Tailoring Co3d and O2p Band Centers to Inhibit Oxygen Escape for Stable 4.6 V LiCoO2 Cathodes

被引:184
作者
Kong, Weijin [1 ]
Zhang, Jicheng [1 ]
Wong, Deniz [2 ]
Yang, Wenyun [3 ]
Yang, Jinbo [3 ]
Schulz, Christian [2 ]
Liu, Xiangfeng [1 ,4 ]
机构
[1] Univ Chinese Acad Sci, Coll Mat Sci & Optoelect Technol, Ctr Mat Sci & Optoelect Engn, Beijing 100049, Peoples R China
[2] Helmholtz Ctr Berlin Mat & Energy, Hahn Meitner Pl 1, D-14109 Berlin, Germany
[3] Peking Univ, State Key Lab Mesoscop Phys, Sch Phys, Beijing 100871, Peoples R China
[4] Univ Chinese Acad Sci, CAS Ctr Excellence Topol Quantum Computat, Beijing 100190, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
band center; energy gap; high voltage LiCoO2; MgF2; doping; oxygen release; LITHIUM COBALT OXIDE; POSITIVE ELECTRODE; THIN-FILM; REDOX; LI; BATTERY; GENERATION;
D O I
10.1002/anie.202112508
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
High-voltage LiCoO2 delivers a high capacity but sharp fading is a critical issue, and the capacity decay mechanism is also poorly understood. Herein, we clarify that the escape of surface oxygen and Li-insulator Co3O4 formation are the main causes for the capacity fading of 4.6 V LiCoO2. We propose the inhibition of the oxygen escape for achieving stable 4.6 V LiCoO2 by tailoring the Co3d and O2p band center and enlarging their band gap with MgF2 doping. This enhances the ionicity of the Co-O bond and the redox activity of Co and improves cation migration reversibility. The inhibition of oxygen escape suppresses the formation of Li-insulator Co3O4 and maintains the surface structure integrity. Mg acts as a pillar, providing a stable and enlarged channel for fast Li+ intercalation/extraction. The modulated LiCoO2 shows almost zero strain and achieves a record capacity retention at 4.6 V: 92 % after 100 cycles at 1C and 86.4 % after 1000 cycles at 5C.
引用
收藏
页码:27102 / 27112
页数:11
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