WO2005020258A1 - Chip solid electrolyte capacitor and production method of the same - Google Patents
Chip solid electrolyte capacitor and production method of the same Download PDFInfo
- Publication number
- WO2005020258A1 WO2005020258A1 PCT/JP2004/012228 JP2004012228W WO2005020258A1 WO 2005020258 A1 WO2005020258 A1 WO 2005020258A1 JP 2004012228 W JP2004012228 W JP 2004012228W WO 2005020258 A1 WO2005020258 A1 WO 2005020258A1
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- WIPO (PCT)
- Prior art keywords
- anode
- solid electrolyte
- chip solid
- capacitor
- electrolyte capacitor
- Prior art date
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- 239000003990 capacitor Substances 0.000 title claims abstract description 174
- 239000007784 solid electrolyte Substances 0.000 title claims abstract description 103
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 13
- 238000000465 moulding Methods 0.000 claims abstract description 12
- 239000002184 metal Substances 0.000 claims description 52
- 229910052751 metal Inorganic materials 0.000 claims description 49
- 239000004065 semiconductor Substances 0.000 claims description 46
- 239000000758 substrate Substances 0.000 claims description 26
- 229920005989 resin Polymers 0.000 claims description 25
- 239000011347 resin Substances 0.000 claims description 25
- 239000000956 alloy Substances 0.000 claims description 19
- 229910045601 alloy Inorganic materials 0.000 claims description 19
- 238000000034 method Methods 0.000 claims description 17
- 239000002322 conducting polymer Substances 0.000 claims description 15
- 229920001940 conductive polymer Polymers 0.000 claims description 15
- 229910052782 aluminium Inorganic materials 0.000 claims description 14
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 14
- 125000004432 carbon atom Chemical group C* 0.000 claims description 12
- YADSGOSSYOOKMP-UHFFFAOYSA-N dioxolead Chemical compound O=[Pb]=O YADSGOSSYOOKMP-UHFFFAOYSA-N 0.000 claims description 10
- 239000000463 material Substances 0.000 claims description 10
- 238000007747 plating Methods 0.000 claims description 10
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 9
- 125000000217 alkyl group Chemical group 0.000 claims description 9
- 125000004122 cyclic group Chemical group 0.000 claims description 9
- 239000011888 foil Substances 0.000 claims description 9
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 9
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical group [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 claims description 9
- 239000010936 titanium Substances 0.000 claims description 9
- 229910052719 titanium Inorganic materials 0.000 claims description 9
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 8
- 229910052802 copper Inorganic materials 0.000 claims description 8
- 239000010949 copper Substances 0.000 claims description 8
- 229910052757 nitrogen Inorganic materials 0.000 claims description 8
- 229910052715 tantalum Inorganic materials 0.000 claims description 8
- 150000001875 compounds Chemical class 0.000 claims description 7
- 239000007769 metal material Substances 0.000 claims description 7
- 239000010955 niobium Substances 0.000 claims description 7
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 claims description 7
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 6
- QXYJCZRRLLQGCR-UHFFFAOYSA-N dioxomolybdenum Chemical compound O=[Mo]=O QXYJCZRRLLQGCR-UHFFFAOYSA-N 0.000 claims description 6
- 239000002019 doping agent Substances 0.000 claims description 6
- 238000010030 laminating Methods 0.000 claims description 6
- NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Chemical compound O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 claims description 6
- 229910044991 metal oxide Inorganic materials 0.000 claims description 6
- 150000002739 metals Chemical class 0.000 claims description 6
- 229910052758 niobium Inorganic materials 0.000 claims description 6
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 6
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 6
- DZKDPOPGYFUOGI-UHFFFAOYSA-N tungsten(iv) oxide Chemical compound O=[W]=O DZKDPOPGYFUOGI-UHFFFAOYSA-N 0.000 claims description 6
- 229920000642 polymer Polymers 0.000 claims description 5
- -1 polyoxyphenylene Polymers 0.000 claims description 5
- 239000000203 mixture Substances 0.000 claims description 4
- 229920000123 polythiophene Polymers 0.000 claims description 4
- 229920006395 saturated elastomer Polymers 0.000 claims description 4
- 238000006467 substitution reaction Methods 0.000 claims description 4
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 claims description 3
- 229920001609 Poly(3,4-ethylenedioxythiophene) Polymers 0.000 claims description 3
- 239000004734 Polyphenylene sulfide Substances 0.000 claims description 3
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 3
- 125000003545 alkoxy group Chemical group 0.000 claims description 3
- 229920001577 copolymer Polymers 0.000 claims description 3
- 229910052742 iron Inorganic materials 0.000 claims description 3
- 229910000484 niobium oxide Inorganic materials 0.000 claims description 3
- 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 description 3
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims description 3
- 229920000767 polyaniline Polymers 0.000 claims description 3
- 229920000414 polyfuran Polymers 0.000 claims description 3
- 229920000069 polyphenylene sulfide Polymers 0.000 claims description 3
- 229920000128 polypyrrole Polymers 0.000 claims description 3
- 229930195734 saturated hydrocarbon Natural products 0.000 claims description 3
- 229910000679 solder Inorganic materials 0.000 claims description 3
- 125000001424 substituent group Chemical group 0.000 claims description 3
- 238000005486 sulfidation Methods 0.000 claims description 3
- 229910052717 sulfur Inorganic materials 0.000 claims description 3
- 125000004434 sulfur atom Chemical group 0.000 claims description 3
- UGNWTBMOAKPKBL-UHFFFAOYSA-N tetrachloro-1,4-benzoquinone Chemical compound ClC1=C(Cl)C(=O)C(Cl)=C(Cl)C1=O UGNWTBMOAKPKBL-UHFFFAOYSA-N 0.000 claims description 3
- PCCVSPMFGIFTHU-UHFFFAOYSA-N tetracyanoquinodimethane Chemical compound N#CC(C#N)=C1C=CC(=C(C#N)C#N)C=C1 PCCVSPMFGIFTHU-UHFFFAOYSA-N 0.000 claims description 3
- 229910052718 tin Inorganic materials 0.000 claims description 3
- 125000004417 unsaturated alkyl group Chemical group 0.000 claims description 3
- 239000010410 layer Substances 0.000 description 54
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 11
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 10
- 230000032683 aging Effects 0.000 description 9
- 230000000052 comparative effect Effects 0.000 description 9
- 229910052709 silver Inorganic materials 0.000 description 9
- 239000004332 silver Substances 0.000 description 9
- WABPQHHGFIMREM-UHFFFAOYSA-N lead(0) Chemical compound [Pb] WABPQHHGFIMREM-UHFFFAOYSA-N 0.000 description 8
- 239000000243 solution Substances 0.000 description 8
- 239000000843 powder Substances 0.000 description 7
- 238000005245 sintering Methods 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
- 229910052799 carbon Inorganic materials 0.000 description 5
- 229910052759 nickel Inorganic materials 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 4
- 239000003822 epoxy resin Substances 0.000 description 4
- 229920000647 polyepoxide Polymers 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000008151 electrolyte solution Substances 0.000 description 3
- 150000004706 metal oxides Chemical class 0.000 description 3
- 239000011148 porous material Substances 0.000 description 3
- 238000007711 solidification Methods 0.000 description 3
- 230000008023 solidification Effects 0.000 description 3
- 239000002344 surface layer Substances 0.000 description 3
- 239000004925 Acrylic resin Substances 0.000 description 2
- 229920000178 Acrylic resin Polymers 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 229920000180 alkyd Polymers 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 2
- 239000012298 atmosphere Substances 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 230000002950 deficient Effects 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 238000007598 dipping method Methods 0.000 description 2
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 2
- 229910052737 gold Inorganic materials 0.000 description 2
- 239000010931 gold Substances 0.000 description 2
- 229940046892 lead acetate Drugs 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000005011 phenolic resin Substances 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 238000007493 shaping process Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- YMMGRPLNZPTZBS-UHFFFAOYSA-N 2,3-dihydrothieno[2,3-b][1,4]dioxine Chemical compound O1CCOC2=C1C=CS2 YMMGRPLNZPTZBS-UHFFFAOYSA-N 0.000 description 1
- GKWLILHTTGWKLQ-UHFFFAOYSA-N 2,3-dihydrothieno[3,4-b][1,4]dioxine Chemical compound O1CCOC2=CSC=C21 GKWLILHTTGWKLQ-UHFFFAOYSA-N 0.000 description 1
- JAJIPIAHCFBEPI-UHFFFAOYSA-N 9,10-dioxoanthracene-1-sulfonic acid Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2S(=O)(=O)O JAJIPIAHCFBEPI-UHFFFAOYSA-N 0.000 description 1
- MMNWSHJJPDXKCH-UHFFFAOYSA-N 9,10-dioxoanthracene-2-sulfonic acid Chemical compound C1=CC=C2C(=O)C3=CC(S(=O)(=O)O)=CC=C3C(=O)C2=C1 MMNWSHJJPDXKCH-UHFFFAOYSA-N 0.000 description 1
- USFZMSVCRYTOJT-UHFFFAOYSA-N Ammonium acetate Chemical compound N.CC(O)=O USFZMSVCRYTOJT-UHFFFAOYSA-N 0.000 description 1
- 239000005695 Ammonium acetate Substances 0.000 description 1
- 229910000881 Cu alloy Inorganic materials 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 229940043376 ammonium acetate Drugs 0.000 description 1
- 235000019257 ammonium acetate Nutrition 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000001413 cellular effect Effects 0.000 description 1
- 239000003985 ceramic capacitor Substances 0.000 description 1
- 238000005234 chemical deposition Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 230000020169 heat generation Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910052734 helium Inorganic materials 0.000 description 1
- 239000001307 helium Substances 0.000 description 1
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
- 150000003949 imides Chemical class 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 239000011812 mixed powder Substances 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 230000035882 stress Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 238000001721 transfer moulding Methods 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
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
- H01G2/00—Details of capacitors not covered by a single one of groups H01G4/00-H01G11/00
- H01G2/10—Housing; Encapsulation
- H01G2/103—Sealings, e.g. for lead-in wires; Covers
-
- 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
- H01G9/022—Electrolytes; Absorbents
- H01G9/025—Solid electrolytes
- H01G9/028—Organic semiconducting electrolytes, e.g. TCNQ
-
- 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
- H01G9/15—Solid electrolytic capacitors
Definitions
- Provisional application Serial No. 60/498,596 filed August 29, 2003 under the provision of 35 U.S.C. Section 111(b), pursuant to 35 U.S.C. Section 119(e) (1) .
- the present invention relates to a chip solid electrolyte capacitor having good properties such as large capacitance per unit volume and low equivalent series resistance (ESR) and a production method of the same.
- ESR equivalent series resistance
- a capacitor in the periphery of central processing unit (CPU) used for personal computers and the like is required to have high capacitance and low ESR so as to suppress the fluctuation of voltage and reduce the heat generation at the passing of a high ripple current.
- a chip aluminum solid electrolyte capacitor and a chip tantalum solid electrolyte capacitor are known .
- the chip solid electrolyte capacitor is manufactured by producing a solid electrolyte capacitor element where an oxide dielectric film layer, a semiconductor layer and an electrically conducting layer are sequentially stacked to form a cathode part on a surface excluding the anode part at one end of an anode substrate comprising a valve-acting metal foil having fine pores in the surface layer, an anode substrate comprising a sintered body having fine pores in the inside, or an anode substrate comprising this sintered body to which a metal wire is connected, connecting a part of the anode part and a part of the cathode part to an anode terminal and a cathode terminal, respectively, and molding the capacitor element with a jacket while partially leaving outside a part of the both anode and cathode terminals .
- a conventionally known chip solid electrolyte capacitor has a structure that a cathode part (3) of a solid electrolyte capacitor element (1) is provided by stacking a semiconductor layer and an electrically conducting layer in this order on a sintered body comprising a valve-acting metal having formed on the surface thereof an oxide dielectric film layer, a part of the cathode part is placed on a cathode terminal (4), a part of the anode lead (2) (anode part) connected to the sintered body is placed on an anode terminal (5), each part is electrically and mechanically connected, and the entirety is sealed with a jacketing resin while leaving outside only respective bottom faces of the anode and cathode terminals (4a, 5a) to form a jacket (6) (see, JP-A- 2003-68576 (the term "JP-A" as used herein means an "unexamined published Japanese patent application”)) (in Fig.
- FIG. 1 is a perspective view of a chip solid electrolyte capacitor or the present invention, showing the state where a part of the anode part and a part of the cathode part of a solid electrolyte capacitor element having an anode lead (anode part) are laid on each of the anode and cathode terminals.
- Fig. 2 is a plane cross-sectional view (A) and a side cross-sectional view (B) of the solid electrolyte capacitor of Fig. 1.
- Fig. 3 is a perspective view of a conventional chip solid electrolyte capacitor.
- the present invention relates to a chip solid electrolyte capacitor, a production method of the same and electronic devices using the chip solid electrolyte capacitor, which are described below. 1.
- a chip solid electrolyte capacitor obtained by connecting a part of the anode part and a part of the cathode part of a capacitor element to an anode terminal and a cathode terminal, respectively, and jacket-molding the capacitor element excluding a part or the whole of respective bottom faces or bottom and side faces of the anode and cathode terminals, wherein the connection face of the cathode terminal to the capacitor element is larger than the entire face of the capacitor element in the side connected to the cathode terminal.
- valve-acting metal or electrically conducting oxide is tantalum, aluminum, niobium, titanium, an alloy mainly comprising such a valve- acting metal or niobium oxide, or a mixture of two or more members selected from these valve-acting metals, alloys and electrically conducting oxides.
- the organic semiconductor is at least one member selected from an organic semiconductor comprising benzopyrroline tetramer and chloranil, an organic semiconductor mainly comprising tetrathiotetracene, an organic semiconductor mainly comprising tetracyanoquino- dimethane, and an organic semiconductor mainly comprising an electrically conducting polymer obtained by doping a dopant to a polymer containing a repeating unit represented by the following formula (1) or (2):
- R 1 to R 4 each independently represents a hydrogen atom, an alkyl group having from 1 to 6 carbon atoms or an alkoxy group having from 1 to 6 carbon atoms
- X represents an oxygen atom, a sulfur atom or a nitrogen atom
- R 5 is present only when X is a nitrogen atom, and represents a hydrogen atom or an alkyl group having from 1 to 6 carbon atoms
- each of the pairs of R 1 and R 2 , and R 3 and R 4 may combine with each other to form a cyclic structure.
- R 6 and R 7 each independently represents a hydrogen atom, a linear or branched, saturated or unsaturated alkyl group having from 1 to 6 carbon atoms, or a substituent for forming at least one 5-, 6- or 7-membered saturated hydrocarbon cyclic structure containing two oxygen atoms when the alkyl groups are combined with each other at an arbitrary position, and the cyclic structure includes a structure having a vinylene bond which may be substituted, and a phenylene structure which may be substituted. 18.
- the inorganic semiconductor is at least one compound selected from molybdenum dioxide, tungsten dioxide, lead dioxide and manganese dioxide. 21.
- Fig. 1 is a schematic view (perspective view) showing one example of the chip solid electrolyte capacitor of the present invention
- Fig. 2(A) is a plane cross-sectional view of Fig. 1
- Fig. 2(B) is a side cross-sectional view (in Figs. 1 and 2, the portions of both anode and cathode terminals are drawn by exaggerating the size) .
- the chip solid electrolyte capacitor of this example has a structure that a cathode part (3) of a solid electrolyte capacitor element (1) is formed by stacking an oxide dielectric layer, a semiconductor layer and an electrically conducting layer in this order on a surface of an anode substrate comprising a valve-acting metal or an electrically conducting oxide and being connected with an anode lead (2), a part of the cathode part is placed on a cathode terminal (4), a part of the anode part lead (2) is placed on an anode terminal (5), each part is electrically and mechanically connected, and then the capacitor element is jacketed (6) by resin molding while leaving outside bottom faces (4a, 4b) and side face (4c) of the both anode and cathode terminals.
- the capacitor element for use in the present invention is produced based on an anode substrate comprising a valve-acting metal or an electrically conducting oxide.
- the valve-acting metal or electrically conducting oxide include tantalum, aluminum, niobium, titanium, an alloy mainly comprising such a valve-acting metal or niobium oxide, and a mixture of two or more members selected from these valve-acting metals, alloys and electrically conducting oxides.
- the valve-acting metal, alloy, electrically conducting compound or the like may be used after subjecting a part thereof to at least one treatment selected from carbidation, phosphation, boronation, nitridation and sulfidation.
- the anode substrate for use in the present invention is a valve-acting metal foil or sheet having fine pores in the surface layer or a sintered body obtained by shaping the powder of valve-acting metal or electrically conducting oxide and then sintering the shaped article.
- the surface area of the sintered body can be varied by appropriately selecting the shaping pressure and sintering conditions (temperature and time) . After the sintering, the sintered body surface may be chemically and/or electrically etched to further increase the surface area of the sintered body.
- a part of the anode substrate is used as an anode part. A distal end of the anode substrate may be assigned to the anode part or as shown in Fig.
- a metal wire (2) or foil may be connected to a part of the anode substrate and used as the anode part.
- the metal wire (or metal foil) may be connected after the sintered body is produced, or a part of the metal wire (or metal foil) may be embedded at the molding before the production of the sintered body and then sintered, thereby making a connection.
- Examples of the kind of the metal wire (or metal foil) include tantalum, niobium, aluminum, titanium, alloys mainly comprising such a metal, and these metals and alloys which are partially oxidized and/or nitrided.
- the diameter of the metal wire is usually 1 mm or less and in the case of a metal foil, the thickness is usually 1 mm or less.
- the anode part and the remaining part of the anode substrate may be insulated by attaching an insulating resin like a hair band to the boundary therebetween before forming the semiconductor layer.
- the oxide dielectric film layer which is formed on the entirety or part of the anode substrate surface excluding the anode part in the present invention include a dielectric layer mainly comprising at least one member selected from metal oxides such as Ta 2 0 5 , A1 2 0 3 , Ti0 2 and Nb 2 0 5 .
- the dielectric layer can be obtained by electrochemically forming the anode substrate in an electrolytic solution.
- a dielectric layer obtained by mixing a dielectric layer mainly comprising at least one member selected from metal oxides and a dielectric layer for use in ceramic capacitors may be used (WO00/75943) .
- Representative examples of the semiconductor layer which is formed on the dielectric layer in the present invention include at least one compound selected from organic semiconductors and inorganic semiconductors.
- organic semiconductors include an organic semiconductor comprising benzopyrroline tetramer and chloranil, an organic semiconductor mainly comprising tetrathiotetracene, an organic semiconductor mainly comprising tetracyanoquinodimethane, and an organic semiconductor mainly comprising an electrically conducting polymer obtained by doping a dopant to a polymer containing a repeating unit represented by the following formula (1) or (2) :
- R 1 to R 4 each independently represents a hydrogen atom, an alkyl group having from 1 to 6 carbon atoms or an alkoxy group having from 1 to 6 carbon atoms
- X represents an oxygen atom, a sulfur atom or a nitrogen atom
- R 5 is present only when X is a nitrogen atom and represents a hydrogen atom or an alkyl group having from 1 to 6 carbon atoms
- each of the pairs of R 1 and R 2 , and R 3 and R 4 may combine with each other to form a cyclic structure.
- Preferred examples of the electrically conducting polymer containing a repeating unit represented by formula (1) include an electrically conducting polymer containing a structure unit represented by the following formula (3) as a repeating unit:
- R 6 and R 7 each independently represents a hydrogen atom, a linear or branched, saturated or unsaturated alkyl group having from 1 to 6 carbon atoms, or a substituent for forming at least one 5-, 6- or 7-membered saturated hydrocarbon cyclic structure containing two oxygen atoms when the alkyl groups are combined with each other at an arbitrary position.
- the cyclic structure includes a structure having a vinylene bond which may be substituted, and a phenylene structure which may be substituted.
- the electrically conducting polymer containing such a chemical structure is electrically charged and a dopant is doped thereto.
- known dopants can be used without limitation.
- Examples of the polymer containing a repeating unit represented by formula (1), (2) or (3) include polyaniline, polyoxyphenylene, polyphenylene sulfide, polythiophene, polyfuran, polypyrrole, polymethylpyrrole, and substitution derivatives and copolymers thereof.
- preferred are polypyrrole, polythiophene and substitution derivatives thereof (e.g., poly (3, 4-ethylenedioxythiophene) ) .
- Specific examples of the inorganic semiconductors include at least one compound selected from molybdenum dioxide, tungsten dioxide, lead dioxide and manganese dioxide, etc.
- the capacitor produced can have a small ESR value and this is preferred.
- conventionally known methods such as a method using electrolytic polymerization (see, JP-A-60-37114) , method using electrolytic polymerization of an anode substrate treated with an oxidizing agent (see, Japanese Patent No. 2,054,506), and method using chemical deposition (see, Japanese Patent No. 2,044,334) may be employed.
- an electrically conducting layer is provided on the semiconductor layer formed by the above-described method or the like.
- the electrically conducting layer can be formed, for example, by the solidification of electrically conducting paste, plating, vapor deposition of metal, or adhesion of heat-resistant electrically conducting resin film.
- Preferred examples of the electrically conducting paste include silver paste, copper paste, aluminum paste, carbon paste and nickel paste, and these may be used individually or in combination of two or more thereof. In the case of using two or more pastes, the pastes may be mixed or may be superposed one on another as separate layers .
- the electrically conducting paste applied is then solidified by allowing it to stand in air or under heating.
- the electrically conducting paste mainly comprises resin and electrically conducting powder such as metal.
- a solvent for dissolving the resin or a hardening agent for the resin is added, and the solvent dissipates at the time of solidification.
- the resin various known resins are used, such as alkyd resin, acrylic resin, epoxy resin, phenol resin, imide resin, fluororesin, ester resin, imidamide resin, amide resin and styrene resin.
- the electrically conducting powder at least one member selected from powder of silver, copper, aluminum, gold, carbon, nickel or an alloy mainly comprising such a metal, coated powder having such a metal on the surface layer, and mixed powder thereof is used. The content of the electrically conducting powder is usually from 40 to 97 mass?.
- the electrically conducting paste may be used after mixing thereto powder of the above- described electrically conducting polymer or metal oxide for forming the semiconductor layer.
- the plating include nickel plating, copper plating, silver plating and aluminum plating.
- the metal vapor-deposited include aluminum, nickel, copper and silver.
- an electrically conducting layer is formed by stacking carbon paste and silver paste in this order on the anode substrate having formed thereon the semiconductor layer.
- a solid electrolyte capacitor element where a cathode part is formed by stacking layers up to the electrically conducting layer on the anode substrate is produced.
- a part of the anode part and a part of the cathode part of the solid electrolyte capacitor element are connected to an anode terminal and a cathode terminal respectively, which are described later, and thereafter, the capacitor element is sealed with a jacket while leaving outside a part or the whole of the bottom face or bottom and side faces of each terminal, whereby a chip solid electrolyte capacitor is produced.
- the top face (the face which actually comes into contact with the capacitor element) of the cathode terminal is the same or larger in the size than the cathode terminal-connected face of the solid electrolyte capacitor element and it is preferable that the bottom face parts of both the anode and cathode terminals have nearly the same size.
- the term "cathode terminal-connected face of the solid electrolyte capacitor element" means the entire face in the side connected to the cathode terminal out of the faces of the capacitor element in which a cathode layer is formed.
- the produced solid electrolyte capacitor can have a minimum ESR value. Furthermore, in the present invention, only the sizes of top and bottom faces of the cathode terminal are changed but no extra material of limiting the height of a substrate as in the capacitor of JP-A-8-148386 publication is used and therefore, the size in the height direction of the capacitor element enclosed in the jacket of the chip solid electrolyte capacitor need not be decreased, so that the capacitance of the capacitor can be maximized.
- the cathode terminal differing in the shape between top and bottom faces can be produced by working a metal material, but in the case of simultaneously producing a large number of chip solid electrolyte capacitors, the anode and cathode terminals are usually produced from a lead frame comprising a repeated pattern of anode and cathode terminals and after jacketing, cut at predetermined positions to be made into desired shapes. Therefore, in order to facilitate the cutting, for example, a metal having a predetermined shape may be laminated on a flat lead frame having a uniform thickness, so that the lead frame can have a large thickness only in the portions corresponding to the anode and cathode terminals.
- a method for producing the thinner part of the lead frame a method of making the desired part thin by pressing may be used.
- the material of the anode and cathode terminals for example, iron, copper, aluminum or an alloy mainly comprising such a metal is used.
- Each of the anode and cathode terminals may be partially or entirely plated with solder, tin, titanium, silver, gold or the like.
- a primer plating such as nickel or copper may be provided.
- different materials may be used for the anode and cathode terminals so as to cope with the diversification of sound quality when using the produced chip solid electrolyte capacitor for an audio device.
- the bottom face parts of the anode and cathode terminals are made to have nearly the same size, this ensures compatibility with the bottom face part of conventional chip solid electrolyte capacitors and the land shape of a circuit board where the capacitor is mounted need not be changed.
- multiple solid electrolyte capacitor elements may be placed on the anode and cathode terminals and in this case, the size of the top face of the cathode terminal may be sufficient if it is larger than the cathode terminal-connected faces of the multiple capacitor elements .
- the solid electrolyte capacitor element of the present invention is jacketed, for example, with a resin mold, resin case or metallic jacket case and thereby, can be completed as a capacitor product for various uses.
- a chip solid electrolyte capacitor jacketed with a resin mold is preferred, because reduction in the size and in the cost can be simply achieved.
- a known resin for use in the molding of a solid electrolyte capacitor such as epoxy resin, phenol resin and alkyd resin, can be employed.
- Each resin is preferably a low-stress resin, so that the molding stress on the capacitor element generated at the molding can be mitigated.
- a transfer machine is preferably used for the production machine for performing the molding with resin.
- the thus-produced solid electrolyte capacitor may be subjected to an aging treatment so as to repair the thermal and/or physical deterioration of the dielectric layer, which is caused at the formation of electrically conducting layer or at the jacketing.
- the aging is performed by applying a predetermined voltage (usually, within two times the rated voltage) to the solid electrolyte capacitor.
- the optimal values of aging time and temperature vary depending on the kind and capacitance of capacitor and the rated voltage and therefore, are determined by previously performing an experiment, but the aging time is usually from several minutes to several days and the aging temperature is usually 300°C or less by taking account of heat deterioration of the voltage-applying jig.
- the aging may be performed in an air atmosphere or a gas atmosphere such as argon, nitrogen or helium and may be performed under reduced pressure, atmospheric pressure or applied pressure, but when the aging is performed while supplying water vapor or after water vapor is supplied, the stabilization of a dielectric layer sometimes proceeds.
- Examples of the method for supplying the water vapor include a method of supplying water vapor from a water reservoir placed in the aging furnace by using the heat.
- the method of applying a voltage it can be designed to pass an arbitrary current such as direct current, alternating current having an arbitrary waveform, alternating current superposed on direct current and pulse current. It is also possible to once stop the voltage application on the way of aging and again apply a voltage.
- the chip solid electrolyte capacitor produced in the present invention can be preferably used for circuits requiring a high-capacitance and low ESR capacitor, such as a central processing circuit and a power source circuit. These circuits can be used in various digital devices such as a personal computer, server, camera, game machine, DVD equipment, AV equipment and cellular phone, and electronic devices such as various power sources.
- the chip solid electrolyte capacitor produced in the present invention has a high capacitance and good ESR performance and therefore, by using this chip solid electrolyte capacitor, electronic circuits and electronic devices having high reliability can be obtained.
- the present invention provides a chip solid electrolyte capacitor in which the connection face of the cathode terminal to the capacitor element is larger than the entire face of the capacitor element in the side connected to the cathode terminal and the bottom face parts of the cathode and anode terminals have nearly the same size and which is obtained by jacket-molding the capacitor element while leaving outside a part of the bottom face or bottom and side faces of the anode and cathode terminals. According to the present invention, a chip solid electrolyte capacitor with large capacitance and good ESR can be obtained.
- Example 1 and Comparative Example 1 By using tantalum powder having CV (product of capacitance and electrochemical voltage) of 130,000 ⁇ F «V/g, sintered bodies in a size of 4.5x0.95x3.0 mm were produced (sintering temperature: 1,300°C, sintering time: 20 minutes, density of the sintered body: 6.3 g/cm 3 , Ta lead wire: 0.24 mm ⁇ ; a part of the Ta lead wire was embedded in the sintered body to run in parallel to the longitudinal direction of the 4.5 mm dimension and the lead wire part protruded from the sintered body was used as the anode part) .
- CV product of capacitance and electrochemical voltage
- the sintered body to serve as the anode excluding a part of the lead wire was dipped in an aqueous 1% phosphoric acid solution and electrochemically formed at 80°C for 8 hours by applying a voltage of 9 V between the anode and a Ta plate electrode as the cathode to form an oxide dielectric film layer composed of Ta 2 0 5 .
- the solid electrolyte capacitor was jacketed with epoxy resin by transfer molding while leaving outside all of bottom faces and side faces of the anode and cathode both terminals and the lead frame was cut at a flat part of the lead frame, namely, at the side face of the jacketed body to produce a chip solid electrolyte capacitor in a size of 7.3x4.3x1.8 mm (Example 1) .
- a chip solid electrolyte capacitor was produced in the same manner as in Example 1 except that in the end part of the lead frame on which the cathode part of the capacitor element was to be laid in Example 1, a metal strip having a width of 3.4 mm, a length of 1.4 mm and a thickness of 100 ⁇ m and being made of the same material as that of the lead frame was welded while aligning the width to come flush with the distal end (in this case, when coplanarly projected, a gap of 4.5 mm was present between the pair of the end parts) (Comparative Example 1) .
- Example 2 and Comparative Example 2 By using 0.048 g of partially nitrided niobium powder (nitrogen amount: 10,000 ppm, total oxygen amount: 91,000 ppm resulting from natural oxidation of the surface) having
- the sintered body was dipped in an electrolytic solution of water and 20% ethylene glycol, where ethylenedioxythiophene (used in the form of an aqueous solution having a monomer concentration lower than the saturated concentration) and anthraquinone- sulfonic acid were dissolved, and for forming a semiconductor layer, a direct current of 30 ⁇ A was passed between the anode assigned to the lead wire of the sintered body and a tantalum electrode disposed in the electrolytic solution used as the negative electrode, at room temperature for 45 minutes.
- ethylenedioxythiophene used in the form of an aqueous solution having a monomer concentration lower than the saturated concentration
- anthraquinone- sulfonic acid were dissolved, and for forming a semiconductor layer, a direct current of 30 ⁇ A was passed between the anode assigned to the lead wire of the sintered body and a tantalum electrode disposed in the electrolytic solution used as the negative electrode, at room temperature for 45 minutes.
- the sintered body was then pulled up, washed, dried and subjected to re- electrochemical formation (80°C, 30 minutes, 14 V) in an aqueous 0.1% acetic acid solution to repair the LC-causing defects in the fine electrically defective portions of the dielectric layer.
- the sintered body was washed with water and dried to form a semiconductor layer working as the cathode.
- carbon paste and silver paste comprising 10 mass parts of acrylic resin and 90 mass parts of silver powder were sequentially stacked to complete the cathode layer, thereby producing a solid electrolyte capacitor element.
- Example 1 and Comparative Example 1 chip solid electrolyte capacitors were produced in the same manner as in Example 1 and Comparative Example 1 (capacitors of Example 2 and Comparative Example 2) .
- the capacitance, ESR value and LC value were measured according to the following methods and the results (average value) obtained are shown in Table 1.
- Capacitance of capacitor The capacitance was measured at room temperature and 120 Hz by using an LCR measuring meter manufactured by Hewlett Packard.
- ESR Value The equivalent series resistance of a capacitor was measured at 100 kHz.
- LC Value After continuously applying a predetermined direct current voltage (2.5 V for Example 1 and Comparative Example 1, and 4 V for Example 2 and Comparative Example 2) between the terminals of the produced capacitor for 30 seconds at room temperature, the LC value was measured. TABLE 1
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Abstract
Description
Claims
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
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US10/568,713 US7355842B2 (en) | 2003-08-20 | 2004-08-19 | Chip solid electrolyte capacitor and production method of the same |
EP04772184A EP1661150A4 (en) | 2003-08-20 | 2004-08-19 | Chip solid electrolyte capacitor and production method of the same |
Applications Claiming Priority (4)
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JP2003296276 | 2003-08-20 | ||
JP2003-296276 | 2003-08-20 | ||
US49859603P | 2003-08-29 | 2003-08-29 | |
US60/498,596 | 2003-08-29 |
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WO2005020258A1 true WO2005020258A1 (en) | 2005-03-03 |
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PCT/JP2004/012228 WO2005020258A1 (en) | 2003-08-20 | 2004-08-19 | Chip solid electrolyte capacitor and production method of the same |
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US (1) | US7355842B2 (en) |
EP (1) | EP1661150A4 (en) |
WO (1) | WO2005020258A1 (en) |
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US20060256506A1 (en) * | 2005-04-27 | 2006-11-16 | Showa Denko K.K. | Solid electrolyte capacitor and process for producing same |
JP4832053B2 (en) | 2005-11-01 | 2011-12-07 | 三洋電機株式会社 | Manufacturing method of solid electrolytic capacitor |
WO2009012124A2 (en) * | 2007-07-18 | 2009-01-22 | Cabot Corporation | Niobium suboxide- and niobium-tantalum-oxide-powders and capacitor anodes produced thereof |
JP4964102B2 (en) * | 2007-11-26 | 2012-06-27 | 三洋電機株式会社 | Solid electrolytic capacitor |
KR102052763B1 (en) * | 2014-11-07 | 2019-12-05 | 삼성전기주식회사 | Tantalum capacitor and method of preparing the same |
WO2020112954A1 (en) * | 2018-11-29 | 2020-06-04 | Avx Corporation | Solid electrolytic capacitor containing a sequential vapor-deposited dielectric film |
Citations (5)
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JPH05343272A (en) * | 1992-06-09 | 1993-12-24 | Showa Denko Kk | Solid electrolytic capacitor |
JP2000323357A (en) * | 1999-05-07 | 2000-11-24 | Matsushita Electric Ind Co Ltd | Chip type solid electrolytic capacitor |
JP2002367862A (en) * | 2001-04-05 | 2002-12-20 | Rohm Co Ltd | Solid electrolytic capacitor and method for manufacturing the same |
JP2003133177A (en) * | 2001-08-16 | 2003-05-09 | Sanyo Electric Co Ltd | Solid electrolytic capacitor and manufacturing method therefor |
JP2003142337A (en) * | 2001-08-22 | 2003-05-16 | Showa Denko Kk | Capacitor |
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US3579813A (en) * | 1968-12-23 | 1971-05-25 | Matsuo Electric Co | Method of making electronic components on comblike metal fingers and severing the fingers |
US3588629A (en) * | 1969-05-07 | 1971-06-28 | Sprague Electric Co | Electrolytic capacitor with support members as terminals |
DE2509856B2 (en) * | 1975-03-06 | 1979-03-01 | Standard Elektrik Lorenz Ag, 7000 Stuttgart | Method for attaching connections to electrical components and components with at least one punched connection |
JPS6037114A (en) | 1983-08-09 | 1985-02-26 | 昭和電工株式会社 | Solid electrolytic condenser |
US4488204A (en) * | 1983-11-01 | 1984-12-11 | Union Carbide Corporation | Device for use in making encapsulated chip capacitor assemblies |
JPH0766901B2 (en) | 1985-09-03 | 1995-07-19 | 昭和電工株式会社 | Solid electrolytic capacitor and manufacturing method thereof |
GB2186752A (en) * | 1986-02-15 | 1987-08-19 | Stc Plc | Fuse for electronic component |
JPH0682592B2 (en) | 1989-06-05 | 1994-10-19 | 昭和電工株式会社 | Method for manufacturing solid electrolytic capacitor |
JP2921416B2 (en) | 1994-11-25 | 1999-07-19 | 日本電気株式会社 | Solid electrolytic capacitor and method of manufacturing the same |
US6185090B1 (en) * | 1997-01-29 | 2001-02-06 | Vishay Sprague, Inc. | Method for doping sintered tantalum and niobium pellets with nitrogen |
JP2001244145A (en) * | 2000-02-25 | 2001-09-07 | Rohm Co Ltd | Solid electrolytic capacitor |
US6625009B2 (en) * | 2001-04-05 | 2003-09-23 | Rohm Co., Ltd. | Solid electrolytic capacitor and method of making the same |
JP2003068576A (en) | 2001-08-30 | 2003-03-07 | Rohm Co Ltd | Structure of surface mounted solid electrolytic capacitor and manufacturing method therefor |
EP1665301B1 (en) * | 2003-09-26 | 2018-12-12 | Showa Denko K.K. | Production method of a capacitor |
-
2004
- 2004-08-19 EP EP04772184A patent/EP1661150A4/en not_active Withdrawn
- 2004-08-19 US US10/568,713 patent/US7355842B2/en not_active Expired - Lifetime
- 2004-08-19 WO PCT/JP2004/012228 patent/WO2005020258A1/en active Application Filing
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JPH05343272A (en) * | 1992-06-09 | 1993-12-24 | Showa Denko Kk | Solid electrolytic capacitor |
JP2000323357A (en) * | 1999-05-07 | 2000-11-24 | Matsushita Electric Ind Co Ltd | Chip type solid electrolytic capacitor |
JP2002367862A (en) * | 2001-04-05 | 2002-12-20 | Rohm Co Ltd | Solid electrolytic capacitor and method for manufacturing the same |
JP2003133177A (en) * | 2001-08-16 | 2003-05-09 | Sanyo Electric Co Ltd | Solid electrolytic capacitor and manufacturing method therefor |
JP2003142337A (en) * | 2001-08-22 | 2003-05-16 | Showa Denko Kk | Capacitor |
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See also references of EP1661150A4 * |
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US7355842B2 (en) | 2008-04-08 |
EP1661150A1 (en) | 2006-05-31 |
US20060221556A1 (en) | 2006-10-05 |
EP1661150A4 (en) | 2009-05-27 |
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