Charge-Compensation-Driven Failure Mechanism of Ni Redox in Fe-Rich Ni/Fe/Mn-Based O3-Type Layered Oxide Sodium-Ion Cathodes
For cathode materials of sodium-ion batteries, O3-type Ni/Fe/Mn-based (Na-NFM) layered oxides have garnered extensive attention because of high economic viability, environmental friendliness, and the potential for high energy density. Among them, Fe-rich compositions exhibit higher initial charge capacity and lower bill-of-material costs, while they fade rapidly and exhibit low initial coulombic efficiency, hindering their commercialization prospects. In this work, we investigate the failure of Fe-rich Na-NFM materials through X-ray absorption spectroscopy methods. The results reveal a combined failure mechanism that encompasses not only the conventional theory of Fe migration but also an abnormal Ni-redox deterioration, which has not yet been reported. More factors related to the failure of Fe-rich Na-NFM layered oxides are discussed in detail. These findings are expected to inspire targeted research efforts toward Fe-rich Na-NFM materials, thereby accelerating the practical application of sodium-ion batteries.
Authors
- Yoshiharu Uchimoto (ORCID: https://orcid.org/0000-0002-1491-2647)
- Kentaro Yamamoto (ORCID: https://orcid.org/0000-0002-8739-4246)
- Xiaobo Ji (ORCID: https://orcid.org/0000-0002-5405-7913)
- Chunxiao Zhang (ORCID: https://orcid.org/0000-0001-5300-6025)
- Hongshuai Hou (ORCID: https://orcid.org/0000-0001-8201-4614)
- Weifeng F. Wei (ORCID: https://orcid.org/0000-0002-3088-6549)
- Yanchang Wang (ORCID: https://orcid.org/0000-0001-6782-0570)
- Datong Zhang (ORCID: https://orcid.org/0000-0002-2886-9758)
- Yao Xiao (ORCID: https://orcid.org/0000-0002-2820-2937)
- Jiangnan Huang
Institutions
- Central South University (CN)
- Kyoto University (JP)
Publication Details
- Journal
- The Journal of Physical Chemistry Letters
- Published
- 2024-10-24
- DOI
- https://doi.org/10.1021/acs.jpclett.4c02461
- Citations
- 9
- Primary Topic
- Advancements in Battery Materials
- Type
- article
- Field-Weighted Citation Impact
- 1.88