Author/Authors :
Rastgoo-Deylami، Mohadese نويسنده Department of Chemistry, Amirkabir University of Technology, Tehran, Iran , , Javanbakht، Mehran نويسنده , , Ghaem، Mehdi نويسنده Renewable Energy Research Center, Amirkabir University of Technology, Tehran, Iran , , Omidvar، Hamid نويسنده Renewable Energy Research Center, Amirkabir University of Technology, Tehran, Iran , , Ghafarian، Hossein نويسنده Department of Chemistry, Amirkabir University of Technology, Tehran, Iran ,
Abstract :
A controllable synthesis of flower-like lithium iron phosphate LiFePO4 (LFP) was
obtained via a two-stage heating during hydrothermal process. In the first stage, the
temperature was held at 105 °C (LFP1), 120 °C (LFP2), 150 °C (LFP3) and 190 °C (LFP4)
for 5 h. In the final stage, the temperature was held constant at 400 °C under H2/N2
atmosphere for 4 h. To increase the electrochemical reversibility and electronic conductivity,
LFP is treated with polyethylene glycol (PEG) as the templating agent and carbon sources for
the as-prepared materials. This is to obtain a modified LFP cathode with optimum electrical
contact between the electroactive materials and the carbon-filled electrode matrix which is
found to be effective in terms of raising the electrochemical performance of the Li-ion
batteries. Results show that as the first-stage temperature increased, the corresponding
electrochemical performance of the resulting sample has been increased up to a temperature
of 150 °C. Galvanostatic charge-discharge test indicates that flower-like LiFePO4/C
composite, LFP3, exhibits initial discharge capacity of 118 mAh g-1 at 0.1C rates. The
performance improvement was attributed to a reduction of the thickness and particle size of
the flower-like LiFePO4 particles. Results of X-ray diffraction (XRD) revealed that the
structure of the latter represents phase of the ordered olivine structure without any impurities.
Cyclic voltammetry indicates that the improvement in redox cycling could be attributed to an
increase of the electrochemical active surface area (ECSA) and the related increase in microporosity
as evidenced by SEM analysis.