Optimization of the lithium-ion cell electrolyte composition through the use of the LiTDI salt

被引:33
作者
Niedzicki, L. [1 ]
Karpierz, E. [1 ]
Bitner, A. [1 ]
Kasprzyk, M. [1 ]
Zukowska, G. Z. [1 ]
Marcinek, M. [1 ]
Wieczorek, W. [1 ]
机构
[1] Warsaw Univ Technol, Fac Chem, PL-00664 Warsaw, Poland
关键词
lithium; LiTDI; conductivity; association; solvent mixture; PC-EC SOLUTIONS; POLYMER ELECTROLYTES; PHASE-DIAGRAMS; LI BATTERIES; CONDUCTIVITY; CARBONATES; VISCOSITY; DEC;
D O I
10.1016/j.electacta.2013.11.134
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Optimization of electrolyte composition for future traction batteries is presented in this paper. Extensive systematic studies of electrochemical performance, material utility and subsequently cost are reported in order to obtain optimal combination. Lithium salt of TDI anion (4,5-dicyano-2-trifluoromethanoimidazole) is used due to its superior thermal stability (compared to other commercially available lithium salts), stability in case of moisture presence, electrochemical stability and possible material savings when used in electrolyte. Critical selection of solvent mixtures is made with respect to the price of components. Conductivity dependence of salt concentration is shown. For all studied systems the increased conductivity region is observed in the salt low and broad concentration range of 0.3 to 0.8 mol kg(-1). The structural and rheological explanation of the mentioned feature is performed. Lithium cation transference numbers are measured for highly conductive samples and used as the secondary parameter in the optimization procedure. The highest values are recorded for the very low salt content: 0.31 mol kg(-1) LiTDI in EC:DMC (1:2 weight ratio) (sigma=5.09 mS cm(-1), t(Li+)= 0.622) and 0.4 mol kg(-1) LiTDI in EC:DMC:DME (8:16:1 weight ratio) (sigma = 6.17 mS cm(-1), t(Li+). = 0.648) giving the opportunity to substantial material savings in batteries. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:224 / 229
页数:6
相关论文
共 25 条
[1]   CHARACTERIZATION OF ETHER ELECTROLYTES FOR RECHARGEABLE LITHIUM CELLS [J].
ABRAHAM, KM ;
GOLDMAN, JL ;
NATWIG, DL .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1982, 129 (11) :2404-2409
[2]  
[Anonymous], 2011, DAVID CO REPORT LITH
[3]  
[Anonymous], 2011, PIKE RES REPORT LITH
[4]   Electrode-solution interactions in Li-ion batteries: a short summary and new insights [J].
Aurbach, D .
JOURNAL OF POWER SOURCES, 2003, 119 :497-503
[5]   FILMING MECHANISM OF LITHIUM-CARBON ANODES IN ORGANIC AND INORGANIC ELECTROLYTES [J].
BESENHARD, JO ;
WINTER, M ;
YANG, J ;
BIBERACHER, W .
JOURNAL OF POWER SOURCES, 1995, 54 (02) :228-231
[6]  
Boukamp B. A., EQUIVALENT CIRCUIT V
[7]   STEADY-STATE CURRENT FLOW IN SOLID BINARY ELECTROLYTE CELLS [J].
BRUCE, PG ;
VINCENT, CA .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1987, 225 (1-2) :1-17
[8]  
Cluzel C., 2012, Cost and performance of EV batteries
[9]   Liquid-solid phase diagrams of ternary and quaternary organic carbonates [J].
Ding, MS .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2004, 151 (05) :A731-A738
[10]   Conductivity and viscosity of PC-DEC and PC-EC solutions of LiBF4 [J].
Ding, MS .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2004, 151 (01) :A40-A47