Minwook Park

Photoresponsive Carbohydrate-based Giant Surfactants: Automatic Vertical Alignment of Nematic Liquid Crystal for the Remote-Controllable Optical Device

Photoresponsive carbohydrate-based giant surfactants (abbreviated as CELAnD-OH) were specifically designed and synthesized for the automatic vertical alignment (VA) layer of nematic (N) liquid crystal (LC), which can be applied for the fabrication of remote-controllable optical devices. Without the conventional polymer-based LC alignment process, a perfect VA layer was automatically constructed by directly adding the 0.1 wt % CELA1D-OH in the N-LC media. The programmed CELA1D-OH giant surfactants in the N-LC media gradually diffused onto the substrates of LC cell and self-assembled to the expanded monolayer structure, which can provide enough empty spaces for N-LC molecules to crawl into the empty zones for the construction of VA layer. On the other hand, the CELA3D-OH giant surfactants forming the condensed monolayer structure on the substrates exhibited a planar alignment (PA) rather than a VA. Upon tuning the wavelength of light, the N-LC alignments were reversibly switched between VA and PA in the remote-controllable LC optical devices. Based on the experimental results, it was realized that understanding the interactions between N-LC molecules and amphiphilic giant surfactants is critical to design the suitable materials for the automatic LC alignment.

Dual Photo‐functionalized Amphiphile for Photo‐reversible Liquid Crystal Alignments

Without the conventional polymer-based liquid crystal (LC) alignment process, a newly synthesized dual photo-functionalized amphiphile (abbreviated as ADMA1 ) was successfully applied as a robust photo-reversible LC alignment layer by self-assembly and photo-polymerization. The LC alignment layer constructed by directly adding dual photo-functionalized amphiphiles into LC media significantly cuts the manufacturing cost as well as opens new doors for the fabrication of novel electro-optical devices.

Self-Assembled Hierarchical Superstructures from the Benzene-1,3,5-Tricarboxamide Supramolecules for the Fabrication of Remote-Controllable Actuating and Rewritable Films

The well-defined hierarchical superstructures constructed by the self-assembly of programmed supramolecules can be organized for the fabrication of remote-controllable actuating and rewritable films. To realize this concept, we newly designed and synthesized a benzene-1,3,5-tricarboxamide (BTA) derivative (abbreviated as BTA-3AZO) containing photoresponsive azobenzene (AZO) mesogens on the periphery of the BTA core. BTA-3AZO was first self-assembled to nanocolumns mainly driven by the intermolecular hydrogen-bonds between BTA cores, and these self-assembled nanocolumns were further self-organized laterally to form the low-ordered hexagonal columnar liquid crystal (LC) phase below the isotropization temperature. Upon cooling, a lamello-columnar crystal phase emerged at room temperature via a highly ordered lamello-columnar LC phase. The three-dimensional (3D) organogel networks consisted of fibrous and lamellar superstructures were fabricated in the BTA-3AZO cyclohexane-methanol solutions. By tuning the wavelength of light, the shape and color of the 3D networked thin films were remote-controlled by the conformational changes of azobenzene moieties in the BTA-3AZO. The demonstrations of remote-controllable 3D actuating and rewritable films with the self-assembled hierarchical BTA-3AZO thin films can be stepping stones for the advanced flexible optoelectronic devices.

Butterfly-Shaped Diphenylpyrimidine Molecule: Tunable Photophysical Properties by Molecular Self-Assembly Pathways

To understand the relationships between chemical structures, molecular packing structures, and photophysical properties of organic materials, a butterfly shaped diphenylpyrimidine molecule (abbreviated as DPP-6C12) was newly synthesized [Park, M.; Choi, Y.-J.; Kim, D.-Y.; Hwang, S.-H.; Jeong, K.-U. Cryst. Growth Des. 2015, 15, 900-906]. By breaking the molecular symmetry and coplanarity of DPP-6C12, peculiar monotropic phase transitions were observed. Based on two-dimensional wide-angle X-ray diffraction and selected area electron diffraction, the molecular packing structures of ordered phases were identified, which were further confirmed by the computer simulations in the real and reciprocal spaces. Finally, we demonstrated that the photophysical properties of DPP-6C12 can be tuned by controlling the molecular packing structures with simple thermal treatments.

Multifunctional Optical Thin Films Fabricated by the Photopolymerization of Uniaxially Oriented Lyotropic Liquid Crystal Monomers for Electro-Optical Devices

A multifunctional optical thin film (MOTF) is fabricated by coating the newly synthesized perylene-based reactive mesogen (PBRM) and stabilized by the subsequent photopolymerization. Based on the spectroscopic results combined with morphological observations, it is found that nematic liquid crystal (NLC) is aligned parallel to the molecular long axis of PBRM not only due to the long-range physical anchoring effect but also due to the short-range molecular physical interactions between alignment layer and NLC molecules. From the electro-optical properties of LC test cells fabricated with the PBRM MOTF, it is clearly demonstrated that the PBRM MOTF can work as the planar LC alignment layer as well as the in-cell coatable polarizer. The coatable PBRM MOTF from lyotropic chromonic reactive mesogens can pave a new way for the flexible optoelectronic devices.

Interfacial Engineering for the Synergistic Enhancement of Thermal Conductivity of Discotic Liquid Crystal Composites

To develop an advanced heat transfer composite, a deeper understanding of the interfacial correlation between matrix and filler is of paramount importance. To verify the effect of interfacial correlations on the thermal conductivity, the conductive fillers such as expanded graphite (EG) and boron nitride (BN) are introduced in the discotic liquid crystal (DLC)-based polymeric matrix. The DLC matrix exhibits better interfacial affinity with EG compared to BN because of the strong π-π interactions between EG and DLC. Thanks to its excellent interfacial affinity, the EG-DLC composites show a synergistic increment in thermal conducting performance.

Stimuli-responsive liquid crystal physical gels based on the hierarchical superstructures of benzene-1,3,5-tricarboxamide macrogelators

For the fabrication of rewritable electro-optic devices, we prepared randomly dispersed liquid crystal physical gels (LCPG) by constructing a well-defined hierarchical superstructure of a benzene-1,3,5-tricarboxamide (BTA)-based macrogelator (abbreviated BTA3AZO) in a host nematic (N) LC medium. The programmed BTA3AZO macrogelator in the NLC medium built up three-dimensional networks not only by hydrogen-bonding between BTA cores but also by nanophase separations between BTA3AZOs and NLCs. On the basis of the anisotropic optical properties of LCPGs, it was realized that a light scattering state of BTA3AZO LCPGs can be switched to a transmittance state under a fairly low driving voltage (22 V) compared with those (around 100 V) of polymer-based systems. The lower driving voltage of BTA3AZO LCPGs should be mainly due to the formation of self-assembled BTA3AZO nanocolumn networks (only 1 wt%) which were finely dispersed in the NLC medium as well as the good affinity between NLCs and azobenzene mesogens (AZOs) which also responded to the applied electric fields. The BTA3AZO LCPGs can be remote-controlled by utilizing the trans–cis photoisomerization of the azobenzene moieties in the LCPGs. Additionally, the rewritable electro-optical properties of BTA3AZO LCPGs allowed us to demonstrate remote-controllable light shutters.

Construction of Polymer-Stabilized Automatic MultiDomain Vertical Molecular Alignment Layers with Pretilt Angles by Photopolymerizing Dendritic Monomers under Electric Fields

The synthesized itaconic acid-based dendritic amphiphile (Ita3C12) monomers and the methacryl polyhedral oligomeric silsesquioxane (MAPOSS) cross-linkers were directly introduced for the construction of automatic vertical alignment (auto-VA) layers in the host nematic liquid crystal (NLC) medium. The auto-VA layer can be stabilized by irradiating UV light. For the automatic fabrication of a polymer-stabilized multidomain VA (PS auto-MDVA) layer with a pretilt angle, Ita3C12 and MAPOSS were photopolymerized under the electric field by irradiating UV light on the multidomain electrode cell. Mainly because of the pretilted NLC at zero voltage, the electro-optic properties of the PS auto-MDVA cell were dramatically improved. From the morphological observations combined with surface chemical analyses, it was found that various sizes of protrusions on the solid substrates were automatically constructed by the two-step mechanisms. We demonstrated the PS auto-MDVA cell with the enhancement of electro-optic properties as a single-step process and investigated how the protrusions were automatically developed during the polymer stabilization.

Viewing angle compensation of vertical alignment liquid crystal display using a triphenylene-based discotic reactive mesogen

We synthesised a triphenylene-based discotic reactive mesogen 2,3,6,7,10,11-hexakis(but-3-enyloxy)triphenylene (HABET) and investigated its performance as the compensation film for a vertical alignment-liquid crystal display (VA-LCD). The HABET molecule has a negative birefringence with an extraordinary refractive index (ne) that is smaller than the ordinary refractive index (no). The optic axis of the HABET is parallel to the ne direction and was vertically aligned to function as a negative C-plate. We measured the refractive indices and birefringence of the HABET layer in the visible wavelength range. Using the experimental data, we simulated the viewing angle property of the VA-LCD with the HABET negative C-plate and a positive A-plate. The viewing angle property of the VA-LCD with the HABET compensation film was wider than those without the compensation film and those using triacetylcellulose films.

Electro-Optical Characteristics and Analysis of 1×1 mm 2 Large-Area InGaN/GaN Green LED

We investigated the effects of piezoelectric field on the electro-absorption characteristics in InGaN/GaN multiple-quantum well (MQW) green light emitting diodes (LED). Double crystal X-ray diffraction measurement was performed to study the crystalline property and indium (In) composition in the MQW active layer. To measure the electro-luminescence and electro-reflectance (ER) spectroscopy, we fabricated the large-area green LED chip. The piezoelectric field inside the LED structure was evaluated from the Vcomp in active layer by the ER spectra. Finally, we analyzed the electro-absorption characteristics of the green LED by using the photo-current spectroscopy.