Constructing LiF-Dominated Interphases with Polymer Interwoven Outer Layer Enables Long-Term Cycling of Si Anodes

• Published in: ACS nano Vol. 18; no. 10; pp. 7666 - 7676
• Main Authors: Yang, Yaozong, Wang, Jie, Li, Zhaolin, Yang, Zhao, Wang, Bo, Zhao, Hailei
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 12.03.2024
• Subjects: silicon anode; electrode−electrolyte interphase; trans-difluoroethylene carbonate; lithium-ion battery; electrolyte additive
• ISSN: 1936-0851; 1936-086X
• DOI: 10.1021/acsnano.4c00998

Constructing a robust solid electrolyte interphase (SEI) is extremely critical to developing high-energy-density silicon (Si)-based lithium-ion batteries. However, it is still elusive how to accurately manipulate the chemical composition and structure of the SEI layer. Herein, a LiF-dominated SEI film intertwined by a highly elastic polymer is achieved by regulating the defluorination mechanism of the fluorinated carbonate additive on the Si electrode surface. The experimental and computational results confirm that the decomposition route of trans-difluoroethylene carbonate (DFEC) molecules can be significantly altered in the presence of lithium difluoro­(oxalato)­borate (LiDFOB) additive. The induction of direct defluorination of DFEC step by LiDFOB, as opposed to the breaking of C–O bonds without LiDFOB addition, is crucial in ensuring the exclusive formation of LiF-dominated SEI and maintaining the cyclic structure of DFEC. The defluorinated DFEC easily polymerizes to form poly­(vinylene carbonate), enhancing the elasticity of the SEI. The resulting LiF-dominated SEI film with a polymer interwoven outer layer shows enhanced ionic conductivity and mechanical stability, which can effectively accelerate electrode reaction kinetics and maintain the structural stability of the Si electrode. As a result, the Si electrode with the electrolyte containing the designed dual-additive exhibits superior cycling stability and excellent rate performance, delivering a high reversible capacity of 1487.3 mAh g–1 after 1000 cycles at 2 A g–1.