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液晶性和机械变形对负泊松比液晶弹性体分子弛豫的影响

Influence of Liquid Crystallinity and Mechanical Deformation on the Molecular Relaxations of an Auxetic Liquid Crystal Elastomer.

作者信息

Raistrick Thomas, Reynolds Matthew, Gleeson Helen F, Mattsson Johan

机构信息

School of Physics and Astronomy, University of Leeds, Leeds LS2 9JT, UK.

出版信息

Molecules. 2021 Dec 2;26(23):7313. doi: 10.3390/molecules26237313.

Abstract

Liquid Crystal Elastomers (LCEs) combine the anisotropic ordering of liquid crystals with the elastic properties of elastomers, providing unique physical properties, such as stimuli responsiveness and a recently discovered molecular auxetic response. Here, we determine how the molecular relaxation dynamics in an acrylate LCE are affected by its phase using broadband dielectric relaxation spectroscopy, calorimetry and rheology. Our LCE is an excellent model system since it exhibits a molecular auxetic response in its nematic state, and chemically identical nematic or isotropic samples can be prepared by cross-linking. We find that the glass transition temperatures (Tg) and dynamic fragilities are similar in both phases, and the T-dependence of the α relaxation shows a crossover at the same T* for both phases. However, for T>T*, the behavior becomes Arrhenius for the nematic LCE, but only more Arrhenius-like for the isotropic sample. We provide evidence that the latter behavior is related to the existence of pre-transitional nematic fluctuations in the isotropic LCE, which are locked in by polymerization. The role of applied strain on the relaxation dynamics and mechanical response of the LCE is investigated; this is particularly important since the molecular auxetic response is linked to a mechanical Fréedericksz transition that is not fully understood. We demonstrate that the complex Young's modulus and the α relaxation time remain relatively unchanged for small deformations, whereas for strains for which the auxetic response is achieved, significant increases are observed. We suggest that the observed molecular auxetic response is coupled to the strain-induced out-of-plane rotation of the mesogen units, in turn driven by the increasing constraints on polymer configurations, as reflected in increasing elastic moduli and α relaxation times; this is consistent with our recent results showing that the auxetic response coincides with the emergence of biaxial order.

摘要

液晶弹性体(LCEs)将液晶的各向异性有序性与弹性体的弹性特性相结合,具有独特的物理性质,如刺激响应性和最近发现的分子负泊松比响应。在此,我们使用宽带介电弛豫光谱、量热法和流变学来确定丙烯酸酯LCE中的分子弛豫动力学如何受其相的影响。我们的LCE是一个出色的模型系统,因为它在向列相状态下表现出分子负泊松比响应,并且可以通过交联制备化学性质相同的向列相或各向同性样品。我们发现两个相中的玻璃化转变温度(Tg)和动态脆性相似,并且α弛豫的T依赖性在两个相的相同T处出现交叉。然而,对于T>T,向列相LCE的行为变为阿累尼乌斯型,但各向同性样品仅更类似于阿累尼乌斯型。我们提供证据表明,后一种行为与各向同性LCE中预过渡向列相涨落的存在有关,这些涨落在聚合过程中被锁定。研究了施加应变对LCE弛豫动力学和力学响应的作用;这一点尤为重要,因为分子负泊松比响应与尚未完全理解的机械弗雷德里克斯转变有关。我们证明,对于小变形,复杨氏模量和α弛豫时间保持相对不变,而对于实现负泊松比响应的应变,则观察到显著增加。我们认为,观察到的分子负泊松比响应与介晶单元的应变诱导面外旋转相关,而这又由聚合物构型上不断增加的限制所驱动,这反映在弹性模量和α弛豫时间的增加上;这与我们最近的结果一致,即负泊松比响应与双轴有序的出现相吻合。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f95/8659252/1b90d0fb2b15/molecules-26-07313-g001.jpg

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