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Extraordinary pseudocapacitive energy storage triggered by phase transformation in hierarchical vanadium oxides

Author

Listed:
  • Bo-Tian Liu

    (Jilin University)

  • Xiang-Mei Shi

    (Jilin University)

  • Xing-You Lang

    (Jilin University)

  • Lin Gu

    (Chinese Academy of Sciences)

  • Zi Wen

    (Jilin University)

  • Ming Zhao

    (Jilin University)

  • Qing Jiang

    (Jilin University)

Abstract

Pseudocapacitance holds great promise for improving energy densities of electrochemical supercapacitors, but state-of-the-art pseudocapacitive materials show capacitances far below their theoretical values and deliver much lower levels of electrical power than carbon-based materials due to poor cation accessibility and/or long-range electron transferability. Here we show that in situ corundum-to-rutile phase transformation in electron-correlated vanadium sesquioxide can yield nonstoichiometric rutile vanadium dioxide layers that are composed of highly sodium ion accessible oxygen-deficiency quasi-hexagonal tunnels sandwiched between conductive rutile slabs. This unique structure serves to boost redox and intercalation kinetics for extraordinary pseudocapacitive energy storage in hierarchical isomeric vanadium oxides, leading to a high specific capacitance of ~1856 F g–1 (almost sixfold that of the pristine vanadium sesquioxide and dioxide) and a bipolar charge/discharge capability at ultrafast rates in aqueous electrolyte. Symmetric wide voltage window pseudocapacitors of vanadium oxides deliver a power density of ~280 W cm–3 together with an exceptionally high volumetric energy density of ~110 mWh cm–3 as well as long-term cycling stability.

Suggested Citation

  • Bo-Tian Liu & Xiang-Mei Shi & Xing-You Lang & Lin Gu & Zi Wen & Ming Zhao & Qing Jiang, 2018. "Extraordinary pseudocapacitive energy storage triggered by phase transformation in hierarchical vanadium oxides," Nature Communications, Nature, vol. 9(1), pages 1-9, December.
  • Handle: RePEc:nat:natcom:v:9:y:2018:i:1:d:10.1038_s41467-018-03700-3
    DOI: 10.1038/s41467-018-03700-3
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