WO2013027548A1 - 液晶表示装置の製造方法 - Google Patents
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- WO2013027548A1 WO2013027548A1 PCT/JP2012/069561 JP2012069561W WO2013027548A1 WO 2013027548 A1 WO2013027548 A1 WO 2013027548A1 JP 2012069561 W JP2012069561 W JP 2012069561W WO 2013027548 A1 WO2013027548 A1 WO 2013027548A1
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- G—PHYSICS
- G02—OPTICS
- G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
- G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
- G02F1/01—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour
- G02F1/13—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells
- G02F1/133—Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
- G02F1/1333—Constructional arrangements; Manufacturing methods
- G02F1/1337—Surface-induced orientation of the liquid crystal molecules, e.g. by alignment layers
- G02F1/13378—Surface-induced orientation of the liquid crystal molecules, e.g. by alignment layers by treatment of the surface, e.g. embossing, rubbing or light irradiation
- G02F1/133788—Surface-induced orientation of the liquid crystal molecules, e.g. by alignment layers by treatment of the surface, e.g. embossing, rubbing or light irradiation by light irradiation, e.g. linearly polarised light photo-polymerisation
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K19/00—Liquid crystal materials
- C09K19/04—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
- C09K19/06—Non-steroidal liquid crystal compounds
- C09K19/08—Non-steroidal liquid crystal compounds containing at least two non-condensed rings
- C09K19/30—Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
- C09K19/3001—Cyclohexane rings
- C09K19/3003—Compounds containing at least two rings in which the different rings are directly linked (covalent bond)
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K19/00—Liquid crystal materials
- C09K19/52—Liquid crystal materials characterised by components which are not liquid crystals, e.g. additives with special physical aspect: solvents, solid particles
- C09K19/54—Additives having no specific mesophase characterised by their chemical composition
- C09K19/56—Aligning agents
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- G—PHYSICS
- G02—OPTICS
- G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
- G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
- G02F1/01—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour
- G02F1/13—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells
- G02F1/133—Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
- G02F1/1333—Constructional arrangements; Manufacturing methods
- G02F1/1337—Surface-induced orientation of the liquid crystal molecules, e.g. by alignment layers
- G02F1/133711—Surface-induced orientation of the liquid crystal molecules, e.g. by alignment layers by organic films, e.g. polymeric films
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- G—PHYSICS
- G02—OPTICS
- G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
- G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
- G02F1/01—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour
- G02F1/13—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells
- G02F1/133—Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
- G02F1/1333—Constructional arrangements; Manufacturing methods
- G02F1/1339—Gaskets; Spacers; Sealing of cells
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- G—PHYSICS
- G02—OPTICS
- G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
- G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
- G02F1/01—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour
- G02F1/13—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells
- G02F1/133—Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
- G02F1/1333—Constructional arrangements; Manufacturing methods
- G02F1/1341—Filling or closing of cells
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K19/00—Liquid crystal materials
- C09K19/04—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
- C09K19/06—Non-steroidal liquid crystal compounds
- C09K19/08—Non-steroidal liquid crystal compounds containing at least two non-condensed rings
- C09K19/30—Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
- C09K19/3001—Cyclohexane rings
- C09K19/3003—Compounds containing at least two rings in which the different rings are directly linked (covalent bond)
- C09K2019/3004—Cy-Cy
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- G—PHYSICS
- G02—OPTICS
- G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
- G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
- G02F1/01—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour
- G02F1/13—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells
- G02F1/133—Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
- G02F1/1333—Constructional arrangements; Manufacturing methods
- G02F1/1337—Surface-induced orientation of the liquid crystal molecules, e.g. by alignment layers
- G02F1/133711—Surface-induced orientation of the liquid crystal molecules, e.g. by alignment layers by organic films, e.g. polymeric films
- G02F1/133715—Surface-induced orientation of the liquid crystal molecules, e.g. by alignment layers by organic films, e.g. polymeric films by first depositing a monomer
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- G—PHYSICS
- G02—OPTICS
- G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
- G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
- G02F1/01—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour
- G02F1/13—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells
- G02F1/133—Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
- G02F1/1333—Constructional arrangements; Manufacturing methods
- G02F1/1337—Surface-induced orientation of the liquid crystal molecules, e.g. by alignment layers
- G02F1/133738—Surface-induced orientation of the liquid crystal molecules, e.g. by alignment layers for homogeneous alignment
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- G—PHYSICS
- G02—OPTICS
- G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
- G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
- G02F1/01—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour
- G02F1/13—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells
- G02F1/133—Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
- G02F1/1333—Constructional arrangements; Manufacturing methods
- G02F1/1341—Filling or closing of cells
- G02F1/13415—Drop filling process
Definitions
- the present invention relates to a method for manufacturing a liquid crystal display device. More specifically, the present invention relates to a method for manufacturing a liquid crystal display device suitable for forming a polymer layer for improving characteristics on a horizontal alignment film formed by photo-alignment processing.
- a liquid crystal display is a display device that controls transmission / blocking of light (display on / off) by controlling the orientation of liquid crystal molecules having birefringence.
- LCD display methods include a vertical alignment (VA) mode in which liquid crystal molecules having negative dielectric anisotropy are vertically aligned with respect to the substrate surface, and a liquid crystal having positive or negative dielectric anisotropy.
- VA vertical alignment
- IPS In-plane switching
- FFS fringe field switching
- an alignment stabilization technique using a polymer hereinafter also referred to as PS (Polymer Sustained) technique
- PS Polymer Sustained
- a liquid crystal composition mixed with polymerizable components such as polymerizable monomers and oligomers is sealed between substrates.
- a monomer is polymerized in a state where the liquid crystal molecules are tilted by applying a voltage between the substrates to form a polymer.
- liquid crystal molecules tilted at a predetermined pretilt angle can be obtained, and the orientation direction of the liquid crystal molecules can be defined in a certain direction.
- the monomer a material that is polymerized by heat, light (ultraviolet rays) or the like is selected.
- a polymerization initiator for initiating the polymerization reaction of the monomer may be mixed into the liquid crystal composition (see, for example, Patent Document 4).
- the photo-alignment technique is a technique that uses an active material for light as the material of the alignment film, and irradiates the formed film with light rays such as ultraviolet rays, thereby generating alignment regulating force in the alignment film.
- Non-Patent Document 1 A paper that succeeded in obtaining good results has been published (for example, see Non-Patent Document 1).
- the current photo-alignment technology is mainly introduced for mass production of TVs using a vertical alignment film such as VA mode, and is still introduced for mass production of TVs using a horizontal alignment film such as IPS mode. Not. This is because the use of a horizontal alignment film causes a large amount of image sticking in the liquid crystal display. Burn-in means that when the same voltage is continuously applied to a part of the liquid crystal cell for a certain period of time and then the entire display is changed to another display, the voltage is continuously applied and the voltage is not applied. It is a phenomenon that looks different in brightness.
- FIG. 6 is a schematic view showing a state of image sticking of an IPS mode liquid crystal cell manufactured by performing a photo-alignment process.
- the brightness is greatly different between the voltage (AC) application part and the voltage (AC) non-application part, and it can be seen that intense image sticking occurs in the voltage (AC) application part.
- FIG. 7 is a schematic view showing a state of image sticking of an IPS mode liquid crystal cell manufactured by introducing a photo-alignment process and adopting a PS process. As shown in FIG. 7, it can be seen that the brightness is almost the same between the voltage (AC) application part and the voltage (AC) non-application part, and the image sticking in the voltage (AC) application part is improved. Thus, the image sticking is greatly improved by adding the PS process to the conventional method.
- the improvement effect by the PS process is particularly effective when an alignment film formed from a material having photoactivity is used, for example, a photoinactive material. It was found that the effect of improvement by the PS process cannot be obtained when the rubbing method is performed on the alignment film formed from or when the alignment process itself is not performed.
- FIG. 8 is a schematic diagram for comparing polymerization states of polymerizable monomers when the PS process is performed with an alignment film formed of a photo-inactive material
- FIG. 9 is formed of a photo-active material. It is the schematic diagram which compares the mode of superposition
- the liquid crystal composition filled between the pair of substrates and the pair of substrates is irradiated with light such as ultraviolet rays, and the polymerizable monomer 33 in the liquid crystal layer, 43 starts chain polymerization such as radical polymerization, and the polymer is deposited on the surface of the alignment films 32 and 42 on the liquid crystal layer 30 side to control the alignment of liquid crystal molecules (hereinafter also referred to as PS layer). Is formed.
- the alignment film 42 When the alignment film 42 is inactive to light, the polymerizable monomer 43 a in the liquid crystal layer 30 excited by light irradiation is uniformly generated in the liquid crystal layer 30 as shown in FIG.
- the excited polymerizable monomer 43 b undergoes photopolymerization, and a polymer layer is formed by phase separation at the interface between the alignment film 42 and the liquid crystal layer 30. That is, in the PS process, there is a process in which the polymerizable monomer 43b excited in the bulk moves to the interface between the alignment film 42 and the liquid crystal layer 30 after photopolymerization.
- the alignment film 32 when the alignment film 32 is active with respect to light, a larger amount of the polymerizable monomer 33b in the excited state is formed as shown in FIG. This is because light absorption occurs in the alignment film 32 due to light irradiation, and the excitation energy is transmitted to the polymerizable monomer 33a.
- the polymerizable monomer 33a close to the alignment film 32 receives the excitation energy and is in an excited state. It is easy to change to the polymerizable monomer 33b. That is, the polymerizable monomer 33 a in the liquid crystal layer excited by light irradiation is unevenly distributed near the interface between the alignment film 32 and the liquid crystal layer 30 and exists in a larger amount.
- the alignment film 32 when the alignment film 32 is active with respect to light, the process in which the excited polymerizable monomer 33b moves to the interface between the alignment film 32 and the liquid crystal layer 30 after photopolymerization can be ignored. Therefore, the polymerization reaction and the formation rate of the polymer layer are improved, and a PS layer having a stable orientation regulating force can be formed.
- FIG. 10 is a schematic diagram showing a state when a polymerizable monomer is polymerized with respect to the vertical alignment film.
- FIG. 11 is a schematic diagram showing a state in which a polymerizable monomer is polymerized with respect to the horizontal alignment film.
- the photoactive group 52 constituting the vertical alignment film is indirectly in contact with the liquid crystal molecules 54 and the polymerizable monomer 53 via the hydrophobic group 55, and the light Passing of excitation energy from the active group 52 to the polymerizable monomer 53 hardly occurs.
- the alignment film is a horizontal alignment film
- the photoactive group 62 constituting the horizontal alignment film directly contacts the liquid crystal molecules 64 and the polymerizable monomer 63. Excitation energy is easily transferred to the functional monomer 63. Therefore, the polymerization reaction and the formation rate of the polymer layer are improved, and a PS layer having a stable orientation regulating force can be formed.
- the PS process is performed on an alignment film formed from a photoactive material and when the alignment film is a horizontal alignment film, the transfer of excitation energy is greatly improved and the occurrence of image sticking. Can be greatly reduced.
- FIG. 12 is a photographic diagram showing a state where display unevenness occurs on the outer periphery of the display area in the liquid crystal display panel. Since the sealing material is applied along the outer edge of the substrate, display unevenness occurs along the outer periphery of the display area.
- Such display unevenness is caused, for example, when a PS alignment process is performed using a vertical alignment film, or when a horizontal alignment film is simply formed using a photoactive material without performing the PS conversion process. Such a defect does not occur, and occurs peculiarly when the PS process is performed on the horizontal alignment film using the photoactive material. This difference seems to be due to the difference in reactivity at which PS polymerization occurs. The reactivity of the horizontal alignment film using a photoactive material is very high, and therefore polymerization may proceed due to a factor different from the original PS process.
- the present invention has been made in view of the above situation, and manufacture of a liquid crystal display device that makes it difficult to cause display unevenness in the vicinity of a seal when a PS process is performed on a horizontal alignment film using a photoactive material. It is intended to provide a method.
- the inventors of the present invention have made extensive studies on such problems, and as a PS process, paying attention to the point that it is effective to initiate polymerization by light irradiation, and as a sealing material, a monomer Display unevenness occurs around the display area due to light irradiation for seal curing by using a material that is cured by irradiation with light having a wavelength longer than the absorption wavelength of the material or a material that is cured by being heated. It was found that it can be suppressed. Furthermore, it has been found that unevenness around the display area can be further improved by setting the monomer concentration contained in the liquid crystal composition to a range in which image sticking can be suppressed and exposing the display area while shading (masking) the display area.
- Another aspect of the present invention includes a step of forming a horizontal alignment film containing a photoactive material on at least one of a pair of substrates, a liquid crystal material and a monomer on one of the pair of substrates.
- a liquid crystal display device manufacturing method hereinafter also referred to as a second manufacturing method of the present invention).
- a step of applying a sealing material onto the substrate, a step of bonding the pair of substrates, a step of curing the sealing material, and a liquid crystal composition containing a liquid crystal material and a monomer are vacuum injected between the pair of substrates.
- a process for forming the liquid crystal display device hereinafter also referred to as a third manufacturing method of the present invention).
- a step of forming a horizontal alignment film containing a photoactive material on at least one of the pair of substrates, a liquid crystal material on one substrate of the pair of substrates, and a liquid crystal A step of dropping a liquid crystal composition containing 0.4% by weight or less of the monomer with respect to the entire composition; and the monomer of the monomer with respect to the sealing material applied along the outer edge of one of the pair of substrates. Irradiating the liquid crystal composition sealed between the pair of substrates with a step of irradiating light having a wavelength longer than 10 nm from the absorption wavelength end while shielding the display region to cure the sealing material. And a step of polymerizing the monomer to form a polymer layer for controlling the alignment of adjacent liquid crystal molecules on the horizontal alignment film (hereinafter also referred to as a fourth manufacturing method of the present invention). Say.)
- the components of the liquid crystal display manufacturing method are not particularly limited by other components as long as such components are formed as essential.
- a manufacturing method of the liquid crystal display device and a preferable method thereof will be described in detail.
- a method in which two or more preferable methods for manufacturing the liquid crystal display device described below are combined is also a preferable method for manufacturing the liquid crystal display device.
- the first to fourth manufacturing methods of the present invention include a step of forming a horizontal alignment film containing a photoactive material on at least one of a pair of substrates.
- a horizontal alignment film containing a photoactive material is formed on both of the pair of substrates.
- the horizontal alignment film refers to a film that aligns adjacent liquid crystal molecules substantially horizontally with respect to the horizontal alignment film surface.
- the alignment types of the liquid crystal display devices manufactured by the above manufacturing methods are IPS type, FFS type, OCB (Optically Compensated Bend) type, and TN (Twisted Nematic) type that can use a horizontal alignment film.
- STN Super Twisted Nematic
- FLC Fluorescence Chemical
- PDLC Polymer Dispersed Liquid Crystal
- PNLC Polymer Network Liquid Crystal
- the IPS type or the FFS type is preferable, and a desired orientation can be achieved by a single irradiation of polarized light from the front of the substrate. Therefore, the process is simple and the mass productivity is excellent.
- the FFS type has a flat electrode (solid electrode) in addition to the slit electrode, for example, when the substrates are bonded using an electrostatic chuck, the solid electrode is used as the liquid crystal layer. Since it can be used as a shielding wall that prevents high voltage applied to the film, it is particularly excellent in increasing the efficiency of the manufacturing process.
- the orientation type is also suitable for a form in which a multi-domain structure is formed on at least one of the pair of substrates in order to improve viewing angle characteristics.
- the multi-domain structure is different in the alignment mode of liquid crystal molecules (for example, the bend direction in OCB and the twist direction in TN and STN) or the alignment direction when no voltage is applied, when voltage is applied, or both.
- the horizontal alignment film includes a photoactive material.
- a photoactive material for the horizontal alignment film material for example, when the photopolymerization is performed on the monomer, the base film material is excited, and excitation energy or radical transfer occurs to the monomer. The reactivity can be improved.
- a photo-alignment treatment that imparts alignment characteristics can be performed by irradiating light under certain conditions.
- the polymer film having the property of controlling the alignment of the liquid crystal by the photo-alignment treatment is also referred to as a photo-alignment film.
- the photoactive material examples include a photochromic compound material, a dye material, a fluorescent material, a phosphorescent material, and a photoalignment film material.
- the photoactive materials include terphenyl derivatives, naphthalene derivatives, phenanthrene derivatives, tetracene derivatives, spiropyran derivatives, spiroperimidine derivatives, viologen derivatives, diarylethene derivatives, anthraquinone derivatives, azobenzene derivatives, cinnamoyl derivatives, chalcone derivatives, cinnamate derivatives, coumarin derivatives. It preferably contains at least one chemical structure selected from the group consisting of stilbene derivatives and anthracene derivatives.
- the benzene ring contained in these derivatives may be a heterocyclic ring.
- the “derivative” means one substituted with a specific atom or functional group and one incorporated into a molecular structure as a monovalent or divalent functional group. It does not matter whether these derivatives are in the molecular structure of the polymer main chain, in the molecular structure of the polymer side chain, monomer or oligomer.
- the monomer or oligomer having these photoactive functional groups is contained in the horizontal alignment film material (preferably 3% by weight or more), the polymer itself constituting the horizontal alignment film may be photoinactive.
- the polymer constituting the horizontal alignment film is preferably polysiloxane, polyamic acid or polyimide from the viewpoint of heat resistance.
- the polymer constituting the horizontal alignment film may contain a cyclobutane skeleton.
- the photoactive material is more preferably a photoalignment film material.
- the photo-alignment film is a polymer film having a property of causing anisotropy in the film by irradiation with polarized light or non-polarized light and generating alignment regulating force in the liquid crystal. It does not matter whether the photo-alignment film material is a single polymer or a mixture containing further molecules as long as it has the aforementioned properties.
- the polymer containing a functional group capable of photo-orientation may have a form in which a further low molecule such as an additive or a further polymer that is photoinactive is contained.
- the form in which the additive containing the functional group which can be photo-aligned is mixed with the photo-inactive polymer may be sufficient.
- the photo-alignment film material a material that causes a photodecomposition reaction, a photoisomerization reaction, or a photodimerization reaction is selected. Compared with the photolysis reaction, the photoisomerization reaction and the photodimerization reaction are generally excellent in mass productivity because they can be oriented with a long wavelength and a small irradiation dose.
- a typical material that causes a photolysis reaction is a material containing a compound having a cyclobutane skeleton.
- the material for forming the photo-alignment film preferably includes a compound having a functional group of photoisomerization type, photodimerization type, or both.
- Typical materials that cause a photoisomerization reaction or a photodimerization reaction are azobenzene derivatives, cinnamoyl derivatives, chalcone derivatives, cinnamate derivatives, coumarin derivatives, diarylethene derivatives, stilbene derivatives, and anthracene derivatives.
- the photoisomerization type or photodimerization type functional group is more preferably a cinnamate group or a derivative thereof. These functional groups are particularly excellent in reactivity.
- the benzene ring contained in these functional groups may be a heterocyclic ring.
- the horizontal alignment film is preferably a photo-alignment film that has been subjected to photo-alignment treatment with ultraviolet rays, visible light, or both. Since the alignment of the liquid crystal is fixed by the formation of the PS layer, it is not necessary to prevent ultraviolet rays or visible light from entering the liquid crystal layer after the manufacturing process, and the range of selection of the manufacturing process is widened. Moreover, it is preferable that the said horizontal alignment film is a photo-alignment film by which the photo-alignment process was carried out by polarization or non-polarization.
- the alignment regulating force by the horizontal alignment film is mainly determined by the type of photo-alignment film material (photo functional group). Depending on the type of light, light irradiation time, light irradiation intensity, type of photo functional group, etc. The orientation azimuth, the pretilt angle, etc. can be adjusted.
- a liquid crystal composition containing a liquid crystal material and a monomer of 1.0% by weight or less with respect to the entire liquid crystal composition is dropped onto one of the pair of substrates.
- the sealing material by irradiating light with a wavelength longer than the absorption wavelength end of the monomer the polymerization reaction of the monomer that starts polymerization by ultraviolet light is prevented, and display unevenness that occurs along the outer edge of the display area is prevented. be able to.
- the “absorption wavelength end” is a wavelength located at the end of the absorption wavelength range of the monomer, and specifically, a measurement target at a concentration of 1.4 ⁇ 10 ⁇ 4 mol / L in chloroform. This is the wavelength at which the absorbance (Absorbance / cm) is 0.01 or less in the absorbance measurement using light having an optical path length of 10 mm.
- the absorption wavelength end of the monomer can be determined by using, for example, a visible-ultraviolet absorption spectrum measuring device V7100 (manufactured by JASCO Corporation).
- light having a wavelength longer than 40 nm longer than the absorption wavelength end of the monomer is irradiated by light having a wavelength slightly longer than the wavelength at the absorption wavelength end of the monomer. This point will be described in detail in an evaluation test described later.
- the second production method of the present invention includes a step of dropping a liquid crystal composition containing a liquid crystal material and a monomer on one of the pair of substrates, and along an outer edge of the one of the pair of substrates. And the step of curing the sealing material by applying heat without applying light to the sealing material applied. By applying heat, in the step of curing the sealing material, the polymerization reaction of the monomer that initiates polymerization by light can be prevented, and display unevenness that occurs along the outer edge of the display region can be prevented. In the second production method of the present invention, it is necessary to use a PS monomer whose polymerization does not proceed sufficiently by heat.
- a liquid crystal layer is formed between a pair of substrates using a liquid crystal dropping (ODF) method.
- ODF liquid crystal dropping
- a third manufacturing method of the present invention includes a step of applying a sealing material on the substrate along an outer edge of one of the pair of substrates, a step of bonding the pair of substrates, and the sealing material.
- a pair of substrates bonded together by a sealing material is immersed in a dish in which a liquid crystal material is stored in a vacuum state, and then the atmospheric pressure is changed to an internal / external pressure difference and A method of injecting a liquid crystal material using capillary action.
- the liquid crystal material can be filled, and the problem that the PS process proceeds by light irradiation for curing the sealing material does not occur in the first place.
- a liquid crystal composition containing a liquid crystal material and a monomer of 0.4% by weight or less with respect to the entire liquid crystal composition is dropped onto one of the pair of substrates. Irradiating the sealing material applied along the outer edge of one of the pair of substrates with a wavelength of 10 nm or more longer than the absorption wavelength end of the monomer while shielding the display region, And a step of curing the sealing material.
- the concentration of the monomer contained in the liquid crystal composition is reduced, and further, the display area is shielded during irradiation, so that even if the sealing material is cured with light of a shorter wavelength, the display is performed.
- the liquid crystal composition sealed between the pair of substrates is irradiated with light, the monomer is polymerized, and close to the horizontal alignment film. Forming a polymer layer for controlling alignment of liquid crystal molecules. Due to the contrivances described above, the polymerization of the monomer that initiates the polymerization by light irradiation is hindered in the sealing material curing step, so that the polymer layer can be formed without causing display unevenness.
- the polymer layer is formed by polymerizing monomers contained in the liquid crystal composition, and controls alignment of adjacent liquid crystal molecules.
- the monomer starts polymerization upon irradiation with light to form a polymer layer.
- the polymerizable functional group of the monomer is preferably an acrylate group, a methacrylate group, a vinyl group, or a vinyloxy group.
- an acrylate group or a methacrylate group is preferable.
- An acrylate group or a methacrylate group has a high radical generation probability and is effective in shortening the manufacturing tact time.
- the number of polymerizable functional groups possessed by the monomer is preferably 2 or more.
- the reaction efficiency increases, so that polymerization by light irradiation in a short time becomes possible.
- the number of polymerizable functional groups in the monomer is too large, the number of polymerizable functional groups that the monomer has is more preferably in consideration of the point that the molecular weight is increased and the monomer is difficult to dissolve in the liquid crystal. 4 or less.
- the polymerization reaction for forming the PS layer is not particularly limited.
- Any of the “chain polymerization” in which monomers are successively bound to the active species generated from the above and chain-grown is included.
- Examples of the sequential polymerization include polycondensation and polyaddition.
- Examples of the chain polymerization include radical polymerization, ionic polymerization (anionic polymerization, cationic polymerization, etc.) and the like.
- the horizontal alignment film is a photo-alignment film
- the light for forming the PS layer that is, the polymer is polymerized to form a polymer layer that controls the alignment of adjacent liquid crystal molecules on the horizontal alignment film.
- the light used in the step is preferably linearly polarized light. This is because the photo-alignment film is considered to deteriorate the orientation due to the influence of light for curing the sealing material.
- linearly polarized light when forming the PS layer after the step of curing the sealing material, the alignment of the liquid crystal adjacent to the photo-alignment film and the polymer layer can be improved, and as a result, the contrast ratio can be improved. it can.
- the alignment regulating force of the horizontal alignment film can be improved.
- the occurrence of display burn-in can be greatly reduced, and the display quality can be greatly improved.
- the polymer layer is formed. Is formed in a shape having a pretilt alignment with respect to the liquid crystal molecules.
- the electrode is preferably a transparent electrode.
- Examples of such an electrode material include translucent materials such as indium tin oxide (ITO: Indium Tin Oxide) and indium zinc oxide (IZO).
- ITO Indium Tin Oxide
- IZO indium zinc oxide
- the liquid crystal composition preferably contains liquid crystal molecules containing multiple bonds other than the conjugated double bond of the benzene ring in the molecular structure.
- a functional group having multiple bonds such as an alkenyl group
- the progress of the PS reaction can be further promoted. This is probably because the multiple bonds of the liquid crystal molecules themselves can be activated by light, and secondly, they can be transporters that can exchange activation energy and radicals. It is done.
- the liquid crystal molecules may be either one having positive dielectric anisotropy (positive type) or one having negative dielectric anisotropy (negative type).
- the liquid crystal molecules are preferably nematic liquid crystal molecules having high symmetry in the liquid crystal layer. Examples of the molecular skeleton of the liquid crystal molecule include those having a structure in which two ring structures and a group bonded to the ring structure are linearly connected.
- the multiple bond does not include a conjugated double bond of a benzene ring. This is because the benzene ring is poor in reactivity.
- the said liquid crystal molecule may have the conjugated double bond of a benzene ring, and this bond is not specifically excluded.
- the liquid crystal composition may be a mixture of a plurality of types. In order to ensure reliability, improve the response speed, and adjust the liquid crystal phase temperature range, elastic constant, dielectric anisotropy and refractive index anisotropy, the liquid crystal composition is a mixture of a plurality of liquid crystal molecules. It is possible.
- the multiple bond is preferably a double bond, and is preferably contained in an ester group or an alkenyl group.
- the double bond is more reactive than the triple bond.
- the multiple bond may be a triple bond.
- the triple bond is preferably contained in a cyano group.
- the liquid crystal molecules preferably have two or more types of the multiple bonds.
- the liquid crystal molecules preferably include at least one molecular structure selected from the group consisting of the following formulas (1-1) to (1-6). Particularly preferred is a molecular structure comprising the following formula (1-4).
- the polymerization reaction of the monomer added to the liquid crystal composition by the curing process of the sealing material does not proceed, so that display unevenness does not occur along the formation site of the sealing material, and display quality such as image sticking is achieved.
- a liquid crystal display device with little deterioration can be obtained.
- FIG. 2 is a schematic cross-sectional view of a liquid crystal display device manufactured by the method for manufacturing a liquid crystal display device of Examples 1 to 12, showing a state before the PS polymerization step.
- FIG. 3 is a schematic cross-sectional view of a liquid crystal display device manufactured by the method for manufacturing a liquid crystal display device of Examples 1 to 12, and shows a state after the PS polymerization step.
- 3 is a schematic plan view of a slit-containing electrode substrate of Example 1.
- FIG. It is a graph which shows the absorption spectrum of the compound represented by following Chemical formula (5), and the compound represented by following Chemical formula (6).
- a liquid crystal display device manufactured by the method for manufacturing a liquid crystal display device of Examples 1 to 12 is a display device including a liquid crystal cell, and is used for a TV panel, digital signage, a medical monitor, an electronic book, a PC monitor, and a tablet terminal. It can be suitably used for panels, panels for mobile phone terminals, and the like.
- FIG. 1 and 2 are schematic cross-sectional views of liquid crystal display devices manufactured by the liquid crystal display device manufacturing methods of Examples 1 to 12.
- FIG. FIG. 1 shows before the PS polymerization step
- FIG. 2 shows after the PS polymerization step.
- the liquid crystal display device includes an array substrate 10, a color filter substrate 20, and a liquid crystal layer 30 sandwiched between a pair of substrates including the array substrate 10 and the color filter substrate 20.
- the array substrate 10 includes an insulating transparent substrate 11 made of glass or the like, and further includes various wirings formed on the transparent substrate 11, pixel electrodes, common electrodes, TFTs, and the like.
- the color filter substrate 20 includes an insulating transparent substrate 21 made of glass or the like, a color filter formed on the transparent substrate 21, a black matrix, and the like. For example, in the IPS mode, an electrode is formed only on the array substrate 10, but in another mode, etc., an electrode is formed on both the array substrate 10 and the color filter substrate 20 as necessary. Is formed.
- the array substrate 10 includes a horizontal alignment film 12, and the color filter substrate 20 also includes a horizontal alignment film 22.
- the horizontal alignment films 12 and 22 are films mainly composed of polyimide, polyamide, polyvinyl, polysiloxane, and the like. By forming the horizontal alignment film, the liquid crystal molecules that are adjacent to each other are substantially aligned with respect to the horizontal alignment film surface. It can be oriented horizontally.
- the horizontal alignment films 12 and 22 include a photoactive material, for example, a material including a compound having a photoactive functional group as described above.
- the polymerizable monomer 3 is present in the liquid crystal layer 30 before the PS polymerization step. Then, the polymerizable monomer 3 starts to be polymerized by the PS polymerization process, and becomes the PS layers 13 and 23 on the horizontal alignment films 12 and 22 as shown in FIG. Improve power.
- the polymerizable monomer 3 may be used by mixing a plurality of types.
- the PS layers 13 and 23 inject a liquid crystal composition containing a liquid crystal material and a polymerizable monomer between the array substrate 10 and the color filter substrate 20 to irradiate the liquid crystal layer 30 with a certain amount of light, It can be formed by polymerizing the polymerizable monomer 3. At this time, by performing polymerization in a state where a voltage equal to or higher than the threshold is applied to the liquid crystal layer 30, PS layers 13 and 23 having a shape along the initial inclination of the liquid crystal molecules are formed. PS layers 13 and 23 having high properties can be obtained. In addition, you may add a polymerization initiator to a liquid-crystal composition as needed.
- Examples of the polymerizable monomer 3 that can be used in Examples 1 to 12 include one or more monomers having a monofunctional or polyfunctional polymerizable group having a ring structure. Examples of such a monomer include the following chemical formula (2);
- R 1 represents —R 2 —Sp 1 —P 1 group, hydrogen atom, halogen atom, —CN group, —NO 2 group, —NCO group, —NCS group, —OCN group, —SCN group, —SF 5 group. Or a linear or branched alkyl group having 1 to 12 carbon atoms.
- P 1 represents a polymerizable group.
- Sp 1 represents a linear, branched or cyclic alkylene group or alkyleneoxy group having 1 to 6 carbon atoms, or a direct bond.
- Hydrogen atoms R 1 has may be substituted by a fluorine atom or a chlorine atom.
- the —CH 2 — group of R 1 is an —O— group, —S— group, —NH— group, —CO— group, —COO— group, —OCO— group unless an oxygen atom and a sulfur atom are adjacent to each other.
- —O—COO— group —OCH 2 — group, —CH 2 O— group, —SCH 2 — group, —CH 2 S— group, —N (CH 3 ) — group, —N (C 2 H 5 ) — Group, —N (C 3 H 7 ) — group, —N (C 4 H 9 ) — group, —CF 2 O— group, —OCF 2 — group, —CF 2 S— group, —SCF 2 — Group, —N (CF 3 ) — group, —CH 2 CH 2 — group, —CF 2 CH 2 — group, —CH 2 CF 2 — group, —CF 2 CF 2 — group, —CH ⁇ CH— group, It may be substituted with a —CF ⁇ CF— group, —C ⁇ C— group, —CH ⁇ CH—COO— group, or —OCO—CH ⁇ CH— group.
- R 2 represents —O— group, —S— group, —NH— group, —CO— group, —COO— group, —OCO— group, —O—COO— group, —OCH 2 — group, —CH 2 O— group, —SCH 2 — group, —CH 2 S— group, —N (CH 3 ) — group, —N (C 2 H 5 ) — group, —N (C 3 H 7 ) — group, —N (C 4 H 9 ) — group, —CF 2 O— group, —OCF 2 — group, —CF 2 S— group, —SCF 2 — group, —N (CF 3 ) — group, —CH 2 CH 2 — Group, —CF 2 CH 2 — group, —CH 2 CF 2 — group, —CF 2 CF 2 — group, —CH ⁇ CH— group, —CF ⁇ CF— group, —C ⁇ C— group, —CH ⁇ It
- a 1 and A 2 are the same or different and each represents 1,2-phenylene group, 1,3-phenylene group, 1,4-phenylene group, naphthalene-1,4-diyl group, naphthalene-1,5-diyl group , Naphthalene-2,6-diyl group, 1,4-cyclohexylene group, 1,4-cyclohexenylene group, 1,4-bicyclo [2.2.2] octylene group, piperidine-1,4-diyl group , Naphthalene-2,6-diyl group, decahydronaphthalene-2,6-diyl group, 1,2,3,4-tetrahydronaphthalene-2,6-diyl group, indane-1,3-diyl group, indane- 1,5-diyl group), indan-2,5-diyl group, phenanthrene-1,6-diyl group, phenanthrene-1,8
- the —CH 2 — groups of A 1 and A 2 may be substituted with —O— groups or —S— groups as long as they are not adjacent to each other.
- a hydrogen atom of A 1 and A 2 is substituted with a fluorine atom, a chlorine atom, a —CN group, or an alkyl group having 1 to 6 carbon atoms, an alkoxy group, an alkylcarbonyl group, an alkoxycarbonyl group, or an alkylcarbonyloxy group. It may be.
- Z is the same or different and represents an —O— group, —S— group, —NH— group, —CO— group, —COO— group, —OCO— group, —O—COO— group, —OCH 2 — group.
- n is 0, 1 or 2.
- P 1 is the same or different and represents a polymerizable group.
- Part or all of the hydrogen atoms of the benzene ring are substituted with halogen atoms, or alkyl groups or alkoxy groups having 1 to 12 carbon atoms.
- any or all of the hydrogen atoms of the alkyl group or alkoxy group having 1 to 12 carbon atoms may be substituted with a halogen atom. Is mentioned.
- the monomers represented by the above chemical formulas (3-1) to (3-5) are compounds that cause photocleavage upon irradiation with ultraviolet light and generate radicals. Therefore, the polymerization reaction can be performed without a polymerization initiator. It is possible to proceed, and it is possible to prevent deterioration in display quality such as burn-in caused by the polymerization initiator remaining after the PS process is completed.
- Examples of P 1 include an acryloyloxy group, a methacryloyloxy group, a vinyl group, a vinyloxy group, an acryloylamino group, and a methacryloylamino group.
- Examples of other polymerizable monomers 3 that can be used in Examples 1 to 12 include the following chemical formulas (4-1) to (4-8);
- R 3 and R 4 may be the same or different and each represents a —Sp 2 —P 2 group, a hydrogen atom, a halogen atom, —CN group, —NO 2 group, —NCO group, —NCS group, —OCN group, —SCN group , —SF 5 group, or a linear or branched alkyl group having 1 to 12 carbon atoms, an aralkyl group, or a phenyl group. At least one of R 3 and R 4 includes a —Sp 2 —P 2 group.
- P 2 represents a polymerizable group.
- Sp 2 represents a linear, branched or cyclic alkylene group or alkyleneoxy group having 1 to 6 carbon atoms, or a direct bond.
- R 3 and R 4 is a linear or branched alkyl group having 1 to 12 carbon atoms, an aralkyl group, or a phenyl group
- the hydrogen atom that at least one of R 3 and R 4 has is ,
- a fluorine atom, a chlorine atom or a —Sp 2 —P 2 group may be substituted.
- the —CH 2 — group possessed by R 1 and R 2 is an —O— group, —S— group, —NH— group, —CO— group, —COO— unless an oxygen atom, sulfur atom and nitrogen atom are adjacent to each other.
- Part or all of the hydrogen atoms of the benzene ring may be substituted with a halogen atom, or an alkyl group or alkoxy group having 1 to 12 carbon atoms.
- part or all of the hydrogen atoms of the alkyl group or alkoxy group having 1 to 12 carbon atoms may be substituted with a halogen atom.
- Examples of P 2 include an acryloyloxy group, a methacryloyloxy group, a vinyl group, a vinyloxy group, an acryloylamino group, and a methacryloylamino group.
- the compounds represented by the above chemical formulas (4-1) to (4-8) are compounds that generate radicals by extracting hydrogen when irradiated with visible light, so that the polymerization reaction can be performed even without a polymerization initiator. It is possible to proceed, and it is possible to prevent deterioration of display quality such as image sticking caused by the polymerization initiator remaining even after the PS process is completed.
- a sealant 81 is provided between the array substrate 10 and the color filter substrate 20 along the outer edges of these substrates.
- the sealing material 81 for example, a resin that is cured by light or heat is used.
- the liquid crystal layer 30 is formed by bonding the array substrate 10 and the color filter substrate 20 with the sealant 81 with the liquid crystal composition sandwiched therebetween. Since the PS process is performed after the sealing material is attached, the sealing material 81 is formed on the horizontal alignment films 12 and 22 as shown in FIG. 2, but the PS layers 13 and 23 are surrounded by the sealing material 81. Formed in the region.
- the array substrate 10, the liquid crystal layer 30, and the color filter substrate 20 are laminated in this order from the back side of the liquid crystal display device to the observation surface side to form a liquid crystal cell.
- a linear polarizing plate is provided on the back side of the array substrate 10 and the observation surface side of the color filter substrate 20.
- a retardation plate may be further arranged to form a circularly polarizing plate.
- the liquid crystal display device may be any of a transmission type, a reflection type, and a reflection / transmission type.
- the liquid crystal display device further includes a backlight.
- the backlight is disposed on the back side of the liquid crystal cell, and is disposed such that light is transmitted through the array substrate 10, the liquid crystal layer 30, and the color filter substrate 20 in this order.
- the array substrate 10 includes a reflection plate for reflecting external light. Further, at least in a region where reflected light is used as a display, the polarizing plate of the color filter substrate 20 needs to be a circularly polarizing plate.
- the liquid crystal display device includes a color filter on array (COA) that forms a color filter on an array substrate, or a black matrix on array (BOA) that forms a black matrix on an array substrate. It is good also as a form.
- COA color filter on array
- BOA black matrix on array
- a monochrome display or a field sequential color method may be used, and in that case, a color filter need not be arranged.
- the liquid crystal layer 30 is filled with a liquid crystal material having a characteristic of being oriented in a specific direction when a constant voltage is applied.
- the orientation of the liquid crystal molecules in the liquid crystal layer 30 is controlled by applying a voltage higher than a threshold value.
- GC-MS Gas-Chromatograph-Mass-Spectrometry
- TOF-SIMS Time-of-Flight-Secondary-Ion-Mass-Spectrometry
- Example 1 is an example of manufacturing an FFS mode liquid crystal cell.
- Example 1 corresponds to the first production method of the present invention.
- a TFT substrate (FFS substrate) having a slit electrode and a flat electrode (solid electrode) and a counter substrate having a color filter are prepared, and a polyvinyl cinnamate solution as a material of a horizontal alignment film is prepared on each substrate.
- the size of the TFT substrate is 10 inches.
- One of the slit electrode and the solid electrode is a signal electrode, and the other is a common electrode.
- FIG. 3 is a schematic plan view of the electrode substrate with slit according to the first embodiment. The double-headed arrow in FIG.
- the slit 71a of the slit electrode has a V-shape, the width L of the slit 71a of the slit electrode is 3 ⁇ m, and the distance S between the slits 71a is 5 ⁇ m.
- a polyvinyl cinnamate solution was prepared by dissolving polyvinyl cinnamate to 3% by weight in a solvent in which N-methyl-2-pyrrolidone and ethylene glycol monobutyl ether were mixed in equal amounts.
- the film thickness of the alignment film after baking was 75 nm on the slit electrode in the display area (active area) of the TFT substrate. Further, it was 85 nm in the display area (active area) of the color filter substrate.
- a photospacer was formed on the counter substrate so that the thickness of the liquid crystal layer in the display region (active area) was 3.5 ⁇ m.
- the bottom diameter of the photo spacer was 12 ⁇ m. The bottom diameter is defined as the diameter of the portion of the photospacer that is in contact with the immediate lower layer of the alignment film.
- the surface of each substrate was irradiated with linearly polarized ultraviolet rays as an alignment treatment from the normal direction of the substrate so as to be 5 J / cm 2 at a wavelength of 313 nm.
- the degree of polarization of the linearly polarized light at this time was 30: 1.
- the angle formed between the length direction of the slit electrode and the polarization direction was 10 °.
- the liquid crystal molecules 74 have an orientation in a direction substantially perpendicular to the polarization direction of the linearly polarized ultraviolet light when no voltage is applied, and the slit electrodes are applied when a voltage exceeding the threshold is applied. It has orientation in a direction substantially perpendicular to the length direction.
- a heat-visible light combined sealing material (World Rock: manufactured by Kyoritsu Chemical Industry Co., Ltd.) was drawn on the TFT substrate along the outer edge of the TFT substrate using a dispenser.
- a liquid crystal composition containing a liquid crystal material and a monomer was dropped onto the counter substrate.
- the liquid crystal composition MLC-6610 (manufactured by Merck & Co., Inc.), the liquid crystal molecule trans-4-propyl-4′-vinyl-1,1′-bicyclohexane having an alkenyl group is added to the entire liquid crystal composition.
- the amount of biphenyl-4,4′-diylbis (2-methyl acrylate) represented by the following chemical formula (5) as a monomer is 1.0% by weight with respect to the entire liquid crystal composition. What was added to was used.
- the absorption wavelength end of the monomer represented by the following chemical formula (5) is 325 nm, and is a compound in which polymerization does not proceed sufficiently by light of 365 nm or more or heat.
- the arrangement of the two types of substrates was adjusted so that the polarization directions of the irradiated ultraviolet rays coincided with each other, and these were bonded together.
- the pressure was applied to the bonded substrates at a pressure of 0.5 kgf / cm 2 , and the seal was cured using an ultra-high pressure UV lamp (USH-500D: manufactured by USHIO INC.).
- a filter for cutting light having a wavelength of 380 nm or less was disposed between the bonded substrate and the ultra-high pressure UV lamp so that ultraviolet rays were not irradiated onto the substrate.
- the above steps were all performed under a yellow fluorescent lamp so that the ultraviolet light from the fluorescent lamp was not exposed in the liquid crystal cell. Further, immediately before the next PS treatment, the liquid crystal cell was heated at 130 ° C. for 40 minutes, and the charge removal treatment was performed carefully.
- Example 2 A liquid crystal cell was produced by the same process as in Example 1 except that the types of monomers were different.
- Example 2 corresponds to the first production method of the present invention.
- a liquid crystal composition trans-4-propyl-4′-vinyl-1,1′-bicyclohexane having an alkenyl group is used for MLC-6610 (manufactured by Merck).
- the phenanthrene-2,7-diylbis (2-methyl acrylate) represented by the following chemical formula (6) as a monomer is 1.0% by weight with respect to the whole liquid crystal composition. What was added so that it might become% was used.
- the absorption wavelength end of the monomer represented by the following chemical formula (6) is 360 nm, and is a compound whose polymerization does not proceed sufficiently by light of 405 nm or more or heat.
- FIG. 4 is a graph showing absorption spectra of the compound represented by the chemical formula (5) and the compound represented by the chemical formula (6).
- a visible-ultraviolet absorption spectrum measuring device V7100 manufactured by JASCO Corporation was used.
- Example 3 In Example 3, except that a thermosetting sealing material (HC1413FP: manufactured by Mitsui Chemicals, Inc.) was used as the sealing material, and no ultra-high pressure UV lamp was applied to cure the sealing material.
- a liquid crystal cell was produced by the same process as in Example 1.
- Example 3 corresponds to the second production method of the present invention. When this liquid crystal cell was used to assemble a liquid crystal display panel and the display was visually confirmed, a good display with little unevenness of alignment was obtained.
- Comparative Example 1 In order to cure the sealing material without using a filter that cuts light with a wavelength of 380 nm or less, using a heat-ultraviolet combined sealing material (Photorec S-WB: manufactured by Sekisui Chemical Co., Ltd.) as the sealing material A liquid crystal cell was assembled in the same manner as in Example 3 except that UV irradiation was performed using an ultra-high pressure UV lamp (USH-500D: manufactured by USHIO INC.). Confirmed over the entire display area.
- a heat-ultraviolet combined sealing material (Photorec S-WB: manufactured by Sekisui Chemical Co., Ltd.) as the sealing material
- a liquid crystal cell was assembled in the same manner as in Example 3 except that UV irradiation was performed using an ultra-high pressure UV lamp (USH-500D: manufactured by USHIO INC.). Confirmed over the entire display area.
- Comparative Example 2 When the sealing material was cured, a quartz glass plated with chrome was disposed to shield the display area, and the display area was not irradiated with ultraviolet light. As shown in FIG. 12, uneven orientation along the sealing material (the outer periphery of the display area) was confirmed.
- Example 4 is an example of manufacturing an FFS mode liquid crystal cell.
- Example 4 corresponds to the third production method of the present invention.
- As the material of the slit electrode 71 and the solid electrode 72 a translucent material was used.
- the slit 71a of the slit electrode has a V-shape, the width L of the slit 71a of the slit electrode is 3 ⁇ m, and the distance S between the slits 71a is 5 ⁇ m.
- a polyvinyl cinnamate solution was prepared by dissolving polyvinyl cinnamate to 3% by weight in a solvent in which N-methyl-2-pyrrolidone and ethylene glycol monobutyl ether were mixed in equal amounts.
- the film thickness of the alignment film after baking was 75 nm on the slit electrode in the display area (active area) of the TFT substrate. Further, it was 85 nm in the display area (active area) of the color filter substrate.
- a photospacer was formed on the counter substrate so that the thickness of the liquid crystal layer in the display region (active area) was 3.5 ⁇ m.
- the bottom diameter of the photo spacer was 12 ⁇ m. The bottom diameter is defined by the diameter of the layer immediately below the alignment film and the portion of the photo spacer.
- each substrate was irradiated with linearly polarized ultraviolet rays as an alignment treatment from the normal direction of the substrate so as to be 5 J / cm 2 at a wavelength of 313 nm.
- the angle formed by the length direction of the slit electrode and the polarization direction was 10 °.
- a heat-ultraviolet combined seal material (Photorec S-WB: manufactured by Sekisui Chemical Co., Ltd.) was drawn on the TFT substrate along the outer edge of the TFT substrate using a dispenser. At this time, as the drawing pattern, an injection port was provided in part so that the liquid crystal composition could be injected in a later step.
- the arrangement of the two types of substrates was adjusted so that the polarization directions of the irradiated ultraviolet rays coincided with each other, and these were bonded together.
- the pressure was applied to the bonded substrates at a pressure of 0.5 kgf / cm 2 , and the seal was cured using an ultra-high pressure UV lamp (USH-500D: manufactured by USHIO INC.). Thereafter, heating was continued at 130 ° C. for 40 minutes while continuing to pressurize, thereby further curing the seal.
- USH-500D manufactured by USHIO INC.
- a liquid crystal composition containing a liquid crystal material and a monomer was injected between the pair of substrates using a vacuum injection (Dip) method.
- the same liquid crystal composition as in Example 1 was used.
- the injection port of the cell was sealed with an epoxy adhesive (Araldite AR-S30: manufactured by Nichiban Co., Ltd.).
- the above steps were all performed under a yellow fluorescent lamp so that the ultraviolet light from the fluorescent lamp was not exposed in the liquid crystal cell. Further, immediately before the next PS treatment, the liquid crystal cell was heated at 130 ° C. for 40 minutes, and the charge removal treatment was performed carefully.
- Comparative Example 3 As a liquid crystal injection method, a liquid crystal cell was assembled by the same method as in Example 4 except that the liquid crystal dropping method was used instead of the vacuum injection method (that is, the same as Comparative Example 1), and the display was visually confirmed. As shown in FIG. 12, uneven orientation along the sealing material (the outer periphery of the display area) was confirmed.
- Example 5 a liquid crystal cell was completed in the same manner as in Example 1 except that a polyimide solution having a cyclobutane skeleton was used as the alignment film material and the conditions for the alignment treatment were used.
- the alignment film material was applied to the substrate and dried under the same conditions as in Example 1.
- the surface of each substrate was irradiated with linearly polarized ultraviolet rays as an alignment treatment from the normal direction of each substrate so as to be 500 mJ / cm 2 at a wavelength of 254 nm. Thereby, the alignment film material applied on the substrate caused a photodecomposition reaction, and a horizontal alignment film was formed.
- Evaluation test 1 In order to verify how much the wavelength of light for curing the sealing material affects the polymerization of the monomer when the compound represented by the chemical formula (5) is used as a monomer, Reference Examples 1 to 4 liquid crystal cells were produced and tested.
- Reference example 1 A set of raw glass substrates having no electrode or the like was prepared, and a polyvinyl cinnamate solution serving as a material for the horizontal alignment film was applied onto each substrate by a spin coating method.
- a polyvinyl cinnamate solution was prepared by dissolving polyvinyl cinnamate to 3% by weight in a solvent in which N-methyl-2-pyrrolidone and ethylene glycol monobutyl ether were mixed in equal amounts.
- each substrate was irradiated with linearly polarized ultraviolet rays as an alignment treatment from the normal direction of the substrate so as to be 5 J / cm 2 at a wavelength of 313 nm.
- thermosetting sealing material (HC1413FP: manufactured by Mitsui Chemicals, Inc.) was drawn on one substrate along the outer edge of the one substrate using a screen plate. At this time, as the drawing pattern, an injection port was provided in part so that the liquid crystal composition could be injected in a later step.
- the pressure was applied to the bonded substrates at a pressure of 0.5 kgf / cm 2 , and the seal was cured using an ultra-high pressure UV lamp (USH-500D: manufactured by USHIO INC.). Thereafter, heating was continued at 130 ° C. for 60 minutes while continuing to pressurize, thereby further curing the seal.
- USH-500D manufactured by USHIO INC.
- a liquid crystal composition including a liquid crystal material and a monomer was injected between the pair of substrates using a vacuum injection method.
- the liquid crystal composition the liquid crystal molecule trans-4-propyl-4′-vinyl-1,1′-bicyclohexane was 5% by weight with respect to the entire liquid crystal composition, with respect to MLC-6610 (manufactured by Merck).
- a monomer in which biphenyl-4,4′-diylbis (2-methyl acrylate) was added as a monomer in an amount of 0.3% by weight based on the entire liquid crystal composition was used.
- the injection port of the cell was sealed with an epoxy adhesive (Araldite AR-S30: manufactured by Nichiban Co., Ltd.).
- the electrodes were short-circuited so that the liquid crystal alignment was not disturbed by the external field, and the surface of the glass substrate was subjected to charge removal treatment. At this point, the liquid crystal molecules are fluidly aligned.
- the entire liquid crystal cell was irradiated with light of 2 J / cm 2 through a 340 nm band pass filter using an ultrahigh pressure UV lamp (USH-500D: manufactured by USHIO INC.) As a light source.
- an ultrahigh pressure UV lamp USH-500D: manufactured by USHIO INC.
- the liquid crystal cell of Reference Example 1 thus prepared was heated at 130 ° C. for 40 minutes and subjected to realignment treatment. As a result, PS polymerization proceeded in the liquid crystal composition, and the liquid crystal alignment was fixed. Had to hold.
- Reference example 2 Reference Example 1 except that an ultra-high pressure UV lamp (USH-500D: manufactured by Ushio Electric Co., Ltd.) was used as a light source and the entire liquid crystal cell was irradiated with 2 J / cm 2 of light through a 360 nm bandpass filter and the PS process was performed.
- a liquid crystal cell of Reference Example 2 was produced using the same method as described above. When this liquid crystal cell was heated at 130 ° C. for 40 minutes and subjected to realignment treatment, PS polymerization proceeded in the liquid crystal composition, and the alignment of the liquid crystal was fixed, and the liquid crystal retained the fluid alignment. .
- an ultra-high pressure UV lamp USH-500D: manufactured by Ushio Electric Co., Ltd.
- Reference example 3 Reference Example 1 except that the entire liquid crystal cell was irradiated with 2 J / cm 2 of light through a 365 nm band pass filter using an ultra-high pressure UV lamp (USH-500D: manufactured by USHIO INC.) As a light source.
- a liquid crystal cell of Reference Example 3 was produced using the same method as described above. When this liquid crystal cell was heated at 130 ° C. for 40 minutes and subjected to a realignment treatment, the liquid crystal canceled the flow alignment and became uniform uniaxial alignment.
- Reference example 4 Reference Example 1 except that an ultra high pressure UV lamp (USH-500D: manufactured by USHIO INC.) Was used as a light source, and the entire liquid crystal cell was irradiated with 2 J / cm 2 of light through a 370 nm bandpass filter and the PS process was performed.
- a liquid crystal cell of Reference Example 4 was produced using the same method as described above. When this liquid crystal cell was heated at 130 ° C. for 40 minutes and subjected to a realignment treatment, the liquid crystal canceled the flow alignment and became uniform uniaxial alignment.
- Evaluation test 2 In order to verify how much the wavelength of light for curing the sealing material affects the polymerization of the monomer when the compound represented by the chemical formula (6) is used as a monomer, Reference Examples 5 to 8 liquid crystal cells were produced and tested.
- Reference Example 5 Using the compound represented by the chemical formula (6) as a monomer, and using an ultra-high pressure UV lamp (USH-500D: manufactured by Ushio Inc.) as a light source, light of 2 J / cm 2 is liquid crystal through a 380 nm band pass filter.
- a liquid crystal cell of Reference Example 5 was produced using the same method as Reference Example 1 except that the entire cell was irradiated and the PS step was performed. When this liquid crystal cell was heated at 130 ° C. for 40 minutes and subjected to realignment treatment, PS polymerization proceeded in the liquid crystal composition, and the alignment of the liquid crystal was fixed, and the liquid crystal retained the fluid alignment. .
- Reference Example 6 Reference Example 5 except that the entire liquid crystal cell was irradiated with 2 J / cm 2 of light through a 390 nm band pass filter using an ultra-high pressure UV lamp (USH-500D: manufactured by USHIO INC.) As a light source.
- a liquid crystal cell of Reference Example 6 was produced using the same method. When this liquid crystal cell was heated at 130 ° C. for 40 minutes and subjected to realignment treatment, PS polymerization proceeded in the liquid crystal composition, and the alignment of the liquid crystal was fixed, and the liquid crystal retained the fluid alignment. .
- Reference Example 7 Reference Example 5 except that the entire liquid crystal cell was irradiated with 2 J / cm 2 light through a 400 nm bandpass filter using an ultra-high pressure UV lamp (USH-500D: manufactured by USHIO INC.) As a light source.
- a liquid crystal cell of Reference Example 7 was produced using the same method. When this liquid crystal cell was heated at 130 ° C. for 40 minutes and subjected to a realignment treatment, the liquid crystal canceled the flow alignment and became uniform uniaxial alignment.
- Reference Example 8 Reference Example 5 except that the ultra high pressure UV lamp (USH-500D: manufactured by USHIO INC.) Was used as the light source and the entire liquid crystal cell was irradiated with 2 J / cm 2 of light through a 420 nm bandpass filter and the PS process was performed.
- a liquid crystal cell of Reference Example 8 was produced using the same method. When this liquid crystal cell was heated at 130 ° C. for 40 minutes and subjected to a realignment treatment, the liquid crystal canceled the flow alignment and became uniform uniaxial alignment.
- FIG. 5 is a graph showing that the absorption wavelength differs between when the monomer is dissolved in the liquid crystal and when the monomer is dissolved in a solvent such as chloroform.
- the absorption spectrum of a molecule floating in a vacuum or a solvent with a molecule existing in an aggregated state such as a solid the absorption spectrum of the solid becomes broader as shown in FIG. This is because the interaction between molecules is stronger in the solid than in the liquid.
- the monomer is dissolved in the liquid crystal, and the interaction with the liquid crystal molecules having a large number of polar groups and electrons. Seems to be working hard. Therefore, the monomer can take more various molecular conformations or electronically excited states. As a result, the absorption spectrum of the monomer in the liquid crystal becomes broader than that of the monomer dissolved in a solvent such as chloroform, and the absorption wavelength. It is considered that the end has a longer wavelength. Then, it can be estimated from the results of the evaluation tests 1 and 2 that the value of the long wavelength is about +40 nm.
- seal curing when seal curing is performed with light having a wavelength of about 40 nm longer than the absorption wavelength end of the monomer, seal curing may be insufficient depending on the type of monomer.
- the absorption wavelength end of phenanthrene-2,7-diylbis (2-methylacrylate) represented by the chemical formula (6) used in Example 2 is 360 nm, and the light used for seal curing becomes visible light.
- the sealing material is cured with visible light, it is preferable that light having a wavelength shorter than +40 nm can be used because the tact time of the curing process becomes longer. That is, it is more preferable that the light used for seal curing has a shorter wavelength than +40 nm while being longer than the absorption wavelength end of the monomer.
- the present inventors conducted extensive studies and found that the monomer concentration was set to 1.0% by weight or less, and the display area was shielded during irradiation, thereby sealing with light having a shorter wavelength. It has been found that display unevenness hardly occurs along the outer edge of the display area even if the material is cured. By this method, the degree of cure of the sealing material is increased and the peel strength is improved, and since the seal curing is completed with a low irradiation dose, the tact time can be shortened. This is the idea of the fourth manufacturing method of the present invention described above. Examples are shown below.
- Example 6 The content of the monomer contained in the liquid crystal composition is 0.4% by weight with respect to the entire liquid crystal composition, and light having a wavelength of 335 nm or less is emitted between the bonded substrate and the ultrahigh pressure UV lamp. A filter to be cut and quartz glass plated with chrome for shielding the display area were arranged so that ultraviolet rays were not irradiated to the display area. Others were carried out in the same manner as in Example 1.
- a liquid crystal display panel was assembled using the liquid crystal cell thus prepared, and the display was visually confirmed. As a result, a good display with no alignment unevenness and little image sticking was obtained.
- Example 7 The content of the monomer contained in the liquid crystal composition is 0.4% by weight based on the whole liquid crystal composition, and the monomer includes phenanthrene-2,7-diylbis (2-methyl) represented by the above chemical formula (6).
- Acrylate and between the bonded substrate and the ultra-high pressure UV lamp, a filter that cuts off light with a wavelength of 370 nm or less and quartz glass that is plated with chromium to shield the display area This was carried out in the same manner as in Example 1 except that it was arranged so that the display area was not irradiated with ultraviolet rays.
- a liquid crystal display panel was assembled using the liquid crystal cell thus prepared, and the display was visually confirmed. As a result, a good display with no alignment unevenness and little image sticking was obtained.
- Evaluation test 3 In order to verify how much the wavelength of light for curing the sealant affects the polymerization of the monomer when the compound represented by the chemical formula (5) is used as a monomer, Reference Examples 9 to Twelve liquid crystal cells were produced and tested.
- Reference Example 9 The use of the compound represented by the chemical formula (5) as a monomer, and the content of the monomer contained in the liquid crystal composition is 0.4% by weight with respect to the entire liquid crystal composition.
- USH-500D (made by USHIO ELECTRIC CO., LTD.) was used as a light source, passed through a 315 nm bandpass filter, the display area was shielded, and 1 J / cm 2 of light was applied to the entire liquid crystal cell, and the PS process was performed.
- a liquid crystal cell of Reference Example 9 was produced using the same method as in Reference Example 1. When this liquid crystal cell was heated at 130 ° C. for 40 minutes and subjected to realignment treatment, PS polymerization progressed in the region along the sealing material in the liquid crystal composition (the outer edge of the display region), and the alignment of the liquid crystal was fixed. And retained the flow orientation.
- Reference Example 10 Using an ultra high pressure UV lamp (USH-500D: manufactured by USHIO INC.) As a light source, passing through a 325 nm bandpass filter, shielding the display area, irradiating the entire liquid crystal cell with 1 J / cm 2 light, and performing the PS process A liquid crystal cell of Reference Example 10 was produced using the same method as in Reference Example 9 except that. When this liquid crystal cell was heated at 130 ° C. for 40 minutes and subjected to realignment treatment, PS polymerization progressed in the region along the sealing material in the liquid crystal composition (the outer edge of the display region), and the alignment of the liquid crystal was fixed. And retained the flow orientation.
- USH-500D manufactured by USHIO INC.
- Reference Example 11 Using an ultra-high pressure UV lamp (USH-500D: manufactured by USHIO INC.) As a light source, passing through a 335 nm bandpass filter, shielding the display area, irradiating the entire liquid crystal cell with 1 J / cm 2 light, and performing the PS process A liquid crystal cell of Reference Example 11 was produced using the same method as in Reference Example 9 except that. When this liquid crystal cell was heated at 130 ° C. for 40 minutes and subjected to a realignment treatment, the liquid crystal canceled the flow alignment and became uniform uniaxial alignment.
- USH-500D manufactured by USHIO INC.
- Reference Example 12 Using an ultra-high pressure UV lamp (USH-500D: manufactured by USHIO INC.) As a light source, passing through a 345 nm bandpass filter, shielding the display area of the liquid crystal cell, irradiating the entire liquid crystal cell with 1 J / cm 2 , PS A liquid crystal cell of Reference Example 12 was produced using the same method as in Reference Example 9 except that the steps were performed. When this liquid crystal cell was heated at 130 ° C. for 40 minutes and subjected to a realignment treatment, the liquid crystal canceled the flow alignment and became uniform uniaxial alignment.
- USH-500D manufactured by USHIO INC.
- Evaluation test 4 In order to verify how much the wavelength of light for curing the sealing material affects the polymerization of the monomer when the compound represented by the chemical formula (6) is used as a monomer, Reference Examples 13 to Sixteen liquid crystal cells were produced and tested.
- Reference Example 13 Using the compound represented by the above chemical formula (6) as a monomer, and using a super high pressure UV lamp (USH-500D: manufactured by USHIO INC.) As a light source, passing through a 350 nm bandpass filter and shielding the display area.
- a liquid crystal cell of Reference Example 13 was produced using the same method as Reference Example 9 except that the entire liquid crystal cell was irradiated with 1 J / cm 2 of light and the PS step was performed. When this liquid crystal cell was heated at 130 ° C. for 40 minutes and subjected to realignment treatment, PS polymerization proceeded in the region along the sealing material in the liquid crystal composition (the outer edge of the display region), and the alignment of the liquid crystal was fixed. And retained the flow orientation.
- Reference Example 14 Using an ultra-high pressure UV lamp (USH-500D: manufactured by USHIO INC.) As a light source, passing through a 360 nm bandpass filter, shielding the display area, irradiating the entire liquid crystal cell with 1 J / cm 2 light, and performing the PS process A liquid crystal cell of Reference Example 14 was produced using the same method as in Reference Example 9 except that. When this liquid crystal cell was heated at 130 ° C. for 40 minutes and subjected to realignment treatment, PS polymerization progressed in the region along the sealing material in the liquid crystal composition (the outer edge of the display region), and the alignment of the liquid crystal was fixed. And retained the flow orientation.
- USH-500D manufactured by USHIO INC.
- Reference Example 15 Using an ultra-high pressure UV lamp (USH-500D: manufactured by USHIO INC.) As a light source, passing through a 370 nm bandpass filter, shielding the display area, irradiating the entire liquid crystal cell with 1 J / cm 2 light, and performing the PS process A liquid crystal cell of Reference Example 15 was produced using the same method as in Reference Example 9 except that. When this liquid crystal cell was heated at 130 ° C. for 40 minutes and subjected to a realignment treatment, the liquid crystal canceled the flow alignment and became uniform uniaxial alignment.
- USH-500D manufactured by USHIO INC.
- Reference Example 16 Using an ultra-high pressure UV lamp (USH-500D: manufactured by USHIO INC.) As a light source, passing through a 380 nm bandpass filter, shielding the display area, irradiating the entire liquid crystal cell with 1 J / cm 2 light, and performing the PS process A liquid crystal cell of Reference Example 16 was produced using the same method as in Reference Example 9 except that. When this liquid crystal cell was heated at 130 ° C. for 40 minutes and subjected to a realignment treatment, the liquid crystal canceled the flow alignment and became uniform uniaxial alignment.
- USH-500D manufactured by USHIO INC.
- Evaluation test 5 In order to verify how much the wavelength of light for curing the sealing material affects the polymerization of the monomer when the compound represented by the chemical formula (5) is used as a monomer, Reference Examples 17 to Twenty liquid crystal cells were produced and tested.
- Reference Example 17 The use of the compound represented by the chemical formula (5) as a monomer, and the content of the monomer contained in the liquid crystal composition is 1.0% by weight with respect to the entire liquid crystal composition, USH-500D (made by USHIO ELECTRIC CO., LTD.) Was used as a light source, passed through a 315 nm bandpass filter, the display area was shielded, and 1 J / cm 2 of light was applied to the entire liquid crystal cell, and the PS process was performed.
- a liquid crystal cell of Reference Example 17 was produced using the same method as in Reference Example 1. When this liquid crystal cell was heated at 130 ° C. for 40 minutes and subjected to realignment treatment, PS polymerization progressed in the region along the sealing material in the liquid crystal composition (the outer edge of the display region), and the alignment of the liquid crystal was fixed. And retained the flow orientation.
- Reference Example 18 Using an ultra high pressure UV lamp (USH-500D: manufactured by USHIO INC.) As a light source, passing through a 325 nm bandpass filter, shielding the display area, irradiating the entire liquid crystal cell with 1 J / cm 2 light, and performing the PS process A liquid crystal cell of Reference Example 18 was produced using the same method as in Reference Example 17 except that. When this liquid crystal cell was heated at 130 ° C. for 40 minutes and subjected to realignment treatment, PS polymerization progressed in the region along the sealing material in the liquid crystal composition (the outer edge of the display region), and the alignment of the liquid crystal was fixed. And retained the flow orientation.
- USH-500D manufactured by USHIO INC.
- Reference Example 19 Using an ultra-high pressure UV lamp (USH-500D: manufactured by USHIO INC.) As a light source, passing through a 335 nm bandpass filter, shielding the display area, irradiating the entire liquid crystal cell with 1 J / cm 2 light, and performing the PS process A liquid crystal cell of Reference Example 19 was produced using the same method as in Reference Example 17 except that. When this liquid crystal cell was heated at 130 ° C. for 40 minutes and subjected to a realignment treatment, the liquid crystal canceled the flow alignment and became uniform uniaxial alignment.
- USH-500D manufactured by USHIO INC.
- Reference Example 20 Using an ultra-high pressure UV lamp (USH-500D: manufactured by USHIO INC.) As a light source, passing through a 345 nm bandpass filter, shielding the display area of the liquid crystal cell, irradiating the entire liquid crystal cell with 1 J / cm 2 , PS A liquid crystal cell of Reference Example 20 was produced using the same method as in Reference Example 17 except that the steps were performed. When this liquid crystal cell was heated at 130 ° C. for 40 minutes and subjected to a realignment treatment, the liquid crystal canceled the flow alignment and became uniform uniaxial alignment.
- USH-500D manufactured by USHIO INC.
- Evaluation test 6 In order to verify how much the wavelength of light for curing the sealant affects the polymerization of the monomer when the compound represented by the chemical formula (6) is used as a monomer, Reference Examples 21 to 24 liquid crystal cells were produced and tested.
- Reference Example 21 Using the compound represented by the chemical formula (6) as a monomer, and passing a 350 nm bandpass filter using an ultra-high pressure UV lamp (USH-500D: manufactured by USHIO INC.) As a light source, and shielding the display area A liquid crystal cell of Reference Example 21 was produced using the same method as Reference Example 17 except that the entire liquid crystal cell was irradiated with 1 J / cm 2 of light and the PS step was performed. When this liquid crystal cell was heated at 130 ° C. for 40 minutes and subjected to realignment treatment, PS polymerization progressed in the region along the sealing material in the liquid crystal composition (the outer edge of the display region), and the alignment of the liquid crystal was fixed. And retained the flow orientation.
- an ultra-high pressure UV lamp USH-500D: manufactured by USHIO INC.
- Reference Example 22 Using an ultra-high pressure UV lamp (USH-500D: manufactured by USHIO INC.) As a light source, passing through a 360 nm bandpass filter, shielding the display area, irradiating the entire liquid crystal cell with 1 J / cm 2 light, and performing the PS process A liquid crystal cell of Reference Example 22 was produced using the same method as in Reference Example 17 except that. When this liquid crystal cell was heated at 130 ° C. for 40 minutes and subjected to realignment treatment, PS polymerization progressed in the region along the sealing material in the liquid crystal composition (the outer edge of the display region), and the alignment of the liquid crystal was fixed. And retained the flow orientation.
- USH-500D manufactured by USHIO INC.
- Reference Example 23 Using an ultra-high pressure UV lamp (USH-500D: manufactured by USHIO INC.) As a light source, passing through a 370 nm bandpass filter, shielding the display area, irradiating the entire liquid crystal cell with 1 J / cm 2 light, and performing the PS process A liquid crystal cell of Reference Example 23 was produced using the same method as in Reference Example 17 except that. When this liquid crystal cell was heated at 130 ° C. for 40 minutes and subjected to a realignment treatment, the liquid crystal canceled the flow alignment and became uniform uniaxial alignment.
- USH-500D manufactured by USHIO INC.
- Reference Example 24 Using an ultra-high pressure UV lamp (USH-500D: manufactured by USHIO INC.) As a light source, passing through a 380 nm bandpass filter, shielding the display area, irradiating the entire liquid crystal cell with 1 J / cm 2 light, and performing the PS process A liquid crystal cell of Reference Example 24 was produced in the same manner as in Reference Example 17 except that. When this liquid crystal cell was heated at 130 ° C. for 40 minutes and subjected to a realignment treatment, the liquid crystal canceled the flow alignment and became uniform uniaxial alignment.
- USH-500D manufactured by USHIO INC.
- Example 8 In Example 1, non-polarized ultraviolet rays were irradiated when the liquid crystal cell was subjected to PS treatment.
- a UV-B ultraviolet lamp FHF32-UVB: manufactured by Sankyo Electric Co., Ltd.
- FHF32-UVB manufactured by Sankyo Electric Co., Ltd.
- the degree of polarization at this time was 10: 1.
- the polarization direction is the same direction as the polarization when the alignment treatment is performed on the photo-alignment film. Except for these, a liquid crystal cell was produced in the same manner as in Example 1. As a result, a uniform uniaxially aligned liquid crystal cell was obtained, and the orientation of the liquid crystal was further improved as compared with Example 1.
- the contrast ratio increased by about 10%.
- Example 9 A liquid crystal cell was produced in the same manner as in Example 2 except that the same linearly polarized ultraviolet light as in Example 8 was irradiated during the PS treatment. As a result, a liquid crystal cell in which the liquid crystal was uniaxially aligned without unevenness was obtained. The alignment of the liquid crystal was improved as compared with Example 2, and the contrast ratio was increased by about 10% compared to Example 2.
- Example 10 A liquid crystal cell was produced in the same manner as in Example 5 except that the same linearly polarized ultraviolet light as in Example 8 was irradiated during the PS treatment. As a result, a liquid crystal cell in which the liquid crystal was uniaxially aligned without unevenness was obtained. The alignment of the liquid crystal was improved as compared with Example 5, and the contrast ratio was increased by about 5% compared to Example 5.
- Example 11 A liquid crystal cell was produced in the same manner as in Example 6 except that the same linearly polarized ultraviolet light as in Example 8 was irradiated during PS treatment. As a result, a liquid crystal cell in which the liquid crystal was uniaxially aligned without unevenness was obtained. The alignment of the liquid crystal was improved as compared with Example 6, and the contrast ratio was increased by about 10% with respect to Example 6.
- Example 12 A liquid crystal cell was produced in the same manner as in Example 7 except that the same linearly polarized ultraviolet light as in Example 8 was irradiated during the PS treatment. As a result, a liquid crystal cell in which the liquid crystal was uniaxially aligned without unevenness was obtained. The orientation of the liquid crystal was improved as compared with Example 7, and the contrast ratio was increased by about 10% compared to Example 7.
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Abstract
Description
R1は、-R2-Sp1-P1基、水素原子、ハロゲン原子、-CN基、-NO2基、-NCO基、-NCS基、-OCN基、-SCN基、-SF5基、又は、炭素数1~12の直鎖状若しくは分枝状のアルキル基である。
P1は、重合性基を表す。
Sp1は、炭素数1~6の直鎖状、分枝状若しくは環状のアルキレン基若しくはアルキレンオキシ基、又は、直接結合を表す。
R1が有する水素原子は、フッ素原子又は塩素原子に置換されていてもよい。
R1が有する-CH2-基は、酸素原子及び硫黄原子が互いに隣接しない限り-O-基、-S-基、-NH-基、-CO-基、-COO-基、-OCO-基、-O-COO-基、-OCH2-基、-CH2O-基、-SCH2-基、-CH2S-基、-N(CH3)-基、-N(C2H5)-基、-N(C3H7)-基、-N(C4H9)-基、-CF2O-基、-OCF2-基、-CF2S-基、-SCF2-基、-N(CF3)-基、-CH2CH2-基、-CF2CH2-基、-CH2CF2-基、-CF2CF2-基、-CH=CH-基、-CF=CF-基、-C≡C-基、-CH=CH-COO-基、又は、-OCO-CH=CH-基で置換されていてもよい。
R2は、-O-基、-S-基、-NH-基、-CO-基、-COO-基、-OCO-基、-O-COO-基、-OCH2-基、-CH2O-基、-SCH2-基、-CH2S-基、-N(CH3)-基、-N(C2H5)-基、-N(C3H7)-基、-N(C4H9)-基、-CF2O-基、-OCF2-基、-CF2S-基、-SCF2-基、-N(CF3)-基、-CH2CH2-基、-CF2CH2-基、-CH2CF2-基、-CF2CF2-基、-CH=CH-基、-CF=CF-基、-C≡C-基、-CH=CH-COO-基、-OCO-CH=CH-基、又は、直接結合を表す。
A1及びA2は、同一又は異なって、1,2-フェニレン基、1,3-フェニレン基、1,4-フェニレン基、ナフタレン-1,4-ジイル基、ナフタレン-1,5-ジイル基、ナフタレン-2,6-ジイル基、1,4-シクロヘキシレン基、1,4-シクロヘキセニレン基、1,4-ビシクロ[2.2.2]オクチレン基、ピペリジン-1,4-ジイル基、ナフタレン-2,6-ジイル基、デカヒドロナフタレン-2,6-ジイル基、1,2,3,4-テトラヒドロナフタレン-2,6-ジイル基、インダン-1,3-ジイル基、インダン-1,5-ジイル基)、インダン-2,5-ジイル基、フェナントレン-1,6-ジイル基、フェナントレン-1,8-ジイル基、フェナントレン-2,7-ジイル基、フェナントレン-3,6-ジイル基、アントラセン-1,5‐ジイル基、アントラセン-1,8-ジイル基、アントラセン-2,6-ジイル基、又は、アントラセン-2,7-ジイル基を表す。
A1及びA2が有する-CH2-基は、互いに隣接しない限り-O-基又は-S-基で置換されていてもよい。
A1及びA2が有する水素原子は、フッ素原子、塩素原子、-CN基、又は、炭素数1~6のアルキル基、アルコキシ基、アルキルカルボニル基、アルコキシカルボニル基若しくはアルキルカルボニルオキシ基で置換されていてもよい。
Zは、同一又は異なって、-O-基、-S-基、-NH-基、-CO-基、-COO-基、-OCO-基、-O-COO-基、-OCH2-基、-CH2O-基、-SCH2-基、-CH2S-基、-N(CH3)-基、-N(C2H5)-基、-N(C3H7)-基、-N(C4H9)-基、-CF2O-基、-OCF2-基、-CF2S-基、-SCF2-基、-N(CF3)-基、-CH2CH2-基、-CF2CH2-基、-CH2CF2-基、-CF2CF2-基、-CH=CH-基、-CF=CF-基、-C≡C-基、-CH=CH-COO-基、-OCO-CH=CH-基、又は、直接結合を表す。
nは0、1又は2である。)
で表される化合物が挙げられる。
R3及びR4は、同一又は異なって、-Sp2-P2基、水素原子、ハロゲン原子、-CN基、-NO2基、-NCO基、-NCS基、-OCN基、-SCN基、-SF5基、又は、炭素数1~12の直鎖状若しくは分枝状のアルキル基、アラルキル基若しくはフェニル基を表す。
R3及びR4の少なくとも一方は、-Sp2-P2基を含む。
P2は、重合性基を表す。
Sp2は、炭素数1~6の直鎖状、分枝状若しくは環状のアルキレン基若しくはアルキレンオキシ基、又は、直接結合を表す。
R3及びR4の少なくとも一方が、炭素数1~12の直鎖状又は分枝状のアルキル基、アラルキル基又はフェニル基であるとき、上記R3及びR4の少なくとも一方が有する水素原子は、フッ素原子、塩素原子又は-Sp2-P2基に置換されていてもよい。
R1及びR2が有する-CH2-基は、酸素原子、硫黄原子及び窒素原子が互いに隣接しない限り-O-基、-S-基、-NH-基、-CO-基、-COO-基、-OCO-基、-O-COO-基、-OCH2-基、-CH2O-基、-SCH2-基、-CH2S-基、-N(CH3)-基、-N(C2H5)-基、-N(C3H7)-基、-N(C4H9)-基、-CF2O-基、-OCF2-基、-CF2S-基、-SCF2-基、-N(CF3)-基、-CH2CH2-基、-CF2CH2-基、-CH2CF2-基、-CF2CF2-基、-CH=CH-基、-CF=CF-基、-C≡C-基、-CH=CH-COO-基、又は、-OCO-CH=CH-基で置換されていてもよい。
ベンゼン環が有する水素原子の一部又は全部は、ハロゲン原子、又は、炭素数1~12のアルキル基若しくはアルコキシ基に置換されていてもよい。また、上記炭素数1~12のアルキル基若しくはアルコキシ基が有する水素原子の一部又は全部は、ハロゲン原子に置換されていてもよい。)
で表されるいずれかの化合物が挙げられる。
実施例1は、FFSモードの液晶セルの作製例である。また、実施例1は、本発明の第一の製造方法に相当する。スリット入り電極と平板状の電極(ベタ電極)とを有するTFT基板(FFS基板)と、カラーフィルタを有する対向基板とを用意し、水平配向膜の材料となるポリビニルシンナメート溶液をそれぞれの基板上にスピンコート法により塗布した。TFT基板の大きさは10インチである。上記スリット入り電極とベタ電極とでは、一方が信号電極となり、他方が共通電極となる。図3は、実施例1のスリット入り電極基板の平面模式図である。図3の両矢印は、照射偏光方向(ネガ型液晶分子を用いる場合)を示す。スリット入り電極71及びベタ電極72の材料としては、透光性の材料を用いた。また、スリット入り電極のスリット71aの形状はV字状とし、スリット入り電極のスリット71aの幅Lは3μm、スリット71a間距離Sは5μmとした。ポリビニルシンナメート溶液は、N-メチル-2-ピロリドンとエチレングリコールモノブチルエーテルを等量で混合した溶媒に、ポリビニルシンナメートが全体の3重量%となるように溶かして調製した。
モノマーの種類が異なることを除き、実施例1と同じ工程により、液晶セルを作製した。実施例2は、本発明の第一の製造方法に相当する。具体的には、液晶組成物としては、MLC-6610(メルク社製)に対し、アルケニル基を有する液晶性分子trans-4-プロピル-4’-ビニル-1,1’-ビシクロヘキサンを液晶組成物全体に対して5重量%となるように、かつモノマーとして下記化学式(6)で表されるフェナントレン-2,7-ジイルビス(2-メチルアクリレート)を液晶組成物全体に対して1.0重量%となるように添加したものを用いた。なお、下記化学式(6)で表されるモノマーの吸収波長端は、360nmであり、405nm以上の光、又は、熱によって重合が充分に進行しない化合物である。
実施例3においては、シール材として熱硬化シール材(HC1413FP:三井化学社製)を用いたこと、及び、シール材を硬化させるための超高圧UVランプによる紫外線の照射を行わなかったことを除き、実施例1と同じ工程により、液晶セルを作製した。実施例3は、本発明の第二の製造方法に相当する。この液晶セルを用いて液晶表示パネルを組み立て、表示を目視にて確認したところ、配向ムラがなく焼き付きの少ない良好な表示が得られた。
シール材として熱-紫外線併用シール材(フォトレックS-WB:積水化学工業社製)を使用し、かつ380nm以下の波長の光をカットするフィルタを配置することなく、シール材を硬化させるために超高圧UVランプ(USH-500D:ウシオ電機社製)による紫外線の照射を行ったこと以外は、実施例3と同様の方法で液晶セルを組み立て、表示を目視にて確認したところ、配向ムラが表示領域全体で確認された。
シール材を硬化させる際に、表示領域を遮光するためにクロムでメッキされた石英ガラスを配置し、紫外線が表示領域に照射されないようにしたこと以外は、比較例1と同様に実施したところ、図12で示したような、シール材(表示領域の外周)に沿った配向ムラが確認された。
実施例4は、FFSモードの液晶セルの作製例である。実施例4は、本発明の第三の製造方法に相当する。スリット入り電極と平板状の電極(ベタ電極)とをTFT基板(FFS基板)と、カラーフィルタを有する対向基板とを用意し、水平配向膜の材料となるポリビニルシンナメート溶液をそれぞれの基板上にスピンコート法により塗布した。TFT基板の大きさは10インチである。スリット入り電極71及びベタ電極72の材料としては、透光性の材料を用いた。また、スリット入り電極のスリット71aの形状はV字状とし、スリット入り電極のスリット71aの幅Lは3μm、スリット71a間距離Sは5μmとした。ポリビニルシンナメート溶液は、N-メチル-2-ピロリドンとエチレングリコールモノブチルエーテルを等量で混合した溶媒に、ポリビニルシンナメートが全体の3重量%となるように溶かして調製した。
液晶注入法として、真空注入法ではなく液晶滴下法を用いたこと以外は、実施例4と同様の方法で液晶セルを組み立て(すなわち、比較例1と同じ)、表示を目視にて確認したところ、図12で示したような、シール材(表示領域の外周)に沿った配向ムラが確認された。
実施例5では、配向膜材料としてシクロブタン骨格を有するポリイミド溶液を用いたこと、及び、配向処理の条件以外は、実施例1と同様にして液晶セルを完成させた。配向膜材料の基板への塗布及び乾燥は、実施例1と同様の条件とした。各基板の表面に対し、配向処理として直線偏光紫外線を、波長254nmにおいて500mJ/cm2となるように、各基板の法線方向から照射した。これにより、基板上に塗布された配向膜材料が光分解反応を起こし、水平配向膜が形成された。
上記化学式(5)で表される化合物をモノマーとして用いたときに、シール材を硬化させる光の波長がどの程度であればモノマーの重合に影響が出るかを検証するために、参考例1~4の液晶セルを作製して実験を行った。
電極等を有しない素ガラス基板を一組用意し、水平配向膜の材料となるポリビニルシンナメート溶液をそれぞれの基板上にスピンコート法により塗布した。ポリビニルシンナメート溶液は、N-メチル-2-ピロリドンとエチレングリコールモノブチルエーテルを等量で混合した溶媒に、ポリビニルシンナメートが全体の3重量%となるように溶かして調製した。
超高圧UVランプ(USH-500D:ウシオ電機社製)を光源として、360nmバンドパスフィルターを通して2J/cm2の光を、液晶セル全体に照射し、PS工程を行ったこと以外は、参考例1と同様の方法を用いて参考例2の液晶セルを作製した。この液晶セルを130℃で40分間加熱し、再配向処理を行ったところ、液晶組成物中ではPS重合が進んで液晶の配向が固定化されており、液晶は流動配向を保持してしまった。
超高圧UVランプ(USH-500D:ウシオ電機社製)を光源として、365nmバンドパスフィルターを通して2J/cm2の光を、液晶セル全体に照射し、PS工程を行ったこと以外は、参考例1と同様の方法を用いて参考例3の液晶セルを作製した。この液晶セルを130℃で40分間加熱し、再配向処理を行ったところ、液晶は流動配向を解消し、ムラのない一軸配向となった。
超高圧UVランプ(USH-500D:ウシオ電機社製)を光源として、370nmバンドパスフィルターを通して2J/cm2の光を、液晶セル全体に照射し、PS工程を行ったこと以外は、参考例1と同様の方法を用いて参考例4の液晶セルを作製した。この液晶セルを130℃で40分間加熱し、再配向処理を行ったところ、液晶は流動配向を解消し、ムラのない一軸配向となった。
上記化学式(6)で表される化合物をモノマーとして用いたときに、シール材を硬化させる光の波長がどの程度であればモノマーの重合に影響が出るかを検証するために、参考例5~8の液晶セルを作製して実験を行った。
モノマーとして上記化学式(6)で表される化合物を用いたこと、及び、超高圧UVランプ(USH-500D:ウシオ電機社製)を光源として、380nmバンドパスフィルターを通して2J/cm2の光を液晶セル全体に照射し、PS工程を行ったこと以外は、参考例1と同様の方法を用いて参考例5の液晶セルを作製した。この液晶セルを130℃で40分間加熱し、再配向処理を行ったところ、液晶組成物中ではPS重合が進んで液晶の配向が固定化されており、液晶は流動配向を保持してしまった。
超高圧UVランプ(USH-500D:ウシオ電機社製)を光源として、390nmバンドパスフィルターを通して2J/cm2の光を液晶セル全体に照射し、PS工程を行ったこと以外は、参考例5と同様の方法を用いて参考例6の液晶セルを作製した。この液晶セルを130℃で40分間加熱し、再配向処理を行ったところ、液晶組成物中ではPS重合が進んで液晶の配向が固定化されており、液晶は流動配向を保持してしまった。
超高圧UVランプ(USH-500D:ウシオ電機社製)を光源として、400nmバンドパスフィルターを通して2J/cm2の光を液晶セル全体に照射し、PS工程を行ったこと以外は、参考例5と同様の方法を用いて参考例7の液晶セルを作製した。この液晶セルを130℃で40分間加熱し、再配向処理を行ったところ、液晶は流動配向を解消し、ムラのない一軸配向となった。
超高圧UVランプ(USH-500D:ウシオ電機社製)を光源として、420nmバンドパスフィルターを通して2J/cm2の光を液晶セル全体に照射し、PS工程を行ったこと以外は、参考例5と同様の方法を用いて参考例8の液晶セルを作製した。この液晶セルを130℃で40分間加熱し、再配向処理を行ったところ、液晶は流動配向を解消し、ムラのない一軸配向となった。
液晶組成物に含まれるモノマーの含有量を、液晶組成物全体に対して0.4重量%とし、更に、貼り合わせた基板と超高圧UVランプとの間には、335nm以下の波長の光をカットするフィルタと、表示領域を遮光するためにクロムでメッキされた石英ガラスを配置し、紫外線が表示領域に照射されないようにした。その他は実施例1と同様に実施した。
液晶組成物に含まれるモノマーの含有量を、液晶組成物全体に対して0.4重量%とし、モノマーには、上記化学式(6)で表されるフェナントレン-2,7-ジイルビス(2-メチルアクリレート)を使用し、更に、貼り合わせた基板と超高圧UVランプとの間には、370nm以下の波長の光をカットするフィルタと、表示領域を遮光するためにクロムでメッキされた石英ガラスを配置し、紫外線が表示領域に照射されないようにしたこと以外は、実施例1と同様に実施した。
上記化学式(5)で表される化合物をモノマーとして用いたときに、シール材を硬化させる光の波長がどの程度であればモノマーの重合に影響が出るかを検証するために、参考例9~12の液晶セルを作製して実験を行った。
モノマーとして上記化学式(5)で表される化合物を用いたこと、及び、液晶組成物に含まれるモノマーの含有量を、液晶組成物全体に対して0.4重量%とし、超高圧UVランプ(USH-500D:ウシオ電機社製)を光源として、315nmバンドパスフィルターを通し、表示領域を遮光して、1J/cm2の光を液晶セル全体に照射し、PS工程を行ったこと以外は、参考例1と同様の方法を用いて参考例9の液晶セルを作製した。この液晶セルを130℃で40分間加熱し、再配向処理を行ったところ、液晶組成物中のシール材に沿った領域(表示領域の外縁)においてはPS重合が進んで液晶の配向が固定化され、流動配向を保持してしまった。
超高圧UVランプ(USH-500D:ウシオ電機社製)を光源として、325nmバンドパスフィルターを通し、表示領域を遮光して、1J/cm2の光を液晶セル全体に照射し、PS工程を行ったこと以外は、参考例9と同様の方法を用いて参考例10の液晶セルを作製した。この液晶セルを130℃で40分間加熱し、再配向処理を行ったところ、液晶組成物中のシール材に沿った領域(表示領域の外縁)においてはPS重合が進んで液晶の配向が固定化され、流動配向を保持してしまった。
超高圧UVランプ(USH-500D:ウシオ電機社製)を光源として、335nmバンドパスフィルターを通し、表示領域を遮光して、1J/cm2の光を液晶セル全体に照射し、PS工程を行ったこと以外は、参考例9と同様の方法を用いて参考例11の液晶セルを作製した。この液晶セルを130℃で40分間加熱し、再配向処理を行ったところ、液晶は流動配向を解消して、ムラのない一軸配向となった。
超高圧UVランプ(USH-500D:ウシオ電機社製)を光源として、345nmバンドパスフィルターを通し、液晶セルの表示領域を遮光して、1J/cm2の光を液晶セル全体に照射し、PS工程を行ったこと以外は、参考例9と同様の方法を用いて参考例12の液晶セルを作製した。この液晶セルを130℃で40分間加熱し、再配向処理を行ったところ、液晶は流動配向を解消して、ムラのない一軸配向となった。
上記化学式(6)で表される化合物をモノマーとして用いたときに、シール材を硬化させる光の波長がどの程度であればモノマーの重合に影響が出るかを検証するために、参考例13~16の液晶セルを作製して実験を行った。
モノマーとして上記化学式(6)で表される化合物を用いたこと、及び、超高圧UVランプ(USH-500D:ウシオ電機社製)を光源として、350nmバンドパスフィルターを通し、表示領域を遮光して、1J/cm2の光を液晶セル全体に照射し、PS工程を行ったこと以外は、参考例9と同様の方法を用いて参考例13の液晶セルを作製した。この液晶セルを130℃で40分間加熱し、再配向処理を行ったところ、液晶組成物中のシール材に沿った領域(表示領域の外縁)においてはPS重合が進んで液晶の配向が固定化され、流動配向を保持してしまった。
超高圧UVランプ(USH-500D:ウシオ電機社製)を光源として、360nmバンドパスフィルターを通し、表示領域を遮光して、1J/cm2の光を液晶セル全体に照射し、PS工程を行ったこと以外は、参考例9と同様の方法を用いて参考例14の液晶セルを作製した。この液晶セルを130℃で40分間加熱し、再配向処理を行ったところ、液晶組成物中のシール材に沿った領域(表示領域の外縁)においてはPS重合が進んで液晶の配向が固定化され、流動配向を保持してしまった。
超高圧UVランプ(USH-500D:ウシオ電機社製)を光源として、370nmバンドパスフィルターを通し、表示領域を遮光して、1J/cm2の光を液晶セル全体に照射し、PS工程を行ったこと以外は、参考例9と同様の方法を用いて参考例15の液晶セルを作製した。この液晶セルを130℃で40分間加熱し、再配向処理を行ったところ、液晶は流動配向を解消して、ムラのない一軸配向となった。
超高圧UVランプ(USH-500D:ウシオ電機社製)を光源として、380nmバンドパスフィルターを通し、表示領域を遮光して、1J/cm2の光を液晶セル全体に照射し、PS工程を行ったこと以外は、参考例9と同様の方法を用いて参考例16の液晶セルを作製した。この液晶セルを130℃で40分間加熱し、再配向処理を行ったところ、液晶は流動配向を解消して、ムラのない一軸配向となった。
上記化学式(5)で表される化合物をモノマーとして用いたときに、シール材を硬化させる光の波長がどの程度であればモノマーの重合に影響が出るかを検証するために、参考例17~20の液晶セルを作製して実験を行った。
モノマーとして上記化学式(5)で表される化合物を用いたこと、及び、液晶組成物に含まれるモノマーの含有量を、液晶組成物全体に対して1.0重量%とし、超高圧UVランプ(USH-500D:ウシオ電機社製)を光源として、315nmバンドパスフィルターを通し、表示領域を遮光して、1J/cm2の光を液晶セル全体に照射し、PS工程を行ったこと以外は、参考例1と同様の方法を用いて参考例17の液晶セルを作製した。この液晶セルを130℃で40分間加熱し、再配向処理を行ったところ、液晶組成物中のシール材に沿った領域(表示領域の外縁)においてはPS重合が進んで液晶の配向が固定化され、流動配向を保持してしまった。
超高圧UVランプ(USH-500D:ウシオ電機社製)を光源として、325nmバンドパスフィルターを通し、表示領域を遮光して、1J/cm2の光を液晶セル全体に照射し、PS工程を行ったこと以外は、参考例17と同様の方法を用いて参考例18の液晶セルを作製した。この液晶セルを130℃で40分間加熱し、再配向処理を行ったところ、液晶組成物中のシール材に沿った領域(表示領域の外縁)においてはPS重合が進んで液晶の配向が固定化され、流動配向を保持してしまった。
超高圧UVランプ(USH-500D:ウシオ電機社製)を光源として、335nmバンドパスフィルターを通し、表示領域を遮光して、1J/cm2の光を液晶セル全体に照射し、PS工程を行ったこと以外は、参考例17と同様の方法を用いて参考例19の液晶セルを作製した。この液晶セルを130℃で40分間加熱し、再配向処理を行ったところ、液晶は流動配向を解消して、ムラのない一軸配向となった。
超高圧UVランプ(USH-500D:ウシオ電機社製)を光源として、345nmバンドパスフィルターを通し、液晶セルの表示領域を遮光して、1J/cm2の光を液晶セル全体に照射し、PS工程を行ったこと以外は、参考例17と同様の方法を用いて参考例20の液晶セルを作製した。この液晶セルを130℃で40分間加熱し、再配向処理を行ったところ、液晶は流動配向を解消して、ムラのない一軸配向となった。
上記化学式(6)で表される化合物をモノマーとして用いたときに、シール材を硬化させる光の波長がどの程度であればモノマーの重合に影響が出るかを検証するために、参考例21~24の液晶セルを作製して実験を行った。
モノマーとして上記化学式(6)で表される化合物を用いたこと、及び、超高圧UVランプ(USH-500D:ウシオ電機社製)を光源として、350nmバンドパスフィルターを通し、表示領域を遮光して、1J/cm2の光を液晶セル全体に照射し、PS工程を行ったこと以外は、参考例17と同様の方法を用いて参考例21の液晶セルを作製した。この液晶セルを130℃で40分間加熱し、再配向処理を行ったところ、液晶組成物中のシール材に沿った領域(表示領域の外縁)においてはPS重合が進んで液晶の配向が固定化され、流動配向を保持してしまった。
超高圧UVランプ(USH-500D:ウシオ電機社製)を光源として、360nmバンドパスフィルターを通し、表示領域を遮光して、1J/cm2の光を液晶セル全体に照射し、PS工程を行ったこと以外は、参考例17と同様の方法を用いて参考例22の液晶セルを作製した。この液晶セルを130℃で40分間加熱し、再配向処理を行ったところ、液晶組成物中のシール材に沿った領域(表示領域の外縁)においてはPS重合が進んで液晶の配向が固定化され、流動配向を保持してしまった。
超高圧UVランプ(USH-500D:ウシオ電機社製)を光源として、370nmバンドパスフィルターを通し、表示領域を遮光して、1J/cm2の光を液晶セル全体に照射し、PS工程を行ったこと以外は、参考例17と同様の方法を用いて参考例23の液晶セルを作製した。この液晶セルを130℃で40分間加熱し、再配向処理を行ったところ、液晶は流動配向を解消して、ムラのない一軸配向となった。
超高圧UVランプ(USH-500D:ウシオ電機社製)を光源として、380nmバンドパスフィルターを通し、表示領域を遮光して、1J/cm2の光を液晶セル全体に照射し、PS工程を行ったこと以外は、参考例17と同様の方法を用いて参考例24の液晶セルを作製した。この液晶セルを130℃で40分間加熱し、再配向処理を行ったところ、液晶は流動配向を解消して、ムラのない一軸配向となった。
実施例1では液晶セルをPS処理する際に無偏光紫外線を照射したが、本実施例では、UV-B紫外線ランプ(FHF32-UVB:三共電気社製)にフィルム偏光板を組み合わせて1.5J/cm2の直線偏光紫外線を照射した。この時の偏光度は10:1であった。偏光方向は、光配向膜へ配向処理した際の偏光と同じ方向である。これら以外は実施例1と同様の方法で液晶セルを作製したところ、ムラのない一軸配向した液晶セルが得られ、更に実施例1よりも液晶の配向性が改善して、実施例1に対してコントラスト比が10%程度上昇した。
PS処理する際に実施例8と同様の直線偏光紫外線を照射した以外は、実施例2と同様の方法で液晶セルを作製したところ、液晶がムラなく一軸配向した液晶セルが得られ、更に実施例2よりも液晶の配向性が改善して、実施例2に対してコントラスト比が10%程度上昇した。
PS処理する際に実施例8と同様の直線偏光紫外線を照射した以外は、実施例5と同様の方法で液晶セルを作製したところ、液晶がムラなく一軸配向した液晶セルが得られ、更に実施例5よりも液晶の配向性が改善して、実施例5に対してコントラスト比が5%程度上昇した。
PS処理する際に実施例8と同様の直線偏光紫外線を照射した以外は、実施例6と同様の方法で液晶セルを作製したところ、液晶がムラなく一軸配向した液晶セルが得られ、更に実施例6よりも液晶の配向性が改善して、実施例6に対してコントラスト比が10%程度上昇した。
PS処理する際に実施例8と同様の直線偏光紫外線を照射した以外は、実施例7と同様の方法で液晶セルを作製したところ、液晶がムラなく一軸配向した液晶セルが得られ、更に実施例7よりも液晶の配向性が改善して、実施例7に対してコントラスト比が10%程度上昇した。
10:アレイ基板
11、21:透明基板
12、22:水平配向膜
13、23:PS層(ポリマー層)
20:カラーフィルタ基板
30:液晶層
32、42:配向膜
33a、43a:重合性モノマー(未励起)
33b、43b:重合性モノマー(励起状態)
52:光活性基(垂直配向膜分子)
54、64、74:液晶分子
55:疎水基
62:光活性基(水平配向膜分子)
71:スリット入り電極
71a:スリット
72:ベタ電極
81:シール材
Claims (15)
- 一対の基板の少なくとも一方の基板に光活性材料を含む水平配向膜を形成する工程と、
該一対の基板の一方の基板上に、液晶材料と、液晶組成物全体に対して1.0重量%以下のモノマーとを含有する液晶組成物を滴下する工程と、
該一対の基板の一方の基板の外縁に沿って塗布されたシール材に対し、該モノマーの吸収波長端より40nm以上長波長の光を照射して、シール材を硬化させる工程と、
該一対の基板間に封止された、該液晶組成物に光を照射し、該モノマーを重合させて、該水平配向膜上に、近接する液晶分子を配向制御するポリマー層を形成する工程とを有する
ことを特徴とする液晶表示装置の製造方法。 - 一対の基板の少なくとも一方の基板に光活性材料を含む水平配向膜を形成する工程と、
該一対の基板の一方の基板上に、液晶材料とモノマーとを含有する液晶組成物を滴下する工程と、
該一対の基板の一方の基板の外縁に沿って塗布されたシール材に対し、光照射は行わず、熱を加えてシール材を硬化させる工程と、
該一対の基板間に封止された、該液晶組成物に光を照射し、該モノマーを重合させて、該水平配向膜上に、近接する液晶分子を配向制御するポリマー層を形成する工程とを有する
ことを特徴とする液晶表示装置の製造方法。 - 一対の基板の少なくとも一方の基板に光活性材料を含む水平配向膜を形成する工程と、
該一対の基板の一方の基板の外縁に沿って、該基板上にシール材を塗布する工程と、
該一対の基板を貼り合わせる工程と、
該シール材を硬化させる工程と、
該一対の基板間に、液晶材料とモノマーとを含有する液晶組成物を真空注入する工程と、
該一対の基板間に封止された、該液晶組成物に光を照射し、該モノマーを重合させて、該水平配向膜上に、近接する液晶分子を配向制御するポリマー層を形成する工程とを有する
ことを特徴とする液晶表示装置の製造方法。 - 一対の基板の少なくとも一方の基板に光活性材料を含む水平配向膜を形成する工程と、
該一対の基板の一方の基板上に、液晶材料と、液晶組成物全体に対して0.4重量%以下のモノマーとを含有する液晶組成物を滴下する工程と、
該一対の基板の一方の基板の外縁に沿って塗布されたシール材に対し、該モノマーの吸収波長端より10nm以上長波長の光を、表示領域を遮光しながら照射して、シール材を硬化させる工程と、
該一対の基板間に封止された、該液晶組成物に光を照射し、該モノマーを重合させて、該水平配向膜上に、近接する液晶分子を配向制御するポリマー層を形成する工程とを有する
ことを特徴とする液晶表示装置の製造方法。 - 前記光活性材料は、光配向膜材料であることを特徴とする請求項1~4のいずれかに記載の液晶表示装置の製造方法。
- 前記光配向膜材料は、シクロブタン骨格を有する化合物を含むことを特徴とする請求項5記載の液晶表示装置の製造方法。
- 前記光配向膜材料は、光異性化型、光二量化型、又は、その両方の官能基を有する化合物を含むことを特徴とする請求項5記載の液晶表示装置の製造方法。
- 前記光異性化型又は光二量化型の官能基は、シンナメート基又はその誘導体であることを特徴とする請求項7記載の液晶表示装置の製造方法。
- 前記モノマーを重合させて、水平配向膜上に、近接する液晶分子を配向制御するポリマー層を形成する工程に用いられる光は、直線偏光であることを特徴とする請求項5~8のいずれかに記載の液晶表示装置の製造方法。
- 前記モノマーの重合性官能基は、アクリレート基、メタクリレート基、ビニル基、又は、ビニロキシ基であることを特徴とする請求項1~9のいずれかに記載の液晶表示装置の製造方法。
- 前記液晶組成物は、分子構造にベンゼン環の共役二重結合以外の多重結合を含む液晶分子を含有することを特徴とする請求項1~10のいずれかに記載の液晶表示装置の製造方法。
- 前記多重結合は、二重結合であることを特徴とする請求項11記載の液晶表示装置の製造方法。
- 前記二重結合は、アルケニル基に含まれていることを特徴とする請求項12記載の液晶表示装置の製造方法。
- 前記液晶層の配向型は、IPS型、FFS型、OCB型、TN型、STN型、FLC型、又は、PDLC型であることを特徴とする請求項1~13のいずれかに記載の液晶表示装置の製造方法。
- 前記一対の基板の少なくとも一方は、マルチドメイン構造を有することを特徴とする請求項14記載の液晶表示装置の製造方法。
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Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2015041006A (ja) * | 2013-08-22 | 2015-03-02 | スタンレー電気株式会社 | 液晶光学素子及びその製造方法 |
US20170205669A1 (en) * | 2014-05-23 | 2017-07-20 | Dic Corporation | Image display device and oriented material used in same |
KR20180030998A (ko) * | 2015-07-14 | 2018-03-27 | 메르크 파텐트 게엠베하 | 중합체 안정화된 액정 디스플레이에서 odf 얼룩을 감소시키는 방법 |
KR20180057666A (ko) * | 2015-09-23 | 2018-05-30 | 메르크 파텐트 게엠베하 | 중합체 안정화된 액정 디스플레이에서 선경사각을 제어하는 방법 |
JP2019113675A (ja) * | 2017-12-22 | 2019-07-11 | Dic株式会社 | 液晶表示素子の製造方法 |
JP2019219609A (ja) * | 2018-06-22 | 2019-12-26 | 株式会社ジャパンディスプレイ | 液晶パネルおよび電気光学装置 |
Families Citing this family (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR101663563B1 (ko) * | 2009-12-24 | 2016-10-07 | 엘지디스플레이 주식회사 | 액정표시장치의 제조방법 |
TWI510847B (zh) * | 2013-12-24 | 2015-12-01 | Innolux Corp | 液晶顯示裝置 |
CN105093689A (zh) * | 2015-07-17 | 2015-11-25 | 深圳市华星光电技术有限公司 | 彩色滤光片整合晶体管式液晶面板及其制造方法 |
JP2017062396A (ja) * | 2015-09-25 | 2017-03-30 | 旭硝子株式会社 | 光学素子の製造方法および光学素子 |
JP6037070B1 (ja) * | 2016-02-22 | 2016-11-30 | 大日本印刷株式会社 | 調光セル |
KR102512756B1 (ko) * | 2016-05-04 | 2023-03-23 | 삼성디스플레이 주식회사 | 윈도우 부재 및 이를 포함하는 표시 장치 |
WO2018008581A1 (ja) * | 2016-07-04 | 2018-01-11 | シャープ株式会社 | 液晶表示装置、及び、液晶表示装置の製造方法 |
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WO2018180852A1 (ja) * | 2017-03-28 | 2018-10-04 | シャープ株式会社 | 液晶表示装置、及び、液晶表示装置の製造方法 |
JP2019056825A (ja) * | 2017-09-21 | 2019-04-11 | シャープ株式会社 | 液晶回折格子、液晶組成物、液晶回折格子の製造方法、及び、ワイヤグリッド偏光子 |
WO2021039219A1 (ja) * | 2019-08-23 | 2021-03-04 | Jsr株式会社 | 液晶表示装置 |
CN115220267B (zh) * | 2022-08-01 | 2023-07-25 | 南京大学 | 一种液晶注液多孔光滑表面构建方法及其微流控应用 |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2009265308A (ja) * | 2008-04-24 | 2009-11-12 | Sony Corp | 液晶表示素子 |
WO2011040397A1 (ja) * | 2009-10-02 | 2011-04-07 | 積水化学工業株式会社 | 液晶表示装置の製造方法 |
Family Cites Families (26)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP3874871B2 (ja) * | 1997-02-10 | 2007-01-31 | シャープ株式会社 | 液晶表示装置の製造方法 |
US6177972B1 (en) | 1999-02-04 | 2001-01-23 | International Business Machines Corporation | Polymer stabilized in-plane switched LCD |
US7113241B2 (en) * | 2001-08-31 | 2006-09-26 | Sharp Kabushiki Kaisha | Liquid crystal display and method of manufacturing the same |
US6952252B2 (en) | 2001-10-02 | 2005-10-04 | Fujitsu Display Technologies Corporation | Substrate for liquid crystal display and liquid crystal display utilizing the same |
JP4237977B2 (ja) | 2001-10-02 | 2009-03-11 | シャープ株式会社 | 液晶表示装置 |
JP4175826B2 (ja) | 2002-04-16 | 2008-11-05 | シャープ株式会社 | 液晶表示装置 |
JP4472263B2 (ja) | 2003-03-20 | 2010-06-02 | シャープ株式会社 | 液晶表示装置の製造方法 |
CN100401170C (zh) * | 2003-10-08 | 2008-07-09 | 夏普株式会社 | 液晶显示面板的制造方法和紫外线照射装置 |
JP4744801B2 (ja) | 2003-12-18 | 2011-08-10 | 富士通株式会社 | 液晶表示装置およびその製造方法 |
KR20050094011A (ko) * | 2004-03-17 | 2005-09-26 | 비오이 하이디스 테크놀로지 주식회사 | 고분자 네크워크 액정 배열 방법 |
JP4387276B2 (ja) * | 2004-09-24 | 2009-12-16 | シャープ株式会社 | 液晶表示装置 |
JP2006145992A (ja) | 2004-11-22 | 2006-06-08 | Sharp Corp | 液晶表示装置及びその製造方法 |
JP2007072042A (ja) * | 2005-09-06 | 2007-03-22 | Sanyo Epson Imaging Devices Corp | 液晶表示素子の製造方法 |
US7667795B2 (en) * | 2006-07-18 | 2010-02-23 | Chunghwa Picture Tubes, Ltd. | Color filter substrate and liquid crystal display panel |
JP5073297B2 (ja) * | 2007-01-25 | 2012-11-14 | 三菱電機株式会社 | 液晶表示パネル及び液晶表示パネルの製造方法 |
JP5288729B2 (ja) * | 2007-05-23 | 2013-09-11 | 株式会社ジャパンディスプレイセントラル | 液晶表示装置 |
US8114310B2 (en) | 2007-10-22 | 2012-02-14 | Merck Patent Gmbh | Liquid-crystal display |
EP2065361B1 (de) | 2007-11-30 | 2014-12-17 | Merck Patent GmbH | Polymerisierbare Verbindungen |
JP2009258425A (ja) * | 2008-04-17 | 2009-11-05 | Sharp Corp | 液晶表示装置の製造方法 |
CN102076821B (zh) * | 2008-06-27 | 2015-06-17 | 默克专利股份有限公司 | 液晶介质 |
RU2011143816A (ru) * | 2009-03-30 | 2013-05-10 | Шарп Кабусики Кайся | Жидкокристаллическое дисплейное устройство, способ получения жидкокристаллического дисплейного устройства, композиция для получения полимерного слоя и композиция для получения жидкокристаллического слоя |
CN102378938B (zh) * | 2009-04-06 | 2015-05-13 | 夏普株式会社 | 液晶显示装置、液晶显示装置的制造方法、聚合物层形成用组合物和液晶层形成用组合物 |
KR101755597B1 (ko) * | 2009-05-29 | 2017-07-07 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 액정 표시 장치의 제작 방법 |
JP5165667B2 (ja) | 2009-11-17 | 2013-03-21 | 友達光電股▲ふん▼有限公司 | 液晶表示装置及びその製造方法 |
WO2012050178A1 (ja) * | 2010-10-14 | 2012-04-19 | シャープ株式会社 | 液晶表示装置 |
WO2013024749A1 (ja) | 2011-08-12 | 2013-02-21 | シャープ株式会社 | 液晶表示装置 |
-
2012
- 2012-08-01 US US14/240,418 patent/US9405153B2/en not_active Expired - Fee Related
- 2012-08-01 TW TW101127894A patent/TWI537643B/zh not_active IP Right Cessation
- 2012-08-01 CN CN201280041399.7A patent/CN103748507B/zh active Active
- 2012-08-01 WO PCT/JP2012/069561 patent/WO2013027548A1/ja active Application Filing
- 2012-08-01 JP JP2013529945A patent/JP5620006B2/ja not_active Expired - Fee Related
-
2016
- 2016-06-10 US US15/178,684 patent/US9671650B2/en active Active
-
2017
- 2017-05-03 US US15/585,237 patent/US9864236B2/en active Active
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2009265308A (ja) * | 2008-04-24 | 2009-11-12 | Sony Corp | 液晶表示素子 |
WO2011040397A1 (ja) * | 2009-10-02 | 2011-04-07 | 積水化学工業株式会社 | 液晶表示装置の製造方法 |
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2015041006A (ja) * | 2013-08-22 | 2015-03-02 | スタンレー電気株式会社 | 液晶光学素子及びその製造方法 |
US20170205669A1 (en) * | 2014-05-23 | 2017-07-20 | Dic Corporation | Image display device and oriented material used in same |
KR20180030998A (ko) * | 2015-07-14 | 2018-03-27 | 메르크 파텐트 게엠베하 | 중합체 안정화된 액정 디스플레이에서 odf 얼룩을 감소시키는 방법 |
JP2018527606A (ja) * | 2015-07-14 | 2018-09-20 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツングMerck Patent Gesellschaft mit beschraenkter Haftung | ポリマー安定化液晶ディスプレイにおけるodfムラを低減する方法 |
KR102625383B1 (ko) * | 2015-07-14 | 2024-01-17 | 메르크 파텐트 게엠베하 | 중합체 안정화된 액정 디스플레이에서 odf 얼룩을 감소시키는 방법 |
KR20180057666A (ko) * | 2015-09-23 | 2018-05-30 | 메르크 파텐트 게엠베하 | 중합체 안정화된 액정 디스플레이에서 선경사각을 제어하는 방법 |
JP2018534630A (ja) * | 2015-09-23 | 2018-11-22 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツングMerck Patent Gesellschaft mit beschraenkter Haftung | ポリマー安定化液晶ディスプレイにおいてプレチルト角を制御する方法 |
KR102654469B1 (ko) * | 2015-09-23 | 2024-04-08 | 메르크 파텐트 게엠베하 | 중합체 안정화된 액정 디스플레이에서 선경사각을 제어하는 방법 |
JP2019113675A (ja) * | 2017-12-22 | 2019-07-11 | Dic株式会社 | 液晶表示素子の製造方法 |
JP7091652B2 (ja) | 2017-12-22 | 2022-06-28 | Dic株式会社 | 液晶表示素子の製造方法 |
JP2019219609A (ja) * | 2018-06-22 | 2019-12-26 | 株式会社ジャパンディスプレイ | 液晶パネルおよび電気光学装置 |
JP7195779B2 (ja) | 2018-06-22 | 2022-12-26 | 株式会社ジャパンディスプレイ | 液晶パネル、電気光学装置および液晶パネルの製造方法 |
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US20170235192A1 (en) | 2017-08-17 |
TWI537643B (zh) | 2016-06-11 |
CN103748507B (zh) | 2016-08-24 |
JPWO2013027548A1 (ja) | 2015-03-19 |
TW201312215A (zh) | 2013-03-16 |
US20160282678A1 (en) | 2016-09-29 |
US9671650B2 (en) | 2017-06-06 |
US9405153B2 (en) | 2016-08-02 |
US9864236B2 (en) | 2018-01-09 |
JP5620006B2 (ja) | 2014-11-05 |
CN103748507A (zh) | 2014-04-23 |
US20140213137A1 (en) | 2014-07-31 |
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