Electrochemical AFM Observation of the HOPG Edge Plane in Ethylene Carbonate-Based Electrolytes Containing Film-Forming Additives

被引:34
作者
Domi, Yasuhiro [1 ]
Ochida, Manabu [1 ]
Tsubouchi, Shigetaka [1 ]
Nakagawa, Hiroe [1 ]
Yamanaka, Toshiro [1 ]
Doi, Takayuki [1 ]
Abe, Takeshi [2 ]
Ogumia, Zempachi [1 ]
机构
[1] Kyoto Univ, Off Soc Acad Collaborat Innovat, Kyoto 6110011, Japan
[2] Kyoto Univ, Grad Sch Engn, Nishikyo Ku, Kyoto 6158510, Japan
关键词
LITHIUM-ION BATTERIES; GRAPHITE NEGATIVE ELECTRODE; ORIENTED PYROLYTIC-GRAPHITE; ATOMIC-FORCE MICROSCOPY; SURFACE-REACTIONS; INTERCALATION; SOLVENT; ROUGHNESS; SULFITE; SLOPE;
D O I
10.1149/2.059208jes
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The effects of film-forming additives in electrolyte solutions on the formation of a surface film on edge plane pyrolytic graphite electrodes in lithium ion batteries were investigated by electrochemical atomic force microscopy (AFM). Surface films were formed at around 1.2 V through reductive decomposition of the additives including vinyl ethylene carbonate. The thickness of the surface films, ca. 20 nm, was less than half of that for an electrolyte with no additives, and remained unchanged after the second potential cycle. Most of the surface films could be scraped off by repeated scanning of the surface in contact-mode AFM. However, a very thin surface layer, which was in close contact with the edge plane, remained even after repeated scans by AFM. No precipitate was observed on the scraped part in the subsequent potential cycle, indicating that the remaining thin surface layer could act effectively as a passivating film for the edge plane graphite electrode. Such a passivating surface layer was found to be formed uniformly over the entire surface of the edge plane. These results clearly indicate that surface films with high passivation ability can be effectively formed on the edge plane during the initial cycle by the presence of film-forming additives in electrolytes. (C) 2012 The Electrochemical Society. [DOI: 10.1149/2.059208jes] All rights reserved.
引用
收藏
页码:A1292 / A1297
页数:6
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