Transmission polarized optical microscopy of short-pitch cholesteric liquid crystal shells

We recently demonstrated that colloidal crystal arrangements of monodisperse droplets or shells of planar-aligned cholesteric liquid crystal exhibit intricate patterns of circularly polarized reflection spots of different colors. The spots appear as a result of photonic cross communication between droplets, hence the patterns reflect the macroscopic arrangement of droplets or shells. Apart from being an interesting optical phenomenon, it offers attractive application opportunities in photonics and beyond, due to the unique characteristics of the patterns. It turns out that the optical quality of shells is much enhanced compared to that of droplets, hence we focus our attention primarily on shells, of varying thickness. Here we analyze and explain the intriguing textures arising when studying planar-aligned short-pitch cholesteric shells in transmission polarizing optical microscopy. In this case, the texture reflects the properties of each individual shell, without any sign of cross communication, yet also this pattern holds some fascinating mysteries. These can only be elucidated by considering all the peculiar optical properties of cholesterics together, as well as the unusual situation given by the spherical shell geometry

Tuneable Multicoloured Patterns From Photonic Cross Communication Between Cholesteric Liquid Crystal Droplets

Monodisperse droplets of planar-aligned cholesteric (N*) liquid crystal exhibit an intriguing capacity for photonic cross-communication, giving rise to colourful patterns that depend sensitively on the N* pitch, droplet positions and illuminated area. The phenomenon results from a combination of omnidirectional selective reflection of N* droplets—which thus act as spherically symmetric self-assembled photonic crystals—and total internal reflection at the continuous phase surface. We outline how the unique optical properties can be employed in numerous applications

Through the Spherical Looking-Glass: Asymmetry Enables Multicolored Internal Reflection in Cholesteric Liquid Crystal Shells

Spheres of cholesteric liquid crystal generate dynamic patterns due to selec- tive reflection from a helical structure subject to continuously curved bounda- ries. So far the patterns are investigated exclusively as function of reflections at the sphere exterior. Here it is shown that the cholesteric shells in a microfluidics produced double emulsion enable also a sequence of internal reflections if the shells have sufficiently thin top and thick bottom. While such asymmetry is promoted by buoyancy when the internal droplet has lower density than the liquid crystal, the elasticity of the cholesteric helix prefers a symmetric shell geometry, acting against gravity. This subtle balance can hide the internal reflections for long time. Eventually, however, the asymmetry is established, revealing a new class of photonic patterns characterized by colored sharp concentric rings. With the complete knowledge of the diverse light-reflecting behavior of cholesteric liquid crystal shells, and utilizing the tunability of the structure period by, e.g., temperature, electric field, or expo- sure to various chemical species as well as polymer stabilization for making the shells long-term stable, they may be developed into remarkable new optical elements for photonics, sensing, or security pattern generation

Dynamic tuning of the director field in liquid crystal shells using block copolymers

When an orientationally ordered system, like a nematic liquid crystal (LC), is confined on a self-closing spherical shell, topological constraints arise with intriguing consequences that depend critically on how the LC is aligned in the shell. We demonstrate reversible dynamic tuning of the alignment, and thereby the topology, of nematic LC shells stabilized by the nonionic amphiphilic block copolymer Pluronic F127. Deep in the nematic phase, the director (the average molecule orientation) is tangential to the interface, but upon approaching the temperature TNI of the nematic– isotropic transition, the director realigns to normal. We link this to a delicate interplay between an interfacial tension that is nearly independent of director orientation, and the configurationdependent elastic deformation energy of an LC confined in a shell. The process is primarily triggered by the heating-induced reduction of the nematic order parameter, hence realignment temperatures differ by several tens of degrees between LCs with high and low TNI , respectively. The temperature of realignment is always lower on the positive-curved shell outside than at the negative-curved inside, yielding a complex topological reconfiguration on heating. Complementing experimental investigations with mathematical modeling and computer simulations, we identify and investigate three different trajectories, distinguished by their configurations of topological defects in the initial tangential-aligned shell. Our results uncover a new aspect of the complex response of LCs to curved confinement, demonstrating that the order of the LC itself can influence the alignment and thereby the topology of the system. They also reveal the potential of amphiphilic block copolymer stabilizers for enabling continuous tunability of LC shell configuration, opening doors for in-depth studies of topological dynamics as well as novel applications in, e.g., sensing and programmed soft actuators

Elucidating the fine details of cholesteric liquid crystal shell reflection patterns

Clusters of planar-aligned short-pitch cholesteric liquid crystal spheres generate dynamic colourful patterns due to multiple selective reflections from the radially oriented cholesteric helices in neighbour shells at varying distances. These photonic communication patterns were widely investigated for the cases of both droplets and shells, demonstrating not only intriguing optical phenomena but also potential for applications as new optical elements for photonics, sensing or security pattern generation. However, the optics of these clusters is truly complex and until now only the strongest and most fundamental reflections have been analysed and explained. In this report, we elucidate the origin of a number of more subtle reflections and we explain the extension in space of various spots as well as their internal colour variations

Sub-second dynamic phototuning of alignment in azodendrimer-doped nematic liquid crystal shells

The alignment of nematic liquid crystal 5CB in micron-thick shells, suspended in and containing aqueous liquid phases, can be rapidly switched between radial (homeotropic) and tangential (planar) director field by doping them with a photoresponsive dendrimer with multiple azobenzene moieties in the branches. The dendrimer spontaneously segregates to the inner as well as outer shell interfaces, folding into an amphiphilic conformation irrespective of the sign of interface curvature. The branches are directed into the liquid crystal, inducing a homeotropic ground state. Upon UV irradiation, the trans-cis isomerization of azobenzene triggers immediate switching to planar alignment. The very fast realignment and the simultaneous response throughout the shell leads to an initially random planar director field, with many topological defects of both positive and negative signs becoming visible within a second of irradiation. All but two +1 defects quickly annihilate, and the remaining defect pair moves up towards the thinnest part of the shell to form the planar steady state. By illuminating with visible light the homeotropic alignment is quickly recovered. By exchanging the solvent used for assisting the dendrimer dissolution, also dynamic phase separation phenomena can be studied in the shells, revealing that the dendrimer solubility in 5CB is greater in the UV-induced cis state than in the trans ground state

Liquid crystals in micron-scale droplets, shells and fibers

peer reviewedThe extraordinary responsiveness and large diversity of self-assembled structures of liquid crystals are well documented and they have been extensively used in devices like displays. For long, this application route strongly influenced academic research, which frequently focused on the performance of liquid crystals in display-like geometries, typically between flat, rigid substrates of glass or similar solids. Today a new trend is clearly visible, where liquid crystals confined within curved, often soft and flexible, interfaces are in focus. Innovation in microfluidic technology has opened for high-throughput production of liquid crystal droplets or shells with exquisite monodispersity, and modern characterization methods allow detailed analysis of complex director arrangements. The introduction of electrospinning in liquid crystal research has enabled encapsulation in optically transparent polymeric cylinders with very small radius, allowing studies of confinement effects that were not easily accessible before. It also opened the prospect of functionalizing textile fibers with liquid crystals in the core, triggering activities that target wearable devices with true textile form factor for seamless integration in clothing. Together, these developments have brought issues center stage that might previously have been considered esoteric, like the interaction of topological defects on spherical surfaces, saddle-splay curvature-induced spontaneous chiral symmetry breaking, or the non-trivial shape changes of curved liquid crystal elastomers with non-uniform director fields that undergo a phase transition to an isotropic state. The new research thrusts are motivated equally by the intriguing soft matter physics showcased by liquid crystals in these unconventional geometries, and by the many novel application opportunities that arise when we can reproducibly manufacture these systems on a commercial scale. This review attempts to summarize the current understanding of liquid crystals in spherical and cylindrical geometry, the state of the art of producing such samples, as well as the perspectives for innovative applications that have been put forward.R-AGR-0505 - IRP15 - UNIQUE (20150401-20180331) - LAGERWALL Ja

Chapter 6 MARINE BIODIVERSITY IN KOREA: A REVIEW OF MACROZOOBENTHIC ASSEMBLAGES, THEIR DISTRIBUTIONS, AND LONG-TERM COMMUNITY CHANGES FROM HUMAN IMPACTS

oceanography, climate change, reefs, marine science, marine conservation, marine researc

Tuning Self-Assembly in Liquid Crystal shells: from Interfacial- to Polymer-stabilization

Liquid crystals form a subclass of soft materials which is easily influenced and deformed by a surface, an interface and the geometry. Of particular interest, in this thesis, is the confinement of liquid crystals in shell geometry, imposing real or virtual defects that the liquid crystal cannot avoid. With the help of microfluidics, we prepare our research platform, liquid crystal shells, which contain and are surrounded by aqueous phases. In order to maintain such a shell structure in the aqueous phases, immiscible with the liquid crystal, appropriate stabilization is required. Here we explore two different pathways of interfacial stabilization and polymer stabilization and their impact on liquid crystal self-assembly. We primarily use either a polymeric or an ionic surfactant dissolving in water to stabilize shells and tune boundary conditions of shells. Depending on symmetrically or asymmetrically imposed boundary conditions, the nematic–isotropic phase transition appears as a single transi- tion or separated into two steps. We propose that the latter phenomenon can be understood as a result of an ordering-enhancing effect by surfactants. The nematic–smectic A phase transition is also investigated under varying boundary conditions. With a precise temperature control, we explore equilibrium smectic structures and introduce a new arrangement of focal conic arrays in shell geometry. Beyond stabilizing the shell from the shell exterior, but we also incorporate a photosensitive surface agent within the shell, enabling dynamic and reversible photoswitching of the liquid crystal alignment in real time. However, shells with interfacial stabilization cannot survive more than several weeks due to their intrinsic fluid interfaces. In particular, a liquid crystal shell can serve as a permeable mem- brane which lets the constituents of aqueous phases pass through, giving a significant influence on the liquid crystalline order. To tame liquid crystal self-assembly and make the shell struc- ture permanent, we use photopolymerization to stabilize the shells. With only 5% monomer, the entire configuration of each liquid crystal shell is locked and shell lifetime extends beyond several months. The liquid crystalline order is visualized on the nanoscale via the polymer network and we further demonstrate that the shell configurations can be a unique template for creating complex polymer networks. Finally a new experimental approach is introduced to making ultrathin shells and several issues on shell instability and alignment determination are addressed

The Diabetes Epidemic in Korea

Diabetes is one of the foremost public health issues worldwide that can lead to complications in many organ systems, and has become a significant cause of morbidity and mortality in Korea. According to data from the National Health Insurance Service (NHIS), about 2.7 million Koreans (8.0%) aged 30 years or older had type 2 diabetes mellitus (T2DM) in 2013. The prevalence of T2DM increased with age and rose from 5.6% in 2006 to 8.0% in 2013. Using data based on The Health Screening Service of the NHIS, 25% of Korean adults were reported to have prediabetes in 2013. The prevalence of an impaired fasting glucose tended to increase over time from 21.5% in 2006 to 25.0% in 2013. Even though nationwide health screening has been regularly conducted as a public service, the proportion of undiagnosed cases of diabetes was still reported to be on the higher side in the latest study. Based on the results of these epidemic studies, further actions will be needed to effectively implement lifestyle changes on a social level and increase measures for the early detection of diabetes to stem the tide of the epidemic