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Daniel A. Paterson

Publications and source records attributed to Daniel A. Paterson.

3 recordsLinked to original sources

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

Distinct differences in the nanoscale behaviors of the twist-bend liquid crystal phase of a flexible linear trimer and homologous dimer

We synthesized the liquid crystal dimer and trimer members of a series of flexible linear oligomers and characterized their microscopic and nanoscopic properties using resonant soft x-ray scattering and a number of other experimental techniques. On the microscopic scale, the twist-bend phases of the dimer and trimer appear essentially identical. However, while the liquid crystal dimer exhibits a temperature-dependent variation of its twist-bend helical pitch varying from 100 - 170 Å on heating, the trimer exhibits an essentially temperature-independent pitch of 66 Å, significantly shorter than those reported for other twist-bend forming materials in the literature. We attribute this to a specific combination of intrinsic conformational bend of the trimer molecules and a sterically favorable intercalation of the trimers over a commensurate fraction (two-thirds) of the molecular length. We develop a geometric model of the twist-bend phase for these materials with the molecules arranging into helical chain structures, and we fully determine their respective geometric parameters.

cond-mat.soft

Electrically tunable selective reflection of light from ultraviolet to visible and infrared by heliconical cholesterics

Cholesteric liquid crystals with helicoidal molecular architecture are known for their ability to selectively reflect light with the wavelength that is determined by the periodicity of molecular orientations. Here we demonstrate that by using a cholesteric with oblique helicoidal(heliconical) structure, as opposed to the classic right-angle helicoid, one can vary the wavelength of selectively reflected light in a broad spectral range, from ultraviolet to visible and infrared (360-1520 nm for the same chemical composition) by simply adjusting the electric field applied parallel to the helicoidal axis. The effect exists in a wide temperature range (including the room temperatures) and thus can enable many applications that require dynamically controlled transmission and reflection of electromagnetic waves, from energy-saving smart windows to tunable organic lasers, reflective color display, and transparent see-through displays.

cond-mat.soft