Archimedean polyhedron LiCoO2 for ultrafast rechargeable Li-ion batteries

被引:10
|
作者
Zhang, Fengchu [1 ]
Dong, Jinyang [2 ,3 ]
Yi, Ding [1 ]
Xia, Jing [4 ]
Lu, Zongjing [5 ,6 ]
Yang, Yang [1 ]
Wang, Xi [1 ]
机构
[1] Beijing Jiaotong Univ, Sch Sci, Dept Phys, Beijing 100044, PR, Peoples R China
[2] Sch Mat Sci, Beijing Key Lab Environm Sci & Engn, Beijing 100081, PR, Peoples R China
[3] Sch Mat Sci, Beijing Inst Technol, Beijing 100081, PR, Peoples R China
[4] Tianjin Univ, Inst Mol Plus, Tianjin 300072, PR, Peoples R China
[5] Tianjin Univ, Sch Chem Engn & Technol, Tianjin 300072, PR, Peoples R China
[6] Tianjin Univ, Collaborat Innovat Ctr Chem Sci & Engn Tianjin, Tianjin 300072, PR, Peoples R China
基金
中国国家自然科学基金;
关键词
Lithium-ion batteries; Archimedean polyhedron; Twin boundary; Ultrahigh rate; Electron; ion transport; TOTAL-ENERGY CALCULATIONS; STABLE CATHODE MATERIAL; HIGH-RATE PERFORMANCE; ELASTIC BAND METHOD; LITHIUM; LINI1/3CO1/3MN1/3O2; OXIDE; DELITHIATION; CHALLENGES; MIGRATION;
D O I
10.1016/j.cej.2021.130122
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Internal interfaces within electrode materials play crucial roles in the rate capability of lithium cobalt oxide (LiCoO2) based batteries. In this work, we apply an acetate-assisted molten-salt method to synthesize Archimedean concave cuboctahedron-shaped LiCoO2 (ACO-LiCoO2), which possesses abundant built-in 109.5 degrees twin boundaries (TBs) originating from its O3 stacking pattern. The ACO-LiCoO2 cathode material presents outstanding rate capability, including an ultra-high discharge capacity of over 151 mAh/g at 5C and a discharge capacity of 136 mAh/g at 50C (1C = 140 mA/g). Density functional theory (DFT) calculations reveal that the coherent TBs not only introduce Co-3dz2 orbitals in the forbidden band, resulting in higher electrical conductivity, they also provide new migration pathways for faster Li-ion diffusion, compared to commercial LiCoO2. The TB-rich ACO-LiCoO2 material might pave the way for the design of ultrafast rechargeable Li-ion batteries.
引用
收藏
页数:7
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