Study of the formation and evolution of solid electrolyte interface via in-situ electrochemical impedance spectroscopy

• Published in: Applied surface science Vol. 596; p. 153572
• Main Authors: Wang, Peng, Yan, De, Wang, Caiyun, Ding, Hao, Dong, Hong, Wang, Jie, Wu, Shumin, Cui, Xiaoling, Li, Chunlei, Zhao, Dongni, Li, Shiyou
• Format: Journal Article
• Language: English
• Published: Elsevier B.V 15.09.2022
• Subjects: Difluoro(Oxalato)borate; Film forming mechanism; In-situ lithium electrochemical impedance spectroscopy; Solid electrolyte interface; In-situ lithium electrochemical impedance spectroscopy; Difluoro(Oxalato)borate; Solid electrolyte interface; Film forming mechanism
• ISSN: 0169-4332; 1873-5584
• DOI: 10.1016/j.apsusc.2022.153572

[Display omitted] •A potential resolved in-situ electrochemical impedance technique was built.•The solid electrolyte interface layer still be formed and decomposed after long cycle.•The contribution of the interface layer compounds to impedance was distinguished. An understanding of the formation and evolution of the solid electrolyte interface (SEI) layer is still a challenge for lithium ion batteries due to its complexity and non-uniformity. Herein, an in-situ electrochemical technique, named potential resolved in-situ electrochemical impedance spectroscopy (PRIs-EIS), have developed to correlate the Nyquist and Bode plot changes with the voltammetric scan, which is then used to determine the correspondence between circuit components and SEI layer composition. Moreover, the formation and re-oxidation of organic compounds in the SEI layer are studied in conjunction with the electrochemical quartz crystal microbalance characteristics. In particular, it is shown that more inorganic compounds accumulate in the SEI layer as the cycle continues, repairing the pore structure, but decreasing the toughness of the SEI layer. The PRIs-EIS technique is shown to be a powerful, useful and cost-effective tool to illuminate the interfacial reaction mechanism, and the results from this technique aid in the evaluation and design of electrolyte systems.