CA2497451A1 - Organic species that facilitate charge transfer to or from nanostructures - Google Patents
Organic species that facilitate charge transfer to or from nanostructures Download PDFInfo
- Publication number
- CA2497451A1 CA2497451A1 CA002497451A CA2497451A CA2497451A1 CA 2497451 A1 CA2497451 A1 CA 2497451A1 CA 002497451 A CA002497451 A CA 002497451A CA 2497451 A CA2497451 A CA 2497451A CA 2497451 A1 CA2497451 A1 CA 2497451A1
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- CA
- Canada
- Prior art keywords
- composition
- nanostructure
- moiety
- substituent
- matrix
- 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.)
- Abandoned
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- 239000002086 nanomaterial Substances 0.000 title claims description 271
- 238000012546 transfer Methods 0.000 title claims description 10
- 239000000203 mixture Substances 0.000 claims abstract description 408
- 239000002159 nanocrystal Substances 0.000 claims abstract description 127
- 239000011159 matrix material Substances 0.000 claims abstract description 109
- 238000000034 method Methods 0.000 claims abstract description 83
- 125000001424 substituent group Chemical group 0.000 claims description 134
- 238000005859 coupling reaction Methods 0.000 claims description 72
- -1 2-ethylhexyl moiety Chemical group 0.000 claims description 68
- 230000008878 coupling Effects 0.000 claims description 68
- 238000010168 coupling process Methods 0.000 claims description 68
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 claims description 54
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims description 42
- 239000002243 precursor Substances 0.000 claims description 42
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical group CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 claims description 41
- 239000000126 substance Substances 0.000 claims description 40
- 239000011541 reaction mixture Substances 0.000 claims description 39
- 125000003118 aryl group Chemical group 0.000 claims description 29
- 229930192474 thiophene Natural products 0.000 claims description 23
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 21
- 125000000217 alkyl group Chemical group 0.000 claims description 21
- 230000004048 modification Effects 0.000 claims description 19
- 238000012986 modification Methods 0.000 claims description 19
- 150000001345 alkine derivatives Chemical group 0.000 claims description 16
- HSFWRNGVRCDJHI-UHFFFAOYSA-N Acetylene Chemical compound C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 claims description 15
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims description 14
- 150000001412 amines Chemical class 0.000 claims description 14
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 claims description 14
- 230000021615 conjugation Effects 0.000 claims description 13
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 claims description 12
- 230000003993 interaction Effects 0.000 claims description 12
- 150000003577 thiophenes Chemical class 0.000 claims description 11
- KDKYADYSIPSCCQ-UHFFFAOYSA-N but-1-yne Chemical compound CCC#C KDKYADYSIPSCCQ-UHFFFAOYSA-N 0.000 claims description 10
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 9
- ILLHQJIJCRNRCJ-UHFFFAOYSA-N dec-1-yne Chemical compound CCCCCCCCC#C ILLHQJIJCRNRCJ-UHFFFAOYSA-N 0.000 claims description 9
- 125000006575 electron-withdrawing group Chemical group 0.000 claims description 9
- 150000003573 thiols Chemical group 0.000 claims description 9
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 8
- KWTSZCJMWHGPOS-UHFFFAOYSA-M chloro(trimethyl)stannane Chemical compound C[Sn](C)(C)Cl KWTSZCJMWHGPOS-UHFFFAOYSA-M 0.000 claims description 8
- 229920001940 conductive polymer Polymers 0.000 claims description 8
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 8
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 8
- 230000002194 synthesizing effect Effects 0.000 claims description 8
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 7
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims description 7
- 125000003342 alkenyl group Chemical group 0.000 claims description 7
- 150000001502 aryl halides Chemical group 0.000 claims description 7
- IJOOHPMOJXWVHK-UHFFFAOYSA-N chlorotrimethylsilane Chemical compound C[Si](C)(C)Cl IJOOHPMOJXWVHK-UHFFFAOYSA-N 0.000 claims description 7
- RMBPEFMHABBEKP-UHFFFAOYSA-N fluorene Chemical compound C1=CC=C2C3=C[CH]C=CC3=CC2=C1 RMBPEFMHABBEKP-UHFFFAOYSA-N 0.000 claims description 7
- 150000004820 halides Chemical group 0.000 claims description 7
- NIHNNTQXNPWCJQ-UHFFFAOYSA-N o-biphenylenemethane Natural products C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 claims description 7
- 125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 claims description 7
- CSHWQDPOILHKBI-UHFFFAOYSA-N peryrene Natural products C1=CC(C2=CC=CC=3C2=C2C=CC=3)=C3C2=CC=CC3=C1 CSHWQDPOILHKBI-UHFFFAOYSA-N 0.000 claims description 7
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims description 7
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 claims description 7
- 238000010438 heat treatment Methods 0.000 claims description 6
- 229910000073 phosphorus hydride Inorganic materials 0.000 claims description 6
- 229920000301 poly(3-hexylthiophene-2,5-diyl) polymer Polymers 0.000 claims description 6
- 229920000767 polyaniline Polymers 0.000 claims description 6
- 230000000379 polymerizing effect Effects 0.000 claims description 6
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 6
- CGHIBGNXEGJPQZ-UHFFFAOYSA-N 1-hexyne Chemical compound CCCCC#C CGHIBGNXEGJPQZ-UHFFFAOYSA-N 0.000 claims description 5
- IBXNCJKFFQIKKY-UHFFFAOYSA-N 1-pentyne Chemical compound CCCC#C IBXNCJKFFQIKKY-UHFFFAOYSA-N 0.000 claims description 5
- 229920000265 Polyparaphenylene Polymers 0.000 claims description 5
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 5
- LXCYSACZTOKNNS-UHFFFAOYSA-N diethoxy(oxo)phosphanium Chemical compound CCO[P+](=O)OCC LXCYSACZTOKNNS-UHFFFAOYSA-N 0.000 claims description 5
- YVXHZKKCZYLQOP-UHFFFAOYSA-N hept-1-yne Chemical compound CCCCCC#C YVXHZKKCZYLQOP-UHFFFAOYSA-N 0.000 claims description 5
- 230000007246 mechanism Effects 0.000 claims description 5
- OSSQSXOTMIGBCF-UHFFFAOYSA-N non-1-yne Chemical compound CCCCCCCC#C OSSQSXOTMIGBCF-UHFFFAOYSA-N 0.000 claims description 5
- UMIPWJGWASORKV-UHFFFAOYSA-N oct-1-yne Chemical compound CCCCCCC#C UMIPWJGWASORKV-UHFFFAOYSA-N 0.000 claims description 5
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 5
- 229920000123 polythiophene Polymers 0.000 claims description 5
- MWWATHDPGQKSAR-UHFFFAOYSA-N propyne Chemical compound CC#C MWWATHDPGQKSAR-UHFFFAOYSA-N 0.000 claims description 5
- 150000001336 alkenes Chemical class 0.000 claims description 4
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 4
- 229910052751 metal Inorganic materials 0.000 claims description 4
- 239000002184 metal Substances 0.000 claims description 4
- 229910004613 CdTe Inorganic materials 0.000 claims description 3
- 238000003477 Sonogashira cross-coupling reaction Methods 0.000 claims description 3
- 239000013626 chemical specie Substances 0.000 claims description 3
- 150000003003 phosphines Chemical class 0.000 claims description 3
- 150000003007 phosphonic acid derivatives Chemical class 0.000 claims description 3
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-M acrylate group Chemical group C(C=C)(=O)[O-] NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 2
- 239000003574 free electron Substances 0.000 claims description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-M methacrylate group Chemical group C(C(=C)C)(=O)[O-] CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 claims description 2
- 238000006619 Stille reaction Methods 0.000 claims 1
- 230000002152 alkylating effect Effects 0.000 claims 1
- 229920000642 polymer Polymers 0.000 abstract description 41
- 150000003384 small molecules Chemical class 0.000 abstract description 3
- 238000003786 synthesis reaction Methods 0.000 description 68
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 62
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 62
- 230000015572 biosynthetic process Effects 0.000 description 59
- 239000002070 nanowire Substances 0.000 description 49
- 239000000463 material Substances 0.000 description 39
- 239000002904 solvent Substances 0.000 description 33
- 229910052786 argon Inorganic materials 0.000 description 31
- 239000000543 intermediate Substances 0.000 description 30
- 238000006243 chemical reaction Methods 0.000 description 23
- 229940093499 ethyl acetate Drugs 0.000 description 20
- 235000019439 ethyl acetate Nutrition 0.000 description 20
- 238000001704 evaporation Methods 0.000 description 20
- 239000003446 ligand Substances 0.000 description 20
- 239000004065 semiconductor Substances 0.000 description 20
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 19
- 238000013459 approach Methods 0.000 description 17
- 241000894007 species Species 0.000 description 17
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 16
- 101150041968 CDC13 gene Proteins 0.000 description 15
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 15
- 239000013078 crystal Substances 0.000 description 14
- 238000006116 polymerization reaction Methods 0.000 description 14
- 238000002360 preparation method Methods 0.000 description 14
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 13
- 150000001875 compounds Chemical class 0.000 description 13
- 238000000746 purification Methods 0.000 description 11
- 238000005160 1H NMR spectroscopy Methods 0.000 description 10
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 10
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 10
- 239000002073 nanorod Substances 0.000 description 10
- 239000000243 solution Substances 0.000 description 10
- 239000004094 surface-active agent Substances 0.000 description 10
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 9
- 238000000576 coating method Methods 0.000 description 9
- 238000004770 highest occupied molecular orbital Methods 0.000 description 9
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 8
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 8
- 239000004809 Teflon Substances 0.000 description 8
- 229920006362 Teflon® Polymers 0.000 description 8
- 239000002114 nanocomposite Substances 0.000 description 8
- 239000002105 nanoparticle Substances 0.000 description 8
- 239000003921 oil Substances 0.000 description 8
- 235000019198 oils Nutrition 0.000 description 8
- 239000012044 organic layer Substances 0.000 description 8
- 239000004054 semiconductor nanocrystal Substances 0.000 description 8
- UHYPYGJEEGLRJD-UHFFFAOYSA-N cadmium(2+);selenium(2-) Chemical compound [Se-2].[Cd+2] UHYPYGJEEGLRJD-UHFFFAOYSA-N 0.000 description 7
- 238000003818 flash chromatography Methods 0.000 description 7
- 238000004768 lowest unoccupied molecular orbital Methods 0.000 description 7
- PIBWKRNGBLPSSY-UHFFFAOYSA-L palladium(II) chloride Chemical compound Cl[Pd]Cl PIBWKRNGBLPSSY-UHFFFAOYSA-L 0.000 description 7
- 238000003756 stirring Methods 0.000 description 7
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
- 125000002355 alkine group Chemical group 0.000 description 6
- 239000012267 brine Substances 0.000 description 6
- 229910052799 carbon Inorganic materials 0.000 description 6
- UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Chemical compound CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 description 6
- 238000002347 injection Methods 0.000 description 6
- 239000007924 injection Substances 0.000 description 6
- 230000008569 process Effects 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 6
- 239000007787 solid Substances 0.000 description 6
- 239000011877 solvent mixture Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 5
- 239000003054 catalyst Substances 0.000 description 5
- 239000011248 coating agent Substances 0.000 description 5
- 238000004132 cross linking Methods 0.000 description 5
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 5
- 235000019341 magnesium sulphate Nutrition 0.000 description 5
- TZSZZENYCISATO-WIOPSUGQSA-N rodatristat Chemical compound CCOC(=O)[C@@H]1CC2(CN1)CCN(CC2)c1cc(O[C@H](c2ccc(Cl)cc2-c2ccccc2)C(F)(F)F)nc(N)n1 TZSZZENYCISATO-WIOPSUGQSA-N 0.000 description 5
- 229920006395 saturated elastomer Polymers 0.000 description 5
- 229910052938 sodium sulfate Inorganic materials 0.000 description 5
- 235000011152 sodium sulphate Nutrition 0.000 description 5
- BPLUKJNHPBNVQL-UHFFFAOYSA-N triphenylarsine Chemical compound C1=CC=CC=C1[As](C=1C=CC=CC=1)C1=CC=CC=C1 BPLUKJNHPBNVQL-UHFFFAOYSA-N 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- WEFVEIXIKPJCOB-UHFFFAOYSA-N CCCCCCCCC#CC1=CC=C[S+]1[SnH3] Chemical compound CCCCCCCCC#CC1=CC=C[S+]1[SnH3] WEFVEIXIKPJCOB-UHFFFAOYSA-N 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- LQZMLBORDGWNPD-UHFFFAOYSA-N N-iodosuccinimide Chemical compound IN1C(=O)CCC1=O LQZMLBORDGWNPD-UHFFFAOYSA-N 0.000 description 4
- 238000005481 NMR spectroscopy Methods 0.000 description 4
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 4
- 125000000304 alkynyl group Chemical group 0.000 description 4
- 235000019270 ammonium chloride Nutrition 0.000 description 4
- 230000008901 benefit Effects 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
- KAKZBPTYRLMSJV-UHFFFAOYSA-N butadiene group Chemical group C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 4
- 239000000470 constituent Substances 0.000 description 4
- 239000008367 deionised water Substances 0.000 description 4
- 238000000605 extraction Methods 0.000 description 4
- 230000005525 hole transport Effects 0.000 description 4
- 239000010410 layer Substances 0.000 description 4
- ZCSHNCUQKCANBX-UHFFFAOYSA-N lithium diisopropylamide Chemical compound [Li+].CC(C)[N-]C(C)C ZCSHNCUQKCANBX-UHFFFAOYSA-N 0.000 description 4
- 229910003002 lithium salt Inorganic materials 0.000 description 4
- 159000000002 lithium salts Chemical class 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 229910000027 potassium carbonate Inorganic materials 0.000 description 4
- 239000012266 salt solution Substances 0.000 description 4
- 229910002027 silica gel Inorganic materials 0.000 description 4
- 239000000741 silica gel Substances 0.000 description 4
- 239000000377 silicon dioxide Substances 0.000 description 4
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 4
- 235000019345 sodium thiosulphate Nutrition 0.000 description 4
- 238000006467 substitution reaction Methods 0.000 description 4
- 239000000758 substrate Substances 0.000 description 4
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 4
- STBLNCCBQMHSRC-BATDWUPUSA-N (2s)-n-[(3s,4s)-5-acetyl-7-cyano-4-methyl-1-[(2-methylnaphthalen-1-yl)methyl]-2-oxo-3,4-dihydro-1,5-benzodiazepin-3-yl]-2-(methylamino)propanamide Chemical compound O=C1[C@@H](NC(=O)[C@H](C)NC)[C@H](C)N(C(C)=O)C2=CC(C#N)=CC=C2N1CC1=C(C)C=CC2=CC=CC=C12 STBLNCCBQMHSRC-BATDWUPUSA-N 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 229920000106 Liquid crystal polymer Polymers 0.000 description 3
- 239000004977 Liquid-crystal polymers (LCPs) Substances 0.000 description 3
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- 230000000712 assembly Effects 0.000 description 3
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- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 3
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- 125000002534 ethynyl group Chemical class [H]C#C* 0.000 description 3
- 125000000524 functional group Chemical group 0.000 description 3
- 125000005647 linker group Chemical group 0.000 description 3
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- UAOUIVVJBYDFKD-XKCDOFEDSA-N (1R,9R,10S,11R,12R,15S,18S,21R)-10,11,21-trihydroxy-8,8-dimethyl-14-methylidene-4-(prop-2-enylamino)-20-oxa-5-thia-3-azahexacyclo[9.7.2.112,15.01,9.02,6.012,18]henicosa-2(6),3-dien-13-one Chemical compound C([C@@H]1[C@@H](O)[C@@]23C(C1=C)=O)C[C@H]2[C@]12C(N=C(NCC=C)S4)=C4CC(C)(C)[C@H]1[C@H](O)[C@]3(O)OC2 UAOUIVVJBYDFKD-XKCDOFEDSA-N 0.000 description 2
- SHAHPWSYJFYMRX-GDLCADMTSA-N (2S)-2-(4-{[(1R,2S)-2-hydroxycyclopentyl]methyl}phenyl)propanoic acid Chemical compound C1=CC([C@@H](C(O)=O)C)=CC=C1C[C@@H]1[C@@H](O)CCC1 SHAHPWSYJFYMRX-GDLCADMTSA-N 0.000 description 2
- YJLIKUSWRSEPSM-WGQQHEPDSA-N (2r,3r,4s,5r)-2-[6-amino-8-[(4-phenylphenyl)methylamino]purin-9-yl]-5-(hydroxymethyl)oxolane-3,4-diol Chemical compound C=1C=C(C=2C=CC=CC=2)C=CC=1CNC1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O YJLIKUSWRSEPSM-WGQQHEPDSA-N 0.000 description 2
- WWTBZEKOSBFBEM-SPWPXUSOSA-N (2s)-2-[[2-benzyl-3-[hydroxy-[(1r)-2-phenyl-1-(phenylmethoxycarbonylamino)ethyl]phosphoryl]propanoyl]amino]-3-(1h-indol-3-yl)propanoic acid Chemical compound N([C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)O)C(=O)C(CP(O)(=O)[C@H](CC=1C=CC=CC=1)NC(=O)OCC=1C=CC=CC=1)CC1=CC=CC=C1 WWTBZEKOSBFBEM-SPWPXUSOSA-N 0.000 description 2
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Classifications
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- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/58—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving labelled substances
- G01N33/588—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving labelled substances with semiconductor nanocrystal label, e.g. quantum dots
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- B82Y10/00—Nanotechnology for information processing, storage or transmission, e.g. quantum computing or single electron logic
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- B82Y15/00—Nanotechnology for interacting, sensing or actuating, e.g. quantum dots as markers in protein assays or molecular motors
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- 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
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
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- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G9/00—Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
- H01G9/20—Light-sensitive devices
- H01G9/2059—Light-sensitive devices comprising an organic dye as the active light absorbing material, e.g. adsorbed on an electrode or dissolved in solution
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K30/00—Organic devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation
- H10K30/10—Organic devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation comprising heterojunctions between organic semiconductors and inorganic semiconductors
- H10K30/15—Sensitised wide-bandgap semiconductor devices, e.g. dye-sensitised TiO2
- H10K30/151—Sensitised wide-bandgap semiconductor devices, e.g. dye-sensitised TiO2 the wide bandgap semiconductor comprising titanium oxide, e.g. TiO2
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- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K30/00—Organic devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation
- H10K30/50—Photovoltaic [PV] devices
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- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P70/00—Climate change mitigation technologies in the production process for final industrial or consumer products
- Y02P70/50—Manufacturing or production processes characterised by the final manufactured product
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- Health & Medical Sciences (AREA)
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| US40872202P | 2002-09-05 | 2002-09-05 | |
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| US45223203P | 2003-03-04 | 2003-03-04 | |
| US60/452,232 | 2003-03-04 | ||
| PCT/US2003/027847 WO2004022714A2 (en) | 2002-09-05 | 2003-09-04 | Organic species that facilitate charge transfer to or from nanostructures |
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Families Citing this family (237)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6919119B2 (en) * | 2000-05-30 | 2005-07-19 | The Penn State Research Foundation | Electronic and opto-electronic devices fabricated from nanostructured high surface to volume ratio thin films |
| US7205048B2 (en) * | 2001-09-17 | 2007-04-17 | Invitrogen Corporation | Functionalized fluorescent nanocrystal compositions and methods of making |
| US8294025B2 (en) * | 2002-06-08 | 2012-10-23 | Solarity, Llc | Lateral collection photovoltaics |
| US7253017B1 (en) | 2002-06-22 | 2007-08-07 | Nanosolar, Inc. | Molding technique for fabrication of optoelectronic devices |
| US7291782B2 (en) * | 2002-06-22 | 2007-11-06 | Nanosolar, Inc. | Optoelectronic device and fabrication method |
| US6946597B2 (en) * | 2002-06-22 | 2005-09-20 | Nanosular, Inc. | Photovoltaic devices fabricated by growth from porous template |
| US7594982B1 (en) | 2002-06-22 | 2009-09-29 | Nanosolar, Inc. | Nanostructured transparent conducting electrode |
| WO2004027822A2 (en) | 2002-09-05 | 2004-04-01 | Nanosys, Inc. | Oriented nanostructures and methods of preparing |
| US7572393B2 (en) * | 2002-09-05 | 2009-08-11 | Nanosys Inc. | Organic species that facilitate charge transfer to or from nanostructures |
| JP2005538573A (ja) * | 2002-09-05 | 2005-12-15 | ナノシス・インク． | ナノ構造及びナノ複合材をベースとする組成物 |
| US7083586B2 (en) * | 2003-02-03 | 2006-08-01 | Dj Orthopedics, Llc | Patellofemoral brace |
| US6936761B2 (en) * | 2003-03-29 | 2005-08-30 | Nanosolar, Inc. | Transparent electrode, optoelectronic apparatus and devices |
| US7511217B1 (en) | 2003-04-19 | 2009-03-31 | Nanosolar, Inc. | Inter facial architecture for nanostructured optoelectronic devices |
| US7645934B1 (en) | 2003-04-29 | 2010-01-12 | Nanosolar, Inc. | Nanostructured layer and fabrication methods |
| US7462774B2 (en) * | 2003-05-21 | 2008-12-09 | Nanosolar, Inc. | Photovoltaic devices fabricated from insulating nanostructured template |
| US7605327B2 (en) * | 2003-05-21 | 2009-10-20 | Nanosolar, Inc. | Photovoltaic devices fabricated from nanostructured template |
| US7422790B1 (en) | 2003-09-04 | 2008-09-09 | Nanosys, Inc. | Methods of processing nanocrystals, and compositions, devices and systems including same |
| FR2862955B1 (fr) * | 2003-12-02 | 2006-03-10 | Commissariat Energie Atomique | Nanocristaux inorganiques a couche de revetement organique, leur procede de preparation, et materiaux constitues par ceux-ci. |
| EP1733077B1 (en) * | 2004-01-15 | 2018-04-18 | Samsung Electronics Co., Ltd. | Nanocrystal doped matrixes |
| US7645397B2 (en) * | 2004-01-15 | 2010-01-12 | Nanosys, Inc. | Nanocrystal doped matrixes |
| EP1738378A4 (en) | 2004-03-18 | 2010-05-05 | Nanosys Inc | NANOFIBRE SURFACE BASED CAPACITORS |
| US20050214190A1 (en) * | 2004-03-25 | 2005-09-29 | Seoul National University | Method of synthesizing nanorods by reaction of metal-surfactant complexes injected using a syringe pump |
| US7773404B2 (en) | 2005-01-07 | 2010-08-10 | Invisage Technologies, Inc. | Quantum dot optical devices with enhanced gain and sensitivity and methods of making same |
| KR101185613B1 (ko) | 2004-04-27 | 2012-09-24 | 더 보오드 오브 트러스티스 오브 더 유니버시티 오브 일리노이즈 | 소프트 리소그래피용 복합 패터닝 장치 |
| US20080055581A1 (en) * | 2004-04-27 | 2008-03-06 | Rogers John A | Devices and methods for pattern generation by ink lithography |
| GB0409877D0 (en) | 2004-04-30 | 2004-06-09 | Univ Manchester | Preparation of nanoparticle materials |
| WO2006076036A2 (en) * | 2004-05-25 | 2006-07-20 | The Trustees Of The University Of Pennsylvania | Nanostructure assemblies, methods and devices thereof |
| KR101260981B1 (ko) | 2004-06-04 | 2013-05-10 | 더 보오드 오브 트러스티스 오브 더 유니버시티 오브 일리노이즈 | 인쇄가능한 반도체소자들의 제조 및 조립방법과 장치 |
| US7943491B2 (en) | 2004-06-04 | 2011-05-17 | The Board Of Trustees Of The University Of Illinois | Pattern transfer printing by kinetic control of adhesion to an elastomeric stamp |
| US7521292B2 (en) | 2004-06-04 | 2009-04-21 | The Board Of Trustees Of The University Of Illinois | Stretchable form of single crystal silicon for high performance electronics on rubber substrates |
| US7799699B2 (en) | 2004-06-04 | 2010-09-21 | The Board Of Trustees Of The University Of Illinois | Printable semiconductor structures and related methods of making and assembling |
| US8217381B2 (en) | 2004-06-04 | 2012-07-10 | The Board Of Trustees Of The University Of Illinois | Controlled buckling structures in semiconductor interconnects and nanomembranes for stretchable electronics |
| TWI406890B (zh) * | 2004-06-08 | 2013-09-01 | Sandisk Corp | 奈米結構之沉積後包封：併入該包封體之組成物、裝置及系統 |
| US7968273B2 (en) | 2004-06-08 | 2011-06-28 | Nanosys, Inc. | Methods and devices for forming nanostructure monolayers and devices including such monolayers |
| JP5000510B2 (ja) | 2004-06-08 | 2012-08-15 | ナノシス・インク． | ナノ構造単層の形成方法および形成デバイスならびにかかる単層を含むデバイス |
| US8563133B2 (en) | 2004-06-08 | 2013-10-22 | Sandisk Corporation | Compositions and methods for modulation of nanostructure energy levels |
| WO2005122293A2 (en) * | 2004-06-08 | 2005-12-22 | Princeton University | Formation of ordered thin films of organics on metal oxide surfaces |
| US7776758B2 (en) | 2004-06-08 | 2010-08-17 | Nanosys, Inc. | Methods and devices for forming nanostructure monolayers and devices including such monolayers |
| US8088483B1 (en) | 2004-06-08 | 2012-01-03 | Nanosys, Inc. | Process for group 10 metal nanostructure synthesis and compositions made using same |
| JPWO2005123637A1 (ja) * | 2004-06-17 | 2008-04-10 | 独立行政法人理化学研究所 | 単結晶、ナノ配線用材料、電子素子、および、ナノ配線用材料の製造方法 |
| EP1622178A1 (en) * | 2004-07-29 | 2006-02-01 | Ecole Polytechnique Federale De Lausanne (Epfl) | 2,2 -Bipyridine ligand, sensitizing dye and dye sensitized solar cell |
| US7247670B2 (en) * | 2004-08-24 | 2007-07-24 | General Electric Company | Nanotubes and methods of dispersing and separating nanotubes |
| US7794600B1 (en) * | 2004-08-27 | 2010-09-14 | Nanosys, Inc. | Purification of nanocrystal solutions by chromatography |
| US7365395B2 (en) * | 2004-09-16 | 2008-04-29 | Nanosys, Inc. | Artificial dielectrics using nanostructures |
| US8558311B2 (en) | 2004-09-16 | 2013-10-15 | Nanosys, Inc. | Dielectrics using substantially longitudinally oriented insulated conductive wires |
| US8089152B2 (en) * | 2004-09-16 | 2012-01-03 | Nanosys, Inc. | Continuously variable graded artificial dielectrics using nanostructures |
| CA2578359A1 (en) * | 2004-09-17 | 2006-11-09 | Nanosys, Inc. | Nanostructured thin films and their uses |
| US8278011B2 (en) | 2004-12-09 | 2012-10-02 | Nanosys, Inc. | Nanostructured catalyst supports |
| EP2432058B8 (en) | 2004-12-09 | 2013-09-11 | Nanosys, Inc. | Nanowire-based membrane electrode assemblies for fuel cells |
| US7939218B2 (en) * | 2004-12-09 | 2011-05-10 | Nanosys, Inc. | Nanowire structures comprising carbon |
| US7842432B2 (en) * | 2004-12-09 | 2010-11-30 | Nanosys, Inc. | Nanowire structures comprising carbon |
| US7811479B2 (en) * | 2005-02-07 | 2010-10-12 | The Trustees Of The University Of Pennsylvania | Polymer-nanocrystal quantum dot composites and optoelectronic devices |
| WO2006124625A2 (en) * | 2005-05-12 | 2006-11-23 | Nanosys, Inc. | Use of nanoparticles in film formation and as solder |
| US9297092B2 (en) * | 2005-06-05 | 2016-03-29 | Qd Vision, Inc. | Compositions, optical component, system including an optical component, devices, and other products |
| US8845927B2 (en) * | 2006-06-02 | 2014-09-30 | Qd Vision, Inc. | Functionalized nanoparticles and method |
| WO2006138671A2 (en) * | 2005-06-17 | 2006-12-28 | Illuminex Corporation | Photovoltaic wire |
| US20090050204A1 (en) * | 2007-08-03 | 2009-02-26 | Illuminex Corporation. | Photovoltaic device using nanostructured material |
| US20100193768A1 (en) * | 2005-06-20 | 2010-08-05 | Illuminex Corporation | Semiconducting nanowire arrays for photovoltaic applications |
| US20070001581A1 (en) * | 2005-06-29 | 2007-01-04 | Stasiak James W | Nanostructure based light emitting devices and associated methods |
| GB2472542B (en) | 2005-08-12 | 2011-03-23 | Nanoco Technologies Ltd | Nanoparticles |
| JP4982675B2 (ja) * | 2005-08-31 | 2012-07-25 | 国立大学法人九州工業大学 | 電解質組成物および色素増感太陽電池 |
| GB0522027D0 (en) * | 2005-10-28 | 2005-12-07 | Nanoco Technologies Ltd | Controlled preparation of nanoparticle materials |
| CN101563801B (zh) | 2005-11-21 | 2013-03-27 | 纳米系统公司 | 含碳的纳米线结构体 |
| US8796544B2 (en) * | 2005-12-14 | 2014-08-05 | Massachusetts Institute Of Technology | Bio-sensitized solar cells (BSSC) |
| EP1989744A1 (en) * | 2006-02-16 | 2008-11-12 | Solexant Corporation | Nanoparticle sensitized nanostructured solar cells |
| JP2009527876A (ja) * | 2006-02-17 | 2009-07-30 | ソレクサント・コーポレイション | ナノ構造のエレクトロルミネセンスデバイス及びディスプレイ |
| EP1991723A2 (en) | 2006-03-03 | 2008-11-19 | The Board Of Trustees Of The University Of Illinois | Methods of making spatially aligned nanotubes and nanotube arrays |
| WO2008070028A2 (en) * | 2006-12-01 | 2008-06-12 | Qd Vision, Inc. | Improved composites and devices including nanoparticles |
| US8849087B2 (en) | 2006-03-07 | 2014-09-30 | Qd Vision, Inc. | Compositions, optical component, system including an optical component, devices, and other products |
| US7524746B2 (en) * | 2006-03-13 | 2009-04-28 | Evident Technologies, Inc. | High-refractive index materials comprising semiconductor nanocrystal compositions, methods of making same, and applications therefor |
| AU2007314229A1 (en) * | 2006-03-23 | 2008-05-08 | Solexant Corp. | Photovoltaic device containing nanoparticle sensitized carbon nanotubes |
| WO2007112088A2 (en) * | 2006-03-24 | 2007-10-04 | Qd Vision, Inc. | Hyperspectral imaging device |
| WO2008060704A2 (en) * | 2006-06-02 | 2008-05-22 | Innovalight, Inc. | Photoactive materials containing group iv nanostructures and optoelectronic devices made therefrom |
| US9212056B2 (en) * | 2006-06-02 | 2015-12-15 | Qd Vision, Inc. | Nanoparticle including multi-functional ligand and method |
| US7442575B2 (en) * | 2006-09-29 | 2008-10-28 | Texas Christian University | Method of manufacturing semiconductor nanowires |
| US7816669B1 (en) * | 2006-10-13 | 2010-10-19 | Hewlett-Packard Development Company, L.P. | Light emitting system and methods for controlling nanocrystal distribution therein |
| US20080142075A1 (en) * | 2006-12-06 | 2008-06-19 | Solexant Corporation | Nanophotovoltaic Device with Improved Quantum Efficiency |
| US20080246076A1 (en) * | 2007-01-03 | 2008-10-09 | Nanosys, Inc. | Methods for nanopatterning and production of nanostructures |
| US20090136785A1 (en) * | 2007-01-03 | 2009-05-28 | Nanosys, Inc. | Methods for nanopatterning and production of magnetic nanostructures |
| CN101617406B (zh) | 2007-01-17 | 2011-04-20 | 伊利诺伊大学评议会 | 通过基于印刷的组装制造的光学系统 |
| ITMI20070217A1 (it) | 2007-02-07 | 2008-08-08 | Consiglio Nazionale Ricerche | Transistori a film sottile organico composti e procedimenti per la loro realizzazione e loro uso come sensori in fase gassosa |
| KR101430261B1 (ko) * | 2007-02-23 | 2014-08-14 | 삼성전자주식회사 | 유기 실리콘 나노클러스터, 이의 제조방법, 이를 이용한박막형성 방법 |
| DE102007009790A1 (de) | 2007-02-27 | 2008-08-28 | Bayer Technology Services Gmbh | Hybride organische Solarzellen mit von photoaktiven Oberflächenmodifikatoren umgebenen Halbleiter-Nanopartikeln |
| US20100155749A1 (en) * | 2007-03-19 | 2010-06-24 | Nanosys, Inc. | Light-emitting diode (led) devices comprising nanocrystals |
| US20100110728A1 (en) | 2007-03-19 | 2010-05-06 | Nanosys, Inc. | Light-emitting diode (led) devices comprising nanocrystals |
| CN101641424B (zh) * | 2007-03-19 | 2013-12-04 | 纳米系统公司 | 用于包封纳米晶体的方法 |
| US8563348B2 (en) * | 2007-04-18 | 2013-10-22 | Nanoco Technologies Ltd. | Fabrication of electrically active films based on multiple layers |
| US20100044676A1 (en) * | 2008-04-18 | 2010-02-25 | Invisage Technologies, Inc. | Photodetectors and Photovoltaics Based on Semiconductor Nanocrystals |
| EP2432015A1 (en) | 2007-04-18 | 2012-03-21 | Invisage Technologies, Inc. | Materials, systems and methods for optoelectronic devices |
| US8525287B2 (en) | 2007-04-18 | 2013-09-03 | Invisage Technologies, Inc. | Materials, systems and methods for optoelectronic devices |
| US20080264479A1 (en) | 2007-04-25 | 2008-10-30 | Nanoco Technologies Limited | Hybrid Photovoltaic Cells and Related Methods |
| EP2171763A2 (en) * | 2007-06-26 | 2010-04-07 | Solarity, Inc. | Lateral collection photovoltaics |
| US8784701B2 (en) | 2007-11-30 | 2014-07-22 | Nanoco Technologies Ltd. | Preparation of nanoparticle material |
| KR101735575B1 (ko) * | 2008-02-25 | 2017-05-15 | 나노코 테크놀로지스 리미티드 | 반도체 나노입자 캐핑물질 |
| CN103872002B (zh) | 2008-03-05 | 2017-03-01 | 伊利诺伊大学评议会 | 可拉伸和可折叠的电子器件 |
| JP5285062B2 (ja) * | 2008-03-19 | 2013-09-11 | シャープ株式会社 | 光増感素子及びそれを用いた太陽電池 |
| US8470701B2 (en) | 2008-04-03 | 2013-06-25 | Advanced Diamond Technologies, Inc. | Printable, flexible and stretchable diamond for thermal management |
| US8203195B2 (en) | 2008-04-18 | 2012-06-19 | Invisage Technologies, Inc. | Materials, fabrication equipment, and methods for stable, sensitive photodetectors and image sensors made therefrom |
| WO2009129540A1 (en) * | 2008-04-18 | 2009-10-22 | Invisage Technologies, Inc. | Photodetectors and photovoltaics based on semiconductor nanocrystals |
| WO2010005707A1 (en) | 2008-06-16 | 2010-01-14 | The Board Of Trustees Of The University Of Illinois | Medium scale carbon nanotube thin film integrated circuits on flexible plastic substrates |
| GB0813273D0 (en) * | 2008-07-19 | 2008-08-27 | Nanoco Technologies Ltd | Method for producing aqueous compatible nanoparticles |
| DE102008035559A1 (de) | 2008-07-30 | 2010-02-11 | Rupert Goihl | Elektrolumineszenz oder Photovoltaikquelle |
| GB0814458D0 (en) * | 2008-08-07 | 2008-09-10 | Nanoco Technologies Ltd | Surface functionalised nanoparticles |
| US8389862B2 (en) | 2008-10-07 | 2013-03-05 | Mc10, Inc. | Extremely stretchable electronics |
| US8886334B2 (en) | 2008-10-07 | 2014-11-11 | Mc10, Inc. | Systems, methods, and devices using stretchable or flexible electronics for medical applications |
| US8097926B2 (en) | 2008-10-07 | 2012-01-17 | Mc10, Inc. | Systems, methods, and devices having stretchable integrated circuitry for sensing and delivering therapy |
| US8372726B2 (en) | 2008-10-07 | 2013-02-12 | Mc10, Inc. | Methods and applications of non-planar imaging arrays |
| WO2010042653A1 (en) | 2008-10-07 | 2010-04-15 | Mc10, Inc. | Catheter balloon having stretchable integrated circuitry and sensor array |
| US9006133B2 (en) | 2008-10-24 | 2015-04-14 | Oned Material Llc | Electrochemical catalysts for fuel cells |
| GB0820101D0 (en) * | 2008-11-04 | 2008-12-10 | Nanoco Technologies Ltd | Surface functionalised nanoparticles |
| US8540889B1 (en) | 2008-11-19 | 2013-09-24 | Nanosys, Inc. | Methods of generating liquidphobic surfaces |
| GB0821122D0 (en) * | 2008-11-19 | 2008-12-24 | Nanoco Technologies Ltd | Semiconductor nanoparticle - based light emitting devices and associated materials and methods |
| US8343575B2 (en) | 2008-12-30 | 2013-01-01 | Nanosys, Inc. | Methods for encapsulating nanocrystals and resulting compositions |
| US10214686B2 (en) | 2008-12-30 | 2019-02-26 | Nanosys, Inc. | Methods for encapsulating nanocrystals and resulting compositions |
| US11198270B2 (en) | 2008-12-30 | 2021-12-14 | Nanosys, Inc. | Quantum dot films, lighting devices, and lighting methods |
| WO2010087842A1 (en) * | 2009-01-30 | 2010-08-05 | Hewlett-Packard Development Company | Polymer and polymer-nanoparticle compositions |
| JP2009182333A (ja) * | 2009-02-05 | 2009-08-13 | Sony Corp | 電子デバイス及びその製造方法 |
| GB0901857D0 (en) * | 2009-02-05 | 2009-03-11 | Nanoco Technologies Ltd | Encapsulated nanoparticles |
| CN104387772B (zh) | 2009-05-01 | 2017-07-11 | 纳米系统公司 | 用于纳米结构体分散的官能化基质 |
| JP5686988B2 (ja) * | 2009-05-04 | 2015-03-18 | シャープ株式会社 | 燃料電池用膜電極複合体に用いられる触媒層、それを用いる燃料電池用膜電極複合体、燃料電池、およびその製造方法 |
| TWI592996B (zh) | 2009-05-12 | 2017-07-21 | 美國伊利諾大學理事會 | 用於可變形及半透明顯示器之超薄微刻度無機發光二極體之印刷總成 |
| KR102067922B1 (ko) | 2009-05-19 | 2020-01-17 | 원드 매터리얼 엘엘씨 | 배터리 응용을 위한 나노구조화된 재료 |
| GB0916700D0 (en) * | 2009-09-23 | 2009-11-04 | Nanoco Technologies Ltd | Semiconductor nanoparticle-based materials |
| GB0916699D0 (en) * | 2009-09-23 | 2009-11-04 | Nanoco Technologies Ltd | Semiconductor nanoparticle-based materials |
| US9723122B2 (en) | 2009-10-01 | 2017-08-01 | Mc10, Inc. | Protective cases with integrated electronics |
| US9936574B2 (en) | 2009-12-16 | 2018-04-03 | The Board Of Trustees Of The University Of Illinois | Waterproof stretchable optoelectronics |
| US10918298B2 (en) | 2009-12-16 | 2021-02-16 | The Board Of Trustees Of The University Of Illinois | High-speed, high-resolution electrophysiology in-vivo using conformal electronics |
| US10441185B2 (en) | 2009-12-16 | 2019-10-15 | The Board Of Trustees Of The University Of Illinois | Flexible and stretchable electronic systems for epidermal electronics |
| US20110232717A1 (en) * | 2010-02-18 | 2011-09-29 | OneSun, LLC | Semiconductors compositions for dye-sensitized solar cells |
| KR101257152B1 (ko) * | 2010-03-16 | 2013-04-23 | 엘에스전선 주식회사 | 반도전성 조성물 및 이를 이용한 전력 케이블 |
| CN104224171B (zh) | 2010-03-17 | 2017-06-09 | 伊利诺伊大学评议会 | 基于生物可吸收基质的可植入生物医学装置 |
| GB201005601D0 (en) | 2010-04-01 | 2010-05-19 | Nanoco Technologies Ltd | Ecapsulated nanoparticles |
| US8916947B2 (en) | 2010-06-08 | 2014-12-23 | Invisage Technologies, Inc. | Photodetector comprising a pinned photodiode that is formed by an optically sensitive layer and a silicon diode |
| US8519444B2 (en) | 2010-09-10 | 2013-08-27 | Taiwan Semiconductor Manufacturing Company, Ltd. | Modified design rules to improve device performance |
| GB2484743B (en) * | 2010-10-23 | 2014-10-15 | Univ Montfort | Organic photoconductive material |
| KR102098682B1 (ko) | 2010-11-10 | 2020-05-22 | 나노시스, 인크. | 양자 도트 필름들, 조명 디바이스들, 및 조명 방법들 |
| US9442285B2 (en) | 2011-01-14 | 2016-09-13 | The Board Of Trustees Of The University Of Illinois | Optical component array having adjustable curvature |
| US9765934B2 (en) | 2011-05-16 | 2017-09-19 | The Board Of Trustees Of The University Of Illinois | Thermally managed LED arrays assembled by printing |
| WO2012158832A2 (en) | 2011-05-16 | 2012-11-22 | Qd Vision, Inc. | Method for preparing semiconductor nanocrystals |
| WO2012166686A2 (en) | 2011-05-27 | 2012-12-06 | Mc10, Inc. | Electronic, optical and/or mechanical apparatus and systems and methods for fabricating same |
| EP2713863B1 (en) | 2011-06-03 | 2020-01-15 | The Board of Trustees of the University of Illionis | Conformable actively multiplexed high-density surface electrode array for brain interfacing |
| WO2013028253A1 (en) | 2011-08-19 | 2013-02-28 | Qd Vision, Inc. | Semiconductor nanocrystals and methods |
| JP5888976B2 (ja) * | 2011-09-28 | 2016-03-22 | 富士フイルム株式会社 | 導電性組成物、導電性部材およびその製造方法、タッチパネル並びに太陽電池 |
| WO2013078249A1 (en) | 2011-11-22 | 2013-05-30 | Qd Vision Inc. | Method of making quantum dots |
| US10008631B2 (en) | 2011-11-22 | 2018-06-26 | Samsung Electronics Co., Ltd. | Coated semiconductor nanocrystals and products including same |
| WO2013078245A1 (en) | 2011-11-22 | 2013-05-30 | Qd Vision, Inc. | Method of making quantum dots |
| WO2013078242A1 (en) | 2011-11-22 | 2013-05-30 | Qd Vision, Inc. | Methods for coating semiconductor nanocrystals |
| WO2013078247A1 (en) | 2011-11-22 | 2013-05-30 | Qd Vision, Inc. | Methods of coating semiconductor nanocrystals, semiconductor nanocrystals, and products including same |
| JP6231489B2 (ja) | 2011-12-01 | 2017-11-15 | ザ ボード オブ トラスティーズ オブ ザ ユニヴァーシティー オブ イリノイ | プログラム可能な変化を被るように設計された遷移デバイス |
| CN104205368B (zh) | 2012-02-05 | 2018-08-07 | 三星电子株式会社 | 半导体纳米晶体、其制备方法、组合物、以及产品 |
| WO2013149181A1 (en) | 2012-03-30 | 2013-10-03 | The Board Of Trustees Of The University Of Illinois | Appendage mountable electronic devices conformable to surfaces |
| WO2013151142A1 (ja) * | 2012-04-05 | 2013-10-10 | コニカミノルタ株式会社 | 有機光電変換素子およびこれを用いた太陽電池 |
| US9139770B2 (en) | 2012-06-22 | 2015-09-22 | Nanosys, Inc. | Silicone ligands for stabilizing quantum dot films |
| TWI596188B (zh) | 2012-07-02 | 2017-08-21 | 奈米系統股份有限公司 | 高度發光奈米結構及其製造方法 |
| US9171794B2 (en) | 2012-10-09 | 2015-10-27 | Mc10, Inc. | Embedding thin chips in polymer |
| WO2014079532A1 (de) * | 2012-11-20 | 2014-05-30 | Merck Patent Gmbh | Formulierung in hochreinem l?sungsmittel zur herstellung elektronischer vorrichtungen |
| CA2905883C (en) | 2013-03-14 | 2021-09-14 | William P. Freeman | Alkyl-acid ligands for nanocrystals |
| JP6250785B2 (ja) | 2013-03-14 | 2017-12-20 | ナノシス・インク． | 無溶媒量子ドット交換方法 |
| CA2905913C (en) | 2013-03-14 | 2021-07-13 | Nanosys, Inc. | Polyhedral oligomeric silsesquioxane nanocrystal stabilization ligands |
| US9617472B2 (en) | 2013-03-15 | 2017-04-11 | Samsung Electronics Co., Ltd. | Semiconductor nanocrystals, a method for coating semiconductor nanocrystals, and products including same |
| CN105765428A (zh) | 2013-10-17 | 2016-07-13 | 纳米系统公司 | 发光二极管(led)器件 |
| WO2015069640A1 (en) | 2013-11-05 | 2015-05-14 | Nanosys, Inc. | Backlight unit for display devices adapted to reduce light leakage |
| CN106103645B (zh) | 2014-03-10 | 2019-05-28 | 3M创新有限公司 | 包括硫醇取代的有机硅的复合纳米粒子 |
| CN106164219B (zh) | 2014-04-02 | 2019-03-01 | 3M创新有限公司 | 包含硫醚配体的复合纳米粒子 |
| KR20230048161A (ko) | 2014-07-16 | 2023-04-10 | 나노시스, 인크. | 양자점용 실리콘 리간드 |
| KR101798755B1 (ko) | 2015-03-12 | 2017-11-16 | 주식회사 엘지화학 | 광학 필름용 조성물 및 이를 포함하는 광학 필름 |
| US10984735B2 (en) | 2015-04-17 | 2021-04-20 | Nanosys, Inc. | White point uniformity in display devices |
| MX2017015586A (es) | 2015-06-01 | 2018-08-23 | Univ Illinois | Sistemas electronicos miniaturizados con capacidades de energia inalambrica y comunicacion de campo cercano. |
| BR112017025616A2 (pt) | 2015-06-01 | 2018-08-07 | Univ Illinois | abordagem alternativa à captação de uv |
| WO2017030857A1 (en) | 2015-08-19 | 2017-02-23 | 3M Innovative Properties Company | Perfluoroether-stabilized quantum dots |
| KR20180052679A (ko) | 2015-09-09 | 2018-05-18 | 나노시스, 인크. | 청색 방출을 갖는 고 발광 무카드뮴 나노결정 |
| EP3350284B1 (en) | 2015-09-15 | 2019-02-27 | 3M Innovative Properties Company | Additive stabilized composite nanoparticles |
| EP3350285A1 (en) | 2015-09-15 | 2018-07-25 | 3M Innovative Properties Company | Additive stabilized composite nanoparticles |
| US10925543B2 (en) | 2015-11-11 | 2021-02-23 | The Board Of Trustees Of The University Of Illinois | Bioresorbable silicon electronics for transient implants |
| EP3377591A1 (en) | 2015-11-18 | 2018-09-26 | 3M Innovative Properties Company | Copolymeric stabilizing carrier fluid for nanoparticles |
| US9658489B1 (en) | 2015-12-31 | 2017-05-23 | Nanosys, Inc. | Backlight units for display devices |
| WO2017127302A1 (en) | 2016-01-19 | 2017-07-27 | Nanosys, Inc. | Inp quantum dots with gap and alp shells and method of producing the same |
| WO2017142781A1 (en) | 2016-02-17 | 2017-08-24 | 3M Innovative Properties Company | Matrix for quantum dot film article |
| CN108699433B (zh) | 2016-02-17 | 2020-08-14 | 3M创新有限公司 | 具有稳定含氟化合物共聚物的量子点 |
| US20170250322A1 (en) | 2016-02-26 | 2017-08-31 | Nanosys, Inc. | Low Cadmium Content Nanostructure Compositions and Uses Thereof |
| KR20180128956A (ko) | 2016-04-01 | 2018-12-04 | 쓰리엠 이노베이티브 프로퍼티즈 컴파니 | 플루오로케미칼 안정화제를 갖는 양자점 |
| US20170306227A1 (en) | 2016-04-26 | 2017-10-26 | Nanosys, Inc. | Stable inp quantum dots with thick shell coating and method of producing the same |
| EP3242333B1 (en) * | 2016-05-03 | 2020-09-09 | Nokia Technologies Oy | An apparatus and method of forming an apparatus comprising a graphene field effect transistor |
| JP7062600B2 (ja) | 2016-05-19 | 2022-05-06 | ナノシス・インク． | 高輝度ナノ構造体のためのコア／シェル量子ドット形態の改良法 |
| WO2017200824A1 (en) | 2016-05-20 | 2017-11-23 | 3M Innovative Properties Company | Quantum dots with mixed amine and thiol ligands |
| WO2017214107A1 (en) | 2016-06-06 | 2017-12-14 | Nanosys, Inc. | Method for synthesizing core shell nanocrystals at high temperatures |
| KR20190031505A (ko) | 2016-07-20 | 2019-03-26 | 쓰리엠 이노베이티브 프로퍼티즈 컴파니 | 양자점을 위한 안정화 스티렌계 중합체 |
| WO2018017514A1 (en) | 2016-07-20 | 2018-01-25 | 3M Innovative Properties Company | Stabilizing styrenic polymer for quantum dots |
| CN109790454A (zh) | 2016-09-19 | 2019-05-21 | 3M创新有限公司 | 用官能氨基有机硅稳定的荧光纳米粒子 |
| US11320577B2 (en) | 2016-10-31 | 2022-05-03 | Nanosys, Inc. | Radiation absorbing element for increasing color gamut of quantum dot based display devices |
| US10782014B2 (en) | 2016-11-11 | 2020-09-22 | Habib Technologies LLC | Plasmonic energy conversion device for vapor generation |
| US20180223182A1 (en) | 2017-01-31 | 2018-08-09 | Nanosys, Inc. | Rapid thickening of aminosilicones to promote emulsion stability and adhesion of uv-curable quantum dot enhancement film emulsions |
| WO2018167645A1 (en) | 2017-03-14 | 2018-09-20 | 3M Innovative Properties Company | Additive stabilized composite nanoparticles |
| WO2018208807A1 (en) | 2017-05-10 | 2018-11-15 | Nanosys, Inc. | Silicone copolymers as emulsification additives for quantum dot resin premix |
| US11407937B2 (en) | 2017-05-10 | 2022-08-09 | Nanosys, Inc. | In-situ cross-linking of emulsified quantum dot-containing domains within a carrier resin |
| WO2018226654A1 (en) | 2017-06-05 | 2018-12-13 | Austin Smith | Acid stabilization of quantum dot-resin concentrates and premixes |
| WO2018226925A1 (en) | 2017-06-07 | 2018-12-13 | Nanosys, Inc. | Thiolated hydrophilic ligands for improved quantum dot reliability in resin films |
| US10919770B2 (en) | 2017-06-23 | 2021-02-16 | Nanosys, Inc. | Homogeneous anaerobically stable quantum dot concentrates |
| CN110799623B (zh) * | 2017-06-29 | 2023-06-27 | 默克专利股份有限公司 | 包含半导体发光纳米颗粒的组合物 |
| BR112020001032A2 (pt) | 2017-07-16 | 2020-07-14 | Massachusetts Institute Of Technology | estrutura de matriz de microagulhas e método para fornecer identificação e/ou tatuagem e/ou distribuição de um agente terapêutico, profilático ou de diagnóstico |
| WO2019035957A1 (en) | 2017-08-16 | 2019-02-21 | Nanosys, Inc. | PEG-BASED LIGANDS HAVING IMPROVED DISPERSION CAPABILITY AND IMPROVED PERFORMANCE |
| US11092850B2 (en) | 2017-08-25 | 2021-08-17 | Nanosys, Inc. | Using multiple excitation wavelengths in nanostructure based display devices |
| US10935842B2 (en) | 2017-08-25 | 2021-03-02 | Nanosys, Inc. | Nanostructure based display devices |
| US11029559B2 (en) | 2017-08-25 | 2021-06-08 | Nanosys, Inc. | Nanostructure based display devices |
| WO2019072938A1 (en) | 2017-10-10 | 2019-04-18 | Katholieke Universiteit Leuven | PLATE-GUIDE LIGHT |
| KR20200074197A (ko) | 2017-10-25 | 2020-06-24 | 나노시스, 인크. | 두꺼운 쉘 코팅을 갖는 안정적인 InP 양자 도트들 및 그것을 제조하는 방법 |
| TWI778156B (zh) | 2017-10-27 | 2022-09-21 | 美商納諾西斯有限公司 | 應用多官能配位體改善量子點墨水的性能及穩定性 |
| US20190273178A1 (en) | 2018-03-05 | 2019-09-05 | Nanosys, Inc. | Decreased Photon Reabsorption in Emissive Quantum Dots |
| EP3844240B1 (en) | 2018-05-30 | 2024-02-14 | Shoei Chemical Inc. | Method for synthesis of blue-emitting znse1-xtex alloy nanocrystals |
| US11434423B2 (en) | 2018-06-29 | 2022-09-06 | Nanosys, Inc. | Wavelength tuning of ZnSe quantum dots using In3+ salts as dopants |
| CN110780486A (zh) | 2018-07-24 | 2020-02-11 | 纳米系统公司 | 使用具有集成光学元件的量子点改善显示效率的方法 |
| WO2020040982A1 (en) | 2018-08-21 | 2020-02-27 | Nanosys, Inc. | Quantum dots with charge-transporting ligands |
| US11428988B2 (en) | 2018-08-31 | 2022-08-30 | Nanosys, Inc. | Increasing color gamut performance and efficiency in quantum dot color conversion layers |
| EP3898885B1 (en) | 2019-01-24 | 2023-12-27 | Shoei Chemical Inc. | Small molecule passivation of quantum dots for increased quantum yield |
| CN113330095A (zh) | 2019-01-24 | 2021-08-31 | 纳米系统公司 | 用于增强蓝光吸收的薄壳量子点 |
| TWI827791B (zh) | 2019-02-05 | 2024-01-01 | 日商昭榮化學工業股份有限公司 | 以熔融鹽化學合成無機奈米結構之方法、奈米結構及包含該奈米結構之顯示裝置 |
| CN113710773A (zh) | 2019-04-15 | 2021-11-26 | 纳米系统公司 | 提高磷化铟量子点量子产率的方法 |
| WO2020214930A1 (en) | 2019-04-19 | 2020-10-22 | Nanosys, Inc. | Flexible electroluminescent devices |
| JP2022531290A (ja) | 2019-05-08 | 2022-07-06 | ナノシス・インク． | 光抽出効率を向上させたナノ構造ベースの表示装置 |
| US10927294B2 (en) | 2019-06-20 | 2021-02-23 | Nanosys, Inc. | Bright silver based quaternary nanostructures |
| KR20220035152A (ko) | 2019-07-11 | 2022-03-21 | 나노시스, 인크. | 입방체 형상 및 플루오라이드 패시베이션을 갖는 청색 발광 나노결정들 |
| CN114867818A (zh) | 2019-08-12 | 2022-08-05 | 纳米系统公司 | 具有低半峰全宽的蓝光发射ZnSe1-xTex合金纳米晶体的合成 |
| JP2022547849A (ja) | 2019-09-11 | 2022-11-16 | ナノシス・インク． | インクジェット印刷のためのナノ構造インク組成物 |
| WO2021141945A1 (en) | 2020-01-06 | 2021-07-15 | Nanosys, Inc. | Rohs compliant mixed quantum dot films |
| EP4073203A2 (en) | 2020-01-08 | 2022-10-19 | Nanosys, Inc. | Quantum dots with donor-acceptor ligands |
| KR20210149950A (ko) * | 2020-06-02 | 2021-12-10 | 삼성디스플레이 주식회사 | 양자점 조성물, 발광 소자 및 이의 제조 방법 |
| KR20230036133A (ko) | 2020-07-08 | 2023-03-14 | 나노시스, 인크. | 박형 금속 산화물 코팅들을 포함하는 qd들을 갖는 디바이스들의 성능을 개선하는 방법 |
| EP4217439A1 (en) | 2020-09-28 | 2023-08-02 | Nanosys, Inc. | Thermally stable polythiol ligands with pendant solubilizing moieties |
| JP2023551766A (ja) | 2020-10-22 | 2023-12-13 | ナノシス・インク． | ハイブリッド輸送層を有する電界発光デバイス |
| TW202230848A (zh) | 2020-10-22 | 2022-08-01 | 美商納諾西斯有限公司 | 具有有機傳輸層的電致發光裝置 |
| KR20230136124A (ko) | 2020-12-22 | 2023-09-26 | 나노시스, 인크. | 밝은 은 기반 4원 나노구조를 포함하는 필름 |
| WO2022212517A1 (en) | 2021-04-01 | 2022-10-06 | Nanosys, Inc. | Stable aigs films |
| WO2023287886A1 (en) | 2021-07-13 | 2023-01-19 | Nanosys, Inc. | Tunable illumination device |
| US20230229087A1 (en) | 2022-01-19 | 2023-07-20 | Nanosys, Inc. | Uv-curable quantum dot formulations |
| WO2023157814A1 (ja) * | 2022-02-17 | 2023-08-24 | 日産化学株式会社 | フェニルホスホン酸エステルおよびフェニルホスホン酸化合物の製造方法 |
| WO2023183619A1 (en) | 2022-03-25 | 2023-09-28 | Nanosys, Inc. | Silica composite microparticles comprising nanostructures |
| WO2023220050A1 (en) | 2022-05-09 | 2023-11-16 | Nanosys, Inc. | Microled-based display device and method of manufacturing same |
Family Cites Families (48)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2002A (en) * | 1841-03-12 | Tor and planter for plowing | ||
| US2004A (en) * | 1841-03-12 | Improvement in the manner of constructing and propelling steam-vessels | ||
| JP2584288B2 (ja) * | 1988-08-31 | 1997-02-26 | 富士写真フイルム株式会社 | 電子写真感光体 |
| US5225495A (en) * | 1991-07-10 | 1993-07-06 | Richard C. Stewart, II | Conductive polymer film formation using initiator pretreatment |
| JPH07502479A (ja) | 1991-11-22 | 1995-03-16 | ザ リージェンツ オブ ザ ユニバーシティ オブ カリフォルニア | 自己集合性単一層を使って固体無機表面に共有結合した半導体微少結晶 |
| US5505928A (en) | 1991-11-22 | 1996-04-09 | The Regents Of University Of California | Preparation of III-V semiconductor nanocrystals |
| US6320200B1 (en) * | 1992-06-01 | 2001-11-20 | Yale University | Sub-nanoscale electronic devices and processes |
| US5434288A (en) * | 1992-12-01 | 1995-07-18 | Monsanto Company | PLA2 inhibitors |
| US6048616A (en) | 1993-04-21 | 2000-04-11 | Philips Electronics N.A. Corp. | Encapsulated quantum sized doped semiconductor particles and method of manufacturing same |
| US5504323A (en) | 1993-12-07 | 1996-04-02 | The Regents Of The University Of California | Dual function conducting polymer diodes |
| DE69416428T2 (de) | 1993-12-29 | 1999-09-16 | Ecole Polytech | Photoelektrochemische zelle und elektrolyt für diese zelle |
| US5690807A (en) | 1995-08-03 | 1997-11-25 | Massachusetts Institute Of Technology | Method for producing semiconductor particles |
| US6649129B1 (en) | 1995-11-13 | 2003-11-18 | Teledyne Tekmar Company | Method and apparatus for concentrating a VOC sample |
| US6036774A (en) | 1996-02-26 | 2000-03-14 | President And Fellows Of Harvard College | Method of producing metal oxide nanorods |
| US5897945A (en) | 1996-02-26 | 1999-04-27 | President And Fellows Of Harvard College | Metal oxide nanorods |
| EP0792688A1 (en) | 1996-03-01 | 1997-09-03 | Dow Corning Corporation | Nanoparticles of silicon oxide alloys |
| US6721083B2 (en) * | 1996-07-19 | 2004-04-13 | E Ink Corporation | Electrophoretic displays using nanoparticles |
| JP3504079B2 (ja) * | 1996-08-31 | 2004-03-08 | 株式会社東芝 | 半導体発光ダイオード素子の製造方法 |
| JP4049839B2 (ja) * | 1996-11-08 | 2008-02-20 | 昭和電工株式会社 | 帯電防止処理材の製造方法 |
| US5997832A (en) | 1997-03-07 | 1999-12-07 | President And Fellows Of Harvard College | Preparation of carbide nanorods |
| US6413489B1 (en) | 1997-04-15 | 2002-07-02 | Massachusetts Institute Of Technology | Synthesis of nanometer-sized particles by reverse micelle mediated techniques |
| EP0983282B1 (en) | 1997-05-07 | 2003-11-12 | Ecole Polytechnique Federale De Lausanne | Metal complex photosensitizer and photovoltaic cell |
| EP0917208A1 (en) | 1997-11-11 | 1999-05-19 | Universiteit van Utrecht | Polymer-nanocrystal photo device and method for making the same |
| US6322901B1 (en) | 1997-11-13 | 2001-11-27 | Massachusetts Institute Of Technology | Highly luminescent color-selective nano-crystalline materials |
| US5990479A (en) | 1997-11-25 | 1999-11-23 | Regents Of The University Of California | Organo Luminescent semiconductor nanocrystal probes for biological applications and process for making and using such probes |
| GB9815271D0 (en) * | 1998-07-14 | 1998-09-09 | Cambridge Display Tech Ltd | Particles and devices comprising particles |
| US6251303B1 (en) | 1998-09-18 | 2001-06-26 | Massachusetts Institute Of Technology | Water-soluble fluorescent nanocrystals |
| AU1311900A (en) | 1998-10-09 | 2000-05-01 | Trustees Of Columbia University In The City Of New York, The | Solid-state photoelectric device |
| US6244988B1 (en) * | 1999-06-28 | 2001-06-12 | David H. Delman | Interactive exercise system and attachment module for same |
| JP2001085713A (ja) * | 1999-09-14 | 2001-03-30 | Fuji Photo Film Co Ltd | 光電変換素子および太陽電池 |
| US6225198B1 (en) | 2000-02-04 | 2001-05-01 | The Regents Of The University Of California | Process for forming shaped group II-VI semiconductor nanocrystals, and product formed using process |
| US6306736B1 (en) | 2000-02-04 | 2001-10-23 | The Regents Of The University Of California | Process for forming shaped group III-V semiconductor nanocrystals, and product formed using process |
| US6399224B1 (en) | 2000-02-29 | 2002-06-04 | Canon Kabushiki Kaisha | Conjugated polymers with tunable charge injection ability |
| KR100360308B1 (ko) * | 2000-07-03 | 2002-11-18 | 한국화학연구원 | 아세틸렌기를 포함하는 유기화합물, 그 화합물을 이용한증착중합법, 그 방법에 의하여 제조된 증착중합 박막 및그 박막을 사용한 전기 발광소자 |
| US20020010645A1 (en) * | 2000-07-12 | 2002-01-24 | David Hagen | Backend commerce engine |
| JP2002050779A (ja) * | 2000-08-03 | 2002-02-15 | Fuji Photo Film Co Ltd | 光電変換素子、それを用いた光電池およびその製造方法 |
| EP2360298A3 (en) | 2000-08-22 | 2011-10-05 | President and Fellows of Harvard College | Method for depositing a semiconductor nanowire |
| US6649138B2 (en) * | 2000-10-13 | 2003-11-18 | Quantum Dot Corporation | Surface-modified semiconductive and metallic nanoparticles having enhanced dispersibility in aqueous media |
| WO2002035580A2 (en) | 2000-10-24 | 2002-05-02 | Molecular Electronics Corporation | Three-terminal field-controlled molecular devices |
| US6899829B2 (en) * | 2000-11-30 | 2005-05-31 | Shipley Company, L.L.C. | Conductive polymer colloidal compositions with selectivity for non-conductive surfaces |
| EP1215205B1 (en) * | 2000-12-08 | 2007-11-21 | Sony Deutschland GmbH | Tuned multifunctional linker molecules for electronic charge transport through organic-inorganic composite structures and use thereof |
| KR101008294B1 (ko) | 2001-03-30 | 2011-01-13 | 더 리전트 오브 더 유니버시티 오브 캘리포니아 | 나노구조체 및 나노와이어의 제조 방법 및 그로부터 제조되는 디바이스 |
| TWI245795B (en) * | 2001-08-17 | 2005-12-21 | Merck Patent Gmbh | Mono-, oligo- and polyalkylidenefluorenes and their use as charge transport materials |
| US7777303B2 (en) * | 2002-03-19 | 2010-08-17 | The Regents Of The University Of California | Semiconductor-nanocrystal/conjugated polymer thin films |
| US20040026684A1 (en) | 2002-04-02 | 2004-02-12 | Nanosys, Inc. | Nanowire heterostructures for encoding information |
| US7081210B2 (en) * | 2002-04-22 | 2006-07-25 | Konica Minolta Holdings, Inc. | Organic semiconductor composition |
| WO2004022637A2 (en) | 2002-09-05 | 2004-03-18 | Nanosys, Inc. | Nanocomposites |
| JP2005538573A (ja) | 2002-09-05 | 2005-12-15 | ナノシス・インク． | ナノ構造及びナノ複合材をベースとする組成物 |
-
2003
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- 2003-09-04 US US10/656,910 patent/US6949206B2/en not_active Expired - Lifetime
- 2003-09-04 WO PCT/US2003/027847 patent/WO2004022714A2/en active Search and Examination
- 2003-09-04 KR KR1020057003694A patent/KR101032672B1/ko active IP Right Grant
- 2003-09-04 CA CA002497451A patent/CA2497451A1/en not_active Abandoned
- 2003-09-04 AU AU2003272275A patent/AU2003272275A1/en not_active Abandoned
- 2003-09-04 EP EP03754451A patent/EP1537187B1/en not_active Expired - Lifetime
- 2003-09-04 TW TW092124460A patent/TW200422374A/zh unknown
-
2005
- 2005-05-16 US US11/130,296 patent/US7572395B2/en active Active
- 2005-05-16 US US11/130,303 patent/US7438833B2/en active Active
-
2008
- 2008-09-09 US US12/206,935 patent/US7943064B2/en not_active Expired - Lifetime
-
2009
- 2009-12-18 JP JP2009288058A patent/JP5306163B2/ja not_active Expired - Fee Related
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| AU2003272275A1 (en) | 2004-03-29 |
| JP2010150546A (ja) | 2010-07-08 |
| JP5306163B2 (ja) | 2013-10-02 |
| TW200422374A (en) | 2004-11-01 |
| EP1537187B1 (en) | 2012-08-15 |
| WO2004022714A3 (en) | 2005-04-14 |
| KR101032672B1 (ko) | 2011-05-06 |
| US20050205849A1 (en) | 2005-09-22 |
| US20040178390A1 (en) | 2004-09-16 |
| US20090050854A1 (en) | 2009-02-26 |
| US7572395B2 (en) | 2009-08-11 |
| EP1537187A4 (en) | 2008-03-05 |
| EP1537187A2 (en) | 2005-06-08 |
| US6949206B2 (en) | 2005-09-27 |
| AU2003272275A8 (en) | 2004-03-29 |
| KR20050062771A (ko) | 2005-06-27 |
| WO2004022714A2 (en) | 2004-03-18 |
| US7943064B2 (en) | 2011-05-17 |
| US7438833B2 (en) | 2008-10-21 |
| US20050205850A1 (en) | 2005-09-22 |
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