WO2004075220A1 - 固体電解コンデンサ及びその製造方法 - Google Patents
固体電解コンデンサ及びその製造方法 Download PDFInfo
- Publication number
- WO2004075220A1 WO2004075220A1 PCT/JP2004/001905 JP2004001905W WO2004075220A1 WO 2004075220 A1 WO2004075220 A1 WO 2004075220A1 JP 2004001905 W JP2004001905 W JP 2004001905W WO 2004075220 A1 WO2004075220 A1 WO 2004075220A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- electrolytic capacitor
- solid electrolytic
- polymerization
- capacitor according
- solid electrolyte
- Prior art date
Links
- 239000003990 capacitor Substances 0.000 title claims abstract description 138
- 239000007787 solid Substances 0.000 title claims abstract description 120
- 238000000034 method Methods 0.000 title claims description 30
- 238000004519 manufacturing process Methods 0.000 title claims description 23
- 239000007784 solid electrolyte Substances 0.000 claims abstract description 95
- 229920001940 conductive polymer Polymers 0.000 claims abstract description 56
- 229910052751 metal Inorganic materials 0.000 claims abstract description 20
- 239000002184 metal Substances 0.000 claims abstract description 20
- -1 naphthalene sulfonate compound Chemical class 0.000 claims abstract description 12
- 238000006116 polymerization reaction Methods 0.000 claims description 156
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 92
- 150000001875 compounds Chemical class 0.000 claims description 63
- 239000000178 monomer Substances 0.000 claims description 31
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 claims description 28
- 150000002989 phenols Chemical class 0.000 claims description 24
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 17
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 claims description 12
- 239000000126 substance Substances 0.000 claims description 12
- FJKROLUGYXJWQN-UHFFFAOYSA-N 4-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 claims description 11
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims description 10
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 9
- 239000007788 liquid Substances 0.000 claims description 9
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 claims description 7
- 239000003960 organic solvent Substances 0.000 claims description 7
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 claims description 6
- 229930192474 thiophene Natural products 0.000 claims description 6
- CHZCERSEMVWNHL-UHFFFAOYSA-N 2-hydroxybenzonitrile Chemical compound OC1=CC=CC=C1C#N CHZCERSEMVWNHL-UHFFFAOYSA-N 0.000 claims description 5
- IQUPABOKLQSFBK-UHFFFAOYSA-N 2-nitrophenol Chemical group OC1=CC=CC=C1[N+]([O-])=O IQUPABOKLQSFBK-UHFFFAOYSA-N 0.000 claims description 5
- 239000002736 nonionic surfactant Substances 0.000 claims description 4
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims description 3
- 239000004020 conductor Substances 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims 3
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims 2
- 239000005711 Benzoic acid Substances 0.000 claims 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims 1
- 235000010233 benzoic acid Nutrition 0.000 claims 1
- 150000002828 nitro derivatives Chemical class 0.000 claims 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract description 14
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 abstract description 14
- 229910052799 carbon Inorganic materials 0.000 abstract description 14
- 229910052709 silver Inorganic materials 0.000 abstract description 14
- 239000004332 silver Substances 0.000 abstract description 14
- 239000000243 solution Substances 0.000 description 79
- 229920000642 polymer Polymers 0.000 description 30
- 239000011888 foil Substances 0.000 description 29
- 230000000694 effects Effects 0.000 description 28
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 26
- 238000000605 extraction Methods 0.000 description 21
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 20
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 20
- 239000002019 doping agent Substances 0.000 description 19
- 239000002904 solvent Substances 0.000 description 17
- 230000000052 comparative effect Effects 0.000 description 14
- BTJIUGUIPKRLHP-UHFFFAOYSA-N 4-nitrophenol Chemical compound OC1=CC=C([N+]([O-])=O)C=C1 BTJIUGUIPKRLHP-UHFFFAOYSA-N 0.000 description 13
- 239000007864 aqueous solution Substances 0.000 description 13
- 229910052782 aluminium Inorganic materials 0.000 description 12
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 12
- 235000019441 ethanol Nutrition 0.000 description 12
- AMWRITDGCCNYAT-UHFFFAOYSA-L hydroxy(oxo)manganese;manganese Chemical compound [Mn].O[Mn]=O.O[Mn]=O AMWRITDGCCNYAT-UHFFFAOYSA-L 0.000 description 12
- 230000000977 initiatory effect Effects 0.000 description 10
- 239000004094 surface-active agent Substances 0.000 description 10
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 9
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 9
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 238000010586 diagram Methods 0.000 description 9
- 230000001965 increasing effect Effects 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 7
- 238000010438 heat treatment Methods 0.000 description 7
- 229920000767 polyaniline Polymers 0.000 description 7
- DKGAVHZHDRPRBM-UHFFFAOYSA-N tertiry butyl alcohol Natural products CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 7
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 6
- 230000007423 decrease Effects 0.000 description 6
- 230000006866 deterioration Effects 0.000 description 6
- 239000007800 oxidant agent Substances 0.000 description 6
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 6
- 125000001424 substituent group Chemical group 0.000 description 6
- 230000009257 reactivity Effects 0.000 description 5
- 125000000542 sulfonic acid group Chemical group 0.000 description 5
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 description 5
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
- 101150086735 Lmo1 gene Proteins 0.000 description 4
- 101100511353 Xenopus laevis lmo3 gene Proteins 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 150000001298 alcohols Chemical class 0.000 description 4
- UDHMTPILEWBIQI-UHFFFAOYSA-N butyl naphthalene-1-sulfonate;sodium Chemical compound [Na].C1=CC=C2C(S(=O)(=O)OCCCC)=CC=CC2=C1 UDHMTPILEWBIQI-UHFFFAOYSA-N 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 238000011049 filling Methods 0.000 description 4
- 229910052715 tantalum Inorganic materials 0.000 description 4
- YMMGRPLNZPTZBS-UHFFFAOYSA-N 2,3-dihydrothieno[2,3-b][1,4]dioxine Chemical compound O1CCOC2=C1C=CS2 YMMGRPLNZPTZBS-UHFFFAOYSA-N 0.000 description 3
- BMRVLXHIZWDOOK-UHFFFAOYSA-N 2-butylnaphthalene-1-sulfonic acid Chemical compound C1=CC=CC2=C(S(O)(=O)=O)C(CCCC)=CC=C21 BMRVLXHIZWDOOK-UHFFFAOYSA-N 0.000 description 3
- 229940090248 4-hydroxybenzoic acid Drugs 0.000 description 3
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 3
- 229920001609 Poly(3,4-ethylenedioxythiophene) Polymers 0.000 description 3
- 230000000996 additive effect Effects 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 239000003822 epoxy resin Substances 0.000 description 3
- 125000000623 heterocyclic group Chemical group 0.000 description 3
- MIVBAHRSNUNMPP-UHFFFAOYSA-N manganese(2+);dinitrate Chemical compound [Mn+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O MIVBAHRSNUNMPP-UHFFFAOYSA-N 0.000 description 3
- 150000002739 metals Chemical class 0.000 description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-N phosphoric acid Substances OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 3
- 229920000647 polyepoxide Polymers 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 2
- 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 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
- ROSDCCJGGBNDNL-UHFFFAOYSA-N [Ta].[Pb] Chemical compound [Ta].[Pb] ROSDCCJGGBNDNL-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 2
- 239000003792 electrolyte Substances 0.000 description 2
- 230000008030 elimination Effects 0.000 description 2
- 238000003379 elimination reaction Methods 0.000 description 2
- 239000011737 fluorine Substances 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 238000007654 immersion Methods 0.000 description 2
- 239000011244 liquid electrolyte Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 239000005518 polymer electrolyte Substances 0.000 description 2
- WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 description 2
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- VZSRBBMJRBPUNF-UHFFFAOYSA-N 2-(2,3-dihydro-1H-inden-2-ylamino)-N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]pyrimidine-5-carboxamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C(=O)NCCC(N1CC2=C(CC1)NN=N2)=O VZSRBBMJRBPUNF-UHFFFAOYSA-N 0.000 description 1
- DNUYOWCKBJFOGS-UHFFFAOYSA-N 2-[[10-(2,2-dicarboxyethyl)anthracen-9-yl]methyl]propanedioic acid Chemical compound C1=CC=C2C(CC(C(=O)O)C(O)=O)=C(C=CC=C3)C3=C(CC(C(O)=O)C(O)=O)C2=C1 DNUYOWCKBJFOGS-UHFFFAOYSA-N 0.000 description 1
- CETWDUZRCINIHU-UHFFFAOYSA-N 2-heptanol Chemical compound CCCCCC(C)O CETWDUZRCINIHU-UHFFFAOYSA-N 0.000 description 1
- FWMKPJYJDJSEHR-UHFFFAOYSA-N 2-propylnaphthalene-1-sulfonic acid Chemical compound C1=CC=CC2=C(S(O)(=O)=O)C(CCC)=CC=C21 FWMKPJYJDJSEHR-UHFFFAOYSA-N 0.000 description 1
- GSSXLFACIJSBOM-UHFFFAOYSA-N 2h-pyran-2-ol Chemical compound OC1OC=CC=C1 GSSXLFACIJSBOM-UHFFFAOYSA-N 0.000 description 1
- SGHBRHKBCLLVCI-UHFFFAOYSA-N 3-hydroxybenzonitrile Chemical compound OC1=CC=CC(C#N)=C1 SGHBRHKBCLLVCI-UHFFFAOYSA-N 0.000 description 1
- RTZZCYNQPHTPPL-UHFFFAOYSA-N 3-nitrophenol Chemical compound OC1=CC=CC([N+]([O-])=O)=C1 RTZZCYNQPHTPPL-UHFFFAOYSA-N 0.000 description 1
- CVNOWLNNPYYEOH-UHFFFAOYSA-N 4-cyanophenol Chemical compound OC1=CC=C(C#N)C=C1 CVNOWLNNPYYEOH-UHFFFAOYSA-N 0.000 description 1
- FLDCSPABIQBYKP-UHFFFAOYSA-N 5-chloro-1,2-dimethylbenzimidazole Chemical compound ClC1=CC=C2N(C)C(C)=NC2=C1 FLDCSPABIQBYKP-UHFFFAOYSA-N 0.000 description 1
- 239000001741 Ammonium adipate Substances 0.000 description 1
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 1
- VTLYFUHAOXGGBS-UHFFFAOYSA-N Fe3+ Chemical compound [Fe+3] VTLYFUHAOXGGBS-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 235000019293 ammonium adipate Nutrition 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- RATMLZHGSYTFBL-UHFFFAOYSA-N azanium;6-hydroxy-6-oxohexanoate Chemical compound N.OC(=O)CCCCC(O)=O RATMLZHGSYTFBL-UHFFFAOYSA-N 0.000 description 1
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000003985 ceramic capacitor Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000005868 electrolysis reaction Methods 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000002563 ionic surfactant Substances 0.000 description 1
- 229910000358 iron sulfate Inorganic materials 0.000 description 1
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- IJFXRHURBJZNAO-UHFFFAOYSA-N meta--hydroxybenzoic acid Natural products OC(=O)C1=CC=CC(O)=C1 IJFXRHURBJZNAO-UHFFFAOYSA-N 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- DGVVJWXRCWCCOD-UHFFFAOYSA-N naphthalene;hydrate Chemical compound O.C1=CC=CC2=CC=CC=C21 DGVVJWXRCWCCOD-UHFFFAOYSA-N 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 125000004957 naphthylene group Chemical group 0.000 description 1
- 229910052758 niobium Inorganic materials 0.000 description 1
- 239000010955 niobium Substances 0.000 description 1
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229940079877 pyrogallol Drugs 0.000 description 1
- 238000000197 pyrolysis Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000008439 repair process Effects 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 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
- H01G9/0029—Processes of manufacture
- H01G9/0036—Formation of the solid electrolyte layer
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
- H01G11/54—Electrolytes
- H01G11/56—Solid electrolytes, e.g. gels; Additives therein
-
- 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
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/13—Energy storage using capacitors
Definitions
- the present invention relates to a solid electrolytic capacitor and a method for manufacturing the same.
- the present invention relates to a solid electrolytic capacitor used for various electronic devices and a method for manufacturing the same.
- the capacitors used in these devices also have low impedance in the high-frequency range, and there is an increasing demand for smaller and larger capacitors.
- plastic film capacitors, my-power capacitors, multilayer ceramic capacitors, and the like have been used.
- aluminum dry electrolytic capacitors aluminum solid electrolytic capacitors, and latex solid electrolytic capacitors.
- Aluminum dry electrolytic capacitors use an etched aluminum anode foil and cathode foil with a separator interposed between them to form a device, which is impregnated with a liquid electrolyte.
- a solid electrolyte is used to improve the characteristics of the aluminum dry electrolytic capacitor.
- a method for manufacturing a solid electrolyte will be described. That is, the anode body is immersed in a manganese nitrate solution, and is thermally decomposed in a high-temperature furnace at about 250 to 350 ° C. to form a manganese oxide layer acting as a solid electrolyte. I have.
- This capacitor has a solid electrolyte and has no drawbacks such as electrolyte leakage at high temperatures, capacity reduction due to dry-up, and functional deterioration caused by solidification at low temperatures, and has better frequency characteristics and temperature than liquid electrolytes. It shows the characteristics.
- Japanese Patent Application Laid-Open No. 2-130906 discloses that a conductive polymer is obtained by polymerizing a polymerizable monomer such as pyrrole or thiophene in order to increase the conductivity of a solid electrolyte.
- a solid electrolytic capacitor using the same as a solid electrolyte is disclosed.
- a method for forming a solid electrolyte of a solid electrolytic capacitor using a conductive polymer as the solid electrolyte will be described.
- a precoat layer made of a conductive material such as manganese oxide or a conductive polymer is formed on the surface of a dielectric oxide film of a valve metal.
- electrolytic polymerization in which power is supplied from the outside in a polymerization solution containing a polymerizable monomer and a dopant, or (2) chemical polymerization, which is immersed in a polymerization solution containing an oxidizing agent to form a conductive polymer.
- a solid electrolyte made of a conductive polymer is formed.
- a solid electrolytic capacitor of the present invention comprises: an anode body made of a valve metal having a surface formed with a dielectric oxide film layer; and a solid electrolyte layer made of a conductive polymer formed on the oxide film. And a cathode layer formed on the solid electrolyte layer.
- the solid electrolyte layer contains a naphthalenesulfonic acid-based compound, whereby it is possible to obtain a solid electrolytic capacitor having excellent characteristics even at high temperature and high humidity. It has the effect of becoming.
- the method for manufacturing a solid electrolytic capacitor of the present invention comprises: an anode body made of a valve metal having a dielectric oxide film layer formed on a surface thereof; and a solid electrolyte layer made of a conductive polymer formed on the oxide film.
- a solid electrolyte capacitor having a cathode layer formed on the solid electrolyte layer, wherein the polymerizable monomer forming the conductive polymer, a naphthalenesulfonic acid-based compound, and a polymerization solution containing water;
- the solid electrolyte layer is formed on the oxide film layer by a chemical polymerization method or an electrolytic polymerization method.
- the solid electrolyte layer has excellent leakage current characteristics and ESR and capacitance characteristics under high humidity.
- a body electrolytic capacitor can be provided. BRIEF DESCRIPTION OF THE FIGURES
- FIG. 1 is a sectional view showing an outline of a solid electrolytic condenser according to one embodiment of the present invention.
- FIG. 2 is a characteristic diagram showing the relationship between the content of a dopant compound and ESR characteristics.
- Figure 3 is a characteristic diagram showing the relationship between the amount of paraditrophenol added to the polymerization solution and the change in ESR characteristics.
- Figure 4 is a characteristic diagram showing the relationship between the amount of sulfuric acid added to the polymerization solution and the capacitance characteristics or ESR characteristics.
- Figure 5 is a characteristic diagram showing the relationship between the amount of 2-propanol added to the polymerization solution and the leakage current characteristics or polymerization time.
- FIG. 6 is a characteristic diagram showing the relationship between the electropolymerization voltage and ESR characteristics or polymerization time.
- FIG. 7 is a characteristic diagram showing a relationship between a molar concentration ratio of a dopant and sulfuric acid and a capacitance characteristic.
- FIG. 8 is a characteristic diagram showing the relationship between the surface tension of the polymerization solution and the capacitance characteristics.
- Figure 9 is a characteristic diagram showing the relationship between the amount of paraditrophenol added to the polymerization solution and the ESR characteristics.
- Figure 10 is a characteristic diagram showing the relationship between the electropolymerization voltage and ESR characteristics or polymerization time.
- the solid electrolytic capacitor of the present invention has a configuration in which at least the compound (I) is doped in a solid electrolyte layer made of a conductive polymer. This has the effect that a solid electrolytic capacitor having excellent characteristics even under high temperature and high humidity can be obtained. This is because a dopant having a carboxylic acid in a molecule is excellent in chemical conversion properties, and thus a solid electrolytic capacitor having excellent leakage current characteristics and excellent ESR characteristics in a high-temperature, high-humidity environment can be obtained. In addition, a compound having a small steric hindrance, such as compound (I), can form a solid electrolyte layer composed of a dense conductive polymer, and a solid electrolytic capacitor having excellent initial capacitance characteristics. Is considered to be obtained.
- the doping amount of the compound (I) is preferably from 0.05 to 0.5 mol per 1 mol of the monomer forming the solid electrolyte layer made of the conductive polymer. This has the effect of enabling more excellent ESR and impedance characteristics as a solid electrolytic capacitor.
- the doping amount of the compound (I) is less than 0.05 mol 1 with respect to the monomer lmo 1 forming the solid electrolyte layer composed of the conductive polymer, the obtained conductive polymer has a low conductivity. Therefore, when the doping amount of the compound (I) exceeds 0.5 mol, the excess dopant acts as a steric hindrance, and the regularity of the conductive polymer main chain is reduced, resulting in a decrease in the ESR characteristic. Is not preferred because it leads to a decrease in
- the monomers that form the solid electrolyte layer made of conductive polymer are pyrrole and thiophene. It is preferable to be selected from at least one of butane, furan, aniline or a derivative thereof. This has the effect of providing high conductivity and obtaining a solid electrolytic capacitor having excellent impedance characteristics in a high frequency range.
- the phenol derivative has an effect of enhancing the order of the polymer skeleton. This has the effect that a stable solid electrolytic capacitor can be obtained even under higher temperature conditions.
- the phenol derivative is preferably selected from at least one of nitrophenol, cyanophanol, hydroxybenzoic acid, and hydroxyphenol.
- the phenol derivatives used here include 0-nitrophenol, m-nitrophenol, p-nitrophenol, o-cyanophenol, m-cyanophenol, p-cyanophenol, o-hydroxybenzoic acid, and m-hydroxybenzoic acid. Acids, p-hydroxybenzoic acid, o-hydroxyphenol, m-hydroxyphenol, and p-hydroxyphenol.
- sulfuric acid is doped in a part of a solid electrolyte layer made of a conductive polymer.
- sulfuric acid is considered to be incorporated into the conductive polymer as a dopant, so if such a compound having a small steric hindrance in its molecular structure is incorporated, the filling rate of the formed polymer changes. By doing so, it is possible to produce a solid electrolytic capacitor having a high capacitance extraction rate.
- a solid electrolyte layer made of a conductive polymer is formed by using water as a main solvent, a polymerizable monomer and a compound (I ) Is used to form a conductive polymer layer using a polymerization solution containing at least.
- water especially electrolytic weight
- the compound (I) has an effect of obtaining a solid electrolytic capacitor having more excellent leakage current characteristics, ESR under high humidity, and electrostatic capacitance characteristics.
- the polymerizable monomer is selected from at least one of pyrrole, thiophene, aniline and derivatives thereof. This has the effect of obtaining higher conductivity and obtaining a solid electrolytic capacitor having excellent impedance characteristics in a high frequency range.
- At least one of a phenol derivative, sulfuric acid and alcohols can be added to the polymerization solution.
- an excellent capacity extraction efficiency can be obtained, and the solid electrolyte layer made of a conductive polymer having stable film quality can be formed.
- the phenol derivative is preferably selected from at least one of nitrophenol, cyanophenol, hydroxybenzoic acid, and hydroxyphenol, and the concentration of the phenol derivative in the polymerization solution is preferably from 0.01 to 0.1 mol. Since the phenol derivative enhances the order of the polymer skeleton, it has an effect that it is possible to form a solid electrolyte layer having excellent ESR and capacitance characteristics under high temperature and high humidity.
- the concentration of the phenol derivative in the polymerization solution is less than 0.0 lmo1, the heat resistance is lowered due to the low order of the polymer formed, and the phenol derivative in the polymerization solution is not dissolved.
- the concentration exceeds 0.1 lmo1 the polymerization speed is increased, the polymerization current is concentrated on the edge, and the thickness of the polymer layer becomes non-uniform, and the leakage occurs due to the stress when the capacitor element is laminated. It is not preferable because current characteristics are deteriorated. It is preferable that the concentration of sulfuric acid in the polymerization liquid is 0.01 to lwt%.
- the doping of sulfuric acid changes the degree of filling of the formed polymer, and has the effect of enabling the formation of a solid electrolyte layer exhibiting more excellent capacity extraction efficiency. If the concentration of sulfuric acid in the polymerization solution is less than 0.01 wt%, the effect on the capacity extraction rate is not sufficient, while the concentration of sulfuric acid in the polymerization solution exceeds lwt%. In this case, the sulfuric acid is eluted under high humidity and the ESR and the capacitance characteristics under high humidity are remarkably deteriorated.
- the alcohols preferably have 1 to 4 carbon atoms and a concentration in the polymerization solution of 0.5 to 20 wt%.
- the organic solvents used herein include methyl alcohol, ethyl alcohol, n-propyl alcohol, 2-propyl alcohol, n_butyl alcohol, 21-butyl alcohol, 3-butyl alcohol, tert-butyl alcohol, Examples include acetonitrile, acetone, tetrahydrofuran, ethylene glycol, ⁇ -butyltyl lactone, dimethylformamide, and dimethyl sulfoxide.
- concentration of alcohols in the polymerization solution is less than 0.5 wt%, polymerization current concentrates on the edge, and the thickness of the polymer layer becomes non-uniform.
- concentration of alcohols in the polymer solution exceeds 2 wt%, the polymerization speed decreases and the polymerization time becomes longer, resulting in a rapid increase in productivity. It is not preferable because it deteriorates.
- the formation of the solid electrolyte layer made of a conductive polymer can be performed by electrolytic polymerization.
- Conducting electrolytic polymerization forms a conductive polymer with high steric order, which makes it possible to form a solid electrolyte layer with a uniform polymerized film thickness and high electrical conductivity. Has an action.
- the voltage at the time of electrolytic polymerization is preferably 1 to 3 V. Thereby, the reactivity can be controlled by the voltage, so that the solid electrolyte layer having a high capacity extraction characteristic can be formed.
- the solid electrolyte layer made of a conductive polymer contains at least a polymerizable monomer, a naphthylene sulfonic acid-based compound (hereinafter, referred to as compound ( ⁇ )) and sulfuric acid using water as a main solvent.
- the molar concentration ratio of the compound ( ⁇ ) to sulfuric acid in the above polymerization solution is lower than 50: 1, the effect of improving the capacity extraction rate cannot be obtained, and the sulfuric acid concentration is lower than 4: 1.
- a high concentration is not preferable because phenomena such as a decrease in capacity and deterioration of ESR characteristics are observed at high temperature and high humidity.
- the surface tension can improve the wettability with the dielectric oxide film by the use of 7 0 X 1 0- 3 N / m or less of the polymerization solution, further excellent capacity draw-out rate is obtained, et al.
- the effect of capacity drawer ratio improved by making the above-mentioned sulfuric acid addition and the surface tension 7 0 X 1 0 one 3 N Zm below are obtained only when using the compound ([pi).
- alkylnaphthylene sulfonic acid when alkylnaphthylene sulfonic acid is used, no effect of increasing the capacity extraction rate is seen. Note that this is due to the difference in dopant, the state of formation of the conductive polymer, or the difference in the ease of concentration of the conductive polymer on the edge of the pit in the roughened valve metal. It is thought to be due to this.
- nonionic surfactant examples include an acetyldaricol-based surfactant, a silicone-based surfactant, a polyoxyalkylene glycol-based surfactant, and a fluorine-based surfactant.
- a conductive polymer having stable film quality can be formed.
- the phenol derivative is selected from at least one of nitrophenol, cyanophenol, hydroxybenzoic acid, and hydroxyphenol, and the phenol derivative is contained in the polymerization solution. It is preferable that the concentration be 0.0001 to 0.2mo1. As a result, the phenol derivative enhances the order of the polymer skeleton, so that It has the effect of being able to form a solid electrolyte layer having excellent SR and capacitance characteristics.
- the concentration of the phenol derivative in the polymerization solution is less than 0.001 lmo1
- the heat resistance is reduced due to the low order of the polymer formed, and the phenol derivative in the polymerization solution is not dissolved.
- the concentration exceeds 0.2 mol
- the polymerization speed is increased, the polymerization current is concentrated on the edge portion, and the thickness of the polymer layer becomes non-uniform. This is not preferable because the leakage current characteristics are reduced by the stress.
- the present invention provides a solid electrolytic capacitor in which a dielectric oxide film, a solid electrolyte layer made of a conductive polymer, and a cathode layer are sequentially formed on the surface of an anode body made of a valve metal, wherein the conductive polymer is at least a compound It is characterized in that (I) has a doped configuration. Since the dopant having a carboxylic acid in the molecule has excellent chemical conversion properties, a solid electrolytic capacitor having excellent leakage current characteristics and characteristics in a high-temperature and high-humidity environment can be obtained by doping the compound (I). be able to.
- a solid electrolyte layer comprising water as a main solvent, at least a polymerizable monomer, a compound ( ⁇ ) and sulfuric acid, and a molar concentration ratio of the compound ( ⁇ ) and sulfuric acid of 50: 1 to 4: 1, and surface tension 7 0 X 1 0 - by so as to form by performing electrolytic polymerization using at 3 NZM less polymer solution, as it can obtain an excellent solid electrolytic capacitor of the capacitive pull out rate is there.
- FIG. 1 is a sectional view showing the concept of a solid electrolytic capacitor according to one embodiment of the present invention.
- a dielectric oxide film layer 2 is formed on the surface of the anode 1 using an aluminum-etched foil or a tantalum sintered body with a lead as the anode 1.
- a solid electrolyte layer 3 made of a conductive polymer is formed, and subsequently, a solid electrolyte layer 3 is formed from the carbon layer 4 and the silver layer 5.
- the solid electrolytic capacitor according to the embodiment can be obtained by forming a cathode lead portion and using a not-shown epoxy resin to package the package.
- a 3 mm ⁇ 4 mm aluminum etch foil 1 with a lead was used as an anode.
- An aluminum-etched foil is immersed in a 3% aqueous solution of ammonium adipate, and anodized at an applied voltage of 12 V and an aqueous solution temperature of 7 Ot for 60 minutes to form a dielectric oxide film 2 on the surface of the aluminum-etched foil did.
- Anodized aluminum-etched foil 1 is immersed in a 30% aqueous solution of manganese nitrate, lifted up by bow I, air-dried, and finally subjected to a thermal decomposition treatment at 300 ° C for 10 minutes to form a solid electrolyte layer 3
- a manganese oxide layer serving as a part was formed.
- Anodized aluminum foil was anodized in the same manner as in Example 1 to form a dielectric oxide film layer 2.
- Anodized aluminum etched foil is made of water-soluble polyaniline By immersing in a 5% solution and performing heat treatment at 200 ° C. for 10 minutes, a conductive layer to be a part of the solid electrolyte layer 3 was formed.
- a polymerization solution was prepared.
- a solid electrolytic capacitor was produced in the same manner as in Example 1 except for the polymerization liquid.
- a polymerization initiation electrode was brought close to the element surface, and electrolytic polymerization was performed at a liquid temperature of 25 and a polymerization voltage of 2 V to form a solid electrolyte layer. Thereafter, a carbon layer and a silver layer were formed in the same manner as in Example 1, and a cathode lead portion formed of the carbon layer and the silver layer was formed, followed by providing an exterior, thereby producing ten solid electrolytic capacitors.
- the anode is molded with tantalum powder embedded so that a part of the tantalum lead wire is exposed, and then sintered to obtain an anode body 1.4 mm thick, 3.0 mm wide and 3.8 mm long.
- This anode body was immersed in a phosphoric acid aqueous solution and formed at a voltage of 20 V to form a dielectric oxide film layer on the surface of the anode state.
- the surface of the solid electrolyte layer was impregnated with an aqueous solution containing 2 wt% of carbon particles and 2 wt% of pyrogallol, adjusted to pH 10 by adding ammonia, dried at 150 ° C., and dried at 150 ° C. Was formed. Thereafter, a conductor layer of silver paste was formed to obtain a capacitor element.
- a tantalum lead wire and an anode terminal are connected, and a cathode terminal is connected to the cathode layer of the capacitor element via a conductive adhesive, and a part of the anode terminal and a part of the cathode terminal are connected.
- a solid electrolytic capacitor was fabricated by coating with an exterior resin so as to be exposed (D size: 7.3 ⁇ 4.3 ⁇ 2.8 mm).
- Example 5 Using the method shown in Example 5, a dielectric oxide film layer was formed on an anode body made of tantalum.
- the anode body on which the oxide film was formed was immersed in a polymerization solution consisting of an ethylene glycol aqueous solution obtained by mixing a heterocyclic monomer, pyrrole, and sodium butyl naphthalenesulfonate, for 5 minutes and then pulled up. As a result, a solid electrolyte layer was formed.
- Other conditions were the same as in Example 5 to fabricate a solid electrolytic capacitor (D size: 7.3 ⁇ 4.3 ⁇ 2.8 mm).
- Table 1 shows the ESR characteristics of the solid electrolytic condensers of Examples 1 to 5 and Comparative Examples 1 and 2 after the test with initial values and humidity resistance (60 ° C, 90%, 6.3 V, 500 hours). .
- the ESR characteristics were measured at 100 kHz.
- Comparative Example 1 significantly deteriorates the ESR characteristics in the moisture resistance load test as compared with Examples 1 to 4. This shows that sodium butyl naphthalenesulfonate used as a dopant markedly deteriorates the ESR characteristics in a moisture resistance load test, whereas compound (I) has a high chemical conversion property to aluminum. From the comparison between Example 1 and Example 2, the same ESR characteristics can be obtained even when the conductive layer that is a part of the solid electrolyte is a water-soluble polyaniline layer. You can see that.
- Example 1 shows that when the solvent of the polymerization solution was ethanol, the ESR characteristics in the moisture resistance load test tended to be lower than in Example 1, so that water was used as the main solvent. It turns out that it is effective to use. Further, in Example 4 in which the solid electrolyte layer was formed by chemical polymerization using an oxidizing agent, the same ESR characteristics as in Example 1 could not be obtained. This indicates that the characteristics of the obtained solid electrolytic capacitor are more excellent when the electrolytic polymerization is used than when the chemical polymerization method is used.
- Example 1 With Comparative Example 1 and Example 5 with Comparative Example 2, it is difficult to form a dense conductive polymer layer when a noble dopant such as sodium butyl naphthalenesulfonate is used. Therefore, it can be seen that the initial capacitance characteristics are significantly deteriorated.
- a noble dopant such as sodium butyl naphthalenesulfonate
- Example 2 the content of the compound (I) relative to 1 mol of the monomer forming the conductive polymer was 0.001, 0.01, 0.05, 0.1, 0.5, 0.5. 10 solid electrolytic capacitors were produced in the same manner as in Example 2 except that the value was changed to 7 mo1.
- Table 2 and Fig. 2 show the relationship between the compound (I) content and the ESR characteristics of the initial value of the manufactured solid electrolytic capacitor.
- the ESR characteristics were measured at 100 kHz.
- a solid electrolytic capacitor with a compound (I) content of 0.05 to 0.5 mol per 1 mol of the monomer forming the conductive polymer has excellent ESR characteristics.
- the addition amount is less than 0.05 mo 1 or more than 0.5 mo 1, the ESR characteristics tend to deteriorate. Therefore, in order to enable more excellent ESR and impedance characteristics as a capacitor by using the compound (I), the content of the compound (I) in the conductive polymer must be 1 mol of the monomer forming the conductive polymer. It is preferable to adjust the ratio to 0.05 to 0.5 mol with respect to 1.
- Example 1 by adding paranitrophenol to the polymerization solution for forming the solid electrolyte, 0.001, 0.005, 0.01, 0.05, 0.1, and 0.2 mol, the conductivity was increased.
- Ten solid electrolytic capacitors were produced in the same manner as in Example 1 except that paranitrophenol was added to a part of the molecule.
- Example 1 In Example 1 described above, 0.0005, 0.01, 0.1, 1.0, 1.5, 2. Owt% of sulfuric acid was added to the polymerization solution for forming the solid electrolyte, thereby increasing the conductivity.
- Ten solid electrolytic capacitors were manufactured in the same manner as in Example 1 except that sulfuric acid was doped in a part of the capacitors.
- Table 4 and Fig. 4 show the initial capacitance characteristics of the solid electrolytic capacitor and the ESR characteristics before and after the humidity resistance load (60 ° C, 90%, 6.3 V, 500 hours) test.
- the capacitance characteristics were measured at 120 kHz, and the ESR characteristics were measured at 100 kHz.
- the right vertical axis shows the capacitance
- the left vertical axis shows the ESR characteristics
- the horizontal axis shows the amount of sulfuric acid added.
- solid electrolytic capacitors with a paranitrophenol addition of 0.01 to 0.1 mo1 have excellent ESR characteristics, less than 0.01 mo1 and more than 0.1 mo1. In some cases, the ESR characteristics tend to deteriorate. Therefore, in order for paranitrophenol to increase the order of the polymer skeleton and to obtain a solid electrolytic capacitor that is stable even at high temperatures, the amount of paranitrophenol added should be in the range of 0.01 to 0.1 lmo1. Is preferred.
- the solid electrolytic capacitors containing sulfuric acid in an amount of 0.01-: L wt% have excellent capacitance and characteristics under high humidity.
- 0.0 lw of sulfuric acid added If it is less than t%, the capacitance is low, while if it exceeds lwt%, the ESR characteristics tend to deteriorate in the moisture resistance test. Therefore, in order to obtain a solid electrolytic capacitor having a high capacity extraction rate by changing the filling rate of the formed polymer and to obtain a solid electrolytic capacitor having excellent moisture resistance, the amount of sulfuric acid added should be 0.01 to 1 ⁇ 1. %.
- Each of the solid electrolytic capacitors was manufactured in the same manner as in Example 1 except that 0.1, 0.5, 1, 10, 20, and 3 Owt% of 2-propanol was added to the polymerization solution for forming a solid electrolyte. Ten were produced.
- Table 5 and Fig. 5 show the initial leakage current characteristics (6.3 V, 1 minute value) of this solid electrolytic capacitor.
- the right vertical axis shows the polymerization time
- the left vertical axis shows the leakage current characteristics
- the horizontal axis shows the amount of 2-propanol added.
- the amount of 2-propanol added when the amount of 2-propanol added is 0.5 to 20 wt%, the solid electrolytic capacitor shows excellent leakage current characteristics. If it is less than 0.5 wt%, the leakage current characteristics tend to deteriorate. On the other hand, when the amount of 2-propanol exceeds 2 Owt%, the polymerizability deteriorates and the polymerization time becomes longer. Therefore, by adding an organic solvent such as alcohol to the polymer solution, the reactivity of the polymerization reaction is suppressed, the concentration of current on the edge portion is prevented, and the surface shape of the formed conductive polymer is improved. In order to obtain a solid electrolytic capacitor having excellent leakage current characteristics, it is preferable that the amount of 2-propanol be in the range of 0.5 to 2 O wt%.
- Example 10 solid electrolytic capacitors were produced in the same manner as in Example 1 except that the polymerization voltage of electrolytic polymerization was set to 0.5, 1, 2, 3, and 5 V.
- Table 6 and Fig. 6 show the ESR characteristics of the initial values of this solid electrolytic capacitor. The ESR characteristics were measured at 100 kHz. In FIG. 6, the right vertical axis shows the polymerization time, the left vertical axis shows the initial ESR characteristics, and the horizontal axis shows the polymerization voltage.
- Figure 6 shows that solid electrolytic capacitors with a polymerization voltage of 1 to 3 V have excellent ESR characteristics. If it is less than IV, polymerization does not proceed rapidly, and if it exceeds 3 V, a dense polymer is not formed and the ESR characteristics tend to deteriorate. Therefore, in order to control the reaction by the polymerization voltage and obtain a solid electrolytic capacitor having excellent ESR characteristics, the polymerization voltage is preferably in the range of 1 to 3 V.
- Example 11 A 3 mm ⁇ 4 mm aluminum-etched foil 1 to which a lead was attached was used as an anode.
- An aluminum-etched foil is immersed in a 3% aqueous solution of ammonium adipic acid, and anodized at an applied voltage of 6 V and an aqueous solution temperature of 70 ° C for 60 minutes to form a dielectric oxide film on the surface of the aluminum-etched foil.
- Anodized aluminum-etched foil 1 is immersed in a 30% aqueous solution of manganese nitrate, lifted up with bow I, air-dried, and finally subjected to a pyrolysis treatment at 300 for 10 minutes to form solid electrolyte layer 3.
- a manganese oxide layer to be a part was formed.
- a solid electrolyte layer is formed on the manganese oxide layer.
- a compound having 0.5 mol / L of ethylenedimethylxylthiophene monomer and one hydroxyl group and one sulfonic acid group as substituents ( ⁇ ) 0. ImolZL and sulfuric acid 0. OlmolZL and water as a main solvent Is added to the polymerization solution containing, and the surface tension is adjusted to 60 XI O ⁇ NZm to prepare a polymerization solution for forming a solid electrolyte.
- Example 11 a compound having one hydroxyl group and two sulfonic acid groups as substituents ( ⁇ ) 0.1 lmol / L, sulfuric acid 0.01 mol 1
- an external electrode 6 for initiating polymerization was brought close to the surface of the aluminum-etched foil 1 in this polymerization solution, and a solid electrolyte layer was formed by performing electropolymerization at a polymerization voltage of 2.5 V.
- a solid electrolytic capacitor was fabricated.
- Example 13 In Example 11, after forming the dielectric oxide film layer, the conductive oxide which becomes a part of the solid electrolyte layer is formed by immersing in a 5% aqueous polyaniline solution and performing heat treatment at 200 ° C. for 5 minutes. A layer was formed. Next, a polymer solution containing pyrrole monomer (0.2 mol ZL) and a compound having one oxygen and one sulfonic acid group as a substituent (1) 0.05 mol 1 ZL, sulfuric acid 0.01 mol 1 ZL, and a main solvent water containing n A polymer solution for forming a solid electrolyte was prepared in which the surface tension was adjusted to 60 ⁇ 10 3 NZm by adding butyl alcohol.
- a solid electrolyte layer was formed in the same manner as in Example 11 except that an external electrode for initiating polymerization was brought close to the surface of the aluminum-etched foil, and electrolytic polymerization was performed at a polymerization voltage of 2 V to form a solid electrolyte layer.
- a capacitor was manufactured.
- Example 11 after forming the dielectric oxide film layer, the conductive layer serving as a part of the solid electrolyte layer was formed by immersing in a 5% aqueous polyaniline solution and performing heat treatment at 200 for 5 minutes. Formed. Next, a polymer solution containing 0.2 mol ZL of pyrrole monomer and a compound having one sulfonic acid group as a substituent ( ⁇ ) 0.0 Smol ZL, sulfuric acid 0.01 Mol ZL, and water as a main solvent Then, i-propyl alcohol was added thereto to adjust the surface tension to 60 ⁇ 1 CT 3 NZm to prepare a polymerization solution for forming a solid electrolyte.
- a solid electrolytic capacitor was prepared in the same manner as in Example 11 except that an external electrode for initiating polymerization was brought close to the surface of the aluminum-etched foil in this polymerization solution, and a solid electrolyte layer was formed by performing electropolymerization at a polymerization voltage of 2 V. Was prepared.
- Example 11 a compound having 0.2 mol 1 / L of pyrrole monomer and two sulfonic acid groups as substituents ( ⁇ ) 0.05 mol 1 ZL and sulfuric acid.
- a polymerization solution for forming a solid electrolyte was prepared by adding a silicon-based surfactant to the polymerization solution containing the solution and adjusting the surface tension to 60 ⁇ 10 ⁇ 3 N / m.
- a solid electrode was formed in the same manner as in Example 11 except that an external electrode for initiating polymerization was brought close to the surface of the aluminum-etched foil, and an electrolytic polymerization was performed at a polymerization voltage of 2 V to form a solid electrolyte layer.
- An electrolytic capacitor was manufactured.
- a dielectric oxide film layer 2 was formed on the outer surface of the aluminum-etched foil 1 serving as the anode in the same manner as in Example 11 above, it was immersed in a 5% aqueous polyaniline solution at 200 ° C. for 5 minutes. By performing the heat treatment, a conductive layer to be a part of the solid electrolyte layer was formed.
- a carbon layer 4 is formed by applying and drying carbon as a cathode extraction layer
- a silver layer 5 is formed by further applying and drying a silver paste.
- the carbon layer and the silver layer are combined to form a cathode extraction section. did.
- 10 solid electrolytic capacitors were manufactured by packaging using an epoxy resin (not shown).
- a dielectric oxide film layer was formed on the outer surface of the aluminum-etched foil serving as the anode in the same manner as in Example 11 above, the film was immersed in a 5% aqueous polyaniline solution. By performing the heat treatment for a minute, a conductive layer which became a part of the solid electrolyte layer was formed.
- a polymerization solution for forming a solid electrolyte which was an aqueous solution containing 0.2 mol 1 L of a pyrol monomer and 0.05 mol 1 ZL of propylnaphthalenesulfonic acid, was prepared.
- the polymerization initiating electrode was brought close to the surface of the capacitor element, and electrolytic polymerization was performed at a polymerization voltage of 2 V to form a solid electrolyte layer. Thereafter, a carbon layer and a silver layer were formed, a cathode lead portion formed of the carbon layer and the silver layer was formed, and then externally provided, thereby producing ten solid electrolytic capacitors.
- the aluminum oxide foil was immersed in a 5% aqueous polyaniline solution. By conducting a heat treatment at 0 for 5 minutes, a conductive layer to be a part of the solid electrolyte layer was formed. Thereafter, n-butyl alcohol is added to a polymerization solution containing 0.2 mol 1 / L of a pyrrole monomer, 0.05 mol 1 of butyl naphthalene sulfonic acid, and water as a main solvent to increase the surface tension to 60 mol / L.
- a polymer solution for forming a solid electrolyte adjusted to X 1 C ⁇ NZm was prepared ⁇ .
- the polymerization initiating electrode was brought close to the surface of the capacitor element, and electrolytic polymerization was performed at a polymerization voltage of 2 V to form a solid electrolyte layer.
- a cathode lead-out portion composed of a carbon layer and a silver layer was formed, and then exterior was provided, thereby producing 10 solid electrolytic capacitors.
- Table 7 shows the characteristics of the initial values of the solid electrolytic capacitors of Examples 11 to 16 and Comparative Examples 3 and 4. The ESR characteristics were measured at 100 kHz.
- Example 1 1 to 1 6 and from the comparison of Comparative Example 3, the compound ([pi) and 7 0 X 1 0- 3 NZM following the child the surface tension of the polymerization solution using sulfuric acid as de one dopant This shows that a solid electrolytic capacitor having excellent capacitance characteristics can be obtained.
- Example 13 Comparative Example 4
- an excellent capacity extraction rate can be obtained particularly when the compound ( ⁇ ) and sulfuric acid are used as dopants.
- Example 14 was carried out in the same manner as in Example 14 except that the addition amount of sulfuric acid to the compound ( ⁇ ) was changed to 100: 1, 50: 1, 10: 1, 5: 1, 4: 1, 2: 1 in molar ratio. In the same manner as in Example 14, ten solid electrolytic capacitors were produced.
- Figure 7 shows the initial values of this solid electrolytic capacitor and the capacitance characteristics after 1000 hours of application of the 85 ⁇ 85% rated voltage.
- Example 14 butyl naphthalene sulfonic acid was used in place of the compound ( ⁇ ), and the amount of sulfuric acid was changed with respect to butyl naphthylene sulfonic acid in a molar ratio of 100: 1, 50 by changing the amount of sulfuric acid. : 1, 10: 1, 5: 1, 4:
- the solid electrolytic capacitor 1 was manufactured in the same manner as in Example 14 except that it was changed to 1, 2: 1.
- Figure 7 shows the initial values of this solid electrolytic capacitor and the capacitance characteristics after 1000 hours of application of the 85% rated voltage at 85 ° C and 85 ° C.
- the effect of increasing the capacity extraction rate by adding sulfuric acid is particularly obtained when the compound ( ⁇ ) is used.
- naphthyl having an alkyl group such as butyl naphthalene sulfonic acid is used. If evening with sulfone acid it can be seen that not obtain the effect of the capacity draw-out rate increased as follows 70 X 10- 3 N / m additives and surface tension sulfuric acid. This is because these naphthene sulfonic acids have surface activity This is considered to be because the polymer is likely to be concentrated on the edge of the pit where the valve metal has been roughened due to too high a property to form a polymer.
- the compound ([pi) 5 0 adding at least one molar, and the surface tension 7 0 X 1 0- 3 NZm less Need to be used. Further, in order to obtain a solid electrolytic capacitor with less deterioration in a high-temperature, high-humidity environment, it is preferable to adjust the molar concentration ratio of sulfuric acid to the compound (II) in the polymerization solution to 4: 1 or less.
- Example 1 3 n-blanking evening By changing the addition amount of Nord, the surface tension of the polymerization mixture 4 0 X 1 0- 3, 5 0 X 1 0 -3, 5 5 X 1 0- 3, 6 the solid electrolyte at 0 X 1 0- 3, 6 5 X 1 0 "3, 7 0 X 1 0- 3, 7 3 X 1 0- 3 NZm and except for changing example 1 3 same as the method Ten capacitors were produced.
- Figure 8 shows the initial capacitance characteristics of this solid electrolytic capacitor.
- the solid electrolytic capacitor can be obtained having excellent capacity characteristics by the surface tension of the polymer solution 7 0 X 1 0 one 3 NZM below.
- methyl alcohol Ichiru instead of 2 one-propanol as the organic solvent, ethyl alcohol, n- propyl alcohol, n- butyl alcohol, 2-heptyl Alcohol, tri-butyl alcohol, tert-butyl alcohol, acetonitrile, acetone, tetrahydrofuran, ethylene glycol and tert-butyl lactone can be added.
- nonionic surfactants such as acetyldaricol-based surfactants, silicon-based surfactants, polyoxyalkylendalicol-based surfactants, and fluorine-based surfactants.
- Example 14 paranitrophenol was added to the polymerization solution for forming a solid electrolyte in the form of 0.01, 0.005, 0.01, 0.05, 0.1, 0.2, 0. . 3 mo
- Ten solid electrolytic capacitors were produced in the same manner as in Example 14 except that 1 was added, and paranitrophenol was added to a part of the conductive polymer.
- Figure 9 shows the initial values of this solid electrolytic capacitor and the ESR characteristics after the high-temperature no-load (125 500 hours) test. The ESR characteristics were measured at 100 kHz. As is clear from Fig.
- the solid electrolytic capacitor with the addition amount of paranitrophenol of 0.001 to 0.2 mo 1 has excellent ESR characteristics, and the case of less than 0.001 mo 1 and more than 0.2 mo 1 There is a tendency for ESR characteristics to deteriorate. Therefore, in order for paranitrophenol to increase the order of the polymer skeleton and obtain a stable solid electrolytic capacitor even under high temperature conditions, the amount of paranitrophenol added should be in the range of 0.001 to 0.2 mol. Is preferred.
- FIG. 10 shows the ESR characteristics of the initial value of this solid electrolytic capacitor. The ESR characteristics were measured at 100 kHz.
- the right vertical axis shows the polymerization time
- the left vertical axis shows the initial ESR characteristics
- the horizontal axis shows the polymerization voltage.
- the polymerization voltage is preferably in the range of 1 to 3 V.
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Abstract
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US10/512,568 US7289313B2 (en) | 2003-02-19 | 2004-02-19 | Solid electrolytic capacitor and method for manufacturing same |
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JP2003041109A JP4019968B2 (ja) | 2003-02-19 | 2003-02-19 | 固体電解コンデンサ及びその製造方法 |
JP2003080280A JP4063116B2 (ja) | 2003-03-24 | 2003-03-24 | 固体電解コンデンサの製造方法 |
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US8083920B2 (en) * | 2008-03-31 | 2011-12-27 | Sanyo Electric Co., Ltd | Method for manufacturing solid electrolytic capacitor |
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KR101087902B1 (ko) * | 2007-06-26 | 2011-11-30 | 데이카 가부시키가이샤 | 도전성 고분자 합성용 산화제겸 도판트, 이의 알콜 용액, 도전성 고분자 및 고체 전해 콘덴서 |
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WO2006085601A1 (ja) * | 2005-02-08 | 2006-08-17 | Tayca Corporation | 導電性高分子用ドーパント溶液、導電性高分子用酸化剤兼ドーパント溶液、導電性組成物および固体電解コンデンサ |
US7651637B2 (en) | 2005-02-08 | 2010-01-26 | Tayca Corporation | Dopant solution for an electroconductive polymer, an oxidant and dopant solution for an electroconductive polymer, an electroconductive composition and a solid electrolytic capacitor |
KR101144526B1 (ko) | 2005-02-08 | 2012-05-11 | 엔이씨 도낀 가부시끼가이샤 | 도전성 고분자용 도판트 용액, 도전성 고분자용 산화제겸도판트 용액, 도전성 조성물 및 고체 전해 컨덴서 |
TWI425528B (zh) * | 2005-02-08 | 2014-02-01 | Tayca Corp | 導電性高分子用摻雜劑溶液、導電性高分子用氧化劑兼摻雜劑溶液、導電性組成物及固體電解電容 |
US8083920B2 (en) * | 2008-03-31 | 2011-12-27 | Sanyo Electric Co., Ltd | Method for manufacturing solid electrolytic capacitor |
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TWI285385B (en) | 2007-08-11 |
US7289313B2 (en) | 2007-10-30 |
US20050237696A1 (en) | 2005-10-27 |
TW200425190A (en) | 2004-11-16 |
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