scholarly journals Structural and Electrochemical Characterization of PureLiFePO4and Nanocomposite C-LiFePO4Cathodes for Lithium Ion Rechargeable Batteries

2009 ◽  
Vol 2009 ◽  
pp. 1-10 ◽  
Author(s):  
Arun Kumar ◽  
R. Thomas ◽  
N. K. Karan ◽  
J. J. Saavedra-Arias ◽  
M. K. Singh ◽  
...  

Pure lithium iron phosphate (LiFePO4) and carbon-coatedLiFePO4(C-LiFePO4) cathode materials were synthesized for Li-ion batteries. Structural and electrochemical properties of these materials were compared. X-ray diffraction revealed orthorhombic olivine structure. Micro-Raman scattering analysis indicates amorphous carbon, and TEM micrographs show carbon coating onLiFePO4particles. Ex situ Raman spectrum of C-LiFePO4at various stages of charging and discharging showed reversibility upon electrochemical cycling. The cyclic voltammograms ofLiFePO4and C-LiFePO4showed only a pair of peaks corresponding to the anodic and cathodic reactions. The first discharge capacities were 63, 43, and 13 mAh/g for C/5, C/3, and C/2, respectively forLiFePO4where as in case of C-LiFePO4that were 163, 144, 118, and 70 mAh/g for C/5, C/3, C/2, and 1C, respectively. The capacity retention of pureLiFePO4was 69% after 25 cycles where as that of C-LiFePO4was around 97% after 50 cycles. These results indicate that the capacity and the rate capability improved significantly upon carbon coating.

2013 ◽  
Vol 739 ◽  
pp. 21-25 ◽  
Author(s):  
Xiang Yin Mo ◽  
Xiao San Feng ◽  
Yi Ding ◽  
Cai Rong Kang

Carbon-coated, bismuth-doped, lithium iron phosphates, LiFe1xBixPO4(0x0.05), have been synthesized by a solid-state reaction method. From the optimization, the carbon-coated LiFe0.95Bi0.05PO4phase showed superior performances in terms of phase purity and high discharge capacity. The structural, morphological, and electrochemical properties were studied and compared to carbon-coated, LiFePO4. The Li/LiFe0.95Bi0.05PO4with carbon coating cell delivered an initial discharge capacity of 145 mAh/g and was 30 mAh/g higher than the Li/LiFePO4with carbon coating cell. Cyclic voltammetry revealed excellent reversibility of the LiFe0.95Bi0.05PO4with carbon coating material. High rate capability studies were also performed and showed a capacity retention over 93% during the cycling. It was concluded that substituted Bi ion play an important role in enhancing battery performance of the LiFePO4material through improving the kinetics of the lithium insertion/extraction reaction on the electrode.


Author(s):  
A. Srinivas Kumar ◽  
T. V. S. L. Satyavani ◽  
M. Senthilkumar ◽  
P. S. V. Subba Rao

Lithium iron phosphate (LiFePO4) for lithium-ion batteries is considered as perfect cathode material for various military applications, especially underwater combat vehicles. For deployment at high rate applications, the low conductivity of LiFePO4 needs to be improved. Cationic substitution of niobium in the native carbon coated LiFePO4 is one of the methods to enhance the conductivity. In the present work, how the niobium doped solid solution could be formed is studied. Nanopowders of LiFePO4/C and Li1−xNbxFePO4/C (x = 0.05, 0.1, 0.15, 0.16) are synthesized from precursors using microwave synthesis. The solid solution formation up to (x = 0.15) Li1−xNbxFePO4/C without impurity phases is confirmed by X-ray diffraction (XRD) pattern and Fourier transform infrared spectroscopic (FTIR) results. Particle distribution is obtained by scanning electron microscope from the synthesized powders. Energy dispersive X-ray spectrometer (EDS) results qualitatively confirmed the presence of niobium. Also, direct current (dc) conductivities are measured using sintered pellets and activation energies are calculated using Arrhenius equation. The dependence of conductivity and activation energy of LiFePO4/C on variation of niobium doping is investigated in this study. CR2032 type coin cells are fabricated with the synthesized materials and subjected to cyclic voltammetry studies, rate capability and cycle life studies. Diffusion coefficients are obtained from electrochemical impedance spectroscopy studies. It is observed that room temperature dc conductivity improved by niobium doping when compared to LiFePO4/C (0.379 × 10−2 S/cm) and is maximum for Li0.9Nb0.1FePO4/C (40.58 × 10−2 S/cm). It is also observed that diffusion coefficient of Li+ in Li0.9Nb0.1FePO4/C (13.306 × 10−9 cm2 s−1) improved by two orders of magnitude in comparison with the pure LiFePO4 (10 − 12 cm2 s−1) and carbon-coated nano LiFePO4/C (0.632 × 10−11 cm2 s−1). Cells with Li0.9Nb0.1FePO4/C are able to deliver useful capacity of around 104 mAh/g at 10 C rate. More than 500 cycles are achieved with Li0.9Nb0.1FePO4/C at 20 C rate.


2006 ◽  
Vol 973 ◽  
Author(s):  
Shijun Wang ◽  
M. Stanley Whittingham

ABSTRACTThis study focusses on optimizing the parameters of the hydrothermal synthesis to produce iron phosphates for lithium ion batteries, with an emphasis on pure LiFePO4 with the olivine structure and compounds containing a higher iron:phosphate ratio. Lithium iron phosphate (LiFePO4) is a promising cathode candidate for lithium ion batteries due to its high theoretical capacity, environmentally benign and the low cost of starting materials. Well crystallized LiFePO4 can be successfully synthesized at temperatures above 150 °C. The addition of a reducing agent, such as hydrazine, is essential to minimize the oxidation of ferrous (Fe2+) to ferric (Fe3+) in the final compound. The morphology of LiFePO4 is highly dependent on the pH of the initial solution. This study also investigated the lipscombite iron phosphates of formula Fe1.33PO4OH. This compound has a log-like structure formed by Fe-O octahedral chains. The chains are partially occupied by the Fe3+ sites, and these iron atoms and some of the vacancies can be substituted by other cations. Most of the protons can be ion-exchanged for lithium, and the electrochemical capacity is much increased.


2009 ◽  
Vol 194 (1) ◽  
pp. 486-493 ◽  
Author(s):  
Hidehiko Nozaki ◽  
Katsuhide Nagaoka ◽  
Kazuhito Hoshi ◽  
Naoto Ohta ◽  
Michio Inagaki

2019 ◽  
Vol 300 ◽  
pp. 18-25 ◽  
Author(s):  
Hye-Jung Kim ◽  
Geun-Hyeong Bae ◽  
Sang-Min Lee ◽  
Jou-Hyeon Ahn ◽  
Jae-Kwang Kim

2011 ◽  
Vol 1363 ◽  
Author(s):  
Yixu Wang ◽  
Hsiao-Ying Shadow Huang

ABSTRACTThe need for the development and deployment of reliable and efficient energy storage devices, such as lithium-ion rechargeable batteries, is becoming increasingly important due to the scarcity of petroleum. In this work, we provide an overview of commercially available cathode materials for Li-ion rechargeable batteries and focus on characteristics that give rise to optimal energy storage systems for future transportation modes. The study shows that the development of lithium-iron-phosphate (LiFePO4) batteries promises an alternative to conventional lithiumion batteries, with their potential for high energy capacity and power density, improved safety, and reduced cost. This work contributes to the fundamental knowledge of lithium-ion battery cathode materials and helps with the design of better rechargeable batteries, and thus leads to economic and environmental benefits.


2014 ◽  
Vol 262 ◽  
pp. 25-29 ◽  
Author(s):  
Jae-Kwang Kim ◽  
Dul-Sun Kim ◽  
Du-Hyun Lim ◽  
Aleksandar Matic ◽  
Ghanshyam S. Chauhan ◽  
...  

2015 ◽  
Vol 3 (5) ◽  
pp. 2043-2049 ◽  
Author(s):  
Zhang Jinli ◽  
Wang Jiao ◽  
Liu Yuanyuan ◽  
Nie Ning ◽  
Gu Junjie ◽  
...  

A novel composite of LiFePO4 with phosphorus-doped carbon layers has been prepared via a simple hydrothermal method using glucose as the carbon source to generate a carbon coating and triphenylphosphine as the phosphorus source.


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