Morphology-Tuned Porous Lithium-Rich Cathode Materials Synthesized via a Solvothermal Approach for Li-Ion Battery Application

被引:0
|
作者
Shao, Yijia [1 ,2 ]
Li, Chaozhong [1 ,2 ]
Li, Luoqian [1 ,2 ]
Liu, Jian [3 ]
Liao, Shijun [1 ,2 ]
机构
[1] South China Univ Technol, Key Lab Fuel Cell Technol Guangdong Prov, Guangzhou 510641, Peoples R China
[2] South China Univ Technol, Guangdong Univ, Key Lab New Energy Technol, Sch Chem & Chem Engn, Guangzhou 510641, Peoples R China
[3] Univ British Columbia, Fac Appl Sci, Sch Engn, Kelowna, BC V1V 1V7, Canada
基金
中国国家自然科学基金;
关键词
lithium-rich manganese-based layered oxides; cathode materials; multisolvent solvothermal reaction; electrochemical performance; morphology and structure engineering; OXYGEN REDOX; CHALLENGES; OXIDES; MN; 3D; CO;
D O I
10.1021/acsaem.2c03971
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 layered oxides (LMR) are considered one of the most promising cathode materials for the next generation of high-energy lithium-ion batteries for transportation and energy storage applications. However, the irreversible phase transition from a layered to a spinel structure coupled with the anion redox reaction leads to severe capacity degradation and voltage attenuation, hindering practical applications of LMR materials. In this work, we developed a superior LMR cathode material through a structure engineering strategy via a multisolvent solvothermal method. The resultant LMR cathode, with uniform particle size and porous structure, achieved a specific energy density of similar to 933.00 Wh kg-1 (similar to 267.48 mAh g-1) at 0.2C and a capacity retention of similar to 80% after 300 cycles in a voltage range of 2.0-4.8 V at 1C. We further revealed that the excellent performance of our LMR cathode is due to the abundant diffusion pathways, faster lithium-ion diffusion kinetics, and stable crystalline structure. Thus, this study is encouraging and provides an avenue for developing high-energy lithium-ion batteries.
引用
收藏
页码:2531 / 2540
页数:10
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