Reinforcing Particle Architectural Stability of Li‐Rich Cathode With Enhanced Anionic Redox Reaction Reversibility

ABSTRACT Lithium‐rich layered oxides (LRLOs) promise exceptional energy densities (∼1000 Wh kg −1 ) but suffer from coupled structural and chemical instabilities that impede their commercialization. While atomic scale regulation of anionic redox reaction (ARR) reversibility has been extensively explored, the mesoscale architectural degradation, which is exacerbated by detrimental porous structures inherited from precursors, remains critical yet overlooked. Herein, a cross‐scale synergistic strategy was introduced to simultaneously reinforce the mesoscale particle architecture and stabilize the atomic‐scale charge compensation in LRLOs. By incorporating fluorine to modulate the local electronic environment, the surface energy of the active (010) facets is selectively lowered, driving a profound morphological transformation of primary particles from plate‐like to equiaxed. This thermodynamic reconstruction effectively disrupts the adverse precursor‐inherited porosity, yielding highly compact secondary particles with accelerated Li + diffusion kinetics. Simultaneously, at the atomic scale, the strengthened transition metal‐oxygen (TM‐O) covalency suppresses excessive oxygen activation, thereby enhancing reversibility of the ARR. Benefiting from this synergistic architectural and chemical modulation, the cathode exhibits a 6.8% increase in Coulombic efficiency and delivers exceptional long‐term stability with capacity retention of 88.8% after 950 cycles. For Ah‐level full cells, 96.3% of reversible capacity after 1500 cycles under high‐voltage is achieved.

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Journal
Angewandte Chemie
Published
2026-08-14
DOI
https://doi.org/10.1002/ange.6490997
Primary Topic
Advancements in Battery Materials
Type
article
Field-Weighted Citation Impact
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article

Reinforcing Particle Architectural Stability of Li‐Rich Cathode With Enhanced Anionic Redox Reaction Reversibility

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Angewandte Chemie
Advancements in Battery Materials
article

Reinforcing Particle Architectural Stability of Li‐Rich Cathode With Enhanced Anionic Redox Reaction Reversibility

Yinguo Xiao, Yizhen Huang, Yi Jin, Bixian Ying, Tao Zeng, Huaqiang Chen, Qingsong Wang, Guifan Zeng, Jia‐Wei Wang, Chunpu Li, S. Schuppler, Changming Qu, Jiyuan Xue, Fanghua Ning, Chunjing Hu, Chao Li, Kang Zhang, Yu Qiao, Shi‐Gang Sun, Peter Nagel, Maolin Yang, Peng Zhang, Tian Qiu, Yuan Tian, Wei Li
article en

Abstract

ABSTRACT Lithium‐rich layered oxides (LRLOs) promise exceptional energy densities (∼1000 Wh kg −1 ) but suffer from coupled structural and chemical instabilities that impede their commercialization. While atomic scale regulation of anionic redox reaction (ARR) reversibility has been extensively explored, the mesoscale architectural degradation, which is exacerbated by detrimental porous structures inherited from precursors, remains critical yet overlooked. Herein, a cross‐scale synergistic strategy was introduced to simultaneously reinforce the mesoscale particle architecture and stabilize the atomic‐scale charge compensation in LRLOs. By incorporating fluorine to modulate the local electronic environment, the surface energy of the active (010) facets is selectively lowered, driving a profound morphological transformation of primary particles from plate‐like to equiaxed. This thermodynamic reconstruction effectively disrupts the adverse precursor‐inherited porosity, yielding highly compact secondary particles with accelerated Li + diffusion kinetics. Simultaneously, at the atomic scale, the strengthened transition metal‐oxygen (TM‐O) covalency suppresses excessive oxygen activation, thereby enhancing reversibility of the ARR. Benefiting from this synergistic architectural and chemical modulation, the cathode exhibits a 6.8% increase in Coulombic efficiency and delivers exceptional long‐term stability with capacity retention of 88.8% after 950 cycles. For Ah‐level full cells, 96.3% of reversible capacity after 1500 cycles under high‐voltage is achieved.

Angewandte Chemie
Karlsruhe Institute of Technology (DE), FIZ Karlsruhe – Leibniz Institute for Information Infrastructure (DE), Xiamen University (CN), Battery Park (US), Quzhou College of Technology (CN), Augenstern (DE), Ningde Normal University (CN), Kerntechnische Entsorgung Karlsruhe (Germany) (DE), Peking University Shenzhen Hospital (CN), Collaborative Innovation Center of Chemistry for Energy Materials (CN), Sustainable Energy Systems (United Kingdom) (GB), University of Bayreuth (DE), East China Normal University (CN)
National Natural Science Foundation of China, Fundamental Research Funds for the Central Universities
Affordable and clean energy
Openalex Percentile: Top 18%
Advancements in Battery Materials
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