Electronic structural changes of the electrochemically Li-ion deintercalated LiNi0.8Co0.15Al0.05O2 cathode material investigated by X-ray absorption spectroscopy

被引:84
作者
Yoon, Won-Sub [1 ]
Chung, Kyung Yoon [1 ]
McBreen, James [1 ]
Fischer, Daniel A. [2 ]
Yang, Xiao-Qing [1 ]
机构
[1] Brookhaven Natl Lab, Dept Chem, Upton, NY 11973 USA
[2] Natl Inst Stand & Technol, Gaithersburg, MD 20899 USA
关键词
soft X-ray absorption spectroscopy; LiNi0.8Co0.15Al0.05O2; lithium rechargeable batteries; XAS;
D O I
10.1016/j.jpowsour.2007.06.214
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
In situ hard X-ray absorption spectroscopy (XAS) at metal K-edges and soft XAS at 0 K-edge and metal L-edges have been carried out during the first charging process for the layered Li1-xNi0.8Co0.15Al0.05O2 cathode material. The metal K-edge XAS results show that the major charge compensation at the metal site during Li-ion deintercalation is achieved by the oxidation of Ni ions, while the cobalt ions remain mostly unchanged in the Co3+ state. Ni L-II,L-III-edge and O K-edge XAS results in both the fluorescence yield (FY) and partial electron yield (PEY) modes show that substantial amount of Ni ions at the surface of LiNi0.8Co0.15Al0.05O2 powders exist as Ni2+, whereas most of Ni ions in the bulk are in the form of Ni3+. Therefore, if the PEY mode, which is a surface-sensitive technique, is used alone, the interpretation of the results is limited to the surface structures only. In order to get the full picture of both the surface and the bulk, the FY mode and PEY mode should be used simultaneously. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:1015 / 1020
页数:6
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