2 research outputs found

    Hierarchical Striped Walls Constructed by the Photopolymerization of Discotic Reactive Building Blocks in the Anisotropic Liquid Crystal Solvents

    No full text
    A triphenylene-based reactive mesogenic molecule (abbreviated as HABET) was newly designed and synthesized as a programmed building block to construct the striped walls by the photopolymerization in the anisotropic liquid crystal (LC) solvents. On the basis of thermal, scattering and microscopic analyses, it was found that HABET formed three ordered structures: a columnar hexagonal LC phase (Φ<sub>H</sub>), a tilted columnar hexagonal LC phase (Φ<sub>T</sub>) and a highly ordered columnar oblique crystal phase (Φ<sub>OK</sub>). The microscopic molecular orientations in the hierarchical superstructures were controlled in the anisotropic LC solvents with the help of surface anchoring forces, while the dimensions of the striped wall morphologies were determined by the patterned photomasks. The long axis of self-assembled columns in the striped walls was perpendicular to the surface alignment direction regardless of the photomask direction. Additionally, it was realized that the shapes of water drops as well as the surface water contact angles can be tuned by the hierarchical superstructures and morphologies of the polymerized HABET networks. The anisotropic hierarchical superstructures and morphologies concurrently fabricated during the polymerization in the anisotropic LC medium can offer a potential pathway for liquid transportation in the microfluidic devices

    Flexible and Patterned Thin Film Polarizer: Photopolymerization of Perylene-based Lyotropic Chromonic Reactive Mesogens

    No full text
    A perylene-based reactive mesogen (DAPDI) forming a lyotropic chromonic liquid crystal (LCLC) phase was newly designed and synthesized for the fabrication of macroscopically oriented and patterned thin film polarizer (TFP) on the flexible polymer substrates. The anisotropic optical property and molecular self-assembly of DAPDI were investigated by the combination of microscopic, scattering and spectroscopic techniques. The main driving forces of molecular self-assembly were the face-to-face π–π intermolecular interaction among aromatic cores and the nanophase separation between hydrophilic ionic groups and hydrophobic aromatic cores. Degree of polarization for the macroscopically oriented and photopolymerized DAPDI TFP was estimated to be 99.81% at the <i><b>λ</b></i><sub>max</sub> = 491 nm. After mechanically shearing the DAPDI LCLC aqueous solution on the flexible polymer substrates, we successfully fabricated the patterned DAPDI TFP by etching the unpolymerized regions selectively blocked by a photomask during the photopolymerization process. Chemical and mechanical stabilities were confirmed by the solvent and pencil hardness tests, and its surface morphology was further investigated by optical microscopy, atomic force microscopy, and three-dimensional surface nanoprofiler. The flexible and patterned DAPDI TFP with robust chemical and mechanical stabilities can be a stepping stone for the advanced flexible optoelectronic devices
    corecore