Yin Yanli, Arca Elisabetta, Wang Luning, Yang Guang, Schnabel Manuel, Cao Lei, Xiao Chuanxiao, Zhou Hongyao, Liu Ping, Nanda Jagjit, Teeter Glenn, Eichhorn Bryan, Xu Kang, Burrell Anthony, Ban Chunmei
National Renewable Energy Laboratory, Golden, Colorado 80401, United States.
University of Maryland, College Park, Maryland 20742, United States.
ACS Appl Mater Interfaces. 2020 Jun 10;12(23):26593-26600. doi: 10.1021/acsami.0c03799. Epub 2020 May 29.
A stable solid electrolyte interphase (SEI) has been proven to be a key enabler to most advanced battery chemistries, where the reactivity between the electrolyte and the anode operating beyond the electrolyte stability limits must be kinetically suppressed by such SEIs. The graphite anode used in state-of-the-art Li-ion batteries presents the most representative SEI example. Because of similar operation potentials between graphite and silicon (Si), a similar passivation mechanism has been thought to apply on the Si anode when using the same carbonate-based electrolytes. In this work, we found that the chemical formation process of a proto-SEI on Si is closely entangled with incessant SEI decomposition, detachment, and reparation, which lead to continuous lithium consumption. Using a special galvanostatic protocol designed to observe the SEI formation prior to Si lithiation, we were able to deconvolute the electrochemical formation of such dynamic SEI from the morphology and mechanical complexities of Si and showed that a pristine Si anode could not be fully passivated in carbonate-based electrolytes.
稳定的固体电解质界面(SEI)已被证明是大多数先进电池化学体系的关键促成因素,在这些体系中,电解质与运行超出电解质稳定性极限的阳极之间的反应性必须通过此类SEI在动力学上加以抑制。目前最先进的锂离子电池中使用的石墨阳极就是最具代表性的SEI实例。由于石墨和硅(Si)之间的工作电位相似,因此人们认为在使用相同的碳酸盐基电解质时,类似的钝化机制也适用于硅阳极。在这项工作中,我们发现硅上原生SEI的化学形成过程与SEI的持续分解、脱离和修复紧密纠缠在一起,这导致锂的持续消耗。通过使用一种特殊的恒电流协议来观察硅锂化之前的SEI形成过程,我们能够从硅的形态和机械复杂性中解卷积这种动态SEI的电化学形成过程,并表明原始的硅阳极在碳酸盐基电解质中无法完全钝化。