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具有实际参数的碳酸盐电解质中薄锂金属电极的性质

Properties of Thin Lithium Metal Electrodes in Carbonate Electrolytes with Realistic Parameters.

作者信息

Zhang Jian, Shi Jiayan, Wen Xiaoyu, Zhao Yifan, Guo Juchen

机构信息

Program of Materials Science and Engineering, University of California-Riverside, Riverside, California 92521, United States.

Department of Chemical and Environmental Engineering, University of California-Riverside, Riverside, California 92521, United States.

出版信息

ACS Appl Mater Interfaces. 2020 Jul 22;12(29):32863-32870. doi: 10.1021/acsami.0c09730. Epub 2020 Jul 9.

DOI:10.1021/acsami.0c09730
PMID:32584024
Abstract

To understand the baseline performance of lithium (Li) anode in liquid electrolytes, the electrochemical and physical properties of the Li anode are studied with realistic parameters, including thin thickness (50 μm), practical areal capacity (1-4 mA h cm), practical areal current (0.5-2 mA cm), and low electrolyte/capacity ratio. Two different Li salts, lithium hexafluorophosphate (LiPF) and lithium bis(fluorosulfonyl)imide (LiFSI), are used to probe the effects of the electrolyte chemistry and concentration. The cycling of Li/Li symmetric cells, combined with the scanning electron microscopic investigation, demonstrates that the soft-short of Li/Li cells is induced by the continuous volume expansion of Li electrodes during cycling instead of dendrites. The volume change of a Li electrode is dictated by the depth of deposition and stripping (i.e., areal capacity) and the electrolyte/capacity ratio, with no strong correlation with the type of Li salt and concentration. On the other hand, the average Coulombic efficiency (CE) measurement demonstrates inherent correlation with the type of Li salt and its concentration in the electrolyte. Li electrode surface chemical analysis indicates that the fluoride-rich surface layer formed in the LiPF electrolyte can be detrimental to both CE and Li deposition-stripping overpotential.

摘要

为了解锂(Li)负极在液体电解质中的基础性能,采用实际参数研究了Li负极的电化学和物理性质,包括薄厚度(50μm)、实际面积容量(1 - 4 mA h cm)、实际面积电流(0.5 - 2 mA cm)以及低电解质/容量比。使用两种不同的锂盐,六氟磷酸锂(LiPF)和双(氟磺酰)亚胺锂(LiFSI),来探究电解质化学性质和浓度的影响。Li/Li对称电池的循环,结合扫描电子显微镜研究表明,Li/Li电池的软短路是由循环过程中Li电极的持续体积膨胀而非枝晶引起的。Li电极的体积变化由沉积和剥离深度(即面积容量)以及电解质/容量比决定,与锂盐类型和浓度没有强相关性。另一方面,平均库仑效率(CE)测量表明其与锂盐类型及其在电解质中的浓度存在内在相关性。Li电极表面化学分析表明,在LiPF电解质中形成的富含氟化物的表面层可能对CE和Li沉积 - 剥离过电位都不利。

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