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Insight into pulse-charging for lithium plating-free fast-charging lithium-ion batteries
被引:17
|作者:
Jeong, Yeon Tae
[1
,2
]
Shin, Hong Rim
[3
]
Lee, Jinhong
[1
]
Ryu, Myung-Hyun
[1
]
Choi, Sinho
[4
]
Kim, Hansung
[2
]
Jung, Kyu-Nam
[1
]
Lee, Jong-Won
[5
]
机构:
[1] Korea Inst Energy Res KIER, Renewable Energy Inst, 152 Gajeong Ro, Daejeon 34129, South Korea
[2] Yonsei Univ, Dept Chem & Biomol Engn, 50 Yonsei Ro, Seoul 03722, South Korea
[3] Daegu Gyeongbuk Inst Sci & Technol DGIST, Dept Energy Sci & Engn, 333 Techno Jungang Daero, Daegu 42988, South Korea
[4] Korea Inst Energy Res KIER, Ulsan Adv Energy Technol R&D Ctr, 25 Techno saneop Ro 55beon Gil, Ulsan 44776, South Korea
[5] Hanyang Univ, Div Mat Sci & Engn, 222 Wangsimni Ro, Seoul 04763, South Korea
关键词:
Lithium -ion battery;
Fast;
-charging;
Lithium plating;
Pulse;
Charging protocol;
COULOMBIC EFFICIENCY;
CYCLE LIFE;
DEPOSITION;
ELECTRODE;
BEHAVIOR;
D O I:
10.1016/j.electacta.2023.142761
中图分类号:
O646 [电化学、电解、磁化学];
学科分类号:
081704 ;
摘要:
In recent years, tremendous efforts have been devoted to searching for the fast-charging methodology of lithiumion battery (LIB) with widespread practical application of the electric vehicles, since the uncontrolled Li plating on the graphite anode under the fast-charging condition can lead the accelerated capacity decay and cause the safety issues of LIB. Here, we present mechanistic insights into the pulse-current-based fast-charging to aid with suppressing Li plating on the graphite anode. Compared with a conventional fast-charging protocol of the constant current method, the full-cell assembled with graphite anode and LiNi0.6Co0.2Mn0.2O2 cathode exhibits the improved fast-charging capability and cycle performance under the pulse-charging protocol. In particular, the graphite anode after prolonged 300 cycles shows a clean surface free of plated Li, which confirms that the pulse-charging protocol effectively inhibits Li plating on the anode even under fast-charging conditions. Furthermore, the physics-based numerical modeling results demonstrate that the pulse-current redistributes the accumulated Li+ species at the electrolyte/anode interface periodically, which mitigates the anode potential drop and prevents consequent Li plating.
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