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具有三明治结构的高拉伸共轭聚合物/弹性体共混薄膜

Highly Stretchable Conjugated Polymer/Elastomer Blend Films with Sandwich Structure.

作者信息

Qin Ru, Wu Yin, Ding Zicheng, Zhang Rui, Yu Jifa, Huang Wenliang, Liu Dongle, Lu Guanghao, Liu Shengzhong Frank, Zhao Kui, Han Yanchun

机构信息

Key Laboratory of Applied Surface and Colloid Chemistry, National Ministry of Education, Shaanxi Key Laboratory for Advanced Energy Devices, Shaanxi Engineering Lab for Advanced Energy Technology, Institute for Advanced Energy Materials, School of Materials Science and Engineering, Shaanxi Normal University, Xi'an, 710119, China.

Department of Physics, Chemistry and Biology (IFM), Linköping University, Linköping, 58183, Sweden.

出版信息

Macromol Rapid Commun. 2024 Jan;45(1):e2300240. doi: 10.1002/marc.202300240. Epub 2023 Jun 21.

Abstract

The physical blending of high-mobility conjugated polymers with ductile elastomers provides a simple way to realize high-performance stretchable films. However, how to control the morphology of the conjugated polymer and elastomer blend film and its response to mechanical fracture processes during stretching are not well understood. Herein, a sandwich structure is constructed in the blend film based on a conjugated polymer poly[(5-fluoro-2,1,3-benzothiadiazole-4,7-diyl)(4,4-dihexadecyl-4H-cyclopenta[2,1-b:3,4-b″]dithiophene-2,6-diyl)(6-fluoro-2,1,3-benzothiadiazole-4,7-diyl)(4,4-dihexadecyl-4H-cyclopenta[2,1-b:3,4-b″]dithiophene-2,6-diyl)] (PCDTFBT) and an elastomer polystyrene-block-poly(ethylene-ran-butylene)-block-polystyrene (SEBS). The sandwich structure is composed of a PCDTFBT:SEBS mixed layer laminated with a PCDTFBT-rich layer at both the top and bottom surfaces. During stretching, the external strain energy can be effectively dissipated by the deformation of the crystalline PCDTFBT domains and amorphous SEBS phases and the recrystallization of the PCDTFBT chains. This endows the blend film with excellent ductility, with a large crack onset strain exceeding 1100%, and minimized the electrical degradation of the blend film at a large strain. This study indicates that the electrical and mechanical performance of conjugated polymer/elastomer blend films can be improved by manipulating their microstructure.

摘要

将高迁移率共轭聚合物与韧性弹性体进行物理共混,为实现高性能可拉伸薄膜提供了一种简单的方法。然而,如何控制共轭聚合物与弹性体共混薄膜的形态及其在拉伸过程中对机械断裂过程的响应,目前还不太清楚。在此,基于共轭聚合物聚[(5-氟-2,1,3-苯并噻二唑-4,7-二亚基)(4,4-二十六烷基-4H-环戊[2,1-b:3,4-b″]二噻吩-2,6-二亚基)(6-氟-2,1,3-苯并噻二唑-4,7-二亚基)(4,4-二十六烷基-4H-环戊[2,1-b:3,4-b″]二噻吩-2,6-二亚基)](PCDTFBT)和弹性体聚苯乙烯-嵌段-聚(乙烯-无规-丁烯)-嵌段-聚苯乙烯(SEBS),在共混薄膜中构建了一种三明治结构。该三明治结构由一个PCDTFBT:SEBS混合层以及在其上下表面层压的富含PCDTFBT的层组成。在拉伸过程中,外部应变能可通过结晶PCDTFBT域和无定形SEBS相的变形以及PCDTFBT链的再结晶而有效耗散。这赋予了共混薄膜优异的延展性,其大裂纹起始应变超过1100%,并在大应变下使共混薄膜的电性能降解最小化。这项研究表明,通过控制共轭聚合物/弹性体共混薄膜的微观结构,可以改善其电学和力学性能。

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