High Energy Density Shape Memory Polymers Using Strain-Induced Supramolecular Nanostructures

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dc.contributor.authorCooper, Christopher B.ko
dc.contributor.authorNikzad, Shaylako
dc.contributor.authorYan, Hongpingko
dc.contributor.authorOchiai, Yutoko
dc.contributor.authorLai, Jian-Chengko
dc.contributor.authorYu, Zhiaoko
dc.contributor.authorChen, Ganko
dc.contributor.authorKang, Jiheongko
dc.contributor.authorBao, Zhenanko
dc.date.accessioned2021-12-29T06:41:20Z-
dc.date.available2021-12-29T06:41:20Z-
dc.date.created2021-12-28-
dc.date.created2021-12-28-
dc.date.issued2021-10-
dc.identifier.citationACS CENTRAL SCIENCE, v.7, no.10, pp.1657 - 1667-
dc.identifier.issn2374-7943-
dc.identifier.urihttp://hdl.handle.net/10203/291424-
dc.description.abstractShape memory polymers are promising materials in many emerging applications due to their large extensibility and excellent shape recovery. However, practical application of these polymers is limited by their poor energy densities (up to similar to 1 MJ/m(3)). Here, we report an approach to achieve a high energy density, one-way shape memory polymer based on the formation of strain-induced supramolecular nanostructures. As polymer chains align during strain, strong directional dynamic bonds form, creating stable supramolecular nanostructures and trapping stretched chains in a highly elongated state. Upon heating, the dynamic bonds break, and stretched chains contract to their initial disordered state. This mechanism stores large amounts of entropic energy (as high as 19.6 MJ/m(3) or 17.9 J/g), almost six times higher than the best previously reported shape memory polymers while maintaining near 100% shape recovery and fixity. The reported phenomenon of strain-induced supramolecular structures offers a new approach toward achieving high energy density shape memory polymers.-
dc.languageEnglish-
dc.publisherAMER CHEMICAL SOC-
dc.titleHigh Energy Density Shape Memory Polymers Using Strain-Induced Supramolecular Nanostructures-
dc.typeArticle-
dc.identifier.wosid000713057800011-
dc.identifier.scopusid2-s2.0-85115615961-
dc.type.rimsART-
dc.citation.volume7-
dc.citation.issue10-
dc.citation.beginningpage1657-
dc.citation.endingpage1667-
dc.citation.publicationnameACS CENTRAL SCIENCE-
dc.identifier.doi10.1021/acscentsci.1c00829-
dc.contributor.localauthorKang, Jiheong-
dc.contributor.nonIdAuthorCooper, Christopher B.-
dc.contributor.nonIdAuthorNikzad, Shayla-
dc.contributor.nonIdAuthorYan, Hongping-
dc.contributor.nonIdAuthorOchiai, Yuto-
dc.contributor.nonIdAuthorLai, Jian-Cheng-
dc.contributor.nonIdAuthorYu, Zhiao-
dc.contributor.nonIdAuthorChen, Gan-
dc.contributor.nonIdAuthorBao, Zhenan-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordPlusTHERMOPLASTIC ELASTOMERS-
dc.subject.keywordPlusBEHAVIOR-
dc.subject.keywordPlusUREA-
dc.subject.keywordPlusPLASTICITY-
dc.subject.keywordPlusNETWORKS-
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