Partially ordered glass-forming phases – relaxation processes and cold crystallization

IF 5.2 2区 化学 Q2 CHEMISTRY, PHYSICAL
Maria Massalska-Arodź, Ewa Juszyńska-Gałązka
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Abstract

This review paper concerns the dielectric, calorimetric and optical studies of the chosen liquid crystal materials exhibiting the new class of the partially ordered glasses, where the partial order of the molecules in the glass-forming mesophases survives vitrification. Features of dynamics of the polar molecules observed on approaching the glass transition have been analysed: In the liquid-like glass-forming phases of the nematic, cholesteric and ferroelectric smectic order of molecules the super-Arrhenius temperature dependence of the structural α-relaxation observed in isotropic liquids has been confirmed. On the contrary, in the glass-forming solid-like smectic phases and the orientationally and conformationally disordered (ODIC and CONDIS) crystal phases the Arrhenius behaviour of the molecular dynamics has been found. In the most of the glass phases the Arrhenius secondary relaxation related to the librations/intra molecular motions has been evidenced. The kinetics of the isothermal and non-isothermal cold crystallization processes going on after de-vitrification (softening) of the partially ordered glass has been successfully analysed basing on the Avrami and the Ozawa models. The correlation between dynamic and thermodynamic features has been successfully checked for several compounds. In addition, the influence of the partial order of molecules on the phase polymorphism and molecular dynamics is discussed for three chosen liquid crystals under confinement. The findings enhance our understanding of nucleation/vitrification and molecular mobility in anisotropic soft matter systems, what is important for ensuring the thermal and structural stability of functional liquid crystalline materials.
部分有序玻璃形成相——松弛过程和冷结晶
本文综述了所选液晶材料的介电学、量热学和光学研究,这些材料显示了一类新的部分有序玻璃,其中玻璃形成中间相中的部分有序分子在玻璃化过程中幸存下来。分析了极性分子在接近玻璃化转变时所观察到的动力学特征:在向列相、胆甾相和铁电近晶序分子的类液体玻璃化相中,证实了各向同性液体中观察到的结构α-弛豫的超阿累尼乌斯温度依赖性。相反,在形成玻璃的类固晶相和取向和构象无序(ODIC和CONDIS)晶体相中发现了分子动力学的阿伦尼乌斯行为。在大多数玻璃相中,与分子内运动有关的阿伦尼乌斯二次弛豫已被证实。基于Avrami和Ozawa模型,成功地分析了部分有序玻璃脱玻璃(软化)后的等温和非等温冷结晶过程的动力学。对几种化合物的动力学和热力学特征之间的相关性已经成功地进行了检验。此外,还讨论了分子偏序对三种液晶在约束条件下相多态性和分子动力学的影响。这些发现增强了我们对各向异性软物质体系的成核/玻璃化和分子迁移率的理解,这对确保功能液晶材料的热稳定性和结构稳定性具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Molecular Liquids
Journal of Molecular Liquids 化学-物理:原子、分子和化学物理
CiteScore
10.30
自引率
16.70%
发文量
2597
审稿时长
78 days
期刊介绍: The journal includes papers in the following areas: – Simple organic liquids and mixtures – Ionic liquids – Surfactant solutions (including micelles and vesicles) and liquid interfaces – Colloidal solutions and nanoparticles – Thermotropic and lyotropic liquid crystals – Ferrofluids – Water, aqueous solutions and other hydrogen-bonded liquids – Lubricants, polymer solutions and melts – Molten metals and salts – Phase transitions and critical phenomena in liquids and confined fluids – Self assembly in complex liquids.– Biomolecules in solution The emphasis is on the molecular (or microscopic) understanding of particular liquids or liquid systems, especially concerning structure, dynamics and intermolecular forces. The experimental techniques used may include: – Conventional spectroscopy (mid-IR and far-IR, Raman, NMR, etc.) – Non-linear optics and time resolved spectroscopy (psec, fsec, asec, ISRS, etc.) – Light scattering (Rayleigh, Brillouin, PCS, etc.) – Dielectric relaxation – X-ray and neutron scattering and diffraction. Experimental studies, computer simulations (MD or MC) and analytical theory will be considered for publication; papers just reporting experimental results that do not contribute to the understanding of the fundamentals of molecular and ionic liquids will not be accepted. Only papers of a non-routine nature and advancing the field will be considered for publication.
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