{"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 , Yuxin Gao , Yingying Lai , Chengyan Zhang , Wenbo Jia , 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 , Yuxin Gao , Yingying Lai , Chengyan Zhang , Wenbo Jia , 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}
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.
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.