电解质
红外线的
傅里叶变换红外光谱
硅
纳米尺度
无定形固体
纳米
材料科学
同步加速器
红外光谱学
分析化学(期刊)
化学工程
化学
纳米技术
电极
光电子学
光学
物理化学
结晶学
有机化学
物理
工程类
复合材料
作者
Andrew Dopilka,Jonathan M. Larson,Robert Kostecki
标识
DOI:10.1021/acsenergylett.4c03255
摘要
The solid electrolyte interphase (SEI) is a critical component in Li-ion batteries; however, its nanoscale structure and composition and unstable nature make it difficult to characterize and ascertain primary functional mechanisms. We use operando nanoscale Fourier transform infrared spectroscopy (nano-FTIR) with a broadband synchrotron IR source to study the SEI formation on a thin-film Si electrode at nanometer-scale spatial resolution as a function of time and voltage. By probing the Si/carbonate electrolyte interface through a 25 nm-thick amorphous Si window/electrode, we detect molecular vibrational modes within a 10s of nanometers region adjacent to the Si surface and observe that PF6– anions react to form LiF at 0.5 V. Spatially resolved nano-FTIR spectra showcase subtle nanoscale heterogeneities in the initial solid/liquid interface and the resulting deposited LiF. With its nanoscale resolution and high chemical specificity, operando nano-FTIR provides unique insights into the dynamics and heterogeneous formation of SEIs and opens opportunities for connecting nanoscale interfacial properties to bulk performance metrics.
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