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Anisotropic and self-healing hydrogels with multi-responsive actuating capability

机译:具有多响应驱动能力的各向异性和自修复水凝胶

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摘要

Inspired by smart biological tissues, artificial muscle-like actuators offer fascinating prospects due to their distinctive shape transformation and self-healing function under external stimuli. However, further practical application is hindered by the lack of simple and general routes to fabricate ingenious soft materials with anisotropic responsiveness. Here, we describe a general in situ polymerization strategy for the fabrication of anisotropic hydrogels composed of highly-ordered lamellar network crosslinked by the metal nanostructure assemblies, accompanied with remarkably anisotropic performances on mechanical, optical, de-swelling and swelling behaviors. Owing to the dynamic thiolate-metal coordination as healing motifs, the composites exhibit rapid and efficient multi-responsive self-healing performance under NIR irradiation and low pH condition. Dependent on well-defined anisotropic structures, the hydrogel presents controllable solvent-responsive mechanical actuating performance. Impressively, the integrated device through a healing-induced assembly way can deliver more complicated, elaborate forms of actuation, demonstrating its great potentials as superior soft actuators like smart robots.
机译:受智能生物组织的启发,类肌肉样的致动器因其独特的形状转换和在外部刺激下的自我修复功能而备受瞩目。然而,由于缺乏简单且通用的方法来制造具有各向异性响应性的新颖的柔软材料而阻碍了进一步的实际应用。在这里,我们描述了一种一般的原位聚合策略,用于制备由水有序的层状网络(由金属纳米结构组件交联)组成的各向异性水凝胶,并在机械,光学,消肿和溶胀行为方面具有明显的各向异性。由于动态的硫醇盐-金属配位作为修复基序,该复合材料在近红外辐射和低pH条件下显示出快速有效的多响应自修复性能。取决于明确定义的各向异性结构,水凝胶具有可控的溶剂响应性机械驱动性能。令人印象深刻的是,通过愈合诱导的组装方式,该集成设备可以提供更复杂,更精细的驱动形式,证明了其作为智能机器人等高级软驱动器的巨大潜力。

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