电解质
电化学
成核
纳米团簇
电化学电池
扫描透射电子显微镜
锂(药物)
玻璃碳
纳米尺度
电池(电)
化学
电极
纳米技术
化学工程
材料科学
透射电子显微镜
循环伏安法
物理化学
有机化学
功率(物理)
内分泌学
工程类
物理
医学
量子力学
作者
Robert L. Sacci,Jennifer M. Black,Nina Balke,Nancy J. Dudney,Karren L. More,Raymond R. Unocic
出处
期刊:Nano Letters
[American Chemical Society]
日期:2015-02-23
卷期号:15 (3): 2011-2018
被引量:199
摘要
The performance characteristics of Li-ion batteries are intrinsically linked to evolving nanoscale interfacial electrochemical reactions. To probe the mechanisms of solid electrolyte interphase (SEI) formation and to track Li nucleation and growth mechanisms from a standard organic battery electrolyte (LiPF6 in EC:DMC), we used in situ electrochemical scanning transmission electron microscopy (ec-S/TEM) to perform controlled electrochemical potential sweep measurements while simultaneously imaging site-specific structures resulting from electrochemical reactions. A combined quantitative electrochemical measurement and STEM imaging approach is used to demonstrate that chemically sensitive annular dark field STEM imaging can be used to estimate the density of the evolving SEI and to identify Li-containing phases formed in the liquid cell. We report that the SEI is approximately twice as dense as the electrolyte as determined from imaging and electron scattering theory. We also observe site-specific locations where Li nucleates and grows on the surface and edge of the glassy carbon electrode. Lastly, this report demonstrates the investigative power of quantitative nanoscale imaging combined with electrochemical measurements for studying fluid-solid interfaces and their evolving chemistries.
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