JP5558708B2 - マルチカラーoledディスプレイ - Google Patents
マルチカラーoledディスプレイ Download PDFInfo
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- JP5558708B2 JP5558708B2 JP2008509018A JP2008509018A JP5558708B2 JP 5558708 B2 JP5558708 B2 JP 5558708B2 JP 2008509018 A JP2008509018 A JP 2008509018A JP 2008509018 A JP2008509018 A JP 2008509018A JP 5558708 B2 JP5558708 B2 JP 5558708B2
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- 239000000463 material Substances 0.000 claims description 99
- 239000000758 substrate Substances 0.000 claims description 23
- 239000010410 layer Substances 0.000 description 159
- 125000003118 aryl group Chemical group 0.000 description 45
- 239000002019 doping agent Substances 0.000 description 28
- 238000000151 deposition Methods 0.000 description 23
- -1 porphyrin compounds Chemical class 0.000 description 22
- 230000003595 spectral effect Effects 0.000 description 22
- 229910052751 metal Inorganic materials 0.000 description 21
- 239000002184 metal Substances 0.000 description 21
- 125000000217 alkyl group Chemical group 0.000 description 20
- 238000002834 transmittance Methods 0.000 description 20
- 238000001429 visible spectrum Methods 0.000 description 18
- 125000004432 carbon atom Chemical group C* 0.000 description 17
- 150000001875 compounds Chemical class 0.000 description 17
- 238000000034 method Methods 0.000 description 17
- 238000000059 patterning Methods 0.000 description 17
- 125000001424 substituent group Chemical group 0.000 description 17
- 230000005525 hole transport Effects 0.000 description 16
- 239000011159 matrix material Substances 0.000 description 13
- 239000007983 Tris buffer Substances 0.000 description 10
- 238000004519 manufacturing process Methods 0.000 description 10
- MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 description 10
- 125000005259 triarylamine group Chemical group 0.000 description 10
- 230000008021 deposition Effects 0.000 description 9
- 229910052757 nitrogen Inorganic materials 0.000 description 9
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical group C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 8
- 239000004020 conductor Substances 0.000 description 8
- 125000001072 heteroaryl group Chemical group 0.000 description 8
- 125000000623 heterocyclic group Chemical group 0.000 description 8
- 229910052739 hydrogen Inorganic materials 0.000 description 8
- 239000001257 hydrogen Substances 0.000 description 8
- 239000000203 mixture Substances 0.000 description 8
- 239000012044 organic layer Substances 0.000 description 8
- 238000001228 spectrum Methods 0.000 description 8
- 125000003545 alkoxy group Chemical group 0.000 description 7
- 229910052782 aluminium Inorganic materials 0.000 description 7
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 7
- REDXJYDRNCIFBQ-UHFFFAOYSA-N aluminium(3+) Chemical compound [Al+3] REDXJYDRNCIFBQ-UHFFFAOYSA-N 0.000 description 7
- 230000000903 blocking effect Effects 0.000 description 7
- 238000002347 injection Methods 0.000 description 7
- 239000007924 injection Substances 0.000 description 7
- 125000001624 naphthyl group Chemical group 0.000 description 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 6
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical class C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 6
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 6
- 230000008901 benefit Effects 0.000 description 6
- 230000005540 biological transmission Effects 0.000 description 6
- 239000003086 colorant Substances 0.000 description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 6
- 150000004982 aromatic amines Chemical class 0.000 description 5
- 125000000732 arylene group Chemical group 0.000 description 5
- 125000004429 atom Chemical group 0.000 description 5
- 125000004093 cyano group Chemical group *C#N 0.000 description 5
- 229920000553 poly(phenylenevinylene) Polymers 0.000 description 5
- 230000006798 recombination Effects 0.000 description 5
- 238000005215 recombination Methods 0.000 description 5
- 125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 4
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 description 4
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 4
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 4
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 4
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 4
- 229910052783 alkali metal Inorganic materials 0.000 description 4
- 150000001340 alkali metals Chemical class 0.000 description 4
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 4
- 150000001342 alkaline earth metals Chemical class 0.000 description 4
- 125000004104 aryloxy group Chemical group 0.000 description 4
- 125000000319 biphenyl-4-yl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 description 4
- 229910052733 gallium Inorganic materials 0.000 description 4
- 229910052738 indium Inorganic materials 0.000 description 4
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 description 4
- 230000031700 light absorption Effects 0.000 description 4
- 229910052744 lithium Inorganic materials 0.000 description 4
- 229910052749 magnesium Inorganic materials 0.000 description 4
- 239000011777 magnesium Substances 0.000 description 4
- 239000011368 organic material Substances 0.000 description 4
- 125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 description 4
- 229920003227 poly(N-vinyl carbazole) Polymers 0.000 description 4
- 125000003107 substituted aryl group Chemical group 0.000 description 4
- 229910052726 zirconium Inorganic materials 0.000 description 4
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 3
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 3
- 125000002947 alkylene group Chemical group 0.000 description 3
- 150000001454 anthracenes Chemical class 0.000 description 3
- ZYGHJZDHTFUPRJ-UHFFFAOYSA-N benzo-alpha-pyrone Natural products C1=CC=C2OC(=O)C=CC2=C1 ZYGHJZDHTFUPRJ-UHFFFAOYSA-N 0.000 description 3
- 125000006267 biphenyl group Chemical group 0.000 description 3
- 125000000753 cycloalkyl group Chemical group 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 239000000975 dye Substances 0.000 description 3
- 238000000295 emission spectrum Methods 0.000 description 3
- 230000005281 excited state Effects 0.000 description 3
- 239000010408 film Substances 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- 229910052731 fluorine Inorganic materials 0.000 description 3
- 239000011737 fluorine Substances 0.000 description 3
- ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 description 3
- 125000002541 furyl group Chemical group 0.000 description 3
- 150000002739 metals Chemical class 0.000 description 3
- IBHBKWKFFTZAHE-UHFFFAOYSA-N n-[4-[4-(n-naphthalen-1-ylanilino)phenyl]phenyl]-n-phenylnaphthalen-1-amine Chemical group C1=CC=CC=C1N(C=1C2=CC=CC=C2C=CC=1)C1=CC=C(C=2C=CC(=CC=2)N(C=2C=CC=CC=2)C=2C3=CC=CC=C3C=CC=2)C=C1 IBHBKWKFFTZAHE-UHFFFAOYSA-N 0.000 description 3
- 229960003540 oxyquinoline Drugs 0.000 description 3
- CSHWQDPOILHKBI-UHFFFAOYSA-N peryrene Natural products C1=CC(C2=CC=CC=3C2=C2C=CC=3)=C3C2=CC=CC3=C1 CSHWQDPOILHKBI-UHFFFAOYSA-N 0.000 description 3
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 3
- 125000003367 polycyclic group Chemical group 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 125000004076 pyridyl group Chemical group 0.000 description 3
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 description 3
- 238000007789 sealing Methods 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 150000003518 tetracenes Chemical class 0.000 description 3
- 125000001544 thienyl group Chemical group 0.000 description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
- NGQSLSMAEVWNPU-YTEMWHBBSA-N 1,2-bis[(e)-2-phenylethenyl]benzene Chemical class C=1C=CC=CC=1/C=C/C1=CC=CC=C1\C=C\C1=CC=CC=C1 NGQSLSMAEVWNPU-YTEMWHBBSA-N 0.000 description 2
- ZMLPKJYZRQZLDA-UHFFFAOYSA-N 1-(2-phenylethenyl)-4-[4-(2-phenylethenyl)phenyl]benzene Chemical class C=1C=CC=CC=1C=CC(C=C1)=CC=C1C(C=C1)=CC=C1C=CC1=CC=CC=C1 ZMLPKJYZRQZLDA-UHFFFAOYSA-N 0.000 description 2
- 125000001637 1-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C(*)=C([H])C([H])=C([H])C2=C1[H] 0.000 description 2
- STTGYIUESPWXOW-UHFFFAOYSA-N 2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline Chemical compound C=12C=CC3=C(C=4C=CC=CC=4)C=C(C)N=C3C2=NC(C)=CC=1C1=CC=CC=C1 STTGYIUESPWXOW-UHFFFAOYSA-N 0.000 description 2
- 239000005725 8-Hydroxyquinoline Substances 0.000 description 2
- VFUDMQLBKNMONU-UHFFFAOYSA-N 9-[4-(4-carbazol-9-ylphenyl)phenyl]carbazole Chemical group C12=CC=CC=C2C2=CC=CC=C2N1C1=CC=C(C=2C=CC(=CC=2)N2C3=CC=CC=C3C3=CC=CC=C32)C=C1 VFUDMQLBKNMONU-UHFFFAOYSA-N 0.000 description 2
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- JLVVSXFLKOJNIY-UHFFFAOYSA-N Magnesium ion Chemical compound [Mg+2] JLVVSXFLKOJNIY-UHFFFAOYSA-N 0.000 description 2
- 229920001609 Poly(3,4-ethylenedioxythiophene) Polymers 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- PTFCDOFLOPIGGS-UHFFFAOYSA-N Zinc dication Chemical compound [Zn+2] PTFCDOFLOPIGGS-UHFFFAOYSA-N 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 125000000033 alkoxyamino group Chemical group 0.000 description 2
- 125000003282 alkyl amino group Chemical group 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 125000001769 aryl amino group Chemical group 0.000 description 2
- 125000005605 benzo group Chemical group 0.000 description 2
- 239000004305 biphenyl Substances 0.000 description 2
- 125000006268 biphenyl-3-yl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C1=C([H])C(*)=C([H])C([H])=C1[H] 0.000 description 2
- 229910052796 boron Inorganic materials 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 125000001309 chloro group Chemical group Cl* 0.000 description 2
- 229920001940 conductive polymer Polymers 0.000 description 2
- 229960000956 coumarin Drugs 0.000 description 2
- 235000001671 coumarin Nutrition 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- 125000004986 diarylamino group Chemical group 0.000 description 2
- BKMIWBZIQAAZBD-UHFFFAOYSA-N diindenoperylene Chemical group C12=C3C4=CC=C2C2=CC=CC=C2C1=CC=C3C1=CC=C2C3=CC=CC=C3C3=CC=C4C1=C32 BKMIWBZIQAAZBD-UHFFFAOYSA-N 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- GVEPBJHOBDJJJI-UHFFFAOYSA-N fluoranthene Chemical compound C1=CC(C2=CC=CC=C22)=C3C2=CC=CC3=C1 GVEPBJHOBDJJJI-UHFFFAOYSA-N 0.000 description 2
- 239000007850 fluorescent dye Substances 0.000 description 2
- 125000001153 fluoro group Chemical group F* 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 230000005283 ground state Effects 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 125000005843 halogen group Chemical group 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 125000005842 heteroatom Chemical group 0.000 description 2
- 150000002431 hydrogen Chemical class 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 229910052741 iridium Inorganic materials 0.000 description 2
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 description 2
- FQHFBFXXYOQXMN-UHFFFAOYSA-M lithium;quinolin-8-olate Chemical compound [Li+].C1=CN=C2C([O-])=CC=CC2=C1 FQHFBFXXYOQXMN-UHFFFAOYSA-M 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 description 2
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 description 2
- 125000005561 phenanthryl group Chemical group 0.000 description 2
- 229920002098 polyfluorene Polymers 0.000 description 2
- 239000002861 polymer material Substances 0.000 description 2
- 229920000123 polythiophene Polymers 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 125000001725 pyrenyl group Chemical group 0.000 description 2
- 125000006413 ring segment Chemical group 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 125000000547 substituted alkyl group Chemical group 0.000 description 2
- 239000010409 thin film Substances 0.000 description 2
- 239000012780 transparent material Substances 0.000 description 2
- TVIVIEFSHFOWTE-UHFFFAOYSA-K tri(quinolin-8-yloxy)alumane Chemical compound [Al+3].C1=CN=C2C([O-])=CC=CC2=C1.C1=CN=C2C([O-])=CC=CC2=C1.C1=CN=C2C([O-])=CC=CC2=C1 TVIVIEFSHFOWTE-UHFFFAOYSA-K 0.000 description 2
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- 0 *c(cc1*2)cc(*)c1N=C2C1=Cc(cc(*)c(N(*)*)c2*)c2OC1=* Chemical compound *c(cc1*2)cc(*)c1N=C2C1=Cc(cc(*)c(N(*)*)c2*)c2OC1=* 0.000 description 1
- 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 description 1
- XNCMQRWVMWLODV-UHFFFAOYSA-N 1-phenylbenzimidazole Chemical compound C1=NC2=CC=CC=C2N1C1=CC=CC=C1 XNCMQRWVMWLODV-UHFFFAOYSA-N 0.000 description 1
- YPUFOHGCKCFWAW-UHFFFAOYSA-N 2-n,6-n-dinaphthalen-1-yl-2-n,6-n-dinaphthalen-2-ylnaphthalene-2,6-diamine;2-n,2-n,6-n,6-n-tetrakis(4-methylphenyl)naphthalene-2,6-diamine;2-n,2-n,6-n,6-n-tetranaphthalen-1-ylnaphthalene-2,6-diamine Chemical compound C1=CC(C)=CC=C1N(C=1C=C2C=CC(=CC2=CC=1)N(C=1C=CC(C)=CC=1)C=1C=CC(C)=CC=1)C1=CC=C(C)C=C1.C1=CC=C2C(N(C=3C=C4C=CC(=CC4=CC=3)N(C=3C=C4C=CC=CC4=CC=3)C=3C4=CC=CC=C4C=CC=3)C3=CC4=CC=CC=C4C=C3)=CC=CC2=C1.C1=CC=C2C(N(C=3C=C4C=CC(=CC4=CC=3)N(C=3C4=CC=CC=C4C=CC=3)C=3C4=CC=CC=C4C=CC=3)C=3C4=CC=CC=C4C=CC=3)=CC=CC2=C1 YPUFOHGCKCFWAW-UHFFFAOYSA-N 0.000 description 1
- HXWWMGJBPGRWRS-CMDGGOBGSA-N 4- -2-tert-butyl-6- -4h-pyran Chemical group O1C(C(C)(C)C)=CC(=C(C#N)C#N)C=C1\C=C\C1=CC(C(CCN2CCC3(C)C)(C)C)=C2C3=C1 HXWWMGJBPGRWRS-CMDGGOBGSA-N 0.000 description 1
- AHDTYXOIJHCGKH-UHFFFAOYSA-N 4-[[4-(dimethylamino)-2-methylphenyl]-phenylmethyl]-n,n,3-trimethylaniline Chemical compound CC1=CC(N(C)C)=CC=C1C(C=1C(=CC(=CC=1)N(C)C)C)C1=CC=CC=C1 AHDTYXOIJHCGKH-UHFFFAOYSA-N 0.000 description 1
- MAGFQRLKWCCTQJ-UHFFFAOYSA-M 4-ethenylbenzenesulfonate Chemical compound [O-]S(=O)(=O)C1=CC=C(C=C)C=C1 MAGFQRLKWCCTQJ-UHFFFAOYSA-M 0.000 description 1
- YXYUIABODWXVIK-UHFFFAOYSA-N 4-methyl-n,n-bis(4-methylphenyl)aniline Chemical compound C1=CC(C)=CC=C1N(C=1C=CC(C)=CC=1)C1=CC=C(C)C=C1 YXYUIABODWXVIK-UHFFFAOYSA-N 0.000 description 1
- LQYYDWJDEVKDGB-XPWSMXQVSA-N 4-methyl-n-[4-[(e)-2-[4-[(e)-2-[4-(4-methyl-n-(4-methylphenyl)anilino)phenyl]ethenyl]phenyl]ethenyl]phenyl]-n-(4-methylphenyl)aniline Chemical compound C1=CC(C)=CC=C1N(C=1C=CC(\C=C\C=2C=CC(\C=C\C=3C=CC(=CC=3)N(C=3C=CC(C)=CC=3)C=3C=CC(C)=CC=3)=CC=2)=CC=1)C1=CC=C(C)C=C1 LQYYDWJDEVKDGB-XPWSMXQVSA-N 0.000 description 1
- MEIBOBDKQKIBJH-UHFFFAOYSA-N 4-methyl-n-[4-[1-[4-(4-methyl-n-(4-methylphenyl)anilino)phenyl]-4-phenylcyclohexyl]phenyl]-n-(4-methylphenyl)aniline Chemical compound C1=CC(C)=CC=C1N(C=1C=CC(=CC=1)C1(CCC(CC1)C=1C=CC=CC=1)C=1C=CC(=CC=1)N(C=1C=CC(C)=CC=1)C=1C=CC(C)=CC=1)C1=CC=C(C)C=C1 MEIBOBDKQKIBJH-UHFFFAOYSA-N 0.000 description 1
- ZOKIJILZFXPFTO-UHFFFAOYSA-N 4-methyl-n-[4-[1-[4-(4-methyl-n-(4-methylphenyl)anilino)phenyl]cyclohexyl]phenyl]-n-(4-methylphenyl)aniline Chemical compound C1=CC(C)=CC=C1N(C=1C=CC(=CC=1)C1(CCCCC1)C=1C=CC(=CC=1)N(C=1C=CC(C)=CC=1)C=1C=CC(C)=CC=1)C1=CC=C(C)C=C1 ZOKIJILZFXPFTO-UHFFFAOYSA-N 0.000 description 1
- MVIXNQZIMMIGEL-UHFFFAOYSA-N 4-methyl-n-[4-[4-(4-methyl-n-(4-methylphenyl)anilino)phenyl]phenyl]-n-(4-methylphenyl)aniline Chemical group C1=CC(C)=CC=C1N(C=1C=CC(=CC=1)C=1C=CC(=CC=1)N(C=1C=CC(C)=CC=1)C=1C=CC(C)=CC=1)C1=CC=C(C)C=C1 MVIXNQZIMMIGEL-UHFFFAOYSA-N 0.000 description 1
- VIZUPBYFLORCRA-UHFFFAOYSA-N 9,10-dinaphthalen-2-ylanthracene Chemical class C12=CC=CC=C2C(C2=CC3=CC=CC=C3C=C2)=C(C=CC=C2)C2=C1C1=CC=C(C=CC=C2)C2=C1 VIZUPBYFLORCRA-UHFFFAOYSA-N 0.000 description 1
- VIJYEGDOKCKUOL-UHFFFAOYSA-N 9-phenylcarbazole Chemical compound C1=CC=CC=C1N1C2=CC=CC=C2C2=CC=CC=C21 VIJYEGDOKCKUOL-UHFFFAOYSA-N 0.000 description 1
- 229910001316 Ag alloy Inorganic materials 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
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- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K71/00—Manufacture or treatment specially adapted for the organic devices covered by this subclass
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- H10K85/324—Metal complexes comprising a group IIIA element, e.g. Tris (8-hydroxyquinoline) gallium [Gaq3] comprising aluminium, e.g. Alq3
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Description
a)赤色画素と青色画素のために基板上に設けられたマゼンタ色発光層と、少なくとも緑色画素を生成させるためにその基板上に設けられた緑色発光層と;
b)上記マゼンタ色発光層と作用的関係があってそれぞれ赤色画素と青色画素を生成させる第1のカラー・フィルタと第2のカラー・フィルタを備えるOLEDディスプレイによって達成される。
Q1とQ2は、独立に、芳香族第三級アミン部分の中から選択され、
Gは、炭素-炭素結合の結合基(例えば、アリーレン基、シクロアルキレン基、アルキレン基など)である。
R1とR2は、それぞれ独立に、水素原子、アリール基、アルキル基のいずれかを表わすか、R1とR2は、合わさって、シクロアルキル基を完成させる原子を表わし;
R3とR4は、それぞれ独立にアリール基を表わし、そのアリール基は、構造式(C):
R5とR6は、独立に、アリール基の中から選択される。一実施態様では、R5とR6のうちの少なくとも一方は、多環式縮合環基(例えばナフタレン)を含んでいる。
それぞれのAreは、独立に選択したアリーレン基(例えばフェニレン部分またはアントラセン部分)であり;
nは1〜4の中から選択され;
Ar、R7、R8、R9は、独立に選択したアリール基である。
1,1-ビス(4-ジ-p-トリルアミノフェニル)シクロヘキサン;
1,1-ビス(4-ジ-p-トリルアミノフェニル)-4-フェニルシクロヘキサン;
4,4'-ビス(ジフェニルアミノ)クアテルフェニル;
ビス(4-ジメチルアミノ-2-メチルフェニル)-フェニルメタン;
トリ(p-トリル)アミン;
4-(ジ-p-トリルアミノ)-4'-[4-(ジ-p-トリルアミノ)-スチリル]スチルベン;
N,N,N',N'-テトラ-p-トリル-4,4'-ジアミノビフェニル;
N,N,N',N'-テトラフェニル-4,4'-ジアミノビフェニル;
N-フェニルカルバゾール;
ポリ(N-ビニルカルバゾール);
N,N'-ジ-1-ナフタレニル-N,N'-ジフェニル-4,4'-ジアミノビフェニル;
4,4'-ビス[N-(1-ナフチル)-N-フェニルアミノ]ビフェニル(NPB)
4,4'-ビス[N-(1-ナフチル)-N-(2-ナフチル)アミノ]ビフェニル(TNB)
4,4"-ビス[N-(1-ナフチル)-N-フェニルアミノ]-p-テルフェニル
4,4'-ビス[N-(2-ナフチル)-N-フェニルアミノ]ビフェニル
4,4'-ビス[N-(3-アセナフテニル)-N-フェニルアミノ]ビフェニル
1,5-ビス[N-(1-ナフチル)-N-フェニルアミノ]ナフタレン
4,4'-ビス[N-(9-アントリル)-N-フェニルアミノ]ビフェニル
4,4"-ビス[N-(1-アントリル)-N-フェニルアミノ]-p-テルフェニル
4,4'-ビス[N-(2-フェナントリル)-N-フェニルアミノ]ビフェニル
4,4'-ビス[N-(8-フルオランテニル)-N-フェニルアミノ]ビフェニル
4,4'-ビス[N-(2-ピレニル)-N-フェニルアミノ]ビフェニル
4,4'-ビス[N-(2-ナフトアセニル)-N-フェニルアミノ]ビフェニル
4,4'-ビス[N-(2-ペリレニル)-N-フェニルアミノ]ビフェニル
4,4'-ビス[N-(1-コロネニル)-N-フェニルアミノ]ビフェニル
2,6-ビス(ジ-p-トリルアミノ)ナフタレン
2,6-ビス[ジ-(1-ナフチル)アミノ]ナフタレン
2,6-ビス[N-(1-ナフチル)-N-(2-ナフチル)アミノ]ナフタレン
N,N,N',N'-テトラ(2-ナフチル)-4,4"-ジアミノ-p-テルフェニル
4,4'-ビス{N-フェニル-N-[4-(1-ナフチル)-フェニル]アミノ}ビフェニル
4,4'-ビス[N-フェニル-N-(2-ピレニル)アミノ]ビフェニル
2,6-ビス[N,N-ジ(2-ナフチル)アミノ]フルオレン
1,5-ビス[N-(1-ナフチル)-N-フェニルアミノ]ナフタレン。
CO-1:アルミニウムトリスオキシン[別名、トリス(8-キノリノラト)アルミニウム(III)]
CO-2:マグネシウムビスオキシン[別名、ビス(8-キノリノラト)マグネシウム(II)]
CO-3:ビス[ベンゾ{f}-8-キノリノラト]亜鉛(II)
CO-4:ビス(2-メチル-8-キノリノラト)アルミニウム(III)-μ-オキソ-ビス(2-メチル-8-キノリノラト)アルミニウム(III)
CO-5:インジウムトリスオキシン[別名、トリス(8-キノリノラト)インジウム]
CO-6:アルミニウムトリス(5-メチルオキシン)[別名、トリス(5-メチル-8-キノリノラト)アルミニウム(III)]
CO-7:リチウムオキシン[別名、(8-キノリノラト)リチウム(I)]
CO-8:ガリウムオキシン[別名、トリス(8-キノリノラト)ガリウム(III)]
CO-9:ジルコニウムオキシン[別名、テトラ(8-キノリノラト)ジルコニウム(IV)]
R1〜R6は各環上の1個以上の置換基を著わし、各置換基の選択は、個別に、以下のカテゴリー:
カテゴリー1:水素、または炭素原子が1〜24個のアルキル;
カテゴリー2:炭素原子が5〜20個のアリールまたは置換されたアリール;
カテゴリー3:4〜24個の炭素原子を持ち、縮合芳香族環または縮合芳香族環系を完成させる炭化水素;
カテゴリー4:単結合を通じて結合されるか、縮合複素芳香族環系を完成させる 5〜24個の炭素原子を持つヘテロアリールまたは置換されたヘテロアリール(チアゾリル、フリル、チエニル、ピリジル、キノリニル、または他の複素環系);
カテゴリー5:炭素原子を1〜24個持つアルコキシアミノ、アルキルアミノ、アリールアミノ;
カテゴリー6:フルオロ、クロロ、ブロモ、シアノ
の中からなされる。
Y1〜Y5は、ヒドロ、アルキル、置換されたアルキル、アリール、置換されたアリールの中から独立に選択した1つ以上の基であり;
Y1〜Y5は、独立に非環式基を含むか、ペアで結合して1つ以上の縮合環を形成するが、Y3とY5がともに縮合環を形成することはない。
R1、R2、R3、R4、R5、R6は各環上の1個以上の置換基を表わし、各置換基の選択は、個別に、以下のカテゴリー:
グループ1:水素、または炭素原子が1〜24個のアルキル;
グループ2:炭素原子が5〜20個のアリールまたは置換されたアリール;
グループ3:アントラセニル、ピレニル、ペリレニルいずれかの縮合芳香族環を完成させるのに必要な4〜24個の炭素原子;
グループ4:フリル、チエニル、ピリジル、キノリニル、または他の複素環系の縮合複素芳香族環系を完成させるのに必要な 5〜24個の炭素原子を持つヘテロアリールまたは置換されたヘテロアリール;
グループ5:炭素原子を1〜24個持つアルコキシアミノ、アルキルアミノ、アリールアミノ;
グループ6:フッ素、塩素、臭素、シアノ
の中からなされる。
nは3〜8の整数であり;
Zは、O、NR、Sのいずれかであり;
R'は、水素;1〜24個の炭素原子を含むアルキル(例えばプロピル、t-ブチル、ヘプチルなど);5〜20個の炭素原子を含むアリール、またはヘテロ原子で置換されたアリール(例えばフェニル、ナフチル、フリル、チエニル、ピリジル、キノリニルや、他の複素環系);ハロ(クロロ、フルオロなど);縮合芳香族環を完成させるのに必要な原子のいずれかであり;
Lは、アルキル、アリール、置換されたアルキル、置換されたアリールのいずれかを含んでいて複数のベンズアゾールを共役または非共役に結合させる結合単位である。
R1〜R8はHである。
R9は、脂肪族炭素環のメンバーを有する縮合環を含まないナフチル基である。ただしR9とR10は同じではなく、アミンとイオウ化合物を含んでいない。R9は、1つ以上の縮合環をさらに備えていて芳香族縮合環系(例えばフェナントリル、ピレニル、フルオランテン、ペリレン)を形成している置換されたナフチル基であるか、1個以上の置換基(例えばフッ素、シアノ基、ヒドロキシ基、アルキル基、アルコキシ基、アリールオキシ基、アリール基、複素環式オキシ基、カルボキシ基、トリメチルシリル基)で置換されたナフチル基であるか、縮合した2つの環からなる置換されていないナフチル基であることが好ましい。R9は、パラ位が置換された2-ナフチルまたは1-ナフチルか、パラ位が置換されていない2-ナフチルまたは1-ナフチルであることが好ましい。
R10は、脂肪族炭素環のメンバーを有する縮合環を含まないビフェニル基である。R10は、置換されていて芳香族縮合環(例えばナフチル、フェナントリル、ペリレン)を形成しているビフェニル基か、1個以上の置換基(例えばフッ素、シアノ基、ヒドロキシ基、アルキル基、アルコキシ基、アリールオキシ基、アリール基、複素環式オキシ基、カルボキシ基、トリメチルシリル基)で置換されたビフェニル基か、置換されていないビフェニル基であることが好ましい。R10は、置換されていない4-ビフェニルまたは3-ビフェニルか、縮合環を含まない他のフェニル環で置換されていて三フェニル環系を形成している4-ビフェニルまたは3-ビフェニルか、2-ビフェニルであることが好ましい。特に有用なのは、9-(2-ナフチル)-10-(4-ビフェニル)アントラセンである。
AとA'は、独立に、少なくとも1個の窒素を含む6員の芳香族環系に対応するアジン環系を表わし;
(Xa)nと(Xb)mは、独立に選択した1個以上の置換基を表わし、非環式置換基を含んでいるか、合わさってAまたはA’と縮合した環を形成し;
mとnは、独立に0〜4であり;
ZaとZbは、独立に選択した置換基であり;
1、2、3、4、1’、2’、3’、4’は、炭素原子または窒素原子として独立に選択され;
Xa、Xb、Za、Zb、1、2、3、4、1’、2’、3’、4’は、青色の光を出すように選択される。
XはOまたはSであり、R1、R2、R3、R6は、独立に、水素、アルキル、アリールのいずれかが可能であり;
R4とR5は、独立に、アルキルまたはアリールであるか;R3とR4が合わさって、またはR5とR6が合わさって、またはその両方でシクロアルキル基を完成させる原子を表わす。
CO-1:アルミニウムトリスオキシン[別名、トリス(8-キノリノラト)アルミニウム(III)]
CO-2:マグネシウムビスオキシン[別名、ビス(8-キノリノラト)マグネシウム(II)]
CO-3:ビス[ベンゾ{f}-8-キノリノラト]亜鉛(II)
CO-4:ビス(2-メチル-8-キノリノラト)アルミニウム(III)-μ-オキソ-ビス(2-メチル-8-キノリノラト)アルミニウム(III)
CO-5:インジウムトリスオキシン[別名、トリス(8-キノリノラト)インジウム]
CO-6:アルミニウムトリス(5-メチルオキシン)[別名、トリス(5-メチル-8-キノリノラト)アルミニウム(III)]
CO-7:リチウムオキシン[別名、(8-キノリノラト)リチウム(I)]
CO-8:ガリウムオキシン[別名、トリス(8-キノリノラト)ガリウム(III)]
CO-9:ジルコニウムオキシン[別名、テトラ(8-キノリノラト)ジルコニウム(IV)]
11a 画素
11b 画素
11c 画素
11d 画素
12 画素群
14 画素群
100 基板
110a 第1の電極
110b 第1の電極
110c 第1の電極
110d 第1の電極
122 正孔輸送層
123a マゼンタ色発光層
123c 緑色発光層
124 電子輸送層
130 第2の電極
140a カラー・フィルタ
140b カラー・フィルタ
140c カラー・フィルタ
160 光透過率曲線
162 光透過率曲線
170 相対的発光曲線
172 光透過率曲線
174 光透過率曲線
210a 外部発光
210b 外部発光
210c 外部発光
210d 外部発光
220a 内部発光
220b 内部発光
220c 内部発光
220d 内部発光
Claims (3)
- 少なくとも赤色画素と、緑色画素と、青色画素とを有するOLEDディスプレイであって、
a)赤色画素と青色画素のために基板上に設けられた、青色光を出す材料と赤色光を出す材料とを用いて形成されたマゼンタ色発光層と、少なくとも緑色画素を生成させるためにその基板上に設けられた緑色発光層と;
b)上記マゼンタ色発光層と作用的関係があってそれぞれ赤色画素と青色画素を生成させる第1のカラー・フィルタと第2のカラー・フィルタを備えるOLEDディスプレイ。 - 上記マゼンタ色発光層と上記緑色発光層とが部分的に重なることにより追加の白色画素を提供する、請求項1に記載のOLEDディスプレイ。
- 上記マゼンタ色発光層が、上記赤色画素と上記青色画素と上記白色画素の間で連続であり、上記緑色発光層が、上記緑色画素と上記白色画素の間で連続である、請求項2に記載のOLEDディスプレイ。
Applications Claiming Priority (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US11/113,484 US7471041B2 (en) | 2005-04-25 | 2005-04-25 | OLED multicolor displays |
US11/113,915 US7436113B2 (en) | 2005-04-25 | 2005-04-25 | Multicolor OLED displays |
US11/113,484 | 2005-04-25 | ||
US11/113,915 | 2005-04-25 | ||
US11/315,827 US7602119B2 (en) | 2005-04-25 | 2005-12-22 | OLED with magenta and green emissive layers |
US11/315,827 | 2005-12-22 | ||
PCT/US2006/015538 WO2006116346A2 (en) | 2005-04-25 | 2006-04-19 | Multicolor oled displays |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2008539555A JP2008539555A (ja) | 2008-11-13 |
JP2008539555A5 JP2008539555A5 (ja) | 2009-04-16 |
JP5558708B2 true JP5558708B2 (ja) | 2014-07-23 |
Family
ID=36793420
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JP2008509019A Withdrawn JP2008539556A (ja) | 2005-04-25 | 2006-04-19 | マルチカラーoledディスプレイ |
JP2008509018A Active JP5558708B2 (ja) | 2005-04-25 | 2006-04-19 | マルチカラーoledディスプレイ |
JP2008508929A Active JP5350781B2 (ja) | 2005-04-25 | 2006-04-19 | マルチカラーoledディスプレイ |
JP2012156174A Active JP5457512B2 (ja) | 2005-04-25 | 2012-07-12 | マルチカラーoledディスプレイ |
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JP2008509019A Withdrawn JP2008539556A (ja) | 2005-04-25 | 2006-04-19 | マルチカラーoledディスプレイ |
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JP2008508929A Active JP5350781B2 (ja) | 2005-04-25 | 2006-04-19 | マルチカラーoledディスプレイ |
JP2012156174A Active JP5457512B2 (ja) | 2005-04-25 | 2012-07-12 | マルチカラーoledディスプレイ |
Country Status (5)
Country | Link |
---|---|
US (1) | US7602119B2 (ja) |
EP (3) | EP1875510B1 (ja) |
JP (4) | JP2008539556A (ja) |
DE (3) | DE602006014815D1 (ja) |
WO (3) | WO2006116346A2 (ja) |
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KR101189154B1 (ko) * | 2006-06-08 | 2012-11-09 | 삼성디스플레이 주식회사 | 유기 발광 표시 장치 |
US20080157659A1 (en) * | 2006-12-28 | 2008-07-03 | Shiva Prakash | Electronic device including an organic device layer |
JP4479737B2 (ja) * | 2007-03-07 | 2010-06-09 | セイコーエプソン株式会社 | 発光装置およびその製造方法ならびに電子機器 |
JP4529988B2 (ja) | 2007-03-08 | 2010-08-25 | セイコーエプソン株式会社 | 発光装置ならびに電子機器 |
US8183767B2 (en) * | 2007-07-06 | 2012-05-22 | Canon Kabushiki Kaisha | Display apparatus and imaging system using the same |
JP2009037886A (ja) * | 2007-08-02 | 2009-02-19 | Seiko Epson Corp | 有機エレクトロルミネッセンス装置 |
KR20090063469A (ko) * | 2007-12-14 | 2009-06-18 | 삼성전자주식회사 | 유기박막 트랜지스터 표시판, 이의 제조 방법, 및 유기박막트랜지스터 표시판을 갖는 표시장치 |
JP5491383B2 (ja) * | 2008-03-19 | 2014-05-14 | 出光興産株式会社 | アントラセン誘導体、発光材料および有機エレクトロルミネッセンス素子 |
US8053770B2 (en) * | 2008-10-14 | 2011-11-08 | Universal Display Corporation | Emissive layer patterning for OLED |
TWI386688B (zh) * | 2009-01-08 | 2013-02-21 | Au Optronics Corp | 顯示器及其顯示面板與彩色濾光片 |
US20120161172A1 (en) * | 2009-07-06 | 2012-06-28 | Pioneer Corporation | Display device and method for manufacturing the same |
US8877356B2 (en) * | 2009-07-22 | 2014-11-04 | Global Oled Technology Llc | OLED device with stabilized yellow light-emitting layer |
DE102009042680A1 (de) * | 2009-09-23 | 2011-03-24 | Merck Patent Gmbh | Organische Elektrolumineszenzvorrichtung |
JP5609058B2 (ja) * | 2009-10-22 | 2014-10-22 | ソニー株式会社 | 表示装置 |
KR101125570B1 (ko) * | 2009-12-04 | 2012-03-22 | 삼성모바일디스플레이주식회사 | 유기 발광 장치 |
JP5431280B2 (ja) * | 2010-09-24 | 2014-03-05 | 株式会社東芝 | 有機elディスプレイ |
JP2012204164A (ja) * | 2011-03-25 | 2012-10-22 | Sony Corp | 有機el表示装置およびその製造方法 |
TWI562424B (en) | 2011-03-25 | 2016-12-11 | Semiconductor Energy Lab Co Ltd | Light-emitting panel, light-emitting device, and method for manufacturing the light-emitting panel |
JP5837316B2 (ja) * | 2011-03-25 | 2015-12-24 | 株式会社Joled | 有機el表示装置およびその製造方法 |
JP2013012477A (ja) * | 2011-06-28 | 2013-01-17 | Cbrite Inc | ハイブリッドのフルカラー・アクティブ・マトリクス有機発光ディスプレイ |
JP5927601B2 (ja) * | 2011-09-07 | 2016-06-01 | 株式会社Joled | 発光パネル、表示装置および電子機器 |
KR101407309B1 (ko) * | 2011-11-15 | 2014-06-16 | 엘지디스플레이 주식회사 | 유기 전계 발광 표시 패널 및 그의 제조 방법 |
KR101931770B1 (ko) * | 2011-11-30 | 2018-12-24 | 삼성디스플레이 주식회사 | 마스크 조립체 및 유기 발광 표시장치 |
JP6031649B2 (ja) * | 2012-01-19 | 2016-11-24 | 株式会社Joled | 有機電界発光装置、有機電界発光装置の製造方法および電子機器 |
TWI508279B (zh) | 2012-01-19 | 2015-11-11 | Joled Inc | 顯示器及其製造方法,單元,轉印方法,有機電致發光單元及其製造方法,以及電子裝置 |
JP2012156136A (ja) * | 2012-03-09 | 2012-08-16 | Sony Corp | 有機発光表示装置 |
KR102022698B1 (ko) * | 2012-05-31 | 2019-11-05 | 삼성디스플레이 주식회사 | 표시 패널 |
KR101954973B1 (ko) * | 2012-09-19 | 2019-03-08 | 삼성디스플레이 주식회사 | 유기 발광 표시 장치 |
CN104756601B (zh) * | 2012-10-30 | 2018-06-12 | 株式会社半导体能源研究所 | 发光面板、显示装置以及发光面板的制造方法 |
KR101990312B1 (ko) | 2012-12-31 | 2019-06-18 | 엘지디스플레이 주식회사 | 유기전계발광표시장치 및 그 제조방법 |
US10243023B2 (en) | 2013-01-18 | 2019-03-26 | Universal Display Corporation | Top emission AMOLED displays using two emissive layers |
US9385168B2 (en) * | 2013-01-18 | 2016-07-05 | Universal Display Corporation | High resolution low power consumption OLED display with extended lifetime |
US10580832B2 (en) | 2013-01-18 | 2020-03-03 | Universal Display Corporation | High resolution low power consumption OLED display with extended lifetime |
US9590017B2 (en) | 2013-01-18 | 2017-03-07 | Universal Display Corporation | High resolution low power consumption OLED display with extended lifetime |
US10304906B2 (en) | 2013-01-18 | 2019-05-28 | Universal Display Corporation | High resolution low power consumption OLED display with extended lifetime |
US10229956B2 (en) * | 2013-01-18 | 2019-03-12 | Universal Display Corporation | High resolution low power consumption OLED display with extended lifetime |
JP5849981B2 (ja) * | 2013-03-25 | 2016-02-03 | ソニー株式会社 | 表示装置および電子機器 |
KR102178256B1 (ko) | 2013-03-27 | 2020-11-12 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 발광 소자, 발광 장치, 전자 기기, 및 조명 장치 |
KR102060013B1 (ko) * | 2013-04-24 | 2019-12-30 | 삼성디스플레이 주식회사 | 유기 발광 표시 장치 |
KR20150014007A (ko) * | 2013-07-25 | 2015-02-06 | 삼성전자주식회사 | 이미지 센서 및 이를 포함하는 촬상 장치 |
JP2015069758A (ja) * | 2013-09-27 | 2015-04-13 | 株式会社ジャパンディスプレイ | 有機el表示装置 |
TWI515891B (zh) | 2013-11-01 | 2016-01-01 | 友達光電股份有限公司 | 顯示面板 |
JP2015138612A (ja) * | 2014-01-21 | 2015-07-30 | 株式会社ジャパンディスプレイ | 有機エレクトロルミネセンス表示装置 |
KR102320578B1 (ko) * | 2014-04-25 | 2021-11-02 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 발광 장치, 전자 기기, 및 조명 장치 |
US10700134B2 (en) | 2014-05-27 | 2020-06-30 | Universal Display Corporation | Low power consumption OLED display |
CN113299710A (zh) * | 2014-05-27 | 2021-08-24 | 环球展览公司 | 具有延长寿命的高分辨率低功耗oled显示器 |
KR102305143B1 (ko) | 2014-08-20 | 2021-09-28 | 삼성디스플레이 주식회사 | 표시 장치 및 이의 제조 방법 |
CN112992992A (zh) | 2014-10-01 | 2021-06-18 | 索尼公司 | 显示装置和电子设备 |
US10263050B2 (en) | 2015-09-18 | 2019-04-16 | Universal Display Corporation | Hybrid display |
US9818804B2 (en) | 2015-09-18 | 2017-11-14 | Universal Display Corporation | Hybrid display |
CN109076672B (zh) * | 2016-04-14 | 2020-06-23 | 夏普株式会社 | 显示装置及其制造方法 |
CN106373989B (zh) * | 2016-11-24 | 2019-10-22 | 上海天马有机发光显示技术有限公司 | 一种有机发光显示面板、电子设备以及制作方法 |
CN107068886B (zh) * | 2017-05-12 | 2019-01-25 | 京东方科技集团股份有限公司 | 有机电致发光器件及其制作方法、发光装置 |
KR20190033816A (ko) * | 2017-09-22 | 2019-04-01 | 삼성전자주식회사 | 디스플레이 패널 및 이를 포함하는 디스플레이 장치 |
US10797112B2 (en) | 2018-07-25 | 2020-10-06 | Universal Display Corporation | Energy efficient OLED TV |
KR102678994B1 (ko) * | 2019-07-03 | 2024-07-01 | 한국전자통신연구원 | 표시 장치 및 그 제조 방법 |
KR20220009651A (ko) * | 2020-07-16 | 2022-01-25 | 엘지디스플레이 주식회사 | 유기발광표시장치 |
WO2022172981A1 (ja) * | 2021-02-12 | 2022-08-18 | ソニーセミコンダクタソリューションズ株式会社 | 表示装置および電子機器 |
Family Cites Families (32)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4800375A (en) | 1986-10-24 | 1989-01-24 | Honeywell Inc. | Four color repetitive sequence matrix array for flat panel displays |
JP2584490B2 (ja) | 1988-06-13 | 1997-02-26 | 三菱電機株式会社 | マトリクス型カラ−液晶表示装置 |
US5276380A (en) | 1991-12-30 | 1994-01-04 | Eastman Kodak Company | Organic electroluminescent image display device |
US5550066A (en) | 1994-12-14 | 1996-08-27 | Eastman Kodak Company | Method of fabricating a TFT-EL pixel |
JPH0992465A (ja) * | 1995-09-22 | 1997-04-04 | Fuji Electric Co Ltd | 電場発光素子 |
JPH09274991A (ja) * | 1996-04-08 | 1997-10-21 | Fuji Electric Co Ltd | 多色発光エレクトロルミネッセンス装置 |
JPH1012379A (ja) * | 1996-06-24 | 1998-01-16 | Idemitsu Kosan Co Ltd | 多色発光装置およびその製造方法 |
JPH11354273A (ja) * | 1998-06-09 | 1999-12-24 | Idemitsu Kosan Co Ltd | 多色発光装置 |
GB9818092D0 (en) | 1998-08-19 | 1998-10-14 | Cambridge Display Tech Ltd | Display devices |
US20010043043A1 (en) | 2000-01-07 | 2001-11-22 | Megumi Aoyama | Organic electroluminescent display panel and organic electroluminescent device used therefor |
US6570584B1 (en) | 2000-05-15 | 2003-05-27 | Eastman Kodak Company | Broad color gamut display |
JP2002175879A (ja) * | 2000-12-08 | 2002-06-21 | Tdk Corp | 有機elディスプレイパネルおよびそれに用いる有機el素子 |
JP4644938B2 (ja) * | 2001-01-15 | 2011-03-09 | ソニー株式会社 | 有機電界発光素子 |
US7012588B2 (en) | 2001-06-05 | 2006-03-14 | Eastman Kodak Company | Method for saving power in an organic electroluminescent display using white light emitting elements |
US20020191130A1 (en) | 2001-06-19 | 2002-12-19 | Wei-Chen Liang | Color display utilizing combinations of four colors |
US6815723B2 (en) | 2001-12-28 | 2004-11-09 | Semiconductor Energy Laboratory Co., Ltd. | Light emitting device, method of manufacturing the same, and manufacturing apparatus therefor |
US6872472B2 (en) * | 2002-02-15 | 2005-03-29 | Eastman Kodak Company | Providing an organic electroluminescent device having stacked electroluminescent units |
JP4069745B2 (ja) * | 2002-12-26 | 2008-04-02 | 株式会社デンソー | 有機elパネル |
JP2004296136A (ja) * | 2003-03-25 | 2004-10-21 | Tdk Corp | 積層薄膜el素子およびその製造方法並びにelパネル |
KR100490322B1 (ko) * | 2003-04-07 | 2005-05-17 | 삼성전자주식회사 | 유기전계발광 표시장치 |
US6919681B2 (en) * | 2003-04-30 | 2005-07-19 | Eastman Kodak Company | Color OLED display with improved power efficiency |
US6771028B1 (en) * | 2003-04-30 | 2004-08-03 | Eastman Kodak Company | Drive circuitry for four-color organic light-emitting device |
JP4895490B2 (ja) * | 2003-09-30 | 2012-03-14 | 三洋電機株式会社 | 有機elパネル |
TWI263184B (en) | 2003-09-30 | 2006-10-01 | Sanyo Electric Co | Electroluminescence display device |
US20050116615A1 (en) | 2003-09-30 | 2005-06-02 | Shoichiro Matsumoto | Light emissive display device |
JP4716699B2 (ja) * | 2003-09-30 | 2011-07-06 | 三洋電機株式会社 | 有機elパネル |
JP4731865B2 (ja) * | 2003-10-03 | 2011-07-27 | 株式会社半導体エネルギー研究所 | 発光装置 |
US7439670B2 (en) * | 2005-02-03 | 2008-10-21 | Eastman Kodak Company | Making multicolor OLED displays |
US7142179B2 (en) * | 2005-03-23 | 2006-11-28 | Eastman Kodak Company | OLED display device |
US7436113B2 (en) * | 2005-04-25 | 2008-10-14 | Eastman Kodak Company | Multicolor OLED displays |
TWI296181B (en) * | 2005-08-01 | 2008-04-21 | Univision Technology Inc | Full color organic electroluminescent display device with low power consumption |
TWI283549B (en) * | 2005-09-30 | 2007-07-01 | Univision Technology Inc | Organic electroluminescent display device with improved color saturation and method of fabricating the same |
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JP2012195310A (ja) | 2012-10-11 |
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EP1875509B1 (en) | 2010-06-09 |
DE602006014815D1 (de) | 2010-07-22 |
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