US20070025064A1 - Solid electrolytic capacitor element, manufacturing method therefor, and solid electrolytic capacitor - Google Patents
Solid electrolytic capacitor element, manufacturing method therefor, and solid electrolytic capacitor Download PDFInfo
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- US20070025064A1 US20070025064A1 US11/483,834 US48383406A US2007025064A1 US 20070025064 A1 US20070025064 A1 US 20070025064A1 US 48383406 A US48383406 A US 48383406A US 2007025064 A1 US2007025064 A1 US 2007025064A1
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- electrolytic capacitor
- solid electrolytic
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- 239000007787 solid Substances 0.000 title claims abstract description 80
- 238000004519 manufacturing process Methods 0.000 title claims description 25
- 239000010410 layer Substances 0.000 claims abstract description 123
- 239000002344 surface layer Substances 0.000 claims abstract description 67
- 229910052758 niobium Inorganic materials 0.000 claims abstract description 47
- 239000010955 niobium Substances 0.000 claims abstract description 47
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 claims abstract description 47
- 229910000484 niobium oxide Inorganic materials 0.000 claims abstract description 26
- URLJKFSTXLNXLG-UHFFFAOYSA-N niobium(5+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[Nb+5].[Nb+5] URLJKFSTXLNXLG-UHFFFAOYSA-N 0.000 claims abstract description 26
- 229910052715 tantalum Inorganic materials 0.000 claims abstract description 22
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 claims abstract description 22
- 238000000034 method Methods 0.000 claims description 45
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- 238000002048 anodisation reaction Methods 0.000 claims description 2
- PQXKHYXIUOZZFA-UHFFFAOYSA-M lithium fluoride Chemical compound [Li+].[F-] PQXKHYXIUOZZFA-UHFFFAOYSA-M 0.000 claims 6
- NROKBHXJSPEDAR-UHFFFAOYSA-M potassium fluoride Chemical compound [F-].[K+] NROKBHXJSPEDAR-UHFFFAOYSA-M 0.000 claims 4
- OAXJZQMFWBIRKF-UHFFFAOYSA-N ethyl 3-methyl-4-nitrobenzoate Chemical compound CCOC(=O)C1=CC=C([N+]([O-])=O)C(C)=C1 OAXJZQMFWBIRKF-UHFFFAOYSA-N 0.000 claims 3
- 235000003270 potassium fluoride Nutrition 0.000 claims 2
- 239000011698 potassium fluoride Substances 0.000 claims 2
- PUZPDOWCWNUUKD-UHFFFAOYSA-M sodium fluoride Chemical compound [F-].[Na+] PUZPDOWCWNUUKD-UHFFFAOYSA-M 0.000 claims 2
- 235000013024 sodium fluoride Nutrition 0.000 claims 1
- 239000011775 sodium fluoride Substances 0.000 claims 1
- 229920001940 conductive polymer Polymers 0.000 abstract description 19
- 239000002245 particle Substances 0.000 abstract description 19
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- 230000000052 comparative effect Effects 0.000 description 15
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- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
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- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 6
- 239000000853 adhesive Substances 0.000 description 6
- 230000001070 adhesive effect Effects 0.000 description 6
- 229910052709 silver Inorganic materials 0.000 description 6
- 239000004332 silver Substances 0.000 description 6
- 238000005476 soldering Methods 0.000 description 6
- BPUBBGLMJRNUCC-UHFFFAOYSA-N oxygen(2-);tantalum(5+) Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[Ta+5].[Ta+5] BPUBBGLMJRNUCC-UHFFFAOYSA-N 0.000 description 5
- 229920000128 polypyrrole Polymers 0.000 description 5
- 229910001936 tantalum oxide Inorganic materials 0.000 description 5
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 229910002804 graphite Inorganic materials 0.000 description 3
- 239000010439 graphite Substances 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 229910052719 titanium Inorganic materials 0.000 description 3
- 239000010936 titanium Substances 0.000 description 3
- YLZOPXRUQYQQID-UHFFFAOYSA-N 3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-1-[4-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]piperazin-1-yl]propan-1-one Chemical compound N1N=NC=2CN(CCC=21)CCC(=O)N1CCN(CC1)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F YLZOPXRUQYQQID-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- GBPYGZIYERGMPX-UHFFFAOYSA-L [F-].[K+].[Li+].[F-] Chemical compound [F-].[K+].[Li+].[F-] GBPYGZIYERGMPX-UHFFFAOYSA-L 0.000 description 2
- PRUIQAWJIWCEKX-UHFFFAOYSA-L [K+].[F-].[K+].[F-].[Li+] Chemical compound [K+].[F-].[K+].[F-].[Li+] PRUIQAWJIWCEKX-UHFFFAOYSA-L 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
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- 230000000694 effects Effects 0.000 description 2
- 239000003792 electrolyte Substances 0.000 description 2
- AMWRITDGCCNYAT-UHFFFAOYSA-L hydroxy(oxo)manganese;manganese Chemical compound [Mn].O[Mn]=O.O[Mn]=O AMWRITDGCCNYAT-UHFFFAOYSA-L 0.000 description 2
- YSGRCOUULWWFIQ-UHFFFAOYSA-K lithium dipotassium sodium trifluoride Chemical compound [K+].[F-].[K+].[F-].[Na+].[F-].[Li+] YSGRCOUULWWFIQ-UHFFFAOYSA-K 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
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- NIPNSKYNPDTRPC-UHFFFAOYSA-N N-[2-oxo-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 NIPNSKYNPDTRPC-UHFFFAOYSA-N 0.000 description 1
- 229910001257 Nb alloy Inorganic materials 0.000 description 1
- 229910001362 Ta alloys Inorganic materials 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 239000003989 dielectric material Substances 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 229920000767 polyaniline Polymers 0.000 description 1
- 229920000123 polythiophene Polymers 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
Images
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G9/00—Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
- H01G9/004—Details
- H01G9/008—Terminals
- H01G9/012—Terminals specially adapted for solid capacitors
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G9/00—Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
- H01G9/004—Details
- H01G9/04—Electrodes or formation of dielectric layers thereon
- H01G9/042—Electrodes or formation of dielectric layers thereon characterised by the material
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G9/00—Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
- H01G9/004—Details
- H01G9/04—Electrodes or formation of dielectric layers thereon
- H01G9/048—Electrodes or formation of dielectric layers thereon characterised by their structure
- H01G9/052—Sintered electrodes
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G9/00—Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
- H01G9/15—Solid electrolytic capacitors
Definitions
- the present invention relates to a solid electrolytic capacitor element, a manufacturing method therefor, and a solid electrolytic capacitor.
- FIG. 8 is a cross-sectional view for illustrating a structure of a conventional solid electrolytic capacitor. The structure of the conventional solid electrolytic capacitor will be described in reference to FIG. 8 .
- an anode 101 comprises an anode lead 101 a made of tantalum and a rectangular block shaped base body 101 c comprised of a porous sintered body made from niobium particles, and the anode lead 101 a is partially embedded in the base body 101 c.
- an oxide layer 102 is formed so as to cover an area surrounding the base body 101 c.
- the oxide layer 102 functions as a dielectric layer.
- an electrically conductive polymer layer 103 made of polypyrrole or the like is formed so as to cover an area surrounding the oxide layer 102 .
- the electrically conductive polymer layer 103 functions as an electrolyte layer.
- a cathode 104 is formed, which is laminated with a first electrically conductive layer 104 a containing carbon particles formed so as to cover an area surrounding the electrically conductive polymer layer 103 and a second electrically conductive layer 104 b containing silver particles formed so as to cover an area surrounding the first electrically conductive layer 104 a.
- an electrically conductive adhesive layer 105 is formed, onto which a cathode terminal 106 is further formed.
- An anode terminal 107 is connected onto the anode lead 101 a , which is exposed from the base body 101 c and the oxide layer 102 .
- a mold-packaging resin 108 is formed around the cathode 104 , the cathode terminal 106 and the anode terminal 107 such that respective edges of the cathode terminal 106 and the anode terminal 107 can be led outside.
- the conventional solid electrolytic capacitor is thus configured.
- FIGS. 9 to 13 are cross-sectional views for illustrating a fabrication process of the conventional solid electrolytic capacitor.
- the fabrication process of the conventional solid electrolytic capacitor having the structure configured as above is now described.
- the anode 101 comprising the anode lead 101 a made of tantalum and the rectangular block shaped base body 101 c comprised of the porous sintered body made from niobium particles is formed.
- the base body 101 c is formed by heat treatment process in vacuum a molding made from niobium particles, in which the anode lead 101 a is partially embedded.
- the anode 101 is anodized in an aqueous solution such as a phosphoric acid solution to thereby form the oxide layer 102 on the base body 101 c so as to cover the area surrounding the base body 101 c as shown in FIG. 10 .
- an aqueous solution such as a phosphoric acid solution
- the electrically conductive polymer layer 103 made of polypyrrole or the like is formed onto the oxide layer 102 by polymerization or the like so as to cover the area surrounding the oxide layer 102 .
- a carbon paste is coated onto the electrically conductive polymer layer 103 so as to cover the area surrounding the electrically conductive polymer layer 103 , and then dried to thereby form the first electrically conductive layer 104 a containing carbon particles.
- a silver paste is coated on the first electrically conductive layer 104 a so as to cover the area surrounding the first electrically conductive layer 104 a , and then dried to thereby form the second electrically conductive layer 104 b containing silver particles. This allows the cathode 104 , which is laminated with the first electrically conductive layer 104 a and the second electrically conductive layer 104 b , to be formed so as to cover the area surrounding the electrically conductive polymer layer 103 .
- the cathode terminal 106 is bonded to the top surface of the area surrounding the cathode 104 through the electrically conductive adhesive. Further, drying the electrically conductive adhesive allows the electrically conductive adhesive layer 105 to be formed, through which the cathode 104 and the cathode terminal 106 are interconnected. Also, the anode terminal 107 is welded onto the anode lead 101 a exposed from the base body 101 c and the oxide layer 102 .
- the mold-packaging resin 108 is formed around the cathode 104 , the cathode terminal 106 and the anode terminal 107 such that the respective edges of the cathode terminal 106 and the anode terminal 107 can be led outside.
- FIG. 14 is a schematic cross-sectional view for illustrating a condition of the oxide layer near the anode lead in the conventional solid electrolytic capacitor.
- the oxide layer 102 is formed on the surface of the anode lead 101 a at positions of spaces that exist between the anode lead 101 a and the base body 101 c due to the base body 101 c comprised of the porous sintered body, as well as on the surface of the base body 101 c.
- the anode lead 101 a is made of tantalum
- an oxide layer 102 a made of tantalum oxide is formed on the anode lead.
- the base body 101 c is made of niobium
- an oxide layer 102 b made of niobium oxide is formed on the base body 101 c.
- the oxide layer 102 is in a condition of a mixture of the oxide layer 102 a made of tantalum oxide and the oxide layer 102 b made of niobium oxide.
- the above conventional solid electrolytic capacitor can achieve large electrostatic capacitance because the oxide layer 102 is comprised of niobium oxide except for an area in the vicinity of the interface between the anode lead 101 a and the base body 101 c as described.
- the oxide layer 102 in the vicinity of the interface between the anode lead 101 a and the base body 101 c is in the condition of the mixture of the oxide layer 102 a made of tantalum oxide and the oxide layer 102 b made of niobium oxide, and therefore stress due to the difference in thermal expansion coefficient between the oxide layer 102 a made of tantalum oxide and the oxide layer 102 b made of niobium oxide arises during heat treatment process such as reflow soldering process.
- heat treatment process such as reflow soldering process.
- problems that the oxide layer 102 is likely to be peeled off from the anode lead 101 a and the base body 101 c and that cracks are likely to be generated inside of the oxide layer 102 .
- leakage current between the cathode 104 formed on the oxide layer 102 and the anode 101 is likely to be increased.
- the present invention has been made in order to solve the problems described above, and it is therefore one object of the present invention to provide a solid electrolytic capacitor element or a solid electrolytic capacitor having low leakage current.
- Another object of the present invention is to provide a method for manufacturing the solid electrolytic capacitor element having low leakage current.
- the solid electrolytic capacitor element comprises: an oxide layer that is formed on an anode and contains niobium oxide; and a cathode formed on the oxide layer, wherein the anode has: an anode lead; a surface layer that is formed on the anode lead and contains niobium; and a base body that is formed on the surface layer and comprised of a porous sintered body containing niobium.
- the anode has the anode lead and the base body containing niobium formed on the anode lead as described above, and therefore the oxide layer containing niobium oxide formed on the anode is also formed on a surface of the base body as well as on a surface of the anode lead at positions of spaces existing between the anode lead and the base body.
- the oxide layer is formed on the surface layer containing niobium. That is, at the positions of the spaces, the oxide layer containing niobium oxide is formed on the surface layer and the base body both containing niobium.
- the oxide layer containing niobium oxide is unlikely to be peeled off from the surface layer and the base body both containing niobium even during heat treatment process such as reflow soldering process, and cracks inside of the oxide layer are also unlikely to be generated.
- an increase in leakage current between the cathode formed on the oxide layer and the anode can be suppressed, so that a solid electrolytic capacitor element with low leakage current can easily be obtained.
- the anode lead contains tantalum and the anode lead around which the base body is not formed has thereon a region not formed with the surface layer.
- the anode lead contains tantalum, a first region formed with the surface layer is formed on the anode lead, and a terminal is formed outside of the first region.
- Configuring as described allows a tantalum base material, which is more chemically stable than niobium and is unlikely to be oxidized, to be exposed in a region on the anode lead where the base body and the surface layer are not formed, and therefore an oxide coating is unlikely to be formed on the region during heat treatment process.
- a film thickness of the surface layer falls within the range of 0.01 ⁇ m to 2 ⁇ m.
- a measurement of the film thickness of the surface layer is performed by an energy dispersive X-ray analysis (EDX) method.
- EDX energy dispersive X-ray analysis
- Configuring as described enables a stress arising between the anode lead and the oxide layer to be sufficiently suppressed and adhesiveness of the surface layer on the anode lead to be improved, and therefore peeling off of the oxide layer and cracks in it are unlikely to be generated. This enables leakage current to be further reduced.
- the above-described surface layer suppresses a leakage current between the cathode and the anode to be less than 600 ⁇ A, and more preferably less than 300 ⁇ A.
- the method for manufacturing the solid electrolytic capacitor element according to the present invention comprises the steps of forming on an anode lead a surface layer containing niobium; forming on the surface layer an anode having a base body comprised of a porous sintered body containing niobium; forming on the anode by anodization an oxide layer containing niobium oxide; and forming a cathode on the oxide layer.
- the step of forming the surface layer containing niobium may comprise cathodic reduction in molten lithium fluoride-sodium fluoride-potassium fluoride-potassium hexafluoroniobate (LiF-NaF-KF-K2NbF6) systems.
- the step of forming the surface layer containing niobium may comprise cathodic reduction in any of molten lithium fluoride-potassium fluoride-potassium hexafluoroniobate (LiF-KF-K2NbF6) systems or molten lithium fluoride-potassium hexafluoroniobate (LiF-K2NbF6) systems.
- surfaces of the anode lead having the surface layer containing niobium and the base body that is formed on the anode lead and comprised of a porous sintered body containing niobium are formed thereon with the oxide layer containing niobium oxide, so that the oxide layer containing niobium oxide can be readily formed also at positions of spaces existing between the anode lead and the base body.
- the oxide layer containing niobium oxide is unlikely to be peeled off from the surface layer and the base body both containing niobium even during heat treatment process such as reflow soldering process, and cracks inside of the oxide layer are also unlikely to be generated.
- an increase in leakage current between the cathode formed on the oxide layer and the anode can be suppressed, so that a solid electrolytic capacitor with low leakage current can easily be manufactured.
- the solid electrolytic capacitor according to the present invention comprises: an oxide layer that is formed on an anode and contains niobium oxide; and a cathode formed on the oxide layer, wherein the anode has: an anode lead; a surface layer that is formed on the anode lead and contains niobium; and a base body that is formed on the surface layer and comprised of a porous sintered body containing niobium, the base body being, an anode terminal is formed on the anode, a cathode terminal is formed on the cathode, and a mold-packaging resin is formed such that respective edges of the anode terminal and the cathode terminal are led outside.
- the oxide layer containing niobium oxide is unlikely to be peeled off from the surface layer and the base body both containing niobium even during heat treatment process such as reflow soldering process, and cracks inside of the oxide layer are also unlikely to be generated.
- an increase in leakage current between the cathode formed on the oxide layer and the anode can be suppressed, so that a solid electrolytic capacitor with low leakage current can easily be obtained.
- FIG. 1 is a cross-sectional view for illustrating a structure of a solid electrolytic capacitor according to Example 1 of the present invention.
- FIG. 2 is a cross-sectional view for illustrating a first step in a fabrication process of the solid electrolytic capacitor according to Example 1 of the present invention.
- FIG. 3 is a cross-sectional view for illustrating a second step in the fabrication process of the solid electrolytic capacitor according to Example 1 of the present invention.
- FIG. 4 is a cross-sectional view for illustrating a third step in the fabrication process of the solid electrolytic capacitor according to Example 1 of the present invention.
- FIG. 5 is a cross-sectional view for illustrating a fourth step in the fabrication process of the solid electrolytic capacitor according to Example 1 of the present invention.
- FIG. 6 is a cross-sectional view for illustrating a fifth step in the fabrication process of the solid electrolytic capacitor according to Example 1 of the present invention.
- FIG. 7 is a schematic cross-sectional view for illustrating a condition of an oxide layer near an anode lead in the solid electrolytic capacitor according to Example 1 of the present invention.
- FIG. 8 is a cross-sectional view for illustrating a structure of a conventional solid electrolytic capacitor.
- FIG. 9 is a cross-sectional view for illustrating a first step in a fabrication process of the conventional solid electrolytic capacitor.
- FIG. 10 is a cross-sectional view for illustrating a second step in the fabrication process of the conventional solid electrolytic capacitor.
- FIG. 11 is a cross-sectional view for illustrating a third step in the fabrication process of the conventional solid electrolytic capacitor.
- FIG. 12 is a cross-sectional view for illustrating a fourth step in the fabrication process of the conventional solid electrolytic capacitor.
- FIG. 13 is a cross-sectional view for illustrating a fifth step in the fabrication process of the conventional solid electrolytic capacitor.
- FIG. 14 is a schematic cross-sectional view for illustrating a condition of an oxide layer near an anode lead in the conventional solid electrolytic capacitor.
- FIG. 1 is a cross-sectional view for illustrating a structure of a solid electrolytic capacitor according to Example 1 of the present invention.
- an anode 1 comprises an anode lead 1 a made of tantalum, a surface layer 1 b made of niobium having a film thickness of approximately 0.1 ⁇ m formed on the anode lead 1 a and a rectangular block shaped base body 1 c with a size of approximately 3.3 mm ⁇ approx. 2.7 mm ⁇ approx. 1.7 mm comprised of a porous sintered body made from niobium particles having an average particle size of approximately 2 ⁇ m, and the anode lead 1 a is partially embedded in the base body 1 c .
- the surface layer 1 b is not formed on an edge 1 d of the anode lead 1 a where the anode lead 1 a is not embedded in the base body 1 c , and therefore a tantalum base material is exposed there.
- the edge 1 d is one example of a “region where a surface layer is not formed” according to the present invention.
- an oxide layer 2 made of niobium oxide is formed so as to cover an area surrounding the anode 1 .
- the oxide layer 2 functions as a so-called dielectric layer.
- an electrically conductive polymer layer 3 made of polypyrrole is formed so as to cover an area surrounding the oxide layer 2 .
- the electrically conductive polymer layer 3 functions as a so-called electrolyte layer.
- a cathode 4 is formed, which is laminated with a first electrically conductive layer 4 a containing graphite particles formed so as to cover an area surrounding the electrically conductive polymer layer 3 and a second electrically conductive layer 4 b containing silver particles formed so as to cover an area surrounding the first electrically conductive layer 4 a.
- an electrically conductive adhesive layer 5 is formed, onto which a cathode terminal 6 is further formed. Also, the edge 1 d of the anode lead 1 a where the anode lead 1 a is not embedded in the base body 1 c is exposed from the surface layer 1 b , the base body 1 c and the oxide layer 2 , and an anode terminal 7 is connected onto the edge 1 d . Further, a mold-packaging resin 8 is formed around the cathode 4 , the cathode terminal 6 and the anode terminal 7 such that respective edges of the cathode terminal 6 and the anode terminal 7 can be led outside.
- the solid electrolytic capacitor according to Example 1 of the present invention is thus configured.
- FIGS. 2 to 6 are cross-sectional views for illustrating a fabrication process of the solid electrolytic capacitor according Example 1 of the present invention.
- the fabrication process of the solid electrolytic capacitor having the structure illustrated above according to Example 1 of the present invention is now described.
- the surface layer 1 b made of niobium having a film thickness of approximately 0.1 ⁇ m was formed on the anode lead 1 a by cathodically reducing the anode lead 1 a for approximately 3 minutes in lithium fluoride-sodium fluoride-potassium fluoride-potassium hexafluoroniobate (LiF-NaF-KF-K 2 NbF 6 ) systems that had been heated at approximately 550° C. to be thereby molten.
- the film thickness of the surface layer 1 b may be identified by an energy dispersive X-ray analysis (EDX) method or the like.
- EDX energy dispersive X-ray analysis
- the anode 1 comprising the anode lead 1 a and the rectangular block shaped base body 1 c with a size of approximately 3.3 mm ⁇ approx. 2.7 mm ⁇ approx. 1.7 mm comprised of a porous sintered body made from niobium particles having an average particle size of approximately 2 ⁇ m was formed.
- the base body 1 c was formed by heat treatment process in vacuum a molding comprised of niobium particles in which the other edge of the anode lead 1 a was embedded.
- the anode 1 was anodized in an approximately 0.5 wt. % phosphoric acid solution, which was held at approximately 60° C., by applying a constant voltage of approximately 10 V for approximately 8 hours, whereby the oxide layer 2 made of niobium oxide was formed so as to cover the area surrounding the base body 1 as shown in FIG. 3 .
- the electrically conductive polymer layer 3 made of polypyrrole was formed on the oxide layer 2 by polymerization or the like so as to cover the area surrounding the oxide layer 2 .
- a graphite paste was coated onto the electrically conductive polymer layer 3 so as to cover the area surrounding the electrically conductive polymer layer 3 , and then dried at approximately 80° C. for approximately 30 minutes to thereby form the first electrically conductive layer 4 a containing graphite particles.
- a silver paste was coated on the first electrically conductive layer 4 a so as to cover the area surrounding the first electrically conductive layer 4 a , and then dried at approximately 170° C. for approximately 30 minutes to thereby form the second electrically conductive layer 4 b containing silver particles. This allowed the cathode 4 , which was laminated with the first electrically conductive layer 4 a and the second electrically conductive layer 4 b , to be formed so as to cover the area surrounding the electrically conductive polymer layer 3 .
- an electrically conductive adhesive had been coated in an amount of approximately 2 mg on the cathode terminal 6 made from iron foil of which a thickness was approximately 0.1 mm and a surface was nickel-plated, the cathode terminal 6 was bonded to the top surface of the area surrounding the cathode 4 through the electrically conductive adhesive. Further, drying the electrically conductive adhesive at approximately 60° C. for approximately 30 minutes allowed the electrically conductive adhesive layer 5 to be formed, through which the cathode 4 and the cathode terminal 6 were interconnected.
- the anode terminal 7 made from iron foil of which a thickness was approximately 0.1 mm and a surface was nickel-plated was welded onto the edge 1 d of the anode lead 1 a where the anode lead 1 a was exposed from the surface layer 1 b , the base body 1 c , and the oxide layer 2 .
- the mold-packaging resin 8 was formed around the cathode 4 , the cathode terminal 6 and the anode terminal 7 such that the respective edges of the cathode terminal 6 and the anode terminal 7 were able to be led outside.
- the solid electrolytic capacitor according to Example 1 was thus fabricated as shown in FIG. 1 .
- a condition in which the cathode terminal 6 and the anode terminal 7 are formed and the mold-packaging resin 8 is formed around the cathode 4 , the cathode terminal 6 and the anode terminal 7 is referred to as a solid electrolytic capacitor, and also, a prior condition as an element in which the terminals have not been connected is referred to as a solid electrolytic capacitor element.
- FIG. 7 is a schematic cross-sectional view for illustrating a condition of the oxide layer near the anode lead in the solid electrolytic capacitor according to Example 1 of the present invention.
- the oxide layer 2 formed on the anode 1 is also formed on the surfaces of the surface layer 1 b and the base body 1 c at positions of spaces that exist between the anode lead 1 a and the base body 1 c due to the base body 1 c comprised of the porous sintered body.
- the oxide layer 2 containing niobium oxide is unlikely to be peeled off from the surface layer 1 b and the base body 1 c even during heat treatment process such as reflow soldering process, and cracks inside of the oxide layer 2 are also unlikely to be generated.
- an increase in leakage current between the cathode 4 formed on the oxide layer 2 and the anode 1 can be suppressed, so that the leakage current can be decreased.
- the anode lead 1 a is made of tantalum and a tantalum base material is exposed at the edge 1 d of the anode lead 1 a where the anode lead 1 a is exposed from the base body 1 c and the oxide layer 2 , so that an oxide coating is unlikely to be formed on the edge 1 d .
- This enables a satisfactory electrical connection between the anode lead 1 a and the anode terminal 8 to be made when the anode terminal 8 is connected onto the edge 1 d , so that ESR can be reduced.
- the oxide layer 2 containing niobium oxide is formed by anodizing the anode 1 having the above configuration, the oxide layer 2 containing niobium oxide can readily be formed also on the surface layer 1 b and the base body 1 c both containing niobium at the positions of the spaces existing between the anode lead 1 a and the base body 1 c .
- the oxide layer 2 containing niobium oxide is unlikely to be peeled off from the surface layer 1 b and the base body 1 c even during heat treatment process such as reflow soldering process, and cracks inside of the oxide layer 2 are also unlikely to be generated.
- an increase in leakage current between the cathode 4 formed on the oxide layer 2 and the anode 1 can be suppressed, so that a solid electrolytic capacitor with low leakage current can easily be manufactured.
- Comparative Example 1 the conventional electrolytic capacitor shown in FIG. 8 was fabricated.
- Comparative Example 1 the solid electrolytic capacitor similar to that in Example 1 was fabricated, except that the capacitor in Comparative Example 1 employed the anode lead made of tantalum onto which the surface layer in Example 1 was not formed.
- Comparative Example 2 a solid electrolytic capacitor similar to that in Comparative Example 1 was fabricated, except that the capacitor in Comparative Example 2 employed an anode lead made of niobium, instead of the anode lead made of tantalum in Comparative Example 1.
- Example 1 As listed in Table 1, it has turned out that the solid electrolytic capacitor in Example 1 exhibits a large reduction in leakage current in comparison with those in Comparative Examples 1 and 2.
- Example 2 solid electrolytic capacitors similar to that in Example 1 were fabricated, except that a film thickness of the surface layer 1 b was varied in Example 2 by varying a time period for cathodically reducing the anode lead 1 a in molten LiF-NaF-KF-K2NbF6 systems in Example 1 in the range of approximately 10 seconds to approximately 2 hours 30 minutes as shown in Table 2.
- Example 2 Similarly to the case of Example 1, a film thickness of the surface layer 1 b was measured by EDX and a leakage current was also measured. Measurement results are listed in Table 2. TABLE 4 Cathodic reduction Surface layer Leakage time thickness ( ⁇ m) current ( ⁇ A) Example 2 10 seconds 0.005 560 Example 2 15 seconds 0.0075 480 Example 2 20 seconds 0.01 270 Example 2 2 minutes 0.05 230 Example 1 3 minutes 0.1 200 Example 2 15 minutes 0.5 200 Example 2 30 minutes 1.0 210 Example 2 1 hour 2.0 210 Example 2 1 hour 30 minutes 3.0 460 Example 2 2 hours 30 minutes 5.0 540
- the film thickness of the surface layer 1 b is varied in the range of approximately 0.005 ⁇ m to approximately 5.0 ⁇ m, depending on the variation in the time period for the cathodic reduction, and in this range, any of the capacitors exhibits a lower leakage current than those in Comparative Examples 1 and 2. Also, it has turned out that in the case where the film thickness of the surface layer 1 b falls within the range of approximately 0.01 ⁇ m to approximately 2.0 ⁇ m, the leakage current is particularly low.
- the surface layer 1 b made of niobium was employed; however, the present invention is not limited to this, but the surface layer 1 b may contain another element such as tantalum, titanium, or nitrogen, besides niobium.
- the surface layer 1 b was formed by the cathodic reduction performed in molten LiF-NaF-KF-K2NbF6 systems; however, the present invention is not limited to this, but another molten salt containing niobium such as lithium fluoride-potassium fluoride-potassium hexafluoroniobate (LiF-KF-K 2 NbF 6 ) systems or lithium fluoride-potassium hexafluoroniobate (LiF-K 2 NbF 6 ) systems may be employed, or alternatively the layer may be formed by another thin film fabrication method. Also, after the fabrication of the surface layer 1 b by the use of one of above methods, a heat treatment may be performed in a nitrogen atmosphere.
- a heat treatment may be performed in a nitrogen atmosphere.
- the anode lead 1 a made of tantalum was employed; however, the present invention is not limited to this, but the anode lead 1 a may be comprised of, for example, a tantalum alloy containing another metal, such as niobium or titanium, or another element such as nitrogen, in addition to tantalum.
- the porous sintered body made from niobium particles was employed as the base body 1 c ; however, the present invention is not limited to this, but the base body 1 c may be comprised of a porous sintered body made from, for example, niobium alloy particles containing another metal such as tantalum or titanium, or another element such as nitrogen, in addition to niobium.
- the oxide layer 2 was formed by anodizing the anode 1 in an aqueous solution; however, the present invention is not limited to this, but the oxide layer 2 may be formed by another method.
- the electrically conductive polymer layer 3 made of polypyrrole was formed; however, the present invention is not limited to this, but another electrically conductive polymer such as polythiophene or polyaniline may be employed, or alternatively another electrically conductive material such as manganese oxide may be employed.
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Abstract
Description
- The present invention relates to a solid electrolytic capacitor element, a manufacturing method therefor, and a solid electrolytic capacitor.
- In recent years, a solid electrolytic capacitor has been requiring the decrease in size and the increase in capacitance, and a solid electrolytic capacitor using niobium oxide having a large dielectric constant have been proposed, instead of using aluminum oxide or tantalum oxide as a dielectric material. An example of such proposal includes Japanese published unexamined patent application No. 2000-68157.
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FIG. 8 is a cross-sectional view for illustrating a structure of a conventional solid electrolytic capacitor. The structure of the conventional solid electrolytic capacitor will be described in reference toFIG. 8 . - As shown in
FIG. 8 , in the conventional solid electrolytic capacitor, ananode 101 comprises an anode lead 101 a made of tantalum and a rectangular block shaped base body 101 c comprised of a porous sintered body made from niobium particles, and the anode lead 101 a is partially embedded in the base body 101 c. - Onto the
anode 101, anoxide layer 102 is formed so as to cover an area surrounding the base body 101 c. Theoxide layer 102 functions as a dielectric layer. - Onto the
oxide layer 102, an electricallyconductive polymer layer 103 made of polypyrrole or the like is formed so as to cover an area surrounding theoxide layer 102. The electricallyconductive polymer layer 103 functions as an electrolyte layer. Onto the electricallyconductive polymer layer 103, acathode 104 is formed, which is laminated with a first electrically conductive layer 104 a containing carbon particles formed so as to cover an area surrounding the electricallyconductive polymer layer 103 and a second electrically conductive layer 104 b containing silver particles formed so as to cover an area surrounding the first electrically conductive layer 104 a. - Onto the top surface of an area surrounding the
cathode 104, an electrically conductiveadhesive layer 105 is formed, onto which acathode terminal 106 is further formed. Ananode terminal 107 is connected onto the anode lead 101 a, which is exposed from the base body 101 c and theoxide layer 102. Further, a mold-packaging resin 108 is formed around thecathode 104, thecathode terminal 106 and theanode terminal 107 such that respective edges of thecathode terminal 106 and theanode terminal 107 can be led outside. The conventional solid electrolytic capacitor is thus configured. - FIGS. 9 to 13 are cross-sectional views for illustrating a fabrication process of the conventional solid electrolytic capacitor. In reference to FIGS. 9 to 13, the fabrication process of the conventional solid electrolytic capacitor having the structure configured as above is now described.
- First, as shown in
FIG. 9 , theanode 101 comprising the anode lead 101 a made of tantalum and the rectangular block shaped base body 101 c comprised of the porous sintered body made from niobium particles is formed. The base body 101 c is formed by heat treatment process in vacuum a molding made from niobium particles, in which the anode lead 101 a is partially embedded. - Then, the
anode 101 is anodized in an aqueous solution such as a phosphoric acid solution to thereby form theoxide layer 102 on the base body 101 c so as to cover the area surrounding the base body 101 c as shown inFIG. 10 . - Subsequently, as shown in
FIG. 11 , the electricallyconductive polymer layer 103 made of polypyrrole or the like is formed onto theoxide layer 102 by polymerization or the like so as to cover the area surrounding theoxide layer 102. - Subsequently, as shown in
FIG. 12 , a carbon paste is coated onto the electricallyconductive polymer layer 103 so as to cover the area surrounding the electricallyconductive polymer layer 103, and then dried to thereby form the first electrically conductive layer 104 a containing carbon particles. After that, a silver paste is coated on the first electrically conductive layer 104 a so as to cover the area surrounding the first electrically conductive layer 104 a, and then dried to thereby form the second electrically conductive layer 104 b containing silver particles. This allows thecathode 104, which is laminated with the first electrically conductive layer 104 a and the second electrically conductive layer 104 b, to be formed so as to cover the area surrounding the electricallyconductive polymer layer 103. - Subsequently, as shown in
FIG. 13 , after an electrically conductive adhesive has been coated onto thecathode terminal 106, thecathode terminal 106 is bonded to the top surface of the area surrounding thecathode 104 through the electrically conductive adhesive. Further, drying the electrically conductive adhesive allows the electrically conductiveadhesive layer 105 to be formed, through which thecathode 104 and thecathode terminal 106 are interconnected. Also, theanode terminal 107 is welded onto the anode lead 101 a exposed from the base body 101 c and theoxide layer 102. - Finally, as shown in
FIG. 8 , the mold-packaging resin 108 is formed around thecathode 104, thecathode terminal 106 and theanode terminal 107 such that the respective edges of thecathode terminal 106 and theanode terminal 107 can be led outside. -
FIG. 14 is a schematic cross-sectional view for illustrating a condition of the oxide layer near the anode lead in the conventional solid electrolytic capacitor. Referring toFIG. 14 , in the conventional solid electrolytic capacitor, theoxide layer 102 is formed on the surface of the anode lead 101 a at positions of spaces that exist between the anode lead 101 a and the base body 101 c due to the base body 101 c comprised of the porous sintered body, as well as on the surface of the base body 101 c. Note that because the anode lead 101 a is made of tantalum, an oxide layer 102 a made of tantalum oxide is formed on the anode lead. On the other hand, because the base body 101 c is made of niobium, an oxide layer 102 b made of niobium oxide is formed on the base body 101 c. For this reason, in the spaces existing between the anode lead 101 a and the base body 101 c, theoxide layer 102 is in a condition of a mixture of the oxide layer 102 a made of tantalum oxide and the oxide layer 102 b made of niobium oxide. - The above conventional solid electrolytic capacitor can achieve large electrostatic capacitance because the
oxide layer 102 is comprised of niobium oxide except for an area in the vicinity of the interface between the anode lead 101 a and the base body 101 c as described. - However, in the above conventional solid electrolytic capacitor, the
oxide layer 102 in the vicinity of the interface between the anode lead 101 a and the base body 101 c is in the condition of the mixture of the oxide layer 102 a made of tantalum oxide and the oxide layer 102 b made of niobium oxide, and therefore stress due to the difference in thermal expansion coefficient between the oxide layer 102 a made of tantalum oxide and the oxide layer 102 b made of niobium oxide arises during heat treatment process such as reflow soldering process. For this reason, there have arisen problems that theoxide layer 102 is likely to be peeled off from the anode lead 101 a and the base body 101 c and that cracks are likely to be generated inside of theoxide layer 102. As a result, there has arisen another problem that leakage current between thecathode 104 formed on theoxide layer 102 and theanode 101 is likely to be increased. - The present invention has been made in order to solve the problems described above, and it is therefore one object of the present invention to provide a solid electrolytic capacitor element or a solid electrolytic capacitor having low leakage current.
- Another object of the present invention is to provide a method for manufacturing the solid electrolytic capacitor element having low leakage current.
- In order to accomplish the above objects, the solid electrolytic capacitor element comprises: an oxide layer that is formed on an anode and contains niobium oxide; and a cathode formed on the oxide layer, wherein the anode has: an anode lead; a surface layer that is formed on the anode lead and contains niobium; and a base body that is formed on the surface layer and comprised of a porous sintered body containing niobium.
- In the solid electrolytic capacitor element according to the present invention, the anode has the anode lead and the base body containing niobium formed on the anode lead as described above, and therefore the oxide layer containing niobium oxide formed on the anode is also formed on a surface of the base body as well as on a surface of the anode lead at positions of spaces existing between the anode lead and the base body.
- Note that because the anode lead is formed thereon with the surface layer containing niobium, the oxide layer is formed on the surface layer containing niobium. That is, at the positions of the spaces, the oxide layer containing niobium oxide is formed on the surface layer and the base body both containing niobium.
- For this reason, the oxide layer containing niobium oxide is unlikely to be peeled off from the surface layer and the base body both containing niobium even during heat treatment process such as reflow soldering process, and cracks inside of the oxide layer are also unlikely to be generated. As a result, an increase in leakage current between the cathode formed on the oxide layer and the anode can be suppressed, so that a solid electrolytic capacitor element with low leakage current can easily be obtained.
- Preferably, in the above-described solid electrolytic capacitor element, the anode lead contains tantalum and the anode lead around which the base body is not formed has thereon a region not formed with the surface layer. In other words, the anode lead contains tantalum, a first region formed with the surface layer is formed on the anode lead, and a terminal is formed outside of the first region.
- Configuring as described allows a tantalum base material, which is more chemically stable than niobium and is unlikely to be oxidized, to be exposed in a region on the anode lead where the base body and the surface layer are not formed, and therefore an oxide coating is unlikely to be formed on the region during heat treatment process.
- This enables a satisfactory electrical connection between the anode lead and the anode terminal to be made when the anode terminal is connected onto the region, so that a solid electrolytic capacitor element with low equivalent series resistance (ESR) can be obtained.
- Preferably, in the solid electrolytic capacitor element, a film thickness of the surface layer falls within the range of 0.01 μm to 2 μm. A measurement of the film thickness of the surface layer is performed by an energy dispersive X-ray analysis (EDX) method.
- Configuring as described enables a stress arising between the anode lead and the oxide layer to be sufficiently suppressed and adhesiveness of the surface layer on the anode lead to be improved, and therefore peeling off of the oxide layer and cracks in it are unlikely to be generated. This enables leakage current to be further reduced.
- Also, the above-described surface layer suppresses a leakage current between the cathode and the anode to be less than 600 μA, and more preferably less than 300 μA.
- Further, the method for manufacturing the solid electrolytic capacitor element according to the present invention comprises the steps of forming on an anode lead a surface layer containing niobium; forming on the surface layer an anode having a base body comprised of a porous sintered body containing niobium; forming on the anode by anodization an oxide layer containing niobium oxide; and forming a cathode on the oxide layer.
- The step of forming the surface layer containing niobium may comprise cathodic reduction in molten lithium fluoride-sodium fluoride-potassium fluoride-potassium hexafluoroniobate (LiF-NaF-KF-K2NbF6) systems. Alternatively, the step of forming the surface layer containing niobium may comprise cathodic reduction in any of molten lithium fluoride-potassium fluoride-potassium hexafluoroniobate (LiF-KF-K2NbF6) systems or molten lithium fluoride-potassium hexafluoroniobate (LiF-K2NbF6) systems.
- In the method for manufacturing the solid electrolytic capacitor element, as described above, surfaces of the anode lead having the surface layer containing niobium and the base body that is formed on the anode lead and comprised of a porous sintered body containing niobium are formed thereon with the oxide layer containing niobium oxide, so that the oxide layer containing niobium oxide can be readily formed also at positions of spaces existing between the anode lead and the base body.
- For this reason, the oxide layer containing niobium oxide is unlikely to be peeled off from the surface layer and the base body both containing niobium even during heat treatment process such as reflow soldering process, and cracks inside of the oxide layer are also unlikely to be generated. As a result, an increase in leakage current between the cathode formed on the oxide layer and the anode can be suppressed, so that a solid electrolytic capacitor with low leakage current can easily be manufactured.
- Also, the solid electrolytic capacitor according to the present invention comprises: an oxide layer that is formed on an anode and contains niobium oxide; and a cathode formed on the oxide layer, wherein the anode has: an anode lead; a surface layer that is formed on the anode lead and contains niobium; and a base body that is formed on the surface layer and comprised of a porous sintered body containing niobium, the base body being, an anode terminal is formed on the anode, a cathode terminal is formed on the cathode, and a mold-packaging resin is formed such that respective edges of the anode terminal and the cathode terminal are led outside.
- For this reason, the oxide layer containing niobium oxide is unlikely to be peeled off from the surface layer and the base body both containing niobium even during heat treatment process such as reflow soldering process, and cracks inside of the oxide layer are also unlikely to be generated. As a result, an increase in leakage current between the cathode formed on the oxide layer and the anode can be suppressed, so that a solid electrolytic capacitor with low leakage current can easily be obtained.
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FIG. 1 is a cross-sectional view for illustrating a structure of a solid electrolytic capacitor according to Example 1 of the present invention. -
FIG. 2 is a cross-sectional view for illustrating a first step in a fabrication process of the solid electrolytic capacitor according to Example 1 of the present invention. -
FIG. 3 is a cross-sectional view for illustrating a second step in the fabrication process of the solid electrolytic capacitor according to Example 1 of the present invention. -
FIG. 4 is a cross-sectional view for illustrating a third step in the fabrication process of the solid electrolytic capacitor according to Example 1 of the present invention. -
FIG. 5 is a cross-sectional view for illustrating a fourth step in the fabrication process of the solid electrolytic capacitor according to Example 1 of the present invention. -
FIG. 6 is a cross-sectional view for illustrating a fifth step in the fabrication process of the solid electrolytic capacitor according to Example 1 of the present invention. -
FIG. 7 is a schematic cross-sectional view for illustrating a condition of an oxide layer near an anode lead in the solid electrolytic capacitor according to Example 1 of the present invention. -
FIG. 8 is a cross-sectional view for illustrating a structure of a conventional solid electrolytic capacitor. -
FIG. 9 is a cross-sectional view for illustrating a first step in a fabrication process of the conventional solid electrolytic capacitor. -
FIG. 10 is a cross-sectional view for illustrating a second step in the fabrication process of the conventional solid electrolytic capacitor. -
FIG. 11 is a cross-sectional view for illustrating a third step in the fabrication process of the conventional solid electrolytic capacitor. -
FIG. 12 is a cross-sectional view for illustrating a fourth step in the fabrication process of the conventional solid electrolytic capacitor. -
FIG. 13 is a cross-sectional view for illustrating a fifth step in the fabrication process of the conventional solid electrolytic capacitor. -
FIG. 14 is a schematic cross-sectional view for illustrating a condition of an oxide layer near an anode lead in the conventional solid electrolytic capacitor. - Examples of the present invention will hereinafter be described in reference to the drawings.
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FIG. 1 is a cross-sectional view for illustrating a structure of a solid electrolytic capacitor according to Example 1 of the present invention. - As shown in
FIG. 1 , in the rectangular block shaped solid electrolytic capacitor according to Example 1 of the present invention, ananode 1 comprises an anode lead 1 a made of tantalum, a surface layer 1 b made of niobium having a film thickness of approximately 0.1 μm formed on the anode lead 1 a and a rectangular block shaped base body 1 c with a size of approximately 3.3 mm×approx. 2.7 mm×approx. 1.7 mm comprised of a porous sintered body made from niobium particles having an average particle size of approximately 2 μm, and the anode lead 1 a is partially embedded in the base body 1 c. Also, the surface layer 1 b is not formed on an edge 1 d of the anode lead 1 a where the anode lead 1 a is not embedded in the base body 1 c, and therefore a tantalum base material is exposed there. In addition, the edge 1 d is one example of a “region where a surface layer is not formed” according to the present invention. - Onto the
anode 1, anoxide layer 2 made of niobium oxide is formed so as to cover an area surrounding theanode 1. Theoxide layer 2 functions as a so-called dielectric layer. - Onto the
oxide layer 2, an electricallyconductive polymer layer 3 made of polypyrrole is formed so as to cover an area surrounding theoxide layer 2. The electricallyconductive polymer layer 3 functions as a so-called electrolyte layer. Onto the electricallyconductive polymer layer 3, acathode 4 is formed, which is laminated with a first electrically conductive layer 4 a containing graphite particles formed so as to cover an area surrounding the electricallyconductive polymer layer 3 and a second electrically conductive layer 4 b containing silver particles formed so as to cover an area surrounding the first electrically conductive layer 4 a. - Onto the top surface of an area surrounding the
cathode 4, an electrically conductiveadhesive layer 5 is formed, onto which acathode terminal 6 is further formed. Also, the edge 1 d of the anode lead 1 a where the anode lead 1 a is not embedded in the base body 1 c is exposed from the surface layer 1 b, the base body 1 c and theoxide layer 2, and ananode terminal 7 is connected onto the edge 1 d. Further, a mold-packaging resin 8 is formed around thecathode 4, thecathode terminal 6 and theanode terminal 7 such that respective edges of thecathode terminal 6 and theanode terminal 7 can be led outside. The solid electrolytic capacitor according to Example 1 of the present invention is thus configured. - FIGS. 2 to 6 are cross-sectional views for illustrating a fabrication process of the solid electrolytic capacitor according Example 1 of the present invention. In reference to FIGS. 2 to 6, the fabrication process of the solid electrolytic capacitor having the structure illustrated above according to Example 1 of the present invention is now described.
- First, as shown in
FIG. 2 , the surface layer 1 b made of niobium having a film thickness of approximately 0.1 μm was formed on the anode lead 1 a by cathodically reducing the anode lead 1 a for approximately 3 minutes in lithium fluoride-sodium fluoride-potassium fluoride-potassium hexafluoroniobate (LiF-NaF-KF-K2NbF6) systems that had been heated at approximately 550° C. to be thereby molten. The film thickness of the surface layer 1 b may be identified by an energy dispersive X-ray analysis (EDX) method or the like. The cathodic reduction was performed without immersing one edge 1 d of the anode lead 1 a, whereby the tantalum base material was exposed at the edge 1 d. - Then, the
anode 1 comprising the anode lead 1 a and the rectangular block shaped base body 1 c with a size of approximately 3.3 mm×approx. 2.7 mm×approx. 1.7 mm comprised of a porous sintered body made from niobium particles having an average particle size of approximately 2 μm was formed. The base body 1 c was formed by heat treatment process in vacuum a molding comprised of niobium particles in which the other edge of the anode lead 1 a was embedded. - Subsequently, the
anode 1 was anodized in an approximately 0.5 wt. % phosphoric acid solution, which was held at approximately 60° C., by applying a constant voltage of approximately 10 V for approximately 8 hours, whereby theoxide layer 2 made of niobium oxide was formed so as to cover the area surrounding thebase body 1 as shown inFIG. 3 . - Subsequently, as shown in
FIG. 4 , the electricallyconductive polymer layer 3 made of polypyrrole was formed on theoxide layer 2 by polymerization or the like so as to cover the area surrounding theoxide layer 2. - Subsequently, as shown in
FIG. 5 , a graphite paste was coated onto the electricallyconductive polymer layer 3 so as to cover the area surrounding the electricallyconductive polymer layer 3, and then dried at approximately 80° C. for approximately 30 minutes to thereby form the first electrically conductive layer 4 a containing graphite particles. After that, a silver paste was coated on the first electrically conductive layer 4 a so as to cover the area surrounding the first electrically conductive layer 4 a, and then dried at approximately 170° C. for approximately 30 minutes to thereby form the second electrically conductive layer 4 b containing silver particles. This allowed thecathode 4, which was laminated with the first electrically conductive layer 4 a and the second electrically conductive layer 4 b, to be formed so as to cover the area surrounding the electricallyconductive polymer layer 3. - Subsequently, as shown in
FIG. 6 , after an electrically conductive adhesive had been coated in an amount of approximately 2 mg on thecathode terminal 6 made from iron foil of which a thickness was approximately 0.1 mm and a surface was nickel-plated, thecathode terminal 6 was bonded to the top surface of the area surrounding thecathode 4 through the electrically conductive adhesive. Further, drying the electrically conductive adhesive at approximately 60° C. for approximately 30 minutes allowed the electrically conductiveadhesive layer 5 to be formed, through which thecathode 4 and thecathode terminal 6 were interconnected. - Also, the
anode terminal 7 made from iron foil of which a thickness was approximately 0.1 mm and a surface was nickel-plated was welded onto the edge 1 d of the anode lead 1 a where the anode lead 1 a was exposed from the surface layer 1 b, the base body 1 c, and theoxide layer 2. - Finally, as shown in
FIG. 1 , the mold-packaging resin 8 was formed around thecathode 4, thecathode terminal 6 and theanode terminal 7 such that the respective edges of thecathode terminal 6 and theanode terminal 7 were able to be led outside. The solid electrolytic capacitor according to Example 1 was thus fabricated as shown inFIG. 1 . - In addition, in the present invention, a condition in which the
cathode terminal 6 and theanode terminal 7 are formed and the mold-packaging resin 8 is formed around thecathode 4, thecathode terminal 6 and theanode terminal 7 is referred to as a solid electrolytic capacitor, and also, a prior condition as an element in which the terminals have not been connected is referred to as a solid electrolytic capacitor element. -
FIG. 7 is a schematic cross-sectional view for illustrating a condition of the oxide layer near the anode lead in the solid electrolytic capacitor according to Example 1 of the present invention. Referring toFIG. 7 , in the solid electrolytic capacitor according to Example 1 of the present invention, theoxide layer 2 formed on theanode 1 is also formed on the surfaces of the surface layer 1 b and the base body 1 c at positions of spaces that exist between the anode lead 1 a and the base body 1 c due to the base body 1 c comprised of the porous sintered body. Because the surface layer 1 b and the base body 1 c contain niobium, theoxide layer 2 containing niobium oxide is unlikely to be peeled off from the surface layer 1 b and the base body 1 c even during heat treatment process such as reflow soldering process, and cracks inside of theoxide layer 2 are also unlikely to be generated. As a result, an increase in leakage current between thecathode 4 formed on theoxide layer 2 and theanode 1 can be suppressed, so that the leakage current can be decreased. - Also, in the above-described Example 1, the anode lead 1 a is made of tantalum and a tantalum base material is exposed at the edge 1 d of the anode lead 1 a where the anode lead 1 a is exposed from the base body 1 c and the
oxide layer 2, so that an oxide coating is unlikely to be formed on the edge 1 d. This enables a satisfactory electrical connection between the anode lead 1 a and theanode terminal 8 to be made when theanode terminal 8 is connected onto the edge 1 d, so that ESR can be reduced. - Further, in the above-described Example 1, because the
oxide layer 2 containing niobium oxide is formed by anodizing theanode 1 having the above configuration, theoxide layer 2 containing niobium oxide can readily be formed also on the surface layer 1 b and the base body 1 c both containing niobium at the positions of the spaces existing between the anode lead 1 a and the base body 1 c. For this reason, theoxide layer 2 containing niobium oxide is unlikely to be peeled off from the surface layer 1 b and the base body 1 c even during heat treatment process such as reflow soldering process, and cracks inside of theoxide layer 2 are also unlikely to be generated. As a result, an increase in leakage current between thecathode 4 formed on theoxide layer 2 and theanode 1 can be suppressed, so that a solid electrolytic capacitor with low leakage current can easily be manufactured. - As the next step, in order to examine an effect of Example 1 of the present invention, the following comparative experiments were performed.
- In Comparative Example 1, the conventional electrolytic capacitor shown in
FIG. 8 was fabricated. - In other word, in Comparative Example 1, the solid electrolytic capacitor similar to that in Example 1 was fabricated, except that the capacitor in Comparative Example 1 employed the anode lead made of tantalum onto which the surface layer in Example 1 was not formed.
- In Comparative Example 2, a solid electrolytic capacitor similar to that in Comparative Example 1 was fabricated, except that the capacitor in Comparative Example 2 employed an anode lead made of niobium, instead of the anode lead made of tantalum in Comparative Example 1.
- Also, leakage current measurements were performed on the solid electrolytic capacitors in the above Example 1, and Comparative Examples 1 and 2.
- In the leakage current measurements, after heat treatment process of each of the fabricated solid electrolytic capacitors had been performed at approximately 240° C. for approximately 5 minutes, a constant voltage of approximately 5 V was applied between the cathode terminal and the anode terminal and a current value observed approximately 20 seconds after the application was measured on each capacitor. Measurement results are listed in Table 1.
TABLE 1 Leakage current (μA) Example 1 200 Comparative Example 1 600 Comparative Example 2 800 - As listed in Table 1, it has turned out that the solid electrolytic capacitor in Example 1 exhibits a large reduction in leakage current in comparison with those in Comparative Examples 1 and 2.
- As the next step, an effect of a film thickness of the surface layer 1 b in the solid electrolytic capacitor in Example 1 of the present invention was examined.
- In other words, solid electrolytic capacitors similar to that in Example 1 were fabricated, except that a film thickness of the surface layer 1 b was varied in Example 2 by varying a time period for cathodically reducing the anode lead 1 a in molten LiF-NaF-KF-K2NbF6 systems in Example 1 in the range of approximately 10 seconds to approximately 2 hours 30 minutes as shown in Table 2.
- Similarly to the case of Example 1, a film thickness of the surface layer 1 b was measured by EDX and a leakage current was also measured. Measurement results are listed in Table 2.
TABLE 4 Cathodic reduction Surface layer Leakage time thickness (μm) current (μA) Example 2 10 seconds 0.005 560 Example 2 15 seconds 0.0075 480 Example 2 20 seconds 0.01 270 Example 2 2 minutes 0.05 230 Example 1 3 minutes 0.1 200 Example 2 15 minutes 0.5 200 Example 2 30 minutes 1.0 210 Example 2 1 hour 2.0 210 Example 2 1 hour 30 minutes 3.0 460 Example 2 2 hours 30 minutes 5.0 540 - As listed in Table 2, the film thickness of the surface layer 1 b is varied in the range of approximately 0.005 μm to approximately 5.0 μm, depending on the variation in the time period for the cathodic reduction, and in this range, any of the capacitors exhibits a lower leakage current than those in Comparative Examples 1 and 2. Also, it has turned out that in the case where the film thickness of the surface layer 1 b falls within the range of approximately 0.01 μm to approximately 2.0 μm, the leakage current is particularly low.
- In addition, the examples disclosed herein should be considered exemplary in all aspects, and not as a limitation on the present invention. The scope of the present invention is defined not by the above description of the examples but by the appended claims, and further includes meanings equivalent to the claims and any modifications within the scope of the claims.
- Also, in the above-described examples, the surface layer 1 b made of niobium was employed; however, the present invention is not limited to this, but the surface layer 1 b may contain another element such as tantalum, titanium, or nitrogen, besides niobium.
- For example, in the examples, the surface layer 1 b was formed by the cathodic reduction performed in molten LiF-NaF-KF-K2NbF6 systems; however, the present invention is not limited to this, but another molten salt containing niobium such as lithium fluoride-potassium fluoride-potassium hexafluoroniobate (LiF-KF-K2NbF6) systems or lithium fluoride-potassium hexafluoroniobate (LiF-K2NbF6) systems may be employed, or alternatively the layer may be formed by another thin film fabrication method. Also, after the fabrication of the surface layer 1 b by the use of one of above methods, a heat treatment may be performed in a nitrogen atmosphere.
- Further, in the above-described examples, the anode lead 1 a made of tantalum was employed; however, the present invention is not limited to this, but the anode lead 1 a may be comprised of, for example, a tantalum alloy containing another metal, such as niobium or titanium, or another element such as nitrogen, in addition to tantalum.
- Still further, in the above-described examples, the porous sintered body made from niobium particles was employed as the base body 1 c; however, the present invention is not limited to this, but the base body 1 c may be comprised of a porous sintered body made from, for example, niobium alloy particles containing another metal such as tantalum or titanium, or another element such as nitrogen, in addition to niobium.
- Still further, in the above-described examples, the
oxide layer 2 was formed by anodizing theanode 1 in an aqueous solution; however, the present invention is not limited to this, but theoxide layer 2 may be formed by another method. - Still further, in the above-described examples, the electrically
conductive polymer layer 3 made of polypyrrole was formed; however, the present invention is not limited to this, but another electrically conductive polymer such as polythiophene or polyaniline may be employed, or alternatively another electrically conductive material such as manganese oxide may be employed.
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US20070232012A1 (en) * | 2006-03-31 | 2007-10-04 | Sanyo Electric Co., Ltd. | Solid electrolytic capacitor |
US20220076895A1 (en) * | 2018-11-29 | 2022-03-10 | KYOCERA AVX Components Corporation | Solid Electrolytic Capacitor Containing A Sequential Vapor-Deposited Dielectric Film |
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JP4776522B2 (en) * | 2006-12-20 | 2011-09-21 | 三洋電機株式会社 | Solid electrolytic capacitor |
JP2010251716A (en) * | 2009-03-25 | 2010-11-04 | Rohm Co Ltd | Solid electrolytic capacitor, and method of manufacturing the same |
KR20130027785A (en) * | 2011-09-08 | 2013-03-18 | 삼성전기주식회사 | Tantalum capacitor |
CN110246695B (en) * | 2015-02-27 | 2021-10-12 | 松下知识产权经营株式会社 | Solid electrolytic capacitor |
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JPS5441456A (en) * | 1977-09-08 | 1979-04-02 | Nippon Electric Co | Method of manufacturing solid electrolyte condenser |
JPH04159705A (en) * | 1990-10-23 | 1992-06-02 | Nec Corp | Solid-state electrolytic condenser |
JPH05283297A (en) * | 1992-03-31 | 1993-10-29 | Nippon Steel Corp | Chip-shaped solid electrolytic capacitor |
JP3196832B2 (en) * | 1998-05-15 | 2001-08-06 | 日本電気株式会社 | Solid electrolytic capacitor and method of manufacturing the same |
JP3973299B2 (en) | 1998-08-26 | 2007-09-12 | 昭和電工株式会社 | Capacitor |
JP4422258B2 (en) * | 1999-11-30 | 2010-02-24 | 昭和電工株式会社 | Capacitor |
JP3984519B2 (en) * | 2001-08-22 | 2007-10-03 | 昭和電工株式会社 | Capacitor |
JP2004014667A (en) * | 2002-06-05 | 2004-01-15 | Matsushita Electric Ind Co Ltd | Solid electrolytic capacitor |
JP2004247550A (en) * | 2003-02-14 | 2004-09-02 | Matsushita Electric Ind Co Ltd | Solid electrolytic capacitor |
JP4131709B2 (en) * | 2003-03-28 | 2008-08-13 | 三洋電機株式会社 | Manufacturing method of solid electrolytic capacitor |
JP4360680B2 (en) * | 2003-11-10 | 2009-11-11 | 昭和電工株式会社 | Niobium powder for capacitors, sintered niobium and capacitors |
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2006
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US20070232012A1 (en) * | 2006-03-31 | 2007-10-04 | Sanyo Electric Co., Ltd. | Solid electrolytic capacitor |
US20080084652A1 (en) * | 2006-03-31 | 2008-04-10 | Sanyo Electric Co., Ltd. | Solid Electrolytic Capacitor |
US7362561B2 (en) * | 2006-03-31 | 2008-04-22 | Sanyo Electric Co., Ltd. | Solid electrolytic capacitor |
US7471504B2 (en) * | 2006-03-31 | 2008-12-30 | Sanyo Electric Co., Ltd. | Solid electrolytic capacitor |
US20220076895A1 (en) * | 2018-11-29 | 2022-03-10 | KYOCERA AVX Components Corporation | Solid Electrolytic Capacitor Containing A Sequential Vapor-Deposited Dielectric Film |
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US7177141B1 (en) | 2007-02-13 |
CN1905103A (en) | 2007-01-31 |
JP2011193035A (en) | 2011-09-29 |
JP5232899B2 (en) | 2013-07-10 |
CN1905103B (en) | 2012-04-18 |
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