LIQUID CRYSTAL DISPLAY DEVICE AND METHOD FOR PRODUCING SAME
20180321560 ยท 2018-11-08
Inventors
Cpc classification
G02F1/1368
PHYSICS
G02F1/134363
PHYSICS
H01L27/1214
ELECTRICITY
G02F1/134372
PHYSICS
H01L27/1218
ELECTRICITY
G02F1/133788
PHYSICS
C09K2323/02
CHEMISTRY; METALLURGY
International classification
G02F1/1337
PHYSICS
H01L27/12
ELECTRICITY
G02F1/1335
PHYSICS
G02F1/1368
PHYSICS
Abstract
A liquid crystal display device includes: upper and lower substrates; a liquid crystal layer and a sealing material between the upper and lower substrates, the liquid crystal layer containing liquid crystal molecules and the sealing material sealing the liquid crystal layer; and alignment control layers for controlling alignment of the liquid crystal molecules, one between the upper substrate and the liquid crystal layer and one between the lower substrate and the liquid crystal layer, wherein the upper and lower substrates are in direct contact with the sealing material, the alignment control layers contain a polymer having a structure derived from a polarized light-absorbing monomer having a polarized light-absorbing skeleton and at least two reactive functional groups, and the polarized light-absorbing skeleton includes a cinnamoyl skeleton.
Claims
1. A liquid crystal display device comprising: upper and lower substrates; a liquid crystal layer and a sealing material between the upper and lower substrates, the liquid crystal layer containing liquid crystal molecules and the sealing material sealing the liquid crystal layer; and alignment control layers for controlling alignment of the liquid crystal molecules, one between the upper substrate and the liquid crystal layer and one between the lower substrate and the liquid crystal layer, wherein the upper and lower substrates are in direct contact with the sealing material, the alignment control layers contain a polymer having a structure derived from a polarized light-absorbing monomer having a polarized light-absorbing skeleton and at least two reactive functional groups, and the polarized light-absorbing skeleton includes a cinnamoyl skeleton.
2. The liquid crystal display device according to claim 1, wherein the polarized light-absorbing skeleton is a chalcone skeleton.
3. The liquid crystal display device according to claim 1, wherein the reactive functional group is a (meth)acrylate group.
4. The liquid crystal display device according to claim 3, wherein the monomer has a structure in which the (meth)acrylate group is directly bonded to a benzene ring.
5. The liquid crystal display device according to claim 1, wherein the alignment control layers align the liquid crystal molecules in a direction substantially parallel to main surfaces of the upper and lower substrates when no voltage is applied.
6. A method for producing a liquid crystal display device, comprising: step (1) of forming a liquid crystal layer containing liquid crystal molecules and a polarized light-absorbing monomer between a pair of substrates bonded by a sealing material; step (2) of forming layers, one between the liquid crystal layer and one substrate and one between the liquid crystal layer and the other substrate, by irradiating the liquid crystal layer with polarized light to dimerize the polarized light-absorbing monomer and phase-separate the resulting dimer from the liquid crystal layer; and step (3) of forming alignment control layers for controlling alignment of the liquid crystal molecules by irradiating the liquid crystal layer with polarized light, with the temperature of the liquid crystal layer set to T.sub.N-I or higher, where T.sub.N-I indicates the phase transition temperature between a nematic phase and an isotropic phase of the liquid crystal molecules contained in the liquid crystal layer, wherein the polarized light-absorbing monomer has a polarized light-absorbing skeleton and at least two reactive functional groups, and the polarized light-absorbing skeleton includes a cinnamoyl skeleton.
Description
BRIEF DESCRIPTION OF DRAWINGS
[0020]
[0021]
[0022]
[0023]
[0024]
[0025]
[0026]
[0027]
[0028]
[0029]
[0030]
DESCRIPTION OF EMBODIMENTS
[0031] The present invention is described in more detail in the following embodiments with reference to the drawings, but is not limited to these embodiments. The features of each embodiment may be appropriately combined or modified without departing from the gist of the present invention.
[0032] As used herein, the polarized light-absorbing monomer means a monomer having a polarized light-absorbing functional group in the molecule. The polarized light-absorbing monomer according to the present invention has the following properties because of the presence of a cinnamoyl skeleton therein. Specifically, the polarized light-absorbing monomer dissolves in the liquid crystal and is phase-separated from a liquid crystal layer when dimerized as the liquid crystal layer is irradiated with polarized ultraviolet light, and such a dimer formed under specific conditions deposits on the substrates. The specific conditions may include, for example, temperature changes and adsorption to inorganic compounds. In addition, the polarized light-absorbing functional group means a functional group that absorbs polarized light when irradiated with polarized light having a specific wavelength in an ultraviolet wavelength region and/or a visible light wavelength region.
[0033] In addition, a mode in which liquid crystal molecules are aligned in a direction substantially parallel to the main surfaces of the substrates when no voltage is applied is also referred to as the horizontal alignment mode. Being substantially parallel means that, for example, the pre-tilt angle of liquid crystal molecules is in the range of 0 to 5 from the main surfaces of the substrates. A mode in which liquid crystal molecules are aligned in a direction substantially perpendicular to the main surfaces of the substrates when no voltage is applied is also referred to as a vertical alignment mode. Being substantially perpendicular means that, for example, the pre-tilt angle of liquid crystal molecules is in the range of 85 to 90 from the main surfaces of the substrates. The room temperature is a temperature in the range of 15 C. to 30 C. The pre-tilt angle is measured by a crystal rotation method using a device (model number: OMS-AF2) available from Chuo Seiki Kabushiki Kaisha.
[0034] The following embodiments mainly describe a case where a horizontal alignment mode is achieved, but the present invention is also applicable to a case where a vertical alignment mode is achieved.
Embodiment 1
[0035]
[0036] The lower substrate 10 includes the glass substrate 11 as a supporting substrate and thin-film transistor elements (a TFT array substrate 13) suitably disposed on the glass substrate 11. The lower substrate 10 also includes pixel electrodes 15p and a common electrode (not shown) on the same layer or different layers in some portions on an insulating film that covers the TFT array substrate 13. Here, the pixel electrodes and a common electrode being on the same layer or different layers means that the pixel electrodes and the common electrode are in contact with the same component (e.g., the liquid crystal layer 30 or the insulating film) on the liquid crystal layer 30 side and/or the side opposite to the liquid crystal layer 30 side of the pixel electrodes and the common electrode. Indium tin oxide (ITO) or indium zinc oxide (IZO) can be suitably used as a material of the pixel electrodes and the common electrode. The upper substrate 20 does not include electrodes but it includes the glass substrate 21 as a supporting substrate and components such as a color filter layer CF (optionally with a black matrix BM on the same layer) suitably disposed on the glass substrate 21. In addition, the lower substrate 10 and the upper substrate 20 do not include conventional alignment films (e.g., the alignment films 717 and 727 in
[0037] Unlike conventional liquid crystal display devices, the liquid crystal display device of Embodiment 1 includes substantially no portions where the alignment films adhere to the sealing material, and the sealing material is in direct contact with the substrates. Thus, it is possible to increase the adhesion strength of the sealing material to the substrate, resulting in a liquid crystal display device in which the sealing material is not easily peeled from the upper and lower substrates even when the device has a narrow frame. In addition, in the liquid crystal display device of Embodiment 1, the alignment control layers are not exposed to the outside environment, thus preventing a situation where moisture or the like enters from the edge of the alignment films exposed to the outside environment.
[0038] The alignment control layers 19 and 29 control the alignment of the liquid crystal molecules, and are formed as the polarized light-absorbing monomer having a polarized light-absorbing skeleton and at least two reactive functional groups, which has been added to the liquid crystal layer 30, is phase-separated from the liquid crystal layer 30 and polymerized. The horizontal alignment mode can be achieved with the alignment control layers 19 and 29.
[0039] The polarized light-absorbing monomer (hereinafter also simply referred to as the monomer) is required to be soluble in the liquid crystal.
[0040] The solubility of the monomer in the liquid crystal largely depends on the structure of a core portion (central portion). Monomers commonly used in photo-alignment films have a photoreactive group in the core portion, and their alignment is induced by a photoreaction. Examples of the photoreactive group include azobenzene groups that induce molecular alignment by polarized photoreaction, and photo-crosslinkable groups such as a cinnamic acid group, a chalcone group, a coumarin group, and anthracene group. However, monomers having an azo-based photo-functional group hardly dissolve in the liquid crystal. Among materials that induce dimerization, anthracene-based materials have low solubility in the liquid crystal, and only an amount of about 0.1% by mass or less dissolves in the liquid crystal. In contrast, materials having a cinnamoyl skeleton (C.sub.6H.sub.5CHCHCO) are highly compatible with the liquid crystal.
[0041] Among compounds having a cinnamoyl skeleton, cinnamic acid represented by the following formula has one benzene ring, and can be used as a monomer according to the present invention when two or more reactive functional groups are bonded to the benzene ring.
##STR00001##
[0042] In particular, the chalcone skeleton has two benzene rings, and a monomer having a chalcone skeleton is easily rendered multifunctional. When the monomer is a bifunctional monomer having a chalcone skeleton, preferably, one or more reactive functional groups are bonded to each of the two benzene rings of the chalcone skeleton.
[0043] The monomer according to the present invention has a polarized light-absorbing skeleton and at least two reactive functional groups. Preferably, the core portion of the monomer is a polarized light-absorbing skeleton, and at least two reactive functional groups are directly bonded to the core portion.
(Core Portion of Monomer)
[0044] The core portion of the monomer is preferably a polarized light-absorbing skeleton.
[0045] In order to form the alignment control layers that easily align the liquid crystal molecules by polarized light, the polarized light-absorbing skeleton as the core portion has a cinnamoyl skeleton. The polarized light-absorbing skeleton is preferably a chalcone skeleton. The benzene rings of the chalcone skeleton provide a rigid structure to the monomer.
[0046] It is essential that the core portion should dissolve in the liquid crystal, so that azo-based monomers used in photo-alignment films cannot be used as the core portion.
(Spacer Portion)
[0047] The monomer forms the alignment control layers after polymerization. Having an ability to control the alignment of the liquid crystal molecules means that the alignment control layers strongly interact with the liquid crystal molecules, and when the liquid crystal molecules move under the effect of the electric field, stress is imparted to deform the alignment control layers. If a spacer (e.g., alkyl spacer) is present between the core portion and the reactive functional group and if the spacer is long, the alignment control layers will be easily deformed. In the present invention, preferably, the monomer does not include such a spacer. For example, preferably, the monomer has a structure in which the reactive functional group such as a (meth)acrylate group is directly bonded to a benzene ring. The (meth)acrylate group refers an acrylate group, a methacrylate group, or both of these groups.
(Reactive Functional Group)
[0048] When the monomer has only one reactive functional group, polymerization of the monomer forms an easily deformable, linear polymer in which carbon-carbon bonds are one-dimensionally connected. The monomer having only one reactive functional group may reduce the voltage holding ratio of the liquid crystal.
[0049] In the present invention, as described above, since the polarized light-absorbing monomer has at least two reactive functional groups, polymerization of the polarized light-absorbing monomer results in the formation of a polymer having a network structure, making it possible to form a stable alignment control layers that are not highly soluble in the liquid crystal and that are not easily deformed by an external shock.
[0050] The reactive functional group is preferably one having a reactive unsaturated bond, more preferably a (meth)acrylate group, for example. For example, the monomer preferably has two (meth)acrylate groups.
[0051] Preferably, the monomer has a chalcone skeleton in which a reactive functional group such as methacrylate and/or acrylate is directly bonded to each benzene ring constituting the chalcone skeleton. A polymer formed from the monomer suitably forms alignment control layers. For example, 2-methyl acrylic acid 4-{3-[4-(2-methyl-acryloyloxy)-phenyl]-acryloyl}-phenyl ester represented by the following formula is particularly preferred. The monomer has a structure in which one methacrylate group is bonded to each of the two benzene rings constituting the chalcone skeleton.
##STR00002##
[0052] The molecular structure having methacrylate and/or acrylate directly bonded to the benzene rings generates radicals due to Fries rearrangement upon irradiation with ultraviolet light. The radicals initiate polymerization, and a polymer layer is formed from a dimer deposited on the substrate surface as described later. The polymer that forms a polymer layer has a high molecular weight and a three-dimensional network structure. Thus, the polymer does not easily dissolve in the liquid crystal, remains stable as is the case with a conventional alignment film even when the liquid crystal panel is subjected to an external shock or the like, and can stably align the liquid crystal molecules.
[0053] Thus, the liquid crystal display device of Embodiment 1 includes stable alignment control layers formed on the substrates and eliminates an unstable state associated with alignment control layers including a low molecular material.
[0054] Next, a method for producing the liquid crystal display device of Embodiment 1 is described.
[0055] According to the method for producing the liquid crystal display device of Embodiment 1, preferably, a bifunctional monomer having a chalcone skeleton is used as a monomer in an amount of about 0.1 to 10% by mass in the entire liquid crystal mixture (100% by mass) constituting the liquid crystal layer. If the amount is less than 0.1% by mass, the alignment control layer may not be formed on the entire interface between the liquid crystal layer and each substrate, failing to sufficiently control the alignment of the liquid crystal molecules. If the amount is more than 10% by mass, the polarized light-absorbing monomer will highly likely remain in the liquid crystal layer after the post-process, which may affect the performance such as reliability. For example, the monomer may precipitate, impairing the display performance of the liquid crystal panel.
[0056] The amount is preferably 0.3% by mass or more, more preferably 1% by mass or more. Meanwhile, the amount is preferably 5% by mass or less.
[0057] With regard to the substrates, as is the case with conventional liquid crystal panels, one substrate may include color filters, and the other substrate may have a structure in which the potential of the pixel electrodes can be controlled by switching elements such as TFTs. However, unlike conventional methods for producing liquid crystal panels, alignment films are not formed on the substrates.
[0058] After an agent for forming a sealing material is applied to one substrate, specifically to the outer periphery of a region corresponding to the liquid crystal panel, the substrate and the other substrate are bonded together such that they face each other. Thus, a pair of substrates is formed with a space sealed by the sealing material inside. The space sealed between the pair of substrates is rendered vacuum. Then, an inlet for injecting a liquid crystal mixture containing the monomer into the space is dipped in the liquid crystal mixture to inject the liquid crystal mixture into the space.
[0059] Instead of injecting the liquid crystal mixture as described above, the liquid crystal and the monomer may be added dropwise to one substrate, and then the substrate may be bonded to the other substrate in a vacuum chamber.
[0060] The sealing material may be one that is cured by heat or ultraviolet light, or by both heat and ultraviolet light.
[0061] After injection (or dropwise addition) of the liquid crystal, the liquid crystal layer is irradiated with polarized ultraviolet light while the temperature of the liquid crystal layer is in the range of room temperature (e.g., 20 C.) to T.sub.N-I+5 C. so as to dimerize the added monomer and phase-separate the resulting dimer from the liquid crystal layer to deposit the dimer on the substrates, thus forming dimer layers. The phase transition temperature ( C.) between the nematic phase and the isotropic phase of the liquid crystal molecules is indicated by T.sub.N-I (also referred to as NI point). The dimer layers can function as alignment control layers that horizontally align the liquid crystal molecules in a predetermined direction. Further, the dimer layers are irradiated with polarized ultraviolet light to polymerize the dimer to form alignment control layers. While the liquid crystal is heated to the isotropic phase (i.e., the liquid crystal is heated to a temperature equal to or higher than the phase transition temperature T.sub.N-I between the nematic phase and the isotropic phase of the liquid crystal molecules) so that the interaction between the dimer layers and the liquid crystal molecules is reduced to allow the alignment control layers to easily perform alignment, the dimer layers are irradiated with polarized ultraviolet light. Polarized ultraviolet light is emitted in the direction from the lower substrate with no color filters to the upper substrate. Subsequently, as the temperature is lowered to room temperature, the liquid crystal molecules are aligned by the alignment control layers. The temperature of the liquid crystal layer when irradiating the dimer layers with polarized ultraviolet light is preferably T.sub.N-I or higher of the liquid crystal material used. Meanwhile, the temperature is preferably T.sub.N-I+5 C. or lower. Even if the temperature of the liquid crystal panel is increased in the range of T.sub.N-I to T.sub.N-I+5 C., the dimer layer will not dissolve in the liquid crystal. This is because a polymer having a network structure is formed in the dimer layer by irradiation with polarized ultraviolet light and such a polymer no longer dissolves in the liquid crystal layer.
[0062] The liquid crystal may be either one having positive anisotropy of dielectric constant or one negative anisotropy of dielectric constant. In addition, T.sub.N-I of the liquid crystal molecules is not particularly limited, and the liquid crystal having any T.sub.N-I can be used. Yet, since there are cases where the liquid crystal layer is heated to a temperature equal to or higher than T.sub.N-I upon irradiation with polarized ultraviolet light, T.sub.N-I of the liquid crystal molecules is preferably below the glass-transition temperature of the sealing material.
[0063] After formation of the polymer, the temperature of the liquid crystal panel is cooled to room temperature, and components such as a polarizing plate and a backlight are suitably disposed. As a result, a transverse electric field mode liquid crystal display device in which the liquid crystal molecules are aligned substantially parallel to the main surfaces of the lower substrate and the upper substrates when no voltage is applied can be obtained.
[0064] As described above, the liquid crystal display device of Embodiment 1 can be suitably used not only as a vertical alignment mode liquid crystal display device but also as a horizontal alignment mode liquid crystal display device. In the case of the horizontal alignment mode, modes such as the IPS mode and the FFS mode are the main streams. The liquid crystal display device of Embodiment 1 can achieve not only the IPS mode and the FFS mode but also an electrically controlled birefringence (ECB) mode. Hereafter, the electrode structure of a horizontal alignment mode liquid crystal display device is described with more detail.
[0065]
[0066] The IPS mode liquid crystal display device shown in
[0067]
Embodiment 2
[0068]
[0069] The liquid crystal display device according to Embodiment 1 includes color filters and a black matrix disposed on the upper substrate. The color filters hardly transmit ultraviolet light, and the black matrix also does not transmit ultraviolet light. Thus, ultraviolet light to polymerize the monomer is emitted in the direction from the lower substrate (array substrate) with no color filters to the upper substrate.
[0070] The lower substrate has many light-blocking regions due to metal conductive lines constituting the TFT array. Thus, polymerization of the monomer in the liquid crystal by irradiation with ultraviolet light takes time. In addition, since the light-blocking portions interfere with the formation of the alignment control layers, there may be a wide light-blocking region where the alignment control layers cannot be formed. If such a case occurs, the liquid crystal molecules in the display region (on the pixel electrodes) may cause alignment defect.
[0071] Thus, in Embodiment 2, color filters CF are disposed on a lower substrate 310. As shown in
[0072] The upper substrate 320 of Embodiment 2 does not include any structures that block ultraviolet light. Thus, ultraviolet light to polymerize the monomer in the liquid crystal can be efficiently emitted in the direction from the upper substrate 320 to the lower substrate. In addition, since there are no shaded portions, the alignment control layers can be easily formed on the entire substrates.
[0073] The liquid crystal display device and the production method thereof of Embodiment 2 are the same as in Embodiment 1, except that the color filters CF are disposed on the lower substrate 310 instead of the upper substrate 320 and ultraviolet light to polymerize the monomer in the liquid crystal is emitted in the direction from the upper substrate 320 to the lower substrate. Such a liquid crystal display device including the color filters disposed on the lower substrate 310 can also achieve not only the vertical alignment mode but also the horizontal alignment mode with alignment control layers 319 and 329.
Embodiment 3
[0074]
[0075] In the liquid crystal display device of Embodiment 3, the color filters CF are coated with an overcoat in order to prevent passage of impurities from the color filters. Since the adhesion of the sealing material S to an overcoat 424 is lower than the adhesion of the sealing material directly attached to the substrates, the overcoat 424 should not be disposed under the sealing material S (e.g., see JP 2010-8534 A).
[0076] As shown in
[0077] It is possible to produce a vertical alignment mode (e.g., VA, vertical ECB, or vertical TN mode) liquid crystal display device using any of the liquid crystal display devices of the embodiments described above. Also in such a liquid crystal display device, the sealing material can be in direct contact with the upper substrate and the lower substrate, without conventional alignment films disposed between the sealing material and the upper and lower substrates. Thus, it is possible to produce a liquid crystal display device in which the sealing material is not easily peeled from the upper and lower substrates even when the device has a narrow frame.
Comparative Embodiment 1
[0078] Azobenzene-based materials are widely known materials for use in photo-alignment films (e.g., K. Ichimura, Y. Suzuki, and T. Seki, Langmuir, 4. 1214 (1988)).
[0079] In the case where a multifunctional monomer is dissolved in the liquid crystal to be photopolymerized so as to form alignment control layers and the alignment control layers are used to align the liquid crystal as in Embodiment 1 described above, a compound represented by the following formula may be suggested, for example.
##STR00003##
[0080] The molecular size is preferably smaller for dissolution in the liquid crystal. The alkyl spacer portion between the core portion and the reactive functional group is preferably shorter (or absent) to prevent the polymerized polymer from being deformed by stress. Thus, the molecule has a structure including only one azobenzene in which a methacrylate group is directly bonded to each benzene ring constituting the azobenzene.
[0081] Attempts were made to dissolve the compound in the liquid crystal, but only less than 0.05% by mass of the compound dissolved in the entire liquid crystal layer. Thus, the compound could not be used to align the liquid crystal molecules.
Additional Remarks
[0082] Examples of preferred aspects of the liquid crystal display device of the present invention are listed below. These examples may be appropriately combined without departing from the gist of the present invention.
[0083] In the present invention, the pair of substrates is in direct contact with the sealing material without an alignment film therebetween. The pair of substrates does not include conventional alignment films. Examples of components constituting the surface layer of each substrate which is in direct contact with the sealing material include supporting substrates (e.g., glass substrates), electrodes, and an insulating film. In view of enhancing the adhesion strength, a structure in which the glass substrates are in direct contact with the sealing material is preferred.
[0084] The polarized light-absorbing skeleton is preferably a chalcone skeleton.
[0085] Preferably, the reactive functional group contains a reactive unsaturated bond. More preferably, the reactive functional group contains a reactive double bond. The reactive double bond is further preferably a carbon-carbon double bond.
[0086] The reactive functional group is preferably a (meth)acrylate group.
[0087] The alignment control layers preferably align the liquid crystal molecules in a direction substantially parallel to the main surfaces of the upper and lower substrates when no voltage is applied. Thus, a horizontal alignment mode liquid crystal display device can be achieved. In one preferred embodiment of the present invention, the liquid crystal display device of the present invention is a horizontal alignment mode liquid crystal display device. The horizontal alignment mode may be, for example, an IPS mode, an FFS mode, or an ECB mode. The positive or negative anisotropy of dielectric constant of the liquid crystal can be selected to be best suited for each mode.
[0088] The alignment control layers may align the liquid crystal molecules in the direction substantially perpendicular to the main surfaces of the pair of substrates when no voltage is applied. Thus, a vertical alignment mode liquid crystal display device can be achieved. In another preferred embodiment of the present invention, the liquid crystal display device of the present invention is a vertical alignment mode liquid crystal display device. The vertical alignment mode maybe, for example, a vertical ECB mode, a 4-domain vertical ECB mode, a TBA (Transverse Bent Alignment) mode, a VA mode, a MVA (Multi-domain Vertical Alignment) mode, or a 4-domain vertical TN (Twisted Nematic) mode. The positive or negative anisotropy of dielectric constant of the liquid crystal can be selected to be best suited for each mode.
[0089] The polarized light-absorbing monomer may have a carboxy group, a hydroxyl group, or an amine group. Among these groups, the carboxy group is particularly preferred.
[0090] The liquid crystal material contained in the liquid crystal layer may have positive anisotropy of dielectric constant. In such a case, the major axis of each liquid crystal molecule is aligned along the line of electric force when voltage is applied, so that the alignment can be more easily controlled, further improving the high-speed response.
[0091] Examples of preferred aspects of the method for producing the liquid crystal display device of the present invention are listed below. These examples may be appropriately combined or modified without departing from the gist of the present invention.
[0092] The present invention may relate to a method for producing a liquid crystal display device, including: step (1) of forming a liquid crystal layer containing liquid crystal molecules and a polarized light-absorbing monomer between a pair of substrates bonded by a sealing material; step (2) of forming layers, one between the liquid crystal layer and one substrate and one between the liquid crystal layer and the other substrate, by irradiating the liquid crystal layer with polarized light to dimerize the polarized light-absorbing monomer and phase-separate the resulting dimer from the liquid crystal layer; and step (3) of forming alignment control layers for controlling alignment of the liquid crystal molecules by irradiating the liquid crystal layer with polarized light, with the temperature of the liquid crystal layer set to T.sub.N-I or higher, where T.sub.N-I indicates the phase transition temperature between a nematic phase and an isotropic phase of the liquid crystal molecules contained in the liquid crystal layer, wherein the polarized light-absorbing monomer has a polarized light-absorbing skeleton and at least two reactive functional groups, and the polarized light-absorbing skeleton includes a cinnamoyl skeleton.
[0093] In the present invention, the polarized light for irradiation in step (3) is preferably polarized ultraviolet light, particularly preferably linearly polarized ultraviolet light. Irradiation conditions of the polarized light can be appropriately set according to the composition of the polarized light-absorbing monomer.
[0094] In step (3), the liquid crystal layer may be irradiated with polarized light with the temperature of the layer set in the range of T.sub.N-I to T.sub.N-I+5 C.
[0095] Steps (1) to (3) may be performed at a constant temperature without changing the temperature of the liquid crystal layer. For example, the temperature of the liquid crystal layer in steps (1) to (3) is preferably constant in the range of T.sub.N-I to T.sub.N-I+5 C. without changing. This enables easy production of the liquid crystal display device of the present invention.
[0096] Step (1) may be performed with the temperature of the liquid crystal layer set to T.sub.N-I or higher, and step (2) may be performed with the temperature of the liquid crystal layer lowered from T.sub.N-I or higher to below T.sub.N-I. This enables suitable formation of the alignment control layers owing to the effect that causes the polarized light-absorbing monomer to dissolve in the liquid crystal material at a temperature of T.sub.N-I or higher and to phase-separate from the liquid crystal layer at a temperature below T.sub.N-I.
[0097] Step (2) may be performed with the polarized light-absorbing monomer being adsorbed to an inorganic compound constituting the surface layer of each substrate of the pair. This enables suitable formation of the alignment control layers owing to the effect that causes the polarized light-absorbing monomer to be adsorbed to the inorganic compound.
REFERENCE SIGNS LIST
[0098] 10, 110, 210, 310, 410, 710, 810, 910: lower substrate [0099] 11, 21, 111, 121, 211, 221, 311, 321, 411, 421, 711, 721, 811, 821, 911, 921: glass substrate [0100] 13, 313, 413: TFT array substrate [0101] 15p, 115p, 215p, 315p, 415p: pixel electrode [0102] 15c, 115c, 215c, 315c: common electrode [0103] 19, 29, 119, 129, 219, 229, 319, 329, 419, 429: alignment control layer [0104] 20, 120, 220, 320, 420, 720, 820, 920: upper substrate [0105] 30, 130, 230, 330, 430, 730, 830, 930: liquid crystal layer [0106] 424: overcoat [0107] 700: liquid crystal display device [0108] 717, 727, 817, 827, 917, 927: alignment film [0109] BM: black matrix [0110] CF: color filter layer [0111] DE: drain electrode [0112] GE: gate electrode [0113] GL: gate bus line [0114] S: sealing material [0115] SC: semiconductor layer [0116] SE: source electrode [0117] SL: source bus line [0118] Rf: frame region