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Review-High-Capacity Li[Ni1-xCox/2Mnx/2]O2 (x=0.1, 0.05, 0) Cathodes for Next-Generation Li-Ion Battery
被引:132
作者:
Yoon, Chong S.
[1
]
Choi, Moon Ho
[2
]
Lim, Byung-Beom
[2
]
Lee, Eung-Ju
[2
]
Sun, Yang-Kook
[2
]
机构:
[1] Hanyang Univ, Dept Mat Sci & Engn, Seoul 133791, South Korea
[2] Hanyang Univ, Dept Energy Engn, Seoul 133791, South Korea
基金:
新加坡国家研究基金会;
关键词:
POSITIVE ELECTRODE MATERIALS;
X-RAY-DIFFRACTION;
ELECTROCHEMICAL PROPERTIES;
CRYSTAL-STRUCTURE;
THERMAL-STABILITY;
LITHIUM NICKELATE;
LINIO2;
BEHAVIOR;
R(3)OVER-BAR-M;
PERFORMANCE;
D O I:
10.1149/2.0101514jes
中图分类号:
O646 [电化学、电解、磁化学];
学科分类号:
081704 ;
摘要:
LiNiO2 with theoretical capacity of 275 mAh g(-1) is regarded as a promising cathode material for Li-ion batteries, but its potential capacity has not been fully realized due to the severe capacity loss in the first charge/discharge cycle. Via co-precipitation method, we synthesized Li[Ni0.90Co0.05Mn0.05]O-2, Li[Ni0.95Co0.025Mn0.025]O-2, and LiNiO2 which delivered 221, 230, and 240 mAh g(-1) respectively, when cycled from 2.7 to 4.3 V vs. Li-0/Li+ at 0.1 C and retained similar to 70% of the initial capacity after 100 cycles. To date, such high reversible capacities are not yet to be reported from the Ni-rich Li[Ni1-x-yCoxMny]O-2 cathodes. The observed high capacities were attributed to the presence of a rock salt phase from severe cation mixing and excess Li ions in the host structure. It is believed that the rock salt phase stabilized the host structure in the delithiated state while the excess Li allowed the Li ions percolated through the rock salt phase which would be electrochemically inactive otherwise. (C) 2015 The Electrochemical Society. All rights reserved.
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页码:A2483 / A2489
页数:7
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