JP2012524834A - 導電性ポリマー組成物およびそれから作製されたフィルム - Google Patents
導電性ポリマー組成物およびそれから作製されたフィルム Download PDFInfo
- Publication number
- JP2012524834A JP2012524834A JP2012507410A JP2012507410A JP2012524834A JP 2012524834 A JP2012524834 A JP 2012524834A JP 2012507410 A JP2012507410 A JP 2012507410A JP 2012507410 A JP2012507410 A JP 2012507410A JP 2012524834 A JP2012524834 A JP 2012524834A
- Authority
- JP
- Japan
- Prior art keywords
- dispersion
- oxide
- acid
- polymer
- group
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 229920001940 conductive polymer Polymers 0.000 title claims abstract description 59
- 239000000203 mixture Substances 0.000 title abstract description 26
- 239000006185 dispersion Substances 0.000 claims abstract description 67
- 239000002253 acid Substances 0.000 claims abstract description 61
- 229920000642 polymer Polymers 0.000 claims abstract description 61
- 239000002245 particle Substances 0.000 claims abstract description 12
- 229920006120 non-fluorinated polymer Polymers 0.000 claims abstract 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical group O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 34
- 239000002105 nanoparticle Substances 0.000 claims description 30
- 229920001577 copolymer Polymers 0.000 claims description 29
- 239000000377 silicon dioxide Substances 0.000 claims description 13
- 229920000128 polypyrrole Polymers 0.000 claims description 11
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 claims description 11
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 claims description 10
- 229920001609 Poly(3,4-ethylenedioxythiophene) Polymers 0.000 claims description 8
- 229920000767 polyaniline Polymers 0.000 claims description 8
- 150000007513 acids Chemical class 0.000 claims description 7
- JHRWWRDRBPCWTF-OLQVQODUSA-N captafol Chemical compound C1C=CC[C@H]2C(=O)N(SC(Cl)(Cl)C(Cl)Cl)C(=O)[C@H]21 JHRWWRDRBPCWTF-OLQVQODUSA-N 0.000 claims description 7
- 125000000542 sulfonic acid group Chemical group 0.000 claims description 7
- 229930192474 thiophene Natural products 0.000 claims description 7
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 claims description 6
- 229920000123 polythiophene Polymers 0.000 claims description 6
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 5
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims description 4
- JKQOBWVOAYFWKG-UHFFFAOYSA-N molybdenum trioxide Chemical compound O=[Mo](=O)=O JKQOBWVOAYFWKG-UHFFFAOYSA-N 0.000 claims description 4
- 229960004643 cupric oxide Drugs 0.000 claims description 3
- PFZLGKHSYILJTH-UHFFFAOYSA-N thieno[2,3-c]thiophene Chemical compound S1C=C2SC=CC2=C1 PFZLGKHSYILJTH-UHFFFAOYSA-N 0.000 claims description 3
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 claims description 3
- AUUAIQGEFIEHRO-UHFFFAOYSA-N 1,1,2,2-tetrafluoro-2-[1,1,1,2,3,3-hexafluoro-3-(1,2,2-trifluoroethenoxy)propan-2-yl]oxyethanesulfonic acid Chemical compound OS(=O)(=O)C(F)(F)C(F)(F)OC(F)(C(F)(F)F)C(F)(F)OC(F)=C(F)F AUUAIQGEFIEHRO-UHFFFAOYSA-N 0.000 claims description 2
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical group FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 claims description 2
- WTFWZOSMUGZKNZ-UHFFFAOYSA-N 1H-indol-7-amine Chemical compound NC1=CC=CC2=C1NC=C2 WTFWZOSMUGZKNZ-UHFFFAOYSA-N 0.000 claims description 2
- LUNUNJFSHKSXGQ-UHFFFAOYSA-N 4-Aminoindole Chemical compound NC1=CC=CC2=C1C=CN2 LUNUNJFSHKSXGQ-UHFFFAOYSA-N 0.000 claims description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 2
- 239000005977 Ethylene Substances 0.000 claims description 2
- XHCLAFWTIXFWPH-UHFFFAOYSA-N [O-2].[O-2].[O-2].[O-2].[O-2].[V+5].[V+5] Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[V+5].[V+5] XHCLAFWTIXFWPH-UHFFFAOYSA-N 0.000 claims description 2
- 125000005336 allyloxy group Chemical group 0.000 claims description 2
- KOPBYBDAPCDYFK-UHFFFAOYSA-N caesium oxide Chemical compound [O-2].[Cs+].[Cs+] KOPBYBDAPCDYFK-UHFFFAOYSA-N 0.000 claims description 2
- 229910001942 caesium oxide Inorganic materials 0.000 claims description 2
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 claims description 2
- SIWVEOZUMHYXCS-UHFFFAOYSA-N oxo(oxoyttriooxy)yttrium Chemical compound O=[Y]O[Y]=O SIWVEOZUMHYXCS-UHFFFAOYSA-N 0.000 claims description 2
- BPUBBGLMJRNUCC-UHFFFAOYSA-N oxygen(2-);tantalum(5+) Chemical class [O-2].[O-2].[O-2].[O-2].[O-2].[Ta+5].[Ta+5] BPUBBGLMJRNUCC-UHFFFAOYSA-N 0.000 claims description 2
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 claims description 2
- 229920002580 poly(selenophene-2,5-diyl) polymer Polymers 0.000 claims description 2
- 229910001954 samarium oxide Inorganic materials 0.000 claims description 2
- 229940075630 samarium oxide Drugs 0.000 claims description 2
- FKTOIHSPIPYAPE-UHFFFAOYSA-N samarium(iii) oxide Chemical compound [O-2].[O-2].[O-2].[Sm+3].[Sm+3] FKTOIHSPIPYAPE-UHFFFAOYSA-N 0.000 claims description 2
- 235000012239 silicon dioxide Nutrition 0.000 claims description 2
- 229910052814 silicon oxide Inorganic materials 0.000 claims description 2
- 229910001936 tantalum oxide Inorganic materials 0.000 claims description 2
- 150000005087 tellurophenes Chemical class 0.000 claims description 2
- 239000004408 titanium dioxide Substances 0.000 claims description 2
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 claims description 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 2
- 229910001935 vanadium oxide Inorganic materials 0.000 claims description 2
- 239000011787 zinc oxide Substances 0.000 claims description 2
- 229910001928 zirconium oxide Inorganic materials 0.000 claims description 2
- GWTYBAOENKSFAY-UHFFFAOYSA-N 1,1,1,2,2-pentafluoro-2-(1,2,2-trifluoroethenoxy)ethane Chemical compound FC(F)=C(F)OC(F)(F)C(F)(F)F GWTYBAOENKSFAY-UHFFFAOYSA-N 0.000 claims 1
- OUPSAGJPSYBVNO-UHFFFAOYSA-N 1,1,1,2,3,3-hexafluoro-3-(1,1,2,2-tetrafluoroethoxy)-2-(1,2,2-trifluoroethenoxy)propane Chemical compound FC(F)C(F)(F)OC(F)(F)C(F)(C(F)(F)F)OC(F)=C(F)F OUPSAGJPSYBVNO-UHFFFAOYSA-N 0.000 claims 1
- 229910052787 antimony Inorganic materials 0.000 claims 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 claims 1
- 230000003647 oxidation Effects 0.000 claims 1
- 238000007254 oxidation reaction Methods 0.000 claims 1
- 150000003460 sulfonic acids Chemical class 0.000 claims 1
- NMFKEMBATXKZSP-UHFFFAOYSA-N thieno[3,2-b]thiophene Chemical compound S1C=CC2=C1C=CS2.S1C=CC2=C1C=CS2 NMFKEMBATXKZSP-UHFFFAOYSA-N 0.000 claims 1
- 239000010410 layer Substances 0.000 description 121
- 239000000463 material Substances 0.000 description 59
- 239000000178 monomer Substances 0.000 description 53
- -1 hydrogen ions Chemical class 0.000 description 51
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 47
- 239000010408 film Substances 0.000 description 43
- 125000000217 alkyl group Chemical group 0.000 description 33
- 229910052739 hydrogen Inorganic materials 0.000 description 31
- 239000001257 hydrogen Substances 0.000 description 31
- RZXLPPRPEOUENN-UHFFFAOYSA-N Chlorfenson Chemical compound C1=CC(Cl)=CC=C1OS(=O)(=O)C1=CC=C(Cl)C=C1 RZXLPPRPEOUENN-UHFFFAOYSA-N 0.000 description 26
- 230000006870 function Effects 0.000 description 25
- 238000002347 injection Methods 0.000 description 25
- 239000007924 injection Substances 0.000 description 25
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 24
- 238000000034 method Methods 0.000 description 24
- 230000002378 acidificating effect Effects 0.000 description 19
- 239000002131 composite material Substances 0.000 description 19
- 125000003118 aryl group Chemical group 0.000 description 18
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 18
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 16
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 15
- 229910052757 nitrogen Inorganic materials 0.000 description 15
- 239000002243 precursor Substances 0.000 description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
- URLKBWYHVLBVBO-UHFFFAOYSA-N Para-Xylene Chemical group CC1=CC=C(C)C=C1 URLKBWYHVLBVBO-UHFFFAOYSA-N 0.000 description 14
- 150000007942 carboxylates Chemical class 0.000 description 14
- 150000001875 compounds Chemical class 0.000 description 14
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 13
- 125000003342 alkenyl group Chemical group 0.000 description 13
- 229910052751 metal Inorganic materials 0.000 description 13
- 239000002184 metal Substances 0.000 description 13
- 239000000523 sample Substances 0.000 description 12
- 230000000052 comparative effect Effects 0.000 description 11
- 238000000151 deposition Methods 0.000 description 11
- 229910052717 sulfur Inorganic materials 0.000 description 11
- UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 10
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 10
- 125000002947 alkylene group Chemical group 0.000 description 10
- 230000005525 hole transport Effects 0.000 description 10
- 239000007788 liquid Substances 0.000 description 10
- 230000005855 radiation Effects 0.000 description 10
- 239000004065 semiconductor Substances 0.000 description 10
- 239000004593 Epoxy Substances 0.000 description 9
- 101001102158 Homo sapiens Phosphatidylserine synthase 1 Proteins 0.000 description 9
- 102100039298 Phosphatidylserine synthase 1 Human genes 0.000 description 9
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 9
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 9
- 239000003960 organic solvent Substances 0.000 description 9
- 229910052711 selenium Inorganic materials 0.000 description 9
- 239000011669 selenium Substances 0.000 description 9
- 229910000077 silane Inorganic materials 0.000 description 9
- 239000007787 solid Substances 0.000 description 9
- 229910052714 tellurium Inorganic materials 0.000 description 9
- 125000002723 alicyclic group Chemical group 0.000 description 8
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 8
- 229910052731 fluorine Inorganic materials 0.000 description 8
- 229910052736 halogen Inorganic materials 0.000 description 8
- 150000002367 halogens Chemical class 0.000 description 8
- 125000001424 substituent group Chemical group 0.000 description 8
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 7
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 7
- 239000000654 additive Substances 0.000 description 7
- 125000004450 alkenylene group Chemical group 0.000 description 7
- 125000003545 alkoxy group Chemical group 0.000 description 7
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 7
- 230000008901 benefit Effects 0.000 description 7
- 125000004432 carbon atom Chemical group C* 0.000 description 7
- 239000011737 fluorine Substances 0.000 description 7
- 239000011521 glass Substances 0.000 description 7
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 6
- 125000002877 alkyl aryl group Chemical group 0.000 description 6
- 125000006350 alkyl thio alkyl group Chemical group 0.000 description 6
- 125000003710 aryl alkyl group Chemical group 0.000 description 6
- 125000001589 carboacyl group Chemical group 0.000 description 6
- 125000001153 fluoro group Chemical group F* 0.000 description 6
- ZAHSNWXGKUBLHM-UHFFFAOYSA-N hydroperoxy(hydroxy)silane Chemical compound OO[SiH2]O ZAHSNWXGKUBLHM-UHFFFAOYSA-N 0.000 description 6
- 238000005259 measurement Methods 0.000 description 6
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 6
- 229910052760 oxygen Inorganic materials 0.000 description 6
- 238000006116 polymerization reaction Methods 0.000 description 6
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 6
- 239000010409 thin film Substances 0.000 description 6
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical group OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 5
- 229920000144 PEDOT:PSS Polymers 0.000 description 5
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 5
- 229910052783 alkali metal Inorganic materials 0.000 description 5
- 150000001340 alkali metals Chemical class 0.000 description 5
- 125000004183 alkoxy alkyl group Chemical group 0.000 description 5
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 5
- 125000003282 alkyl amino group Chemical group 0.000 description 5
- 125000004644 alkyl sulfinyl group Chemical group 0.000 description 5
- 125000004390 alkyl sulfonyl group Chemical group 0.000 description 5
- 125000004414 alkyl thio group Chemical group 0.000 description 5
- 125000006615 aromatic heterocyclic group Chemical group 0.000 description 5
- 125000005135 aryl sulfinyl group Chemical group 0.000 description 5
- 125000004391 aryl sulfonyl group Chemical group 0.000 description 5
- 125000005110 aryl thio group Chemical group 0.000 description 5
- 125000004104 aryloxy group Chemical group 0.000 description 5
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 5
- 239000004020 conductor Substances 0.000 description 5
- 230000001186 cumulative effect Effects 0.000 description 5
- 125000004663 dialkyl amino group Chemical group 0.000 description 5
- 238000009826 distribution Methods 0.000 description 5
- 125000004404 heteroalkyl group Chemical group 0.000 description 5
- 229920001519 homopolymer Polymers 0.000 description 5
- 239000001301 oxygen Substances 0.000 description 5
- 125000004430 oxygen atom Chemical group O* 0.000 description 5
- 230000008569 process Effects 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 239000011593 sulfur Substances 0.000 description 5
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 4
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 4
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 4
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 239000002019 doping agent Substances 0.000 description 4
- 230000007062 hydrolysis Effects 0.000 description 4
- 238000006460 hydrolysis reaction Methods 0.000 description 4
- 239000011777 magnesium Substances 0.000 description 4
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 4
- 239000012044 organic layer Substances 0.000 description 4
- 230000001590 oxidative effect Effects 0.000 description 4
- PORWMNRCUJJQNO-UHFFFAOYSA-N tellurium atom Chemical group [Te] PORWMNRCUJJQNO-UHFFFAOYSA-N 0.000 description 4
- 238000004402 ultra-violet photoelectron spectroscopy Methods 0.000 description 4
- 0 *1C=C(*C=C*2)C2=C1 Chemical compound *1C=C(*C=C*2)C2=C1 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000007983 Tris buffer Substances 0.000 description 3
- 230000009471 action Effects 0.000 description 3
- 239000012736 aqueous medium Substances 0.000 description 3
- 125000000732 arylene group Chemical group 0.000 description 3
- 125000004429 atom Chemical group 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- 229910052791 calcium Inorganic materials 0.000 description 3
- 239000011575 calcium Substances 0.000 description 3
- 150000001768 cations Chemical class 0.000 description 3
- 239000002800 charge carrier Substances 0.000 description 3
- 239000000084 colloidal system Substances 0.000 description 3
- 229920000547 conjugated polymer Polymers 0.000 description 3
- 230000008021 deposition Effects 0.000 description 3
- 125000005549 heteroarylene group Chemical group 0.000 description 3
- 239000003446 ligand Substances 0.000 description 3
- 229920002521 macromolecule Polymers 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 150000003384 small molecules Chemical class 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- OBTWBSRJZRCYQV-UHFFFAOYSA-N sulfuryl difluoride Chemical compound FS(F)(=O)=O OBTWBSRJZRCYQV-UHFFFAOYSA-N 0.000 description 3
- VJYJJHQEVLEOFL-UHFFFAOYSA-N thieno[3,2-b]thiophene Chemical compound S1C=CC2=C1C=CS2 VJYJJHQEVLEOFL-UHFFFAOYSA-N 0.000 description 3
- 238000012546 transfer Methods 0.000 description 3
- IYZMXHQDXZKNCY-UHFFFAOYSA-N 1-n,1-n-diphenyl-4-n,4-n-bis[4-(n-phenylanilino)phenyl]benzene-1,4-diamine Chemical compound C1=CC=CC=C1N(C=1C=CC(=CC=1)N(C=1C=CC(=CC=1)N(C=1C=CC=CC=1)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 IYZMXHQDXZKNCY-UHFFFAOYSA-N 0.000 description 2
- VQGHOUODWALEFC-UHFFFAOYSA-N 2-phenylpyridine Chemical compound C1=CC=CC=C1C1=CC=CC=N1 VQGHOUODWALEFC-UHFFFAOYSA-N 0.000 description 2
- FSEXLNMNADBYJU-UHFFFAOYSA-N 2-phenylquinoline Chemical compound C1=CC=CC=C1C1=CC=C(C=CC=C2)C2=N1 FSEXLNMNADBYJU-UHFFFAOYSA-N 0.000 description 2
- 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 2
- DHDHJYNTEFLIHY-UHFFFAOYSA-N 4,7-diphenyl-1,10-phenanthroline Chemical compound C1=CC=CC=C1C1=CC=NC2=C1C=CC1=C(C=3C=CC=CC=3)C=CN=C21 DHDHJYNTEFLIHY-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 2
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 2
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 2
- 238000004833 X-ray photoelectron spectroscopy Methods 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
- 150000001342 alkaline earth metals Chemical class 0.000 description 2
- 125000003368 amide group Chemical group 0.000 description 2
- 150000001448 anilines Chemical class 0.000 description 2
- 229910052788 barium Inorganic materials 0.000 description 2
- 229910052792 caesium Inorganic materials 0.000 description 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 2
- 125000002843 carboxylic acid group Chemical group 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000007334 copolymerization reaction Methods 0.000 description 2
- 238000007766 curtain coating Methods 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- 238000003618 dip coating Methods 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- 238000005401 electroluminescence Methods 0.000 description 2
- 238000005538 encapsulation Methods 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 125000001033 ether group Chemical group 0.000 description 2
- 229920002313 fluoropolymer Polymers 0.000 description 2
- 238000007756 gravure coating Methods 0.000 description 2
- 238000007646 gravure printing Methods 0.000 description 2
- 125000004474 heteroalkylene group Chemical group 0.000 description 2
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 description 2
- 238000007641 inkjet printing Methods 0.000 description 2
- 229910052809 inorganic oxide Inorganic materials 0.000 description 2
- 238000005342 ion exchange Methods 0.000 description 2
- 229910052741 iridium Inorganic materials 0.000 description 2
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 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 2
- 150000002825 nitriles Chemical class 0.000 description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 description 2
- 229910052755 nonmetal Inorganic materials 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 150000002902 organometallic compounds Chemical class 0.000 description 2
- 125000002524 organometallic group Chemical group 0.000 description 2
- 125000005010 perfluoroalkyl group Chemical group 0.000 description 2
- 230000000737 periodic effect Effects 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 229920000172 poly(styrenesulfonic acid) Polymers 0.000 description 2
- 125000003367 polycyclic group Chemical group 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 150000003233 pyrroles Chemical class 0.000 description 2
- 238000010791 quenching Methods 0.000 description 2
- 230000000171 quenching effect Effects 0.000 description 2
- 230000006798 recombination Effects 0.000 description 2
- 238000005215 recombination Methods 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 238000007650 screen-printing Methods 0.000 description 2
- 125000003748 selenium group Chemical group *[Se]* 0.000 description 2
- 229910052709 silver Inorganic materials 0.000 description 2
- 239000004332 silver Substances 0.000 description 2
- 238000007764 slot die coating Methods 0.000 description 2
- 238000004528 spin coating Methods 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 125000004434 sulfur atom Chemical group 0.000 description 2
- 150000003577 thiophenes Chemical class 0.000 description 2
- ODHXBMXNKOYIBV-UHFFFAOYSA-N triphenylamine Chemical compound C1=CC=CC=C1N(C=1C=CC=CC=1)C1=CC=CC=C1 ODHXBMXNKOYIBV-UHFFFAOYSA-N 0.000 description 2
- 238000007740 vapor deposition Methods 0.000 description 2
- 230000000007 visual effect Effects 0.000 description 2
- ICPSWZFVWAPUKF-UHFFFAOYSA-N 1,1'-spirobi[fluorene] Chemical compound C1=CC=C2C=C3C4(C=5C(C6=CC=CC=C6C=5)=CC=C4)C=CC=C3C2=C1 ICPSWZFVWAPUKF-UHFFFAOYSA-N 0.000 description 1
- FNQJDLTXOVEEFB-UHFFFAOYSA-N 1,2,3-benzothiadiazole Chemical compound C1=CC=C2SN=NC2=C1 FNQJDLTXOVEEFB-UHFFFAOYSA-N 0.000 description 1
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 description 1
- YCFOLQSTUQNCAS-UHFFFAOYSA-N 1-phenyl-2h-isoindole Chemical class C=12C=CC=CC2=CNC=1C1=CC=CC=C1 YCFOLQSTUQNCAS-UHFFFAOYSA-N 0.000 description 1
- VMAUSAPAESMXAB-UHFFFAOYSA-N 2,3-bis(4-fluorophenyl)quinoxaline Chemical compound C1=CC(F)=CC=C1C1=NC2=CC=CC=C2N=C1C1=CC=C(F)C=C1 VMAUSAPAESMXAB-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
- STTGYIUESPWXOW-UHFFFAOYSA-N 2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline Chemical compound C=12C=CC3=C(C=4C=CC=CC=4)C=C(C)N=C3C2=NC(C)=CC=1C1=CC=CC=C1 STTGYIUESPWXOW-UHFFFAOYSA-N 0.000 description 1
- TUFKHKZLBZWCAW-UHFFFAOYSA-N 2-(1-ethenoxypropan-2-yloxy)ethanesulfonyl fluoride Chemical compound C=COCC(C)OCCS(F)(=O)=O TUFKHKZLBZWCAW-UHFFFAOYSA-N 0.000 description 1
- LCPVQAHEFVXVKT-UHFFFAOYSA-N 2-(2,4-difluorophenoxy)pyridin-3-amine Chemical compound NC1=CC=CN=C1OC1=CC=C(F)C=C1F LCPVQAHEFVXVKT-UHFFFAOYSA-N 0.000 description 1
- RFJVDJWCXSPUBY-UHFFFAOYSA-N 2-(difluoromethylidene)-4,4,5-trifluoro-5-(trifluoromethyl)-1,3-dioxolane Chemical compound FC(F)=C1OC(F)(F)C(F)(C(F)(F)F)O1 RFJVDJWCXSPUBY-UHFFFAOYSA-N 0.000 description 1
- RIKNNBBGYSDYAX-UHFFFAOYSA-N 2-[1-[2-(4-methyl-n-(4-methylphenyl)anilino)phenyl]cyclohexyl]-n,n-bis(4-methylphenyl)aniline Chemical compound C1=CC(C)=CC=C1N(C=1C(=CC=CC=1)C1(CCCCC1)C=1C(=CC=CC=1)N(C=1C=CC(C)=CC=1)C=1C=CC(C)=CC=1)C1=CC=C(C)C=C1 RIKNNBBGYSDYAX-UHFFFAOYSA-N 0.000 description 1
- GEQBRULPNIVQPP-UHFFFAOYSA-N 2-[3,5-bis(1-phenylbenzimidazol-2-yl)phenyl]-1-phenylbenzimidazole Chemical compound C1=CC=CC=C1N1C2=CC=CC=C2N=C1C1=CC(C=2N(C3=CC=CC=C3N=2)C=2C=CC=CC=2)=CC(C=2N(C3=CC=CC=C3N=2)C=2C=CC=CC=2)=C1 GEQBRULPNIVQPP-UHFFFAOYSA-N 0.000 description 1
- IXHWGNYCZPISET-UHFFFAOYSA-N 2-[4-(dicyanomethylidene)-2,3,5,6-tetrafluorocyclohexa-2,5-dien-1-ylidene]propanedinitrile Chemical compound FC1=C(F)C(=C(C#N)C#N)C(F)=C(F)C1=C(C#N)C#N IXHWGNYCZPISET-UHFFFAOYSA-N 0.000 description 1
- SVQOKUWDNBOKFD-UHFFFAOYSA-N 2-ethenoxyethanesulfonyl fluoride Chemical compound FS(=O)(=O)CCOC=C SVQOKUWDNBOKFD-UHFFFAOYSA-N 0.000 description 1
- OXPDQFOKSZYEMJ-UHFFFAOYSA-N 2-phenylpyrimidine Chemical compound C1=CC=CC=C1C1=NC=CC=N1 OXPDQFOKSZYEMJ-UHFFFAOYSA-N 0.000 description 1
- YSYRISKCBOPJRG-UHFFFAOYSA-N 4,5-difluoro-2,2-bis(trifluoromethyl)-1,3-dioxole Chemical compound FC1=C(F)OC(C(F)(F)F)(C(F)(F)F)O1 YSYRISKCBOPJRG-UHFFFAOYSA-N 0.000 description 1
- YGBCLRRWZQSURU-UHFFFAOYSA-N 4-[(diphenylhydrazinylidene)methyl]-n,n-diethylaniline Chemical compound C1=CC(N(CC)CC)=CC=C1C=NN(C=1C=CC=CC=1)C1=CC=CC=C1 YGBCLRRWZQSURU-UHFFFAOYSA-N 0.000 description 1
- VXEGSRKPIUDPQT-UHFFFAOYSA-N 4-[4-(4-methoxyphenyl)piperazin-1-yl]aniline Chemical compound C1=CC(OC)=CC=C1N1CCN(C=2C=CC(N)=CC=2)CC1 VXEGSRKPIUDPQT-UHFFFAOYSA-N 0.000 description 1
- KBXXZTIBAVBLPP-UHFFFAOYSA-N 4-[[4-(diethylamino)-2-methylphenyl]-(4-methylphenyl)methyl]-n,n-diethyl-3-methylaniline Chemical compound CC1=CC(N(CC)CC)=CC=C1C(C=1C(=CC(=CC=1)N(CC)CC)C)C1=CC=C(C)C=C1 KBXXZTIBAVBLPP-UHFFFAOYSA-N 0.000 description 1
- 125000000590 4-methylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 1
- SFBHJDZYFDQEEY-UHFFFAOYSA-N 9-cyclobutylcarbazole Chemical compound C1CCC1N1C2=CC=CC=C2C2=CC=CC=C21 SFBHJDZYFDQEEY-UHFFFAOYSA-N 0.000 description 1
- VIJYEGDOKCKUOL-UHFFFAOYSA-N 9-phenylcarbazole Chemical compound C1=CC=CC=C1N1C2=CC=CC=C2C2=CC=CC=C21 VIJYEGDOKCKUOL-UHFFFAOYSA-N 0.000 description 1
- 229920001621 AMOLED Polymers 0.000 description 1
- 239000005964 Acibenzolar-S-methyl Substances 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 239000003341 Bronsted base Substances 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229910018068 Li 2 O Inorganic materials 0.000 description 1
- YHBTXTFFTYXOFV-UHFFFAOYSA-N Liquid thiophthene Chemical compound C1=CSC2=C1C=CS2 YHBTXTFFTYXOFV-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 229920000557 Nafion® Polymers 0.000 description 1
- 238000006411 Negishi coupling reaction Methods 0.000 description 1
- YXLXNENXOJSQEI-UHFFFAOYSA-L Oxine-copper Chemical class [Cu+2].C1=CN=C2C([O-])=CC=CC2=C1.C1=CN=C2C([O-])=CC=CC2=C1 YXLXNENXOJSQEI-UHFFFAOYSA-L 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 229920000265 Polyparaphenylene Polymers 0.000 description 1
- 229910052772 Samarium Inorganic materials 0.000 description 1
- 238000006069 Suzuki reaction reaction Methods 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
- 229910052768 actinide Inorganic materials 0.000 description 1
- 150000001255 actinides Chemical class 0.000 description 1
- 230000002730 additional effect Effects 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 150000004703 alkoxides Chemical class 0.000 description 1
- 125000005210 alkyl ammonium group Chemical group 0.000 description 1
- 125000005227 alkyl sulfonate group Chemical group 0.000 description 1
- 125000000304 alkynyl group Chemical group 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 229940024548 aluminum oxide Drugs 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 150000001454 anthracenes Chemical class 0.000 description 1
- 229910000410 antimony oxide Inorganic materials 0.000 description 1
- 229920003235 aromatic polyamide Polymers 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- ZYGHJZDHTFUPRJ-UHFFFAOYSA-N benzo-alpha-pyrone Natural products C1=CC=C2OC(=O)C=CC2=C1 ZYGHJZDHTFUPRJ-UHFFFAOYSA-N 0.000 description 1
- 229910052790 beryllium Inorganic materials 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 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 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- XZCJVWCMJYNSQO-UHFFFAOYSA-N butyl pbd Chemical compound C1=CC(C(C)(C)C)=CC=C1C1=NN=C(C=2C=CC(=CC=2)C=2C=CC=CC=2)O1 XZCJVWCMJYNSQO-UHFFFAOYSA-N 0.000 description 1
- KKGZSDRHWZATTM-UHFFFAOYSA-N c1c[o]c2c1[IH]C=C2 Chemical compound c1c[o]c2c1[IH]C=C2 KKGZSDRHWZATTM-UHFFFAOYSA-N 0.000 description 1
- 239000003990 capacitor Substances 0.000 description 1
- 125000004556 carbazol-9-yl group Chemical group C1=CC=CC=2C3=CC=CC=C3N(C12)* 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000011203 carbon fibre reinforced carbon Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000003729 cation exchange resin Substances 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000005229 chemical vapour deposition Methods 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 150000001846 chrysenes Chemical class 0.000 description 1
- 238000001246 colloidal dispersion Methods 0.000 description 1
- 239000002322 conducting polymer Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 239000011258 core-shell material Substances 0.000 description 1
- 235000001671 coumarin Nutrition 0.000 description 1
- 125000000332 coumarinyl group Chemical class O1C(=O)C(=CC2=CC=CC=C12)* 0.000 description 1
- 125000000392 cycloalkenyl group Chemical group 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- JAONJTDQXUSBGG-UHFFFAOYSA-N dialuminum;dizinc;oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[Al+3].[Al+3].[Zn+2].[Zn+2] JAONJTDQXUSBGG-UHFFFAOYSA-N 0.000 description 1
- 150000004891 diazines Chemical class 0.000 description 1
- 125000001664 diethylamino group Chemical group [H]C([H])([H])C([H])([H])N(*)C([H])([H])C([H])([H])[H] 0.000 description 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
- 238000001312 dry etching Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000002296 dynamic light scattering Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000011263 electroactive material Substances 0.000 description 1
- 238000000921 elemental analysis Methods 0.000 description 1
- 238000000295 emission spectrum Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- BHHBQJFPDCNFMI-UHFFFAOYSA-N ethene;1-propoxypropane Chemical group C=C.CCCOCCC BHHBQJFPDCNFMI-UHFFFAOYSA-N 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- RMBPEFMHABBEKP-UHFFFAOYSA-N fluorene Chemical compound C1=CC=C2C3=C[CH]C=CC3=CC2=C1 RMBPEFMHABBEKP-UHFFFAOYSA-N 0.000 description 1
- JVZRCNQLWOELDU-UHFFFAOYSA-N gamma-Phenylpyridine Natural products C1=CC=CC=C1C1=CC=NC=C1 JVZRCNQLWOELDU-UHFFFAOYSA-N 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910021480 group 4 element Inorganic materials 0.000 description 1
- 229910021478 group 5 element Inorganic materials 0.000 description 1
- 229910021476 group 6 element Inorganic materials 0.000 description 1
- 229910052735 hafnium Inorganic materials 0.000 description 1
- VBJZVLUMGGDVMO-UHFFFAOYSA-N hafnium atom Chemical compound [Hf] VBJZVLUMGGDVMO-UHFFFAOYSA-N 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
- HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical group FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- 229910003437 indium oxide Inorganic materials 0.000 description 1
- AMGQUBHHOARCQH-UHFFFAOYSA-N indium;oxotin Chemical compound [In].[Sn]=O AMGQUBHHOARCQH-UHFFFAOYSA-N 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000012212 insulator Substances 0.000 description 1
- RUTXIHLAWFEWGM-UHFFFAOYSA-H iron(3+) sulfate Chemical compound [Fe+3].[Fe+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O RUTXIHLAWFEWGM-UHFFFAOYSA-H 0.000 description 1
- 229910000360 iron(III) sulfate Inorganic materials 0.000 description 1
- 229910052747 lanthanoid Inorganic materials 0.000 description 1
- 150000002602 lanthanoids Chemical class 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- PQXKHYXIUOZZFA-UHFFFAOYSA-M lithium fluoride Inorganic materials [Li+].[F-] PQXKHYXIUOZZFA-UHFFFAOYSA-M 0.000 description 1
- 125000000040 m-tolyl group Chemical group [H]C1=C([H])C(*)=C([H])C(=C1[H])C([H])([H])[H] 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 239000002923 metal particle Substances 0.000 description 1
- 238000005649 metathesis reaction Methods 0.000 description 1
- QLOAVXSYZAJECW-UHFFFAOYSA-N methane;molecular fluorine Chemical group C.FF QLOAVXSYZAJECW-UHFFFAOYSA-N 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- JGOAZQAXRONCCI-SDNWHVSQSA-N n-[(e)-benzylideneamino]aniline Chemical compound C=1C=CC=CC=1N\N=C\C1=CC=CC=C1 JGOAZQAXRONCCI-SDNWHVSQSA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- NIHNNTQXNPWCJQ-UHFFFAOYSA-N o-biphenylenemethane Natural products C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 description 1
- 229920000620 organic polymer Polymers 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
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 description 1
- HTJNDQNBKKHPAQ-UHFFFAOYSA-N oxotin zirconium Chemical compound [Sn]=O.[Zr] HTJNDQNBKKHPAQ-UHFFFAOYSA-N 0.000 description 1
- SOQBVABWOPYFQZ-UHFFFAOYSA-N oxygen(2-);titanium(4+) Chemical class [O-2].[O-2].[Ti+4] SOQBVABWOPYFQZ-UHFFFAOYSA-N 0.000 description 1
- 238000000059 patterning Methods 0.000 description 1
- CBHCDHNUZWWAPP-UHFFFAOYSA-N pecazine Chemical compound C1N(C)CCCC1CN1C2=CC=CC=C2SC2=CC=CC=C21 CBHCDHNUZWWAPP-UHFFFAOYSA-N 0.000 description 1
- 125000005003 perfluorobutyl group Chemical group FC(F)(F)C(F)(F)C(F)(F)C(F)(F)* 0.000 description 1
- FVDOBFPYBSDRKH-UHFFFAOYSA-N perylene-3,4,9,10-tetracarboxylic acid Chemical compound C=12C3=CC=C(C(O)=O)C2=C(C(O)=O)C=CC=1C1=CC=C(C(O)=O)C2=C1C3=CC=C2C(=O)O FVDOBFPYBSDRKH-UHFFFAOYSA-N 0.000 description 1
- 150000002979 perylenes Chemical class 0.000 description 1
- 238000006552 photochemical reaction Methods 0.000 description 1
- 238000004838 photoelectron emission spectroscopy Methods 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 238000005240 physical vapour deposition Methods 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920003227 poly(N-vinyl carbazole) Polymers 0.000 description 1
- 229920000553 poly(phenylenevinylene) Polymers 0.000 description 1
- 229920000548 poly(silane) polymer Polymers 0.000 description 1
- 229920001798 poly[2-(acrylamido)-2-methyl-1-propanesulfonic acid] polymer Polymers 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920002098 polyfluorene Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 150000004032 porphyrins Chemical class 0.000 description 1
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 1
- VXPLXMJHHKHSOA-UHFFFAOYSA-N propham Chemical compound CC(C)OC(=O)NC1=CC=CC=C1 VXPLXMJHHKHSOA-UHFFFAOYSA-N 0.000 description 1
- 150000003220 pyrenes Chemical class 0.000 description 1
- 150000003252 quinoxalines Chemical class 0.000 description 1
- 229910052761 rare earth metal Inorganic materials 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 230000027756 respiratory electron transport chain Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- KZUNJOHGWZRPMI-UHFFFAOYSA-N samarium atom Chemical compound [Sm] KZUNJOHGWZRPMI-UHFFFAOYSA-N 0.000 description 1
- 150000005082 selenophenes Chemical class 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 239000005049 silicon tetrachloride Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- CHQMHPLRPQMAMX-UHFFFAOYSA-L sodium persulfate Substances [Na+].[Na+].[O-]S(=O)(=O)OOS([O-])(=O)=O CHQMHPLRPQMAMX-UHFFFAOYSA-L 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- 125000005504 styryl group Chemical group 0.000 description 1
- 125000000547 substituted alkyl group Chemical group 0.000 description 1
- 125000000565 sulfonamide group Chemical group 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
- 238000005211 surface analysis Methods 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- TXEYQDLBPFQVAA-UHFFFAOYSA-N tetrafluoromethane Chemical group FC(F)(F)F TXEYQDLBPFQVAA-UHFFFAOYSA-N 0.000 description 1
- VLLMWSRANPNYQX-UHFFFAOYSA-N thiadiazole Chemical compound C1=CSN=N1.C1=CSN=N1 VLLMWSRANPNYQX-UHFFFAOYSA-N 0.000 description 1
- 150000004867 thiadiazoles Chemical class 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 229910001887 tin oxide Inorganic materials 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 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 1
- 125000005259 triarylamine group Chemical group 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
- 239000012808 vapor phase Substances 0.000 description 1
- 238000003631 wet chemical etching Methods 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- YVTHLONGBIQYBO-UHFFFAOYSA-N zinc indium(3+) oxygen(2-) Chemical compound [O--].[Zn++].[In+3] YVTHLONGBIQYBO-UHFFFAOYSA-N 0.000 description 1
- 229960001296 zinc oxide Drugs 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Images
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B1/00—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
- H01B1/06—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances
- H01B1/12—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances organic substances
- H01B1/124—Intrinsically conductive polymers
- H01B1/127—Intrinsically conductive polymers comprising five-membered aromatic rings in the main chain, e.g. polypyrroles, polythiophenes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y30/00—Nanotechnology for materials or surface science, e.g. nanocomposites
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/02—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques
- C08J3/03—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in aqueous media
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L101/00—Compositions of unspecified macromolecular compounds
- C08L101/12—Compositions of unspecified macromolecular compounds characterised by physical features, e.g. anisotropy, viscosity or electrical conductivity
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L65/00—Compositions of macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain; Compositions of derivatives of such polymers
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B1/00—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
- H01B1/06—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances
- H01B1/12—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances organic substances
- H01B1/122—Ionic conductors
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B1/00—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
- H01B1/06—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances
- H01B1/12—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances organic substances
- H01B1/124—Intrinsically conductive polymers
- H01B1/128—Intrinsically conductive polymers comprising six-membered aromatic rings in the main chain, e.g. polyanilines, polyphenylenes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G2261/30—Monomer units or repeat units incorporating structural elements in the main chain
- C08G2261/32—Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain
- C08G2261/322—Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain non-condensed
- C08G2261/3223—Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain non-condensed containing one or more sulfur atoms as the only heteroatom, e.g. thiophene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G2261/50—Physical properties
- C08G2261/51—Charge transport
- C08G2261/512—Hole transport
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G2261/70—Post-treatment
- C08G2261/79—Post-treatment doping
- C08G2261/794—Post-treatment doping with polymeric dopants
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2300/00—Characterised by the use of unspecified polymers
- C08J2300/12—Polymers characterised by physical features, e.g. anisotropy, viscosity or electrical conductivity
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2365/00—Characterised by the use of macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain; Derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2427/00—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers
- C08J2427/02—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers not modified by chemical after-treatment
- C08J2427/12—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
- C08J2427/18—Homopolymers or copolymers of tetrafluoroethylene
-
- 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
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/34—Silicon-containing compounds
- C08K3/36—Silica
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L25/00—Compositions of, homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Compositions of derivatives of such polymers
- C08L25/18—Homopolymers or copolymers of aromatic monomers containing elements other than carbon and hydrogen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L27/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
- C08L27/02—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L27/12—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
- C08L27/18—Homopolymers or copolymers or tetrafluoroethene
-
- 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
- Y10S977/00—Nanotechnology
- Y10S977/70—Nanostructure
- Y10S977/773—Nanoparticle, i.e. structure having three dimensions of 100 nm or less
Landscapes
- Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Nanotechnology (AREA)
- General Physics & Mathematics (AREA)
- Materials Engineering (AREA)
- Crystallography & Structural Chemistry (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- Composite Materials (AREA)
- Dispersion Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Electroluminescent Light Sources (AREA)
- Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)
- Conductive Materials (AREA)
- Electrodes Of Semiconductors (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US17239609P | 2009-04-24 | 2009-04-24 | |
| US61/172,396 | 2009-04-24 | ||
| PCT/US2010/032175 WO2010124166A2 (en) | 2009-04-24 | 2010-04-23 | Electrically conductive polymer compositions and films made therefrom |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2012524834A true JP2012524834A (ja) | 2012-10-18 |
| JP2012524834A5 JP2012524834A5 (enExample) | 2013-03-28 |
Family
ID=43011760
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012507410A Pending JP2012524834A (ja) | 2009-04-24 | 2010-04-23 | 導電性ポリマー組成物およびそれから作製されたフィルム |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US8945427B2 (enExample) |
| EP (1) | EP2421919A4 (enExample) |
| JP (1) | JP2012524834A (enExample) |
| KR (1) | KR101581991B1 (enExample) |
| CN (1) | CN102395627B (enExample) |
| TW (1) | TW201100482A (enExample) |
| WO (1) | WO2010124166A2 (enExample) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2014189114A1 (ja) * | 2013-05-23 | 2014-11-27 | 富士フイルム株式会社 | 有機半導体組成物および有機薄膜トランジスタならびに電子ペーパーおよびディスプレイデバイス |
| WO2014189116A1 (ja) * | 2013-05-23 | 2014-11-27 | 富士フイルム株式会社 | 有機半導体組成物および有機薄膜トランジスタならびに電子ペーパーおよびディスプレイデバイス |
| KR20170125902A (ko) * | 2015-03-03 | 2017-11-15 | 닛산 가가쿠 고교 가부시키 가이샤 | 정공 캐리어 화합물 및 중합체 산을 함유하는 조성물, 및 그의 용도 |
| WO2017195559A1 (ja) * | 2016-05-10 | 2017-11-16 | 日立化成株式会社 | 電荷輸送性材料、有機エレクトロニクス素子、及び有機エレクトロルミネセンス素子 |
| WO2018135582A1 (ja) * | 2017-01-18 | 2018-07-26 | 日産化学工業株式会社 | インク組成物 |
| WO2018135580A1 (ja) * | 2017-01-18 | 2018-07-26 | 日産化学工業株式会社 | 電荷輸送性ワニス及びそれを用いる電荷輸送性薄膜 |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR102197160B1 (ko) * | 2013-05-27 | 2020-12-31 | 메르크 파텐트 게엠베하 | 유기 전자 소자용 전자 주입층에 사용하기 위한 개선된 전자 수송 조성물 |
| CN103865263B (zh) * | 2014-01-09 | 2016-05-11 | 常州大学 | 一种有机-无机复合红外隐身材料的制备方法 |
| CN105098073B (zh) * | 2014-05-07 | 2018-11-09 | 中国科学院苏州纳米技术与纳米仿生研究所 | 金属氧化物-导电聚合物-醇组合物、其制备方法及应用 |
| CN106663542B (zh) * | 2014-05-21 | 2019-01-08 | 凯米特电子公司 | 具有充电时间降低添加剂和功函数改良剂的电容器 |
| KR102677529B1 (ko) * | 2017-06-20 | 2024-06-24 | 닛산 가가쿠 가부시키가이샤 | 비수계 잉크 조성물 |
| KR20200132914A (ko) * | 2018-03-15 | 2020-11-25 | 닛산 가가쿠 가부시키가이샤 | 전하수송성 조성물 |
| CN109841697B (zh) * | 2019-03-29 | 2020-10-16 | 陕西师范大学 | 一种基于CuO/Se复合材料薄膜的太阳能电池 |
| JP6881541B2 (ja) * | 2019-10-09 | 2021-06-02 | ダイキン工業株式会社 | 含フッ素ポリマーを含有する組成物および架橋物 |
| US11773212B2 (en) | 2020-03-03 | 2023-10-03 | Lg Energy Solution, Ltd. | Preparation method of polymer |
| US11339246B2 (en) | 2020-03-03 | 2022-05-24 | Lg Energy Solution, Ltd. | Preparation method of polymer |
| CN117866438A (zh) * | 2024-03-11 | 2024-04-12 | 彩虹高新材料(莱阳)有限公司 | 一种改性聚醚砜树脂及其制备方法 |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2006500461A (ja) * | 2002-09-24 | 2006-01-05 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | 電子工学用途のための、ポリマー酸コロイドを用いて製造された水分散性ポリアニリン |
| WO2007145977A1 (en) * | 2006-06-05 | 2007-12-21 | E. I. Du Pont De Nemours And Company | Process for making an organic electronic device |
| WO2009018009A1 (en) * | 2007-07-27 | 2009-02-05 | E. I. Du Pont De Nemours And Company | Aqueous dispersions of electrically conducting polymers containing inorganic nanoparticles |
| JP2010514904A (ja) * | 2006-12-29 | 2010-05-06 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | 導電性ポリマーの高仕事関数および高導電率組成物 |
| JP2011517468A (ja) * | 2008-03-19 | 2011-06-09 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | 導電性ポリマー組成物およびそれから作製されたフィルム |
| JP2012524831A (ja) * | 2009-04-21 | 2012-10-18 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | 導電性ポリマー組成物およびそれから作製されたフィルム |
Family Cites Families (168)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3282875A (en) | 1964-07-22 | 1966-11-01 | Du Pont | Fluorocarbon vinyl ether polymers |
| US4358545A (en) | 1980-06-11 | 1982-11-09 | The Dow Chemical Company | Sulfonic acid electrolytic cell having flourinated polymer membrane with hydration product less than 22,000 |
| US4433082A (en) | 1981-05-01 | 1984-02-21 | E. I. Du Pont De Nemours And Company | Process for making liquid composition of perfluorinated ion exchange polymer, and product thereof |
| US5378402A (en) | 1982-08-02 | 1995-01-03 | Raychem Limited | Polymer compositions |
| US4552927A (en) | 1983-09-09 | 1985-11-12 | Rockwell International Corporation | Conducting organic polymer based on polypyrrole |
| JPS62119237A (ja) | 1985-11-20 | 1987-05-30 | Agency Of Ind Science & Technol | 導電性有機高分子化合物用ド−パント |
| US4731408A (en) | 1985-12-20 | 1988-03-15 | Polaroid Corporation | Processable conductive polymers |
| US4940525A (en) | 1987-05-08 | 1990-07-10 | The Dow Chemical Company | Low equivalent weight sulfonic fluoropolymers |
| US4795543A (en) | 1987-05-26 | 1989-01-03 | Transducer Research, Inc. | Spin coating of electrolytes |
| US5160457A (en) | 1987-08-07 | 1992-11-03 | Allied-Signal Inc. | Thermally stable forms of electrically conductive polyaniline |
| US5069820A (en) | 1987-08-07 | 1991-12-03 | Allied-Signal Inc. | Thermally stable forms of electrically conductive polyaniline |
| JPH01132052A (ja) | 1987-08-10 | 1989-05-24 | Nitto Denko Corp | 導電性有機重合体電池 |
| DE3843412A1 (de) | 1988-04-22 | 1990-06-28 | Bayer Ag | Neue polythiophene, verfahren zu ihrer herstellung und ihre verwendung |
| FR2632979B1 (fr) | 1988-06-16 | 1990-09-21 | Commissariat Energie Atomique | Procede de preparation d'un polymere conducteur mixte ionique et electronique et polymeres obtenus par ce procede |
| US4973391A (en) | 1988-08-30 | 1990-11-27 | Osaka Gas Company, Ltd. | Composite polymers of polyaniline with metal phthalocyanine and polyaniline with organic sulfonic acid and nafion |
| JPH02249221A (ja) | 1989-03-23 | 1990-10-05 | Asahi Glass Co Ltd | 固体電解コンデンサ |
| GB8909011D0 (en) | 1989-04-20 | 1989-06-07 | Friend Richard H | Electroluminescent devices |
| DE59010247D1 (de) | 1990-02-08 | 1996-05-02 | Bayer Ag | Neue Polythiophen-Dispersionen, ihre Herstellung und ihre Verwendung |
| EP0443861B2 (en) | 1990-02-23 | 2008-05-28 | Sumitomo Chemical Company, Limited | Organic electroluminescence device |
| US5185100A (en) | 1990-03-29 | 1993-02-09 | Allied-Signal Inc | Conductive polymers formed from conjugated backbone polymers doped with non-oxidizing protonic acids |
| BE1008036A3 (fr) | 1990-08-30 | 1996-01-03 | Solvay | Melanges de polymeres polaires et de polymeres conducteurs dedopes, procedes d'obtention de ces melanges et utilisation de ces melanges pour fabriquer des dispositifs electroniques optoelectriques, electrotechniques et electromecaniques. |
| FR2666443A1 (fr) | 1990-08-31 | 1992-03-06 | Commissariat Energie Atomique | Materiau a base de polymere conducteur electronique comprenant des particules magnetiques et son procede de fabrication. |
| JP3056522B2 (ja) | 1990-11-30 | 2000-06-26 | 三菱レイヨン株式会社 | 金属―導電性高分子複合微粒子及びその製造方法 |
| JP3265431B2 (ja) | 1991-11-05 | 2002-03-11 | 第一工業製薬株式会社 | 固体電解コンデンサ |
| US5463005A (en) | 1992-01-03 | 1995-10-31 | Gas Research Institute | Copolymers of tetrafluoroethylene and perfluorinated sulfonyl monomers and membranes made therefrom |
| JPH05255576A (ja) | 1992-03-12 | 1993-10-05 | Nippon Chibagaigii Kk | 面状発熱体及びその製造法 |
| EP0593111B1 (en) | 1992-10-14 | 1998-06-17 | Agfa-Gevaert N.V. | Antistatic coating composition |
| DE4334390C2 (de) | 1993-10-08 | 1999-01-21 | Nat Science Council | Verfahren zur Herstellung eines verarbeitbaren, leitfähigen, kolloidalen Polymeren |
| US5537000A (en) | 1994-04-29 | 1996-07-16 | The Regents, University Of California | Electroluminescent devices formed using semiconductor nanocrystals as an electron transport media and method of making such electroluminescent devices |
| JP2001506393A (ja) | 1994-09-06 | 2001-05-15 | フィリップス エレクトロニクス ネムローゼ フェンノートシャップ | 導電性ポリマー製の透明な構造を付与した電極層を有するエレクトロルミネセント装置 |
| US5567356A (en) | 1994-11-07 | 1996-10-22 | Monsanto Company | Emulsion-polymerization process and electrically-conductive polyaniline salts |
| JP3798484B2 (ja) | 1995-11-15 | 2006-07-19 | インターナショナル・ビジネス・マシーンズ・コーポレーション | 架橋導電性ポリマー及びその前駆物質 |
| DE19543205A1 (de) | 1995-11-20 | 1997-05-22 | Bayer Ag | Zwischenschicht in elektrolumineszierenden Anordnungen enthaltend feinteilige anorganische Partikel |
| US5798170A (en) | 1996-02-29 | 1998-08-25 | Uniax Corporation | Long operating life for polymer light-emitting diodes |
| DE19627069A1 (de) | 1996-07-05 | 1998-01-08 | Bayer Ag | Elektrolumineszierende Anordnungen unter Verwendung von lamellaren Elektroden |
| CA2268629A1 (en) | 1996-10-15 | 1998-04-23 | E.I. Du Pont De Nemours And Company | Compositions containing particles of highly fluorinated ion exchange polymer |
| CN1170321C (zh) | 1996-11-12 | 2004-10-06 | 国际商业机器公司 | 导电聚合物图形及其作为电极或电接触的应用 |
| CA2704986C (fr) | 1996-12-30 | 2013-04-09 | Hydro-Quebec | Utilisation d'un compose ionique derive du malononitrile comme photoinitiateur, amorceur radicalaire ou catalyseur dans les procedes de polymerisation, ou comme colorant cationique |
| JP2001509206A (ja) | 1997-01-22 | 2001-07-10 | イー・アイ・デユポン・ドウ・ヌムール・アンド・カンパニー | 過フッ化炭化水素化合物でのポリマーのグラフト化 |
| DE69835366T2 (de) | 1997-03-31 | 2007-07-19 | Daikin Industries, Ltd. | Verfahren zur herstellung von perfluorvinylethersulfonsäure-derivaten |
| US6599631B2 (en) | 2001-01-26 | 2003-07-29 | Nanogram Corporation | Polymer-inorganic particle composites |
| US6303238B1 (en) | 1997-12-01 | 2001-10-16 | The Trustees Of Princeton University | OLEDs doped with phosphorescent compounds |
| JP2001508121A (ja) | 1997-11-05 | 2001-06-19 | コーニンクレッカ フィリップス エレクトロニクス エヌ ヴィ | 酸化状態にある共役重合体 |
| JP4236719B2 (ja) | 1997-12-17 | 2009-03-11 | 昭和電工株式会社 | 固体電解コンデンサ及びその製造方法 |
| DE19757542A1 (de) | 1997-12-23 | 1999-06-24 | Bayer Ag | Siebdruckpaste zur Herstellung elektrisch leitfähiger Beschichtungen |
| AU2492599A (en) | 1998-02-02 | 1999-08-16 | Uniax Corporation | Organic diodes with switchable photosensitivity |
| US6866946B2 (en) | 1998-02-02 | 2005-03-15 | Dupont Displays, Inc. | High resistance polyaniline useful in high efficiency pixellated polymer electronic displays |
| US6100324A (en) | 1998-04-16 | 2000-08-08 | E. I. Du Pont De Nemours And Company | Ionomers and ionically conductive compositions |
| JP3937113B2 (ja) | 1998-06-05 | 2007-06-27 | 日産化学工業株式会社 | 有機−無機複合導電性ゾル及びその製造法 |
| US6210790B1 (en) | 1998-07-15 | 2001-04-03 | Rensselaer Polytechnic Institute | Glass-like composites comprising a surface-modified colloidal silica and method of making thereof |
| US6830828B2 (en) | 1998-09-14 | 2004-12-14 | The Trustees Of Princeton University | Organometallic complexes as phosphorescent emitters in organic LEDs |
| US6097147A (en) | 1998-09-14 | 2000-08-01 | The Trustees Of Princeton University | Structure for high efficiency electroluminescent device |
| US6187522B1 (en) | 1999-03-25 | 2001-02-13 | Eastman Kodak Company | Scratch resistant antistatic layer for imaging elements |
| US20040217877A1 (en) | 1999-05-04 | 2004-11-04 | William Kokonaski | Flexible electronic display and wireless communication system |
| EP2306495B1 (en) | 1999-05-13 | 2017-04-19 | The Trustees of Princeton University | Very high efficiency organic light emitting devices based on electrophosphorescence |
| US20020099119A1 (en) | 1999-05-27 | 2002-07-25 | Bradley D. Craig | Water-borne ceramer compositions and antistatic abrasion resistant ceramers made therefrom |
| KR100302326B1 (ko) | 1999-06-09 | 2001-09-22 | 윤덕용 | 폴리비닐알콜-실란커플링제를 이용한 무-유기 공중합체 및 그의제조방법 |
| JP2001006878A (ja) | 1999-06-22 | 2001-01-12 | Matsushita Electric Ind Co Ltd | 薄膜el素子およびその駆動方法 |
| US6324091B1 (en) | 2000-01-14 | 2001-11-27 | The Regents Of The University Of California | Tightly coupled porphyrin macrocycles for molecular memory storage |
| US6620494B2 (en) | 1999-07-03 | 2003-09-16 | Ten Cate Enbi B.V. | Conductive roller |
| US6593690B1 (en) | 1999-09-03 | 2003-07-15 | 3M Innovative Properties Company | Large area organic electronic devices having conducting polymer buffer layers and methods of making same |
| WO2001038219A1 (en) | 1999-11-24 | 2001-05-31 | Tda Research, Inc. | Combustion synthesis of single walled nanotubes |
| JP3656244B2 (ja) | 1999-11-29 | 2005-06-08 | 株式会社豊田中央研究所 | 高耐久性固体高分子電解質及びその高耐久性固体高分子電解質を用いた電極−電解質接合体並びにその電極−電解質接合体を用いた電気化学デバイス |
| AU1807201A (en) | 1999-12-01 | 2001-06-12 | Trustees Of Princeton University, The | Complexes of form L2MX as phosphorescent dopants for organic leds |
| JP2004500449A (ja) | 1999-12-02 | 2004-01-08 | デュポン ディスプレイズ インコーポレイテッド | 高効率のピクセル化ポリマー電子ディスプレイにおいて有用な高抵抗ポリアニリン |
| US6821645B2 (en) | 1999-12-27 | 2004-11-23 | Fuji Photo Film Co., Ltd. | Light-emitting material comprising orthometalated iridium complex, light-emitting device, high efficiency red light-emitting device, and novel iridium complex |
| JP2001270999A (ja) | 2000-01-19 | 2001-10-02 | Mitsubishi Rayon Co Ltd | 架橋性導電性組成物、耐水性導電体及びその形成方法 |
| KR20010095437A (ko) | 2000-03-30 | 2001-11-07 | 윤덕용 | 발광물질/점토 나노복합소재를 이용한 유기 전기 발광 소자 |
| US6706963B2 (en) | 2002-01-25 | 2004-03-16 | Konarka Technologies, Inc. | Photovoltaic cell interconnection |
| JP2001325831A (ja) | 2000-05-12 | 2001-11-22 | Bando Chem Ind Ltd | 金属コロイド液、導電性インク、導電性被膜及び導電性被膜形成用基底塗膜 |
| US20020038999A1 (en) | 2000-06-20 | 2002-04-04 | Yong Cao | High resistance conductive polymers for use in high efficiency pixellated organic electronic devices |
| US20020036291A1 (en) | 2000-06-20 | 2002-03-28 | Parker Ian D. | Multilayer structures as stable hole-injecting electrodes for use in high efficiency organic electronic devices |
| CN1239561C (zh) | 2000-06-26 | 2006-02-01 | 爱克发-格法特公司 | 包含聚噻吩的可再分散性胶乳 |
| US6632472B2 (en) | 2000-06-26 | 2003-10-14 | Agfa-Gevaert | Redispersable latex comprising a polythiophene |
| US6670645B2 (en) | 2000-06-30 | 2003-12-30 | E. I. Du Pont De Nemours And Company | Electroluminescent iridium compounds with fluorinated phenylpyridines, phenylpyrimidines, and phenylquinolines and devices made with such compounds |
| US20020121638A1 (en) | 2000-06-30 | 2002-09-05 | Vladimir Grushin | Electroluminescent iridium compounds with fluorinated phenylpyridines, phenylpyrimidines, and phenylquinolines and devices made with such compounds |
| JP5241053B2 (ja) | 2000-08-11 | 2013-07-17 | ザ、トラスティーズ オブ プリンストン ユニバーシティ | 有機金属化合物及び放射移行有機電気燐光体 |
| JP2002082082A (ja) | 2000-09-07 | 2002-03-22 | Matsushita Refrig Co Ltd | 臭気センサー及びその製造方法 |
| JP4154140B2 (ja) | 2000-09-26 | 2008-09-24 | キヤノン株式会社 | 金属配位化合物 |
| JP4154139B2 (ja) | 2000-09-26 | 2008-09-24 | キヤノン株式会社 | 発光素子 |
| US6515314B1 (en) | 2000-11-16 | 2003-02-04 | General Electric Company | Light-emitting device with organic layer doped with photoluminescent material |
| EP1231251A1 (en) | 2001-02-07 | 2002-08-14 | Agfa-Gevaert | Thin film inorganic light emitting diode |
| JP4300028B2 (ja) | 2001-02-08 | 2009-07-22 | 旭化成株式会社 | 有機ドメイン/無機ドメイン複合材料及びその用途 |
| US6756474B2 (en) | 2001-02-09 | 2004-06-29 | E. I. Du Pont De Nemours And Company | Aqueous conductive dispersions of polyaniline having enhanced viscosity |
| US7074885B2 (en) * | 2001-05-03 | 2006-07-11 | E.I. Du Pont De Nemours And Company | Electroactive fluorene copolymers and devices made with such polymers |
| DE10126860C2 (de) | 2001-06-01 | 2003-05-28 | Siemens Ag | Organischer Feldeffekt-Transistor, Verfahren zu seiner Herstellung und Verwendung zum Aufbau integrierter Schaltungen |
| US6784016B2 (en) | 2001-06-21 | 2004-08-31 | The Trustees Of Princeton University | Organic light-emitting devices with blocking and transport layers |
| US6875523B2 (en) | 2001-07-05 | 2005-04-05 | E. I. Du Pont De Nemours And Company | Photoactive lanthanide complexes with phosphine oxides, phosphine oxide-sulfides, pyridine N-oxides, and phosphine oxide-pyridine N-oxides, and devices made with such complexes |
| JP4223393B2 (ja) | 2001-07-13 | 2009-02-12 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | 高度にフッ素化されたイオン交換ポリマーを溶解させる方法 |
| US6777515B2 (en) | 2001-07-13 | 2004-08-17 | I. Du Pont De Nemours And Company | Functional fluorine-containing polymers and ionomers derived therefrom |
| US6924047B2 (en) | 2001-07-18 | 2005-08-02 | E.I. Du Pont De Nemours And Company | Luminescent lanthanide complexes with imine ligands and devices made with such complexes |
| KR101178643B1 (ko) | 2001-07-27 | 2012-09-07 | 에이일이삼 시스템즈 인코포레이티드 | 배터리 구조, 자기 조직화 구조 및 관련 방법 |
| US6627333B2 (en) | 2001-08-15 | 2003-09-30 | Eastman Kodak Company | White organic light-emitting devices with improved efficiency |
| US7112368B2 (en) | 2001-11-06 | 2006-09-26 | E. I. Du Pont De Nemours And Company | Poly(dioxythiophene)/poly(acrylamidoalkyslufonic acid) complexes |
| US7166368B2 (en) | 2001-11-07 | 2007-01-23 | E. I. Du Pont De Nemours And Company | Electroluminescent platinum compounds and devices made with such compounds |
| AU2002356479A1 (en) | 2001-11-30 | 2003-06-10 | Acreo Ab | Electrochemical sensor |
| EP1326260A1 (en) | 2001-12-11 | 2003-07-09 | Agfa-Gevaert | Material for making a conductive pattern |
| JP2003187983A (ja) | 2001-12-17 | 2003-07-04 | Ricoh Co Ltd | 有機elトランジスタ |
| JP4299144B2 (ja) | 2001-12-26 | 2009-07-22 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | フッ素化フェニルピリジン、フェニルピリミジン、およびフェニルキノリンを含むエレクトロルミネッセンスイリジウム化合物ならびにこのような化合物を用いて製造されるデバイス |
| JP2003217862A (ja) | 2002-01-18 | 2003-07-31 | Honda Motor Co Ltd | 有機エレクトロルミネッセンス素子 |
| JP4363050B2 (ja) | 2002-01-31 | 2009-11-11 | 住友化学株式会社 | 有機エレクトロルミネッセンス素子 |
| JP2005526876A (ja) | 2002-03-01 | 2005-09-08 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | 添加剤を含有する有機導電性ポリマーの印刷 |
| US6923881B2 (en) | 2002-05-27 | 2005-08-02 | Fuji Photo Film Co., Ltd. | Method for producing organic electroluminescent device and transfer material used therein |
| JP4288895B2 (ja) | 2002-06-04 | 2009-07-01 | コニカミノルタホールディングス株式会社 | 有機エレクトロルミネッセンスの製造方法 |
| US20040004433A1 (en) | 2002-06-26 | 2004-01-08 | 3M Innovative Properties Company | Buffer layers for organic electroluminescent devices and methods of manufacture and use |
| JP3606855B2 (ja) | 2002-06-28 | 2005-01-05 | ドン ウン インターナショナル カンパニー リミテッド | 炭素ナノ粒子の製造方法 |
| US7572879B2 (en) * | 2002-07-11 | 2009-08-11 | Air Products And Chemicals, Inc. | Fluorinated alkyl substituted-thieno[3,4-b]thiophene monomers and polymers therefrom |
| US6963005B2 (en) | 2002-08-15 | 2005-11-08 | E. I. Du Pont De Nemours And Company | Compounds comprising phosphorus-containing metal complexes |
| US7118836B2 (en) | 2002-08-22 | 2006-10-10 | Agfa Gevaert | Process for preparing a substantially transparent conductive layer configuration |
| US6977390B2 (en) | 2002-08-23 | 2005-12-20 | Agfa Gevaert | Layer configuration comprising an electron-blocking element |
| US20040092700A1 (en) | 2002-08-23 | 2004-05-13 | Che-Hsiung Hsu | Methods for directly producing stable aqueous dispersions of electrically conducting polyanilines |
| JP2004082395A (ja) | 2002-08-23 | 2004-03-18 | Eamex Co | 積層体形成方法及び積層体 |
| US7307276B2 (en) | 2002-08-23 | 2007-12-11 | Agfa-Gevaert | Layer configuration comprising an electron-blocking element |
| US7033646B2 (en) | 2002-08-29 | 2006-04-25 | E. I. Du Pont De Nemours And Company | High resistance polyaniline blend for use in high efficiency pixellated polymer electroluminescent devices |
| AU2002337064A1 (en) | 2002-09-02 | 2004-03-19 | Agfa-Gevaert | New 3,4-alkylenedioxythiophenedioxide compounds and polymers comprising monomeric units thereof |
| US7317047B2 (en) | 2002-09-24 | 2008-01-08 | E.I. Du Pont De Nemours And Company | Electrically conducting organic polymer/nanoparticle composites and methods for use thereof |
| WO2004029128A2 (en) | 2002-09-24 | 2004-04-08 | E.I. Du Pont De Nemours And Company | Water dispersible polythiophenes made with polymeric acid colloids |
| CN100540628C (zh) | 2002-09-24 | 2009-09-16 | E.I.内穆尔杜邦公司 | 导电有机聚合物/纳米微粒组合物及其应用方法 |
| US7371336B2 (en) | 2002-09-24 | 2008-05-13 | E.I. Du Pont Nemours And Company | Water dispersible polyanilines made with polymeric acid colloids for electronics applications |
| AU2003274121A1 (en) | 2002-10-07 | 2004-04-23 | Agfa-Gevaert | 3,4-alkylenedioxythiophene compounds and polymers thereof |
| US6717358B1 (en) | 2002-10-09 | 2004-04-06 | Eastman Kodak Company | Cascaded organic electroluminescent devices with improved voltage stability |
| US6793197B2 (en) | 2003-01-30 | 2004-09-21 | Fisher Controls International, Inc. | Butterfly valve |
| TWI373483B (en) | 2003-04-22 | 2012-10-01 | Du Pont | Water dispersible polythiophenes made with polymeric acid colloids |
| US7390438B2 (en) | 2003-04-22 | 2008-06-24 | E.I. Du Pont De Nemours And Company | Water dispersible substituted polydioxythiophenes made with fluorinated polymeric sulfonic acid colloids |
| WO2004105150A1 (en) | 2003-05-19 | 2004-12-02 | E.I. Dupont De Nemours And Company | Hole transport composition |
| JP2007528907A (ja) | 2003-06-27 | 2007-10-18 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | トリフルオロスチレン含有化合物、およびポリマー電解質膜におけるそれらの使用 |
| EP1507298A1 (en) | 2003-08-14 | 2005-02-16 | Sony International (Europe) GmbH | Carbon nanotubes based solar cells |
| WO2005024853A1 (ja) | 2003-09-08 | 2005-03-17 | Sumitomo Metal Mining Co., Ltd. | 透明導電積層体とそれを用いた有機el素子、及びそれらの製造方法 |
| US7618704B2 (en) | 2003-09-29 | 2009-11-17 | E.I. Du Pont De Nemours And Company | Spin-printing of electronic and display components |
| US7105237B2 (en) | 2003-10-01 | 2006-09-12 | The University Of Connecticut | Substituted thieno[3,4-B]thiophene polymers, method of making, and use thereof |
| JP4600284B2 (ja) | 2003-10-28 | 2010-12-15 | 住友金属鉱山株式会社 | 透明導電積層体とその製造方法及び透明導電積層体を用いたデバイス |
| TWI365218B (en) | 2003-11-17 | 2012-06-01 | Sumitomo Chemical Co | Conjugated oligomers or polymers based on crosslinkable arylamine compounds |
| US20050209392A1 (en) | 2003-12-17 | 2005-09-22 | Jiazhong Luo | Polymer binders for flexible and transparent conductive coatings containing carbon nanotubes |
| US7960587B2 (en) | 2004-02-19 | 2011-06-14 | E.I. Du Pont De Nemours And Company | Compositions comprising novel compounds and electronic devices made with such compositions |
| US7365230B2 (en) | 2004-02-20 | 2008-04-29 | E.I. Du Pont De Nemours And Company | Cross-linkable polymers and electronic devices made with such polymers |
| US7112369B2 (en) | 2004-03-02 | 2006-09-26 | Bridgestone Corporation | Nano-sized polymer-metal composites |
| US7351358B2 (en) | 2004-03-17 | 2008-04-01 | E.I. Du Pont De Nemours And Company | Water dispersible polypyrroles made with polymeric acid colloids for electronics applications |
| US7338620B2 (en) | 2004-03-17 | 2008-03-04 | E.I. Du Pont De Nemours And Company | Water dispersible polydioxythiophenes with polymeric acid colloids and a water-miscible organic liquid |
| US7250461B2 (en) | 2004-03-17 | 2007-07-31 | E. I. Du Pont De Nemours And Company | Organic formulations of conductive polymers made with polymeric acid colloids for electronics applications, and methods for making such formulations |
| EP1730215B1 (en) | 2004-03-18 | 2017-08-16 | Enthone GmbH | A composition comprising a conductive polymer in colloidal form and carbon |
| US7455793B2 (en) | 2004-03-31 | 2008-11-25 | E.I. Du Pont De Nemours And Company | Non-aqueous dispersions comprising electrically doped conductive polymers and colloid-forming polymeric acids |
| US20050222333A1 (en) | 2004-03-31 | 2005-10-06 | Che-Hsiung Hsu | Aqueous electrically doped conductive polymers and polymeric acid colloids |
| US7354532B2 (en) | 2004-04-13 | 2008-04-08 | E.I. Du Pont De Nemours And Company | Compositions of electrically conductive polymers and non-polymeric fluorinated organic acids |
| US7378040B2 (en) | 2004-08-11 | 2008-05-27 | Eikos, Inc. | Method of forming fluoropolymer binders for carbon nanotube-based transparent conductive coatings |
| US20060051401A1 (en) | 2004-09-07 | 2006-03-09 | Board Of Regents, The University Of Texas System | Controlled nanofiber seeding |
| CN100583485C (zh) | 2004-09-24 | 2010-01-20 | 普莱克斯托尼克斯公司 | 含杂原子立体规则性聚(3-取代噻吩)的光电池 |
| US7211824B2 (en) | 2004-09-27 | 2007-05-01 | Nitto Denko Corporation | Organic semiconductor diode |
| US7388235B2 (en) | 2004-09-30 | 2008-06-17 | The United States Of America As Represented By The Secretary Of The Navy | High electron mobility transistors with Sb-based channels |
| KR100882503B1 (ko) | 2004-10-06 | 2009-02-06 | 한국과학기술연구원 | 염료감응 태양전지용 고효율 대향전극 및 그 제조방법 |
| US7569158B2 (en) | 2004-10-13 | 2009-08-04 | Air Products And Chemicals, Inc. | Aqueous dispersions of polythienothiophenes with fluorinated ion exchange polymers as dopants |
| WO2006073968A2 (en) | 2004-12-30 | 2006-07-13 | E. I. Dupont De Nemours And Company | Derivatized 3,4-alkylenedioxythiophene monomers, methods of making them, and use thereof |
| US7985490B2 (en) | 2005-02-14 | 2011-07-26 | Samsung Mobile Display Co., Ltd. | Composition of conducting polymer and organic opto-electronic device employing the same |
| US7593004B2 (en) | 2005-06-02 | 2009-09-22 | Eastman Kodak Company | Touchscreen with conductive layer comprising carbon nanotubes |
| US7645497B2 (en) | 2005-06-02 | 2010-01-12 | Eastman Kodak Company | Multi-layer conductor with carbon nanotubes |
| KR101294905B1 (ko) * | 2005-06-27 | 2013-08-09 | 이 아이 듀폰 디 네모아 앤드 캄파니 | 전기 전도성 중합체 조성물 |
| WO2007002681A2 (en) | 2005-06-27 | 2007-01-04 | E. I. Du Pont De Nemours And Company | Electrically conductive polymer compositions |
| US7727421B2 (en) | 2005-06-27 | 2010-06-01 | E. I. Du Pont De Nemours And Company Dupont Displays Inc | Electrically conductive polymer compositions |
| KR101294892B1 (ko) | 2005-06-27 | 2013-08-09 | 이 아이 듀폰 디 네모아 앤드 캄파니 | 전기 전도성 중합체 조성물 |
| WO2007002740A2 (en) | 2005-06-28 | 2007-01-04 | E. I. Du Pont De Nemours And Company | Buffer compositions |
| CN101208369B (zh) | 2005-06-28 | 2013-03-27 | E.I.内穆尔杜邦公司 | 高功函数透明导体 |
| EP1913604A4 (en) | 2005-06-28 | 2011-07-20 | Du Pont | ANODE BICOUCHE |
| US8216680B2 (en) | 2006-02-03 | 2012-07-10 | E I Du Pont De Nemours And Company | Transparent composite conductors having high work function |
| JP2009534831A (ja) | 2006-04-18 | 2009-09-24 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | 高エネルギーポテンシャル二重層組成物 |
| US8153029B2 (en) | 2006-12-28 | 2012-04-10 | E.I. Du Pont De Nemours And Company | Laser (230NM) ablatable compositions of electrically conducting polymers made with a perfluoropolymeric acid applications thereof |
| US20080251768A1 (en) | 2007-04-13 | 2008-10-16 | Che-Hsiung Hsu | Electrically conductive polymer compositions |
| US20080283800A1 (en) * | 2007-05-18 | 2008-11-20 | Che Hsiung Hsu | Electrically conductive polymer compositions and films made therefrom |
| US8241526B2 (en) | 2007-05-18 | 2012-08-14 | E I Du Pont De Nemours And Company | Aqueous dispersions of electrically conducting polymers containing high boiling solvent and additives |
| US8461758B2 (en) * | 2008-12-19 | 2013-06-11 | E I Du Pont De Nemours And Company | Buffer bilayers for electronic devices |
-
2010
- 2010-04-23 KR KR1020117027924A patent/KR101581991B1/ko active Active
- 2010-04-23 CN CN201080017846.6A patent/CN102395627B/zh active Active
- 2010-04-23 JP JP2012507410A patent/JP2012524834A/ja active Pending
- 2010-04-23 US US13/265,002 patent/US8945427B2/en active Active
- 2010-04-23 EP EP10767815.3A patent/EP2421919A4/en not_active Withdrawn
- 2010-04-23 WO PCT/US2010/032175 patent/WO2010124166A2/en not_active Ceased
- 2010-04-23 TW TW99112912A patent/TW201100482A/zh unknown
Patent Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2006500461A (ja) * | 2002-09-24 | 2006-01-05 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | 電子工学用途のための、ポリマー酸コロイドを用いて製造された水分散性ポリアニリン |
| WO2007145977A1 (en) * | 2006-06-05 | 2007-12-21 | E. I. Du Pont De Nemours And Company | Process for making an organic electronic device |
| JP2010514904A (ja) * | 2006-12-29 | 2010-05-06 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | 導電性ポリマーの高仕事関数および高導電率組成物 |
| WO2009018009A1 (en) * | 2007-07-27 | 2009-02-05 | E. I. Du Pont De Nemours And Company | Aqueous dispersions of electrically conducting polymers containing inorganic nanoparticles |
| JP2010534739A (ja) * | 2007-07-27 | 2010-11-11 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | 無機ナノ粒子を含有する導電性ポリマーの水性分散体 |
| JP2011517468A (ja) * | 2008-03-19 | 2011-06-09 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | 導電性ポリマー組成物およびそれから作製されたフィルム |
| JP2012524831A (ja) * | 2009-04-21 | 2012-10-18 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | 導電性ポリマー組成物およびそれから作製されたフィルム |
Cited By (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2014189116A1 (ja) * | 2013-05-23 | 2014-11-27 | 富士フイルム株式会社 | 有機半導体組成物および有機薄膜トランジスタならびに電子ペーパーおよびディスプレイデバイス |
| JPWO2014189114A1 (ja) * | 2013-05-23 | 2017-02-23 | 富士フイルム株式会社 | 有機半導体組成物および有機薄膜トランジスタならびに電子ペーパーおよびディスプレイデバイス |
| JPWO2014189116A1 (ja) * | 2013-05-23 | 2017-02-23 | 富士フイルム株式会社 | 有機半導体組成物および有機薄膜トランジスタならびに電子ペーパーおよびディスプレイデバイス |
| WO2014189114A1 (ja) * | 2013-05-23 | 2014-11-27 | 富士フイルム株式会社 | 有機半導体組成物および有機薄膜トランジスタならびに電子ペーパーおよびディスプレイデバイス |
| KR20170125902A (ko) * | 2015-03-03 | 2017-11-15 | 닛산 가가쿠 고교 가부시키 가이샤 | 정공 캐리어 화합물 및 중합체 산을 함유하는 조성물, 및 그의 용도 |
| KR102499662B1 (ko) * | 2015-03-03 | 2023-02-15 | 닛산 가가쿠 가부시키가이샤 | 정공 캐리어 화합물 및 중합체 산을 함유하는 조성물, 및 그의 용도 |
| JP2021061445A (ja) * | 2016-05-10 | 2021-04-15 | 昭和電工マテリアルズ株式会社 | 電荷輸送性材料、有機エレクトロニクス素子、及び有機エレクトロルミネセンス素子 |
| WO2017195559A1 (ja) * | 2016-05-10 | 2017-11-16 | 日立化成株式会社 | 電荷輸送性材料、有機エレクトロニクス素子、及び有機エレクトロルミネセンス素子 |
| JP7425418B2 (ja) | 2016-05-10 | 2024-01-31 | 株式会社レゾナック | 電荷輸送性材料、有機エレクトロニクス素子、及び有機エレクトロルミネセンス素子 |
| JP2022123002A (ja) * | 2016-05-10 | 2022-08-23 | 昭和電工マテリアルズ株式会社 | 電荷輸送性材料、有機エレクトロニクス素子、及び有機エレクトロルミネセンス素子 |
| JPWO2017195559A1 (ja) * | 2016-05-10 | 2019-03-22 | 日立化成株式会社 | 電荷輸送性材料、有機エレクトロニクス素子、及び有機エレクトロルミネセンス素子 |
| KR20190104212A (ko) * | 2017-01-18 | 2019-09-06 | 닛산 가가쿠 가부시키가이샤 | 잉크 조성물 |
| JP2019192928A (ja) * | 2017-01-18 | 2019-10-31 | 日産化学株式会社 | 電荷輸送性ワニス及びそれを用いる電荷輸送性薄膜 |
| JPWO2018135582A1 (ja) * | 2017-01-18 | 2019-11-07 | 日産化学株式会社 | インク組成物 |
| CN110268540A (zh) * | 2017-01-18 | 2019-09-20 | 日产化学株式会社 | 墨液组合物 |
| JP2022022288A (ja) * | 2017-01-18 | 2022-02-03 | 日産化学株式会社 | インク組成物 |
| JP7077944B2 (ja) | 2017-01-18 | 2022-05-31 | 日産化学株式会社 | インク組成物 |
| CN110268540B (zh) * | 2017-01-18 | 2022-07-01 | 日产化学株式会社 | 墨液组合物 |
| JPWO2018135580A1 (ja) * | 2017-01-18 | 2019-01-24 | 日産化学株式会社 | 電荷輸送性ワニス及びそれを用いる電荷輸送性薄膜 |
| WO2018135580A1 (ja) * | 2017-01-18 | 2018-07-26 | 日産化学工業株式会社 | 電荷輸送性ワニス及びそれを用いる電荷輸送性薄膜 |
| KR102564836B1 (ko) * | 2017-01-18 | 2023-08-09 | 닛산 가가쿠 가부시키가이샤 | 잉크 조성물 |
| WO2018135582A1 (ja) * | 2017-01-18 | 2018-07-26 | 日産化学工業株式会社 | インク組成物 |
Also Published As
| Publication number | Publication date |
|---|---|
| US20120145966A1 (en) | 2012-06-14 |
| KR20120000113A (ko) | 2012-01-03 |
| US8945427B2 (en) | 2015-02-03 |
| WO2010124166A3 (en) | 2011-02-17 |
| TW201100482A (en) | 2011-01-01 |
| WO2010124166A2 (en) | 2010-10-28 |
| CN102395627B (zh) | 2015-04-01 |
| KR101581991B1 (ko) | 2015-12-31 |
| EP2421919A2 (en) | 2012-02-29 |
| CN102395627A (zh) | 2012-03-28 |
| EP2421919A4 (en) | 2014-01-22 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US8945427B2 (en) | Electrically conductive polymer compositions and films made therefrom | |
| JP5411249B2 (ja) | 導電性ポリマー組成物およびそれから作製されたフィルム | |
| US8945426B2 (en) | Electrically conductive polymer compositions for coating applications | |
| JP2010534739A (ja) | 無機ナノ粒子を含有する導電性ポリマーの水性分散体 | |
| JP2011529115A (ja) | 無機ナノ粒子を含有する導電性ポリマーの水性分散体 | |
| JP5587980B2 (ja) | 導電性ポリマー組成物およびそれから作製されたフィルム | |
| JP2011510484A (ja) | 電子デバイスのための緩衝二層 | |
| US8785913B2 (en) | Buffer bilayers for electronic devices | |
| US8216685B2 (en) | Buffer bilayers for electronic devices |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20130201 |
|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20130201 |
|
| A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20130729 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20130806 |
|
| A02 | Decision of refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A02 Effective date: 20140107 |