WO2016086887A1 - Mélange organique, composé le contenant, et dispositif électronique organique et son application - Google Patents
Mélange organique, composé le contenant, et dispositif électronique organique et son application Download PDFInfo
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- WO2016086887A1 WO2016086887A1 PCT/CN2015/096330 CN2015096330W WO2016086887A1 WO 2016086887 A1 WO2016086887 A1 WO 2016086887A1 CN 2015096330 W CN2015096330 W CN 2015096330W WO 2016086887 A1 WO2016086887 A1 WO 2016086887A1
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- Prior art keywords
- organic
- group
- mixture according
- electron
- organic mixture
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims abstract description 62
- 150000001875 compounds Chemical class 0.000 title claims abstract description 23
- 239000000463 material Substances 0.000 claims abstract description 85
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 claims description 48
- -1 cyclic aromatic hydrocarbon Chemical class 0.000 claims description 40
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims description 25
- 125000003118 aryl group Chemical group 0.000 claims description 25
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 claims description 16
- 125000001072 heteroaryl group Chemical group 0.000 claims description 15
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims description 15
- 239000011159 matrix material Substances 0.000 claims description 15
- YNPNZTXNASCQKK-UHFFFAOYSA-N phenanthrene Chemical compound C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 claims description 15
- UJOBWOGCFQCDNV-UHFFFAOYSA-N 9H-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 claims description 12
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 11
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims description 10
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 claims description 10
- 230000000903 blocking effect Effects 0.000 claims description 10
- 125000004122 cyclic group Chemical group 0.000 claims description 10
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims description 10
- 150000002894 organic compounds Chemical class 0.000 claims description 10
- 239000011368 organic material Substances 0.000 claims description 10
- 229930192474 thiophene Natural products 0.000 claims description 10
- 229910052757 nitrogen Inorganic materials 0.000 claims description 9
- FCEHBMOGCRZNNI-UHFFFAOYSA-N 1-benzothiophene Chemical compound C1=CC=C2SC=CC2=C1 FCEHBMOGCRZNNI-UHFFFAOYSA-N 0.000 claims description 8
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 claims description 8
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 8
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 claims description 8
- DZBUGLKDJFMEHC-UHFFFAOYSA-N acridine Chemical compound C1=CC=CC2=CC3=CC=CC=C3N=C21 DZBUGLKDJFMEHC-UHFFFAOYSA-N 0.000 claims description 8
- 125000006575 electron-withdrawing group Chemical group 0.000 claims description 8
- 229910052739 hydrogen Inorganic materials 0.000 claims description 8
- AWJUIBRHMBBTKR-UHFFFAOYSA-N isoquinoline Chemical compound C1=NC=CC2=CC=CC=C21 AWJUIBRHMBBTKR-UHFFFAOYSA-N 0.000 claims description 8
- XSCHRSMBECNVNS-UHFFFAOYSA-N quinoxaline Chemical compound N1=CC=NC2=CC=CC=C21 XSCHRSMBECNVNS-UHFFFAOYSA-N 0.000 claims description 8
- 125000000217 alkyl group Chemical group 0.000 claims description 7
- 125000006615 aromatic heterocyclic group Chemical group 0.000 claims description 7
- IYYZUPMFVPLQIF-UHFFFAOYSA-N dibenzothiophene Chemical compound C1=CC=C2C3=CC=CC=C3SC2=C1 IYYZUPMFVPLQIF-UHFFFAOYSA-N 0.000 claims description 7
- 239000001257 hydrogen Substances 0.000 claims description 7
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 7
- VEPOHXYIFQMVHW-XOZOLZJESA-N 2,3-dihydroxybutanedioic acid (2S,3S)-3,4-dimethyl-2-phenylmorpholine Chemical compound OC(C(O)C(O)=O)C(O)=O.C[C@H]1[C@@H](OCCN1C)c1ccccc1 VEPOHXYIFQMVHW-XOZOLZJESA-N 0.000 claims description 6
- 150000001336 alkenes Chemical class 0.000 claims description 6
- 150000001345 alkine derivatives Chemical class 0.000 claims description 6
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 6
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 claims description 6
- 235000010290 biphenyl Nutrition 0.000 claims description 6
- 239000004305 biphenyl Substances 0.000 claims description 6
- TXCDCPKCNAJMEE-UHFFFAOYSA-N dibenzofuran Chemical compound C1=CC=C2C3=CC=CC=C3OC2=C1 TXCDCPKCNAJMEE-UHFFFAOYSA-N 0.000 claims description 6
- 230000005669 field effect Effects 0.000 claims description 6
- 125000004404 heteroalkyl group Chemical group 0.000 claims description 6
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 6
- 229910052717 sulfur Inorganic materials 0.000 claims description 6
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 claims description 5
- GJCOSYZMQJWQCA-UHFFFAOYSA-N 9H-xanthene Chemical compound C1=CC=C2CC3=CC=CC=C3OC2=C1 GJCOSYZMQJWQCA-UHFFFAOYSA-N 0.000 claims description 5
- 238000000862 absorption spectrum Methods 0.000 claims description 5
- 125000001931 aliphatic group Chemical group 0.000 claims description 5
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 5
- VVVPGLRKXQSQSZ-UHFFFAOYSA-N indolo[3,2-c]carbazole Chemical compound C1=CC=CC2=NC3=C4C5=CC=CC=C5N=C4C=CC3=C21 VVVPGLRKXQSQSZ-UHFFFAOYSA-N 0.000 claims description 5
- 229960005544 indolocarbazole Drugs 0.000 claims description 5
- QDLAGTHXVHQKRE-UHFFFAOYSA-N lichenxanthone Natural products COC1=CC(O)=C2C(=O)C3=C(C)C=C(OC)C=C3OC2=C1 QDLAGTHXVHQKRE-UHFFFAOYSA-N 0.000 claims description 5
- 229910052698 phosphorus Inorganic materials 0.000 claims description 5
- 229910052710 silicon Inorganic materials 0.000 claims description 5
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 claims description 4
- KTZQTRPPVKQPFO-UHFFFAOYSA-N 1,2-benzoxazole Chemical compound C1=CC=C2C=NOC2=C1 KTZQTRPPVKQPFO-UHFFFAOYSA-N 0.000 claims description 4
- YJTKZCDBKVTVBY-UHFFFAOYSA-N 1,3-Diphenylbenzene Chemical group C1=CC=CC=C1C1=CC=CC(C=2C=CC=CC=2)=C1 YJTKZCDBKVTVBY-UHFFFAOYSA-N 0.000 claims description 4
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- BNRDGHFESOHOBF-UHFFFAOYSA-N 1-benzoselenophene Chemical compound C1=CC=C2[se]C=CC2=C1 BNRDGHFESOHOBF-UHFFFAOYSA-N 0.000 claims description 4
- OLGGLCIDAMICTA-UHFFFAOYSA-N 2-pyridin-2-yl-1h-indole Chemical compound N1C2=CC=CC=C2C=C1C1=CC=CC=N1 OLGGLCIDAMICTA-UHFFFAOYSA-N 0.000 claims description 4
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical group [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 4
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 claims description 4
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 claims description 4
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 4
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 claims description 4
- FBVBNCGJVKIEHH-UHFFFAOYSA-N [1]benzofuro[3,2-b]pyridine Chemical compound C1=CN=C2C3=CC=CC=C3OC2=C1 FBVBNCGJVKIEHH-UHFFFAOYSA-N 0.000 claims description 4
- WIUZHVZUGQDRHZ-UHFFFAOYSA-N [1]benzothiolo[3,2-b]pyridine Chemical compound C1=CN=C2C3=CC=CC=C3SC2=C1 WIUZHVZUGQDRHZ-UHFFFAOYSA-N 0.000 claims description 4
- 125000002029 aromatic hydrocarbon group Chemical group 0.000 claims description 4
- RFRXIWQYSOIBDI-UHFFFAOYSA-N benzarone Chemical compound CCC=1OC2=CC=CC=C2C=1C(=O)C1=CC=C(O)C=C1 RFRXIWQYSOIBDI-UHFFFAOYSA-N 0.000 claims description 4
- 125000005605 benzo group Chemical group 0.000 claims description 4
- 229910052796 boron Inorganic materials 0.000 claims description 4
- DHFABSXGNHDNCO-UHFFFAOYSA-N dibenzoselenophene Chemical compound C1=CC=C2C3=CC=CC=C3[se]C2=C1 DHFABSXGNHDNCO-UHFFFAOYSA-N 0.000 claims description 4
- 229910052731 fluorine Inorganic materials 0.000 claims description 4
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 4
- 239000003960 organic solvent Substances 0.000 claims description 4
- WCPAKWJPBJAGKN-UHFFFAOYSA-N oxadiazole Chemical compound C1=CON=N1 WCPAKWJPBJAGKN-UHFFFAOYSA-N 0.000 claims description 4
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- 125000004430 oxygen atom Chemical group O* 0.000 claims description 4
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- 125000004434 sulfur atom Chemical group 0.000 claims description 4
- VLLMWSRANPNYQX-UHFFFAOYSA-N thiadiazole Chemical compound C1=CSN=N1.C1=CSN=N1 VLLMWSRANPNYQX-UHFFFAOYSA-N 0.000 claims description 4
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- WJFKNYWRSNBZNX-UHFFFAOYSA-N 10H-phenothiazine Chemical compound C1=CC=C2NC3=CC=CC=C3SC2=C1 WJFKNYWRSNBZNX-UHFFFAOYSA-N 0.000 claims description 3
- TZMSYXZUNZXBOL-UHFFFAOYSA-N 10H-phenoxazine Chemical compound C1=CC=C2NC3=CC=CC=C3OC2=C1 TZMSYXZUNZXBOL-UHFFFAOYSA-N 0.000 claims description 3
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- 238000002189 fluorescence spectrum Methods 0.000 claims description 3
- CTAPFRYPJLPFDF-UHFFFAOYSA-N isoxazole Chemical compound C=1C=NOC=1 CTAPFRYPJLPFDF-UHFFFAOYSA-N 0.000 claims description 3
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- XDJOIMJURHQYDW-UHFFFAOYSA-N phenalene Chemical compound C1=CC(CC=C2)=C3C2=CC=CC3=C1 XDJOIMJURHQYDW-UHFFFAOYSA-N 0.000 claims description 3
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- 238000012360 testing method Methods 0.000 description 1
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
- 239000003451 thiazide diuretic agent Substances 0.000 description 1
- ZMZDMBWJUHKJPS-UHFFFAOYSA-M thiocyanate group Chemical group [S-]C#N ZMZDMBWJUHKJPS-UHFFFAOYSA-M 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Images
Classifications
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
Definitions
- the present invention relates to the field of electroluminescent materials, and in particular to an organic mixture, a composition comprising the same, an organic electronic device, and an application of an organic mixture in an organic electronic device, particularly in an organic electroluminescent device. .
- the invention further relates to an organic electronic device comprising the organic mixture of the invention, and a process for the preparation thereof.
- the organic mixture provided by the present invention comprises an organic material H1 and an organic fluorescent material E1, wherein the triplet level T1 (H1) of the H1 is greater than or equal to the triplet level T1 (E1) of E1. And the difference between the singlet level and the triplet level of E1, ⁇ (S1(E1)-T1(E1)) ⁇ 0.35eV.
- Ar 1 to Ar 9 may be independently selected from the group consisting of:
- ETM is sometimes referred to as an n-type organic semiconductor material.
- suitable ETM materials are not subject to special As a limitation, any metal complex or organic compound may be used as the ETM as long as they can transport electrons.
- Preferred organic ETM materials may be selected from the group consisting of tris(8-hydroxyquinoline)aluminum (AlQ3), phenazine, Phenanthroline, Anthracene, Phenanthrene, Fluorene, and Bifluorene, Spiro-bifluorene, Phenylene-vinylene, triazine, triazole, imidazole, pyrene, Perylene, Trans-Indenofluorene, cis-Indenon fluorene, Dibenzol-indenofluorene, Indenonaphthalene, Benzanthracene and their derivatives .
- H1 is selected from the group consisting of triplet matrix materials.
- H1 is selected from the group consisting of singlet matrix materials.
- Examples of singlet emitters based on vinylamines and arylamines are also preferred examples and can be found in the following patent documents: WO 2006/000388, WO 2006/058737, WO 2006/000389, WO 2007/065549, WO 2007 /115610, US 7250532 B2, DE 102005058557 A1, CN 1583691 A, JP 08053397 A, US 6251531 B1, US 2006/210830 A, EP 1957606 A1 and US 2008/0113101 A1, the entire contents of which are hereby incorporated by reference. This article is incorporated herein by reference.
- polycyclic aromatic hydrocarbon compounds in particular derivatives of the following compounds: for example, 9,10-di(2-naphthoquinone) (9,10-di(2-naphthylanthracene) ), naphthalene, tetraphenyl, xanthene, phenanthrene, perylene such as 2,5,8,11-tetra-t-butylperylene, indenoperylene, phenylenes
- r 0, 1, 2, 3 or 4;
- s 0, 1, 2, 3, 4o or 5;
- organic ETM material is a polymer with electron transport capability, including conjugated polymers and non-co-polymers. Yoke polymer.
- the invention further relates to the use of an organic electronic device according to the invention in various electronic devices, including but not limited to display devices, illumination devices, light sources, sensors and the like.
- H1-1, H1-2, and H1-3 were purchased from Jilin Orient Photoelectric Material Co., Ltd., and they were advanced and purified before use.
- the synthesis methods of E1-1 and E1-2 are all prior art, and the references in the prior art are not described in detail herein.
- E1-1 can be found in Chem. Mater. Vol 25p 3766
- E1-2 can be found in Chem. Comm. Vol 48p958.
- HOMO(eV) ((HOMO(G) ⁇ 27.212)-0.9899)/1.1206
- EML organic light-emitting layer, 40 nm: according to the composition of Table 2, hot evaporation in high vacuum (1 ⁇ 10 -6 mbar);
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- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Electroluminescent Light Sources (AREA)
Abstract
L'invention concerne un mélange organique, un composé le contenant, et un dispositif électronique organique et son application ; le mélange organique comprend une matière de corps H1, et une matière émettrice de lumière fluorescente organique E1 ; le niveau d'énergie triplet de H1 est supérieur ou égal au niveau d'énergie triplet T1(E1) de E1, et en ce qui concerne la différence entre le niveau d'énergie singulet et le niveau d'énergie triplet de E1, Δ(S1(E1) - T1(E1)) ≤ 0,35 eV. L'invention permet d'obtenir un dispositif électroluminescent qui possède de faibles coûts de fabrication, un rendement élevé, et un large spectre.
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Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
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US20170250351A1 (en) * | 2016-02-25 | 2017-08-31 | Japan Display Inc. | Material for organic electroluminescent display device and organic electroluminescent display device |
CN109791982A (zh) * | 2016-11-23 | 2019-05-21 | 广州华睿光电材料有限公司 | 有机混合物、有机组合物、有机电子器件及其制备方法 |
USRE47654E1 (en) | 2010-01-15 | 2019-10-22 | Idemitsu Koasn Co., Ltd. | Organic electroluminescence device |
US20200083460A1 (en) * | 2017-12-29 | 2020-03-12 | Kunshan Go-Visionox Opto-Electronics Co., Ltd. | Organic electroluminescent devices and preparation methods thereof |
CN111247133A (zh) * | 2017-12-14 | 2020-06-05 | 广州华睿光电材料有限公司 | 咔唑三苯有机化合物、高聚物、混合物、组合物及其应用 |
CN111326665A (zh) * | 2018-12-17 | 2020-06-23 | 固安鼎材科技有限公司 | 一种新材料及其电致发光器件 |
CN112262127A (zh) * | 2018-06-15 | 2021-01-22 | 三星显示有限公司 | 杂环化合物和包括该杂环化合物的有机发光器件 |
US11482681B2 (en) | 2018-07-27 | 2022-10-25 | Idemitsu Kosan Co., Ltd. | Compound, material for organic electroluminescence element, organic electroluminescence element, and electronic device |
Families Citing this family (1)
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CN110746409B (zh) * | 2018-12-10 | 2023-10-17 | 广州华睿光电材料有限公司 | 有机化合物、混合物、组合物及电子器件和应用 |
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CN102709485A (zh) * | 2011-09-30 | 2012-10-03 | 昆山维信诺显示技术有限公司 | 一种有机电致发光器件及其制备方法 |
CN103740359A (zh) * | 2013-12-27 | 2014-04-23 | 深圳市华星光电技术有限公司 | 热激活延迟荧光材料、其合成方法及使用该热激活延迟荧光材料的oled器件 |
WO2014166585A1 (fr) * | 2013-04-08 | 2014-10-16 | Merck Patent Gmbh | Dispositif électroluminescent organique |
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CN103985822B (zh) * | 2014-05-30 | 2017-05-10 | 广州华睿光电材料有限公司 | 有机混合物、包含其的组合物、有机电子器件及应用 |
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- 2015-12-03 CN CN201580065949.2A patent/CN107004778B/zh active Active
- 2015-12-03 WO PCT/CN2015/096330 patent/WO2016086887A1/fr active Application Filing
Patent Citations (3)
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CN102709485A (zh) * | 2011-09-30 | 2012-10-03 | 昆山维信诺显示技术有限公司 | 一种有机电致发光器件及其制备方法 |
WO2014166585A1 (fr) * | 2013-04-08 | 2014-10-16 | Merck Patent Gmbh | Dispositif électroluminescent organique |
CN103740359A (zh) * | 2013-12-27 | 2014-04-23 | 深圳市华星光电技术有限公司 | 热激活延迟荧光材料、其合成方法及使用该热激活延迟荧光材料的oled器件 |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
USRE47654E1 (en) | 2010-01-15 | 2019-10-22 | Idemitsu Koasn Co., Ltd. | Organic electroluminescence device |
US20170250351A1 (en) * | 2016-02-25 | 2017-08-31 | Japan Display Inc. | Material for organic electroluminescent display device and organic electroluminescent display device |
CN109791982A (zh) * | 2016-11-23 | 2019-05-21 | 广州华睿光电材料有限公司 | 有机混合物、有机组合物、有机电子器件及其制备方法 |
CN109791982B (zh) * | 2016-11-23 | 2023-10-17 | 广州华睿光电材料有限公司 | 有机混合物、有机组合物、有机电子器件及其制备方法 |
CN111247133A (zh) * | 2017-12-14 | 2020-06-05 | 广州华睿光电材料有限公司 | 咔唑三苯有机化合物、高聚物、混合物、组合物及其应用 |
US20200083460A1 (en) * | 2017-12-29 | 2020-03-12 | Kunshan Go-Visionox Opto-Electronics Co., Ltd. | Organic electroluminescent devices and preparation methods thereof |
CN112262127A (zh) * | 2018-06-15 | 2021-01-22 | 三星显示有限公司 | 杂环化合物和包括该杂环化合物的有机发光器件 |
US11482681B2 (en) | 2018-07-27 | 2022-10-25 | Idemitsu Kosan Co., Ltd. | Compound, material for organic electroluminescence element, organic electroluminescence element, and electronic device |
CN111326665A (zh) * | 2018-12-17 | 2020-06-23 | 固安鼎材科技有限公司 | 一种新材料及其电致发光器件 |
CN111326665B (zh) * | 2018-12-17 | 2023-08-22 | 固安鼎材科技有限公司 | 一种新材料及其电致发光器件 |
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