Mechanisms of the Photomechanical Response in Thin-Film Dye-Doped Glassy Polymers.

IF 4.9 3区 工程技术 Q1 POLYMER SCIENCE Polymers Pub Date : 2025-01-20 DOI:10.3390/polym17020254
Zoya Ghorbanishiadeh, Ankita Bhuyan, Bojun Zhou, Morteza Sheibani Karkhaneh, Mark G Kuzyk
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Abstract

This work aims to determine the mechanism of the photomechanical response of poly(Methyl methacrylate) polymer doped with the photo-isomerizable dye Disperse Red 1 using the non-isomerizable dye Disperse Orange 11 as a control to isolate photoisomerization. Samples are free-standing thin films with thickness that is small compared with the optical skin depth to assure uniform illumination and photomechanical response throughout their volume, which differentiates these studies from most others. Polarization-dependent measurements of the photomechanical stress response are used to deconvolute the contributions of angular hole burning, molecular reorientation and photothermal heating. While photo-isomerization of dopant molecules is commonly observed in dye-doped polymers, the shape changes of a molecule might not couple strongly to the host polymer through steric mechanical interactions, thus not contributing substantially to a macroscopic shape change. To gain insights into the effectiveness of such mechanical coupling, we directly probe the dopant molecules using dichroism measurements simultaneously while measuring the photomechanical response and find mechanical coupling to be small enough to make photothermal heating-mediated by the transfer of optical energy as heat to the polymer-the dominant mechanism. We also predict the fraction of light energy converted to mechanical energy using a model whose parameters are thermodynamic material properties that are measured with independent experiments. We find that in the thin-film geometry, these dye-doped glassy polymers are as efficient as any other material but their large Young's modulus relative to other organic materials, such as liquid crystal elastomers, makes them suitable in applications that require mechanically strong materials. The mechanical properties and the photomechanical response of thin films are observed to be significantly different than in fibers, suggesting that the geometry of the material and surface effects might play an important role.

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薄膜染料掺杂玻璃聚合物的光力学响应机制。
本工作旨在确定掺杂光异构染料分散红1的聚甲基丙烯酸甲酯聚合物的光力学响应机制,以非光异构染料分散橙11为对照,分离光异构。样品是独立的薄膜,其厚度与光学皮肤深度相比很小,以确保均匀的照明和整个体积的光电响应,这将这些研究与大多数其他研究区别开来。光力学应力响应的偏振相关测量用于解卷积角孔燃烧、分子重定向和光热加热的贡献。虽然在染料掺杂聚合物中通常观察到掺杂分子的光异构化,但分子的形状变化可能不会通过空间机械相互作用与宿主聚合物强烈耦合,因此不会对宏观形状变化做出实质性贡献。为了深入了解这种机械耦合的有效性,我们在测量光力学响应的同时,使用二色性测量直接探测掺杂分子,并发现机械耦合足够小,使得光热加热(由光能作为热量传递给聚合物)成为主要机制。我们还使用一个模型来预测光能转换为机械能的比例,该模型的参数是通过独立实验测量的热力学材料特性。我们发现,在薄膜几何结构中,这些染料掺杂的玻璃聚合物与任何其他材料一样高效,但它们相对于其他有机材料(如液晶弹性体)的杨氏模量较大,使它们适用于需要机械强度材料的应用。观察到薄膜的力学性能和光力学响应明显不同于纤维,这表明材料的几何形状和表面效应可能起重要作用。
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来源期刊
Polymers
Polymers POLYMER SCIENCE-
CiteScore
8.00
自引率
16.00%
发文量
4697
审稿时长
1.3 months
期刊介绍: Polymers (ISSN 2073-4360) is an international, open access journal of polymer science. It publishes research papers, short communications and review papers. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. Therefore, there is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. Polymers provides an interdisciplinary forum for publishing papers which advance the fields of (i) polymerization methods, (ii) theory, simulation, and modeling, (iii) understanding of new physical phenomena, (iv) advances in characterization techniques, and (v) harnessing of self-assembly and biological strategies for producing complex multifunctional structures.
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