Red Sea Star-Inspired, Rapid Underwater Self-Healing Polyurethane Based on Dual Hydrophobic Units and Tandem Dynamic Bonds

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.

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Publication Details

Journal
Macromolecules
Published
2025-04-25
DOI
https://doi.org/10.1021/acs.macromol.4c03007
Citations
13
Primary Topic
Polymer composites and self-healing
Type
article
Field-Weighted Citation Impact
7.89

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article

Red Sea Star-Inspired, Rapid Underwater Self-Healing Polyurethane Based on Dual Hydrophobic Units and Tandem Dynamic Bonds

Haofeng Qiu, Jin Zhu, Minghui Cui, Wu Bin Ying et al.
13 citations
Macromolecules
Polymer composites and self-healing
7.89
article

Red Sea Star-Inspired, Rapid Underwater Self-Healing Polyurethane Based on Dual Hydrophobic Units and Tandem Dynamic Bonds

Haofeng Qiu, Jin Zhu, Minghui Cui, Wu Bin Ying, Shijie Qiu, Fenglong Li, Jing Chen, Chao Chen, Kyung Jin Lee, Xiaolin Wang
article en
13 citations

Abstract

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.

MacromoleculesVol. 58(10)
Korea Advanced Institute of Science and Technology (KR), Chungnam National University (KR), Chinese Academy of Sciences (CN), Theranostics (New Zealand) (NZ), Ningbo Medical Center Lihuili Hospital (CN), Ningbo Institute of Industrial Technology (CN)
National Natural Science Foundation of China, National Research Foundation of Korea
Life below water
Openalex Percentile: Top 2%
Polymer composites and self-healing
7.89
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