High-entropy Li-rich layered oxide cathode for Li-ion batteries

被引:7
作者
Kim, Jaemin [1 ]
Yang, Songge [1 ]
Zhong, Yu [1 ]
Tompsett, Geoffrey [1 ]
Jeong, Seonghun [2 ,3 ]
Mun, Junyoung [2 ,3 ]
Sunariwal, Neelam [4 ]
Cabana, Jordi [4 ]
Yang, Zhenzhen [5 ]
Wang, Yan [1 ]
机构
[1] Worcester Polytech Inst, Dept Mech Engn, Worcester, MA 01609 USA
[2] Sungkyunkwan Univ, Sch Adv Mat Sci & Engn, Suwon 16419, South Korea
[3] Sungkyunkwan Univ, SKKU Inst Energy Sci & Technol SIEST, Suwon 16419, South Korea
[4] Univ Illinois, Dept Chem, Chicago, IL 60607 USA
[5] Argonne Natl Lab, Chem Sci & Engn Div, Lemont, IL 60439 USA
基金
美国国家科学基金会;
关键词
Li-ion batteries; Li-rich layered oxides; Non-equimolar high-entropy oxides; Cathode materials; HIGH-ENERGY; VOLTAGE-FADE; LITHIUM; OXYGEN; DEGRADATION; SURFACE; PERFORMANCE; TRANSITION; DIFFUSION; ORIGIN;
D O I
10.1016/j.jpowsour.2024.235915
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
High-entropy oxides (HEOs) are emerging as promising cathode materials for Li-ion batteries (LIBs) due to their stable solid-state phase and compositional flexibility. Herein, we investigate the structural and electrochemical properties of a novel non-equimolar high-entropy cathode material, termed high-entropy Li-rich layered oxide (HE-LLO, Li1.15Na0.05Ni0.19Mn0.56Fe0.02Mg0.02Al0.02O1.97F0.03), in comparison to a pristine Li-rich layered oxide (PR-LLO, Li1.2Ni0.2Mn0.6O2). The incorporation of multiple cations (Na+, Al3+, Mg2+, Fe3+) and anion (F-) into HE-LLO introduces compositional diversity, enhancing structural stability through the entropy stabilization effect. Theoretical calculations confirm a significantly higher configurational entropy in HE-LLO compared to PRLLO, supporting its high-entropy nature. Electrochemical evaluations demonstrate that HE-LLO exhibits considerable capacity retention, preserving 76.8 % of its discharge capacity at 0.5C after 200 cycles, compared to only 36.2 % for PR-LLO. Even under high-temperature conditions, HE-LLO outperformed PR-LLO, maintaining 76.1 % of its discharge capacity after 100 cycles at 5C, while PR-LLO retained only 12.4 %. These enhancements are attributed to the improved phase reversibility and higher Li+ ion diffusion coefficients of HE-LLO, validated by ex-situ characterizations using a synchrotron X-ray technique, along with density functional theory (DFT) calculations. These findings highlight the promise of non-equimolar HEOs as a novel design strategy for highperformance cathode materials.
引用
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页数:11
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