WO2010116564A1 - 液晶表示装置、液晶表示装置の製造方法、重合体層形成用組成物、及び、液晶層形成用組成物 - Google Patents
液晶表示装置、液晶表示装置の製造方法、重合体層形成用組成物、及び、液晶層形成用組成物 Download PDFInfo
- Publication number
- WO2010116564A1 WO2010116564A1 PCT/JP2009/069565 JP2009069565W WO2010116564A1 WO 2010116564 A1 WO2010116564 A1 WO 2010116564A1 JP 2009069565 W JP2009069565 W JP 2009069565W WO 2010116564 A1 WO2010116564 A1 WO 2010116564A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- liquid crystal
- display device
- crystal display
- polymerization initiator
- radical polymerization
- Prior art date
Links
Images
Classifications
-
- G—PHYSICS
- G02—OPTICS
- G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
- G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
- G02F1/01—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour
- G02F1/13—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells
- G02F1/133—Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
- G02F1/1333—Constructional arrangements; Manufacturing methods
- G02F1/1337—Surface-induced orientation of the liquid crystal molecules, e.g. by alignment layers
- G02F1/133711—Surface-induced orientation of the liquid crystal molecules, e.g. by alignment layers by organic films, e.g. polymeric films
-
- G—PHYSICS
- G02—OPTICS
- G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
- G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
- G02F1/01—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour
- G02F1/13—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells
- G02F1/133—Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
- G02F1/1333—Constructional arrangements; Manufacturing methods
- G02F1/1337—Surface-induced orientation of the liquid crystal molecules, e.g. by alignment layers
- G02F1/133711—Surface-induced orientation of the liquid crystal molecules, e.g. by alignment layers by organic films, e.g. polymeric films
- G02F1/133715—Surface-induced orientation of the liquid crystal molecules, e.g. by alignment layers by organic films, e.g. polymeric films by first depositing a monomer
-
- G—PHYSICS
- G02—OPTICS
- G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
- G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
- G02F1/01—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour
- G02F1/13—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells
- G02F1/133—Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
- G02F1/1333—Constructional arrangements; Manufacturing methods
- G02F1/1337—Surface-induced orientation of the liquid crystal molecules, e.g. by alignment layers
- G02F1/13378—Surface-induced orientation of the liquid crystal molecules, e.g. by alignment layers by treatment of the surface, e.g. embossing, rubbing or light irradiation
- G02F1/133788—Surface-induced orientation of the liquid crystal molecules, e.g. by alignment layers by treatment of the surface, e.g. embossing, rubbing or light irradiation by light irradiation, e.g. linearly polarised light photo-polymerisation
Definitions
- the present invention relates to a liquid crystal display device, a method for producing a liquid crystal display device, a composition for forming a polymer layer, and a composition for forming a liquid crystal layer. More specifically, a liquid crystal display device having a polymer layer formed on an alignment film, a method for producing the liquid crystal display device, a composition for forming a polymer layer suitable for forming a polymer layer, and a composition for forming a liquid crystal layer It is about things.
- a liquid crystal display is a display device that controls transmission / blocking of light (display on / off) by controlling the orientation of liquid crystal molecules having birefringence.
- LCD display methods include vertical alignment (VA) mode in which liquid crystal molecules having negative dielectric anisotropy are aligned perpendicular to the substrate surface, and liquid crystal molecules having positive dielectric anisotropy.
- VA vertical alignment
- IPS in-plane switching
- MVA Multi-domain Vertical Alignment
- liquid crystal molecules having negative dielectric anisotropy and providing banks (linear protrusions) and electrode extraction parts (slits) as alignment regulating structures.
- the liquid crystal alignment azimuth at the time of voltage application can be controlled to a plurality of azimuths without applying rubbing treatment to the alignment film, and the viewing angle characteristics are excellent.
- the conventional MVA-LCD there is room for improvement in that the upper part of the protrusion and the upper part of the slit become the boundary of the alignment division of the liquid crystal molecules, the transmittance during white display is lowered, and a dark line may be seen in the display. was there.
- a pretilt angle providing technique using a polymer as a method for obtaining an LCD capable of high brightness and high-speed response (see, for example, Patent Documents 1 and 2).
- a liquid crystal composition in which polymerizable components such as polymerizable monomers and oligomers are mixed is sealed between substrates, and a voltage is applied between the substrates to tilt (tilt) the liquid crystal molecules.
- the monomer is polymerized to form a polymer.
- liquid crystal molecules tilted at a predetermined pretilt angle can be obtained, and the orientation direction of the liquid crystal molecules can be defined in a certain direction.
- the monomer a material that is polymerized by heat, light (ultraviolet rays) or the like is selected.
- the polymerization initiator for starting the polymerization reaction of a monomer may be mixed in a liquid crystal composition.
- a liquid crystal layer composition containing a liquid crystal material, a polymerizable monomer, and a polymerization initiator is injected between a pair of substrates to cause a polymerization reaction under predetermined conditions to cause an alignment film. Even when the polymer layer was formed on the top, it was found that the finished liquid crystal display device sometimes showed burn-in and there was room for further improvement.
- the present invention has been made in view of the above-described present situation, and an object thereof is to provide a liquid crystal display device with reduced burn-in.
- the inventors of the present invention have studied various causes of image sticking in the liquid crystal display device, and have focused on components contained in the liquid crystal layer after the polymerization reaction. Even after a series of polymerization reactions are completed, it is found that unreacted monomers and polymerization initiators remain in the liquid crystal layer, and unreacted monomers remain in the liquid crystal layer. In this case, the unreacted monomer slowly starts the polymerization reaction due to the influence of the backlight light in the general usage mode after completion or the influence of the inspection aging process after the assembly process, and as a result, the pretilt It was found that the liquid crystal display had burned in due to the change of the corners.
- the present inventors have conducted further intensive studies. As a result, the burn-in caused by the change in the pretilt angle can be seen in a liquid crystal display by adjusting the concentration of the polymerization initiator in the liquid crystal layer to a certain level or less.
- the inventors have arrived at the present invention by conceiving that the cause of burn-in can be solved and the above-mentioned problems can be solved brilliantly.
- the present invention is a liquid crystal display device including a pair of substrates and a liquid crystal layer sandwiched between the pair of substrates, wherein at least one of the pair of substrates includes an alignment film and the alignment film
- the polymer layer is formed by polymerization in which the polymerizable monomer starts to react with a polymerization initiator that is 1 mol% or less with respect to the polymerizable monomer. is there.
- the control mode of the liquid crystal layer provided in the liquid crystal display device of the present invention is not particularly limited, such as a twisted nematic (TN) mode, a VA mode, and an IPS mode.
- one or both of the pair of substrates is an MVA mode, 4D-RTN (4 domain Reverse TN) provided with an alignment control structure such as a protrusion made of a dielectric and / or a slit provided in the electrode.
- an alignment control structure such as a protrusion made of a dielectric and / or a slit provided in the electrode.
- one of the pair of substrates provided in the liquid crystal display device of the present invention is used as an array substrate and the other as a color filter substrate.
- the array substrate includes a plurality of pixel electrodes, whereby the alignment of the liquid crystal is controlled on a pixel-by-pixel basis.
- the color filter substrate is, for example, a color filter composed of R (red), G (green), B (blue), etc. is arranged at a position where it overlaps with the pixel electrode of the array substrate, and the display color is displayed in units of pixels. Be controlled.
- the alignment film refers to a film that aligns adjacent liquid crystal molecules in a certain direction, and includes any film that does not undergo alignment treatment and that that performs alignment treatment.
- An example of the alignment film is a resin film.
- a vertical alignment film formed using a general vertical alignment film material or a horizontal alignment film formed using a general horizontal alignment film material is used for the alignment film without performing an alignment process. Also good.
- the alignment treatment means for performing the alignment treatment include rubbing treatment and photo-alignment treatment.
- At least one of the pair of substrates provided in the liquid crystal display device of the present invention has a polymer layer on the alignment film, and the polymer layer is formed by a polymerization initiator that is 1 mol% or less with respect to the polymerizable monomer.
- the polymerizable monomer is formed by polymerization that initiates the reaction.
- the polymerization initiator is 0.1 mol% or less with respect to the polymerizable monomer, and more preferably, the polymerization initiator is 0.01 mol% or less with respect to the polymerizable monomer.
- the polymer layer included in the liquid crystal display device of the present invention is composed of a polymer formed by the polymerization reaction initiated by the action of the polymerization initiator, so that the pretilt caused by the remaining unpolymerized monomer is caused.
- the seizure based on the change in angle is suppressed and a polymer layer having a high crosslinking density is obtained by performing a sufficient polymerization reaction, the seizure based on the change in the pretilt angle due to external stress is suppressed.
- the polymerizable monomer include a polymerizable monomer that initiates a polymerization reaction upon irradiation with light, a polymerizable monomer that initiates a polymerization reaction upon heating, and the like, and as a result, a polymer layer is formed.
- a radical polymerization initiator is mentioned as said polymerization initiator
- a radical polymerization is mentioned as said polymerization.
- the polymer layer allows the alignment film to be regularly tilted in a fixed direction with respect to adjacent liquid crystal molecules without performing an alignment treatment. For example, when a polymer layer is formed by polymerizing a monomer in a state where the liquid crystal molecules are pretilt-aligned, the polymer layer is in contact with the liquid crystal molecules regardless of whether or not the alignment film is aligned. Thus, it is formed in a form having a structure for pretilt alignment.
- the configuration of the liquid crystal display device of the present invention is not particularly limited by other components as long as such components are essential.
- the polymer layer is formed by light irradiation, the polymerizable monomer is polymerized by light irradiation, the polymerization initiator is a radical polymerization initiator, and the polymerization is radical polymerization by light irradiation. preferable. Thereby, the polymerization reaction can be easily started at room temperature.
- the radical polymerization is composed of three elementary reactions of an initiation reaction, a growth reaction, and a termination reaction, and usually has the following radical polymerization reaction mechanism.
- the radical polymerization initiator When the polymerization initiator is a radical polymerization initiator, the radical polymerization initiator preferably has a function of stopping radical polymerization.
- the reaction rate of the radical polymerization reaction is greatly improved, so that unreacted monomers are less likely to remain, and image sticking based on changes in the pretilt angle is suppressed.
- radicals when the monomer contained in the liquid crystal layer undergoes radical polymerization based on the radical polymerization initiator, radicals remain at the end of the formed polymer, and this causes residual DC voltage in the alignment film and the polymer layer. It can be a cause.
- the radical polymerization initiator causes the initiation reaction by bonding with the monomer and can further stop the radical polymerization reaction by bonding with the terminal of the polymer, the radical is introduced into the polymer constituting the polymer layer. It can be made difficult to remain, and the residual DC voltage accumulated in the alignment film and the polymer layer can be reduced. As a result, the occurrence of image sticking based on the residual DC voltage can be suppressed.
- the molecular weight distribution of the polymer constituting the polymer layer is preferably 8 or less.
- the molecular weight distribution is defined by the weight average molecular weight / number average molecular weight of the polymer. If the molecular weight distribution of the polymer is 8 or less, it means that the polymerization has progressed sufficiently, and image sticking based on a change in the pretilt angle is suppressed.
- the molecular weight distribution can be measured using, for example, a gel permeation chromatography method (GPC: Gel Permeation Chromatography).
- GPC Gel Permeation Chromatography
- the radical polymerization initiator has the following general formula (1):
- R represents H, C n H 2n + 1 or C n H 2n CF 3 , and n is an integer of 1 to 18). It is preferable to initiate polymerization by generating radicals with ultraviolet light.
- the radical polymerization initiator includes the following general formulas (3-1) to (3-8);
- the radical polymerization initiator has the following general formula (5):
- R represents C n H 2n + 1 , n is an integer of 1 to 18, and A represents an aromatic compound. It is preferable to generate a radical by light and initiate polymerization.
- the radical polymerization is represented by the following reaction formula (8);
- the radical polymerization initiator has the following general formula (9);
- the radical polymerization initiator includes the following general formulas (10-1) to (10-17);
- R represents any of CH 3 , C 2 H 5 , C 6 H 13 , C 10 H 21 and C 12 H 25 ) and the following general formulas (11-1) to (11-3) ;
- Each of the pair of substrates has an electrode, and the polymer layer is formed by polymerization of a polymerizable monomer in a state where a voltage higher than a threshold is applied to the liquid crystal layer through the electrode. It is preferable.
- the polymer layer is formed by polymerization performed in a state where a voltage higher than a threshold is applied to the liquid crystal layer, that is, in a state where the inclination of the liquid crystal molecules in the liquid crystal layer is changed from when no voltage is applied. Therefore, since the surface shape of the polymer layer has a shape along the inclination of the liquid crystal molecules after the change, the pretilt alignment of the liquid crystal molecules is further stabilized, and the liquid crystal when the voltage application state is switched. An improvement in the propagation speed of the molecular gradient, that is, an improvement in the response speed can be realized.
- the alignment film is preferably made of a material containing a compound having a photoreactive functional group.
- the alignment film is preferably a photo-alignment film composed of a material imparted with alignment with liquid crystal molecules by light irradiation. Since the photo-alignment process is a non-contact type alignment process, the orientation imparted by the photo-alignment process can be adjusted by the irradiation angle of the light, the wavelength of the irradiation light, the intensity, etc. A 4D-RTN configuration that defines four different orientation directions can be easily obtained.
- the photoreactive functional group is preferably a cinnamate group, a chalcone group, a tolan group, a coumarin group, or an azobenzene group. These photoreactive functional groups can be formed relatively easily on the side chain of the polymer, and are also excellent in reactivity.
- the alignment film is preferably composed of a copolymer including a monomer unit having a side chain containing a photoreactive functional group and a monomer unit having a side chain not containing a photoreactive functional group.
- the alignment film preferably aligns the liquid crystal molecules in the liquid crystal layer vertically when no voltage is applied. Since the alignment film has such characteristics, the response speed of a liquid crystal display device using a liquid crystal molecule having negative dielectric anisotropy such as VA mode and MVA mode can be increased.
- the alignment film preferably tilts the liquid crystal molecules in the liquid crystal layer in an oblique direction with respect to the normal direction to the alignment film surface when no voltage is applied.
- Such an alignment film can be obtained by subjecting a general resin material, vertical alignment film material, or horizontal alignment film material to an alignment process such as a rubbing process or an optical alignment process.
- the polymer layer acts in a direction to increase the alignment regulating force of the alignment film, leading to a reduction in image sticking. In this case, it is not necessary to perform the polymerization step while applying a voltage higher than the threshold value to the liquid crystal layer.
- the same seizure prevention effect as that in the case of performing the polymerization step while applying the above voltage can be obtained.
- the liquid crystal display device includes a plurality of pixels, and a region of the liquid crystal layer corresponding to one of the pixels is divided into a plurality of regions having different alignment directions. Preferably it is. By forming multiple regions with different alignment directions of liquid crystal molecules in one pixel region, the same view can be ensured even when viewing the display screen from different angles. Angular characteristics are improved.
- alignment dividing means include alignment control structures such as linear bank-like projections made of dielectric on the electrodes, means for forming linear slits formed in the electrodes, photo-alignment Examples include means for adjusting the light irradiation angle when forming the film to change the orientation of the pretilt angle of the alignment film.
- the plurality of regions are preferably four regions. By dividing into four, the viewing angle characteristics are improved in a balanced manner even when the viewing angle is tilted in any of the upward, downward, left and right directions with respect to the normal direction of the display screen.
- a method of manufacturing the liquid crystal display device of the present invention using the feature of forming a polymer layer on the alignment film as described above includes a pair of substrates and a liquid crystal layer sandwiched between the pair of substrates.
- a manufacturing method of a liquid crystal display device wherein the manufacturing method is a step of forming an alignment film on at least one of the pair of substrates and 1 mol% or less with respect to the polymerizable monomer on the alignment film.
- a method for producing a liquid crystal display device comprising the step of initiating radical polymerization of a polymerizable monomer with a radical polymerization initiator to form a polymer layer is preferred.
- the ratio of the radical polymerization initiator to the monomer in the above production method is adjusted to 1 mol% or less, it is possible to suppress the remaining unreacted polymerization monomer compared to the case where no radical polymerization initiator is added.
- a polymer layer having a high crosslink density can be obtained, seizure due to a change in pretilt angle can be prevented.
- by preparing the radical polymerization initiator at a low concentration it is possible to reduce the residual DC voltage caused by the remaining radicals, and from this point, the effect of preventing seizure can be obtained.
- the radical polymerization initiator in the above production method preferably has a function of stopping radical polymerization. Since the radical polymerization initiator also has a function of stopping the polymerization reaction by binding to the end of the polymer, it is difficult for radicals to remain in the polymer constituting the alignment film and the polymer layer. Therefore, it is possible to prevent the residual DC voltage from being accumulated, and to prevent the occurrence of image sticking based on the residual DC voltage.
- the step of forming the polymer layer in the above production method is preferably a step of forming a polymer layer by polymerizing a polymerizable monomer with a voltage applied to the liquid crystal layer in a voltage higher than a threshold value.
- the step of forming the alignment film in the manufacturing method preferably includes a step of performing an alignment treatment by irradiating light.
- the step of performing the alignment treatment by irradiating light since the contact type treatment such as rubbing is not performed, the possibility of damage to the structure (for example, TFT) under the alignment film can be reduced.
- the orientation imparted by the photo-alignment treatment can be adjusted by the light irradiation angle, the wavelength of light to be irradiated, the intensity, and the like, 4D-RTN that defines four different orientation directions within one pixel. Therefore, the process of obtaining a wide viewing angle can be performed relatively easily.
- a method for manufacturing a liquid crystal display device of the present invention includes the pair of substrates.
- a method for producing a liquid crystal display device in which the molecular weight distribution of the polymer is 8 or less can be mentioned. As described above, when the molecular weight distribution of the polymer is 8 or less, it means that the polymerization is sufficiently progressed, and the image sticking based on the change in the pretilt angle is suppressed.
- the production method preferably includes a step of dissolving the monomer and a polymerization initiator having a concentration of 1 mol% or less in the liquid crystal material before the step of forming the polymer layer.
- a concentration of 1 mol% or less in the liquid crystal material As described above, by setting the above concentration, it is possible to suppress the unreacted polymerization monomer from remaining and to obtain a polymer layer having a high crosslink density. Can be prevented.
- the step of forming the polymer layer is a step of forming a polymer layer on the vertical alignment film by starting polymerization by an initiation reaction with a polymerization initiator in a voltage application state higher than a threshold with respect to the liquid crystal layer. Is preferred. As a result, the pretilt alignment of the liquid crystal molecules is further stabilized, and the propagation speed of the liquid crystal molecules when the voltage application state is switched, that is, the response speed is improved, particularly in the VA mode, the MVA mode, etc. This is realized by a type using liquid crystal molecules having dielectric anisotropy.
- the manufacturing method preferably includes a step of performing an alignment treatment by irradiating light to an alignment film formed of a material including a compound having a photoreactive functional group.
- the photo-alignment process can be easily performed, and a 4D-RTN that defines four different orientation directions in one pixel depending on the light irradiation angle, the wavelength of light to be irradiated, the intensity, and the like. The form can be easily obtained.
- the photoreactive functional group is preferably a cinnamate group, a chalcone group, a tolan group, a coumarin group, or an azobenzene group. As described above, these photoreactive functional groups can be formed relatively easily on the side chain of the polymer, and are excellent in reactivity.
- the alignment film is preferably composed of a copolymer including a monomer unit having a side chain containing a photoreactive functional group and a monomer unit having a side chain not containing a photoreactive functional group.
- the present invention also provides a polymer layer forming composition comprising a polymerizable monomer and a polymerization initiator, wherein the concentration of the polymerization initiator is 1 mol% or less with respect to the polymerizable monomer. It is also a composition for use.
- the ratio of the polymerization initiator is 0.1 mol% or less with respect to the polymerizable monomer, and more preferably, the ratio of the polymerization initiator is 0.01 mol% or less with respect to the polymerizable monomer. It is.
- a ratio of the polymerization initiator to the polymerizable monomer at a low concentration for example, when a polymer layer made of the composition for forming a polymer layer of the present invention is formed on an alignment film of a liquid crystal display device Since a polymer layer having a high crosslinking density can be obtained while suppressing the unpolymerized monomer from remaining, a polymer layer in which the change in the pretilt angle hardly occurs afterwards can be obtained. As a result, it is possible to obtain a liquid crystal display device that is excellent in response speed and hardly burns in.
- composition of the composition for forming a polymer layer of the present invention is not particularly limited by other components as long as such components are formed as essential.
- examples of the polymer layer forming composition include a composition that forms a polymer layer by light irradiation.
- the polymerizable monomer is a monomer that is polymerized by light irradiation, and the polymerization initiator is preferably a radical polymerization initiator. Thereby, the polymerization reaction can be easily started at room temperature.
- the polymerization initiator preferably has a function of stopping the polymerization.
- a polymer layer is formed by using a polymerization initiator that has a function of causing an initiation reaction by binding to a monomer and stopping a polymerization reaction by binding to a terminal of a polymer. It is possible to make it difficult for radicals to remain in the polymer to be retained, and to suppress the accumulation of residual DC voltage in the alignment film and the polymer layer.
- a polymer layer made of the polymer layer forming composition of this embodiment is formed on the alignment film of the liquid crystal display device, the occurrence of image sticking based on the residual DC voltage can be suppressed.
- the present invention is also a liquid crystal layer forming composition comprising the polymer layer forming composition and a liquid crystal material.
- the liquid crystal display device of the present invention includes a polymer layer formed on the alignment film using a radical polymerization initiator having a low concentration relative to the monomer, image sticking is unlikely to occur.
- Embodiment 1 is an example of the liquid crystal display device of the present invention produced using the polymer layer forming composition and the liquid crystal layer forming composition of the present invention.
- the liquid crystal display device according to Embodiment 1 includes a polymer layer formed by radical polymerization of a polymerizable monomer by light irradiation on an alignment film. By forming such a polymer layer, the alignment of the liquid crystal is controlled.
- the polymer layer thus formed on the alignment film is also referred to as a PSA (Polymer Sustained Alignment) layer.
- radical polymerization is initiated by the action of a radical polymerization initiator.
- the composition (liquid crystal layer forming composition) used for forming the liquid crystal layer in Embodiment 1 is a composition (polymer layer forming composition) containing a polymerizable monomer and a radical polymerization initiator in addition to the liquid crystal material.
- concentration of the radical polymerization initiator relative to the polymerizable monomer is adjusted to 1 mol% or less.
- the reaction rate of the polymerization reaction does not increase, and there is a high possibility that unreacted monomers remain in the liquid crystal layer. Then, the unreacted monomer slowly starts the polymerization reaction due to the influence of the backlight light in the general use mode after completion or the aging process for inspection after the assembly process.
- the size of the pretilt angle of the applied PSA layer changes, and image sticking tends to occur.
- a PSA layer having a low crosslinking density is obtained. Therefore, the size of the pretilt angle of the PSA layer is easily changed under the influence of elastic energy of liquid crystal molecules, Image burn-in tends to occur.
- the concentration of the radical polymerization initiator with respect to the polymerizable monomer is as high as 2 mol% or more and not all the radical polymerization initiator is consumed by the radical polymerization reaction, due to the influence of the radical site of the radical polymerization initiator, Residual DC voltage is likely to occur in the alignment film and the PSA layer. Further, if a DC voltage remains in the alignment film and the PSA layer, image sticking tends to occur.
- Embodiment 1 since the addition amount of the radical polymerization initiator is adjusted to a low concentration, both image sticking based on the change in the pretilt angle and image sticking based on the residual DC voltage can be suppressed. . Even at a low concentration, the addition of a radical polymerization initiator starts the polymerization reaction and increases the rate of progress of the polymerization reaction, leading to improved throughput.
- the light irradiation for starting the radical polymerization reaction is preferably performed in a state where a voltage equal to or higher than a threshold is applied to the liquid crystal layer.
- Embodiment 1 as the polymerizable monomer, for example, those represented by the following general formula (I) can be used.
- P 1 -S 1 -A 1- (Z 1 -A 2 ) n -S 2 -P 2 (I) (Wherein P 1 and P 2 represent the same or different acrylate group, methacrylate group, acrylamide group, methacrylamide group, vinyl group, vinyloxy group or epoxy group.
- a 1 and A 2 are 1,4-phenylene.
- S 1 and S 2 are the same or different — (CH 2 ) m — (0 ⁇ m ⁇ 6) , — (CH 2 —CH 2 —O) m — (0 ⁇ m ⁇ 6), or P 1 and A 1 , A 1 and P 2 or A 2 and P 2 are directly bonded hydrogen atoms .
- a 1 and A 2 have the The androgenic group or a methyl group may be substituted.
- Examples of the radical polymerization initiator that can be used in Embodiment 1 include compounds represented by the following chemical formulas (3-1) to (3-8).
- the compounds used in the above chemical formulas (3-1) to (3-8) or the above reaction formula (8) are compounds that do not generate a gas such as carbon dioxide (CO 2 ) when radical polymerization starts.
- the radical polymerization initiator used in Embodiment 1 is a very suitable material from the viewpoint of suppressing seizure. The relationship between gas generation and image sticking will be described in Example 1 below.
- Examples of the radical polymerization initiator having higher solubility in the liquid crystal layer in Embodiment 1 include compounds represented by the following chemical formulas (4-1) to (4-3).
- Any of the compounds represented by the above chemical formulas (4-1) to (4-3) has a 1,4-phenylene group at one or both ends serving as a polymerization initiation point. Is highly soluble.
- the liquid crystal display device of Embodiment 1 includes an array substrate 10, a color filter substrate 20, and a liquid crystal layer 30 sandwiched between a pair of substrates including the array substrate 10 and the color filter substrate 20.
- the array substrate 10 includes an insulating transparent substrate made of glass or the like, and further includes a support substrate 11 including various wirings, pixel electrodes, TFTs, and the like formed on the transparent substrate.
- the color filter substrate 20 includes an insulating transparent substrate made of glass or the like, and a support substrate 21 including a color filter, a black matrix, a common electrode, and the like formed on the transparent substrate.
- the array substrate 10 includes an alignment film 12 on the support substrate 11, and the color filter substrate 20 includes an alignment film 22 on the support substrate 21.
- the alignment films 12 and 22 are films mainly composed of polyimide, polyamide, polyvinyl, polysiloxane, and the like, and by forming the alignment film, liquid crystal molecules before voltage application are pretilt aligned (initial tilt) in a certain direction. be able to. In the VA mode, these alignment films 12 and 22 are preferably vertical alignment films having a pretilt angle of 80 ° or more.
- a monomer may be added to the alignment films 12 and 22. Even if the alignment film containing the polymer composed of the monomer is not energized even when energized, it is difficult to cause a change in the change in the pretilt angle.
- the polymerizable monomer represented by the above formula (I) is By forming the alignment film by adding it at a concentration of 5 to 20 mol% with respect to the monomer constituting the alignment film polymer, an alignment film having better alignment stability can be obtained.
- the liquid crystal display device according to Embodiment 1 is linear when viewed from the normal direction with respect to the support substrate surface in the pixel electrode of the support substrate 11 and / or in the common electrode of the support substrate 21. Having a slit.
- a PSA layer that functions as an alignment film that imparts pretilt alignment to liquid crystal molecules can be formed by initiating radical polymerization reaction of the polymerization monomer by light irradiation.
- the dielectric is linear when viewed from the normal direction with respect to the support substrate surface on the pixel electrode and / or the common electrode.
- a body protrusion may be formed.
- the liquid crystal molecules are inclined obliquely toward the dielectric protrusion when no voltage is applied. Therefore, even when the voltage higher than the threshold is not applied to the liquid crystal layer 30, the PSA that functions as an alignment film that imparts pretilt alignment to the liquid crystal molecules when the polymerization monomer starts radical polymerization reaction by light irradiation.
- a layer can be formed.
- the material of the dielectric protrusion include resist resins such as polyimide and novolac.
- the liquid crystal display device has both a linear slit provided in the pixel electrode or the common electrode and a linear dielectric protrusion provided on the pixel electrode and / or the common electrode.
- a linear slit provided in the pixel electrode or the common electrode
- a linear dielectric protrusion provided on the pixel electrode and / or the common electrode.
- only the linear slit is used without using the dielectric protrusion. It is preferable to use it.
- the slits and / or the dielectric protrusions are preferably arranged so as to extend in an oblique direction (for example, about 45 ° or 135 °) with respect to each side of the pixel electrode.
- the slit and / or the dielectric protrusion has a bent portion, and is U-shaped, V-shaped, W-shaped or a combination thereof when viewed from the normal direction with respect to the support substrate surface. It is preferable from the viewpoint of widening the viewing angle characteristics.
- a polymerizable monomer 41 exists in the liquid crystal layer 30 before the PSA polymerization step. Then, the polymerizable monomer 41 starts to be polymerized by the PSA polymerization process, and becomes the PSA layers 13 and 23 on the alignment films 12 and 22 as shown in FIG. Improve. However, if unreacted polymerizable monomer remains in the liquid crystal layer 30, polymerization occurs again by irradiation of backlight light in the aging process or the like, and the tilt angle of the already formed PSA layer may be changed. is there.
- the PSA layers 13 and 23 are composed of a liquid crystal layer forming composition obtained by adding a polymer layer forming composition containing a polymerizable monomer and a radical polymerization initiator to a liquid crystal material, as an array substrate and a color filter substrate. And the liquid crystal layer 30 is irradiated with a certain amount of light to radically polymerize the polymerizable monomer. At this time, a PSA layer with higher alignment stability can be obtained by performing light irradiation in a state where a voltage equal to or higher than the threshold is applied to the liquid crystal layer 30.
- the array substrate 10, the liquid crystal layer 30, and the color filter substrate 20 are stacked in this order from the back side of the liquid crystal display device toward the observation surface side.
- a polarizing plate is provided on the back side of the support substrate 11 included in the array substrate 10.
- a polarizing plate is also provided on the observation surface side of the support substrate 21 included in the color filter substrate 20.
- a retardation plate may be further arranged for these polarizing plates, and the polarizing plate may be a circularly polarizing plate.
- the liquid crystal display device may be any of a transmission type, a reflection type, and a reflection / transmission type. If it is a transmission type or a reflection / transmission type, the liquid crystal display device of Embodiment 1 further includes a backlight. The backlight is arranged on the further back side of the array substrate 10, and is arranged so that light passes through the array substrate 10, the liquid crystal layer 30, and the color filter substrate 20 in this order.
- the array substrate 10 includes a reflection plate for reflecting external light. Further, at least in a region where reflected light is used as a display, the polarizing plate of the color filter substrate 20 needs to be a circularly polarizing plate provided with a so-called ⁇ / 4 retardation plate.
- the liquid crystal display device according to the first embodiment may be in the form of a color filter-on-array including a color filter on the array substrate 10.
- the liquid crystal display device according to the first embodiment may be a monochrome display. In that case, the color filter does not need to be arranged.
- the liquid crystal layer 30 is filled with a liquid crystal material having a characteristic of being oriented in a specific direction when a constant voltage is applied.
- the orientation of the liquid crystal molecules in the liquid crystal layer 30 is controlled by applying a voltage equal to or higher than a threshold value, and the control mode of the liquid crystal molecules of the liquid crystal display device according to the first embodiment is one or both of the pair of substrates. Is a mode having a slit provided in the electrode, and a wide viewing angle is realized.
- the liquid crystal display device is disassembled, and nuclear magnetic resonance analysis (NMR: Nuclear Magnetic Resonance), Fourier transform infrared spectroscopy (FT-IR), mass spectrometry (MS: Analyzing the components of the alignment film, analyzing the components of the PSA layer forming monomer or radical polymerization initiator contained in the liquid crystal layer, and forming the PSA layer present in the PSA layer by performing chemical analysis using mass spectrometry Analysis of monomer components, the amount of PSA layer forming monomer or radical polymerization initiator contained in the liquid crystal layer, the presence ratio of the PSA layer forming monomer or radical polymerization initiator in the PSA layer, etc. it can.
- NMR Nuclear Magnetic Resonance
- FT-IR Fourier transform infrared spectroscopy
- MS mass spectrometry
- Example 1 Hereinafter, an example in which a liquid crystal cell included in the liquid crystal display device according to Embodiment 1 is actually manufactured will be described.
- a pair of support substrates is prepared, a polyimide-based solution as a material for the vertical alignment film is applied to the surfaces of the pair of support substrates, pre-baked at 80 ° C., and subsequently at 200 ° C. Post bake was performed.
- each of the pixel electrodes included in the pair of support substrates is provided with a plurality of slits that are linear when viewed from the normal direction with respect to the support substrate surface.
- a seal is applied to one support substrate, beads are dispersed on the other support substrate, a pair of support substrates are bonded together, and a negative dielectric anisotropy is provided between the pair of support substrates.
- a liquid crystal layer forming composition containing a liquid crystal material was injected.
- the composition for forming a liquid crystal layer used in this example includes a bifunctional monomer represented by a compound represented by the following chemical formula (12), a radical polymerization initiator represented by a compound represented by the following chemical formula (13), and A sample containing a bifunctional monomer represented by a compound represented by the following chemical formula (12) and a radical polymerization initiator represented by a compound represented by the following chemical formula (14), and the following chemical formula (12 ) And a bifunctional monomer represented by a compound represented by the following formula (15) and two radical polymerization initiators (benzophenone and N, N-diethylaniline) represented by the following chemical formula (15), respectively,
- the concentration of the radical polymerization initiator relative to the concentration of the bifunctional monomer is 0.01 mol%, 0.1 mol%, 1 mol%, 2.5 mol%, Beauty, were produced in total 15 kinds of samples were prepared with 5 mole%.
- the following chemical reaction formula (16) shows a state in which the radical polymerization initiator represented by the compound represented by the chemical formula (13) is irradiated with ultraviolet rays to form radicals.
- the following chemical reaction formula (17) shows a state in which the radical polymerization initiator represented by the compound represented by the chemical formula (14) is irradiated with ultraviolet rays to form radicals.
- carbon dioxide (CO 2 ) is generated as radicals are formed.
- the following chemical reaction formula (18) shows a state in which two radical polymerization initiators represented by the compound represented by the chemical formula (15) are irradiated with ultraviolet rays to form radicals.
- the pair of supporting substrates into which the liquid crystal layer forming composition has been injected are heated and quenched at 130 ° C., and further, black light (with a peak wavelength at 300 to 350 nm is applied while applying a voltage higher than the threshold value).
- black light (with a peak wavelength at 300 to 350 nm is applied while applying a voltage higher than the threshold value).
- a certain ultraviolet ray was irradiated for 20 minutes to carry out the polymerization reaction of the bifunctional monomer, thereby completing each liquid crystal cell in which the PSA layer was formed on the vertical alignment film.
- VHR Voltage : Holding Ratio
- Residual DC (Direct Current) voltage pretilt angle change amount
- VHR was measured under the conditions of 1V and 70 ° C.
- the residual DC voltage was measured by a flicker elimination method with a DC offset voltage of 1 V and 40 ° C.
- the amount of change in the pretilt angle was calculated by subtracting the pretilt angle before the backlight light irradiation from the pretilt angle after the backlight light irradiation energization.
- liquid crystal cell similar to the sample of this example, except that it does not contain a radical polymer in the liquid crystal layer forming composition was prepared as a reference cell for comparison with these samples.
- the amount of tilt angle change based on VHR, residual DC voltage, and backlight light irradiation energization was measured.
- Table 1 is a table showing the measurement results of VHR (%) after irradiating backlight light for about 100 hours using each of the above samples.
- Table 2 is a table showing the measurement results of the residual DC voltage (mV) after irradiating the backlight for about 100 hours using each of the above samples.
- the value of the residual DC voltage is a measured value one hour after the DC voltage is applied.
- the compounds represented by the chemical formulas (13) and (15) were used as radical polymerization initiators at the start of the polymerization reaction.
- the example in which the compound represented by the chemical formula (14) is used as a radical polymerization initiator at the start of the polymerization reaction the residual DC voltage is determined using the compound represented by the chemical formula (14) as a radical polymerization initiator. In the example used, it was confirmed to be larger. This is presumably because the compound represented by the chemical formula (14) generated carbon dioxide (CO 2 ) in the radical polymerization initiation reaction, and the gas density mixed in the liquid crystal layer increased.
- the radical polymerization initiator When the concentration was 0.01 mol%, the residual DC voltage was 100 (mV) or less, and good results were obtained for improvement in image sticking.
- the residual DC voltage is 100 or less regardless of the value as long as it is 1 mol% or less. Good results were obtained for improvement in image sticking.
- Table 3 is a table showing the measurement results of the amount of change in pretilt angle (°) when AC energization is performed at 5 V while irradiating backlight light for about 100 hours using each of the above samples.
- the liquid crystal cell after the measurement was disassembled and the molecular weight distribution of the polymer layer was evaluated by GPC.
- a polymer was obtained using the polymerization initiator represented by the chemical formulas (13), (14) and (15).
- the molecular weight distribution of the polymer forming the layer was 5 in all cases, and the molecular weight distribution of the polymer forming the polymer layer under the condition without the polymerization initiator was 15 or more.
- the concentration of the radical polymerization initiator is 0.1 mol% than when it is 1 mol%, the effect of suppressing the decrease in VHR and the increase in residual DC voltage can be obtained. It was found that when the content was 0.01 mol% than when 0.1 mol%, the effect of further suppressing the decrease in VHR and the increase in the residual DC voltage was obtained.
- Embodiment 2 is an example of the liquid crystal display device of the present invention produced using the polymer layer forming composition and the liquid crystal layer forming composition of the present invention. Similar to the liquid crystal display device according to the first embodiment, the liquid crystal display device according to the second embodiment includes a PSA layer formed by radical polymerization of a polymerizable monomer on the alignment film, but the alignment film is subjected to an alignment treatment. Is used, which is different from the liquid crystal display device according to the first embodiment in that the pretilt angle is not less than 80 ° and less than 90 °. The liquid crystal display device according to the second embodiment is substantially the same as the liquid crystal display device according to the first embodiment with respect to the configuration other than the alignment film.
- the PSA layer when the PSA layer is formed, it is preferable to irradiate light with a voltage higher than a threshold applied to the liquid crystal layer, but since the alignment treatment is performed, the liquid crystal layer On the other hand, a PSA layer having a relatively high alignment regulating force can be obtained without irradiating light with a voltage higher than the threshold applied.
- a monomer may be added to the alignment film material.
- a method of performing a photo-alignment process as the alignment process that is, a method of forming a photo-alignment film will be described in detail.
- a solution in which a photo-alignment film material having a photoreactive functional group is dissolved in a solvent is applied onto a support substrate on which the alignment film is formed by a printing method or the like, pre-baked, further baked, and the solvent component is evaporated.
- the photofunctional group may be either a photobonding type or a photolytic type.
- the compound having a photoreactive functional group include a polyamide compound represented by the following general formula (19) and a polyimide compound represented by the following general formula (20).
- the functional group represented by Z in the following general formula functions as a photoreactive functional group.
- X represents any one of the following general formulas (21-1) to (21-8)
- Y represents any one of the following general formulas (22-1) to (22-15)
- Z represents (A functional group containing a photoreactive functional group represented by any one of the following general formulas (23-1) to (23-6), where m represents the number of repeating structures in parentheses and is a positive integer.)
- X represents any one of the following general formulas (21-1) to (21-8)
- Y represents any one of the following general formulas (22-1) to (22-15)
- Z represents (A functional group containing a photoreactive functional group represented by any one of the following general formulas (23-1) to (23-6), where m represents the number of repeating structures in parentheses and is a positive integer.)
- the photo-alignment film material used in Embodiment 2 may be a copolymer (copolymer) having a side chain having a photoreactive functional group and a side chain not having a photoreactive functional group.
- a copolymer examples include compounds represented by the following chemical formula (24) or (25).
- X represents any one of the above general formulas (21-1) to (21-8)
- Y represents any one of the above general formulas (22-1) to (22-15)
- Z represents The functional group containing the photoreactive functional group of any one of the above general formulas (23-1) to (23-6) is represented
- W represents any one of the following general formulas (26-1) to (26-6).
- M represents the composition ratio of the monomer units in the copolymer and is a numerical value from 0 to 1
- n represents a degree of polymerization and is a positive integer
- D in the following general formulas (26-1) to (26-6)
- E are selected from the group consisting of the same or different O, CO, COO, OCO, NHCO, CONH, S, two phenylene groups bonded directly to each other, a methylene group, and an alkylene group having 2 to 6 carbon atoms. Indicates a divalent group.
- X represents any one of the above general formulas (21-1) to (21-8)
- Y1 represents any one of the above general formulas (22-1) to (22-15)
- Y2 represents Represents a divalent organic group having an alicyclic skeleton having 4 to 40 carbon atoms
- Z represents a functional group containing any one of the photoreactive functional groups represented by the general formulas (23-1) to (23-6).
- Q represents O, CO, COO, OCO, NHCO, S, or a phenylene group and Y2 are directly bonded
- m represents a composition ratio of monomer units in the copolymer and is from 0 to 1.
- N is a positive integer representing the degree of polymerization, and examples corresponding to the portion V include the following general formulas (27-1) to (27-8).
- A is a phenylene group or groups on both sides of A are directly bonded to each other.
- B or C each independently represents O, CO, COO, OCO, NHCO, CONH, S, Ar-Ar-CH2- (Ar is a phenylene group), a methylene group, or an alkylene group having 2 to 6 carbon atoms. And a divalent group selected from a phenylene group.)
- the photo-alignment film is formed by irradiating a certain amount of, for example, ultraviolet rays, preferably polarized ultraviolet rays, from an oblique direction.
- the magnitude of the pretilt angle imparted to the liquid crystal molecules by the photo-alignment film can be adjusted by the light irradiation time, the light irradiation intensity, the wavelength of the irradiated light, the type of the photofunctional group, and the like.
- the orientation processing direction is made different between the pair of substrates so as to be orthogonal to each other, and one pixel is divided into four domains (Domain 4D-RTN (Reverse Twisted Nematic) mode).
- Domain 4D-RTN Reverse Twisted Nematic
- the viewing angle is greatly improved.
- 4D-RTN high-precision pretilt control is required, but according to the liquid crystal display device of Embodiment 2, a pretilt with excellent stability can be obtained due to the influence of the PSA layer formed on the alignment film. Therefore, sufficient alignment stability can be obtained even when 4D-RTN is used.
- the liquid crystal display device is disassembled, and is subjected to nuclear magnetic resonance analysis (NMR: Nuclear Magnetic Resonance), Fourier transform infrared spectroscopy (FT-IR), mass spectrometry (MS: Analysis of the components of the alignment film, analysis of the PSA layer forming monomer or radical polymerization initiator component contained in the liquid crystal layer, and the PSA layer forming monomer present in the PSA layer by chemical analysis using mass spectrometry Analysis of the components, the amount of the PSA layer forming monomer or radical polymerization initiator contained in the liquid crystal layer, the abundance ratio of the PSA layer forming monomer or radical polymerization initiator in the PSA layer, and the like can be confirmed.
- NMR Nuclear Magnetic Resonance
- FT-IR Fourier transform infrared spectroscopy
- MS mass spectrometry
- Example 2 Hereinafter, an example in which a liquid crystal cell included in the liquid crystal display device according to the second embodiment is actually manufactured will be described.
- a pair of support substrates is prepared, a polyimide-based solution as a material for the vertical alignment film is applied to the surfaces of the pair of support substrates, prebaked at 80 ° C., and subsequently at 200 ° C. Post bake was performed.
- photo-alignment treatment was performed by irradiating with ultraviolet polarized light having a wavelength near 300 nm at a dose of 100 mJ / cm 2 from a direction oblique to 40 to 50 ° with respect to the support substrate surface.
- a liquid crystal layer forming composition containing a liquid crystal material was injected.
- the composition for forming a liquid crystal layer used in this example is represented by a bifunctional monomer represented by the compound represented by the chemical formula (12) and a compound represented by the chemical formula (13), as in Example 1.
- benzophenone and N, N-diethylaniline were added in equimolar%.
- the above mol% is the amount of each of benzophenone and N, N-diethylaniline added.
- the pair of supporting substrates into which the composition for forming a liquid crystal layer is inserted is rapidly heated and cooled at 130 ° C., and further, black light (ultraviolet light having a peak wavelength at 300 to 350 nm) is applied with no voltage applied. ) For 20 minutes to carry out the polymerization reaction of the bifunctional monomer, thereby completing each liquid crystal cell in which the PSA layer was formed on the vertical alignment film.
- the completed liquid crystal cells were subjected to backlight irradiation at 5 V for about 100 hours, and the voltage holding ratio (VHR), the residual DC voltage, and the tilt angle change amount for each of the liquid crystal cells after irradiation were set. It was measured.
- VHR voltage holding ratio
- VHR was measured under the conditions of 1V and 70 ° C.
- the residual DC voltage was measured by a flicker elimination method with a DC offset voltage of 1 V and 40 ° C.
- the amount of change in the pretilt angle was calculated by subtracting the tilt angle before the backlight light irradiation from the tilt angle after the backlight light irradiation energization.
- liquid crystal cell similar to the sample of this example, except that it does not contain a radical polymer in the liquid crystal layer forming composition was prepared as a reference cell for comparison with these samples.
- the amount of change in tilt angle based on VHR, residual DC voltage, and backlight irradiation energization was measured.
- Table 4 is a table showing the measurement results of VHR (%) after irradiating backlight light for about 100 hours using each of the above samples.
- Table 5 is a table showing the measurement results of the residual DC voltage (mV) after irradiating the backlight for about 100 hours using each of the above samples.
- the value of the residual DC voltage is a measured value one hour after the DC voltage is applied.
- the compounds represented by the chemical formulas (13) and (15) were used as radical polymerization initiators at the start of the polymerization reaction.
- the example in which the compound represented by the chemical formula (14) is used as a radical polymerization initiator at the start of the polymerization reaction the residual DC voltage is determined using the compound represented by the chemical formula (14) as a radical polymerization initiator. In the example used, it was confirmed to be larger. This is presumably because the compound represented by the chemical formula (14) generated carbon dioxide (CO 2 ) in the radical polymerization initiation reaction, and the gas density mixed in the liquid crystal layer increased.
- the concentration of the radical polymerization initiator is 0.01.
- the residual DC voltage was 100 (mV) or less, and a good result was obtained for improvement of image sticking.
- Table 6 is a table showing the measurement results of the tilt angle change amount (°) when AC energization is performed for about 100 hours at 5 V while irradiating backlight light, using each of the above samples.
- the liquid crystal cell after the measurement was disassembled and the molecular weight distribution of the polymer layer was evaluated by GPC.
- a polymer was obtained using the polymerization initiator represented by the chemical formulas (13), (14) and (15).
- the molecular weight distribution of the polymer forming the layer was 5 in all cases, and the molecular weight distribution of the polymer forming the polymer layer under the condition without the polymerization initiator was 15 or more.
- the concentration of the radical polymerization initiator is 0.1 mol% than when it is 1 mol%, the effect of suppressing the decrease in VHR and the increase in residual DC voltage can be obtained. It was found that when the content was 0.01 mol% than when 0.1 mol%, the effect of further suppressing the decrease in VHR and the increase in the residual DC voltage was obtained.
- the alignment film By using an alignment film that has been subjected to an alignment treatment, even if the polymer layer is formed by a polymerization reaction in a state where no voltage is applied to the liquid crystal layer, the alignment film has a sufficient alignment regulating force. It was found that this was effective in reducing seizure.
- Embodiment 3 is an example of the liquid crystal display device of the present invention produced using the polymer layer forming composition and the liquid crystal layer forming composition of the present invention.
- the liquid crystal display device according to the third embodiment includes a PSA layer formed by radical polymerization of a polymerizable monomer on an alignment film, like the liquid crystal display devices according to the first and second embodiments.
- the radical polymerization initiator used for initiating the polymerization reaction is different from the first and second embodiments in that it is also a polymerization terminator for terminating the radical polymerization.
- such a radical polymerization initiator that also functions as a polymerization terminator is also referred to as an iniferter.
- the liquid crystal display device according to the third embodiment is substantially the same as the liquid crystal display device according to the first or second embodiment, except for the PSA layer.
- the alignment film that has not been subjected to the alignment treatment as in the first embodiment may be used, or the alignment film that has been subjected to the optical alignment treatment as in the second embodiment may be used.
- the iniferter causes an initiation reaction by bonding with a monomer, and further stops the radical polymerization reaction by bonding with the end of the polymer.
- This makes it difficult for radicals to remain in the polymer constituting the polymer layer, so that the residual DC voltage accumulated in the alignment film and the polymer layer can be reduced. Therefore, according to the liquid crystal display device of Embodiment 3, it is possible to suppress the occurrence of image sticking based on the residual DC voltage.
- Examples of the iniferter that can be used in Embodiment 3 include compounds represented by the following chemical formulas (10-1) to (10-17).
- R represents any of CH 3 , C 2 H 5 , C 6 H 13 , C 10 H 21, and C 12 H 25.
- the compounds represented by the above chemical formulas (10-1) to (10-17) serving as iniferters are compounds that do not generate a gas such as carbon dioxide (CO 2 ) when radical polymerization starts.
- the iniferter used in Form 3 is a suitable material from the viewpoint of suppressing seizure.
- Examples of the iniferter having higher solubility in the liquid crystal layer in Embodiment 3 include compounds represented by the following chemical formulas (11-1) to (11-3).
- Any of the compounds represented by the chemical formulas (11-1) to (11-3) has a phenyl group or a 1,4-phenylene group at one or both ends serving as a polymerization initiation point.
- High solubility in liquid crystal material By using a radical polymerization initiator having high solubility in the liquid crystal material in this way, the iniferter is consumed more efficiently, so the reaction rate of the polymerization reaction can be further improved and unreacted monomers can remain. Can be further reduced.
- the liquid crystal display device is disassembled, and is subjected to nuclear magnetic resonance analysis (NMR: Nuclear Magnetic Resonance), Fourier transform infrared spectroscopy (FT-IR), mass spectrometry (MS: Analysis of the components of the alignment film, analysis of the PSA layer forming monomer or iniferter component contained in the liquid crystal layer, and the components of the PSA layer forming monomer present in the PSA layer by chemical analysis using mass spectrometry Analysis, the amount of the PSA layer forming monomer or iniferter contained in the liquid crystal layer, the abundance ratio of the PSA layer forming monomer or iniferter in the PSA layer, and the like can be confirmed.
- NMR Nuclear Magnetic Resonance
- FT-IR Fourier transform infrared spectroscopy
- MS mass spectrometry
- Example 3 Hereinafter, an example in which a liquid crystal cell included in the liquid crystal display device according to Embodiment 3 is actually manufactured will be described.
- a pair of support substrates is prepared, a polyimide-based solution as a material for the vertical alignment film is applied to the surfaces of the pair of support substrates, prebaked at 80 ° C., and subsequently at 200 ° C. Post bake was performed.
- the composition for forming a liquid crystal layer used in this example includes a bifunctional monomer (M) represented by the compound represented by the chemical formula (12) and an iniferter represented by the compound represented by the following chemical formula (28). And the concentration of the iniferter with respect to the bifunctional monomer concentration is 0.01 mol%, 0.1 mol%, 1 mol%, 2.5 mol%, and 5 mol%. A total of five types of samples prepared as described above were prepared.
- M represents a monomer
- m and n represent a positive integer.
- the radical polymerization reaction in Example 3 begins with the iniferter forming a radical by irradiating the iniferter with ultraviolet rays, as shown in the chemical reaction formula (29-1).
- the iniferter that has become a radical bonds with the monomer (M) to start radical polymerization of the monomer (M), and the monomer (M)
- radical polymerization connecting a plurality of thiocarbamate proceeds, a thiocarbamate group is covalently bonded to the radical at the end of the radical polymerization.
- the thiocarbamate group is dissociated as shown by the chemical reaction formula (29-3), and again the monomer.
- the polymerization reaction (M) proceeds. That is, in the chemical reaction formula (29-3), the thiocarbamate group plays a role of chain transfer. Then, such binding and dissociation of the thiocarbamate group are repeatedly performed. Finally, the thiocarbamate group is covalently bonded to the radical at the radical polymerization terminal, and the radical polymerization reaction is stopped.
- an iniferter that repeats the start and stop of polymerization in terms of keeping the radical concentration low in a system containing a monomer and / or polymer having a radical end dissolved in the liquid crystal layer. Residual DC voltage can be hardly generated in the alignment film and the PSA layer, and as a result, occurrence of burn-in can be prevented. Further, since no gas such as carbon dioxide (CO 2 ) is generated in the polymerization reaction, the occurrence of image sticking is prevented from this point.
- CO 2 carbon dioxide
- Example 3 a pair of support substrates into which a composition for forming a liquid crystal layer containing an iniferter is injected is heated and cooled at 130 ° C., and a voltage higher than a threshold is applied to the liquid crystal layer.
- the liquid crystal cell in which the PSA layer was formed on the vertical alignment film was obtained by irradiating with black light (ultraviolet light having a peak wavelength at 300 to 350 nm) for 20 minutes and performing the polymerization reaction of the bifunctional monomer (M). Each completed.
- black light ultraviolet light having a peak wavelength at 300 to 350 nm
- the completed liquid crystal cells were irradiated with backlight light at 5 V for about 100 hours, and each liquid crystal cell after irradiation was subjected to voltage holding ratio (VHR), residual DC voltage, and change in pretilt angle. The amount was measured.
- VHR voltage holding ratio
- VHR was measured under conditions of 1V and 70 ° C.
- the residual DC voltage was measured by a flicker elimination method with a DC offset voltage of 1 V and 40 ° C.
- the amount of change in the pretilt angle was calculated by subtracting the tilt angle before the backlight light irradiation from the tilt angle after the backlight light irradiation energization.
- liquid crystal cell similar to the sample of this example except that no iniferter is included in the composition for forming a liquid crystal layer was prepared as a reference cell for comparison with these samples, and VHR was obtained in the same manner.
- the amount of change in the pretilt angle based on the residual DC voltage and the backlight light irradiation energization was measured.
- Table 7 is a table showing the measurement results of VHR (%) after irradiating backlight light for 100 hours using the above samples.
- Table 8 is a table showing the measurement results of the residual DC voltage (mV) after irradiating backlight light for about 100 hours using each of the above samples.
- the value of the residual DC voltage is a measured value one hour after the DC voltage is applied.
- the residual DC voltage is 100 (mV) or less at 1 mol% or less. As a result, good results were obtained for improvement in image sticking.
- Table 9 is a table showing the measurement results of the tilt angle change amount (°) when AC energization is performed at 5 V while irradiating backlight light for about 100 hours using each of the above samples.
- the amount of change in the pretilt angle was an order of magnitude greater in the example in which the iniferter was not added at all. The value was confirmed. Due to the function of stopping the polymerization reaction by the iniferter, it was confirmed that the possibility of new polymerization by irradiation of the backlight is greatly reduced, and as a result, it has a great effect on suppressing the change of the tilt angle.
- the liquid crystal cell after the measurement was disassembled, and the molecular weight distribution of the polymer layer was evaluated by GPC.
- the molecular weight distribution of the polymer in which the polymer layer was formed under the condition that there was no iniferter was 15 or more.
- the iniferter by mixing the iniferter with the monomer in the composition for forming the liquid crystal layer, the occurrence of image sticking based on the change in the pretilt angle can be greatly reduced, and the amount of iniferter mixed can be polymerized. It was found that the occurrence of image sticking based on the residual DC voltage can be suppressed by adjusting the amount to 1 mol% or less with respect to the functional monomer. Further, when the concentration of the iniferter is 0.1 mol% than when it is 1 mol%, the effect of suppressing the decrease in VHR and the increase in the residual DC voltage can be obtained. It was found that when the content was 0.01 mol% than when it was 1 mol%, the effect of further suppressing the decrease in VHR and the increase in the residual DC voltage was obtained.
Landscapes
- Physics & Mathematics (AREA)
- Nonlinear Science (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Mathematical Physics (AREA)
- Chemical & Material Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- General Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Liquid Crystal (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Polymerisation Methods In General (AREA)
Abstract
Description
実施形態1は、本発明の重合体層形成用組成物及び液晶層形成用組成物を用いて作製を行った本発明の液晶表示装置の一例である。実施形態1に係る液晶表示装置は、配向膜上に重合性モノマーが光照射によりラジカル重合することによって形成された重合体層を備える。このような重合体層を形成することで液晶の配向を制御する。以下、このように配向膜上に形成された重合体層をPSA(Polymer Sustained Alignment)層ともいう。
P1-S1-A1-(Z1-A2)n-S2-P2 (I)
(式中、P1及びP2は、同一若しくは異なるアクリレート基、メタクリレート基、アクリルアミド基、メタクリルアミド基、ビニル基、ビニロキシ基又はエポキシ基を表す。A1及びA2は、1,4-フェニレン基、ナフタレン-2,6-ジイル基、アントラセン-2,6-ジイル基又はフェナントレン-2,6-ジイル基を表す。Z1は、COO、OCO若しくはO、又は、A1とA2若しくはA2とA2とが直接結合していることを表す。nは、0、1又は2である。S1及びS2は、同一若しくは異なる-(CH2)m-(0≦m≦6)、-(CH2-CH2-O)m-(0≦m≦6)、又は、P1とA1、A1とP2若しくはA2とP2とが直接結合していることを表す。A1及びA2が有する水素原子は、ハロゲン基又はメチル基に置換されていてもよい。)
以下、実施形態1に係る液晶表示装置が備える液晶セルを実際に作製した例を示す。まず、一対の支持基板を用意し、垂直配向膜の材料となるポリイミド系溶液を一対の支持基板の表面にそれぞれ塗布し、80℃の条件下でプリベークを行い、続いて200℃の条件下でポストベークを行った。なお、上記一対の支持基板が有する画素電極のそれぞれには、支持基板面に対して法線方向から見たときに線状となる複数のスリットが設けられている。
実施形態2は、本発明の重合体層形成用組成物及び液晶層形成用組成物を用いて作製を行った本発明の液晶表示装置の一例である。実施形態2に係る液晶表示装置は、実施形態1に係る液晶表示装置と同様、配向膜上に重合性モノマーがラジカル重合することによって形成されたPSA層を備えるが、配向処理がなされた配向膜が用いられており、それによってプレチルト角が80°以上90°未満となっている点で、実施形態1に係る液晶表示装置と異なっている。なお、実施形態2に係る液晶表示装置は、配向膜以外の構成については、実施形態1に係る液晶表示装置とほぼ同様である。また、実施形態2においても、PSA層を形成する際には、液晶層に対し閾値以上の電圧を印加した状態で光の照射を行うことが好ましいが、配向処理を施しているため、液晶層に対し閾値以上の電圧を印加した状態で光の照射を行わなくとも、比較的高い配向規制力を有するPSA層を得ることができる。
以下、実施形態2に係る液晶表示装置が備える液晶セルを実際に作製した例を示す。まず、一対の支持基板を用意し、垂直配向膜の材料となるポリイミド系溶液を一対の支持基板の表面にそれぞれ塗布し、80℃の条件下でプリベークを行い、続いて200℃の条件下でポストベークを行った。
実施形態3は、本発明の重合体層形成用組成物及び液晶層形成用組成物を用いて作製を行った本発明の液晶表示装置の一例である。実施形態3に係る液晶表示装置は、実施形態1及び実施形態2に係る液晶表示装置と同様、配向膜上に重合性モノマーがラジカル重合することによって形成されたPSA層を備えるが、重合性モノマーの重合反応を開始するために用いられるラジカル重合開始剤が、更に、ラジカル重合を停止させる重合停止剤でもある点で、実施形態1及び実施形態2と異なっている。以下、このように重合停止剤としても機能するラジカル重合開始剤を、イニファーター(Iniferter)ともいう。実施形態3に係る液晶表示装置は、PSA層以外の構成については、実施形態1又は実施形態2に係る液晶表示装置とほぼ同様である。実施形態3においては、配向膜として、実施形態1のように配向処理されていないものを用いたとしても、実施形態2のように光配向処理がなされたものを用いたとしてもよい。また、実施形態3においても、必ずしも液晶層に対し閾値以上の電圧を印加した状態で光の照射を行う必要はないが、配向膜に高い配向安定性を付与する観点からは、液晶層に対し閾値以上の電圧を印加した状態で光の照射を行うことが好ましい。
以下、実施形態3に係る液晶表示装置が備える液晶セルを実際に作製した例を示す。まず、一対の支持基板を用意し、垂直配向膜の材料となるポリイミド系溶液を一対の支持基板の表面にそれぞれ塗布し、80℃の条件下でプリベークを行い、続いて200℃の条件下でポストベークを行った。
11,21:支持基板
12,22:配向膜
13,23:PSA層(重合体層)
20:カラーフィルタ基板
30:液晶層
41:重合性モノマー
Claims (32)
- 一対の基板と、該一対の基板間に挟持された液晶層とを備える液晶表示装置であって、
該一対の基板の少なくとも一方は、配向膜、及び、該配向膜上に重合体層を有し、
該重合体層は、重合性モノマーに対して1モル%以下である重合開始剤によって重合性モノマーが反応を開始する重合で形成されたものである
ことを特徴とする液晶表示装置。 - 前記重合体層は、光照射により形成され、
前記重合性モノマーは、光照射により重合し、
前記重合開始剤は、ラジカル重合開始剤であり、
前記重合は、光照射によるラジカル重合である
ことを特徴とする請求項1記載の液晶表示装置。 - 前記ラジカル重合開始剤は、ラジカル重合を停止させる機能を有することを特徴とする請求項2記載の液晶表示装置。
- 前記一対の基板は、いずれも電極を有し、
前記重合体層は、該電極を通じて液晶層に対して閾値以上の電圧が印加された状態での重合性モノマーの重合で形成されたものである
ことを特徴とする請求項1~3のいずれかに記載の液晶表示装置。 - 前記配向膜は、光反応性官能基を有する化合物を含む材料で構成されていることを特徴とする請求項1~4のいずれかに記載の液晶表示装置。
- 前記配向膜は、樹脂膜であることを特徴とする請求項1~5のいずれかに記載の液晶表示装置。
- 前記重合体層を構成する重合体の分子量分布は8以下であることを特徴とする請求項1記載の液晶表示装置。
- 前記重合開始剤は、ラジカル重合開始剤であり、
前記重合は、ラジカル重合である
ことを特徴とする請求項7記載の液晶表示装置。 - 前記ラジカル重合開始剤は、ラジカル重合を停止させる機能を有することを特徴とする請求項8記載の液晶表示装置。
- 前記配向膜は、電圧無印加時に液晶層内の液晶分子を垂直配向させることを特徴とする請求項1~15のいずれかに記載の液晶表示装置。
- 前記配向膜は、光反応性官能基を有する化合物を含む材料で構成されていることを特徴とする請求16記載の液晶表示装置。
- 前記光反応性官能基は、シンナメート基、カルコン基、トラン基、クマリン基又はアゾベンゼン基であることを特徴とする請求項17記載の液晶表示装置。
- 前記配向膜は、光反応性官能基を含む側鎖を有するモノマー単位と、光反応性官能基を含まない側鎖を有するモノマー単位とを含む共重合体で構成されていることを特徴とする請求項16~18のいずれかに記載の液晶表示装置。
- 前記配向膜は、電圧無印加時に、液晶層内の液晶分子を、配向膜表面に対する法線方向に対して斜め方向に傾かせるものであることを特徴とする請求項17~19のいずれかに記載の液晶表示装置。
- 前記液晶表示装置は複数の画素を有しており、前記液晶層の、複数の画素のうち一つあたりの画素と対応する領域は、液晶分子を配向方向が互いに異なる複数の領域に分割されていることを特徴とする請求項1~20のいずれかに記載の液晶表示装置。
- 前記複数の領域は、4つの領域であることを特徴とする請求項21記載の液晶表示装置。
- 一対の基板と、該一対の基板間に挟持された液晶層とを備える液晶表示装置の製造方法であって、該製造方法は、該一対の基板の少なくとも一方に配向膜を形成する工程と、該配向膜上に、重合開始剤により開始反応を行った重合体による重合体層を形成する工程を有し、該重合体層を構成する重合体の分子量分布は8以下であることを特徴とする液晶表示装置の製造方法。
- 前記製造方法は、重合体層を形成する工程の前に、モノマーと、モノマーに対して1モル%以下の濃度の重合開始剤を液晶材料に溶解させる工程を有することを特徴とする請求項23記載の液晶表示装置の製造方法。
- 前記重合体層を形成する工程は、液晶層に対して閾値以上の電圧印加状態で、重合開始剤による開始反応により重合を開始し、垂直配向膜上に重合体層を形成する工程であることを特徴とする請求項23又は24記載の液晶表示装置の製造方法。
- 前記製造方法は、光反応性官能基を有する化合物を含む材料で構成されている配向膜に光照射を行って配向処理を行う工程を含むことを特徴とする請求項23又は24記載の液晶表示装置の製造方法。
- 前記光反応性官能基は、シンナメート基、カルコン基、トラン基、クマリン基又はアゾベンゼン基であることを特徴とする請求項26記載の液晶表示装置の製造方法。
- 前記配向膜は、光反応性官能基を含む側鎖を有するモノマー単位と、光反応性官能基を含まない側鎖を有するモノマー単位とを含む共重合体で構成されていることを特徴とする請求項26又は27のいずれかに記載の液晶表示装置の製造方法。
- 重合性モノマー及び重合開始剤を含む重合体層形成用組成物であって、
該重合開始剤の濃度は、重合性モノマーに対して1モル%以下である
ことを特徴とする重合体層形成用組成物。 - 前記重合性モノマーは、光照射により重合するモノマーであり、
前記重合開始剤は、ラジカル重合開始剤である
ことを特徴とする請求項29記載の重合体層形成用組成物。 - 前記重合開始剤は、重合を停止させる機能を有することを特徴とする請求項29又は30記載の重合体層形成用組成物。
- 請求項29~31のいずれかに記載の重合体層形成用組成物と、液晶材料とを含むことを特徴とする液晶層形成用組成物。
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP09843070.5A EP2418536B1 (en) | 2009-04-06 | 2009-11-18 | LIQUID CRYSTAL DISPLAY DEVICE and COMPOSITION FOR FORMING a POLYMER LAYER |
JP2011508186A JP5587294B2 (ja) | 2009-04-06 | 2009-11-18 | 液晶表示装置、液晶表示装置の製造方法、psa層形成用組成物、及び、液晶層形成用組成物 |
US13/263,155 US20120033167A1 (en) | 2009-04-06 | 2009-11-18 | Liquid crystal display device, method for manufacturing liquid crystal display device, composition for forming polymer layer, and composition for forming liquid crystal layer |
CN200980158500.5A CN102378938B (zh) | 2009-04-06 | 2009-11-18 | 液晶显示装置、液晶显示装置的制造方法、聚合物层形成用组合物和液晶层形成用组合物 |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2009-092146 | 2009-04-06 | ||
JP2009092146 | 2009-04-06 | ||
JP2009209690 | 2009-09-10 | ||
JP2009-209690 | 2009-09-10 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2010116564A1 true WO2010116564A1 (ja) | 2010-10-14 |
Family
ID=42935867
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2009/069565 WO2010116564A1 (ja) | 2009-04-06 | 2009-11-18 | 液晶表示装置、液晶表示装置の製造方法、重合体層形成用組成物、及び、液晶層形成用組成物 |
Country Status (5)
Country | Link |
---|---|
US (1) | US20120033167A1 (ja) |
EP (1) | EP2418536B1 (ja) |
JP (1) | JP5587294B2 (ja) |
CN (1) | CN102378938B (ja) |
WO (1) | WO2010116564A1 (ja) |
Cited By (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2012077668A1 (ja) * | 2010-12-06 | 2012-06-14 | シャープ株式会社 | 液晶表示装置及び液晶表示装置の製造方法 |
WO2013018668A1 (ja) * | 2011-08-04 | 2013-02-07 | シャープ株式会社 | 液晶表示装置 |
US20130128204A1 (en) * | 2010-08-03 | 2013-05-23 | Sharp Kabushiki Kaisha | Liquid crystal display device and process for producing liquid crystal display device |
US20130128203A1 (en) * | 2010-08-03 | 2013-05-23 | Sharp Kabushiki Kaisha | Liquid crystal display device and process for producing liquid crystal display device |
WO2013094734A1 (ja) * | 2011-12-22 | 2013-06-27 | 日産化学工業株式会社 | 横電界駆動用液晶表示素子の製造方法 |
US20130286340A1 (en) * | 2010-12-22 | 2013-10-31 | Sharp Kabushiki Kaisha | Liquid crystal alignment agent, liquid crystal display, and method for manufacturing liquid crystal display |
US20140111754A1 (en) * | 2011-06-27 | 2014-04-24 | Sharp Kabushiki Kaisha | Liquid crystal display device and method for manufacturing liquid crystal display device |
JP5620006B2 (ja) * | 2011-08-25 | 2014-11-05 | シャープ株式会社 | 液晶表示装置の製造方法 |
JP2014532104A (ja) * | 2011-10-03 | 2014-12-04 | ロリク アーゲーRolic Ag | 光アライニング材料 |
US9195097B2 (en) | 2010-08-03 | 2015-11-24 | Sharp Kabushiki Kaisha | Liquid crystal display device and process for producing liquid-crystal display device |
US9557605B2 (en) | 2010-10-14 | 2017-01-31 | Merck Patent Gmbh | Method of producing liquid crystal display device |
US9644146B2 (en) | 2010-09-07 | 2017-05-09 | Sharp Kabushiki Kaisha | Composition for forming liquid crystal layer, liquid crystal display device, and method for producing liquid crystal display device |
WO2017170542A1 (ja) * | 2016-03-29 | 2017-10-05 | シャープ株式会社 | 液晶表示装置および液晶表示装置の製造方法 |
US9798179B2 (en) | 2010-10-14 | 2017-10-24 | Merck Patent Gmbh | Liquid crystal display device |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102662274B (zh) * | 2012-05-22 | 2015-07-01 | 深圳市华星光电技术有限公司 | 液晶面板及其液晶配向方法 |
US9115308B2 (en) * | 2012-07-20 | 2015-08-25 | Shenzhen China Star Optoelectronics Technology Co., Ltd | Liquid crystal medium composition of liquid crystal display |
US9759948B2 (en) | 2014-11-10 | 2017-09-12 | Samsung Display Co., Ltd. | Curved liquid crystal display |
JP2017090781A (ja) * | 2015-11-13 | 2017-05-25 | 株式会社ジャパンディスプレイ | 光配向膜用ワニス及び液晶表示装置 |
US11530357B2 (en) * | 2017-07-06 | 2022-12-20 | Sharp Kabushiki Kaisha | Liquid crystal alignment agent and liquid crystal panel |
US11048125B2 (en) * | 2018-03-29 | 2021-06-29 | Sharp Kabushiki Kaisha | Liquid crystal cell and liquid crystal display device |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH10227998A (ja) * | 1997-02-14 | 1998-08-25 | Sharp Corp | 光学素子、偏光素子およびそれらの製造方法、並びに映像表示装置 |
JPH11109393A (ja) * | 1997-10-06 | 1999-04-23 | Nec Corp | 液晶表示装置、その製造方法およびその駆動方法 |
JP2003228050A (ja) * | 2002-02-04 | 2003-08-15 | Fujitsu Display Technologies Corp | 液晶表示装置及びその製造方法 |
JP2005338613A (ja) * | 2004-05-28 | 2005-12-08 | Fujitsu Display Technologies Corp | 液晶表示装置及びその製造方法 |
JP2008076950A (ja) * | 2006-09-25 | 2008-04-03 | Sharp Corp | 液晶表示パネル及びその製造方法 |
JP2009104119A (ja) * | 2007-10-24 | 2009-05-14 | Au Optronics Corp | Psa処理のための混合液晶及び液晶ディスプレイ装置 |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1219651A1 (en) * | 2000-12-29 | 2002-07-03 | Rolic AG | Photoactive copolymer |
CN1327279C (zh) * | 2002-02-04 | 2007-07-18 | 夏普株式会社 | 液晶显示装置及其制造方法 |
JP4744801B2 (ja) * | 2003-12-18 | 2011-08-10 | 富士通株式会社 | 液晶表示装置およびその製造方法 |
JP2006243637A (ja) * | 2005-03-07 | 2006-09-14 | Sharp Corp | 液晶表示装置及びその製造方法 |
JP2008089732A (ja) * | 2006-09-29 | 2008-04-17 | Jsr Corp | 感放射線性樹脂組成物およびカラーフィルタ |
-
2009
- 2009-11-18 US US13/263,155 patent/US20120033167A1/en not_active Abandoned
- 2009-11-18 JP JP2011508186A patent/JP5587294B2/ja not_active Expired - Fee Related
- 2009-11-18 CN CN200980158500.5A patent/CN102378938B/zh not_active Expired - Fee Related
- 2009-11-18 EP EP09843070.5A patent/EP2418536B1/en not_active Not-in-force
- 2009-11-18 WO PCT/JP2009/069565 patent/WO2010116564A1/ja active Application Filing
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH10227998A (ja) * | 1997-02-14 | 1998-08-25 | Sharp Corp | 光学素子、偏光素子およびそれらの製造方法、並びに映像表示装置 |
JPH11109393A (ja) * | 1997-10-06 | 1999-04-23 | Nec Corp | 液晶表示装置、その製造方法およびその駆動方法 |
JP2003228050A (ja) * | 2002-02-04 | 2003-08-15 | Fujitsu Display Technologies Corp | 液晶表示装置及びその製造方法 |
JP2005338613A (ja) * | 2004-05-28 | 2005-12-08 | Fujitsu Display Technologies Corp | 液晶表示装置及びその製造方法 |
JP2008076950A (ja) * | 2006-09-25 | 2008-04-03 | Sharp Corp | 液晶表示パネル及びその製造方法 |
JP2009104119A (ja) * | 2007-10-24 | 2009-05-14 | Au Optronics Corp | Psa処理のための混合液晶及び液晶ディスプレイ装置 |
Non-Patent Citations (1)
Title |
---|
See also references of EP2418536A4 * |
Cited By (25)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9164326B2 (en) | 2010-08-03 | 2015-10-20 | Sharp Kabushiki Kaisha | Liquid crystal display device and process for producing liquid crystal display device |
US20130128204A1 (en) * | 2010-08-03 | 2013-05-23 | Sharp Kabushiki Kaisha | Liquid crystal display device and process for producing liquid crystal display device |
US20130128203A1 (en) * | 2010-08-03 | 2013-05-23 | Sharp Kabushiki Kaisha | Liquid crystal display device and process for producing liquid crystal display device |
US9195097B2 (en) | 2010-08-03 | 2015-11-24 | Sharp Kabushiki Kaisha | Liquid crystal display device and process for producing liquid-crystal display device |
US9164325B2 (en) | 2010-08-03 | 2015-10-20 | Sharp Kabushiki Kaisha | Liquid crystal display device and process for producing liquid crystal display device |
US9644146B2 (en) | 2010-09-07 | 2017-05-09 | Sharp Kabushiki Kaisha | Composition for forming liquid crystal layer, liquid crystal display device, and method for producing liquid crystal display device |
US9798179B2 (en) | 2010-10-14 | 2017-10-24 | Merck Patent Gmbh | Liquid crystal display device |
US9557605B2 (en) | 2010-10-14 | 2017-01-31 | Merck Patent Gmbh | Method of producing liquid crystal display device |
WO2012077668A1 (ja) * | 2010-12-06 | 2012-06-14 | シャープ株式会社 | 液晶表示装置及び液晶表示装置の製造方法 |
US9182632B2 (en) | 2010-12-06 | 2015-11-10 | Sharp Kabushiki Kaisha | Liquid crystal display device and method for manufacturing liquid crystal display device |
US20130286340A1 (en) * | 2010-12-22 | 2013-10-31 | Sharp Kabushiki Kaisha | Liquid crystal alignment agent, liquid crystal display, and method for manufacturing liquid crystal display |
US9239493B2 (en) | 2010-12-22 | 2016-01-19 | Sharp Kabushiki Kaisha | Liquid crystal alignment agent, liquid crystal display, and method for manufacturing liquid crystal display |
US20140111754A1 (en) * | 2011-06-27 | 2014-04-24 | Sharp Kabushiki Kaisha | Liquid crystal display device and method for manufacturing liquid crystal display device |
TWI559057B (zh) * | 2011-06-27 | 2016-11-21 | Merck Patent Gmbh | A liquid crystal display device, and a liquid crystal display device |
US9651828B2 (en) * | 2011-06-27 | 2017-05-16 | Merck Patent Gmbh | Liquid crystal display device and method for manufacturing liquid crystal display device |
US9291857B2 (en) | 2011-08-04 | 2016-03-22 | Sharp Kabushiki Kaisha | Liquid crystal display device |
WO2013018668A1 (ja) * | 2011-08-04 | 2013-02-07 | シャープ株式会社 | 液晶表示装置 |
JPWO2013027548A1 (ja) * | 2011-08-25 | 2015-03-19 | シャープ株式会社 | 液晶表示装置の製造方法 |
JP5620006B2 (ja) * | 2011-08-25 | 2014-11-05 | シャープ株式会社 | 液晶表示装置の製造方法 |
JP2014532104A (ja) * | 2011-10-03 | 2014-12-04 | ロリク アーゲーRolic Ag | 光アライニング材料 |
JPWO2013094734A1 (ja) * | 2011-12-22 | 2015-04-27 | 日産化学工業株式会社 | 横電界駆動用液晶表示素子の製造方法 |
CN104136976A (zh) * | 2011-12-22 | 2014-11-05 | 日产化学工业株式会社 | 横向电场驱动用液晶显示元件的制造方法 |
WO2013094734A1 (ja) * | 2011-12-22 | 2013-06-27 | 日産化学工業株式会社 | 横電界駆動用液晶表示素子の製造方法 |
WO2017170542A1 (ja) * | 2016-03-29 | 2017-10-05 | シャープ株式会社 | 液晶表示装置および液晶表示装置の製造方法 |
US10739645B2 (en) | 2016-03-29 | 2020-08-11 | Sharp Kabushiki Kaisha | Liquid crystal display apparatus and manufacturing method of liquid crystal display apparatus |
Also Published As
Publication number | Publication date |
---|---|
EP2418536B1 (en) | 2014-09-17 |
CN102378938B (zh) | 2015-05-13 |
EP2418536A1 (en) | 2012-02-15 |
JPWO2010116564A1 (ja) | 2012-10-18 |
EP2418536A4 (en) | 2012-11-28 |
JP5587294B2 (ja) | 2014-09-10 |
CN102378938A (zh) | 2012-03-14 |
US20120033167A1 (en) | 2012-02-09 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP5587294B2 (ja) | 液晶表示装置、液晶表示装置の製造方法、psa層形成用組成物、及び、液晶層形成用組成物 | |
EP2416211B1 (en) | Liquid crystal display device, process for producing liquid crystal display device, composition for forming polymer layer, and composition for forming liquid crystal layer | |
US9817274B2 (en) | Method for manufacturing liquid crystal display device | |
TWI578063B (zh) | A liquid crystal display device, and a liquid crystal display device | |
TWI519868B (zh) | Liquid crystal display device | |
US9417482B2 (en) | Liquid crystal display panel and liquid crystal display device | |
WO2012121321A1 (ja) | 液晶表示装置及び液晶表示装置の製造方法 | |
WO2014061755A1 (ja) | 液晶表示装置及び液晶表示装置の製造方法 | |
WO2013002084A1 (ja) | 液晶表示装置及び液晶表示装置の製造方法 | |
WO2012077668A1 (ja) | 液晶表示装置及び液晶表示装置の製造方法 | |
TWI522699B (zh) | Liquid crystal display panel and liquid crystal display device | |
WO2014038431A1 (ja) | 配向膜用重合体、及び、液晶表示装置 | |
KR20160067151A (ko) | 액정 표시 소자 및 액정 표시 소자의 제조 방법 | |
WO2011102041A1 (ja) | 液晶表示装置、液晶表示装置の製造方法、及び、配向膜形成用組成物 | |
WO2013069487A1 (ja) | 液晶表示装置及びその製造方法 | |
KR20240073899A (ko) | 약앵커링 액정 배향제, 액정 표시 소자 및 중합체 | |
WO2013161865A1 (ja) | 液晶表示装置及び液晶表示装置の製造方法 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
WWE | Wipo information: entry into national phase |
Ref document number: 200980158500.5 Country of ref document: CN |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 09843070 Country of ref document: EP Kind code of ref document: A1 |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2011508186 Country of ref document: JP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2009843070 Country of ref document: EP |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
WWE | Wipo information: entry into national phase |
Ref document number: 13263155 Country of ref document: US |