Wenxuan Peng, Jiamin Zhao, Qiuxian Li, Yue Sun, Guoli Du, Fangyuan Tang, Yongfei Liu, Qingdi Hu, Xusheng Li, Shuangxi Nie
{"title":"通过分层网格和离子杂化合作实现的强韧离子凝胶","authors":"Wenxuan Peng, Jiamin Zhao, Qiuxian Li, Yue Sun, Guoli Du, Fangyuan Tang, Yongfei Liu, Qingdi Hu, Xusheng Li, Shuangxi Nie","doi":"10.1002/adfm.202414682","DOIUrl":null,"url":null,"abstract":"Ion-gels, with inherent flexibility, tunable conductivity, and multi-stimulus response, have attracted significant attention in flexible/wearable electronics. However, the design of ion-gels that exhibit both strength and toughness is challenging. In this study, a novel ion-gel design is proposed that mimics the hierarchical meshing structure of leaves in combination with ion hybridization. Polyacrylamide (PAM) is incorporated in TEMPO oxidized cellulose nanofibers (TOCNFs) clusters by in situ polymerization, generating a hydrogel with micro/nanoscale entangled networks. Replacement of water by a metal halide ionic liquid ([BMIm]Zn<sub>x</sub>Cl<sub>y</sub>) in the hydrogel resulted in the formation of an ion hybrid network with supramolecular interactions. The integration of the PAM/TOCNF polymer network with [BMIm]Zn<sub>x</sub>Cl<sub>y</sub> resulted in ion-gels with high strength (5.9 MPa), toughness (22 MJ m<sup>−3</sup>), and enhanced elastic modulus (30 MPa) combined with non-flammability, heat and cold resistance. While having fast responsiveness (36 ms) of sensing signal and stability of power supply even at 4000 cycle collisions. Stable signal output even at high (200 °C) /sub-zero temperatures. The proposed strategy offers a new approach to the material design of flexible/wearable electronics.","PeriodicalId":18,"journal":{"name":"ACS Macro Letters","volume":"20 1","pages":""},"PeriodicalIF":5.1000,"publicationDate":"2024-11-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A Strong and Tough Ion-gel Enabled by Hierarchical Meshing and Ion Hybridizations Collaboration\",\"authors\":\"Wenxuan Peng, Jiamin Zhao, Qiuxian Li, Yue Sun, Guoli Du, Fangyuan Tang, Yongfei Liu, Qingdi Hu, Xusheng Li, Shuangxi Nie\",\"doi\":\"10.1002/adfm.202414682\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Ion-gels, with inherent flexibility, tunable conductivity, and multi-stimulus response, have attracted significant attention in flexible/wearable electronics. However, the design of ion-gels that exhibit both strength and toughness is challenging. In this study, a novel ion-gel design is proposed that mimics the hierarchical meshing structure of leaves in combination with ion hybridization. Polyacrylamide (PAM) is incorporated in TEMPO oxidized cellulose nanofibers (TOCNFs) clusters by in situ polymerization, generating a hydrogel with micro/nanoscale entangled networks. Replacement of water by a metal halide ionic liquid ([BMIm]Zn<sub>x</sub>Cl<sub>y</sub>) in the hydrogel resulted in the formation of an ion hybrid network with supramolecular interactions. The integration of the PAM/TOCNF polymer network with [BMIm]Zn<sub>x</sub>Cl<sub>y</sub> resulted in ion-gels with high strength (5.9 MPa), toughness (22 MJ m<sup>−3</sup>), and enhanced elastic modulus (30 MPa) combined with non-flammability, heat and cold resistance. While having fast responsiveness (36 ms) of sensing signal and stability of power supply even at 4000 cycle collisions. Stable signal output even at high (200 °C) /sub-zero temperatures. The proposed strategy offers a new approach to the material design of flexible/wearable electronics.\",\"PeriodicalId\":18,\"journal\":{\"name\":\"ACS Macro Letters\",\"volume\":\"20 1\",\"pages\":\"\"},\"PeriodicalIF\":5.1000,\"publicationDate\":\"2024-11-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Macro Letters\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://doi.org/10.1002/adfm.202414682\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"POLYMER SCIENCE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Macro Letters","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1002/adfm.202414682","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
A Strong and Tough Ion-gel Enabled by Hierarchical Meshing and Ion Hybridizations Collaboration
Ion-gels, with inherent flexibility, tunable conductivity, and multi-stimulus response, have attracted significant attention in flexible/wearable electronics. However, the design of ion-gels that exhibit both strength and toughness is challenging. In this study, a novel ion-gel design is proposed that mimics the hierarchical meshing structure of leaves in combination with ion hybridization. Polyacrylamide (PAM) is incorporated in TEMPO oxidized cellulose nanofibers (TOCNFs) clusters by in situ polymerization, generating a hydrogel with micro/nanoscale entangled networks. Replacement of water by a metal halide ionic liquid ([BMIm]ZnxCly) in the hydrogel resulted in the formation of an ion hybrid network with supramolecular interactions. The integration of the PAM/TOCNF polymer network with [BMIm]ZnxCly resulted in ion-gels with high strength (5.9 MPa), toughness (22 MJ m−3), and enhanced elastic modulus (30 MPa) combined with non-flammability, heat and cold resistance. While having fast responsiveness (36 ms) of sensing signal and stability of power supply even at 4000 cycle collisions. Stable signal output even at high (200 °C) /sub-zero temperatures. The proposed strategy offers a new approach to the material design of flexible/wearable electronics.
期刊介绍:
ACS Macro Letters publishes research in all areas of contemporary soft matter science in which macromolecules play a key role, including nanotechnology, self-assembly, supramolecular chemistry, biomaterials, energy generation and storage, and renewable/sustainable materials. Submissions to ACS Macro Letters should justify clearly the rapid disclosure of the key elements of the study. The scope of the journal includes high-impact research of broad interest in all areas of polymer science and engineering, including cross-disciplinary research that interfaces with polymer science.
With the launch of ACS Macro Letters, all Communications that were formerly published in Macromolecules and Biomacromolecules will be published as Letters in ACS Macro Letters.