WO2020255913A1 - 有機マンガン化合物からなる化学蒸着用原料及び該化学蒸着用原料を用いた化学蒸着法 - Google Patents
有機マンガン化合物からなる化学蒸着用原料及び該化学蒸着用原料を用いた化学蒸着法 Download PDFInfo
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- WO2020255913A1 WO2020255913A1 PCT/JP2020/023378 JP2020023378W WO2020255913A1 WO 2020255913 A1 WO2020255913 A1 WO 2020255913A1 JP 2020023378 W JP2020023378 W JP 2020023378W WO 2020255913 A1 WO2020255913 A1 WO 2020255913A1
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- vapor deposition
- chemical vapor
- manganese
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- thin film
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- 150000002697 manganese compounds Chemical class 0.000 title claims abstract description 83
- 238000005229 chemical vapour deposition Methods 0.000 title claims abstract description 60
- 238000000034 method Methods 0.000 title claims abstract description 23
- 239000007858 starting material Substances 0.000 title abstract 5
- 239000011572 manganese Substances 0.000 claims abstract description 80
- 229910052748 manganese Inorganic materials 0.000 claims abstract description 77
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 claims abstract description 76
- 239000003446 ligand Substances 0.000 claims abstract description 53
- 239000010409 thin film Substances 0.000 claims abstract description 53
- 230000015572 biosynthetic process Effects 0.000 claims abstract description 32
- 239000001257 hydrogen Substances 0.000 claims abstract description 30
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 30
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 29
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 claims abstract description 25
- 239000012495 reaction gas Substances 0.000 claims abstract description 25
- 125000000058 cyclopentadienyl group Chemical group C1(=CC=CC1)* 0.000 claims abstract description 24
- ZSWFCLXCOIISFI-UHFFFAOYSA-N endo-cyclopentadiene Natural products C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 claims abstract description 24
- 125000001424 substituent group Chemical group 0.000 claims abstract description 21
- 239000007789 gas Substances 0.000 claims abstract description 18
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 10
- 125000006165 cyclic alkyl group Chemical group 0.000 claims abstract description 6
- 239000002994 raw material Substances 0.000 claims description 57
- 239000010408 film Substances 0.000 claims description 44
- 239000000758 substrate Substances 0.000 claims description 16
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 9
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 7
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 4
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 4
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 4
- 125000004122 cyclic group Chemical group 0.000 claims description 2
- 239000000463 material Substances 0.000 claims description 2
- 239000000126 substance Substances 0.000 abstract description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 42
- -1 5 - cyclopentadienyl Chemical group 0.000 description 20
- 239000000243 solution Substances 0.000 description 17
- 239000002904 solvent Substances 0.000 description 17
- 238000000354 decomposition reaction Methods 0.000 description 16
- 150000001875 compounds Chemical class 0.000 description 14
- 238000006243 chemical reaction Methods 0.000 description 11
- 239000007983 Tris buffer Substances 0.000 description 10
- 238000004833 X-ray photoelectron spectroscopy Methods 0.000 description 10
- 238000010438 heat treatment Methods 0.000 description 10
- AMWRITDGCCNYAT-UHFFFAOYSA-L hydroxy(oxo)manganese;manganese Chemical compound [Mn].O[Mn]=O.O[Mn]=O AMWRITDGCCNYAT-UHFFFAOYSA-L 0.000 description 10
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 10
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 9
- 230000008016 vaporization Effects 0.000 description 9
- 229910052799 carbon Inorganic materials 0.000 description 8
- 125000004430 oxygen atom Chemical group O* 0.000 description 8
- 238000009834 vaporization Methods 0.000 description 8
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 7
- 150000002431 hydrogen Chemical class 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- 229910052760 oxygen Inorganic materials 0.000 description 7
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 6
- 239000001301 oxygen Substances 0.000 description 6
- 239000004065 semiconductor Substances 0.000 description 6
- 238000003786 synthesis reaction Methods 0.000 description 6
- 230000004888 barrier function Effects 0.000 description 5
- 239000012159 carrier gas Substances 0.000 description 5
- 229910052757 nitrogen Inorganic materials 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 238000000746 purification Methods 0.000 description 4
- 230000009257 reactivity Effects 0.000 description 4
- 239000000741 silica gel Substances 0.000 description 4
- 229910002027 silica gel Inorganic materials 0.000 description 4
- FAGLEPBREOXSAC-UHFFFAOYSA-N tert-butyl isocyanide Chemical compound CC(C)(C)[N+]#[C-] FAGLEPBREOXSAC-UHFFFAOYSA-N 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000004458 analytical method Methods 0.000 description 3
- 239000012298 atmosphere Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000005530 etching Methods 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 238000005457 optimization Methods 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 238000000231 atomic layer deposition Methods 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 239000011261 inert gas Substances 0.000 description 2
- KQFUCKFHODLIAZ-UHFFFAOYSA-N manganese Chemical compound [Mn].[Mn] KQFUCKFHODLIAZ-UHFFFAOYSA-N 0.000 description 2
- MIVBAHRSNUNMPP-UHFFFAOYSA-N manganese(2+);dinitrate Chemical compound [Mn+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O MIVBAHRSNUNMPP-UHFFFAOYSA-N 0.000 description 2
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- 229910004298 SiO 2 Inorganic materials 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical compound [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000000280 densification Methods 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 229910001882 dioxygen Inorganic materials 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 238000002795 fluorescence method Methods 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- QKOHYQVZNLEAJH-UHFFFAOYSA-N oxomethylidenemanganese Chemical compound O=C=[Mn] QKOHYQVZNLEAJH-UHFFFAOYSA-N 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- 238000005092 sublimation method Methods 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 238000002411 thermogravimetry Methods 0.000 description 1
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F17/00—Metallocenes
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F13/00—Compounds containing elements of Groups 7 or 17 of the Periodic Table
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C16/00—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
- C23C16/06—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the deposition of metallic material
- C23C16/18—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the deposition of metallic material from metallo-organic compounds
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/28—Manufacture of electrodes on semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/268
- H01L21/283—Deposition of conductive or insulating materials for electrodes conducting electric current
- H01L21/285—Deposition of conductive or insulating materials for electrodes conducting electric current from a gas or vapour, e.g. condensation
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/28—Manufacture of electrodes on semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/268
- H01L21/283—Deposition of conductive or insulating materials for electrodes conducting electric current
- H01L21/285—Deposition of conductive or insulating materials for electrodes conducting electric current from a gas or vapour, e.g. condensation
- H01L21/28506—Deposition of conductive or insulating materials for electrodes conducting electric current from a gas or vapour, e.g. condensation of conductive layers
- H01L21/28512—Deposition of conductive or insulating materials for electrodes conducting electric current from a gas or vapour, e.g. condensation of conductive layers on semiconductor bodies comprising elements of Group IV of the Periodic Table
- H01L21/28556—Deposition of conductive or insulating materials for electrodes conducting electric current from a gas or vapour, e.g. condensation of conductive layers on semiconductor bodies comprising elements of Group IV of the Periodic Table by chemical means, e.g. CVD, LPCVD, PECVD, laser CVD
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/70—Manufacture or treatment of devices consisting of a plurality of solid state components formed in or on a common substrate or of parts thereof; Manufacture of integrated circuit devices or of parts thereof
- H01L21/71—Manufacture of specific parts of devices defined in group H01L21/70
- H01L21/768—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics
- H01L21/76801—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics characterised by the formation and the after-treatment of the dielectrics, e.g. smoothing
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/70—Manufacture or treatment of devices consisting of a plurality of solid state components formed in or on a common substrate or of parts thereof; Manufacture of integrated circuit devices or of parts thereof
- H01L21/71—Manufacture of specific parts of devices defined in group H01L21/70
- H01L21/768—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics
- H01L21/76838—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics characterised by the formation and the after-treatment of the conductors
- H01L21/76841—Barrier, adhesion or liner layers
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/70—Manufacture or treatment of devices consisting of a plurality of solid state components formed in or on a common substrate or of parts thereof; Manufacture of integrated circuit devices or of parts thereof
- H01L21/71—Manufacture of specific parts of devices defined in group H01L21/70
- H01L21/768—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics
- H01L21/76838—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics characterised by the formation and the after-treatment of the conductors
- H01L21/76841—Barrier, adhesion or liner layers
- H01L21/76871—Layers specifically deposited to enhance or enable the nucleation of further layers, i.e. seed layers
Definitions
- the present invention relates to a raw material for chemical vapor deposition composed of an organic manganese compound for producing a manganese thin film or a manganese compound thin film by a chemical vapor deposition method. More specifically, the present invention relates to a raw material for chemical vapor deposition, which is composed of an organic manganese compound that does not contain oxygen atoms in its structure and enables manganese film formation with a reducing gas such as hydrogen.
- a barrier layer is often formed under the copper wiring layer in order to suppress electromigration.
- a Ta film, a TaN film, or the like has been applied, but in recent years, in order to improve reliability, the application of a barrier layer using a Mn film or a Cumn alloy film has been studied.
- CVD method chemical vapor deposition method
- ALD method atomic layer deposition method
- organic manganese compounds have been conventionally known as raw materials (precursors) for forming a manganese thin film or a manganese-containing thin film by a chemical vapor deposition method.
- examples of the organic manganese compound as a raw material for chemical vapor deposition include manganese with three coordinations of 2,2,6,6-tetramethyl-3,5-heptadionate, which are ⁇ -diketonato ligands.
- the tris (2,2,6,6-tetramethyl-3,5-heptadionat) manganese shown is known (Non-Patent Document 1 and Non-Patent Document 2).
- Non-Patent Document 3 cyclopentadienyl ligand and carbonyl manganese coordinated, 2 of (eta 5-1-methyl - cyclopentadienyl) tricarbonyl manganese also useful as the organic manganese compound as a chemical vapor deposition raw material It is said that there is (Non-Patent Document 3).
- the conventional raw materials for chemical vapor deposition using the above organic manganese compound as an example satisfy the basic property of being able to form a manganese thin film.
- organic manganese compounds used as raw materials for chemical vapor deposition are also required to have various properties.
- many conventional raw materials for chemical vapor deposition made of organic manganese compounds apply oxygen as a reaction gas, and there is a problem of oxidation of a substrate as a base. Therefore, there is a growing demand for organic manganese compounds capable of forming a film using a reducing gas such as hydrogen as a reaction gas.
- the chemical vapor deposition method is a method in which a raw material compound is vaporized into a raw material gas, which is transported to a substrate and decomposed on the substrate to form a thin film.
- a compound having an appropriately high vapor pressure is preferable.
- a compound having appropriate thermal stability and having excellent handleability that does not easily decompose except on the surface of the substrate is preferable.
- the present invention provides a raw material for chemical vapor deposition, which comprises an organic manganese compound capable of forming a high-quality manganese thin film using a reducing gas such as hydrogen as a reaction gas while having basic characteristics as a raw material for chemical vapor deposition.
- the present invention which solves the above-mentioned problems, is a raw material for chemical vapor deposition for producing a manganese thin film or a manganese compound thin film by a chemical vapor deposition method.
- substituents R 1 to R 5 of the cyclopentadienyl ligand (L1) are hydrogen or linear, branched, or cyclic alkyl groups having 1 to 4 carbon atoms, respectively.
- substituents R 6 isocyanide ligand (L2) is a linear, branched, or cyclic having 1 to 4 alkyl groups of carbon atoms in.
- the organic manganese compound constituting the raw material for chemical vapor deposition according to the present invention is characterized in that an isocyanide ligand and a cyclopentadienyl ligand are applied as ligands.
- the isocyanide ligand is a ligand composed of carbon, hydrogen and nitrogen.
- the cyclopentadienyl ligand is a ligand composed of carbon and hydrogen. Neither ligand contains an oxygen atom.
- ligands other than the isocyanide ligand and the cyclopentadienyl ligand are not coordinated with manganese. Therefore, the organic manganese compound of the present invention does not contain oxygen atoms in its structure. Therefore, the organic manganese compound of the present invention enables the formation of a pure manganese thin film without forming an oxide (manganese oxide).
- organic manganese compound of the present invention ligands having a relatively low carbon number (isocyanide ligand and cyclopentadienyl ligand) are applied, and the carbon number of their substituents is also limited. Has been made. From this point as well, according to the organic manganese compound of the present invention, a high-quality manganese thin film can be formed.
- the organic manganese compound according to the present invention to which the isocyanide ligand is applied has appropriate thermal stability and is highly reactive with hydrogen to conventional compounds. Therefore, hydrogen can be applied as the reaction gas, and a manganese thin film can be formed in a reducing atmosphere.
- the organic manganese compound according to the present invention can highly suppress the oxidation of the substrate and the manganese thin film due to the structural advantages of the complex containing no oxygen atom and the advantages of reactivity in a reducing atmosphere.
- a cyclopentadienyl ligand (L1) is coordinated as a ligand together with an isocyanide ligand.
- the cyclopentadienyl ligand is a well-known ligand in conventional organic manganese compounds and stably binds to manganese. Then, in cooperation with the isocyanide ligand, it contributes to the optimization of the thermal stability of the compound.
- Substituents R 1 to R 5 of the cyclopentadienyl ligand (L1) are hydrogen or linear, branched, or cyclic alkyl groups having 1 or more and 4 or less carbon atoms, respectively.
- the carbon number of the substituent is limited in order to make the vaporization property of the organic manganese compound suitable.
- Examples of the alkyl group having 1 or more and 4 or less carbon atoms include a methyl group, an ethyl group, an n-propyl group, an iso-propyl group, an n-butyl group, a sec-butyl group and a tert-butyl group.
- R 1 to R 5 may all be the same substituent or may be different substituents.
- a particularly preferred embodiment of the cyclopentadienyl ligand in the present invention is a cyclopentadienyl ligand in which all of R 1 to R 5 are hydrogen, or R 1 is a methyl group or an ethyl group, and R all 2 ⁇ R 5 is cyclopentadienyl ligand is hydrogen.
- the organic manganese compound of the present invention is characterized by applying an isocyanide ligand (L2) as a ligand to manganese.
- L2 isocyanide ligand
- the isocyanide ligand contributes to the improvement of the reactivity of the compound and the optimization of the thermal stability.
- R 6 is a substituent of isocyanide ligands are straight chain, branched, or cyclic alkyl group having 1 to 4 carbon atoms in the.
- the alkyl group is used in order to make the molecular weight appropriate while limiting the composition of the ligand coordinating to manganese to carbon, hydrogen and nitrogen. Further, the carbon number is limited in order to make the molecular weight of the compound appropriate and to make the vaporization property and the decomposition property suitable. Substituents with an excessively high number of carbon atoms increase the molecular weight and may affect the vaporization properties of the organic manganese compound.
- R 6 is a substituent isocyanide ligands (L2) include a methyl group, an ethyl group, n- propyl group, iso- propyl, sec- butyl group, n- butyl group, tert- butyl It is one of the groups (2-methylpropyl group).
- the organic manganese compound constituting the raw material for chemical vapor deposition according to the present invention is a manganese metallocene (manganosen: Mn (manganosen: Mn) having the same cyclopentadienyl ligand as the cyclopentadienyl ligand (L1) of the compound to be produced. It can be manufactured by using L1) and 2 ) as raw materials.
- the organic manganese compound of the present invention is synthesized by reacting the manganosen with isocyanide (L2), which is the same as isocyanide (L2) of the compound to be produced, in a stoichiometric amount.
- the organic manganese compound constituting the raw material for chemical vapor deposition according to the invention is a monovalent manganese complex (organic compound).
- This synthesis reaction is a reaction for synthesizing a monovalent manganese complex from manganese, which is a divalent manganese complex.
- no additive such as a catalyst or a reducing agent is required in the reaction system. That is, the synthetic reaction can proceed in a reaction system consisting of only manganosen and an equivalent amount of isocyanide.
- the synthesis reaction proceeds by mixing manganosen and an equivalent amount of isocyanide while using a solvent as needed. This synthetic reaction proceeds at room temperature.
- the solvent is preferably ether (diethyl ether or the like), tetrahydrofuran or alkane (n-hexane, n-pentane or the like).
- the raw material composed of the organic manganese compound described above is vaporized by heating to generate a raw material gas, and the raw material gas is transported onto the surface of the substrate to heat the organic manganese compound. It is decomposed to form a manganese thin film.
- the organic manganese compound applied in the present invention is in a solid state or a liquid state at room temperature depending on its substituent.
- the raw material for chemical vapor deposition composed of the organic manganese compound of the present invention can be easily vaporized by a distillation or sublimation method. Therefore, the organic manganese compound as a raw material can be heated and used as it is. Alternatively, it can be dissolved in an appropriate solvent to form a solution, and the solution can be heated to obtain a raw material gas.
- the heating temperature for vaporizing the raw material is preferably 50 ° C. or higher and 120 ° C. or lower.
- the vaporized raw material merges with an appropriate carrier gas and is transported onto the substrate.
- the organic manganese compound of the present invention uses an inert gas (argon, nitrogen, etc.) as a carrier gas, and manganese can be formed only by heating without using a reaction gas. Since the organic manganese compound of the present invention does not contain oxygen in its structure, it is difficult for oxides to be formed even if it is decomposed by heating, and a manganese thin film can be formed only by heating.
- the above-mentioned raw material gas is preferably transported on the substrate together with the reaction gas.
- the raw material gas is heated on the surface of the substrate together with the reaction gas to form a manganese thin film.
- a reducing gas such as hydrogen can be used as a reaction gas for manganese film formation using the raw material for chemical vapor deposition according to the present invention.
- a reducing gas such as ammonia, hydrazine, and formic acid may be applied as the reaction gas. Since these reaction gases can also serve as carrier gases, the application of the carrier gas composed of the above-mentioned inert gas or the like is not essential.
- the decomposition reaction itself of the organic manganese compound of the present invention can also proceed with oxygen as a reaction gas.
- oxygen gas can be applied as a reaction gas.
- a manganese oxide thin film may be applied.
- the raw material for chemical vapor deposition according to the present invention can also meet such a request.
- the film formation temperature at the time of film formation is preferably 150 ° C. or higher and 400 ° C. or lower. If the temperature is lower than 150 ° C., the decomposition reaction of the organic manganese compound is difficult to proceed, and efficient film formation cannot be performed. On the other hand, if the film formation temperature exceeds 400 ° C., it becomes difficult to form a uniform film, and there is a concern that the substrate may be damaged.
- the film formation temperature is usually adjusted by the heating temperature of the substrate.
- the film formation temperature is more preferably 200 ° C. or higher and 400 ° C. or lower, and further preferably 200 ° C. or higher and 300 ° C. or lower.
- the organic manganese compound constituting the raw material for chemical vapor deposition according to the present invention has improved reactivity with hydrogen or the like due to the optimization of the ligand that coordinates with manganese. Therefore, the reactivity of hydrogen or the like is reduced.
- a manganese thin film can be formed using the gas as a reaction gas. According to the present invention, oxidation of the substrate and oxygen mixing in the thin film can be suppressed at a high level. Then, it becomes possible to form a high-quality manganese thin film in which the oxygen and oxide contents are extremely reduced.
- the organic manganese compound of the present invention also has good vaporization characteristics and decomposition characteristics conventionally required for a raw material for chemical vapor deposition. From the above, the raw material for chemical vapor deposition according to the present invention is useful for forming a barrier layer and a seed layer of a highly miniaturized semiconductor device in recent years.
- TG-DTA curve of the organic manganese compound of Example 1 of the first embodiment TG-DTA curve of the organic manganese compound of Example 2 of the first embodiment.
- TG-DTA curve of the organic manganese compound of Example 3 of the first embodiment TG-DTA curve of the organic manganese compound of Example 4 of the first embodiment.
- Example 1 (eta 5 - cyclopentadienyl) - tris (2-isocyano-2-methylpropane) Synthesis of manganese bis - of (eta 5 cyclopentadienyl) manganese 0.185 g (1.0 mmol) To 10 mL of the diethyl ether solution, 10 mL of the diethyl ether solution of 0.263 g (3.0 mmol) of 2-isocyano-2-methylpropane was added, and the mixture was stirred at 25 ° C. for 30 minutes.
- Example 2 (eta 5 - cyclopentadienyl) - tris (2-isocyanoacetate propane) Synthesis of manganese bis - diethyl ether (eta 5 cyclopentadienyl) manganese 0.185 g (1.0 mmol) solution To 10 mL, 0.207 g (3.0 mmol of diethyl ether solution) of 0.207 g (3.0 mmol) was added, and the mixture was stirred at 25 ° C. for 30 minutes.
- Example 3 (eta 5-1-ethyl-cyclopentadienyl) - tris (2-isocyano-2-methylpropane) Synthesis of bis (eta 5-1-ethyl-cyclopentadienyl) manganese Manganese 7.24 g ( To 70 mL of a diethyl ether solution of 30.0 mmol) was added 30 mL of a diethyl ether solution of 7.48 g (90.0 mmol) of 2-isocyano-2-methylpropane, and the mixture was stirred at 25 ° C. for 30 minutes.
- Example 4 (eta 5-1-ethyl-cyclopentadienyl) - tris (2-isocyanoacetate propane) Synthesis of bis (eta 5-1-ethyl-cyclopentadienyl) manganese Manganese 0.241 g (1.0 To 10 mL of a diethyl ether solution of (mmol), 10 mL of a diethyl ether solution of 0.207 g (3.0 mmol) of 2-isocyanatepropane was added, and the mixture was stirred at 25 ° C. for 30 minutes.
- TG-DTA Thermogravimetric analysis
- an endothermic peak or an exothermic peak due to decomposition of the compound is observed near 200 ° C. on the DTA curve.
- the endothermic peak near 65 ° C. in Example 1 is presumed to be due to melting of the solid compound.
- the decomposition temperatures of the organic manganese compounds of Examples 1 to 4 were 187 ° C. (Example 1), 195 ° C. (Example 2), 187 ° C. (Example 3), and 209 ° C. (Example 4).
- the organic manganese compounds of each example proceed smoothly after the decomposition starts.
- About 15% by mass of metallic manganese was generated as a residue after this decomposition.
- the organic manganese compound produced in this embodiment can be decomposed at a temperature near 200 ° C., and manganese can be smoothly decomposed after decomposition. It was confirmed that it could be precipitated.
- Substrate Si or SiO 2 Film formation temperature: 200 ° C or 300 ° C Sample temperature (vaporization temperature): 80 ° C Carrier gas: Nitrogen (50 sccm) Reaction gas: none (0 sccm) or hydrogen (50 sccm) Chamber pressure: 5 torr, 15 torr, 50 torr Film formation time: 15 min
- a film formation test using tris (2,2,6,6-tetramethyl-3,5-heptadionat) manganese which is a conventional organic manganese compound for chemical vapor deposition. It was.
- This organic manganese compound is prepared by mixing a commercially available reagent manganese nitrate (II) with a 50% ethanol aqueous solution of 2,2,6,6-tetramethyl-3,5-heptadione and adjusting the pH with an aqueous sodium hydroxide solution. Synthesized with.
- the conditions for the film formation test were the same as above, and hydrogen gas was used as the reaction gas.
- the film thickness of the manganese thin film at a plurality of locations was measured by the observation result by SEM (scanning electron microscope) or XRF (X-ray reflection fluorescence method), and the average value was calculated.
- the results of the film formation test are shown in Table 1.
- the organic manganese compound of Example 3 of the present embodiment - by material consisting of ((eta 5-1-ethyl-cyclopentadienyl) tris (2-isocyano-2-methylpropane) manganese), manganese thin It was confirmed that a film can be formed. According to the organic manganese compound of this embodiment, a manganese film can be formed using hydrogen gas as a reaction gas. It was also confirmed that a manganese thin film can be formed only by heating without using hydrogen gas (reaction gas).
- the purity of the manganese thin film formed in the present embodiment was examined by XPS (X-ray photoelectron spectroscopy).
- XPS X-ray photoelectron spectroscopy
- the atomic concentrations of various elements (Mn, O, C, N, Si) in the thickness direction were measured while etching the formed manganese thin film. The etching was performed because it was taken into consideration that the manganese thin film was surface-oxidized by the atmosphere when the substrate was transferred from the CVD apparatus to the XPS analyzer.
- FIG. 6 shows No. 1 in Table 1 obtained from the results of XPS. 3 and No. 5 is a graph comparing the manganese concentration (atomic concentration) and the oxygen concentration (atomic concentration) inside the thin film after etching for 1500 seconds in XPS for the manganese thin film of 5. From FIG. 6, it can be seen that these manganese thin films are composed of pure manganese.
- the raw material composed of the conventional organic manganese compound (tris (2,2,6,6-tetramethyl-3,5-heptadionat) manganese) which is a comparative example
- the manganese thin film could not be formed by hydrogen gas.
- Second Embodiment In this embodiment, to set the substituents R 1 ⁇ R 5 cyclopentadienyl ligand (L1) hydrogen, methyl, n- butyl, the tert- butyl, isocyanide ligands (L2 methyl substituents R 6 in), an iso-propyl, combining a plurality of organic manganese compound to tert- butyl, to evaluate its degradation properties. In addition, a film formation test using some compounds was also carried out.
- the organic manganese compounds of each example produced in the second embodiment can also be decomposed at a temperature of 180 ° C. to 220 ° C. It was also confirmed that manganese was smoothly precipitated after decomposition and manganese was generated as a residue.
- the film formation test was performed on Examples 9 and 11.
- the film formation conditions of the film formation test were the same as those of the first embodiment, and the film thickness (average value) was measured from SEM and XRF. As a result, it was confirmed that a high-purity manganese thin film can be formed even with the organic manganese compound of this embodiment.
- the film thickness of the formed manganese thin film had a sufficient thickness in the range of 10 to 40 nm.
- the organic manganese compound constituting the raw material for chemical vapor deposition according to the present invention has high thermal stability and can form manganese under a reducing reaction gas such as hydrogen. In addition, it has vaporization characteristics suitable as a raw material for chemical vapor deposition.
- the present invention is useful for forming seed layers and barrier layers for various semiconductor devices.
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Abstract
Description
ビス(η5-シクロペンタジエニル)マンガン0.185 g(1.0 mmol)のジエチルエーテル溶液 10 mLに、2-イソシアノ-2-メチルプロパン0.263 g(3.0 mmol)のジエチルエーテル溶液 10 mLを加え、25℃で30分撹拌した。
ビス(η5-シクロペンタジエニル)マンガン0.185 g(1.0 mmol)のジエチルエーテル溶液 10 mLに、2-イソシアノプロパン)0.207 g(3.0 mmolのジエチルエーテル溶液 10 mLを加え、25℃で30分撹拌した。
ビス(η5-1-エチルシクロペンタジエニル)マンガン7.24 g(30.0 mmol)のジエチルエーテル溶液 70 mLに、2-イソシアノ-2-メチルプロパン7.48 g(90.0 mmol)のジエチルエーテル溶液 30 mLを加え、25℃で30分撹拌した。
ビス(η5-1-エチルシクロペンタジエニル)マンガン0.241 g(1.0 mmol)のジエチルエーテル溶液 10 mLに、2-イソシアノプロパン0.207 g(3.0 mmol)のジエチルエーテル溶液 10 mLを加え、25℃で30分撹拌した。
成膜温度:200℃又は300℃
試料温度(気化温度):80℃
キャリアガス:窒素(50sccm)
反応ガス:なし(0sccm)又は水素(50sccm)
チャンバー圧力:5torr、15torr、50torr
成膜時間:15min
Claims (7)
- シクロペンタジエニル配位子(L1)の置換基R1~R5の全てが水素である請求項1記載の化学蒸着用原料。
- シクロペンタジエニル配位子(L1)の置換基R1がメチル基、エチル基、n-プロピル基、iso-プロピル基、n-ブチル基、sec-ブチル基、tert-ブチル基のいずれかであって、R2~R5の全てが水素である請求項1記載の化学蒸着用原料。
- イソシアニド配位子(L2)の置換基R6が、メチル基、エチル基、n-プロピル基、iso-プロピル基、n-ブチル基、sec-ブチル基、tert-ブチル基のいずれかである請求項1~請求項3のいずれかに記載の化学蒸着用原料。
- 有機マンガン化合物からなる原料を気化して原料ガスとし、前記原料ガスを基板表面に導入しつつ加熱するマンガン薄膜又はマンガン化合物薄膜の化学蒸着法において、
前記原料として請求項1~請求項3のいずれかに記載の化学蒸着用原料を用い、前記反応ガスとして水素を用いる化学蒸着法。 - 反応ガスとして還元性ガスを適用し、
原料ガスを前記反応ガスと共に基板表面に導入して加熱する請求項5記載の化学蒸着法。 - 成膜温度を150℃以上400℃以下とする請求項5又は請求項6記載の化学蒸着法。
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US17/615,272 US20220235455A1 (en) | 2019-06-17 | 2020-06-15 | Starting material for chemical vapor deposition composed of organomanganese compound, and chemical vapor deposition method using said starting material for chemical vapor deposition |
JP2021528211A JP7478731B2 (ja) | 2019-06-17 | 2020-06-15 | 有機マンガン化合物からなる化学蒸着用原料及び該化学蒸着用原料を用いた化学蒸着法 |
KR1020217037552A KR20210153114A (ko) | 2019-06-17 | 2020-06-15 | 유기 망간 화합물을 포함하는 화학 증착용 원료 및 해당 화학 증착용 원료를 사용한 화학 증착법 |
CN202080042968.4A CN114008238A (zh) | 2019-06-17 | 2020-06-15 | 由有机锰化合物构成的化学蒸镀用原料和使用该化学蒸镀用原料的化学蒸镀法 |
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Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2013508979A (ja) * | 2009-10-23 | 2013-03-07 | プレジデント アンド フェロウズ オブ ハーバード カレッジ | 相互接続用自己整合バリアおよびキャッピング層 |
WO2013191065A1 (ja) * | 2012-06-18 | 2013-12-27 | 東京エレクトロン株式会社 | マンガン含有膜の形成方法 |
JP2019031508A (ja) * | 2013-06-28 | 2019-02-28 | ウェイン ステイト ユニバーシティー | 基板上に層を形成するための還元剤としてのビス(トリメチルシリル)6員環系および類縁化合物 |
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5130172A (en) * | 1988-10-21 | 1992-07-14 | The Regents Of The University Of California | Low temperature organometallic deposition of metals |
KR20120118060A (ko) * | 2006-11-02 | 2012-10-25 | 어드밴스드 테크놀러지 머티리얼즈, 인코포레이티드 | 금속 박막의 cvd/ald용으로 유용한 안티몬 및 게르마늄 착체 |
GB0700534D0 (en) * | 2007-01-11 | 2007-02-21 | Innospec Ltd | Composition |
CN101680085B (zh) * | 2007-05-21 | 2012-12-05 | 乔治洛德方法研究和开发液化空气有限公司 | 用于半导体领域的钴前体 |
US9660205B2 (en) * | 2007-06-22 | 2017-05-23 | Regents Of The University Of Colorado | Protective coatings for organic electronic devices made using atomic layer deposition and molecular layer deposition techniques |
JP5507909B2 (ja) * | 2009-07-14 | 2014-05-28 | 東京エレクトロン株式会社 | 成膜方法 |
JP2014141739A (ja) * | 2012-12-27 | 2014-08-07 | Tokyo Electron Ltd | 金属マンガン膜の成膜方法、処理システム、電子デバイスの製造方法および電子デバイス |
JP5374779B1 (ja) * | 2013-02-12 | 2013-12-25 | 国立大学法人東北大学 | 太陽電池及び、この太陽電池における酸化物層の形成方法、積層酸化物層の形成方法 |
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JP6548896B2 (ja) * | 2014-12-26 | 2019-07-24 | 株式会社マテリアル・コンセプト | 太陽電池モジュールおよびその製造方法 |
JP6043835B1 (ja) * | 2015-05-12 | 2016-12-14 | 田中貴金属工業株式会社 | 異種複核錯体からなる化学蒸着用原料及び該化学蒸着用原料を用いた化学蒸着法 |
US10787738B2 (en) * | 2016-01-27 | 2020-09-29 | Basf Se | Process for the generation of thin inorganic films |
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Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
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WO2013191065A1 (ja) * | 2012-06-18 | 2013-12-27 | 東京エレクトロン株式会社 | マンガン含有膜の形成方法 |
JP2019031508A (ja) * | 2013-06-28 | 2019-02-28 | ウェイン ステイト ユニバーシティー | 基板上に層を形成するための還元剤としてのビス(トリメチルシリル)6員環系および類縁化合物 |
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