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21.
Dr. Mohamed Alaasar Dr. Marko Prehm Dr. Sebastian Belau Dr. Nerea Sebastián Marharyta Kurachkina Prof. Dr. Alexey Eremin Changlong Chen Prof. Dr. Feng Liu Prof. Dr. Carsten Tschierske 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(25):6362-6377
In recent years, liquid crystals (LCs) responding to light or electrical fields have gained significant importance as multifunctional materials. Herein, two new series of photoswitchable bent-core liquid crystals (BCLCs) derived from 4-cyanoresorcinol as the central core connected to an azobenzene based wing and a phenyl benzoate wing are reported. The self-assembly of these molecules was characterized by differential scanning calorimetry (DSC), polarizing light microscopy (POM), electro-optical, dielectric, second harmonic generation (SHG) studies, and XRD. Depending on the direction of the COO group in the phenyl benzoate wing, core-fluorination, temperature, and the terminal alkyl chain length, cybotactic nematic and lamellar (smectic) LC phases were observed. The coherence length of the ferroelectric fluctuations increases continuously with decreasing temperature and adopts antipolar correlation upon the condensation into superparaelectric states of the paraelectric smectic phases. Finally, long-range polar order develops at distinct phase transitions; first leading to polarization modulated and then to nonmodulated antiferroelectric smectic phases. Conglomerates of chiral domains were observed in the high permittivity ranges of the synclinic tilted paraelectric smectic phases of these achiral molecules, indicating mirror symmetry breaking. Fine-tuning of the molecular structure leads to photoresponsive bent-core (BC)LCs exhibiting a fast and reversible photoinduced change of the mode of the switching between ferroelectric- and antiferroelectric-like as well as a light-induced switching between an achiral and a spontaneous mirror-symmetry-broken LC phase. 相似文献
22.
J. M. Igartua G. Aguirre-Zamalloa I. Ruiz-Larrea M. Couzi A. López-Echarri T. Breczewski 《Journal of Thermal Analysis and Calorimetry》1994,41(6):1211-1215
The specific heat of N(CH3)4CdBr3 from 50 to 300 K has been measured by adiabatic calorimetry, using both static and dynamic methods. The obtained results have permitted a careful study of the ferro-paraelectric phase transition the crystal shows at 160 K. The available spectroscopic data have been used to generate a reliable baseline which accounts for the normal lattice contribution to the specific heat. These results allow for an accurate estimation of the phase transition thermodynamic functions: ΔH=2620 J·mol?1 and ΔS=18.04 J·(mol°C)?1. These high values are in agreement with the predictions of the 6 well potential Frenkel model. 相似文献
23.
Back Cover: Chemical Preparation of Ferroelectric Mesoporous Barium Titanate Thin Films: Drastic Enhancement of Curie Temperature Induced by Mesopore‐Derived Strain (Chem. Eur. J. 36/2014) 下载免费PDF全文
24.
Poly(vinylidene fluoride)(PVDF)/Na+‐MMT composites have been successfully prepared utilizing sodium montmorillonite (Na+‐MMT) via N,N‐dimethylformamide (DMF) solution mixing. The dispersion of Na+‐MMT layers in composites were investigated by transmission electron microscopy (TEM) and X‐ray diffraction (XRD). The effect of adding Na+‐MMT on crystallization behavior of PVDF was specifically studied. The β‐crystalline nucleation effect of Na+‐MMT was investigated and confirmed by differential scanning calorimetry (DSC), XRD, and Fourier transform infrared (FTIR) results. The interaction between PVDF and the surface of Na+‐MMT layers in DMF solution was confirmed by UV‐Vis absorbency. The effect of adding Na+‐MMT on rheological and electrical properties of PVDF/Na+‐MMT composites were also determined. © 2009 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 47: 903–911, 2009 相似文献
25.
Liying Wang Xingzhong Zhao Jiwen Feng 《Journal of Polymer Science.Polymer Physics》2006,44(12):1714-1724
The effects of electron irradiation on the molecular chemical structure, conformation, mobility, and phase transition of vinylidene fluoride (VDF) and trifluoroethylene (TrFE) copolymer have been investigated with variable‐temperature, solid‐state 19F nuclear magnetic resonance (NMR). It has been found that electron irradiation converts all‐trans conformations of both VDF‐rich and TrFE‐containing segments into dynamically mixed trans–gauche conformations accompanied by a simultaneous ferroelectric‐to‐paraelectric (or amorphous) transition. The variable‐temperature 19F magic‐angle‐spinning spectra results show that the paraelectric phase melts at much lower temperatures in irradiated films than in an unirradiated sample. Moreover, 19F NMR relaxation data (spin–lattice relaxation times in both the laboratory and rotating frames) reveal that electron irradiation enhances the molecular motion in paraelectric regions, whereas the molecular motion in a high‐temperature amorphous melt (>100 °C) is more constrained in irradiated films. Besides these physical changes, electron irradiation also induces the formation of several CF3 groups. © 2006 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 44: 1714–1724, 2006 相似文献
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In this paper we report synthesis of phase-pure highly resistive magnetoelectric BiFeO3 thin films on Pt/TiO2/SiO2/Si substrate by using pulsed laser deposition technique. For the first time saturated ferroelectric hysteresis loop has been
observed. It has confirmed the presence of ferroelectricity in BiFeO3 compound. The films exhibit dielectric anomaly near Neel temperature. This anomaly is related to the influence of vanishing
magnetic order on the electric order. In situ domain alignment occurs during observation of the films under transmission electron microscope. 相似文献
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Conjugated polymers consisting of pyrrole or an N‐substituted pyrrole bridged by methine with a mesogenic group were synthesized. Chemical structures of the products were confirmed with IR, NMR, UV–visible (UV–vis) spectroscopy, and gel permeation chromatography analysis. Liquid crystallinity was examined with differential scanning calorimetry measurements and polarizing optical microscopy observations. Liquid crystal domains of the polymer were macroscopically oriented in one direction by an external magnetic force (10 Tesla). The polymer orientation was confirmed by optical microscopy and X‐ray analysis. One of the polymers exhibited a striated fan‐shaped texture when observed with a polarizing optical microscope. This is attributed to the formation of a chiral smectic C (SmC*) phase, which is a property of ferroelectricity. Spontaneous polarization of the polymer occurred at 110 nC/cm2. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 616–629, 2005 相似文献
30.
铁电材料是一类重要的功能材料,铁电元件的小型化、集成化是当今铁电材料发展的一大趋势.但是尺寸效应、表面效应等的存在制约了传统块体铁电材料在纳米尺度下的应用,因而低维度纳米材料中的铁电性能研究成为当前材料科学领域的研究热点之一.本文综述了近年来理论和实验上关于低维铁电材料的探索,包括二维范德瓦耳斯层状铁电材料、共价功能化低维铁电材料、低维钙钛矿材料、外界调控以及二维"铁电金属"等材料的理论预言与实验铁电性的观测;也提出一些物理新机制来解释低维下的铁电性;最后对该领域今后的发展进行了展望. 相似文献