{"title":"硅橡胶和碳基弹性体通过化学和拓扑粘附的耐变形连接","authors":"Daohang Cai and Yanhao Yu","doi":"10.1039/D5TC02022K","DOIUrl":null,"url":null,"abstract":"<p >Integrating silicone rubbers with carbon-based elastomers is a common practice in assembling stretchable electronics, but weak or rigid interfacial linkages often lead to structural failure under deformation. Here, we present a chemical and topological adhesive (CTA) composed of poly(styrene–isobutylene–styrene) (SIBS) and maleic anhydride-grafted polypropylene (PP-<em>g</em>-MAH) to bridge silicone rubbers and carbon-based elastomers. The CTA synergizes covalent bonding (<em>via</em> amine-anhydride reactions) with topological entanglement (enabled by matched chain reptation) and achieves interfacial toughness >200 J m<small><sup>−2</sup></small> through finger-pressing which can be further increased to >600 J m<small><sup>−2</sup></small><em>via</em> hot pressing. The adhered interface can endure 10 000 cycles of 100% stretch and 10 days of exposure to acidic/alkaline solutions (pH 1–13). The CTA applies to various silicone rubbers (<em>e.g.</em>, polydimethylsiloxane (PDMS) and Ecoflex silicone elastomer) and carbon-based elastomers (<em>e.g.</em>, poly(styrene–ethylene–butylene–styrene) (SEBS), poly(styrene–isobutylene–styrene) (SIBS), and poly(styrene–butylene–styrene) (SBS)). This adhesion strategy significantly increases the interfacial toughness of stretchable devices in practical usage, offering a general solution for deformation-tolerant integration of stretchable electronics.</p>","PeriodicalId":84,"journal":{"name":"Journal of Materials Chemistry C","volume":" 32","pages":" 16787-16795"},"PeriodicalIF":5.1000,"publicationDate":"2025-07-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Deformation-tolerant linkage of silicone rubbers and carbon-based elastomers via chemical and topological adhesion†\",\"authors\":\"Daohang Cai and Yanhao Yu\",\"doi\":\"10.1039/D5TC02022K\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Integrating silicone rubbers with carbon-based elastomers is a common practice in assembling stretchable electronics, but weak or rigid interfacial linkages often lead to structural failure under deformation. Here, we present a chemical and topological adhesive (CTA) composed of poly(styrene–isobutylene–styrene) (SIBS) and maleic anhydride-grafted polypropylene (PP-<em>g</em>-MAH) to bridge silicone rubbers and carbon-based elastomers. The CTA synergizes covalent bonding (<em>via</em> amine-anhydride reactions) with topological entanglement (enabled by matched chain reptation) and achieves interfacial toughness >200 J m<small><sup>−2</sup></small> through finger-pressing which can be further increased to >600 J m<small><sup>−2</sup></small><em>via</em> hot pressing. The adhered interface can endure 10 000 cycles of 100% stretch and 10 days of exposure to acidic/alkaline solutions (pH 1–13). The CTA applies to various silicone rubbers (<em>e.g.</em>, polydimethylsiloxane (PDMS) and Ecoflex silicone elastomer) and carbon-based elastomers (<em>e.g.</em>, poly(styrene–ethylene–butylene–styrene) (SEBS), poly(styrene–isobutylene–styrene) (SIBS), and poly(styrene–butylene–styrene) (SBS)). This adhesion strategy significantly increases the interfacial toughness of stretchable devices in practical usage, offering a general solution for deformation-tolerant integration of stretchable electronics.</p>\",\"PeriodicalId\":84,\"journal\":{\"name\":\"Journal of Materials Chemistry C\",\"volume\":\" 32\",\"pages\":\" 16787-16795\"},\"PeriodicalIF\":5.1000,\"publicationDate\":\"2025-07-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Materials Chemistry C\",\"FirstCategoryId\":\"1\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2025/tc/d5tc02022k\",\"RegionNum\":2,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MATERIALS SCIENCE, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Materials Chemistry C","FirstCategoryId":"1","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/tc/d5tc02022k","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
Deformation-tolerant linkage of silicone rubbers and carbon-based elastomers via chemical and topological adhesion†
Integrating silicone rubbers with carbon-based elastomers is a common practice in assembling stretchable electronics, but weak or rigid interfacial linkages often lead to structural failure under deformation. Here, we present a chemical and topological adhesive (CTA) composed of poly(styrene–isobutylene–styrene) (SIBS) and maleic anhydride-grafted polypropylene (PP-g-MAH) to bridge silicone rubbers and carbon-based elastomers. The CTA synergizes covalent bonding (via amine-anhydride reactions) with topological entanglement (enabled by matched chain reptation) and achieves interfacial toughness >200 J m−2 through finger-pressing which can be further increased to >600 J m−2via hot pressing. The adhered interface can endure 10 000 cycles of 100% stretch and 10 days of exposure to acidic/alkaline solutions (pH 1–13). The CTA applies to various silicone rubbers (e.g., polydimethylsiloxane (PDMS) and Ecoflex silicone elastomer) and carbon-based elastomers (e.g., poly(styrene–ethylene–butylene–styrene) (SEBS), poly(styrene–isobutylene–styrene) (SIBS), and poly(styrene–butylene–styrene) (SBS)). This adhesion strategy significantly increases the interfacial toughness of stretchable devices in practical usage, offering a general solution for deformation-tolerant integration of stretchable electronics.
期刊介绍:
The Journal of Materials Chemistry is divided into three distinct sections, A, B, and C, each catering to specific applications of the materials under study:
Journal of Materials Chemistry A focuses primarily on materials intended for applications in energy and sustainability.
Journal of Materials Chemistry B specializes in materials designed for applications in biology and medicine.
Journal of Materials Chemistry C is dedicated to materials suitable for applications in optical, magnetic, and electronic devices.
Example topic areas within the scope of Journal of Materials Chemistry C are listed below. This list is neither exhaustive nor exclusive.
Bioelectronics
Conductors
Detectors
Dielectrics
Displays
Ferroelectrics
Lasers
LEDs
Lighting
Liquid crystals
Memory
Metamaterials
Multiferroics
Photonics
Photovoltaics
Semiconductors
Sensors
Single molecule conductors
Spintronics
Superconductors
Thermoelectrics
Topological insulators
Transistors