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通过光开关主客体相互作用重新配置水凝胶片的高斯曲率

Reconfiguring Gaussian Curvature of Hydrogel Sheets with Photoswitchable Host-Guest Interactions.

作者信息

Kuenstler Alexa S, Lahikainen Markus, Zhou Hantao, Xu Wenwen, Priimagi Arri, Hayward Ryan C

机构信息

Department of Polymer Science and Engineering, University of Massachusetts Amherst, Amherst, Massachusetts 01003, United States.

Smart Photonic Materials, Faculty of Engineering and Natural Sciences, Tampere University, P.O. Box 541F1-33101, Tampere, Finland.

出版信息

ACS Macro Lett. 2020 Aug 18;9(8):1172-1177. doi: 10.1021/acsmacrolett.0c00469. Epub 2020 Jul 31.

DOI:10.1021/acsmacrolett.0c00469
PMID:32864191
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7445929/
Abstract

Photoinduced shape morphing has implications in fields ranging from soft robotics to biomedical devices. Despite considerable effort in this area, it remains a challenge to design materials that can be both rapidly deployed and reconfigured into multiple different three-dimensional forms, particularly in aqueous environments. In this work, we present a simple method to program and rewrite spatial variations in swelling and, therefore, Gaussian curvature in thin sheets of hydrogels using photoswitchable supramolecular complexation of azobenzene pendent groups with dissolved α-cyclodextrin. We show that the extent of swelling can be programmed via the proportion of azobenzene isomers, with a 60% decrease in areal swelling from the all to the predominantly state near room temperature. The use of thin gel sheets provides fast response times in the range of a few tens of seconds, while the shape change is persistent in the absence of light thanks to the slow rate of thermal isomerization. Finally, we demonstrate that a single gel sheet can be programmed with a first swelling pattern via spatially defined illumination with ultraviolet light, then erased with white light, and finally redeployed with a different swelling pattern.

摘要

光致形状变形在从软体机器人到生物医学设备等诸多领域都有应用。尽管在这一领域已经付出了相当大的努力,但设计出既能快速展开又能重新配置成多种不同三维形状的材料,尤其是在水性环境中,仍然是一项挑战。在这项工作中,我们提出了一种简单的方法,利用偶氮苯侧基与溶解的α-环糊精的光开关超分子络合作用,对水凝胶薄片中的溶胀空间变化以及高斯曲率进行编程和重写。我们表明,溶胀程度可以通过偶氮苯异构体的比例来编程,在室温附近,从全反式到主要为顺式状态,面积溶胀减少了60%。使用薄凝胶片可在几十秒的范围内提供快速响应时间,而由于热异构化速率较慢,形状变化在无光的情况下是持久的。最后,我们证明,通过用紫外光进行空间定义照明,可以为单个凝胶片编程第一种溶胀模式,然后用白光擦除,最后用不同的溶胀模式重新展开。

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