Synthesis and electrochemical properties of Na-doped Li 3V 2(PO 4) 3 cathode materials for Li-ion batteries
► Li 3− x Na x V 2(PO 4) 3/C cathodes have been synthesized by using sol–gel method for the first time. ► The Na doping in Li site by Na would be favorable to expanding the lattices and enhancing the electronic conductivities. ► The short Li-Li distance and wide Li-O contact of Li 2.97Na 0.03V 2(PO...
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Published in | Journal of power sources Vol. 196; no. 23; pp. 10169 - 10175 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Elsevier B.V
2011
|
Subjects | |
Online Access | Get full text |
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Summary: | ► Li
3−
x
Na
x
V
2(PO
4)
3/C cathodes have been synthesized by using sol–gel method for the first time. ► The Na doping in Li site by Na would be favorable to expanding the lattices and enhancing the electronic conductivities. ► The short Li-Li distance and wide Li-O contact of Li
2.97Na
0.03V
2(PO
4)
3 improve Li-ion diffusion. ► The partial substitution of Li with Na (
x
=
0.03) is favorable for rate performance and cyclic ability.
Na-doped Li
3−
x
Na
x
V
2(PO
4)
3/C (
x
=
0.00, 0.01, 0.03, and 0.05) compounds have been prepared by using sol–gel method. The Rietveld refinement results indicate that single-phase Li
3−
x
Na
x
V
2(PO
4)
3/C with monoclinic structure can be obtained. Among three Na-doped samples and the undoped one, Li
2.97Na
0.03V
2(PO
4)
3/C sample has the highest electronic conductivity of 6.74
×
10
−3
S
cm
−1. Although the initial specific capacities for all Na-doped samples have no much enhancement at the current rate of 0.2
C, both cycle performance and rate capability have been improved. At the 2.0
C rate, Li
2.97Na
0.03V
2(PO
4)
3/C presents the highest initial capacity of 118.9
mAh
g
−1 and 12% capacity loss after 80 cycles. The partial substitution of Li with Na (
x
=
0.03) is favorable for electrochemical rate and cyclic ability due to the enlargement of Li
3V
2(PO
4)
3 unit cells, optimizing the particle size and morphology, as well as resulting in a higher electronic conductivity. |
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ISSN: | 0378-7753 1873-2755 |
DOI: | 10.1016/j.jpowsour.2011.08.044 |