XPS ANALYSIS FOR THE LITHIUM SURFACE IMMERSED IN GAMMA-BUTYROLACTONE CONTAINING VARIOUS SALTS

被引:85
作者
KANAMURA, K
TAMURA, H
SHIRAISHI, S
TAKEHARA, ZI
机构
[1] Division of Energy and Hydrocarbon Chemistry, Graduate School of Engineering, Kyoto University, Sakyo-ku, Kyoto, 606-01, Yoshida-honmachi
关键词
LITHIUM; GAMMA-BUTYROLACTONE; SURFACE REACTION; X-RAY PHOTOELECTRON SPECTROSCOPY (XPS); BATTERY;
D O I
10.1016/0013-4686(93)E0020-M
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Lithium surfaces immersed in gamma-butyrolactone solutions containing salts were analyzed by X-ray photoelectron spectroscopy. The lithium surface before immersion in electrolyte was covered with the native film that consists of Li2CO3, Li2O and LiOH. During the immersion of lithium in electrolyte, the native film reacted with acid in the electrolyte to form lithium halide on the lithium surface. The formation of lithium halide strongly depended on the kind of salt. The reaction rate of the native film in gamma-butyrolactone containing 1.0 mol dm(-3) LiClO4 or LiAsF6 was much less than that in gamma-butyrolactone containing 1.0 mol dm(-3) LiBF4 or LiPF6. The morphology of lithium deposited on the lithium surface immersed in electrolyte for three days was influenced by the surface state of lithium. The film formed on the lithium surface immersed in gamma-butyrolactone containing 1.0 mol dm(-3) LiPF6 was thinner than those immersed in any other electrolytes. The chemical compositions of the lithium surface immersed in gamma-butyrolactone containing 1.0 mol dm(-3) LiPF6 were different from those of the lithium surface immersed in gamma-butyrolactone containing 1.0 mol dm(-3) LiAsF6, LiClO4, or LiBF4. When gamma-butyrolactone containing 1.0 mol dm(-3) LiPF6 was used as electrolyte, dendrite formation was not observed on lithium immersed in the electrolyte for three days.
引用
收藏
页码:913 / 921
页数:9
相关论文
共 30 条
[1]   THE ELECTROCHEMISTRY OF NOBLE-METAL ELECTRODES IN APROTIC ORGANIC-SOLVENTS CONTAINING LITHIUM-SALTS [J].
AURBACH, D ;
DAROUX, M ;
FAGUY, P ;
YEAGER, E .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1991, 297 (01) :225-244
[2]  
AURBACH D, 1990, ELECTROCHIM ACTA, V35, P625, DOI 10.1016/0013-4686(90)87055-7
[3]  
AURBACH D, 1989, J ELECTROCHEM SOC, V136, P1611, DOI 10.1149/1.2096978
[4]   IDENTIFICATION OF SURFACE-FILMS FORMED ON LITHIUM IN PROPYLENE CARBONATE SOLUTIONS [J].
AURBACH, D ;
DAROUX, ML ;
FAGUY, PW ;
YEAGER, E .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1987, 134 (07) :1611-1620
[5]  
AURBACH D, 1991, J ELECTROCHEM SOC, V138, pL6
[6]  
BRUMMER SB, 1980, LITHIUM NONAQUEOUS B, P130
[7]  
BURROWS B, 1958, J ELECTROCHEM SOC, V115, P1164
[8]  
CARLSON TA, 1975, PHOTOELECTRON AUGER, P349
[9]   POLAROMICROTRIBOMETRIC (PMT) AND SPECTROSCOPIC (INFRARED-XPS) STUDY OF FORMATION AND MODIFICATIONS OF FILMS FORMED ON A POLARIZED PLATINUM-ELECTRODE IN THF-LICLO4 MEDIUM .1. CATHODIC POLARIZATION [J].
DUBOIS, JE ;
TOURILLON, G ;
LACAZE, PC .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1978, 125 (08) :1257-1261
[10]   CYCLABILITY OF THE LITHIUM ELECTRODE [J].
GARREAU, M .
JOURNAL OF POWER SOURCES, 1987, 20 (1-2) :9-17