Preparation and Characterization of Chlorine Doped Li3V2(PO4)(3) as High Rate Cathode Active Material for Lithium Secondary Batteries
- Authors
- Lee, S. N.; Kim, H. S.; An, J. Y.; Amaresh, S.; Lee, Y. G.; Nam, K. W.; Lee, Y. S.
- Issue Date
- Oct-2014
- Publisher
- AMER SCIENTIFIC PUBLISHERS
- Keywords
- Lithium Vanadium Phosphate; Cathode; Anion; Chlorine; Doping; Battery
- Citation
- JOURNAL OF NANOSCIENCE AND NANOTECHNOLOGY, v.14, no.10, pp 7516 - 7520
- Pages
- 5
- Indexed
- SCI
SCIE
SCOPUS
- Journal Title
- JOURNAL OF NANOSCIENCE AND NANOTECHNOLOGY
- Volume
- 14
- Number
- 10
- Start Page
- 7516
- End Page
- 7520
- URI
- https://scholarworks.dongguk.edu/handle/sw.dongguk/23952
- DOI
- 10.1166/jnn.2014.9560
- ISSN
- 1533-4880
1533-4899
- Abstract
- Monoclinic Li3V2(PO4)(2).Cl-99(0.01) was synthesized using the conventional solid state method and the X-ray diffraction pattern was indexed based on P2(1)/n space group. The sharp cyclic voltammetric curves clearly revealed three lithium extraction/insertion processes at approximately 3.64, 3.72, 4.13, and 4.58 V during the anodic scan and 3.96, 3.58, and 3.48 V during the cathodic scan. Charge/discharge studies showed reduced electrolyte decomposition contribution in the case of the chlorine doped Li3V2(PO4)(2.99)Cl-0.01 sample with an initial capacity of 176 mA h g (1) at a 0.1 C current rate. The chlorine doped Li3V2(PO4)(3) sample showed an increased capacity retention with an increase in current rate, even at a very high C-rate (20 C), than the pristine and carbon coated samples. The pristine and carbon coated Li3V2(PO4)(3) samples showed a lower capacity retention of 71% and 84%, respectively, at a current rate of 0.1 C. In contrast, the chlorine doped Li3V2(PO4)(3) sample retained 87% of the initial capacity (176 mA h g(-1)) at the same current rate but with a higher coulombic efficiency of 91%. The enhanced capacity retention for the chlorine doped Li3V2(PO4)(3) was attributed to the reduction in polarization and decreased charge transfer resistance of the electrode.
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Collections - College of Engineering > Department of Energy and Materials Engineering > 1. Journal Articles

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