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Crack Suppression in Conductive Film by Amyloid-Like Protein Aggregation toward Flexible Device.

Authors :
Chen M
Yang F
Chen X
Qin R
Pi H
Zhou G
Yang P
Source :
Advanced materials (Deerfield Beach, Fla.) [Adv Mater] 2021 Nov; Vol. 33 (44), pp. e2104187. Date of Electronic Publication: 2021 Sep 12.
Publication Year :
2021

Abstract

A fatal weakness in flexible electronics is the mechanical fracture that occurs during repetitive fatigue deformation; thus, controlling the crack development of the conductive layer is of prime importance and has remained a great challenge until now. Herein, this issue is tackled by utilizing an amyloid/polysaccharide molecular composite as an interfacial binder. Sodium alginate (SA) can take part in amyloid-like aggregation of the lysozyme, leading to the facile synthesis of a 2D protein/saccharide hybrid nanofilm over an ultralarge area (e.g., >400 cm <superscript>2</superscript> ). The introduction of SA into amyloid-like aggregates significantly enhances the mechanical strength of the hybrid nanofilm, which, with the help of amyloid-mediated interfacial adhesion, effectively diminishes the microcracks in the hybrid nanofilm coating after repetitive bending or stretching. The microcrack-free hybrid nanofilm then shows high interfacial activity to induce electroless deposition of metal in a Kelvin model on a substrate, which noticeably suppresses the formation of microcracks and consequent conductivity loss during the bending and stretching of the metal-coated flexible substrates. This work underlines the significance of amyloid/polysaccharide nanocomposites in the design of interfacial binders for reliable flexible electronic devices and represents an important contribution to mimicking amyloid and polysaccharide-based adhesive cements created by organisms.<br /> (© 2021 Wiley-VCH GmbH.)

Details

Language :
English
ISSN :
1521-4095
Volume :
33
Issue :
44
Database :
MEDLINE
Journal :
Advanced materials (Deerfield Beach, Fla.)
Publication Type :
Academic Journal
Accession number :
34510560
Full Text :
https://doi.org/10.1002/adma.202104187