A solid-state surface-to-bulk modification with a multifunctional modified layer for 4.6 V LiCoO 2

被引:1
|
作者
Shi, Yongzhi [1 ]
Ding, Xiaoliang [1 ]
Wang, Dongxiao [1 ]
Cheng, Hongyu [1 ]
Su, Wei [1 ]
Wang, Rui [2 ]
Lyu, Yingchun [1 ]
Guo, Bingkun [1 ]
机构
[1] Shanghai Univ, Mat Genome Inst, Shanghai 200444, Peoples R China
[2] China Univ Geosci, Fac Mat Sci & Chem, Wuhan 430074, Peoples R China
基金
中国国家自然科学基金;
关键词
4.6V-LiCoO2; Interface reconstruction; LiNbO3; Structure stability; Oxygen release;
D O I
10.1016/j.jpowsour.2024.234998
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
With the attempts of more than 30 years, the current commercial LiCoO 2 (LCO) offers a reversible capacity of 185 mAh g -1 with a cut-off voltage of 4.5 V vs . Li + /Li. Further increasing the cut-off voltage, more lithium -ions can extract, deeply enhancing the capacity and energy density. However, it results in numerous side reactions and a significant decay in battery cycle performance. To address these issues, Nano-LiNbO 3 as a coating agency is introduced by a solid-state surface -to -bulk modification process. To avoid the agglomeration and achieve uneven coating of Nano-LiNbO 3 in the solid-state reaction, polyvinylpyrrolidone (PVP) is introduced as a dispersant, which effectively ensures the uniform and smooth coating along with the carbonization process. The modified LCO sample presents a specific reversible capacity of 215.5 mAh g -1 in the initial cycle and a capacity retention rate of 90 % after 100 cycles at 3 -4.6 V and 0.5 C. Further analysis demonstrate that the LiNbO 3 surface coating layer and the element gradient doping layer provide LCO a stable structure and an inert surface, which improves the surface stability, suppresses the oxygen release and ensures the enhanced electrochemical performance.
引用
收藏
页数:9
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