Microscopic Origin of the Solid Electrolyte Interphase Formation in Fire-Extinguishing Electrolyte: Formation of Pure Inorganic Layer in High Salt Concentration

被引:19
作者
Bouibes, Amine [1 ]
Takenaka, Norio [1 ]
Saha, Soumen [1 ,2 ]
Nagaoka, Masataka [1 ,2 ,3 ]
机构
[1] Nagoya Univ, Grad Sch Informat, Chikusa Ku, Furo Cho, Nagoya, Aichi 4648601, Japan
[2] Kyoto Univ, ESICB, Nishikyo Ku, Kyodai Katsura, Kyoto 6158520, Japan
[3] Japan Sci & Technol Agcy, Core Res Evolut Sci & Technol, Kawaguchi, Saitama 3320012, Japan
基金
日本学术振兴会;
关键词
LITHIUM-ION BATTERIES; SOLVENT-CONTAINING ELECTROLYTES; TRIMETHYL PHOSPHATE; FORMATION MECHANISM; DECOMPOSITION; PERFORMANCE; REDUCTION; STABILITY; METAL; FILM;
D O I
10.1021/acs.jpclett.9b02392
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A highly salt-concentrated (HC) electrolyte based on the nonflammable solvent trimethyl-phosphate (TMP) has recently shown an attractive self-extinguishing property in addition to an excellent charge-discharge performance. However, the microscopic understanding of its solid electrolyte interphase (SEI) layer remains an open question. In this Letter, the red moon (RM) method was used to investigate the molecular mechanism of SEI layer formation depending on lithium bis(fluorosulfonyl)amide (LiFSA) salt concentration in a TMP-based electrolyte and was able to reproduce successfully the experimental observations, i.e., the "bottom-up" formation mechanism with a thinner and denser SEI layer mainly based on salt reduction in the HC electrolyte. The results showed that a pure dense inorganic layer is formed in the HC electrolyte, which should considerably improve the SEI layer stability leading to a longer lifetime in charge-discharge performance. This new microscopic finding should provide an important guide in designing an effective nonflammable electrolyte to develop advanced, safe secondary batteries.
引用
收藏
页码:5949 / 5955
页数:8
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