A new light-driven chiral molecular switch doped in a stable blue phase (BP) liquid crystal allows wide optical tunability of three-dimensional cubic nanostructures with a selective reflection wavelength that is reversibly tuned through the visible region. Moreover, unprecedented reversible light-directed red, green, and blue reflections of the self-organized three-dimensional cubic nanostructure in a single film are demonstrated for the first time. Additionally, unusual isothermal photo-stimulated less ordered BP II to more ordered BP I phase transition was observed in the system.

Halide perovskites have received tremendous attention due to their fantastic optical and electrical properties. Here, circularly polarized light emission is successfully demonstrated using a simple configuration consisting of inorganic perovskite nanocrystals embedded within a predefined handedness cholesteric superstructure stack. The helical structured cholesteric liquid crystal film acts as a selective filter to transform the unpolarized light emission from perovskite nanocrystals into circularly polarized luminescence. The transformation is accompanied by an extraordinary dissymmetry factor (|g lum |) up to 1.6, well-defined handedness, high photoluminescence quantum yield, and full-color availability. Furthermore, the circularly polarized luminescence is angular dependent and can easily be modulated by shifting the overlap of the reflection band and the emission band. The proposed method is more straightforward and powerful than the previous approaches, offering new opportunities in optoelectronic and photonic devices.of turning the unpolarized light emission arising from the perovskite NC layer into fully chiral light emission with a high dissymmetry factor value of ≈1.6. To the best of our knowledge, this is one of the highest values reported for the dissymmetry factor of circularly polarized light emission from perovskite materials.

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This investigation demonstrates an electrically switchable uniformly lying helix (ULH) stable state in cholesteric liquid crystal. A stable ULH state can be achieved by applying the low-frequency (30 Hz) pulse electrical field via an electro-hydrodynamatic effect. The ULH state can be stably maintained with a helical pitch in the visible range (450 nm–630 nm) and exhibit a tunable uniaxial crystal wave plate property under 1 kHz electrical field. The study examines the electro-optical property of ULH state and driving scheme for switching among the three stable states. A multi-stable and electrically switchable cholesteric liquid crystal can provide various optical properties and has extensive potential applications.

Although there have been intense efforts to fabricate large three-dimensional photonic crystals in order to realize their full potential, the technologies developed so far are still beset with various material processing and cost issues. Conventional top-down fabrications are costly and time-consuming, whereas natural self-assembly and bottom-up fabrications often result in high defect density and limited dimensions. Here we report the fabrication of extraordinarily large monocrystalline photonic crystals by controlling the self-assembly processes which occur in unique phases of liquid crystals that exhibit three-dimensional photonic-crystalline properties called liquid-crystal blue phases. In particular, we have developed a gradient-temperature technique that enables three-dimensional photonic crystals to grow to lateral dimensions of ~1 cm (~30,000 of unit cells) and thickness of ~100 μm (~ 300 unit cells). These giant single crystals exhibit extraordinarily sharp photonic bandgaps with high reflectivity, long-range periodicity in all dimensions and well-defined lattice orientation.