A Metastable Oxygen Redox Cathode for Lithium‐Ion Batteries

Abstract Simultaneously harnessing cation and anion redox activities in the cathode is crucial for the development of high energy‐density lithium‐ion batteries. However, achieving long‐term stability for both mechanisms remains a significant challenge due to pronounced anisotropic volume changes at low lithium content, unfavorable cation migration, and oxygen loss. Here, we demonstrate exceptionally stable cation and anion redox behavior in a metastable, cobalt‐free layered oxide, Li 0.693 [Li 0.153 Ni 0.190 Mn 0.657 ]O 2 (LLNMO). After 50 cycles at 50 mA/g (~0.2 C), the cathode retains 97.4 % of its initial capacity (222.4 mAh/g) with negligible voltage decay. This remarkable stability is attributed to its metastable O6‐type structure (R‐3m symmetry) with unique local geometry. The face‐sharing connectivity between lithium layers and alternating transition metal (TM) layers effectively suppresses TM migration‐induced voltage decay during anion redox. Additionally, the structure balances interlayer cation/cation and anion/anion repulsions, resulting in minimal expansion and contraction during de‐/lithiation (<2.3 % along the c ‐axis) and excellent structural reversibility. These findings highlight that layered oxides with a metastable framework are promising cathode candidates for next‐generation ultra‐high‐energy lithium‐ion batteries.

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Publication Details

Journal
Angewandte Chemie
Published
2025-02-04
DOI
https://doi.org/10.1002/ange.202422789
Citations
5
Primary Topic
Advancements in Battery Materials
Type
article
Field-Weighted Citation Impact
3.65
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article

A Metastable Oxygen Redox Cathode for Lithium‐Ion Batteries

Ning Qin, Wilgner Lima da Silva, Joshua M. Stratford, Zhouguang Lu et al.
5 citations
Angewandte Chemie
Advancements in Battery Materials
3.65
article

A Metastable Oxygen Redox Cathode for Lithium‐Ion Batteries

Ning Qin, Wilgner Lima da Silva, Joshua M. Stratford, Zhouguang Lu, R. M. Benito, Ke‐Jin Zhou, Dominic Gardner, Phoebe K. Allan, Sahil Tippireddy, J. B. WILLIAMS, Qingmeng Gan, Chun Zeng, Fangchang Zhang, Fucai Zhang, Wen Luo, Yingzhi Li, Joshua W. Makepeace, Cheng Li, Yanfang Wang, Hongzhi Wang, Zhiqiang Li, Kaili Zhang, Yulin Cao
article en
5 citations

Abstract

Abstract Simultaneously harnessing cation and anion redox activities in the cathode is crucial for the development of high energy‐density lithium‐ion batteries. However, achieving long‐term stability for both mechanisms remains a significant challenge due to pronounced anisotropic volume changes at low lithium content, unfavorable cation migration, and oxygen loss. Here, we demonstrate exceptionally stable cation and anion redox behavior in a metastable, cobalt‐free layered oxide, Li 0.693 [Li 0.153 Ni 0.190 Mn 0.657 ]O 2 (LLNMO). After 50 cycles at 50 mA/g (~0.2 C), the cathode retains 97.4 % of its initial capacity (222.4 mAh/g) with negligible voltage decay. This remarkable stability is attributed to its metastable O6‐type structure (R‐3m symmetry) with unique local geometry. The face‐sharing connectivity between lithium layers and alternating transition metal (TM) layers effectively suppresses TM migration‐induced voltage decay during anion redox. Additionally, the structure balances interlayer cation/cation and anion/anion repulsions, resulting in minimal expansion and contraction during de‐/lithiation (<2.3 % along the c ‐axis) and excellent structural reversibility. These findings highlight that layered oxides with a metastable framework are promising cathode candidates for next‐generation ultra‐high‐energy lithium‐ion batteries.

Angewandte ChemieVol. 137(16)
City University of Hong Kong (HK), Diamond Light Source (GB), Southern University of Science and Technology (CN), Division of Materials Science and Engineering (AU), The Faraday Institution (GB), University of Birmingham (GB)
Openalex Percentile: Top 8%
Advancements in Battery Materials
3.65
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