WO1998008136A1 - Liquid crystal display device - Google Patents
Liquid crystal display device Download PDFInfo
- Publication number
- WO1998008136A1 WO1998008136A1 PCT/EP1997/004501 EP9704501W WO9808136A1 WO 1998008136 A1 WO1998008136 A1 WO 1998008136A1 EP 9704501 W EP9704501 W EP 9704501W WO 9808136 A1 WO9808136 A1 WO 9808136A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- alignment layer
- alignment
- liquid crystal
- display device
- crystal display
- Prior art date
Links
- 239000004973 liquid crystal related substance Substances 0.000 title claims abstract description 48
- 239000000758 substrate Substances 0.000 claims abstract description 18
- 238000000034 method Methods 0.000 claims description 41
- 238000010894 electron beam technology Methods 0.000 claims description 12
- 230000001678 irradiating effect Effects 0.000 claims description 4
- 229920000620 organic polymer Polymers 0.000 claims description 2
- -1 polyimidoamide Polymers 0.000 description 49
- 229920000642 polymer Polymers 0.000 description 45
- 229920002678 cellulose Polymers 0.000 description 13
- 239000001913 cellulose Substances 0.000 description 13
- 210000004027 cell Anatomy 0.000 description 10
- 239000000463 material Substances 0.000 description 10
- 229920002554 vinyl polymer Polymers 0.000 description 9
- 229910052731 fluorine Inorganic materials 0.000 description 7
- 239000004793 Polystyrene Substances 0.000 description 6
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 5
- 230000005684 electric field Effects 0.000 description 5
- 239000011737 fluorine Substances 0.000 description 5
- 229920002223 polystyrene Polymers 0.000 description 5
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 4
- 239000004952 Polyamide Substances 0.000 description 4
- 239000004642 Polyimide Substances 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 229920000058 polyacrylate Polymers 0.000 description 4
- 229920002647 polyamide Polymers 0.000 description 4
- 229920001721 polyimide Polymers 0.000 description 4
- 229920000193 polymethacrylate Polymers 0.000 description 4
- 239000004988 Nematic liquid crystal Substances 0.000 description 3
- 239000004721 Polyphenylene oxide Substances 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 210000002858 crystal cell Anatomy 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 125000001153 fluoro group Chemical group F* 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 3
- 229920003227 poly(N-vinyl carbazole) Polymers 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- 229920000570 polyether Polymers 0.000 description 3
- 229920002635 polyurethane Polymers 0.000 description 3
- 239000004814 polyurethane Substances 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical group [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- 239000002033 PVDF binder Substances 0.000 description 2
- 229920002396 Polyurea Polymers 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- 125000002723 alicyclic group Chemical group 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 125000002029 aromatic hydrocarbon group Chemical group 0.000 description 2
- 235000010290 biphenyl Nutrition 0.000 description 2
- 239000004305 biphenyl Substances 0.000 description 2
- 229940114081 cinnamate Drugs 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 2
- 229910052753 mercury Inorganic materials 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920000515 polycarbonate Polymers 0.000 description 2
- 239000004417 polycarbonate Substances 0.000 description 2
- 229920002776 polycyclohexyl methacrylate Polymers 0.000 description 2
- 229920006254 polymer film Polymers 0.000 description 2
- 229920000098 polyolefin Polymers 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 2
- 229920002981 polyvinylidene fluoride Polymers 0.000 description 2
- 238000004528 spin coating Methods 0.000 description 2
- WBYWAXJHAXSJNI-VOTSOKGWSA-M trans-cinnamate Chemical compound [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 description 2
- LNAZSHAWQACDHT-XIYTZBAFSA-N (2r,3r,4s,5r,6s)-4,5-dimethoxy-2-(methoxymethyl)-3-[(2s,3r,4s,5r,6r)-3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6r)-4,5,6-trimethoxy-2-(methoxymethyl)oxan-3-yl]oxyoxane Chemical compound CO[C@@H]1[C@@H](OC)[C@H](OC)[C@@H](COC)O[C@H]1O[C@H]1[C@H](OC)[C@@H](OC)[C@H](O[C@H]2[C@@H]([C@@H](OC)[C@H](OC)O[C@@H]2COC)OC)O[C@@H]1COC LNAZSHAWQACDHT-XIYTZBAFSA-N 0.000 description 1
- ARHOUOIHKWELMD-UHFFFAOYSA-N 1-ethenyl-3-(trifluoromethyl)benzene Chemical compound FC(F)(F)C1=CC=CC(C=C)=C1 ARHOUOIHKWELMD-UHFFFAOYSA-N 0.000 description 1
- MAGFQRLKWCCTQJ-UHFFFAOYSA-M 4-ethenylbenzenesulfonate Chemical compound [O-]S(=O)(=O)C1=CC=C(C=C)C=C1 MAGFQRLKWCCTQJ-UHFFFAOYSA-M 0.000 description 1
- KFDVPJUYSDEJTH-UHFFFAOYSA-N 4-ethenylpyridine Chemical compound C=CC1=CC=NC=C1 KFDVPJUYSDEJTH-UHFFFAOYSA-N 0.000 description 1
- 229920000623 Cellulose acetate phthalate Polymers 0.000 description 1
- 229920002284 Cellulose triacetate Polymers 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- 229920002153 Hydroxypropyl cellulose Polymers 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 229920002319 Poly(methyl acrylate) Polymers 0.000 description 1
- 229920001665 Poly-4-vinylphenol Polymers 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 229920002873 Polyethylenimine Polymers 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 1
- 125000005428 anthryl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C3C(*)=C([H])C([H])=C([H])C3=C([H])C2=C1[H] 0.000 description 1
- 238000004630 atomic force microscopy Methods 0.000 description 1
- 229920005601 base polymer Polymers 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 125000006267 biphenyl group Chemical group 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 229920006217 cellulose acetate butyrate Polymers 0.000 description 1
- 229940081734 cellulose acetate phthalate Drugs 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 125000005442 diisocyanate group Chemical group 0.000 description 1
- 238000006471 dimerization reaction Methods 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- 239000002019 doping agent Substances 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 150000002430 hydrocarbons Chemical group 0.000 description 1
- 229920003063 hydroxymethyl cellulose Polymers 0.000 description 1
- 229940031574 hydroxymethyl cellulose Drugs 0.000 description 1
- 239000001863 hydroxypropyl cellulose Substances 0.000 description 1
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 description 1
- 238000006317 isomerization reaction Methods 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 125000005561 phenanthryl group Chemical group 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229920005593 poly(benzyl methacrylate) Polymers 0.000 description 1
- 229920001485 poly(butyl acrylate) polymer Polymers 0.000 description 1
- 229920001490 poly(butyl methacrylate) polymer Polymers 0.000 description 1
- 229920003203 poly(dimethylsilylene-co-phenylmethyl- silylene) polymer Polymers 0.000 description 1
- 229920001483 poly(ethyl methacrylate) polymer Polymers 0.000 description 1
- 229920002552 poly(isobornyl acrylate) polymer Polymers 0.000 description 1
- 229920000212 poly(isobutyl acrylate) Polymers 0.000 description 1
- 229920000205 poly(isobutyl methacrylate) Polymers 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
- 229920001197 polyacetylene Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920000120 polyethyl acrylate Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920002720 polyhexylacrylate Polymers 0.000 description 1
- 229920000129 polyhexylmethacrylate Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920001184 polypeptide Polymers 0.000 description 1
- 229920000182 polyphenyl methacrylate Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920005553 polystyrene-acrylate Polymers 0.000 description 1
- 229920003053 polystyrene-divinylbenzene Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 229920002620 polyvinyl fluoride Polymers 0.000 description 1
- 229920002717 polyvinylpyridine Polymers 0.000 description 1
- 102000004196 processed proteins & peptides Human genes 0.000 description 1
- 108090000765 processed proteins & peptides Proteins 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000008707 rearrangement Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000004626 scanning electron microscopy Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 125000005373 siloxane group Chemical group [SiH2](O*)* 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 125000005023 xylyl group Chemical group 0.000 description 1
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
- G02F1/1343—Electrodes
- G02F1/134309—Electrodes characterised by their geometrical arrangement
- G02F1/134363—Electrodes characterised by their geometrical arrangement for applying an electric field parallel to the substrate, i.e. in-plane switching [IPS]
-
- G—PHYSICS
- G02—OPTICS
- G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
- G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
- G02F1/01—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour
- G02F1/13—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells
- G02F1/133—Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
- G02F1/1333—Constructional arrangements; Manufacturing methods
- G02F1/1337—Surface-induced orientation of the liquid crystal molecules, e.g. by alignment layers
- G02F1/133753—Surface-induced orientation of the liquid crystal molecules, e.g. by alignment layers with different alignment orientations or pretilt angles on a same surface, e.g. for grey scale or improved viewing angle
- G02F1/133757—Surface-induced orientation of the liquid crystal molecules, e.g. by alignment layers with different alignment orientations or pretilt angles on a same surface, e.g. for grey scale or improved viewing angle with different alignment orientations
Definitions
- This invention relates to a process for producing a liquid crystal alignment layer and a liquid crystal display device with the use of the same. More particularly, it relates to a liquid crystal display device capable of achieving a wide viewing angle.
- a liquid crystal display device is an electro-optical device containing a liquid crystal material which undergoes changes in the optical characteristics when an electrical field is externally applied thereto.
- IPS(ln-Plane Switching)-TFT for widening the viewing angle of liquid crystal display devices.
- This IPS-TFT mode is characterized by placing parallel electrodes on one substrate and rotating liquid crystal molecules located horizontally to the substrate within this plane to generate "on" state and "off” state (Fig. 1 ) (Nikkei Electronics, Dec. 4, 1995, p. 184). Since the liquid crystals are always aligned in the direction horizontal to the substrate in this mode, the contrast scarcely varies depending on the viewing direction, which makes it possible to achieve a wide viewing angle.
- a liquid crystal alignment layer which is capable of providing a liquid crystal display device having excellent viewing angle characteristics and thus solving the above-mentioned problems and a process for producing the same, as well as a liquid crystal display device with the use of said liquid crystal alignment layer.
- the present inventors have now found that the viewing angle characteristics of an IPS-TFT liquid crystal display device can be further improved by forming at least two regions differing in alignment direction from each other in an alignment layer, thus completing the present invention.
- the present invention provides an IPS-TFT liquid crystal display device characterized in that at least two regions differing in alignment direction from each other are formed in an alignment layer on the substrate of the electrode side.
- a part of the alignment layer has been irradiated with UV light or an electron beam after completion of the aligning process, whereby the alignment direction of the alignment layer within the irradiated region is shifted by about 90° to the alignment direction established by the aligning process.
- the present invention further provides a process for producing an IPS-TFT liquid crystal display device.
- the process comprises the steps of: preparing an alignment layer made of organic polymers; aligning said alignment layer; irradiating a part of the alignment layer with UV light or an electron beam to shift the alignment direction of the alignment layer within the irradiated region by about 90° to the alignment direction established by the aligning process; and assembling the liquid crystal display device using the alignment layer thus obtained as the alignment layer on the substrate of the electrode side.
- the present invention furthermore relates to use of an alignment layer having at least two regions differing in alignment direction from each other in an IPS-TFT liquid crystal display device.
- the alignment layer employed in the method of the present invention is preferably characterized in that a part of said alignment layer has been irradiated with UV light or an electron beam after completion of the aligning process, whereby the alignment direction of the alignment layer within the irradiated region is shifted by about 90° to the alignment direction established by the aligning process.
- an IPS-TFT liquid crystal display device having good contrast and less viewing angle dependency of display characteristics can be produced by forming at least two regions differing in alignment direction from each other in an alignment layer on the substrate of the electrode side.
- the IPS-TFT liquid crystal display device of the present invention can be produced by partly irradiating the surface of an alignment layer with UV light or an electron beam so that the alignment direction of the irradiated region is shifted by about 90°, more particularly 85 to 95°, to the alignment direction established by the aligning process.
- the term "alignment direction of the alignment layer" as used herein means the direction along which the liquid crystal is to be aligned on the surface of the alignment layer.
- irradiated regions and unirradiated regions are alternately arranged along the direction of the electrical field in the alignment layer on the substrate of the electrode side. Such an arrangement allows to form two regions differing in alignment direction by about 90° from each other (i.e.
- Example 2 and Fig. 5 it is also possible to arrange two regions differing in alignment direction from each other vertically to the direction of the electrical field. In this case, it is preferable to arrange these regions in such a manner that the adjacent regions in adjacent dots differ from each other in alignment direction.
- each dot should have at least one pair of each of (a-b) and (c-d) regions. It is preferable that the total area of the (a-b) regions is identical with that of the (c-d) regions.
- the alignment layer material employed in the present invention in which the alignment direction of the irradiated region is shifted by about 90° to the alignment direction established by the aligning process by irradiating with UV light or an electron beam, use can be made of photosensitive polymers having unsaturated bonds in the molecular chain such as polyvinyl cinnamate.
- photosensitive polymers having unsaturated bonds in the molecular chain such as polyvinyl cinnamate.
- the alignment layer employed in the present invention can be obtained by mixing a polymer [polymer (A)], which has such properties as to align the liquid crystal in the direction of the aligning process after completion of the aligning process, with another polymer [polymer (B)], which has such properties as to align the liquid crystal in the direction shifted by about 90° to the direction of the aligning process.
- polymer (A) examples include but are not limited to backbone type polymers such as polyimide, polyamide, polyether, polyester and polyurethane. It is still preferable to use polyimide or polyamide, in particular, those bearing a fluorine and siloxane group. When irradiated with UV light, etc., many of these polymers suffer from a decrease in pretilt angle and thus alignment regulation tends to be weakened.
- polymers (B) examples include polyvinyl, polymethacrylate and polyacrylate having bulky groups in side chain such as polystyrene and polycyclohexyl methacrylate. It is preferable to use polyacenaphthylene, poly-4-vinylpyridine, polyvinyl diphenyl, polyvinyl naphthalene, polyvinyl formal, polyvinylpyridine-N- oxide, polyphenyl methacrylate, polyvinyl carbazole, etc. Polyvinyl cinnamate can also be used. Although many of these polymers (B) would be slightly or not aligned by usual aligning processes, they can establish uniform alignment after irradiation with UV light, etc.
- the appropriate mixing ratio of the polymers (A) to (B) and the irradiation dose of UV light, etc are determined depending on the difference in alignment regulation between these polymers
- the mixing ratio of the polymers (A) to (B) preferably ranges from 1 50 to 50 1
- the alignment regulation by the polymer (A) becomes dominant continuously, even if the alignment layer is irradiated with UV light, etc In this case, the alignment direction is not shifted by about 90°
- the polymers (A) and (B) may be each a mixture of two or more polymers
- the irradiation dose of UV light, etc preferably ranges from 0 01 mJ to 50 J, still preferably from 0.1 mJ to 10 J. If the dose of UV light, etc was too large, the polymers would be oxidized and thus the alignment would be disordered
- the wavelength of UV light, etc preferably ranges from 150 to 450 nm, still preferably from 200 to 400 nm
- the alignment layer employed in the present invention can be produced by forming a polymer film on a glass or plastic substrate provided with a transparent electrode by spin coating or printing in accordance with a method commonly known in the art, then the film is subjected to the aligning process followed by the irradiation with UV light or an electron beam
- the aligning process it is also possible to use nonpolarized UV light which facilitates the production process
- the aligning process is carried out by the rubbing method, though the present invention is not restricted thereto.
- regions with different viewing directions can be formed in a single pixel. These regions can be arbitrarily varied in size and shape by appropriately selecting the mask pattern.
- the mask size is determined depending on the display size. Namely, the mask may have the same size as the display, or a smaller mask may be used by using steppers.
- the pattern size of the mask is preferably several ten to 500 ⁇ m depending on the size of a pixel.
- the alignment layer employed in the present invention can be produced by other multi-domain formation methods known in the art. For example, it is possible to form two regions differing in alignment direction from each other in a single pixel by using photolithographic techniques. By mixing two or more polymers differring in SP value of at least 1 , preferably at least 2, it is also possible to form an alignment layer which can provide at least two different states of liquid crystal alignment by the aligning process in a single direction.
- the liquid crystal alignment layer has microprotrusions on the surface thereof. It is still preferable in these cases that in the liquid crystal alignment layer, at least one of the polymers is a polymer containing siloxane or one containing fluorine.
- the alignment layer has microprotrusions with arbitrary sizes and shapes on the surface thereof. These microprotrusions are from several hundred A to several ⁇ m in size, i.e., in diameter, and from several hundred A to several ⁇ m in height, preferably from several hundred A to several thousand A in height. Size and height of the microprotrusions can be measured by methods well known in the art, e.g., atomic force microscopy or scanning electron microscopy.
- At least one polymer which differs in SP value by 1 or more from other polymers, serves as a base material amounting to 50 % or more of the alignment layer materials while other polymer(s) are used as so-called dopant(s) to be blended with the base, a phase separation is generated by mixing these polymers. As a result, it is believed that the polymer(s) added form microphase separation structures on the base polymer, thus giving microprotrusions.
- the alignment layer can be produced by mixing two or more polymers differing in SP value by at least 1, and forming a film of the resulting mixture on a glass or plastic substrate by spin coating or print coating in accordance with a method commonly known in the art. By forming such alignment layers on both substrates, a liquid crystal display device having two or more alignment states with a high stability and a good reproducibility can be established.
- the polymers to be used as the material for the alignment layer can be selected from, but are not limited to, those commonly employed in organic alignment layers such as polyimide, polyamide, polyurethane, polyester, polycarbonate, polyurea, polyether, polyimidoamide, polypeptide, polyolefins, cellulose and derivatives thereof, polyacrylates, polymethacrylates, polyvinyl such as polystyrenes and polyvinyl alcohol. It is preferable that at least one of the polymers to be used as the material for the alignment layer of the present invention is a polymer containing siloxane or one containing fluorine.
- Polyimide, polyamide, polyurethane, polyester, polycarbonate, polyether, polyimidoamide and polyurea can be obtained by polymerizing monomers (for example, diisocyanate, diol, dicarboxylic acid, diamine, tetracarboxylic anhydride) by a method which has been commonly known by those skilled in the art.
- monomers for example, diisocyanate, diol, dicarboxylic acid, diamine, tetracarboxylic anhydride
- a polymer containing fluorine can be obtained by using a monomer substituted with fluorine atom(s).
- cellulose and derivatives thereof include hydroxypropyl cellulose, cellulose, hydroxymethyl cellulose, cellulose acetate butyrate, cellulose acetate phthalate, cellulose triacetate, methyl cellulose, cellulose acetate, cellulose hydroxypeptide, p-aminobenzyl cellulose, polyethyleneimine cellulose, triethylaminoethyl cellulose, ethyl cellulose, cyanoethylated cellulose, carboxymethylated cellulose, diethylaminohydroxypropylated cellulose, sulfohydroxypropylated cellulose, trimethylaminohydroxy-propylated cellulose and bromoacetyl cellulose.
- polyvinyl and derivatives thereof examples include polystyrene, sodium poly-4- styrene sulfonate, polymethylstyrene, dicarboxy- terminated polystyrene, monocarboxy-terminated polystyrene, polystyrene divinylbenzene, polystyrene methyl methacrylate, 3-trifluoromethylstyrene, polyvinylalcohol, polyvinylbiphenyl, polyvinylbiphenylether, polyvinylcinnamate, polyvinylformal, polyacenaphthylene, polyvinylcarbazole, polyvinylcyclohexyl, polyvinylmethlketone, polyvinylnaphthalene, polyvinylphenol, polyvinylpyridine, polyvinylbutyral, polyvinylidenefluoride, polyvinylpyhdine-N-oxide, polyvinylch
- polyacrylates or polymethacrylates examples include poly(methyl acrylate), poly(methyl methacrylate), poly(ethyl acrylate), poly(ethyl methacrylate), poly(butyl acrylate), poly(butyl methacrylate), poly(isobutyl acrylate), poly(isobutyl methacrylate), poly(t-butyl acrylate), poly(t-butyl methacrylate), poly(hexyl acrylate), poly(hexyl methacrylate), poly(2-ethylbutyl acrylate), poly(2-ethylbutyl methacrylate), poly(benzyl acrylate), poly(benzyl methacrylate), poly(cyclohexyl acrylate), poly(cyclohexyl methacrylate), poly(norbomyl acrylate), poly(norbornyl methacrylate), poly(isobornyl acrylate), poly(isobomyl methacrylate),
- a fluorine-containing polymer can be obtained by introducing fluorine atom(s) into such a polyacrylate or a polymethacrylate.
- polystyrene use can be made of, for example, polyethylene, polypropylene, polyacetylene, polybutadiene, polyvinylidene fluoride and copolymers thereof.
- polysilastyrene, etc. are also usable therefor.
- siloxane-containing polymer use can be made of polymers obtained by reacting a compound represented by the following general formula as a siloxane component. It is preferable to use a block polymer of siloxane with other polymer(s).
- n is an integer of 1 or above;
- R 2 represents a divalent hydrocarbon group
- R 3 represents a monovalent, linear or branched, aliphatic hydrocarbon group having from 1 to 5 carbon atoms or a alicyclic or aromatic hydrocarbon group having from 4 to 14 carbon atoms; and R 4 represents -NH 2 , -OH, -COOH, Ar(COOH) 2 , Ar(CO) 2 O or
- R 2 is a linear alkylene group having from 1 to 10 carbon atoms.
- Ar is preferably an aromatic group having from 4 to 14 carbon atoms.
- Examples of the aliphatic hydrocarbon group usable as R 3 include methyl, ethyl, propyl, isopropyl, n-butyl, t-butyl and pentyl groups.
- Examples of the alicyclic hydrocarbon group include cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl groups.
- Examples of the aromatic hydrocarbon group include phenyl, tolyl, xylyl, biphenyl, naphthyl, anthryl and phenanthryl groups. These aromatic rings may be substituted by, for example, halogen atoms, nitro groups or alkyl groups.
- R 3 may be different from each other. It is preferable that R 3 is a methyl group.
- m is 2 or above, still preferably 8 or above.
- m is not more than 100.
- a polyaramide/polysiloxane copolymer and polyvinyl carbazole were dissolved in N-methylpyrrolidone at a ratio of 1 : 1 to give a concentration of 2.5 % by weight.
- the solution thus obtained was applied onto glass substrates by using a spinner at 2,000 r.p.m. for 20 seconds, and dried at 180°C for 1 hour to form a polymer film having a thickness of about 50 nm. Then the film was aligned by rubbing with a nylon fabric in one direction.
- the alignment layer was irradiated with UV light for 5 minutes by using a lattice-patterned mask (300 ⁇ m x 50 ⁇ m) under a high pressure mercury lamp (105 W) to form an alignment layer having two types of regions adjacent to each other, namely, the UV-irradiated regions (300 ⁇ m x 50 ⁇ m) and unirradiated regions.
- an IPS-TFT cell was assembled using the substrate having the alignment layer thus obtained as the substrate of the electrode side.
- Fig. 3 shows the constitution of the alignment layer and the alignment directions of liquid crystal molecules.
- a pair of an UV-irradiated region (b) and an unirradiated region (a) corresponds to a dot regulated by a TFT device.
- a dot of one (a-b) pair usually corresponds to one of colors R (red), G (green) and B (blue).
- a nematic liquid crystal material (LIXON 5043LC, manufactured by Chisso Petrochemical Co.) was filled into the cell and subjected to a heat treatment. Evaluation of the viewing angle characteristics of this liquid crystal cell indicated that the region with low contrast was narrowed and thus the viewing angle of the cell was widened (Fig. 4).
- Example 2 An IPS-TFT cell was assembled in the same manner as that described in Example 1 , except for using a mask of a pattern size of 150 ⁇ m x 100 ⁇ m and arranging the alignment layer so that the electrical field was applied vertically thereto.
- the alignment layer was arranged so that the adjacent regions in adjacent dots differed from each other in alignment direction.
- Fig. 5 shows the constitution of the alignment layer and the alignment directions of liquid crystal molecules.
- a nematic liquid crystal material (LIXON 5043LC, manufactured by Chisso Petrochemical Co.) was filled into the cell and subjected to a heat treatment.
- An alignment layer was assembled in the same manner as that described in Example 1 and aligned by rubbing in one direction.
- the alignment layer was irradiated with UV light for 5 minutes by using a mask (100 ⁇ m x 37.5 ⁇ m and 150 ⁇ m x 25 ⁇ m) under a high pressure mercury lamp (105 W) so that the UV-irradiated regions and the unirradiated regions were arranged as shown in Fig. 7. Then an
- IPS-TFT cell was assembled using the substrate as the substrate on the electrode side.
- a nematic liquid crystal material (LIXON 5043LC, manufactured by Chisso Petrochemical Co.) was filled into the cell and subjected to a heat treatment. Evaluation of the viewing angle characteristics of this liquid crystal cell indicated that the region with low contrast substantially disappeared and the viewing angle of the cell was further widened (Fig. 8).
- Fig. 1 shows the structure of an IPS-TFT liquid crystal display device.
- Fig. 2 shows the viewing angle characteristics of a conventional IPS-TFT cell.
- Fig. 3 shows the constitution and alignment directions of liquid crystal molecules of the alignment layer of the present invention produced in Example 1. Only the regions b were irradiated with UV light.
- Fig. 4 shows the viewing angle characteristics of the liquid crystal display device of the present invention produced in Example 1.
- Fig. 5 shows the constitution and alignment directions of liquid crystal molecules of the alignment layer of the present invention produced in Example 2. Only the region d was irradiated with UV light.
- Fig. 6 shows the viewing angle characteristics of the liquid crystal display device of the present invention produced in Example 2.
- Fig. 7 shows the constitution of the alignment layer of the present invention produced in Example 3.
- the regions b and d were irradiated with UV light.
- Fig. 8 shows the viewing angle characteristics of the liquid crystal display device of the present invention produced in Example 3.
Landscapes
- Physics & Mathematics (AREA)
- Nonlinear Science (AREA)
- Liquid Crystal (AREA)
- Geometry (AREA)
- Mathematical Physics (AREA)
- Chemical & Material Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- General Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
Abstract
To provide an IPS-TFT liquid crystal display device having a wide viewing angle. Means for solution: an IPS-TFT liquid crystal display device characterized in that at least two regions differing in alignment direction from each other are formed in an alignment layer on the substrate of the electrode side.
Description
Description
Liquid Crystal Display Device
This invention relates to a process for producing a liquid crystal alignment layer and a liquid crystal display device with the use of the same. More particularly, it relates to a liquid crystal display device capable of achieving a wide viewing angle.
A liquid crystal display device is an electro-optical device containing a liquid crystal material which undergoes changes in the optical characteristics when an electrical field is externally applied thereto. Recently, there has been proposed an operating mode called IPS(ln-Plane Switching)-TFT for widening the viewing angle of liquid crystal display devices. This IPS-TFT mode is characterized by placing parallel electrodes on one substrate and rotating liquid crystal molecules located horizontally to the substrate within this plane to generate "on" state and "off" state (Fig. 1 ) (Nikkei Electronics, Dec. 4, 1995, p. 184). Since the liquid crystals are always aligned in the direction horizontal to the substrate in this mode, the contrast scarcely varies depending on the viewing direction, which makes it possible to achieve a wide viewing angle.
Even in this IPS-TFT mode, however, there still remains a region wherein the contrast is low and a gray-scale inversion arises depending on viewing angle (Fig. 2). This problem is caused by the fact that good optical characteristics cannot be obtained in the direction vertical to the longitudinal direction of molecules under applying an electric voltage.
Accordingly, it is an object of the present invention to provide a liquid crystal alignment layer which is capable of providing a liquid crystal display device having excellent viewing angle characteristics and thus solving the above-mentioned problems and a process for producing the same, as well as a liquid crystal display device with the use of said liquid crystal alignment layer.
The present inventors have now found that the viewing angle characteristics of an IPS-TFT liquid crystal display device can be further improved by forming at least two regions differing in alignment direction from each other in an alignment layer, thus completing the present invention.
The present invention provides an IPS-TFT liquid crystal display device characterized in that at least two regions differing in alignment direction from each other are formed in an alignment layer on the substrate of the electrode side. Preferably, in the liquid crystal display device of the present invention, a part of the alignment layer has been irradiated with UV light or an electron beam after completion of the aligning process, whereby the alignment direction of the alignment layer within the irradiated region is shifted by about 90° to the alignment direction established by the aligning process.
The present invention further provides a process for producing an IPS-TFT liquid crystal display device. The process comprises the steps of: preparing an alignment layer made of organic polymers; aligning said alignment layer; irradiating a part of the alignment layer with UV light or an electron beam to shift the alignment direction of the alignment layer within the irradiated region by about 90° to the alignment direction established by the aligning process; and assembling the liquid crystal display device using the alignment layer thus obtained as the alignment layer on the substrate of the electrode side.
The present invention furthermore relates to use of an alignment layer having at least two regions differing in alignment direction from each other in an IPS-TFT liquid crystal display device. The alignment layer employed in the method of the present invention is preferably characterized in that a part of said alignment layer has been irradiated with UV light or an electron beam after completion of the aligning process, whereby the alignment direction of the alignment layer within the irradiated region is shifted by about 90° to the alignment direction established by the aligning process.
According to the present invention, an IPS-TFT liquid crystal display device having good contrast and less viewing angle dependency of display characteristics can be produced by forming at least two regions differing in alignment direction from each other in an alignment layer on the substrate of the electrode side.
The IPS-TFT liquid crystal display device of the present invention can be produced by partly irradiating the surface of an alignment layer with UV light or an electron beam so that the alignment direction of the irradiated region is shifted by about 90°, more particularly 85 to 95°, to the alignment direction established by the aligning process. The term "alignment direction of the alignment layer" as used herein means the direction along which the liquid crystal is to be aligned on the surface of the alignment layer. As shown in Example 1 and Fig. 3, for example, irradiated regions and unirradiated regions are alternately arranged along the direction of the electrical field in the alignment layer on the substrate of the electrode side. Such an arrangement allows to form two regions differing in alignment direction by about 90° from each other (i.e. differing in viewing direction by about 90° from each other) in a single pixel, thus widening the viewing angle. Alternatively, as shown in Example 2 and Fig. 5, it is also possible to arrange two regions differing in alignment direction from each other vertically to the direction of the electrical field. In this case, it is preferable to arrange these regions in such a manner that the adjacent regions in adjacent dots differ from each other in alignment direction.
It is also possible, as shown in Example 3 and Fig. 7, to arrange regions differing in alignment direction from each other by 90° in combination horizontally and vertically to the direction of the electrical field, thus further improving the viewing angle characteristics. In this case, every dot should have at least one pair of each of (a-b) and (c-d) regions. It is preferable that the total area of the (a-b) regions is identical with that of the (c-d) regions.
As the alignment layer material employed in the present invention in which the alignment direction of the irradiated region is shifted by about 90° to the alignment direction established by the aligning process by irradiating with UV light or an electron beam, use can be made of photosensitive polymers having unsaturated
bonds in the molecular chain such as polyvinyl cinnamate. When irradiated with UV light after the aligning process, such a polymer undergoes dimerization or isomerization and thus its alignment direction is shifted by about 90°.
Alternatively, the alignment layer employed in the present invention can be obtained by mixing a polymer [polymer (A)], which has such properties as to align the liquid crystal in the direction of the aligning process after completion of the aligning process, with another polymer [polymer (B)], which has such properties as to align the liquid crystal in the direction shifted by about 90° to the direction of the aligning process.
Examples of the polymer (A) include but are not limited to backbone type polymers such as polyimide, polyamide, polyether, polyester and polyurethane. It is still preferable to use polyimide or polyamide, in particular, those bearing a fluorine and siloxane group. When irradiated with UV light, etc., many of these polymers suffer from a decrease in pretilt angle and thus alignment regulation tends to be weakened.
Examples of the polymer (B) include polyvinyl, polymethacrylate and polyacrylate having bulky groups in side chain such as polystyrene and polycyclohexyl methacrylate. It is preferable to use polyacenaphthylene, poly-4-vinylpyridine, polyvinyl diphenyl, polyvinyl naphthalene, polyvinyl formal, polyvinylpyridine-N- oxide, polyphenyl methacrylate, polyvinyl carbazole, etc. Polyvinyl cinnamate can also be used. Although many of these polymers (B) would be slightly or not aligned by usual aligning processes, they can establish uniform alignment after irradiation with UV light, etc. It still remains unknown why such uniform alignment can be established by irradiation with UV light, etc. It is assumed that the irradiation with energy beams such as UV light might cause a rearrangement of the molecular chains of such a polymer in the direction established by the aligning process. Alternatively, crosslinking might occur in some chemical structures. It is also possible that the terminal group in the side chain of a branched polymer is substituted by vinyl, acrylate, etc. and then the polymer is crosslinked upon UV-irradiation to fix the alignment.
By mixing the polymers (A) and (B) at an appropriate ratio, which is easily established by routine methods known to someone skilled in the art, it is possible to form an alignment layer which has the alignment direction established by the aligning process after completion of the aligning process, and has the alignment direction shifted by about 90° to the direction established by the aligning process after irradiation with UV light or an electron beam Thus, after the aligning process, the alignment regulation by the polymer (B) is weaker than the alignment regulation by the polymer (A) and, therefore, the liquid crystal is aligned in the direction established by the aligning process On the other hand, when irradiated with UV light or an electron beam, the alignment regulation by the polymer (A) is weakened while that by the polymer (B) is strengthened As a result, the alignment direction of the alignment layer is shifted by about 90° to the alignment direction established by the aligning process
The appropriate mixing ratio of the polymers (A) to (B) and the irradiation dose of UV light, etc are determined depending on the difference in alignment regulation between these polymers The mixing ratio of the polymers (A) to (B) preferably ranges from 1 50 to 50 1 When the amount of the polymer (A) is too large, the alignment regulation by the polymer (A) becomes dominant continuously, even if the alignment layer is irradiated with UV light, etc In this case, the alignment direction is not shifted by about 90° The polymers (A) and (B) may be each a mixture of two or more polymers The irradiation dose of UV light, etc preferably ranges from 0 01 mJ to 50 J, still preferably from 0.1 mJ to 10 J. If the dose of UV light, etc was too large, the polymers would be oxidized and thus the alignment would be disordered The wavelength of UV light, etc preferably ranges from 150 to 450 nm, still preferably from 200 to 400 nm
The alignment layer employed in the present invention can be produced by forming a polymer film on a glass or plastic substrate provided with a transparent electrode by spin coating or printing in accordance with a method commonly known in the art, then the film is subjected to the aligning process followed by the irradiation with UV light or an electron beam In the present invention, it is also possible to use nonpolarized UV light which facilitates the production process It is preferable that
the aligning process is carried out by the rubbing method, though the present invention is not restricted thereto. By using a mask in the step of irradiation with UV light or an electron beam, regions with different viewing directions can be formed in a single pixel. These regions can be arbitrarily varied in size and shape by appropriately selecting the mask pattern. The mask size is determined depending on the display size. Namely, the mask may have the same size as the display, or a smaller mask may be used by using steppers. The pattern size of the mask is preferably several ten to 500 μm depending on the size of a pixel.
Alternatively, the alignment layer employed in the present invention can be produced by other multi-domain formation methods known in the art. For example, it is possible to form two regions differing in alignment direction from each other in a single pixel by using photolithographic techniques. By mixing two or more polymers differring in SP value of at least 1 , preferably at least 2, it is also possible to form an alignment layer which can provide at least two different states of liquid crystal alignment by the aligning process in a single direction.
The SP value is a solubility parameter (SP - value δ = (Δ E/V)1 2 wherein Δ E is the molar heat of vaporization and V is the volume fraction (see, e.g, I.H. Hildebrand, R.L Scott, The Solubility of Nonelectrolytes, 3rd Ed., Reinhold, New Yor, 1949). It is the preferable that the liquid crystal alignment layer has microprotrusions on the surface thereof. It is still preferable in these cases that in the liquid crystal alignment layer, at least one of the polymers is a polymer containing siloxane or one containing fluorine.
It is preferable that the alignment layer has microprotrusions with arbitrary sizes and shapes on the surface thereof. These microprotrusions are from several hundred A to several μm in size, i.e., in diameter, and from several hundred A to several μm in height, preferably from several hundred A to several thousand A in height. Size and height of the microprotrusions can be measured by methods well known in the art, e.g., atomic force microscopy or scanning electron microscopy. When at least one polymer, which differs in SP value by 1 or more from other polymers, serves as a base material amounting to 50 % or more of the alignment layer materials while
other polymer(s) are used as so-called dopant(s) to be blended with the base, a phase separation is generated by mixing these polymers. As a result, it is believed that the polymer(s) added form microphase separation structures on the base polymer, thus giving microprotrusions.
The alignment layer can be produced by mixing two or more polymers differing in SP value by at least 1, and forming a film of the resulting mixture on a glass or plastic substrate by spin coating or print coating in accordance with a method commonly known in the art. By forming such alignment layers on both substrates, a liquid crystal display device having two or more alignment states with a high stability and a good reproducibility can be established.
The polymers to be used as the material for the alignment layer can be selected from, but are not limited to, those commonly employed in organic alignment layers such as polyimide, polyamide, polyurethane, polyester, polycarbonate, polyurea, polyether, polyimidoamide, polypeptide, polyolefins, cellulose and derivatives thereof, polyacrylates, polymethacrylates, polyvinyl such as polystyrenes and polyvinyl alcohol. It is preferable that at least one of the polymers to be used as the material for the alignment layer of the present invention is a polymer containing siloxane or one containing fluorine.
Polyimide, polyamide, polyurethane, polyester, polycarbonate, polyether, polyimidoamide and polyurea can be obtained by polymerizing monomers (for example, diisocyanate, diol, dicarboxylic acid, diamine, tetracarboxylic anhydride) by a method which has been commonly known by those skilled in the art.
A polymer containing fluorine can be obtained by using a monomer substituted with fluorine atom(s).
Examples of cellulose and derivatives thereof include hydroxypropyl cellulose, cellulose, hydroxymethyl cellulose, cellulose acetate butyrate, cellulose acetate phthalate, cellulose triacetate, methyl cellulose, cellulose acetate, cellulose hydroxypeptide, p-aminobenzyl cellulose, polyethyleneimine cellulose,
triethylaminoethyl cellulose, ethyl cellulose, cyanoethylated cellulose, carboxymethylated cellulose, diethylaminohydroxypropylated cellulose, sulfohydroxypropylated cellulose, trimethylaminohydroxy-propylated cellulose and bromoacetyl cellulose.
Examples of polyvinyl and derivatives thereof include polystyrene, sodium poly-4- styrene sulfonate, polymethylstyrene, dicarboxy- terminated polystyrene, monocarboxy-terminated polystyrene, polystyrene divinylbenzene, polystyrene methyl methacrylate, 3-trifluoromethylstyrene, polyvinylalcohol, polyvinylbiphenyl, polyvinylbiphenylether, polyvinylcinnamate, polyvinylformal, polyacenaphthylene, polyvinylcarbazole, polyvinylcyclohexyl, polyvinylmethlketone, polyvinylnaphthalene, polyvinylphenol, polyvinylpyridine, polyvinylbutyral, polyvinylidenefluoride, polyvinylpyhdine-N-oxide, polyvinylchloride, polyvinylfluoride and polystyrenesulfonylfluoride.
Examples of the polyacrylates or polymethacrylates include poly(methyl acrylate), poly(methyl methacrylate), poly(ethyl acrylate), poly(ethyl methacrylate), poly(butyl acrylate), poly(butyl methacrylate), poly(isobutyl acrylate), poly(isobutyl methacrylate), poly(t-butyl acrylate), poly(t-butyl methacrylate), poly(hexyl acrylate), poly(hexyl methacrylate), poly(2-ethylbutyl acrylate), poly(2-ethylbutyl methacrylate), poly(benzyl acrylate), poly(benzyl methacrylate), poly(cyclohexyl acrylate), poly(cyclohexyl methacrylate), poly(norbomyl acrylate), poly(norbornyl methacrylate), poly(isobornyl acrylate), poly(isobomyl methacrylate), poly(biphenyl acrylate), poly(biphenyl methacrylate) and copolymers thereof.
A fluorine-containing polymer can be obtained by introducing fluorine atom(s) into such a polyacrylate or a polymethacrylate.
As the polyolefins, use can be made of, for example, polyethylene, polypropylene, polyacetylene, polybutadiene, polyvinylidene fluoride and copolymers thereof. In addition thereto, polysilastyrene, etc. are also usable therefor.
As a siloxane-containing polymer, use can be made of polymers obtained by
reacting a compound represented by the following general formula as a siloxane component. It is preferable to use a block polymer of siloxane with other polymer(s).
wherein m is an integer of 1 or above;
R2 represents a divalent hydrocarbon group;
R3 represents a monovalent, linear or branched, aliphatic hydrocarbon group having from 1 to 5 carbon atoms or a alicyclic or aromatic hydrocarbon group having from 4 to 14 carbon atoms; and R4 represents -NH2, -OH, -COOH, Ar(COOH)2, Ar(CO)2O or
-NHSi(CH3)3, wherein Ar represents an aromatic group.
It is preferable that R2 is a linear alkylene group having from 1 to 10 carbon atoms. Ar is preferably an aromatic group having from 4 to 14 carbon atoms.
Examples of the aliphatic hydrocarbon group usable as R3 include methyl, ethyl, propyl, isopropyl, n-butyl, t-butyl and pentyl groups. Examples of the alicyclic hydrocarbon group include cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl groups. Examples of the aromatic hydrocarbon group include phenyl, tolyl, xylyl, biphenyl, naphthyl, anthryl and phenanthryl groups. These aromatic rings may be substituted by, for example, halogen atoms, nitro groups or alkyl groups. R3 may be different from each other. It is preferable that R3 is a methyl group.
In the above formula, it is preferable that m is 2 or above, still preferably 8 or above. When the polymerization degree of polysiloxane is excessively high, however, there arises a tendency toward deterioration in the strength of the alignment layer material. It is therefore preferable that m is not more than 100.
Examples
To further illustrate the present invention in greater detail, and not by way of limitation, the following Examples will be given.
Example 1
A polyaramide/polysiloxane copolymer and polyvinyl carbazole were dissolved in N-methylpyrrolidone at a ratio of 1 : 1 to give a concentration of 2.5 % by weight. The solution thus obtained was applied onto glass substrates by using a spinner at 2,000 r.p.m. for 20 seconds, and dried at 180°C for 1 hour to form a polymer film having a thickness of about 50 nm. Then the film was aligned by rubbing with a nylon fabric in one direction. Next, the alignment layer was irradiated with UV light for 5 minutes by using a lattice-patterned mask (300 μm x 50 μm) under a high pressure mercury lamp (105 W) to form an alignment layer having two types of regions adjacent to each other, namely, the UV-irradiated regions (300 μm x 50 μm) and unirradiated regions. Then an IPS-TFT cell was assembled using the substrate having the alignment layer thus obtained as the substrate of the electrode side. Fig. 3 shows the constitution of the alignment layer and the alignment directions of liquid crystal molecules. In Fig. 3, a pair of an UV-irradiated region (b) and an unirradiated region (a) corresponds to a dot regulated by a TFT device. A dot of one (a-b) pair usually corresponds to one of colors R (red), G (green) and B (blue).
A nematic liquid crystal material (LIXON 5043LC, manufactured by Chisso Petrochemical Co.) was filled into the cell and subjected to a heat treatment. Evaluation of the viewing angle characteristics of this liquid crystal cell indicated that the region with low contrast was narrowed and thus the viewing angle of the cell was widened (Fig. 4).
Example 2 An IPS-TFT cell was assembled in the same manner as that described in Example 1 , except for using a mask of a pattern size of 150 μm x 100 μm and arranging the alignment layer so that the electrical field was applied vertically thereto. The alignment layer was arranged so that the adjacent regions in adjacent dots differed
from each other in alignment direction. Fig. 5 shows the constitution of the alignment layer and the alignment directions of liquid crystal molecules.
A nematic liquid crystal material (LIXON 5043LC, manufactured by Chisso Petrochemical Co.) was filled into the cell and subjected to a heat treatment.
Evaluation of the viewing angle characteristics of this liquid crystal cell indicated that the region with low contrast was narrowed and thus the viewing angle of the cell was widened (Fig. 6).
Example 3
An alignment layer was assembled in the same manner as that described in Example 1 and aligned by rubbing in one direction. Next, the alignment layer was irradiated with UV light for 5 minutes by using a mask (100 μm x 37.5 μm and 150 μm x 25 μm) under a high pressure mercury lamp (105 W) so that the UV-irradiated regions and the unirradiated regions were arranged as shown in Fig. 7. Then an
IPS-TFT cell was assembled using the substrate as the substrate on the electrode side.
A nematic liquid crystal material (LIXON 5043LC, manufactured by Chisso Petrochemical Co.) was filled into the cell and subjected to a heat treatment. Evaluation of the viewing angle characteristics of this liquid crystal cell indicated that the region with low contrast substantially disappeared and the viewing angle of the cell was further widened (Fig. 8).
Fig. 1 shows the structure of an IPS-TFT liquid crystal display device.
Fig. 2 shows the viewing angle characteristics of a conventional IPS-TFT cell.
Fig. 3 shows the constitution and alignment directions of liquid crystal molecules of the alignment layer of the present invention produced in Example 1. Only the regions b were irradiated with UV light.
Fig. 4 shows the viewing angle characteristics of the liquid crystal display device of the present invention produced in Example 1.
Fig. 5 shows the constitution and alignment directions of liquid crystal molecules of the alignment layer of the present invention produced in Example 2. Only the region d was irradiated with UV light.
Fig. 6 shows the viewing angle characteristics of the liquid crystal display device of the present invention produced in Example 2.
Fig. 7 shows the constitution of the alignment layer of the present invention produced in Example 3. The regions b and d were irradiated with UV light.
Fig. 8 shows the viewing angle characteristics of the liquid crystal display device of the present invention produced in Example 3.
Claims
1. An IPS-TFT liquid crystal display device characterized in that at least two regions differing in alignment direction from each other are formed in an alignment layer on the substrate of the electrode side.
2. A liquid crystal display device as claimed in Claim 1 , characterized in that a part of said alignment layer has been irradiated with UV light or an electron beam after completion of the aligning process, whereby the alignment direction of the alignment layer within the irradiated region is shifted by about 90° to the alignment direction established by the aligning process.
3. A process for producing an IPS-TFT liquid crystal display device comprising the steps of: preparing an alignment layer made of organic polymers; aligning said alignment layer; irradiating a part of the alignment layer with UV light or an electron beam to shift the alignment direction of the alignment layer within the irradiated region by about 90° to the alignment direction established by the aligning process; and assembling the liquid crystal display device using the irradiated alignment layer as the alignment layer on the substrate of the electrode side.
4. Use of an alignment layer having at least two regions differing in alignment direction from each other in an IPS-TFT liquid crystal display device.
5. Use as claimed in Claim 4, characterized in that a part of said alignment layer has been irradiated with UV light or an electron beam after completion of the aligning process, whereby the alignment direction of the alignment layer within the irradiated region is shifted by about 90° to the alignment direction established by the aligning process.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8221087A JPH1062788A (en) | 1996-08-22 | 1996-08-22 | Liquid crystal display element |
JP8/221087 | 1996-08-22 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1998008136A1 true WO1998008136A1 (en) | 1998-02-26 |
Family
ID=16761293
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP1997/004501 WO1998008136A1 (en) | 1996-08-22 | 1997-08-18 | Liquid crystal display device |
Country Status (2)
Country | Link |
---|---|
JP (1) | JPH1062788A (en) |
WO (1) | WO1998008136A1 (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2792736A1 (en) * | 1999-04-21 | 2000-10-27 | Lg Philips Lcd Co Ltd | LIQUID CRYSTAL DISPLAY DEVICE |
EP1067423A3 (en) * | 1999-07-06 | 2003-04-16 | Matsushita Electric Industrial Co., Ltd. | Liquid crystal display and producing method thereof |
EP1063564A4 (en) * | 1998-03-06 | 2005-09-14 | Hitachi Ltd | LIQUID CRYSTAL DISPLAY DEVICE |
US7388639B2 (en) | 2003-12-29 | 2008-06-17 | Lg Display Co., Ltd. | In-plane switching mode liquid crystal display device having multi-domains |
US7599031B2 (en) | 1998-03-06 | 2009-10-06 | Hitachi, Ltd. | Liquid crystal display device |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100306800B1 (en) | 1998-05-29 | 2002-06-20 | 박종섭 | Liquid crystal display and method for fabricating the same |
KR100306799B1 (en) | 1998-05-29 | 2001-11-30 | 박종섭 | Liquid crystal display |
JP2000035572A (en) | 1998-07-16 | 2000-02-02 | Mitsubishi Electric Corp | Liquid crystal display |
KR100543040B1 (en) * | 1998-08-21 | 2006-05-22 | 삼성전자주식회사 | Wide viewing angle liquid crystal display device |
KR100413485B1 (en) * | 2001-07-09 | 2003-12-31 | 엘지.필립스 엘시디 주식회사 | Inplane switching mode liquid crystal display device and method for fabricating the same |
KR100963029B1 (en) | 2003-03-24 | 2010-06-09 | 엘지디스플레이 주식회사 | Method of manufacturing transverse electric field liquid crystal display device |
JP4637248B2 (en) * | 2009-04-16 | 2011-02-23 | シャープ株式会社 | Liquid crystal display device |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE4420585A1 (en) * | 1994-06-13 | 1995-12-14 | Merck Patent Gmbh | Electro-optical system |
-
1996
- 1996-08-22 JP JP8221087A patent/JPH1062788A/en active Pending
-
1997
- 1997-08-18 WO PCT/EP1997/004501 patent/WO1998008136A1/en active Application Filing
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE4420585A1 (en) * | 1994-06-13 | 1995-12-14 | Merck Patent Gmbh | Electro-optical system |
Non-Patent Citations (2)
Title |
---|
AHATANI S ET AL: "Complete suppression of color shift in in-plane switching mode liquid crystal displays with a multidomain structure obtained by unidirectional rubbing", JAPANESE JOURNAL OF APPLIED PHYSICS, PART 2 (LETTERS), 15 JAN. 1997, PUBLICATION OFFICE, JAPANESE JOURNAL APPL. PHYS, JAPAN, vol. 36, no. 1A-B, ISSN 0021-4922, pages L27 - L29, XP002049459 * |
KONDO K: "8.1: INVITED PAPER: WIDE-VIEWING-ANGLE DISPLAYS WITH IN-PLANE SWITCHING MODE OF NEMATIC LCS ADDRESSED BY 13.3-IN. XGA TFTS", SID INTERNATIONAL SYMPOSIUM. DIGEST OF TECHNICAL PAPERS, SAN DIEGO, MAY 12 - 17, 1996, vol. 27, 12 May 1996 (1996-05-12), SOCIETY FOR INFORMATION DISPLAY, pages 81 - 84, XP000621030 * |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1063564A4 (en) * | 1998-03-06 | 2005-09-14 | Hitachi Ltd | LIQUID CRYSTAL DISPLAY DEVICE |
US7599031B2 (en) | 1998-03-06 | 2009-10-06 | Hitachi, Ltd. | Liquid crystal display device |
FR2792736A1 (en) * | 1999-04-21 | 2000-10-27 | Lg Philips Lcd Co Ltd | LIQUID CRYSTAL DISPLAY DEVICE |
US7018687B2 (en) | 1999-04-21 | 2006-03-28 | Lg. Philips Lcd Co., Ltd. | Liquid crystal display device |
EP1067423A3 (en) * | 1999-07-06 | 2003-04-16 | Matsushita Electric Industrial Co., Ltd. | Liquid crystal display and producing method thereof |
US7388639B2 (en) | 2003-12-29 | 2008-06-17 | Lg Display Co., Ltd. | In-plane switching mode liquid crystal display device having multi-domains |
Also Published As
Publication number | Publication date |
---|---|
JPH1062788A (en) | 1998-03-06 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP5587294B2 (en) | Liquid crystal display device, method for producing liquid crystal display device, composition for forming PSA layer, and composition for forming liquid crystal layer | |
US5959707A (en) | Liquid crystal display having domains with different tilted-up directions as well as domains with different twist directions of lc molecules | |
CN104238193B (en) | Directional material, oriented layer, Liquid crystal disply device and its preparation method | |
CN107109050B (en) | Liquid crystal aligning agent, liquid crystal alignment film, and liquid crystal display element | |
WO1998008136A1 (en) | Liquid crystal display device | |
US20030232927A1 (en) | Hybrid polymer materials for liquid crystal alignment layers | |
KR20010024294A (en) | Photocrosslinkable polyimides | |
KR20130057153A (en) | Liquid crystal device alignment layer and methods for manufacturing the same | |
WO2022260048A1 (en) | Weak anchoring liquid crystal aligning agent, liquid cyrstal display element and copolymer | |
KR20160002795A (en) | Method for manufacturing in-plane-switching-type liquid-crystal display element | |
US5795629A (en) | Liquid crystal alignment layer and liquid crystal display device | |
KR100316112B1 (en) | LCD Display | |
JP7552597B2 (en) | In-plane switching liquid crystal display element and method for manufacturing the in-plane switching liquid crystal cell | |
US20050094073A1 (en) | Bistable nematic liquid crystal device | |
US5861198A (en) | Liquid crystal display device | |
US7422778B2 (en) | Photoreactive compound, liquid crystal alignment layer using the compound, method of manufacturing the alignment layer, and liquid crystal display device containing the alignment layer | |
CN118043732A (en) | Weak anchoring liquid crystal aligning agent, liquid crystal display element and polymer | |
KR102864723B1 (en) | Method for manufacturing a patterned liquid crystal display element | |
KR102826665B1 (en) | Method for manufacturing zero-surface anchoring film and liquid crystal display element | |
TW202346543A (en) | Weak-anchoring liquid crystal aligning agent and liquid crystal display element | |
KR20240136415A (en) | Liquid crystal alignment agent and liquid crystal display element | |
WO2023157879A1 (en) | Weak-anchoring liquid crystal aligning agent, and liquid crystal display element | |
WO2022196565A1 (en) | Liquid-crystal composition, liquid-crystal display element production method, and liquid-crystal display element | |
WO2023120726A1 (en) | Weak-anchoring liquid crystal alignment agent, and liquid cyrstal display element | |
JPH1073824A (en) | Production of liquid crystal orienting film and liquid crystal display element using the same |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AK | Designated states |
Kind code of ref document: A1 Designated state(s): JP KR US |
|
AL | Designated countries for regional patents |
Kind code of ref document: A1 Designated state(s): AT BE CH DE DK ES FI FR GB GR IE IT LU MC NL PT SE |
|
DFPE | Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101) | ||
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
NENP | Non-entry into the national phase |
Ref country code: JP Ref document number: 1998510403 Format of ref document f/p: F |
|
122 | Ep: pct application non-entry in european phase |