SearcharxivSearch

arXiv subjects

Yuki Arakawa

Publications and source records attributed to Yuki Arakawa.

4 recordsLinked to original sources

Structure of the twist-bend nematic phase with respect to the orientational molecular order of the thioether-linked dimers

An analysis of the IR absorbance for the segmented functional groups of liquid crystal dimers: mesogen and linker, enabled the orientation order to be determined and information about the dipole interactions in the nematic and twist-bend nematic phases to be obtained. The long axis orientational order increases as the temperature decreases in the nematic phase, although much more slowly than for the classical nematics, and then reverses this trend in the twist-bend nematic phase due to the tilt of the molecules. In the nematic phase, the short axis of the molecule performs an isotropic uniform rotation and has a uniaxial alignment. In the twist-bend nematic phase, however, biaxial ordering occurs and grows significantly in accordance with the helical deformation of the director. Changes in the mean absorbance in the twist-bend nematic phase were observed: a decrease for the longitudinal dipole at the nematic-twist-bend nematic phase transition, thus emphasizing the antiparallel axial interaction of the dipoles, while the absorbance of the transverse dipoles remains unchanged up to 340 K, and then the latter become parallelly correlated.

cond-mat.soft

Increased intermolecular interactions and cluster formation at the onset of the twist-bend nematic phase in thioether cyanobiphenyl-based liquid crystal dimers

Infrared spectroscopy (IR) and quantum chemistry calculations, based on density functional theory (DFT) were used to study the structure and the molecular interactions in the nematic (N) and twist-bend (NTB) phases of thioether-linked dimers. Infrared absorbance measurements were conducted in a polarized beam for homogeneously aligned samples to measure and understand the orientation of the vibrational transition dipole moments in the liquid crystal states. Revealing temperature-dependent changes in the mean IR absorbance in the twist-bend nematic phase were observed. In the transition from the N to the NTB phase, is was found to be associated with a decrease in absorbance for the longitudinal dipoles. This is a result of the antiparallel axial interactions of the dipoles, while the absorbance of the transverse dipoles remained unchanged up to 340 K and then increased and the dipoles correlated in parallel. In order to account for the molecular arrangement in the nematic phase, DFT calculations were conducted for the system nearest to the lateral neighborhoods. Changes in the square of transition dipoles were found to be quite similar to the mean absorbance that was observed in the IR spectra. Interactions of molecules that were dominated by pair formation was observed as well as a shift of the long axes of the molecules relative to each other. The most important observation from the spectroscopic measurements was the sudden increase in the intermolecular interactions as the temperature decreased from the N to the NTB phase. This was evidenced by a significant increase in the correlation of the dipoles that were induced in the dimer cores.

cond-mat.soft

Study of the experimental and simulated vibrational spectra together with conformational analysis for thioether cyanobiphenyl-based liquid crystal dimers

Infrared spectroscopy (IR) and quantum chemistry calculations that are based on the density functional theory (DFT) have been used to study the structure, molecular interactions of the nematic and twist-bend phases for thioether-linked dimers. Infrared absorbance measurements were conducted in a polarized beam for a homogeneously aligned sample in order to obtain more details about the orientation of the vibrational transition dipole moments. The distributions to investigate the structure and conformation of the molecule dihedral angle were calculated. The calculated spectrum was compared with the experimental infrared spectra and as a result, detailed vibrational assignments are reported.

cond-mat.soft

Identification of New Assembly Mode in the Heliconical Nematic Phase via Tender Resonant X-ray Scattering

Helical structures are exciting and are utilized in numerous applications ranging from biotechnology to displays to medicine. Accurate description and understanding of resonance effects in helical structures provides crucial knowledge on molecular packing beyond positional ordering. We exam-ined the manifestation of resonance effects in a nematic phase with heliconical structure, the so called twist bend nematic (NTB) via tender resonant X-ray scattering (TReXS) at the sulfur K-edge. We demonstrate for the first time quantitatively that the energy dependence of the scattering peak in the NTB phase follows the energy dependence of the complex refractive indices measured by X-ray absorption. This allows us to identify a new self-assembly mode for specific sets of liquid crystal dimers in the NTB phase. We anticipate that new avenues in the exploration of complex orientational structures both in static as well as in dynamic modes induced by external stimuli will be pursued.

cond-mat.soft