共 16 条
Li2CO3 in LiNi0.8Co0.15Al0.05O2 cathodes and its effects on capacity and power
被引:272
作者:

Zhuang, GV
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机构: Ernest Orlando Lawrence Berkeley Natl Lab, Environm Energy Technol Div, Berkeley, CA 94720 USA

Chen, GY
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机构: Ernest Orlando Lawrence Berkeley Natl Lab, Environm Energy Technol Div, Berkeley, CA 94720 USA

Shim, J
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机构: Ernest Orlando Lawrence Berkeley Natl Lab, Environm Energy Technol Div, Berkeley, CA 94720 USA

Song, XY
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机构: Ernest Orlando Lawrence Berkeley Natl Lab, Environm Energy Technol Div, Berkeley, CA 94720 USA

Ross, PN
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机构: Ernest Orlando Lawrence Berkeley Natl Lab, Environm Energy Technol Div, Berkeley, CA 94720 USA

Richardson, TJ
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机构:
Ernest Orlando Lawrence Berkeley Natl Lab, Environm Energy Technol Div, Berkeley, CA 94720 USA Ernest Orlando Lawrence Berkeley Natl Lab, Environm Energy Technol Div, Berkeley, CA 94720 USA
机构:
[1] Ernest Orlando Lawrence Berkeley Natl Lab, Environm Energy Technol Div, Berkeley, CA 94720 USA
[2] Ernest Orlando Lawrence Berkeley Natl Lab, Div Sci Mat, Berkeley, CA 94720 USA
关键词:
lithium batteries;
battery power;
battery capacity;
power fade;
capacity fade;
D O I:
10.1016/j.jpowsour.2004.02.030
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:
Lithium carbonate is commonly found on the surfaces of lithiated cathode active materials that have been exposed to air. Long-term exposure of LiNi0.8Co0.15Al0.05O2 electrodes produced a dense Li2CO3 coating, approximately 10 nm in thickness that severely reduced both the accessible capacity and the rate at which the electrodes could be cycled. Ex situ X-ray diffraction patterns of cycled electrodes revealed a bimodal distribution of active material in different states of charge. Particle isolation is proposed to contribute to both capacity and power losses, and possible mechanisms related to the formation of Li2CO3 are discussed. (C) 2004 Elsevier B.V. All rights reserved.
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页码:293 / 297
页数:5
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