Abstract
Na2FePO4F (NFPF) is an attractive sodium-ion cathode owing to its low cost, non-toxicity, and structural robustness, yet its practical deployment is often limited by sluggish Na+ transport and insufficient intrinsic electronic conductivity under high-rate operation. In this work, multiscale charge-transport pathways were constructed in NFPF through a progressive design: partial PO43− substitution with BO33− was employed to regulate the localized electronic structure/defect chemistry and accelerate intrinsic transport, and carbon nanotubes (CNTs) were subsequently incorporated to reinforce electrode-scale electronic percolation and stabilize interfacial charge-transfer processes. As a result, Na2Fe(PO4)0.9(BO3)0.1F/CNTs delivers a high reversible capacity of 124.2 mA h g−1 at 0.1 C and retains 85.32% after 500 cycles at 5C and 78.4% after 1000 cycles at 10 C. Scan-rate CV yields markedly increased apparent diffusion coefficients, consistent with GITT-derived enhancement over most of the voltage window, while DRT-resolved impedance analysis reveals strongly suppressed potential-dependent fluctuations of Rct and RCEI. DFT and EPR analysis further support band-gap narrowing from 3.226 to 2.076 eV and oxygen-vacancy-related defect states. These results highlight multiscale pathway construction via anion-site regulation coupled with conductive-network reinforcement as an effective route to improving the high-rate durability of fluorophosphate cathodes.
| Original language | English |
|---|---|
| Pages (from-to) | 902-912 |
| Number of pages | 11 |
| Journal | Journal of Energy Chemistry |
| Volume | 121 |
| DOIs | |
| Publication status | Published - Oct 2026 |
| Externally published | Yes |
Keywords
- Cycling stability
- Enhanced diffusion kinetics
- High-rate durability
- Polyanion-site substitution
- Sodium ion cathode
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