This study examines the surface-assisted photoalignment effect of dye-doped liquid-crystal films having a homogeneous alignment. Observations made using a polarizing optical microscope, a scanning electronic microscope, and an atomic force microscope confirm that the morphology of laser-induced surface-adsorbed dyes at the command surface strongly affects the orientation of liquid crystals (LC's) in a manner that depends significantly on the intensity and duration of the pumping. In weak-intensity regime, a homogeneous and fine layer of adsorbed dyes competes with a layer of ripple structure in reorienting LC's. These two effects dominantly cause LC's to reorient perpendicular and parallel to the polarization direction of the pump beam in the early and late stages, respectively. In the high-intensity regime, rough and inhomogeneous ribbonlike adsorbents produced by rapid and random aggregation and adsorption form on the top of the preformed microgrooves, reorienting LC's irregularly. This surface morphology does not enable photoalignment.

This study applies a low-cost solvothermal method to synthesize all-inorganic (lead-free cesium tin halide) perovskite quantum dots (AIPQDs) and to fabricate AIPQD-doped lasers with cholesteric liquid crystal (CLC) lasing cavities. The lasers present highly qualified lasing features of low threshold (150 nJ/pulse) and narrow line width (0.20 nm) that are attributed to the conjunction of the suppression of photoluminescence (PL) loss caused by the quantum confinement of AIPQDs and the amplification of PL caused by the band-edge effect of the CLC-distributed feedback resonator. In addition, the lasers possess highly flexible lasing-wavelength tuning features and a long-term stability under storage at room temperature and under high humidity given the protective role of CLC. These advantages are difficult to confer to typical light-emitting perovskite devices. Given these merits, the AIPQD-doped CLC laser device has considerable potential applications in optoelectronic and photonic devices, including lighting, displays, and lasers.

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Eight new chrysogenolides (A-H (1-8)) and seven known (9-15) 3,5-dimethylorsellinic acid derived meroterpenoids were isolated from the solid substrate fermentation cultures of a Huperzia serrata endophytic fungus, Penicillium chrysogenum MT-12. The structures of the new compounds were elucidated by interpretation of spectroscopic and spectrometric data (1D and 2D NMR, IR, and HRESIMS). The absolute configurations of 1-4 were determined by single-crystal X-ray crystallographic analysis, and those of 5-8 were assigned on the basis of experimental and calculated electronic circular dichroism spectra. Compounds 3, 4, 6, 11, and 12 showed inhibition of nitric oxide production in lipopolysaccharide-activated RAW 264.7 macrophage cells with IC values in the range of 4.3-78.2 μM (positive control, indomethacin, IC = 33.6 ± 1.4 μM).

This study investigates high-resolution photoinduced biphotonic holographic gratings in azo-dye-doped liquid crystal films. A biphotonic grating (BG) is formed under the illumination of one linearly polarized green light with the simultaneous irradiation of an interference pattern created by two linearly polarized red lights. This study ascribes the formation of this grating to two mechanisms. One mechanism is the green-light-inducing strong dye absorption followed by adsorption through the trans–cis isomerization; the other mechanism is the inhibition effect of adsorption induced by the red light through the cis–trans inverse isomerization. These produce a twisted nematic structure-modulated pattern, which, in turn, causes the BG. Additional experiments demonstrate that the formed BGs are electrically switchable and thermally erasable.