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Activating Sodium Intercalation in Cation-Deficient Fe3O4 Through Mo Substitution
Shasha Guo1, Mohamed Ait Tamerd1, Changyuan Li1
1Shanghai Key Laboratory for R&D and Application of Metallic Functional Materials, Institute of New Energy for Vehicles, School of Materials Science and Engineering, Tongji University, Shanghai, 201804, China.
Tailoring iron vacancies in magnetite (Fe3O4) via molybdenum doping significantly boosts sodium-ion battery performance. This defect engineering enhances capacity and facilitates faster sodium intercalation for improved energy storage.
Area of Science:
- Materials Science
- Electrochemistry
- Nanotechnology
Background:
- Magnetite (Fe3O4) is a promising, cost-effective anode material for energy storage.
- Sodium-ion batteries face challenges with Na+ intercalation in conversion-type oxides.
- Developing efficient anode materials is crucial for large-scale energy storage.
Purpose of the Study:
- To enhance the electrochemical performance of magnetite anodes in sodium-ion batteries.
- To investigate the role of iron vacancies in Fe3O4 for improved sodium intercalation.
- To establish a method for modulating defective structures in transition metal oxides.
Main Methods:
- Gradient molybdenum (Mo) doping to create controllable Fe vacancies in Fe3O4.
- Pair distribution function (PDF) analysis for local structure elucidation.
- Physical-electrochemical characterizations and theoretical calculations.
Main Results:
- Achieved a vacancy-rich Fe3O4 structure with 7.3% Fe vacancies.
- Enhanced capacity of 127 mAh g-1 after 150 cycles, compared to 37 mAh g-1 for defect-free Fe3O4.
- Mo doping improved electronic conductivity and facilitated Na+ migration.
Conclusions:
- Tailoring Fe vacancies through Mo doping is an effective strategy to enhance sodium-ion battery performance.
- Defective structures in transition metal oxides can activate fast and reversible sodium intercalation.
- This work offers a pathway for designing high-performance sodium-ion batteries.
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