{"title":"Scalable production of critically thin polyethylene films via multistep stretching","authors":"Runlai Li, Zirui Wang, Weilong Sun, He Zhang, Yuwen Zeng, Xiaoxu Zhao, Wenbing Hu, Hua Deng, Kian Ping Loh, Qiang Fu","doi":"10.1038/s44286-024-00139-w","DOIUrl":null,"url":null,"abstract":"Plastic films are among the most used materials. In many applications, both high strength and low thickness are required. The thickness of free-standing plastic films has recently been reduced to micrometres, 200 nm and even 60 nm. Pushing this boundary further faces considerable challenges, as processability conflicts with stability at the ‘ultrathin’ scale (below ~100–200 nm). Here, to overcome this trade-off, we modulated the entanglement density of plastic chains to identify a maximum stretching processing window. Then, relaxation was introduced during stretching to kinetically stabilize the ultrathin film. Combined, polyethylene film thicknesses were reduced to ~12 nm, near its critical thickness. This critically thin polyethylene reveals physical properties different from its bulk counterparts, such as high mechanical strength (113.9 GPa (g cm–3)–1), abnormal interfacial properties and a high aspect ratio near 108. Potential applications of these films include nuclear fusion ignition support and thin breathable epidermal sensors. Our work reveals advanced processing strategies, distinctive properties and broader applications of plastic films near the processing limit. A multistep stretch–relaxation process is used to produce critically thin polyethylene films. Several key physical properties of the polyethylene films are presented, and their potential applications in nuclear fusion and epidermal sensing are highlighted.","PeriodicalId":501699,"journal":{"name":"Nature Chemical Engineering","volume":"1 11","pages":"702-709"},"PeriodicalIF":0.0000,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nature Chemical Engineering","FirstCategoryId":"1085","ListUrlMain":"https://www.nature.com/articles/s44286-024-00139-w","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Plastic films are among the most used materials. In many applications, both high strength and low thickness are required. The thickness of free-standing plastic films has recently been reduced to micrometres, 200 nm and even 60 nm. Pushing this boundary further faces considerable challenges, as processability conflicts with stability at the ‘ultrathin’ scale (below ~100–200 nm). Here, to overcome this trade-off, we modulated the entanglement density of plastic chains to identify a maximum stretching processing window. Then, relaxation was introduced during stretching to kinetically stabilize the ultrathin film. Combined, polyethylene film thicknesses were reduced to ~12 nm, near its critical thickness. This critically thin polyethylene reveals physical properties different from its bulk counterparts, such as high mechanical strength (113.9 GPa (g cm–3)–1), abnormal interfacial properties and a high aspect ratio near 108. Potential applications of these films include nuclear fusion ignition support and thin breathable epidermal sensors. Our work reveals advanced processing strategies, distinctive properties and broader applications of plastic films near the processing limit. A multistep stretch–relaxation process is used to produce critically thin polyethylene films. Several key physical properties of the polyethylene films are presented, and their potential applications in nuclear fusion and epidermal sensing are highlighted.