Abstract
Improving the intrinsic Na+ ion diffusivity of the advanced cathode material Na3V2(PO4)2O2F (NVPOF) has been a fundamental strategy to enhance its Na+ ion storage performance, while challenges remain in structural design and fabrication with specific features targeting the alleviation of migration energy barriers of the Na+ ions at different (de)sodiated states. Herein, K+ ions are introduced into the Na-sites in NVPOF to create Na+ ion vacancies, support the Na+ ion transport channels in the c axis and disrupt the continuity of the crystal structure. This strategy simultaneously reduces the electrostatic repulsive forces on the migrating Na+ ions from neighboring Na+ ions at a sodiated state and energy barriers originating from Na+ ion ordering at a desodiated state. Thus, the obtained NVPOF-K0.05 cathode presents a dramatic enhancement in the rate capability up to 80C (49.1 mA h g−1) and almost no decay in the long cycles at 10C up to 500 cycles (106.7 mA h g−1). The NVPOF-K0.05//Se@C sodium-ion full cell exhibits outstanding energy/power density (430.3 W h kg−1 at 208.3 W kg−1 and 310.5 W h kg−1 at 3357.1 W kg−1) and cycling stability (86.5% capacity retention of 107.1 mA h g−1 after 1000 cycles at 10C).
Original language | English |
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Pages (from-to) | 22105-22113 |
Number of pages | 9 |
Journal | Journal of Materials Chemistry A |
Volume | 10 |
Issue number | 41 |
DOIs | |
Publication status | Published - Sept 19 2022 |
Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2022 The Royal Society of Chemistry.
ASJC Scopus Subject Areas
- General Chemistry
- Renewable Energy, Sustainability and the Environment
- General Materials Science