WO2007089218A2 - High integrity protective coating - Google Patents
High integrity protective coating Download PDFInfo
- Publication number
- WO2007089218A2 WO2007089218A2 PCT/US2005/041660 US2005041660W WO2007089218A2 WO 2007089218 A2 WO2007089218 A2 WO 2007089218A2 US 2005041660 W US2005041660 W US 2005041660W WO 2007089218 A2 WO2007089218 A2 WO 2007089218A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- coating
- composite article
- composition
- high integrity
- substrate
- Prior art date
Links
- 239000011253 protective coating Substances 0.000 title claims abstract description 55
- 239000000203 mixture Substances 0.000 claims abstract description 97
- 239000010410 layer Substances 0.000 claims abstract description 87
- 239000002131 composite material Substances 0.000 claims abstract description 70
- 230000004888 barrier function Effects 0.000 claims abstract description 68
- 238000000151 deposition Methods 0.000 claims abstract description 37
- 238000000034 method Methods 0.000 claims abstract description 25
- 239000011247 coating layer Substances 0.000 claims abstract description 15
- 238000000576 coating method Methods 0.000 claims description 114
- 239000011248 coating agent Substances 0.000 claims description 95
- 239000000758 substrate Substances 0.000 claims description 73
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 31
- 229910052760 oxygen Inorganic materials 0.000 claims description 31
- 239000001301 oxygen Substances 0.000 claims description 31
- 229920005989 resin Polymers 0.000 claims description 27
- 239000011347 resin Substances 0.000 claims description 27
- 230000005693 optoelectronics Effects 0.000 claims description 22
- 230000008021 deposition Effects 0.000 claims description 18
- 239000007789 gas Substances 0.000 claims description 17
- 230000005540 biological transmission Effects 0.000 claims description 15
- 239000003054 catalyst Substances 0.000 claims description 15
- 238000001723 curing Methods 0.000 claims description 11
- 239000000376 reactant Substances 0.000 claims description 11
- 239000004094 surface-active agent Substances 0.000 claims description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 10
- 239000003795 chemical substances by application Substances 0.000 claims description 8
- 230000008569 process Effects 0.000 claims description 7
- 230000006798 recombination Effects 0.000 claims description 7
- 238000005215 recombination Methods 0.000 claims description 7
- 238000006243 chemical reaction Methods 0.000 claims description 6
- 238000004528 spin coating Methods 0.000 claims description 6
- 238000002834 transmittance Methods 0.000 claims description 6
- 229920000515 polycarbonate Polymers 0.000 claims description 5
- 239000004417 polycarbonate Substances 0.000 claims description 5
- 238000003847 radiation curing Methods 0.000 claims description 5
- 239000003822 epoxy resin Substances 0.000 claims description 4
- 229920000647 polyepoxide Polymers 0.000 claims description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 3
- 238000007756 gravure coating Methods 0.000 claims description 3
- 230000001681 protective effect Effects 0.000 claims description 3
- 230000005855 radiation Effects 0.000 claims description 3
- 238000001029 thermal curing Methods 0.000 claims description 3
- 239000000853 adhesive Substances 0.000 claims description 2
- 238000007754 air knife coating Methods 0.000 claims description 2
- 238000007766 curtain coating Methods 0.000 claims description 2
- 238000003618 dip coating Methods 0.000 claims description 2
- 230000008020 evaporation Effects 0.000 claims description 2
- 238000001704 evaporation Methods 0.000 claims description 2
- 238000001125 extrusion Methods 0.000 claims description 2
- 238000007757 hot melt coating Methods 0.000 claims description 2
- 230000005499 meniscus Effects 0.000 claims description 2
- 238000007763 reverse roll coating Methods 0.000 claims description 2
- 238000007777 rotary screen coating Methods 0.000 claims description 2
- 238000007767 slide coating Methods 0.000 claims description 2
- 238000007764 slot die coating Methods 0.000 claims description 2
- 239000007921 spray Substances 0.000 claims description 2
- 239000004925 Acrylic resin Substances 0.000 claims 1
- 229920000178 Acrylic resin Polymers 0.000 claims 1
- 239000004593 Epoxy Substances 0.000 claims 1
- 230000001070 adhesive effect Effects 0.000 claims 1
- 238000009685 knife-over-roll coating Methods 0.000 claims 1
- 238000002156 mixing Methods 0.000 claims 1
- 239000000463 material Substances 0.000 description 19
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 16
- 239000010703 silicon Substances 0.000 description 16
- 229910052710 silicon Inorganic materials 0.000 description 16
- 230000003287 optical effect Effects 0.000 description 13
- 230000007547 defect Effects 0.000 description 10
- 238000000623 plasma-assisted chemical vapour deposition Methods 0.000 description 9
- 239000002243 precursor Substances 0.000 description 9
- 239000000126 substance Substances 0.000 description 7
- 230000003746 surface roughness Effects 0.000 description 7
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- 230000008901 benefit Effects 0.000 description 6
- 230000035699 permeability Effects 0.000 description 6
- 210000002381 plasma Anatomy 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 230000008859 change Effects 0.000 description 5
- 229910010272 inorganic material Inorganic materials 0.000 description 5
- 239000011147 inorganic material Substances 0.000 description 5
- 230000004048 modification Effects 0.000 description 5
- 238000012986 modification Methods 0.000 description 5
- 239000004033 plastic Substances 0.000 description 5
- 229920003023 plastic Polymers 0.000 description 5
- 241000894007 species Species 0.000 description 5
- 230000008033 biological extinction Effects 0.000 description 4
- 239000008199 coating composition Substances 0.000 description 4
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 4
- 229910052753 mercury Inorganic materials 0.000 description 4
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 4
- 239000011368 organic material Substances 0.000 description 4
- 239000000654 additive Substances 0.000 description 3
- 239000002318 adhesion promoter Substances 0.000 description 3
- 229910021529 ammonia Inorganic materials 0.000 description 3
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 229920000139 polyethylene terephthalate Polymers 0.000 description 3
- 239000005020 polyethylene terephthalate Substances 0.000 description 3
- 238000001228 spectrum Methods 0.000 description 3
- 229920002799 BoPET Polymers 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 239000005041 Mylar™ Substances 0.000 description 2
- 229910052581 Si3N4 Inorganic materials 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 229920004738 ULTEM® Polymers 0.000 description 2
- 229920001646 UPILEX Polymers 0.000 description 2
- 238000005299 abrasion Methods 0.000 description 2
- 239000006096 absorbing agent Substances 0.000 description 2
- 239000011358 absorbing material Substances 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 150000001299 aldehydes Chemical class 0.000 description 2
- 150000001335 aliphatic alkanes Chemical class 0.000 description 2
- 150000001336 alkenes Chemical class 0.000 description 2
- 150000001345 alkine derivatives Chemical class 0.000 description 2
- 125000002947 alkylene group Chemical group 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 235000006708 antioxidants Nutrition 0.000 description 2
- 230000000712 assembly Effects 0.000 description 2
- 238000000429 assembly Methods 0.000 description 2
- 230000000903 blocking effect Effects 0.000 description 2
- 239000013590 bulk material Substances 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 238000005229 chemical vapour deposition Methods 0.000 description 2
- 239000007772 electrode material Substances 0.000 description 2
- GCSJLQSCSDMKTP-UHFFFAOYSA-N ethenyl(trimethyl)silane Chemical compound C[Si](C)(C)C=C GCSJLQSCSDMKTP-UHFFFAOYSA-N 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 2
- 230000005525 hole transport Effects 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 150000002431 hydrogen Chemical class 0.000 description 2
- PJXISJQVUVHSOJ-UHFFFAOYSA-N indium(iii) oxide Chemical compound [O-2].[O-2].[O-2].[In+3].[In+3] PJXISJQVUVHSOJ-UHFFFAOYSA-N 0.000 description 2
- 239000002346 layers by function Substances 0.000 description 2
- 230000031700 light absorption Effects 0.000 description 2
- 239000004973 liquid crystal related substance Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 150000004767 nitrides Chemical class 0.000 description 2
- 238000000847 optical profilometry Methods 0.000 description 2
- 238000013086 organic photovoltaic Methods 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 229910052761 rare earth metal Inorganic materials 0.000 description 2
- 150000002910 rare earth metals Chemical class 0.000 description 2
- 238000005546 reactive sputtering Methods 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 2
- 238000004544 sputter deposition Methods 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- 238000000411 transmission spectrum Methods 0.000 description 2
- WJQZZLQMLJPKQH-UHFFFAOYSA-N 2,4-dichloro-6-methylphenol Chemical compound CC1=CC(Cl)=CC(Cl)=C1O WJQZZLQMLJPKQH-UHFFFAOYSA-N 0.000 description 1
- BXGYYDRIMBPOMN-UHFFFAOYSA-N 2-(hydroxymethoxy)ethoxymethanol Chemical compound OCOCCOCO BXGYYDRIMBPOMN-UHFFFAOYSA-N 0.000 description 1
- HIPPBUJQSIICJN-UHFFFAOYSA-N 3385-61-3 Chemical compound C12CC=CC2C2CC(O)C1C2 HIPPBUJQSIICJN-UHFFFAOYSA-N 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- OWYWGLHRNBIFJP-UHFFFAOYSA-N Ipazine Chemical compound CCN(CC)C1=NC(Cl)=NC(NC(C)C)=N1 OWYWGLHRNBIFJP-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 239000004697 Polyetherimide Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- 239000006087 Silane Coupling Agent Substances 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 238000003848 UV Light-Curing Methods 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 238000005524 ceramic coating Methods 0.000 description 1
- 229910010293 ceramic material Inorganic materials 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000013626 chemical specie Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 230000032798 delamination Effects 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 1
- 229910003437 indium oxide Inorganic materials 0.000 description 1
- 238000009616 inductively coupled plasma Methods 0.000 description 1
- 239000011229 interlayer Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- HMMGMWAXVFQUOA-UHFFFAOYSA-N octamethylcyclotetrasiloxane Chemical compound C[Si]1(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O1 HMMGMWAXVFQUOA-UHFFFAOYSA-N 0.000 description 1
- 229920002113 octoxynol Polymers 0.000 description 1
- 229920001601 polyetherimide Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000003678 scratch resistant effect Effects 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- 238000000391 spectroscopic ellipsometry Methods 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 238000004383 yellowing Methods 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/30—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26
- H01L21/31—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26 to form insulating layers thereon, e.g. for masking or by using photolithographic techniques; After treatment of these layers; Selection of materials for these layers
- H01L21/3205—Deposition of non-insulating-, e.g. conductive- or resistive-, layers on insulating layers; After-treatment of these layers
- H01L21/321—After treatment
- H01L21/32115—Planarisation
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K50/00—Organic light-emitting devices
- H10K50/80—Constructional details
- H10K50/84—Passivation; Containers; Encapsulations
- H10K50/844—Encapsulations
- H10K50/8445—Encapsulations multilayered coatings having a repetitive structure, e.g. having multiple organic-inorganic bilayers
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/70—Manufacture or treatment of devices consisting of a plurality of solid state components formed in or on a common substrate or of parts thereof; Manufacture of integrated circuit devices or of parts thereof
- H01L21/71—Manufacture of specific parts of devices defined in group H01L21/70
- H01L21/768—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics
- H01L21/76838—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics characterised by the formation and the after-treatment of the conductors
- H01L21/7684—Smoothing; Planarisation
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L2924/00—Indexing scheme for arrangements or methods for connecting or disconnecting semiconductor or solid-state bodies as covered by H01L24/00
- H01L2924/06—Polymers
- H01L2924/068—Polycarbonate
Definitions
- the invention relates generally to protective coatings. More specifically, the invention relates to protective coatings that arc used in optoelectronic devices.
- Optical and optoelectronic devices that are susceptible to reactive chemical species normally encountered in the environment, require protective coatings with good barrier properties.
- substrates especially polymeric substrates on which these devices may be a manufactured, are not alomically smooth and have surface spikes that are hundreds of nanometers high.
- the exposed surfaces of these devices may be scratched and damaged during fabrication and/or transportation. These surface defects may often limit the performance of these devices. Defects could lead to a short in the device by forming a contact between anode and cathode and pinholes in various functional coatings could help the permeation of moisture, oxygen and possibly other deleterious materials.
- One aspect of this invention is a composite article comprising at least one high integrity protective coating, the high integrity protective coating comprising at least
- Another aspect of the invention is a method for depositing a high integrity protective coating.
- the method comprising the steps of preparing a substantially homogenous resin based planarizing layer composition, providing at least one surface for deposition; depositing the planarizing layer composition on the surface, curing the planarizing layer composition, depositing reaction or recombination products of reacting species on the planarizing layer, and changing the composition of the react ants fed into the reactor chamber during deposition to form an organic-inorganic composition barrier coating layer.
- a further aspect of the invention is a device assembly comprising a device, at least one surface of which is coated with at least one protecting coating.
- FIG. 1 graphically shows light iransmittance through identical substrates having organic-inorganic composition barrier coatings with and without refractive index matching.
- FIG. 2 shows schematically an embodiment of an organic-inorganic composition barrier coating of the present invention.
- FIG. 3 shows light transmittance spectra for an organic-inorganic composition barrier coating of the present invention with varying number of zones and varying zone thicknesses.
- FIG. 4 shows schematically a first embodiment of a composite article with an organic- inorganic composition barrier coating.
- FIG. 5 shows schematically a second embodiment of a composite article with an organic-inorganic composition barrier coating.
- FIG. 6 shows schematically a third embodiment of a composite article with an organic-inorganic composition barrier coating.
- FIG. 7 shows variation in refractive index and extinction coefficient with variation in oxygen mole fraction in precursor feed gas during deposition.
- FlG. 8 shows calculated visible light transmittancc spectra as a function of oxygen mole fraction in feed gas during deposition.
- FIG. 9 shows a perspective view of a portion of a bare substrate obtained using optical profilometry.
- FIG. 10 shows a perspective view of a portion of a substrate with a planarizing layer obtained using optical profilometry.
- FIG. 11 graphically shows water vapor transmittancc rate (WVTR) through identical substrates (a) with a barrier coating of organic-inorganic composition and (b) with a high integrity protective coating in accordance with one aspect of the present invention.
- WVTR water vapor transmittancc rate
- FIG. 12 shows schematically an embodiment of a high integrity protective coating of the present invention.
- FIG. 13 shows schematically a first embodiment of a composite article of the present invention with a high integrity protective coating.
- FIG. 14 shows schematically a second embodiment of a composite article of the present invention with a high integrity protective coating.
- FIG. 15 shows schematically a third embodiment of a composite article composite article of the present invention with a high integrity protective coating.
- the barrier coating of the present invention will be termed interchangeably hereinafter as an "organic-inorganic composition barrier coating,” “barrier coating of organic-inorganic composition,” or simply “organic-inorganic barrier coating.”
- Light emitting and light absorbing materials and electrode materials in optoelectronic devices, especially in organic optoelectronic devices, are all susceptible to attack by reactive species existing in the environment, such as oxygen, water vapor, hydrogen sulfide. SOx, NOK, solvents, etc.
- Barrier coatings engineered to affect light transmission only to a small extent are useful in extending the device lifetime without degrading the overall device efficiency, thus rendering them commercially viable. Desirable barrier properties are achieved in the coating of the present invention by using an organic-inorganic composition and desirable light transmission is achieved by matching refractive indices of inorganic zones and organic zones in the coating.
- One aspect of this invention is a composite article comprising a barrier coating of organic-inorganic composition, the barrier coating having optical properties that are substantially uniform along an axis of light transmission oriented substantially perpendicular to the surface of the coating.
- substantially perpendicular means within 15 degrees cither side of a perpendicular to a tangent drawn at any point on the surface.
- the substantially uniform optical properties provides for a coating with a substantially uniform refractive index.
- “Substantially uniform refractive index” means the refractive index of any zone in the coating is within 10% of any other /one in the coating for a selected wavelength.
- the barrier coating preserves color neutrality by exhibiting substantially uniform light transmission.
- substantially uniform light transmission means at any selected ⁇ vavclength in a selected wavelength range, the transmission is within 10% of the average light transmission for the wavelength range, in other words, the barrier coating does not substantially differentially attenuate wavelengths within the selected wavelength range.
- the barrier coating is constructed with zones of various compositions. The oxygen and water vapor barrier properties are enhanced by the inorganic-organic composition. Optical loss due to interference resulting from differing refractive indices of the zones of various compositions is overcome by depositing substantially uniform refractive-index materials. The desired transmissivity is achieved by matching the refractive indices of zones in the coating.
- any coating used in such a device to enhance other performance parameters does not compromise the optical efficiency due to light absorption or other factors. Therefore it is important that barrier coatings be substantially transparent.
- substantially transparent means allowing a total transmission of at least about 50 percent, preferably at least about 80 percent, and more preferably at least 90 percent, of light in a selected wavelength range.
- the selected wavelength range can be in the visible region, the infrared region, the ultraviolet region or combinations thereof.
- a 5 mil polycarbonate substrate with a hairier coating of the present invention light transmittance along the axis of light transmission is greater than 85% for all wavelengths in the visible light wavelength region about 400 nanometers to about 700 nanometers.
- FlG. 1 compares the visible light transmittance through a substrate with a bam or coating of organic- inorganic composition without refractive index matching (a) with a refractive index matched barrier coating of organic-inorganic composition (b).
- FlG. 1 shows a transmissivity greater than 85% for the visible wavelength with no large amplitude interference fringes for the barrier coating of the present invention. Therefore the barrier coating of the present invention is desirably substantially transparent in the visible wavelength range.
- the barrier coating of the present invention consists of at least one substantially transparent inorganic zone and at least one substantially transparent organic zone having low permeability of oxygen or other reactive materials present in the environment.
- low permeability it is meant that the oxygen permeability is less than about 0.1 cm 3 / ⁇ m 2 day), as measured at 25° C and with a gas containing 21 volume-percent oxygen and the water vapor transmission is less than about 1 g'( ⁇ rrday), as measured at 25° C. and with a gas having 100-percent relative humidity.
- substantially organic zone 12 shows schematically a substantially organic zone 12, a substantially inorganic zone 14 and an organic-inorganic interface zone 16
- substantially organic means the composition is over 90% organic.
- substantially inorganic means the composition is over 90% inorganic.
- any number of zones can be present in the barrier coating, at least two, a substantially organic zone 12 and a substantially inorganic zone 14. is suitable for reduction of moisture, oxygen and other reactive species.
- Typical thickness of respective substantially organic zones 12 is 100 nanometers to 1 micron.
- Typical thickness of respective substantially inorganic zones 14 is 10 nanometers to 100 nanometers.
- Typical thickness of respective transitional zones 16 is 5 nanometers to 30 nanometers.
- the substantially organic zone 12 is of uniform composition.
- the substantially organic zone 12 is of a composition that varies across the thickness of the zone, in another embodiment all substantially organic zones 12 in a barrier coating are of same composition. In another embodiment at least two of the organic zones 32 are of different composition.
- the substantially inorganic zone 14 is of uniform composition.
- the substantially organic zone 14 is of a composition that varies across the thickness of the zone, in another embodiment, all substantially organic zones 14 in a barrier coating are of same composition. In another embodiment at least two of the organic zones 14 are of different composition.
- Other embodiments may include transitional zones 16 that are neither substantially organic nor substantially inorganic. Jt should be clearly understood that the zones are not layers. The zones do not have distinct boundaries,
- a coating of the present invention does not have distinct interfaces at which the composition of the coating changes abruptly.
- the composition of the barrier coating does not necessarily vary nionotonically from one surface to the other surface thereof.
- a monotonicaUy varying composition is only one case of barrier coating of the present invention.
- FlG.3 shows transmission spectra for barrier coatings with varying number of zones and varying organic zone thickness. Transmission spectra as shown in FIG. 3 for barrier coatings with 100 nm silicon oxycarbide substantially organic zone between two 30 nm silicon oxy ⁇ itride substantially inorganic zones (a), with 300 nm silicon oxycarbide substantially organic zone between two 30 nm silicon oxynitride substantially inorganic zones (b).
- Suitable coating compositions of regions across the thickness are organic, and inorganic materials and combinations thereof. These materials are typically reaction or recombination products of reacting plasma species and are deposited onto the substrate surface.
- Organic coating materials typically comprise carbon, hydrogen, oxygen, and optionally other minor elements, such as sulfur, nitrogen, silicon, etc.. depending on the types of reactants. Suitable reactants that result in organic compositions in the coating are straight or branched alkanes, alkenes, alkynes, alcohols, aldehydes, ethers, alkylene oxides, aromatics. etc., having up to 15 carbon atoms.
- Inorganic coating materials typically comprise oxide: nitride; carbide: boride; or combinations thereof of elements of Groups HA. JIlA, IVA, VA, VIA, VIIA, IB. and IfB: metals of Groups HIB. IVB, and VB; and rare-earth metals.
- At least one barrier coating 10 is disposed on at ieast one surface of an element or substrate 20. of the composite article 30.
- at least one barrier coating 10 disposed on at least one surface of more than one element 20 of the composite article.
- at least one barrier coating K encapsulates at least one substrate or element 20 of the composite article 30.
- At least one element is an optoelectronic element.
- the optoelectronic element is an organic clement.
- the optoelectronic element is an electroluminescent element.
- the optoelectronic element is a photoresponsive element.
- a composite article in another embodiment, includes a polymeric substrate and an active element, which is an organic electroluminescent element.
- the composite article may include additional elements such as. but not limited to, an adhesion layer, abrasion resistant layer, chemically resistant layer, photoluminescent layer radiation-absorbing layer, radiation reflective layer, conductive layer, electrode layer, electron transport layer, hole transport layer and charge blocking layer.
- Another aspect of the invention is a method for depositing the barrier coatings of organic-inorganic composition.
- the method comprising the steps of providing at least one surface for deposition, depositing reaction or recombination products of reacting species on the surface, changing the compositions of the reactants fed into the reactor chamber during the deposition to form an organic-inorganic coating with at least one substantially organic zone and at least one substantially inorganic zone, and performing refractive index modification of at least one inorganic zone by varying the precursor gas composition, the refractive index of the inorganic zone being adjusted to provide a substantially uniform refractive index along an axis of light transmission through the barrier coating.
- a bulk material or a substrate having a surface for deposition typically is a single piece or a structure comprising a plurality of adjacent pieces of different materials.
- a substrate include a rigid transparent glass and a flexible or rigid polymeric substrate.
- Non-limiting examples of substrate materials that benefit from having a organic- inorganic composition barrier coating are organic polymeric materials; such as polycthylenetercphthalate ("PET”); polyacrylatcs; polycarbonate; silicone; epoxy resins; silicone-functionuli'/ed epoxy resins; polyester such as Mylar (made by E.I. du Pont de Nemours & Co.); polyimide such as Kapt ⁇ n H or Kapton E (made by du Pont). Apical AV (made by Kanegafugi Chemical Industry Company). Upilex (made by UBE Industries. Ltd.); polycthcrs ⁇ lfones (“PES,” made by Sumitomo); polyetherimide such as Ultem (made by General Electric Company); and polyethylene ⁇ aphthalene (“PEN").
- PET polycthylenetercphthalate
- PES polycthcrs ⁇ lfones
- Ultem made by General Electric Company
- PEN polyethylene ⁇ aphthalene
- the coating can be formed using one of many deposition techniques, such as plasma- enhanced chemical-vapor deposition, radio-frequency plasma-enhanced chemical- vapor deposition, microwave plasma enhanced chemical vapor deposition, expanding thermal-plasma chemical-vapor deposition, sputtering, reactive sputtering, electron- cyclotron-resonancc plasma-enhanced chemical-vapor deposition, inductively- coupled plasma-enhanced chemical-vapor deposition, and combinations thereof.
- deposition techniques such as plasma- enhanced chemical-vapor deposition, radio-frequency plasma-enhanced chemical- vapor deposition, microwave plasma enhanced chemical vapor deposition, expanding thermal-plasma chemical-vapor deposition, sputtering, reactive sputtering, electron- cyclotron-resonancc plasma-enhanced chemical-vapor deposition, inductively- coupled plasma-enhanced chemical-vapor deposition, and combinations thereof.
- deposition techniques such as plasma- enhanced chemical-vapor deposition, radio-frequency plasma-enhanced chemical
- silicon carbide can be deposited on a surface by recombination of plasmas generated from silanc (S1H4) and an organic material, such as methane or xylene.
- Silicon oxycarbide can be deposited from plasmas generated from silanc, methane, and oxygen or silanc and propylene oxide. Silicon oxycarbide also can be deposited from plasmas generated from ⁇ rganosiliconc precursors, such as Vinyl trimethylsilane (VTMS). tetraethoxysilanc (TEOS), hcxamethyldisiloxanc (HMDSO), hcxamethyldisilazane (HMDSN). or octamethylcyclotetrasiloxane (D4).
- VTMS Vinyl trimethylsilane
- TEOS tetraethoxysilanc
- HMDSO hcxamethyldisiloxanc
- HMDSN hcxamethyldisilazane
- Aluminum oxyearbonitride can be deposited from a plasma generated from a mixture of aluminum tartrate and ammonia. Other combinations of reactants may be chosen to obtain a desired coating composition. The choice of particular reactants is within the skills of the artisans.
- a mixed composition of the coating is obtained by changing the compositions of the reacla ⁇ ts Cc ⁇ into the reactor chamber during the deposition of reaction products to form the coating.
- the first rcactant gas can be ammonia
- the second rcactant gas can be silane.
- the relative supply rates of react ant gases are varied during deposition to vary the composition of the deposited material as the coating is built up. If oxygen is used as an additional precursor gas. and the mole fraction of oxygen in the feed gas is increased from zero, the material deposited on the surface changes from silicon nitride to silicon oxynitride. As the oxygen mole fraction in the reactant gas increases, oxygen starts to replace nitrogen in the deposited material. Compositional and structural changes occur with increase in oxygen mole fraction, resulting in refractive index modification as well.
- FIG. 7 shows the variation of refractive index with variation in oxygen mole fraction, for a precursor composition including, ammonia and oxygen.
- a substantially inorganic zone of silicon oxynitride at an oxygen mole fraction of about 0.25. is also deposited such that the refractive index of the inorganic /.one matches the refractive index of the substantially organic zone of silicon oxycarbide. resulting in a barrier coating of organic-inorganic composition with substantially uniform refractive index.
- Fig.7 shows measured optical properties, refractive index (a) and extinction coefficient (b), of inorganic layers deposited with varying oxygen mole fraction, obtained by spectroscopic ellipsometry.
- refractive index of the depositing inorganic material varies from 1.8 to 3.4.
- the interference amplitude can be reduced significantly.
- FIG. 7 also indicates that the extinction coefficient (b) does not change enough to significantly affect the absorption of light through the inorganic layers for thicknesses of inorganic layers used in this invention.
- a region between the substrate or element with the coating and the coating is diffuse, such that there is a gradual change from the composition of the bulk of the substrate or element to the composition of the portion of the coating. Such a transition prevents an abrupt change in the composition and mitigates any chance for delamination of the coating.
- the gradual change of the coating composition is achieved by the gradual change of the precursor composition.
- a further aspect of the invention is a device assembly comprising a device, at least one surface of which is coated with at least one barrier coating, the composition of which varies across the thickness of the coating and has substantially uniform refractive index along the axis of light transmission.
- Such device assemblies include, but are not limited to. liquid crystal displays, light emitting devices, photo-responsive devices, integrated circuits and components of medical diagnostic systems.
- the device assembly may comprise a device disposed on a flexible substantially transparent substrate, said substrate having a first substrate surface and a second substrate surface, at least one of said substrate surface being coated with the barrier coating of the present invention.
- the barrier coatings of the present invention have many advantages, including being robust 'against environmentally reactive species, having desirable optical properties and being easily mass-produced.
- the fundamental advantage of the method of deposition of the present invention is that it enables concurrent control of optical and diffusion properties of barrier coatings by adjusting the deposition parameters.
- the barrier coatings of the present invention would be useful as barrier coatings in many optical and optoelectronic devices including organic light-emitting devices and organic photovoltaic devices.
- Light emitting and light absorbing materials and electrode materials in optoelectronic devices, especially in organic optoelectronic devices, are all susceptible to attack by reactive species existing in the environment, such as oxygen, water vapor etc. Additionally, surface defects such as spikes and point defects on substrates or other functional layers could affect the performance of these devices. Desirable protective properties, to overcome these drawbacks and protect the device, are achieved in a coating of the present invention.
- high integrity protective coating refers to a coating wherein at least one planarizing layer is coupled to at least one organic-inorganic composition barrier coating layer.
- One aspect of this invention is a composite article comprising a high integrity protective coating.
- the high integrity protective coating has at least one planarizing layer and at least one organic-inorganic composition barrier coating layer.
- Organic- inorganic composition hairier coatings are described in reference US Patent Application No. 10/879,468, which is herein incorporated by reference.
- the planarizing layer thickness is in the range of about 1 nanometer to about 100 microns. Often the planarizing layer thickness is in the range of about 100 nanometers to about 10 micron. Very often the planarizing layer thickness is in the range of about 500 nanometers to about 5 microns.
- the high integrity protective coating of the present invention is substantially smooth and substantially defect free.
- the term "average surface roughness” R n is defined as the integral of the absolute value of the roughness profile measured over an evaluation length.
- the term “peak surface roughness” R 1 is the height of the highest peak in the roughness profile over the evaluation length.
- substantially smooth' * means the average surface roughness R,, is less than about 4 nanometers, preferably less than about 2 nanometers and more preferably less than about 0.75 nanometers and the peak surface roughness R p is less than about 10 nanometers, preferably less than 7 nanometers and more preferably less than 5.5 nanometers.
- Substantially defect free means the number of point defects is less than about 100/mi ⁇ T, preferably less than 10/mnf, and more preferably ! ⁇ ' mm".
- Figure 9 shows an optica! profilomctry plot of a bare substrate surface and
- Figure 10 shows an optical profilomctry plot of a substrate surface with a plana ⁇ zing layer in accordance with one aspect of the present invention.
- the high integrity protective coating of the present invention includes at least one planarizing layer and at least one organic-inorganic composition barrier coating, the combination having low permeability of oxygen, water vapor and other reactive materials present in the environment.
- low permeability it is meant that the oxygen permeability is less than about 0.1 cm /(m 2 day). as measured at 25° C and with a gas containing 21 volume-percent oxygen and the water vapor transmission rate is less than about I x 1 C) '2 g/(mfday). as measured at 25° C. and with a gas having 100- percent relative humidity.
- FIG. 1 1 graphically shows water vapor transmittancc rate (WVTR) through identical substrates (a) with an organic-inorganic composition barrier coating and (b) with a high integrity protective coating in accordance with one aspect of the present invention.
- the WVTR measurements shown in Figure 18 were obtained using a system with a detection limit of low Ix I0 "6 g/(m 2 day).
- Figure 18 shows that a substrate with a high integrity protective coating in accordance with one aspect of the present invention, formed by the combination of at least one planarizing layer and at least one organic-inorganic composition barrier coating layer, has a lower WVTR than a similar substrate with only an organic-inorganic composition barrier layer coating.
- a substrate with a high integrity protective coating has a light transmittancc greater than 85% in a selected wavelength range between about 400 nanometers to about 700 nanometers.
- the planarizing layer composition comprises at least one resin.
- the resin is an cpoxy based resin.
- the resin could be a cycloaliphatic resin.
- the resin is an acrylic based resin.
- the planarizing layer composition may further include at least one flexibilizing agent, adhesion promoter, surfactant or catalyst and combinations thereof.
- a flexibilizing agent helps make the planarizing layer less brittle, more flexible reducing cracking or peeling and generally reduce the stress the coating applies to the underlying element or substrate.
- An adhesion promoter helps improve adhesion between the substrate on the coating.
- an adhesion promoter such as an organic silane coupling agent binds to a surface of a substrate or clement and also to the subsequent film applied over the substrate or element.
- a surfactant helps lower the surface energy of the coating, allowing it to wet a substrate or element, and level better, providing a smoother, more uniform coating.
- a planarixing layer composition may be cured.
- the curing may be radiation curing or thermal curing and combinations thereof.
- said radiation curing is ultraviolet curing.
- Other curing mechanisms, including anhydride or amine curing, can also be employed.
- Additives can be incorporated into the planarizing layer to tailor its properties.
- a UV catalyst may be added to the layer composition.
- UV absorbers can be added to protect underlying UV sensitive layers.
- Siloxane additives can be included to make the leveling layer more scratch resistant.
- Antioxidant chemicals such as Ciba Geigy's Irganox hindered amine complexes can also be added to prevent yellowing of the coating and underlying substrate.
- Non-limiting example of substrate materials that benefit from having a high integrity protective coating are organic polymeric materials; such as polyethyleneterephthalate (“PET”); polyacrylatcs: polycarbonate: silicone; cpoxy resins: silicone-functionalized cpoxy resins: polyester such as Mylar (made by E.I. du Pont de Nemours & Co.); polyimidc such as Kapton H or Kapton E (made by du Pont), Apical AV (made by Kanegafugi Chemical Industry Company). Upilex (made by UBE Industries, Ltd.): polyethers ⁇ lfones (“PES.” made by Sumitomo): polycthcrimide such as Ultem (made by General Electric Company); and polyethylenenaphthalene (“PEN").
- PET polyethyleneterephthalate
- polyacrylatcs polycarbonate: silicone
- cpoxy resins silicone-functionalized cpoxy resins: polyester such as Mylar (made by E.I. du Pont de Nemours & Co.);
- Non-limiting examples of eyeloaliphatic cpoxy resins are Dow ERL4221. ERL4299, ERLX4360. UVR60Q and Silar Labs eyeloaliphatic diepoxy disiloxane.
- Non-limiting examples of UV curing agents are Dow UVI-6976, UVJ-6992 Ciba lrgaciire 250, and GE UV9380C.
- UV sensitizers are Lsopropylthioxanthone and ethyl dimethoxyanthraccne.
- thermal catalysts are King Industries CXC-162, CXC-1614. XC-B220 and 3 M FC520.
- Non-limiting examples of surfactants arc OSl Silwet 7001. 7604 GE SF1 188A, SFl 288. SFl 488. BYK-Chemic BYK307 and Dow Triton X.
- Non-limiting examples of flexiblizing agents are Dow DER 732 and 736, cyclohcxane dimethanol. Cejanese TCD alcohol DM. and King Industries KfI ex 148 and 188.
- Non-limiting examples of other additives which can be used are. anti-oxidants such as Ciba Irganox, UV absorbers such as Ciba Tinuvin and leveling agents such as BYK- Chcmie BYK-361.
- anti-oxidants such as Ciba Irganox
- UV absorbers such as Ciba Tinuvin
- leveling agents such as BYK- Chcmie BYK-361.
- Figure 12 shows schematically a high integrity protecth e coating in accordance with one aspect of the present invention.
- At least one high integrity protective coating 10 is disposed on at least one surface of an element or substrate 120. of the composite article 130.
- at least one high integrity protective coating 1 10 disposed on at least one surface of more than one element or substrate 120 of the composite article.
- at least one barrier coating 1 10 encapsulates at least one substrate or element 120 of the composite article 130.
- a high integrity protective coating of the present invention can be applied to various types of substrates.
- the composite article comprises a substrate.
- the substrate can be transparent or opaque.
- the substrate can be rigid or flexible.
- Non-limiting examples of a substrate include a rigid transparent glass and a flexible or rigid polymeric substrate.
- the high integrity protective coating can be applied to cither blank substrate or uncncapsuiatcd optoelectronic device.
- a high integrity protective coating of the present invention may be either optically transparent or opaque.
- a high integrity protective coating of the present invention may be flexible or rigid.
- a high integrity protective coating of the present invention may also provide mechanical protection to underlying substrate and coatings.
- the high integrity protective coating significantly reduces the surface roughness, wherein the average surface roughness is below about 0.75 nanometers and peak surface roughness is less than about 5.5 nanometers, and reduces the surface defect density, wherein the number of point defects is less than about lOO ⁇ nm 2 . of high glass transition temperature (Tg) polycarbonates. Additional functional coating can be deposited on top of the high integrity protective coating of this invention, the high integrity protective coating protecting a device or element from being damaged in subsequent deposition environment.
- Tg glass transition temperature
- a high integrity protective coating can also be used as an etch-stop layer for the conductive coatings such as ITO coatings.
- a planariztng layer may be used as an interlayer between two organic-inorganic composition barrier coatings.
- a high integrity protective coating of the present invention can be used to release the stress between a top inorganic layer and bottom plastic substrate. The other side of a substrate with a high integrity protective coating can be coated with the same or different coating to balance the stress brought by adding of coating.
- At least one element is an optoelectronic element.
- the optoelectronic clement is an organic element.
- the optoelectronic element is an electroluminescent element.
- the optoelectronic element is a photoresponsivc element.
- one embodiment of the composite article of the present invention includes a polymeric substrate and an active element, which is an organic electroluminescent element.
- a bulk material or a substrate having a surface for deposition typically is a single piece or a structure comprising a plurality of adjacent pieces of different materials.
- the composite article may include additional elements such as. but not limited to. an adhesion layer, abrasion resistant layer, chemically resistant layer, photoluminescent layer radiation-absorbing layer, radiation reflective layer, conductive layer, electrode layer, electron transport layer, hole transport layer and charge blocking layer.
- Jn one aspect of the present invention is a method for depositing a high integrity protective coating.
- the method includes the steps preparing a substantially homogenous resin based planari/ing layer composition, providing at least one surface for deposition, depositing the planari/ing layer composition on the surface and curing the planarizing layer composition.
- the deposition of a planarizing layer can be either batch mode process or roll-to-roll mode process, can be selected from the group consisting of reverse roll coating, wire-wound or Mayer rod coating, direct and offset gravure coating, slot die coating, blade coating, hot melt coating, curtain coating, knife o ⁇ er roll coating, extrusion, air knife coating, spray, rotary screen coating, multilayer slide coating, coextrusion, meniscus coating, comma and micrograviire coating, spin coating, dip coating, lithographic process, langmuir process and Hash evaporation.
- the planarizing layer composition comprises at least one resin.
- the resin is an cpoxy based resin.
- the resin is an acrylic based resin.
- the method of the present invention may further include the steps of adding at least one flexibiJizing agent adhesive agent, surfactant or catalyst or combinations thereof in the planarizing layer composition.
- the planarizing layer composition may be cured.
- the curing may be radiation curing or thermal curing. In one aspect of the present invention, said radiation curing is ultraviolet curing.
- the method further includes the steps of depositing reaction or recombination products of reacting species on the planarizing layer, and changing the composition of the rcactants fed into the reactor chamber during deposition to form an organic-inorganic composition barrier coating layer.
- the organic-inorganic composition barrier coating layer may be formed by one of many deposition techniques, such as plasma-enhanced chemical-vapor deposition ("PECVD”). radio-frequency plasma-enhanced chemical-vapor deposition (“RFPECVD”), expanding thermal-plasma chemical-vapor deposilion (“ETPCVD”), sputtering including reactive sputtering, clectron-cyclotron-rcsonance plasma- enhanced chemical-vapor deposition (ECRPECVD”), inductively coupled plasma- enhanced chemical-vapor deposition (“ICPECVD”). or combinations thereof.
- PECVD plasma-enhanced chemical-vapor deposition
- RFPECVD radio-frequency plasma-enhanced chemical-vapor deposition
- EPCVD expanding thermal-plasma chemical-vapor deposilion
- sputtering including reactive sputtering clectron-cyclotron-rcsonance plasma- enhanced chemical-vapor deposition
- ICPECVD inductively coupled plasma- enhanced chemical-vapor deposition
- Organic coating materials typically comprise carbon, hydrogen, oxygen, and optionally other minor elements, such as sulfur, nitrogen, silicon, etc., depending on the types of reactants. Suitable rcactants that result in organic compositions in the coating are straight or branched alkanes. alkenes, alkynes, alcohols, aldehydes, ethers, alkylene oxides, aromatics, etc.. having up to 15 carbon atoms.
- Inorganic and ceramic coating materials typically comprise oxide; nitride; carbide; boridc; or combinations thereof of elements of Groups HA. IHA, IVA, VA.
- VIA, VIlA, IB, and HB metals of Groups IHB. IVB. and VB; and rare-earth metals.
- a further aspect of the invention is a device assembly comprising a device, at least one surface of which is coated with at least one high integrity protective coating.
- Such device assemblies include, but are not limited to. liquid crystal displays, light emitting devices, photo-responsive devices, integrated circuits and components of medical diagnostic systems.
- the device assembly may comprise a device disposed on a flexible substantially transparent substrate, said substrate having a first substrate surface and a second substrate surface, at least one of said substrate surface being coated with the high integrity protective coaling of the present invention.
- a composition comprising 100 parts by weight liquide cycloaliphatic diepoxide (Dow Chemical ERL4221 d), 1 part by weight Octacat UV sensitive catalyst (General Electric UV9392C) and 0.15 parts by weight of a surfactant (3M Fluorad FC430) were blended together, filtered through a 1 micron filter, degassed and applied to a plastic substrate by spin coating. Immediately after coating, the layer was exposed to a mercury arc lamp broadband UV source for 30 seconds which activates the catalyst and then the part was baked m an oven at 125 C for 1 hour to complete the cure of the epoxy resin. An organic-inorganic composition barrier coating layer is deposited over the planarizing layer.
- a composition comprising ERL4299.
- Octacat UV sensitive catalyst General Electric UV9392C
- a surfactant (3M Fluorad FC430)
- a mercury arc lamp broadband UV source for 30 seconds which activates the catalyst and then the part was baked in an oven to complete the cure of the cpoxy resin.
- An organic-inorganic composition barrier coating layer is deposited over the planarizing layer.
- a composition comprising siloxanc containing cpoxy such as Silar Labs Product 2283 (cycloaliphatic cpoxy chsiloxane), Octacat UV sensitive catalyst (General Electric UV9392C) and a surfactant (3M Fluorad FC430) were blended together, filtered through a 1 micron filler, degassed and applied to a plastic substrate by spin coating. Immediately after coating, the layer was exposed to a mercury arc lamp broadband UV source for 30 seconds which activates the catalyst and then the part was baked in an oven to complete the cure of the cpoxy resin. An organic-inorganic composition barrier coating layer is deposited over the planarizing layer.
- a composition comprising liquide cycloaliphatic diepoxide (Dow Chemical ERL4221d).
- Octacat UV sensitive catalyst General Electric UV9392C
- a surfactant 3M Fluorad FC430
- the layer was exposed to a mercury arc lamp broadband UV source for 30 seconds which activates the catalyst and then the part was baked in an oven at 125 C for 1 hour to complete the cure of the cpoxy resin.
- An organic-inorganic composition barrier coating layer is deposited over the planarizing layer.
- composition comprising liquide cycloaliphatic diepoxide (Dow Chemical ERL4221d), Octacat UV sensitive catalyst (General Electric UV9392C) and a surfactant (3M Fluorad FC430) is spin coated over the organic-inorganic composition barrier coating layer.
- a transparent conductive coating comprising tin doped indium oxide (ITO) is then deposited over the second planarizing layer.
Landscapes
- Physics & Mathematics (AREA)
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Optics & Photonics (AREA)
- Inorganic Chemistry (AREA)
- General Physics & Mathematics (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Power Engineering (AREA)
- Computer Hardware Design (AREA)
- Manufacturing & Machinery (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- Laminated Bodies (AREA)
- Electroluminescent Light Sources (AREA)
- Paints Or Removers (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
Abstract
Description
Claims
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP05858693.4A EP1859496B1 (en) | 2004-11-15 | 2005-11-15 | High integrity protective coating |
KR1020147008962A KR101498868B1 (en) | 2004-11-15 | 2005-11-15 | High integrity protective coatings |
CN200580046401.XA CN101142696B (en) | 2004-11-15 | 2005-11-15 | High integrity protective coatings |
JP2007557013A JP5312805B2 (en) | 2004-11-15 | 2005-11-15 | High integrity protective coating |
CA2587922A CA2587922C (en) | 2004-11-15 | 2005-11-15 | High integrity protective coatings |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/988,481 | 2004-11-15 | ||
US10/988,481 US8704211B2 (en) | 2004-06-30 | 2004-11-15 | High integrity protective coatings |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2007089218A2 true WO2007089218A2 (en) | 2007-08-09 |
WO2007089218A3 WO2007089218A3 (en) | 2007-11-08 |
Family
ID=38319542
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2005/041660 WO2007089218A2 (en) | 2004-11-15 | 2005-11-15 | High integrity protective coating |
Country Status (8)
Country | Link |
---|---|
US (1) | US8704211B2 (en) |
EP (1) | EP1859496B1 (en) |
JP (1) | JP5312805B2 (en) |
KR (2) | KR101498868B1 (en) |
CN (1) | CN101142696B (en) |
CA (1) | CA2587922C (en) |
SG (2) | SG160322A1 (en) |
WO (1) | WO2007089218A2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US10787591B2 (en) | 2012-04-30 | 2020-09-29 | The Boeing Company | Composites including silicon-oxy-carbide layers and methods of making the same |
Families Citing this family (30)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6866901B2 (en) * | 1999-10-25 | 2005-03-15 | Vitex Systems, Inc. | Method for edge sealing barrier films |
US20070196682A1 (en) * | 1999-10-25 | 2007-08-23 | Visser Robert J | Three dimensional multilayer barrier and method of making |
US20100330748A1 (en) | 1999-10-25 | 2010-12-30 | Xi Chu | Method of encapsulating an environmentally sensitive device |
US7198832B2 (en) * | 1999-10-25 | 2007-04-03 | Vitex Systems, Inc. | Method for edge sealing barrier films |
US8900366B2 (en) * | 2002-04-15 | 2014-12-02 | Samsung Display Co., Ltd. | Apparatus for depositing a multilayer coating on discrete sheets |
US20060208634A1 (en) * | 2002-09-11 | 2006-09-21 | General Electric Company | Diffusion barrier coatings having graded compositions and devices incorporating the same |
US7648925B2 (en) | 2003-04-11 | 2010-01-19 | Vitex Systems, Inc. | Multilayer barrier stacks and methods of making multilayer barrier stacks |
US7767498B2 (en) | 2005-08-25 | 2010-08-03 | Vitex Systems, Inc. | Encapsulated devices and method of making |
US7571999B2 (en) * | 2005-11-30 | 2009-08-11 | Xerox Corporation | Overcoat compositions, oil-based ink compositions, and processes for ink-jet recording using overcoat and oil-based ink compositions |
US7976899B2 (en) | 2006-10-23 | 2011-07-12 | General Electric Company | Methods for selective deposition of graded materials on continuously fed objects |
AU2006350626B2 (en) * | 2006-11-06 | 2013-09-19 | Agency For Science, Technology And Research | Nanoparticulate encapsulation barrier stack |
US7781031B2 (en) * | 2006-12-06 | 2010-08-24 | General Electric Company | Barrier layer, composite article comprising the same, electroactive device, and method |
US20080138538A1 (en) * | 2006-12-06 | 2008-06-12 | General Electric Company | Barrier layer, composite article comprising the same, electroactive device, and method |
US20080138624A1 (en) * | 2006-12-06 | 2008-06-12 | General Electric Company | Barrier layer, composite article comprising the same, electroactive device, and method |
US8956731B2 (en) * | 2008-02-27 | 2015-02-17 | Dai Nippon Printing Co., Ltd. | Gas barrier sheet |
EP2358529A4 (en) * | 2008-11-17 | 2013-08-28 | 3M Innovative Properties Co | Gradient composition barrier |
JP5788646B2 (en) * | 2009-06-25 | 2015-10-07 | 住友化学株式会社 | Polarizing plate, composite polarizing plate, and liquid crystal display device |
US20110008525A1 (en) * | 2009-07-10 | 2011-01-13 | General Electric Company | Condensation and curing of materials within a coating system |
US9472783B2 (en) * | 2009-10-12 | 2016-10-18 | General Electric Company | Barrier coating with reduced process time |
CN103348502B (en) * | 2011-02-08 | 2016-01-27 | 应用材料公司 | The hybrid method for packing of Organic Light Emitting Diode |
US8525191B2 (en) | 2011-04-01 | 2013-09-03 | Sabic Innovative Plastics Ip B.V. | Optoelectronic devices and coatings therefore |
US8350275B2 (en) | 2011-04-01 | 2013-01-08 | Sabic Innovative Plastics Ip B.V. | Optoelectronic devices and coatings therefore |
US20130014808A1 (en) | 2011-07-14 | 2013-01-17 | Sabic Innovative Plastics Ip B.V. | Photovoltaic modules and methods for making and using the same |
EP2818498B1 (en) * | 2012-02-25 | 2019-03-06 | Mitsubishi Chemical Corporation | Coated film |
KR101903054B1 (en) * | 2012-07-11 | 2018-10-02 | 삼성디스플레이 주식회사 | Organic light emitting display apparatus and the method for manufacturing the same |
CN110010713B (en) | 2013-02-25 | 2020-10-27 | 沙特基础工业全球技术有限公司 | Photovoltaic module assembly |
JP2015050143A (en) * | 2013-09-04 | 2015-03-16 | 積水化学工業株式会社 | Sealant for organic electroluminescent display element |
US20150370409A1 (en) * | 2014-06-18 | 2015-12-24 | International Business Machines Corporation | Disambiguation of touch-based gestures |
CN104332416A (en) * | 2014-08-21 | 2015-02-04 | 京东方科技集团股份有限公司 | Preparation method of flexible display and flexible display |
JP6648467B2 (en) * | 2014-12-25 | 2020-02-14 | 日亜化学工業株式会社 | Light emitting device |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5900285A (en) | 1994-10-27 | 1999-05-04 | Schott Glaswerke | Method of making a vessel having a wall surface having a barrier coating |
US20030104753A1 (en) | 1999-10-25 | 2003-06-05 | Graff Gordon Lee | Method of making encapsulated display devices |
US20030205845A1 (en) | 2002-05-02 | 2003-11-06 | Karl Pichler | Encapsulation for organic light emitting diodes devices |
US20040046497A1 (en) | 2002-09-11 | 2004-03-11 | General Electric Company | Diffusion barrier coatings having graded compositions and devices incorporating the same |
US20040209126A1 (en) | 2001-05-04 | 2004-10-21 | Ziegler John P | O2 and h2o barrier material |
Family Cites Families (33)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2951772A (en) * | 1956-12-10 | 1960-09-06 | Owens Corning Fiberglass Corp | Treatments for fibrous glass used to reinforce resins |
US3536518A (en) * | 1967-03-10 | 1970-10-27 | Johnson & Johnson | Method of applying print pattern of resin to fibrous sheet material |
US4234533A (en) * | 1978-10-31 | 1980-11-18 | Mary Frances Theresa Langlands | Method of bonding spaced sheets by molding resin therebetween |
US4861671A (en) | 1985-10-23 | 1989-08-29 | Kerdix, Inc. | Magneto-optic recording media with protective layer |
US5151318A (en) * | 1989-05-26 | 1992-09-29 | Ciba-Geigy Corporation | Reinforcing material |
JPH03183759A (en) * | 1989-12-12 | 1991-08-09 | Toyobo Co Ltd | Laminated plastic film and its production |
US5194293A (en) * | 1991-12-03 | 1993-03-16 | Foster Brian C | Process for finishing a plastic surface |
KR100283522B1 (en) * | 1993-12-01 | 2001-03-02 | 사토 히로시 | Method of manufacturing magnetic recording medium |
DE4445427C2 (en) * | 1994-12-20 | 1997-04-30 | Schott Glaswerke | Plasma CVD method for producing a gradient layer |
JPH0926596A (en) * | 1995-07-13 | 1997-01-28 | Sharp Corp | Liquid crystal display device and its production |
JPH11129423A (en) | 1997-11-04 | 1999-05-18 | Toray Ind Inc | Polyester film for gas barrier |
CA2290595C (en) * | 1998-03-23 | 2004-06-15 | Presstek, Inc. | Lithographic imaging with constructions having mixed organic/inorganic layers |
JP3897938B2 (en) * | 1998-10-22 | 2007-03-28 | 宇部日東化成株式会社 | Organic-inorganic composite gradient material, its production method and its use |
US6117498A (en) * | 1998-11-13 | 2000-09-12 | International Business Machines Corporation | Single source thermal ablation method for depositing organic-inorganic hybrid films |
US6495208B1 (en) * | 1999-09-09 | 2002-12-17 | Virginia Tech Intellectual Properties, Inc. | Near-room temperature CVD synthesis of organic polymer/oxide dielectric nanocomposites |
US6492026B1 (en) * | 2000-04-20 | 2002-12-10 | Battelle Memorial Institute | Smoothing and barrier layers on high Tg substrates |
JP4581187B2 (en) * | 2000-06-13 | 2010-11-17 | ソニー株式会社 | Manufacturing method of display device |
US6537688B2 (en) | 2000-12-01 | 2003-03-25 | Universal Display Corporation | Adhesive sealed organic optoelectronic structures |
US6614057B2 (en) | 2001-02-07 | 2003-09-02 | Universal Display Corporation | Sealed organic optoelectronic structures |
SG118118A1 (en) * | 2001-02-22 | 2006-01-27 | Semiconductor Energy Lab | Organic light emitting device and display using the same |
US6664137B2 (en) | 2001-03-29 | 2003-12-16 | Universal Display Corporation | Methods and structures for reducing lateral diffusion through cooperative barrier layers |
KR100413450B1 (en) * | 2001-07-20 | 2003-12-31 | 엘지전자 주식회사 | protecting film structure for display device |
US6737753B2 (en) | 2001-09-28 | 2004-05-18 | Osram Opto Semiconductor Gmbh | Barrier stack |
TW519853B (en) | 2001-10-17 | 2003-02-01 | Chi Mei Electronic Corp | Organic electro-luminescent display and its packaging method |
GB0208506D0 (en) | 2002-04-12 | 2002-05-22 | Dupont Teijin Films Us Ltd | Film coating |
US6897474B2 (en) | 2002-04-12 | 2005-05-24 | Universal Display Corporation | Protected organic electronic devices and methods for making the same |
US7268486B2 (en) * | 2002-04-15 | 2007-09-11 | Schott Ag | Hermetic encapsulation of organic, electro-optical elements |
DE10318187B4 (en) * | 2002-05-02 | 2010-03-18 | Osram Opto Semiconductors Gmbh | Encapsulation method for organic light emitting diode devices |
US7048823B2 (en) * | 2002-05-20 | 2006-05-23 | Eastman Kodak Company | Acrylic films prepared by coating methods |
US20040121146A1 (en) * | 2002-12-20 | 2004-06-24 | Xiao-Ming He | Composite barrier films and method |
JP4491196B2 (en) * | 2003-03-31 | 2010-06-30 | 富士フイルム株式会社 | GAS BARRIER LAMINATED FILM, PROCESS FOR PRODUCING THE SAME, AND SUBSTRATE AND IMAGE DISPLAY DEVICE USING THE FILM |
JP4383077B2 (en) * | 2003-03-31 | 2009-12-16 | 大日本印刷株式会社 | Gas barrier substrate |
US7229703B2 (en) | 2003-03-31 | 2007-06-12 | Dai Nippon Printing Co. Ltd. | Gas barrier substrate |
-
2004
- 2004-11-15 US US10/988,481 patent/US8704211B2/en active Active
-
2005
- 2005-11-15 CN CN200580046401.XA patent/CN101142696B/en active Active
- 2005-11-15 WO PCT/US2005/041660 patent/WO2007089218A2/en active Application Filing
- 2005-11-15 KR KR1020147008962A patent/KR101498868B1/en active IP Right Grant
- 2005-11-15 EP EP05858693.4A patent/EP1859496B1/en active Active
- 2005-11-15 JP JP2007557013A patent/JP5312805B2/en active Active
- 2005-11-15 CA CA2587922A patent/CA2587922C/en active Active
- 2005-11-15 KR KR1020077013425A patent/KR20080016779A/en not_active Application Discontinuation
- 2005-11-15 SG SG200907683-7A patent/SG160322A1/en unknown
- 2005-11-15 SG SG2013037791A patent/SG190658A1/en unknown
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5900285A (en) | 1994-10-27 | 1999-05-04 | Schott Glaswerke | Method of making a vessel having a wall surface having a barrier coating |
US20030104753A1 (en) | 1999-10-25 | 2003-06-05 | Graff Gordon Lee | Method of making encapsulated display devices |
US20040209126A1 (en) | 2001-05-04 | 2004-10-21 | Ziegler John P | O2 and h2o barrier material |
US20030205845A1 (en) | 2002-05-02 | 2003-11-06 | Karl Pichler | Encapsulation for organic light emitting diodes devices |
US20040046497A1 (en) | 2002-09-11 | 2004-03-11 | General Electric Company | Diffusion barrier coatings having graded compositions and devices incorporating the same |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US10787591B2 (en) | 2012-04-30 | 2020-09-29 | The Boeing Company | Composites including silicon-oxy-carbide layers and methods of making the same |
Also Published As
Publication number | Publication date |
---|---|
US20060001040A1 (en) | 2006-01-05 |
SG190658A1 (en) | 2013-06-28 |
WO2007089218A3 (en) | 2007-11-08 |
KR20140069093A (en) | 2014-06-09 |
SG160322A1 (en) | 2010-04-29 |
JP2008520477A (en) | 2008-06-19 |
KR101498868B1 (en) | 2015-03-05 |
CA2587922A1 (en) | 2006-05-15 |
KR20080016779A (en) | 2008-02-22 |
JP5312805B2 (en) | 2013-10-09 |
EP1859496B1 (en) | 2018-09-12 |
CA2587922C (en) | 2014-01-28 |
EP1859496A2 (en) | 2007-11-28 |
CN101142696B (en) | 2014-01-29 |
US8704211B2 (en) | 2014-04-22 |
CN101142696A (en) | 2008-03-12 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CA2587922C (en) | High integrity protective coatings | |
US8227984B2 (en) | Barrier coatings | |
CA2457791C (en) | Coatings with low permeation of gases and vapors | |
US8034419B2 (en) | Method for making a graded barrier coating | |
US8691371B2 (en) | Barrier coating and method | |
EP1930966A2 (en) | Barrier layer, composite article comprising the same, electroactive device, and method | |
US11934056B2 (en) | Flexible multi-layered cover lens stacks for foldable displays | |
US20090110892A1 (en) | System and method for making a graded barrier coating | |
US11825570B2 (en) | Heater package | |
KR102141632B1 (en) | Barrier film | |
KR102071915B1 (en) | Method for preparing barrier film | |
US11458703B2 (en) | Barrier film | |
JP2021041608A (en) | Gas barrier film | |
KR20080062597A (en) | Process for preparing plastic substrate |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
WWE | Wipo information: entry into national phase |
Ref document number: 200580046401.X Country of ref document: CN |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2007557013 Country of ref document: JP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2587922 Country of ref document: CA |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2005858693 Country of ref document: EP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 1020077013425 Country of ref document: KR |
|
WWP | Wipo information: published in national office |
Ref document number: 2005858693 Country of ref document: EP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 1020147008962 Country of ref document: KR |