Facile and large-scale chemical synthesis of highly porous secondary submicron/micron-sized NiCo2O4 materials for high-performance aqueous hybrid AC-NiCo2O4 electrochemical capacitors

•A facile and scalable chemical synthesis strategy is proposed.•The NiCo2O4 materials display a high surface area and porosity.•The NiCo2O4 electrode shows a high specific capacitance and rate capability.•The AC-NiCo2O4 capacitor exhibits a high Ragone behavior and high cycling stability. Highly por...

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Published inElectrochimica acta Vol. 107; pp. 494 - 502
Main Authors Ding, Rui, Qi, Li, Jia, Mingjun, Wang, Hongyu
Format Journal Article
LanguageEnglish
Published Elsevier Ltd 01.09.2013
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Abstract •A facile and scalable chemical synthesis strategy is proposed.•The NiCo2O4 materials display a high surface area and porosity.•The NiCo2O4 electrode shows a high specific capacitance and rate capability.•The AC-NiCo2O4 capacitor exhibits a high Ragone behavior and high cycling stability. Highly porous nickel cobaltite (NiCo2O4) materials have been synthesized via a facile and scalable chemical synthesis route. The obtained NiCo2O4 material displays a typical secondary submicron/micron-sized (0.1–2μm) agglomerate morphology, exhibiting large surface area (190.1m2g−1) and high porosity (1.136cm3g−1). The fabricated NiCo2O4 electrode shows high specific capacitance (351Fg−1 at 1Ag−1) and high-rate capability (82.1% capacitance retention at 8Ag−1), which is superior to many reported NiCo2O4 materials. Further, the assembled AC-NiCo2O4 aqueous hybrid capacitor exhibits high power and energy densities (2805Wkg−1, 6.8Whkg−1 at 8Ag−1) and high cycling stability (15% loss after 5000 cycles at 1.5Ag−1). The high-performance of the NiCo2O4 materials is attributed to their large surface area and highly porous structure which contribute to rich surface electroactive sites and easy ions transport pathways for facile electrochemical reactions.
AbstractList Highly porous nickel cobaltite (NiCo2O4) materials have been synthesized via a facile and scalable chemical synthesis route. The obtained NiCo2O4 material displays a typical secondary submicron/micron-sized (0.1a2 mu m) agglomerate morphology, exhibiting large surface area (190.1 m2 ga1) and high porosity (1.136 cm3 ga1). The fabricated NiCo2O4 electrode shows high specific capacitance (351 F ga1 at 1 A ga1) and high-rate capability (82.1% capacitance retention at 8 A ga1), which is superior to many reported NiCo2O4 materials. Further, the assembled AC-NiCo2O4 aqueous hybrid capacitor exhibits high power and energy densities (2805 W kga1, 6.8 Wh kga1 at 8 A ga1) and high cycling stability (15% loss after 5000 cycles at 1.5 A ga1). The high-performance of the NiCo2O4 materials is attributed to their large surface area and highly porous structure which contribute to rich surface electroactive sites and easy ions transport pathways for facile electrochemical reactions.
•A facile and scalable chemical synthesis strategy is proposed.•The NiCo2O4 materials display a high surface area and porosity.•The NiCo2O4 electrode shows a high specific capacitance and rate capability.•The AC-NiCo2O4 capacitor exhibits a high Ragone behavior and high cycling stability. Highly porous nickel cobaltite (NiCo2O4) materials have been synthesized via a facile and scalable chemical synthesis route. The obtained NiCo2O4 material displays a typical secondary submicron/micron-sized (0.1–2μm) agglomerate morphology, exhibiting large surface area (190.1m2g−1) and high porosity (1.136cm3g−1). The fabricated NiCo2O4 electrode shows high specific capacitance (351Fg−1 at 1Ag−1) and high-rate capability (82.1% capacitance retention at 8Ag−1), which is superior to many reported NiCo2O4 materials. Further, the assembled AC-NiCo2O4 aqueous hybrid capacitor exhibits high power and energy densities (2805Wkg−1, 6.8Whkg−1 at 8Ag−1) and high cycling stability (15% loss after 5000 cycles at 1.5Ag−1). The high-performance of the NiCo2O4 materials is attributed to their large surface area and highly porous structure which contribute to rich surface electroactive sites and easy ions transport pathways for facile electrochemical reactions.
Author Ding, Rui
Wang, Hongyu
Qi, Li
Jia, Mingjun
Author_xml – sequence: 1
  givenname: Rui
  surname: Ding
  fullname: Ding, Rui
  email: dingrui@ciac.jl.cn
  organization: State Key Laboratory of Electroanalytical Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, 5625 Renmin Street, Changchun 130022, PR China
– sequence: 2
  givenname: Li
  surname: Qi
  fullname: Qi, Li
  organization: State Key Laboratory of Electroanalytical Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, 5625 Renmin Street, Changchun 130022, PR China
– sequence: 3
  givenname: Mingjun
  surname: Jia
  fullname: Jia, Mingjun
  organization: State Key Laboratory of Theoretical and Computational Chemistry, College of Chemistry, Jilin University, Changchun 130023, PR China
– sequence: 4
  givenname: Hongyu
  surname: Wang
  fullname: Wang, Hongyu
  email: hongyuwang@ciac.jl.cn
  organization: State Key Laboratory of Electroanalytical Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, 5625 Renmin Street, Changchun 130022, PR China
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Keywords Hybrid
Nickel cobaltite
Chemical deposition
Electrochemical capacitors
Porous
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Snippet •A facile and scalable chemical synthesis strategy is proposed.•The NiCo2O4 materials display a high surface area and porosity.•The NiCo2O4 electrode shows a...
Highly porous nickel cobaltite (NiCo2O4) materials have been synthesized via a facile and scalable chemical synthesis route. The obtained NiCo2O4 material...
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SubjectTerms Agglomeration
Capacitance
Capacitors
Chemical deposition
Displays
Electrochemical capacitors
Electrodes
Hybrid
Ion transport
Nickel cobaltite
Porous
Surface area
Synthesis
Title Facile and large-scale chemical synthesis of highly porous secondary submicron/micron-sized NiCo2O4 materials for high-performance aqueous hybrid AC-NiCo2O4 electrochemical capacitors
URI https://dx.doi.org/10.1016/j.electacta.2013.05.114
https://www.proquest.com/docview/1513486217
Volume 107
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