JP2009231336A - Electric double-layer capacitor - Google Patents

Electric double-layer capacitor Download PDF

Info

Publication number
JP2009231336A
JP2009231336A JP2008071494A JP2008071494A JP2009231336A JP 2009231336 A JP2009231336 A JP 2009231336A JP 2008071494 A JP2008071494 A JP 2008071494A JP 2008071494 A JP2008071494 A JP 2008071494A JP 2009231336 A JP2009231336 A JP 2009231336A
Authority
JP
Japan
Prior art keywords
electric double
layer capacitor
double layer
electrode
paste
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP2008071494A
Other languages
Japanese (ja)
Other versions
JP5035993B2 (en
Inventor
Wataru Oizumi
亘 大泉
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Tokin Corp
Original Assignee
NEC Tokin Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by NEC Tokin Corp filed Critical NEC Tokin Corp
Priority to JP2008071494A priority Critical patent/JP5035993B2/en
Publication of JP2009231336A publication Critical patent/JP2009231336A/en
Application granted granted Critical
Publication of JP5035993B2 publication Critical patent/JP5035993B2/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/13Energy storage using capacitors

Landscapes

  • Electric Double-Layer Capacitors Or The Like (AREA)

Abstract

<P>PROBLEM TO BE SOLVED: To provide an electric double-layer capacitor, wherein the dispersion in coating quantity for a paste electrode as a polarizable electrode is suppressed and the dispersion of electrostatic capacity is reduced. <P>SOLUTION: In the unit cell 1 of an electric double-layer capacitor, a pair of a paste-like polarizable electrode 3 (paste electrode 3) containing sulphuric solution, active carbon powder and graphite powder and a collector 2 is arranged opposite to each other, with a separator 4 therebetween, and the weight ratio Wc/Wac of active carbon powder (Wac) to graphite powder (Wc) in the paste electrode 3 is set to 0.005-0.10. <P>COPYRIGHT: (C)2010,JPO&INPIT

Description

本発明は、ICメモリや小型アクチュエータ等のバックアップ用電源として好適に用いられる電気二重層コンデンサに関し、特に静電容量の特性に関するものである。   The present invention relates to an electric double layer capacitor that is suitably used as a backup power source for an IC memory, a small actuator, and the like, and particularly relates to a capacitance characteristic.

電気二重層コンデンサは、固体と液体の界面に生じる電気二重層を利用して蓄電するデバイスであり、その蓄電機構は物理的な電荷のやり取りによるものである。そのため、急速充放電、半永久的寿命などの特長があり、主にICメモリや小型アクチュエータ等のバックアップ用電源に使用されている。また、最近ではハイブリッド自動車の補助電源やエネルギー回生用途への利用にも期待されている。   An electric double layer capacitor is a device that stores electricity by using an electric double layer generated at the interface between a solid and a liquid, and its power storage mechanism is based on the exchange of physical charges. Therefore, it has features such as rapid charge / discharge and semi-permanent lifetime, and is mainly used as a backup power source for IC memories, small actuators and the like. Recently, it is also expected to be used for auxiliary power sources and energy regeneration in hybrid vehicles.

電気二重層コンデンサは使用する電解液によって、水系電解液と非水(有機)系電解液のどちらかの2種類に大きく分別することができる。   The electric double layer capacitor can be largely classified into two types of an aqueous electrolyte and a non-aqueous (organic) electrolyte depending on the electrolyte used.

また、電解液によって材質等の細部が異なるが、電気二重層コンデンサ素子の単位セルの構造としては、次のコイン型の電気二重層コンデンサ等に用いられる板状の単位セルと巻回型の電気二重層コンデンサの単位セルがある。図1に、本発明と従来例の電気二重層コンデンサの単位セルの構造図を示す。小型電気二重層コンデンサの代表的なコイン型の電気二重層コンデンサの場合は、図1に示すように、表面に活性炭を主とする分極性電極3を形成した一対の集電体2の間に、ポリプロピレン不織布などからなるセパレータ4を挟んで、周りにガスケット5を配して電気二重層コンデンサ素子の板状の単位セル1が構成される。この単位セル1を必要枚数積層させて、電解液を含浸させた電気二重層コンデンサ素子を金属容器に収容し、キャップと外部封止用ガスケットにより金属容器に密封してコイン型の電気二重層コンデンサ等が製造されている。   In addition, although the details of the material and the like vary depending on the electrolyte, the unit cell structure of the electric double layer capacitor element is the same as the plate type unit cell used in the following coin type electric double layer capacitor, etc. There is a unit cell of a double layer capacitor. FIG. 1 shows a structural diagram of a unit cell of an electric double layer capacitor according to the present invention and a conventional example. In the case of a typical coin-type electric double layer capacitor of a small electric double layer capacitor, as shown in FIG. 1, between a pair of current collectors 2 having a polarizable electrode 3 mainly composed of activated carbon formed on the surface. A plate-like unit cell 1 of an electric double layer capacitor element is configured by placing a gasket 5 around a separator 4 made of polypropylene nonwoven fabric or the like. The required number of unit cells 1 are stacked, and an electric double layer capacitor element impregnated with an electrolyte solution is accommodated in a metal container, and sealed in a metal container with a cap and an external sealing gasket to form a coin-type electric double layer capacitor Etc. are manufactured.

また、上述の電気二重層コンデンサ素子と比べると比較的大型で大容量の電気二重層コンデンサ素子として、シート状の分極性電極と、集電体、セパレータを積層し、この積層体を渦巻状に巻き回して電解液を含浸させ巻回型の電気二重層コンデンサ素子の単位セルが構成されている。この巻回型の単位セルからなる電気二重層コンデンサ素子に電解液を含浸させ、金属容器に収容し、容器の開口部をキャップで密閉して大容量の電気二重層コンデンサが製造されている。   In addition, a sheet-shaped polarizable electrode, a current collector, and a separator are laminated as a relatively large and large-capacity electric double layer capacitor element as compared with the electric double layer capacitor element described above, and the laminate is spirally formed. A unit cell of a wound type electric double layer capacitor element is formed by winding and impregnating with an electrolytic solution. A large-capacity electric double layer capacitor is manufactured by impregnating an electrolytic solution in an electric double layer capacitor element composed of this wound type unit cell and storing it in a metal container, and sealing the opening of the container with a cap.

次に、コイン型の電気二重層コンデンサ等に用いられる電気二重層コンデンサ素子の板状の単位セル1で、水系電解液を用いた場合について述べる。水系電解液を用いた電気二重層コンデンサの場合は、電気二重層コンデンサ素子にはイオン透過性で非電子伝導性の多孔性のセパレータ4を介して分離された一対の分極性電極3が配置され、また、この分極性電極3の外側には導電性ゴムなどからなる集電体2が配置され、さらに、この分極性電極3の外周には非導電性ゴムなどからなるガスケット5が配置された構造である。   Next, a case where an aqueous electrolyte is used in the plate-shaped unit cell 1 of an electric double layer capacitor element used for a coin-type electric double layer capacitor or the like will be described. In the case of an electric double layer capacitor using an aqueous electrolyte, a pair of polarizable electrodes 3 separated by an ion permeable non-electron conductive porous separator 4 is arranged in the electric double layer capacitor element. The current collector 2 made of conductive rubber or the like is disposed outside the polarizable electrode 3, and the gasket 5 made of non-conductive rubber or the like is disposed on the outer periphery of the polarizable electrode 3. Structure.

この分極性電極3は、活性炭と硫酸水溶液およびバインダーをよく混練してペースト状のペースト体とした分極性電極3(以下、ペースト電極3という)を、非導電性ブチルゴムの中空円形状のガスケット5と導電性ブチルゴムの円盤状の集電体2とを貼り合わせてできた有底円筒状の内側の空間部(凹部)にスキージを用いて塗工することで構成している。   This polarizable electrode 3 is made of a non-conductive butyl rubber hollow circular gasket 5 which is obtained by mixing kneaded activated carbon, a sulfuric acid aqueous solution and a binder into a paste-like paste body. And a disk-shaped current collector 2 made of conductive butyl rubber are applied to a space portion (concave portion) inside a bottomed cylindrical shape using a squeegee.

例えば、特許文献1のように、ポリフッ化ビニリデン等の有機バインダーを添加することで、ペースト電極3の充填密度を大きくしているが、有機バインダーを添加することで、電気二重層コンデンサの内部抵抗が大きくなり、急速充電・大電流放電が難しくなっている。そこで、特許文献2では、バインダーを改善することで内部抵抗の低減を図っていることが記載されているが、バインダーを使用しないペースト電極3についての記載はない。   For example, as in Patent Document 1, the filling density of the paste electrode 3 is increased by adding an organic binder such as polyvinylidene fluoride, but the internal resistance of the electric double layer capacitor is increased by adding the organic binder. , And rapid charging and large current discharge are becoming difficult. Therefore, Patent Document 2 describes that the internal resistance is reduced by improving the binder, but there is no description of the paste electrode 3 that does not use the binder.

また、例えば、特許文献3では、活性炭と硫酸水溶液の電解液とを混練した電極について、電気二重層コンデンサの静電容量の向上を検討しているが、硫酸水溶液の硫酸濃度変化についてのみの検討にとどまっている。   Further, for example, in Patent Document 3, the improvement of the capacitance of the electric double layer capacitor is examined for an electrode obtained by kneading activated carbon and an electrolyte solution of sulfuric acid solution, but only the change in sulfuric acid concentration of the sulfuric acid solution is examined. Stays on.

特開2002−231585号公報JP 2002-231585 A 特開2007−157976号公報JP 2007-157976 A 特開2004−158639号公報JP 2004-158639 A

上記特許文献1のように、有機バインダーを添加することで、電気二重層コンデンサの内部抵抗が大きくなり、急速充電・大電流放電が難しくなることから、有機バインダーを含まないペースト電極にも優位な点がある。しかしながら、バインダーを含まない活性炭と硫酸水溶液からなるペースト電極は、潤滑性が悪く、塗工時において、ガスケットと集電体を貼り合わせてできた凹部の縁に未塗工部が発生しやすくなる。この対策として、スキージを用いて塗工する往復回数を増やして実施しているものの、上記ペースト電極ではこの凹部でのペースト体の塗工量のばらつきは大きくなってしまい、この結果として、単位セルの静電容量ばらつきが大きくなるという問題があった。特に、小型の電気二重層コンデンサにおいては、ガスケットと集電体を貼り合わせてできた凹部がより小さくなるため、上記の問題点は顕著に現れる。   As described in Patent Document 1, the addition of an organic binder increases the internal resistance of the electric double layer capacitor, making rapid charging and large current discharge difficult. Therefore, it is also advantageous for paste electrodes that do not contain an organic binder. There is a point. However, paste electrodes made of activated carbon and sulfuric acid aqueous solution that do not contain a binder have poor lubricity, and uncoated parts are likely to occur at the edges of the recesses formed by bonding the gasket and current collector during coating. . As a countermeasure, although the number of reciprocations to be applied using a squeegee is increased, the paste electrode has a large variation in the coating amount of the paste body in the recess, and as a result, the unit cell There has been a problem that the variation in the capacitance is large. In particular, in a small electric double layer capacitor, the above-mentioned problem appears remarkably because the concave portion formed by bonding the gasket and the current collector becomes smaller.

また、複数個の単位セルを積層して、直列に接続して構成された電気二重層コンデンサにおいては、単位セルの静電容量のばらつきが電気二重層コンデンサとしての静電容量のばらつきに影響を及ぼしてしまう。   In addition, in an electric double layer capacitor configured by stacking a plurality of unit cells and connecting them in series, the variation in the capacitance of the unit cell affects the variation in the capacitance as an electric double layer capacitor. Will affect.

この発明は、以上の点に鑑みてなされたものであり、単位セルに対するペースト電極のペースト体塗工量のばらつきを低下させ、かつ静電容量のばらつきが小さい電気二重層コンデンサを提供することを目的としている。   The present invention has been made in view of the above points, and it is intended to provide an electric double layer capacitor that reduces variations in the amount of paste applied to a unit cell and reduces variations in capacitance. It is aimed.

本発明は、硫酸水溶液を含んだ一対の分極性電極と一対の集電体がセパレータを介して対向配置された電気二重層コンデンサ素子を有する電気二重層コンデンサであって、前記分極性電極が、有機バインダーを含まず、少なくとも硫酸水溶液と活性炭粉末および黒鉛粉末を含む混合物から構成されたことを特徴とする電気二重層コンデンサである。   The present invention is an electric double layer capacitor having an electric double layer capacitor element in which a pair of polarizable electrodes containing an aqueous sulfuric acid solution and a pair of current collectors are arranged to face each other via a separator, the polarizable electrode comprising: An electric double layer capacitor characterized in that it is composed of a mixture containing at least an aqueous sulfuric acid solution, activated carbon powder, and graphite powder without containing an organic binder.

また、本発明は、前記分極性電極を構成する前記活性炭粉末Wacと前記黒鉛粉末Wcの重量比Wc/Wacが0.005〜0.10であることを特徴とする電気二重層コンデンサである。   Further, the present invention is the electric double layer capacitor, wherein a weight ratio Wc / Wac between the activated carbon powder Wac and the graphite powder Wc constituting the polarizable electrode is 0.005 to 0.10.

本発明によれば、水系電解液を用いたペースト電極に活性炭粉末と黒鉛粉末を含有させることで、塗工時において、黒鉛粉末と電解液の水分子の存在によりペースト体の潤滑性が改善し、ガスケットと集電体を貼り合わせてできた凹部にペースト体を充填しやすくなり、電極塗工量のばらつきを抑えることができる。また、これにより、単位セルの静電容量のばらつきを小さくすることができる。   According to the present invention, by including activated carbon powder and graphite powder in a paste electrode using an aqueous electrolyte, the lubricity of the paste body is improved by the presence of water molecules in the graphite powder and the electrolyte during coating. In addition, it becomes easy to fill the recess formed by bonding the gasket and the current collector with the paste body, and the variation in the amount of electrode coating can be suppressed. This also makes it possible to reduce the variation in the capacitance of the unit cells.

図1は、本発明と従来例の電気二重層コンデンサの単位セルの構造図である。本発明の電気二重層コンデンサの単位セル1は、図1のように、集電体2、分極性電極3、セパレータ4、ガスケット5から構成される。分極性電極3(ペースト電極3)および分極性電極3の外側に配置される集電体2は、正極側と負極側とに分けられてセパレータ4で絶縁されている。ここで、セパレータ4を、例えばポリプロピレンの不織布のような多孔質の絶縁シートとすることにより、水系電解液に含まれるイオンの移動を可能とし、充放電可能な構造としている。   FIG. 1 is a structural diagram of a unit cell of an electric double layer capacitor according to the present invention and a conventional example. As shown in FIG. 1, the unit cell 1 of the electric double layer capacitor of the present invention includes a current collector 2, a polarizable electrode 3, a separator 4, and a gasket 5. The current collector 2 disposed outside the polarizable electrode 3 (paste electrode 3) and the polarizable electrode 3 is divided into a positive electrode side and a negative electrode side and insulated by a separator 4. Here, the separator 4 is made of a porous insulating sheet such as a nonwoven fabric of polypropylene, for example, so that the ions contained in the aqueous electrolyte can be moved and charged and discharged.

具体的には、例えば、中空円形状のガスケット5と円盤状の集電体2を貼り合わせ、有底の円筒(凹部)とし、その凹部に、硫酸水溶液と活性炭と黒鉛粉末を含むペースト状のペースト体を塗工してペースト電極3とし、単位セル1の電極の片側を形成する。同様にして、他の電極の片側を形成し、それぞれをセパレータ4を挟んで対向配置させることによって、硫酸水溶液の水系電解液を用いたペースト電極3が封止される。なお、ガスケット5と集電体2の形状は、円形でなく、方形や楕円形等の形状であってもよい。   Specifically, for example, a hollow circular gasket 5 and a disk-shaped current collector 2 are bonded together to form a bottomed cylinder (concave), and in the concave portion, a paste-form containing sulfuric acid aqueous solution, activated carbon, and graphite powder. The paste body is applied to form a paste electrode 3, and one side of the unit cell 1 electrode is formed. Similarly, one side of the other electrode is formed, and each is placed opposite to each other with the separator 4 interposed therebetween, whereby the paste electrode 3 using the aqueous electrolyte solution of sulfuric acid aqueous solution is sealed. Note that the shapes of the gasket 5 and the current collector 2 are not circular, but may be square, elliptical, or the like.

また、ガスケット5には非導電性ブチルゴム等のゴムを用い、集電体2には導電性ブチルゴム等のゴムを用いるとよい。分極性電極3には硫酸水溶液の水系電解液を用いたペースト電極3を用いる。   The gasket 5 may be made of rubber such as non-conductive butyl rubber, and the current collector 2 may be made of rubber such as conductive butyl rubber. For the polarizable electrode 3, a paste electrode 3 using an aqueous electrolyte solution of sulfuric acid aqueous solution is used.

本実施の形態では、硫酸水溶液と活性炭、黒鉛粉末から構成されたペースト電極3を用いる。活性炭には、平均粒子径が4〜14μmのフェノール樹脂系活性炭が好適に用いられ、その他にヤシ殻活性炭等を用いてもよい。黒鉛粉末には、平均粒子径が0.05〜8μmの天然黒鉛、平均粒子径が0.05〜10μmの天然鱗状黒鉛、平均粒子径が0.1〜7μmの人造黒鉛が好適に用いられ、その他にカーボンブラックやケッチェンブラック等を用いてもよい。   In this embodiment, a paste electrode 3 composed of an aqueous sulfuric acid solution, activated carbon, and graphite powder is used. As the activated carbon, phenol resin-based activated carbon having an average particle diameter of 4 to 14 μm is suitably used, and coconut shell activated carbon or the like may be used. As the graphite powder, natural graphite having an average particle size of 0.05 to 8 μm, natural scaly graphite having an average particle size of 0.05 to 10 μm, and artificial graphite having an average particle size of 0.1 to 7 μm are preferably used. In addition, carbon black or ketjen black may be used.

ペースト電極3に黒鉛粉末を添加すると、ペースト体の潤滑性を改善させることができる。これは、次のことから理由付けられる。一般的に、黒鉛は潤滑性に優れた材料として知られている。これは黒鉛の結晶構造に由来しており、黒鉛は六方晶系の六角板状結晶で亀の甲状の層状物質で、この結晶の層毎の内面は強い共有結合であるが、層と層の間は弱いファンデルワールス力で結合している。この弱いファンデルワールス力で結合された層と隣り合う層との間で、これらの層同士が滑ることで潤滑性を発揮する。また、結晶端部には結合の切れた原子が存在し、遊離結合力を有しているため、この遊離結合力を飽和させないと高い潤滑性は保てないが、水系電解液中の水分子が結合端部に吸着するため、遊離結合力が飽和され、潤滑性を有する。   When graphite powder is added to the paste electrode 3, the lubricity of the paste body can be improved. This is because of the following. Generally, graphite is known as a material excellent in lubricity. This is derived from the crystal structure of graphite. Graphite is a hexagonal hexagonal plate-like crystal with a turtle shell-like layered substance, and the inner surface of each layer of this crystal is a strong covalent bond. Are united by weak van der Waals forces. Between the layer joined by this weak van der Waals force and the adjacent layer, these layers slide to exhibit lubricity. In addition, since there is a broken bond atom at the crystal edge and it has free bond strength, high lubricity cannot be maintained unless this free bond force is saturated, but water molecules in the aqueous electrolyte Is adsorbed at the bonding end, so that the free bonding force is saturated and has lubricity.

従って、塗工時において、水系電解液には水分子が存在するため、電極のペースト体をガスケット5と集電体2を貼り合わせてできた凹部の縁にまで充填しやすくなり、電極の塗工量のばらつきを抑えることができる。この結果、単位セル1の静電容量のばらつき小さくすることが可能となる。   Accordingly, since water molecules exist in the aqueous electrolyte during coating, the electrode paste body can be easily filled up to the edge of the recess formed by bonding the gasket 5 and the current collector 2 together. Variations in work can be suppressed. As a result, it is possible to reduce the variation in the capacitance of the unit cell 1.

また、本実施の形態において、ペースト電極3に用いる黒鉛粒子の粒径は0.5〜10μmの範囲であることが好ましい。これは、黒鉛粒子の粒径が10μmより大きな場合、ペースト体の塗工時に塗工面が荒れ、塗工ばらつきが大きくなり、これにより、静電容量が小さくなってしまうためである。また、黒鉛粒子の粒径が0.5μmより小さい場合、通常工業的に入手困難であり、ハンドリングの点からも好ましくない。   Moreover, in this Embodiment, it is preferable that the particle size of the graphite particle used for the paste electrode 3 is the range of 0.5-10 micrometers. This is because when the particle size of the graphite particles is larger than 10 μm, the coating surface becomes rough during coating of the paste body, and the coating variation increases, thereby reducing the capacitance. Moreover, when the particle size of the graphite particles is smaller than 0.5 μm, it is usually difficult to obtain industrially, which is not preferable from the viewpoint of handling.

また、ペースト電極3における活性炭粉末(Wac)と黒鉛粉末(Wc)の重量比Wc/Wacが0.005〜0.10であることが望ましく、特に重量比Wc/Wacが0.03〜0.08であることがより望ましい。すなわち、重量比Wc/Wacが0.005以下の場合、黒鉛の添加量が少ないために良い潤滑性が得られず、電極塗工ばらつきは大きく、また、これと同時に、静電容量のばらつきも大きくなり、好ましくない。一方、重量比Wc/Wacが0.10以上の場合、比表面積が小さくて静電容量を大きくするためには寄与しない黒鉛粉末の混合割合が増え、逆に、それによって、比表面積が大きくて静電容量を大きくするためには寄与する活性炭粉末の混合割合が少なくなり、結果として静電容量が低下してしまい、好ましくない。   The weight ratio Wc / Wac between the activated carbon powder (Wac) and the graphite powder (Wc) in the paste electrode 3 is preferably 0.005 to 0.10, and particularly the weight ratio Wc / Wac is 0.03 to 0.00. It is more desirable to be 08. That is, when the weight ratio Wc / Wac is 0.005 or less, good lubricity cannot be obtained due to the small amount of graphite added, and the electrode coating variation is large. At the same time, the capacitance variation is also large. It becomes large and is not preferable. On the other hand, when the weight ratio Wc / Wac is 0.10 or more, the mixing ratio of the graphite powder that does not contribute to increase the capacitance due to the small specific surface area increases, and conversely, the specific surface area increases. In order to increase the electrostatic capacity, the mixing ratio of the activated carbon powder that contributes decreases, and as a result, the electrostatic capacity decreases, which is not preferable.

(実施例1)
まず、図1に示すように、内径4.5mmかつ外径6.0mmに打ち抜き成形したリング状シートからなる厚さ0.18mmで非導電性ブチルゴムのガスケット5の下面に、直径6.0mmに打ち抜き成形した円盤状シートからなる厚さ0.18mmで導電性ブチルゴムの集電体2を同心円上に配置し、貼り合わせて凹部を有する凹体を形成した。
Example 1
First, as shown in FIG. 1, on the lower surface of a non-conductive butyl rubber gasket 5 made of a ring-shaped sheet punched and molded to an inner diameter of 4.5 mm and an outer diameter of 6.0 mm, a diameter of 6.0 mm A conductive butyl rubber current collector 2 having a thickness of 0.18 mm made of a punched disk-shaped sheet was arranged on a concentric circle and bonded to form a concave body having a concave portion.

次に、平均粒子径が5μmのフェノール樹脂系活性炭(Wac)と平均粒子径が1μmの天然黒鉛粉末(Wc)を重量比Wc/Wac=0.002、0.005、0.01、0.05、0.1、0.5、1.0、1.4で混合した。さらに、この混合物に40%希硫酸水溶液を加えてよく混練し、ペースト状のペースト体とした。分極性電極となるこのペースト体を上記凹体に、スキージを用いて塗工することによって、ペースト電極3を作製した。この塗工を12回繰り返し、塗工前後の重量変化とそのばらつきを調べた。   Next, a weight ratio Wc / Wac = 0.002, 0.005, 0.01, 0.00 is obtained by adding phenol resin-based activated carbon (Wac) having an average particle diameter of 5 μm and natural graphite powder (Wc) having an average particle diameter of 1 μm. Mixed at 05, 0.1, 0.5, 1.0, 1.4. Furthermore, 40% dilute sulfuric acid aqueous solution was added to this mixture and kneaded well to obtain a paste-like paste body. A paste electrode 3 was produced by coating this paste body to be a polarizable electrode on the concave body using a squeegee. This coating was repeated 12 times, and the weight change before and after coating and the variation thereof were examined.

さらに、上記ペースト体を塗工した凹体を一対用意し、厚さ25μmで直径5.0mmのセパレータを介してそれらを重ね合わせた。上下方向より圧力を加え、この圧力を保持した状態でブチルゴム間を熱圧着し、非導電性ブチルゴムからなるガスケット5のブチルゴムの加硫を促して封止を行い、単位セル1を100個作製した。得られた単位セル1の100個の電気二重層コンデンサについて静電容量とそのばらつきを測定した。   Furthermore, a pair of concave bodies coated with the paste body was prepared, and they were overlapped via a separator having a thickness of 25 μm and a diameter of 5.0 mm. Pressure was applied from above and below, and the butyl rubber was thermocompression bonded while maintaining this pressure, and vulcanization of the butyl rubber of the gasket 5 made of non-conductive butyl rubber was promoted for sealing, and 100 unit cells 1 were produced. . The electrostatic capacity and the variation thereof were measured for 100 electric double layer capacitors of the obtained unit cell 1.

(実施例2)
実施例2については、ペースト体を、平均粒子径が5μmのフェノール樹脂系活性炭(Wac)と平均粒径径が0.1、1.0、5.0μmの天然鱗状黒鉛粉末(Wc)を重量比Wc/Wac=0.5で混合して作製した。以下、実施例1と同様に、塗工前後のシートの重量変化とそのばらつきを調べ、単位セル1を100個作製し、得られた単位セル1の100個の電気二重層コンデンサについて電気二重層コンデンサの静電容量とそのばらつきを測定した。
(Example 2)
For Example 2, the paste was weighted with phenol resin activated carbon (Wac) having an average particle diameter of 5 μm and natural scaly graphite powder (Wc) having an average particle diameter of 0.1, 1.0, 5.0 μm. It was prepared by mixing at a ratio Wc / Wac = 0.5. Hereinafter, in the same manner as in Example 1, the change in the weight of the sheet before and after coating and its variation were examined, 100 unit cells 1 were produced, and the 100 electric double layer capacitors of the obtained unit cell 1 were electrically double layered. The capacitance of the capacitor and its variation were measured.

(実施例3)
次に、実施例3については、ペースト体を、平均粒子径が5μmのフェノール樹脂系活性炭(Wac)と平均粒径径が0.1、1.0、5.0μmの人造黒鉛粉末(Wc)を重量比Wc/Wac=0.5で混合して作製した。以下、実施例1と同様に、塗工前後のシートの重量変化とそのばらつきを調べ、単位セル1を100個作製し、得られた単位セル1の100個の電気二重層コンデンサについて電気二重層コンデンサの静電容量とそのばらつきを測定した。
(Example 3)
Next, for Example 3, the paste body was made of phenol resin activated carbon (Wac) having an average particle diameter of 5 μm and artificial graphite powder (Wc) having an average particle diameter of 0.1, 1.0, 5.0 μm. Were mixed at a weight ratio of Wc / Wac = 0.5. Hereinafter, in the same manner as in Example 1, the change in the weight of the sheet before and after coating and its variation were examined, 100 unit cells 1 were produced, and the 100 electric double layer capacitors of the obtained unit cell 1 were electrically double layered. The capacitance of the capacitor and its variation were measured.

(比較例1)
次に、比較例1については、活性炭として平均粒子径が5μmのフェノール樹脂系活性炭(Wac)を用い、黒鉛粉末は添加させずにペースト体を作製した。それ以外は実施例1と同様に、塗工前後のシートの重量変化とそのばらつきを調べ、単位セル1を100個作製し、得られた単位セル1の100個の電気二重層コンデンサについて電気二重層コンデンサの静電容量とそのばらつきを測定した。
(Comparative Example 1)
Next, for Comparative Example 1, a phenol resin activated carbon (Wac) having an average particle size of 5 μm was used as the activated carbon, and a paste was prepared without adding graphite powder. Other than that, like Example 1, the change in the weight of the sheet before and after coating and its variation were examined, 100 unit cells 1 were produced, and the 100 electric double layer capacitors of the obtained unit cell 1 were The capacitance of the multilayer capacitor and its variation were measured.

(実施例4)
次に、実施例4については、ペースト体を、平均粒子径が5μmのヤシ殻活性炭(Wac)と平均粒子径が1.0μmの天然黒鉛粉末、天然鱗状黒鉛粉末、人造黒鉛粉末(Wc)を重量比Wc/Wac=0.5で混合して作製した。以下、実施例1と同様に、塗工前後のシートの重量変化とそのばらつきを調べ、単位セル1を100個作製し、得られた単位セル1の100個の電気二重層コンデンサについて電気二重層コンデンサの静電容量とそのばらつきを測定した。
Example 4
Next, for Example 4, the paste body was made of coconut shell activated carbon (Wac) having an average particle diameter of 5 μm, natural graphite powder, natural scaly graphite powder, and artificial graphite powder (Wc) having an average particle diameter of 1.0 μm. It was prepared by mixing at a weight ratio Wc / Wac = 0.5. Hereinafter, in the same manner as in Example 1, the change in the weight of the sheet before and after coating and its variation were examined, 100 unit cells 1 were produced, and the 100 electric double layer capacitors of the obtained unit cell 1 were electrically double layered. The capacitance of the capacitor and its variation were measured.

(比較例2)
次に、比較例1については、活性炭として平均粒子径が5μmのヤシ殻活性炭(Wac)を用い、黒鉛粉末は添加させずにペースト体を作製した。それ以外は実施例1と同様に、塗工前後のシートの重量変化とそのばらつきを調べ、単位セル1を100個作製し、得られた単位セル1の100個の電気二重層コンデンサについて電気二重層コンデンサの静電容量とそのばらつきを測定した。
(Comparative Example 2)
Next, for Comparative Example 1, a coconut shell activated carbon (Wac) having an average particle diameter of 5 μm was used as the activated carbon, and a paste was prepared without adding graphite powder. Other than that, like Example 1, the change in the weight of the sheet before and after coating and its variation were examined, 100 unit cells 1 were produced, and the 100 electric double layer capacitors of the obtained unit cell 1 were The capacitance of the multilayer capacitor and its variation were measured.

Figure 2009231336
Figure 2009231336

表1に示すように、活性炭粉末(Wac)と黒鉛粉末(Wc)の重量比Wc/Wacが0.005以上のペースト電極を用いることで、電極シートにおける塗工量のばらつきを0.04以下に抑えることができた。また、同様に単位セルの静電容量のばらつきも0.01以下に抑えられることが分かった。重量比Wc/Wacが0.10以上では黒鉛粉末の添加量が増えたため、単位セルの静電容量が減少していることが確認され、黒鉛粉末の添加量の上限値は重量比Wc/Wacが0.10とすることが好ましいと分かった。また、活性炭は、フェノール樹脂系活性炭とヤシ殻活性炭とのいずれを用いても、適量の黒鉛を添加することにより、電極シートにおける塗工量のばらつき、静電容量のばらつきともに抑えられることが分かった。   As shown in Table 1, by using a paste electrode in which the weight ratio Wc / Wac between the activated carbon powder (Wac) and the graphite powder (Wc) is 0.005 or more, the variation in the coating amount in the electrode sheet is 0.04 or less. I was able to suppress it. Similarly, it has been found that the variation in the capacitance of the unit cell can be suppressed to 0.01 or less. When the weight ratio Wc / Wac is 0.10 or more, it is confirmed that the capacitance of the unit cell is decreased because the amount of graphite powder added is increased, and the upper limit of the amount of graphite powder added is the weight ratio Wc / Wac. Was found to be preferably 0.10. In addition, regardless of whether the activated carbon is phenol resin-based activated carbon or coconut shell activated carbon, it can be seen that by adding an appropriate amount of graphite, both variation in the coating amount and capacitance variation in the electrode sheet can be suppressed. It was.

(まとめ)
以上、述べたように、ペースト電極を活性炭粉末と黒鉛粉末の混合物から構成し、活性炭粉末(Wac)と黒鉛粉末(Wc)の重量比Wc/Wacを0.005〜0.10とすることで、静電容量の低下を招くことなく、静電容量のばらつきを小さくすることができる。これは、黒鉛粉末が潤滑性に優れた材料であり、活性炭粉末の隙間に黒鉛が容易に入り込むことができるためである。
(Summary)
As described above, the paste electrode is composed of a mixture of activated carbon powder and graphite powder, and the weight ratio Wc / Wac between the activated carbon powder (Wac) and the graphite powder (Wc) is 0.005 to 0.10. Thus, the variation in capacitance can be reduced without causing a decrease in capacitance. This is because graphite powder is a material with excellent lubricity, and graphite can easily enter the gaps between the activated carbon powders.

本発明と従来例の電気二重層コンデンサの単位セルの構造図。FIG. 3 is a structural diagram of a unit cell of an electric double layer capacitor of the present invention and a conventional example.

符号の説明Explanation of symbols

1 単位セル
2 集電体
3 分極性電極(ペースト電極)
4 セパレータ
5 ガスケット
1 unit cell 2 current collector 3 polarizable electrode (paste electrode)
4 Separator 5 Gasket

Claims (2)

硫酸水溶液を含んだ一対の分極性電極と一対の集電体がセパレータを介して対向配置された電気二重層コンデンサ素子を有する電気二重層コンデンサであって、
前記分極性電極が、有機バインダーを含まず、少なくとも硫酸水溶液と活性炭粉末および黒鉛粉末を含む混合物から構成されたことを特徴とする電気二重層コンデンサ。
An electric double layer capacitor having an electric double layer capacitor element in which a pair of polarizable electrodes containing a sulfuric acid aqueous solution and a pair of current collectors are arranged to face each other via a separator,
The electric double layer capacitor, wherein the polarizable electrode is composed of a mixture containing at least a sulfuric acid aqueous solution, activated carbon powder and graphite powder without containing an organic binder.
前記分極性電極を構成する前記活性炭粉末Wacと前記黒鉛粉末Wcの重量比Wc/Wacが0.005〜0.10であることを特徴とする請求項1記載の電気二重層コンデンサ。   The electric double layer capacitor according to claim 1, wherein a weight ratio Wc / Wac of the activated carbon powder Wac and the graphite powder Wc constituting the polarizable electrode is 0.005 to 0.10.
JP2008071494A 2008-03-19 2008-03-19 Electric double layer capacitor Active JP5035993B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2008071494A JP5035993B2 (en) 2008-03-19 2008-03-19 Electric double layer capacitor

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2008071494A JP5035993B2 (en) 2008-03-19 2008-03-19 Electric double layer capacitor

Publications (2)

Publication Number Publication Date
JP2009231336A true JP2009231336A (en) 2009-10-08
JP5035993B2 JP5035993B2 (en) 2012-09-26

Family

ID=41246452

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2008071494A Active JP5035993B2 (en) 2008-03-19 2008-03-19 Electric double layer capacitor

Country Status (1)

Country Link
JP (1) JP5035993B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2015177975A1 (en) * 2014-05-21 2015-11-26 Ricoh Company, Ltd. Non-aqueous electrolyte storage element

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH027509A (en) * 1988-06-27 1990-01-11 Nec Corp Electric double-layer capacitor

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH027509A (en) * 1988-06-27 1990-01-11 Nec Corp Electric double-layer capacitor

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2015177975A1 (en) * 2014-05-21 2015-11-26 Ricoh Company, Ltd. Non-aqueous electrolyte storage element

Also Published As

Publication number Publication date
JP5035993B2 (en) 2012-09-26

Similar Documents

Publication Publication Date Title
US9960397B2 (en) Aqueous electrolyte energy storage device
JP5085651B2 (en) Capacitor-battery hybrid electrode assembly
AU2012225439B2 (en) Metal free aqueous electrolyte energy storage device
US8526166B2 (en) Lithium ion capacitor
CN108511199B (en) Electrochemical device
JP2013502070A (en) Porous carbon oxide nanocomposite electrodes for high energy density supercapacitors
JP2007280803A (en) Hybrid laminated electrode and hybrid secondary power source using the same
US9159502B2 (en) Supercapacitor with hexacyanometallate cathode, activated carbon anode, and non-aqueous electrolyte
US9666381B2 (en) Asymmetrical supercapacitor with alkaline electrolyte comprising a three-dimensional negative electrode and method for producing same
JPWO2018043375A1 (en) Storage element and method of manufacturing the same
EP3561917B1 (en) Electrode for power storage devices and production method for said electrode
KR101883005B1 (en) Electrode, method for preparing the same, and super capacitor using the same
JP5396216B2 (en) Lead acid battery
JP5035993B2 (en) Electric double layer capacitor
KR20130085551A (en) Manufacturing method of slurry for super capacitor providing enhanced capacitance characteristic and super capacitor manufactured using the same and manufacturing method of super capacitor thereof
JP7030766B2 (en) Electrodes of power storage devices and their manufacturing methods
WO2005076296A1 (en) Electrochemical device and electrode body
KR102028677B1 (en) Multilayer lithium-ion capacitor comprising graphene electrode
KR101493976B1 (en) Manufacturing method of Asymmetrical Super Capacitor with Cylindrical Type
WO2011161832A1 (en) Electrode collector material and production method for same
JP6837868B2 (en) Electrochemical device
JP6523658B2 (en) Intermediate layer material composition for capacitor air battery, electrode having intermediate layer containing the material composition, and capacitor air battery provided with the electrode
JP2019106520A (en) Electric double layer capacitor
KR101205846B1 (en) Lithium ion capacitor having current collector of plate type
KR20140097273A (en) Cell design for high energy density electrochemical double layer capacitors

Legal Events

Date Code Title Description
A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20101110

A977 Report on retrieval

Free format text: JAPANESE INTERMEDIATE CODE: A971007

Effective date: 20120223

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20120229

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20120328

TRDD Decision of grant or rejection written
A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

Effective date: 20120628

A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

A61 First payment of annual fees (during grant procedure)

Free format text: JAPANESE INTERMEDIATE CODE: A61

Effective date: 20120629

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20150713

Year of fee payment: 3

R150 Certificate of patent or registration of utility model

Ref document number: 5035993

Country of ref document: JP

Free format text: JAPANESE INTERMEDIATE CODE: R150

Free format text: JAPANESE INTERMEDIATE CODE: R150

S533 Written request for registration of change of name

Free format text: JAPANESE INTERMEDIATE CODE: R313533

R350 Written notification of registration of transfer

Free format text: JAPANESE INTERMEDIATE CODE: R350

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250