リチウムイオンを含む塩化アルミニウム系室温イオン液体中における天然黒鉛電極の電気化学反応の解析

  • 十和田 潤
    岩手大学大学院工学研究科フロンティア物質機能工学専攻
  • 門磨 義浩
    岩手大学大学院工学研究科フロンティア材料機能工学専攻
  • 嶋田 和明
    岩手大学大学院工学研究科応用化学・生命工学専攻
  • 熊谷 直昭
    岩手大学大学院工学研究科フロンティア材料機能工学専攻
  • 宇井 幸一
    岩手大学大学院工学研究科フロンティア材料機能工学専攻

書誌事項

タイトル別名
  • Analysis of Electrochemical Reactions of Natural Graphite Electrode in Chloroaluminate Type Room-temperature Ionic Liquid Electrolyte Containing Lithium Ion
  • リチウムイオン オ フクム エンカ アルミニウムケイ シツオン イオン エキタイ チュウ ニ オケル テンネン コクエン デンキョク ノ デンキ カガク ハンノウ ノ カイセキ

この論文をさがす

抄録

We have reported that the electrochemical characteristics of a natural graphite (NG-3) electrode in the chloroaluminate type room-temperature ionic liquid containing lithium ion as the electrolyte for non-flammable lithium-ion batteries were improved by employing polyacrylic acid (PAA) as the binder. Therefore, we have analyzed the influence of the binder types on the electrochemical reaction (charge-discharge reaction) of the natural graphite electrode in more detail. The FE-SEM observations showed that the surface morphology of the NG-3 electrode coated with the PAA binder was smooth, whereas that of the NG-3 electrode using poly(vinylidene difluoride) as a binder was rough. The EDX mappings showed that the reduction of SOCl2 and the deposition of Al would be suppressed to some extent during charging by employing the PAA binder; the deposit from the surface of the NG-3 electrode coated with the PAA binder would be exfoliated or disappeared during discharging. Based on the XPS results, it was clarified that Al would be deposited on the surface of the NG-3 electrode during charging. These results clarified that the deposition reaction that was a side reaction was different according to the binder types during initial charging; the exfoliation or the disappearance of the deposit occurred during discharging.

収録刊行物

  • Electrochemistry

    Electrochemistry 81 (6), 432-439, 2013

    公益社団法人 電気化学会

被引用文献 (1)*注記

もっと見る

参考文献 (46)*注記

もっと見る

詳細情報 詳細情報について

問題の指摘

ページトップへ