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Several studies report on the sensitivity of human vision to static spatial sinusoidal achromatic and chromatic contrast variations. However, a Riemannian color difference metric, which includes the spatial and colorimetric properties of sinusoidal gratings, is lacking. Such a metric is important for various applications. Here we report on the development of a new Riemannian metric, for the prediction of detection ellipsoids in color space, for spatial sinusoidal gratings as a function of the grating's size, spatial frequency, luminance and chromaticity. The metric is based on measurements and models of achromatic and isoluminous chromatic contrast sensitivity functions available in literature, and the Riemannian metric for split fields which we reported earlier. We find adequate agreement with various data sets of experimental achromatic and isoluminous chromatic contrast sensitivity functions and with experimentally determined threshold ellipses of isoluminous chromatic Gabor gratings.
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Liquid crystalline polymers are attractive materials for untethered miniature soft robots. When they contain azo dyes, they acquire light-responsive actuation properties. However, the manipulation of such photoresponsive polymers at the micrometer scale remains largely unexplored. Here, uni- and bidirectional rotation and speed control of polymerized azo-containing chiral liquid crystalline photonic microparticles powered by light is reported. The rotation of these polymer particles is first studied in an optical trap experimentally and theoretically. The micro-sized polymer particles respond to the handedness of a circularly polarized trapping laser due to their chirality and exhibit uni- and bidirectional rotation depending on their alignment within the optical tweezers. The attained optical torque causes the particles to spin with a rotation rate of several hertz. The angular speed can be controlled by small structural changes, induced by ultraviolet (UV) light absorption. After switching off the UV illumination, the particle recovers its rotation speed. The results provide evidence of uni- and bidirectional motion and speed control in light-responsive polymer particles and offer a new way to devise light-controlled rotary microengines at the micrometer scale.
ABSTRACT
For the calculation of the color gamut volume and the maximum number of mutually discernible colors, an algorithm based on a Riemannian metric and the densest packing of spheres is proposed. With this algorithm, the color gamut volume was calculated for the conditions of experiments reported in literature. Good agreement was found with the experimental findings of the color gamut volume as a function of the peak luminance. Using the new algorithm, the color gamut volume and the maximum number of mutually discernible colors was calculated for various sets of primary colors corresponding to display standards and various dynamic ranges. Comparisons were made with state-of-the-art methods which are based on the Euclidean metric in approximately uniform color spaces and a simple cubic lattice. It was found that the state-of-the-art methods underestimate the maximum number of mutually discernible colors. However, the relative differences decrease as the primary colors are more saturated. Based on the new algorithm the maximum number of mutually discernible colors was calculated for a range of peak retinal illuminance levels and various sets of primary colors. We found that, for a given set of primary colors, the maximum number of mutually discernible colors is proportional to the logarithm of the ratio of the peak retinal illuminance level and a fitting parameter.
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Understanding the adsorption of polymers onto particles is crucial for many technological and biomedical applications. Even though polymer adsorption on particles is a dynamic process, most experimental techniques can only study the adsorption indirectly, in equilibrium and on the ensemble level. New analysis methods are required to overcome these limitations. We investigated the use of single-particle electrophoresis to study the adsorption kinetics of cationic polymers onto anionic particles and compared the resulting data to a theoretical model. In this approach, the electrophoretic mobility of single polystyrene (PS) particles, exposed to different concentrations of poly(2-guanidinoethyl methacrylate), was measured as a function of time. The polymer adsorption leads to an electrophoretic mobility change of the PS particle over time, from the initial negative value to a positive value at equilibrium. By fitting the kinetics data to the Langmuir model, the adsorption rate, desorption rate and equilibrium constant were determined. Finally, the adsorption kinetics of several other polymers was investigated. This showed that the presented technique enables direct analysis and comparison of the kinetics of polymer adsorption on the single-particle level.
Subject(s)
Models, Theoretical , Polymers , Adsorption , Electrophoresis , CationsABSTRACT
This study shows that, in cells with small thicknesses, the permanent polarization in the ferroelectric nematic phase of RM734 is aligned in the direction opposite to the rubbing direction. The electrode configuration induces an in-plane field near one substrate and a normal field near the other substrate. At low voltages, the permanent polarization rotates parallel to the substrate plane when its original orientation is at an angle with the electric field. The rotation occurs over a distance of more than 100 µm, where the applied electric field is very small. At higher voltages, the polarization aligns perpendicularly to the substrates under the influence of the transverse electric field. After removing the voltage, sometimes a slow reorientation of the polarization can be observed, which is ascribed to the slow release of ionic species. The results provide insight into the complex mechanisms that are involved in the switching of ferroelectric nematic liquid crystals.
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Two-dimensional (2D) semiconductors are primed to realize a variety of photonic devices that rely on the transient properties of photogenerated charges, yet little is known on the change of the refractive index. The associated optical phase changes can be beneficial or undesired depending on the application, but require proper quantification. Measuring optical phase modulation of dilute 2D materials is, however, not trivial with common methods. Here, we demonstrate that 2D colloidal CdSe quantum wells, a useful model system, can modulate the phase of light across a broad spectrum using a femtosecond interferometry method. Next, we develop a toolbox to calculate the time-dependent refractive index of colloidal 2D materials from widely available transient absorption experiments using a modified effective medium algorithm. Our results show that the excitonic features of 2D materials result in broadband, ultrafast, and sizable phase modulation, even extending to the near infrared because of intraband transitions.
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Flat optics based on chiral liquid crystal (CLC) can be achieved using holographic polarization recording with the help of a photoalignment technique to vary the orientation of the optical axis in a thin CLC layer. A variety of reflective diffractive optical components with high efficiency and polarization selectivity can be realized employing this technique. In this work we discuss the use of CLC diffractive lenses in a spectrometer. The functionalities of two mirrors and a linear grating used in a traditional spectrometer are combined into a single holographic CLC component. Circularly polarized light entering through the slit can be reflected and projected onto a linear detector by the CLC component, with over 90% efficiency. This excellent optical functionality can be achieved with a micrometer thin CLC layer, offering the opportunity for device integration.
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It is generally accepted that the perceptual color space is not Euclidean. A new line element for a 3-dimensional Riemannian color space was developed. This line element is based on the Friele line elements and psychophysical color discrimination models, and comprises both the first and second stage of color vision. The line element is expressed in a contrast space based on the MacLeod-Boynton chromaticities. New equations for the contrast thresholds along the cardinal axes and new metric tensor elements were determined. Visual adaptation effects were incorporated into the model. Color discrimination threshold ellipsoids were calculated with the new line element. Adequate agreement with experimental threshold ellipsoids reported in literature was demonstrated. From a comparison with other color difference metrics a better overall predictability of threshold ellipsoids was found with the new line element.
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A thin, waterproof, and stable spatially tunable band reject filter is fabricated based on a chiral nematic liquid crystal polymer. The fabrication method for this filter is new, to the best of our knowledge, and straightforward. The photonic bandgap (PBG) of the proposed filter can be tuned from 350 nm to 760 nm by a mechanical movement of 6.5 mm. The filter reflects almost 50% of unpolarized incident light in the PBG and remains practically transparent for other wavelengths. The filter remains stable for four years and has acceptable resistance to polar protic solvents and thermal stability up to 90°C. The filter can be detached from the glass substrates, to be used as a thin 8-µm free-standing film or to be attached to a flexible substrate. This spatial tunable band reject filter may be used in displays, optical devices, and optical communication.
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Liquid crystal (LC) based geometric phase optical elements are widely used to effectively change the wavefront or propagation direction of light. Using photoalignment, the liquid crystal can be aligned according to the designed pattern, leading to components such as gratings, lenses or general wavefront shaping devices. The functionality and efficiency of the component is strongly influenced by how well the LC follows the imposed alignment pattern. Next to a considerable tilting of the LC at the air interface, we report on the observation of symmetry breaking in polymerized LC polarization gratings. By carefully analyzing the experimental and numerical data for gratings with different periods, we conclude that the non-negligible homeotropic anchoring strength at the air interface is responsible for the tilt angle and the symmetry breaking. The role of anchoring strength at the photoaligned and air interface and other parameters are investigated.
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This paper demonstrates a thin and transparent reflector film for the near infrared, based on chiral nematic liquid crystal (CLC) polymers. Two films reflect almost 50% of unpolarized incident light from 730 to 820 nm and from 880 to 1030 nm, while remaining completely transparent in the visible region with transmittance >90%. An efficient window uses the combination of two reflectors. After exposing two window-cubes for 2 h to direct sunlight, the temperature inside the cube with reflector windows was 4°C lower than in cube with plain windows. This reveals that the infrared (IR) reflectors can effectively control the indoor temperature. These films, which are 8 µm in thickness, can be detached from the glass substrates and used as a free-standing film, or be attached to a flexible optical foil or a solid window. The foils can be applied in buildings, offices, and automobiles to statically reduce the energy consumption required for air conditioning or lighting. The free-standing foils show acceptable resistance to polar protic solvents and are thermally stable up to 100°C.
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Colloidal CdSe quantum rings (QRs) are a recently developed class of nanomaterials with a unique topology. In nanocrystals with more common shapes, such as dots and platelets, the photophysics is consistently dominated by strongly bound electron-hole pairs, so-called excitons, regardless of the charge carrier density. Here, we show that charge carriers in QRs condense into a hot uncorrelated plasma state at high density. Through strong band gap renormalization, this plasma state is able to produce broadband and sizable optical gain. The gain is limited by a second-order, yet radiative, recombination process, and the buildup is counteracted by a charge-cooling bottleneck. Our results show that weakly confined QRs offer a unique system to study uncorrelated electron-hole dynamics in nanoscale materials.
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The electrophoretic mobility of micron-scale particles is of crucial importance in applications related to pharmacy, electronic ink displays, printing, and food technology as well as in fundamental studies in these fields. Particle mobility measurements are often limited in accuracy because they are based on ensemble averages and because a correction for electroosmosis needs to be made based on a model. Single-particle approaches are better suited for examining polydisperse samples, but existing implementations either require multiple measurements to take the effect of electroosmosis into account or are limited in accuracy by short measurement times. In this work, accurate characterization of monodisperse and polydisperse samples is achieved by measuring the electrophoretic mobility on a particle-to-particle basis while suppressing electroosmosis. Electroosmosis can be suppressed by measuring in the middle of a microchannel while applying an AC voltage with a sufficiently high frequency. An accurate measurement of the electrophoretic mobility is obtained by analyzing the oscillating particle motion for 1.5s per particle with a high-speed camera measuring at 850Hz , synchronized to the applied electric field. Attention is paid to take into account the effect of the rolling shutter and the non-uniform sampling in order to obtain the accurate amplitude and phase of the electrophoretic mobility. The accuracy of method is experimentally verified and compared with a commercial apparatus for polystyrene microspheres in water. The method is further demonstrated on a range of particle materials and particle sizes and for a mixture of positively and negatively charged particles.
Subject(s)
Electroosmosis , Electrophoresis , Microspheres , Particle Size , PolystyrenesABSTRACT
Correction for 'Electrokinetics and behavior near the interface of colloidal particles in non-polar dispersions' by Manoj Prasad et al., Soft Matter, 2017, 13, 5604-5612, DOI: .
ABSTRACT
Correction for 'Space charge limited release of charged inverse micelles in non-polar liquids' by Manoj Prasad et al., Phys. Chem. Chem. Phys., 2016, 18, 19289-19298, DOI: .
ABSTRACT
Externally induced color- and shape-changes in micrometer-sized objects are of great interest in novel application fields such as optofluidics and microrobotics. In this work, light and temperature responsive micrometer-sized structural color actuators based on cholesteric liquid-crystalline (CLC) polymer particles are presented. The particles are synthesized by suspension polymerization using a reactive CLC monomer mixture having a light responsive azobenzene dye. The particles exhibit anisotropic spot-like and arc-like reflective colored domains ranging from red to blue. Electron microscopy reveals a multidirectional asymmetric arrangement of the cholesteric layers in the particles and numerical simulations elucidate the anisotropic optical properties. Upon light exposure, the particles show reversible asymmetric shape deformations combined with structural color changes. When the temperature is increased above the liquid crystal-isotropic phase transition temperature of the particles, the deformation is followed by a reduction or disappearance of the reflection. Such dual light and temperature responsive structural color actuators are interesting for a variety of micrometer-sized devices.
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In this work, the design, fabrication and characterization are reported for a distributed Bragg reflector (DBR) filter with a specific wavelength and angular dependency, which aims to improve the light collection from a wavelength-converter-based light source into a smaller angle than the full angle Lambertian emission. The desired design is obtained by optimizing the transmission characteristics of a multi-layer structure. Titania (TiO2) and silica (SiO2) are used as high and low refractive index materials, respectively. The deposition is made by electron beam evaporation without substrate heating, followed by a post-annealing procedure. The optical properties of the evaporated layers are analyzed by ellipsometer and spectrometer measurements. The angular and wavelength dependency of the fabricated DBR is in good agreement with simulations for the designed structure.
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A common technique to realize the gradient electric field profile that is required in liquid crystal tunable lenses is the use of a weakly conductive layer. Thanks to this layer, an applied voltage with a certain frequency allows us to obtain a refractive index profile that is required for the lens operation. Due to the limited degrees of freedom, however, it is not possible to avoid aberrations in a weakly conductive layer-based tunable lens for a continuously tunable focal length. In this work, we discuss the use of additional higher frequency components in the voltage signal to reduce the lens aberrations drastically.
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The adsorption of charged inverse micelles at the electrode-liquid interface has an important effect on field screening and on the voltage drop over diffuse double layers. Recently, we analyzed the behavior of inverse micelles in a nonpolar liquid close to this electrode-liquid interface. For the fluorocarbon/surfactant system under study, we are in the limit of slow adsorption and negligible desorption of inverse micelles on the electrodes. Upon applying a voltage step, this results in a measurable Stern layer buildup in the time range of hours clearly distinguishable from the diffuse double layer buildup, which happens in less than 1 s. This Stern layer buildup manifests itself by a shift in the voltage drop from the diffuse double layer to the Stern layer until the voltage drop over the Stern layers reaches the applied voltage, leaving a zero bulk field without the diffuse double layer. New measurements of the transients of Stern layer buildup show that the buildup of charges in the Stern layer is more complex. We explain the observed transient behavior by introducing an asymmetry in the adsorption rate of charged inverse micelles. We provide an equivalent electrical network, an analytical solution to explain the behavior in more detail, and simulations within the diffuse double layer limit for a range of adsorption rates.
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Patterned liquid crystal (LC) configurations find widespread applications in functional devices such as lenses, gratings, displays and soft-robots. In combination with external stimuli such as an applied electric field, photo-alignment at the surfaces offers an attractive way to stabilize different LC structures in the bulk of a device. Herein, a planar LC cell is developed using a photo-alignment layer at the bottom substrate and a rubbed nylon film at the top substrate. Patterned planar photo-alignment is achieved by modulating the linear polarization with a spatial light modulator (SLM) and projecting the pattern onto the bottom substrate. A ring pattern is written into the photo-alignment layer with a continuous rotation between an inner radius and an outer radius. In the other regions the alignment is parallel to the rubbing direction at the top substrate. Four different LC configurations are observed: structure A in which a ring-shaped region is formed with an out of plane (vertical) orientation perpendicular to the substrate, structure B which has a single disclination loop and a 180° twist at the inner region of the photo-patterned ring (r < rin), structure C which has no discontinuities but a 360° twist in the inner region of the photo-patterned ring (r < rin) and structure D with 2 disclination loops. The LC director configuration for all 4 structures is simulated through finite element (FE) Q-tensor simulations and the optical transmission for each structure is simulated using a generalized beam propagation method.