Self-Healing Micellar Ion Gels Based on Multiple Hydrogen Bonding

© 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Bibliographische Detailangaben
Veröffentlicht in:Advanced materials (Deerfield Beach, Fla.). - 1998. - (2018) vom: 31. Juli, Seite e1802792
1. Verfasser: Tamate, Ryota (VerfasserIn)
Weitere Verfasser: Hashimoto, Kei, Horii, Tatsuhiro, Hirasawa, Manabu, Li, Xiang, Shibayama, Mitsuhiro, Watanabe, Masayoshi
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2018
Zugriff auf das übergeordnete Werk:Advanced materials (Deerfield Beach, Fla.)
Schlagworte:Journal Article block copolymers hydrogen bonds ion gels ionic liquids self-healing
Beschreibung
Zusammenfassung:© 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Ion gels, composed of macromolecular networks filled by ionic liquids (ILs), are promising candidate soft solid electrolytes for use in wearable/flexible electronic devices. In this context, the introduction of a self-healing function would significantly improve the long-term durability of ion gels subject to mechanical loading. Nevertheless, compared to hydrogels and organogels, the self-healing of ion gels has barely investigated been because of there being insufficient understanding of the interactions between polymers and ILs. Herein, a new class of supramolecular micellar ion gel composed of a diblock copolymer and a hydrophobic IL, which exhibits self-healing at room temperature, is presented. The diblock copolymer has an IL-phobic block and a hydrogen-bonding block with hydrogen-bond-accepting and donating units. By combining the IL and the diblock copolymer, micellar ion gels are prepared in which the IL phobic blocks form a jammed micelle core, whereas coronal chains interact with each other via multiple hydrogen bonds. These hydrogen bonds between the coronal chains in the IL endow the ion gel with a high level of mechanical strength as well as rapid self-healing at room temperature without the need for any external stimuli such as light or elevated temperatures
Beschreibung:Date Revised 27.02.2024
published: Print-Electronic
Citation Status Publisher
ISSN:1521-4095
DOI:10.1002/adma.201802792