通过 L-抗坏血酸触发硬水凝胶界面自生长实现生物启发式分层水凝胶致动器

IF 4.1 2区 化学 Q2 POLYMER SCIENCE
Rongnian Xu , Yuxin Gao , Yingying Lai , Chengyan Zhang , Wenbo Jia , Qiangbing Wei
{"title":"通过 L-抗坏血酸触发硬水凝胶界面自生长实现生物启发式分层水凝胶致动器","authors":"Rongnian Xu ,&nbsp;Yuxin Gao ,&nbsp;Yingying Lai ,&nbsp;Chengyan Zhang ,&nbsp;Wenbo Jia ,&nbsp;Qiangbing Wei","doi":"10.1039/d4py00848k","DOIUrl":null,"url":null,"abstract":"<div><div>Stimuli-responsive layered hydrogel actuators are highly attractive for broad applications in soft robots, intelligent devices, <em>etc</em>., owing to their softness, asymmetric responsiveness and deformability. However, current layered hydrogel actuators suffer from serious challenges such as tedious preparation, uncontrollable layer thickness and weak interfacial bonding force. Herein, we put forward a facile and highly efficient self-growing method to prepare a layered hydrogel actuator from a stiff hydrogel substrate by crafting <span>l</span>-ascorbic acid (Vc)-triggered interfacial radical polymerization. The redox reaction between Vc and confined Fe<sup>3+</sup> in the stiff hydrogel substrate could produce Fe<sup>2+</sup> catalysts, resulting in surface catalytically initiated radical polymerization (SCIRP) at room temperature. Various layered hydrogels were prepared rapidly and the thickness of the grown hydrogel layer can be accurately controlled. The obtained layered hydrogel exhibits asymmetric structural layers consisting of a dense layer and a porous layer, as well as a strong interfacial bonding force of about 250 N m<sup>−1</sup> between the porous layer and the stiff substrate. Furthermore, a thermo-responsive layered hydrogel actuator was developed, which showed reversible underwater bending ability in response to temperature changes and can also be designed as a smart manipulator to capture objects underwater. This work provides a novel and feasible approach for the highly efficient and controllable preparation of layered hydrogel actuators, which will find promising applications in the fields of soft robots, intelligent devices, sensors and so on.</div></div>","PeriodicalId":100,"journal":{"name":"Polymer Chemistry","volume":"15 37","pages":"Pages 3787-3794"},"PeriodicalIF":4.1000,"publicationDate":"2024-09-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A bioinspired layered hydrogel actuator vial-ascorbic acid-triggered interfacial self-growth from a stiff hydrogel†\",\"authors\":\"Rongnian Xu ,&nbsp;Yuxin Gao ,&nbsp;Yingying Lai ,&nbsp;Chengyan Zhang ,&nbsp;Wenbo Jia ,&nbsp;Qiangbing Wei\",\"doi\":\"10.1039/d4py00848k\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Stimuli-responsive layered hydrogel actuators are highly attractive for broad applications in soft robots, intelligent devices, <em>etc</em>., owing to their softness, asymmetric responsiveness and deformability. However, current layered hydrogel actuators suffer from serious challenges such as tedious preparation, uncontrollable layer thickness and weak interfacial bonding force. Herein, we put forward a facile and highly efficient self-growing method to prepare a layered hydrogel actuator from a stiff hydrogel substrate by crafting <span>l</span>-ascorbic acid (Vc)-triggered interfacial radical polymerization. The redox reaction between Vc and confined Fe<sup>3+</sup> in the stiff hydrogel substrate could produce Fe<sup>2+</sup> catalysts, resulting in surface catalytically initiated radical polymerization (SCIRP) at room temperature. Various layered hydrogels were prepared rapidly and the thickness of the grown hydrogel layer can be accurately controlled. The obtained layered hydrogel exhibits asymmetric structural layers consisting of a dense layer and a porous layer, as well as a strong interfacial bonding force of about 250 N m<sup>−1</sup> between the porous layer and the stiff substrate. Furthermore, a thermo-responsive layered hydrogel actuator was developed, which showed reversible underwater bending ability in response to temperature changes and can also be designed as a smart manipulator to capture objects underwater. This work provides a novel and feasible approach for the highly efficient and controllable preparation of layered hydrogel actuators, which will find promising applications in the fields of soft robots, intelligent devices, sensors and so on.</div></div>\",\"PeriodicalId\":100,\"journal\":{\"name\":\"Polymer Chemistry\",\"volume\":\"15 37\",\"pages\":\"Pages 3787-3794\"},\"PeriodicalIF\":4.1000,\"publicationDate\":\"2024-09-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Polymer Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S1759995424003140\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"POLYMER SCIENCE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Polymer Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S1759995424003140","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
引用次数: 0

摘要

由于具有柔软性、非对称响应性和可变形性,刺激响应层状水凝胶致动器在软机器人、智能设备等广泛应用中极具吸引力。然而,目前的层状水凝胶致动器存在制备繁琐、层厚不可控、界面结合力弱等问题。在此,我们提出了一种简便、高效的自生长方法,利用 L-抗坏血酸(Vc)触发的界面自由基聚合,从刚性水凝胶基底制备层状水凝胶致动器。Vc 与硬质水凝胶基底中封闭的 Fe3+ 之间的氧化还原反应可产生 Fe2+ 催化剂,从而在室温下实现表面催化引发的自由基聚合(SCIRP)。各种层状水凝胶均可快速制备,且生长的水凝胶层厚度可精确控制。制备出的层状水凝胶具有由致密层和多孔层组成的不对称结构层,多孔层与坚硬基底之间的界面结合力约为 250 N/m。此外,还开发出了一种热响应层状水凝胶致动器,它具有随温度变化而可逆的水下弯曲能力,还可设计成智能机械手,在水下捕捉物体。这项研究为高效、可控地制备层状水凝胶致动器提供了一种新颖、可行的方法,在软机器人、智能设备、传感器等领域具有广阔的应用前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A bioinspired layered hydrogel actuator vial-ascorbic acid-triggered interfacial self-growth from a stiff hydrogel†

A bioinspired layered hydrogel actuator vial-ascorbic acid-triggered interfacial self-growth from a stiff hydrogel†
Stimuli-responsive layered hydrogel actuators are highly attractive for broad applications in soft robots, intelligent devices, etc., owing to their softness, asymmetric responsiveness and deformability. However, current layered hydrogel actuators suffer from serious challenges such as tedious preparation, uncontrollable layer thickness and weak interfacial bonding force. Herein, we put forward a facile and highly efficient self-growing method to prepare a layered hydrogel actuator from a stiff hydrogel substrate by crafting l-ascorbic acid (Vc)-triggered interfacial radical polymerization. The redox reaction between Vc and confined Fe3+ in the stiff hydrogel substrate could produce Fe2+ catalysts, resulting in surface catalytically initiated radical polymerization (SCIRP) at room temperature. Various layered hydrogels were prepared rapidly and the thickness of the grown hydrogel layer can be accurately controlled. The obtained layered hydrogel exhibits asymmetric structural layers consisting of a dense layer and a porous layer, as well as a strong interfacial bonding force of about 250 N m−1 between the porous layer and the stiff substrate. Furthermore, a thermo-responsive layered hydrogel actuator was developed, which showed reversible underwater bending ability in response to temperature changes and can also be designed as a smart manipulator to capture objects underwater. This work provides a novel and feasible approach for the highly efficient and controllable preparation of layered hydrogel actuators, which will find promising applications in the fields of soft robots, intelligent devices, sensors and so on.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Polymer Chemistry
Polymer Chemistry POLYMER SCIENCE-
CiteScore
8.60
自引率
8.70%
发文量
535
审稿时长
1.7 months
期刊介绍: Polymer Chemistry welcomes submissions in all areas of polymer science that have a strong focus on macromolecular chemistry. Manuscripts may cover a broad range of fields, yet no direct application focus is required.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信