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Nataša Vaupotič

Publications and source records attributed to Nataša Vaupotič.

9 recordsLinked to original sources

Helix alignment, chevrons, and edge dislocations in twist-bend ferroelectric nematics

We explore surface alignment and edge dislocations in the recently discovered twist-bend ferroelectric nematic, NTBF, in which the vector of spontaneous polarization follows an oblique helicoidal trajectory around a polar twist-bend axis. In a planar cell, the polar axis aligns at some angle to the rubbing direction to mitigate surface electric charge. We demonstrate that the pseudolayers in planar cells form chevron defects, a hallmark defect of one-dimensionally positionally ordered phases, such as smectic A and smectic C. The polar character of the twist-bend axis prevents the cores of NTBF edge dislocations from splitting into semi-integer disclinations, in stark contrast to dislocations in paraelectric and ferroelectric chiral nematics. The tilt of pseudolayers around the defect core allows us to estimate the elastic penetration length as being close to the pitch of NTBF. Compression/dilation stresses around the core modify the heliconical tilt angle of molecules as evidenced by a substantial variation in local birefringence. The climb of dislocations exhibits high mobility, allowing the system to equilibrate the temperature-dependent pitch. The uncovered properties facilitate the development of NTBF materials for electro-optical applications, such as electrically controlled diffraction lattices and structural colors.

cond-mat.soft↗

Twist Grain Boundary phases in proper ferroelectric liquid crystals realm

The twist-grain-boundary (TGB) phases, characterized by a periodic, helical arrangement of blocks made of polar smectic phases, SmAF and SmCF, have been discovered. They have been observed for rod-like molecules with a strong longitudinal dipole moment, featuring an (S)-2-methylbutyl end group having only weak twisting power, and emerge below the antiferroelectric SmAAF phase, where the lamellar structure is already well established. It is suggested that the structure is governed by electrostatic interactions amplified by weak chiral forces, in striking contrast to the mechanism of TGB phase formation found in non-polar materials. The TGB phases exhibit light selective reflection in the visible range, while the value of electric polarization confirms an almost perfectly ordered dipole alignment.

cond-mat.soft↗

Ferroelectric nematics: Materials with high permittivity or low resistivity?

Two models have recently been proposed for a description of dielectric spectroscopy measurements of ferroelectric nematics (NF) in thin planar capacitors. The polarization-external capacitance Goldstone reorientation mode (PCG model) considers the NF layer between the electrodes as an effective low resistivity material, the resistivity being inversely proportional to the square of polarisation magnitude. The high-ε model considers the NF material as having a huge permittivity due to the ease of polarisation rotation. In this paper we study implications of both models and show, why both models describe majority of the observed dielectric spectroscopy results equally well. We point out differences among the models predictions and explain why some observations can be explained only by the high-ε model. The major difference between the models is that the high-ε model predicts that the increase in the cell thickness can lead to an increase in the frequency range within which capacitors filled with NF material can be used for energy storage while within the PCG model this frequency range reduces with increasing capacitor thickness. Within both models a crucial parameter which determines the behaviour of the capacitors filled with a NF material is parasitic resistance, primarily due to the electrode resistance. We present measurements of electrode resistance and find that in ITO cells it is of the order of few hundred ohms.

cond-mat.mtrl-sci↗

Interpretation of dielectric spectroscopy measurements of ferroelectric nematic liquid crystals

The magnitude of the relative permittivity of the ferroelectric nematic phase (NF) is under a lively scientific discussion since the phase was recently discovered. Dielectric spectroscopy measurements (DSM) give a huge value of relative permittivity, which depends on the cell thickness, but this is argued to result from a misinterpretation of the DSM results. We have conducted DSM using a set of cells differing in thickness of the NF layer, type of electrodes and presence/absence of nanoscale-thick surface layers. To model the DSM results, cells are presented by an equivalent electric circuit that includes a capacitor due to the NF layer with frequency dependent complex relative permittivity, capacitors due to surface layers, and a resistor describing limited conductivity of electrodes. DSM results for different cells with the same liquid crystal in the NF phase, are semi-quantitatively reproduced by the same set of physical parameters if a huge relative permittivity of the NF, which is even orders of magnitude larger than the measured apparent values, is assumed. We show that the capacitance of surface layers should be considered also in cells with no polymer alignment layer on electrodes.

cond-mat.soft↗

Ferroelectric nematic -- isotropic critical end point

A critical end point above which an isotropic phase continuously evolves into a polar (ferroelectric) nematic phase with an increasing electric field is found in a ferroelectric nematic liquid crystalline material. The critical end point is approximately 30 K above the zero-field transition temperature from the isotropic to nematic phase and at an electric field of the order of 10 V/micron. Such systems are interesting from the application point of view because a strong birefringence can be induced in a broad temperature range in an optically isotropic phase.

cond-mat.soft↗

Dielectric response of a ferroelectric nematic liquid crystalline phase in thin cells

We studied dielectric properties of a polar nematic phase (NF) sandwiched between two gold or ITO electrodes, serving as a cell surfaces. In bulk, NF is expected to exhibit a Goldstone mode (phason), because polarization can uniformly rotate with no energy cost. However, because the coupling between the direction of nematic director and polarization is finite, and the confinement, even in the absence of the aligning surface layer, induces some energy cost for a reorientation of polarization, the phason dielectric relaxation frequency is measured in a kHz regime. The phason mode is easily quenched by a bias electric field, which enables fluctuations in the magnitude of polarization to be followed in both, the ferronematic and nematic phases. This amplitude (soft) mode is also influenced by boundary conditions. A theory describing the phase and amplitude fluctuations in the NF phase shows that the free energy of the system and, consequently, the dielectric response are dominated by polarization-related terms with the flexoelectricity being relevant only at a very weak surface anchoring. Contributions due to the nematic elastic terms are always negligible. The model relates the observed low frequency mode to the director fluctuations weakly coupled to polarization fluctuations.

cond-mat.soft↗

Multi-level Chirality in Liquid Crystals Formed by Achiral Molecules

In many biological materials with a hierarchical structure there is an intriguing and unique mechanism responsible for the 'propagation' of order from the molecular to the nano- or micro-scale level. Here we present a much simpler molecular system built of achiral mesogenic dimeric molecules that shows a similar complexity with four levels of structural chirality (i) layer chirality, (ii) helicity of a basic 4-layer repeating unit, (iii) a helix with a pitch of several layers and (iv) mesoscopic helical filaments. As seen in many biological systems, there is a coupling between chirality at different levels. The structures were identified by a combination of hard and soft x-ray diffraction measurements, optical studies and theoretical modelling.

cond-mat.soft↗

Nature of nematic to twist bend nematic phase transition

The critical behavior at the transition from uniform nematic to twist-bend modulated nematic phase is revealed and shown to be well explained by the mean field approximation. The study was performed on a group of materials that exhibit an unusually broad temperature range of the nematic phase above the twist-bend modulated nematic phase, so the critical range in which the order parameter fluctuations are strong and can be experimentally observed is wide. The formation of instantaneous helices is observed already several degrees above the transition temperature, strongly influencing the birefringence of the system. The analysis of a critical part of the birefringence changes provides a set of critical exponents that are consistent with the mean field approximation, indicating a large correlation length of helical fluctuations in the nematic phase.

cond-mat.soft↗

Structure of nanoscale-pitch helical phases: blue phase and twist-bend nematic phase resolved by resonant soft X-ray scattering

Periodic structures of phases with orientational order of molecules, but homogenous electron density distribution: a short pitch cholesteric, blue phase and twist-bend nematic phase, were probed by a resonant soft x-ray scattering (RSoXS) at the carbon K-edge. The theoretical model shows that in case of a simple heliconical nematic structure two resonant signals corresponding to the full and half pitch band should be present, while only the full pitch band is observed in experiment. This suggests that the twist-bend nematic phase has complex structure with a double-helix, built of two interlocked, shifted helices. We confirm that the helical pitch in the twist-bend nematic phase is in a 10 nm range, for both, the chiral and achiral materials. We also show that the symmetry of a blue phase can unambiguously be determined through a resonant enhancement of x-ray diffraction signals, by including polarization effects, which are found to be an important indicator in phase structure determination.

cond-mat.soft↗