物理交联主链邻氟偶氮苯半晶聚合物光致动器,通过简单的热处理具有超大收缩和多重可编程特性

IF 8.2 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY
Lei Wang, Shengkui Ma, Yan Zhou, Zhaoyang Zhang, Huiqi Zhang
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引用次数: 0

摘要

偶氮苯(azo)聚合物光致动器具有多种可编程特性,在许多光驱动应用中具有很高的吸引力,但其开发仍然具有挑战性。在此,我们报告了一种简单而通用的策略,通过简单的热退火,从物理交联的主链邻氟偶氮半晶聚合物中制造出具有多种可重新编程特性(包括光变形模式、光致应力和机械强度)的先进偶氮聚合物光致动器。在温和条件下,以二丙烯酸酯型邻氟偶氮单体与1,4-二硫苏糖醇为原料,采用Michael加成聚合制备了具有可见光诱导反式异构化的邻氟偶氮主链聚合物。它可以很容易地加工成独立的单轴取向薄膜,具有双重物理交联网络(由相邻的二醇单元诱导的氢键和结晶域形成),通过溶液铸造/机械拉伸方法应变高达2483%。在470 nm蓝光照射下,拉伸膜的晶体域被光致破坏,收缩率达到了前所未有的87%。重要的是,通过不同时间的简单热退火,拉伸薄膜的光力学和力学性能都可以很容易地重新编程,从而导致可见光诱导的多种光变形模式(从一维收缩到收缩加弯曲,再到环境温度下的可逆弯曲/不弯曲),并大大提高了单个样品的光致应力和机械强度。主要是由于它们的热退火引起的结晶度和链间氢键相互作用的增强。本文提出的策略为有效地利用物理交联偶氮半晶聚合物制造具有易于调节的光力学和机械性能的可重构光致动器提供了新的可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Physically Cross-Linked Main-Chain Ortho-Fluorinated Azobenzene Semicrystalline Polymer Photoactuators with Ultralarge Contraction and Multiple Reprogrammable Properties via Simple Thermal Annealing

Physically Cross-Linked Main-Chain Ortho-Fluorinated Azobenzene Semicrystalline Polymer Photoactuators with Ultralarge Contraction and Multiple Reprogrammable Properties via Simple Thermal Annealing
Azobenzene (azo) polymer photoactuators with multiple reprogrammable properties are highly appealing for many photodriven applications, but their development remains challenging. Herein, we report a facile yet versatile strategy for fabricating such advanced azo polymer photoactuators with multiple reprogrammable properties (including photodeformation modes, photoinduced stress, and mechanical strength) from a physically cross-linked main-chain ortho-fluorinated azo semicrystalline polymer via simple thermal annealing. The main-chain ortho-fluorinated azo polymer capable of showing visible-light-induced trans–cis isomerization was efficiently prepared via Michael addition polymerization of a diacrylate-type ortho-fluorinated azo monomer and 1,4-dithiothreitol under mild condition. It can be readily processed into free-standing uniaxially oriented films with dual physical cross-linking networks (formed by both the vicinal diol unit-induced hydrogen bonding and crystalline domains) and strains up to 2483% via solution casting/mechanical stretching method. The stretched films could exhibit up to the unprecedented 87% shrinkage due to the photoinduced destruction of the crystalline domains in the stretched films under 470 nm blue light irradiation. Importantly, both the photomechanical and mechanical properties of the stretched films could be easily reprogrammed by their simple thermal annealing for different times, leading to visible-light-induced multiple photodeformation modes (from one-dimensional shrinkage to shrinkage plus bending and further to reversible bending/unbending at ambient temperature) and largely enhanced photoinduced stress and mechanical strength for a single sample, mainly owing to their thermal annealing-induced enhancement in crystallinity and interchain hydrogen bonding interactions. The strategy presented here offers new possibility for efficiently fabricating remoldable photoactuators with easily tunable photomechanical and mechanical properties from physically cross-linked azo semicrystalline polymers.
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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.
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