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
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
相关论文
共 53 条
[1]  
[Anonymous], 1975, Introduction to infrared and Raman spectroscopy
[2]   A short review of failure mechanisms of lithium metal and lithiated graphite anodes in liquid electrolyte solutions [J].
Aurbach, D ;
Zinigrad, E ;
Cohen, Y ;
Teller, H .
SOLID STATE IONICS, 2002, 148 (3-4) :405-416
[3]   Recent studies on the correlation between surface chemistry, morphology, three-dimensional structures and performance of Li and Li-C intercalation anodes in several important electrolyte systems [J].
Aurbach, D ;
Zaban, A ;
Ein-Eli, Y ;
Weissman, I ;
Chusid, O ;
Markovsky, B ;
Levi, M ;
Levi, E ;
Schechter, A ;
Granot, E .
JOURNAL OF POWER SOURCES, 1997, 68 (01) :91-98
[4]   THE SURFACE-CHEMISTRY OF LITHIUM ELECTRODES IN ALKYL CARBONATE SOLUTIONS [J].
AURBACH, D ;
EINELY, Y ;
ZABAN, A .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1994, 141 (01) :L1-L3
[5]   IDENTIFICATION OF SURFACE-FILMS FORMED ON LITHIUM IN DIMETHOXYETHANE AND TETRAHYDROFURAN SOLUTIONS [J].
AURBACH, D ;
DAROUX, ML ;
FAGUY, PW ;
YEAGER, E .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1988, 135 (08) :1863-1871
[6]   On the Surface Chemical Aspects of Very High Energy Density, Rechargeable Li-Sulfur Batteries [J].
Aurbach, Doron ;
Pollak, Elad ;
Elazari, Ran ;
Salitra, Gregory ;
Kelley, C. Scordilis ;
Affinito, John .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2009, 156 (08) :A694-A702
[7]  
Balbuena P.B., 2004, Lithium-Ion Batteries: Solid-Electrolyte Interphase
[8]   Transport properties of ionic liquid electrolytes with organic diluents [J].
Bayley, Paul M. ;
Lane, George H. ;
Rocher, Nathalie M. ;
Clare, Bronya R. ;
Best, Adam S. ;
MacFarlane, Douglas R. ;
Forsyth, Maria .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2009, 11 (33) :7202-7208
[9]   Synthesis and characterization of two ionic liquids with emphasis on their chemical stability towards metallic lithium [J].
Bazito, Fernanda F. C. ;
Kawano, Yoshio ;
Torresi, Roberto M. .
ELECTROCHIMICA ACTA, 2007, 52 (23) :6427-6437
[10]   Ionic Liquids with the Bis(fluorosulfonyl) imide Anion: Electrochemical Properties and Applications in Battery Technology [J].
Best, A. S. ;
Bhatt, A. I. ;
Hollenkamp, A. F. .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2010, 157 (08) :A903-A911