4.8 Article

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

Journal

NATIONAL SCIENCE REVIEW
Volume 8, Issue 5, Pages -

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/nsr/nwaa154

Keywords

biomimetic; elastomers; ultrafast self-healing; bio-integrated electronics; stretchable conductor

Funding

  1. National Natural Science Foundation of China [21991123, 21574019, 21304015, 81671832]
  2. Natural Science Foundation of Shanghai [20ZR1402500, 18ZR1401900]
  3. Shanghai Belt and Road Joint Laboratory of Advanced Fiber and Low-dimension Materials (Donghua University) [18520750400]
  4. Fundamental Research Funds for the Central Universities
  5. DHU Distinguished Young Professor Program [LZA2019001]
  6. Graduate Student Innovation Fund of Donghua University [CUSF-DH-D-2020037]
  7. Shanghai Municipal Key Clinical Specialty Construction Project [shslczdzk01702]
  8. Science and Technology Commission of Shanghai [17DZ2260100]

Ask authors/readers for more resources

Inspired by peptidoglycan, the first room-temperature autonomous self-healing biodegradable and biocompatible elastomers, PSeHCD, were designed with unique properties including ultrafast self-healing, tunable biomimetic mechanical properties, and good biocompatibility. The potential of PSeHCD elastomers was demonstrated as a super-fast self-healing stretchable conductor and motion sensor in bio-integrated electronics applications.
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.

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