A novel dimethyl"sulfoxide/1,3-dioxolane based electrolyte for lithium/carbon fluorides batteries with a high discharge voltage plateau

被引:50
作者
Pang, Chengkai [1 ,2 ]
Ding, Fei [2 ]
Sun, Wenbin [2 ]
Liu, Jiaquan [1 ]
Hao, Mingming [2 ]
Wang, Ying [2 ]
Liu, Xingjiang [1 ,2 ]
Xu, Qiang
机构
[1] Tianjin Univ, Sch Chem Engn & Technol, Dept Appl Chem, Tianjin 300072, Peoples R China
[2] Tianjin Inst Power Sources, Natl Key Lab Sci & Technol Power Sources, Tianjin 300384, Peoples R China
关键词
Lithium/Carbon fluorides batteries; Electrolyte; Dimethyl sulfoxide; Energy density; Discharge voltage; LI-CFX BATTERIES; HIGH-ENERGY; PERFORMANCE; DENSITY; 1,3-DIOXOLANE; SOLVATION; SULFOXIDE; MECHANISM; SOLVENTS; CELLS;
D O I
10.1016/j.electacta.2015.06.004
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
A novel dimethyl sulfoxide/1,3-dioxolane (DMSO/1,3-DO) based electrolyte is proposed for lithium/carbon fluorides (Li/CF) batteries to enhance the discharge voltage plateau and energy density. Conductivities of the electrolyte of 1 mol L-1 LiBF4/DMSO+1,3-DO with different volume ratios are not identical, which have a maximum of 14.85 mS cm(-1). From the tests of galvanostatic discharge, the discharge voltage plateau of the Li/CF. battery with an electrolyte of 1 mol L-1 LiBF4/DMSO+1,3-DO (5:5, v:v) can reach 2.69 V at 0.1 C, delivering a maximum discharge capacity of 831 mAh g-, and the highest energy density of 2196 Wh kg(-1). Compared to Li/CF batteries with an electrolyte of 1 mol LiBF4/PC +DME (5:5, v:v), the energy density of Li/CF. batteries with an electrolyte of 1 mol L-1 LiBF4/DMSO+1,3DO (5:5, v:v) has been improved more than 12%. With the help of XRD, SEM, TEM, EIS, FT-IR and GC-MS analysis, the results of this work suggest that DMS0/1,3-DO based electrolyte can significantly improve the discharge performance of Li/CF. batteries and keep a good electrochemical stability during discharge. The main reason for improvement of discharge performance is decreasing of both the overpotential of electrochemical polarization of CF. cathodes during discharge and the overpotential of ohmic polarization by increasing the ion conductivity of electrolyte. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:230 / 237
页数:8
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