@article{6f86d061025145dfaaf753faf782f83e,
title = "N-type redox-active benzoylpyridinium-substituted supramolecular gel for an organogel-based rechargeable device",
abstract = "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.",
keywords = "Charge storage, Redox-active molecule, Supramolecule",
author = "Kan Hatakeyama-Sato and Rieka Ichinoi and Yoshito Sasada and Yusuke Sasaki and Kenichi Oyaizu and Hiroyuki Nishide",
note = "Funding Information: The work was also partially supported by Grants-in-Aid for Scientific Research (Nos. 17H03072, 18K19120, 18H03921, and 18H05983) from MEXT, Japan. The work was also partially supported by Research Institute for Science and Engineering, Waseda University. K.H.-S. acknowledges financial support from FS research by JXTG Co. Publisher Copyright: {\textcopyright} 2019 The Chemical Society of Japan.",
year = "2019",
doi = "10.1246/cl.190085",
language = "English",
volume = "48",
pages = "555--557",
journal = "Chemistry Letters",
issn = "0366-7022",
publisher = "Chemical Society of Japan",
number = "6",
}