Abstract
The iron-based polyanionic material Na3Fe2(PO4)P2O7 is regarded as an excellent cathode due to its outstanding thermal stability and the three-dimensional (3D) open framework structure with facile sodium-ion transport. However, its inferior electronic conductivity and limited diffusion kinetics deteriorate its rate performance and cyclability. Herein, a rationally designed Ni doping strategy in Na3Fe2(PO4)P2O7 is developed to stabilize the crystal structure and to expand the migration path of Na+. The as-prepared cathode can exhibit a discharge capacity reaching 100.7 mA h g−1 at 0.1C and excellent cycling stability throughout 5000 cycles at 10C. Moreover, it maintains impressive high-temperature sodium storage behavior with negligible capacity degradation after 200 cycles at 1C and 60 °C. A highly reversible single-phase structural evolution is disclosed by in situ X-ray diffraction. Furthermore, the fast ionic/electronic diffusion kinetics is revealed through various electrochemical measurements and density functional theory calculations. © The Royal Society of Chemistry 2023.
| Original language | English |
|---|---|
| Pages (from-to) | 6978-6985 |
| Journal | Journal of Materials Chemistry A |
| Volume | 11 |
| Issue number | 13 |
| Online published | 14 Feb 2023 |
| DOIs | |
| Publication status | Published - 7 Apr 2023 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
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