Unusual Stability of Acetonitrile-Based Superconcentrated Electrolytes for Fast-Charging Lithium-Ion Batteries

被引:1398
作者
Yamada, Yuki [1 ,2 ]
Furukawa, Keizo [1 ]
Sodeyama, Keitaro [2 ,3 ]
Kikuchi, Keisuke [1 ]
Yaegashi, Makoto [1 ]
Tateyama, Yoshitaka [2 ,3 ,4 ]
Yamada, Atsuo [1 ,2 ]
机构
[1] Univ Tokyo, Dept Chem Syst Engn, Bunkyo Ku, Tokyo 1138656, Japan
[2] Kyoto Univ, ESICB, Nishikyo Ku, Kyoto 6158245, Japan
[3] Natl Inst Mat Sci, Int Ctr Mat Nanoarchitecton MANA, Tsukuba, Ibaraki 3050044, Japan
[4] Japan Sci & Technol Agcy JST, PRESTO, Kawaguchi, Saitama 3330012, Japan
关键词
SURFACE-FILM FORMATION; LI-ION; MOLECULAR-DYNAMICS; GRAPHITE ELECTRODE; INTERCALATION; PSEUDOPOTENTIALS; CAPABILITY; CHALLENGES; SOLVATION; LIQUID;
D O I
10.1021/ja412807w
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
The development of a stable, functional electrolyte is urgently required for fast-charging and high-voltage lithium-ion batteries as well as next-generation advanced batteries (e.g., Li-O-2 systems). Acetonitrile (AN) solutions are one of the most promising electrolytes with remarkably high chemical and oxidative stability as well as high ionic conductivity, but its low stability against reduction is a critical problem that hinders its extensive applications. Herein, we report enhanced reductive stability of a superconcentrated AN solution (>4 mol dm(-3)). Applying it to a battery electrolyte, we demonstrate, for the first time, reversible lithium intercalation into a graphite electrode in a reduction-vulnerable AN solvent. Moreover, the reaction kinetics is much faster than in a currently used commercial electrolyte. First-principle calculations combined with spectroscopic analyses reveal that the peculiar reductive stability arises from modified frontier orbital characters unique to such superconcentrated solutions, in which all solvents and anions coordinate to Li+ cations to form a fluid polymeric network of anions and Li+ cations.
引用
收藏
页码:5039 / 5046
页数:8
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