子单位
材料科学
硅
电化学
锂(药物)
透射电子显微镜
电极
无定形固体
非晶硅
纳米技术
图层(电子)
化学工程
结晶学
晶体硅
光电子学
化学
物理化学
工程类
医学
物理
量子力学
内分泌学
作者
Xiao Hua Liu,Jiangwei Wang,Shan Huang,Feifei Fan,Xu Huang,Yang Liu,Sergiy Krylyuk,Jinkyoung Yoo,Shadi A. Dayeh,Albert V. Davydov,Scott X. Mao,S. T. Picraux,Sulin Zhang,Ju Li,Ting Zhu,Jianyu Huang
标识
DOI:10.1038/nnano.2012.170
摘要
In lithium-ion batteries, the electrochemical reaction between the electrodes and lithium is a critical process that controls the capacity, cyclability and reliability of the battery. Despite intensive study, the atomistic mechanism of the electrochemical reactions occurring in these solid-state electrodes remains unclear. Here, we show that in situ transmission electron microscopy can be used to study the dynamic lithiation process of single-crystal silicon with atomic resolution. We observe a sharp interface (~1 nm thick) between the crystalline silicon and an amorphous Li(x)Si alloy. The lithiation kinetics are controlled by the migration of the interface, which occurs through a ledge mechanism involving the lateral movement of ledges on the close-packed {111} atomic planes. Such ledge flow processes produce the amorphous Li(x)Si alloy through layer-by-layer peeling of the {111} atomic facets, resulting in the orientation-dependent mobility of the interfaces.
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