Abstract
The LiV0.96Mn0.04PO4F/C composite was prepared by partial substitution of vanadium with manganese and in situ carbon coating of LiVPO4F via a modified carbothermal reduction route. Rietveld refinement of X-ray diffraction (XRD) patterns shows that the crystalline lattice is smaller than the value reported in the literature. While electron energy loss spectroscopy (EELS) on a selected area of high resolution transmission electron microscopy (HRTEM) demonstrates that Mn is successfully doped into LiVPO4F, X-ray photoelectron spectroscopy (XPS) indicates the co-existence of Mn3+ and Mn4+. With ∼6.29 wt% residual carbon (estimated by thermogravimetric analysis, TGA) included, the specific discharge capacity of LiV0.96Mn0.04PO 4F/C at 0.1 C and 6 C could reach 138 mA h g-1 and 98 mA h g-1, respectively. The capacity retention after 1000 cycles at 1 C is about 90%, corresponding to only 0.01% loss per cycle. Electrochemical impedance spectroscopy (EIS) shows that the charge transfer resistance (R ct) is significantly reduced by Mn substitution, and the lithium diffusion coefficient was calculated to be 1.34 × 10-13 cm 2 s-1, which is an order of magnitude higher than that of pristine LiVPO4F/C. Moreover, LiV0.96Mn 0.04PO4F/C retains 74% of its initial capacity after 500 cycles at 1 C at 65 °C, indicating its potential application at high temperatures.
| Original language | English |
|---|---|
| Pages (from-to) | 2501-2507 |
| Number of pages | 7 |
| Journal | Journal of Materials Chemistry A |
| Volume | 1 |
| Issue number | 7 |
| DOIs | |
| State | Published - 21 Feb 2013 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
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