Multifunctional Phase Change Films with High Mechanical Strength, Thermally Induced Switchable Adhesion, and Shape Recoverability for Infrared Stealth

IF 8.2 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY ACS Applied Materials & Interfaces Pub Date : 2024-12-19 DOI:10.1021/acsami.4c18276
Guangyu Zhu, Wenjing Chen, Xiaowu Hu, Wenxing Luo, Yan Ma, Jue Wang, Sifan Tan, Yifan Huang, Jinghui Fan, Xiongxin Jiang, Qinglin Li
{"title":"Multifunctional Phase Change Films with High Mechanical Strength, Thermally Induced Switchable Adhesion, and Shape Recoverability for Infrared Stealth","authors":"Guangyu Zhu, Wenjing Chen, Xiaowu Hu, Wenxing Luo, Yan Ma, Jue Wang, Sifan Tan, Yifan Huang, Jinghui Fan, Xiongxin Jiang, Qinglin Li","doi":"10.1021/acsami.4c18276","DOIUrl":null,"url":null,"abstract":"The application of organic solid–liquid phase change materials (PCMs) is limited for the leakage problem after phase change and high rigidity. In this work, a novel flexible solid–solid PCM (DXPCM) was synthesized using a block copolymerization process with polyethylene glycol (PEG) as the energy storage segment. The phase transition temperature (from 36.2 to 49.4 °C) and enthalpy (from 83.27 to 123.35 J/g) of DXPCM could be changed through adjusting the molecular weight of PEG. The introduction of hard chain segments endowed DXPCM with excellent flexibility, foldability, and mechanical properties at room temperature. The large number of internal hydrogen bonds and π–π stacking provided DXPCM with interesting thermally induced switchable adhesion and recyclability. The storage and release of elastic potential energy ensured that DXPCM could recover its original shape after being deformed by external forces. It is worth mentioning that DXPCM exhibits excellent infrared stealth capability as it can absorb and release latent heat for a long period of time. In conclusion, this work developed a novel solid–solid phase change film with high mechanical strength, thermally induced switchable adhesion, and shape recovery capability, which has great potential for application in infrared stealth.","PeriodicalId":5,"journal":{"name":"ACS Applied Materials & Interfaces","volume":"50 1","pages":""},"PeriodicalIF":8.2000,"publicationDate":"2024-12-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Materials & Interfaces","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1021/acsami.4c18276","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

The application of organic solid–liquid phase change materials (PCMs) is limited for the leakage problem after phase change and high rigidity. In this work, a novel flexible solid–solid PCM (DXPCM) was synthesized using a block copolymerization process with polyethylene glycol (PEG) as the energy storage segment. The phase transition temperature (from 36.2 to 49.4 °C) and enthalpy (from 83.27 to 123.35 J/g) of DXPCM could be changed through adjusting the molecular weight of PEG. The introduction of hard chain segments endowed DXPCM with excellent flexibility, foldability, and mechanical properties at room temperature. The large number of internal hydrogen bonds and π–π stacking provided DXPCM with interesting thermally induced switchable adhesion and recyclability. The storage and release of elastic potential energy ensured that DXPCM could recover its original shape after being deformed by external forces. It is worth mentioning that DXPCM exhibits excellent infrared stealth capability as it can absorb and release latent heat for a long period of time. In conclusion, this work developed a novel solid–solid phase change film with high mechanical strength, thermally induced switchable adhesion, and shape recovery capability, which has great potential for application in infrared stealth.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
具有高机械强度、热诱导可切换附着力和红外隐身形状可恢复性的多功能相变薄膜
有机固液相变材料由于相变后的泄漏问题和高刚性限制了其应用。本文以聚乙二醇(PEG)为储能段,采用嵌段共聚工艺合成了一种新型柔性固-固PCM (DXPCM)。通过调节PEG的分子量,可以改变DXPCM的相变温度(36.2 ~ 49.4℃)和焓(83.27 ~ 123.35 J/g)。硬链段的引入使DXPCM在室温下具有优异的柔韧性、可折叠性和力学性能。大量的内部氢键和π -π堆叠为DXPCM提供了有趣的热诱导可切换粘附性和可回收性。弹性势能的储存和释放保证了DXPCM在外力作用下变形后能够恢复到原来的形状。值得一提的是,DXPCM具有较长时间吸收和释放潜热的优良红外隐身能力。综上所述,本工作开发了一种具有高机械强度、热诱导可切换粘附和形状恢复能力的新型固-固相变膜,在红外隐身领域具有很大的应用潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
ACS Applied Materials & Interfaces
ACS Applied Materials & Interfaces 工程技术-材料科学:综合
CiteScore
16.00
自引率
6.30%
发文量
4978
审稿时长
1.8 months
期刊介绍: ACS Applied Materials & Interfaces is a leading interdisciplinary journal that brings together chemists, engineers, physicists, and biologists to explore the development and utilization of newly-discovered materials and interfacial processes for specific applications. Our journal has experienced remarkable growth since its establishment in 2009, both in terms of the number of articles published and the impact of the research showcased. We are proud to foster a truly global community, with the majority of published articles originating from outside the United States, reflecting the rapid growth of applied research worldwide.
期刊最新文献
Field-Gradient-Driven Molecular Polarization and Trap-State Modulation in Cross-Linked Polyethylene Dielectrics Heterocations Synergistic Doping for Kinetically Enhanced and Structurally Stable LiMn0.6Fe0.4PO4 Effects of the Annealing Process and Sb Doping on the Microstructure, Thermoelectric Performance, and Mechanical Processability of β-FeSi2 Bimetallic-Gallic Acid Cross-Linked Hydrogels with Cascading Nanozyme Activity Promote Healing of MRSA-Infected Wounds by Modulating the Oxidative Stress Microenvironment D-Camphorsulfonic Acid Modulated Self-Assembled Monolayer for Stable and Efficient Inverted Perovskite Solar Cells.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1