In the patterned vertical alignment ͑PVA͒ cell in which multidomains are formed from the perfect vertical alignment through an oblique field only, the formation of disclinations between liquid crystal ͑LC͒ molecules is inevitable in the presence of an electric field, which lowers transmittance and the response time. In the proposed PVA device, the pretilt angle is formed in four different directions through the polymerization of an UV curable reactive mesogen monomer at the surface. In this way, the reorientation of LC responding to an electric field is well defined, and thus the device shows reduced threshold voltage and much improved response time in all gray scales.
The patterned vertical alignment (PVA) liquid crystal (LC) mode shows a wide viewing angle and a perfect dark state at a normal direction. However, it is inevitable to avoid the formation of disclinations and the movement of defect points during stabilization of LC's reorientation. It is due to fact that the LC directors tilt downward in different directions with collisions between them by the fringe-electric field. Consequently, the transmittance decreases and the response time gets slower. In order to overcome this barrier, the pretilt angles in four different directions are introduced on the substrates utilizing UV-curable reactive mesogen (RM) monomers. According to our studies, concentration of RM, UV curing condition, and applied voltage to the cell are critical to achieve an optimized surface-modified PVA mode which provides the well-defined reorientation of the LCs with respect to an electric field. Moreover, morphological behaviors on surface of substrate depending on curing conditions were investigated in order to confirm the existence of the stabilized polymer.
The orientational distribution in SmA, the switching behavior in SmC*, and the molecular orientation of SmC A * have been investigated by means of polarized Raman scattering due to the C–C stretching of phenyl rings in two antiferroelectric liquid crystals. The scattered intensities, I Z Z (ω) and I Y Z (ω), have been measured between crossed and parallel polars as a function of rotation angle, ω, of homogeneously aligned cells about their surface normal. The order parameters, <P 2> and <P 4>, and then the orientational distribution function in SmA were obtained by utilizing the method of information entropy. The electric-field-induced reorientation was observed in the rotation angle dependence: I Z Z (ω)∝cos 4(ω±Θ), where Θ is the tilt angle of SmC*. The characteristic rotation angle dependence obtained in SmC A * was described as I Z (ω)∝{cos 4(ω+Θ)+cos 4(ω-Θ)}/2. This result supports the molecular orientation of SmC A * so far proposed that the molecules in adjacent layers tilt in the opposite senses.
In this letter we demonstrate the vertical alignment of liquid crystal on inorganic thin film surfaces using the ion beam exposure. Nematic liquid crystal can be aligned vertically by the rotational oblique evaporation of a-SiOx thin films. However, the electro-optic switching behavior of liquid crystal along random directions results in disclination lines. By using the ion beam exposure, we can achieve highly uniform alignment without disclination lines. We found from x-ray diffraction and x-ray photoemission spectroscopy data that the vertical alignment can be achieved when x approaches 1.5 at the a-SiOx film surface. We have shown that the pretilt angle can be controlled by changing ion beam parameters, such as the ion beam energy, the angle of incidence, and the exposure time. We also have shown that a liquid crystal cell aligned vertically by the ion beam exposure exhibits the voltage-transmittance curve similar to that of a rubbed polyimide cell.
Purpose Deformable lung phantoms have been proposed to investigate four‐dimensional (4D) imaging and radiotherapy delivery techniques. However, most phantoms mimic only the lung and tumor without pulmonary airways. The purpose of this study was to develop a reproducible, deformable lung phantom with three‐dimensional (3D)‐printed airways. Methods The phantom consists of: (a) 3D‐printed flexible airways, (b) flexible polyurethane foam infused with iodinated contrast agents, and (c) a motion platform. The airways were simulated using publicly available breath‐hold computed tomography (CT) image datasets of a human lung through airway segmentation, computer‐aided design modeling, and 3D printing with a rubber‐like material. The lung was simulated by pouring liquid expanding foam into a mold with the 3D‐printed airways attached. Iodinated contrast agents were infused into the lung phantom to emulate the density of the human lung. The lung/airways phantom was integrated into our previously developed motion platform, which allows for compression and decompression of the phantom in the superior–inferior direction. We quantified the reproducibility of the density (lung), motion/deformation (lung and airways), and position (airways) using breath‐hold CT scans (with the phantom compressed and decompressed) repeated every two weeks over a 2‐month period as well as 4D CT scans (with the phantom continuously compressed and decompressed) repeated twice over four weeks. The density reproducibility was quantified with a difference image (created by subtracting the rigidly registered baseline and the repeated images) in each of the compressed and decompressed states. Reproducibility of the motion/deformation was evaluated by comparing the baseline displacement vector fields (DVFs) derived from deformable image registration (DIR) between the compressed and decompressed phantom CT images with those of repeated scans and calculating the difference in the displacement vectors. Reproducibility of the airway position was quantified based on DIR between the baseline and repeated images. Results For the breath‐hold CT scans, the mean difference in lung density between baseline and week 8 was −1.3 (standard deviation 33.5) Hounsfield unit (HU) in the compressed state and 0.4 (36.8) HU in the decompressed state, while large local differences were observed around the high‐contrast structures (caused by small misalignments). By visual inspection, the DVFs (between the compressed and decompressed states) at baseline and last time point (week 8 for the breath‐hold CT scans) demonstrated a similar pattern. The mean lengths of displacement vector differences between baseline and week 8 were 0.5 (0.4) mm for the lung and 0.3 (0.2) mm for the airways. The mean airway displacements between baseline and week 8 were 0.6 (0.5) mm in the compressed state and 0.6 (0.4) mm in the decompressed state. We also observed similar results for the 4D CT scans (week 0 vs week 4) as well as for the breath‐hold CT scans at other time points (week 0 vs weeks 2, 4, a...
To investigate feasible treatment planning parameters, we aimed to evaluate the dosimetric and radiobiological impact of the dose calculation algorithm and grid size in the volumetric modulated arc therapy (VMAT) plan for prostate cancer. Twenty patients were selected, and the treatment plans were initially generated with anisotropic analytical algorithm (AAA) and recalculated with Acuros XB (AXB) algorithm. Various dose grids were used for AXB (1, 2, and 3 mm) and AAA (1, 3, and 5 mm) plan. Dosimetric parameters such as homogeneity index (HI) and conformity index (CI), and radiobiological parameters such as tumor control probability (TCP) and normal tissue complication probability (NTCP) were calculated. Significant differences were observed in the planning target volume (PTV) coverage between both algorithms, and the V95%, HI, and CI of AAA were significantly affected by grid (p < 0.01). On 1 mm grid, the mean rectal dose difference between both algorithms was 2.87% of the prescription dose (p < 0.01), which was the highest among the critical organs. The TCP and NTCP of the AAA were higher than those of AXB (p < 0.01). Compared to AXB with 1 mm grid, the 2 mm grid showed comparable dose calculation accuracy with short calculation time. This study found that the PTV and rectum show significant differences according to dose calculation algorithm and grid. Considering the dose calculation performance for heterogeneous area, we recommend AXB with 2 mm grid for improving treatment efficiency of prostate VMAT.
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