|Publication number||US3710167 A|
|Publication date||Jan 9, 1973|
|Filing date||Jul 2, 1970|
|Priority date||Jul 2, 1970|
|Publication number||US 3710167 A, US 3710167A, US-A-3710167, US3710167 A, US3710167A|
|Inventors||Dresner J, Goodman A|
|Original Assignee||Rca Corp|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (7), Non-Patent Citations (1), Referenced by (121), Classifications (11)|
|External Links: USPTO, USPTO Assignment, Espacenet|
Dresner et a1.
[ 1 Jan. 9, 1973 ORGANIC ELEC'IROLIJMINESCENT CELLS HAVING A TUNNEL INJECTION CATHODE  Inventors: Josepli Dresner; Alvin Malcolm Goodman, both of Princeton, NJ.
 Assignee: RCA Corporation  Filed: July 2, 1970  Appl. No.: 51,898
 US. Cl. ..313/l08 A, 313/1095  Int. Cl. n qsggg gz [5 8] Field ofSearch "313/108 A, 109.5 108 D, Y 108 R 561 netei rice ii'i'id' M 0 UNITED STATES PATENTS 3,172,862 3/1965 Gurnee et al. 313/108 AX 3,359,445 12/1967 Roth ..313/l08 A 3,267,317 '8/1966 Fischer.... ..313/l08 D 3,382,394 5/1968 Mehl ..313/l08 5/1960 Fischer ..313/l08 2,938,136 3,116,427 12/1963 Giaever ..3l3/l08 D UX 3,530,325 9/1970 M'ehl ..3 13/108 OTHER PUBLICATIONS. Semiconductor Compounds, by A. Coblenz, Electronics Buyers Guide, June, 1958, R-4, R-5.
Primary Examiner-Palmer C. Demeo Attorney-Glenn H. Bruestle  ABSTRACT An electroluminescent cell comprises an anthracene layer having an anode and cathode thereon. The
cathode of the novel cell is of the tunnel injection type. A typical cathode consists of a 10-100 A. thick 14 Claims, 4 Drawing Figures ORGANIC ELECTROLUMINESCENT CELLS HAVING A TUNNEL INJECTION CATIIODE BACKGROUND OF THE INVENTIONO This invention relates I to improved electroluminescent cells useful as simple light sources or in display devices. It more particularly relates to electroluminescent cells which employ organic phosphors as the luminescent material.
Organic phosphor electroluminescent cells are known in the art. These prior art cells are formed from admixtures of anthracene or other organic phosphor compositions with electrically conductive materials such as metals, graphite or other forms of carbon. The admixture is deposited as a thin layer on a conductive surface. The conductive surface is typically a tin oxide coating applied to a glass substrate. The admixture is coated with an insulating layer such as glycerin and a metal electrode is provided to make electrical contact with the glycerin. Examples of these prior art cells can be found with reference to U.S. Pat. No. 3,173,050 issued to E. F. Gurnee.
Although the voltage and frequency requirements for operating the cells as described above are stated therein to offer an improvement in the then existing art, this improvement has not been sufficient to result in low cost, low voltage cells emitting a brightness which would approach commercial utility.
In order to approach commercial utility the electroluminescent cell should have a long life, improved brightness, simple construction free of shorts and for many device applications, it should be compatible with silicon technology.
SUMMARY OF THE INVENTION An electroluminescent cell comprises a layer of an organic phosphor composition, an anode upon one surface of the layer and a tunnel-injection type cathode upon the other surface of the layer.
BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 is a cross-sectional view of a novel electroluminescent cell.
FIG. 2 is a front elevational view of an embodiment of an electroluminescent cell having a desired luminescent pattern therein.
FIG. 3 is a cross-sectional view of the embodiment shown in FIG. 2 taken along line 33 thereof.
FIG. 4 is a cross-sectional view of an electroluminescent cell employing a glass support for the anode.
DETAILED DESCRIPTION OF THE INVENTION The organic phosphor layers utilized in the present invention comprise a conjugated organic compound of condensed benzene rings. Examples of useful phosphors are anthracene, naphthalene, methyl derivatives of anthracene and anthracene doped with tetracene or other similar fluorescent dyes.
Preferably, the phosphor should be of high purity. For example, a preferred phosphor is anthracene having an electron trap density in the order of 10 traps/cc. The thickness of the phosphor layer should be less than l micrometers (um) and preferably between I and am.
Unlike the cited prior art devices of Gurnee, the phosphor layer of the novel device is free of dispersed conductive particles. Such particles, if they were to exist in the novel device, would induce shorts and absorb light from the phosphor and thereby reduce the efficiency and life of the novel device.
Preferably, the phosphor layer comprises phosphor grains which are mono-crystalline in the direction of current flow. This results in a more efficient cell.
A feature of the novel cells is the use of a tunnel injection cathode for injecting electrons into the phosphor. Such a cathode comprises a base electrode material having a dielectric film of a thickness of less than about A., and generally between 10-100 A., on the surface thereof. The dielectric film is in contact with the phosphor layer of the cell. Preferably the dielectric material has a dielectric constant of less than.
5, but higher dielectric constant films are also suitable.
A preferred tunnel injection cathode has as the electrode material a wafer of n type silicon, preferably degenerate n type silicon. The dielectric film of this cathode is a l0-100 A. thick silicon dioxide layer on a surface of the silicon wafer. This cathode is hereinafter designated as 11 type SiSiO Another useful tunnel injection cathode consists of aluminum, such as an evaporated layer of aluminum, having a lO-lOO A. thick aluminum oxide layer thereon. This cathode is hereinafter designated as Al-Al O The use of such cathodes results in devices which are easy to construct, are compatible with silicon technology, are long-lived and have improved brightness.
The anode of the device, which is a hole injecting contact, may consist of a conductive oxide, such as tin oxide, indium oxide, or a mixture of cuprous oxide and cuprous iodide; a metal, such as gold or platinum; an alloy, such as selenium-tellurium alloy; or a tunnel inject ing contact such as p type silicon having a 10-100 A. thick layers of silicon dioxide thereon. Preferred anodes comprise a transparent copper oxide and copper iodide layer or a conductive oxide such as tin oxide or indium oxide coated with a very thin transparent layer of Te. A Te layer which is a few atoms thick is sufficient.
Although edge emission is possible, for most purposes and in order for the device to emit a greater amount of light, it is preferred that either the anode or the cathode or both be transparent.
Examples of a transparent anode are films of tin oxide coated with a very thin layer of tellurium (preferably a few atoms thick) or tin oxide coated with a thin layer of a copper oxide-copper iodide mixture. A transparent electrode can be obtained by forming it in a mesh-like configuration so that light is freely transmitted through the spaces in the mesh.
In order to control the thickness of the phosphor layer, spacers defining this thickness may be employed. The novel devices make possible the use of spacers which are an integral part of the electrode structure. For example, the silicon dioxide layer of the tunnel injecting cathode can be built up around the periphery of the electroluminescent cell so as to provide a spacer of several microns in thickness which is integral with the tunnel injection area (less than 100 A. thick) of the cell.
Alternatively, the cathode or anode may be formed on a glass support, either with or withouta transparent conductive coating thereon, and the spacer evaporated, sputtered or otherwise formed on this structure.
Referring now to FIG. 1 there is shown a preferred novel electroluminescent cell 4. The novel cell 4 comprises ananthracene layer 6 sandwiched between a cathode 8 and an anode 10. The cathode comprises a degenerate n'type siliconwafer 12 having a silicon dioxide coating 14 thereon. The degenerate silicon wafer typically has a resistivity in the range of 6X10 to lXlO'ohm-cm. The silicon dioxide coating, which may be formed by any of the techniques which are well known in the art, is provided with a thin central region 16 where electron injection occurs by a tunneling mechanism. This thin region is in the order of 10 to 100 A. thick and is preferably less than 50 A. thick. The outer periphery 18 of the silicon dioxide layer is thicker than the central portion 16. This outer periphery 18, which has a typical uniform thickness of from 1 to pm., functions as a spacer to determine the thickness of the anthracene phosphor layer 6 of the cell and to prevent shorts. A preferred technique for forming the silicon dioxide coating for tunnel injection comprises the steps of (l) cleaning the silicon wafer in a boiling ammoniated solution of hydrogen peroxide, (2) etching the cleaned wafer in concentrated HF, (3) oxidizing the etched wafer in a steam atmosphere at 1,100 C., (4) recleaning and re-etching the oxidized wafer, (5) heating the wafer for several minutes at 150 C., (6) oxidizing the. wafer with water vapor at 600 C., and (7) annealing the oxidized wafer at 500 C. in a pure hydrogen atmosphere. This technique is the subject of a U.S. Patent Application filed by Alvin M. Goodman and James M. Breece.
The anthracene layer 6 may be formed by melting finely divided anthracene on the central portion 16 of the silicon dioxide layer 14 and allowing this molten material to crystallize.
j The anode 10, is provided on the anthracene layer 6 on the side opposite the cathode 8. The anode 10 consists of a thin coating of a copper oxide-copper iodide film. This film may be deposited directly on the,
anthracene or alternatively it is deposited on one surface of a conducting glass flat as shown. The copper oxide-copperiodide film is less than 100 A. thick. If the copper oxide-copper iodide film exceeds about 500 A. in thickness, the transmission of light therethrough is reduced such that it is preferably formed in a mesh or crossed-grid pattern so as to allow light to be efficiently emitted from the cell.
In operation, the silicon wafer 12 is connected to negative terminal of a battery and the copper oxidecopper iodide anode layer 10 is connected to the positive terminal of the battery. Electrons are injected into the anthracene layer 6 through the silicon dioxide layer 14 and holes are injected into the anthracene layer 6 from the copper oxide-copper iodide layer 10. Recombination of electron-hole pairs occurs in the anthracene layer 6 resulting in the emission of blue light.
Although the injecting tunnel cathode is shown to comprise n type silicon, p type silicon can also be used. In fact, p type silicon has the advantage that it is easier to deposit p type silicon on glass than n type silicon,
of the invention. In this embodiment, an electrolu-' minescent cell 30 comprises a grid-like anode 32.
formed on a transparent glass support 34, and a silicon dioxide spacer 36 around the periphery of theanode support 34. A 2-3 pm layer 38 of anthracene phosphor is disposed on the anode 32. A cathode structure 40 is positioned over the anthracene to form the complete cell. This cathode structure 40 consists of a wafer 42 of n type silicon having a 2-3 pm thick SiO layer 44 thereon. The SiO, layer 44 is in contact with the anthracene layer 38. The SiO layer 44'has 1 mil. diameter plugs 46 of the 11 type silicon extending completely therethrough. A 10-50 A. thick dielectric SiO, layer 48 is provided on the outer surface of each of the silicon plugs 46 so as to contact the anthracene layer 38. The plugs are formed in a desired pattern, for example, to portray RCA as shown in FIG. 2. Electron injection into this device takes place by tunneling through the dielectric SiO, layer 48 on each of the silicon plugs 46. An alternative and somewhat similar structure to that described with reference to FIGS. 2 and 3 is one in which the silicon dioxide layer 36 has an array of holes therein extending therethrough rather than silicon plugs extending through the SiO, layer as shown in the FIGURES. In this alternative structure, the Si layer is provided with a thin SiO coating (IO- A.) in the region of each hole and the anthracene then fills each hole.
The cell 50 shown in FIG. 4 employs an AlAl O cathode structure 52. The cathode may be formed by vacuum evaporating a layer 54 of aluminum onto a glass substrate 56 and anodizing the surface of the aluminum layer 54 to form an A1 0 layer 58 which is preferably from 10-50 A. thick. The cell 50 is also provided with an anode 60 having spacers 62 the same as that described with reference to FIG. 3. An organic phosphor layer 64 is disposed between and in contact with the anode and cathode.
-Where one desires light emission from the cathode side of the cell, the cathode can be formed in a thin line or mesh pattern. Such a pattern can be formed,.for example, by evaporating the cathode material onto a glass substrate by standard flash evaporation or electron beam evaporation techniques through an appropriate mask.
Although the examples indicate tunnel injection cathodes comprising Al-Al O and SiSiO it should be understood that other metal-metal oxide tunnelinjection cathodes may also be useful, for example, tantalum-tantalum oxide and magnesium-magnesium oxide.
Electroluminescent cells made in accordance with the invention comprising anthracene containing tetracene therein in an amount not exceeding 5 ppm were operated at applied average fields of only approximately 2X10 volts/cm. across the phosphor layer. Light emission was observed at wavelengths between 4,l00-5,400 A. These cells comprised a cathode consisting of a fine grid of aluminum having about a 50 A.
thick film of Al O thereover and an anode consisting of either colloidal platinum paste, copper-copper iodide paste, silver-silver iodide paste, an evaporated conductive selenium-tellurium alloy or a conductive arsenic-tellurium alloy containing a small percentage of selenium therein. The choice of anode did not have a major effect on the efficiency of light emission from the cell but it does affect the speed of response to the applied field. For the applied fields stated above, current densities ranging from 5X10 to 5X10 amp/cm have been observed. The higher current densities correspond to measured surface brightnesses of 60 footlam berts. This may be compared to a brightness of only 10 foot-lamberts for the blue light of a commercial color television kinescope. The quantum efficiency of these cells is between about 0.01-0.04 photons/electron.
Cells having a cathode consisting of n silicon, either as a wafer or a vacuum deposited film, covered with a 20-40 A. thick film of SiO and an evaporated transparent Cu O-Cul anode were also operated at an average field of about 2.5Xl volts/cm. These cells had a current density of l.8 l0' amp./cm. and a quantum efficiency of from about 0.01-0.03 photons/electron. The surface brightness of these cells was estimated to exceed foot-lamberts.
What is claimed is:
1. An electroluminescent cell comprising 1. a cathode structure consisting ofa base of an electrode material selected from the group consisting of silicon and aluminum and having a thick dielectric insulating layer on one surface thereof, said dielectric layer being an oxide of said electrode material, said electrode material extending through said oxide layer to the surface thereof to form a plurality of plug-like protrusions in a predetermined pattern through said oxide layer, and a thin oxide tunnel injection layer over the exposed surfaces of said plug-like protrusions, said oxide being an oxide ofsaid electrode material,
2. a layer of an organic phosphor over and in contact with said tunnel injection layer, and
3. a light transmitting anode structure over and in contact with said phosphor layer and spaced from said cathode structure.
2. The electroluminescent cell recited in claim 1 wherein said organic phosphor composition comprises an organic compound having conjugated condensed benzene rings selected from the group consisting of anthracene, naphthalene, methyl derivatives of anthracene and anthracene doped with a fluorescent dye.
3. The electroluminescent cell recited in claim 1 wherein said organic phosphor has an electron trap density in the order of IO traps/cc. or less.
4. The electroluminescent cell recited in claim 1 wherein said phosphor layer consists of phosphor grains which are monocrystalline in the direction of current flow.
5. The electroluminescent cell recited in claim I wherein said dielectric has dielectric constant of less than 5.
6. The electroluminescent cell recited in claim 1 wherein said electrode material is n-type degenerate silicon and wherein said dielectric layer is SiO having a thickness of from 10-100 A. I
7. The electroluminescent cell recited [I] claim 1 wherein said anode comprises a member selected from the group consisting of a tin oxide, indium oxide, a mixture of cuprous oxide and cuprous iodide, gold, platinum, a selenium-tellurium alloy and p type silicon having a l0-100 A. thick layer of silicon dioxide thereon.
8. The electroluminescent cell recited in claim 1 wherein said anode comprises a transparent film selected from a member of the group consisting of a mixture of copper oxide and copper iodide, tin oxide and indium oxide, said film having a transparent film of tellurium thereover, said tellurium film being no more than several atomic layers thick.
9. The electroluminescent cell recited in claim 1 wherein said anode has a mesh-like configuration.
10. A cell according to claim 1 wherein said phosphor layer is less than 10 micrometers in thickness.
11. A cell according to claim 1 wherein said phosphor layer contains anthracene.
12. A cell according to claim 1 wherein said cathode is spaced from said anode by an additional thickness of the dielectric layer around the periphery of said cell, which thickness defines the thickness of said phosphor layer.
13. A cell according to claim 12 wherein said peripheral dielectric thickness is from 1 to 10 micrometers.
14. An electroluminescent devise comprising:
1. a cathode structure consisting of a. n type silicon having a thick silicon dioxide dielectric insulating layer on one surface thereof, said silicon extending through said silicon dioxide layer to the surface thereof to form a plurality of plug-like protrusions in a predetermined pattern through said silicon dioxide,
b. a thin silicon dioxide tunnel injection layer over the exposed surfaces of said plug-like protrusions,
2. a layer of an organic phosphor over said tunnel-injection layer and,
3. a light transmitting anode structure over and in contact with said phosphor layer and spaced from said cathode structure.
|Cited Patent||Filing date||Publication date||Applicant||Title|
|US2938136 *||Aug 26, 1958||May 24, 1960||Gen Electric||Electroluminescent lamp|
|US3116427 *||Nov 17, 1960||Dec 31, 1963||Gen Electric||Electron tunnel emission device utilizing an insulator between two conductors eitheror both of which may be superconductive|
|US3172862 *||Sep 29, 1960||Mar 9, 1965||Dow Chemical Co||Organic electroluminescent phosphors|
|US3267317 *||Feb 25, 1963||Aug 16, 1966||Rca Corp||Device for producing recombination radiation|
|US3359445 *||Oct 7, 1964||Dec 19, 1967||Dow Chemical Co||Electroluminescent cells|
|US3382394 *||Mar 24, 1965||May 7, 1968||American Cyanamid Co||Electroluminescent process including injection of negative carriers into a crystal of an organic compound|
|US3530325 *||Aug 21, 1967||Sep 22, 1970||American Cyanamid Co||Conversion of electrical energy into light|
|1||*||Semiconductor Compounds, by A. Coblenz, Electronics Buyers Guide, June, 1958, R 4, R 5.|
|Citing Patent||Filing date||Publication date||Applicant||Title|
|US4720432 *||Feb 11, 1987||Jan 19, 1988||Eastman Kodak Company||Electroluminescent device with organic luminescent medium|
|US4725513 *||Mar 3, 1987||Feb 16, 1988||Canon Kabushiki Kaisha||Electroluminescent device|
|US4734338 *||Feb 27, 1987||Mar 29, 1988||Canon Kabushiki Kaisha||Electroluminescent device|
|US4741976 *||Feb 27, 1987||May 3, 1988||Canon Kabushiki Kaisha||Electroluminescent device|
|US4769292 *||Oct 14, 1987||Sep 6, 1988||Eastman Kodak Company||Electroluminescent device with modified thin film luminescent zone|
|US4775820 *||Jul 29, 1985||Oct 4, 1988||Canon Kabushiki Kaisha||Multilayer electroluminescent device|
|US4885211 *||Feb 11, 1987||Dec 5, 1989||Eastman Kodak Company||Electroluminescent device with improved cathode|
|US4950950 *||May 18, 1989||Aug 21, 1990||Eastman Kodak Company||Electroluminescent device with silazane-containing luminescent zone|
|US5409783 *||Feb 24, 1994||Apr 25, 1995||Eastman Kodak Company||Red-emitting organic electroluminescent device|
|US5552678 *||Sep 23, 1994||Sep 3, 1996||Eastman Kodak Company||AC drive scheme for organic led|
|US5554450 *||Mar 8, 1995||Sep 10, 1996||Eastman Kodak Company||Organic electroluminescent devices with high thermal stability|
|US5834100 *||Jun 25, 1996||Nov 10, 1998||Northwestern University||Organic light-emitting dioddes and methods for assembly and emission control|
|US6020078 *||Dec 18, 1998||Feb 1, 2000||Eastman Kodak Company||Green organic electroluminescent devices|
|US6127004 *||Jan 29, 1999||Oct 3, 2000||Eastman Kodak Company||Forming an amorphous fluorocarbon layer in electroluminescent devices|
|US6278237||Mar 13, 1998||Aug 21, 2001||Emagin Corporation||Laterally structured high resolution multicolor organic electroluminescence display device|
|US6351067||Jan 21, 1999||Feb 26, 2002||City University Of Hong Kong||Organic electroluminescent device with improved hole injecting structure|
|US6361886||Dec 9, 1998||Mar 26, 2002||Eastman Kodak Company||Electroluminescent device with improved hole transport layer|
|US6399221||Nov 6, 1998||Jun 4, 2002||Northwestern University||Organic light-emitting diodes and methods for assembly and emission control|
|US6465115||Dec 9, 1998||Oct 15, 2002||Eastman Kodak Company||Electroluminescent device with anthracene derivatives hole transport layer|
|US6517957||May 14, 1998||Feb 11, 2003||Canon Kabushiki Kaisha||Organic compound and electroluminescent device using the same|
|US6534198||May 14, 1998||Mar 18, 2003||Canon Kabushiki Kaisha||Silicon compound, method for making the same, and electroluminescent device using the same|
|US6583557||Apr 24, 2001||Jun 24, 2003||Canon Kabushiki Kaisha||Organic luminescent element|
|US6586119||May 18, 1998||Jul 1, 2003||Canon Kabushiki Kaisha||Luminescent device|
|US6596415||Apr 26, 2001||Jul 22, 2003||Eastman Kodak Company||Electroluminescent device with polyphenyl hydrocarbon hole transport layer|
|US6632544||Feb 22, 2000||Oct 14, 2003||Junji Kido||Aromatic amine derivative, soluble conductive compound, and electroluminscent element|
|US6632545||Feb 22, 2000||Oct 14, 2003||Junji Kido||Electroluminescent element|
|US6636001||Dec 31, 2001||Oct 21, 2003||Canon Kabushiki Kaisha||Organic electronic device and nonlinear device|
|US6664731||Mar 13, 2002||Dec 16, 2003||Canon Kabushiki Kaisha||Charge injection type light emitting device|
|US6699595||Apr 26, 2001||Mar 2, 2004||Eastman Kodak Company||Electroluminescent device with polyphenyl hydrocarbon hole transport layer|
|US6717358||Oct 9, 2002||Apr 6, 2004||Eastman Kodak Company||Cascaded organic electroluminescent devices with improved voltage stability|
|US6821648||Dec 1, 2000||Nov 23, 2004||Junji Kido||Electroluminescent element|
|US6833200||Jan 23, 2003||Dec 21, 2004||Canon Kabushiki Kaisha||Luminescent device with a triarylamine compound|
|US6852250||Aug 1, 2002||Feb 8, 2005||Elecon, Inc.||Compositions produced by solvent exchange methods and articles of manufacture comprising same|
|US6858325||Oct 9, 2002||Feb 22, 2005||Canon Kabushiki Kaisha||Organic compound and electroluminescent device using the same|
|US6869699||Mar 18, 2003||Mar 22, 2005||Eastman Kodak Company||P-type materials and mixtures for electronic devices|
|US6896723||Dec 6, 2002||May 24, 2005||Eastman Kodak Company||Compressed fluid formulation containing hole transporting material|
|US6919140||Jul 10, 2003||Jul 19, 2005||Eastman Kodak Company||Organic electroluminescent devices with high luminance|
|US6927415||Dec 6, 2002||Aug 9, 2005||Eastman Kodak Company||Compressed fluid formulation containing electron transporting material|
|US6939625||Mar 15, 2002||Sep 6, 2005||N˘rthwestern University||Organic light-emitting diodes and methods for assembly and enhanced charge injection|
|US6949879 *||Apr 6, 2000||Sep 27, 2005||Microemissive Displays Limited||Optoelectronic display|
|US6991859||Mar 18, 2003||Jan 31, 2006||Eastman Kodak Company||Cascaded organic electroluminescent devices|
|US7022867||Sep 16, 2002||Apr 4, 2006||Canon Kabushiki Kaisha||Silicon compound and method for making the same|
|US7037599||Feb 28, 2003||May 2, 2006||Eastman Kodak Company||Organic light emitting diodes for production of polarized light|
|US7041608||Feb 6, 2004||May 9, 2006||Eastman Kodak Company||Providing fluorocarbon layers on conductive electrodes in making electronic devices such as OLED devices|
|US7079091||Jan 14, 2003||Jul 18, 2006||Eastman Kodak Company||Compensating for aging in OLED devices|
|US7086918 *||Dec 11, 2002||Aug 8, 2006||Applied Materials, Inc.||Low temperature process for passivation applications|
|US7094121||Jul 1, 2003||Aug 22, 2006||Northwestern University||Organic light-emitting diodes and methods for assembly and emission control|
|US7307380 *||Apr 27, 2005||Dec 11, 2007||Industrial Technology Research Institute||Cathode structure for inverted organic light emitting devices|
|US7768026 *||Aug 3, 2010||Chi Mei Communication Systems, Inc.||Light-emitting diode package and method for fabricating the same|
|US7914908||Nov 2, 2007||Mar 29, 2011||Global Oled Technology Llc||Organic electroluminescent device having an azatriphenylene derivative|
|US7931975||Nov 7, 2008||Apr 26, 2011||Global Oled Technology Llc||Electroluminescent device containing a flouranthene compound|
|US7947974||Mar 25, 2008||May 24, 2011||Global Oled Technology Llc||OLED device with hole-transport and electron-transport materials|
|US7968215||Dec 9, 2008||Jun 28, 2011||Global Oled Technology Llc||OLED device with cyclobutene electron injection materials|
|US7969088||May 4, 2009||Jun 28, 2011||Northwestern University||Method of using silicon molecular components for controlling charge migration and light emission of organic light-emitting diodes|
|US8034465||Jun 20, 2007||Oct 11, 2011||Global Oled Technology Llc||Phosphorescent oled having double exciton-blocking layers|
|US8053094||Jul 2, 2009||Nov 8, 2011||Northwestern University||Organic light-emitting diodes and methods for assembly and enhanced charge injection|
|US8076009||Oct 26, 2007||Dec 13, 2011||Global Oled Technology, Llc.||OLED device with fluoranthene electron transport materials|
|US8088500||Nov 12, 2008||Jan 3, 2012||Global Oled Technology Llc||OLED device with fluoranthene electron injection materials|
|US8101290||Oct 15, 2008||Jan 24, 2012||Technical Institute Of Physics And Chemistry Of Chinese Academy Of Sciences||Organic compound having electron-transporting and/or hole-blocking performance and its use and OLEDs comprising the compound|
|US8102114||Feb 27, 2009||Jan 24, 2012||Global Oled Technology, Llc.||Method of manufacturing an inverted bottom-emitting OLED device|
|US8129039||Oct 26, 2007||Mar 6, 2012||Global Oled Technology, Llc||Phosphorescent OLED device with certain fluoranthene host|
|US8147989||Feb 27, 2009||Apr 3, 2012||Global Oled Technology Llc||OLED device with stabilized green light-emitting layer|
|US8206842||Apr 6, 2009||Jun 26, 2012||Global Oled Technology Llc||Organic element for electroluminescent devices|
|US8216697||Feb 13, 2009||Jul 10, 2012||Global Oled Technology Llc||OLED with fluoranthene-macrocyclic materials|
|US8247088||Aug 28, 2008||Aug 21, 2012||Global Oled Technology Llc||Emitting complex for electroluminescent devices|
|US8324800||Jun 12, 2008||Dec 4, 2012||Global Oled Technology Llc||Phosphorescent OLED device with mixed hosts|
|US8420229||Oct 26, 2007||Apr 16, 2013||Global OLED Technologies LLC||OLED device with certain fluoranthene light-emitting dopants|
|US8431242||Oct 26, 2007||Apr 30, 2013||Global Oled Technology, Llc.||OLED device with certain fluoranthene host|
|US8795855||Jan 30, 2007||Aug 5, 2014||Global Oled Technology Llc||OLEDs having high efficiency and excellent lifetime|
|US8900722||Nov 29, 2007||Dec 2, 2014||Global Oled Technology Llc||OLED device employing alkali metal cluster compounds|
|US8956738||Oct 5, 2009||Feb 17, 2015||Global Oled Technology Llc||Organic element for low voltage electroluminescent devices|
|US9040170||Nov 29, 2005||May 26, 2015||Global Oled Technology Llc||Electroluminescent device with quinazoline complex emitter|
|US9118020||Dec 9, 2009||Aug 25, 2015||Global Oled Technology Llc||Electroluminescent devices including organic eil layer|
|US20010051487 *||Apr 18, 2001||Dec 13, 2001||Yuichi Hashimoto||Method for making organic luminescent device|
|US20030015691 *||Aug 1, 2002||Jan 23, 2003||Elecon, Incorporated||Compositions produced by solvent exchange methods and articles of manufacture comprising same|
|US20030162053 *||Mar 15, 2002||Aug 28, 2003||Marks Tobin J.||Organic light - emitting diodes and methods for assembly and enhanced charge injection|
|US20030207153 *||Jan 23, 2003||Nov 6, 2003||Canon Kabushiki Kaisha||Luminescent device with a triarylamine compound|
|US20030216591 *||Sep 16, 2002||Nov 20, 2003||Kazunori Ueno||Silicon compound and method for making the same|
|US20040043138 *||Aug 21, 2002||Mar 4, 2004||Ramesh Jagannathan||Solid state lighting using compressed fluid coatings|
|US20040043140 *||Nov 20, 2002||Mar 4, 2004||Ramesh Jagannathan||Solid state lighting using compressed fluid coatings|
|US20040092195 *||Jul 1, 2003||May 13, 2004||Marks Tobin J.||Organic light-emitting diodes and methods for assembly and emission control|
|US20040108510 *||Dec 6, 2002||Jun 10, 2004||Eastman Kodak Company||Compressed fluid formulation containing electron transporting material|
|US20040110866 *||Dec 6, 2002||Jun 10, 2004||Eastman Kodak Company||Compressed fluid formulation containing hole transporting material|
|US20040113542 *||Dec 11, 2002||Jun 17, 2004||Applied Materials, Inc.||Low temperature process for passivation applications|
|US20040135749 *||Jan 14, 2003||Jul 15, 2004||Eastman Kodak Company||Compensating for aging in OLED devices|
|US20040170861 *||Feb 28, 2003||Sep 2, 2004||Eastman Kodak Company||Organic light emitting diodes for production of polarized light|
|US20040183066 *||Mar 18, 2003||Sep 23, 2004||Eastman Kodak Company||P-type materials and mixtures for electronic devices|
|US20040185297 *||Mar 18, 2003||Sep 23, 2004||Eastman Kodak Company||Cascaded organic electroluminescent devices|
|US20040240198 *||May 28, 2003||Dec 2, 2004||Van Laar Ronald Joseph||Automated self-illuminating sports & safety helmet|
|US20040258951 *||Dec 22, 2003||Dec 23, 2004||Haghighat R. Ross||Compositions produced by solvent exchange methods and uses thereof|
|US20040258952 *||Dec 22, 2003||Dec 23, 2004||Haghighat R. Ross||Compositions produced by solvent exchange methods and uses thereof|
|US20050014018 *||Jul 10, 2003||Jan 20, 2005||Eastman Kodak Company||Organic electroluminescent devices with high luminance|
|US20050025997 *||Aug 20, 2004||Feb 3, 2005||Canon Kabushiki Kaisha||Luminescent device with a triarylamine compound|
|US20050176230 *||Feb 6, 2004||Aug 11, 2005||Eastman Kodak Company||Providing fluorocarbon layers on conductive electrodes in making electronic devices such as OLED devices|
|US20060082289 *||Apr 27, 2005||Apr 20, 2006||Industrial Technology Research Institute||Cathode structure for inverted organic light emitting devices|
|US20060273713 *||Jun 2, 2005||Dec 7, 2006||Eastman Kodak Company||Process for making an organic light-emitting device|
|US20070122655 *||Nov 29, 2005||May 31, 2007||Eastman Kodak Company||Electroluminescent device with quinazoline complex emitter|
|US20070122657 *||Nov 30, 2005||May 31, 2007||Eastman Kodak Company||Electroluminescent device containing a phenanthroline derivative|
|US20070252522 *||Apr 27, 2006||Nov 1, 2007||Eastman Kodak Company||Electroluminescent device including an anthracene derivative|
|US20080032123 *||Aug 2, 2006||Feb 7, 2008||Spindler Jeffrey P||Dual electron-transporting layer for oled device|
|US20080057183 *||Aug 31, 2006||Mar 6, 2008||Spindler Jeffrey P||Method for lithium deposition in oled device|
|US20080182129 *||Jan 30, 2007||Jul 31, 2008||Klubek Kevin P||Oleds having high efficiency and excellent lifetime|
|US20080284317 *||May 17, 2007||Nov 20, 2008||Liang-Sheng Liao||Hybrid oled having improved efficiency|
|US20080284318 *||May 17, 2007||Nov 20, 2008||Deaton Joseph C||Hybrid fluorescent/phosphorescent oleds|
|US20090102356 *||Oct 15, 2008||Apr 23, 2009||Technical Institute Of Physics And Chemistry Of Chinese Academy Of Sciences||NOVEL ORGANIC COMPOUND HAVING ELECTRON-TRANSPORTING AND/OR HOLE-BLOCKING PERFORMANCE AND ITS USE AND OLEDs COMPRISING THE COMPOUND|
|US20090108734 *||Oct 26, 2007||Apr 30, 2009||Begley William J||Oled device with certain fluoranthene light-emitting dopants|
|US20090108735 *||Oct 26, 2007||Apr 30, 2009||Begley William J||Oled device with fluoranthene electron transport materials|
|US20090108736 *||Oct 26, 2007||Apr 30, 2009||Begley William J||Phosphorescent oled device with certain fluoranthene host|
|US20090110956 *||Oct 26, 2007||Apr 30, 2009||Begley William J||Oled device with electron transport material combination|
|US20090110957 *||Oct 26, 2007||Apr 30, 2009||Begley William J||Oled device with certain fluoranthene host|
|US20090159911 *||Jun 5, 2008||Jun 25, 2009||Chi Mei Communication Systems, Inc.||Light-emitting diode package and method for fabricating the same|
|US20090162612 *||Dec 19, 2007||Jun 25, 2009||Hatwar Tukaram K||Oled device having two electron-transport layers|
|EP0044686A1 *||Jul 13, 1981||Jan 27, 1982||EASTMAN KODAK COMPANY (a New Jersey corporation)||Organic electroluminescent cell, process for manufacturing the cell and its use|
|EP0786925A2||Jan 13, 1997||Jul 30, 1997||Eastman Kodak Company||White light-emitting electroluminescent devices|
|EP0903964A1||Sep 7, 1998||Mar 24, 1999||Eastman Kodak Company||Organic electroluminescent device with inorganic electron transporting layer|
|EP2270897A2||Nov 25, 1999||Jan 5, 2011||Global OLED Technology LLC||Electroluminescent device with antracene derivatives hole transport layer|
|EP2568515A1||Oct 16, 2008||Mar 13, 2013||Global OLED Technology LLC||OLED device with fluoranthene electron transport materials|
|WO2006138075A2||Jun 2, 2006||Dec 28, 2006||Eastman Kodak Co||Organic element for low voltage electroluminescent devices|
|WO2007050301A2||Oct 12, 2006||May 3, 2007||Eastman Kodak Co||Organic element for low voltage electroluminescent devices|
|WO2008010915A2||Jul 5, 2007||Jan 24, 2008||Eastman Kodak Co||Light emitting device containing phosphorescent complex|
|WO2010117886A1||Apr 1, 2010||Oct 14, 2010||Global Oled Technology Llc||Organic element for electroluminescent devices|
|International Classification||H01L51/52, H05B33/12, H05B33/22, H01L51/50|
|Cooperative Classification||H05B33/12, H01L51/5221, H05B33/22|
|European Classification||H05B33/22, H01L51/52B4, H05B33/12|