Room-Temperature Electrodeposition of Mg Metal from Amide Salts Dissolved in Glyme-Ionic Liquid Mixture

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The electrodeposition of Mg metal from an ionic liquid–glyme mixture was investigated at room temperature. The mixture contains a glyme, a simple amide salt Mg(Tf[2]N)[2] (Tf = SO[2]CF[3]), and a quaternary-ammonium Tf2N ionic liquid. Using the mixture bath, substantial cathodic electrodeposition of Mg at a large current density (∼10 mA cm[−2]) was observed, suggesting a change in coordination geometry around Mg[2+] cation together with improved conductivity. By mixing diglyme, the conductivity increased by an order of magnitude (2.5 – 2.6 mS cm[−1]) compared to the glyme-free ionic liquid (0.35 mS cm[−1]) and the viscosity became as low as that of pure glyme. Additionally, potentiostatic electrolysis resulted in a non-dendritic thin film of elemental Mg with metallic luster.

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詳細情報 詳細情報について

  • CRID
    1050564285736767488
  • NII論文ID
    120005385893
  • NII書誌ID
    AA00697016
  • ISSN
    00134651
  • HANDLE
    2433/182934
  • 本文言語コード
    en
  • 資料種別
    journal article
  • データソース種別
    • IRDB
    • CiNii Articles

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