Abstract
Li-rich cathode materials, characterized by dual anionic and cationic redox activities, present a promising pathway to surpass traditional capacity and voltage constraints for high-energy-density batteries. However, the activation of anionic redox often induces lattice oxygen release, precipitating irreversible structural transformations and compromised ion transport dynamics. In this work, a layered-spinel intergrown structure is designed from an ion-exchange process with great tunability, which induces the arrangement of the manganese oxide layer and combines the high-capacity characteristics of the layer structure with superior stability provided by the spinel structure. Benefiting from expanded ion channels, the intergrown structure delivers an initial discharge capacity of 254.3 mAh g−1 at 0.1 C and retains a great high-rate capability of 169.2 mAh g−1 at 5 C, which is superior to the reported Li-rich manganese-based cathode materials. This work delineates a systematic design framework for layered-spinel intergrown architectures, leveraging their synergistic ion transport characteristics to achieve superior electrochemical performance in lithium-ion batteries.
| Original language | English |
|---|---|
| Article number | e15105 |
| Journal | Advanced Functional Materials |
| Volume | 35 |
| Issue number | 52 |
| DOIs | |
| Publication status | Published - 23 Dec 2025 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
Keywords
- Mn-based cathodes
- anionic redox
- intergrown Li─Mn─O structure
- superior ion kinetics
- transition metal vacancies
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