WO2014157181A1 - Plaque de polarisation stratifiée pour un dispositif d'affichage à cristaux liquides à alignement horizontal et dispositif d'affichage à cristaux liquides à alignement horizontal - Google Patents

Plaque de polarisation stratifiée pour un dispositif d'affichage à cristaux liquides à alignement horizontal et dispositif d'affichage à cristaux liquides à alignement horizontal Download PDF

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WO2014157181A1
WO2014157181A1 PCT/JP2014/058243 JP2014058243W WO2014157181A1 WO 2014157181 A1 WO2014157181 A1 WO 2014157181A1 JP 2014058243 W JP2014058243 W JP 2014058243W WO 2014157181 A1 WO2014157181 A1 WO 2014157181A1
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liquid crystal
anisotropic layer
polarizing plate
display device
horizontal alignment
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PCT/JP2014/058243
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English (en)
Japanese (ja)
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上坂　哲也
涼 西村
浩 今福
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Ｊｘ日鉱日石エネルギー株式会社
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Publication of WO2014157181A1 publication Critical patent/WO2014157181A1/fr

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    • G—PHYSICS
    • G02—OPTICS
    • G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B5/00—Optical elements other than lenses
    • G02B5/30—Polarising elements
    • G02B5/3083—Birefringent or phase retarding elements
    • 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
    • G02F1/1343—Electrodes
    • G02F1/134309—Electrodes characterised by their geometrical arrangement
    • G02F1/134363—Electrodes characterised by their geometrical arrangement for applying an electric field parallel to the substrate, i.e. in-plane switching [IPS]
    • 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
    • G02F1/1335—Structural association of cells with optical devices, e.g. polarisers or reflectors
    • G02F1/13363—Birefringent elements, e.g. for optical compensation
    • G02F1/133634—Birefringent elements, e.g. for optical compensation the refractive index Nz perpendicular to the element surface being different from in-plane refractive indices Nx and Ny, e.g. biaxial or with normal optical axis
    • 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
    • G02F2413/00—Indexing scheme related to G02F1/13363, i.e. to birefringent elements, e.g. for optical compensation, characterised by the number, position, orientation or value of the compensation plates
    • G02F2413/02—Number of plates being 2

Definitions

  • the present invention relates to a laminated polarizing plate for a horizontal alignment type liquid crystal display device and a horizontal alignment type liquid crystal display device excellent in viewing angle characteristics.
  • a horizontal alignment mode in which liquid crystal molecules in a liquid crystal cell are aligned in parallel with a substrate surface in an initial state
  • Patent Document 1 When no voltage is applied, liquid crystal molecules are arranged in parallel to the substrate surface, and a black display can be obtained by arranging linearly polarizing plates orthogonally on both sides of the liquid crystal cell.
  • a voltage is applied, the liquid crystal molecules rotate from the direction parallel to the substrate surface to the direction of the electric field, and as a result, a bright display is obtained.
  • black display of a horizontal alignment type liquid crystal display device good black display can be obtained in the front visual field, but there is a problem that light leakage occurs in the oblique visual field and the contrast becomes low.
  • An object of the present invention is to provide a laminated polarizing plate for a horizontal alignment type liquid crystal display device and a horizontal alignment type liquid crystal display device having excellent viewing angle characteristics.
  • the present inventors have found that the object can be achieved by the following laminated polarizing plate for a horizontal alignment type liquid crystal display device and a horizontal alignment type liquid crystal display device using the same.
  • the inventor has completed the present invention. That is, the present invention is as follows.
  • a laminated polarizing plate for a horizontal alignment type liquid crystal display device in which at least a first polarizing plate, a first optically anisotropic layer, and a second optically anisotropic layer are laminated in this order.
  • a laminated polarizing plate for a horizontal alignment type liquid crystal display device wherein the optically anisotropic layer and the second optically anisotropic layer satisfy the following [1].
  • d1 is the thickness of the first optically anisotropic layer
  • nx1 and ny1 are the main refractive index in the first optically anisotropic layer surface for light having a wavelength of 550 nm
  • nx1 is the maximum main refractive index in the surface
  • ny1 represents the main refractive index in the direction orthogonal to nx1
  • nz1 is the main refractive index in the thickness direction for light having a wavelength of 550 nm
  • Rth2 is the retardation in the thickness direction of the second optical anisotropic layer.
  • Second optically anisotropic layer surface for light Nx2 is the main refractive index in the plane
  • ny2 is the main refractive index in the direction perpendicular to nx2
  • nz2 is the main refractive index in the thickness direction for light having a wavelength of 550 nm.
  • a horizontal alignment type liquid crystal display in which at least a first polarizing plate, a first optical anisotropic layer, a second optical anisotropic layer, a horizontal alignment type liquid crystal cell, and a second polarizing plate are arranged in this order.
  • a horizontal alignment type liquid crystal display device wherein the first optical anisotropic layer and the second optical anisotropic layer satisfy the following [1].
  • Rth1 means a retardation value in the thickness direction of the first optically anisotropic layer.
  • d1 is the thickness of the first optically anisotropic layer
  • nx1 and ny1 are the main refractive index in the first optically anisotropic layer surface for light having a wavelength of 550 nm
  • nx1 is the maximum main refractive index in the surface
  • ny1 represents the main refractive index in the direction orthogonal to nx1
  • nz1 is the main refractive index in the thickness direction for light having a wavelength of 550 nm
  • Rth2 is the retardation in the thickness direction of the second optical anisotropic layer.
  • Second optically anisotropic layer surface for light Nx2 is the main refractive index in the plane
  • ny2 is the main refractive index in the direction perpendicular to nx2
  • nz2 is the main refractive index in the thickness direction for light having a wavelength of 550 nm.
  • the horizontal alignment type liquid crystal display device of the present invention has excellent viewing angle characteristics, bright display, and high contrast display in all directions.
  • FIG. 6 is a schematic cross-sectional view of a horizontal alignment type liquid crystal display device used in Example 2.
  • FIG. FIG. 6 is a plan view showing the angular relationship of each component of the horizontal alignment type liquid crystal display device used in Example 2. It is a figure which shows contrast ratio when the horizontal alignment type liquid crystal display device in Example 2 is seen from all directions. It is a figure which shows contrast ratio when the horizontal alignment type liquid crystal display device in Example 3 is seen from all directions. It is a figure which shows contrast ratio when the horizontal alignment type liquid crystal display device in Example 4 is seen from all directions.
  • the laminated polarizing plate for a horizontal alignment type liquid crystal display device of the present invention is a laminated polarizing plate in which a first polarizing plate, a first optical anisotropic layer and a second optical anisotropic layer are laminated in this order.
  • the driving method of the liquid crystal cell is not particularly limited, and is a passive matrix method used for STN-LCDs, an active matrix method using active electrodes such as TFT (Thin Film Transistor) electrodes, TFD (Thin Film Diode) electrodes, and a plasma addressing method. Any driving method may be used.
  • the transparent substrate constituting the liquid crystal cell is not particularly limited as long as the liquid crystal material constituting the liquid crystal layer is aligned in a specific alignment direction.
  • a transparent substrate having the property of aligning the liquid crystal itself a substrate itself lacking alignment ability, but a transparent substrate provided with an alignment film having the property of aligning liquid crystal, etc.
  • ITO can be used for the electrode of a liquid crystal cell.
  • the electrode can usually be provided on the surface of the transparent substrate with which the liquid crystal layer is in contact. When a substrate having an alignment film is used, it can be provided between the substrate and the alignment film.
  • the material exhibiting liquid crystallinity for forming the liquid crystal layer is not particularly limited as long as it has a positive dielectric anisotropy, and various ordinary low-molecular liquid crystal substances and polymer liquid crystals capable of constituting various liquid crystal cells. Materials and mixtures thereof. Moreover, a pigment
  • the horizontal alignment type liquid crystal display device of the present invention can be provided with other constituent members in addition to the constituent members described above.
  • a color liquid crystal display device capable of performing multicolor or full color display with high color purity can be manufactured.
  • the optically anisotropic layer used in the present invention will be described in order.
  • the first optical anisotropic layer for example, a film made of an appropriate polymer such as a cyclic polyolefin such as polycarbonate or norbornene resin, polyvinyl alcohol, polystyrene, polymethyl methacrylate, polypropylene, other polyolefins, polyarylate, or polyamide.
  • Examples thereof include a refractive film, an alignment film made of a liquid crystal material such as a liquid crystal polymer, and a film in which an alignment layer of the liquid crystal material is supported.
  • the positive biaxial optically anisotropic layer has a relationship of nx> nz> ny as a refractive index.
  • the negative biaxial optically anisotropic layer has a relationship of nx> ny> nz as a refractive index.
  • the first optical anisotropic layer and the second optical anisotropic layer have a thickness of the first optical anisotropic layer d1, a maximum principal refractive index in the plane of the first optical anisotropic layer nx1, and
  • the thickness of the second optical anisotropic layer is d2
  • the maximum main refractive index in the plane of the second optical anisotropic layer is nx2
  • the first optical anisotropic layer satisfies the following [2]
  • the second optical anisotropic layer satisfies the following [3].
  • [3] nz2> nx2 ny2
  • Xd1 [nm]) is desirably in the range of 50 nm to 500 nm, preferably 80 nm to 480 nm, and more preferably 100 nm to 450 nm.
  • the retardation value (Rth1) in the thickness direction of the first optically anisotropic layer is preferably 30 nm to 750 nm, more preferably 40 nm to 500 nm, still more preferably 50 nm to 200 nm. When outside the above range, a sufficient viewing angle improvement effect may not be obtained, or unnecessary coloring may occur when viewed from an oblique direction.
  • r is an angle formed by the absorption axis of the first polarizing plate and the slow axis of the first optically anisotropic layer
  • r is preferably in the range of 85 ° to 95 °
  • the angle is more preferably 88 to 92 °, and still more preferably about 90 ° (orthogonal).
  • the absorption axis of the first polarizing plate and the long roll of the first optically anisotropic layer are substantially orthogonal (the crossing angle is within 90 ° ⁇ 5 °, preferably within ⁇ 2 °).
  • the slow axis of the first optical anisotropic layer is It is necessary to arrange in a direction perpendicular to the roll length direction. For that purpose, it is better to produce the first optically anisotropic layer by lateral uniaxial stretching or biaxial stretching.
  • lateral uniaxial stretching or biaxial stretching In general, when manufactured by transverse uniaxial stretching or biaxial stretching, it is known that the refractive index relationship of the retardation film becomes negative biaxiality consisting of nx> ny> nz.
  • the second optical anisotropic layer is preferably made of a homeotropically aligned liquid crystal film in which a liquid crystal material exhibiting positive uniaxiality is homeotropically aligned in a liquid crystal state and then fixed in alignment.
  • selection of a liquid crystal material and an alignment substrate is extremely important for obtaining a liquid crystal film in which the homeotropic alignment of the liquid crystal material is fixed.
  • the liquid crystal material used in the present invention contains at least a side chain type liquid crystalline polymer such as poly (meth) acrylate or polysiloxane as a main constituent component.
  • the side chain type liquid crystal polymer used in the present invention preferably has a polymerizable oxetanyl group at the terminal. More specifically, the side chain obtained by homopolymerizing the (meth) acrylic moiety of the (meth) acrylic compound having an oxetanyl group represented by the formula (1) or copolymerizing with another (meth) acrylic compound.
  • a preferred example is a liquid crystalline polymer material.
  • R 1 represents hydrogen or a methyl group
  • R 2 represents hydrogen, a methyl group or an ethyl group
  • L 1 and L 2 are each independently a single bond, —O—, —O—CO.
  • M represents formula (2), formula (3) or formula (4)
  • n and m each independently represents an integer of 0 to 10.
  • P1 and P2 each independently represent a group selected from formula (5)
  • P3 represents a group selected from formula (6)
  • L3 and L4 each independently represents a single bond. , —CH ⁇ CH—, —C ⁇ C—, —O—, —O—CO— or —CO—O—.
  • the method for synthesizing these (meth) acrylic compounds having an oxetanyl group is not particularly limited, and can be synthesized by applying a method used in a general organic chemical synthesis method. For example, by combining a site having an oxetanyl group and a site having a (meth) acrylic group by means such as Williamson's ether synthesis or ester synthesis using a condensing agent, oxetanyl group and (meth) acrylic group 2 A (meth) acrylic compound having an oxetanyl group having two reactive functional groups can be synthesized.
  • radical polymerization a (meth) acryl compound is dissolved in a solvent such as dimethylformamide (DMF), and 2,2′-azobisisobutyronitrile (AIBN), benzoyl peroxide (BPO), or the like is used as an initiator. And reacting at 60 to 120 ° C. for several hours. Moreover, in order to make the liquid crystal phase appear stably, a copper (I) bromide / 2,2′-bipyridyl system, a 2,2,6,6-tetramethylpiperidinooxy free radical (TEMPO) system, etc. are used. A method of controlling the molecular weight distribution by conducting living radical polymerization as an initiator is also effective. These radical polymerizations are preferably performed under deoxygenation conditions.
  • a solvent such as dimethylformamide (DMF), and 2,2′-azobisisobutyronitrile (AIBN), benzoyl peroxide (BPO), or the like is used as an initiator. And reacting at 60
  • anionic polymerization examples include a method in which a (meth) acrylic compound is dissolved in a solvent such as tetrahydrofuran (THF) and a strong base such as an organic lithium compound, an organic sodium compound, or a Grignard reagent is reacted as an initiator.
  • a solvent such as tetrahydrofuran (THF)
  • a strong base such as an organic lithium compound, an organic sodium compound, or a Grignard reagent
  • the molecular weight distribution can be controlled by optimizing the initiator and the reaction temperature for living anionic polymerization.
  • the (meth) acryl compound to be copolymerized at this time is not particularly limited and may be anything as long as the synthesized polymer substance exhibits liquid crystallinity, but in order to increase the liquid crystallinity of the synthesized polymer substance, A (meth) acrylic compound having a mesogenic group is preferred.
  • a (meth) acrylic compound represented by the following formula can be exemplified as a preferred compound.
  • R represents hydrogen, an alkyl group having 1 to 12 carbon atoms, an alkoxy group having 1 to 12 carbon atoms, or a cyano group.
  • the side chain type liquid crystalline polymer substance preferably contains 5 to 100 mol% of the unit represented by the formula (7), and particularly preferably contains 10 to 100 mol%.
  • the side chain type liquid crystalline polymer substance preferably has a weight average molecular weight of 2,000 to 100,000, particularly preferably 5,000 to 50,000.
  • the liquid crystal material used in the present invention may contain various compounds that can be mixed without impairing liquid crystallinity in addition to the side chain liquid crystalline polymer substance.
  • examples of compounds that can be contained include compounds having a cationic polymerizable functional group such as an oxetanyl group, an epoxy group, and a vinyl ether group, various polymer substances having film-forming ability, and various low-molecular liquid crystal compounds having liquid crystallinity. And polymer liquid crystalline compounds.
  • the side chain liquid crystalline polymer substance is used as a composition, the proportion of the side chain liquid crystalline polymer substance in the entire composition is 10% by mass or more, preferably 30% by mass or more, and more preferably. Is 50 mass% or more. If the content of the side chain type liquid crystalline polymer substance is less than 10% by mass, the concentration of the polymerizable group in the composition becomes low, and the mechanical strength after polymerization becomes insufficient.
  • the liquid crystal material contains a photocation generator and / or a thermal cation generator that generates cations by an external stimulus such as light or heat. If necessary, various sensitizers may be used in combination.
  • the photo cation generator means a compound capable of generating a cation by irradiating with light having an appropriate wavelength, and examples thereof include organic sulfonium salt systems, iodonium salt systems, and phosphonium salt systems. Antimonates, phosphates, borates and the like are preferably used as counter ions of these compounds. Specific examples of the compound include Ar 3 S + SbF 6 ⁇ , Ar 3 P + BF 4 ⁇ , Ar 2 I + PF 6 ⁇ (wherein Ar represents a phenyl group or a substituted phenyl group), and the like. In addition, sulfonic acid esters, triazines, diazomethanes, ⁇ -ketosulfone, iminosulfonate, benzoinsulfonate and the like can also be used.
  • the thermal cation generator is a compound capable of generating a cation by being heated to an appropriate temperature, for example, benzylsulfonium salts, benzylammonium salts, benzylpyridinium salts, benzylphosphonium salts, hydrazinium salts, carboxylic acid esters, Examples thereof include sulfonic acid esters, amine imides, antimony pentachloride-acetyl chloride complexes, diaryliodonium salts-dibenzyloxycopper, and boron halide-tertiary amine adducts.
  • the amount of these cation generators added to the liquid crystal material varies depending on the structure of the mesogenic part and spacer part, the oxetanyl group equivalent, the alignment condition of the liquid crystal, etc. constituting the side chain type liquid crystalline polymer material to be used. However, it is usually 100 mass ppm to 20 mass%, preferably 1000 mass ppm to 10 mass%, more preferably 0.2 mass% to 7 mass%, most preferably based on the side chain type liquid crystalline polymer substance. Is in the range of 0.5% to 5% by weight. If the amount is less than 100 mass ppm, the amount of cations generated may not be sufficient and polymerization may not proceed. If the amount is more than 20 mass%, the remaining cation generator remains in the liquid crystal film. It is not preferable because there is a risk that the light resistance and the like may deteriorate due to an increase in the number of objects.
  • a substrate having a smooth plane is preferable, and examples thereof include a film or sheet made of an organic polymer material, a glass plate, and a metal plate. From the viewpoint of cost and continuous productivity, it is preferable to use a material made of an organic polymer.
  • organic polymer materials include polyvinyl alcohol, polyimide, polyphenylene oxide, polyether ketone, polyether ether ketone, polyester polymers such as polyethylene terephthalate and polyethylene naphthalate, cellulose polymers such as diacetyl cellulose and triacetyl cellulose, Examples include films made of transparent polymers such as polycarbonate polymers and acrylic polymers such as polymethyl methacrylate.
  • styrene polymers such as polystyrene, acrylonitrile / styrene copolymer, olefin polymers such as polyethylene, polypropylene, ethylene / propylene copolymer, cyclopolyolefins having cyclic or norbornene structure, vinyl chloride polymers, nylon and aromatic polyamides.
  • styrene polymers such as polystyrene, acrylonitrile / styrene copolymer, olefin polymers such as polyethylene, polypropylene, ethylene / propylene copolymer, cyclopolyolefins having cyclic or norbornene structure, vinyl chloride polymers, nylon and aromatic polyamides.
  • olefin polymers such as polyethylene, polypropylene, ethylene / propylene copolymer, cyclopolyolefins having cyclic or norbornene structure, vinyl chloride poly
  • imide polymers examples thereof include a film made of a transparent polymer such as a polymer, an epoxy-based polymer, and a blend of the above polymers.
  • plastic films such as triacetyl cellulose, polycarbonate, norbornene polyolefin used as an optical film are used.
  • organic polymer film examples include norbornene such as ZEONOR (trade name, manufactured by ZEON CORPORATION), ZEONEX (trade name, manufactured by ZEON CORPORATION), Arton (trade name, manufactured by JSR Corporation), etc.
  • a plastic film made of a polymer material having a structure is preferable because it has excellent optical properties.
  • a metal film the said film formed from aluminum etc. is mentioned, for example.
  • the material constituting these substrates has a long chain (usually 4 or more carbon atoms, preferably 8 or more) alkyl group, More preferably, the substrate surface has a compound layer having a long-chain alkyl group. Among them, it is preferable to form a layer made of polyvinyl alcohol having a long-chain alkyl group because the formation method is easy.
  • These organic polymer materials may be used alone as a substrate, or may be formed as a thin film on another substrate.
  • rubbing treatment is generally performed by rubbing the substrate with a cloth or the like, but the homeotropic alignment liquid crystal film of the present invention has an alignment structure in which in-plane anisotropy basically does not occur. Therefore, the rubbing process is not necessarily required. However, it is more preferable to perform a weak rubbing treatment from the viewpoint of suppressing repelling when a liquid crystal material is applied.
  • An important setting value that defines the rubbing condition is a peripheral speed ratio. This represents the ratio between the movement speed of the cloth and the movement speed of the substrate when the rubbing cloth is wound around a roll and rubbed while the substrate is rubbed.
  • the weak rubbing treatment usually has a peripheral speed ratio of 50 or less, more preferably 25 or less, and particularly preferably 10 or less.
  • the peripheral speed ratio is greater than 50, the effect of rubbing is too strong, and the liquid crystal material cannot be completely aligned vertically, and there is a possibility that the alignment is tilted in the in-plane direction from the vertical direction.
  • the manufacturing method of a homeotropic alignment liquid crystal film is demonstrated.
  • the method for producing the liquid crystal film is not limited to these, the above-mentioned liquid crystal material is spread on the above-mentioned alignment substrate, and after aligning the liquid crystal material, light irradiation and / or heat treatment is performed. It can manufacture by fixing the said orientation state.
  • the liquid crystal material is spread on the alignment substrate to form the liquid crystal material layer.
  • the liquid crystal material is applied directly on the alignment substrate in a molten state, or the liquid crystal material solution is applied on the alignment substrate, and then the coating film is applied. And drying the solvent to distill off the solvent.
  • the solvent used for preparing the solution is not particularly limited as long as it can dissolve the liquid crystal material of the present invention and can be distilled off under suitable conditions.
  • ketones such as acetone, methyl ethyl ketone, isophorone, and cyclohexanone
  • butoxyethyl Ethers such as alcohol, hexyloxyethyl alcohol, methoxy-2-propanol
  • glycol ethers such as ethylene glycol dimethyl ether and diethylene glycol dimethyl ether
  • esters such as ethyl acetate and ethyl lactate
  • phenols such as phenol and chlorophenol
  • N Amides such as N, N-dimethylformamide, N, N-dimethylacetamide, N-methylpyrrolidone, halogens such as chloroform, tetrachloroethane, dichlorobenzene, etc.
  • Mixed system is preferably used. Further, in order to form a uniform coating film
  • the application method is not particularly limited as long as the uniformity of the coating film is ensured, and a known method may be adopted. It can. Examples thereof include spin coating, die coating, curtain coating, dip coating, and roll coating.
  • a drying step for removing the solvent after the application As long as the uniformity of a coating film is maintained, this drying process can employ
  • the film thickness of the liquid crystal film cannot be generally described because it depends on the method of the liquid crystal display device and various optical parameters, but is usually 0.2 ⁇ m to 10 ⁇ m, preferably 0.3 ⁇ m to 5 ⁇ m, more preferably 0.5 ⁇ m. ⁇ 2 ⁇ m.
  • the film thickness is thinner than 0.2 ⁇ m, there is a possibility that a sufficient viewing angle improvement or brightness enhancement effect cannot be obtained. If it exceeds 10 ⁇ m, the liquid crystal display device may be unnecessarily colored.
  • the liquid crystal material layer formed on the alignment substrate is liquid crystal aligned by a method such as heat treatment, and is cured and fixed by light irradiation and / or heat treatment.
  • the liquid crystal is aligned by the self-alignment ability inherent in the liquid crystal material by heating to the liquid crystal phase expression temperature range of the used liquid crystal material.
  • the conditions for the heat treatment cannot be generally stated because the optimum conditions and limit values vary depending on the liquid crystal phase behavior temperature (transition temperature) of the liquid crystal material to be used, but are usually 10 ° C. to 250 ° C., preferably in the range of 30 ° C. to 160 ° C.
  • the heat treatment is performed at a temperature equal to or higher than the glass transition point (Tg) of the liquid crystal material, more preferably at a temperature higher by 10 ° C. than Tg. If the temperature is too low, the liquid crystal alignment may not proceed sufficiently, and if the temperature is high, the cationic polymerizable reactive group in the liquid crystal material and the alignment substrate may be adversely affected.
  • the heat treatment time is usually in the range of 3 seconds to 30 minutes, preferably 10 seconds to 10 minutes. If the heat treatment time is shorter than 3 seconds, the liquid crystal alignment may not be completed sufficiently, and if the heat treatment time exceeds 30 minutes, the productivity is deteriorated.
  • the liquid crystal material layer is formed into a liquid crystal alignment by a method such as heat treatment
  • the liquid crystal material is cured by a polymerization reaction of oxetanyl groups in the composition while maintaining the liquid crystal alignment state.
  • the curing step is aimed at fixing the liquid crystal alignment state of the completed liquid crystal alignment by a curing (crosslinking) reaction and modifying it into a stronger film.
  • the liquid crystal material of the present invention has a polymerizable oxetanyl group, as described above, it is preferable to use a cationic polymerization initiator (cation generator) for the polymerization (crosslinking) of the reactive group.
  • a cationic polymerization initiator cation generator
  • the polymerization initiator it is preferable to use a photo cation generator rather than a thermal cation generator.
  • the liquid crystal material can be obtained by adding the photo cation generator to the heat treatment for aligning the liquid crystal under dark conditions (light blocking conditions that do not cause the photo cation generator to dissociate). The liquid crystal can be aligned with sufficient fluidity without curing until the alignment stage. Thereafter, the liquid crystal material layer is cured by generating cations by irradiating light from a light source that emits light of an appropriate wavelength.
  • a photocation is generated by irradiating light from a light source such as a metal halide lamp, a high pressure mercury lamp, a low pressure mercury lamp, a xenon lamp, an arc lamp, or a laser having a spectrum in the absorption wavelength region of the photocation generator used. Cleave the generator.
  • the dose per square centimeter is usually in the range of 1 to 2000 mJ, preferably 10 to 1000 mJ, as the cumulative dose. However, this is not the case when the absorption region of the photocation generator and the spectrum of the light source are remarkably different, or when the liquid crystal material itself has the ability to absorb the light source wavelength.
  • the temperature at the time of light irradiation needs to be within a temperature range in which the liquid crystal material takes liquid crystal alignment. In order to sufficiently enhance the curing effect, it is preferable to perform light irradiation at a temperature equal to or higher than Tg of the liquid crystal material.
  • the liquid crystal material layer produced by the above process is a sufficiently strong film.
  • the mesogens are three-dimensionally bonded by the curing reaction, and not only the heat resistance (the upper limit temperature for maintaining the liquid crystal alignment) is improved as compared to before curing, but also scratch resistance, abrasion resistance, crack resistance.
  • the mechanical strength such as property is also greatly improved.
  • As the alignment substrate it is not optically isotropic, or the liquid crystal film to be obtained is finally opaque in the intended use wavelength region, or the alignment substrate is too thick, resulting in problems in actual use.
  • a form transferred from a form formed on an alignment substrate to a stretched film having a retardation function may be used.
  • As a transfer method a known method can be adopted.
  • a liquid crystal film layer is laminated with a substrate different from the alignment substrate via an adhesive or an adhesive, and if necessary, Examples thereof include a method of transferring only a liquid crystal film by performing a surface curing treatment using an adhesive or an adhesive and peeling the alignment substrate from the laminate.
  • the pressure-sensitive adhesive or adhesive used for transfer is not particularly limited as long as it is of optical grade, and generally used ones such as acrylic, epoxy, and urethane can be used.
  • the homeotropic alignment liquid crystal layer obtained as described above can be quantified by measuring the optical phase difference of the liquid crystal layer at an angle inclined from the normal incidence. In the case of homeotropic alignment liquid crystal layers, this retardation value is symmetric with respect to normal incidence.
  • Several methods can be used for measuring the optical phase difference. For example, an automatic birefringence measuring apparatus (manufactured by Oji Scientific Instruments) and a polarizing microscope can be used. This homeotropic alignment liquid crystal layer appears black between the crossed Nicols polarizing plates. Thus, homeotropic orientation was evaluated.
  • the Re2 value and Rth2 value which are optical parameters of the homeotropic alignment liquid crystal film, cannot be generally described because they depend on the type of the liquid crystal display device and various optical parameters, but the homeotropic alignment for monochromatic light of 550 nm
  • the retardation value (Re2) in the plane of the liquid crystal film is preferably 0 nm to 20 nm, more preferably 0 nm to 10 nm, still more preferably 0 nm to 5 nm, and retardation in the thickness direction.
  • the value (Rth2) is preferably from ⁇ 500 to ⁇ 30 nm, more preferably from ⁇ 400 to ⁇ 50 nm, still more preferably from ⁇ 400 to ⁇ 100 nm.
  • the viewing angle improving film of the liquid crystal display device can widen the viewing angle while correcting the color tone of the liquid crystal display.
  • the Rth2 value is larger than ⁇ 30 nm or smaller than ⁇ 500 nm, a sufficient viewing angle improving effect cannot be obtained, or unnecessary coloring may occur when viewed from an oblique direction.
  • the front characteristic of a liquid crystal display element can be improved by making Re2 value into 20 nm or less.
  • the first polarizing plate and the second polarizing plate used in the present invention will be described.
  • the first polarizing plate and the second polarizing plate used in the present invention those having a protective film on one side or both sides of the polarizer are usually used.
  • the first optically anisotropic layer also functions as a protective film.
  • the laminated polarizing plate of the present invention is laminated so that the slow axis of the first optically anisotropic layer and the absorption axis of the first polarizing plate are substantially orthogonal (intersection angle is within 90 ° ⁇ 5 °).
  • a negative biaxial optically anisotropic layer stretched in the width direction it is possible to perform integral production with a roll-to-roll.
  • the polarizer is not particularly limited, and various types can be used.
  • a hydrophilic polymer film such as a polyvinyl alcohol film, a partially formalized polyvinyl alcohol film, an ethylene / vinyl acetate copolymer partially saponified film.
  • polyene-based oriented films such as those obtained by adsorbing dichroic substances such as iodine and dichroic dyes and uniaxially stretched, polyvinyl alcohol dehydrated products and polyvinyl chloride dehydrochlorinated products.
  • dichroic substances such as iodine and dichroic dyes
  • the thickness of the polarizer is not particularly limited, but is generally about 5 to 80 ⁇ m.
  • a polarizer obtained by dyeing a polyvinyl alcohol film with iodine and uniaxially stretching it can be produced, for example, by dyeing polyvinyl alcohol in an aqueous iodine solution and stretching it 3 to 7 times the original length. If necessary, it can be immersed in an aqueous solution of boric acid or potassium iodide. Further, if necessary, the polyvinyl alcohol film may be immersed in water and washed before dyeing. In addition to washing the polyvinyl alcohol film surface with dirt and anti-blocking agents by washing the polyvinyl alcohol film with water, it also has the effect of preventing unevenness such as uneven coloring by swelling the polyvinyl alcohol film. is there.
  • Stretching may be performed after dyeing with iodine, may be performed while dyeing, or may be dyed with iodine after stretching.
  • the film can be stretched in an aqueous solution of boric acid or potassium iodide or in a water bath.
  • the protective film provided on one side or both sides of the polarizer preferably has excellent transparency, mechanical strength, thermal stability, moisture shielding properties, isotropic properties, and the like.
  • the material for the protective film include polyester polymers such as polyethylene terephthalate and polyethylene naphthalate, cellulose polymers such as diacetyl cellulose and triacetyl cellulose, acrylic polymers such as polymethyl methacrylate, polystyrene, acrylonitrile / styrene copolymer, and the like.
  • polyester polymers such as polyethylene terephthalate and polyethylene naphthalate
  • cellulose polymers such as diacetyl cellulose and triacetyl cellulose
  • acrylic polymers such as polymethyl methacrylate, polystyrene, acrylonitrile / styrene copolymer, and the like.
  • styrene polymers such as coalesced (AS resin), polycarbonate polymers, and the like.
  • polyolefin polymers such as polyethylene, polypropylene, ethylene / propylene copolymers, polyolefins having cycloolefin or norbornene structures, vinyl chloride polymers, amide polymers such as nylon and aromatic polyamide, imide polymers, sulfones Polymer, polyether sulfone polymer, polyether ether ketone polymer, polyphenylene sulfide polymer, vinyl alcohol polymer, vinylidene chloride polymer, vinyl butyral polymer, arylate polymer, polyoxymethylene polymer, epoxy polymer, or Examples of the polymer that forms the protective film include blends of the aforementioned polymers.
  • the thickness of the protective film is generally 500 ⁇ m or less, and preferably 1 to 300 ⁇ m. In particular, the thickness is preferably 5 to 200 ⁇ m.
  • the protective film is preferably an optically isotropic substrate.
  • a triacetyl cellulose (TAC) film such as Fujitac (product of Fujifilm) or Konicatak (product of Konica Minolta Opto), Arton film (product of JSR) And ZEONOR film, ZEONEX film (product of ZEON Corporation), cycloolefin polymer, TPX film (product of Mitsui Chemicals), acrylene film (product of Mitsubishi Rayon Co., Ltd.)
  • TAC triacetyl cellulose
  • TPX film product of Mitsui Chemicals
  • acrylene film product of Mitsubishi Rayon Co., Ltd.
  • the protective film which consists of the same polymer material may be used by the front and back, and the protective film which consists of a different polymer material etc. may be used.
  • the polarizer and the protective film are usually in close contact with each other through an aqueous adhesive or the like.
  • aqueous adhesives include polyvinyl alcohol adhesives, gelatin adhesives, vinyl latexes, aqueous polyurethanes, aqueous polyesters, and the like.
  • a hard coat layer As the protective film, a hard coat layer, an antireflection treatment, an anti-sticking treatment, or a treatment subjected to diffusion or anti-glare treatment can be used.
  • Hard coat treatment is performed for the purpose of preventing scratches on the surface of the polarizing plate.
  • a cured film having excellent hardness and slipping properties with an appropriate ultraviolet curable resin such as acrylic or silicone is applied to the protective film. It can be formed by a method of adding to the surface.
  • the antireflection treatment is performed for the purpose of preventing reflection of external light on the surface of the polarizing plate, and can be achieved by forming an antireflection film or the like according to the conventional art. Further, the anti-sticking treatment is performed for the purpose of preventing adhesion with an adjacent layer.
  • Anti-glare treatment is applied for the purpose of preventing external light from being reflected on the surface of the polarizing plate and obstructing the visibility of the light transmitted through the polarizing plate. For example, roughening by sandblasting or embossing. It can be formed by imparting a fine concavo-convex structure to the surface of the protective film by an appropriate method such as a method or a compounding method of transparent fine particles.
  • the fine particles to be included in the formation of the fine surface uneven structure include conductive particles made of silica, alumina, titania, zirconia, tin oxide, indium oxide, cadmium oxide, antimony oxide, and the like having an average particle size of 0.5 to 50 ⁇ m.
  • transparent fine particles such as inorganic fine particles, organic fine particles composed of a crosslinked or uncrosslinked polymer, and the like are used.
  • the amount of fine particles used is generally about 2 to 50 parts by weight, preferably 5 to 25 parts by weight, based on 100 parts by weight of the transparent resin forming the surface fine uneven structure.
  • the antiglare layer may also serve as a diffusion layer (viewing angle expanding function or the like) for diffusing the light transmitted through the polarizing plate to expand the viewing angle.
  • the antireflection layer, antisticking layer, diffusion layer, antiglare layer, and the like can be provided on the protective film itself, or can be provided separately from the transparent protective layer as an optical layer.
  • the first polarizing plate, the first optically anisotropic layer, and the second optically anisotropic layer can be produced by sticking each other through an adhesive layer.
  • the pressure-sensitive adhesive forming the pressure-sensitive adhesive layer is not particularly limited.
  • an acrylic polymer, a silicone-based polymer, a polyester, a polyurethane, a polyamide, a polyether, a fluorine-based or rubber-based polymer is appropriately used as a base polymer.
  • those having excellent optical transparency such as an acrylic pressure-sensitive adhesive, exhibiting appropriate wettability, cohesiveness, and adhesive pressure-sensitive adhesive properties, and being excellent in weather resistance, heat resistance and the like can be preferably used.
  • the pressure-sensitive adhesive layer can be formed by an appropriate method.
  • a pressure-sensitive adhesive solution of about 10 to 40% by weight in which a base polymer or a composition thereof is dissolved or dispersed in a solvent composed of an appropriate solvent alone or a mixture such as toluene and ethyl acetate is prepared.
  • a method in which it is directly attached on the liquid crystal layer by an appropriate development method such as a casting method or a coating method, or an adhesive layer is formed on the separator according to the above and transferred onto the liquid crystal layer Examples include methods.
  • the pressure-sensitive adhesive layer includes, for example, natural and synthetic resins, in particular, tackifier resins, glass fibers, glass beads, metal powder, fillers made of other inorganic powders, pigments, colorants, You may contain the additive added to adhesion layers, such as antioxidant. Moreover, the adhesive layer etc. which contain microparticles
  • the surface treatment means is not particularly limited, and a surface treatment method such as corona discharge treatment, sputtering treatment, low-pressure UV irradiation, or plasma treatment that can maintain the transparency of each optically anisotropic layer can be suitably employed.
  • a surface treatment method such as corona discharge treatment, sputtering treatment, low-pressure UV irradiation, or plasma treatment that can maintain the transparency of each optically anisotropic layer can be suitably employed.
  • corona discharge treatment is good.
  • the horizontal alignment type liquid crystal display device of the present invention includes a laminated polarizing plate of the present invention, a horizontal alignment type liquid crystal composed of at least a first polarizing plate, a first optical anisotropic layer, and a second optical anisotropic layer.
  • the cell and the second polarizing plate are arranged in this order.
  • s is in the range of 85 ° to 95 °, where s is the angle formed by the absorption axis of the first polarizing plate and the absorption axis of the second polarizing plate. Preferably, it is 88 to 92 °, more preferably about 90 ° (orthogonal).
  • s deviates from the upper and lower ranges, light leakage of the horizontal alignment type liquid crystal display device is large and the visibility is remarkably deteriorated.
  • the layers are laminated so as to satisfy ⁇ 5 ° ⁇ t ⁇ 5 °.
  • t is out of the upper and lower ranges, light leakage of the horizontal alignment type liquid crystal display device is large, and the visibility is remarkably deteriorated.
  • a liquid crystal material solution was prepared by filtration through a 0.45 ⁇ m polytetrafluoroethylene filter.
  • the alignment substrate was prepared as follows.
  • a 38 ⁇ m-thick polyethylene naphthalate film (manufactured by Teijin Limited) was cut into a 15 cm square, and a 5% by mass solution of alkyl-modified polyvinyl alcohol (PVA: Kuraray Co., Ltd., MP-203) (the solvent was water and isopropyl A mixed solvent having an alcohol mass ratio of 1: 1) was applied by spin coating, dried on a hot plate at 50 ° C. for 30 minutes, and then heated in an oven at 120 ° C. for 10 minutes. Subsequently, it was rubbed with a rayon rubbing cloth. The film thickness of the obtained PVA layer was 1.2 ⁇ m.
  • the peripheral speed ratio during rubbing was 4.
  • the liquid crystal material solution described above was applied to the alignment substrate thus obtained by spin coating. Next, it was dried on a hot plate at 60 ° C. for 10 minutes and heat-treated in an oven at 150 ° C. for 2 minutes to align the liquid crystal material. Next, the sample is placed in close contact with an aluminum plate heated to 60 ° C., and then a 600 mJ / cm 2 ultraviolet light (however, measured at 365 nm) is irradiated with a high-pressure mercury lamp lamp to cure the liquid crystal material. It was.
  • the obtained liquid crystalline film on the alignment substrate is converted to a triacetyl cellulose (TAC) film via an ultraviolet curable adhesive.
  • TAC triacetyl cellulose
  • an adhesive is applied to a thickness of 5 ⁇ m, laminated with a TAC film, and irradiated with ultraviolet rays from the TAC film side to cure the adhesive. After that, the polyethylene naphthalate film and the PVA layer were peeled off.
  • the obtained optical film (liquid crystal layer / adhesive layer / TAC film) is observed under a polarizing microscope, it has a uniform uniaxial refractive index structure from conoscopic observation with uniform orientation of monodomains without disclination. It was found to be homeotropic alignment.
  • the retardation in the in-plane direction of the TAC film and the liquid crystal layer measured using KOBRA21ADH was 0.5 nm, and the retardation in the thickness direction was ⁇ 119 nm.
  • the retardation of the liquid crystal layer alone was Re2 of 0 nm and Rth2 of It was estimated to be -154 nm.
  • the TAC film of the substrate was removed and only the homeotropic alignment liquid crystal layer was taken out and used when bonded to another substrate.
  • the thickness of the homeotropic alignment liquid crystal layer was 0.9 ⁇ m.
  • the homeotropic alignment liquid crystal layer corresponds to the second optically anisotropic layer.
  • Example 1 The structure of the laminated polarizing plate will be described with reference to FIG.
  • a triacetyl cellulose (TAC) film having a thickness of 40 ⁇ m, a front phase difference of 6 nm, and a thickness direction retardation of 60 nm is bonded as a protective film to one side of the polarizer obtained in Reference Example 1 via a polyvinyl alcohol adhesive.
  • TAC triacetyl cellulose
  • the first polarizing plate 1 was formed.
  • the other side of the first polarizing plate 1 is delayed in the roll width direction produced by lateral uniaxial stretching with the absorption axis of the first polarizing plate 1 having an absorption axis in the roll longitudinal direction via a polyvinyl alcohol adhesive.
  • the first optically anisotropic layer 3 made of norbornene-based resin having a phase axis and the absorption axis of the first polarizing plate 1 and the slow axis of the first optically anisotropic layer 3 are bonded so as to be orthogonal to each other.
  • the 2nd optically anisotropic layer 4 produced by the reference example 2 was bonded together via the acrylic adhesive, and the laminated polarizing plate 5 was obtained.
  • Re1 of the first optical anisotropic layer 3 has a phase difference of 115 nm
  • Rth1 has a phase difference of 103.5 nm.
  • the refractive index in each direction was in the relationship of nx1>ny1> nz1.
  • Example 2 A horizontal alignment type liquid crystal display device used in Example 2 will be described with reference to FIGS.
  • a transparent electrode 7 is formed of a material having a high transmittance made of an ITO layer on the substrate 6, and a liquid crystal layer 9 made of a liquid crystal material having a positive dielectric anisotropy is sandwiched between the transparent electrode 7 and the substrate 8. .
  • a liquid crystal material exhibiting positive dielectric anisotropy is used for the liquid crystal layer 9.
  • the laminated polarizing plate 5 produced in Example 1 was disposed on the display surface side (upper side in the figure) of the horizontal alignment type liquid crystal cell 10.
  • a linearly polarizing plate (SQW-062 manufactured by Sumitomo Chemical Co., Ltd.) was disposed as the second polarizing plate 11 on the back side (lower side of the figure) of the horizontal alignment type liquid crystal cell 10.
  • Rth of triacetyl cellulose used for the support substrate of the linearly polarizing plate was 35 nm.
  • the directions of the absorption axes of the first polarizing plate 1 and the second polarizing plate 11 indicated by arrows in FIG. 3 were 90 degrees and 0 degrees in the plane, respectively.
  • the first optically anisotropic layer 3 is formed of an optical element having an in-plane optical axis and negative biaxial optical anisotropy.
  • the slow axis orientation of the first optically anisotropic layer 3 indicated by an arrow in FIG. 3 is 0 degree, and the in-plane Re1 has a phase difference of 115 nm and the Rth1 has a phase difference of 103.5 nm.
  • the second optically anisotropic layer 4 made of a homeotropic alignment liquid crystal film exhibits a phase difference in which Re2 is 0 nm and Rth2 is ⁇ 154 nm.
  • contrast ratio 4 shows the contrast ratio from all directions, where the transmittance ratio (white display) / (black display) of black display 0V and white display 5V is used as the contrast ratio.
  • Contrast contour lines were set to 6000, 3000, 1000, and 200 in order from the inside.
  • the concentric circles indicate an angle of 20 degrees from the center. Therefore, the outermost circle shows 80 degrees from the center (the same applies to the following figures).
  • Example 3 The in-plane Re1 of the first optically anisotropic layer 3 made of norbornene-based resin is 125 nm, Rth1 is 87.5 nm, and the in-plane Re2 of the second optically anisotropic layer 4 made of homeotropic alignment liquid crystal film is 0 nm.
  • a horizontal alignment type liquid crystal display device was produced in the same manner as in Example 2 except that Rth2 was changed to -134 nm.
  • FIG. 5 shows the contrast ratio from all directions, where the transmittance ratio (white display) / (black display) of black display 0V and white display 5V is used as the contrast ratio. When the contrast ratio was viewed in all directions, it was found that the contrast ratio was high in all directions and good viewing angle characteristics were obtained.
  • Example 4 The in-plane Re1 of the first optically anisotropic layer 3 made of norbornene-based resin is 140 nm, Rth1 is 70 nm, the in-plane Re2 of the second optically anisotropic layer 4 made of homeotropic alignment liquid crystal film is 0 nm, Rth2 A horizontal alignment type liquid crystal display device was produced in the same manner as in Example 2 except that the thickness was ⁇ 113 nm.
  • FIG. 6 shows the contrast ratio from all directions, where the transmittance ratio (white display) / (black display) of black display 0V and white display 5V is used as the contrast ratio. When the contrast ratio was viewed in all directions, it was found that the contrast ratio was high in all directions and good viewing angle characteristics were obtained.
  • FIG. 7 shows the contrast ratio from all directions, with the transmittance ratio (white display) / (black display) of black display 0V and white display 5V as the contrast ratio.
  • the contrast ratio was viewed in all directions, it was found that the viewing angle characteristics deteriorated particularly in the four directions of upper right, upper left, lower right, and lower left.
  • FIG. 8 shows the contrast ratio from all directions, where the transmittance ratio (white display) / (black display) of black display 0V and white display 5V is used as the contrast ratio.
  • the contrast ratio was viewed in all directions, it was found that the viewing angle characteristics deteriorated particularly in the four directions of upper right, upper left, lower right, and lower left.
  • FIG. 9 shows the contrast ratio from all directions, where the transmittance ratio (white display) / (black display) of black display 0V and white display 5V is used as the contrast ratio.
  • the contrast ratio was viewed in all directions, it was found that the viewing angle characteristics deteriorated particularly in the four directions of upper right, upper left, lower right, and lower left.
  • FIG. 10 shows the contrast ratio from all directions, where the transmittance ratio (white display) / (black display) of black display 0V and white display 5V is used as the contrast ratio.
  • the contrast ratio was viewed in all directions, it was found that the viewing angle characteristics deteriorated particularly in the four directions of upper right, upper left, lower right, and lower left.
  • the second optical anisotropic layer 4 is a negative uniaxial TAC film with an in-plane retardation value of 0.5 nm and a thickness direction retardation value of +35 nm.
  • the contrast ratio of the transmittance ratio (white display) / (black display) of black display 0V and white display 5V was measured, it was particularly low in the four directions of upper right, upper left, lower right, and lower left when viewed in all directions. As a result, it was found that the viewing angle characteristics deteriorate.

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  • Geometry (AREA)
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Abstract

L'invention concerne une plaque de polarisation stratifiée qui est destinée à un dispositif d'affichage à cristaux liquides à alignement horizontal, qui a des caractéristiques supérieures de champ de vision, qui provient de la stratification, dans l'ordre donné, d'au moins une première plaque de polarisation, d'une première couche à anisotropie optique et d'une seconde couche à anisotropie optique, et est caractérisée en ce que la première couche à anisotropie optique et la seconde couche à anisotropie optique satisfont la relation suivante [1] : ‑60 nm ≤ Rth1 + Rth2 ≤ 60 nm (où Rth1 est la valeur de retard dans la direction de l'épaisseur du premier film à anisotropie optique, et Rth2 est la valeur de retard dans la direction de l'épaisseur du second film à anisotropie optique).
PCT/JP2014/058243 2013-03-28 2014-03-25 Plaque de polarisation stratifiée pour un dispositif d'affichage à cristaux liquides à alignement horizontal et dispositif d'affichage à cristaux liquides à alignement horizontal WO2014157181A1 (fr)

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JP2006178401A (ja) * 2004-11-29 2006-07-06 Nitto Denko Corp 液晶パネル及び液晶表示装置
JP2006520008A (ja) * 2004-01-09 2006-08-31 エルジー・ケム・リミテッド 負の二軸性位相差フィルムと＋ｃ−プレートを用いた視野角の補償フィルムを含むｉｐｓ液晶表示装置
JP2008051838A (ja) * 2006-08-22 2008-03-06 Fujifilm Corp 光学補償フィルム及び液晶表示装置
JP2010250204A (ja) * 2009-04-20 2010-11-04 Konica Minolta Opto Inc 液晶パネル
JP2013019943A (ja) * 2011-07-07 2013-01-31 Fujifilm Corp Ｉｐｓ又はｆｆｓ型液晶表示装置
JP2013160979A (ja) * 2012-02-07 2013-08-19 Fujifilm Corp Ｉｐｓ又はｆｆｓ型液晶表示装置

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Publication number Priority date Publication date Assignee Title
JP2006520008A (ja) * 2004-01-09 2006-08-31 エルジー・ケム・リミテッド 負の二軸性位相差フィルムと＋ｃ−プレートを用いた視野角の補償フィルムを含むｉｐｓ液晶表示装置
JP2006178401A (ja) * 2004-11-29 2006-07-06 Nitto Denko Corp 液晶パネル及び液晶表示装置
JP2008051838A (ja) * 2006-08-22 2008-03-06 Fujifilm Corp 光学補償フィルム及び液晶表示装置
JP2010250204A (ja) * 2009-04-20 2010-11-04 Konica Minolta Opto Inc 液晶パネル
JP2013019943A (ja) * 2011-07-07 2013-01-31 Fujifilm Corp Ｉｐｓ又はｆｆｓ型液晶表示装置
JP2013160979A (ja) * 2012-02-07 2013-08-19 Fujifilm Corp Ｉｐｓ又はｆｆｓ型液晶表示装置

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