Large Thermally Irreversible Photoinduced Shift of Selective Light Reflection in Hydrazone-Containing Cholesteric Polymer Systems.

Stimuli responsive liquid crystalline polymers are a unique class of so-called "smart" materials demonstrating various types of mesomorphic structures easily controlled by external fields, including light. In the present work we synthesized and studied a comb-shaped hydrazone-containing copolyacrylate exhibited cholesteric liquid crystalline properties with the pitch length of the helix being tuned under irradiation with light. In the cholesteric phase selective light reflection in the near IR spectral range (1650 nm) was measured and a large blue shift of the reflection peak from 1650 nm to 500 nm was found under blue light (428 or 457 nm) irradiation. This shift is related to the Z-E isomerization of photochromic hydrazone-containing groups and it is photochemically reversible. The improved and faster photo-optical response was found after copolymer doping with 10 wt % of low-molar-mass liquid crystal. It is noteworthy that both, the E and Z isomers of hydrazone photochromic group are thermally stable that enable to achieve a pure photoinduced switch without any dark relaxation at any temperatures. The large photoinduced shift of the selective light reflection, together with thermal bistability, makes such systems promising for applications in photonics.

Laser-induced formation of "craters" and "hills" in azobenzene-containing polymethacrylate films.

Functional organic polymer materials with an ability to change their surface topography in response to external contactless stimuli, like light irradiation, have attracted considerable attention. This work is devoted to the study of contactless control of the surface topography and the formation of the surface features in the amorphousized and liquid crystalline films of two azobenzene-containing polymers. The investigated polymers are side-chain polymethacrylates containing azobenzene chromophores with two lateral methyl substituents in ortho-positions and differing in the length of flexible spacer with six and ten methylene units. Two lateral methyl substituents at the azobenzene chromophore ensure high photoresponses of these polymeric samples in the whole visible spectral range. Irradiation of the polymethacrylate films by focused polarized light of green (532 nm) and red (633 nm) lasers induces a specific photodeformation of the film surface. In the case of the green light formation of circular "craters" with anisotropic borders was found, whereas for the red light highly asymmetric "hills" were observed. The possible mechanisms of the surface topography formation and their features are discussed.

Photopatterning of Azobenzene-Containing Liquid Crystalline Triblock Copolymers: Light-Induced Anisotropy and Photostabilization.

Photochromic liquid crystalline block copolymers (PLCBCs) are currently playing a significant role as light-responsive materials because of their light controllable features over multiple length scales. Herein, a study of the photoinduced optical anisotropy derived by the combination of orientation phenomena at molecular and supramolecular levels in a novel kind of side-chain PLCBCs with mesogenic phenyl benzoate groups and pyridine units that is hydrogen bonded with azobenzene-containing phenol is reported. Based on the polymeric architectures and composition, the supramolecular configuration self-organizes in different microphases that affect the material response to the external stimuli. Simple, 1D, polarization holograms are recorded to evaluate the photoinduced birefringence. The first step, light patterning, involves the orientation of the azobenzene units and precedes a thermal treatment that amplifies the induced anisotropy through the cooperative orientation of the mesogenic units. By selective extraction, the azobenzene units can be removed, making the material transparent to the visible light. Excellent photostability of the material birefringence is obtained, whose final value is strongly affected by the block copolymer's architecture. The versatility in the molecular design, the fine control of the photoinduced features by external parameters, and, finally, the possibility to achieve photostability make these materials of great potential for developing optical and photonic devices.

Novel generation of liquid crystalline photo-actuators based on stretched porous polyethylene films.

The preparation of photo-actuators based on stretched porous polyethylene and an azobenzene-containing liquid crystalline polymer network is reported for the first time. It is revealed that this kind of photo-actuator possesses the following advantages: the lack of a need for using aligning coatings and cells preparation, high deformation of the actuator and its complete reversibility, good mechanical properties, and relatively low cost of fabrication. In addition some kinetic and thermodynamic features of the bending and unbending processes have been studied.

A novel type of crown ether-containing metal ions optical sensors based on polymer-stabilized cholesteric liquid crystalline films.

For the first time, the films based on polymer-stabilized cholesteric composites containing crown ether fragments with the optical properties sensitive to the complexation with potassium and barium ions were obtained. The complexation with these ions leads to blue spectral shift of the selective light reflection of planar cholesteric texture of composite films. Peculiarities of spectral changes and kinetics of selective light reflection shift were studied. The proposed approach can be used for the creation of the effective and selective sensor materials for different ions or groups of ions.

Hybrid fluorescent liquid crystalline composites: directed assembly of quantum dots in liquid crystalline block copolymer matrices.

Hybrid fluorescent liquid crystalline (LC) composites containing inorganic quantum dots (QDs) are promising materials for many applications in optics, nanophotonics and display technology, combining the superior emission capability of QDs with the externally controllable optical properties of LCs. In this work, we propose the hybrid LC composites that were obtained by embedding CdSe/ZnS QDs into a series of host LC block copolymers of different architectures by means of a two-stage ligand exchange procedure. The ABA/BAB triblock copolymers and AB diblock copolymers with different polymerization degrees are composed of nematogenic phenyl benzoate acrylic monomer units and poly(4-vinylpyridine) blocks, which are capable of binding to the QD surface. Our results clearly show that the spatial distribution of QDs within composite films as well as the formation of QD aggregates can be programed by varying the structure of the host block copolymer. The obtained composites form a nematic LC phase, with isotropization temperatures being close to those of the initial host block copolymers. In addition, the influence of the molecular architecture of the host block copolymers on fluorescence properties of the obtained composites is considered. The described strategy for the QD assembly should provide a robust and conventional route for the design of highly ordered hierarchical hybrid materials for many practical applications.

Phase Structure Recording in a Nematic Side-Chain Liquid-Crystalline Polymer.

Dye-doped nematic side-chain liquid-crystalline polymers possess extraordinary large optical nonlinearity and ability to store the induced orientational deformations in a glassy state, which makes them a very promising material for photonic applications. In this study, the phase structures were generated and recorded in the bulk of a 50-µm layer of a nematic liquid-crystalline side-chain polymer, containing polyacrylate backbone, spacer having five methylene groups, and phenyl benzoate mesogenic fragment. The polymer was doped with KD-1 azodye. The director field deformations induced by the light beam close to the TEM01 mode were studied for different geometries of light-polymer interaction. The phase modulation depth of 2π was obtained for the 18-µm spacing between intensity peaks. The experimental data were analyzed based on the elastic continuum theory of nematics. The possibility to induce and record positive and negative microlenses in the polymer bulk was shown experimentally.

Order and dynamics of a liquid crystalline dendrimer by means of 2H NMR spectroscopy.

A complete Deuterium NMR study performed on partially deuterated liquid crystalline carbosilane dendrimer is here reported. The dendrimer under investigation shows a SmA phase in a large temperature range from 381 to 293 K, and its mesophasic properties have been previously determined. However, in this work the occurrence of a biphasic region between the isotropic and SmA phases has been put in evidence. The orientational order of the dendrimer, labeled on its lateral mesogenic units, is here evaluated in the whole temperature range by means of (2)H NMR, revealing a peculiar trend at low temperatures (T < 326 K). This aspect has been further investigated by a detailed analysis of the (2)H NMR spectral features, such as the quadrupolar splitting, the line shape, and the line-width, as a function of temperature. In the context of a detailed NMR analysis, relaxation times (T(1) and T(2)) have also been measured, pointing out a slowing down of the dynamics by decreasing the temperature, which determines from one side the spectral changes observed in the NMR spectra, on the other the observation of a minimum in the T(1).

Direct Observation of Changes in Focal Conic Domains of Cholesteric Films Induced by Ultraviolet Irradiation.

The helical supramolecular structure of cholesteric liquid crystalline (LC) films predetermines their outstanding optical properties and the unique nanostructure of their surface. The introduction of photochromic dopants in these films opens up an interesting possibility for creation of smart cholesteric materials with photocontrollable optical and photovariable surface properties. Using atomic force microscopy (AFM), we performed in situ measurements of the surface topography of cyclosiloxane LC cholesteric oligomer films during the cholesteric helix twisting caused by their preliminary ultraviolet (UV) irradiation. A chiral-photochromic isosorbide-based dopant was introduced in the films to control the cholesteric helix pitch by UV-irradiation. The initial films are characterized by planar texture with the presence of focal conic domains having the double-spiral relief on their surface. UV-irradiation of these films leads to the cholesteric helix twisting resulting in a decrease in the surface relief period, and the enlargement of defect areas between the domains. The detailed mechanisms of the rearrangement of the film surface structure due to the cholesteric helix twisting are suggested. They include the rotation and displacement of cholesteric layers in the bulk, and the nucleation of new ones at the surface in defect regions.

Cholesteric Polymer Scaffolds Filled with Azobenzene-Containing Nematic Mixture with Phototunable Optical Properties.

The past two decades witnessed tremendous progress in the field of creation of different types of responsive materials. Cholesteric polymer networks present a very promising class of smart materials due to the combination of the unique optical properties of cholesteric mesophase and high mechanical properties of polymer networks. In the present work we demonstrate the possibility of fast and reversible photocontrol of the optical properties of cholesteric polymer networks. Several cholesteric photopolymerizable mixtures are prepared, and porous cholesteric network films with different helix pitches are produced by polymerization of these mixtures. An effective and simple method of the introduction of photochromic azobenzene-containing nematic mixture capable of isothermal photoinducing the nematic-isotropic phase transition into the porous polymer matrix is developed. It is found that cross-linking density and degree of polymer network filling with a photochromic nematic mixture strongly influence the photo-optical behavior of the obtained composite films. In particular, the densely cross-linked films are characterized by a decrease in selective light reflection bandwidth, whereas weakly cross-linked systems display two processes: the shift of selective light reflection peak and decrease of its width. It is noteworthy that the obtained cholesteric materials are shown to be very promising for the variety applications in optoelectronics and photonics.

Photoinduced Changes of Surface Topography in Amorphous, Liquid-Crystalline, and Crystalline Films of Bent-Core Azobenzene-Containing Substance.

Recently, photofluidization and mass-transfer effects have gained substantial interest because of their unique abilities of photocontrolled manipulation with material structure and physicochemical properties. In this work, the surface topographies of amorphous, nematic, and crystalline films of an azobenzene-containing bent-core (banana-shaped) compound were studied using a special experimental setup combining polarizing optical microscopy and atomic force microscopy. Spin-coating or rapid cooling of the samples enabled the formation of glassy amorphous or nematic films of the substance. The effects of UV and visible-light irradiation on the surface roughness of the films were investigated. It was found that UV irradiation leads to the fast isothermal transition of nematic and crystalline phases into the isotropic phase. This effect is associated with E-Z photoisomerization of the compound accompanied by a decrease of the anisometry of the bent-core molecules. Focused polarized visible-light irradiation (457.9 nm) results in mass-transfer phenomena and induces the formation of so-called "craters" in amorphous and crystalline films of the substance. The observed photofluidization and mass-transfer processes allow glass-forming bent-core azobenzene-containing substances to be considered for the creation of promising materials with photocontrollable surface topographies. Such compounds are of principal importance for the solution of a broad range of problems related to the investigation of surface phenomena in colloid and physical chemistry, such as surface modification for chemical and catalytic reactions, predetermined morphology of surfaces and interfaces in soft matter, and chemical and biochemical sensing.

Surface Relief Changes in Cholesteric Cyclosiloxane Oligomer Films at Different Temperatures.

The development of new approaches for the surface topography control is an important topic as the relief significantly affects physical and chemical properties of surfaces. We studied cholesteric cyclosiloxane oligomeric films on which surface focal conic domains with double-helix pattern were observed by means of AFM. In situ investigation of the dependence of the films topography on temperature showed that the surface relief formation can be effectively managed by varying conditions of thermal treatment. Obtained structures can be frozen by cooling the films below glass-transition temperature.

Stable selective gratings in LC polymer by photoinduced helix pitch modulation.

A cholesteric mixture based on the nematic liquid crystalline side-chain polymer doped with a chiral-photochromic compound was prepared and used as an active medium for creation of stable polarization selective gratings by phototunable modulation of the helix pitch. Such modulation was fabricated in the polymer mixture by a nonpolarized UV-irradiation with spatially modulated intensity that causes E-Z isomerization of a chiral-photochromic dopant, decreasing its helical twisting power. It was shown that the gratings recorded by UV-exposure through a mask are strongly selective to the handedness of circular polarized light. The studied polymer film forms a right-handed helical structure and, correspondingly, the diffraction of only the right-circularly polarized light was found in the transmittance mode. The maximum diffraction efficiencies were found for the wavelength values between the maxima of selective light reflection. The films obtained open very interesting possibilities for further development of materials with stable gratings operating in the entire visible spectral range. Both the position and the width of the spectral range of an efficient diffraction can be easily controlled by the UV exposure and concentration of the dopant. The materials obtained and methods developed can be used for creation of specific diffraction elements for optics and photonics.

Atomic force microscopy study of surface topography of films of cholesteric oligomer- and polymer-based mixtures with photovariable helix pitch.

The surface topography of glass-forming polymers and oligomer cholesteric systems with a phototunable helix pitch was studied. For this purpose several mixtures based on nematic polyacrylate and cholesteric cyclosiloxanes doped with chiral-photochromic dopant were prepared and investigated. The molecules of chiral-photochromic dopant consist of isosorbide chiral moiety and cinnamic C=C double bonds capable of E-Z photoisomerizing. UV irradiation of the planarly oriented films of mixtures leads to dopant photoisomerization and changes of its helical twisting power. During this process irreversible changes of helix pitch values take place, which allows one to obtain the same cholesteric systems with different helix pitch values. The films of the annealed mixtures were studied by atomic force microscopy and transmission electron microscopy. The correlations between the features of surface topography and helix pitch of cholesteric supramolecular structure were found and discussed.

Optically and electrically controlled circularly polarized emission from cholesteric liquid crystal materials doped with semiconductor quantum dots.

Novel types of electro- and photoactive quantum dot-doped cholesteric materials have been engineered. UV-irradiation or electric field application allows one to control the degree of circular polarization and intensity of fluorescence emission by prepared quantum dot-doped liquid crystal films.

Polarization holographic recording in amorphous polymer with photoinduced linear and circular birefringence.

Polarization grating recording in an amorphous and nonchiral azo copolymer has been investigated. The reported study shows that the amorphous polymeric film undergoes a light-guided inhomogeneous supramolecular modification as a consequence of the illumination with proper polarized light patterns, acquiring new functionalities. Both linear and circular, spatially modulated, photoinduced birefringences occur, attaining their peak values in the linearly and circularly polarized regions of the light pattern, respectively. The photoinduced anisotropic structures strongly affect the polarization state of the light propagating through them, and the characterization of their optical diffraction enables measurement of the amplitude of the linear and circular birefringences. The recorded gratings show long-time stability and full reconfigurability functional to the multiple holographic recording.

Liquid crystal codendrimers with a statistical distribution of phenolic and mesogenic groups: behavior as Langmuir and Langmuir-Blodgett films.

The first series of carbosilane liquid crystal codendrimers with groups of different polarity has been synthesized. The chemical structure of the newly synthesized materials and the composition of the codendrimers were studied by NMR spectroscopy and MALDI-TOF MS. It was found that the codendrimers tend to form stable Langmuir films at the air-water surface. The influence of composition and generation number on surface pressure-surface area isotherms and film stability was studied. Brewster angle microscopy confirmed the different phase behavior for monolayers of different codendrimer composition and generation number. It was found that side groups of fifth-generation codendrimers do not segregate, unlike those of lower generations. Langmuir-Blodgett films on solid substrates were obtained by the vertical dipping method. X-ray diffraction showed that the codendrimers with 75% of hydrophobic mesogenic terminal groups formed ordered layers parallel to the substrate.

Cholesteric polymer guest-host mixture with circularly polarized fluorescence: two ways for phototuning of polarization and its intensity.

A photosensitive fluorescent cholesteric guest-host mixture consisting of a nematic polyacrylate, a chiral, photochromic dopant sensitive to UV light, and a fluorescent dopant was prepared. The nematic polyacrylate contains 4-phenyl-4'-methoxybenzoate nematogenic side groups and photochromic 4-cyanoazobenzene side groups. The chiral-photochromic dopant formed by isosorbide and cinnamic acid is capable of E-Z photoisomerization and [2 + 2] photo-cycloaddition under light irradiation. The planarly oriented films possess a selective light reflection in the visible spectral region coinciding with the emission peak of the fluorescent dopant. The fluorescence emitted by the planarly oriented films of the mixture is strongly circularly polarized and characterized by a large value of the dis-symmetry factor. At temperatures below glass transition (T(g)) the polarized light action of an Ar(+) laser (488 nm) leads to the photo-orientation of the azobenzene fragments resulting in a strong and reversible disruption of the selective reflection and a decrease of the dis-symmetry factor of fluorescence. UV irradiation leads to E-Z isomerization and/or [2 + 2] cycloaddition of the chiral-photochromic dopant, causing an irreversible shift of the maximum of the dis-symmetry factor to a long-wavelength spectral region under subsequent annealing at temperatures higher than T(g). Such multifunctional glass-forming guest-host mixtures combining photosensitive and fluorescent properties with the unique optical properties of cholesteric liquid crystals can be considered as promising material for optical data processing technologies and photonic applications.