Converting Li‐Rich Layered Oxide Cathode into Non‐Shrinking Sacrificial Prelithiation Agent

To improve the energy density of Li-ion batteries, conventional sacrificial prelithiation agents (Li<sub>5</sub>FeO<sub>4</sub>, Li<sub>2</sub>O and Li<sub>2</sub>CO<sub>3</sub>, etc.) are introduced to compensate for active lithium loss, but they undergo serious volumetric shrinkage during decomposition, generating voids that compromise electrode architecture integrity and deteriorate electrochemical performance. Herein, the typical Li-rich layered oxide cathode is converted into Li-rich disordered rocksalt oxide (LRDO) prelithiation agent, achieving 330 mAh g<sup>-1</sup> charge capacity and retaining 130 mAh g<sup>-1</sup> reversible capacity (contributing 200 mAh g<sup>-1</sup> irreversible prelithiation capacity). Compared with the layered structure, the cation-disordered structure in LRDO tunes the local oxygen environment, completely activating oxygen-related anionic oxidation activity at lower potential (<4.5 V). Moreover, coupled with a fluorinated electrolyte additive, the nucleophilic oxygen species released during de-lithiation of LRDO are synergistically utilized, constructing a gradient cathode-electrolyte interphase architecture with enhanced interfacial stability during the cell formation process. Most importantly, the phase-transition-free nature of LRDO during prelithiation completely eradicates volume shrinkage, effectively preventing electrode architecture degradation. Furthermore, a long-life graphite||LiFePO<sub>4</sub> pouch cell with high discharge capacity of 150.02 mAh (7.59% higher than without prelithiation) are achieved, maintaining 91.33% capacity after 1800 cycles.

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Publication Details

Journal
Advanced Materials
Published
2025-08-27
DOI
https://doi.org/10.1002/adma.202509827
Citations
7
Primary Topic
Advancements in Battery Materials
Type
article
Field-Weighted Citation Impact
5.11

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article

Converting Li‐Rich Layered Oxide Cathode into Non‐Shrinking Sacrificial Prelithiation Agent

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7 citations
Advanced Materials
Advancements in Battery Materials
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article

Converting Li‐Rich Layered Oxide Cathode into Non‐Shrinking Sacrificial Prelithiation Agent

Yuan Tian, Yang Sun, Zixin Wu, Minye Yang, Juping Xu, Jianhua Yin, Maolin Yang, Qingsong Wang, Niu Liu, Yuanlong Zhu, Baodan Zhang, Jiyuan Xue, Kang Zhang, Yu Qiao, Shi‐Gang Sun, Yilong Chen, Wen Hui Yin, Haiyan Luo, Xin Sun, Yongfu Qiu, Li Li
article en
7 citations

Abstract

To improve the energy density of Li-ion batteries, conventional sacrificial prelithiation agents (Li<sub>5</sub>FeO<sub>4</sub>, Li<sub>2</sub>O and Li<sub>2</sub>CO<sub>3</sub>, etc.) are introduced to compensate for active lithium loss, but they undergo serious volumetric shrinkage during decomposition, generating voids that compromise electrode architecture integrity and deteriorate electrochemical performance. Herein, the typical Li-rich layered oxide cathode is converted into Li-rich disordered rocksalt oxide (LRDO) prelithiation agent, achieving 330 mAh g<sup>-1</sup> charge capacity and retaining 130 mAh g<sup>-1</sup> reversible capacity (contributing 200 mAh g<sup>-1</sup> irreversible prelithiation capacity). Compared with the layered structure, the cation-disordered structure in LRDO tunes the local oxygen environment, completely activating oxygen-related anionic oxidation activity at lower potential (<4.5 V). Moreover, coupled with a fluorinated electrolyte additive, the nucleophilic oxygen species released during de-lithiation of LRDO are synergistically utilized, constructing a gradient cathode-electrolyte interphase architecture with enhanced interfacial stability during the cell formation process. Most importantly, the phase-transition-free nature of LRDO during prelithiation completely eradicates volume shrinkage, effectively preventing electrode architecture degradation. Furthermore, a long-life graphite||LiFePO<sub>4</sub> pouch cell with high discharge capacity of 150.02 mAh (7.59% higher than without prelithiation) are achieved, maintaining 91.33% capacity after 1800 cycles.

Advanced MaterialsVol. 37(45)
Sun Yat-sen University (CN), Chongqing University (CN), Xiamen University (CN), Chinese Academy of Sciences (CN), Dongguan University of Technology (CN), China Spallation Neutron Source (CN), Institute of High Energy Physics (CN), Tan Kah Kee Innovation Laboratory (CN), University of Bayreuth (DE)
National Natural Science Foundation of China, Ministry of Science and Technology of the People's Republic of China, China Postdoctoral Science Foundation, Fundamental Research Funds for the Central Universities
Openalex Percentile: Top 4%
Advancements in Battery Materials
5.11
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