US20150284412A1 - Method for preparing copper organic metal and copper paste - Google Patents
Method for preparing copper organic metal and copper paste Download PDFInfo
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- US20150284412A1 US20150284412A1 US14/744,244 US201514744244A US2015284412A1 US 20150284412 A1 US20150284412 A1 US 20150284412A1 US 201514744244 A US201514744244 A US 201514744244A US 2015284412 A1 US2015284412 A1 US 2015284412A1
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- Prior art keywords
- copper
- organic metal
- solution
- amine based
- preparing
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- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 title claims abstract description 97
- 239000010949 copper Substances 0.000 title claims abstract description 86
- 229910052802 copper Inorganic materials 0.000 title claims abstract description 85
- 229910052751 metal Inorganic materials 0.000 title claims abstract description 59
- 239000002184 metal Substances 0.000 title claims abstract description 59
- 238000000034 method Methods 0.000 title claims abstract description 28
- 150000001412 amines Chemical class 0.000 claims abstract description 30
- 239000003446 ligand Substances 0.000 claims abstract description 23
- 239000000243 solution Substances 0.000 claims description 33
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 15
- 150000003973 alkyl amines Chemical class 0.000 claims description 9
- 150000001879 copper Chemical class 0.000 claims description 7
- 239000000463 material Substances 0.000 claims description 7
- 239000002904 solvent Substances 0.000 claims description 7
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 5
- 239000002253 acid Substances 0.000 claims description 5
- 239000011259 mixed solution Substances 0.000 claims description 5
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 4
- 239000000194 fatty acid Substances 0.000 claims description 4
- 229930195729 fatty acid Natural products 0.000 claims description 4
- 150000004665 fatty acids Chemical class 0.000 claims description 4
- 230000008569 process Effects 0.000 abstract description 13
- 238000009766 low-temperature sintering Methods 0.000 abstract description 2
- 239000006072 paste Substances 0.000 description 25
- 239000002245 particle Substances 0.000 description 10
- 238000005245 sintering Methods 0.000 description 10
- 239000011230 binding agent Substances 0.000 description 6
- JPVYNHNXODAKFH-UHFFFAOYSA-N Cu2+ Chemical compound [Cu+2] JPVYNHNXODAKFH-UHFFFAOYSA-N 0.000 description 5
- 125000000217 alkyl group Chemical group 0.000 description 5
- 229910001431 copper ion Inorganic materials 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 5
- 125000004429 atom Chemical group 0.000 description 4
- 238000005516 engineering process Methods 0.000 description 4
- 239000002105 nanoparticle Substances 0.000 description 4
- 229910052709 silver Inorganic materials 0.000 description 4
- 239000004332 silver Substances 0.000 description 4
- 230000003247 decreasing effect Effects 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000002798 polar solvent Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 230000009467 reduction Effects 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 238000010304 firing Methods 0.000 description 2
- 239000012454 non-polar solvent Substances 0.000 description 2
- 230000009257 reactivity Effects 0.000 description 2
- 0 *COO[Cu](*)(*)(*)(*)*OOC Chemical compound *COO[Cu](*)(*)(*)(*)*OOC 0.000 description 1
- VXQBJTKSVGFQOL-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethyl acetate Chemical compound CCCCOCCOCCOC(C)=O VXQBJTKSVGFQOL-UHFFFAOYSA-N 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- WUOACPNHFRMFPN-UHFFFAOYSA-N alpha-terpineol Chemical compound CC1=CCC(C(C)(C)O)CC1 WUOACPNHFRMFPN-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- SQIFACVGCPWBQZ-UHFFFAOYSA-N delta-terpineol Natural products CC(C)(O)C1CCC(=C)CC1 SQIFACVGCPWBQZ-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 230000007717 exclusion Effects 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000000615 nonconductor Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229940116411 terpineol Drugs 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B63/00—Purification; Separation; Stabilisation; Use of additives
- C07B63/04—Use of additives
-
- 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
- C07F1/00—Compounds containing elements of Groups 1 or 11 of the Periodic Table
- C07F1/08—Copper compounds
-
- 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
- C07F1/00—Compounds containing elements of Groups 1 or 11 of the Periodic Table
- C07F1/005—Compounds containing elements of Groups 1 or 11 of the Periodic Table without C-Metal linkages
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/24—Electrically-conducting paints
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B1/00—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
- H01B1/02—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of metals or alloys
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B1/00—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
- H01B1/20—Conductive material dispersed in non-conductive organic material
- H01B1/22—Conductive material dispersed in non-conductive organic material the conductive material comprising metals or alloys
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B1/00—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
- H01B1/02—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of metals or alloys
- H01B1/026—Alloys based on copper
Definitions
- the present invention relates to a copper organic metal, a method for preparing a copper organic metal, and a copper paste.
- Copper has a specific resistance value similar to that of silver, but the material costs thereof are much less than silver, such that copper is currently used for electric wiring of most electronic components.
- the copper powder is naturally oxidized or oxidized at the time of heat treatment during a sintering process, or the like, such that conductivity thereof is deteriorated.
- Patent Document 1 discloses a technology in which a paste including nano-sized copper particles is sintered at about 350° C. to form a copper metal wiring.
- Patent Document 2 discloses a technology of coating a surface of the copper particle with silver so as to lower the sintering temperature of the copper particle.
- additional preparing processes of coating silver are added, and material costs are increased.
- the paste made of nano-sized metals of the related art only a non-polar solution may be used.
- Other materials such as a binder, or the like, inserted in the process of forming the conductive pattern using the paste are soluble in a polar solvent. Therefore, since the paste including the nano-sized metal of the related art has a limitation in using of the solvent, the degree of freedom in designing of the paste composition is low in view of viscosity control, improvement in dispersibility, or the like of the paste composition.
- An object of the present invention is to provide a copper organic metal capable of being subjected to a low temperature sintering process and having improved conductivity after the sintering process.
- Another object of the present invention is to provide a copper organic metal having large degrees of freedom in its design.
- Still another object of the present invention is to provide a method for preparing the copper organic metal.
- Still another objection of the present invention is to provide a copper paste including the copper organic metal.
- a copper organic metal having a molecular structure expressed by formula 1 as follows:
- R is an alkyl group and L is an amine based ligand.
- the amine based ligand may include alkylamine.
- alkylamine may be any one material selected from R—NH 2 , R—NH—R′ and R 3 —N.
- the amine based ligand may include hydroxyl (—OH) group.
- the amine based ligand may include HO—R—NH 2 .
- a method for preparing a copper organic metal including: preparing a first solution by dissolving alkanoic acid or fatty acid in aqueous sodium hydroxide solution or aqueous potassium hydroxide solution; mixing the first solution and a second solution having a dissolved copper salt therein; and separating and purifying a copper organic metal from the mixed solution including the first solution and the second solution.
- a method for preparing a copper organic metal including: preparing a first solution by dissolving alkanoic acid or fatty acid in an aqueous sodium hydroxide solution or an aqueous potassium hydroxide solution; mixing the first solution and a second solution having a dissolved copper salt therein; separating and purifying a copper organic metal from the mixed solution including the first solution and the second solution; and reacting the separated and purified copper organic metal with amine based solvent.
- the amine based ligand may include alkylamine.
- the alkylamine may be any one material selected from R—NH 2 , R—NH—R and R 3 —N.
- the amine based ligand may include hydroxyl (—OH) group.
- the amine based ligand may include HO—R—NH 2 .
- a copper paste prepared by mixing a general copper powder and the copper organic metal as described above.
- FIG. 1 is a view showing a molecular structure of a copper organic metal according to an exemplary embodiment of the present invention
- FIG. 2 is a view schematically showing a change of a particle state at the time of heating a paste in which a copper powder and the copper organic metal according to the exemplary embodiment of the present invention are mixed;
- FIG. 3 is a flow chart showing a method for preparing the copper organic metal according to an exemplary embodiment of the present invention.
- FIG. 1 is a view showing a molecular structure of a copper organic metal according to an exemplary embodiment of the present invention.
- the copper organic metal according to the exemplary embodiment of the present invention may include a copper atom and two [R—O 2 ] ion-bonded thereto.
- R means an alkyl group.
- hydrophilicity may be increased or hydrophobicity may be increased depending on the number of carbons included in the alkyl group.
- affinity with water thereof is the largest and in the case of applying alkyl group having eight carbon atoms, affinity with alcohol thereof is increased.
- L which is an amine based ligand, is combined with the copper atom.
- the amine based ligand may be alkylamine or amines including a hydroxyl (—OH) group.
- alkylamine may be any one material selected from R—NH 2 , R—NH—R′ and R 3 —N.
- the amines including a hydroxyl (—OH) group may be HO—R—NH 2 .
- the copper organic metal has good reactivity with a non-polar solvent.
- the copper organic metal has good reactivity with a polar solvent.
- the copper organic metal according to another exemplary embodiment of the present invention may allow compatibility with the solvent of the copper organic metal to include polarity or a non-polarity by changing the kind of the amine based ligand, such that at the time of designing the metal paste, the degree of freedom may be increased.
- FIG. 2 is a view schematically showing a change in a particle state at the time of heating a copper powder and a paste mixed with the copper organic metal.
- the copper organic metal 110 allows combinability among the copper powders 10 to be improved to thereby have improved conductivity.
- the amine based ligand is separated from the Cu atom due to the heating.
- a separation of R—CO 2 is promoted, such that a sintering temperature may be further lowered.
- a general copper paste of the related art is constituted to include a copper powder and a binder. At the time of heating and firing it, copper particles may be combined to one another by the binders. However, since the general binders of the related art were all electrical nonconductors, conductivity was decreased in the case in which the binders were positioned among the copper particles.
- the general copper paste of the related art was rapidly oxidized at the time of high temperature firing, such that an oxide film was formed on a surface of the copper particle, thereby decreasing conductivity.
- the copper organic metal according to the exemplary embodiment of the present invention as described above may include the copper ion.
- the copper ion is changed to be the copper atom to be combined between the copper powders, such that conductivity may be improved as compared to the related art.
- R—CO 2 and the amine based ligand included in the organic metal according to the exemplary embodiment of the present invention are separated from the copper ion, oxides presented in the surface of the copper particle are removed, such that conductivity may be further improved.
- the copper paste according to the exemplary embodiment of the present invention may be formed by mixing the general copper powder and the copper organic metal as described above.
- the copper pastes were prepared by varifying the contents of the copper powder and the copper organic metal, and each of the prepared copper pastes was subjected to the sinter process at 200° C. for 1 hour under nitrogen reduction atmosphere and then resistance thereof was measured.
- epoxy ethyl cellulose, terpineol, and butyl carbitol acetate was used as the main binder and solvent.
- the content of the copper organic metal is increased, viscosity of the copper paste is increased. According to the limitation of the permissible density in a process of forming the conductive pattern, the content of the copper organic metal is preferably controlled.
- FIG. 3 is a flow chart showing a method for preparing the copper organic metal according to the exemplary embodiment of the present invention.
- alkanoic acid or fatty add is dissolved in aqueous sodium hydroxide solution or aqueous potassium hydroxide solution to prepare a first solution (S 100 ).
- the first solution is mixed with a second solution having a dissolved copper salt therein (S 110 ).
- [R—CO 2 ] group included in the first solution and the copper atom included in the first solution are ion-bonded to each other, such that the copper organic metal is formed.
- the copper organic metal is separated and purified from the mixed solution including the first solution and the second solution (S 120 ).
- the separated and purified copper organic metal reacts with the amine based solvent, such that the copper atom is combined with the amine based ligand (L), thereby making it possible to complete the copper organic metal.
- the copper organic metal is capable of being subjected to a sintering process below 300° C. under reduction atmosphere, and having improved conductivity after the sintering process as compared to that of the related art.
- the copper organic metal has compatibility with the polar solvent or the non-polar solvent, such that the metal paste including the copper organic metal has improved degrees of freedom in its design.
- the present invention has been described in connection with what is presently considered to be practical exemplary embodiments. Although the exemplary embodiments of the present invention have been described, the present invention may be also used in various other combinations, modifications and environments. In other words, the present invention may be changed or modified within the range of concept of the invention disclosed in the specification, the range equivalent to the disclosure and/or the range of the technology or knowledge in the field to which the present invention pertains.
- the exemplary embodiments described above have been provided to explain the best state in carrying out the present invention. Therefore, they may be carried out in other states known to the field to which the present invention pertains in using other inventions such as the present invention and also be modified in various forms required in specific application fields and usages of the invention. Therefore, it is to be understood that the invention is not limited to the disclosed embodiments. It is to be understood that other embodiments are also included within the spirit and scope of the appended claims.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Dispersion Chemistry (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
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- Manufacture Of Metal Powder And Suspensions Thereof (AREA)
Abstract
The copper organic metal is constituted to combine a copper atom, [R—CO2] and amine based ligand (L), thereby making it possible to be subjected to a low temperature sintering process and having an improved conductivity at the time of forming a conductive pattern.
Description
- This application is a divisional of U.S. application Ser. No. 13/723,908 filed on Dec. 21, 2012, which claims the benefit under 35 U.S.C. Section 119 of Korean Patent Application No. 10-2011-0143417 filed on Dec. 27, 2011 in the Korean Intellectual Property Office, which are hereby incorporated by reference in their entirety.
- 1. Technical Field
- The present invention relates to a copper organic metal, a method for preparing a copper organic metal, and a copper paste.
- 2. Description of the Related Art
- Copper has a specific resistance value similar to that of silver, but the material costs thereof are much less than silver, such that copper is currently used for electric wiring of most electronic components.
- In the case of forming a copper paste using a copper powder, the copper powder is naturally oxidized or oxidized at the time of heat treatment during a sintering process, or the like, such that conductivity thereof is deteriorated.
- Meanwhile, a technology of forming a paste using a nano-sized copper particle and forming a conductive pattern using the paste has been suggested.
- As an example, Patent Document 1 discloses a technology in which a paste including nano-sized copper particles is sintered at about 350° C. to form a copper metal wiring.
- In general, as a sintering temperature increases, oxidation of a metal is intensified, such that conductivity is reduced.
- In order to overcome the reduction in conductivity at the time of the high sintering process as described above, Patent Document 2 discloses a technology of coating a surface of the copper particle with silver so as to lower the sintering temperature of the copper particle. However, additional preparing processes of coating silver are added, and material costs are increased.
- In addition, in the case of forming the paste made of nano-sized metals of the related art, only a non-polar solution may be used. Other materials such as a binder, or the like, inserted in the process of forming the conductive pattern using the paste are soluble in a polar solvent. Therefore, since the paste including the nano-sized metal of the related art has a limitation in using of the solvent, the degree of freedom in designing of the paste composition is low in view of viscosity control, improvement in dispersibility, or the like of the paste composition.
- An object of the present invention is to provide a copper organic metal capable of being subjected to a low temperature sintering process and having improved conductivity after the sintering process.
- Another object of the present invention is to provide a copper organic metal having large degrees of freedom in its design.
- Still another object of the present invention is to provide a method for preparing the copper organic metal.
- Still another objection of the present invention is to provide a copper paste including the copper organic metal.
- According to an exemplary embodiment of the present invention, there is provided a copper organic metal having a molecular structure expressed by formula 1 as follows:
- wherein R is an alkyl group and L is an amine based ligand.
- In this case, the amine based ligand may include alkylamine.
- In addition, the alkylamine may be any one material selected from R—NH2, R—NH—R′ and R3—N.
- In addition, the amine based ligand may include hydroxyl (—OH) group.
- In addition, the amine based ligand may include HO—R—NH2.
- Meanwhile, according to an exemplary embodiment of the present invention, there is provided a method for preparing a copper organic metal including: preparing a first solution by dissolving alkanoic acid or fatty acid in aqueous sodium hydroxide solution or aqueous potassium hydroxide solution; mixing the first solution and a second solution having a dissolved copper salt therein; and separating and purifying a copper organic metal from the mixed solution including the first solution and the second solution.
- In addition, according to an exemplary embodiment of the present invention, there is provided a method for preparing a copper organic metal including: preparing a first solution by dissolving alkanoic acid or fatty acid in an aqueous sodium hydroxide solution or an aqueous potassium hydroxide solution; mixing the first solution and a second solution having a dissolved copper salt therein; separating and purifying a copper organic metal from the mixed solution including the first solution and the second solution; and reacting the separated and purified copper organic metal with amine based solvent.
- The amine based ligand may include alkylamine.
- The alkylamine may be any one material selected from R—NH2, R—NH—R and R3—N.
- The amine based ligand may include hydroxyl (—OH) group.
- The amine based ligand may include HO—R—NH2.
- According to an exemplary embodiment of the present invention, there is provided a copper paste prepared by mixing a general copper powder and the copper organic metal as described above.
- These and/or other aspects of the disclosure will become apparent and more readily appreciated from the following description of the embodiments, taken in conjunction with the accompanying drawings of which:
-
FIG. 1 is a view showing a molecular structure of a copper organic metal according to an exemplary embodiment of the present invention; -
FIG. 2 is a view schematically showing a change of a particle state at the time of heating a paste in which a copper powder and the copper organic metal according to the exemplary embodiment of the present invention are mixed; and -
FIG. 3 is a flow chart showing a method for preparing the copper organic metal according to an exemplary embodiment of the present invention. - Various advantages and features of the present invention and methods accomplishing thereof will become apparent from the following description of embodiments with reference to the accompanying drawings. However, the present invention may be modified in many different forms and it should not be limited to the embodiments set forth herein. These embodiments may be provided so that this disclosure will be thorough and complete, and will fully convey the scope of the invention to those skilled in the art. Like reference numerals throughout the description denote like elements.
- Terms used in the present specification are for explaining the embodiments rather than limiting the present invention. Unless explicitly described to the contrary, a singular form includes a plural form in the present specification. The word “comprise” and variations such as “comprises” or “comprising,” will be understood to imply the inclusion of stated constituents, steps, operations and/or elements but not the exclusion of any other constituents, steps, operations and/or elements.
- Hereinafter, a configuration and an acting effect of exemplary embodiments of the present invention will be described in more detail with reference to the accompanying drawings.
-
FIG. 1 is a view showing a molecular structure of a copper organic metal according to an exemplary embodiment of the present invention. - Referring to
FIG. 1 , the copper organic metal according to the exemplary embodiment of the present invention may include a copper atom and two [R—O2] ion-bonded thereto. Here, R means an alkyl group. - In addition, hydrophilicity may be increased or hydrophobicity may be increased depending on the number of carbons included in the alkyl group.
- For example, in the case of applying the alkyl group having one carbon atom, affinity with water thereof is the largest and in the case of applying alkyl group having eight carbon atoms, affinity with alcohol thereof is increased.
- In addition, L, which is an amine based ligand, is combined with the copper atom.
- Here, the amine based ligand may be alkylamine or amines including a hydroxyl (—OH) group.
- In addition, the alkylamine may be any one material selected from R—NH2, R—NH—R′ and R3—N.
- In addition, the amines including a hydroxyl (—OH) group may be HO—R—NH2.
- In the case in which the amine based ligand includes the alkylamine, the copper organic metal has good reactivity with a non-polar solvent.
- In addition, in the case in which the amine based ligand is amine including a hydroxyl (—OH) group, the copper organic metal has good reactivity with a polar solvent.
- Therefore, the copper organic metal according to another exemplary embodiment of the present invention may allow compatibility with the solvent of the copper organic metal to include polarity or a non-polarity by changing the kind of the amine based ligand, such that at the time of designing the metal paste, the degree of freedom may be increased.
-
FIG. 2 is a view schematically showing a change in a particle state at the time of heating a copper powder and a paste mixed with the copper organic metal. - Referring to
FIG. 2 , in the case of forming the copper paste by mixing ageneral copper powder 10 and a copperorganic metal 110 at a proper ratio, when applying heat below about 300° C., the copperorganic metal 110 allows combinability among the copper powders 10 to be improved to thereby have improved conductivity. - In this case, while the copper organic metal is heated, the copper ion present in a state of Cu (II) in the copper organic metal is separated from R—CO2 to be changed in a state of Cu atom, such that a conductive pattern is formed. Therefore, a sintering process being subjected at a temperature lower than the temperature of the related art is possible due to the reaction in which the copper ion is changed to the Cu atom.
- In addition, in the case of combining the Cu atom with the amine based ligand, the amine based ligand is separated from the Cu atom due to the heating. In this case, when the amine based ligand is separated, a separation of R—CO2 is promoted, such that a sintering temperature may be further lowered.
- A general copper paste of the related art is constituted to include a copper powder and a binder. At the time of heating and firing it, copper particles may be combined to one another by the binders. However, since the general binders of the related art were all electrical nonconductors, conductivity was decreased in the case in which the binders were positioned among the copper particles.
- In addition, the general copper paste of the related art was rapidly oxidized at the time of high temperature firing, such that an oxide film was formed on a surface of the copper particle, thereby decreasing conductivity.
- However, the copper organic metal according to the exemplary embodiment of the present invention as described above may include the copper ion. As the sintering process progresses, the copper ion is changed to be the copper atom to be combined between the copper powders, such that conductivity may be improved as compared to the related art.
- In addition, while R—CO2 and the amine based ligand included in the organic metal according to the exemplary embodiment of the present invention are separated from the copper ion, oxides presented in the surface of the copper particle are removed, such that conductivity may be further improved.
- Meanwhile, the copper paste according to the exemplary embodiment of the present invention may be formed by mixing the general copper powder and the copper organic metal as described above.
- The copper pastes were prepared by varifying the contents of the copper powder and the copper organic metal, and each of the prepared copper pastes was subjected to the sinter process at 200° C. for 1 hour under nitrogen reduction atmosphere and then resistance thereof was measured.
- Here, in order to prepare the copper paste, epoxy, ethyl cellulose, terpineol, and butyl carbitol acetate was used as the main binder and solvent.
-
TABLE 1 Linear resistance according to content of copper organic metal Composition of copper paste (weight ratio of copper Linear resistance powder:copper organic metal) (Ω) 100:0 300 95:5 140 90:10 12 - Referring to Table 1, it may be appreciated that as the content of the copper organic metal is increased, linear resistance is remarkably decreased.
- Meanwhile, as the content of the copper organic metal is increased, viscosity of the copper paste is increased. According to the limitation of the permissible density in a process of forming the conductive pattern, the content of the copper organic metal is preferably controlled.
-
FIG. 3 is a flow chart showing a method for preparing the copper organic metal according to the exemplary embodiment of the present invention. - Referring to
FIG. 3 , first, alkanoic acid or fatty add is dissolved in aqueous sodium hydroxide solution or aqueous potassium hydroxide solution to prepare a first solution (S100). - Next, the first solution is mixed with a second solution having a dissolved copper salt therein (S110).
- At this time, [R—CO2] group included in the first solution and the copper atom included in the first solution are ion-bonded to each other, such that the copper organic metal is formed.
- Next, the copper organic metal is separated and purified from the mixed solution including the first solution and the second solution (S120).
- Thereafter, amine based solvent is added (S130).
- That is, the separated and purified copper organic metal reacts with the amine based solvent, such that the copper atom is combined with the amine based ligand (L), thereby making it possible to complete the copper organic metal.
- According to an exemplary embodiment of the present invention, the copper organic metal is capable of being subjected to a sintering process below 300° C. under reduction atmosphere, and having improved conductivity after the sintering process as compared to that of the related art.
- According to an exemplary embodiment of the present invention, the copper organic metal has compatibility with the polar solvent or the non-polar solvent, such that the metal paste including the copper organic metal has improved degrees of freedom in its design.
- The present invention has been described in connection with what is presently considered to be practical exemplary embodiments. Although the exemplary embodiments of the present invention have been described, the present invention may be also used in various other combinations, modifications and environments. In other words, the present invention may be changed or modified within the range of concept of the invention disclosed in the specification, the range equivalent to the disclosure and/or the range of the technology or knowledge in the field to which the present invention pertains. The exemplary embodiments described above have been provided to explain the best state in carrying out the present invention. Therefore, they may be carried out in other states known to the field to which the present invention pertains in using other inventions such as the present invention and also be modified in various forms required in specific application fields and usages of the invention. Therefore, it is to be understood that the invention is not limited to the disclosed embodiments. It is to be understood that other embodiments are also included within the spirit and scope of the appended claims.
Claims (7)
1. A method for preparing a copper organic metal having an amine based ligand comprising:
preparing a first solution by dissolving alkanoic acid or fatty acid in an aqueous sodium hydroxide solution or an aqueous potassium hydroxide solution;
mixing the first solution and a second solution having a dissolved copper salt therein; and
separating and purifying a copper organic metal from the mixed solution including the first solution and the second solution.
2. A method for preparing a copper organic metal having an amine based ligand comprising:
preparing a first solution by dissolving alkanoic acid or fatty acid in an aqueous sodium hydroxide solution or an aqueous potassium hydroxide solution;
mixing the first solution and a second solution having a dissolved copper salt therein;
separating and purifying a copper organic metal from the mixed solution including the first solution and the second solution; and
reacting the separated and purified copper organic metal with amine based solvent.
3. The method according to claim 2 , wherein the amine based ligand includes alkylamine.
4. The method according to claim 3 , wherein the alkylamine is any one material selected from R—NH2, R—NH—R′ and R3—N.
5. The method according to claim 2 , wherein the amine based ligand includes a hydroxyl (—OH) group.
6. The method according to claim 2 , wherein the amine based ligand includes HO—R—NH2.
7. A copper paste comprising:
a copper powder; and
a copper organic metal prepared by the method for preparing a copper organic metal according to claim 2 .
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US14/744,244 US20150284412A1 (en) | 2011-12-27 | 2015-06-19 | Method for preparing copper organic metal and copper paste |
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KR10-2011-0143417 | 2011-12-27 | ||
KR1020110143417A KR101376913B1 (en) | 2011-12-27 | 2011-12-27 | Copper organic metal, manufacturing mehtod for copper organic metal and copper paste |
US13/723,908 US9090635B2 (en) | 2011-12-27 | 2012-12-21 | Copper organic metal, method for preparing copper organic metal and copper paste |
US14/744,244 US20150284412A1 (en) | 2011-12-27 | 2015-06-19 | Method for preparing copper organic metal and copper paste |
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US14/744,244 Abandoned US20150284412A1 (en) | 2011-12-27 | 2015-06-19 | Method for preparing copper organic metal and copper paste |
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JP (1) | JP2013136577A (en) |
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EP3263248A4 (en) * | 2015-02-27 | 2018-10-17 | Hitachi Chemical Company, Ltd. | Copper-containing particles, conductor-forming composition, method for manufacturing conductor, conductor and device |
KR102357053B1 (en) * | 2018-10-29 | 2022-02-03 | 한국전자통신연구원 | Solder paste |
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KR900003510A (en) | 1988-08-19 | 1990-03-26 | 이영철 | Engine drive system using compressed air |
JP4575617B2 (en) | 2001-04-27 | 2010-11-04 | ナミックス株式会社 | Metal element-containing organic compound paste, its production method and its use |
JP4389148B2 (en) | 2002-05-17 | 2009-12-24 | 日立化成工業株式会社 | Conductive paste |
DE602004018068D1 (en) * | 2003-07-03 | 2009-01-15 | Mec Co Ltd | Copper compound and method of making a thin copper layer therewith |
JP4360981B2 (en) * | 2003-07-03 | 2009-11-11 | メック株式会社 | Method for producing copper thin film |
DE10360046A1 (en) | 2003-12-18 | 2005-07-21 | Basf Ag | Copper (I) formate |
WO2005101427A1 (en) | 2004-04-14 | 2005-10-27 | Sukgyung A.T Co., Ltd | Conducting metal nano particle and nano-metal ink containing it |
JP2007321215A (en) | 2006-06-02 | 2007-12-13 | Nippon Shokubai Co Ltd | Dispersion of metallic nanoparticle and metallic coating film |
JP5205717B2 (en) | 2006-07-04 | 2013-06-05 | セイコーエプソン株式会社 | Copper formate complex, method for producing copper particles, and method for producing wiring board |
EP2048205A4 (en) | 2006-07-28 | 2010-07-21 | Asahi Glass Co Ltd | Dispersion conatining metal fine particles, process for production of the dispersion, and articles having metal films |
KR100814295B1 (en) * | 2006-10-10 | 2008-03-18 | 삼성전기주식회사 | Method for manufacturing cupper nanoparticles and cupper nanoparticles manufactured using the same |
KR100818195B1 (en) | 2006-12-14 | 2008-03-31 | 삼성전기주식회사 | Method for producing metal nanoparticles and metal nanoparticles produced thereby |
KR100935168B1 (en) | 2007-09-21 | 2010-01-06 | 삼성전기주식회사 | Nonaqueous conductive nanoink composition |
JP2009256218A (en) * | 2008-04-14 | 2009-11-05 | Toray Ind Inc | Copper precursor composition, and method of preparing copper film using the same |
CN102119065B (en) | 2008-08-11 | 2014-03-19 | 地方独立行政法人大阪市立工业研究所 | Copper-containing nanoparticle and process for producing same |
JP2010188094A (en) | 2009-02-15 | 2010-09-02 | Fujio Tsukada | Bedding hanger utilizing space over bed |
WO2011057218A2 (en) * | 2009-11-09 | 2011-05-12 | Carnegie Mellon University | Metal ink compositions, conductive patterns, methods, and devices |
JP5311147B2 (en) | 2010-08-25 | 2013-10-09 | 株式会社豊田中央研究所 | Surface-coated metal nanoparticles, production method thereof, and metal nanoparticle paste including the same |
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JP2013136577A (en) | 2013-07-11 |
US20130161571A1 (en) | 2013-06-27 |
CN103183689A (en) | 2013-07-03 |
KR101376913B1 (en) | 2014-03-20 |
US9090635B2 (en) | 2015-07-28 |
KR20130075165A (en) | 2013-07-05 |
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