Twist-grain boundary phase induced by Au nanoparticles in a chiral liquid crystal host

We report on the stabilisation of the liquid-crystalline, twist-grain boundary A (TGB_A) phase in mixtures of a chiral liquid crystal and surface-functionalised spherical Au nanoparticles (NPs) of 10 nm diameter. The results, obtained by calorimetric, optical, small-angle X-ray and plasmon resonance measurements, demonstrate that a TGB_A phase, which is metastable for the pure liquid crystal host, can be effectively stabilised for a 3 K range in the presence of NPs. Moreover, the role of NPs size on the TGB_A stabilisation is briefly discussed.     

Synthesis and properties of phenyl benzoate-based and biphenyl-based liquid crystalline thiol-ene monomers

Novel phenyl benzoate-based and biphenyl-based liquid crystalline thiol-ene monomers were synthesized and their properties investigated. By varying the bridging unit and spacer length, the type of mesophase can be tuned from the low ordered nematic and smectic A phase in the case of the phenyl benzoate-based monomers, to the highly ordered crystal E phase for the biphenyl-based monomers and their corresponding bromo precursors. We investigated the degree of order of the phenyl benzoate-based materials using the Haller method. Possible premature polymerization of these monomers was examined by size exclusion chromatography. The materials exhibit low transition temperatures and a high stability at typical handling times and temperatures. Consequently, these monomers are useful for in situ polymerization with anisotropic inert solvents, which could potentially lead to new architectures and enhanced electro-optical properties of devices. The use of the biphenyl-based monomers appears to be of limited use for polymerizations in anisotropic solution. However, as a result of their intrinsic high degree of molecular order, these monomers form a particularly interesting class of reactive materials that can be bulk polymerized to give main chain polymers with highly defined mechanical and optical or electro-optical properties.     

Fast switching of vertically aligned negative liquid crystals by optically hidden relaxation

We propose a method for fast switching of vertically aligned (VA) negative liquid crystals (LCs) by hiding the relaxation process of LCs. During the turn-off process, a strong in-plane electric field is applied for a short duration of time instead of relying solely on the slow relaxation of LCs. The LC molecules are rotated to the transmission axis of one of the polarisers by the applied in-plane electric field, resulting in turn-off switching that is 5.8 times faster than that of a conventional VA cell. By applying an overdriving scheme, we experimentally obtained a total response time of 3.3 ms.     

Dynamic simulation of Pi-cell liquid crystal displays

The dynamics of π-cell liquid crystal displays was studied by detailed computer simulation. The time evolution of the director configuration and the velocity of flow reveals the mechanism of the fast response of π-cells. The effect of pretilt angle on the dynamics of π-cells was also studied.     

Simulation of mesogenic diruthenium tetracarboxylates: Development of a force field for coordination polymers of the MMX type

A classical molecular mechanics force field, able to simulate coordination polymers (CP) based on ruthenium carboxylates (Ru₂(O₂CR_eq)₄L_ax) (eq = equatorial group containing aliphatic chains, L_ax= axial ligand), has been developed. New parameters extracted from experimental data and quantum calculations on short aliphatic chains model systems were included in the generalized AMBER force field. The proposed parametrization was evaluated using model systems with known structure, containing either short or long aliphatic chains; experimental results were reproduced satisfactorily. This modified force field, although in a preliminary stage, could then be applied to long chain liquid crystalline compounds. The resulting atomistic simulations allowed assessing the relative influence of the factors determining the CP conformation, determinant for the physical properties of these materials. © 2013 Wiley Periodicals, Inc.     

Single crystal synthesis and magnetism of the BaLn2O4 family (Ln = lanthanide)

The series of compounds in the BaLn₂O₄ family (Ln = La–Lu, Y) has been synthesized for the first time in single crystalline form, using a molten metal flux. The series crystallizes in the CaV₂O₄ structure type with primitive orthorhombic symmetry (space group Pnma, #62), and a complete structural study of atomic positions, bonds, angles, and distortions across the lanthanide series is presented. With the exception of the Y, La, Eu, and Lu members, magnetic susceptibility measurements were performed between 2 K and 300 K. BaCe₂O₄ and BaYb₂O₄ display large crystal fields effects and suppression of magnetic ordering. All compounds show signs of magnetic frustration due to the trigonal arrangements of the trivalent lanthanide cations in the structure.     

Wave mixing in coupled phononic crystals via a variable stiffness mechanism

We investigate wave mixing effects in a phononic crystal that couples the wave dynamics of two channels – primary and control ones – via a variable stiffness mechanism. We demonstrate analytically and numerically that the wave transmission in the primary channel can be manipulated by the control channel's signal. We show that the application of control waves allows the selection of a specific mode through the primary channel. We also demonstrate that the mixing of two wave modes is possible whereby a modulation effect is observed. A detailed study of the design parameters is also carried out to optimize the switching capabilities of the proposed system. Finally, we verify that the system can fulfill both switching and amplification functionalities, potentially enabling the realization of an acoustic transistor.     

Colorimetric Chemosensor for Chloramphenicol Based on Colloidal Magnetically Assembled Molecularly Imprinted Photonic Crystals

A novel colorimetric chemosensor with good sensitivity, specificity, and self‐reporting capability for chloramphenicol (CAP ) has been successfully constructed based on colloidal, magnetically assembled photonic crystals coupled with molecular imprinting. The colloidal, magnetically assembled, molecularly imprinted photonic crystals (CMA ‐MIPCs ) were prepared by assembling CAP in magnetic, molecularly imprinted nanohydrogels (MMIHs ) in a magnetic field. The magnetic assembly of photonic crystals and the sensing processes could be completed simultaneously when MMIHs were dispersed in CAP solutions and in a magnetic field, and the response time was less than 1 min. The CAP concentration could be visually determined from the color change of the CMA ‐MIPCs sensor. The diffraction color blue‐shifted from luminous yellow of the blank to purple in a 1.0 mg/mL CAP solution, with a determination limit of 1.0 × 10⁻³ mg/mL. It could provide a new strategy for qualitative or semiquantitative detection of CAP .     

Galvanomagnetic Properties Of Asf5 -Intercalated Highly-Oriented Pyrolytic Graphite (HOPG)

Due to the anisotropy of the conductivity in AsF₅-intercalated HOPG, eddy current methods have to be used for the measurement of transport effects. The measurements yield carrier concentration, mobility and charge transfer for C8nAsF₅ with n=l-4 at temperatures between 4.2K and 300K.