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近晶型液晶4-正丁氧基苯亚甲基-4'-正辛基苯胺(BBOA)中的玻璃化转变动力学和结晶动力学

Glass Transition Dynamics and Crystallization Kinetics in the Smectic Liquid Crystal 4-n-Butyloxybenzylidene-4'-n'-octylaniline (BBOA).

作者信息

Jasiurkowska-Delaporte Małgorzata, Napolitano Simone, Leys Jan, Juszyńska-Gałązka Ewa, Wübbenhorst Micheal, Massalska-Arodź Maria

机构信息

The Henryk Niewodniczanski Institute of Nuclear Physics, Polish Academy of Sciences , Radzikowskiego 152, 31-342 Kraków, Poland.

Department of Physics and Astronomy, Soft Matter and Biophysics Section, KU Leuven , Celestijnenlaan 200D, B-3001 Leuven, Belgium.

出版信息

J Phys Chem B. 2016 Dec 1;120(47):12160-12167. doi: 10.1021/acs.jpcb.6b06303. Epub 2016 Nov 21.

Abstract

The molecular dynamics of 4-n-butyloxybenzylidene-4'-n'-octylaniline (BBOA, abbreviated also as 4O.8) was studied by broadband dielectric spectroscopy (BDS) for samples that were exposed to various thermal treatments. Phase transitions between liquid crystalline phases (N, SmA, SmB, and SmB) were evidenced by abrupt changes in the temperature dependence of the dielectric permittivity spectra and dielectric relaxation times. A particularly complex dynamic behavior was revealed for the highly ordered SmB phase that showed clear evidence for cooperative dynamics of a glass-forming liquid as manifested by a Vogel-Fulcher-Tammann (VFT)-type temperature dependence of its structural relaxation time τ(T). At low temperatures, dependence τ(T) again changes from VFT to Arrhenius behavior, a phenomenon commonly observed for supercooled liquids confined to nanometer length scales and occasionally discussed as strong-fragile transition on heating. In this context, our observation supports the idea of partial orientation disorder in a quenched SmB phase, where the length scale of cooperative motions is restricted to the nanometer size of glassy domains causing the deviation from "bulk" VFT-type behavior. Finally, the isothermal crystallization kinetics of the metastable SmB phase was studied in detail. On the basis of structural information about the SmB and SmB phases, determined by X-ray diffraction, the subtle relation between molecular order and relaxation behavior is discussed.

摘要

通过宽带介电谱(BDS)对经过各种热处理的4-正丁氧基苄叉-4'-正辛基苯胺(BBOA,也简称为4O.8)样品的分子动力学进行了研究。液晶相(N、SmA、SmB和SmB)之间的相变通过介电常数谱和介电弛豫时间的温度依赖性的突然变化得以证明。对于高度有序的SmB相,揭示了一种特别复杂的动力学行为,该相显示出玻璃形成液体协同动力学的明确证据,这表现为其结构弛豫时间τ(T)呈现出Vogel-Fulcher-Tammann(VFT)型温度依赖性。在低温下,τ(T)的依赖性再次从VFT转变为Arrhenius行为,这种现象通常在限制于纳米长度尺度的过冷液体中观察到,并且偶尔在加热时作为强-弱转变进行讨论。在这种情况下,我们的观察结果支持了淬火SmB相中部分取向无序的观点,其中协同运动的长度尺度被限制在玻璃态域的纳米尺寸,从而导致偏离“本体”VFT型行为。最后,详细研究了亚稳SmB相的等温结晶动力学。基于通过X射线衍射确定的SmB和SmB相的结构信息,讨论了分子有序性与弛豫行为之间的微妙关系。

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