Abstract
Fe-based mixed phosphate Na4Fe3(PO4)2P2O7is a promising sodium-ion battery cathode due to its structural stability and cost-effectiveness, yet its capacity is limited by impurity phases and insufficient Fe redox activity. We introduce an electroactive coefficient (η = C/I), where C is the number of redox couples and I is the number of transferred ions per formula unit, as a design metric for high-capacity cathodes. Analysis reveals that Na4Fe3(PO4)2P2O7has a suboptimal η (0.72), prompting a V-doping strategy to enhance multielectron transfer, raising η to 0.85. V doping also triggers a high-spin-to-low-spin transition in Fe2+, shortening Fe–O bonds and increasing the Fe-vacancy formation energy, thus suppressing impurities. The optimized Na3.6Fe2.6V0.4(PO4)2P2O7achieves a record capacity of 124.6 mAh g–1at 0.1 C. This work elucidates phase-pure cathode formation and establishes a universal design principle for high-capacity electrodes.
| Original language | English |
|---|---|
| Pages (from-to) | 39151-39159 |
| Number of pages | 9 |
| Journal | Journal of the American Chemical Society |
| Volume | 147 |
| Issue number | 43 |
| DOIs | |
| State | Published - 29 Oct 2025 |
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