Controllable construction of La2Li0.5Co0.5O4 multifunctional "armor" to stabilize Li-rich layered oxide cathode for high-performance lithium-ion batteries

被引:16
作者
Deng, Xiaoyang [1 ]
Li, Mi [1 ]
Ma, Zizai [2 ,3 ]
Wang, Xiaoguang [1 ,2 ]
机构
[1] Taiyuan Univ Technol, Inst New Carbon Mat, Coll Mat Sci & Engn, Taiyuan 030024, Peoples R China
[2] Shanxi Key Lab Gas Energy Efficient & Clean Utiliz, Taiyuan 030024, Peoples R China
[3] Taiyuan Univ Technol, Coll Chem, Taiyuan 030024, Peoples R China
基金
中国国家自然科学基金;
关键词
lithium-rich manganese-based oxide; lithium-ion batteries; surface modification; electrochemical performance; SURFACE MODIFICATION; LANTHANUM;
D O I
10.1007/s12274-023-5613-2
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Lithium-rich manganese-based cathodes (LR) are valuable cathode materials for the next generation of lithium-ion batteries (LIBs) with high-energy density. However, the fast voltage/capacity decay on cycling is the major obstacle for the practical application induced by the less-than-ideal anionic redox reactions and structure distortion. Herein, in order to tackle these challenges, a perovskite-like La2Li0.5Co0.5O4 (LLCO) material is selected as protective surface to stabilize the Li1.2Mn0.54Ni0.13Co0.13O2 (LR) substrate through wet chemical coating method. Versatile structure/phase characterizations and electrochemical tests exhibit that the LLCO can not only minish the oxygen evolution and enhance the structure stability, but also restrain the electrolyte corrosion and increase the mechanical strength of cathode materials. Moreover, the coated LLCO with high electronic/ionic conductivity dramatically accelerates the energy storage kinetic, thereby displaying the improved rate performance. Specifically, the optimized LR@LLCO sample (1LLCO) exhibits a high capacity of 250.6 mAh.g(-1) after 100 cycles at 0.1 C and excellent capacity retention of 82.6% after 200 cycles at 2 C. This work provides a new idea for the modification of LR cathodes toward commercial high-performance LIBs.
引用
收藏
页码:10634 / 10643
页数:10
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