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Boosting performance of Co-free Li-rich cathode material through regulating the anionic activity by means of the strong Ta[sbnd]O bonding.

Authors :
Wu, Chao
Li, Heng
Cao, Shuang
Li, Zhi
Zeng, Peng
Chen, Jiarui
Zhu, Xitong
Guo, Xiaowei
Chen, Gairong
Chang, Baobao
Shen, Yongqiang
Wang, Xianyou
Source :
Journal of Colloid & Interface Science. Dec2022:Part B, Vol. 628, p1031-1040. 10p.
Publication Year :
2022

Abstract

[Display omitted] Benefiting from the extra contribution of O redox, Co-free Li-rich layered oxides (LRNMO) can satisfy the requirement of high specific capacities. However, during the high-voltage charging process, lattice oxygen being oxidized to O− or O 2 leads to a gradual transition of the structure from layered to spinel phase, capacity and voltage decline, hindering the practical application of LRNMO in the lithium-ion battery. Here, a surface modification strategy of Li 1.2 Ni 0.32 Mn 0.48 O 2-δ doped with Ta5+ ions is proposed, in which the Ta5+ ions occupy the lithium sites of the lattice structure on the surface layer of LRNMO and form a Ta 2 O 5 coating layer. The modified electrode exhibits excellent rate performance and cycling stability, with 94.9% and 85.5% capacity retention rate and voltage retention rate, respectively, after 200 cycles at 1C. Moreover, the initial coulomb efficiency and ionic conductivity of the modified electrode are also apparently enhanced. Simultaneously, the decreased Li/Ni mixing degree of the modified electrode reflects the improvement of the structural stability. Therefore, the modification strategy through strong metal–oxygen bonding to integrate the surface structure to regulate the oxygen activity provides a new direction for the design of high energy density Co-free Li-rich cathode materials. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00219797
Volume :
628
Database :
Academic Search Index
Journal :
Journal of Colloid & Interface Science
Publication Type :
Academic Journal
Accession number :
160888663
Full Text :
https://doi.org/10.1016/j.jcis.2022.08.135