Hydrophilicity-Hydrophobicity Transformation, Thermoresponsive Morphomechanics, and Crack Multifurcation Revealed by AIEgens in Mechanically Strong Hydrogels

© 2021 Wiley-VCH GmbH.

Bibliographische Detailangaben
Veröffentlicht in:Advanced materials (Deerfield Beach, Fla.). - 1998. - 33(2021), 39 vom: 01. Okt., Seite e2101500
1. Verfasser: Hu, Yubing (VerfasserIn)
Weitere Verfasser: Barbier, Lucile, Li, Zhao, Ji, Xiaofan, Le Blay, Heiva, Hourdet, Dominique, Sanson, Nicolas, Lam, Jacky W Y, Marcellan, Alba, Tang, Ben Zhong
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2021
Zugriff auf das übergeordnete Werk:Advanced materials (Deerfield Beach, Fla.)
Schlagworte:Journal Article aggregation-induced emission crack multifurcation hydrophilicity-hydrophobicity transformation microphase separation
Beschreibung
Zusammenfassung:© 2021 Wiley-VCH GmbH.
Biomimetic exploration of stimuli-responsive and crack-resistant hydrogels is of great academic and practical significance, although the rational design of tough hydrogels is limited by insufficient mechanism study due to the lack of imaging techniques to "see" hydrogels at mesoscale level. A series of composite hydrogels with compartmentalized thermal response is designed by incorporating aggregation- and polarity-sensitive fluorescent probes in a poly(N-isopropylacrylamide) (PNIPAM) network grafted with poly(N,N-dimethylacrylamide) side-chains. The fluorescence technique is explored as a powerful tool to directly visualize their hydrophilicity-hydrophobicity transformation and the composition-dependent microphase separation. Based on the morphological observation and mechanical measurements, the concept of morphomechanics with a comprehensive mechanism clarification is proposed. In this regard, the thermoresponsive toughening is attributed to the formation of multiple noncovalent interactions and the conformational changes of PNIPAM chains. The enhanced fracture energy by crack multifurcation is related to the tearing-like disruption of weak interfaces between the separated phases
Beschreibung:Date Revised 04.10.2021
published: Print-Electronic
Citation Status PubMed-not-MEDLINE
ISSN:1521-4095
DOI:10.1002/adma.202101500