共 36 条
Voltage fade mitigation in the cationic dominant lithium-rich NCM cathode
被引:18
作者:
Chandan, Prem
[1
]
Chang, Chung-Chieh
[2
]
Yeh, Kuo-Wei
[2
]
Chiu, Chui-Chang
[2
]
Wu, Dong-Ze
[1
]
Huang, Tzu-Wen
[1
]
Wu, Phillip M.
[1
]
Chi, Po-Wei
[1
]
Hsu, Wei-Fan
[1
]
Su, Kai-Han
[3
]
Lee, Yu-Wen
[4
]
Chang, Hua-Shu
[1
]
Wang, Ming-Jye
[5
]
Wu, Heng-Liang
[4
]
Tang, Horng-Yi
[6
]
Wu, Maw-Kuen
[1
]
机构:
[1] Acad Sinica, Inst Phys, Taipei 11529, Taiwan
[2] Gus Technol Co Ltd, New Taipei City 22175, Taiwan
[3] Natl Taipei Univ Technol, Inst Mechatron Engn, Taipei 10608, Taiwan
[4] Natl Taiwan Univ, Ctr Condensed Matter Sci, Taipei 10617, Taiwan
[5] Acad Sinica, Inst Astron & Astrophys, Taipei 11529, Taiwan
[6] Natl Chi Nan Univ, Dept Appl Chem, Puli 545, Taiwan
关键词:
ANIONIC REDOX;
CYCLING PERFORMANCE;
ION;
NI;
MN;
ELECTRODES;
CAPACITY;
D O I:
10.1038/s42004-019-0223-3
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
In the archetypal lithium-rich cathode compound Li1.2Ni0.13Co0.13Mn0.54O2, a major part of the capacity is contributed from the anionic (O2(-/-)) reversible redox couple and is accompanied by the transition metal ions migration with a detrimental voltage fade. A better understanding of these mutual interactions demands for a new model that helps to unfold the occurrences of voltage fade in lithium-rich system. Here we present an alternative approach, a cationic reaction dominated lithium-rich material Li1.083Ni0.333Co0.083Mn0.5O2, with reduced lithium content to modify the initial band structure, hence similar to 80% and similar to 20% of capacity are contributed by cationic and anionic redox couples, individually. A 400 cycle test with 85% capacity retention depicts the capacity loss mainly arises from the metal ions dissolution. The voltage fade usually from Mn4+/Mn3+ and/or On-/O2- reduction at around 2.5/3.0 V seen in the typical lithium-rich materials is completely eliminated in the cationic dominated cathode material.
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页数:7
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