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使用液体电池电解质的模型硅阳极上固体电解质界面的长期孔隙率

Long term porosity of solid electrolyte interphase on model silicon anodes with liquid battery electrolytes.

作者信息

Grill Jonas, Popovic-Neuber Jelena

机构信息

Department of Energy and Petroleum Engineering, University of Stavanger, Stavanger, Norway.

出版信息

Commun Chem. 2024 Dec 19;7(1):297. doi: 10.1038/s42004-024-01381-2.

Abstract

A stable solid electrolyte interphase (SEI) is of great importance for battery electrodes in terms of cycling as well as for its shelf life. While SEI formation on silicon anodes is generally only studied after the first charge and discharge of cells and initial reaction of electrolyte, we show the formation of a liquid/solid SEI in symmetric cells with silicon electrodes in contact with carbonate and glyme-based electrolytes under close to open circuit conditions and its behavior during long-term ageing. Activation energies of SEIs were measured via temperature-dependent electrochemical impedance spectroscopy (EIS) to study the contribution of liquid/solid phases to ion transport. The effect of different solvents, salts, their concentrations, and final water content of the glyme-electrolyte on the SEI was studied in detail. SEIs formed in cells with glyme-based electrolytes are generally more porous than the ones in cells with carbonate-based electrolytes. The addition of vinylene carbonate to glyme electrolyte is shown to be beneficial for its SEI, as it causes lower and more stable SEI resistances over time. A small amount of water in glyme electrolytes causes a denser SEI without much change in SEI resistance.

摘要

稳定的固体电解质界面(SEI)对于电池电极的循环性能及其储存寿命都非常重要。虽然通常仅在电池首次充放电以及电解质发生初始反应后才研究硅阳极上SEI的形成,但我们展示了在接近开路条件下,含硅电极与碳酸盐和基于甘醇二甲醚的电解质接触的对称电池中液体/固体SEI的形成及其在长期老化过程中的行为。通过温度相关的电化学阻抗谱(EIS)测量SEI的活化能,以研究液体/固体相对离子传输的贡献。详细研究了不同溶剂、盐、其浓度以及甘醇二甲醚电解质的最终含水量对SEI的影响。在含基于甘醇二甲醚电解质的电池中形成的SEI通常比含碳酸盐基电解质的电池中的SEI孔隙率更高。向甘醇二甲醚电解质中添加碳酸亚乙烯酯对其SEI有益,因为随着时间推移,它会导致更低且更稳定的SEI电阻。甘醇二甲醚电解质中少量的水会导致形成更致密的SEI,而SEI电阻变化不大。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82b9/11659429/843ed1bd9345/42004_2024_1381_Fig1_HTML.jpg

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