材料科学
粘附
自愈水凝胶
胶粘剂
复合材料
聚合物
收缩率
图层(电子)
相变
纳米技术
玻璃化转变
高分子化学
量子力学
物理
作者
Chenxu Liu,Tianhui Sun,Wenqing Chen,Hongbo Zeng,Pan Huang,Lin Yang,Yuan Yao,Qiongyao Peng,Ying Hu,Yonggang Meng,Yu Tian,Hongbo Zeng
标识
DOI:10.1002/advs.202507827
摘要
Abstract Hydrogels are well‐known for their antifriction and lubricating properties, particularly in hydrated environments, where their water‐rich polymer networks enable effective friction reduction. However, during the wet‐to‐dry transition, a critical phase is identified during which the microstructures of a polyacrylamide hydrogel layer undergo volumetric shrinkage, leading to extensive interfacial contact and enhanced intermolecular interactions at solid interfaces. This process leads to a sharp increase in friction and adhesion forces. Sliding friction tests show that under a 2 mN load, the shear force peaked at 115 mN, corresponding to a remarkably high friction coefficient of 57.5. By leveraging this wet‐to‐dry transition, strong object gripping is successfully achieved across a range of surfaces. Notably, the hydrogel layer exhibits a high adhesion strength of 3.48 MPa on glass and 3.64 MPa on Si substrates. These findings offer new insights into hydrogel active gripping technologies and provide promising implications for soft robotics and adhesive interfaces.
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