WO2000070405A1 - Ablation enhancement layer - Google Patents
Ablation enhancement layer Download PDFInfo
- Publication number
- WO2000070405A1 WO2000070405A1 PCT/US2000/013031 US0013031W WO0070405A1 WO 2000070405 A1 WO2000070405 A1 WO 2000070405A1 US 0013031 W US0013031 W US 0013031W WO 0070405 A1 WO0070405 A1 WO 0070405A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- layer
- ablatable
- ablation
- metal oxide
- imaging medium
- Prior art date
Links
- 238000002679 ablation Methods 0.000 title claims abstract description 81
- 239000000758 substrate Substances 0.000 claims abstract description 43
- 229910044991 metal oxide Inorganic materials 0.000 claims abstract description 41
- 150000004706 metal oxides Chemical class 0.000 claims abstract description 41
- 238000003384 imaging method Methods 0.000 claims abstract description 39
- 238000010521 absorption reaction Methods 0.000 claims abstract description 16
- 238000002310 reflectometry Methods 0.000 claims abstract description 12
- 238000004519 manufacturing process Methods 0.000 claims abstract description 8
- 238000000034 method Methods 0.000 claims description 42
- 230000008569 process Effects 0.000 claims description 26
- 239000006229 carbon black Substances 0.000 claims description 8
- 230000000694 effects Effects 0.000 claims description 8
- 229910052782 aluminium Inorganic materials 0.000 claims description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 3
- 239000011159 matrix material Substances 0.000 claims description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 claims 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 claims 1
- 229920002451 polyvinyl alcohol Polymers 0.000 claims 1
- 239000010410 layer Substances 0.000 description 150
- 238000000059 patterning Methods 0.000 description 34
- 238000004140 cleaning Methods 0.000 description 21
- 239000000463 material Substances 0.000 description 21
- 238000000608 laser ablation Methods 0.000 description 13
- 239000004973 liquid crystal related substance Substances 0.000 description 13
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 12
- 239000010931 gold Substances 0.000 description 12
- 238000000429 assembly Methods 0.000 description 9
- 230000000712 assembly Effects 0.000 description 9
- 238000000576 coating method Methods 0.000 description 8
- 239000004020 conductor Substances 0.000 description 8
- 239000004033 plastic Substances 0.000 description 7
- 229920003023 plastic Polymers 0.000 description 7
- 239000011521 glass Substances 0.000 description 6
- 238000004544 sputter deposition Methods 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 5
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 5
- 229910052737 gold Inorganic materials 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 239000000377 silicon dioxide Substances 0.000 description 5
- 239000010409 thin film Substances 0.000 description 5
- 238000005229 chemical vapour deposition Methods 0.000 description 4
- 238000000151 deposition Methods 0.000 description 4
- 239000000835 fiber Substances 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 230000003287 optical effect Effects 0.000 description 4
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 4
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 3
- 230000004888 barrier function Effects 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 230000008021 deposition Effects 0.000 description 3
- 238000005137 deposition process Methods 0.000 description 3
- 239000002360 explosive Substances 0.000 description 3
- 229910003437 indium oxide Inorganic materials 0.000 description 3
- PJXISJQVUVHSOJ-UHFFFAOYSA-N indium(iii) oxide Chemical compound [O-2].[O-2].[O-2].[In+3].[In+3] PJXISJQVUVHSOJ-UHFFFAOYSA-N 0.000 description 3
- AMGQUBHHOARCQH-UHFFFAOYSA-N indium;oxotin Chemical compound [In].[Sn]=O AMGQUBHHOARCQH-UHFFFAOYSA-N 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 229910052709 silver Inorganic materials 0.000 description 3
- 239000004332 silver Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- CXKCTMHTOKXKQT-UHFFFAOYSA-N cadmium oxide Inorganic materials [Cd]=O CXKCTMHTOKXKQT-UHFFFAOYSA-N 0.000 description 2
- CFEAAQFZALKQPA-UHFFFAOYSA-N cadmium(2+);oxygen(2-) Chemical compound [O-2].[Cd+2] CFEAAQFZALKQPA-UHFFFAOYSA-N 0.000 description 2
- ZSWFCLXCOIISFI-UHFFFAOYSA-N cyclopentadiene Chemical compound C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 230000009477 glass transition Effects 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- ZKATWMILCYLAPD-UHFFFAOYSA-N niobium pentoxide Inorganic materials O=[Nb](=O)O[Nb](=O)=O ZKATWMILCYLAPD-UHFFFAOYSA-N 0.000 description 2
- URLJKFSTXLNXLG-UHFFFAOYSA-N niobium(5+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[Nb+5].[Nb+5] URLJKFSTXLNXLG-UHFFFAOYSA-N 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- 229910052814 silicon oxide Inorganic materials 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 229920003002 synthetic resin Polymers 0.000 description 2
- 239000000057 synthetic resin Substances 0.000 description 2
- 229910001316 Ag alloy Inorganic materials 0.000 description 1
- 229910001020 Au alloy Inorganic materials 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 description 1
- 241000270711 Malaclemys terrapin Species 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 230000001154 acute effect Effects 0.000 description 1
- 239000002318 adhesion promoter Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 238000000137 annealing Methods 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 230000001413 cellular effect Effects 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 229910052681 coesite Inorganic materials 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 229910052906 cristobalite Inorganic materials 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000004069 differentiation Effects 0.000 description 1
- 230000003467 diminishing effect Effects 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000010408 film Substances 0.000 description 1
- 239000012634 fragment Substances 0.000 description 1
- 229910052733 gallium Inorganic materials 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- 239000002346 layers by function Substances 0.000 description 1
- 238000001755 magnetron sputter deposition Methods 0.000 description 1
- 229910001092 metal group alloy Inorganic materials 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920006393 polyether sulfone Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 238000001552 radio frequency sputter deposition Methods 0.000 description 1
- 238000005546 reactive sputtering Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 238000005201 scrubbing Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 229910052682 stishovite Inorganic materials 0.000 description 1
- 230000007847 structural defect Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 238000002207 thermal evaporation Methods 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 238000002834 transmittance Methods 0.000 description 1
- 229910052905 tridymite Inorganic materials 0.000 description 1
- 238000001947 vapour-phase growth Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/004—Photosensitive materials
- G03F7/09—Photosensitive materials characterised by structural details, e.g. supports, auxiliary layers
-
- 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
- G02F1/13439—Electrodes characterised by their electrical, optical, physical properties; materials therefor; method of making
-
- 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
- G02F1/1345—Conductors connecting electrodes to cell terminals
- G02F1/13458—Terminal pads
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/004—Photosensitive materials
- G03F7/0042—Photosensitive materials with inorganic or organometallic light-sensitive compounds not otherwise provided for, e.g. inorganic resists
- G03F7/0044—Photosensitive materials with inorganic or organometallic light-sensitive compounds not otherwise provided for, e.g. inorganic resists involving an interaction between the metallic and non-metallic component, e.g. photodope systems
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/20—Exposure; Apparatus therefor
- G03F7/2002—Exposure; Apparatus therefor with visible light or UV light, through an original having an opaque pattern on a transparent support, e.g. film printing, projection printing; by reflection of visible or UV light from an original such as a printed image
- G03F7/2014—Contact or film exposure of light sensitive plates such as lithographic plates or circuit boards, e.g. in a vacuum frame
- G03F7/2016—Contact mask being integral part of the photosensitive element and subject to destructive removal during post-exposure processing
- G03F7/202—Masking pattern being obtained by thermal means, e.g. laser ablation
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/26—Processing photosensitive materials; Apparatus therefor
- G03F7/36—Imagewise removal not covered by groups G03F7/30 - G03F7/34, e.g. using gas streams, using plasma
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/24—Ablative recording, e.g. by burning marks; Spark recording
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31678—Of metal
- Y10T428/31692—Next to addition polymer from unsaturated monomers
Definitions
- this invention relates to an ablatable laminar imaging medium having an optimized exposure threshold, and in particular, one wherein said optimized threshold is resultant of the employment therein of an ablation enhancement layer with predefined absorption and reflection values.
- Liquid crystal displays comprise a liquid crystal material sandwiched between two substantially transparent electrode assemblies.
- Touch screen displays of either the resistive or capacitive types comprise a display screen (for example, a cathode ray tube) having superposed thereover two substantially transparent electrode assemblies.
- each of these electrode assemblies typically comprises a substrate on which is deposited a conductive layer thin enough to be substantially transparent.
- substantially transparent is used herein to mean that the electrodes transmit sufficient visible light so that the two superposed electrodes will not substantially obscure, nor substantially distort the color of, a liquid crystal display or touch screen display incorporating the two electrodes.
- the two superposed electrodes typically have a transmittance of at least 80% at 550 nm.
- the substrate is usually glass, whereas touch screen displays usually employ a synthetic resin (plastic) substrate for at least one electrode.
- the conductor is often formed from indium tin oxide or a similar metal oxide.
- the conductor is typically formed by depositing the oxide by sputtering or chemical vapor deposition at a high temperature, and then annealing, also at a high temperature. On glass substrates temperatures in substrates, lower temperatures must be used, with resultant higher electrical resistance in the conductor.
- both liquid crystal displays and touch screen displays may make use of thin film electrodes comprising a metallic conductive layer sandwiched between two layers having high refractive indices; these two layers usually being formed from metal oxides.
- the metallic conductive layer is patterned so as to divide it into a plurality of electrodes, and conductors are attached to each of these electrodes to enable formation of the desired patterns in the liquid crystal material.
- Prior art processes for forming electrodes also often require the use of elevated temperatures of 200°C or more, which in practice requires the use of glass substrates or expensive high temperature plastics (polymers are known which have glass transition temperatures above 225 °C and can thus withstand processing at such temperatures).
- polymers are known which have glass transition temperatures above 225 °C and can thus withstand processing at such temperatures.
- liquid crystal displays for example, in cellular telephones and other mobile electronic devices
- LCD electrode patterns by laser ablation essentially involved the direct pattern-wise removal of portions layers of electrically conductive and insulating materials by exposing said portions to laser light of an intensity and quality (e.g., wavelength) sufficient to completely or partly decompose said material.
- the reaction can be fairly characterized as "explosive” (i.e., on a microscopic level), producing vapor-like or gas-like streams consisting of fragments of the removed material.
- Explosive i.e., on a microscopic level
- an ablatable laminar imaging medium characterized by its incorporation of an ablation enhancement layer, the ablation enhancement layer being composed, configured, and located to effectively reduce the threshold energy requirement for effecting laser ablation.
- the use of the ablation enhancement layer dramatically improves laser ablation efficiency (i.e., faster scan speed, lower exposure energy threshold, and quality), and promotes "cleaner" ablation of the metallic layer(s) in the area of exposure (e.g., well ablated areas with few "ridges", unablated residue, and/or other like ill-defined edges, surfaces, and boundaries).
- the ablatable laminar imaging medium ⁇ which is particularly useful in the manufacture of a substantially transparent electrode assembly — can be defined as comprising: (a) a substrate; (b) a high-index metal oxide layer; (c) an ablatable metallic conductive layer; (d) a high-index conductive metal oxide layer; and (e) an ablation enhancement layer having an IR-absorption greater than the IR-absorption of said high-index conductive metal oxide layer and an IR-reflectivity less than the IR-reflectivity of said high-index conductive metal oxide layer.
- the present invention also provides a new process for dealing with (cf, "cleaning") remnant and/or residual ablation enhancement material left in the course of ablation, which for many applications and products is unwanted.
- the characterizing steps of the inventive method involve the execution of a "cleaning" operation in close connection with a "patterning"
- the new process can be accomplished by either a sequential methodology (i.e., ablation patterning, followed by ablation cleaning) or a continuous methodology (i.e., ablation patterning conducted contemporaneously with ablation cleaning ).
- a sequential methodology i.e., ablation patterning, followed by ablation cleaning
- a continuous methodology i.e., ablation patterning conducted contemporaneously with ablation cleaning
- FIGS. 1 to 5 provide schematic representational illustrations of embodiments of the present invention, wherein: FIG. 1 illustrates in cross-section an ablatable laminar imaging medium 10 according to the present invention;
- FIGS. 2 A to 2C illustrate a method of processing the ablatable laminar imaging medium 10 of FIG. 1, the method involving sequential (i.e., "step-wise") laser imaging and laser cleaning operations;
- FIGS. 3 A to 3B illustrate another method of processing the ablatable laminar imaging medium 10 of FIG. 1, the method involving contemporaneously-executed (cf, continuous) laser imaging and laser cleaning;
- FIG. 4 is a schematic side elevation of an apparatus suited for imaging the ablatable laminar imaging medium 10 of FIG. 1; and
- FIG. 5 is a cross-sectional view taken along the line II -II in FIG.
- the present invention provides means for preventing, reducing, and/or otherwise alleviating the incidence of certain undesirable structural defects in electrode assemblies manufactured according to conventional laser ablation processes. These defects are essentially trace or residual metals or metal oxides left on the electrode assembly by incomplete, inefficient, and/or unfocused ablation patterning, and/or inadequate post-patterning cleaning. Such residue will — if the incidence is high ⁇ produce an unacceptable level of electrical shorts (cf, dark pixels) in a fully assembled flat panel display product.
- the means disclosed herein target inefficiencies occurring at both the ablation patterning stage and the subsequent cleaning stage. that ablation can be performed more efficiently, at a lower energy threshold, and with greater control, when using an ablatable laminar imaging medium 10 that incorporates therein an ablation enhancement layer 100.
- the primary function of the ablation enhancement layer 100 typically the top layer of said medium
- the ablatable laminar imaging medium 10 comprises a base 212 (i.e., a substrate 120, coated or otherwise) a high-index metal oxide layer 134, an ablatable metallic conductive layer 130, a high index conductive metal oxide layer 132, and an ablation enhancement layer 100 configured to have an IR-absorption (i.e., the absorption of infrared irradiation) greater than the IR-absorption of the high-index conductive metal oxide layer 132 and an IR-reflectivity (i.e., reflection of infrared irradiation) less than the IR-reflectivity of said high-index conductive metal oxide layer 132.
- IR-absorption i.e., the absorption of infrared irradiation
- IR-reflectivity i.e., reflection of infrared irradiation
- the ablation enhancement layer 100 should generally be located in close proximity to the electrode-forming layers 213, though there is no absolute requirement that the structures be physically adjacent. In other words, they should be in sufficiently close proximity in the sense that the transfer of energy from one to the other is assured, a condition that will not necessarily be defeated if intermediate functional layers or coatings are present. 100, those skilled in the art will appreciate that several materials and compositional configurations can be used to effect the aforementioned optical properties. Regardless, the presently contemplated materials for the ablation enhancement layer 100 include carbon black, IR dyes, Al, Au, Pt, or Cu. Carbon black dispersed in a water-soluble polymeric matrix is generally preferred.
- the substrate 120 used in the present process may be formed of any material having sufficient mechanical integrity and a surface smooth enough to permit the formation of electrodes thereon.
- the substrate must, like the other layers of the electrode assembly be sufficiently transparent to allow its use in a liquid crystal display.
- Glass substrates may be used, but it is generally preferred that the substrate be formed from a synthetic resin.
- Preferred resins for this purpose include polycarbonate and poly(b/5 , (cyclopentadiene) condensate)s, such as the material sold by Lonza AG, M ⁇ nchensteinerstrasse 38, CH-4002 Basel, Switzerland under the trademark "TRANSPHAN".
- This material is a film of a polymer sold by Japan Synthetic Rubber Co. Ltd., 2-11- 24 Tsukiji, Tokyo 104, Japan under the trademark "ARTON”; this polymer is stated by the manufacturer to be of the formula:
- substrates which may be useful in the present invention, include poly ether sulfones and poly (alky l)acrylates.
- the substrate 120 may be provided with coatings on one or both surfaces to act as gas and moisture barriers, and/or to improve the hardness and scratch resistance of the substrate and or to improve the adhesion of the high index layer to the substrate.
- coatings 122 and 124 As shown in FIG. 1, it has been useful coatings 122 and 124.
- Such hard coatings 122 and 124 will typically have a thickness of from about 1 to about 15 ⁇ m, preferably from about 2 to about 4 ⁇ m and may be provided by free radical polymerization (initiated either thermally or by ultra-violet radiation) of an appropriate polymerization material.
- An especially preferred hard coating is the acrylic coating sold under the trademark "TERRAPIN” by Tekra Corporation, 6700 West Lincoln Avenue, New Berlin, Wisconsin 53151.
- a thin (typically 10-30 nm) layer of silica (SiO x ) to act as a gas and moisture barrier for the eventual liquid crystal display assembly, and to act as an adhesion promoter to improve the adhesion of the high index layer. See, barrier layer 140 in FIG. 1.
- SiO x silica
- barrier layer 140 in FIG. 1.
- silica layers are often deposited by chemical vapor deposition or sputtering of silicon in an oxygen atmosphere, so that the material deposited does not precisely conform to the stoichiometric formula SiO 2 of pure silica.
- the substrate there are deposited on the substrate, in order, the high-index metal oxide layer 134, the ablatable metallic conductive layer 130, the high-index conductive metal oxide layer 132, and the ablation enhancement layer 100.
- the layers are preferably deposited by sputtering or by chemical vapor deposition, with dc sputtering being especially preferred, although RF, magnetron and reactive sputtering and low-pressure, plasma-enhanced and laser-enhanced chemical vapor deposition may also be used.
- each of the three layers should be effected at a temperature not greater than about 170°C in order to prevent damage to the plastic substrate; the temperature limit of course varies with the exact substrate employed and in the case of the aforementioned TRANSPHAN substrate, this temperature should not be greater than 160-165°C.
- the high-index metal oxide layer 134 adjacent the substrate 120 may be electrically insulating or conductive, though the latter — despite the use of ablation enhancement layer 100 ⁇ is still generally preferred as a matter of caution, since the use of an insulating high index layer can only further ensure that, should any portion of this high index layer 134 remain between adjacent electrodes after the patterning step, this remaining portion will not cause an electrical short between the electrodes.
- a conductive high index layer 134 may be used for applications where the demand for such safeguards are more relaxed.
- the high-index layer 134 is typically formed from a metal oxide, preferred oxides for this purpose being indium oxide (In 2 O 3 ), titanium dioxide (TiO ), cadmium oxide (CdO), gallium indium oxide, niobium pentoxide (Nb 2 O 5 ), indium tin oxide and tin dioxide (SnO ).
- a metal oxide preferred oxides for this purpose being indium oxide (In 2 O 3 ), titanium dioxide (TiO ), cadmium oxide (CdO), gallium indium oxide, niobium pentoxide (Nb 2 O 5 ), indium tin oxide and tin dioxide (SnO ).
- the conductivity of such metal oxide layers can be controlled over several orders of magnitude by varying the conditions under which the oxide layer is deposited.
- the relevant conditions include temperature, reactor pressure, partial pressure of oxygen, dc bias and deposition rate. Doping may also be used to control the conductivity of the insulating from about 20 to about 80 nm.
- the refractive index needed in the high-index metal oxide layer 134 adjacent the substrate 120 (and in the high index conductive metal oxide layer 132) will vary somewhat depending upon the other layers present in the final flat panel display product in which the electrode assembly of the present invention is to be incorporated.
- the refractive index of the high index layers 134 and 132 measured at 550 nm, will exceed 1.6, and the refractive indices of the preferred metal oxide high index layers can readily be made to exceed 1.9, as described in the papers mentioned above.
- the ablatable metallic conductive layer 130 may be formed from any metal or metal alloy capable of being deposited by the deposition process employed and having sufficient conductivity to provide the required low resistance in the final electrode assembly.
- the composition and configuration of layer 130 must also provide absorptivity to the irradiation used for patterning at a level sufficient to allow the explosive reactions involved in ablation to occur at the designated and desired threshold energies.
- the conductive layer comprises at least one of gold, silver and a gold/silver alloy (for example, the alloy described in U.S. Patent No. 4,234,654).
- this layer 130 comprise a layer of silver coated on one or both sides with a thinner layer of gold, e.g., less than one monolayer. For example, a 10 nm layer of silver sandwiched between two 1 nm layers of gold has been found to give good results.
- the overall thickness of the ablatable metallic conductive layer 130 will typically be in the range of about 5 to about 20 nm.
- the preferred materials and processes for forming the high-index conductive metal oxide layer 132 are the same as those for forming high-index metal oxide layer 134, except of course that the conditions used to deposit the layer 132 should be varied, if need be, so as to give the layer 132 at least partial conductivity.
- the resistance of layers used in electrode assemblies is normally measured over the whole surface of the assembly, and in the present case it has been found that using a 400 ohms/square, and desirably from about 100 to about 200 ohms per square, gives satisfactory results.
- the thickness of the layer 132 is desirably in the range of about 20 to about 100 nm. Examples of combinations of ablatable electrode-forming layers
- ITO indium tin oxide
- ITO 40-42 nm Ag, 9- 10 nm/Au, 1 - 1.5 nm ITO, 47 nm
- ITO 40-42 nm Au, 1 nm/Ag, 10 nm/ Au 1 nm ITO, 47 nm
- ablation enhancement layer 100 is deposited over the top high-index conductive layer 132.
- ablation enhancement layer 100 there is no absolute requirement that ablation enhancement layer 100 be adjacent to electrode-forming layers 213. With the ablation enhancement layer 100, it is possible to ablate non-conducting layers such as an intermediate metal-oxide layer 101 having poor absorption in IR, e.g., 2-4 ⁇ m layers of ITO only-type structures. This does not require a metallic layer underneath the non-conducting layer, since energy absorption in the ablation enhancement layer 100 is adequate to remove several microns of lower conductivity or non-conducting metal oxide.
- non-conducting layers such as an intermediate metal-oxide layer 101 having poor absorption in IR, e.g., 2-4 ⁇ m layers of ITO only-type structures. This does not require a metallic layer underneath the non-conducting layer, since energy absorption in the ablation enhancement layer 100 is adequate to remove several microns of lower conductivity or non-conducting metal oxide.
- the ablation enhancement layer 100 is also relevant is the location of the ablation enhancement layer 100 on the top surface of the ablatable laminar imaging medium 10. While there is no absolute requirement that this layer be the exposed, uppermost surface of medium 10, in view of its functionality, the layer should, if this is not to be the case, nevertheless be positioned such that during the expected imagewise exposure of medium 10, exposure irradiation will be incident upon the layer 100, before incidence upon the ablatable electrode-forming layers 213.
- the aforementioned ingredients of ablation enhancement layer 100 should be formulated to still allow passage of exposure irradiation therethrough.
- carbon black is a preferred ingredient, it should not be formulated to create a layer with an optical density so high that all exposure energy is absorbed in the ablation enhancement layer 100. In general, only trace amounts of carbon black will be necessary to produce absorptivity and reflectivity parameters better than otherwise available, for example, with the use of expected configurations of high index conductive metal oxide layer 132.
- the ablation enhancement layer 100 is material only during the imagewise patterning of ablatable laminar imaging assembly
- another of the considerations in its configuration is the selection of materials best suited to facilitate its removal (cf, "cleaning") after ablation patterning.
- the formulation of "easily removable" compositions is within the ability of those skilled in the art.
- carbon black formulations can be either solvent-based or water-based, in which case, post-patterning cleaning can be occasioned by an alcohol rinse (for the former) or a simple water rinse (for the latter).
- a release layer 101 which when treated to an appropriate rinse, disperses, dissolves, or otherwise degrades, thereby "undercutting" said ablation enhancement layer 100.
- the patterning In patterning a desired electrode structure into ablatable laminar imaging medium 10, it is important that the patterning extend completely through both the high-index conductive metal oxide layer 132 and the ablatable metallic conductive layer 130 to ensure that there are no short circuits between adjacent electrodes, a result facilitated by the use of the ablation enhancement layer 100.
- the patterning will usually extend completely through the high index layer 134 adjacent the substrate; however, as already indicated, it is still desirably essential that the high index layer have sufficient resistance to prevent unwanted current leakage between adjacent electrodes should any portion of the high index layer remain after patterning.
- the preferred technique for patterning is to use an infrared laser emitting in the range of about 700 to about 1200 nm.
- the infrared radiation is, after passing through the ablation enhancement layer 100, absorbed primarily within the ablatable metallic conductive layer 130, leading to rapid and reliable patterning of this layer 130.
- the laser used for the laser ablation is a fiber laser employing a double-clad optic fiber, as described for example in U.S. Patents Nos. 4,815,079; 5,268,978; 5,373,576 and 5,418,880.
- the energy required for patterning the electrode assembly is about 800 mJ cm " , so that using a fiber laser with a 6 W output and an 8.5 ⁇ m spot radius (measured and patterns approximately 400 cm per minute of the substrate.
- the laser beam is scanned in a raster pattern over the substrate while being modulated under the control of digital signals from a raster image processor.
- This technique has the advantage that it requires only the preparation of a digital image of the proposed electrode pattern, so that the apparatus can change patterns with essentially no down time.
- FIGS. 2A-2C and FIGS. 3A-3B Two processes by which this can be accomplished — constituting the earlier-mentioned means for improving ablation efficiencies at the "cleaning" stage ⁇ are illustrated schematically in FIGS. 2A-2C and FIGS. 3A-3B.
- imaging medium 10 is illustrated as comprising ablation enhancement layer 100, electrode forming layers 213, and the substrate 212, without detailed illustration of their more particular laminar construction.
- the intensity of this first radiant exposure hvi should be of a level sufficient to effect ablation of the unwanted plug of electrode forming layer 213, which — as a consequence of the explosive character of the ablation reaction ⁇ will result also in the removal of the overlying portions of the ablation enhancement layer 100.
- Step 1, illustrated in FIG. 2A is simply the aforedescribed patterning process.
- ablation enhancement layer 100 are removed (cf, cleaned) or made more easily removable by exposure to a second exposure to radiant energy, hv , this exposure being of a substantially lower intensity than hvi.
- ablation enhancement layer 100 will be configured to have a lower threshold than electrode forming layers 213, this second exposure — when done at the appropriate, sufficiently lower intensity ⁇ should produce an ablation effect in layer 100, without ablating or otherwise compromising electrode forming layers 213.
- a final cleaning step (cf, "rinsing") should be followed to remove blasted residue, as well as — in cases where the second exposure is conducted to weaken only remnants of layer 100 ⁇ to finally remove that layer.
- exposure is continuous and constant. Differentiation in respect of effecting ablation of the enhancement layer 100 only, or in concert with the ablation of electrode-forming layers 213, is effected principally by maintaining continuously active background exposure throughout the patterning operation.
- the background exposure should be of an intensity effecting only the removal (or removability) of only ablation enhancement layer 100.
- the intensity is raised to level sufficient to effect its ablation. Intensity is lowered back to the background level when ablation of that portion is complete.
- AOM acousto-optic-modulator
- the AOM contrast ratio is made equal to the ratio of the patterning to cleaning powers (hvi: hv 2 ). contaminated with redeposited debris from the ablation and surface residue. It has been found that the surface of the assembly can be effectively cleaned by washing it with water, desirably containing a surface active agent; gentle scrubbing of the surface assists in the cleaning process without harming the final electrode assembly.
- the electrode assembly thus formed may be for use in a passive type liquid crystal display, a touch screen display or other flat panel display.
- the electrode assemblies of the present invention can readily be formed having greater than 80% transparency at 550 nm, and less than 10 ohms per square sheet resistance. Such electrode assemblies are readily incorporated into liquid crystal display assemblies of commercial quality.
- Figures 4 and 5 show schematically a preferred apparatus for carrying out the patterning step of the process.
- the apparatus (generally designated 105) shown in Figures 4 and 5 of the accompanying drawings is an internal drum laser ablation device; alternatively an external drum or flat bed device may be used.
- the apparatus 105 comprises a base 11 carrying at its opposed ends two upstanding end plates 12 and 14.
- a cylindrical drum 16 is fixedly mounted between the end plates 12 and 14. (Part of the drum 16 is broken away in Figure 4 to show the remaining parts of the apparatus 10.)
- a rod 18 is fixed between the end plates 12 and 14 and a fiber laser unit 20 is slideably mounted on this rod.
- the laser unit 20 is also engaged with a lead screw 22 which extends below and parallel to the rod 18.
- the laser unit 20 comprises a laser and a rotating mirror (neither component is shown separately in Figure 4), which causes the laser beam 24 to emerge from the laser unit at an acute angle axis, thereby directing this beam around the internal surface of the drum 16.
- the lead screw 22 is rotated synchronously with the mirror of the laser unit 20 so that, as the beam 24 rotates, the laser unit 20 moves horizontally along the axis of the drum 16, so that the beam 24 describes a helical path along the internal surface of the drum 16.
- a sheet 26 of coated substrate is held by a vacuum device (not shown) against the internal surface of the drum 16 so that the beam 24 passes in a raster pattern over the sheet 26.
- the operation of the laser unit 20 is controlled by a computerized control unit (not shown) so as to produce the desired pattern on the sheet 26.
Abstract
Description
Claims
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2000618784A JP2002544568A (en) | 1999-05-14 | 2000-05-12 | Ablation enhancement layer |
AU47124/00A AU4712400A (en) | 1999-05-14 | 2000-05-12 | Ablation enhancement layer |
EP00928971A EP1183570A1 (en) | 1999-05-14 | 2000-05-12 | Ablation enhancement layer |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US13431899P | 1999-05-14 | 1999-05-14 | |
US60/134,318 | 1999-05-14 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2000070405A1 true WO2000070405A1 (en) | 2000-11-23 |
WO2000070405A9 WO2000070405A9 (en) | 2004-10-14 |
Family
ID=22462810
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2000/013031 WO2000070405A1 (en) | 1999-05-14 | 2000-05-12 | Ablation enhancement layer |
Country Status (7)
Country | Link |
---|---|
US (2) | US6485839B1 (en) |
EP (1) | EP1183570A1 (en) |
JP (1) | JP2002544568A (en) |
KR (1) | KR100755810B1 (en) |
CN (1) | CN100354727C (en) |
AU (1) | AU4712400A (en) |
WO (1) | WO2000070405A1 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2354900A2 (en) * | 2008-11-14 | 2011-08-10 | LG Innotek Co., Ltd. | Touch screen and manufacturing method thereof |
EP2354899A2 (en) * | 2008-11-14 | 2011-08-10 | LG Innotek Co., Ltd. | Touch screen and manufacturing method thereof |
Families Citing this family (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6699352B2 (en) | 1999-01-25 | 2004-03-02 | Henry Sawatsky | Decorative and protective system for wares |
CN100354727C (en) * | 1999-05-14 | 2007-12-12 | 3M创新有限公司 | Ablation enhancement layer |
US6828067B2 (en) * | 2001-04-13 | 2004-12-07 | Precision Coatings, Inc. | Ablatable direct write imaging medium |
US20060138104A1 (en) * | 2001-05-25 | 2006-06-29 | Devore Paul W | Fuel cell and liquid container sealant removal system |
KR100503603B1 (en) | 2003-03-11 | 2005-07-26 | 엘지전자 주식회사 | Method of driving plasma display panel |
KR100509763B1 (en) * | 2003-03-11 | 2005-08-25 | 엘지전자 주식회사 | Front filter of plasma display panel |
US20040188150A1 (en) * | 2003-03-25 | 2004-09-30 | 3M Innovative Properties Company | High transparency touch screen |
JP2005011793A (en) * | 2003-05-29 | 2005-01-13 | Sony Corp | Manufacturing method of structure of lamination, lamination structure, display element and display device |
US20050067740A1 (en) * | 2003-09-29 | 2005-03-31 | Frederick Haubensak | Wafer defect reduction by short pulse laser ablation |
US8264466B2 (en) * | 2006-03-31 | 2012-09-11 | 3M Innovative Properties Company | Touch screen having reduced visibility transparent conductor pattern |
IN2012DN02446A (en) * | 2009-09-22 | 2015-08-21 | First Solar Inc | |
KR101621340B1 (en) * | 2009-10-23 | 2016-05-16 | 엠-솔브 리미티드 | Capacitive touch panels |
TWI474377B (en) * | 2010-03-25 | 2015-02-21 | Winsky Technology Ltd | A method of patterning a substrate and a method of manufacturing a capacitive touch panel |
CN102236484B (en) * | 2010-04-30 | 2015-03-11 | 永恒科技有限公司 | Method for patterning substrate and method for manufacturing capacitive touch panel |
US8482713B2 (en) * | 2011-02-04 | 2013-07-09 | Apple Inc. | Laser processing of display components for electronic devices |
US9425571B2 (en) * | 2012-01-06 | 2016-08-23 | Johnson & Johnson Vision Care, Inc. | Methods and apparatus to form electrical interconnects on ophthalmic devices |
US9703139B2 (en) | 2012-09-20 | 2017-07-11 | Apple Inc. | Methods for trimming polarizers in displays |
US8988636B2 (en) | 2012-09-20 | 2015-03-24 | Apple Inc. | Methods for trimming polarizers in displays |
US9753317B2 (en) | 2012-12-21 | 2017-09-05 | Apple Inc. | Methods for trimming polarizers in displays using edge protection structures |
JP2018093180A (en) * | 2016-11-03 | 2018-06-14 | アイメック・ヴェーゼットウェーImec Vzw | Method for patterning amorphous semiconductor layer |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4234654A (en) * | 1978-07-11 | 1980-11-18 | Teijin Limited | Heat wave-reflective or electrically conductive laminated structure |
EP0733931A2 (en) * | 1995-03-22 | 1996-09-25 | Toppan Printing Co., Ltd. | Multilayered conductive film, and transparent electrode substrate and liquid crystal device using the same |
WO1997000777A2 (en) * | 1995-06-23 | 1997-01-09 | Sun Chemical Corporation | Digital laser imagable lithographic printing plates |
JPH09171188A (en) * | 1995-12-18 | 1997-06-30 | Ulvac Japan Ltd | Lamination type transparent conductive film |
US5879861A (en) * | 1996-04-23 | 1999-03-09 | Agfa-Gevaert, N.V. | Method for making a lithographic printing plate wherein an imaging element is used that comprises a thermosensitive mask |
Family Cites Families (44)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3065169D1 (en) | 1979-08-31 | 1983-11-10 | Teijin Ltd | Heat wave-reflective or electrically conductive laminated structure |
GB2083726A (en) * | 1980-09-09 | 1982-03-24 | Minnesota Mining & Mfg | Preparation of multi-colour prints by laser irradiation and materials for use therein |
JPS5761553A (en) | 1980-09-25 | 1982-04-14 | Toray Industries | Laminated film |
FR2499744B1 (en) | 1981-01-05 | 1986-07-04 | Commissariat Energie Atomique | MATRIX DISPLAY DEVICE COMPRISING TWO FAMILIES OF LINED ELECTRODES AND ITS DRIVING METHOD |
EP0077672B1 (en) | 1981-10-19 | 1986-06-25 | Teijin Limited | Selectively light transmitting film and preformed laminar structure |
JPS5910988A (en) | 1982-07-12 | 1984-01-20 | ホシデン株式会社 | Color liquid crystal display |
JPH0637872B2 (en) * | 1984-12-14 | 1994-05-18 | 株式会社東芝 | How to start a hydraulic turbine |
US4775549A (en) * | 1984-12-19 | 1988-10-04 | Matsushita Electric Industrial Co., Ltd. | Method of producing a substrate structure for a large size display panel and an apparatus for producing the substrate structure |
US4815079A (en) | 1987-12-17 | 1989-03-21 | Polaroid Corporation | Optical fiber lasers and amplifiers |
US4973572A (en) * | 1987-12-21 | 1990-11-27 | Eastman Kodak Company | Infrared absorbing cyanine dyes for dye-donor element used in laser-induced thermal dye transfer |
US4804975A (en) * | 1988-02-17 | 1989-02-14 | Eastman Kodak Company | Thermal dye transfer apparatus using semiconductor diode laser arrays |
US4931158A (en) | 1988-03-22 | 1990-06-05 | The Regents Of The Univ. Of Calif. | Deposition of films onto large area substrates using modified reactive magnetron sputtering |
US5343216A (en) | 1989-01-31 | 1994-08-30 | Sharp Kabushiki Kaisha | Active matrix substrate and active matrix display apparatus |
NO894656L (en) | 1989-02-07 | 1990-08-08 | Autodisplay As | PROCEDURE FOR MANUFACTURING AN ELECTRICAL DESIGN ON A SUBSTRATE. |
DE3925970A1 (en) | 1989-08-05 | 1991-02-07 | Hoechst Ag | ELECTRICALLY CONDUCTIVE POLYMERS AND THEIR USE AS AN ORIENTATION LAYER IN LIQUID CRYSTAL SWITCHING AND DISPLAY ELEMENTS |
JP2875363B2 (en) | 1990-08-08 | 1999-03-31 | 株式会社日立製作所 | Liquid crystal display |
NL9002769A (en) | 1990-12-17 | 1992-07-16 | Philips Nv | METHOD FOR MANUFACTURING AN IMAGE WINDOW FOR AN IMAGE DISPLAY DEVICE |
US5164565A (en) | 1991-04-18 | 1992-11-17 | Photon Dynamics, Inc. | Laser-based system for material deposition and removal |
US5244770A (en) * | 1991-10-23 | 1993-09-14 | Eastman Kodak Company | Donor element for laser color transfer |
JP2581373B2 (en) * | 1992-04-27 | 1997-02-12 | 双葉電子工業株式会社 | Method for manufacturing transparent conductive film wiring board |
US5353705A (en) * | 1992-07-20 | 1994-10-11 | Presstek, Inc. | Lithographic printing members having secondary ablation layers for use with laser-discharge imaging apparatus |
JP2794369B2 (en) | 1992-12-11 | 1998-09-03 | キヤノン株式会社 | Liquid crystal element |
US5268978A (en) | 1992-12-18 | 1993-12-07 | Polaroid Corporation | Optical fiber laser and geometric coupler |
US5373576A (en) | 1993-05-04 | 1994-12-13 | Polaroid Corporation | High power optical fiber |
US5354633A (en) * | 1993-09-22 | 1994-10-11 | Presstek, Inc. | Laser imageable photomask constructions |
WO1995013566A1 (en) | 1993-11-10 | 1995-05-18 | Xmr, Inc. | Method for back-side photo-induced ablation for making a color filter, or the like |
KR0124958B1 (en) | 1993-11-29 | 1997-12-11 | 김광호 | Thin film transistor for crystal liquid & manufacturing method of the same |
US5528402A (en) * | 1994-02-07 | 1996-06-18 | Parker; William P. | Addressable electrohologram employing electro-optic layer and patterned conductor between two electrodes |
US5418880A (en) | 1994-07-29 | 1995-05-23 | Polaroid Corporation | High-power optical fiber amplifier or laser device |
JPH08257770A (en) | 1995-03-20 | 1996-10-08 | Hitachi Ltd | Method and device for developing ablation |
IL114137A (en) * | 1995-06-13 | 1998-12-06 | Scitex Corp Ltd | Ir ablateable driographic printing plates and methods for making same |
JPH0980221A (en) | 1995-09-13 | 1997-03-28 | Hitachi Ltd | Color filter substrate for liquid crystal display element and its production |
JPH0990327A (en) | 1995-09-26 | 1997-04-04 | Sharp Corp | Liquid crystal display element and its production |
JPH09152618A (en) * | 1995-11-30 | 1997-06-10 | Sony Corp | Production of planar display panel |
JPH09152567A (en) | 1995-11-30 | 1997-06-10 | Hitachi Ltd | Formation of resist patterns and apparatus therefor |
US5691063A (en) * | 1996-02-29 | 1997-11-25 | Flex Products, Inc. | Laser imageable tuned optical cavity thin film and printing plate incorporating the same |
JPH10217421A (en) * | 1996-05-27 | 1998-08-18 | Mitsubishi Chem Corp | Photosensitive lithographic printing plate without laser direct dampening water |
JPH10100303A (en) * | 1996-06-07 | 1998-04-21 | Nippon Sheet Glass Co Ltd | Substrate fitted with transparent conductive film and display element using the same |
JPH09325365A (en) | 1996-06-07 | 1997-12-16 | Hitachi Ltd | Production of liquid crystal display element and liquid crystal display device |
US5783364A (en) * | 1996-08-20 | 1998-07-21 | Presstek, Inc. | Thin-film imaging recording constructions incorporating metallic inorganic layers and optical interference structures |
JPH1070151A (en) | 1996-08-26 | 1998-03-10 | Ricoh Co Ltd | Method and apparatus for arraying conductive particle |
JP4099841B2 (en) * | 1998-01-09 | 2008-06-11 | 凸版印刷株式会社 | Transparent electrode |
US6379509B2 (en) | 1998-01-20 | 2002-04-30 | 3M Innovative Properties Company | Process for forming electrodes |
CN100354727C (en) * | 1999-05-14 | 2007-12-12 | 3M创新有限公司 | Ablation enhancement layer |
-
2000
- 2000-05-12 CN CNB008075468A patent/CN100354727C/en not_active Expired - Fee Related
- 2000-05-12 WO PCT/US2000/013031 patent/WO2000070405A1/en active Application Filing
- 2000-05-12 AU AU47124/00A patent/AU4712400A/en not_active Abandoned
- 2000-05-12 JP JP2000618784A patent/JP2002544568A/en active Pending
- 2000-05-12 US US09/570,074 patent/US6485839B1/en not_active Expired - Lifetime
- 2000-05-12 EP EP00928971A patent/EP1183570A1/en not_active Withdrawn
- 2000-05-12 KR KR1020017014488A patent/KR100755810B1/en active IP Right Grant
-
2002
- 2002-06-13 US US10/170,843 patent/US6689544B2/en not_active Expired - Lifetime
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4234654A (en) * | 1978-07-11 | 1980-11-18 | Teijin Limited | Heat wave-reflective or electrically conductive laminated structure |
EP0733931A2 (en) * | 1995-03-22 | 1996-09-25 | Toppan Printing Co., Ltd. | Multilayered conductive film, and transparent electrode substrate and liquid crystal device using the same |
WO1997000777A2 (en) * | 1995-06-23 | 1997-01-09 | Sun Chemical Corporation | Digital laser imagable lithographic printing plates |
JPH09171188A (en) * | 1995-12-18 | 1997-06-30 | Ulvac Japan Ltd | Lamination type transparent conductive film |
US5879861A (en) * | 1996-04-23 | 1999-03-09 | Agfa-Gevaert, N.V. | Method for making a lithographic printing plate wherein an imaging element is used that comprises a thermosensitive mask |
Non-Patent Citations (2)
Title |
---|
CHU P Y Z ET AL: "42.2: A NEW CONDUCTOR STRUCTURE FOR PLASTIC LCD APPLICATIONS UTILIZING ALL DRY DIGITAL LASER PATTERNING", SID INTERNATIONAL SYMPOSIUM DIGEST OF TECHNICAL PAPERS,US,SANTA ANA, CA: SID, vol. 29, 17 May 1998 (1998-05-17), pages 1099 - 1101, XP000792579, ISSN: 0098-966X * |
PATENT ABSTRACTS OF JAPAN vol. 1997, no. 10 31 October 1997 (1997-10-31) * |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2354900A2 (en) * | 2008-11-14 | 2011-08-10 | LG Innotek Co., Ltd. | Touch screen and manufacturing method thereof |
EP2354899A2 (en) * | 2008-11-14 | 2011-08-10 | LG Innotek Co., Ltd. | Touch screen and manufacturing method thereof |
EP2354900A4 (en) * | 2008-11-14 | 2013-03-27 | Lg Innotek Co Ltd | Touch screen and manufacturing method thereof |
EP2354899A4 (en) * | 2008-11-14 | 2013-03-27 | Lg Innotek Co Ltd | Touch screen and manufacturing method thereof |
US8842083B2 (en) | 2008-11-14 | 2014-09-23 | Lg Innotek Co., Ltd. | Touch screen and manufacturing method thereof |
US9152256B2 (en) | 2008-11-14 | 2015-10-06 | Lg Innotek Co., Ltd. | Touch screen and method of manufacturing the same |
Also Published As
Publication number | Publication date |
---|---|
KR100755810B1 (en) | 2007-09-07 |
EP1183570A1 (en) | 2002-03-06 |
CN1350658A (en) | 2002-05-22 |
CN100354727C (en) | 2007-12-12 |
US6485839B1 (en) | 2002-11-26 |
KR20020026163A (en) | 2002-04-06 |
JP2002544568A (en) | 2002-12-24 |
WO2000070405A9 (en) | 2004-10-14 |
US20020195435A1 (en) | 2002-12-26 |
AU4712400A (en) | 2000-12-05 |
US6689544B2 (en) | 2004-02-10 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US6689544B2 (en) | Ablation enhancement layer | |
EP1056596B1 (en) | Process for forming electrodes | |
US6617541B1 (en) | Laser etching method | |
US6602790B2 (en) | Method for patterning a multilayered conductor/substrate structure | |
TWI489189B (en) | Glass substrate and liquid crystal display device with shading film | |
CN101626901A (en) | Method for depositing an inorganic layer to a thermal transfer layer | |
CN114089600A (en) | Capacitive input device, method of manufacturing the same, and image display device | |
JP3345089B2 (en) | Method for manufacturing color filter substrate | |
JPH10332930A (en) | Manufacture of color filter | |
JP2002333538A (en) | Optical waveguide forming method, electrodeposition liquid used for it, and optical waveguide manufacturing apparatus | |
US20020122649A1 (en) | Light waveguide forming method, electrolyte solution, light waveguide forming apparatus and light waveguide | |
EP1962295A1 (en) | Transparent substrate with thin film and method for manufacturing transparent substrate with circuit pattern wherein such transparent substrate with thin film is used | |
JPH086070A (en) | Production of liquid crystal display element | |
JP3464473B2 (en) | Display device | |
KR101506734B1 (en) | Device and method for ito patterning | |
KR102122426B1 (en) | Coating layer patterning method using laser and sacrificial layer | |
JP2005527858A (en) | Laser structuring of electro-optic systems | |
Chien et al. | Fabrication of the crystalline ITO pattern by picosecond laser with a diffractive optical element | |
Hsiung | Femtosecond laser-induced crystallization of amorphous indium tin oxide film on glass substrate for patterning applications | |
JPS6094726A (en) | Processing method for translucent conductive film |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
WWE | Wipo information: entry into national phase |
Ref document number: 00807546.8 Country of ref document: CN |
|
AK | Designated states |
Kind code of ref document: A1 Designated state(s): AE AG AL AM AT AT AU AZ BA BB BG BR BY CA CH CN CR CU CZ CZ DE DE DK DK DM DZ EE EE ES FI FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX NO NZ PL PT RO RU SD SE SG SI SK SK SL TJ TM TR TT TZ UA UG UZ VN YU ZA ZW |
|
AL | Designated countries for regional patents |
Kind code of ref document: A1 Designated state(s): GH GM KE LS MW SD SL SZ TZ UG ZW AM AZ BY KG KZ MD RU TJ TM AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE BF BJ CF CG CI CM GA GN GW ML MR NE SN TD TG |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
DFPE | Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101) | ||
WWE | Wipo information: entry into national phase |
Ref document number: 2000928971 Country of ref document: EP |
|
ENP | Entry into the national phase |
Ref document number: 2000 618784 Country of ref document: JP Kind code of ref document: A |
|
WWE | Wipo information: entry into national phase |
Ref document number: 1020017014488 Country of ref document: KR |
|
WWP | Wipo information: published in national office |
Ref document number: 2000928971 Country of ref document: EP |
|
REG | Reference to national code |
Ref country code: DE Ref legal event code: 8642 |
|
WWP | Wipo information: published in national office |
Ref document number: 1020017014488 Country of ref document: KR |
|
COP | Corrected version of pamphlet |
Free format text: PAGES 2-18, DESCRIPTION, REPLACED BY CORRECT PAGES 2-18 |