Directional Natural Rubber Latex–Polyacrylamide/Graphene–PNIPAM Bi-Hydrogel for Programmable Complex Stimuli-Responsive Actuations

IF 4.7 2区 化学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY
Xueliang Feng, , , Jie-Wei Wong, , , Mingjin Yang, , , Qing Zhang, , , Xiaoxue Liao, , , Daquan Kek, , , Zhenzhong Liu*, , , Jize Liu, , , Chunxin Ma*, , , Qingrong Wei, , and , Tuck-Whye Wong*, 
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Abstract

Intelligent hydrogels can provide various biomimetic actuations in response to external stimuli, but it is still difficult to program their actuating complexity, which severely limits their further applications. Herein, a stimuli-responsive actuating bi-hydrogel with a directional negative layer and a homogeneous positive layer has been explored. The stretched natural rubber latex–polyacrylamide (NRL-PAAm) hydrogel layer can partly maintain this directional structure, which can further integrate with the photothermal-responsive graphene-poly(N-isopropylacrylamide) (G-PNIPAM) hydrogel layer to obtain the anisotropic bilayer hydrogel. First of all, different from bilayer PNIPAM-based hydrogels, which commonly only achieve two-dimensional (2D) complex actuations, this bi-hydrogel can achieve various not only 2D but also three-dimensional (3D) complex programmable actuations, especially because of its double anisotropy of both bilayer and directional structures. Furthermore, this bi-hydrogel can own a rapid actuating speed reaching 27.7°/s of bending and 18.0°/s of folding in response to non-contact near-infrared (NIR) irradiation, mainly owing to the high photothermal conversion efficiency of composited graphene. Last but not least, thanks to the highly enhanced mechanical performance of the directional NRL-PAAm hydrogel layer, this bi-hydrogel is robust, reaching 4.0 times the tensile strength of pure G-PNIPAM, which owns a relatively powerful force to lift more than 50 times its self-weight. This work provides a promising intelligent hydrogel integrating programmable 2D/3D complex actuation, rapid actuating speed, and powerful force, which will also inspire exploration of other soft intelligent materials.

Abstract Image

定向天然橡胶乳胶-聚丙烯酰胺/石墨烯- pnipam双水凝胶用于可编程复杂刺激响应驱动
智能水凝胶可以响应外部刺激提供各种仿生驱动,但其驱动复杂性仍然难以编程,这严重限制了其进一步应用。本文研究了一种具有定向负层和均匀正层的刺激响应驱动双水凝胶。拉伸后的天然橡胶乳胶-聚丙烯酰胺(NRL-PAAm)水凝胶层可以部分保持这种定向结构,进一步与光热响应型石墨烯-聚(n -异丙基丙烯酰胺)(G-PNIPAM)水凝胶层结合,得到各向异性双层水凝胶。首先,与基于双层pnipam的水凝胶通常只能实现二维(2D)复杂驱动不同,这种双水凝胶不仅可以实现二维(2D)复杂驱动,还可以实现三维(3D)复杂可编程驱动,特别是由于其双层和定向结构的双各向异性。此外,该双水凝胶在非接触式近红外(NIR)照射下具有27.7°/s的弯曲和18.0°/s的折叠驱动速度,这主要得益于复合石墨烯的高光热转换效率。最后但并非最不重要的是,由于定向NRL-PAAm水凝胶层的机械性能得到了高度增强,这种双水凝胶非常坚固,抗拉强度是纯G-PNIPAM的4.0倍,后者拥有相对强大的力量,可以提升超过其自重50倍的重量。本工作提供了一种具有可编程2D/3D复杂驱动、驱动速度快、力大等特点的有前景的智能水凝胶,也将对其他软智能材料的探索产生启发。
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来源期刊
CiteScore
7.20
自引率
6.00%
发文量
810
期刊介绍: ACS Applied Polymer Materials is an interdisciplinary journal publishing original research covering all aspects of engineering, chemistry, physics, and biology relevant to applications of polymers. The journal is devoted to reports of new and original experimental and theoretical research of an applied nature that integrates fundamental knowledge in the areas of materials, engineering, physics, bioscience, polymer science and chemistry into important polymer applications. The journal is specifically interested in work that addresses relationships among structure, processing, morphology, chemistry, properties, and function as well as work that provide insights into mechanisms critical to the performance of the polymer for applications.
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