Effects of Na+ contents on electrochemical properties of Li1.2Ni0.13Co0.13Mn0.54O2 cathode materials

被引:56
作者
Qiu, Bao [1 ]
Wang, Jun [1 ]
Xia, Yonggao [1 ]
Liu, Yuanzhuang [1 ]
Qin, Laifen [1 ]
Yao, Xiayin [1 ]
Liu, Zhaoping [1 ]
机构
[1] Chinese Acad Sci, Ningbo Inst Mat Technol & Engn, Ningbo 315201, Zhejiang, Peoples R China
关键词
Cathode material; Sodium-ions content; Layered lithium-excess; Solid solution; Lithium-ion batteries; ELECTRODE MATERIALS; HIGH-CAPACITY; ION; COPRECIPITATION;
D O I
10.1016/j.jpowsour.2013.04.047
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
The Li1.2-xNaxNi0.13Co0.13Mn0.54O2 (0 <= x <= 0.1) cathode materials have been synthesized by a solid-state reaction method. The effects of the Na+ contents on the structure, surface components and electrochemical performance are studied by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and electrochemical techniques. The XRD data indicate that the Li(1.2-x)Na(x)Ni(0.13)Co(0.13)Mb(0.54)O(2) samples evolve from a sole layered structure.(0 <= x <= 0.02) to a mixture of Na+-contained layered structure (0.02 < x <= 0.1), which would transform into the single layered structure after the initial charge and discharge process. XPS data demonstrate that some of the Na+ ions could be reversibly de-/re-intercalated for the Li1.2-xNaxNi0.13Co0.13Mn0.54O2 materials. An electrochemical test reveals that a small amount of Na+ (x <= 0.02) in the Li(1.2-x)Na(x)Ni(0.13)Co(0.13)Mb(0.54)O(2) materials can significantly increase the rate capacity, yet the capacity retention becomes worse. We also find that the capacity retention increases with the Na+ contents. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:530 / 535
页数:6
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