Blue phases are types of liquid crystal phases that appear in a temperature range between a chiral nematic phase and an isotropic liquid phase. Because blue phases have a three-dimensional cubic structure with lattice periods of several hundred nanometres, they exhibit selective Bragg reflections in the range of visible light corresponding to the cubic lattice. From the viewpoint of applications, although blue phases are of interest for fast light modulators or tunable photonic crystals, the very narrow temperature range, usually less than a few kelvin, within which blue phases exist has always been a problem. Here we show the stabilization of blue phases over a temperature range of more than 60 K including room temperature (260–326 K). Furthermore, we demonstrate an electro-optical switching with a response time of the order of 10−4 s for the stabilized blue phases at room temperature.

Polymer-stabilized liquid crystal blue phases

Organic semiconducting oligomers for use in thin film transistors.

An object is to provide a semiconductor device of which a manufacturing process is not complicated and by which cost can be suppressed, by forming a thin film transistor using an oxide semiconductor film typified by zinc oxide, and a manufacturing method thereof. For the semiconductor device, a gate electrode is formed over a substrate; a gate insulating film is formed covering the gate electrode; an oxide semiconductor film is formed over the gate insulating film; and a first conductive film and a second conductive film are formed over the oxide semiconductor film. The oxide semiconductor film has at least a crystallized region in a channel region.

Semiconductor device, and manufacturing method thereof

In the 21st century, soft materials will become more important as functional materials because of their dynamic nature. Although soft materials are not as highly durable as hard materials, such as metals, ceramics, and engineering plastics, they can respond well to stimuli and the environment. The introduction of order into soft materials induces new dynamic functions. Liquid crystals are ordered soft materials consisting of self-organized molecules and can potentially be used as new functional materials for electron, ion, or molecular transporting, sensory, catalytic, optical, and bio-active materials. For this functionalization, unconventional materials design is required. Herein, we describe new approaches to the functionalization of liquid crystals and show how the design of liquid crystals formed by supramolecular assembly and nano-segregation leads to the formation of a variety of new self-organized functional materials.

Functional liquid-crystalline assemblies: self-organized soft materials.

The photopolymerization of mixtures of multifunctional thiols and enes is an efficient method for the rapid production of films and thermoset plastics with unprecedented physical and mechanical properties. One of the major obstacles in traditional free-radical photopolymerization is essentially eliminated in thiol–ene polymerizations because the polymerization occurs in air almost as rapidly as in an inert atmosphere. Virtually any type of ene will participate in a free-radical polymerization process with a multifunctional thiol. Hence, it is possible to tailor materials with virtually any combination of properties required for a particular application. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 5301–5338, 2004

https://www.onlinelibrary.wiley.com/doi/pdf/10.1002/pola.20366

Thiol–enes: Chemistry of the past with promise for the future

We report the first observation of cholesteric blue phases in chiral anisotropic polymer networks. In two-component mixtures of a chiral and a non-chiral diacrylate, we observed typical textures of BPI, BPII and BPIII phases. By photopolymerization of these materials at constant temperature we obtained blue phase networks. After polymerization, the blue phases were stored, which enabled us to further study them without any temperature control.

Observation of blue phases in chiral networks

CHOLESTERIC liquid crystals, in which the orientation of the molecules varies in a helical fashion, are used for optical filtering of circularly polarized light, for example in liquidcrystal displays. They reflect circularly polarized incident light of the same handed ness as the cholesteric helix, and in a wavelength band that depends on the helical pitch (repeat distance). This pitch can be selected by careful design of the liquidcrystal molecules or by mixing cholesteric materials with nematic (linearly oriented) liquid crystals, which tend to increase the pitch. Stable optical filters are produced by crosslinking the cholesteric molecules by photopolymerization1; these filters typically have a reflection wavelength bandwidth of ∼50 nm. Here we show that, by introducing a gradient in the pitch of the cholesteric helix, we can obtain reflection of one of the two circularly polarized components over the entire visible spectrum. Polarizers with such broadband reflectivity would greatly improve the light yield and energy efficiency of liquidcrystal display devices.

Wide-band reflective polarizers from cholesteric polymer networks with a pitch gradient

In Vivo Chemistry for Pretargeted Tumor Imaging in Live Mice

Well-defined gradients in molecular alignment have been used as tools to generate large amplitude, light-induced deformations in stiff polymer networks. These systems are reversible, monolithic and based on a simple one-step self-assembly process. To fabricate the actuators, diacrylate dopants containing azobenzene moieties were blended with liquid crystalline diacrylate hosts and photopolymerized in a twisted configuration. The resulting twisted networks were heavily crosslinked with room temperature elastic moduli on the order of 1 GPa. Regardless of the temperature with respect to the glass transitions, subsequent exposure to UV radiation induced anisotropic expansion/contraction, and simple variations in geometry were used to generate uniaxial bending or helical coiling deformation modes. Because mechanical energy is directly related to elastic modulus, these systems are expected to provide significantly greater work output than contemporary polymer actuator materials.

Johan Lub

Papers

Observation of blue phases in chiral networks

Wide-band reflective polarizers from cholesteric polymer networks with a pitch gradient

In Vivo Chemistry for Pretargeted Tumor Imaging in Live Mice

Large amplitude light-induced motion in high elastic modulus polymer actuators

Highly reactive trans-cyclooctene tags with improved stability for Diels-Alder chemistry in living systems.