KR100762014B1 - 유기이온염을 포함하는 전도성 고분자 조성물 및 이를이용한 유기 광전 소자 - Google Patents
유기이온염을 포함하는 전도성 고분자 조성물 및 이를이용한 유기 광전 소자 Download PDFInfo
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- KR100762014B1 KR100762014B1 KR1020060068867A KR20060068867A KR100762014B1 KR 100762014 B1 KR100762014 B1 KR 100762014B1 KR 1020060068867 A KR1020060068867 A KR 1020060068867A KR 20060068867 A KR20060068867 A KR 20060068867A KR 100762014 B1 KR100762014 B1 KR 100762014B1
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- South Korea
- Prior art keywords
- group
- conductive polymer
- polymer composition
- alkyl
- ester
- Prior art date
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- 229920001940 conductive polymer Polymers 0.000 title claims abstract description 81
- 239000000203 mixture Substances 0.000 title claims abstract description 58
- 150000003839 salts Chemical class 0.000 title abstract description 14
- 230000005693 optoelectronics Effects 0.000 title description 2
- -1 heteroalkyl ester Chemical class 0.000 claims abstract description 69
- 125000001072 heteroaryl group Chemical group 0.000 claims abstract description 22
- 125000004404 heteroalkyl group Chemical group 0.000 claims abstract description 20
- 125000003118 aryl group Chemical group 0.000 claims abstract description 18
- 125000000524 functional group Chemical group 0.000 claims abstract description 17
- 239000002904 solvent Substances 0.000 claims abstract description 15
- 125000000923 (C1-C30) alkyl group Chemical group 0.000 claims abstract description 13
- 125000004446 heteroarylalkyl group Chemical group 0.000 claims abstract description 13
- 125000003710 aryl alkyl group Chemical group 0.000 claims abstract description 12
- 125000004104 aryloxy group Chemical group 0.000 claims abstract description 12
- 125000005553 heteroaryloxy group Chemical group 0.000 claims abstract description 12
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 11
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims abstract description 11
- 150000007860 aryl ester derivatives Chemical class 0.000 claims abstract description 10
- 125000004405 heteroalkoxy group Chemical group 0.000 claims abstract description 10
- 150000001450 anions Chemical class 0.000 claims abstract description 5
- 229910052731 fluorine Inorganic materials 0.000 claims abstract description 5
- 229910052794 bromium Inorganic materials 0.000 claims abstract description 4
- 229910052801 chlorine Inorganic materials 0.000 claims abstract description 4
- 229910052740 iodine Inorganic materials 0.000 claims abstract description 4
- 125000000129 anionic group Chemical group 0.000 claims abstract 2
- 125000000217 alkyl group Chemical group 0.000 claims description 22
- 239000003431 cross linking reagent Substances 0.000 claims description 19
- 125000004185 ester group Chemical group 0.000 claims description 15
- 238000000034 method Methods 0.000 claims description 15
- 125000001424 substituent group Chemical group 0.000 claims description 15
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims description 12
- 125000005842 heteroatom Chemical group 0.000 claims description 11
- 229910052739 hydrogen Inorganic materials 0.000 claims description 11
- 239000001257 hydrogen Substances 0.000 claims description 11
- 229910052717 sulfur Inorganic materials 0.000 claims description 11
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 claims description 10
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 10
- 229910052760 oxygen Inorganic materials 0.000 claims description 10
- 229910052698 phosphorus Inorganic materials 0.000 claims description 10
- 229920000642 polymer Polymers 0.000 claims description 9
- 125000003837 (C1-C20) alkyl group Chemical group 0.000 claims description 8
- 125000006736 (C6-C20) aryl group Chemical group 0.000 claims description 8
- 229910052757 nitrogen Inorganic materials 0.000 claims description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 7
- 238000010382 chemical cross-linking Methods 0.000 claims description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 7
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims description 6
- 229920002873 Polyethylenimine Polymers 0.000 claims description 5
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 claims description 5
- 125000005264 aryl amine group Chemical group 0.000 claims description 5
- 229910052736 halogen Inorganic materials 0.000 claims description 5
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims description 4
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims description 4
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 claims description 4
- 239000007788 liquid Substances 0.000 claims description 4
- 239000000178 monomer Substances 0.000 claims description 4
- 125000000168 pyrrolyl group Chemical group 0.000 claims description 4
- 239000007787 solid Substances 0.000 claims description 4
- 239000004593 Epoxy Substances 0.000 claims description 3
- 229920000877 Melamine resin Polymers 0.000 claims description 3
- 125000004429 atom Chemical group 0.000 claims description 3
- 150000002367 halogens Chemical class 0.000 claims description 3
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 claims description 3
- 239000012528 membrane Substances 0.000 claims description 3
- 229930192474 thiophene Natural products 0.000 claims description 3
- 229910015892 BF 4 Inorganic materials 0.000 claims description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 2
- 229910021115 PF 6 Inorganic materials 0.000 claims description 2
- 239000002202 Polyethylene glycol Substances 0.000 claims description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 2
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 claims description 2
- 125000005907 alkyl ester group Chemical group 0.000 claims description 2
- 150000005840 aryl radicals Chemical class 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims description 2
- 229920000767 polyaniline Polymers 0.000 claims description 2
- 229920001223 polyethylene glycol Polymers 0.000 claims description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 2
- 239000008096 xylene Substances 0.000 claims description 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 2
- 125000006716 (C1-C6) heteroalkyl group Chemical group 0.000 claims 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 claims 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 claims 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 claims 1
- 238000010791 quenching Methods 0.000 abstract description 2
- 230000000171 quenching effect Effects 0.000 abstract description 2
- 239000010410 layer Substances 0.000 description 87
- 238000002347 injection Methods 0.000 description 25
- 239000007924 injection Substances 0.000 description 25
- 239000010408 film Substances 0.000 description 21
- 239000000463 material Substances 0.000 description 19
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 18
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 17
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 14
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 12
- 238000006243 chemical reaction Methods 0.000 description 11
- 229920001609 Poly(3,4-ethylenedioxythiophene) Polymers 0.000 description 10
- 230000005525 hole transport Effects 0.000 description 10
- 239000000758 substrate Substances 0.000 description 10
- 230000001629 suppression Effects 0.000 description 9
- 238000004519 manufacturing process Methods 0.000 description 8
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 7
- 230000015572 biosynthetic process Effects 0.000 description 7
- 125000004432 carbon atom Chemical group C* 0.000 description 7
- 229910052799 carbon Inorganic materials 0.000 description 6
- 239000011259 mixed solution Substances 0.000 description 6
- 238000001953 recrystallisation Methods 0.000 description 6
- 239000000377 silicon dioxide Substances 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 238000003786 synthesis reaction Methods 0.000 description 6
- 239000000872 buffer Substances 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- 239000002019 doping agent Substances 0.000 description 5
- 229910001495 sodium tetrafluoroborate Inorganic materials 0.000 description 4
- 238000004528 spin coating Methods 0.000 description 4
- MCTWTZJPVLRJOU-UHFFFAOYSA-N 1-methyl-1H-imidazole Chemical compound CN1C=CN=C1 MCTWTZJPVLRJOU-UHFFFAOYSA-N 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 229910052791 calcium Inorganic materials 0.000 description 3
- 150000001721 carbon Chemical group 0.000 description 3
- 150000003949 imides Chemical class 0.000 description 3
- IBHBKWKFFTZAHE-UHFFFAOYSA-N n-[4-[4-(n-naphthalen-1-ylanilino)phenyl]phenyl]-n-phenylnaphthalen-1-amine Chemical compound 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
- 150000002894 organic compounds Chemical class 0.000 description 3
- 239000012044 organic layer Substances 0.000 description 3
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 3
- 125000006413 ring segment Chemical group 0.000 description 3
- 239000010409 thin film Substances 0.000 description 3
- PAMIQIKDUOTOBW-UHFFFAOYSA-N 1-methylpiperidine Chemical compound CN1CCCCC1 PAMIQIKDUOTOBW-UHFFFAOYSA-N 0.000 description 2
- UINDRJHZBAGQFD-UHFFFAOYSA-O 2-ethyl-3-methyl-1h-imidazol-3-ium Chemical compound CCC1=[NH+]C=CN1C UINDRJHZBAGQFD-UHFFFAOYSA-O 0.000 description 2
- ITQTTZVARXURQS-UHFFFAOYSA-N 3-methylpyridine Chemical compound CC1=CC=CN=C1 ITQTTZVARXURQS-UHFFFAOYSA-N 0.000 description 2
- MAGFQRLKWCCTQJ-UHFFFAOYSA-M 4-ethenylbenzenesulfonate Chemical compound [O-]S(=O)(=O)C1=CC=C(C=C)C=C1 MAGFQRLKWCCTQJ-UHFFFAOYSA-M 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 0 CC1N(C)C(*)(C2CCCCCCC2)N(C)C1* Chemical compound CC1N(C)C(*)(C2CCCCCCC2)N(C)C1* 0.000 description 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 2
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 2
- 229910013528 LiN(SO2 CF3)2 Inorganic materials 0.000 description 2
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 125000003277 amino group Chemical group 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
- 150000001491 aromatic compounds Chemical class 0.000 description 2
- 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 2
- RDHPKYGYEGBMSE-UHFFFAOYSA-N bromoethane Chemical compound CCBr RDHPKYGYEGBMSE-UHFFFAOYSA-N 0.000 description 2
- 238000012512 characterization method Methods 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- NIHNNTQXNPWCJQ-UHFFFAOYSA-N fluorene Chemical compound C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 description 2
- 239000011737 fluorine Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 239000010931 gold Substances 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- AMGQUBHHOARCQH-UHFFFAOYSA-N indium;oxotin Chemical compound [In].[Sn]=O AMGQUBHHOARCQH-UHFFFAOYSA-N 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 150000004866 oxadiazoles Chemical class 0.000 description 2
- ATGUVEKSASEFFO-UHFFFAOYSA-N p-aminodiphenylamine Chemical compound C1=CC(N)=CC=C1NC1=CC=CC=C1 ATGUVEKSASEFFO-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
- 239000003495 polar organic solvent Substances 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 125000005504 styryl group Chemical group 0.000 description 2
- 238000012546 transfer Methods 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
- UHXOHPVVEHBKKT-UHFFFAOYSA-N 1-(2,2-diphenylethenyl)-4-[4-(2,2-diphenylethenyl)phenyl]benzene Chemical compound C=1C=C(C=2C=CC(C=C(C=3C=CC=CC=3)C=3C=CC=CC=3)=CC=2)C=CC=1C=C(C=1C=CC=CC=1)C1=CC=CC=C1 UHXOHPVVEHBKKT-UHFFFAOYSA-N 0.000 description 1
- WECOUKMONWFOGF-UHFFFAOYSA-N 1-[2-[3,5-bis[2-(9h-carbazol-1-yl)-5-methoxyphenyl]phenyl]-4-methoxyphenyl]-9h-carbazole Chemical compound C12=CC=CC=C2NC2=C1C=CC=C2C1=CC=C(OC)C=C1C1=CC(C=2C(=CC=C(OC)C=2)C=2C=3NC4=CC=CC=C4C=3C=CC=2)=CC(C=2C(=CC=C(OC)C=2)C=2C=3NC4=CC=CC=C4C=3C=CC=2)=C1 WECOUKMONWFOGF-UHFFFAOYSA-N 0.000 description 1
- PRUCJKSKYARXJB-UHFFFAOYSA-N 1-[2-[3,5-bis[2-(9h-carbazol-1-yl)phenyl]phenyl]phenyl]-9h-carbazole Chemical compound C12=CC=CC=C2NC2=C1C=CC=C2C1=CC=CC=C1C1=CC(C=2C(=CC=CC=2)C=2C=3NC4=CC=CC=C4C=3C=CC=2)=CC(C=2C(=CC=CC=2)C=2C=3NC4=CC=CC=C4C=3C=CC=2)=C1 PRUCJKSKYARXJB-UHFFFAOYSA-N 0.000 description 1
- AHBDIQVWSLNELJ-UHFFFAOYSA-N 1-[3,5-bis(9h-carbazol-1-yl)phenyl]-9h-carbazole Chemical group C12=CC=CC=C2NC2=C1C=CC=C2C1=CC(C=2C=3NC4=CC=CC=C4C=3C=CC=2)=CC(C2=C3NC=4C(C3=CC=C2)=CC=CC=4)=C1 AHBDIQVWSLNELJ-UHFFFAOYSA-N 0.000 description 1
- DBDOZRBRAYSLFX-UHFFFAOYSA-N 1-[4-[4-(9h-carbazol-1-yl)-2-methylphenyl]-3-methylphenyl]-9h-carbazole Chemical group N1C2=CC=CC=C2C2=C1C(C=1C=C(C(=CC=1)C=1C(=CC(=CC=1)C=1C3=C(C4=CC=CC=C4N3)C=CC=1)C)C)=CC=C2 DBDOZRBRAYSLFX-UHFFFAOYSA-N 0.000 description 1
- IERDDDBDINUYCD-UHFFFAOYSA-N 1-[4-[4-(9h-carbazol-1-yl)phenyl]phenyl]-9h-carbazole Chemical group C12=CC=CC=C2NC2=C1C=CC=C2C(C=C1)=CC=C1C(C=C1)=CC=C1C1=C2NC3=CC=CC=C3C2=CC=C1 IERDDDBDINUYCD-UHFFFAOYSA-N 0.000 description 1
- HLVFKOKELQSXIQ-UHFFFAOYSA-N 1-bromo-2-methylpropane Chemical compound CC(C)CBr HLVFKOKELQSXIQ-UHFFFAOYSA-N 0.000 description 1
- MPPPKRYCTPRNTB-UHFFFAOYSA-N 1-bromobutane Chemical compound CCCCBr MPPPKRYCTPRNTB-UHFFFAOYSA-N 0.000 description 1
- IQQRAVYLUAZUGX-UHFFFAOYSA-N 1-butyl-3-methylimidazolium Chemical compound CCCCN1C=C[N+](C)=C1 IQQRAVYLUAZUGX-UHFFFAOYSA-N 0.000 description 1
- AVFZOVWCLRSYKC-UHFFFAOYSA-N 1-methylpyrrolidine Chemical compound CN1CCCC1 AVFZOVWCLRSYKC-UHFFFAOYSA-N 0.000 description 1
- GKWLILHTTGWKLQ-UHFFFAOYSA-N 2,3-dihydrothieno[3,4-b][1,4]dioxine Chemical compound O1CCOC2=CSC=C21 GKWLILHTTGWKLQ-UHFFFAOYSA-N 0.000 description 1
- YLYPIBBGWLKELC-RMKNXTFCSA-N 2-[2-[(e)-2-[4-(dimethylamino)phenyl]ethenyl]-6-methylpyran-4-ylidene]propanedinitrile Chemical compound C1=CC(N(C)C)=CC=C1\C=C\C1=CC(=C(C#N)C#N)C=C(C)O1 YLYPIBBGWLKELC-RMKNXTFCSA-N 0.000 description 1
- RKVIAZWOECXCCM-UHFFFAOYSA-N 2-carbazol-9-yl-n,n-diphenylaniline Chemical compound C1=CC=CC=C1N(C=1C(=CC=CC=1)N1C2=CC=CC=C2C2=CC=CC=C21)C1=CC=CC=C1 RKVIAZWOECXCCM-UHFFFAOYSA-N 0.000 description 1
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- OGGKVJMNFFSDEV-UHFFFAOYSA-N 3-methyl-n-[4-[4-(n-(3-methylphenyl)anilino)phenyl]phenyl]-n-phenylaniline Chemical compound 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
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- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- 229910016036 BaF 2 Inorganic materials 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
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- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 241000284156 Clerodendrum quadriloculare Species 0.000 description 1
- 239000004971 Cross linker Substances 0.000 description 1
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- 229920000144 PEDOT:PSS Polymers 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
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- 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
- H10K85/10—Organic polymers or oligomers
- H10K85/111—Organic polymers or oligomers comprising aromatic, heteroaromatic, or aryl chains, e.g. polyaniline, polyphenylene or polyphenylene vinylene
- H10K85/113—Heteroaromatic compounds comprising sulfur or selene, e.g. polythiophene
- H10K85/1135—Polyethylene dioxythiophene [PEDOT]; Derivatives thereof
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/17—Amines; Quaternary ammonium compounds
- C08K5/18—Amines; Quaternary ammonium compounds with aromatically bound amino groups
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
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- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
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- C—CHEMISTRY; METALLURGY
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- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
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- 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
- H10K85/649—Aromatic compounds comprising a hetero atom
- H10K85/654—Aromatic compounds comprising a hetero atom comprising only nitrogen as heteroatom
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- H—ELECTRICITY
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- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K50/00—Organic light-emitting devices
- H10K50/10—OLEDs or polymer light-emitting diodes [PLED]
- H10K50/17—Carrier injection layers
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- 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]
- H10K50/17—Carrier injection layers
- H10K50/171—Electron injection layers
Abstract
Description
Claims (14)
- 전도성 고분자, 하기 화학식 2 내지 화학식 5에서 선택되는 하나 이상의 유기 이온염 및 용매를 포함하는 유기 광전 소자용 전도성 고분자 조성물.(상기 R1과 R2는 독립적으로 C1-C30의 알킬기; C1-C30의 헤테로알킬기; C1-C30의 알콕시기; C1-C30의 헤테로알콕시기; C6-C30의 아릴기, C6-C30의 아릴알킬기, C6-C30의 아릴옥시기, C2-C30의 헤테로아릴기, C2-C30의 헤테로아릴알킬기; C2-C30의 헤테로아릴옥시기; C5-C20의 사이클로알킬기; C2-C30의 헤테로사이클로알킬기; C1-C30의 알킬에스테르기; C1-C30의 헤테로알킬에스테르기; C6-C30의 아릴에스테르기; 및 C2-C30의 헤테로아릴에스테르기로 이루어진 군에서 선택되며 각 작용기 내의 수소는 할로겐 등 다른 작용기로 치환될 수 있고,상기 R3 내지 R12는 독립적으로 C1-C30의 알킬기; C1-C30의 헤테로알킬기; C1-C30의 알콕시기; C1-C30의 헤테로알콕시기; C6-C30의 아릴기; C6-C30의 아릴알킬기; C6-C30의 아릴옥시기; C2-C30의 헤테로아릴기; C2-C30의 헤테로아릴알킬기; C2-C30의 헤테로아릴옥시기; C5-C20의 사이클로알킬기; C2-C30의 헤테로사이클로알 킬기; C1-C30의 알킬에스테르기; C1-C30의 헤테로알킬에스테르기; C6-C30의 아릴에스테르기; 및 C2-C30의 헤테로아릴에스테르기로 이루어진 군에서 선택되며, 각 작용기 내의 수소는 할로겐 등 다른 작용기로 치환될 수 있으며,X-는 음이온 작용기로서, X는 F, Cl, Br, I, BF4, PF6, 또는 (CnF2n +1SO2)2N (n은 1 내지 50의 자연수) 등 음이온이 되었을 때 안정화될 수 있는 원자 또는 분자이다.)
- 제 1 항에 있어서,상기 유기이온염은 상기 전도성 고분자 및 용매 100 중량부에 대하여 상기 유기 이온염이 상온에서 액체인 경우 0.05 내지 30중량부 첨가되는 것을 특징으로 하는 유기 광전 소자용 전도성 고분자 조성물.
- 제 1 항에 있어서,상기 유기이온염은 상기 전도성 고분자 및 용매 100 중량부에 대하여 상기 유기이온염이 상온에서 고체인 경우 0.05 내지 50 중량부 첨가되는 것을 특징으로 하는 유기 광전 소자용 전도성 고분자 조성물.
- 제 1 항에 있어서,상기 전도성 고분자는 하기 화학식 6으로 표시되는 폴리아닐린 또는 그 유도체 또는 하기 화학식 7로 표시되는 피롤, 티오펜 또는 그 유도체를 단량체로 하여 중합한 것을 특징으로 하는 유기 광전 소자용 전도성 고분자 조성물.(X는 NH; N, O, S 또는 P와 같은 헤테로 원자에 C1-C20의 알킬기 또는 C6-C20의 아릴기가 결합된 것이고,상기 Ra, Rb, Rc, Rd는 각각 독립적으로 수소; C1-C30의 알킬기; C1-C30의 헤테로알킬기; C1-C30의 알콕시기; C1-C30의 헤테로알콕시기; C6-C30의 아릴기; C6-C30의 아릴알킬기; C6-C30의 아릴옥시기; C6-C30의 아릴아민기; C6-C30의 피롤기; C6-C30의 티오펜기; C2-C30의 헤테로아릴기; C2-C30의 헤테로아릴알킬기; C2-C30의 헤테로아릴옥시기; C5-C20의 사이클로알킬기; C2-C30의 헤테로사이클로알킬기; C1-C30의 알킬에스테르기; C1-C30의 헤테로알킬에스테르기; C6-C30의 아릴에스테르기; 및 C2-C30의 헤테로아릴에스테르기로 이루어진 군에서 선택되는 하나이며 각 작용기 내의 수소는 다른 작용기로 치환될 수 있고,상기 Re, Rf은 각각 독립적으로 NH; N, O, S 또는 P와 같은 헤테로 원자에 C1-C20의 알킬기 또는 C6-C20의 아릴기가 결합된 것; C1-C30의 알킬기; C6-C30의 아릴기; C1-C30의 알콕시기; C1-C30의 헤테로알킬기; C1-C30의 헤테로알콕시기; C6-C30의 아릴알킬기; C6-C30의 아릴옥시기; C6-C30의 아릴아민기; C6-C30의 피롤기; C6-C30의 티오펜기; C2-C30의 헤테로아릴기; C2-C30의 헤테로아릴알킬기; C2-C30의 헤테로아릴옥시기; C5-C20의 사이클로알킬기; C2-C30의 헤테로사이클로알킬기; C1-C30의 알킬에스테르기; C1-C30의 헤테로알킬에스테르기; C6-C30의 아릴에스테르기; 및 C2-C30의 헤테로아릴에스테르기로 이루어진 군에서 선택되는 하나이며 각 작용기 내의 수소는 다른 작용기로 치환될 수 있다)
- 제 1 항에 있어서,상기 전도성 고분자는 하기 화학식 8로 표시되는 단량체를 중합한 것을 특징으로 하는 유기 광전 소자용 전도성 고분자 조성물.(X는 NH, N, O, S 또는 P와 같은 헤테로 원자에 C1-C20의 알킬기 또는 C6-C20의 아릴기가 결합된 것이고,Y는 NH, N, O, S 또는 P와 같은 헤테로 원자에 C1-C20의 알킬기 또는 C6-C20의 아릴기가 결합된 것이고,m과 n은 각각 독립적이고 0 내지 9의 정수이다.Z는 -(CH2)x-CRgRh-(CH2)y이고, Rg 및 Rh는 각각 독립적으로 H, C1-C20의 알킬 라디칼, C6-C14의 아릴 라디칼 및 -CH2-ORi 중에서 선택되는 하나이며, 이때, Ri는 H, C1-C6의 알킬산, C1-C6의 알킬에스테르, C1-C6의 헤테로알킬산 및 C1-C6의 알킬술포닉산 중에서 선택되는 하나이며, 각 작용기 내의 수소는 다른 치환기로 치환될 수 있다.)
- 제 1 항에 있어서,상기 용매는 물, 알코올, 디메틸포름아미드(DMF), 디메틸술폭사이드, 톨루엔, 크실렌, 및 클로로벤젠으로 이루어지는 군에서 선택되는 하나 이상의 용매를 포함하는 것을 특징으로 하는 유기 광전 소자용 전도성 고분자 조성물.
- 제 1 항에 있어서,상기 전도성 고분자 조성물은 물리적 가교제 또는 화학적 가교제를 더 포함하는 것을 특징으로 하는 유기 광전 소자용 전도성 고분자 조성물.
- 제 7 항에 있어서,상기 물리적 가교제는 글리세롤, 부탄올, 폴리비닐알코올, 폴리에틸렌글리콜, 폴리에틸렌이민, 및 폴리비닐피롤리돈으로 이루어진 군에서 선택되는 하나 이상인 것을 특징으로 하는 유기 광전 소자용 전도성 고분자 조성물.
- 제 7 항에 있어서,상기 화학적 가교제는 테트라에틸옥시실란, 폴리아지리딘, 멜라민계 고분자, 및 에폭시계 고분자로 이루어진 군에서 선택되는 하나 이상인 것을 특징으로 하는 유기 광전 소자용 전도성 고분자 조성물.
- 제 7 항에 있어서,상기 물리적 가교제는 상기 제 1 항의 전도성 고분자 조성물 100 중량부에 대하여 0.001 내지 5 중량부가 포함되는 것을 특징으로 하는 유기 광전 소자용 전도성 고분자 조성물.
- 제 7 항에 있어서,상기 화학적 가교제는 상기 제1항의 전도성 고분자 조성물 100 중량부에 대하여 0.001 내지 50 중량부가 포함되는 것을 특징으로 하는 유기 광전 소자용 전도성 고분자 조성물.
- 상기 제 1 항 내지 제 11 항 중 어느 한 항의 전도성 고분자 조성물에 의해 형성되는 유기 광전 소자용 전도성 고분자 조성물막.
- 제 4 항의 전도성 고분자 100중량부에 대해서 화학식 2 내지 화학식 5에서 선택되는 하나 이상의 유기 이온염 0.05 내지 50중량부를 포함하는 전도성 고분자 조성물막.
- 제 12 항의 전도성 고분자 조성물막을 포함하는 유기 광전 소자.
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
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KR1020060068867A KR100762014B1 (ko) | 2006-07-24 | 2006-07-24 | 유기이온염을 포함하는 전도성 고분자 조성물 및 이를이용한 유기 광전 소자 |
TW096126573A TWI361811B (en) | 2006-07-24 | 2007-07-20 | Conductive polymer composition comprising organic ionic salt and optoelectronic device using the same |
US11/782,025 US20080017852A1 (en) | 2006-07-24 | 2007-07-24 | Conductive Polymer Composition Comprising Organic Ionic Salt and Optoelectronic Device Using the Same |
JP2007192546A JP4686510B2 (ja) | 2006-07-24 | 2007-07-24 | 有機塩を含む伝導性高分子組成物及びこれを用いた有機光電素子 |
DE102007034309A DE102007034309A1 (de) | 2006-07-24 | 2007-07-24 | Leitfähige Polymerzusammensetzung, umfassend ein organisches ionisches Salz, sowie eine optoelektronische Vorrichtung, in der diese verwendet wird |
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KR100881234B1 (ko) * | 2007-11-30 | 2009-02-05 | 제일모직주식회사 | 수분산 전도성 고분자 화합물 및 이를 포함하는 유기 광전소자 |
US8747702B2 (en) | 2009-12-29 | 2014-06-10 | Cheil Industries, Inc. | Conductive polymer, conductive polymer composition, conductive polymer layer, and organic photoelectric device including the conductive polymer layer |
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KR101111435B1 (ko) * | 2009-03-11 | 2012-02-16 | 광 석 서 | 정공주입층 및 정공수송층 재료로 사용가능한 화합물 및 이를 이용한 유기발광소자 |
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GB201317966D0 (en) | 2013-10-10 | 2013-11-27 | Univ Manchester | Nanoparticles |
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EP2876141A1 (en) * | 2013-11-21 | 2015-05-27 | Solvay SA | Conductive polymer composition and layer made therefrom |
US20160312006A1 (en) * | 2013-12-11 | 2016-10-27 | Rhodia Operations | Polymer compositions, films, gels, and foams containing sulfonylimide salts, and electronic devices containing such films, gels, and foams |
DE102015103895A1 (de) * | 2015-03-17 | 2016-09-22 | Osram Oled Gmbh | Verfahren zum Herstellen eines organischen Bauelements |
US11499007B2 (en) * | 2016-01-15 | 2022-11-15 | The Board Of Trustees Of The Leland Stanford Junior University | Highly stretchable, transparent, and conductive polymer |
CN108063001B (zh) * | 2017-12-07 | 2020-12-01 | 南京邮电大学 | 一种薄膜电极及其制作方法与应用 |
CN111303590B (zh) * | 2020-02-01 | 2021-11-23 | 华南理工大学 | 一种用于pedot:pss改性的有机离子盐添加剂及其应用 |
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US8747702B2 (en) | 2009-12-29 | 2014-06-10 | Cheil Industries, Inc. | Conductive polymer, conductive polymer composition, conductive polymer layer, and organic photoelectric device including the conductive polymer layer |
Also Published As
Publication number | Publication date |
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TW200806703A (en) | 2008-02-01 |
TWI361811B (en) | 2012-04-11 |
JP4686510B2 (ja) | 2011-05-25 |
US20080017852A1 (en) | 2008-01-24 |
JP2008038147A (ja) | 2008-02-21 |
DE102007034309A1 (de) | 2008-05-08 |
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