胶粘剂
自愈水凝胶
材料科学
粘附
纳米技术
仿生学
软机器人
软质材料
复合材料
计算机科学
机器人
人工智能
高分子化学
图层(电子)
作者
Zhen Yang,Xingwei Yang,Rong Long,Jianyu Li
出处
期刊:Langmuir
[American Chemical Society]
日期:2021-06-03
卷期号:37 (23): 7097-7106
被引量:12
标识
DOI:10.1021/acs.langmuir.1c00696
摘要
The ability to modulate the adhesion of soft materials on-demand is desired for broad applications ranging from tissue repair to soft robotics. Research effort has been focused on the chemistry and architecture of interfaces, leaving the mechanics of soft adhesives overlooked. Stimuli-responsive mechanisms of smart hydrogels could be leveraged for achieving stimuli-responsive hydrogel adhesives that respond mechanically to external stimuli. Such stimuli-responsive hydrogel adhesives involve complex chemomechanical coupling and interfacial fracture phenomena, calling for mechanistic understanding to enable rational design. Here, we combine experimental, computational, and analytical approaches to study a thermo-responsive hydrogel adhesive. Experimentally, we show that the adhesion and mechanical properties of a stimuli-responsive hydrogel adhesive are both enhanced by the application of a stimulus. Our analysis further reveals that the enhanced adhesion stems from the increased fracture energy of the bulk hydrogel and the insignificant residual stress on the adhesive–tissue interface. This study presents a framework for designing stimuli-responsive hydrogel adhesives based on the modulation of bulk properties and sheds light on the development of smart adhesives with tunable mechanics.
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