Ionic Liquid Electrolyte for Lithium Metal Batteries: Physical, Electrochemical, and Interfacial Studies of N-Methyl-N-butylmorpholinium Bis(fluorosulfonyl)imide

被引:83
|
作者
Lane, George H. [1 ,2 ]
Bayley, Paul M. [3 ]
Clare, Bronya R. [2 ]
Best, Adam S. [1 ]
MacFarlane, Douglas R. [2 ]
Forsyth, Maria [3 ]
Hollenkamp, Anthony F. [1 ]
机构
[1] CSIRO Energy Technol, Clayton, Vic 3168, Australia
[2] Monash Univ, Sch Chem, Clayton, Vic 3800, Australia
[3] Monash Univ, Dept Mat Engn, Clayton, Vic 3800, Australia
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2010年 / 114卷 / 49期
关键词
SECONDARY BATTERIES; PHYSICOCHEMICAL PROPERTIES; LITHIATED GRAPHITE; SURFACE-CHEMISTRY; SELF-DIFFUSION; TEMPERATURE; SALT; LI; IMIDAZOLIUM; TETRAHYDROFURAN;
D O I
10.1021/jp1054809
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
The ionic liquid (IL) N-methyl-N-butylmorpholinium bis(fluorosulfonyl)imide (C(4)mmor FSI) is examined from physical and electrochemical perspectives. Pulsed field gradient NMR spectroscopy shows that ion diffusivities are low compared with similar, non-ethereal ILs. Ionicity values indicate that above room temperature, less than 50% of ions contribute to conductivity. Lithium cycling in symmetrical cells using a C(4)mmor FSI-based electrolyte is best demonstrated at elevated temperatures. Specific capacities of 130 mAh g(-1) are achieved in a Li-LiFePO4 battery at 85 degrees C. FT-IR spectroscopic investigations of lithium electrodes suggest the presence of alkoxide species in the solid electrolyte interphase (SEI), implying a ring-opening reaction of C(4)mmor with lithium metal. In contrast, the SET derived from N-methyl-N-propylpiperidinium FSI lacks the alkoxide signature but shows signs of alkyl unsaturation, and the activation energy for Li+ transport through this SEI is slightly lower than that for the C(4)mmor-derived SEI Our detailed findings give insight into the capabilities and limitations of rechargeable lithium metal batteries utilizing a C(4)mmor FSI electrolyte.
引用
收藏
页码:21775 / 21785
页数:11
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