Hydrated ion diffusion-driven interfacial adhesion and failure mechanisms in electroadhesion hydrogels: A digital image correlation-based investigation

IF 13.2 1区 工程技术 Q1 ENGINEERING, CHEMICAL
Yaqian Liu, Wenyue Xie, Xiaocen Duan, Jiayi Chen, Zuoying Yuan, Guojun Ji, Jianyong Huang
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引用次数: 0

Abstract

The electroadhesion strategy driven by hydrated ion diffusion in functional hydrogels enables controllable soft interface adhesion, offering a new solution for smart interfacial interactions. This is crucial for various engineering applications such as tissue repair, soft robotics, and wearable electronics. However, the intrinsic mechanisms of interfacial adhesion and failure associated with the electroadhesion strategy remain unclear. With an incremental digital image correlation (DIC) technique, we comprehensively investigated the spatiotemporal dynamics of interfacial deformation and failure modulated by electrically controllable hydrated ion diffusion in electroadhesive hydrogels. We also visualized the spatiotemporal evolution of mechanical properties near adhesion interfaces, including interfacial toughness, initial elastic modulus, and nominal secant modulus, under various electrical stimulations. Furthermore, we recognized the transition of adhered specimens from adhesive failure to cohesive failure, driven by the applied external electrical stimulation. This work not only presents a DIC-based characterization method for quantifying the mechanical responses of adhesive interfaces in functional hydrogels, but also provides insights into how electrically regulated hydrated ions dominate interfacial adhesion and failure dynamics in electroadhesive hydrogels, which paves the way to guide the design of future high-performance electroadhesive hydrogels.
电黏附水凝胶中水合离子扩散驱动的界面黏附和失效机制:基于数字图像相关的研究
功能水凝胶中由水合离子扩散驱动的电粘附策略实现了可控制的软界面粘附,为智能界面相互作用提供了新的解决方案。这对于组织修复、软机器人和可穿戴电子产品等各种工程应用至关重要。然而,与电粘附策略相关的界面粘附和失效的内在机制仍不清楚。采用增量数字图像相关(DIC)技术,全面研究了电黏附水凝胶中可控水合离子扩散对界面变形和破坏的时空动态影响。我们还可视化了在各种电刺激下粘附界面附近力学性能的时空演变,包括界面韧性、初始弹性模量和标称割线模量。此外,我们认识到粘附试样从粘附破坏到内聚破坏的转变,是由外加电刺激驱动的。这项工作不仅提出了一种基于dic的表征方法来量化功能水凝胶中粘附界面的力学响应,而且还提供了电调节水合离子如何主导电粘附水凝胶中的界面粘附和失效动力学的见解,为指导未来高性能电粘附水凝胶的设计铺平了道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Chemical Engineering Journal
Chemical Engineering Journal 工程技术-工程:化工
CiteScore
21.70
自引率
9.30%
发文量
6781
审稿时长
2.4 months
期刊介绍: The Chemical Engineering Journal is an international research journal that invites contributions of original and novel fundamental research. It aims to provide an international platform for presenting original fundamental research, interpretative reviews, and discussions on new developments in chemical engineering. The journal welcomes papers that describe novel theory and its practical application, as well as those that demonstrate the transfer of techniques from other disciplines. It also welcomes reports on carefully conducted experimental work that is soundly interpreted. The main focus of the journal is on original and rigorous research results that have broad significance. The Catalysis section within the Chemical Engineering Journal focuses specifically on Experimental and Theoretical studies in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. These studies have industrial impact on various sectors such as chemicals, energy, materials, foods, healthcare, and environmental protection.
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