Peptidoglycan-inspired autonomous ultrafast self-healing bio-friendly elastomers for bio-integrated electronics

Abstract Elastomers are essential for stretchable electronics, which have become more and more important in bio-integrated devices. To ensure high compliance with the application environment, elastomers are expected to resist, and even self-repair, mechanical damage, while being friendly to the huma...

Full description

Saved in:
Bibliographic Details
Published inNational science review Vol. 8; no. 5; p. nwaa154
Main Authors Zhang, Luzhi, Liang, Jiahui, Jiang, Chenyu, Liu, Zenghe, Sun, Lijie, Chen, Shuo, Xuan, Huixia, Lei, Dong, Guan, Qingbao, Ye, Xiaofeng, You, Zhengwei
Format Journal Article
LanguageEnglish
Published China Oxford University Press 01.05.2021
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Abstract Elastomers are essential for stretchable electronics, which have become more and more important in bio-integrated devices. To ensure high compliance with the application environment, elastomers are expected to resist, and even self-repair, mechanical damage, while being friendly to the human body. Herein, inspired by peptidoglycan, we designed the first room-temperature autonomous self-healing biodegradable and biocompatible elastomers, poly(sebacoyl 1,6-hexamethylenedicarbamate diglyceride) (PSeHCD) elastomers. The unique structure including alternating ester-urethane moieties and bionic hybrid crosslinking endowed PSeHCD elastomers superior properties including ultrafast self-healing, tunable biomimetic mechanical properties, facile reprocessability, as well as good biocompatibility and biodegradability. The potential of the PSeHCD elastomers was demonstrated as a super-fast self-healing stretchable conductor (21 s) and motion sensor (2 min). This work provides a new design and synthetic principle of elastomers for applications in bio-integrated electronics. Superfast autonomous self-healing biocompatible and biodegradable elastomers were developed based on unique alternating ester-urethane moieties and bionic hybrid crosslinking networks, showing great potential for stretchable electronics.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
Equally contributed to this work.
ISSN:2095-5138
2053-714X
DOI:10.1093/nsr/nwaa154