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原位电势表征揭示聚合物固态锂电池界面降解机理

陈博文a,b, 徐克b, 陈琪a,b,*, 陈立桅c   

  1. a中国科学技术大学 纳米技术与纳米仿生学院 合肥 230026;
    b中国科学院 苏州纳米技术与纳米仿生研究所 创新实验室 苏州 215123;
    c上海交通大学 化学与化工学院 物质科学原位中心 上海 200240
  • 投稿日期:2024-09-09
  • 基金资助:
    项目受苏州市科技项目(Grant No. SSD2023005)资助.

In-situ potential characterization reveals the interface degradation mechanism of solid-state polymer lithium batteries

Chen Bowena,b, Xu Keb, Chen Qia,b,*, Chen Liweic   

  1. aSchool of Nano-Tech and Nano-Bionics, University of Science and Technology of China, Hefei 230026, China;
    bi-Lab, Suzhou Institute of Nano-Tech and Nano-Bionics, Chinese Academy of Sciences, Suzhou 215123, China;
    cIn-situ Center for Physical Sciences, School of Chemistry and Chemical Engineering, Shanghai Jiao Tong University, Shanghai 200240, China)
  • Received:2024-09-09
  • Contact: *E-mail: qchen2011@sinano.ac.cn; Tel.: 0512-62872723
  • Supported by:
    Project supported by the Suzhou Science and Technology Program (Grant No. SSD2023005).

Solid-state polymer electrolyte lithium metal batteries (SPE-LIBs) with high energy density and safety have been widely concerned as the next generation of lithium batteries. In recent years, the ion transport mechanism of SPE has been extensively studied, resulting in a significant increase in its ionic conductivity and lithium transference number. However, SPE has poor cycling stability when used with high-voltage cathodes, limiting its further development. Therefore, it is important to understand the mechanism of battery performance degradation in high-voltage systems. In this work, first, the SPE was prepared by photopolymerization using 1-butyl-3-vinylimidazolium bis((trifluorompropyl)sulfonyl)imide, vinylethylene carbonate and poly(ethylene glycol) diacrylate. The LiFePO4(LFP)||SPE||Li battery was prepared by the in-situ polymerization method. This battery has an initial discharge specific capacity of 159.6 mAh·g-1 at room temperature, and the capacity retention rate reaches 95% after 145 cycles, indicating that the cell has a low interface impedance and the electrolyte has a high ionic conductivity. Then, in-situ Scanning Kelvin Probe Force Microscopy was used to characterize the interfacial potential of the cross-section of batteries with two different cathodes, which was prepared by argon ion beam polishing, during charging. Compared with the LFP cathode, the LiNi0.6Co0.2Mn0.2O2(NCM) cathode with higher electrochemical reaction potential has a greater potential difference between the cathode and the electrolyte after charging. As a result, it indicates that the energy level of high-voltage cathode materials changes greatly during the charging process, which makes the electrolyte materials easy to lose electrons preferentially and cause degradation side reactions. Combined with electrochemical impedance spectroscopy and laser confocal Raman spectroscopy to characterize the interfacial structure of the SPE-LIB. It found that side reactions would destroy the structure of the cathode electrolyte interphase, resulting in a significant increase in the interfacial impedance and the attenuation of the battery capacity. The electrolyte degradation mechanism of SPE-LIBs under high-voltage systems was revealed through in-situ characterization, which provided guidance for improving the cycling stability with the high-voltage cathodes.

Key words: solid-state lithium batteries, solid-state polymer electrolyte, in-situ characterization, scanning probe microscopy, electrolyte degradation