CA2905913C - Polyhedral oligomeric silsesquioxane nanocrystal stabilization ligands - Google Patents
Polyhedral oligomeric silsesquioxane nanocrystal stabilization ligands Download PDFInfo
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- CA2905913C CA2905913C CA2905913A CA2905913A CA2905913C CA 2905913 C CA2905913 C CA 2905913C CA 2905913 A CA2905913 A CA 2905913A CA 2905913 A CA2905913 A CA 2905913A CA 2905913 C CA2905913 C CA 2905913C
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- 239000003446 ligand Substances 0.000 title claims abstract description 70
- 239000002159 nanocrystal Substances 0.000 title description 33
- 230000006641 stabilisation Effects 0.000 title description 2
- 238000011105 stabilization Methods 0.000 title description 2
- 239000002096 quantum dot Substances 0.000 claims abstract description 110
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims abstract description 20
- 239000000203 mixture Substances 0.000 claims abstract description 12
- -1 isooctyl Chemical group 0.000 claims description 70
- 125000000217 alkyl group Chemical group 0.000 claims description 52
- 125000003118 aryl group Chemical group 0.000 claims description 23
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 22
- 125000002947 alkylene group Chemical group 0.000 claims description 20
- 125000003342 alkenyl group Chemical group 0.000 claims description 17
- 125000000304 alkynyl group Chemical group 0.000 claims description 16
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 13
- 229910052739 hydrogen Inorganic materials 0.000 claims description 12
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 12
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 11
- 229910052710 silicon Inorganic materials 0.000 claims description 9
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Chemical group CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 claims description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 7
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 5
- 125000001624 naphthyl group Chemical group 0.000 claims description 5
- 125000000640 cyclooctyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 claims description 4
- 125000005073 adamantyl group Chemical group C12(CC3CC(CC(C1)C3)C2)* 0.000 claims description 2
- 125000002178 anthracenyl group Chemical group C1(=CC=CC2=CC3=CC=CC=C3C=C12)* 0.000 claims description 2
- 125000001204 arachidyl 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])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])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- 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 2
- 125000003438 dodecyl 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])C([H])([H])C([H])([H])* 0.000 claims description 2
- 125000002960 margaryl 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])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])[H] 0.000 claims description 2
- 125000001421 myristyl 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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 125000001196 nonadecyl 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])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])C([H])([H])[H] 0.000 claims description 2
- 125000001400 nonyl 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])C([H])([H])[H] 0.000 claims description 2
- 125000002868 norbornyl group Chemical group C12(CCC(CC1)C2)* 0.000 claims description 2
- 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 2
- 125000000913 palmityl 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])C([H])([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 2
- 125000002958 pentadecyl 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])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 2
- 125000004079 stearyl 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])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])[H] 0.000 claims description 2
- 125000002889 tridecyl 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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 125000002948 undecyl 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])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims 1
- 239000002086 nanomaterial Substances 0.000 abstract description 21
- 150000001412 amines Chemical class 0.000 abstract description 13
- 230000002829 reductive effect Effects 0.000 abstract description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 66
- 238000006243 chemical reaction Methods 0.000 description 54
- 239000000243 solution Substances 0.000 description 51
- 238000004458 analytical method Methods 0.000 description 29
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 27
- 239000000463 material Substances 0.000 description 27
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 26
- 239000011159 matrix material Substances 0.000 description 22
- 239000003039 volatile agent Substances 0.000 description 21
- 239000003054 catalyst Substances 0.000 description 20
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 18
- UHYPYGJEEGLRJD-UHFFFAOYSA-N cadmium(2+);selenium(2-) Chemical compound [Se-2].[Cd+2] UHYPYGJEEGLRJD-UHFFFAOYSA-N 0.000 description 17
- 239000000047 product Substances 0.000 description 17
- 230000015572 biosynthetic process Effects 0.000 description 16
- 238000003786 synthesis reaction Methods 0.000 description 16
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 15
- 238000005033 Fourier transform infrared spectroscopy Methods 0.000 description 15
- 229910052757 nitrogen Inorganic materials 0.000 description 15
- 229920000642 polymer Polymers 0.000 description 15
- 239000010410 layer Substances 0.000 description 14
- 238000000034 method Methods 0.000 description 14
- 238000012546 transfer Methods 0.000 description 14
- 239000004971 Cross linker Substances 0.000 description 13
- 229910003460 diamond Inorganic materials 0.000 description 13
- 239000010432 diamond Substances 0.000 description 13
- 238000004821 distillation Methods 0.000 description 13
- 125000004404 heteroalkyl group Chemical group 0.000 description 13
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 13
- 238000000746 purification Methods 0.000 description 13
- 239000011257 shell material Substances 0.000 description 13
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 12
- 238000005481 NMR spectroscopy Methods 0.000 description 12
- UVPNNMSOKAULIN-UHFFFAOYSA-N O1[Si](O)(C2CCCC2)O[Si](O2)(C3CCCC3)O[Si](O)(C3CCCC3)O[Si](O3)(C4CCCC4)O[Si](O)(C4CCCC4)O[Si]1(C1CCCC1)O[Si]23C1CCCC1 Chemical compound O1[Si](O)(C2CCCC2)O[Si](O2)(C3CCCC3)O[Si](O)(C3CCCC3)O[Si](O3)(C4CCCC4)O[Si](O)(C4CCCC4)O[Si]1(C1CCCC1)O[Si]23C1CCCC1 UVPNNMSOKAULIN-UHFFFAOYSA-N 0.000 description 12
- 229910004613 CdTe Inorganic materials 0.000 description 11
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 11
- 229910052793 cadmium Inorganic materials 0.000 description 10
- 229920001296 polysiloxane Polymers 0.000 description 10
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 9
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 9
- 239000011162 core material Substances 0.000 description 9
- 239000000178 monomer Substances 0.000 description 9
- 239000004065 semiconductor Substances 0.000 description 9
- 238000005160 1H NMR spectroscopy Methods 0.000 description 8
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 8
- 125000004429 atom Chemical group 0.000 description 8
- 150000001875 compounds Chemical class 0.000 description 8
- 239000003921 oil Substances 0.000 description 8
- 239000002245 particle Substances 0.000 description 8
- 125000001424 substituent group Chemical group 0.000 description 8
- 239000004094 surface-active agent Substances 0.000 description 8
- VEDJZFSRVVQBIL-UHFFFAOYSA-N trisilane Chemical compound [SiH3][SiH2][SiH3] VEDJZFSRVVQBIL-UHFFFAOYSA-N 0.000 description 8
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 7
- 238000005102 attenuated total reflection Methods 0.000 description 7
- 235000011089 carbon dioxide Nutrition 0.000 description 7
- 238000010790 dilution Methods 0.000 description 7
- 239000012895 dilution Substances 0.000 description 7
- 230000012010 growth Effects 0.000 description 7
- 239000001257 hydrogen Substances 0.000 description 7
- 229910052751 metal Inorganic materials 0.000 description 7
- 239000002184 metal Substances 0.000 description 7
- 229910052697 platinum Inorganic materials 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 229910020175 SiOH Inorganic materials 0.000 description 6
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical group [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 6
- 229910002808 Si–O–Si Inorganic materials 0.000 description 6
- 150000008064 anhydrides Chemical class 0.000 description 6
- 238000005516 engineering process Methods 0.000 description 6
- 239000000284 extract Substances 0.000 description 6
- 229910052738 indium Inorganic materials 0.000 description 6
- 230000003287 optical effect Effects 0.000 description 6
- 239000002243 precursor Substances 0.000 description 6
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 6
- 150000003254 radicals Chemical class 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- YXFVVABEGXRONW-JGUCLWPXSA-N toluene-d8 Chemical compound [2H]C1=C([2H])C([2H])=C(C([2H])([2H])[2H])C([2H])=C1[2H] YXFVVABEGXRONW-JGUCLWPXSA-N 0.000 description 6
- 229940086542 triethylamine Drugs 0.000 description 6
- WUMMIJWEUDHZCL-UHFFFAOYSA-N 3-prop-2-enyloxolane-2,5-dione Chemical compound C=CCC1CC(=O)OC1=O WUMMIJWEUDHZCL-UHFFFAOYSA-N 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 5
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- 125000004432 carbon atom Chemical group C* 0.000 description 5
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- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 description 5
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- 239000011550 stock solution Substances 0.000 description 5
- 230000007306 turnover Effects 0.000 description 5
- YBNMDCCMCLUHBL-UHFFFAOYSA-N (2,5-dioxopyrrolidin-1-yl) 4-pyren-1-ylbutanoate Chemical compound C=1C=C(C2=C34)C=CC3=CC=CC4=CC=C2C=1CCCC(=O)ON1C(=O)CCC1=O YBNMDCCMCLUHBL-UHFFFAOYSA-N 0.000 description 4
- 229910017115 AlSb Inorganic materials 0.000 description 4
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 4
- 229910002601 GaN Inorganic materials 0.000 description 4
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- 238000004639 Schlenk technique Methods 0.000 description 4
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- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- 229910052796 boron Inorganic materials 0.000 description 4
- QABCGOSYZHCPGN-UHFFFAOYSA-N chloro(dimethyl)silicon Chemical compound C[Si](C)Cl QABCGOSYZHCPGN-UHFFFAOYSA-N 0.000 description 4
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- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 4
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- 238000007429 general method Methods 0.000 description 4
- NDJKXXJCMXVBJW-UHFFFAOYSA-N heptadecane Chemical compound CCCCCCCCCCCCCCCCC NDJKXXJCMXVBJW-UHFFFAOYSA-N 0.000 description 4
- 125000004474 heteroalkylene group Chemical group 0.000 description 4
- DCAYPVUWAIABOU-UHFFFAOYSA-N hexadecane Chemical compound CCCCCCCCCCCCCCCC DCAYPVUWAIABOU-UHFFFAOYSA-N 0.000 description 4
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- KQCGMVTVEQZXGM-UHFFFAOYSA-N oxolane-2,5-dione silane Chemical compound [SiH4].O=C1CCC(=O)O1 KQCGMVTVEQZXGM-UHFFFAOYSA-N 0.000 description 3
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Classifications
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
- C09K11/08—Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials
- C09K11/88—Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials containing selenium, tellurium or unspecified chalcogen elements
- C09K11/881—Chalcogenides
- C09K11/883—Chalcogenides with zinc or cadmium
-
- 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
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/14—Polysiloxanes containing silicon bound to oxygen-containing groups
-
- 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
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/22—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen
- C08G77/26—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen nitrogen-containing groups
-
- 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
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/38—Polysiloxanes modified by chemical after-treatment
-
- 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
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/38—Polysiloxanes modified by chemical after-treatment
- C08G77/382—Polysiloxanes modified by chemical after-treatment containing atoms other than carbon, hydrogen, oxygen or silicon
- C08G77/388—Polysiloxanes modified by chemical after-treatment containing atoms other than carbon, hydrogen, oxygen or silicon containing nitrogen
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
- C09K11/02—Use of particular materials as binders, particle coatings or suspension media therefor
- C09K11/025—Use of particular materials as binders, particle coatings or suspension media therefor non-luminescent particle coatings or suspension media
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- General Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Silicon Polymers (AREA)
- Luminescent Compositions (AREA)
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| US9139770B2 (en) * | 2012-06-22 | 2015-09-22 | Nanosys, Inc. | Silicone ligands for stabilizing quantum dot films |
| US9005480B2 (en) | 2013-03-14 | 2015-04-14 | Nanosys, Inc. | Method for solventless quantum dot exchange |
| JP5895958B2 (ja) * | 2014-02-20 | 2016-03-30 | 横浜ゴム株式会社 | 偏波保持光ファイバー用接着剤組成物 |
| US10442823B2 (en) | 2014-10-07 | 2019-10-15 | Nbd Nanotechnologies, Inc. | Functionalized F-POSS monomer compositions and uses thereof |
| EP3268412A4 (en) * | 2015-03-09 | 2018-10-24 | Nbd Nanotechnologies, Inc. | Functionalized f-poss monomer compositions and uses thereof |
| TWI723092B (zh) | 2015-12-02 | 2021-04-01 | 美商奈米系統股份有限公司 | 量子點封裝技術 |
| TW201729901A (zh) | 2015-12-02 | 2017-09-01 | 奈米系統股份有限公司 | 於顯示裝置中基於量子點之色轉換層 |
| JP6621226B2 (ja) * | 2016-02-15 | 2019-12-18 | 国立研究開発法人産業技術総合研究所 | シロキサン及びその製造方法 |
| JP7202352B2 (ja) * | 2017-07-11 | 2023-01-11 | ティーシーエル テクノロジー グループ コーポレーション | 量子ドット及び量子ドットの製造方法 |
| CN109671837B (zh) * | 2017-10-17 | 2021-08-10 | 乐金显示有限公司 | 发光体以及包括其的发光膜、发光二极管和发光装置 |
| KR102712599B1 (ko) * | 2017-10-17 | 2024-10-02 | 엘지디스플레이 주식회사 | 발광체, 이를 포함하는 발광 필름, 발광다이오드 및 발광장치 |
| JP6959119B2 (ja) * | 2017-12-04 | 2021-11-02 | 信越化学工業株式会社 | 量子ドット及びその製造方法、並びに樹脂組成物、波長変換材料、発光素子 |
| KR102713384B1 (ko) | 2018-01-11 | 2024-10-08 | 삼성전자주식회사 | 양자점 집단과 이를 포함하는 조성물 |
| US11472911B2 (en) | 2018-01-17 | 2022-10-18 | Cardiac Pacemakers, Inc. | End-capped polyisobutylene polyurethane |
| CN108832014B (zh) * | 2018-06-22 | 2020-12-25 | 南京邮电大学通达学院 | 基于CdTe/CdS量子点的发光二极管及其制备方法 |
| CN109735203B (zh) * | 2018-12-25 | 2021-01-29 | 陕西科技大学 | 一种半封闭笼状三官能环氧醚基poss组合料、涂料及制备方法 |
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| KR102286274B1 (ko) | 2019-06-07 | 2021-08-05 | 주식회사 신아티앤씨 | 카르복시기를 포함하는 (메타)아크릴레이트 구조의 양자점 리간드용 화합물, 상기 화합물로 형성된 리간드를 포함하는 양자점 입자, 상기 양자점 입자를 포함하는 양자점 입자 조성물, 및 상기 화합물의 제조방법 |
| KR102071688B1 (ko) | 2019-06-07 | 2020-04-01 | 주식회사 신아티앤씨 | 티올기와, 하이드록시기 또는 카르복시기를 포함하는 양자점 리간드를 포함하는 양자점 입자, 상기 양자점 입자를 포함하는 양자점 입자 조성물, 및 상기 양자점 리간드의 제조방법 |
| KR102207329B1 (ko) | 2020-01-06 | 2021-01-25 | 주식회사 신아티앤씨 | 티올기와, 하이드록시기 또는 카르복시기를 포함하는 양자점 리간드를 포함하는 양자점 입자, 상기 양자점 입자를 포함하는 양자점 입자 조성물, 및 상기 양자점 리간드의 제조방법 |
| KR102207331B1 (ko) | 2020-06-03 | 2021-01-28 | 주식회사 신아티앤씨 | 카르복시기를 포함하는 (메타)아크릴레이트 구조의 양자점 리간드용 화합물, 상기 화합물로 형성된 리간드를 포함하는 양자점 입자, 상기 양자점 입자를 포함하는 양자점 입자 조성물, 및 상기 화합물의 제조방법 |
| KR102174457B1 (ko) | 2020-06-03 | 2020-11-04 | 주식회사 신아티앤씨 | 카르복시기를 포함하는 (메타)아크릴레이트 구조의 양자점 리간드용 화합물, 상기 화합물로 형성된 리간드를 포함하는 양자점 입자, 상기 양자점 입자를 포함하는 양자점 입자 조성물, 및 상기 화합물의 제조방법 |
| KR102207330B1 (ko) | 2020-06-03 | 2021-01-28 | 주식회사 신아티앤씨 | 카르복시기를 포함하는 (메타)아크릴레이트 구조의 양자점 리간드용 화합물, 상기 화합물로 형성된 리간드를 포함하는 양자점 입자, 상기 양자점 입자를 포함하는 양자점 입자 조성물, 및 상기 화합물의 제조방법 |
| JP7335520B2 (ja) * | 2021-06-21 | 2023-08-30 | 日亜化学工業株式会社 | 波長変換部材、発光装置及び画像表示装置 |
| KR20220169985A (ko) * | 2021-06-21 | 2022-12-29 | 삼성디스플레이 주식회사 | 양자점, 상기 양자점의 제조방법, 상기 양자점을 포함한 조성물, 상기 양자점을 포함한 광학 부재 및 상기 양자점을 포함한 전자 장치 |
| JP7734616B2 (ja) * | 2022-03-30 | 2025-09-05 | 日鉄ケミカル＆マテリアル株式会社 | アミノ化合物、当該アミノ化合物を用いたポリアミド酸及びポリイミド、並びにこれらの製造方法 |
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| US6501091B1 (en) | 1998-04-01 | 2002-12-31 | Massachusetts Institute Of Technology | Quantum dot white and colored light emitting diodes |
| 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 |
| ATE491230T1 (de) | 2000-10-04 | 2010-12-15 | Univ Arkansas | Synthese von kolloidalen metall chalcogenide nanokristallen |
| DE10220853A1 (de) * | 2002-05-08 | 2003-11-20 | Creavis Tech & Innovation Gmbh | Funktionalisierte polyedrische oligomere Silizium-Sauerstoff-Cluster als Vernetzer |
| US7572393B2 (en) | 2002-09-05 | 2009-08-11 | Nanosys Inc. | Organic species that facilitate charge transfer to or from nanostructures |
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2014
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- 2014-03-13 JP JP2016501860A patent/JP6283092B2/ja active Active
- 2014-03-13 CN CN201480022802.0A patent/CN105143235B/zh active Active
- 2014-03-13 EP EP14774527.7A patent/EP2970341B1/en active Active
- 2014-03-13 WO PCT/US2014/025486 patent/WO2014159936A1/en not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| JP6283092B2 (ja) | 2018-02-21 |
| JP2016521251A (ja) | 2016-07-21 |
| EP2970341A1 (en) | 2016-01-20 |
| CN105143235B (zh) | 2018-06-08 |
| KR102204761B1 (ko) | 2021-01-18 |
| US9133394B2 (en) | 2015-09-15 |
| CA2905913A1 (en) | 2014-10-02 |
| EP2970341A4 (en) | 2016-09-07 |
| WO2014159936A1 (en) | 2014-10-02 |
| US20140275598A1 (en) | 2014-09-18 |
| CN105143235A (zh) | 2015-12-09 |
| KR20150128988A (ko) | 2015-11-18 |
| EP2970341B1 (en) | 2020-07-29 |
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