Large format ultracapacitors and method of assembly

Abstract
A capacitor includes a plurality of electrode substrates, with each of the plurality of electrode substrates having a coated portion and an uncoated portion. The coated portion is coated with a coating material that includes a high surface area activated carbon material, a water soluble binder selected from the group consisting of: poly vinyl alcohol, poly acrylic acid, polymethacrylic acid, polyethylene oxide, polyacrylamide, poly-N-isopropylearylamide, poly-N,N-dimethylacrylamide, polyethyleneimine, polyoxyethylene, polyvinylsulfonic acid, poly(2-methoxyethoxyethoxyethylene), butadiene-acrylonitrile, and combinations thereof, and a water soluble thickener. A separator is inserted between adjacent substrates of the plurality of electrode substrates. The capacitor further includes an electrolyte. A method of manufacturing the capacitor is also provided.
Description
BACKGROUND OF THE INVENTION

Commonly used binders in the fabrication of commercial ultracapacitor electrodes include polyvinyledene fluoride (PVDF), ethylene-propylene, diene (EPDM), as well as other materials. The binders consist of one or more polymers, which are generally insoluble in water. Hence, organic solvent such as N-methyl pyrrolidone (NMP) is being used to dissolve these binders to fabricate electrodes. Some disadvantages of using organic solvents are that they are relatively higher in cost, they can possess negative environmental impacts, and pose disposal issues. Further, PVDF is highly unstable and tends to break down at high temperatures.


Accordingly, there is a need for water soluble binders to fabricate electrodes for ultracapacitors.


SUMMARY OF THE INVENTION

Briefly, the present invention provides a capacitor comprising a plurality of electrode substrates, with each of the plurality of electrode substrates having a coated portion and an uncoated portion. The coated portion is an electrode material comprised of activated carbon material with high surface area, a water soluble binder selected from the group consisting of: poly vinyl alcohol, poly acrylic acid, polymethacrylic acid, polyethylene oxide, polyacrylamide, poly-N-isopropylearylamide, poly-N,N-dimethylacrylamide, polyethyleneimine, polyoxyethylene, polyvinylsulfonic acid, poly(2-methoxyethoxyethoxyethylene), butadiene-acrylonitrile, and combinations thereof, and a water soluble thickener. A separator is inserted between adjacent substrates of the plurality of electrode substrates. The capacitor further includes an electrolyte.


The present invention also provides a method of manufacturing a large format capacitor. The method comprises the steps of forming a slurry that contains activated carbon material with high surface area, a water soluble binder selected from the group consisting of: poly vinyl alcohol, poly acrylic acid, polymethacrylic acid, polyethylene oxide, polyacrylamide, poly-N-isopropylearylamide, poly-N,N-dimethylacrylamide, polyethyleneimine, polyoxyethylene, polyvinylsulfonic acid, poly(2-methoxyethoxyethoxyethylene), butadiene-acrylonitrile, and combinations thereof, a water soluble thickener (if necessary) and water; coating a substrate with the slurry; and drying the coating onto the substrate.





BRIEF DESCRIPTION OF THE DRAWINGS

The foregoing summary, as well as the following detailed description of the invention, will be better understood when read in conjunction with the appended drawings. For the purpose of illustrating the invention, certain embodiments of the present invention are shown in the drawings. It should be understood, however, that the invention is not limited to the precise arrangements shown. The present invention will hereinafter be described in conjunction with the appended drawing figures wherein like numerals denote like elements. In the drawings:



FIG. 1 is a schematic view of a capacitor according to an exemplary embodiment of the present invention;



FIG. 2 is a sectional view of an exemplary capacitor configuration according to an exemplary embodiment of the present invention; and



FIG. 3 is a flowchart of exemplary steps performed to manufacture the capacitor of FIGS. 1 and 2.





DETAILED DESCRIPTION OF EXEMPLARY EMBODIMENTS

The ensuing detailed description provides preferred exemplary embodiments only, and is not intended to limit the scope, applicability, or configuration of the invention. Rather, the ensuing detailed description of the preferred exemplary embodiments will provide those skilled in the art with an enabling description for implementing the preferred exemplary embodiments of the invention. It is understood that various changes may be made in the function and arrangement of elements without departing from the spirit and scope of the invention, as set forth in the appended claims.


To aid in describing the invention, directional terms are used in the specification and claims to describe portions of the present invention (e.g., upper, lower, left, right, etc.). These directional definitions are merely intended to assist in describing and claiming the invention and are not intended to limit the invention in any way. In addition, reference numerals that are introduced in the specification in association with a drawing figure may be repeated in one or more subsequent figures without additional description in the specification in order to provide context for other features. Generally, the following disclosure refers to electrodes for ultracapacitors using water soluble binders and a method of manufacturing large size ultracapacitors using the above electrodes.


Referring to FIG. 1, an ultracapacitor 100 according to an exemplary embodiment of the present invention is shown. Ultracapacitor 100 includes a plurality of metallic electrode substrates 102. Each of the plurality of electrode substrates 102 has a coated portion 102a and an uncoated portion 102b. Substrate 102 is coated with a coating material 104, forming coated portion 102a. Substrate 102 may be aluminum, carbon coated aluminum foil, and any polymer primed aluminum foil (with or without carbon) or any other suitable material.


Coating 104 includes an activated carbon material with high surface area 106 mixed with a water soluble binder 108 and water to form a slurry. A water soluble thickener 110 may be added to the slurry to thicken the slurry for application onto electrode substrates 102. Additionally, a conductive additive or additives selected from the group consisting of carbon black, acetylene black, carbon fibers, coke, high surface area carbon and graphite may optionally be added to the slurry.


Exemplary high surface area activated carbon material 106 may be activated carbon, activated carbon nano foam, or other suitable carbon-based material. The amount of carbon in the slurry ranges between about 60 and about 95 weight percent. An exemplary surface area of activated carbon material 106 may be between about 100 to be about 2500 square meters per gram (m2/g).


Exemplary water soluble binder 108 may be selected from the group consisting of: poly vinyl alcohol, poly acrylic acid, polymethacrylic acid, polyethylene oxide, polyacrylamide, poly-N-isopropylacrylamide, poly-N,N-dimethylacrylamide, polyethyleneimine, polyoxyethylene, polyvinylsulfonic acid, poly(2-methoxyethoxyethoxyethylene), butadiene-acrylonitrile, carboxymethylcellulose, (CMC), polyvinylpyrrolidone, poly(allylamine), xanthan gum, guar gum, chitosan, polyvinyl acetate, gelatin, casein, styrene butadiene rubber (SBR), butadiene-acrylonitrile, rubber (NBR) hydrogenated NBR (HNBR), epichlorhydrin rubber (CHR), acrylate rubber (ACM), a cellulose from the group consisting of natural cellulose, physically and for chemically modified cellulose, natural polysaccharides, chemically and for physically modified polysaccharides, hydroxy methyl cellulose and methyl ethyl hydroxy cellulose, poly(carboxylic acid) and combinations and/or copolymers thereof.


Exemplary poly(carboxylic acids) are: polylactic acid (PLA), polyacrylic acid, polysuccinic acid, poly maleic acid and anhydride, poly furoic (pyromucic acid), poly fumaric acid, poly sorbic acid, poly linoleic acid, poly linolenic acid, poly glutamic acid, poly methacrylic acid, poly licanic acid, poly glycolic acid, poly aspartic acid, poly amic acid, poly formic acid, poly acetic acid, poly propoionic acid, poly butyric acid, poly sebacic acid, and copolymers thereof. When using poly(carboxylic acids), the pH of binder 108 can be neutralized by adding LiOH or other suitable material. The weight percent of binder in the slurry ranges between about 1 and about 20 percent.


Exemplary water soluble thickener 110 may be selected from the group consisting of natural cellulose, physically and/or chemically modified cellulose, natural polysaccharides, chemically and/or physically modified polysaccharides, carboxymethyl cellulose, hydroxy methyl cellulose and methyl ethyl hydroxy cellulose. The total solid weight percent of the thickener in the slurry ranges between about 1 and about 5 weight percent such that the weight percentage of the carbon, the binder, the thickener, and the conductive additive equals 100 percent. Water is added to the solid components to form the slurry such that the weight percent of the water in the slurry ranges between about 20 and about 70 percent.


The slurry is coated onto coated portion 102a of electrode substrates 102 and dried until the moisture level is less than 1000 parts per million (ppm) or more preferably less than 200 ppm in the electrode 102a. After drying, electrode substrates 102 are cut into desired size and shaped electrodes 112, with uncoated portion 102b formed into terminal tabs 114. Electrodes 112 are stacked on top of each other, with a separator 120 inserted between adjacent electrodes 112, forming an electrode stack 116. Separator 120 may be a micro porous material such as, for example polyethylene or polypropylene-type separator or plasticized polymer type separators which are bonded to the electrodes. Separator 120 extends beyond coating 102a as shown in FIG. 1 to prevent direct contact between adjacent electrodes 102.


Terminal tabs 114 are alternated on different sides of adjacent electrodes 112, with terminal tabs 114a on one side of ultracapacitor 100 being “positive” terminal tabs 114a and terminal tabs 114b on the other side of ultracapacitor 100 being “negative” terminal tabs 114b. Terminal tabs 114a and 114b both extend from the same side (i.e., top) of ultracapacitor 100, resulting in less complexity in connecting terminal tabs 114 to an electrical circuit than having one set of terminal tabs extending from the top of ultracapacitor 100 and the other terminal tabs extending from the bottom of ultracapacitor 100.


An equal number of positive terminal tabs 114a as negative terminal tabs 114b are provided, with positive terminal tabs 114a coupled to each other in parallel and negative terminal tabs 114b coupled to each other in parallel as well to form a capacitive circuit, or bundle. Ultracapacitor 100 may include multiple bundles, with the multiple bundles coupled together in series to achieve a desired capacitor voltage.


Referring to FIG. 2, the bundles are enclosed in packaging that includes a pressure regulated large format cell pouch 130. Cell pouch 130 includes a metallic lamination, with the inside of pouch 130 being formed from a heat sealable material, such as, for example, an aluminum pouch bag material supplied by Showa Denko, Japan.


Positive terminal tabs 114a are coupled to a positive terminal 132 inside cell pouch 130 and negative terminal tabs 114b are coupled to a negative terminal 134, also inside cell pouch 130. The feature of providing these couplings inside cell pouch 130 provides improved safety and eliminates hazards during handling of ultracapacitor 100.


An insulator block 140 provides structure and a pass-through for terminals 132, 134 in a hermetic fashion. Insulator block 140 provides for sealing of cell pouch 130 to seal around the pass-throughs for terminals 132, 134. An exemplary packaging is disclosed in U.S. patent application Ser. No. 12/729,790, which is owned by the assignee of the present invention and is incorporated herein by reference in its entirety as though fully set forth.


Referring back to FIG. 1, ultracapacitor 100 further includes an electrolyte 142 that is inserted into cell pouch 130. The electrolyte 142 may be an aqueous or a non-aqueous medium with an appropriate salt. An exemplary organic electrolyte may be tetraethylammonium tetrafluoroborate (TEABF4) in acetonitrile (ACN) or propylene carbonate (PC).


Cell pouch 130 may be stored in a housing assembly 146. An exemplary housing assembly 146 is a nested heatsink housing assembly disclosed in U.S. patent application Ser. No. 12/730,642, which is owned by the assignee of the present invention and is incorporated herein by reference in its entirety as though fully set forth. The ultracapacitor 100 according to the present invention has a capacity of between about 30 and about 40 Farads.


Referring to the flowchart 500 of FIG. 3, an exemplary method of manufacturing ultracapacitor 100 is provided. In step 502, a slurry is formed comprised of high surface area activated carbon material 106, water soluble binder 108, water soluble thickener 110, and water. In step 504, substrate 114 is coated with the slurry and in step 506, the coating is dried onto the substrate 114.


In step 508, a plurality of the substrates 114 are stacked on top of each other, while separating adjacent substrates from each other with micro porous separator material 120, forming a stack. In step 510, the stack is inserted into cell pouch 130 and in step 512, electrolyte 142 is added to the stack in cell pouch 130.


While the principles of the invention have been described above in connection with preferred embodiments, it is to be clearly understood that this description is made only by way of example and not as a limitation of the scope of the invention.

Claims
  • 1. A capacitor comprising: a plurality of electrode substrates, each of the plurality of electrode substrates having a coated portion and an uncoated portion, the coated portion being coated with a coating material comprising: an activated carbon material with high surface area;a water soluble binder selected from the group consisting of poly vinyl alcohol, poly acrylic acid, polymethacrylic acid, polyethylene oxide, polyacrylamide, poly-N-isopropylearylamide, poly-N,N-dimethylacrylamide, polyethyleneimine, polyoxyethylene, polyvinylsulfonic acid, poly(2-methoxyethoxyethoxyethylene), butadiene-acrylonitrile, and combinations thereof; anda water soluble thickener;a separator inserted between adjacent substrates of the plurality of electrode substrates; andan electrolyte.
  • 2. The capacitor according to claim 1, wherein the water soluble binder comprises poly acrylic acid.
  • 3. The capacitor according to claim 1, wherein the water soluble binder comprises polymethacrylic acid.
  • 4. The capacitor according to claim 1, wherein the water soluble binder comprises polyethylene oxide.
  • 5. The capacitor according to claim 1, wherein the water soluble binder comprises polyacrylamide.
  • 6. The capacitor according to claim 1, wherein the water soluble binder comprises poly-N-isopropylearylamide.
  • 7. The capacitor according to claim 1, wherein the water soluble binder comprises poly-N,N-dimethylacrylamide.
  • 8. The capacitor according to claim 1, wherein the water soluble binder comprises polyethyleneimine.
  • 9. The capacitor according to claim 1, wherein the water soluble binder comprises polyoxyethylene.
  • 10. The capacitor according to claim 1, wherein the water soluble binder comprises polyvinylsulfonic acid.
  • 11. The capacitor according to claim 1, wherein the water soluble binder comprises poly(2-methoxyethoxyethoxyethylene).
  • 12. The capacitor according to claim 1, wherein the water soluble binder comprises butadiene-acrylonitrile.
  • 13. The capacitor according to claim 1, wherein the activated carbon material comprises activated carbon nano foam.
  • 14. The capacitor according to claim 1, wherein the activated carbon material has a surface area between about 100 square meters per gram and about 2,500 square meters per gram.
  • 15. The capacitor according to claim 1, having a capacitance of above about 30 Farads.
  • 16. The capacitor according to claim 1, wherein the electrolyte comprises an aqueous medium.
  • 17. The capacitor according to claim 1, wherein the electrolyte comprises a non-aqueous medium.
  • 18. The capacitor according to claim 1, wherein the coating further comprises a conductive additive.
  • 19. A method comprising the steps of: a) forming a slurry comprised of: a high surface area activated carbon material;a water soluble binder selected from the group consisting of: poly vinyl alcohol, poly acrylic acid, polymethacrylic acid, polyethylene oxide, polyacrylamide, poly-N-isopropylearylamide, poly-N,N-dimethylacrylamide, polyethyleneimine, polyoxyethylene, polyvinylsulfonic acid, poly(2-methoxyethoxyethoxyethylene), butadiene-acrylonitrile, and combinations thereof;a water soluble thickener; andwater;b) coating a substrate with the slurry; andc) drying the coating onto the substrate.
  • 20. The method according to claim 19, further comprising the steps of: d) stacking a plurality of the substrates on top of each other, while separating adjacent substrates from each other with a micro porous separator material;e) inserting the stack into a pouch; andf) adding an electrolyte to the stack in the pouch.
US Referenced Citations (97)
Number Name Date Kind
3625759 Williams Dec 1971 A
4664883 Melody et al. May 1987 A
5150283 Yoshida et al. Sep 1992 A
5175222 Betso Dec 1992 A
5514488 Hake et al. May 1996 A
5557497 Ivanov et al. Sep 1996 A
5707756 Inoue et al. Jan 1998 A
5795558 Aoki et al. Aug 1998 A
5866279 Wada et al. Feb 1999 A
5897955 Drumheller Apr 1999 A
6007947 Mayer Dec 1999 A
6031712 Kurihara et al. Feb 2000 A
6159636 Wang et al. Dec 2000 A
6183908 Miyasaka et al. Feb 2001 B1
6235427 Idota et al. May 2001 B1
6282081 Takabayashi et al. Aug 2001 B1
6372387 Kawakami et al. Apr 2002 B1
6399246 Vandayburg et al. Jun 2002 B1
6497979 Iijima et al. Dec 2002 B1
6602742 Maletin et al. Aug 2003 B2
6616903 Poles et al. Sep 2003 B2
6627252 Nanjundiah et al. Sep 2003 B1
6697249 Maletin et al. Feb 2004 B2
6770397 Maeda et al. Aug 2004 B1
6811911 Peled et al. Nov 2004 B1
6852449 Nagata et al. Feb 2005 B2
6881517 Kanzaki et al. Apr 2005 B1
6946007 Bendale et al. Sep 2005 B2
6955694 Bendale et al. Oct 2005 B2
6987663 Merker et al. Jan 2006 B2
7027292 Anzai et al. Apr 2006 B2
7052629 Maeda et al. May 2006 B2
7052803 Kato et al. May 2006 B2
7083829 Hoke et al. Aug 2006 B2
7227737 Mitchell et al. Jun 2007 B2
7267907 Kim Sep 2007 B2
7316864 Nakayama et al. Jan 2008 B2
7393476 Shiozaki et al. Jul 2008 B2
7419745 Chaturvedi et al. Sep 2008 B2
7422826 Xing et al. Sep 2008 B2
7425386 Takezawa et al. Sep 2008 B2
7481991 Kawasato et al. Jan 2009 B2
7508651 Mitchell et al. Mar 2009 B2
7531272 Park et al. May 2009 B2
7547491 Ham et al. Jun 2009 B2
7558050 Roh et al. Jul 2009 B2
7570478 Terada et al. Aug 2009 B2
7749658 Isono et al. Jul 2010 B2
7914704 Yamakawa et al. Mar 2011 B2
20020110732 Coustier et al. Aug 2002 A1
20030091883 Peled et al. May 2003 A1
20030118904 Hosokawa et al. Jun 2003 A1
20030138696 Peres et al. Jul 2003 A1
20030172509 Maletin et al. Sep 2003 A1
20040020763 Kanzaki et al. Feb 2004 A1
20040023115 Kato et al. Feb 2004 A1
20040121232 Kato et al. Jun 2004 A1
20040234850 Watarai et al. Nov 2004 A1
20050069763 Hong et al. Mar 2005 A1
20050074669 Park et al. Apr 2005 A1
20050142446 Yamamoto et al. Jun 2005 A1
20050238958 Kim Oct 2005 A1
20060058462 Kim et al. Mar 2006 A1
20060166093 Zaghib et al. Jul 2006 A1
20060194116 Suzuki et al. Aug 2006 A1
20060228627 Nakayama et al. Oct 2006 A1
20060275661 Kim et al. Dec 2006 A1
20070055023 Han et al. Mar 2007 A1
20070264568 Ryu et al. Nov 2007 A1
20070264573 Yamada et al. Nov 2007 A1
20070292765 Inoue et al. Dec 2007 A1
20080089006 Zhong et al. Apr 2008 A1
20080090138 Vu et al. Apr 2008 A1
20080118834 Yew et al. May 2008 A1
20080118840 Yew et al. May 2008 A1
20080160415 Wakita et al. Jul 2008 A1
20080212260 Roh et al. Sep 2008 A1
20080254362 Raffaelle et al. Oct 2008 A1
20080299461 Kim Dec 2008 A1
20090080141 Eilertsen Mar 2009 A1
20090148772 Kawasato et al. Jun 2009 A1
20090155694 Park Jun 2009 A1
20090214952 Wakita et al. Aug 2009 A1
20090220678 Kono et al. Sep 2009 A1
20090258296 Kawasato et al. Oct 2009 A1
20090268377 Choi et al. Oct 2009 A1
20090317718 Imachi et al. Dec 2009 A1
20100009258 Hasegawa et al. Jan 2010 A1
20100047690 Tsuchiya et al. Feb 2010 A1
20100075229 Atsuki et al. Mar 2010 A1
20100112441 Fukumine et al. May 2010 A1
20100117031 Akagi et al. May 2010 A1
20100136430 Lee Jun 2010 A1
20100140554 Oki et al. Jun 2010 A1
20100143799 Park Jun 2010 A1
20110009553 Heller et al. Jan 2011 A1
20110045168 Seo et al. Feb 2011 A1
Foreign Referenced Citations (9)
Number Date Country
573266 Dec 1993 EP
1172878 Jan 2002 EP
62270337 Nov 1987 JP
8069791 Mar 1996 JP
10208729 Aug 1998 JP
11149929 Jun 1999 JP
2002226505 Aug 2002 JP
2004185826 Jul 2004 JP
2007142579 Dec 2007 WO
Related Publications (1)
Number Date Country
20110141661 A1 Jun 2011 US