Abstract
A series of LiFe1-xVxPO4/C samples have been successfully prepared using a two-step solid-state reaction route. The effect of vanadium incorporation on the performance of LiFePO4 has systematically been investigated with X-ray diffraction, Raman spectroscopy, charge/discharge measurements, and cyclic voltammetry tests. It is found that V incorporation significantly enhances the electrochemical performance of LiFe-PO4. Particularly, the LiFePO4/C sample with 5 at. % vanadium doping exhibits the best performance with a specific discharge capacity of 129 mAh g-1 at 5.0 C after 50 cycles; the capacity retention ratio is higher than 97.5% at all C rates from 0.1 to 5.0 C. X-ray absorption spectroscopy results show that the valence of V in LiFe0.95V0.05PO4/C is between +3 and +4. It is confirmed that the samples with x ≤ 0.03 are in single phase, whereas the samples with 0.05 ≤ x < 1.00 contain two impurity phases: Li3V2 (PO4)3 and LiVOPO4. A clear feature of vanadium incorporation in LiFePO 4 has been specified.
Original language | English (US) |
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Pages (from-to) | 13520-13527 |
Number of pages | 8 |
Journal | Journal of Physical Chemistry C |
Volume | 115 |
Issue number | 27 |
DOIs | |
State | Published - Jul 14 2011 |
All Science Journal Classification (ASJC) codes
- Electronic, Optical and Magnetic Materials
- General Energy
- Physical and Theoretical Chemistry
- Surfaces, Coatings and Films