N-type redox-active benzoylpyridinium-substituted supramolecular gel for an organogel-based rechargeable device

Kan Hatakeyama-Sato, Rieka Ichinoi, Yoshito Sasada, Yusuke Sasaki, Kenichi Oyaizu, Hiroyuki Nishide

研究成果: Article査読

1 被引用数 (Scopus)

抄録

A supramolecular benzoylpyridinium-substituted cyclohexanediamine gelator with n-type redox properties was synthesized. The gelator formed a robust supramolecular network consisting of cyclohexanediamine units. In the organogel, the stable redox reactions of the benzoylpyridinium moieties led to a reversible charge/discharge at 1.05V (vs. Fc/Fc+). A supramolecule- based rechargeable device was fabricated using TEMPO- and benzoylpyridinium-substituted gelators as the cathode and anode, respectively, giving rise to a flexible, transparent, and even self-healable battery.

本文言語English
ページ(範囲)555-557
ページ数3
ジャーナルChemistry Letters
48
6
DOI
出版ステータスPublished - 2019

ASJC Scopus subject areas

  • Chemistry(all)

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