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We investigated the electrostatic behavior of ferroelectric liquid droplets exposed to the pyroelectric field of a lithium niobate ferroelectric crystal substrate. The ferroelectric liquid is a nematic liquid crystal, in which almost complete polar ordering of the molecular dipoles generates an internal macroscopic polarization locally collinear to the mean molecular long axis. Upon entering the ferroelectric phase by reducing the temperature from the nematic phase, the liquid crystal droplets become electromechanically unstable and disintegrate by the explosive emission of fluid jets. These jets are mostly interfacial, spreading out on the substrate surface, and exhibit fractal branching out into smaller streams to eventually disrupt, forming secondary droplets. We understand this behavior as a manifestation of the Rayleigh instability of electrically charged fluid droplets, expected when the electrostatic repulsion exceeds the surface tension of the fluid. In this case, the charges are due to the bulk polarization of the ferroelectric fluid, which couples to the pyroelectric polarization of the underlying lithium niobate substrate through its fringing field and solid-fluid interface coupling. Since the ejection of fluid does not neutralize the droplet surfaces, they can undergo multiple explosive events as the temperature decreases.
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Ferroelectric nematic liquid crystals are a class of recently discovered fluid materials formed by highly polar molecules that spontaneously align along a common direction, giving rise to a macroscopic polarization P. Since the polarization vector is locally collinear to the optical axis n, the study of the spatial patterns of n enables deducing the structure of P. We have carried on such topological study on ferroelectric nematic droplets confined between two solid ferroelectric substrates both when the droplet is in equilibrium and during a jet-emission phase that takes place when the solid surfaces become sufficiently charged. We find that in equilibrium the droplet splits in striped domains in which P has alternating directions. When these domains extend close to the droplets' perimeter, P adopts a π-twisted structure to minimize accumulation of polarization charges. As the substrate surface charge is increased above threshold, fluid jets are emitted with a quasi-periodic pattern, a behaviour suggesting that their location is governed by an electrofluidic instability on the droplets' rim, in turn indicating the absence of specific trigger points. Soon after their emission, the jet periodicity is lost; some jets retract while other markedly grow. In this second regime, jets that grow are those that more easily connect to polar domains with P along the jet axis. Occasionally, ejection of isolated spikes also occurs, revealing locations where polarization charges have accumulated because of topological patterns extending on length scales smaller than the typical domain size.
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Correction for 'Surface alignment of ferroelectric nematic liquid crystals' by Federico Caimi et al., Soft Matter, 2021, 17, 8130-8139, https://doi.org/10.1039/D1SM00734C.
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The success of nematic liquid crystals in displays and optical applications is due to the combination of their optical uniaxiality, fluidity, elasticity, responsiveness to electric fields and controllable coupling of the molecular orientation at the interface with solid surfaces. The discovery of a polar nematic phase opens new possibilities for liquid crystal-based applications, but also requires a new study of how this phase couples with surfaces. Here we explore the surface alignment of the ferroelectric nematic phase by testing different rubbed and unrubbed substrates that differ in coupling strength and anchoring orientation and find a variety of behaviors - in terms of nematic orientation, topological defects and electric field response - that are specific to the ferroelectric nematic phase and can be understood as a consequence of the polar symmetry breaking. In particular, we show that by using rubbed polymer surfaces it is easy to produce cells with a planar polar preferential alignment and that cell electrostatics (e.g. grounding the electrodes) has a remarkable effect on the overall homogeneity of the ferroelectric ordering.
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A Berry phase is revealed for circularly polarized light when it is Bragg reflected by a chiral liquid-crystal medium of the same handedness. By using a chiral nematic layer we demonstrate that if the input plane of the layer is rotated with respect to a fixed reference frame, a geometric phase effect occurs for the circularly polarized light reflected by the periodic helical structure of the medium. Theory and numerical simulations are supported by an experimental observation, disclosing novel applications in the field of optical manipulation and fundamental optical phenomena.
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The motion of ferroelectric liquid sessile droplets deposited on a ferroelectric lithium niobate substrate can be controlled by a light beam of moderate intensity irradiating the substrate at a distance of several droplet diameters from the droplet itself. The ferroelectric liquid is a nematic liquid crystal, in which almost complete polar ordering of the molecular dipoles generates an internal macroscopic polarization locally collinear to the mean molecular long axis. Upon entering the ferroelectric phase, droplets are either attracted toward the center of the beam or repelled, depending on the side of the lithium niobate exposed to light irradiation. Moreover, moving the beam results in walking the ferroelectric droplet over long distances on the substrate. This behavior is understood as due to the coupling between the polarization of the ferroelectric droplet and the polarization photoinduced in the irradiated region of the lithium niobate substrate. Indeed, the effect is not observed in the conventional nematic phase, suggesting the crucial role of the ferroelectric liquid crystal polarization.
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Accurately measuring mechanical displacements is essential for a vast portion of current technologies. Several optical techniques accomplish this task, allowing for non-contact sensing even below the diffraction limit. Here we introduce an optical encoding technique, dubbed "linear photonic gears", that enables ultra-sensitive measurements of a transverse displacement by mapping it into the polarization rotation of a laser beam. In ordinary ambient conditions, we measure the relative shift between two objects with a resolution of 400 pm. We argue that a resolution of 50 pm should be achievable with existing state-of-the-art technologies. Our single-optical-path scheme is intrinsically stable and it could be implemented as a compact sensor, using cost effective integrated optics. We anticipate it may have a strong impact on both research and industry.
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We analyze the angular steering of self-confined light beams, i.e., spatial solitons, in nematic liquid crystals exploiting both their electro-optic response and reorientational nonlinearity. A bias-induced interface is obtained with comb electrodes in a planar cell, applying two distinct voltages to control the spatial distribution of the optic axis. The configuration allows spatial solitons to propagate in a plane and maximize their deflection via refraction and total internal reflection, with an overall deflection of 70° in standard E7.
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Electrically driven nematic liquid crystals layers are ideal contexts for studying the interactions of local topological defects, umbilical defects. In homogeneous samples the number of defects is expected to decrease inversely proportional to time as a result of defect-pair interaction law, so-called coarsening process. Experimentally, we characterize the coarsening dynamics in samples containing glass beads as spacers and show that the inclusion of such imperfections changes the exponent of the coarsening law. Moreover, we demonstrate that beads that are slightly deformed alter the surrounding molecular distribution and attract vortices of both topological charges, thus, presenting a mainly quadrupolar behavior. Theoretically, based on a model of vortices diluted in a dipolar medium, a 2/3 exponent is inferred, which is consistent with the experimental observations.
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Random lasers are resonator-less light sources where feedback stems from recurrent scattering at the expense of spatial profile and directionality. Suitably-doped nematic liquid crystals can random lase when optically pumped near resonance(s); moreover, through molecular reorientation within the transparency region, they support self-guided optical spatial solitons, i.e., light-induced waveguides. Here, we synergistically combine solitons and collinear pumping in weakly scattering dye-doped nematic liquid crystals, whereby random lasing and self-confinement concur to beaming the emission, with several improved features: all-optical switching driven by a low-power input, laser directionality and smooth output profile with high-conversion efficiency, externally controlled angular steering. Such effects make soliton-assisted random lasers an outstanding route towards application-oriented random lasers.