In situ X-ray absorption spectroscopic study of Li-rich layered cathode material Li[Ni0.17Li0.2Co0.07Mn0.56]O2

被引:178
作者
Ito, Atsushi [1 ]
Sato, Yuichi [2 ]
Sanada, Takashi [3 ]
Hatano, Masaharu [1 ]
Horie, Hideaki [1 ]
Ohsawa, Yasuhiko [1 ]
机构
[1] Nissan Motor Co Ltd, Nissan Res Ctr, Kanagawa 2378523, Japan
[2] Kanagawa Univ, Fac Engn, Dept Mat & Life Chem, Kanagawa Ku, Yokohama, Kanagawa 2218686, Japan
[3] NISSAN ARC LTD, Kanagawa 2370061, Japan
关键词
Cathode material; Li[Ni0.17Li0.2Co0.07Mn0.56]O-2; In situ X-ray absorption spectroscopy; LOCAL-STRUCTURE; ANOMALOUS CAPACITY; BATTERY CATHODE; LITHIUM; OXIDES; EXTRACTION; LIMN2O4; MN; NI; CO;
D O I
10.1016/j.jpowsour.2010.09.105
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
Although Li-rich solid-solution layered materials Li2MnO3-LiMO2 (M = Co, Ni, etc.) are expected as large capacity lithium insertion cathodes, the fundamental charge-discharge reaction mechanism of these materials is not clear. Therefore the change in valence states of Ni, Co and Mn of Li[Ni0.17Li0.2Co0.07Mn0.56]O-2 during charge-discharge was examined in detail using in situ X-ray absorption spectroscopy (XAS), which includes both X-ray absorption near-edge structure (XANES) and extended X-ray absorption fine structure (EXAFS) measurements. Since the Mn K edge shift during charge-discharge was not clear to determine the valence change of Mn, the Mn K pre-edge shift was examined during charge-discharge. In our measurements, only a small shift of the Mn K pre-edge toward lower energy was observed on discharge from 4.8 to 2.0V. This corresponds to a decrease of the Mn valence from 4+ to approximately 3.6+. However, this shift cannot explain the large reversible capacity of this material and thus strongly suggests the participation of oxygen in the reversible charge-discharge reaction of this material. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:6828 / 6834
页数:7
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