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Interfacial Radical Reaction Enables High-Performance Graphite Anode for Potassium-Ion Batteries
Jianhao Lin1, Xiaobo Ding1, Xinyue Zeng2
1School of Environment and Energy, Guangdong Provincial Key Laboratory of Advanced Energy Storage Materials, South China University of Technology, Guangzhou, 510006, P.R. China.
A novel interfacial radical reaction enhances graphite anodes for potassium-ion batteries (PIBs). This modification improves stability and kinetics, enabling high performance for large-scale energy storage.
Area of Science:
- Materials Science
- Electrochemistry
- Energy Storage
Background:
- Potassium-ion batteries (PIBs) are crucial for large-scale energy storage.
- Graphite anodes face challenges with solid electrolyte interface (SEI) stability and K+-solvent co-intercalation, limiting cycling stability and reaction kinetics.
Purpose of the Study:
- To develop a stable and efficient graphite anode for PIBs.
- To overcome the limitations of SEI instability and K+-solvent co-intercalation.
Main Methods:
- A mechanochemical-induced radical reaction between graphite and Spiro-O8 radicals was employed.
- A uniform organic layer was constructed on graphite, facilitating KFSI salt decomposition to form an inorganic-rich outer layer.
Main Results:
- The modified graphite anode demonstrated enhanced K+ transport kinetics and inhibited K+-solvent co-intercalation.
- The Spiro-O8 inner film accommodated volume changes during cycling.
- Achieved reversible capacity of 241.0 mAh g-1 at 100 mA g-1, with 147.2 mAh g-1 at 1 A g-1.
- Exhibited stable cycling over 600 cycles with 89.4% capacity retention.
Conclusions:
- The interfacial radical reaction provides a new strategy for stabilizing graphite anodes in PIBs.
- This approach significantly enhances cycling stability and rate capability for high-performance PIBs.
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