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Antimony Doping Enabled Radially Aligned Microstructure in LiNi0.91Co0.06Al0.03O2 Cathode for High‐Voltage and Low‐Temperature Lithium Battery.

Authors :
Lv, Yao
Huang, Shifei
Zhang, Jinhui
Kang, Guohuang
Liu, Yanru
Li, Nanrui
Liang, Yinxuan
Zhong, Xiaoyun
Jia, Tianqi
Ouyang, Yunfei
Qin, Peiwu
Kang, Feiyu
Zhang, Jiujun
Cao, Yidan
Source :
Advanced Functional Materials. 7/10/2024, Vol. 34 Issue 28, p1-11. 11p.
Publication Year :
2024

Abstract

Ni‐rich layered oxide cathode material with Ni contents greater than 90% is considered as a highly promising candidate for lithium‐ion batteries (LIBs) owing to its remarkable specific capacity and cost‐efficiency. However, severe capacity degradation caused by the structural collapse and interfacial instability with electrolyte under high voltage greatly hinders the practical application. Here, an antimony (Sb)‐doped LiNi0.91Co0.06Al0.03O2 (Sb‐NCA91) cathode is proposed, where the Sb doping modifies the morphology of primary particles and enables the radially aligned microstructure. This unique microstructure can disperse the anisotropic mechanical stress caused by the H2‐H3 phase transformation, and mitigate the shrinkage and expansion of the primary particles during high‐voltage and low‐temperature cycling, thus inhibiting the formation of microcracks and structural deterioration. Meanwhile, the closely arranged radial spokes allow fast ion transport in the secondary particles and effectively improve the rate performance and low‐temperature performance of the cathodes. As a result, the Sb modified cathode demonstrates superior capacity retention of ≈84% at 1 C after 200 cycles in 2.7–4.5 V at 25 °C, while the pristine NCA91 cathode only retains ≈79%. Additionally, the capacity retention at −20 °C is significantly increased from ≈61% (NCA91) to ≈88% (Sb‐NCA91) after 100 cycles. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
1616301X
Volume :
34
Issue :
28
Database :
Academic Search Index
Journal :
Advanced Functional Materials
Publication Type :
Academic Journal
Accession number :
178355016
Full Text :
https://doi.org/10.1002/adfm.202312284