Viewing angle controllable fringe and in-plane switching vertical alignment LCD

A viewing angle controllable fringe and in-plane switching vertical alignment liquid crystal display (LCD) structure has been proposed. To realise the change from wide viewing angle (WVA) to narrow viewing angle (NVA) in a single LCD panel, the bias voltage is applied on the common electrode, and NVA can decreases with the increasing bias voltage. In WVA mode, the viewing angle cone (contrast ratio larger than 1000:1) is almost 70° and the contrast ratio is larger than 100:1 in arbitrary azimuthal directions. In NVA mode, the viewing angle cone (10:1) can continuously and uniformly change from 40° to 20°.     

Fabrication of homogenously self-alignment fringe-field switching mode liquid crystal cell without using a conventional alignment layer

We propose a novel method to fabricate a uniaxially homogeneous alignment of liquid crystal (LC) molecules without using a conventional alignment layer such as polyimide film. The method produces the polymer alignment layer (PAL) by polymerisation of the monomer including in the LC layer above the T_NI of the LC material. The fringe-field switching (FFS) mode LC cell with the PAL (FFS-PAL-LC cell) produced from the monomer 4,4?-di-mehacryloyl-oxy chalcone (4,4?-DMOCh) exhibited enough level of alignment state and electro-optical property compared with the FFS-LC cell having the conventional polyimide-type alignment layer. We can expect that the FFS-PAL-LC cell is useful for next-generation displays such as flexible liquid crystal displays (LCDs) because the method does not need high-temperature process of over 200°C.     

Investigation on ion movement in the fringe-field switching mode depending on resistivity of alignment layer and dielectric anisotropic sign of liquid crystal

Adsorption and desorption of ions at interface between liquid crystal and alignment layer in liquid crystal displays play a crucial role in residual direct current voltage associated with image sticking. In this article, the dependency of such adsorption and desorption of ions on resistivity of alignment layer and sign of liquid crystal dielectric anisotropy in the fringe-field liquid crystal cell has been investigated. Our studies show that the time constant of ions during adsorption and desorption depends upon resistivity and dielectric constant of liquid crystal and alignment layer, and most strongly influenced by the resistivity of alignment layer such that the one with lower resistivity in two orders shows much faster adsorption and desorption at the interface than that of the one with higher resistivity.     

Surface polymer-stabilised in-plane field driven vertical alignment liquid crystal device

In-plane field driven vertical alignment device using a liquid crystal with positive dielectric anisotropy has been studied. In the device, the distance between inter-digital electrodes needs to be increased to achieve higher transmittance; however, such a design results in an increase in operating voltage and slower response time. In this work, we use polymer stabilisation technique, which generates surface tilt angle other than 90^o, to improve upon these drawbacks. As a result, the proposed device shows lower operating voltage and faster response time while keeping transmittance at the same level, compared to those prior to polymer stabilisation.     

Polarised UV-induced homogeneous alignment for fringe-field switching liquid crystal display with a new azobenzene monomer

A novel preparation method of homogeneous alignment polymer film (HAPF) was proposed by polymerisation of the monomer, 4,4?-di-methacryloyl-oxy azobenzene (4,4?-DMOAz), being dissolved in the liquid crystal (LC) material of positive dielectric anisotropy. For obtaining the homogeneous alignment, exposure of the polarised UV light was carried out to the LC cell above the nematic to isotropic transition temperature of the LC material. The fringe-field switching (FFS) mode LC cell with the HAPF formed from the monomer 4,4?-DMOAz (FFS-HAPF-LC cell) exhibited enough level of alignment state, electro-optical and response properties compared with the FFS-LC cell carrying the conventional polyimide-type alignment layer. FFS-HAPF-LC cell can be expected to be useful for next-generation displays such as flexible LC displays.     

Fast switching and luminance-controlled fringe-field switching liquid crystal device for vehicle display

ABSTRACT

Liquid crystal displays (LCDs) for vehicle displays should exhibit a fast response time in wide temperature range and wide-viewing angle in horizontal and downward directions without grey-scale inversion but limited brightness in the upward direction because the display images can be reproduced in the front window glass of a vehicle, affecting driver’s front visibility. Currently, fringe-field switching (FFS) liquid crystal device is widely commercialised for high resolution and wide-viewing-angle LCD; however, it needs to improve response times and limit the display brightness in the upward direction. As a solution, we propose a homogeneously aligned liquid crystal device in which liquid crystal director does tilt as well as twist deformation in a confined area by both vertical- and fringe-electric fields, exhibiting about two times faster decay response time than that of conventional FFS mode with suppressed luminance in the upward direction. The proposed liquid crystal device can be applied to LCDs for vehicle displays.     

Optimisation of alignment materials for minimising residual retardation in in-plane switching liquid crystal display

The light leakage in a black state of in-plane switching (IPS) liquid crystal display (LCD) associated with rubbing process has been investigated. The mechanical rubbing process with a cloth caused orientation disorders in the liquid crystal directors and these partial orientation disorders result in residual retardations of the IPS LCD, causing the light leakages at the black state. In this study, we theoretically estimated how the light leakage is associated with the rubbing uniformity using 2 × 2 Jones matrix equation and also experimentally confirmed how it is associated with structural properties of the alignment layer. The light leakage was clearly reduced in the alignment layer with reduced crystallinity and flexibility.     

Fast switching of vertically aligned negative liquid crystals by optically hidden relaxation

We propose a method for fast switching of vertically aligned (VA) negative liquid crystals (LCs) by hiding the relaxation process of LCs. During the turn-off process, a strong in-plane electric field is applied for a short duration of time instead of relying solely on the slow relaxation of LCs. The LC molecules are rotated to the transmission axis of one of the polarisers by the applied in-plane electric field, resulting in turn-off switching that is 5.8 times faster than that of a conventional VA cell. By applying an overdriving scheme, we experimentally obtained a total response time of 3.3 ms.     

Continuous viewing angle controllable patterned vertical alignment liquid crystal display

A continuous viewing angle switchable patterned vertical alignment liquid crystal display (PVA-LCD) with circle polarisers is proposed. In wide viewing angle (WVA) mode, the viewing cone with contrast ratio larger than 1000:1 is extended to 50° and the contrast ratio larger than 100:1 is extended to 80°. Meanwhile, the viewing cone with contrast ratio more than 10:1 is limited to 40° in all direction for narrow viewing angle (NVA) mode. The viewing angle of the display can be controlled by applying a bias voltage on the common electrode. With the increasing bias voltage, the viewing angle cone with contrast ratio more than 10:1 can be changed from 40° to 20°. The proposed PVA-LCD has high transmittance (~93%) under the circle polarisers because the dead zone in the normal PVA-LCD with linear polarisers is eliminated.     

Synthesis of novel soluble rubbing-resistant polyimides used as liquid crystal vertical alignment layers

A novel functional diamine N12, containing triphenylamine moiety, biphenyl, tert-butyl substituents and long alkyl chain, N,N-bis(4-aminophenyl)-p-(3,5-di-tert-butyl-4-dodecyloxy phenyl) aniline (N12), was synthesised and characterised. A series of polyimides (PIs) were prepared based on 2,2?-bis(trifluoromethyl)benzidine, 4,4?-oxydiphthalicanhydride and different contents of N12 via a conventional two-step procedure that included a ring-opening polyaddition to gain polyamic acids, followed by chemical cyclodehydration. The chemical structures of the intermediates, diamines and PIs were characterised by Fourier transform infrared spectroscopy and nuclear magnetic resonance spectroscopy. All of the PIs were amorphous and exhibited good solubility in both polar aprotic solvents and some low boiling point solvents. PIs containing different content of N12 could induce highly uniform vertical alignment of liquid crystals (LCs). More importantly, PIs derived from N12 showed a good rubbing resistance. Besides, all PI films showed high transmittance in the wavelength range 400–700 nm and good thermal stabilities. Such PIs could be suitable candidates for alignment layers used in the manufacture of high-performance vertical alignment mode LC displays.     

Fabrication of vertical alignment liquid crystal cell without forming a conventional polyimide-alignment layer

Two series of asymmetric banana-shaped compounds have been synthesized and studied. In the 1,3-phenylene bis[4-(4′-alkoxybenzoyloxy)]benzoate series the lack of symmetry was derived solely from the difference in length of the two terminal alkoxy chains. In the 3,4′-biphenylene bis[4-(4′-alkoxybenzoyloxy)]benzoate series the asymmetric nature originates from the 3,4′-substitution of the central biphenyl group and from the difference in length of the two terminal chains. All the melting points of the asymmetrical compounds in the series with the central phenyl unit are lower than those of the symmetrical compounds. The liquid crystalline B₁ or B₂ phase was retained in all cases. In the series with the central biphenyl unit the compounds with the shortest chain attached to the para-position of the central biphenyl unit have the lowest melting points. A significant lowering of the melting points in comparison with the symmetrically substituted compounds, however, could not be achieved. All the compounds of both series show a layer spacing which is comparable to those of the symmetrically substituted parent compounds. The observed switching behaviour of both the symmetric and asymmetric compounds with a B₂ phase was antiferroelectric.     

Development of non-reactive fluorine-rich biphenyl molecules and their incorporation into a PDLC system

Novel highly fluorinated molecules containing biphenyl moieties were synthesized via N,N ′-dicyclohexylcarbodiimide esterification reactions. Chemical structures were confirmed by FTIR, NMR and elemental analysis. These non-reactive fluorinated molecules were added in increasing concentrations to a pentaacrylate-based polymer dispersed liquid crystal formulation and thin films were made by homogeneous illumination with a white light source. Refractive index and dynamic scattering measurements, in addition to direct polymerization attempts, indicate that the fluorinated compounds are non-reactive in the photopolymerization process. Electro-optic measurements suggest that the fluorinated molecules preferentially occupy the interface between the crosslinked polymer matrix and the liquid crystal domains. As a consequence, threshold voltages are lowered and relaxation times increased.     

Investigation on newly designed low resistivity polyimide-type alignment layer for reducing DC image sticking of in-plane switching liquid crystal display

Soluble polyimide-type alignment layer is widely used in in-plane switching (IPS) liquid crystal display (LCD) because of its excellent reliability owing to high imidisation ratio during long-term driving, high voltage-holding ratio and low ion density. Nevertheless, it exhibits slow direct current (DC) discharging property due to its high resistivity, causing significant DC image-sticking problem. In this study, we doped inorganic salt to control the resistivity of soluble polyimide-type alignment layer and found that this approach reduced DC image sticking greatly without any loss of reliability property in IPS-LCD.     

Synthesis of photosensitive polyimide for liquid crystal alignment under non-polarised UV ageing lamp irradiation and a study on the possible mechanism of alignment

ABSTRACT

A new photosensitive polyimide (PI) was successfully synthesised via esterification of PI containing hydroxyl groups with cinnamoyl chloride (CL). The cinnamate (CA) group contents of the PI was up to 90%. The PI films could induce uniform parallel alignment of liquid crystal (LC) molecules after the non-polarised ultraviolet ageing lamp exposure, which reduce the cost significantly compared with polarised ultraviolet light equipment. In addition, the PI exhibited good thermal stability. Meanwhile, the possible mechanism of PI alignment films induced by NPUVL was discussed in some detail.     

Preparation and characterization of a novel polyimide liquid crystal vertical alignment layer

A series of diamines with a side chain containing rigid biphenyl unit and nonpolar alkoxy side end group [4-alkoxy-biphenol-3′,5′-diaminobenzoate] (Cm-BBDA, m = 4, 6, 12) were synthesized and their chemical structures were confirmed by Fourier Transform Infrared Spectroscopy (FT-IR) and nuclear magetic resonance spectroscopy (¹H NMR). Then three polyimides (PIs) were prepared by copolymerization of pyromellitic dianhydride (PMDA), 4,4′-methylenedianiline (MDA) and Cm-BBDA in N-methyl-2-pyrrolodone (NMP), and chemical structures of all PIs were confirmed by FT-IR. Structural identification of all poly(amic acid)s (PAA) was performed by ¹H NMR. Liquid crystal (LC) cells were fabricated using these PIs as the alignment layer for characterization of the alignment properties of LCs. It was found that the planar alignment was obtained when PI with side chain containing alkoxy side end group of 4 carbon atoms was employed and the vertical alignment was observed when alkoxy side end groups of 6 or 12 carbon atoms were included. A uniform vertical alignment was validated by polarizing microscopy. It was testified that LC vertical alignment possessed high thermal stability.     

UV-induced vertical alignment liquid crystal cell with two species of monomers having vertical-alignment-induced side-chain group and phenanthrene group

We propose the method for formation of the vertical alignment polymer film by polymerisation of the monomers being dissolved in the liquid crystal (LC) material. For obtaining the vertical alignment, combination of the two monomers, 4-(4?-octyloxy-biphenyl-4-yloxy)-butyl ester (AOBBE) and 2,7-dimethacryloyl-oxy-phenanthrene (DMAPhen), was found to be useful.

The monomer DMAPhen initiates the polymerisation under UV light exposure, and the AOBBE unit induces the vertical alignment without generating any alignment defects. The monomer DMAPhen is useful for maintaining the high voltage holding ratio and low residual direct current voltage after UV light exposure because the molecules of DMAPhen do not remain in the LC layer.     

Achieving a robust homogenously aligned liquid crystal layer with reactive mesogen for in-plane switching liquid crystal displays

Uniformly aligned liquid crystals (LCs) are of crucial importance in a practical application, such as displays, phase modulators and virtual reality devices. Although an alignment layer using polyimide-type polymers can almost perfectly align the LCs, polymer-stabilisation at the surface using pre-mixed monomers has been attempted to reduce the fabrication process, i.e. eliminating the alignment layer, thereby reducing the fabrication cost. Here, we propose an approach to achieve a homogeneous alignment of LCs by controlling the molecular structure of reactive monomers mixed in LCs without using conventional polyimide alignment layer. The result shows an excellent initial dark state and acceptable electro-optic performance which implies that the polymer stabilisation at the surface successfully anchors the homogenous orientation of LCs. We believe that the proposed fabrication method can contribute to cost-effective fabrication process by eliminating an alignment layer with no fabrication step of a surface treatment.     

Fabrication of vertically aligned liquid crystal cell without using a conventional alignment layer

We propose a novel method to fabricate a vertical alignment (VA) of liquid crystal (LC) molecules without using a conventional alignment layer such as polyimide film. The method produces the vertical alignment polymer layer (VAPL) by polymerisation of a monomer or mixed monomers including in the LC layer above T_NI of the LC material. The VA mode LC cell with the VAPL (VAPL-LC cell) produced from the mixed monomers of acrylic acid 4-(4?-octyloxy-biphenyl-4-yloxy)-butyl ester and 1,2-bis-(4-methacryloxy-phenyl)-2,2-dimethoxy-ethane-1-one exhibited enough level of alignment state and electro-optical property with high voltage holding ratio. We can expect that the VAPL-LC cell is useful for next-generation displays such as flexible liquid crystal displays because the method does not need the process including high temperature over 200°C.     

Preparation and characterization of photo-decomposable ester-containing semi-alicyclic polyimide alignment layers for potential applications in in-plane switching thin-film transistor liquid crystal display devices

Poly(amic acid)s (PAAs) alignment agents have been prepared from the alicyclic dianhydrides, including 1,2,3,4-cyclobutanetetracarboxylic dianhydride (CBDA, I), 1,3-dimethyl-1,2,3,4-cyclobutanetetracarboxylic dianhydride (DMCBDA, II), and ester-linked aromatic diamines, including 4-aminophenyl-4′-aminobenzoate (APAB, a) and bis(4-aminophenyl)terephthalate (BPTP, b), respectively. The derived PAAs, including PAA-I_a (CBDA-APAB), PAA-I_b (CBDA-BPTP), and PAA-II_a (DMCBDA-APAB) exhibited the preferable molecular weights, while the PAA-II_b (DMCBDA-BPTP) showed the low one due to the low polymerization reactivity both for the DMCBDA dianhydride and the BPTP diamine. All the PAA solutions except PAA-II_b were adopted as the alignment components to fabricate liquid crystal (LC) minicells with a mode of in-plane switching (IPS). The polyimides (PI) alignment layers derived from the thermal dehydration reaction of the PAA precursors at 230°C for 30 min showed good alignments effects to the LC molecules, which exhibited the pretilt angles (θ_p) from 0.09 to 0.15° after being exposed by the linear polarized ultraviolet light sources with the wavelength of 254 nm. In addition, the PI alignment layers afforded good optoelectronic features to the minicells, including the voltage holding ratio values over 97% at room temperature, and the residual direct circuit voltages lower than 1.0 V. The anchoring energy results indicated that the PI-II_a (DMCBDA-APAB) alignment layer showed the highest interaction with the LC molecules, and thus exhibited the highest threshold voltage (V_th) in the voltage-transmittance (V-T) measurements for the minicells.     

Ferroelectric liquid crystals from banana-shaped achiral molecules with vinyl end groups

Banana-shaped achiral compounds, the 1,3-phenylene bis[4-(alkenyloxyphenyliminomethyl)benzoate]s, were synthesized with varying length of the alkenyl group; their ferroelectric properties are described. The smectic mesophases, including a switchable chiral smectic C (SmC*) phase, were characterized by differential scanning calorimetry, polarizing optical microscopy and the triangular wave method. The presence of vinyl groups at the ends of the linear side-wings in the banana-shaped achiral molecules, containing a Schiff's base mesogen, induced a decrease in melting temperature and formation of the switchable SmC* phase in the melt. The compound having the octenyloxy group exhibited a spontaneous polarization of 120 nC cm^?2 on reversal of an applied electric field.