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Electrochemical Characterization of Li1.07V0.83Fe0.1O2 ANODE Material for Li-ION Batteries
Recently a novel compounds based on layered LiV1-yMyO2 (M = Li, Fe, Cr) were found to be promising anode materials for Li-ion technology [1-3], as they exhibit long low-voltage plateau vs. metallic lithium, and higher volumetric capacity than commonly used graphite-based anode materials.
This work presents synthesis and evaluation of electrochemical properties of Li1.07V0.83Fe0.1O2, in particular open circuit voltage (OCV) and XRD analysis at different discharge (lithium content) stages.
EXPERIMENTAL
Li1.07V0.83Fe0.1O2 was synthesized using a high-temperature solid-state reaction method with Li2CO3, V2O3 and Fe2O3 taken as substrates. Stoichiometric amounts of reactants were milled in a high efficiency mill. Obtained powder was pressed into pellets and sintered in two steps: 1) at 800 °C for 10 h in Ar and 2) at 1050 °C for 12 h in 5 vol.% of H2 in Ar, followed by quenching.
Structural studies were performed in 10-110° range with CuKα radiation using Panalytical Empyrean diffractometer, followed by Rietveld refinement of identified structures.
Electrical conductivity was measured using 4-probe AC technique in -60°C to 70°C temperature range.
Electrochemical studies were done in Li/Li+/ Li1.07V0.83Fe0.1O2 cells constructed using CR2032-type containers. 1M solution of LiPF6in EC/DEC (in 1:1 ratio) was used as the electrolyte. For the positive electrode powder of active material was used (mass ≈ 50mg). OCV values were assumed as voltages of batteries after discharging to designated compositions followed by at least 24 h of relaxation.
RESULTS AND DISCUSSION
XRD analysis shown that the material is single phase and exhibits layered R-3m α-NaFeO2 type structure.
Electrical conductivity values are almost two order of magnitude higher than for materials with no iron substitution.
Discharge characteristics upon load shown step-like character, distinctly different than in Li1.07V0.93O2with shorter and right-shifted low voltage plateau.
ACKNOWLEDGMENT
This work was supported by NCN grant no. NCN 2011/02/A/ST5/00447.
REFERENCES
[1] A. R. Armstrong, C. Lyness, P. M. Panchmatia, M. S. Islam, P. G. Bruce, Nature Mater. 10
(2011) 223-229
[2] W.-T. Kim, Y. U. Jeong, H. C. Choi, Y. J. Lee, Y. J. Kim, J. H. Song, J. Power Sources 221
(2013) 366-371.
[3] X. Ma, G. Hautier, A. Jain, R. Doe, G. Ceder, J. Electrochem. Soc., 160 (2013) A279-A284.