CN101682002A - 杂化荧光/磷光oled - Google Patents
杂化荧光/磷光oled Download PDFInfo
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- CN101682002A CN101682002A CN200880016387A CN200880016387A CN101682002A CN 101682002 A CN101682002 A CN 101682002A CN 200880016387 A CN200880016387 A CN 200880016387A CN 200880016387 A CN200880016387 A CN 200880016387A CN 101682002 A CN101682002 A CN 101682002A
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- 239000000463 material Substances 0.000 claims abstract description 267
- 238000004770 highest occupied molecular orbital Methods 0.000 claims abstract description 60
- 125000006850 spacer group Chemical group 0.000 claims abstract description 15
- 125000003118 aryl group Chemical group 0.000 claims description 64
- 150000001875 compounds Chemical class 0.000 claims description 64
- 230000005540 biological transmission Effects 0.000 claims description 57
- 229910052799 carbon Inorganic materials 0.000 claims description 38
- 125000004432 carbon atom Chemical group C* 0.000 claims description 31
- 239000001257 hydrogen Substances 0.000 claims description 31
- 229910052739 hydrogen Inorganic materials 0.000 claims description 31
- 125000000217 alkyl group Chemical group 0.000 claims description 29
- 125000004429 atom Chemical group 0.000 claims description 25
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 21
- 229910052782 aluminium Inorganic materials 0.000 claims description 20
- 229910052733 gallium Inorganic materials 0.000 claims description 19
- 125000003107 substituted aryl group Chemical group 0.000 claims description 17
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 claims description 16
- 239000004411 aluminium Substances 0.000 claims description 16
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 16
- 125000001072 heteroaryl group Chemical group 0.000 claims description 16
- 229910052760 oxygen Inorganic materials 0.000 claims description 15
- 239000001301 oxygen Substances 0.000 claims description 15
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 14
- 125000003983 fluorenyl group Chemical class C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 claims description 12
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 11
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 11
- 229910052731 fluorine Inorganic materials 0.000 claims description 11
- 239000011737 fluorine Substances 0.000 claims description 11
- 125000004122 cyclic group Chemical group 0.000 claims description 10
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 9
- 239000000460 chlorine Substances 0.000 claims description 9
- 229910052801 chlorine Inorganic materials 0.000 claims description 9
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 6
- 230000015572 biosynthetic process Effects 0.000 claims description 6
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 6
- 229910052794 bromium Inorganic materials 0.000 claims description 6
- 125000000033 alkoxyamino group Chemical group 0.000 claims description 5
- 125000003282 alkyl amino group Chemical group 0.000 claims description 5
- 125000001769 aryl amino group Chemical group 0.000 claims description 5
- 150000002576 ketones Chemical class 0.000 claims description 3
- 239000010410 layer Substances 0.000 description 296
- -1 aphthacene Chemical compound 0.000 description 104
- 239000002585 base Substances 0.000 description 57
- 229910052741 iridium Inorganic materials 0.000 description 51
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 48
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 description 41
- 229910052757 nitrogen Inorganic materials 0.000 description 38
- 230000005284 excitation Effects 0.000 description 36
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 31
- 230000005525 hole transport Effects 0.000 description 28
- 230000027756 respiratory electron transport chain Effects 0.000 description 27
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 25
- 239000002019 doping agent Substances 0.000 description 24
- VQGHOUODWALEFC-UHFFFAOYSA-N 2-phenylpyridine Chemical compound C1=CC=CC=C1C1=CC=CC=N1 VQGHOUODWALEFC-UHFFFAOYSA-N 0.000 description 23
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 23
- 238000004768 lowest unoccupied molecular orbital Methods 0.000 description 23
- 238000000034 method Methods 0.000 description 23
- UJOBWOGCFQCDNV-UHFFFAOYSA-N 9H-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 description 22
- 150000001721 carbon Chemical group 0.000 description 22
- PQXKHYXIUOZZFA-UHFFFAOYSA-M lithium fluoride Chemical compound [Li+].[F-] PQXKHYXIUOZZFA-UHFFFAOYSA-M 0.000 description 22
- 229910052751 metal Inorganic materials 0.000 description 22
- 239000002184 metal Substances 0.000 description 22
- 125000000623 heterocyclic group Chemical group 0.000 description 19
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 18
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical class C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 17
- MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 description 17
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 16
- 230000004888 barrier function Effects 0.000 description 15
- 230000000903 blocking effect Effects 0.000 description 15
- 238000002347 injection Methods 0.000 description 15
- 239000007924 injection Substances 0.000 description 15
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 14
- 239000000203 mixture Substances 0.000 description 14
- 238000000465 moulding Methods 0.000 description 14
- 125000005259 triarylamine group Chemical group 0.000 description 14
- 239000011248 coating agent Substances 0.000 description 13
- 238000000576 coating method Methods 0.000 description 13
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 12
- 150000002475 indoles Chemical class 0.000 description 12
- 239000003446 ligand Substances 0.000 description 12
- 238000005215 recombination Methods 0.000 description 12
- 125000001624 naphthyl group Chemical group 0.000 description 11
- 239000012044 organic layer Substances 0.000 description 11
- 238000000151 deposition Methods 0.000 description 10
- 230000008021 deposition Effects 0.000 description 10
- 229920000642 polymer Polymers 0.000 description 10
- 150000004982 aromatic amines Chemical class 0.000 description 9
- MILUBEOXRNEUHS-UHFFFAOYSA-N iridium(3+) Chemical compound [Ir+3] MILUBEOXRNEUHS-UHFFFAOYSA-N 0.000 description 9
- 239000004305 biphenyl Substances 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 8
- 229910052736 halogen Inorganic materials 0.000 description 8
- 238000004020 luminiscence type Methods 0.000 description 8
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Substances [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 8
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 8
- 125000001544 thienyl group Chemical group 0.000 description 8
- REDXJYDRNCIFBQ-UHFFFAOYSA-N aluminium(3+) Chemical compound [Al+3] REDXJYDRNCIFBQ-UHFFFAOYSA-N 0.000 description 7
- 235000010290 biphenyl Nutrition 0.000 description 7
- 238000005401 electroluminescence Methods 0.000 description 7
- 238000002474 experimental method Methods 0.000 description 7
- 150000002367 halogens Chemical class 0.000 description 7
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 7
- 230000006798 recombination Effects 0.000 description 7
- 238000012546 transfer Methods 0.000 description 7
- VDULMXJUOWIPGE-UHFFFAOYSA-N 1-phenylisoquinoline quinoline Chemical compound N1=CC=CC2=CC=CC=C12.C1(=CC=CC=C1)C1=NC=CC2=CC=CC=C12 VDULMXJUOWIPGE-UHFFFAOYSA-N 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 6
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 6
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 6
- 239000002800 charge carrier Substances 0.000 description 6
- 125000002541 furyl group Chemical group 0.000 description 6
- SIOXPEMLGUPBBT-UHFFFAOYSA-N picolinic acid Chemical class OC(=O)C1=CC=CC=N1 SIOXPEMLGUPBBT-UHFFFAOYSA-N 0.000 description 6
- 125000003367 polycyclic group Chemical group 0.000 description 6
- 125000005493 quinolyl group Chemical group 0.000 description 6
- 125000001424 substituent group Chemical group 0.000 description 6
- 229910052726 zirconium Inorganic materials 0.000 description 6
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 5
- 150000001412 amines Chemical class 0.000 description 5
- 150000001450 anions Chemical class 0.000 description 5
- 239000010406 cathode material Substances 0.000 description 5
- 230000021615 conjugation Effects 0.000 description 5
- 230000008878 coupling Effects 0.000 description 5
- 238000010168 coupling process Methods 0.000 description 5
- 238000005859 coupling reaction Methods 0.000 description 5
- 239000010408 film Substances 0.000 description 5
- 239000011521 glass Substances 0.000 description 5
- 229910052744 lithium Inorganic materials 0.000 description 5
- 239000011777 magnesium Substances 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 230000003287 optical effect Effects 0.000 description 5
- KDLHZDBZIXYQEI-UHFFFAOYSA-N palladium Substances [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 5
- 229910052697 platinum Inorganic materials 0.000 description 5
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 229920002554 vinyl polymer Polymers 0.000 description 5
- 238000004057 DFT-B3LYP calculation Methods 0.000 description 4
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 4
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 4
- 125000003545 alkoxy group Chemical group 0.000 description 4
- 125000001118 alkylidene group Chemical group 0.000 description 4
- 125000004104 aryloxy group Chemical group 0.000 description 4
- 150000001716 carbazoles Chemical class 0.000 description 4
- 230000008859 change Effects 0.000 description 4
- 239000004020 conductor Substances 0.000 description 4
- 125000000753 cycloalkyl group Chemical group 0.000 description 4
- 238000009792 diffusion process Methods 0.000 description 4
- 230000005283 ground state Effects 0.000 description 4
- CECAIMUJVYQLKA-UHFFFAOYSA-N iridium 1-phenylisoquinoline Chemical compound [Ir].C1=CC=CC=C1C1=NC=CC2=CC=CC=C12.C1=CC=CC=C1C1=NC=CC2=CC=CC=C12.C1=CC=CC=C1C1=NC=CC2=CC=CC=C12 CECAIMUJVYQLKA-UHFFFAOYSA-N 0.000 description 4
- 229910052749 magnesium Inorganic materials 0.000 description 4
- 239000011159 matrix material Substances 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
- 125000004433 nitrogen atom Chemical group N* 0.000 description 4
- 238000005457 optimization Methods 0.000 description 4
- 229910052763 palladium Inorganic materials 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
- 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 4
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 4
- HRGDZIGMBDGFTC-UHFFFAOYSA-N platinum(2+) Chemical compound [Pt+2] HRGDZIGMBDGFTC-UHFFFAOYSA-N 0.000 description 4
- 125000000547 substituted alkyl group Chemical group 0.000 description 4
- 150000003852 triazoles Chemical class 0.000 description 4
- XNCMQRWVMWLODV-UHFFFAOYSA-N 1-phenylbenzimidazole Chemical compound C1=NC2=CC=CC=C2N1C1=CC=CC=C1 XNCMQRWVMWLODV-UHFFFAOYSA-N 0.000 description 3
- PNEYBMLMFCGWSK-UHFFFAOYSA-N Alumina Chemical compound [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 3
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 3
- HDDYZBALTSRZPD-UHFFFAOYSA-N NCC=1C=C(C=CC1)N(C1=CC=CC=C1)C1=C(C=CC=C1)N(C1=CC=CC=C1)C1=CC=CC=C1 Chemical class NCC=1C=C(C=CC1)N(C1=CC=CC=C1)C1=C(C=CC=C1)N(C1=CC=CC=C1)C1=CC=CC=C1 HDDYZBALTSRZPD-UHFFFAOYSA-N 0.000 description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
- 239000005864 Sulphur Substances 0.000 description 3
- DGEZNRSVGBDHLK-UHFFFAOYSA-N [1,10]phenanthroline Chemical group C1=CN=C2C3=NC=CC=C3C=CC2=C1 DGEZNRSVGBDHLK-UHFFFAOYSA-N 0.000 description 3
- 229910052783 alkali metal Inorganic materials 0.000 description 3
- 150000001340 alkali metals Chemical class 0.000 description 3
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 description 3
- 239000010405 anode material Substances 0.000 description 3
- 125000005428 anthryl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C3C(*)=C([H])C([H])=C([H])C3=C([H])C2=C1[H] 0.000 description 3
- 238000013459 approach Methods 0.000 description 3
- UFVXQDWNSAGPHN-UHFFFAOYSA-K bis[(2-methylquinolin-8-yl)oxy]-(4-phenylphenoxy)alumane Chemical compound [Al+3].C1=CC=C([O-])C2=NC(C)=CC=C21.C1=CC=C([O-])C2=NC(C)=CC=C21.C1=CC([O-])=CC=C1C1=CC=CC=C1 UFVXQDWNSAGPHN-UHFFFAOYSA-K 0.000 description 3
- 229910052796 boron Inorganic materials 0.000 description 3
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000012937 correction Methods 0.000 description 3
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- 238000001704 evaporation Methods 0.000 description 3
- 230000008020 evaporation Effects 0.000 description 3
- 229920002313 fluoropolymer Polymers 0.000 description 3
- 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 3
- 229910052738 indium Inorganic materials 0.000 description 3
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 description 3
- MRNHPUHPBOKKQT-UHFFFAOYSA-N indium;tin;hydrate Chemical compound O.[In].[Sn] MRNHPUHPBOKKQT-UHFFFAOYSA-N 0.000 description 3
- 238000003475 lamination Methods 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 150000002790 naphthalenes Chemical class 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 238000007639 printing Methods 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 125000001725 pyrenyl group Chemical group 0.000 description 3
- 229910052710 silicon Inorganic materials 0.000 description 3
- 125000004646 sulfenyl group Chemical group S(*)* 0.000 description 3
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 3
- 125000003944 tolyl group Chemical group 0.000 description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 2
- SNTWKPAKVQFCCF-UHFFFAOYSA-N 2,3-dihydro-1h-triazole Chemical compound N1NC=CN1 SNTWKPAKVQFCCF-UHFFFAOYSA-N 0.000 description 2
- 125000000590 4-methylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 2
- QCRMNYVCABKJCM-UHFFFAOYSA-N 5-methyl-2h-pyran Chemical compound CC1=COCC=C1 QCRMNYVCABKJCM-UHFFFAOYSA-N 0.000 description 2
- NEGKJMRDAJYBPM-UHFFFAOYSA-N 9-(4-carbazol-9-ylphenyl)-3-n,3-n,6-n,6-n-tetraphenylcarbazole-3,6-diamine Chemical class C1=CC=CC=C1N(C=1C=C2C3=CC(=CC=C3N(C=3C=CC(=CC=3)N3C4=CC=CC=C4C4=CC=CC=C43)C2=CC=1)N(C=1C=CC=CC=1)C=1C=CC=CC=1)C1=CC=CC=C1 NEGKJMRDAJYBPM-UHFFFAOYSA-N 0.000 description 2
- HDKRDRXHKYTCCZ-UHFFFAOYSA-N 9-(4-carbazol-9-ylphenyl)-n,n-diphenylcarbazol-3-amine Chemical compound C1=CC=CC=C1N(C=1C=C2C3=CC=CC=C3N(C=3C=CC(=CC=3)N3C4=CC=CC=C4C4=CC=CC=C43)C2=CC=1)C1=CC=CC=C1 HDKRDRXHKYTCCZ-UHFFFAOYSA-N 0.000 description 2
- LTUJKAYZIMMJEP-UHFFFAOYSA-N 9-[4-(4-carbazol-9-yl-2-methylphenyl)-3-methylphenyl]carbazole Chemical compound C12=CC=CC=C2C2=CC=CC=C2N1C1=CC=C(C=2C(=CC(=CC=2)N2C3=CC=CC=C3C3=CC=CC=C32)C)C(C)=C1 LTUJKAYZIMMJEP-UHFFFAOYSA-N 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 2
- UVUNZHNCNUFPQA-UHFFFAOYSA-K C(C)(=O)CC(C(=O)[O-])=O.[Ir+3].C(C)(=O)CC(C(=O)[O-])=O.C(C)(=O)CC(C(=O)[O-])=O Chemical compound C(C)(=O)CC(C(=O)[O-])=O.[Ir+3].C(C)(=O)CC(C(=O)[O-])=O.C(C)(=O)CC(C(=O)[O-])=O UVUNZHNCNUFPQA-UHFFFAOYSA-K 0.000 description 2
- UAWSFVGZNFBYOC-UHFFFAOYSA-N C1(=CC=CC=C1)N(C1=CC(=CC=C1)CN)C1=C(C=CC=C1)C1=CC=CC=C1 Chemical group C1(=CC=CC=C1)N(C1=CC(=CC=C1)CN)C1=C(C=CC=C1)C1=CC=CC=C1 UAWSFVGZNFBYOC-UHFFFAOYSA-N 0.000 description 2
- XUXUEXXDYVBRGS-UHFFFAOYSA-N CC1=C(C=C(C(=C1)N(C1=CC=CC=C1)C1=CC(=CC=C1)CN)C)NC1=C(C=C(C(=C1)C)N(C1=CC=CC=C1)C1=CC(=CC=C1)CN)C Chemical compound CC1=C(C=C(C(=C1)N(C1=CC=CC=C1)C1=CC(=CC=C1)CN)C)NC1=C(C=C(C(=C1)C)N(C1=CC=CC=C1)C1=CC(=CC=C1)CN)C XUXUEXXDYVBRGS-UHFFFAOYSA-N 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- 238000003775 Density Functional Theory Methods 0.000 description 2
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 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
- HBBGRARXTFLTSG-UHFFFAOYSA-N Lithium ion Chemical compound [Li+] HBBGRARXTFLTSG-UHFFFAOYSA-N 0.000 description 2
- JLVVSXFLKOJNIY-UHFFFAOYSA-N Magnesium ion Chemical compound [Mg+2] JLVVSXFLKOJNIY-UHFFFAOYSA-N 0.000 description 2
- ZGHJDJQFPCSKPY-UHFFFAOYSA-N N-naphthalen-1-yl-N-(2-phenylphenyl)naphthalen-2-amine Chemical group C1(=CC=CC2=CC=CC=C12)N(C1=CC2=CC=CC=C2C=C1)C1=C(C=CC=C1)C1=CC=CC=C1 ZGHJDJQFPCSKPY-UHFFFAOYSA-N 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
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- H10K50/11—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers
- H10K50/125—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers specially adapted for multicolour light emission, e.g. for emitting white light
- H10K50/13—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers specially adapted for multicolour light emission, e.g. for emitting white light comprising stacked EL layers within one EL unit
- H10K50/131—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers specially adapted for multicolour light emission, e.g. for emitting white light comprising stacked EL layers within one EL unit with spacer layers between the electroluminescent layers
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Abstract
Description
实施例 | 发光效率(cd/A) | 外部量子效率(%) | CIE(x,y) |
1-1(本发明) | 9.55 | 10.70 | 0.298,0.182 |
1-2(对比) | 6.89 | 6.35 | 0.216,0.173 |
1-3(对比) | 6.69 | 5.78 | 0.182,0.166 |
1-4(对比) | 6.82 | 5.49 | 0.175,0.179 |
实施例 | 发光效率(cd/A) | 外部量子效率(%) | CIE(x,y) |
2-1(本发明) | 39.2 | 14.2 | 0.232,0.425 |
2-2(对比) | 23.3 | 8.82 | 0.226,0.401 |
2-3(对比) | 20.7 | 8.52 | 0.210,0.362 |
2-4(对比) | 13.8 | 6.61 | 0.183,0.301 |
2-5(对比) | 11.4 | 5.71 | 0.175,0.284 |
Claims (11)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US11/749,899 | 2007-05-17 | ||
US11/749,899 US20080284318A1 (en) | 2007-05-17 | 2007-05-17 | Hybrid fluorescent/phosphorescent oleds |
PCT/US2008/005911 WO2008143791A1 (en) | 2007-05-17 | 2008-05-08 | Hybrid fluorescent/phosphorescent oleds |
Publications (2)
Publication Number | Publication Date |
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CN101682002A true CN101682002A (zh) | 2010-03-24 |
CN101682002B CN101682002B (zh) | 2011-11-23 |
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Application Number | Title | Priority Date | Filing Date |
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CN2008800163872A Active CN101682002B (zh) | 2007-05-17 | 2008-05-08 | 杂化荧光/磷光oled |
Country Status (5)
Country | Link |
---|---|
US (1) | US20080284318A1 (zh) |
EP (1) | EP2147473A1 (zh) |
CN (1) | CN101682002B (zh) |
TW (1) | TW200904943A (zh) |
WO (1) | WO2008143791A1 (zh) |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102024909A (zh) * | 2010-09-27 | 2011-04-20 | 电子科技大学 | 一种发光稳定的有机电致发光器件及其制备方法 |
CN102738402A (zh) * | 2011-03-31 | 2012-10-17 | 海洋王照明科技股份有限公司 | 一种白光电致发光器件 |
CN103187537A (zh) * | 2011-12-31 | 2013-07-03 | 昆山维信诺显示技术有限公司 | 一种高效白光有机电致发光器件 |
CN104979482A (zh) * | 2014-04-07 | 2015-10-14 | 柯尼卡美能达株式会社 | 有机电致发光元件及电子器件 |
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- 2008-05-08 CN CN2008800163872A patent/CN101682002B/zh active Active
- 2008-05-16 TW TW097118193A patent/TW200904943A/zh unknown
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CN101682002B (zh) | 2011-11-23 |
TW200904943A (en) | 2009-02-01 |
US20080284318A1 (en) | 2008-11-20 |
WO2008143791A1 (en) | 2008-11-27 |
EP2147473A1 (en) | 2010-01-27 |
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