Volume 108
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Wang, T., Wang, Y., Zeng, J., Li, B., Feng, H., Shen, Y., . . . Zhou, Y. (2026). Porous Ni-rich cathode material constructed by K+ and F− co-doping. Particuology, 108, 218-229. https://doi.org/10.1016/j.partic.2025.10.024
Porous Ni-rich cathode material constructed by K+ and F co-doping
Tongtong Wang a b c d, Yumin Wang a b c d, Jinbo Zeng a b c d *, Bo Li a b c d *, Haitao Feng a b c d, Yue Shen a b c d, Chunxi Hai e, Kaisheng Xia f, Yuan Zhou e *
a Key Laboratory of Green and High-end Utilization of Salt Lake Resources, Qinghai Institute of Salt Lakes, Chinese Academy of Sciences, Xining, 810008, China
b Qinghai Engineering and Technology Research Center of Comprehensive Utilization of Salt Lake Resources, Xining, 810008, China
c Qinghai Provincial Key Laboratory of Resources and Chemistry of Salt Lakes, Xining, 810008, China
d University of Chinese Academy of Sciences, Beijing, 100049, China
e College of Materials and Chemistry & Chemical Engineering, Chengdu University of Technology, Chengdu, 610059, China
f Faculty of Materials Science and Chemistry, China University of Geosciences, Wuhan, 430074, China
10.1016/j.partic.2025.10.024
Volume 108, January 2026, Pages 218-229
Received 17 September 2025, Revised 24 October 2025, Accepted 28 October 2025, Available online 10 November 2025, Version of Record 3 December 2025.
E-mail: jinbozeng@isl.ac.cn; libo@isl.ac.cn; yzhou712@sina.com

Highlights

• Larger angular polyhedron primary particles were found.

• Porous Ni-rich cathode material was constructed.

• The K+ and F co-doping leads to a porous and more stable structure.

• The facile low-cost co-doping is ideal for industrial applications.


Abstract

Ni-rich cathode materials for lithium-ion batteries have attracted much attention due to their high capacity and low cost; however, they are structurally and thermodynamically unstable, and their cycling performance also needs to be further improved to meet the needs of large-scale commercial applications. Herein, a synergistic K+ and F co-doping strategy is used to enhance performance of Ni-rich LiNi0.8Co0.1Mn0.1O2 cathode material. Trace surface K+ doping forms large polyhedral primary particles with sharp edges, hindering dense aggregation and promoting uniform internal porosity within secondary particles. Bulk F doping stabilizes the structure. This co-doping, combined with the porous architecture, significantly improves electrolyte infiltration, shortens Li+ pathways, reduces Li+/Ni2+ disordering, and lowers Li+ migration barriers, facilitates a stable cathode electrolyte interface (CEI), mitigates polarization and suppresses lattice oxygen loss. The optimized KF30 sample delivers 173.0 mAh g−1 at 8 C (111 % of undoped KF00 capacity). After 200 cycles at 1 C, it retains 170.5 mAh g−1 (88.39 % retention), outperforming KF00 by 12.36 %. This strategy provides a cost-effective approach to boost Ni-rich cathode stability and electrochemical properties for lithium-ion batteries.

Graphical abstract
Keywords
Porous material; K+ and F co-doping; Ni-rich cathode material; Electrochemical performance; Lithium-ion batteries