Abstract
The practical application of vanadium-based cathodes in aqueous zinc-ion batteries is primarily hindered by their limited rate performance and rapid capacity fading. Herein, we report a strategy to overcome these limitations by fabricating phosphorus-substituted V2O3 nanofibers within an N-doped carbon matrix (P-V2O3@NCNFs) through a combination of electrospinning and thermal phosphorylation. Our findings demonstrate that the incorporation of phosphorus anions effectively tunes the electronic configuration of V2O3, which significantly facilitates Zn2+ transport and reinforces the structural framework. By virtue of an optimal phosphorus doping level, the P-V2O3@NCNFs electrode achieves a high reversible capacity of 494.65 mAh g−1 at 0.1 A g−1, sustains 284.81 mAh g−1 at 1.0 A g−1, and demonstrates long-term cycling stability, highlighting the promise of anion doping as a powerful strategy to develop advanced cathodes for next-generation energy storage.
| Original language | English |
|---|---|
| Article number | 240785 |
| Journal | Journal of Power Sources |
| Volume | 689 |
| DOIs | |
| State | Published - 15 Oct 2026 |
| Externally published | Yes |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
Keywords
- Aqueous zinc-ion batteries
- Phosphorus doping
- Pseudocapacitance
- Reaction kinetics
- VOcathode
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