4.8 Article

Mechano-responsive hydrogen-bonding array of thermoplastic polyurethane elastomer captures both strength and self-healing

Journal

NATURE COMMUNICATIONS
Volume 12, Issue 1, Pages -

Publisher

NATURE RESEARCH
DOI: 10.1038/s41467-021-20931-z

Keywords

-

Funding

  1. KRICT [SS2042-10, BSF20-254]
  2. National Research Foundation of Korea (NRF) - Ministry of Science, ICT & Future Planning [2018R1C1B6000966, 2019R1C1C1003888, 2020R1C1C1009340]
  3. National Research Foundation of Korea [5199990514442, 2020R1C1C1009340, 2018R1C1B6000966] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

Ask authors/readers for more resources

Self-repairable materials aim to replicate the curable and resilient properties of biological tissue, but often face challenges due to the conflicting properties of self-healing and toughening. In this study, authors introduced a tough and strong carbonate-type thermoplastic polyurethane elastomer that self-heals at ambient temperature.
Self-repairable materials strive to emulate curable and resilient biological tissue; however, their performance is currently insufficient for commercialization purposes because mending and toughening are mutually exclusive. Herein, we report a carbonate-type thermoplastic polyurethane elastomer that self-heals at 35 degrees C and exhibits a tensile strength of 43MPa; this elastomer is as strong as the soles used in footwear. Distinctively, it has abundant carbonyl groups in soft-segments and is fully amorphous with negligible phase separation due to poor hard-segment stacking. It operates in dual mechano-responsive mode through a reversible disorder-to-order transition of its hydrogen-bonding array; it heals when static and toughens when dynamic. In static mode, non-crystalline hard segments promote the dynamic exchange of disordered carbonyl hydrogen-bonds for self-healing. The amorphous phase forms stiff crystals when stretched through a transition that orders inter-chain hydrogen bonding. The phase and strain fully return to the pre-stressed state after release to repeat the healing process. Self-healing materials strive to emulate curable and resilient biological tissue but their performance is often insufficient for commercial applications because self-healing and toughening are mutually exclusive properties. Here, the authors report a tough and strong carbonate-type thermoplastic polyurethane elastomer that self-heals at ambient temperature.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available