Ultrathin liquid crystal films showed a nematic to isotropic transition when exposed to solvent vapour for a short duration while a reverse isotropic to nematic transition was observed when the film was isolated from the solvent exposure. The phase transitions were associated with the appearance and fading of surface patterns as the solvent molecules diffused into and out of the film matrix, resulting in the destruction or restoration of the orientational order. A long-time solvent vapour exposure caused the dewetting of the film on the surface, which was demonstrated by the formation of holes and their growth in size with the progress of time. Even at this stage, withdrawal of the solvent exposure produced an array of nematic fingers, which nearly self-healed the dewetted holes. The change in contact angle due to the phase transition coupled with the imbalance of osmotic pressure across the contact line due to the differential rate of solvent evaporation from the film and the hole helped the fingers to grow towards the centre of the hole. The appearance of the fingers upon withdrawal of the solvent exposure and their disappearance upon exposure to solvent were also found to be a nearly reversible process. These findings could significantly contribute to the development of vapour sensors and self-healing surfaces using liquid crystal thin films.
Chemical pattern directed spin-dewetting of a macroscopic droplet composed of a dilute organic solution of liquid crystal (LC) formed an ordered array of micro- and nanoscale LC droplets. Controlled evaporation of the spin-dewetted droplets through vacuum drying could further miniaturize the size to the level of ∼90 nm. The size, periodicity, and spacing of these mesoscale droplets could be tuned with the variations in the initial loading of LC in the organic solution, the strength of the centripetal force on the droplet, and the duration of the evaporation. A simple theoretical model was developed to predict the spacing between the spin-dewetted droplets. The patterned LC droplets showed a reversible phase transition from nematic to isotropic and vice versa with the periodic exposure of a solvent vapor and its removal. A similar phase transition behavior was also observed with the periodic increase or reduction of temperature, suggesting their usefulness as vapor or temperature sensors. Interestingly, when the spin-dewetted droplets were confined between a pair of electrodes and an external electric field was applied, the droplets situated at the hydrophobic patches showed light-reflecting properties under the polarization microscopy highlighting their importance in the development of micro- or nanoscale LC displays. The digitized LC droplets, which were stationary otherwise, showed dielectrophoretic locomotion under the guidance of the external electric field beyond a threshold intensity of the field. Remarkably, the motion of these droplets could be restricted to the hydrophilic zones, which were confined between the hydrophobic patches of the chemically patterned surface. The findings could significantly contribute in the development of futuristic vapor or temperature sensors, light reflectors, and self-propellers using the micro- or nanoscale digitized LC droplets.
Solvent vapor exposure could transform a crystalline or smectic liquid crystal (LC) film into nematic and isotropic phases under ambient conditions. The average time for such phase transitions is found to linearly reduce with an increase in vapor pressure and reduction in the molecular weight of solvents. Such responses of solvent vapor-annealed phase transitions of a nanoparticle-loaded LC droplet were then converted into an electrical signal, wherein the electrical resistance reduced (increased) with time upon destruction (restoration) of the orientational order of the LC matrix. Variation in the electrical response was used to identify the volatile organic vapors, phase transition of LCs, rate of diffusion−absorption of solvent into LCs, and rate of desorption−evaporation of solvent from LCs. Pattern-directed phase transitions on physically heterogeneous surfaces showed a faster (slower) kinetics on thinner (thicker) patterns. However, for chemically heterogeneous surfaces, weaker (stronger) anchoring of LCs on hydrophobic (hydrophilic) patches ensured a faster (slower) transition.
A single-step room-temperature fabrication method is presented to develop a collection of ordered LC micro-/nanodroplets over a large surface area.
Pathways to fabricate self-organized nanostructures have been identified exploiting the instabilities of ultrathin (<100 nm) polystyrene (PS) film on the polydimethylsiloxane (PDMS) substrates loaded with discrete and closely packed gold nanoparticles (AuNPs). The AuNPs were deposited on the PDMS substrates by chemical treatment, and the size and periodicity of the AuNPs were varied before coating the PS films. The study unveils that the physicochemical heterogeneity created by the AuNPs on the PDMS surface could guide the hole-formation, influence the average spacing between the holes formed at the initial dewetting stage, and affects the spacing and periodicity of the droplets formed at the end of the dewetting phase. The size and spacing of the holes and the droplets could be tuned by varying the nanoparticle loading on the PDMS substrate. Interestingly, as compared to the dewetting of PS films on the homogeneous PDMS surfaces, the AuNP guided dewetted patterns show ten-fold miniaturization, leading to the formation of the micro-holes and nanodroplets. The spacing between the droplets could also see a ten-fold reduction resulting in high-density random patterns on the PDMS substrate. Further, the use of a physicochemical substrate with varying density of physicochemical heterogeneities could impose a long-range order to the dewetted patterns to develop a gradient surface. The reported results can be of significance in the fabrication of high-density nanostructures exploiting the self-organized instabilities of thin polymers films.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.