posted on 2025-04-25, 18:47authored byFenglong Li, Haofeng Qiu, Chao Chen, Xiaolin Wang, Minghui Cui, Shijie Qiu, Kyung Jin Lee, Jing Chen, Wu Bin Ying, Jin Zhu
Red sea stars exhibit an extraordinary
underwater self-healing
capability driven by fibrinolytic enzyme secretion, enabling survival
in challenging marine environments. Inspired by this biological mechanism,
we developed a polyurethane (DSFPU-3) capable of rapid underwater
self-healing. By integrating dual hydrophobic units (alkyl side chains
and fluorine groups) with tandem dynamic bonds (disulfide and imine
bonds), DSFPU-3 achieved a water contact angle of 99.3° and maintained
stable microphase structures and micromorphology even after 4-day
water soaking. The synergistic effect of hydrophobic units and dynamic
bonds enabled self-healing at a speed exceeding 33.33 μm/h,
achieving 98% efficiency and allowing the material to endure significant
mechanical stress post-healing. Small-molecule modeling experiments
and rheological analyses validated the bond exchange mechanisms of
the tandem dynamic bonds, underscoring their critical role in accelerating
the self-healing process. This study presents a novel strategy for
fabricating rapid underwater self-healing polyurethanes, representing
a significant advancement in their application under aquatic conditions.