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    Ferrous Nitrate–Nickel Oxide (Fe(NO3)2–NiO) Nanospheres Incorporated With Carbon Black and Polyvinylidenefluoride for Supercapacitor Applications

    Source: Journal of Electrochemical Energy Conversion and Storage:;2019:;volume( 016 ):;issue: 003::page 31008
    Author:
    Muzaffar, Aqib
    ,
    Muthusamy, Keerthana
    ,
    Basheer Ahamed, M.
    DOI: 10.1115/1.4042727
    Publisher: American Society of Mechanical Engineers (ASME)
    Abstract: Ferrous nitrate/nickel oxide {Fe(NO3)2–NiO} nanocomposite was synthesized via two-step facile hydrothermal route. The nanocomposite exhibits crystalline structure as unveiled by X-ray diffraction (XRD) pattern, while as the scanning electron microscope (SEM) images divulge spherical morphologies for both Fe(NO3)2 as well as NiO nanoparticles differentiating from each other in size. Cyclic voltammetry (CV), galvanostatic charge–discharge (GCD), and electrochemical impedance spectroscopy (EIS) techniques were used to investigate supercapacitive behavior of the symmetrically fabricated nanocomposite electrode configuration using aqueous KOH as the electrolyte. The CV analyses demonstrate dominant electrical double layer capacitance (EDLC) behavior in the potential range of 0–1 V. From charge–discharge curves, the maximum specific capacitance calculated was 460 F g−1 corresponding to the energy density of 16 W h kg−1 at a high power density of 250 W kg−1. EIS data affiliate well with the CV and GCD results justifying the maximum contribution of specific capacitance due to double layer capacitance. The nanocomposite retained 84% of its original capacitance after 1000 cycles and yielded maximum efficiency of 78%.
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      Ferrous Nitrate–Nickel Oxide (Fe(NO3)2–NiO) Nanospheres Incorporated With Carbon Black and Polyvinylidenefluoride for Supercapacitor Applications

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    http://yetl.yabesh.ir/yetl1/handle/yetl/4257954
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    contributor authorMuzaffar, Aqib
    contributor authorMuthusamy, Keerthana
    contributor authorBasheer Ahamed, M.
    date accessioned2019-09-18T09:01:17Z
    date available2019-09-18T09:01:17Z
    date copyright3/13/2019 12:00:00 AM
    date issued2019
    identifier issn2381-6872
    identifier otherjeecs_016_03_031008.pdf
    identifier urihttp://yetl.yabesh.ir/yetl1/handle/yetl/4257954
    description abstractFerrous nitrate/nickel oxide {Fe(NO3)2–NiO} nanocomposite was synthesized via two-step facile hydrothermal route. The nanocomposite exhibits crystalline structure as unveiled by X-ray diffraction (XRD) pattern, while as the scanning electron microscope (SEM) images divulge spherical morphologies for both Fe(NO3)2 as well as NiO nanoparticles differentiating from each other in size. Cyclic voltammetry (CV), galvanostatic charge–discharge (GCD), and electrochemical impedance spectroscopy (EIS) techniques were used to investigate supercapacitive behavior of the symmetrically fabricated nanocomposite electrode configuration using aqueous KOH as the electrolyte. The CV analyses demonstrate dominant electrical double layer capacitance (EDLC) behavior in the potential range of 0–1 V. From charge–discharge curves, the maximum specific capacitance calculated was 460 F g−1 corresponding to the energy density of 16 W h kg−1 at a high power density of 250 W kg−1. EIS data affiliate well with the CV and GCD results justifying the maximum contribution of specific capacitance due to double layer capacitance. The nanocomposite retained 84% of its original capacitance after 1000 cycles and yielded maximum efficiency of 78%.
    publisherAmerican Society of Mechanical Engineers (ASME)
    titleFerrous Nitrate–Nickel Oxide (Fe(NO3)2–NiO) Nanospheres Incorporated With Carbon Black and Polyvinylidenefluoride for Supercapacitor Applications
    typeJournal Paper
    journal volume16
    journal issue3
    journal titleJournal of Electrochemical Energy Conversion and Storage
    identifier doi10.1115/1.4042727
    journal fristpage31008
    journal lastpage031008-6
    treeJournal of Electrochemical Energy Conversion and Storage:;2019:;volume( 016 ):;issue: 003
    contenttypeFulltext
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