WO2008013069A1 - Dispositif el - Google Patents
Dispositif el Download PDFInfo
- Publication number
- WO2008013069A1 WO2008013069A1 PCT/JP2007/063971 JP2007063971W WO2008013069A1 WO 2008013069 A1 WO2008013069 A1 WO 2008013069A1 JP 2007063971 W JP2007063971 W JP 2007063971W WO 2008013069 A1 WO2008013069 A1 WO 2008013069A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- shell
- core portion
- core
- shell layer
- layer
- Prior art date
Links
- 239000002096 quantum dot Substances 0.000 claims abstract description 23
- 239000000463 material Substances 0.000 claims abstract description 17
- 239000011258 core-shell material Substances 0.000 claims abstract description 11
- 230000005684 electric field Effects 0.000 claims description 13
- 239000011230 binding agent Substances 0.000 claims description 9
- 239000002245 particle Substances 0.000 claims description 8
- 239000002800 charge carrier Substances 0.000 claims description 5
- 238000002156 mixing Methods 0.000 claims description 2
- 239000000969 carrier Substances 0.000 description 10
- 239000004065 semiconductor Substances 0.000 description 8
- 239000010419 fine particle Substances 0.000 description 6
- 239000010931 gold Substances 0.000 description 6
- 239000000758 substrate Substances 0.000 description 6
- 238000000034 method Methods 0.000 description 5
- 239000011521 glass Substances 0.000 description 4
- 239000012535 impurity Substances 0.000 description 4
- 239000004743 Polypropylene Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- UHYPYGJEEGLRJD-UHFFFAOYSA-N cadmium(2+);selenium(2-) Chemical compound [Se-2].[Cd+2] UHYPYGJEEGLRJD-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000007791 liquid phase Substances 0.000 description 3
- 238000004020 luminiscence type Methods 0.000 description 3
- 238000000103 photoluminescence spectrum Methods 0.000 description 3
- 238000004544 sputter deposition Methods 0.000 description 3
- 238000001308 synthesis method Methods 0.000 description 3
- -1 Polyethylene Polymers 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- BPUBBGLMJRNUCC-UHFFFAOYSA-N oxygen(2-);tantalum(5+) Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[Ta+5].[Ta+5] BPUBBGLMJRNUCC-UHFFFAOYSA-N 0.000 description 2
- 238000005424 photoluminescence Methods 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- SBIBMFFZSBJNJF-UHFFFAOYSA-N selenium;zinc Chemical compound [Se]=[Zn] SBIBMFFZSBJNJF-UHFFFAOYSA-N 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 229910001936 tantalum oxide Inorganic materials 0.000 description 2
- ZMBHCYHQLYEYDV-UHFFFAOYSA-N trioctylphosphine oxide Chemical compound CCCCCCCCP(=O)(CCCCCCCC)CCCCCCCC ZMBHCYHQLYEYDV-UHFFFAOYSA-N 0.000 description 2
- YBNMDCCMCLUHBL-UHFFFAOYSA-N (2,5-dioxopyrrolidin-1-yl) 4-pyren-1-ylbutanoate Chemical compound C=1C=C(C2=C34)C=CC3=CC=CC4=CC=C2C=1CCCC(=O)ON1C(=O)CCC1=O YBNMDCCMCLUHBL-UHFFFAOYSA-N 0.000 description 1
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 description 1
- KXJGSNRAQWDDJT-UHFFFAOYSA-N 1-acetyl-5-bromo-2h-indol-3-one Chemical compound BrC1=CC=C2N(C(=O)C)CC(=O)C2=C1 KXJGSNRAQWDDJT-UHFFFAOYSA-N 0.000 description 1
- 229910015999 BaAl Inorganic materials 0.000 description 1
- 229910004613 CdTe Inorganic materials 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 229910001218 Gallium arsenide Inorganic materials 0.000 description 1
- 229910004262 HgTe Inorganic materials 0.000 description 1
- 101100476480 Mus musculus S100a8 gene Proteins 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 229910052581 Si3N4 Inorganic materials 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 229910007709 ZnTe Inorganic materials 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 238000003618 dip coating Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000001194 electroluminescence spectrum Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 230000005284 excitation Effects 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 230000005283 ground state Effects 0.000 description 1
- 229910000449 hafnium oxide Inorganic materials 0.000 description 1
- WIHZLLGSGQNAGK-UHFFFAOYSA-N hafnium(4+);oxygen(2-) Chemical compound [O-2].[O-2].[Hf+4] WIHZLLGSGQNAGK-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- 238000000608 laser ablation Methods 0.000 description 1
- 239000003446 ligand Substances 0.000 description 1
- 238000001748 luminescence spectrum Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000013307 optical fiber Substances 0.000 description 1
- SIWVEOZUMHYXCS-UHFFFAOYSA-N oxo(oxoyttriooxy)yttrium Chemical compound O=[Y]O[Y]=O SIWVEOZUMHYXCS-UHFFFAOYSA-N 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920005990 polystyrene resin Polymers 0.000 description 1
- 238000013139 quantization Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 238000007650 screen-printing Methods 0.000 description 1
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000004528 spin coating Methods 0.000 description 1
- 229940071182 stannate Drugs 0.000 description 1
- 230000003746 surface roughness Effects 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000001771 vacuum deposition Methods 0.000 description 1
- 238000007738 vacuum evaporation Methods 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
- H05B33/00—Electroluminescent light sources
- H05B33/12—Light sources with substantially two-dimensional radiating surfaces
- H05B33/14—Light sources with substantially two-dimensional radiating surfaces characterised by the chemical or physical composition or the arrangement of the electroluminescent material, or by the simultaneous addition of the electroluminescent material in or onto the light source
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
- C09K11/02—Use of particular materials as binders, particle coatings or suspension media therefor
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
- C09K11/08—Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials
- C09K11/56—Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials containing sulfur
- C09K11/562—Chalcogenides
- C09K11/565—Chalcogenides with zinc cadmium
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
- C09K11/08—Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials
- C09K11/88—Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials containing selenium, tellurium or unspecified chalcogen elements
- C09K11/881—Chalcogenides
- C09K11/883—Chalcogenides with zinc or cadmium
Definitions
- the present invention relates to an EL element (electric mouth luminescence element) of a type that emits light by injecting carriers into luminescent particles by applying an alternating electric field.
- the second semiconductor fine particles are made of the first semiconductor. Dispersed in the continuous phase. When an alternating electric field is applied to the EL element, carriers generated from the first semiconductor collide with the second semiconductor fine particles, and the second semiconductor fine particles are excited to emit light when returning to the ground state. Arise.
- Patent Document 1 Japanese Patent Laid-Open No. 2003-249373
- Patent Document 2 Japanese Patent Laid-Open No. 2003-173878
- Patent Document 1 cannot realize the light emission efficiency expected to reduce the carrier injection efficiency into the fine particles of the second semiconductor. This is because the scattering of carriers due to impurities mixed during the formation of the light emitting layer and the low continuity at the interface between the first semiconductor and the second semiconductor fine particles, resulting in a decrease in the “quantum confinement effect”. It is thought to be due to this.
- a first aspect of the present invention is an EL device in which a light emitting layer includes a quantum dot having a core-shell structure in which a surface of a core portion is covered with a shell layer, and emits light by applying an alternating electric field.
- the layer is made of a material having a larger band gap than the material of the core portion, and the shell
- This is an EL device with a film thickness of 5 nm to 100 nm.
- a second aspect of the present invention is an EL device in which the light emitting layer includes a quantum dot having a core-shell structure in which the surface of the core portion is covered with a shell layer, and emits light by applying an alternating electric field.
- the layer is made of a material having a band gap larger than that of the material of the core portion, and is an EL element that emits light when intrinsic charge carriers existing in the shell layer are supplied to the core portion.
- a third aspect of the present invention is the EL device according to the first or second aspect, wherein the light-emitting layer has core-shell structured particles mixed with a binder material.
- a fourth aspect of the present invention is the EL element according to the third aspect, wherein the binder material is a dielectric.
- a fifth aspect of the present invention is the EL device according to any one of the first to third aspects, in which the quantum dot has an organic side chain outside the shell.
- a sixth aspect of the present invention is the EL device according to any one of the first to fifth aspects, wherein the core portion has a particle size of 1 to: LOnm.
- the core portion and the carrier injection that are hardly affected by the contamination of impurities during the formation of the light-emitting layer can be obtained by a simple manufacturing method.
- the continuity of the interface of the shell layer as a layer can be ensured, and carriers present in the shell layer can be efficiently injected into the core portion.
- the EL element (electric aperture luminescence element) according to this embodiment has a configuration in which a first insulating layer, a light emitting layer, and a second insulating layer are sequentially stacked between a pair of electrodes.
- an Au (gold) metal electrode and an ITO (indium stannate) transparent electrode can be used as the pair of electrodes.
- the Au electrode is formed by vacuum evaporation using a normal resistance heating evaporation source.
- the ITO electrode used is a film formed on a glass substrate. You may form by sputtering method and other well-known means.
- the two insulating layers are formed, for example, by sputtering or the like using silicon nitride, tantalum oxide, silicon oxide, yttrium oxide, alumina, hafnium oxide, or norium tantalum oxide. be able to.
- the light emitting layer also constitutes only a core-shell quantum dot force. This eliminates the need to uniformly disperse the particles in the needle and reduces the possibility of impurities being mixed. However, if it is difficult to form a light-emitting layer using only core-shell quantum dots, it is advisable to improve the adhesion to the insulating layer by mixing with a binder.
- the core-shell structure quantum dot has a structure in which the surface of the core portion is covered with a shell layer.
- the material and the particle size are appropriately determined according to the emission wavelength required for the EL element.
- the particle size of the core portion is formed in a spherical shape by a known method (for example, a wet chemical synthesis method (liquid phase synthesis method), a laser ablation method), which is preferably selected based on a force within the range of 1 to lOnm.
- the Chenole layer is composed of ZnS, ZnSe, CaS, SrS, BaS, CaGa S, SrGa S, ZnM
- a material having a large band gap is used, for example, formed by a liquid phase synthesis method, a vapor deposition method, an aerosol deposition method or a spray coating method.
- the quantum dot obtained by the liquid phase synthesis method usually has a ligand having an organic side chain force around the shell layer so that the solvent dispersibility is high.
- the supply power of intrinsic charge carriers to the core portion is a shell layer formed around the core portion. It will not contribute. Therefore, the quantum dots can be used for the light emitting layer while the organic side chain exists around the shell layer.
- the specific charge carriers supplied to the core portion are naturally supplied from the shell layer formed around the core portion, but the adjacent quantum dots or remote quantum dot shells are used. Even layer strength will be supplied.
- a dielectric is preferred from the viewpoint of application of an alternating electric field.
- epoxy resin vinylidene fluoride resin, cyanocellulose, cyanopolyvinyl alcohol, Polyethylene, polypropylene, polystyrene resin, and silicone resin can be used.
- the binder can be formed by a relatively simple film formation method such as spin coating, screen printing, dip coating, or spray coating.
- the EL device of this embodiment is excited and emits light by applying an alternating electric field between a pair of electrodes and injecting carriers into the core portion.
- the injected carriers exist in the shell layer.
- the shell layer can have a predetermined thickness and an alternating electric field can be generated at a predetermined period.
- the predetermined thickness of the shell layer is 5 ⁇ ! It is selected from the range of ⁇ 10 Onm, and the predetermined period can be selected so that only the carriers existing in the shell can be injected into the core portion in combination with the predetermined film thickness.
- Example 1 of the above embodiment will be described.
- An ITO electrode formed on a glass substrate (crystallite size film thickness; approximately lOOnm, surface roughness Ra; approximately 50nm) is used.
- a TaO film was grown as an insulating layer and the substrate was grown at room temperature using a high-frequency magnetron 'sputtering apparatus.
- the film thickness of the insulating layer was about 400 nm.
- CdSe (core part) ZZnS (shell layer) quantum dots having a CoreZShell structure surface-modified with TOPO (trioctylphosphine oxide) are dispersed in a cyanoethylcellulose solution (binder). Was spin-coated and dried to form a film.
- the substrate temperature during drying can be selected from room temperature to around 200 ° C However, it is preferably 100 ° C or lower. This is because if it is too high, the light emission activity of the quantum dots deteriorates.
- the thickness of the deposited film was about 1 ⁇ m.
- an insulating layer TaO film was grown to a thickness of about 400 ⁇ m, and an Au electrode having a thickness of about 500 nm was formed by vacuum deposition using a shadow mask.
- TaO Z CdSe (core diameter: about 5.2 nm) ZZnS (shell thickness: about 15 nm) quantum dot-cyanoethyl cellulose binder) ZTaO ZAu is laminated in this order to form an EL device.
- An EL spectrum single peak centered around 600 nm, which is the emission color originating from the quantization level of the quantum dot core, was obtained.
- the photoluminescence (PL) of the EL device was measured using a fluorescence spectrophotometer FP-6500DS manufactured by JASCO Corporation using monochromatic light with a wavelength of 350 nm as excitation light. All sample temperatures at the time of measurement are room temperature. At this time, the PL spectrum of the used raw material dispersion was also measured. The EL measurement was performed by applying a low-frequency sine wave voltage between the ITO and Au electrodes.
- Example 2 CdSe (core part) ZZnS (shell layer) quantum dots having a CoreZShell structure surface-modified with TOPO (trioctylphosphine oxide) in Example 1 described above! Instead of, EL elements were formed in the same manner except that InP (core part) ZZnSe (shell layer) quantum dots having a CoreZShell structure surface-modified with TOPO were used.
- the quantum dots used in Example 2 had a core diameter of about 2.6 nm and a shell thickness of about 12 nm.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Electroluminescent Light Sources (AREA)
- Luminescent Compositions (AREA)
Abstract
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2008526727A JPWO2008013069A1 (ja) | 2006-07-28 | 2007-07-13 | El素子 |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2006-205625 | 2006-07-28 | ||
JP2006205625 | 2006-07-28 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2008013069A1 true WO2008013069A1 (fr) | 2008-01-31 |
Family
ID=38981382
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2007/063971 WO2008013069A1 (fr) | 2006-07-28 | 2007-07-13 | Dispositif el |
Country Status (3)
Country | Link |
---|---|
JP (1) | JPWO2008013069A1 (fr) |
CN (1) | CN101449626A (fr) |
WO (1) | WO2008013069A1 (fr) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2015107790A1 (fr) * | 2014-01-16 | 2015-07-23 | コニカミノルタ株式会社 | Élément électroluminescent |
WO2015114679A1 (fr) * | 2014-01-29 | 2015-08-06 | 株式会社ダイセル | Conjugué à base de boîtes quantiques, élément de conversion de longueur d'onde contenant le conjugué, dispositif de conversion photoélectrique, et cellule photovoltaïque |
WO2020174604A1 (fr) * | 2019-02-27 | 2020-09-03 | シャープ株式会社 | Élément électroluminescent et dispositif d'affichage l'utilisant |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103715370B (zh) | 2013-12-26 | 2017-08-08 | 合肥京东方光电科技有限公司 | 微胶囊的制备方法 |
CN104701430B (zh) * | 2015-02-10 | 2017-12-08 | 河南大学 | 一种改善量子点发光二极管寿命的方法 |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2000228285A (ja) * | 1999-02-05 | 2000-08-15 | Matsushita Electric Ind Co Ltd | 多色発光分散型elランプ |
WO2004081141A1 (fr) * | 2003-03-11 | 2004-09-23 | Philips Intellectual Property & Standards Gmbh | Diode electroluminescente a points quantiques |
JP2005505428A (ja) * | 2001-10-02 | 2005-02-24 | クァンタム・ドット・コーポレイション | 半導体ナノ粒子合成方法 |
JP2005132947A (ja) * | 2003-10-30 | 2005-05-26 | Konica Minolta Medical & Graphic Inc | 無機エレクトロルミネッセンス用蛍光体、その製造方法および無機エレクトロルミネッセンス素子 |
WO2005071764A1 (fr) * | 2004-01-23 | 2005-08-04 | Hoya Corporation | Dispositif electroluminescent a points quantiques et procede de fabrication de celui-ci |
-
2007
- 2007-07-13 WO PCT/JP2007/063971 patent/WO2008013069A1/fr active Application Filing
- 2007-07-13 JP JP2008526727A patent/JPWO2008013069A1/ja active Pending
- 2007-07-13 CN CNA2007800183208A patent/CN101449626A/zh active Pending
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2000228285A (ja) * | 1999-02-05 | 2000-08-15 | Matsushita Electric Ind Co Ltd | 多色発光分散型elランプ |
JP2005505428A (ja) * | 2001-10-02 | 2005-02-24 | クァンタム・ドット・コーポレイション | 半導体ナノ粒子合成方法 |
WO2004081141A1 (fr) * | 2003-03-11 | 2004-09-23 | Philips Intellectual Property & Standards Gmbh | Diode electroluminescente a points quantiques |
JP2005132947A (ja) * | 2003-10-30 | 2005-05-26 | Konica Minolta Medical & Graphic Inc | 無機エレクトロルミネッセンス用蛍光体、その製造方法および無機エレクトロルミネッセンス素子 |
WO2005071764A1 (fr) * | 2004-01-23 | 2005-08-04 | Hoya Corporation | Dispositif electroluminescent a points quantiques et procede de fabrication de celui-ci |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2015107790A1 (fr) * | 2014-01-16 | 2015-07-23 | コニカミノルタ株式会社 | Élément électroluminescent |
JPWO2015107790A1 (ja) * | 2014-01-16 | 2017-03-23 | コニカミノルタ株式会社 | 電界発光素子 |
US9773993B2 (en) | 2014-01-16 | 2017-09-26 | Konica Minolta, Inc. | Electroluminescence element |
WO2015114679A1 (fr) * | 2014-01-29 | 2015-08-06 | 株式会社ダイセル | Conjugué à base de boîtes quantiques, élément de conversion de longueur d'onde contenant le conjugué, dispositif de conversion photoélectrique, et cellule photovoltaïque |
US9796920B2 (en) | 2014-01-29 | 2017-10-24 | Daicel Corporation | Quantum dot composite and wavelength conversion element, photoelectric conversion device, and solar cell having the composite |
WO2020174604A1 (fr) * | 2019-02-27 | 2020-09-03 | シャープ株式会社 | Élément électroluminescent et dispositif d'affichage l'utilisant |
Also Published As
Publication number | Publication date |
---|---|
JPWO2008013069A1 (ja) | 2009-12-17 |
CN101449626A (zh) | 2009-06-03 |
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