{"title":"双可逆热致变色和热响应光致发光电离胶,具有高拉伸性,低滞后和优异的热机械稳定性","authors":"Yushu Liu, Yajie Li, Fangzheng Zuo, Zhuoyou Gao and Hongzan Song*, ","doi":"10.1021/acs.macromol.5c00887","DOIUrl":null,"url":null,"abstract":"<p >Stretchable ionogels with thermoresponsive capabilities are garnering substantial attention owing to their potential applications in the fields of smart displays, soft robotics, and wearable ionotronics. Nevertheless, the application of traditional thermoresponsive ionogels in complex scenes remains a challenge because of the single response mechanism and poor thermomechanical stability. Herein, a simple strategy for the construction of high-stretchable and low-hysteresis ionogels with doubly reversible thermochromic and thermoresponsive photoluminescent properties is proposed. Taking advantage of the synergistic effect of poly(hydroxyethyl acrylate) (PHEA) and polyethylene glycol monomethyl ether (mPEG) in the ionic liquid (IL), doubly reversible thermochromic ionogels with both upper critical solution temperature (UCST) and lower critical solution temperature (LCST) phase behaviors are prepared. Simultaneously, doubly reversible thermoresponsive multiple photoluminescent behaviors are realized by the confined-domain cross-link-enhanced emission (CEE) effect. The synergistic effect of hierarchical micro/nanophase-separated structures and entanglement of polymer chains endow the ionogel with high stretchability (1070%), low hysteresis (<3.0%), outstanding temperature tolerance (−80–300 °C), excellent ionic conductivity (up to 2.57 mS/cm), and extraordinary thermomechanical stability (25–200 C). Ionogel-based wearable thermo-mechano-multimodal sensors can detect various human motions sensitively, showing great promise in multifunctional wearable ionotronics.</p>","PeriodicalId":51,"journal":{"name":"Macromolecules","volume":"58 14","pages":"7245–7257"},"PeriodicalIF":5.2000,"publicationDate":"2025-07-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Doubly Reversible Thermochromic and Thermoresponsive Photoluminescent Ionogels with High Stretchability, Low Hysteresis, and Excellent Thermomechanical Stability\",\"authors\":\"Yushu Liu, Yajie Li, Fangzheng Zuo, Zhuoyou Gao and Hongzan Song*, \",\"doi\":\"10.1021/acs.macromol.5c00887\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Stretchable ionogels with thermoresponsive capabilities are garnering substantial attention owing to their potential applications in the fields of smart displays, soft robotics, and wearable ionotronics. Nevertheless, the application of traditional thermoresponsive ionogels in complex scenes remains a challenge because of the single response mechanism and poor thermomechanical stability. Herein, a simple strategy for the construction of high-stretchable and low-hysteresis ionogels with doubly reversible thermochromic and thermoresponsive photoluminescent properties is proposed. Taking advantage of the synergistic effect of poly(hydroxyethyl acrylate) (PHEA) and polyethylene glycol monomethyl ether (mPEG) in the ionic liquid (IL), doubly reversible thermochromic ionogels with both upper critical solution temperature (UCST) and lower critical solution temperature (LCST) phase behaviors are prepared. Simultaneously, doubly reversible thermoresponsive multiple photoluminescent behaviors are realized by the confined-domain cross-link-enhanced emission (CEE) effect. The synergistic effect of hierarchical micro/nanophase-separated structures and entanglement of polymer chains endow the ionogel with high stretchability (1070%), low hysteresis (<3.0%), outstanding temperature tolerance (−80–300 °C), excellent ionic conductivity (up to 2.57 mS/cm), and extraordinary thermomechanical stability (25–200 C). Ionogel-based wearable thermo-mechano-multimodal sensors can detect various human motions sensitively, showing great promise in multifunctional wearable ionotronics.</p>\",\"PeriodicalId\":51,\"journal\":{\"name\":\"Macromolecules\",\"volume\":\"58 14\",\"pages\":\"7245–7257\"},\"PeriodicalIF\":5.2000,\"publicationDate\":\"2025-07-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Macromolecules\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.macromol.5c00887\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"POLYMER SCIENCE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Macromolecules","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.macromol.5c00887","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
Doubly Reversible Thermochromic and Thermoresponsive Photoluminescent Ionogels with High Stretchability, Low Hysteresis, and Excellent Thermomechanical Stability
Stretchable ionogels with thermoresponsive capabilities are garnering substantial attention owing to their potential applications in the fields of smart displays, soft robotics, and wearable ionotronics. Nevertheless, the application of traditional thermoresponsive ionogels in complex scenes remains a challenge because of the single response mechanism and poor thermomechanical stability. Herein, a simple strategy for the construction of high-stretchable and low-hysteresis ionogels with doubly reversible thermochromic and thermoresponsive photoluminescent properties is proposed. Taking advantage of the synergistic effect of poly(hydroxyethyl acrylate) (PHEA) and polyethylene glycol monomethyl ether (mPEG) in the ionic liquid (IL), doubly reversible thermochromic ionogels with both upper critical solution temperature (UCST) and lower critical solution temperature (LCST) phase behaviors are prepared. Simultaneously, doubly reversible thermoresponsive multiple photoluminescent behaviors are realized by the confined-domain cross-link-enhanced emission (CEE) effect. The synergistic effect of hierarchical micro/nanophase-separated structures and entanglement of polymer chains endow the ionogel with high stretchability (1070%), low hysteresis (<3.0%), outstanding temperature tolerance (−80–300 °C), excellent ionic conductivity (up to 2.57 mS/cm), and extraordinary thermomechanical stability (25–200 C). Ionogel-based wearable thermo-mechano-multimodal sensors can detect various human motions sensitively, showing great promise in multifunctional wearable ionotronics.
期刊介绍:
Macromolecules publishes original, fundamental, and impactful research on all aspects of polymer science. Topics of interest include synthesis (e.g., controlled polymerizations, polymerization catalysis, post polymerization modification, new monomer structures and polymer architectures, and polymerization mechanisms/kinetics analysis); phase behavior, thermodynamics, dynamic, and ordering/disordering phenomena (e.g., self-assembly, gelation, crystallization, solution/melt/solid-state characteristics); structure and properties (e.g., mechanical and rheological properties, surface/interfacial characteristics, electronic and transport properties); new state of the art characterization (e.g., spectroscopy, scattering, microscopy, rheology), simulation (e.g., Monte Carlo, molecular dynamics, multi-scale/coarse-grained modeling), and theoretical methods. Renewable/sustainable polymers, polymer networks, responsive polymers, electro-, magneto- and opto-active macromolecules, inorganic polymers, charge-transporting polymers (ion-containing, semiconducting, and conducting), nanostructured polymers, and polymer composites are also of interest. Typical papers published in Macromolecules showcase important and innovative concepts, experimental methods/observations, and theoretical/computational approaches that demonstrate a fundamental advance in the understanding of polymers.