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    Effect of Niobium Doping on Electrochemical Properties of Microwave Synthesized Carbon Coated Nanolithium Iron Phosphate for High Rate Underwater Applications

    Source: Journal of Electrochemical Energy Conversion and Storage:;2019:;volume( 016 ):;issue: 002::page 21002
    Author:
    Kumar, A. Srinivas
    ,
    Satyavani, T. V. S. L.
    ,
    Senthilkumar, M.
    ,
    Subba Rao, P. S. V.
    DOI: 10.1115/1.4041454
    Publisher: The American Society of Mechanical Engineers (ASME)
    Abstract: 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.
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      Effect of Niobium Doping on Electrochemical Properties of Microwave Synthesized Carbon Coated Nanolithium Iron Phosphate for High Rate Underwater Applications

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    http://yetl.yabesh.ir/yetl1/handle/yetl/4256204
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    contributor authorKumar, A. Srinivas
    contributor authorSatyavani, T. V. S. L.
    contributor authorSenthilkumar, M.
    contributor authorSubba Rao, P. S. V.
    date accessioned2019-03-17T10:34:11Z
    date available2019-03-17T10:34:11Z
    date copyright10/19/2018 12:00:00 AM
    date issued2019
    identifier issn2381-6872
    identifier otherjeecs_016_02_021002.pdf
    identifier urihttp://yetl.yabesh.ir/yetl1/handle/yetl/4256204
    description abstractLithium 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.
    publisherThe American Society of Mechanical Engineers (ASME)
    titleEffect of Niobium Doping on Electrochemical Properties of Microwave Synthesized Carbon Coated Nanolithium Iron Phosphate for High Rate Underwater Applications
    typeJournal Paper
    journal volume16
    journal issue2
    journal titleJournal of Electrochemical Energy Conversion and Storage
    identifier doi10.1115/1.4041454
    journal fristpage21002
    journal lastpage021002-8
    treeJournal of Electrochemical Energy Conversion and Storage:;2019:;volume( 016 ):;issue: 002
    contenttypeFulltext
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