Effects of copper trifluoromethanesulphonate as an additive to propylene carbonate-based electrolyte for lithium-ion batteries

被引:18
作者
Wu, MS [1 ]
Chiang, PCJ [1 ]
Lin, JC [1 ]
Lee, JT [1 ]
机构
[1] Ind Technol Res Inst, Mat Res Labs, Hsinchu 310, Taiwan
关键词
copper trifluoromethanesulphonate additive; propylene carbonate; lithium-ion batteries; electrolyte; AC impedance;
D O I
10.1016/j.electacta.2004.04.029
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Addition of copper trifluoromethanesulphonate (CuTF) to propylene carbonate (PC)-based electrolyte effectively suppresses the cointercalation and decomposition of PC in the mesocarbon microbeads (MCMB) electrodes during the first lithiation process. During the first charging cycle, copper ions are reduced at a higher potential (2 V versus Li/Li+) than the potential of PC cointercalation and decomposition (0.6-0.8 V versus Li/Li+), and predominately form a porous copper layer over the MCMB surface, thereby obstructing PC to cointercalate. An increase in reversible capacity can be achieved by increasing the amount of CuTF. However, above a critical value, the copper layer inhibits the intercalation of lithium ions and lowers the capacity. The AC impedance data reveal that the passivation film and the charge-transfer resistance are both increased when the deposited copper is in excess. An optimum result may be obtained when the addition is approximately 5 wt.%. CuTF is a possibility for PC-based electrolyte additive in lithium-ion batteries. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4379 / 4386
页数:8
相关论文
共 27 条
[1]   THE CATHODIC DECOMPOSITION OF PROPYLENE CARBONATE IN LITHIUM BATTERIES [J].
ARAKAWA, M ;
YAMAKI, JI .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1987, 219 (1-2) :273-280
[2]   Review of selected electrode-solution interactions which determine the performance of Li and Li ion batteries [J].
Aurbach, D .
JOURNAL OF POWER SOURCES, 2000, 89 (02) :206-218
[3]   On the use of vinylene carbonate (VC) electrolyte solutions for Li-ion as an additive to batteries [J].
Aurbach, D ;
Gamolsky, K ;
Markovsky, B ;
Gofer, Y ;
Schmidt, M ;
Heider, U .
ELECTROCHIMICA ACTA, 2002, 47 (09) :1423-1439
[4]   CATHODIC REDUCTION OF GRAPHITE IN ORGANIC SOLUTIONS OF ALKALI AND NR4+ SALTS [J].
BESENHAR.JO ;
FRITZ, HP .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1974, 53 (02) :329-333
[5]   ELECTROCHEMICAL PREPARATION AND PROPERTIES OF IONIC ALKALI METAL- AND NR4-GRAPHITE INTERCALATION COMPOUNDS IN ORGANIC ELECTROLYTES [J].
BESENHARD, JO .
CARBON, 1976, 14 (02) :111-115
[6]   Effect of surface structure on the irreversible capacity of various graphitic carbon electrodes [J].
Chung, GC ;
Jun, SH ;
Lee, KY ;
Kim, MH .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1999, 146 (05) :1664-1671
[7]   ELECTROCHEMICAL DECOMPOSITION OF PROPYLENE CARBONATE ON GRAPHITE [J].
DEY, AN ;
SULLIVAN, BP .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1970, 117 (02) :222-&
[8]   CONDUCTIVITY OF ELECTROLYTES FOR RECHARGEABLE LITHIUM BATTERIES [J].
DUDLEY, JT ;
WILKINSON, DP ;
THOMAS, G ;
LEVAE, R ;
WOO, S ;
BLOM, H ;
HORVATH, C ;
JUZKOW, MW ;
DENIS, B ;
JURIC, P ;
AGHAKIAN, P ;
DAHN, JR .
JOURNAL OF POWER SOURCES, 1991, 35 (01) :59-82
[9]   STUDIES OF LITHIUM INTERCALATION INTO CARBONS USING NONAQUEOUS ELECTROCHEMICAL-CELLS [J].
FONG, R ;
VONSACKEN, U ;
DAHN, JR .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1990, 137 (07) :2009-2013
[10]   Nano-scale copper-coated graphite as anode material for lithium-ion batteries [J].
Guo, K ;
Pan, Q ;
Wang, L ;
Fang, S .
JOURNAL OF APPLIED ELECTROCHEMISTRY, 2002, 32 (06) :679-685