KR100584917B1 - 유기전계발광소자 - Google Patents
유기전계발광소자 Download PDFInfo
- Publication number
- KR100584917B1 KR100584917B1 KR1019990058093A KR19990058093A KR100584917B1 KR 100584917 B1 KR100584917 B1 KR 100584917B1 KR 1019990058093 A KR1019990058093 A KR 1019990058093A KR 19990058093 A KR19990058093 A KR 19990058093A KR 100584917 B1 KR100584917 B1 KR 100584917B1
- Authority
- KR
- South Korea
- Prior art keywords
- organic
- layer
- cathode electrode
- metal
- light emitting
- Prior art date
Links
- 239000010410 layer Substances 0.000 claims abstract description 135
- 229910052751 metal Inorganic materials 0.000 claims abstract description 40
- 239000002184 metal Substances 0.000 claims abstract description 40
- 150000002894 organic compounds Chemical class 0.000 claims abstract description 33
- 150000001875 compounds Chemical class 0.000 claims abstract description 29
- -1 rare earth metal ions Chemical class 0.000 claims abstract description 27
- 125000002524 organometallic group Chemical group 0.000 claims abstract description 20
- 239000012044 organic layer Substances 0.000 claims abstract description 16
- 229910021645 metal ion Inorganic materials 0.000 claims abstract description 9
- 229910052761 rare earth metal Inorganic materials 0.000 claims abstract description 9
- 229910001413 alkali metal ion Inorganic materials 0.000 claims abstract description 6
- 229910001420 alkaline earth metal ion Inorganic materials 0.000 claims abstract description 6
- 229910052782 aluminium Inorganic materials 0.000 claims description 19
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 19
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 6
- 229910052710 silicon Inorganic materials 0.000 claims description 6
- 239000010703 silicon Substances 0.000 claims description 6
- 239000010936 titanium Substances 0.000 claims description 6
- 229910045601 alloy Inorganic materials 0.000 claims description 5
- 239000000956 alloy Substances 0.000 claims description 5
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 4
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims description 4
- 229910052706 scandium Inorganic materials 0.000 claims description 4
- SIXSYDAISGFNSX-UHFFFAOYSA-N scandium atom Chemical compound [Sc] SIXSYDAISGFNSX-UHFFFAOYSA-N 0.000 claims description 4
- 229910052719 titanium Inorganic materials 0.000 claims description 4
- 229910052727 yttrium Inorganic materials 0.000 claims description 4
- VWQVUPCCIRVNHF-UHFFFAOYSA-N yttrium atom Chemical compound [Y] VWQVUPCCIRVNHF-UHFFFAOYSA-N 0.000 claims description 4
- 229910052726 zirconium Inorganic materials 0.000 claims description 4
- 238000002347 injection Methods 0.000 abstract description 45
- 239000007924 injection Substances 0.000 abstract description 45
- 239000000463 material Substances 0.000 abstract description 10
- 238000004519 manufacturing process Methods 0.000 abstract description 9
- 230000004888 barrier function Effects 0.000 abstract description 8
- 239000007769 metal material Substances 0.000 abstract 1
- 230000005525 hole transport Effects 0.000 description 16
- 238000000151 deposition Methods 0.000 description 12
- 238000000034 method Methods 0.000 description 12
- 239000000758 substrate Substances 0.000 description 10
- 230000015572 biosynthetic process Effects 0.000 description 9
- 239000011521 glass Substances 0.000 description 8
- PQXKHYXIUOZZFA-UHFFFAOYSA-M lithium fluoride Chemical compound [Li+].[F-] PQXKHYXIUOZZFA-UHFFFAOYSA-M 0.000 description 8
- 229920000642 polymer Polymers 0.000 description 8
- 150000002484 inorganic compounds Chemical class 0.000 description 7
- 229910010272 inorganic material Inorganic materials 0.000 description 7
- 229910052744 lithium Inorganic materials 0.000 description 7
- 150000002739 metals Chemical class 0.000 description 7
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 6
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 description 6
- 239000010408 film Substances 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 5
- 230000008021 deposition Effects 0.000 description 5
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical group C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 5
- 239000007772 electrode material Substances 0.000 description 5
- 150000002500 ions Chemical class 0.000 description 5
- 239000011777 magnesium Substances 0.000 description 5
- PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical group C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 5
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 4
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 description 4
- ZSWFCLXCOIISFI-UHFFFAOYSA-N cyclopentadiene Chemical compound C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 description 4
- 239000002019 doping agent Substances 0.000 description 4
- 229910052749 magnesium Inorganic materials 0.000 description 4
- 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 4
- 150000002910 rare earth metals Chemical class 0.000 description 4
- 238000001771 vacuum deposition Methods 0.000 description 4
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 3
- PJANXHGTPQOBST-VAWYXSNFSA-N Stilbene Natural products C=1C=CC=CC=1/C=C/C1=CC=CC=C1 PJANXHGTPQOBST-VAWYXSNFSA-N 0.000 description 3
- 229910052783 alkali metal Inorganic materials 0.000 description 3
- 150000001339 alkali metal compounds Chemical class 0.000 description 3
- 150000001340 alkali metals Chemical class 0.000 description 3
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 3
- 150000001341 alkaline earth metal compounds Chemical class 0.000 description 3
- 150000001342 alkaline earth metals Chemical class 0.000 description 3
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 3
- 239000010406 cathode material Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 3
- 150000002909 rare earth metal compounds Chemical class 0.000 description 3
- 238000006722 reduction reaction Methods 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 238000004544 sputter deposition Methods 0.000 description 3
- 235000021286 stilbenes Nutrition 0.000 description 3
- 125000005504 styryl group Chemical group 0.000 description 3
- 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 2
- KLCLIOISYBHYDZ-UHFFFAOYSA-N 1,4,4-triphenylbuta-1,3-dienylbenzene Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)=CC=C(C=1C=CC=CC=1)C1=CC=CC=C1 KLCLIOISYBHYDZ-UHFFFAOYSA-N 0.000 description 2
- XJKSTNDFUHDPQJ-UHFFFAOYSA-N 1,4-diphenylbenzene Chemical group C1=CC=CC=C1C1=CC=C(C=2C=CC=CC=2)C=C1 XJKSTNDFUHDPQJ-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
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 description 2
- SULWTXOWAFVWOY-PHEQNACWSA-N 2,3-bis[(E)-2-phenylethenyl]pyrazine Chemical class C=1C=CC=CC=1/C=C/C1=NC=CN=C1\C=C\C1=CC=CC=C1 SULWTXOWAFVWOY-PHEQNACWSA-N 0.000 description 2
- 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 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- HBBGRARXTFLTSG-UHFFFAOYSA-N Lithium ion Chemical compound [Li+] HBBGRARXTFLTSG-UHFFFAOYSA-N 0.000 description 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 2
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 2
- 239000007983 Tris buffer Substances 0.000 description 2
- DGEZNRSVGBDHLK-UHFFFAOYSA-N [1,10]phenanthroline Chemical compound C1=CN=C2C3=NC=CC=C3C=CC2=C1 DGEZNRSVGBDHLK-UHFFFAOYSA-N 0.000 description 2
- DZBUGLKDJFMEHC-UHFFFAOYSA-N acridine Chemical compound C1=CC=CC2=CC3=CC=CC=C3N=C21 DZBUGLKDJFMEHC-UHFFFAOYSA-N 0.000 description 2
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 2
- 238000013475 authorization Methods 0.000 description 2
- 235000010290 biphenyl Nutrition 0.000 description 2
- 239000004305 biphenyl Substances 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- WDECIBYCCFPHNR-UHFFFAOYSA-N chrysene Chemical compound C1=CC=CC2=CC=C3C4=CC=CC=C4C=CC3=C21 WDECIBYCCFPHNR-UHFFFAOYSA-N 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 229920000547 conjugated polymer Polymers 0.000 description 2
- VPUGDVKSAQVFFS-UHFFFAOYSA-N coronene Chemical compound C1=C(C2=C34)C=CC3=CC=C(C=C3)C4=C4C3=CC=C(C=C3)C4=C2C3=C1 VPUGDVKSAQVFFS-UHFFFAOYSA-N 0.000 description 2
- AMGQUBHHOARCQH-UHFFFAOYSA-N indium;oxotin Chemical compound [In].[Sn]=O AMGQUBHHOARCQH-UHFFFAOYSA-N 0.000 description 2
- 239000003446 ligand Substances 0.000 description 2
- 229910001416 lithium ion Inorganic materials 0.000 description 2
- 150000002736 metal compounds Chemical class 0.000 description 2
- UHVLDCDWBKWDDN-UHFFFAOYSA-N n-phenyl-n-[4-[4-(n-pyren-2-ylanilino)phenyl]phenyl]pyren-2-amine Chemical group C1=CC=CC=C1N(C=1C=C2C=CC3=CC=CC4=CC=C(C2=C43)C=1)C1=CC=C(C=2C=CC(=CC=2)N(C=2C=CC=CC=2)C=2C=C3C=CC4=CC=CC5=CC=C(C3=C54)C=2)C=C1 UHVLDCDWBKWDDN-UHFFFAOYSA-N 0.000 description 2
- 150000004866 oxadiazoles Chemical class 0.000 description 2
- 229930184652 p-Terphenyl Natural products 0.000 description 2
- GPRIERYVMZVKTC-UHFFFAOYSA-N p-quaterphenyl Chemical group C1=CC=CC=C1C1=CC=C(C=2C=CC(=CC=2)C=2C=CC=CC=2)C=C1 GPRIERYVMZVKTC-UHFFFAOYSA-N 0.000 description 2
- 125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 description 2
- YNPNZTXNASCQKK-UHFFFAOYSA-N phenanthrene Chemical compound C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 description 2
- RDOWQLZANAYVLL-UHFFFAOYSA-N phenanthridine Chemical compound C1=CC=C2C3=CC=CC=C3C=NC2=C1 RDOWQLZANAYVLL-UHFFFAOYSA-N 0.000 description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
- BBEAQIROQSPTKN-UHFFFAOYSA-N pyrene Chemical compound C1=CC=C2C=CC3=CC=CC4=CC=C1C2=C43 BBEAQIROQSPTKN-UHFFFAOYSA-N 0.000 description 2
- XSCHRSMBECNVNS-UHFFFAOYSA-N quinoxaline Chemical compound N1=CC=NC2=CC=CC=C21 XSCHRSMBECNVNS-UHFFFAOYSA-N 0.000 description 2
- 150000005838 radical anions Chemical class 0.000 description 2
- VSZWPYCFIRKVQL-UHFFFAOYSA-N selanylidenegallium;selenium Chemical compound [Se].[Se]=[Ga].[Se]=[Ga] VSZWPYCFIRKVQL-UHFFFAOYSA-N 0.000 description 2
- 229910052709 silver Inorganic materials 0.000 description 2
- 239000004332 silver Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 229910052712 strontium Inorganic materials 0.000 description 2
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 2
- IATRAKWUXMZMIY-UHFFFAOYSA-N strontium oxide Chemical compound [O-2].[Sr+2] IATRAKWUXMZMIY-UHFFFAOYSA-N 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- IFLREYGFSNHWGE-UHFFFAOYSA-N tetracene Chemical compound C1=CC=CC2=CC3=CC4=CC=CC=C4C=C3C=C21 IFLREYGFSNHWGE-UHFFFAOYSA-N 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
- 238000007740 vapor deposition Methods 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- UWRZIZXBOLBCON-VOTSOKGWSA-N (e)-2-phenylethenamine Chemical class N\C=C\C1=CC=CC=C1 UWRZIZXBOLBCON-VOTSOKGWSA-N 0.000 description 1
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 1
- NGQSLSMAEVWNPU-YTEMWHBBSA-N 1,2-bis[(e)-2-phenylethenyl]benzene Chemical compound C=1C=CC=CC=1/C=C/C1=CC=CC=C1\C=C\C1=CC=CC=C1 NGQSLSMAEVWNPU-YTEMWHBBSA-N 0.000 description 1
- OURODNXVJUWPMZ-UHFFFAOYSA-N 1,2-diphenylanthracene Chemical compound C1=CC=CC=C1C1=CC=C(C=C2C(C=CC=C2)=C2)C2=C1C1=CC=CC=C1 OURODNXVJUWPMZ-UHFFFAOYSA-N 0.000 description 1
- BCMCBBGGLRIHSE-UHFFFAOYSA-N 1,3-benzoxazole Chemical compound C1=CC=C2OC=NC2=C1 BCMCBBGGLRIHSE-UHFFFAOYSA-N 0.000 description 1
- 150000000183 1,3-benzoxazoles Chemical class 0.000 description 1
- QKLPIYTUUFFRLV-YTEMWHBBSA-N 1,4-bis[(e)-2-(2-methylphenyl)ethenyl]benzene Chemical compound CC1=CC=CC=C1\C=C\C(C=C1)=CC=C1\C=C\C1=CC=CC=C1C QKLPIYTUUFFRLV-YTEMWHBBSA-N 0.000 description 1
- BCASZEAAHJEDAL-PHEQNACWSA-N 1,4-bis[(e)-2-(4-methylphenyl)ethenyl]benzene Chemical compound C1=CC(C)=CC=C1\C=C\C(C=C1)=CC=C1\C=C\C1=CC=C(C)C=C1 BCASZEAAHJEDAL-PHEQNACWSA-N 0.000 description 1
- LWGPQZLNJIVUIC-UHFFFAOYSA-N 1,4-bis[2-(2-ethylphenyl)ethenyl]benzene Chemical compound CCC1=CC=CC=C1C=CC(C=C1)=CC=C1C=CC1=CC=CC=C1CC LWGPQZLNJIVUIC-UHFFFAOYSA-N 0.000 description 1
- SWYYRSGBEBXIRE-UHFFFAOYSA-N 1,4-bis[2-(3-ethylphenyl)ethenyl]benzene Chemical compound CCC1=CC=CC(C=CC=2C=CC(C=CC=3C=C(CC)C=CC=3)=CC=2)=C1 SWYYRSGBEBXIRE-UHFFFAOYSA-N 0.000 description 1
- XBDQJALUKGQTAV-UHFFFAOYSA-N 1,4-bis[2-(3-methylphenyl)ethenyl]benzene Chemical compound CC1=CC=CC(C=CC=2C=CC(C=CC=3C=C(C)C=CC=3)=CC=2)=C1 XBDQJALUKGQTAV-UHFFFAOYSA-N 0.000 description 1
- MNCMBBIFTVWHIP-UHFFFAOYSA-N 1-anthracen-9-yl-2,2,2-trifluoroethanone Chemical group C1=CC=C2C(C(=O)C(F)(F)F)=C(C=CC=C3)C3=CC2=C1 MNCMBBIFTVWHIP-UHFFFAOYSA-N 0.000 description 1
- UVHXEHGUEKARKZ-UHFFFAOYSA-N 1-ethenylanthracene Chemical compound C1=CC=C2C=C3C(C=C)=CC=CC3=CC2=C1 UVHXEHGUEKARKZ-UHFFFAOYSA-N 0.000 description 1
- GUPMCMZMDAGSPF-UHFFFAOYSA-N 1-phenylbuta-1,3-dienylbenzene Chemical compound C=1C=CC=CC=1[C](C=C[CH2])C1=CC=CC=C1 GUPMCMZMDAGSPF-UHFFFAOYSA-N 0.000 description 1
- UIWLITBBFICQKW-UHFFFAOYSA-N 1h-benzo[h]quinolin-2-one Chemical compound C1=CC=C2C3=NC(O)=CC=C3C=CC2=C1 UIWLITBBFICQKW-UHFFFAOYSA-N 0.000 description 1
- 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 description 1
- OWTKICLARQLANW-UHFFFAOYSA-N 2,5-bis(2-pyren-1-ylethenyl)pyrazine Chemical compound C1=C2C(C=CC3=NC=C(N=C3)C=CC=3C4=CC=C5C=CC=C6C=CC(C4=C65)=CC=3)=CC=C(C=C3)C2=C2C3=CC=CC2=C1 OWTKICLARQLANW-UHFFFAOYSA-N 0.000 description 1
- ZGXQLVRLPJXTIK-LQIBPGRFSA-N 2,5-bis[(e)-2-(4-methoxyphenyl)ethenyl]pyrazine Chemical compound C1=CC(OC)=CC=C1\C=C\C(N=C1)=CN=C1\C=C\C1=CC=C(OC)C=C1 ZGXQLVRLPJXTIK-LQIBPGRFSA-N 0.000 description 1
- PAJSTGVSGZWCGO-UHFFFAOYSA-N 2,5-bis[2-(4-ethylphenyl)ethenyl]pyrazine Chemical compound C1=CC(CC)=CC=C1C=CC(N=C1)=CN=C1C=CC1=CC=C(CC)C=C1 PAJSTGVSGZWCGO-UHFFFAOYSA-N 0.000 description 1
- BFQSAUNFPAHVRZ-UHFFFAOYSA-N 2,5-bis[2-(4-methylphenyl)ethenyl]pyrazine Chemical compound C1=CC(C)=CC=C1C=CC(N=C1)=CN=C1C=CC1=CC=C(C)C=C1 BFQSAUNFPAHVRZ-UHFFFAOYSA-N 0.000 description 1
- BDMRRCGWWDZRRG-UHFFFAOYSA-N 2-[2-(4-chlorophenyl)ethenyl]benzo[e][1,3]benzoxazole Chemical compound C1=CC(Cl)=CC=C1C=CC(O1)=NC2=C1C=CC1=CC=CC=C21 BDMRRCGWWDZRRG-UHFFFAOYSA-N 0.000 description 1
- JDDDDNVALGZAMR-UHFFFAOYSA-N 2-[4-[2-(1h-benzimidazol-2-yl)ethenyl]phenyl]-1h-benzimidazole Chemical compound C1=CC=C2NC(C=CC=3C=CC(=CC=3)C=3NC4=CC=CC=C4N=3)=NC2=C1 JDDDDNVALGZAMR-UHFFFAOYSA-N 0.000 description 1
- XFPKINQJEVMALK-UHFFFAOYSA-N 2-[4-[4-(1,3-benzoxazol-2-yl)phenyl]phenyl]-1,3-benzoxazole Chemical group C1=CC=C2OC(C3=CC=C(C=C3)C3=CC=C(C=C3)C=3OC4=CC=CC=C4N=3)=NC2=C1 XFPKINQJEVMALK-UHFFFAOYSA-N 0.000 description 1
- SMRCQMRVIVSYOX-UHFFFAOYSA-N 2-[5-[5,7-bis(2-methylbutan-2-yl)-1,3-benzoxazol-2-yl]-1,3,4-thiadiazol-2-yl]-5,7-bis(2-methylbutan-2-yl)-1,3-benzoxazole Chemical compound CCC(C)(C)C1=CC(C(C)(C)CC)=C2OC(C3=NN=C(S3)C=3OC4=C(C=C(C=C4N=3)C(C)(C)CC)C(C)(C)CC)=NC2=C1 SMRCQMRVIVSYOX-UHFFFAOYSA-N 0.000 description 1
- HNPLZFFFNHWZPM-UHFFFAOYSA-N 2-[5-[5,7-bis(2-methylbutan-2-yl)-1,3-benzoxazol-2-yl]-3,4-diphenylthiophen-2-yl]-5,7-bis(2-methylbutan-2-yl)-1,3-benzoxazole Chemical compound N=1C2=CC(C(C)(C)CC)=CC(C(C)(C)CC)=C2OC=1C=1SC(C=2OC3=C(C=C(C=C3N=2)C(C)(C)CC)C(C)(C)CC)=C(C=2C=CC=CC=2)C=1C1=CC=CC=C1 HNPLZFFFNHWZPM-UHFFFAOYSA-N 0.000 description 1
- MUMFNDFRZDYMNG-UHFFFAOYSA-N 2-[5-[5,7-bis(2-methylbutan-2-yl)-1,3-benzoxazol-2-yl]thiophen-2-yl]-5,7-bis(2-methylbutan-2-yl)-1,3-benzoxazole Chemical compound CCC(C)(C)C1=CC(C(C)(C)CC)=C2OC(C3=CC=C(S3)C=3OC4=C(C=C(C=C4N=3)C(C)(C)CC)C(C)(C)CC)=NC2=C1 MUMFNDFRZDYMNG-UHFFFAOYSA-N 0.000 description 1
- TZUPZYHCGXBTIJ-UHFFFAOYSA-N 2-ethyl-1,4-bis[2-(2-methylphenyl)ethenyl]benzene Chemical compound C=1C=C(C=CC=2C(=CC=CC=2)C)C(CC)=CC=1C=CC1=CC=CC=C1C TZUPZYHCGXBTIJ-UHFFFAOYSA-N 0.000 description 1
- SVNTXZRQFPYYHV-UHFFFAOYSA-N 2-methyl-1,4-bis[2-(2-methylphenyl)ethenyl]benzene Chemical compound CC1=CC=CC=C1C=CC(C=C1C)=CC=C1C=CC1=CC=CC=C1C SVNTXZRQFPYYHV-UHFFFAOYSA-N 0.000 description 1
- 125000004398 2-methyl-2-butyl group Chemical group CC(C)(CC)* 0.000 description 1
- MVLOINQUZSPUJS-UHFFFAOYSA-N 2-n,2-n,6-n,6-n-tetrakis(4-methylphenyl)naphthalene-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 MVLOINQUZSPUJS-UHFFFAOYSA-N 0.000 description 1
- MATLFWDVOBGZFG-UHFFFAOYSA-N 2-n,2-n,6-n,6-n-tetranaphthalen-1-ylnaphthalene-2,6-diamine Chemical compound 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 MATLFWDVOBGZFG-UHFFFAOYSA-N 0.000 description 1
- DJIXFCSAUCLVLK-UHFFFAOYSA-N 2-n,2-n,6-n,6-n-tetranaphthalen-2-yl-9h-fluorene-2,6-diamine Chemical compound C1=CC=CC2=CC(N(C=3C=C4C=CC=CC4=CC=3)C3=CC=C4CC5=CC(=CC=C5C4=C3)N(C=3C=C4C=CC=CC4=CC=3)C=3C=C4C=CC=CC4=CC=3)=CC=C21 DJIXFCSAUCLVLK-UHFFFAOYSA-N 0.000 description 1
- FZTBAQBBLSYHJZ-UHFFFAOYSA-N 2-phenyl-1,3-oxazol-4-ol Chemical compound OC1=COC(C=2C=CC=CC=2)=N1 FZTBAQBBLSYHJZ-UHFFFAOYSA-N 0.000 description 1
- CCMLIFHRMDXEBM-UHFFFAOYSA-N 2-phenyl-1,3-thiazol-4-ol Chemical compound OC1=CSC(C=2C=CC=CC=2)=N1 CCMLIFHRMDXEBM-UHFFFAOYSA-N 0.000 description 1
- HJJXCBIOYBUVBH-UHFFFAOYSA-N 2-phenyl-1h-benzimidazol-4-ol Chemical compound N1C=2C(O)=CC=CC=2N=C1C1=CC=CC=C1 HJJXCBIOYBUVBH-UHFFFAOYSA-N 0.000 description 1
- VHRHRMPFHJXSNR-UHFFFAOYSA-N 2-phenylpyridin-3-ol Chemical compound OC1=CC=CN=C1C1=CC=CC=C1 VHRHRMPFHJXSNR-UHFFFAOYSA-N 0.000 description 1
- JMTMSDXUXJISAY-UHFFFAOYSA-N 2H-benzotriazol-4-ol Chemical compound OC1=CC=CC2=C1N=NN2 JMTMSDXUXJISAY-UHFFFAOYSA-N 0.000 description 1
- MGADZUXDNSDTHW-UHFFFAOYSA-N 2H-pyran Chemical compound C1OC=CC=C1 MGADZUXDNSDTHW-UHFFFAOYSA-N 0.000 description 1
- OGGKVJMNFFSDEV-UHFFFAOYSA-N 3-methyl-n-[4-[4-(n-(3-methylphenyl)anilino)phenyl]phenyl]-n-phenylaniline Chemical group CC1=CC=CC(N(C=2C=CC=CC=2)C=2C=CC(=CC=2)C=2C=CC(=CC=2)N(C=2C=CC=CC=2)C=2C=C(C)C=CC=2)=C1 OGGKVJMNFFSDEV-UHFFFAOYSA-N 0.000 description 1
- HQPIRXQACTZROS-UHFFFAOYSA-N 4-[2-(1h-benzimidazol-2-yl)ethenyl]benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1C=CC1=NC2=CC=CC=C2N1 HQPIRXQACTZROS-UHFFFAOYSA-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
- DUSWRTUHJVJVRY-UHFFFAOYSA-N 4-methyl-n-[4-[2-[4-(4-methyl-n-(4-methylphenyl)anilino)phenyl]propan-2-yl]phenyl]-n-(4-methylphenyl)aniline Chemical compound C1=CC(C)=CC=C1N(C=1C=CC(=CC=1)C(C)(C)C=1C=CC(=CC=1)N(C=1C=CC(C)=CC=1)C=1C=CC(C)=CC=1)C1=CC=C(C)C=C1 DUSWRTUHJVJVRY-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
- XIQGFRHAIQHZBD-UHFFFAOYSA-N 4-methyl-n-[4-[[4-(4-methyl-n-(4-methylphenyl)anilino)phenyl]-phenylmethyl]phenyl]-n-(4-methylphenyl)aniline Chemical compound C1=CC(C)=CC=C1N(C=1C=CC(=CC=1)C(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 XIQGFRHAIQHZBD-UHFFFAOYSA-N 0.000 description 1
- UYEBVQUTQHTYOU-UHFFFAOYSA-N 5-methyl-2-[4-[2-(5-methyl-1,3-benzoxazol-2-yl)ethenyl]phenyl]-1,3-benzoxazole Chemical compound CC1=CC=C2OC(C3=CC=C(C=C3)C=CC=3OC4=CC=C(C=C4N=3)C)=NC2=C1 UYEBVQUTQHTYOU-UHFFFAOYSA-N 0.000 description 1
- XPLXHDHGYSONMX-UHFFFAOYSA-N 5-methyl-2-[5-(5-methyl-1,3-benzoxazol-2-yl)thiophen-2-yl]-1,3-benzoxazole Chemical compound CC1=CC=C2OC(C3=CC=C(S3)C=3OC4=CC=C(C=C4N=3)C)=NC2=C1 XPLXHDHGYSONMX-UHFFFAOYSA-N 0.000 description 1
- CFNMUZCFSDMZPQ-GHXNOFRVSA-N 7-[(z)-3-methyl-4-(4-methyl-5-oxo-2h-furan-2-yl)but-2-enoxy]chromen-2-one Chemical compound C=1C=C2C=CC(=O)OC2=CC=1OC/C=C(/C)CC1OC(=O)C(C)=C1 CFNMUZCFSDMZPQ-GHXNOFRVSA-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
- VESMRDNBVZOIEN-UHFFFAOYSA-N 9h-carbazole-1,2-diamine Chemical compound C1=CC=C2C3=CC=C(N)C(N)=C3NC2=C1 VESMRDNBVZOIEN-UHFFFAOYSA-N 0.000 description 1
- 229930192334 Auxin Natural products 0.000 description 1
- ROFVEXUMMXZLPA-UHFFFAOYSA-N Bipyridyl Chemical group N1=CC=CC=C1C1=CC=CC=N1 ROFVEXUMMXZLPA-UHFFFAOYSA-N 0.000 description 1
- HKZHJLHKUPHYSX-UHFFFAOYSA-N C1(=CC2=CC=C3C=CC4=CC=C5C=CC6=CC=C1C1=C6C5=C4C3=C21)N(C2=CC=CC=C2)C2=CC=C(C=C2)C2=CC=C(C=C2)N(C2=CC1=CC=C3C=CC4=CC=C5C=CC6=CC=C2C2=C6C5=C4C3=C12)C1=CC=CC=C1.C1(=CC2=CC=C3C=CC4=CC=C5C=CC6=CC=C1C1=C6C5=C4C3=C21)N(C2=CC=CC=C2)C2=CC=C(C=C2)C2=CC=C(C=C2)N(C2=CC1=CC=C3C=CC4=CC=C5C=CC6=CC=C2C2=C6C5=C4C3=C12)C1=CC=CC=C1 Chemical group C1(=CC2=CC=C3C=CC4=CC=C5C=CC6=CC=C1C1=C6C5=C4C3=C21)N(C2=CC=CC=C2)C2=CC=C(C=C2)C2=CC=C(C=C2)N(C2=CC1=CC=C3C=CC4=CC=C5C=CC6=CC=C2C2=C6C5=C4C3=C12)C1=CC=CC=C1.C1(=CC2=CC=C3C=CC4=CC=C5C=CC6=CC=C1C1=C6C5=C4C3=C21)N(C2=CC=CC=C2)C2=CC=C(C=C2)C2=CC=C(C=C2)N(C2=CC1=CC=C3C=CC4=CC=C5C=CC6=CC=C2C2=C6C5=C4C3=C12)C1=CC=CC=C1 HKZHJLHKUPHYSX-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 description 1
- 239000002841 Lewis acid Substances 0.000 description 1
- 229910000861 Mg alloy Inorganic materials 0.000 description 1
- NRCMAYZCPIVABH-UHFFFAOYSA-N Quinacridone Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C=C1C(=O)C3=CC=CC=C3NC1=C2 NRCMAYZCPIVABH-UHFFFAOYSA-N 0.000 description 1
- 229910052772 Samarium Inorganic materials 0.000 description 1
- XBDYBAVJXHJMNQ-UHFFFAOYSA-N Tetrahydroanthracene Natural products C1=CC=C2C=C(CCCC3)C3=CC2=C1 XBDYBAVJXHJMNQ-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- XIVOUNPJCNJBPR-UHFFFAOYSA-N acridin-1-ol Chemical compound C1=CC=C2C=C3C(O)=CC=CC3=NC2=C1 XIVOUNPJCNJBPR-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 150000005010 aminoquinolines Chemical class 0.000 description 1
- 150000001454 anthracenes Chemical class 0.000 description 1
- 239000002363 auxin Substances 0.000 description 1
- 125000005605 benzo group Chemical group 0.000 description 1
- 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 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 1
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 1
- 239000000292 calcium oxide Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000010549 co-Evaporation Methods 0.000 description 1
- 229920001940 conductive polymer Polymers 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- 238000003618 dip coating Methods 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 230000005684 electric field Effects 0.000 description 1
- 239000012777 electrically insulating material Substances 0.000 description 1
- 238000001194 electroluminescence spectrum Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- GVEPBJHOBDJJJI-UHFFFAOYSA-N fluoranthrene Natural products C1=CC(C2=CC=CC=C22)=C3C2=CC=CC3=C1 GVEPBJHOBDJJJI-UHFFFAOYSA-N 0.000 description 1
- GNBHRKFJIUUOQI-UHFFFAOYSA-N fluorescein Chemical compound O1C(=O)C2=CC=CC=C2C21C1=CC=C(O)C=C1OC1=CC(O)=CC=C21 GNBHRKFJIUUOQI-UHFFFAOYSA-N 0.000 description 1
- 239000006081 fluorescent whitening agent Substances 0.000 description 1
- 229910052733 gallium Inorganic materials 0.000 description 1
- RBTKNAXYKSUFRK-UHFFFAOYSA-N heliogen blue Chemical compound [Cu].[N-]1C2=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=NC([N-]1)=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=N2 RBTKNAXYKSUFRK-UHFFFAOYSA-N 0.000 description 1
- 150000002391 heterocyclic compounds Chemical class 0.000 description 1
- 150000004678 hydrides Chemical class 0.000 description 1
- NPZTUJOABDZTLV-UHFFFAOYSA-N hydroxybenzotriazole Substances O=C1C=CC=C2NNN=C12 NPZTUJOABDZTLV-UHFFFAOYSA-N 0.000 description 1
- 150000002466 imines Chemical class 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 description 1
- SEOVTRFCIGRIMH-UHFFFAOYSA-N indole-3-acetic acid Chemical compound C1=CC=C2C(CC(=O)O)=CNC2=C1 SEOVTRFCIGRIMH-UHFFFAOYSA-N 0.000 description 1
- 238000007641 inkjet printing Methods 0.000 description 1
- 150000007517 lewis acids Chemical class 0.000 description 1
- DZVCFNFOPIZQKX-LTHRDKTGSA-M merocyanine Chemical compound [Na+].O=C1N(CCCC)C(=O)N(CCCC)C(=O)C1=C\C=C\C=C/1N(CCCS([O-])(=O)=O)C2=CC=CC=C2O\1 DZVCFNFOPIZQKX-LTHRDKTGSA-M 0.000 description 1
- 229910001092 metal group alloy Inorganic materials 0.000 description 1
- WLDXVGCMDLRPHA-UHFFFAOYSA-N n,n-diphenyl-4-[4-(n-phenylanilino)phenyl]aniline;9-phenylcarbazole Chemical compound C1=CC=CC=C1N1C2=CC=CC=C2C2=CC=CC=C21.C1=CC=CC=C1N(C=1C=CC(=CC=1)C=1C=CC(=CC=1)N(C=1C=CC=CC=1)C=1C=CC=CC=1)C1=CC=CC=C1 WLDXVGCMDLRPHA-UHFFFAOYSA-N 0.000 description 1
- BBDFECYVDQCSCN-UHFFFAOYSA-N n-(4-methoxyphenyl)-4-[4-(n-(4-methoxyphenyl)anilino)phenyl]-n-phenylaniline Chemical group C1=CC(OC)=CC=C1N(C=1C=CC(=CC=1)C=1C=CC(=CC=1)N(C=1C=CC=CC=1)C=1C=CC(OC)=CC=1)C1=CC=CC=C1 BBDFECYVDQCSCN-UHFFFAOYSA-N 0.000 description 1
- PNDZMQXAYSNTMT-UHFFFAOYSA-N n-(4-naphthalen-1-ylphenyl)-4-[4-(n-(4-naphthalen-1-ylphenyl)anilino)phenyl]-n-phenylaniline Chemical group C1=CC=CC=C1N(C=1C=CC(=CC=1)C=1C2=CC=CC=C2C=CC=1)C1=CC=C(C=2C=CC(=CC=2)N(C=2C=CC=CC=2)C=2C=CC(=CC=2)C=2C3=CC=CC=C3C=CC=2)C=C1 PNDZMQXAYSNTMT-UHFFFAOYSA-N 0.000 description 1
- OMQCLPPEEURTMR-UHFFFAOYSA-N n-[4-[4-(n-fluoranthen-8-ylanilino)phenyl]phenyl]-n-phenylfluoranthen-8-amine Chemical group C1=CC=CC=C1N(C=1C=C2C(C=3C=CC=C4C=CC=C2C=34)=CC=1)C1=CC=C(C=2C=CC(=CC=2)N(C=2C=CC=CC=2)C=2C=C3C(C=4C=CC=C5C=CC=C3C=45)=CC=2)C=C1 OMQCLPPEEURTMR-UHFFFAOYSA-N 0.000 description 1
- BLFVVZKSHYCRDR-UHFFFAOYSA-N n-[4-[4-(n-naphthalen-2-ylanilino)phenyl]phenyl]-n-phenylnaphthalen-2-amine Chemical group C1=CC=CC=C1N(C=1C=C2C=CC=CC2=CC=1)C1=CC=C(C=2C=CC(=CC=2)N(C=2C=CC=CC=2)C=2C=C3C=CC=CC3=CC=2)C=C1 BLFVVZKSHYCRDR-UHFFFAOYSA-N 0.000 description 1
- LUBWJINDFCNHLI-UHFFFAOYSA-N n-[4-[4-(n-perylen-2-ylanilino)phenyl]phenyl]-n-phenylperylen-2-amine Chemical group C1=CC=CC=C1N(C=1C=C2C=3C=CC=C4C=CC=C(C=34)C=3C=CC=C(C2=3)C=1)C1=CC=C(C=2C=CC(=CC=2)N(C=2C=CC=CC=2)C=2C=C3C=4C=CC=C5C=CC=C(C=45)C=4C=CC=C(C3=4)C=2)C=C1 LUBWJINDFCNHLI-UHFFFAOYSA-N 0.000 description 1
- TUPXWIUQIGEYST-UHFFFAOYSA-N n-[4-[4-(n-phenanthren-2-ylanilino)phenyl]phenyl]-n-phenylphenanthren-2-amine Chemical group C1=CC=CC=C1N(C=1C=C2C(C3=CC=CC=C3C=C2)=CC=1)C1=CC=C(C=2C=CC(=CC=2)N(C=2C=CC=CC=2)C=2C=C3C(C4=CC=CC=C4C=C3)=CC=2)C=C1 TUPXWIUQIGEYST-UHFFFAOYSA-N 0.000 description 1
- NBHXGUASDDSHGV-UHFFFAOYSA-N n-[4-[4-[4-(n-naphthalen-1-ylanilino)phenyl]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)C=2C=CC(=CC=2)N(C=2C=CC=CC=2)C=2C3=CC=CC=C3C=CC=2)C=C1 NBHXGUASDDSHGV-UHFFFAOYSA-N 0.000 description 1
- RJSTZCQRFUSBJV-UHFFFAOYSA-N n-[4-[4-[n-(1,2-dihydroacenaphthylen-3-yl)anilino]phenyl]phenyl]-n-phenyl-1,2-dihydroacenaphthylen-3-amine Chemical group C1=CC(C2=3)=CC=CC=3CCC2=C1N(C=1C=CC(=CC=1)C=1C=CC(=CC=1)N(C=1C=CC=CC=1)C=1C=2CCC3=CC=CC(C=23)=CC=1)C1=CC=CC=C1 RJSTZCQRFUSBJV-UHFFFAOYSA-N 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- 229910052755 nonmetal Inorganic materials 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- WCPAKWJPBJAGKN-UHFFFAOYSA-N oxadiazole Chemical compound C1=CON=N1 WCPAKWJPBJAGKN-UHFFFAOYSA-N 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- DGBWPZSGHAXYGK-UHFFFAOYSA-N perinone Chemical compound C12=NC3=CC=CC=C3N2C(=O)C2=CC=C3C4=C2C1=CC=C4C(=O)N1C2=CC=CC=C2N=C13 DGBWPZSGHAXYGK-UHFFFAOYSA-N 0.000 description 1
- 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 1
- KELCFVWDYYCEOQ-UHFFFAOYSA-N phenanthridin-1-ol Chemical compound C1=CC=CC2=C3C(O)=CC=CC3=NC=C21 KELCFVWDYYCEOQ-UHFFFAOYSA-N 0.000 description 1
- 229920003227 poly(N-vinyl carbazole) Polymers 0.000 description 1
- 229920000548 poly(silane) polymer Polymers 0.000 description 1
- 229920000767 polyaniline Polymers 0.000 description 1
- 125000003367 polycyclic group Chemical group 0.000 description 1
- 150000004032 porphyrins Chemical class 0.000 description 1
- LISFMEBWQUVKPJ-UHFFFAOYSA-N quinolin-2-ol Chemical compound C1=CC=C2NC(=O)C=CC2=C1 LISFMEBWQUVKPJ-UHFFFAOYSA-N 0.000 description 1
- 150000005839 radical cations Chemical class 0.000 description 1
- 238000011946 reduction process Methods 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 229910052701 rubidium Inorganic materials 0.000 description 1
- IGLNJRXAVVLDKE-UHFFFAOYSA-N rubidium atom Chemical compound [Rb] IGLNJRXAVVLDKE-UHFFFAOYSA-N 0.000 description 1
- 229910001952 rubidium oxide Inorganic materials 0.000 description 1
- CWBWCLMMHLCMAM-UHFFFAOYSA-M rubidium(1+);hydroxide Chemical compound [OH-].[Rb+].[Rb+] CWBWCLMMHLCMAM-UHFFFAOYSA-M 0.000 description 1
- YYMBJDOZVAITBP-UHFFFAOYSA-N rubrene Chemical compound C1=CC=CC=C1C(C1=C(C=2C=CC=CC=2)C2=CC=CC=C2C(C=2C=CC=CC=2)=C11)=C(C=CC=C2)C2=C1C1=CC=CC=C1 YYMBJDOZVAITBP-UHFFFAOYSA-N 0.000 description 1
- KZUNJOHGWZRPMI-UHFFFAOYSA-N samarium atom Chemical compound [Sm] KZUNJOHGWZRPMI-UHFFFAOYSA-N 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- FZHAPNGMFPVSLP-UHFFFAOYSA-N silanamine Chemical class [SiH3]N FZHAPNGMFPVSLP-UHFFFAOYSA-N 0.000 description 1
- 238000004528 spin coating Methods 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 229930192474 thiophene Natural products 0.000 description 1
- IBBLKSWSCDAPIF-UHFFFAOYSA-N thiopyran Chemical compound S1C=CC=C=C1 IBBLKSWSCDAPIF-UHFFFAOYSA-N 0.000 description 1
- NZFNXWQNBYZDAQ-UHFFFAOYSA-N thioridazine hydrochloride Chemical compound Cl.C12=CC(SC)=CC=C2SC2=CC=CC=C2N1CCC1CCCCN1C NZFNXWQNBYZDAQ-UHFFFAOYSA-N 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc 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
- H10K50/00—Organic light-emitting devices
- H10K50/80—Constructional details
- H10K50/805—Electrodes
- H10K50/82—Cathodes
-
- 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
- H05B33/26—Light sources with substantially two-dimensional radiating surfaces characterised by the composition or arrangement of the conductive material used as an electrode
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K50/00—Organic light-emitting devices
- H10K50/10—OLEDs or polymer light-emitting diodes [PLED]
- H10K50/14—Carrier transporting layers
- H10K50/16—Electron transporting layers
- H10K50/165—Electron transporting layers comprising dopants
-
- 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
- H10K85/30—Coordination compounds
-
- 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
- H10K85/30—Coordination compounds
- H10K85/321—Metal complexes comprising a group IIIA element, e.g. Tris (8-hydroxyquinoline) gallium [Gaq3]
- H10K85/324—Metal complexes comprising a group IIIA element, e.g. Tris (8-hydroxyquinoline) gallium [Gaq3] comprising aluminium, e.g. Alq3
-
- 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
- H10K85/631—Amine compounds having at least two aryl rest on at least one amine-nitrogen atom, e.g. triphenylamine
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S428/00—Stock material or miscellaneous articles
- Y10S428/917—Electroluminescent
Landscapes
- Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Electroluminescent Light Sources (AREA)
Abstract
Description
Claims (4)
- 음극전극과 상기 음극전극에 대향하는 양극전극과의 사이에 유기화합물로 구성되는 적어도 하나의 발광층을 포함하는 유기전계발광소자에 있어서,상기 음극전극에 인접하며, 알칼리금속이온, 알칼리토금속이온 및 희토류금속이온으로 구성되는 그룹으로부터 선택된 적어도 하나의 부재(member)를 함유하는 유기금속착체화합물과 전자수송성유기화합물의 혼합층으로 구성되는 유기층을 포함하며,상기 음극전극은, 상기 혼합층의 상기 유기금속착체화합물에 함유되는 금속이온을 진공중에서 해당 금속으로 환원할 수 있는 금속을 포함하는 유기전계발광소자.
- 제 1항에 있어서, 상기 혼합층은 상기 유기금속착체화합물과 상기 전자수송성유기화합물의 공증착에 의해 형성되는 층인 것을 특징으로 하는 유기전계발광소자.
- 제 1항에 있어서, 상기 음극전극을 형성하는 데 사용되는 금속은 알루미늄, 지르코늄, 티타늄, 이트륨, 스칸듐 및 실리콘 중 하나인 것을 특징으로 하는 유기전계발광소자.
- 제 1항에 있어서, 상기 음극전극을 형성하는 데 사용되는 금속은 알루미늄, 지르코늄, 티타늄, 이트륨, 스칸듐 및 실리콘 중의 적어도 어느 하나를 함유하는 합금인 것을 특징으로 하는 유기전계발광소자.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP35789998A JP4505067B2 (ja) | 1998-12-16 | 1998-12-16 | 有機エレクトロルミネッセント素子 |
JP10-357899 | 1998-12-16 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR20000048161A KR20000048161A (ko) | 2000-07-25 |
KR100584917B1 true KR100584917B1 (ko) | 2006-05-29 |
Family
ID=18456513
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019990058093A KR100584917B1 (ko) | 1998-12-16 | 1999-12-15 | 유기전계발광소자 |
Country Status (8)
Country | Link |
---|---|
US (1) | US6396209B1 (ko) |
EP (1) | EP1011155B1 (ko) |
JP (1) | JP4505067B2 (ko) |
KR (1) | KR100584917B1 (ko) |
CN (1) | CN100372144C (ko) |
AT (1) | ATE242548T1 (ko) |
DE (1) | DE69908537T2 (ko) |
TW (1) | TW435052B (ko) |
Families Citing this family (127)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB0128074D0 (en) * | 2001-11-23 | 2002-01-16 | Elam T Ltd | Doped lithium quinolate |
JP4514841B2 (ja) | 1998-02-17 | 2010-07-28 | 淳二 城戸 | 有機エレクトロルミネッセント素子 |
JP4505067B2 (ja) * | 1998-12-16 | 2010-07-14 | 淳二 城戸 | 有機エレクトロルミネッセント素子 |
EP1173049B1 (en) * | 2000-02-02 | 2015-05-27 | Mitsubishi Chemical Corporation | Organic electroluminescent element |
KR100329571B1 (ko) * | 2000-03-27 | 2002-03-23 | 김순택 | 유기 전자 발광소자 |
KR20010104215A (ko) * | 2000-05-12 | 2001-11-24 | 야마자끼 순페이 | 발광장치 제작방법 |
CN101026226B (zh) * | 2000-09-07 | 2011-09-14 | 出光兴产株式会社 | 有机电场发光元件 |
DE10152655B4 (de) * | 2000-10-17 | 2013-10-02 | Samsung Display Co., Ltd. | Verfahren zur Herstellung einer organischen Elektrolumineszenz-Vorrichtung |
SG138466A1 (en) | 2000-12-28 | 2008-01-28 | Semiconductor Energy Lab | Luminescent device |
TW545080B (en) | 2000-12-28 | 2003-08-01 | Semiconductor Energy Lab | Light emitting device and method of manufacturing the same |
TW518909B (en) * | 2001-01-17 | 2003-01-21 | Semiconductor Energy Lab | Luminescent device and method of manufacturing same |
TW519770B (en) * | 2001-01-18 | 2003-02-01 | Semiconductor Energy Lab | Light emitting device and manufacturing method thereof |
KR100392707B1 (ko) * | 2001-01-29 | 2003-07-28 | 주식회사모나미 | 유기 전기 발광소자 및 그 제조방법 |
SG118110A1 (en) | 2001-02-01 | 2006-01-27 | Semiconductor Energy Lab | Organic light emitting element and display device using the element |
US20020139303A1 (en) | 2001-02-01 | 2002-10-03 | Shunpei Yamazaki | Deposition apparatus and deposition method |
TWI225312B (en) * | 2001-02-08 | 2004-12-11 | Semiconductor Energy Lab | Light emitting device |
US20030010288A1 (en) * | 2001-02-08 | 2003-01-16 | Shunpei Yamazaki | Film formation apparatus and film formation method |
TW550672B (en) * | 2001-02-21 | 2003-09-01 | Semiconductor Energy Lab | Method and apparatus for film deposition |
SG118118A1 (en) * | 2001-02-22 | 2006-01-27 | Semiconductor Energy Lab | Organic light emitting device and display using the same |
US6841932B2 (en) * | 2001-03-08 | 2005-01-11 | Xerox Corporation | Display devices with organic-metal mixed layer |
KR100841850B1 (ko) | 2001-08-09 | 2008-06-27 | 이데미쓰 고산 가부시키가이샤 | 유기 전자 발광 표시 장치 및 이의 구동 방법 |
KR100495407B1 (ko) | 2001-08-20 | 2005-06-14 | 티디케이가부시기가이샤 | 유기el소자 및 그 제조방법 |
US6734457B2 (en) * | 2001-11-27 | 2004-05-11 | Semiconductor Energy Laboratory Co., Ltd. | Light emitting device |
US6723445B2 (en) * | 2001-12-31 | 2004-04-20 | Canon Kabushiki Kaisha | Organic light-emitting devices |
AU2002323418A1 (en) | 2002-04-08 | 2003-10-27 | The University Of Southern California | Doped organic carrier transport materials |
US20030230980A1 (en) * | 2002-06-18 | 2003-12-18 | Forrest Stephen R | Very low voltage, high efficiency phosphorescent oled in a p-i-n structure |
US7254331B2 (en) * | 2002-08-09 | 2007-08-07 | Micron Technology, Inc. | System and method for multiple bit optical data transmission in memory systems |
WO2004028217A1 (ja) * | 2002-09-20 | 2004-04-01 | Idemitsu Kosan Co., Ltd. | 有機エレクトロルミネッセンス素子 |
JP2004172090A (ja) | 2002-10-31 | 2004-06-17 | Seiko Epson Corp | エレクトロルミネッセンス装置の製造方法及びエレクトロルミネッセンス装置、並びに電子機器 |
JP4350996B2 (ja) | 2002-11-26 | 2009-10-28 | 日東電工株式会社 | 有機エレクトロルミネッセンス素子、面光源および表示装置 |
JP3900125B2 (ja) * | 2002-11-26 | 2007-04-04 | セイコーエプソン株式会社 | 有機エレクトロルミネッセンス装置の製造方法 |
JP2004193011A (ja) * | 2002-12-12 | 2004-07-08 | Fuji Photo Film Co Ltd | 有機電界発光素子 |
JP4683924B2 (ja) * | 2002-12-19 | 2011-05-18 | 株式会社半導体エネルギー研究所 | 発光材料、電界発光素子、及び発光装置 |
GB0230072D0 (en) * | 2002-12-24 | 2003-01-29 | Elam T Ltd | Electroluminescent materials and devices |
US20050129978A1 (en) * | 2002-12-25 | 2005-06-16 | Semiconductor Energy Laboratory Co., Ltd. | Electroluminescent device and method of manufacturing thereof |
WO2004068910A1 (ja) * | 2003-01-24 | 2004-08-12 | Semiconductor Energy Laboratory Co. Ltd. | 発光装置及びその製造方法、並びに前記発光装置を用いた電気機器 |
JP4466064B2 (ja) * | 2003-02-17 | 2010-05-26 | セイコーエプソン株式会社 | 電気光学装置の製造方法 |
JP2004311403A (ja) * | 2003-03-27 | 2004-11-04 | Seiko Epson Corp | エレクトロルミネセンス素子及びその製造方法 |
US6703180B1 (en) * | 2003-04-16 | 2004-03-09 | Eastman Kodak Company | Forming an improved stability emissive layer from a donor element in an OLED device |
KR100560778B1 (ko) * | 2003-04-17 | 2006-03-13 | 삼성에스디아이 주식회사 | 유기 전계 발광 디스플레이 장치 |
US7092206B2 (en) * | 2003-06-25 | 2006-08-15 | Hitachi Global Storage Technologies Netherlands B.V. | Magnetic head with magnetic layers of differing widths and third pole with reduced thickness |
JP4683829B2 (ja) * | 2003-10-17 | 2011-05-18 | 淳二 城戸 | 有機エレクトロルミネッセント素子及びその製造方法 |
JP4476594B2 (ja) | 2003-10-17 | 2010-06-09 | 淳二 城戸 | 有機エレクトロルミネッセント素子 |
JP4243237B2 (ja) | 2003-11-10 | 2009-03-25 | 淳二 城戸 | 有機素子、有機el素子、有機太陽電池、及び、有機fet構造、並びに、有機素子の製造方法 |
EP1548856A3 (en) | 2003-12-26 | 2012-08-08 | Nitto Denko Corporation | Electroluminescence device, planar light source and display using the same |
JP4276109B2 (ja) * | 2004-03-01 | 2009-06-10 | ローム株式会社 | 有機エレクトロルミネッセント素子 |
JP4175273B2 (ja) | 2004-03-03 | 2008-11-05 | セイコーエプソン株式会社 | 積層型有機エレクトロルミネッセンス素子の製造方法及び表示装置 |
JP2005294124A (ja) | 2004-04-01 | 2005-10-20 | Seiko Epson Corp | 有機エレクトロルミネッセンス装置及び有機エレクトロルミネッセンス装置の製造方法ならびに電子機器 |
JP4925569B2 (ja) * | 2004-07-08 | 2012-04-25 | ローム株式会社 | 有機エレクトロルミネッセント素子 |
EP1624502B1 (en) * | 2004-08-04 | 2015-11-18 | Semiconductor Energy Laboratory Co., Ltd. | Light-emitting element, display device, and electronic appliance |
US8026510B2 (en) * | 2004-10-20 | 2011-09-27 | Dai Nippon Printing Co., Ltd. | Organic electronic device and method for producing the same |
CN100395618C (zh) * | 2004-12-25 | 2008-06-18 | 鸿富锦精密工业(深圳)有限公司 | 金属络合物、光源与背光模组 |
US7887876B2 (en) * | 2004-12-29 | 2011-02-15 | Dupont Displays Inc. | Organic electronic device and method to manufacture same |
KR101097300B1 (ko) * | 2005-01-08 | 2011-12-23 | 삼성모바일디스플레이주식회사 | 전자 샤워 처리된 정공 주입층을 포함하는 유기 전계 발광소자 및 그 제조방법 |
TWI256855B (en) * | 2005-02-16 | 2006-06-11 | Au Optronics Corp | Silane compound, organic electroluminescent device and displaying panel using the same |
EP1866983A4 (en) | 2005-02-28 | 2009-10-21 | Semiconductor Energy Lab | COMPOSITE MATERIAL AND ITS USE IN A LIGHT-EMITTING ELEMENT, A LIGHT-EMITTING DEVICE AND AN ELECTRONIC DEVICE |
US20060204784A1 (en) * | 2005-03-10 | 2006-09-14 | Begley William J | Organic light-emitting devices with mixed electron transport materials |
US7517595B2 (en) | 2005-03-10 | 2009-04-14 | Eastman Kodak Company | Electroluminescent devices with mixed electron transport materials |
US20060246315A1 (en) * | 2005-04-27 | 2006-11-02 | Begley William J | Phosphorescent oled with mixed electron transport materials |
US20060286405A1 (en) | 2005-06-17 | 2006-12-21 | Eastman Kodak Company | Organic element for low voltage electroluminescent devices |
US20060286402A1 (en) * | 2005-06-17 | 2006-12-21 | Eastman Kodak Company | Organic element for low voltage electroluminescent devices |
JP4305425B2 (ja) * | 2005-07-20 | 2009-07-29 | セイコーエプソン株式会社 | 電子デバイスおよび電子機器 |
US7563518B2 (en) * | 2005-07-28 | 2009-07-21 | Eastman Kodak Company | Low voltage organic electroluminescent element |
US20070048545A1 (en) * | 2005-08-31 | 2007-03-01 | Eastman Kodak Company | Electron-transporting layer for white OLED device |
US20070046189A1 (en) * | 2005-08-31 | 2007-03-01 | Eastman Kodak Company | Intermediate connector for a tandem OLED device |
JP4548301B2 (ja) * | 2005-10-21 | 2010-09-22 | セイコーエプソン株式会社 | 有機発光素子の製造方法 |
US20070092753A1 (en) * | 2005-10-26 | 2007-04-26 | Eastman Kodak Company | Organic element for low voltage electroluminescent devices |
US8956738B2 (en) * | 2005-10-26 | 2015-02-17 | Global Oled Technology Llc | Organic element for low voltage electroluminescent devices |
US20070092754A1 (en) * | 2005-10-26 | 2007-04-26 | Eastman Kodak Company | Organic element for low voltage electroluminescent devices |
US20070092755A1 (en) * | 2005-10-26 | 2007-04-26 | Eastman Kodak Company | Organic element for low voltage electroluminescent devices |
US20070092759A1 (en) * | 2005-10-26 | 2007-04-26 | Begley William J | Organic element for low voltage electroluminescent devices |
US7767317B2 (en) * | 2005-10-26 | 2010-08-03 | Global Oled Technology Llc | Organic element for low voltage electroluminescent devices |
US20070099810A1 (en) * | 2005-10-27 | 2007-05-03 | Hiroshi Matsunaga | Cleaning liquid and cleaning method |
US20070252516A1 (en) * | 2006-04-27 | 2007-11-01 | Eastman Kodak Company | Electroluminescent devices including organic EIL layer |
JP5268249B2 (ja) | 2005-12-14 | 2013-08-21 | キヤノン株式会社 | 有機発光素子の製造方法 |
JP4770699B2 (ja) * | 2005-12-16 | 2011-09-14 | ソニー株式会社 | 表示素子 |
TWI333803B (en) * | 2006-01-13 | 2010-11-21 | Au Optronics Corp | Organic electro-luminescence device |
JP4273132B2 (ja) * | 2006-04-03 | 2009-06-03 | セイコーエプソン株式会社 | 有機発光素子の製造方法 |
US9118020B2 (en) * | 2006-04-27 | 2015-08-25 | Global Oled Technology Llc | Electroluminescent devices including organic eil layer |
US20080032123A1 (en) * | 2006-08-02 | 2008-02-07 | Spindler Jeffrey P | Dual electron-transporting layer for oled device |
GB0625865D0 (en) | 2006-12-29 | 2007-02-07 | Oled T Ltd | Electro-optical or opto-electronic device |
US20080176099A1 (en) * | 2007-01-18 | 2008-07-24 | Hatwar Tukaram K | White oled device with improved functions |
US8795855B2 (en) * | 2007-01-30 | 2014-08-05 | Global Oled Technology Llc | OLEDs having high efficiency and excellent lifetime |
KR100879476B1 (ko) * | 2007-09-28 | 2009-01-20 | 삼성모바일디스플레이주식회사 | 유기 발광 소자 |
US20090110956A1 (en) * | 2007-10-26 | 2009-04-30 | Begley William J | Oled device with electron transport material combination |
US8076009B2 (en) * | 2007-10-26 | 2011-12-13 | Global Oled Technology, Llc. | OLED device with fluoranthene electron transport materials |
US8431242B2 (en) * | 2007-10-26 | 2013-04-30 | Global Oled Technology, Llc. | OLED device with certain fluoranthene host |
US8420229B2 (en) * | 2007-10-26 | 2013-04-16 | Global OLED Technologies LLC | OLED device with certain fluoranthene light-emitting dopants |
KR20090050369A (ko) * | 2007-11-15 | 2009-05-20 | 삼성모바일디스플레이주식회사 | 유기 발광 소자 |
KR101481822B1 (ko) * | 2007-12-07 | 2015-01-13 | 엘지디스플레이 주식회사 | 유기발광다이오드 및 이를 구비한 유기전계발광 표시장치 |
KR20090062602A (ko) * | 2007-12-13 | 2009-06-17 | 삼성모바일디스플레이주식회사 | 유기 발광 표시 장치 및 그의 제조 방법 |
US20090162612A1 (en) * | 2007-12-19 | 2009-06-25 | Hatwar Tukaram K | Oled device having two electron-transport layers |
US20090162644A1 (en) * | 2007-12-19 | 2009-06-25 | Ricks Michele L | Organic element for low voltage electroluminescent devices |
KR100918401B1 (ko) | 2007-12-24 | 2009-09-24 | 삼성모바일디스플레이주식회사 | 유기 발광 소자 |
KR100922755B1 (ko) * | 2007-12-28 | 2009-10-21 | 삼성모바일디스플레이주식회사 | 유기 발광 소자 |
KR100894066B1 (ko) | 2007-12-28 | 2009-04-24 | 삼성모바일디스플레이 주식회사 | 유기 발광 소자 |
KR101367465B1 (ko) * | 2008-01-21 | 2014-02-25 | 주식회사 엘지화학 | 유기 발광 소자 및 이의 제조방법 |
KR20090082778A (ko) | 2008-01-28 | 2009-07-31 | 삼성모바일디스플레이주식회사 | 유기전계발광소자 및 그 제조방법 |
KR100922759B1 (ko) * | 2008-02-26 | 2009-10-21 | 삼성모바일디스플레이주식회사 | 유기 발광 소자 |
KR100922760B1 (ko) * | 2008-03-03 | 2009-10-21 | 삼성모바일디스플레이주식회사 | 유기 발광 소자 |
KR100898075B1 (ko) | 2008-03-04 | 2009-05-18 | 삼성모바일디스플레이주식회사 | 유기 발광 소자 |
KR20090131550A (ko) * | 2008-06-18 | 2009-12-29 | 삼성모바일디스플레이주식회사 | 유기 발광 소자 |
DE102008056391B4 (de) | 2008-09-26 | 2021-04-01 | Osram Oled Gmbh | Organisches elektronisches Bauelement und Verfahren zu dessen Herstellung |
JP2012504847A (ja) * | 2008-10-01 | 2012-02-23 | エルジー・ケム・リミテッド | 有機発光素子およびその製造方法 |
US7931975B2 (en) * | 2008-11-07 | 2011-04-26 | Global Oled Technology Llc | Electroluminescent device containing a flouranthene compound |
US8088500B2 (en) * | 2008-11-12 | 2012-01-03 | Global Oled Technology Llc | OLED device with fluoranthene electron injection materials |
US7968215B2 (en) * | 2008-12-09 | 2011-06-28 | Global Oled Technology Llc | OLED device with cyclobutene electron injection materials |
DE102008064200A1 (de) | 2008-12-22 | 2010-07-01 | Merck Patent Gmbh | Organische Elektrolumineszenzvorrichtung |
US8216697B2 (en) * | 2009-02-13 | 2012-07-10 | Global Oled Technology Llc | OLED with fluoranthene-macrocyclic materials |
US20100244677A1 (en) * | 2009-03-31 | 2010-09-30 | Begley William J | Oled device containing a silyl-fluoranthene derivative |
US8206842B2 (en) * | 2009-04-06 | 2012-06-26 | Global Oled Technology Llc | Organic element for electroluminescent devices |
CN102484921A (zh) | 2009-07-23 | 2012-05-30 | 株式会社钟化 | 有机电致发光元件 |
KR101877581B1 (ko) * | 2010-06-18 | 2018-07-11 | 유디씨 아일랜드 리미티드 | 피리딘 화합물 및 8-히드록시퀴놀리노레이토 알칼리 토금속 또는 알칼리 금속 착물의 층을 포함하는 유기 전자 소자 |
KR101877580B1 (ko) * | 2010-06-18 | 2018-08-09 | 유디씨 아일랜드 리미티드 | 디벤조푸란 화합물 및 8-히드록시퀴놀리노레이토 알칼리 토금속 또는 알칼리 금속 착물의 층을 포함하는 유기 전자 소자 |
KR20120128483A (ko) * | 2011-05-17 | 2012-11-27 | 삼성디스플레이 주식회사 | 유기 발광 장치 |
CN103548172B (zh) * | 2011-10-05 | 2017-08-04 | 株式会社Lg化学 | 有机发光器件及其制造方法 |
JP5889730B2 (ja) | 2012-06-27 | 2016-03-22 | Lumiotec株式会社 | 有機エレクトロルミネッセント素子及び照明装置 |
KR20140008126A (ko) * | 2012-07-10 | 2014-01-21 | 삼성디스플레이 주식회사 | 유기 발광 장치 |
KR102023028B1 (ko) * | 2012-09-14 | 2019-09-23 | 삼성디스플레이 주식회사 | 포스핀 옥사이드계 화합물 및 이를 포함한 유기 발광 소자 |
KR102167041B1 (ko) * | 2013-08-14 | 2020-10-19 | 삼성디스플레이 주식회사 | 헤테로고리 화합물 및 이를 포함한 유기 발광 소자 |
CN103700775B (zh) * | 2013-12-31 | 2017-08-25 | 北京维信诺科技有限公司 | 一种有机电致发光器件及其制备方法 |
KR102562894B1 (ko) | 2015-12-28 | 2023-08-04 | 삼성디스플레이 주식회사 | 유기 발광 소자 |
KR102547685B1 (ko) | 2016-02-22 | 2023-06-27 | 삼성디스플레이 주식회사 | 유기 발광 소자 |
JP2018152485A (ja) * | 2017-03-14 | 2018-09-27 | セイコーエプソン株式会社 | 発光素子、発光装置、光源、認証装置および電子機器 |
KR20190141053A (ko) | 2018-06-12 | 2019-12-23 | 삼성디스플레이 주식회사 | 헤테로시클릭 화합물 및 이를 포함한 유기 발광 소자 |
TW202110821A (zh) * | 2019-07-26 | 2021-03-16 | 日商半導體能源研究所股份有限公司 | 發光器件、發光裝置、電子裝置、照明設備及化合物 |
KR20220027352A (ko) * | 2020-08-26 | 2022-03-08 | 삼성디스플레이 주식회사 | 발광 소자 및 이를 포함하는 전자 장치 |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5719467A (en) * | 1995-07-27 | 1998-02-17 | Hewlett-Packard Company | Organic electroluminescent device |
JPH10270171A (ja) * | 1997-01-27 | 1998-10-09 | Junji Kido | 有機エレクトロルミネッセント素子 |
JPH10270172A (ja) * | 1997-01-27 | 1998-10-09 | Junji Kido | 有機エレクトロルミネッセント素子 |
EP1011155A2 (en) * | 1998-12-16 | 2000-06-21 | Junji Kido | Organic electroluminescent deivce |
Family Cites Families (66)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4539507A (en) | 1983-03-25 | 1985-09-03 | Eastman Kodak Company | Organic electroluminescent devices having improved power conversion efficiencies |
US4720432A (en) | 1987-02-11 | 1988-01-19 | Eastman Kodak Company | Electroluminescent device with organic luminescent medium |
JPH0288689A (ja) | 1988-09-26 | 1990-03-28 | Mitsubishi Kasei Corp | 電界発光素子 |
CA2005289A1 (en) | 1988-12-14 | 1990-06-14 | Chishio Hosokawa | Electroluminescence device |
JPH02289676A (ja) | 1989-01-13 | 1990-11-29 | Ricoh Co Ltd | 電界発光素子 |
JP2651233B2 (ja) | 1989-01-20 | 1997-09-10 | 出光興産株式会社 | 薄膜有機el素子 |
JPH02196885A (ja) | 1989-01-25 | 1990-08-03 | Asahi Chem Ind Co Ltd | 有機電界発光素子 |
JPH02213088A (ja) * | 1989-02-13 | 1990-08-24 | Nec Corp | 有機薄膜el素子及びその製造方法 |
US5130603A (en) | 1989-03-20 | 1992-07-14 | Idemitsu Kosan Co., Ltd. | Organic electroluminescence device |
JP2879080B2 (ja) | 1989-03-23 | 1999-04-05 | 株式会社リコー | 電界発光素子 |
JPH07119408B2 (ja) | 1989-03-28 | 1995-12-20 | 出光興産株式会社 | 有機エレクトロルミネッセンス素子 |
JPH02255789A (ja) | 1989-03-29 | 1990-10-16 | Asahi Chem Ind Co Ltd | 有機電場発光素子 |
JP2554771B2 (ja) | 1989-12-28 | 1996-11-13 | 出光興産株式会社 | 芳香族ジメチリディン化合物 |
JPH07119409B2 (ja) * | 1990-03-19 | 1995-12-20 | 凸版印刷株式会社 | 有機薄膜el素子 |
JPH03296595A (ja) | 1990-04-13 | 1991-12-27 | Kao Corp | 有機薄膜エレクトロルミネッセンス素子 |
JP2997021B2 (ja) | 1990-08-10 | 2000-01-11 | パイオニア株式会社 | 有機エレクトロルミネッセンス素子 |
JP2891783B2 (ja) | 1991-02-06 | 1999-05-17 | パイオニア株式会社 | 有機エレクトロルミネッセンス素子 |
JP2891784B2 (ja) | 1991-02-06 | 1999-05-17 | パイオニア株式会社 | 有機エレクトロルミネッセンス素子 |
JPH05202011A (ja) | 1992-01-27 | 1993-08-10 | Toshiba Corp | オキサジアゾール誘導体 |
JPH0649079A (ja) | 1992-04-02 | 1994-02-22 | Idemitsu Kosan Co Ltd | シラナミン誘導体およびその製造方法並びに該シラナミン誘導体を用いたel素子 |
JPH06107648A (ja) | 1992-09-29 | 1994-04-19 | Ricoh Co Ltd | 新規なオキサジアゾール化合物 |
JPH0625659A (ja) | 1992-07-07 | 1994-02-01 | Idemitsu Kosan Co Ltd | ホスファミン誘導体、その製造方法およびそれを用いたエレクトロルミネッセンス素子 |
JP3341090B2 (ja) | 1992-07-27 | 2002-11-05 | 株式会社リコー | オキサジアゾール誘導体ならびにその製造法 |
JP3228301B2 (ja) | 1992-09-07 | 2001-11-12 | 出光興産株式会社 | 有機エレクトロルミネッセンス素子 |
JP3163589B2 (ja) | 1992-09-21 | 2001-05-08 | 出光興産株式会社 | 有機エレクトロルミネッセンス素子 |
JPH06206865A (ja) | 1992-10-14 | 1994-07-26 | Chisso Corp | 新規アントラセン化合物と該化合物を用いる電界発光素子 |
JP3287421B2 (ja) | 1992-10-19 | 2002-06-04 | 出光興産株式会社 | 有機エレクトロルミネッセンス素子 |
JPH06145146A (ja) | 1992-11-06 | 1994-05-24 | Chisso Corp | オキシネイト誘導体 |
JP3366401B2 (ja) | 1992-11-20 | 2003-01-14 | 出光興産株式会社 | 白色有機エレクトロルミネッセンス素子 |
JPH06203963A (ja) | 1993-01-08 | 1994-07-22 | Idemitsu Kosan Co Ltd | 有機エレクトロルミネッセンス素子 |
JPH06215874A (ja) | 1993-01-20 | 1994-08-05 | Idemitsu Kosan Co Ltd | 有機エレクトロルミネッセンス素子 |
JP3419534B2 (ja) | 1993-02-10 | 2003-06-23 | 靖彦 城田 | トリスアリールアミノベンゼン誘導体、有機el素子用化合物および有機el素子 |
JP3211994B2 (ja) | 1993-03-26 | 2001-09-25 | 出光興産株式会社 | 4官能スチリル化合物およびその製造法 |
JP3214674B2 (ja) | 1993-03-26 | 2001-10-02 | 出光興産株式会社 | 新規スチリル化合物,その製造法およびそれからなる有機エレクトロルミネッセンス素子 |
JPH06293778A (ja) | 1993-04-05 | 1994-10-21 | Idemitsu Kosan Co Ltd | シラナミン誘導体およびその製造方法 |
JP3549555B2 (ja) | 1993-10-04 | 2004-08-04 | 株式会社リコー | 新規なピレン誘導体ならびにその製造方法 |
JP3220950B2 (ja) | 1993-11-01 | 2001-10-22 | 保土谷化学工業株式会社 | ベンジジン化合物 |
JP3574860B2 (ja) | 1993-11-01 | 2004-10-06 | 保土谷化学工業株式会社 | テトラフェニルベンジジン化合物 |
JPH07145116A (ja) | 1993-11-25 | 1995-06-06 | Nisshinbo Ind Inc | 芳香族ジアミン化合物 |
JPH07157473A (ja) | 1993-12-06 | 1995-06-20 | Chisso Corp | トリアジン誘導体、その製造法及びそれを用いた電界発光素子 |
JP3539995B2 (ja) | 1993-12-21 | 2004-07-07 | 株式会社リコー | オキサジアゾール化合物およびその製造法 |
JP3300827B2 (ja) | 1993-12-21 | 2002-07-08 | 株式会社リコー | オキサジアゾール化合物およびその製造法 |
JP3594642B2 (ja) | 1993-12-24 | 2004-12-02 | 保土谷化学工業株式会社 | ジアミノジフェニル化合物及び該化合物を用いた有機電界発光素子 |
JP3496080B2 (ja) | 1993-12-24 | 2004-02-09 | 株式会社リコー | オキサジアゾール誘導体およびその製造方法 |
JP3579746B2 (ja) | 1994-02-07 | 2004-10-20 | チッソ株式会社 | ジフェニルアミン誘導体 |
JP3828595B2 (ja) | 1994-02-08 | 2006-10-04 | Tdk株式会社 | 有機el素子 |
JPH07268317A (ja) | 1994-03-31 | 1995-10-17 | Toray Ind Inc | 発光素子 |
US6064355A (en) | 1994-05-24 | 2000-05-16 | Texas Instruments Incorporated | Method and apparatus for playback with a virtual reality system |
JP3593717B2 (ja) | 1994-08-04 | 2004-11-24 | 東洋インキ製造株式会社 | 新規なトリフェニルアミン誘導体、その製造方法及び用途 |
JP3593719B2 (ja) | 1994-08-04 | 2004-11-24 | 東洋インキ製造株式会社 | 新規なトリフェニルアミン誘導体、その製造方法及び用途 |
JP3593718B2 (ja) | 1994-08-04 | 2004-11-24 | 東洋インキ製造株式会社 | 新規なトリフェニルアミン誘導体、その製造方法及び用途 |
DE69526614T2 (de) | 1994-09-12 | 2002-09-19 | Motorola, Inc. | Lichtemittierende Vorrichtungen die Organometallische Komplexe enthalten. |
JP3261945B2 (ja) * | 1994-10-14 | 2002-03-04 | 東洋インキ製造株式会社 | エレクトロルミネッセンス素子封止用積層体およびエレクトロルミネッセンス素子封止構造体 |
JP3231970B2 (ja) | 1995-01-31 | 2001-11-26 | 東京応化工業株式会社 | 回転カップ式塗布方法及び塗布装置 |
JP2931229B2 (ja) * | 1995-02-13 | 1999-08-09 | 出光興産株式会社 | 有機エレクトロルミネッセンス素子 |
JP3412076B2 (ja) * | 1995-03-08 | 2003-06-03 | 株式会社リコー | 有機el素子 |
JP3518047B2 (ja) * | 1995-05-02 | 2004-04-12 | 凸版印刷株式会社 | 有機薄膜el素子 |
JPH09129376A (ja) * | 1995-10-30 | 1997-05-16 | Idemitsu Kosan Co Ltd | 有機el素子 |
JPH09272865A (ja) * | 1996-04-08 | 1997-10-21 | Toyo Ink Mfg Co Ltd | 有機エレクトロルミネッセンス素子用電子注入材料およびそれを用いた有機エレクトロルミネッセンス素子 |
JP4024327B2 (ja) * | 1996-07-03 | 2007-12-19 | 出光興産株式会社 | 有機el発光装置 |
US5955834A (en) * | 1996-08-02 | 1999-09-21 | The Ohio State University | Light emitting devices utilizing high work function electrodes |
US5844363A (en) * | 1997-01-23 | 1998-12-01 | The Trustees Of Princeton Univ. | Vacuum deposited, non-polymeric flexible organic light emitting devices |
JP3669783B2 (ja) * | 1996-08-21 | 2005-07-13 | 三井化学株式会社 | 有機電界発光素子 |
US5965281A (en) * | 1997-02-04 | 1999-10-12 | Uniax Corporation | Electrically active polymer compositions and their use in efficient, low operating voltage, polymer light-emitting diodes with air-stable cathodes |
JP4038833B2 (ja) * | 1997-05-21 | 2008-01-30 | 三菱化学株式会社 | 有機電界発光素子 |
JP4514841B2 (ja) | 1998-02-17 | 2010-07-28 | 淳二 城戸 | 有機エレクトロルミネッセント素子 |
-
1998
- 1998-12-16 JP JP35789998A patent/JP4505067B2/ja not_active Expired - Lifetime
-
1999
- 1999-12-10 TW TW088121623A patent/TW435052B/zh not_active IP Right Cessation
- 1999-12-13 US US09/459,830 patent/US6396209B1/en not_active Expired - Lifetime
- 1999-12-15 EP EP99125041A patent/EP1011155B1/en not_active Expired - Lifetime
- 1999-12-15 KR KR1019990058093A patent/KR100584917B1/ko active IP Right Grant
- 1999-12-15 AT AT99125041T patent/ATE242548T1/de not_active IP Right Cessation
- 1999-12-15 DE DE69908537T patent/DE69908537T2/de not_active Expired - Lifetime
- 1999-12-16 CN CNB991277708A patent/CN100372144C/zh not_active Expired - Lifetime
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5719467A (en) * | 1995-07-27 | 1998-02-17 | Hewlett-Packard Company | Organic electroluminescent device |
JPH10270171A (ja) * | 1997-01-27 | 1998-10-09 | Junji Kido | 有機エレクトロルミネッセント素子 |
JPH10270172A (ja) * | 1997-01-27 | 1998-10-09 | Junji Kido | 有機エレクトロルミネッセント素子 |
EP1011155A2 (en) * | 1998-12-16 | 2000-06-21 | Junji Kido | Organic electroluminescent deivce |
US6396209B1 (en) * | 1998-12-16 | 2002-05-28 | International Manufacturing And Engineering Services Co., Ltd. | Organic electroluminescent device |
Also Published As
Publication number | Publication date |
---|---|
EP1011155B1 (en) | 2003-06-04 |
CN1261760A (zh) | 2000-08-02 |
JP2000182774A (ja) | 2000-06-30 |
ATE242548T1 (de) | 2003-06-15 |
TW435052B (en) | 2001-05-16 |
CN100372144C (zh) | 2008-02-27 |
JP4505067B2 (ja) | 2010-07-14 |
US6396209B1 (en) | 2002-05-28 |
EP1011155A3 (en) | 2001-05-23 |
EP1011155A2 (en) | 2000-06-21 |
DE69908537D1 (de) | 2003-07-10 |
KR20000048161A (ko) | 2000-07-25 |
DE69908537T2 (de) | 2004-04-29 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
KR100584917B1 (ko) | 유기전계발광소자 | |
KR100533341B1 (ko) | 유기전기장발광성소자 | |
US6013384A (en) | Organic electroluminescent devices | |
KR100641880B1 (ko) | 유기전기장발광성소자 | |
EP1089361B1 (en) | Organic electroluminescent device and method of controlling emission spectrum | |
JP4486713B2 (ja) | 有機エレクトロルミネッセント素子 | |
JP4729154B2 (ja) | 有機エレクトロルミネッセント素子、有機エレクトロルミネッセント素子群及びその発光スペクトルの制御方法 | |
JP4824848B2 (ja) | 有機エレクトロルミネッセント素子、有機エレクトロルミネッセント素子群及びその発光スペクトルの特定方法 | |
KR100922760B1 (ko) | 유기 발광 소자 | |
US20050084713A1 (en) | Organic electroluminescent device and production process thereof | |
KR20090092112A (ko) | 유기 발광 소자 | |
JP2007525023A (ja) | 有機電場発光デバイスにおける結晶化抑制材料の使用 | |
KR20090131550A (ko) | 유기 발광 소자 | |
JP4825296B2 (ja) | 有機エレクトロルミネッセント素子 | |
JP4820902B2 (ja) | 有機エレクトロルミネッセント素子及びその発光スペクトルの制御方法 | |
JPH10270167A (ja) | 新規発光材料、新規電子輸送材料およびそれを用いた有機el素子 | |
KR19980081742A (ko) | 유기 전계발광 소자 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A201 | Request for examination | ||
E701 | Decision to grant or registration of patent right | ||
GRNT | Written decision to grant | ||
FPAY | Annual fee payment |
Payment date: 20130415 Year of fee payment: 8 |
|
FPAY | Annual fee payment |
Payment date: 20140428 Year of fee payment: 9 |
|
FPAY | Annual fee payment |
Payment date: 20150216 Year of fee payment: 10 |
|
FPAY | Annual fee payment |
Payment date: 20160126 Year of fee payment: 11 |
|
FPAY | Annual fee payment |
Payment date: 20170202 Year of fee payment: 12 |
|
FPAY | Annual fee payment |
Payment date: 20180220 Year of fee payment: 13 |
|
FPAY | Annual fee payment |
Payment date: 20190520 Year of fee payment: 14 |