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Vacancy-Enabled O3 Phase Stabilization for Manganese-Rich Layered Sodium Cathodes
Biwei Xiao1, Yichao Wang2, Sha Tan3
1Energy & Environment Directorate, Pacific Northwest National Laboratory, Richland, WA, 99352, USA.
Angewandte Chemie (International Ed. in English)
|January 22, 2021
Summary
Researchers developed a novel O3 phase sodium cathode from manganese-rich layered oxides, overcoming capacity fade issues common in P2 phase materials for sodium-ion batteries.
Area of Science:
- Materials Science
- Electrochemistry
- Energy Storage
Background:
- Manganese-rich layered oxides are promising low-cost, high-capacity cathode materials for sodium-ion batteries.
- Existing P2 phase materials often exhibit rapid capacity degradation, limiting their practical application.
Purpose of the Study:
- To develop a stable O3 phase sodium cathode from a Li and Mn-rich layered material.
- To investigate the role of transition metal and oxygen vacancies in enhancing electrochemical performance.
Main Methods:
- Synthesis of a Li and Mn-rich layered material.
- Electrochemical exchange of sodium and lithium ions.
- Characterization of phase stability and electrochemical cycling.
Main Results:
- The developed material primarily maintains the O3 phase during cycling, exhibiting a full sodiation capacity of approximately 220 mAh g⁻¹.
- Achieved a specific capacity of ~160 mAh g⁻¹ between 2-3.8 V with over 86% capacity retention after 250 cycles.
- Pre-formed vacancies facilitate reversible transition metal migration, creating metastable states that prevent O3-P3 phase transitions.
Conclusions:
- The novel O3 phase cathode demonstrates enhanced stability and capacity retention for sodium-ion batteries.
- The engineered vacancies and resulting phase stabilization are key to overcoming the limitations of traditional P2 phase materials.
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