Abstract
Ti at the oxidation states of Ti3+ and Ti4+, was used to enhance the performance of Na3V2(PO4)2F2O by partially substituting vanadium. After doping Ti, the crystallographic volume is decreased due to the less radii of Ti3+/4+, and the valence of Ti is demonstrated identical to V. During sodium insertion in Ti-doped Na3V2(PO4)2F2O, the two discharge plateaus split into three because of the rearrangement of local redox environment. Consequently, the optimized Na3V0.96Ti0.04(PO4)2F2O shows a specific capacity of 123 and 63 mA·h/g at 0.1C and 20C, respectively. After 350 cycles at 0.5C, the capacity is gradually reduced corresponding to a retention of 71.05%. The significantly improved performance is attributed to the rapid electrochemical kinetics, and showcases the strategy of replacing V3+/4+ with Ti3+/4+ for high-performance vanadium-based oxyfluorophosphates.
| Original language | English |
|---|---|
| Pages (from-to) | 243-256 |
| Number of pages | 14 |
| Journal | Transactions of Nonferrous Metals Society of China (English Edition) |
| Volume | 35 |
| Issue number | 1 |
| DOIs | |
| State | Published - Jan 2025 |
Keywords
- cathode
- energy storage
- sodium battery
- sodium vanadium oxyfluorophosphate
- titanium doping