| Literature DB >> 23042490 |
Xiao Hua Liu1, Jiang Wei Wang, Shan Huang, Feifei Fan, Xu Huang, Yang Liu, Sergiy Krylyuk, Jinkyoung Yoo, Shadi A Dayeh, Albert V Davydov, Scott X Mao, S Tom Picraux, Sulin Zhang, Ju Li, Ting Zhu, Jian Yu Huang.
Abstract
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.Entities:
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Year: 2012 PMID: 23042490 DOI: 10.1038/nnano.2012.170
Source DB: PubMed Journal: Nat Nanotechnol ISSN: 1748-3387 Impact factor: 39.213