Abstract
A high-rate of oxygen redox assisted by cobalt in layered sodium-based compounds is achieved. The rationally designed Na0.6[Mg0.2Mn0.6Co0.2]O2 exhibits outstanding electrode performance, delivering a discharge capacity of 214 mAh g−1 (26 mA g−1) with capacity retention of 87% after 100 cycles. High rate performance is also achieved at 7C (1.82 A g−1) with a capacity of 107 mAh g−1. Surprisingly, the Na0.6[Mg0.2Mn0.6Co0.2]O2 compound is able to deliver capacity for 1000 cycles at 5C (at 1.3 A g−1), retaining 72% of its initial capacity of 108 mAh g−1. X-ray absorption spectroscopy analysis of the O K-edge indicates the oxygen-redox species (O2−/1−) is active during cycling. First-principles calculations show that the addition of Co reduces the bandgap energy from ≈2.65 to ≈0.61 eV and that overlapping of the Co 3d and O 2p orbitals facilitates facile electron transfer, enabling the long-term reversibility of the oxygen redox, even at high rates. To the best of the authors' knowledge, this is the first report on high-rate oxygen redox in sodium-based cathode materials, and it is believed that the findings will open a new pathway for the use of oxygen-redox-based materials for sodium-ion batteries.
Original language | English |
---|---|
Article number | 1901181 |
Journal | Advanced Energy Materials |
Volume | 9 |
Issue number | 32 |
DOIs | |
Publication status | Published - Jan 1 2019 |
Externally published | Yes |
Keywords
- DFT
- Mn-rich
- oxygen redox
- P2-type layered cathodes
- sodium-ion batteries
ASJC Scopus subject areas
- Renewable Energy, Sustainability and the Environment
- General Materials Science