JP2009010000A - Capacitor and manufacturing method thereof - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a capacitor that can increase capacity and has low ESR. <P>SOLUTION: The capacitor comprises: an anode that is made of a valve metal and forms irregularities on the surface; a dielectric layer formed while the surface of the anode is oxidized; and a cathode that is formed on the surface of the dielectric layer and has a solid electrolyte layer containing a π-conjugate-system conductive polymer and polyanion. In the capacitor, one portion or entire portion of the surface at the cathode side of the dielectric layer is treated by a polymer A having a specific chemical structure. <P>COPYRIGHT: (C)2009,JPO&INPIT

Description

  The present invention relates to a capacitor such as an aluminum electrolytic capacitor, a tantalum electrolytic capacitor, a niobium electrolytic capacitor, and a manufacturing method thereof.

 In recent years, with the digitization of electronic devices, capacitors used in electronic devices are required to reduce impedance (equivalent series resistance: ESR) in a high frequency region. Conventionally, in order to meet this requirement, an oxide film of valve metal such as aluminum, tantalum, or niobium is used as a dielectric, and a π-conjugated conductive polymer film such as polypyrrole or polythiophene is formed on this surface to form a cathode. This capacitor is used.

As shown in Patent Document 1, this capacitor is made of a valve metal, an anode having irregularities formed on the surface, a dielectric layer formed by oxidizing the surface of the anode, and a solid electrolyte in the dielectric layer. A layer and a cathode on which a cathode conductive layer is laminated are generally used.
As a method for forming a film of a π-conjugated conductive polymer, an electrolytic polymerization method (see Patent Document 2) and a chemical oxidative polymerization method (see Patent Document 3) are widely known.
However, in the electropolymerization method, it is necessary to previously form an electroconductive layer made of manganese oxide on the anode surface, which is very complicated, and manganese oxide has low conductivity and high conductivity. There was a problem that the effect of using a π-conjugated conductive polymer was weakened.
On the other hand, in the chemical oxidation polymerization method, the polymerization time is long, and it is necessary to repeat the polymerization in order to ensure the thickness of the film, so that the production efficiency of the capacitor is low and the conductivity is also low.
Therefore, in Patent Document 4, a method for forming a coating film by preparing a water-soluble polyaniline by chemically oxidatively polymerizing aniline in the presence of a polyanion having a sulfo group, a carboxy group or the like, and applying and drying the aqueous polyaniline solution. Has been proposed.
JP 2003-37024 A JP-A-63-158829 JP 63-173313 A JP-A-7-105718

Generally, a capacitor having a small size and a high capacitance is required. However, it is difficult to increase the capacity of a capacitor having a polyaniline solution coating described in Patent Document 4 as a solid electrolyte layer. Further, in capacitors, there is a demand for further reduction in ESR.
An object of the present invention is to provide a capacitor capable of realizing a high capacity and having a low ESR. It is another object of the present invention to provide a capacitor manufacturing method that can realize a high capacity and can manufacture a capacitor with low ESR with high productivity.

  As a result of investigations by the present inventors, a high capacitance cannot be obtained when a solution containing a π-conjugated conductive polymer and a polyanion is applied. It was estimated that this was because the aqueous solution contained did not penetrate deep into the dielectric layer. From this, as a result of studying a method for increasing the affinity for the π-conjugated conductive polymer and polyanion on the surface of the dielectric layer, the following capacitor and the manufacturing method thereof were invented.

That is, the present invention includes the following aspects.
[1] An anode made of a valve metal and having irregularities formed on the surface thereof, a dielectric layer formed by oxidizing the surface of the anode, and formed on the surface of the dielectric layer. In a capacitor having a cathode with a solid electrolyte layer containing molecules and polyanions,
Part or all of the surface on the cathode side of the dielectric layer is treated with a polymer (A) having one or more chemical structures selected from the group consisting of the following (a) to (f): Capacitor.
(R ¹ represents a hydrogen atom or an alkyl group.)

[2] The capacitor according to [1], wherein a high conductivity agent is added to the polymer (A) used for the treatment of the cathode side surface of the dielectric layer.

[3] A dielectric layer forming step of forming a dielectric layer by oxidizing the surface of the anode made of a valve metal and having irregularities formed on the surface;
The surface of the dielectric layer is a polymer (A) having a pH of 3 to 12 at 25 ° C. and having one or more chemical structures selected from the group consisting of the following (a) to (f) or the polymer (A): A treatment step of treating with a treatment liquid containing the compound (B) to be formed;
A solid that forms a solid electrolyte layer by applying a conductive polymer solution containing a π-conjugated conductive polymer, a polyanion and a solvent on the surface of the dielectric layer treated with the polymer (A) or the compound (B). A method for manufacturing a capacitor, comprising: an electrolyte layer forming step.
(R ¹ represents a hydrogen atom or an alkyl group.)

[4] The method for manufacturing a capacitor according to [3], wherein the treatment liquid further includes a high conductivity agent.

The capacitor of the present invention can realize high capacity and has low ESR.
According to the method for manufacturing a capacitor of the present invention, it is possible to realize a high capacity and to manufacture a capacitor with low ESR with high productivity.

"Capacitor"
Hereinafter, an embodiment of the capacitor of the present invention will be described.
FIG. 1 is a diagram illustrating a configuration of a capacitor according to the present embodiment. The capacitor 10 is roughly configured to include an anode 11 made of a valve metal, a dielectric layer 12 formed by oxidizing the surface of the anode 11, and a cathode 13 formed on the dielectric layer 12. Yes.

<Anode>
Examples of the valve metal forming the anode 11 include aluminum, tantalum, niobium, titanium, hafnium, zirconium, zinc, tungsten, bismuth, and antimony. Of these, aluminum, tantalum, and niobium are preferable.
As a specific example of the anode 11, an aluminum foil is etched to increase the surface area, and then the surface is oxidized, or the surface of a sintered body of tantalum particles and niobium particles is oxidized to form a porous pellet. The thing which was done is mentioned. The anode 11 treated in this way has irregularities formed on the surface.

<Dielectric layer>
The dielectric layer 12 is formed, for example, by anodizing the surface of the anode 11 in an electrolytic solution such as an aqueous solution of ammonium adipate. Therefore, as shown in FIG. 1, the dielectric layer 12 is formed along the unevenness of the surface of the anode 11.

In this embodiment, the surface of the dielectric layer 12 on the cathode 13 side is treated with the polymer (A). Therefore, the polymer (A) 14 exists on the surface of the dielectric layer 12 on the cathode 13 side.
Moreover, since the ESR of the capacitor 10 can be further lowered in the polymer (A) used for the treatment of the surface of the dielectric layer 12 on the cathode 13 side, it is preferable that a high conductivity agent described later is added. When a highly conductive agent is added to the polymer (A), the highly conductive agent is also present on the surface of the dielectric layer 12 on the cathode 13 side.

(Polymer (A))
The polymer (A) is a polymer having one or more chemical structures selected from the group consisting of the above (a) to (f). R ¹ represents a hydrogen atom or an alkyl group (for example, methyl group, ethyl group, propyl group, butyl group, etc.).

Examples of the polymer having the chemical structure (a) include polyesters such as polyethylene terephthalate, polybutylene terephthalate, and polyethylene naphthalate.
Examples of the polymer having the chemical structure (b) include polyacrylic polyurethane, polyester polyurethane, polyether polyurethane, and polyurea.
Examples of the polymer having the chemical structure (c) include polyamides such as polyamide 6, polyamide 6,6, polyamide 12, and polyamide 11, polyimide, polyamideimide, and polyimide silicone.
Examples of the polymer having the chemical structure (d) include an acrylic resin.
Examples of the polymer having the chemical structure (e) include polyvinyl alcohol and phenol resin.
Examples of the polymer having the chemical structure (f) include polyether, polyvinyl ether, and polyhydroxyalkyl acrylate.

  Examples of the polyether include diethylene glycol, triethylene glycol, oligoethylene glycol, triethylene glycol monochlorohydrin, diethylene glycol monochlorohydrin, oligoethylene glycol monochlorohydrin, triethylene glycol monobromhydrin, diethylene glycol monobromhydrin, oligoethylene. Glycol monobromohydrin, polyethylene glycol, polyethylene oxide, triethylene glycol / dimethyl ether, tetraethylene glycol / dimethyl ether, diethylene glycol / dimethyl ether, diethylene glycol / diethyl ether, diethylene glycol / dibutyl ether, dipropylene glycol / tripropylene glycol, polypropylene Glycol, polypropylene dioxide, polyoxyethylene alkyl ether, polyoxyethylene glycerin fatty acid ester, polyoxyethylene fatty acid amide, ethylene glycol di (meth) acrylate, diethylene glycol di (meth) acrylate, triethylene glycol di (meth) acrylate, Examples include polyethylene glycol di (meth) acrylate, neopentyl glycol di (meth) acrylate, ethylene oxide modified trimethylolpropane triacrylate, ethylene oxide modified pentaerythritol triacrylate, ethylene oxide modified pentaerythritol tetraacrylate, and the like.

  In addition to the above polymers, for example, fluorine resins such as polyvinylidene fluoride, polyvinyl fluoride, polytetrafluoroethylene, ethylene tetrafluoroethylene copolymer, and polychlorotrifluoroethylene; vinyl resins such as polyvinyl butyral, polyvinyl acetate, and polyvinyl chloride An epoxy resin, a xylene resin, an aramid resin, a melamine resin, and the like can also be used.

<Cathode>
The cathode 13 includes a solid electrolyte layer 13a and a cathode conductive layer 13b made of carbon, silver, aluminum or the like formed on the solid electrolyte layer 13a.
(Solid electrolyte layer)
The solid electrolyte layer 13 a is a layer containing a π-conjugated conductive polymer and a polyanion, and is formed on the dielectric layer 12 on the cathode 13 side.

[Π-conjugated conductive polymer]
The π-conjugated conductive polymer can be used as long as the main chain is an organic polymer having a π-conjugated system. Examples thereof include polypyrroles, polythiophenes, polyacetylenes, polyphenylenes, polyphenylene vinylenes, polyanilines, polyacenes, polythiophene vinylenes, and copolymers thereof.

  Specific examples of such π-conjugated conductive polymers include polypyrrole, poly (N-methylpyrrole), poly (3-methylpyrrole), poly (3-ethylpyrrole), and poly (3-n-propylpyrrole). ), Poly (3-butylpyrrole), poly (3-octylpyrrole), poly (3-decylpyrrole), poly (3-dodecylpyrrole), poly (3,4-dimethylpyrrole), poly (3,4 Dibutylpyrrole), poly (3-carboxypyrrole), poly (3-methyl-4-carboxypyrrole), poly (3-methyl-4-carboxyethylpyrrole), poly (3-methyl-4-carboxybutylpyrrole), Poly (3-hydroxypyrrole), poly (3-methoxypyrrole), poly (3-ethoxypyrrole), poly (3-butoxypyrrole), poly 3-hexyloxypyrrole), poly (3-methyl-4-hexyloxypyrrole), poly (3-methyl-4-hexyloxypyrrole), polythiophene, poly (3-methylthiophene), poly (3-ethylthiophene) , Poly (3-propylthiophene), poly (3-butylthiophene), poly (3-hexylthiophene), poly (3-heptylthiophene), poly (3-octylthiophene), poly (3-decylthiophene), poly (3-dodecylthiophene), poly (3-octadecylthiophene), poly (3-bromothiophene), poly (3-chlorothiophene), poly (3-iodothiophene), poly (3-cyanothiophene), poly (3 -Phenylthiophene), poly (3,4-dimethylthiophene), poly (3,4-dibuty) Ruthiophene), poly (3-hydroxythiophene), poly (3-methoxythiophene), poly (3-ethoxythiophene), poly (3-butoxythiophene), poly (3-hexyloxythiophene), poly (3-heptyl) Oxythiophene), poly (3-octyloxythiophene), poly (3-decyloxythiophene), poly (3-dodecyloxythiophene), poly (3-octadecyloxythiophene), poly (3,4-dihydroxythiophene), Poly (3,4-dimethoxythiophene), poly (3,4-diethoxythiophene), poly (3,4-dipropoxythiophene), poly (3,4-dibutoxythiophene), poly (3,4-dihexyl) Oxythiophene), poly (3,4-diheptyloxythiophene), poly (3 4-dioctyloxythiophene), poly (3,4-didecyloxythiophene), poly (3,4-didodecyloxythiophene), poly (3,4-ethylenedioxythiophene), poly (3,4-propylene) Dioxythiophene), poly (3,4-butenedioxythiophene), poly (3-methyl-4-methoxythiophene), poly (3-methyl-4-ethoxythiophene), poly (3-carboxythiophene), poly (3-methyl-4-carboxythiophene), poly (3-methyl-4-carboxyethylthiophene), poly (3-methyl-4-carboxybutylthiophene), polyaniline, poly (2-methylaniline), poly (3 -Isobutylaniline), poly (2-anilinesulfonic acid), poly (3-anilinesulfonic acid), etc. It is below.

  Among these, one or two selected from polypyrrole, polythiophene, poly (N-methylpyrrole), poly (3-methylthiophene), poly (3-methoxythiophene), and poly (3,4-ethylenedioxythiophene) A (co) polymer consisting of seeds is preferably used from the viewpoint of resistance and reactivity. Furthermore, polypyrrole and poly (3,4-ethylenedioxythiophene) are more preferable because they have higher conductivity and improved heat resistance.

  The content of the π-conjugated conductive polymer in the solid electrolyte layer 13a is preferably 1% by mass or more and more preferably 5% by mass or more because the function as the capacitor 10 can be sufficiently exhibited. .

[Polyanion]
The polyanion is a homopolymer or copolymer selected from substituted or unsubstituted polyalkylene, substituted or unsubstituted polyalkenylene, substituted or unsubstituted polyimide, substituted or unsubstituted polyamide, substituted or unsubstituted polyester And having a structural unit having an anionic group and optionally having a structural unit having no anionic group.
The polyanion not only solubilizes the π-conjugated conductive polymer in a solvent, but also functions as a dopant for the π-conjugated conductive polymer.

Here, polyalkylene is a polymer whose main chain is composed of repeating methylene.
Polyalkenylene is a polymer composed of structural units containing one or more unsaturated bonds (vinyl groups) in the main chain. Among these, substituted or unsubstituted butenylene is preferable because of the interaction between the unsaturated bond and the π-conjugated conductive polymer and the ease of synthesis using substituted or unsubstituted butadiene as a starting material.

As polyimide, pyromellitic dianhydride, biphenyltetracarboxylic dianhydride, benzophenonetetracarboxylic dianhydride, 2,2 ′, 3,3′-tetracarboxydiphenyl ether dianhydride, 2,2 ′-[ Examples include polyimides from anhydrides such as 4,4′-di (dicarboxyphenyloxy) phenyl] propane dianhydride and diamines such as oxydiamine, paraphenylenediamine, metaphenylenediamine, and benzophenonediamine.
Examples of the polyamide include polyamide 6, polyamide 6,6, polyamide 6,10 and the like.
Examples of the polyester include polyethylene terephthalate and polybutylene terephthalate.

When the polyanion has a substituent, examples of the substituent include an alkyl group, a hydroxy group, an amino group, a cyano group, a phenyl group, a phenol group, an ester group, an alkoxy group, and a carbonyl group. In view of solubility in a solvent, heat resistance, compatibility with a resin, and the like, an alkyl group, a hydroxy group, a phenol group, and an ester group are preferable.
Alkyl groups can increase solubility and dispersibility in polar or nonpolar solvents, compatibility and dispersibility in resins, and hydroxy groups form hydrogen bonds with other hydrogen atoms. It can be made easy, and the solubility in an organic solvent, the compatibility with a resin, the dispersibility, and the adhesiveness can be increased. In addition, the cyano group and the hydroxyphenyl group can increase the compatibility and solubility in the polar resin, and can also increase the heat resistance.
Among the above substituents, an alkyl group, a hydroxy group, an ester group, and a cyano group are preferable.

Examples of the alkyl group include chain alkyl groups such as methyl, ethyl, propyl, butyl, isobutyl, t-butyl, pentyl, hexyl, octyl, decyl, and dodecyl, and cycloalkyl groups such as cyclopropyl, cyclopentyl, and cyclohexyl. . In consideration of solubility in an organic solvent, dispersibility in a resin, steric hindrance, and the like, an alkyl group having 1 to 12 carbon atoms is more preferable.
Examples of the hydroxy group include a hydroxy group directly bonded to the main chain of the polyanion or a hydroxy group bonded via another functional group. Examples of other functional groups include an alkyl group having 1 to 7 carbon atoms, an alkenyl group having 2 to 7 carbon atoms, an amide group, and an imide group. The hydroxy group is substituted at the end or in these functional groups. Among these, a hydroxy group bonded to the terminal of an alkyl group having 1 to 6 carbon atoms bonded to the main chain is more preferable from the viewpoint of compatibility with a resin and solubility in an organic solvent.
Examples of the ester group include an alkyl ester group directly bonded to the main chain of the polyanion, an aromatic ester group, and an alkyl ester group or an aromatic ester group having another functional group interposed therebetween.
The cyano group includes a cyano group directly bonded to the main chain of the polyanion, a cyano group bonded to the terminal of the alkyl group having 1 to 7 carbon atoms bonded to the main chain of the polyanion, and 2 to 2 carbon atoms bonded to the main chain of the polyanion. And a cyano group bonded to the terminal of 7 alkenyl group.

  The anion group of the polyanion may be a functional group capable of undergoing chemical oxidation doping to the π-conjugated conductive polymer. Among them, from the viewpoint of ease of production and stability, a monosubstituted sulfate group, A monosubstituted phosphate group, a phosphate group, a carboxy group, a sulfo group and the like are preferable. Furthermore, a sulfo group and a monosubstituted sulfate group are more preferable from the viewpoint of the doping effect of the functional group on the π-conjugated conductive polymer.

Specific examples of polyanions include polyvinyl sulfonic acid, polystyrene sulfonic acid, polyallyl sulfonic acid, polyacryl sulfonic acid, polymethacryl sulfonic acid, poly (2-acrylamido-2-methylpropane sulfonic acid), polyisoprene sulfonic acid, poly Acrylic acid etc. are mentioned. These homopolymers may be sufficient and 2 or more types of copolymers may be sufficient.
Of these, polyacrylsulfonic acid and polymethacrylsulfonic acid can alleviate thermal decomposition of the π-conjugated conductive polymer by absorbing thermal energy and decomposing by itself. Therefore, it is excellent in heat resistance and environmental resistance.

[High conductivity agent]
Since the solid electrolyte layer 13a can reduce the ESR of the capacitor 10, it is preferable that the solid electrolyte layer 13a contains a high conductivity agent that acts on the π-conjugated conductive polymer to improve the conductivity of the solid electrolyte layer 13a.
Examples of the highly conductive agent include nitrogen-containing aromatic cyclic compounds, compounds having two or more hydroxy groups, compounds having two or more carboxy groups, one or more hydroxy groups, and one or more carboxy groups. Examples thereof include a compound having a group, a compound having an amide group, a compound having an imide group, a lactam compound, a compound having a glycidyl group, an acrylic compound, and a water-soluble organic solvent.

-Nitrogen-containing aromatic cyclic compound A nitrogen-containing aromatic cyclic compound has an aromatic ring containing at least one nitrogen atom, and the nitrogen atom in the aromatic ring is in the aromatic ring. It has a conjugated relationship with other atoms. In order to become a conjugated relationship, the nitrogen atom and other atoms form an unsaturated bond. Alternatively, even if the nitrogen atom does not directly form an unsaturated bond with another atom, it may be adjacent to the other atom that forms the unsaturated bond. This is because an unshared electron pair existing on a nitrogen atom can form a pseudo conjugate relationship with an unsaturated bond formed between other atoms.
The nitrogen-containing aromatic cyclic compound preferably has both a nitrogen atom having a conjugated relationship with another atom and a nitrogen atom adjacent to the other atom forming the unsaturated bond.

Examples of such nitrogen-containing aromatic cyclic compounds include pyridines and derivatives thereof containing one nitrogen atom, imidazoles and derivatives thereof containing two nitrogen atoms, pyrimidines and derivatives thereof, and pyrazines. And derivatives thereof, triazines containing three nitrogen atoms, and derivatives thereof. From the viewpoint of solvent solubility and the like, pyridines and derivatives thereof, imidazoles and derivatives thereof, and pyrimidines and derivatives thereof are preferable.
Nitrogen-containing aromatic cyclic compounds are those in which substituents such as alkyl groups, hydroxy groups, carboxy groups, cyano groups, phenyl groups, phenol groups, oxycarbonyl groups, alkoxy groups, and carbonyl groups are introduced into the ring. However, it may be not introduced. The ring may be polycyclic.

  Specific examples of pyridines and derivatives thereof include pyridine, 2-methylpyridine, 3-methylpyridine, 4-methylpyridine, 4-ethylpyridine, N-vinylpyridine, 2,4-dimethylpyridine, 2,4. , 6-trimethylpyridine, 3-cyano-5-methylpyridine, 2-pyridinecarboxylic acid, 6-methyl-2-pyridinecarboxylic acid, 4-pyridinecarboxaldehyde, 4-aminopyridine, 2,3-diaminopyridine, 2 , 6-diaminopyridine, 2,6-diamino-4-methylpyridine, 4-hydroxypyridine, 4-pyridinemethanol, 2,6-dihydroxypyridine, 2,6-pyridinedimethanol, methyl 6-hydroxynicotinate, 2 -Hydroxy-5-pyridinemethanol, ethyl 6-hydroxynicotinate, 4-pi Lysine methanol, 4-pyridineethanol, 2-phenylpyridine, 3-methylquinoline, 3-ethylquinoline, quinolinol, 2,3-cyclopentenopyridine, 2,3-cyclohexanopyridine, 1,2-di (4- Pyridyl) ethane, 1,2-di (4-pyridyl) propane, 2-pyridinecarboxaldehyde, 2-pyridinecarboxylic acid, 2-pyridinecarbonitrile, 2,3-pyridinedicarboxylic acid, 2,4-pyridinedicarboxylic acid, Examples include 2,5-pyridinedicarboxylic acid, 2,6-pyridinedicarboxylic acid, and 3-pyridinesulfonic acid.

  Specific examples of imidazoles and derivatives thereof include imidazole, 2-methylimidazole, 2-propylimidazole, 2-undecylimidazole, 2-phenylimidazole, N-methylimidazole, N-vinylimidazole, and N-allylimidazole. 1- (2-hydroxyethyl) imidazole (N-hydroxyethylimidazole), 2-ethyl-4-methylimidazole, 1,2-dimethylimidazole, 1-benzyl-2-methylimidazole, 1-benzyl-2-phenyl Imidazole, 1-cyanoethyl-2-methylimidazole, 1-cyanoethyl-2-ethyl-4-methylimidazole, 2-phenyl-4,5-dihydroxymethylimidazole, 1-acetylimidazole, 4,5-imidazoledicarbo Acid, dimethyl 4,5-imidazole dicarboxylate, benzimidazole, 2-aminobenzimidazole, 2-aminobenzimidazole-2-sulfonic acid, 2-amino-1-methylbenzimidazole, 2-hydroxybenzimidazole , 2- (2-pyridyl) benzimidazole and the like.

  Specific examples of pyrimidines and derivatives thereof include 2-amino-4-chloro-6-methylpyrimidine, 2-amino-6-chloro-4-methoxypyrimidine, 2-amino-4,6-dichloropyrimidine, 2-amino-4,6-dihydroxypyrimidine, 2-amino-4,6-dimethylpyrimidine, 2-amino-4,6-dimethoxypyrimidine, 2-aminopyrimidine, 2-amino-4-methylpyrimidine, 4,6 -Dihydroxypyrimidine, 2,4-dihydroxypyrimidine-5-carboxylic acid, 2,4,6-triaminopyrimidine, 2,4-dimethoxypyrimidine, 2,4,5-trihydroxypyrimidine, 2,4-pyrimidinediol, etc. Is mentioned.

  Specific examples of the pyrazines and derivatives thereof include pyrazine, 2-methylpyrazine, 2,5-dimethylpyrazine, pyrazinecarboxylic acid, 2,3-pyrazinedicarboxylic acid, 5-methylpyrazinecarboxylic acid, pyrazineamide, 5 -Methylpyrazine amide, 2-cyanopyrazine, aminopyrazine, 3-aminopyrazine-2-carboxylic acid, 2-ethyl-3-methylpyrazine, 2,3-dimethylpyrazine, 2,3-diethylpyrazine and the like.

  Specific examples of triazines and derivatives thereof include 1,3,5-triazine, 2-amino-1,3,5-triazine, 3-amino-1,2,4-triazine, and 2,4-diamino. -6-phenyl-1,3,5-triazine, 2,4,6-triamino-1,3,5-triazine, 2,4,6-tris (trifluoromethyl) -1,3,5-triazine, 2,4,6-tri-2-pyridine-1,3,5-triazine, 3- (2-pyridine) -5,6-bis (4-phenylsulfonic acid) -1,2,4-triazine disodium 3- (2-pyridine) -5,6-diphenyl-1,2,4-triazine, 3- (2-pyridine) -5,6-diphenyl-1,2,4-triazine-ρ, ρ′- Disodium disulphonate, 2-hydroxy-4,6-dichloro -1,3,5-triazine and the like.

Since a non-shared electron pair exists in the nitrogen atom in the nitrogen-containing aromatic cyclic compound, a substituent or a proton is easily coordinated or bonded on the nitrogen atom. When a substituent or proton is coordinated or bonded to a nitrogen atom, it tends to have a cationic charge on the nitrogen atom. Here, since the nitrogen atom and other atoms have a conjugated relationship, the cation charge generated by the coordination or bonding of a substituent or a proton on the nitrogen atom is contained in the nitrogen-containing aromatic ring. Once diffused, it will exist in a stable form.
For this reason, in the nitrogen-containing aromatic cyclic compound, a substituent may be introduced into the nitrogen atom to form a nitrogen-containing aromatic cyclic compound cation. Further, a salt may be formed by combining the cation and the anion. Even if it is a salt, the same effect as a nitrogen-containing aromatic cyclic compound which is not a cation is exhibited.
The substituent introduced into the nitrogen atom of the nitrogen-containing aromatic cyclic compound includes a hydrogen atom, an alkyl group, a hydroxy group, a carboxy group, a cyano group, a phenyl group, a phenol group, an oxycarbonyl group, an alkoxy group, and a carbonyl group. Etc. As the kind of the substituent, the substituent shown above can be introduced.

  The content of the nitrogen-containing aromatic cyclic compound is preferably in the range of 0.1 to 100 mol, more preferably in the range of 0.5 to 30 mol, with respect to 1 mol of the anion group unit of the polyanion. A range of 1 to 10 moles is particularly preferable from the viewpoint of physical properties and conductivity of the solid electrolyte layer 13a. When the content of the nitrogen-containing aromatic cyclic compound is less than 0.1 mol, the interaction between the nitrogen-containing aromatic cyclic compound, the polyanion and the conjugated conductive polymer tends to be weak, and the conductivity May be insufficient. In addition, when the nitrogen-containing aromatic cyclic compound exceeds 100 moles, the content of the conjugated conductive polymer decreases, and it is difficult to obtain sufficient conductivity, and the physical properties of the solid electrolyte layer 13a change. There are things to do.

-Compound having two or more hydroxy groups Examples of the compound having two or more hydroxy groups include propylene glycol, 1,3-butylene glycol, 1,4-butylene glycol, glycerin, diglycerin, D-glucose, D-glucitol, isoprene glycol, dimethylolpropionic acid, butanediol, 1,5-pentanediol, 1,6-hexanediol, 1,9-nonanediol, neopentyl glycol, trimethylolethane, trimethylolpropane, pentaerythritol Polyhydric aliphatic alcohols such as dipentaerythritol, thiodiethanol, glucose, tartaric acid, D-glucaric acid and glutaconic acid;
Polymer alcohols such as polyvinyl alcohol, cellulose, polysaccharides, sugar alcohols;
1,4-dihydroxybenzene, 1,3-dihydroxybenzene, 2,3-dihydroxy-1-pentadecylbenzene, 2,4-dihydroxyacetophenone, 2,5-dihydroxyacetophenone, 2,4-dihydroxybenzophenone, 2,6 -Dihydroxybenzophenone, 3,4-dihydroxybenzophenone, 3,5-dihydroxybenzophenone, 2,4'-dihydroxydiphenylsulfone, 2,2 ', 5,5'-tetrahydroxydiphenylsulfone, 3,3', 5,5 '-Tetramethyl-4,4'-dihydroxydiphenylsulfone, hydroxyquinonecarboxylic acid and its salts, 2,3-dihydroxybenzoic acid, 2,4-dihydroxybenzoic acid, 2,5-dihydroxybenzoic acid, 2,6- Dihydroxybenzoic acid, 3,5-di Droxybenzoic acid, 1,4-hydroquinonesulfonic acid and its salts, 4,5-hydroxybenzene-1,3-disulfonic acid and its salts, 1,5-dihydroxynaphthalene, 1,6-dihydroxynaphthalene, 2,6- Dihydroxynaphthalene, 2,7-dihydroxynaphthalene, 2,3-dihydroxynaphthalene, 1,5-dihydroxynaphthalene-2,6-dicarboxylic acid, 1,6-dihydroxynaphthalene-2,5-dicarboxylic acid, 1,5-dihydroxy Naphthoic acid, 1,4-dihydroxy-2-naphthoic acid phenyl ester, 4,5-dihydroxynaphthalene-2,7-disulfonic acid and its salts, 1,8-dihydroxy-3,6-naphthalenedisulfonic acid and its salts, 6,7-Dihydroxy-2-naphthalenesulfonic acid and its 1,2,3-trihydroxybenzene (pyrogallol), 1,2,4-trihydroxybenzene, 5-methyl-1,2,3-trihydroxybenzene, 5-ethyl-1,2,3-tri Hydroxybenzene, 5-propyl-1,2,3-trihydroxybenzene, trihydroxybenzoic acid, trihydroxyacetophenone, trihydroxybenzophenone, trihydroxybenzaldehyde, trihydroxyanthraquinone, 2,4,6-trihydroxybenzene, tetra Examples thereof include aromatic compounds such as hydroxy-p-benzoquinone, tetrahydroxyanthraquinone, methyl garlic acid (methyl gallate) and ethyl garlic acid (ethyl gallate), and potassium hydroquinone sulfonate.

  The content of the compound having two or more hydroxy groups is preferably in the range of 0.05 to 50 mol and more preferably in the range of 0.3 to 10 mol with respect to 1 mol of the anion group unit of the polyanion. More preferred. If the content of the compound having two or more hydroxy groups is less than 0.05 mol with respect to 1 mol of the anion group unit of the polyanion, conductivity and heat resistance may be insufficient. Further, when the content of the compound having two or more hydroxy groups is more than 50 moles per mole of the anion group unit of the polyanion, the content of the π-conjugated conductive polymer in the solid electrolyte layer 13a is small. Thus, it is difficult to obtain sufficient conductivity, and the physical properties of the solid electrolyte layer 13a may change.

When a compound having two or more hydroxy groups is included as the high conductivity agent, the conductivity of the solid electrolyte layer 13a can be further increased for the following reason.
The π-conjugated conductive polymer in the solid electrolyte layer 13a is in a highly oxidized state, and a part of the π-conjugated conductive polymer is easily oxidized and deteriorated by heat or the like. Therefore, it is considered that radicals are generated and the deterioration proceeds due to radical chains. However, it is presumed that a compound having two or more hydroxy groups can block the radical chain by radical scavenging of the hydroxy groups and suppress the progress of deterioration, and as a result, the conductivity becomes higher.

-Compound having two or more carboxy groups Examples of the compound having two or more carboxy groups include maleic acid, fumaric acid, itaconic acid, citraconic acid, malonic acid, 1,4-butanedicarboxylic acid, succinic acid, tartaric acid, Aliphatic carboxylic acid compounds such as adipic acid, D-glucaric acid, glutaconic acid and citric acid;
Phthalic acid, terephthalic acid, isophthalic acid, tetrahydrophthalic anhydride, 5-sulfoisophthalic acid, 5-hydroxyisophthalic acid, methyltetrahydrophthalic anhydride, 4,4'-oxydiphthalic acid, biphenyltetracarboxylic dianhydride, benzophenone tetra Aromatic carboxylic acid compounds in which at least one carboxy group is bonded to an aromatic ring, such as carboxylic dianhydride, naphthalene dicarboxylic acid, trimellitic acid, pyromellitic acid; diglycolic acid, oxydibutyric acid Thiodiacetic acid (thiodiacetic acid), thiodibutyric acid, iminodiacetic acid, iminobutyric acid and the like.

  The compound having two or more carboxy groups is preferably in the range of 0.1 to 30 mol, more preferably in the range of 0.3 to 10 mol, relative to 1 mol of the anion group unit of the polyanion. When the content of the compound having two or more carboxy groups is less than 0.1 mol relative to 1 mol of the anion group unit of the polyanion, conductivity and heat resistance may be insufficient. Further, when the content of the compound having two or more carboxy groups is more than 30 moles relative to 1 mole of the anion group unit of the polyanion, the content of the π-conjugated conductive polymer in the solid electrolyte layer 13a decreases. However, it is difficult to obtain sufficient conductivity, and the physical properties of the solid electrolyte layer 13a may change.

-A compound having one or more hydroxy groups and one or more carboxy groups As a compound having one or more hydroxy groups and one or more carboxy groups, tartaric acid, glyceric acid, dimethylolbutanoic acid, dimethylolpropanoic acid , D-glucaric acid, glutaconic acid and the like.

  The content of the compound having one or more hydroxy groups and one or more carboxy groups is preferably 1 to 5,000 parts by mass with respect to 100 parts by mass in total of the polyanion and the π-conjugated conductive polymer. 50 to 500 parts by mass is more preferable. When the content of the compound having one or more hydroxy groups and one or more carboxy groups is less than 1 part by mass, conductivity and heat resistance may be insufficient. In addition, when the content of the compound having one or more hydroxy groups and one or more carboxy groups exceeds 5,000 parts by mass, the content of the π-conjugated conductive polymer in the solid electrolyte layer 13a decreases. Again, it is difficult to obtain sufficient conductivity.

Amide Compound A compound having an amide group is a monomolecular compound having an amide bond represented by —CO—NH— (the CO moiety is a double bond) in the molecule. That is, as the amide compound, for example, a compound having functional groups at both ends of the bond, a compound in which a cyclic compound is bonded to one end of the bond, urea and urea derivatives in which the functional groups at both ends are hydrogen Etc.
Specific examples of amide compounds include acetamide, malonamide, succinamide, maleamide, fumaramide, benzamide, naphthamide, phthalamide, isophthalamide, terephthalamide, nicotinamide, isonicotinamide, 2-fluamide, formamide, N-methylformamide, propionamide , Propioluamide, butyramide, isobutylamide, methacrylamide, palmitoamide, stearylamide, oleamide, oxamide, glutaramide, adipamide, cinnamamide, glycolamide, lactamide, glyceramide, tartaramide, citrulamide, glyoxylamide, pyruvamide, acetoacetamide, dimethyl Acetamide, benzylamide, anthranilamide, ethylenediamine Laacetamide, diacetamide, triacetamide, dibenzamide, tribenzamide, rhodanine, urea, 1-acetyl-2-thiourea, biuret, butylurea, dibutylurea, 1,3-dimethylurea, 1,3-diethylurea and These derivatives are mentioned.

  Moreover, acrylamide can also be used as an amide compound. As acrylamide, N-methylacrylamide, N-methylmethacrylamide, N-ethylacrylamide, N-ethylmethacrylamide, N, N-dimethylacrylamide, N, N-dimethylmethacrylamide, N, N-diethylacrylamide, N, Examples thereof include N-diethyl methacrylamide, 2-hydroxyethyl acrylamide, 2-hydroxyethyl methacrylamide, N-methylol acrylamide, N-methylol methacrylamide and the like.

  The molecular weight of the amide compound is preferably 46 to 10,000, more preferably 46 to 5,000, and particularly preferably 46 to 1,000.

  The content of the amide compound is preferably 1 to 5,000 parts by mass and more preferably 50 to 500 parts by mass with respect to 100 parts by mass in total of the polyanion and the π-conjugated conductive polymer. When the content of the amide compound is less than 1 part by mass, conductivity and heat resistance may be insufficient. On the other hand, when the content of the amide compound exceeds 5,000 parts by mass, the content of the π-conjugated conductive polymer in the solid electrolyte layer 13a decreases, and it is difficult to obtain sufficient conductivity.

-Imide compound As an amide compound, since electroconductivity becomes higher, the monomolecular compound (henceforth an imide compound) which has an imide bond is preferable. Examples of the imide compound include phthalimide and phthalimide derivatives, succinimide and succinimide derivatives, benzimide and benzimide derivatives, maleimide and maleimide derivatives, naphthalimide and naphthalimide derivatives from the skeleton.

Moreover, although an imide compound is classified into an aliphatic imide, an aromatic imide, etc. by the kind of functional group of both terminal, an aliphatic imide is preferable from a soluble viewpoint.
Furthermore, the aliphatic imide compound is classified into a saturated aliphatic imide compound having an unsaturated bond between carbons in the molecule and an unsaturated aliphatic imide compound having an unsaturated bond between carbons in the molecule.
The saturated aliphatic imide compound is a compound represented by R ¹¹ —CO—NH—CO—R ¹² , and is a compound in which both R ¹¹ and R ¹² are saturated hydrocarbons. Specifically, cyclohexane-1,2-dicarboximide, allantoin, hydantoin, barbituric acid, alloxan, glutarimide, succinimide, 5-butylhydantoic acid, 5,5-dimethylhydantoin, 1-methylhydantoin, 1,5 , 5-trimethylhydantoin, 5-hydantoin acetic acid, N-hydroxy-5-norbornene-2,3-dicarboximide, semicarbazide, α, α-dimethyl-6-methylsuccinimide, bis [2- (succinimidooxycarbonyloxy) Ethyl] sulfone, α-methyl-α-propylsuccinimide, cyclohexylimide and the like.
The unsaturated aliphatic imide compound is a compound represented by R ¹¹ —CO—NH—CO—R ¹² , and one or both of R ¹¹ and R ¹² are one or more unsaturated bonds. Specific examples are 1,3-dipropylene urea, maleimide, N-methylmaleimide, N-ethylmaleimide, N-hydroxymaleimide, 1,4-bismaleimide butane, 1,6-bismaleimide hexane, 1,8-bis. Maleimide octane, N-carboxyheptylmaleimide and the like can be mentioned.

  The molecular weight of the imide compound is preferably 60 to 5,000, more preferably 70 to 1,000, and particularly preferably 80 to 500.

  The content of the imide compound is preferably 10 to 10,000 parts by mass, more preferably 50 to 5,000 parts by mass with respect to 100 parts by mass in total of the π-conjugated conductive polymer and the polyanion. . If the addition amount of the amide compound and the imide compound is less than the lower limit, the effect of the addition of the amide compound and the imide compound is lowered, which is not preferable. Moreover, when the said upper limit is exceeded, since the electroconductive fall resulting from the fall of (pi) conjugated system conductive polymer concentration will occur, it is unpreferable.

-Lactam compound A lactam compound is an intramolecular cyclic amide of aminocarboxylic acid, and a part of the ring is -CO-NR- (R is hydrogen or an arbitrary substituent). However, one or more carbon atoms in the ring may be replaced with an unsaturated or heteroatom.
Examples of the lactam compound include pentano-4-lactam, 4-pentanelactam-5-methyl-2-pyrrolidone, 5-methyl-2-pyrrolidinone, hexano-6-lactam, 6-hexane lactam and the like.

  The content of the lactam compound is preferably 10 to 10,000 parts by mass, and more preferably 50 to 5000 parts by mass with respect to 100 parts by mass in total of the π-conjugated conductive polymer and the polyanion. If the amount of the lactam compound added is less than the lower limit, the effect of the addition of the lactam compound is reduced, which is not preferable. Moreover, when the said upper limit is exceeded, since the electroconductive fall resulting from the fall of (pi) conjugated system conductive polymer concentration will occur, it is unpreferable.

-Compound having glycidyl group Examples of the compound having glycidyl group include ethyl glycidyl ether, butyl glycidyl ether, t-butyl glycidyl ether, allyl glycidyl ether, benzyl glycidyl ether, glycidyl phenyl ether, bisphenol A, diglycidyl ether, acrylic Examples thereof include glycidyl compounds such as acid glycidyl ether and methacrylic acid glycidyl ether.

  The content of the compound having a glycidyl group is preferably 10 to 10,000 parts by mass, and more preferably 50 to 5000 parts by mass with respect to 100 parts by mass in total of the π-conjugated conductive polymer and the polyanion. When the amount of the compound having a glycidyl group is less than the lower limit, the effect of adding the compound having a glycidyl group is undesirably reduced. Moreover, when the said upper limit is exceeded, since the electroconductive fall resulting from the fall of (pi) conjugated system conductive polymer concentration will occur, it is unpreferable.

Acrylic compounds Acrylic acid, 2-hydroxyethyl methacrylate, 2-hydroxypropyl methacrylate, n-butoxyethyl methacrylate, n-butoxyethylene glycol methacrylate, methoxytriethylene glycol methacrylate, methoxypolyethylene glycol methacrylate, 2-hydroxyethyl acrylate, 2- Monofunctional (meth) acrylate compounds such as hydroxypropyl acrylate, n-butoxyethyl acrylate, n-butoxyethylene glycol acrylate, methoxytriethylene glycol acrylate, methoxypolyethylene glycol acrylate, ethylene glycol di (meth) acrylate, diethylene glycol di (meth) Acrylate, triethylene glycol di (meth) acrylate Relate, bifunctional (meth) acrylates such as polyethylene glycol di (meth) acrylate, neopentyl glycol di (meth) acrylate, glycerin di (meth) acrylate, ethylene glycol diglycidyl ether, glycidyl ether, diethylene glycol diglycidyl ether, triethylene Glycidyl ethers such as glycol diglycidyl ether, polyethylene glycol diglycidyl ether, propylene glycidyl ether, tripropylene glycidyl ether, polypropylene glycidyl ether, glycerin diglycidyl ether, 2-methacryloyloxyethyl succinic acid, glycidyl methacrylate, trimethylolpropane tri Acrylate, ethylene oxide modified trimethylolpropane triac Rate, ethylene oxide-modified pentaerythritol triacrylate, ethylene oxide modified pentaerythritol tetraacrylate and the like.

  The content of the acrylic compound is preferably 10 to 100,000 parts by mass, and more preferably 50 to 10,000 parts by mass with respect to 100 parts by mass in total of the π-conjugated conductive polymer and the polyanion. It is not preferable that the amount of the acrylic compound added is less than the lower limit because the effect of the acrylic compound addition is reduced. Moreover, when the said upper limit is exceeded, since the electroconductive fall resulting from the fall of (pi) conjugated system conductive polymer concentration will occur, it is unpreferable.

Water-soluble organic solvent Examples of the water-soluble organic solvent include N-methyl-2-pyrrolidone, N-methylacetamide, N, N-dimethylformamide, N, N-dimethylacetamide, dimethyl sulfoxide, hexamethylene phosphortriamide, Polar solvents such as N-vinylpyrrolidone, N-vinylformamide, N-vinylacetamide, phenols such as cresol, phenol, xylenol, ethylene glycol, diethylene glycol, triethylene glycol, propylene glycol, dipropylene glycol, 1,3-butylene Glycol, 1,4-butylene glycol, glycerin, diglycerin, D-glucose, D-glucitol, isoprene glycol, butanediol, 1,5-pentanediol, 1,6-hexanediol , Polyhydric aliphatic alcohols such as 1,9-nonanediol and neopentyl glycol, carbonate compounds such as ethylene carbonate and propylene carbonate, ether compounds such as dioxane and diethyl ether, dialkyl ether, propylene glycol dialkyl ether, polyethylene glycol Examples include chain ethers such as dialkyl ether and polypropylene glycol dialkyl ether, heterocyclic compounds such as 3-methyl-2-oxazolidinone, nitrile compounds such as acetonitrile, glutaronitrile, methoxyacetonitrile, propionitrile, and benzonitrile. . These solvents may be used alone or as a mixture of two or more.

[Dopant]
The solid electrolyte layer 13a may contain a dopant other than the polyanion in order to improve the conductivity of the π-conjugated conductive polymer.
As the dopant, halogen compounds, Lewis acids, proton acids, and the like are used. Specifically, organic acids such as organic carboxylic acids and organic sulfonic acids, organic cyano compounds, fullerenes, hydrogenated fullerenes, fullerene hydroxides, and carboxyl oxidations. Examples include fullerene and sulfonated fullerene.

Examples of organic acids include alkylbenzene sulfonic acid, alkyl naphthalene sulfonic acid, alkyl naphthalene disulfonic acid, naphthalene sulfonic acid formalin polycondensate, melamine sulfonic acid formalin polycondensate, naphthalene disulfonic acid, naphthalene trisulfonic acid, dinaphthylmethane disulfonic acid, Anthraquinone sulfonic acid, anthraquinone disulfonic acid, anthracene sulfonic acid, pyrene sulfonic acid, acetic acid, oxalic acid, benzoic acid, phthalic acid, maleic acid, fumaric acid, malonic acid and the like can be mentioned. These metal salts can also be used.
As the organic cyano compound, a compound containing two or more cyano groups in a conjugated bond can be used. Examples include tetracyanoethylene, tetracyanoethylene oxide, tetracyanobenzene, dichlorodicyanobenzoquinone (DDQ), tetracyanoquinodimethane, and tetracyanoazanaphthalene.

  The ratio of the π-conjugated conductive polymer to the dopant is preferably 97: 3 to 10:90 as a molar ratio of π-conjugated conductive polymer: dopant. Even if there are more or less dopants, the conductivity tends to decrease.

  In the solid electrolyte layer 13a in the present invention, a polymer component, a surfactant, a dispersant, a silane coupling agent, and the like may be included as necessary.

(Cathode conductive layer)
The cathode conductive layer 13b of the cathode 13 can be made of, for example, carbon, silver, aluminum, or the like. The cathode conductive layer 13b made of carbon, silver or the like can be formed from a conductive paste containing a conductor such as carbon or silver. The cathode conductive layer 13b made of aluminum can be formed from an aluminum foil.
Further, a separator may be disposed between the dielectric layer 12 and the cathode conductive layer 13b as necessary.

The capacitor 10 described above is obtained by forming the solid electrolyte layer 13a on the surface of the dielectric layer 12 that has been treated with the polymer (A) and has increased affinity for the π-conjugated conductive polymer. In such a capacitor 10, since the π-conjugated conductive polymer enters deep inside the dielectric layer 12, high capacity can be realized.
Moreover, the layer of the polymer (A) is formed on part or all of the surface of the dielectric layer 12 by the treatment with the treatment liquid containing the polymer (A). The dielectric layer 12, which is a metal oxide, and the π-conjugated conductive polymer and polyanion have poor affinity, but as a result of the formation of the polymer (A) layer, the π-conjugated conductive polymer and polyanion This improves the affinity and improves the adhesion. As a result, the ESR of the capacitor 10 can be lowered.

"Capacitor manufacturing method"
Next, an embodiment of a method for manufacturing a capacitor according to the present invention will be described.
<Dielectric layer forming process>
In the method for manufacturing the capacitor 10 according to this embodiment, first, the dielectric layer 12 is formed by oxidizing the surface of the anode 11 made of a valve metal in the dielectric layer forming step.
Examples of the method for oxidizing the surface of the anode 11 include a method of anodizing the surface of the anode 11 in an electrolytic solution such as an aqueous solution of ammonium adipate.

<Processing process>
Next, in the treatment step, the surface of the dielectric layer 12 is treated with a treatment liquid containing the polymer (A) or the compound (B) that forms the polymer (A). As a method of treating the surface of the dielectric layer 12 with a treatment liquid containing the polymer (A) or the compound (B), the treatment liquid is applied to the surface of the dielectric layer 12 by a known application method such as coating, dipping, or spraying. The method of apply | coating can be taken.

Moreover, when the process liquid containing a compound (B) is apply | coated, it heat-drys after application | coating.
The temperature for drying after the treatment is preferably 40 to 150 ° C. If temperature is 40 degreeC or more, drying time can be shortened, and if it is 150 degrees C or less, the energy amount used at the time of drying can be restrained low.
When the compound (B) is contained in the treatment liquid, the compound (B) is thermally polymerized into a polymer (A) at the time of drying. If various polymerization initiators are added as required, thermal polymerization at this time is promoted.

(Processing liquid)
The pH of the treatment liquid is 3 to 12, and preferably 4 to 10. Even if the pH of the treatment liquid is less than 3 or more than 12, the dielectric layer 12 or the members constituting the capacitor 10 may be corroded. The pH of the treatment liquid may be adjusted by appropriately adding known acidic compounds and alkaline compounds.

As a compound (B), the acrylic monomer or acrylic oligomer in case a polymer (A) is an acrylic resin is mentioned, for example.
As the acrylic monomer, (meth) acrylate, methyl (meth) acrylate, ethyl (meth) acrylate, alkyl (meth) acrylate such as n-butyl (meth) acrylate, (meth) acrylic compound having one or more hydroxy groups Examples thereof include (meth) acrylic compounds having one or more alkoxy groups, acrylamide, methacrylamide and the like.

Furthermore, as a (meth) acryl compound having one or more hydroxy groups, for example, 2-hydroxyethyl methacrylate, 2-hydroxypropyl methacrylate, 2-hydroxyethyl acrylate, 2-hydroxypropyl acrylate, glycerin di (meth) acrylate Etc.
Examples of the (meth) acrylic compound having one or more alkoxy groups include n-butoxyethyl methacrylate, n-butoxyethylene glycol methacrylate, methoxytriethylene glycol methacrylate, methoxypolyethylene glycol methacrylate, n-butoxyethyl acrylate, n- Examples include butoxyethylene glycol acrylate, methoxytriethylene glycol acrylate, and methoxypolyethylene glycol acrylate.

  When the polymer (A) is a polyester, the compound (B) is a dicarboxylic acid compound or a polyhydric alcohol compound. When the polymer (A) is a polyether, the compound (B) is a polyhydric alcohol compound.

The treatment liquid may contain a solvent. When the treatment liquid contains a solvent, the solvent is selected so as to dissolve the polymer (A) or the compound (B). As the solvent, water and / or an organic solvent is used. Examples of the organic solvent include N-methyl-2-pyrrolidone, N, N-dimethylformamide, N, N-dimethylacetamide, dimethyl sulfoxide, hexamethylene phosphortriamide, N-vinylpyrrolidone, N-vinylformamide, N- Polar solvents such as vinylacetamide, phenols such as cresol, phenol, xylenol, alcohols such as methanol, ethanol, propanol, butanol, ethylene glycol, diethylene glycol, triethylene glycol, propylene glycol, dipropylene glycol, 1,3-butylene Glycol, 1,4-butylene glycol, glycerin, diglycerin, D-glucose, D-glucitol, isoprene glycol, butanediol, 1,5-pentanediol, 1 6-hexanediol, 1,9-nonanediol, polyhydric aliphatic alcohols such as neopentyl glycol, ketones such as acetone and methyl ethyl ketone, hydrocarbons such as hexane, benzene and toluene, carboxylic acids such as formic acid and acetic acid Carbonate compounds such as ethylene carbonate and propylene carbonate, ether compounds such as dioxane and diethyl ether, chain ethers such as ethylene glycol dialkyl ether, propylene glycol dialkyl ether, polyethylene glycol dialkyl ether and polypropylene glycol dialkyl ether, 3-methyl- Heterocyclic compounds such as 2-oxazolidinone, nitrile compounds such as acetonitrile, glutaronitrile, methoxyacetonitrile, propionitrile, and benzonitrile And the like. These solvents may be used alone, as a mixture of two or more kinds, or as a mixture with other solvents.
Among these solvents, water or an alcohol solvent is preferable because of its low environmental burden.
In addition, when a compound (B) is a liquid compound, it is not necessary to contain a solvent. That is, the treatment liquid may consist of the compound (B).

  The concentration of the polymer (A) or compound (B) in the treatment liquid when the treatment liquid contains a solvent is preferably 0.1 to 50% by mass, more preferably 0.3 to 30% by mass. preferable. If the concentration is less than the lower limit, it may not be possible to increase the capacity, and if it exceeds the upper limit, it tends to be difficult to apply or ESR tends to increase.

[Alkaline compounds]
In terms of reducing the ESR of the capacitor 10, it is preferable that the treatment liquid contains an alkaline compound.
As the alkaline compound, known inorganic alkali compounds and organic alkali compounds can be used. Examples of the inorganic alkali compound include sodium hydroxide, potassium hydroxide, calcium hydroxide, ammonia and the like.
As the organic alkali compound, a nitrogen-containing aromatic cyclic compound (aromatic amine), an aliphatic amine, a metal alkoxide, or the like can be suitably used.
Examples of the nitrogen-containing aromatic cyclic compound include those described above.
Examples of the aliphatic amine compound include ethylamine, n-octylamine, diethylamine, diisobutylamine, methylethylamine, trimethylamine, triethylamine, allylamine, 2-ethylaminoethanol, 2,2′-iminodiethanol, N-ethylethylenediamine, and the like. Can be mentioned.
Examples of the metal alkoxide include sodium alkoxide such as sodium methoxide and sodium ethoxide, potassium alkoxide and calcium alkoxide.

  Since the treatment liquid can lower the ESR of the capacitor 10, it is preferable that the treatment liquid further contains the high conductivity agent.

<Solid electrolyte formation process>
Next, in the solid electrolyte layer forming step, a conductive polymer solution is applied on the surface of the dielectric layer 12 treated with the treatment liquid to form the solid electrolyte layer 13a.
As a method for applying the conductive polymer solution, for example, a method in which the conductive polymer solution is applied to the surface of the dielectric layer 12 by a known coating apparatus, or a conductive polymer solution is known to the surface of the dielectric layer 12. For example, a method of spraying with a spraying device, and a method of immersing an element having the dielectric layer 12 in a conductive polymer solution. Moreover, you may make it a pressure reduction state at the time of application | coating as needed.
After application of the conductive polymer solution, it is preferably dried by a known drying method such as hot air drying.

Here, the conductive polymer solution is obtained, for example, by polymerizing a precursor monomer of a π-conjugated conductive polymer in the presence of a polyanion.
As a specific example of polymerizing a precursor monomer of a π-conjugated conductive polymer in the presence of a polyanion, first, the polyanion is dissolved in a solvent that can dissolve the polyanion, and the resulting solution is dissolved in a π-conjugated conductive polymer. Add molecular precursor monomers. Next, an oxidizing agent is added to polymerize the precursor monomer, and then the surplus oxidizing agent and precursor monomer are separated and purified to obtain a conductive polymer solution.
According to such polymerization, the π-conjugated conductive polymer grows so as to form a salt with the polyanion. Therefore, the obtained π-conjugated conductive polymer forms a complex with the polyanion.

Examples of the precursor monomer of the π-conjugated conductive polymer include pyrroles and derivatives thereof, thiophenes and derivatives thereof, anilines and derivatives thereof, and the like.
Any oxidizing agent may be used as long as it can oxidize the precursor monomer to obtain a π-conjugated conductive polymer. Examples thereof include ammonium peroxodisulfate (ammonium persulfate), sodium peroxodisulfate (persulfate). Sodium), peroxodisulfates such as potassium peroxodisulfate (potassium persulfate), transition metal compounds such as ferric chloride, ferric sulfate, ferric nitrate, cupric chloride, boron trifluoride Metal halide compounds such as aluminum chloride, metal oxides such as silver oxide and cesium oxide, peroxides such as hydrogen peroxide and ozone, organic peroxides such as benzoyl peroxide, oxygen, and the like.

  The solvent used in the production of the π-conjugated conductive polymer is not particularly limited as long as it is a solvent that can dissolve or disperse the precursor monomer and can maintain the oxidizing power of the oxidizing agent. For example, those similar to those contained in the treatment liquid are used.

According to the above method for producing a π-conjugated conductive polymer, the pH of the resulting π-conjugated conductive polymer solution becomes acidic, but in that case, the ESR of the obtained capacitor 10 tends to increase. . Therefore, it is preferable to add an alkaline compound to the conductive polymer solution to adjust the pH to 3-13.
As the alkaline compound, the same compounds as those contained in the treatment liquid are used, but among the alkaline compounds, nitrogen-containing aromatic cyclic compounds are preferable. If the alkaline compound is a nitrogen-containing aromatic cyclic compound, de-doping of the polyanion from the π-conjugated conductive molecule can be prevented in particular, and the conductivity of the solid electrolyte layer 13a can be improved to lower the ESR. be able to.

<Cathode conductive layer forming step>
After forming the solid electrolyte layer 13a, a method of forming a cathode conductive layer 13b by impregnating an electrolytic solution as needed and then applying a carbon paste or a silver paste, or a cathode such as an aluminum foil through a separator. Capacitor 10 can be obtained by forming cathode 13 by a method of disposing conductive layer 13b.
When a separator is used, a single or mixed nonwoven fabric such as cellulose fiber, glass fiber, polypropylene fiber, polyester fiber, polyamide fiber, carbonized nonwoven fabric obtained by carbonizing these, or the like is used as the separator.

In the manufacturing method of the capacitor 10 described above, the surface of the dielectric layer 12 is treated with a treatment liquid containing the polymer (A) or the compound (B), so that the π-conjugated conductive polymer on the surface of the dielectric layer 12 is obtained. The affinity for can be improved. As a result, when the conductive polymer is applied to the surface of the dielectric layer 12, the conductive polymer solution can be penetrated deep into the inside of the dielectric layer 12. Therefore, since the solid electrolyte layer 13a can be formed in a wide area, the capacity of the capacitor 10 can be increased.
Further, by treating the surface of the dielectric layer 12 with a treatment liquid containing the polymer (A), a layer of the polymer (A) is formed on a part or all of the surface of the dielectric layer 12. The dielectric layer 12, which is a metal oxide, and the π-conjugated conductive polymer and polyanion have poor affinity, but as a result of the formation of the polymer (A) layer, the π-conjugated conductive polymer and polyanion The affinity is improved and the adhesion is increased. As a result, the ESR of the obtained capacitor 10 can be lowered.
Moreover, since the method for manufacturing the capacitor 10 described above is a method of forming the solid electrolyte layer 13a with a solution containing a π-conjugated conductive polymer, the capacitor 10 can be manufactured with high productivity.

  Note that the present invention is not limited to the above-described embodiments. In the embodiment described above, the cathode is formed by providing the cathode conductive layer after forming the solid electrolyte layer to obtain the capacitor. However, in the present invention, the timing for providing the cathode conductive layer is not limited to this. For example, after disposing the cathode conductive layer so as to face the dielectric layer, the surface of the dielectric layer may be treated with a treatment liquid, and then the solid electrolyte layer may be formed. In that case, it is preferable to arrange a separator between the cathode conductive layer and the dielectric layer.

Hereinafter, the present invention will be described in more detail with reference to examples.
(1) Preparation of conductive polymer solution (Preparation Example 1) Preparation of conductive polymer solution (I) 14.2 g of 3,4-ethylenedioxythiophene and 27.5 g of polystyrene sulfonic acid (mass average molecular weight About 150,000) in 2000 ml of ion-exchanged water and mixed at 20 ° C.
While keeping the mixed solution thus obtained at 20 ° C. and stirring, 29.64 g of ammonium persulfate and 8.0 g of ferric sulfate oxidation catalyst solution dissolved in 200 ml of ion exchange water were added for 3 hours. The reaction was stirred.
The resulting reaction solution was dialyzed to remove unreacted monomers and oxidants to obtain an aqueous solution of about 1.5% by mass of polystyrenesulfonic acid poly (3,4-ethylenedioxythiophene).
10 g of polyethylene glycol 400 was added to 10 g of the polystyrene sulfonate poly (3,4-ethylenedioxythiophene) aqueous solution and dispersed to obtain a conductive polymer solution (I).

Preparation Example 2 Preparation of Conductive Polymer Solution (II) 0.5 g of imidazole was added to 110 g of the conductive polymer solution (I) to obtain a conductive polymer solution (II) having a pH of 9.

(2) Preparation of polymer solution (Preparation Example 3) Preparation of polyester solution (I) 10 g of an aqueous polyester solution (solid content concentration 25% by mass, plus coat RZ-105 manufactured by Kyoyo Chemical Co., Ltd.) was mixed with 90 g of ion-exchanged water. The polyester solution (I) having a pH value of 6 at 25 ° C. was prepared.

(Preparation Example 4) Preparation of Polyester Solution (II) 90 g of ion-exchanged water was mixed with 10 g of an aqueous polyester solution (solid content concentration 25% by mass, Plus Coat RZ-105 manufactured by Kyoyo Chemical Co., Ltd.) and 0.1 g of imidazole. A polyester solution (II) having a pH value of 9 at 25 ° C. was prepared.

(Preparation Example 5) Preparation of polyurethane solution (I) 90 g of ion-exchanged water was mixed with 10 g of an aqueous polyurethane solution (solid content concentration 40 mass%, R-9660 manufactured by Enomoto Kasei Co., Ltd.), and the pH value at 25 ° C. 8 polyurethane solution (I) was prepared.

(Preparation example 6) Preparation of polyurethane solution (II) 90 g of ion-exchanged water was mixed with 10 g of an aqueous polyurethane solution (solid content concentration 38% by mass, HYBRIDUR870 manufactured by Air Products), and the pH value at 25 ° C was 8. A polyurethane solution (II) was prepared.

(Preparation Example 7) Preparation of polyurethane solution (III) In 90 g of ion-exchanged water, 10 g of polyurethane aqueous solution (solid content concentration 38% by mass, HYBRIDUR870 manufactured by Air Products), 2 g of 2-hydroxyethylacrylamide were mixed, A polyurethane solution (III) having a pH value of 8 at 25 ° C. was prepared.

(Preparation Example 8) Preparation of polyurethane solution (IV) In 90 g of ion-exchanged water, 10 g of an aqueous polyurethane solution (solid content concentration 40 mass%, R-9660 manufactured by Enomoto Kasei Co., Ltd.), 2 g of 2-hydroxyacrylamide, 0.2 g Was mixed with triethylamine to prepare a polyurethane solution (IV) having a pH value of 12 at 25 ° C.

(Preparation Example 9) Preparation of polyacryl / polyurethane copolymer solution 90 g of ethanol was mixed with 10 g of polyacryl / polyurethane copolymer alcohol solution (solid content concentration 40% by mass, 3041MA manufactured by Taisei Fine Chemical Co., Ltd.) A polyacryl / polyurethane copolymer solution having a pH value of 7 at 25 ° C. was prepared.

(Preparation Example 10) Preparation of Epoxy Resin Solution 95 g of ethanol was mixed with 5 g of an epoxy resin (Epicoat 828 manufactured by Yuka Shell Epoxy Co., Ltd., solid content concentration: 100% by mass), and an epoxy having a pH value of 7 at 25 ° C. A resin solution was prepared.

Preparation Example 11 Preparation of Polyvinyl Alcohol Solution 5 g of polyvinyl alcohol (PVA JM05 manufactured by Shin-Etsu Chemical Co., Ltd.) was mixed with 95 g of ion exchange water to prepare a polyvinyl alcohol solution having a pH value of 7 at 25 ° C.

(Preparation example 12) Preparation of polyethylene glycol solution 5 g of polyethylene glycol 600 was mixed with 95 g of ion-exchanged water to prepare a polyethylene glycol solution having a pH value of 7 at 25 ° C.

(Preparation Example 13) Preparation of polyethylene glycol acrylate solution (I) In 9.5 g of ion-exchanged water, 5 g of polyethylene glycol acrylate (14EG-A manufactured by Kyoeisha Chemical Co., Ltd.) was mixed, and the pH value at 25 ° C was 7. A polyethylene glycol acrylate solution (I) was prepared.

Preparation Example 14 Preparation of Polyethylene Glycol Acrylate Solution (II) 9.5 g of ion exchange water was mixed with 5 g of polyethylene glycol acrylate (Kyoeisha Chemical Co., Ltd. 14EG-A) and 0.1 g of vinyl imidazole. A polyethylene glycol acrylate solution (II) having a pH value of 7 at 0 ° C. was prepared.

(Preparation Example 15) Preparation of Polyethylene Glycol Diglycidyl Solution 5 g of polyethylene glycol diglycidyl ether (Epolite 400E manufactured by Kyoeisha Chemical Co., Ltd.) is mixed with 9.5 g of ion-exchanged water, and a polyethylene having a pH value of 7 at 25 ° C. A glycol diglycidyl solution was prepared.

(3) Manufacture of capacitors (Manufacturing Example 1)
After connecting the anode lead terminal to the etched aluminum foil (anode foil), a voltage of 100 V was applied in an aqueous solution of 10% by weight ammonium adipate to form (oxidize) the dielectric layer on both sides of the aluminum foil. An anode foil was obtained by forming.
Next, on both surfaces of the anode foil, opposed aluminum cathode foils with cathode lead terminals welded were laminated via a cellulose separator, and this was wound into a cylindrical shape to obtain a capacitor element.

Example 1
The capacitor element was immersed in the polyester solution (I) prepared in Preparation Example 3 under reduced pressure, and then dried for 10 minutes with a hot air dryer at 120 ° C. Subsequently, the capacitor element was immersed in the conductive polymer solution (I) prepared in Preparation Example 1 under reduced pressure, and then dried with a hot air dryer at 120 ° C. for 30 minutes. Further, the immersion in the conductive polymer solution (I) was repeated three times to form a solid electrolyte layer containing a π-conjugated conductive polymer on the surface of the dielectric layer.
Next, a capacitor element on which a solid electrolyte layer was formed was loaded into an aluminum case and sealed with a sealing rubber to produce a capacitor.
About the produced capacitor, the initial value of the electrostatic capacitance in 120 Hz and the equivalent series resistance (ESR) in 100 kHz was measured using LCZ meter 2345 (made by NF circuit design block company). The results are shown in Table 1. Note that ESR is an index of impedance.

(Example 2)
A capacitor was produced in the same manner as in Example 1 except that the conductive polymer solution (II) was used instead of the conductive polymer solution (I). Further, the electrostatic capacity and ESR were measured in the same manner as in Example 1. The results are shown in Table 2.

(Example 3)
A capacitor was produced in the same manner as in Example 1 except that the polyester solution (II) was used instead of the polyester solution (I). Further, the electrostatic capacity and ESR were measured in the same manner as in Example 1. The results are shown in Table 1.

Example 4
A capacitor was produced in the same manner as in Example 1 except that the polyurethane solution (I) was used instead of the polyester solution (I). Further, the electrostatic capacity and ESR were measured in the same manner as in Example 1. The results are shown in Table 1.

(Example 5)
A capacitor was produced in the same manner as in Example 1 except that the polyurethane solution (II) was used instead of the polyester solution (I). Further, the electrostatic capacity and ESR were measured in the same manner as in Example 1. The results are shown in Table 1.

(Example 6)
A capacitor was produced in the same manner as in Example 1 except that the polyurethane solution (III) was used instead of the polyester solution (I). Further, the electrostatic capacity and ESR were measured in the same manner as in Example 1. The results are shown in Table 1.

(Example 7)
A capacitor was produced in the same manner as in Example 1 except that the polyurethane solution (IV) was used instead of the polyester solution (I). Further, the electrostatic capacity and ESR were measured in the same manner as in Example 1. The results are shown in Table 1.

(Example 8)
A capacitor was produced in the same manner as in Example 1 except that a polyacryl / polyurethane copolymer solution was used instead of the polyester solution (I). Further, the electrostatic capacity and ESR were measured in the same manner as in Example 1. The results are shown in Table 1.

Example 9
A capacitor was produced in the same manner as in Example 1 except that an epoxy resin solution was used instead of the polyester solution (I). Further, the electrostatic capacity and ESR were measured in the same manner as in Example 1. The results are shown in Table 1.

(Example 10)
A capacitor was produced in the same manner as in Example 1 except that a polyvinyl alcohol solution was used instead of the polyester solution (I). Further, the electrostatic capacity and ESR were measured in the same manner as in Example 1. The results are shown in Table 1.

Example 11
A capacitor was produced in the same manner as in Example 2 except that the polyester solution (II) was used instead of the polyester solution (I). Further, the electrostatic capacity and ESR were measured in the same manner as in Example 1. The results are shown in Table 2.

Example 12
A capacitor was produced in the same manner as in Example 2 except that the polyurethane solution (I) was used instead of the polyester solution (I). Further, the electrostatic capacity and ESR were measured in the same manner as in Example 1. The results are shown in Table 2.

(Example 13)
A capacitor was produced in the same manner as in Example 2 except that the polyurethane solution (II) was used instead of the polyester solution (I). Further, the electrostatic capacity and ESR were measured in the same manner as in Example 1. The results are shown in Table 2.

(Example 14)
A capacitor was produced in the same manner as in Example 2 except that the polyurethane solution (III) was used instead of the polyester solution (I). Further, the electrostatic capacity and ESR were measured in the same manner as in Example 1. The results are shown in Table 2.

(Example 15)
A capacitor was produced in the same manner as in Example 2 except that the polyurethane solution (IV) was used instead of the polyester solution (I). Further, the electrostatic capacity and ESR were measured in the same manner as in Example 1. The results are shown in Table 2.

(Example 16)
A capacitor was produced in the same manner as in Example 2 except that a polyacryl / polyurethane copolymer solution was used instead of the polyester solution (I). Further, the electrostatic capacity and ESR were measured in the same manner as in Example 1. The results are shown in Table 2.

(Example 17)
A capacitor was produced in the same manner as in Example 2 except that an epoxy resin solution was used instead of the polyester solution (I). Further, the electrostatic capacity and ESR were measured in the same manner as in Example 1. The results are shown in Table 2.

(Example 18)
A capacitor was produced in the same manner as in Example 2 except that a polyvinyl alcohol solution was used instead of the polyester solution (I). Further, the electrostatic capacity and ESR were measured in the same manner as in Example 1. The results are shown in Table 2.

Example 19
A capacitor was produced in the same manner as in Example 1 except that a polyethylene glycol solution was used instead of the polyester solution (I). Further, the electrostatic capacity and ESR were measured in the same manner as in Example 1. The results are shown in Table 3.

(Example 20)
A capacitor was produced in the same manner as in Example 1 except that the polyethylene glycol acrylate solution (I) was used instead of the polyester solution (I). Further, the electrostatic capacity and ESR were measured in the same manner as in Example 1. The results are shown in Table 3.

(Example 21)
A capacitor was produced in the same manner as in Example 1 except that the polyethylene glycol acrylate solution (II) was used instead of the polyester solution (I). Further, the electrostatic capacity and ESR were measured in the same manner as in Example 1. The results are shown in Table 3.

(Example 22)
A capacitor was produced in the same manner as in Example 1 except that a polyethylene glycol diglycidyl solution was used instead of the polyester solution (I). Further, the electrostatic capacity and ESR were measured in the same manner as in Example 1. The results are shown in Table 3.

(Example 23)
A capacitor was produced in the same manner as in Example 2 except that a polyethylene glycol solution was used instead of the polyester solution (I). Further, the electrostatic capacity and ESR were measured in the same manner as in Example 1. The results are shown in Table 4.

(Example 24)
A capacitor was produced in the same manner as in Example 2 except that the polyethylene glycol acrylate solution (I) was used instead of the polyester solution (I). Further, the electrostatic capacity and ESR were measured in the same manner as in Example 1. The results are shown in Table 4.

(Example 25)
A capacitor was produced in the same manner as in Example 2 except that the polyethylene glycol acrylate solution (II) was used instead of the polyester solution (I). Further, the electrostatic capacity and ESR were measured in the same manner as in Example 1. The results are shown in Table 4.

(Example 26)
A capacitor was produced in the same manner as in Example 2 except that a polyethylene glycol diglycidyl solution was used instead of the polyester solution (I). Further, the electrostatic capacity and ESR were measured in the same manner as in Example 1. The results are shown in Table 4.

(Comparative Example 1)
A capacitor was produced in the same manner as in Example 1 except that the capacitor element was not immersed in the polyester solution (I) in the production of the capacitor of Example 1. Further, the electrostatic capacity and ESR were measured in the same manner as in Example 1. The results are shown in Tables 1 and 3.

(Comparative Example 2)
A capacitor was produced in the same manner as in Example 2 except that the capacitor element was not immersed in the polyester solution (I) in the production of the capacitor of Example 2. Further, the electrostatic capacity and ESR were measured in the same manner as in Example 1. The results are shown in Table 2 and Table 4.

The capacitors of Examples 1 to 26 obtained by treating the surface of the dielectric layer with the treatment liquid containing the polymer (A) achieved high capacity and had low ESR. Moreover, the capacitors of Examples 11 to 18 and 23 to 26 obtained using the conductive polymer solution containing imidazole had lower ESR.
On the other hand, the capacitors of Comparative Examples 1 and 2 obtained without treating the dielectric layer surface with the treatment liquid had a low capacitance.

It is sectional drawing which shows one example of embodiment in the capacitor | condenser of this invention.

Explanation of symbols

10 Capacitor 11 Anode 12 Dielectric Layer 13 Cathode 13a Solid Electrolyte Layer 13b Cathode Conductive Layer 14 Polymer (A)

Claims (4)

An anode made of a valve metal and having an irregular surface formed thereon, a dielectric layer formed by oxidizing the surface of the anode, and a π-conjugated conductive polymer and polyanion formed on the surface of the dielectric layer A capacitor having a solid electrolyte layer comprising:
Part or all of the surface on the cathode side of the dielectric layer is treated with a polymer (A) having one or more chemical structures selected from the group consisting of the following (a) to (f): Capacitor.

(R ¹ represents a hydrogen atom or an alkyl group.)   The capacitor according to claim 1, wherein a high conductivity agent is added to the polymer (A) used for the treatment of the cathode side surface of the dielectric layer. A dielectric layer forming step of forming a dielectric layer by oxidizing the surface of the anode made of a valve metal and having irregularities formed on the surface;
The surface of the dielectric layer is a polymer (A) having a pH of 3 to 12 at 25 ° C. and having one or more chemical structures selected from the group consisting of the following (a) to (f) or the polymer (A): A treatment step of treating with a treatment liquid containing the compound (B) to be formed;
A solid that forms a solid electrolyte layer by applying a conductive polymer solution containing a π-conjugated conductive polymer, a polyanion and a solvent on the surface of the dielectric layer treated with the polymer (A) or the compound (B). A method for manufacturing a capacitor, comprising: an electrolyte layer forming step.

(R ¹ represents a hydrogen atom or an alkyl group.)   The method for manufacturing a capacitor according to claim 3, wherein the treatment liquid further includes a high conductivity agent.

Images