材料科学
粘附
氢键
渗透(战争)
胶粘剂
韧性
水下
纳米技术
复合材料
化学物理
分子动力学
超分子化学
化学工程
变形(气象学)
承压水
跳跃的
深水
氢
作者
Gang Lü,Rui Ma,Jian Lü,Yuanhao Chang,Ming Li,Eduardo Saiz
出处
期刊:Science Advances
[American Association for the Advancement of Science]
日期:2025-11-05
卷期号:11 (45): eaea3097-eaea3097
被引量:6
标识
DOI:10.1126/sciadv.aea3097
摘要
Underwater adhesion has long been limited by interfacial water's paradoxical role as both bonding mediator and failure initiator. We present a confined hydration adhesive tape (CHAT) that harnesses water as a molecular architect through spatial hydration management. By confining water penetration to sub-8-micrometer depths, we create a dynamic interface where hydration-activated hydrogen bonds enable adaptive, high-density interfacial connections, and hydrophobic nanodomains maintain bulk integrity via entropic water exclusion. This orchestrated hydration yields an interfacial toughness of 6 kilojoules per square meter (>1.8× literature benchmarks; 1.4 to 3.8× commercial tapes), while preserving stability across harsh conditions (pH 1 and 13, 3.5% saline). Multiscale experiments and simulations reveal water's triple role as a hydrogen bond catalyst at the interface, a dynamical reorganizer of supramolecular networks, and a mechanical decoupler of interfacial adhesion/bulk cohesion. By establishing interfacial water as a design variable rather than a compromise, CHAT opens avenues for marine, biomedical, and industrial applications where water-resistant adhesion is critical.
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