Synthesis of poly(TEMPO-substituted glycidyl ether) by utilizing t-BuOK/18-crown-6 for an organic cathode-active material

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    Abstract

    A nitroxide radical-substituted polyether, poly(TEMPO-substituted glycidyl ether) (PTGE), was synthesized using a potassium tert-butoxide/18-crown-6 initiator. The presence of 18-crown-6 effected significant improvement in the reactivity of the chain end, thus allowing the polymerization to proceed at moderate temperatures to suppress the deactivation of the pendant nitroxide group. A high molecular-weight polyether with a theoretical radical concentration was first obtained in high yield. Charging and discharging cyclability was much improved by cross-linking, which helped the electrode-active material stay on a current collector during the electrolysis. The polymer/vapor-grown carbon nanofiber composite electrode exhibited a redox capacity comparable to the formula weight-based theoretical density over 10<sup>3</sup> cycles and fast charging/discharging capability up to a rate of 60 C which corresponded to full charging and discharging in 60 s. The redox capacity was almost maintained for a composite layer with a remarkably high polymer ratio of 90 %, which demonstrated the presence of effective percolation network of the carbon nanofiber due likely to the affinity of the polyether to the carbon material.

    Original languageEnglish
    Pages (from-to)90-96
    Number of pages7
    JournalMacromolecular Symposia
    Volume351
    Issue number1
    DOIs
    Publication statusPublished - 2015 May 1

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    Keywords

    • anionic ring-opening polymerization
    • electrode-active material
    • nitroxide radical
    • polyether
    • redox polymer

    ASJC Scopus subject areas

    • Organic Chemistry
    • Materials Chemistry
    • Polymers and Plastics
    • Condensed Matter Physics

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