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In Situ Measurement of Solid Electrolyte Interphase Evolution on Silicon Anodes Using Atomic Force Microscopy

机译:原子力显微镜硅阳极固体电解质差异转化的原位测量

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摘要

In situ measurements of the growth of solid electrolyte interphase (SEI) layer on silicon and the lithiation-induced volume changes in silicon in lithium ion half-cells are reported. Thin film amorphous silicon electrodes are fabricated in a configuration that allows unambiguous separation of the total thickness change into contribution from SEI thickness and silicon volume change. Electrodes are assembled into a custom-designed electrochemical cell, which is integrated with an atomic force microscope. The electrodes are subjected to constant potential lithiation/delithiation at a sequence of potential values and the thickness measurements are made at each potential after equilibrium is reached. Experiments are carried out with two electrolytes-1.2 M lithium hexafluoro-phosphate (LiPF6) in ethylene carbonate (EC) and 1.2 M LiPF6 in propylene carbonate (PC)-to investigate the influence of electrolyte composition on SEI evolution. It is observed that SEI formation occurs predominantly during the first lithiation and the maximum SEI thickness is approximate to 17 and 10 nm respectively for EC and PC electrolytes. This study also presents the measured Si expansion ratio versus equilibrium potential and charge capacity versus equilibrium potential; both relationships display hysteresis, which is explained in terms of the stress-potential coupling in silicon.
机译:据报道,原位测量硅上的固体电解质间(SEI)层的生长及锂离子半电池中硅中的锂诱导的体积变化。薄膜非晶硅电极以配置的构造制造,该构造允许将总厚度的明确分离变为来自SEI厚度和硅容积变化的贡献。电极组装成定制设计的电化学电池,其与原子力显微镜集成在一起。在达到达到平衡后,电极经受恒定潜在的锂电层/脱位,并且在达到平衡后,在每个电位下进行厚度测量。实验用两个电解质-1.2M六氟 - 磷酸锂(LIPF6)在碳酸亚乙酯(EC)和1.2M LiPF6中进行 - 研究电解质组合物对SEI演化的影响。观察到,SEI形成主要在第一锂化期间主要发生,并且对于EC和PC电解质,最大SEI厚度分别近似为17和10nm。本研究还提出了测量的Si膨胀比与平衡电位和充电容量相比平衡势;这两种关系显示滞后,这就是硅中的应力势耦合而解释的。

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