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Supramolecular Association of a Block Copolymer via Strong Hydrogen Bonding to Form Self-Healable Ionogels.

作者信息

Kim Seungjun, Park Soeun, Kim Min Su, Lee Hyeonji, Lee Hyeji, Lee Keun Hyung, Kim Myungwoong

机构信息

Department of Chemistry and Chemical Engineering, Inha University, Incheon 22212, Republic of Korea.

出版信息

ACS Appl Mater Interfaces. 2024 Sep 25;16(38):51459-51468. doi: 10.1021/acsami.4c09988. Epub 2024 Sep 12.

DOI:10.1021/acsami.4c09988
PMID:39264059
Abstract

The drive to enhance the operational durability and reliability of stretchable and wearable electronic and electrochemical devices has led to the exploration of self-healing materials that can recover from both physical and functional failures. In the present study, we fabricated a self-healable solid polymer electrolyte, referred to as an ionogel, using reversible hydrogen bonding between the ureidopyrimidone units of a block copolymer (BCP) network swollen in an ionic liquid (IL). The BCP consisted of poly(styrene--(methyl acrylate--ureidopyrimidone methacrylate)) [poly(S--(MA--UPyMA)], with the IL-phobic polystyrene forming micellar cores that were interconnected via intercorona hydrogen bonding between the ureidopyrimidone units. By precisely regulating the molecular weight and the composition of the hydrogen-bondable motifs, the mechanical, electrical, and self-healing characteristics of the ionogel were systematically evaluated. The resulting ionogel samples exhibited suitable stretchability, ionic conductivity, and room-temperature self-healability due to reversible hydrogen bonding. To highlight the applicability of the self-healing ionogel as a high-capacitance gate insulator, an electrolyte-gated transistor (EGT) was fabricated using a poly(3-hexylthiophene-2,5-diyl) semiconductor, and the performance of the EGT was fully recovered from a complete cut without any external stimuli.

摘要

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