Effect of Li2CO3 additive on gas generation in lithium-ion batteries

被引:203
作者
Shin, JS
Han, CH
Jung, UH
Lee, SI
Kim, HJ
Kim, K [1 ]
机构
[1] Korea Univ, Div Chem & Mol Engn, Dept Chem, Seoul 136701, South Korea
[2] Korea Univ, Dept Chem Engn, Seoul 136701, South Korea
[3] LG Chem Ltd, Battery Res Ctr, Taejon 305380, South Korea
关键词
Li-ion batteries; additives; gas generation; SEI; Li2CO3;
D O I
10.1016/S0378-7753(02)00039-3
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
To elucidate the mechanism of gas generation during charge-discharge cycling of a lithium-ion cell, the generated gases and passive films on the carbon electrode are examined by means of gas chromatography (GC) and Fourier transform infrared (FTIR) spectroscopy. In ethyl carbonate/dimethyl carbonate and ethyl carbonate/diethyl carbonate 1 M LiPF6 electrolytes, the detected gaseous products are CO2, CO, CH4, C2H4, C2H6, etc. The FTIR spectrum of the surface of the carbon electrode shows bands which correspond to Li2CO3, ROCO2Li, (ROCO2Li)(2), and RCO2Li. These results suggest that gas evolution is caused by electrode decomposition, reactive trace impurities, and electrolyte reduction. The surface of the electrode is composed of electrolyte reduction products. When 0.05 M Li2CO3 is added as an electrolyte additive, the total volume of generated gases is reduced, and the discharge capacity and the conductivity of lithium-ions are increased. These results can be explained by a more compact and thin 'solid electrolyte interface' film on the carbon electrode formed by Li2CO3, which effectively prevents solvent co-intercalation and carbon exfoliation. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:47 / 52
页数:6
相关论文
共 29 条
[1]   MIXED ETHER ELECTROLYTES FOR SECONDARY LITHIUM BATTERIES WITH IMPROVED LOW-TEMPERATURE PERFORMANCE [J].
ABRAHAM, KM ;
PASQUARIELLO, DM ;
MARTIN, FJ .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1986, 133 (04) :661-666
[2]   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
[3]   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
[4]   THE STUDY OF ELECTROLYTE-SOLUTIONS BASED ON ETHYLENE AND DIETHYL CARBONATES FOR RECHARGEABLE LI BATTERIES .2. GRAPHITE-ELECTRODES [J].
AURBACH, D ;
EINELI, Y ;
MARKOVSKY, B ;
ZABAN, A ;
LUSKI, S ;
CARMELI, Y ;
YAMIN, H .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1995, 142 (09) :2882-2890
[5]   IMPEDANCE SPECTROSCOPY OF NONACTIVE METAL-ELECTRODES AT LOW POTENTIALS IN PROPYLENE CARBONATE SOLUTIONS - A COMPARISON TO STUDIES OF LI ELECTRODES [J].
AURBACH, D ;
ZABAN, A .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1994, 141 (07) :1808-1819
[6]   THE CORRELATION BETWEEN THE SURFACE-CHEMISTRY AND THE PERFORMANCE OF LI-CARBON INTERCALATION ANODES FOR RECHARGEABLE ROCKING-CHAIR TYPE BATTERIES [J].
AURBACH, D ;
EINELI, Y ;
CHUSID, O ;
CARMELI, Y ;
BABAI, M ;
YAMIN, H .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1994, 141 (03) :603-611
[7]   THE USE OF EQCM FOR THE STUDY OF NONACTIVE METAL-ELECTRODES IN PROPYLENE CARBONATE-LIASF6 SOLUTIONS - SIGNIFICANCE OF THE DATA OBTAINED [J].
AURBACH, D ;
ZABAN, A .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1995, 142 (07) :L108-L111
[8]  
BESENHARD JO, 1993, J POWER SOURCES, V43, P413
[9]   Electrochemical impedance analysis for lithium ion intercalation into graphitized carbons [J].
Chang, YC ;
Sohn, HJ .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2000, 147 (01) :50-58
[10]   CO2 REDUCTION AT PLATINUM, GOLD AND GLASSY-CARBON ELECTRODES IN ACETONITRILE - AN INSITU FTIR STUDY [J].
CHRISTENSEN, PA ;
HAMNETT, A ;
MUIR, AVG ;
FREEMAN, NA .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1990, 288 (1-2) :197-215