Sun Jinran, Chen Guodong, Wang Bo, Li Jiedong, Xu Gaojie, Wu Tianyuan, Tang Yongfu, Dong Shanmu, Huang Jianyu, Cui Guanglei
Qingdao Industrial Energy Storage Research Institute, Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Sciences, Qingdao, 266101, Shandong, China.
Shandong Energy Institute, Qingdao, 266101, Shandong, China.
Angew Chem Int Ed Engl. 2024 Aug 19;63(34):e202406198. doi: 10.1002/anie.202406198. Epub 2024 Jul 24.
As a highly promising next-generation high-specific capacity anode, the industrial-scale utilization of micron silicon has been hindered by the issue of pulverization during cycling. Although numerous studies have demonstrated the effectiveness of regulating the inorganic components of the solid electrolyte interphase (SEI) in improving pulverization, the evolution of most key inorganic components in the SEI and their correlation with silicon failure mechanisms remain ambiguous. This study provides a clear and direct correlation between the lithium hydride (LiH) in the SEI and the degree of micron silicon pulverization in the battery system. The reverse lithiation behavior of LiH on micron silicon during de-lithiation exacerbates the localized stress in silicon particles and contributes to particle pulverization. This work successfully proposes a novel approach to decouple the SEI from electrochemical performance, which can be significant to decipher the evolution of critical SEI components at varied battery anode interfaces and analyze their corresponding failure mechanisms.
作为一种极具潜力的下一代高比容量负极材料,微米硅的工业规模应用因循环过程中的粉化问题而受到阻碍。尽管众多研究已证明调节固体电解质界面(SEI)的无机成分在改善粉化方面的有效性,但SEI中大多数关键无机成分的演变及其与硅失效机制的相关性仍不明确。本研究明确了电池系统中SEI中的氢化锂(LiH)与微米硅粉化程度之间的直接关联。脱锂过程中LiH在微米硅上的反向锂化行为加剧了硅颗粒中的局部应力,导致颗粒粉化。这项工作成功提出了一种将SEI与电化学性能解耦的新方法,这对于解读不同电池负极界面处关键SEI成分的演变及其相应的失效机制具有重要意义。