Concentrated Electrolytes for Enhanced Stability of Al-Alloy Negative Electrodes in Li-Ion Batteries

被引:31
作者
Chan, Averey K. [1 ,2 ]
Tatara, Ryoichi [3 ,6 ]
Feng, Shuting [4 ]
Karayaylali, Pinar [5 ]
Lopez, Jeffrey [3 ]
Stephens, Ifan E. L. [2 ]
Shao-Horn, Yang [1 ,3 ,5 ]
机构
[1] MIT, Dept Mat Sci & Engn, Cambridge, MA 02139 USA
[2] Imperial Coll London, Dept Mat, Royal Sch Mines Bldg, London SW7 2AZ, England
[3] MIT, Res Lab Elect, Cambridge, MA 02139 USA
[4] MIT, Dept Chem Engn, Cambridge, MA 02139 USA
[5] MIT, Dept Mech Engn, Cambridge, MA 02139 USA
[6] Yokohama Natl Univ, Dept Chem & Biotechnol, Hodogaya Ku, 79-5 Tokiwadai, Yokohama, Kanagawa 2408501, Japan
基金
美国国家科学基金会;
关键词
SUPERCONCENTRATED ELECTROLYTES; PHYSICOCHEMICAL PROPERTIES; ELECTROCHEMICAL REACTIONS; LITHIUM INTERCALATION; TRANSPORT-PROPERTIES; 3-ELECTRODE SETUPS; SOLVENT ACTIVITY; ALUMINUM FOIL; SOLVATION; GRAPHITE;
D O I
10.1149/2.0581910jes
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Replacing graphite with alloying Al negative electrodes would allow for the development of high energy density Li-ion batteries. However, large volume changes associated with the alloying/dealloying process often result in pulverization of the electrode and rapid capacity fade during cycling due to the continuous formation of solid electrolyte interphase (SEI) layers and loss of electronic contact. In this study, we report that increasing salt concentration in the electrolyte to >5 mol dm(-3) led to enhanced capacity retention during cycling of Li-Al half-cells, which was accompanied by nearly constant impedance for the Al electrode in lithium bis(fluorosulfonyl) imide (LiFSI)/dimethyl carbonate (DMC) 1:1.1 (mol/mol) superconcentrated electrolyte. X-ray photoelectron spectroscopy (XPS) revealed that a potential hold in the superconcentrated electrolyte formed an SEI layer with a greater LiF concentration than in standard 1 mol dm(-3) solution. This was supported by Raman spectroscopy of LiFSI solutions in DMC, supplemented with density functional theory calculations, which showed an increased driving force for the reduction of FSI- anions to form LiF from Li+-coordinated DMC complexes with increasing salt concentration. Therefore, the enhanced capacity retention and stability can be attributed to the stability of LiF-rich SEI layers which limit carbonate reduction and charge transfer impedance growth. (c) The Author(s) 2019. Published by ECS.
引用
收藏
页码:A1867 / A1874
页数:8
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