Ultracapacitor electroyte

Abstract

The invention relates to an ultracapacitor and to a method of making an ultracapacitor. The ultracapacitor of the invention includes two solid, nonporous current collectors, two porous electrodes separating the collectors, a porous separator between the electrodes and an electrolyte occupying the pores in the electrodes and separator. The electrolyte includes a cyclic carbonate solvent, a cyclic ester solvent and an electrolyte salt. The invention also relates to a stack of ultracapacitor cells.

Description

BACKGROUND OF THE INVENTION

Capacitors are storage devices that store electrical energy on an electrode surface. Electrochemical cells create an electrical charge at electrodes by chemical reaction. The ability to store or create electrical charge is a function of electrode surface area in both applications. Ultracapacitors, sometimes referred to as double layer capacitors, are a third type of storage device. An ultracapacitor creates and stores energy by microscopic charge separation at an electrical chemical interface between electrode and electrolyte.

Ultracapacitors are able to store more energy per weight than traditional capacitors and they typically deliver the energy at a higher power rating than many rechargeable batteries. Ultracapacitors comprise two porous electrodes that are isolated from electrical contact by a porous separator. The separator and the electrodes are impregnated with an electrolytic solution, which allows ionic current to flow between the electrodes while preventing electronic current from discharging the cell. Each electrode is in intimate contact with a current collector. One purpose of the current collector is to reduce ohmic loss. If the current collectors are nonporous, they can also be used as part of the capacitor case and seal.

When electric potential is applied to an ultracapacitor cell, ionic current flows due to the attraction of anions to the positive electrode and cations to the negative electrode. Upon reaching the electrode surface, the ionic charge accumulates to create a layer at the solid liquid interface region. This is accomplished by absorption of the charge species themselves and by realignment of dipoles of the solvent molecule. The absorbed charge is held in this region by opposite charges in the solid electrode to generate an electrode potential. This potential increases in a generally linear fashion with the quantity of charge species or ions stored on the electrode surfaces. During discharge, the electrode potential or voltage that exists across the ultracapacitor electrodes causes ionic current to flow as anions are discharged from the surface of the positive electrode and cations are discharged from the surface of the negative electrode while an electronic current flows through an external circuit between electrode current collectors.

In summary, the ultracapacitor stores energy by separation of positive and negative charges at the interface between electrode and electrolyte. An electrical double layer at this location consists of sorbed ions on the electrode as well as solvated ions. Proximity between the electrodes and solvated ions is limited by a separation sheath to create positive and negative charges separated by a distance which produces a true capacitance in the electrical sense.

During use, an ultracapacitor cell is discharged by connecting the electrical connectors to an electrical device such as a portable radio, an electric motor, light emitting diode or other electrical device. The ultracapacitor is not a primary cell but can be recharged. The process of charging and discharging may be repeated over and over. For example, after discharging an ultracapacitor by powering an electrical device, the ultracapacitor can be recharged by supplying potential to the connectors.

The physical processes involved in energy storage in an ultracapacitor are distinctly different from the electrochemical oxidation/reduction processes responsible for charge storage in batteries. Further unlike parallel plate capacitors, ultracapacitors store charge at an atomic level between electrode and electrolyte. The double layer charge storage mechanism of an ultracapacitor is highly efficient and can produce high specific capacitance, up to several hundred Farads per cubic centimeter.

Ultracapacitor electrolytes must exhibit good ionic conductivity and must be highly soluble and chemically and electrochemically stable. Additionally, the electrolyte must be low in cost for commercial production. Nonaqueous electrolyte based ultracapacitors are of interest because they have much larger decomposition voltage limit compared to aqueous electrolyte systems. The energy that can be stored in a nonaqueous ultracapacitor can be greatly increased over that of aqueous systems. However, organic electrolytes are much less conductive compared to aqueous electrolytes. This contributes to a relatively high resistance and limits ultracapacitor use for high power applications. Further, high internal resistance causes a high internal loss of stored energy. This increases the cost of an ultracapacitor because of the concomitant requirement of enlarged electrode.

It would be advantageous to provide nonaqueous ultracapacitors with reduced internal resistance. A number of solvent systems have been extensively investigated toward this end. A common system utilizes propylene carbonate (“PC”) for its moderately good conductivity and reasonably wide potential window. PC is the most common solvent used in nonaqueous ultracapacitors.

The present invention provides an improved electrolyte composition characterized by increased conductivity and lower resistance which in turn provides performance enhancement and cost reduction in an ultracapacitor.

SUMMARY OF THE INVENTION

The invention relates to an ultracapacitor and to a method of making an ultracapacitor. The ultracapacitor of the invention comprises two solid, nonporous current collectors, two porous electrodes separating the collectors, a porous separator between the electrodes and an electrolyte occupying the pores in the electrodes and separator. The electrolyte comprises (i) a cyclic carbonate solvent and (ii) a cyclic ester solvent and an electrolyte salt. The invention also relates to a stack of ultracapacitor cells with an electrolyte comprising (i) a cyclic carbonate solvent and (ii) a cyclic ester solvent and an electrolyte salt.

The method of the invention comprises providing a multilayer structure comprising two solid, nonporous current collectors, two porous electrodes separating the current collectors, a porous separator between the electrodes and an electrolyte occupying the pores in the electrodes and separator. The electrolyte comprises (i) a cyclic carbonate solvent and (ii) a cyclic ester solvent and an electrolyte salt. The multilayer structure is sealed to form the ultracapacitor.

In another aspect, the invention relates to a method of making a stack of ultracapacitor cells. In this method, a plurality of bipolar double layer ultracapacitor cells is provided in stacked relationship. A non-porous current collector is provided between each cell with each current collector having adjoining polarized electrodes of different cells bonded thereto. The electrodes and separators are saturated with an electrolyte comprising (i) a cyclic carbonate solvent and (ii) a cyclic ester solvent and an electrolyte salt. The cells, current collectors and separators are sealed to form the stack of ultracapacitor cells.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a front sectional view of an ultracapacitor;

FIG. 2 is a front sectional view of a series stack of ultracapacitor cells;

FIG. 3 is a cross-sectional view of an exemplary apparatus for sealing an ultracapacitor; and

FIG. 4 is a top cross-sectional view of a separator of a sealed ultracapacitor.

DETAILED DESCRIPTION OF THE INVENTION

The electrolyte composition of the invention may be used in a wide variety of ultracapacitors such as described in U.S. Pat. Nos. 5,464,453; 5,420,747; 5,150,283; 5,136,472; and 4,803,597; as well as PCT Application WO96/11486 (PCT/US95/12772; Apr. 18, 1996), all of which are incorporated herein by reference. FIGS. 1 and 2 herein, are based on PCT Application WO 96/11486 and show a non-limiting example of an ultracapacitor made by the method of the present invention. In all of the Figures of this application, like structures are identified by the same numbers.

Referring to FIG. 1 , ultracapacitor 10 includes a nonconductive enclosing body 12 , a pair of carbon electrodes 14 and 16 , an electronic porous separator layer 18 , an electrolyte 20 , a pair of conductive layers which are current collectors 22 and 24 and electrical leads 26 and 28 , extending from the current collectors 22 and 24 . One of the pair of current collectors 22 and 24 is attached to the back of each electrode 14 and 16 . In FIG. 1 , electrodes 14 and 16 can each represent a plurality of electrodes so long as the electrodes are porous to electrolyte flow.

The current collectors 22 , 24 commonly are made of aluminum because of its conductivity and cost. In the drawings, the current collectors 22 and 24 are thin layers of aluminum foil. However, the electrodes can be any suitable conductive material.

The electronic separator 18 is preferably made from a highly porous material which acts as an electronic insulator between the carbon electrodes 14 and 16 . The separator 18 assures that opposing electrodes 14 and 16 are never in contact with one another. Contact between electrodes can result in a short circuit and rapid depletion of the charges stored in the electrodes. The porous nature of the separator 18 allows movement of ions in the electrolyte 20 . A wide variety of types and arrangements of separation layers can be employed, as those of ordinary skill in the electrochemical arts realize. Separation layers are usually made from nonconductive materials such as cellulosic materials; glass fiber; polymers such as polyesters or polyolefins; and the like. In those embodiments in which the separator layers will be in contact with sealant material, they should have a porosity sufficient to permit the passage of sealant and should be resistant to the chemical components in the sealant. In a typical ultracapacitor, the separator layers have a thickness in the range of about 0.5 mil to about 10 mils. Preferred separators 18 are porous polypropylene and tissue cellulosic materials. The electrolyte 20 is a composition according to the present invention comprising (i) a cyclic carbonate solvent and (ii) a cyclic ester solvent and an electrolyte salt. While it is known that electrolyte conductivity can be enhanced by the use of mixed solvents, the present invention relates to a particular mixed system, and more particularly to a ternary system that exhibits improved performance and lower cost as compared to known mixed solvent systems.

The preferred cyclic carbonates (i) have 5 to 8 carbon atoms. Examples of the cyclic carbonates include 1,2-butylene carbonate, 2,3-butylene carbonate, 1,2-pentene carbonate, 2,3-pentene carbonate and propylene carbonate. Propylene is most preferred.

Preferred cyclic esters (ii) are esters having 3 to 8 carbon atoms. Examples of the cyclic esters include β-butyrolactone, γ-butyrolactone, γ-valerolactone and δ-valerolactone. The most preferred cyclic ester is γ-butyrolactone.

A two solvent component system of the invention comprises (i) the cyclic carbonate solvent and (ii) the cyclic ester solvent in proportions of about 1:4 to about 4:1, preferably about 2:1 to about 1:2 and most preferably about 1:1.

Further, the electrolyte of the invention can be a three component solvent system comprising (i) a cyclic carbonate solvent, (ii) a cyclic ester solvent and (iii) at least one additional aprotic organic solvent and an electrolyte salt. The at least one additional aprotic organic solvent (iii) can be a different cyclic carbonate from (i) or a different cyclic esters from (ii) as defined above. The at least one additional aprotic organic solvent (iii) can also be a chain ether, a cyclic ether or a chain carbonate solvent. The preferred chain ethers have 4 to 8 carbon atoms. Examples of the chain ethers include dimethoxyethane, diethoxyethane, methoxyethoxyethane, dibutoxyethane, dimethoxypropane, diethoxypropane and methoxyethoxypropane. The preferred cyclic ethers have 3 to 8 carbon atoms. Examples of the cyclic ethers include tetrahydofuran, 2-methyl-tetrahydrofuran, 1,3-dioxolan, 1,2-dioxolan, 2-methyldioxolan and 4-methyl-dioxolan. Preferably the at least one additional aprotic organic solvent (iii) is a chain carbonate. The preferred chain carbonates have 3 to 8 carbon atoms. Examples of the chain carbonates include dimethyl carbonate, diethyl carbonate, dipropyl carbonate, methyl ethyl carbonate, methyl propyl carbonate and ethyl propyl carbonate. The most preferred chain carbonate is dimethyl carbonate.

A three component solvent system of the invention comprises (i) the cyclic carbonate solvent, (ii) the cyclic ester solvent and (iii) the at least one additional aprotic organic solvent in proportions of about 4:4:1 to about 1:1:4, preferably about 2:2:1 to about 1:1:2 and most preferably about 1:1:1.

Further, the electrolyte solvents of the present invention can include other solvent components including other aprotic organic solvents including the cyclic ester, chain carbonate, cyclic carbonate, chain ether and/or cyclic ether solvents aforesaid. Other exemplary organic solvent components for electrolyte 20 include but are not limited to nitriles such as acetonitrile, acrylonitrile and propionitrile; sulfoxides such as dimethyl, diethyl, ethyl methyl and benzylmethyl sulfoxide; amides such as dimethyl formamide and pyrrolidones such as N-methylpyrrolidone.

Suitable electrolyte salts include quaternary ammonium salts such as tetraethylammonium tetraflouroborate ((Et) 4 NBF 4 ), hexasubstituted guanidinium salts such as disclosed in U.S. Pat. No. 5,726,856, the disclosure of which is incorporated herein by reference, and lithium salts such as disclosed by Ue et al., Mobility and Ionic Association of Lithium Salts in a Propylene Carbonate-Ethyl Carbonate Mixed Solvent, Electrochem. Soc ., vol. 142, No. 8, August 1995, the disclosure of which is incorporated herein by reference. The salt can be present in the electrolyte with a molar concentration of about 0.1 M to about 1.5M, preferably about 0.5M to about 1.5 M, and most preferably about 1.0M to about 1.5M.

In a preferred embodiment, the electrodes 14 , 16 in FIG. 1 , are both carbon electrodes on aluminum current collectors. The electrode can be fabricated by a forming process or by pressing electrode materials in a die and slurry pasting or screen printing carbon as a paste with a liquid phase binder/fluidizer. The liquid phase may be water or an electrolyte solvent with or without a thinner such as acetone. Both dry and wet electrode formations may include a binder such as polymers, starches, Teflon® particles or Teflon® dispersions in water.

The enclosing body 12 can be any known enclosure means commonly used with ultracapacitors. It is an advantage to minimize the weight of the packaging means to maximize the energy density of the ultracapacitor. Packaged ultracapacitors are typically expected to weigh 1.25 to 2 times more than the unpackaged ultracapacitor. The electrical leads 26 and 28 extend from the current collectors 22 and 24 through the enclosing body 12 and are adapted for connection with an electrical circuit (not shown).

Ultracapacitor 10 of FIG. 1 includes a bipolar double layer cell 30 that includes two solid, nonporous current collectors 22 , 24 , two porous electrodes 14 , 16 separating the current collectors 22 , 24 and a porous separator 18 between the electrodes 14 , 16 and an electrolyte 20 occupying pores in the electrodes 14 , 16 and separator 18 . Individual ultracapacitor cells can be stacked in series to increase operating voltage. The optimum design is to have adjacent cells separated with only a single current collector. This collector is nonporous so that no electrolytic solution is shared between cells. This type of design is called bipolar and is illustrated in FIG. 2 of the drawings. In a bipolar double layer capacitor, one side of the current collector contacts a positive electrode and the other side contacts a negative electrode of an adjacent cell.

A series stack 40 of the high performance bipolar double layer cells 30 (A, B, C and D) is illustrated in FIG. 2 . In FIG. 2 , each pair of polarized carbon electrodes, 14 , 16 is separated with a separator 18 . A current collector 32 is attached at one surface to charged electrode 14 of a first cell. Attached to an opposite surface of the current collector 32 , is an oppositely charged electrode 16 of a second cell. If one side of the current collector 32 is in contact with the negative electrode for a first capacitor cell “A,” then the other side of the same current collector 32 is in contact with a positive electrode for an adjacent cell “B.” A sufficient amount of an electrolyte 20 is introduced such that the electrolyte 20 saturates the electrodes 14 and 16 and separator 18 within each cell. Exterior current collectors 22 and 24 are placed at each end of the stack.

The internal current collectors 32 of the series stack of cells are preferably nonporous layers of aluminum foil designed to separate the electrolyte 20 between adjacent cells. The exterior current collectors are also nonporous such that they can be used as part of the external capacitor case seal, if necessary. The electronic separator 18 is located between the opposing carbon electrodes 14 and 16 within a particular capacitor cell. The electronic separator 18 allows ionic conduction via charged ions in the electrolyte.

The ultracapacitor cell can be constructed by placing the layers of conductor, electrode and separator along with electrolyte within an enclosing body. The structure can then be subjected to pressure to seal the layers within the enclosing body. Alternatively, the enclosing body can be subjected to pressure and vacuum. The vacuum acts to remove gases while the ultracapacitor is sealed. Alternatively, the ultracapacitor cell can be constructed by providing adhesive between layers and applying pressure and or heat throughout the adhesive to seal the cell.

FIG. 3 depicts one, non-limiting illustration of an apparatus and method of sealing an ultracapacitor or series stack of ultracapacitor cells according to the present invention. Referring to FIG. 3 , structure 50 is a frame, platform, or other construction but is often a press as described below. An enclosable region is depicted in FIG. 3 as recess 52 , in which an ultracapacitor series stack 40 is disposed. The embodiment illustrated in FIG. 3 permits application of vacuum while the ultracapacitor is being sealed. Primary vacuum tube 60 communicates with recess 52 . A collapsible membrane 64 can be fastened over the ultracapacitor to maintain a vacuum while the cell is being sealed by pressing.

FIG. 3 shows an ultracapacitor cell disposed in the recess area of the press 50 . The cell includes a separator system, comprising an upper separator layer 42 and a lower separator layer 44 . Sealant portions 46 and 48 are disposed in a peripheral area between the bottom surface of separator 42 and the top surface of separator 44 . “Peripheral” refers to the boundary area of the separator layers. In general, this area should be as small as possible. This boundary area is designated as element 68 in FIG. 4 . FIG. 4 provides a top, cross-sectional view of a separator layer similar to layer 44 of FIG. 3 , after sealant has spread to some extent by the action of pressure and, optionally, heat, as described below. The boundary area 68 surrounds the primary section 66 of a separator layer.

Many different types of sealants can be used in the present invention and the term is meant to encompass, “glues”, or “pastes.” Sealants are described, for example, in the Kirk - Othmer Encyclopedia of Chemical Technology, 3rd Edition, Vol.1, pp.488-508 (1978), and in The Condensed Chemical Dictionary, 10th Edition, 1981, Van Nostrand Reinhold Company. In general, the selected sealant should be chemically resistant to electrolyte. It should also be capable of withstanding operating temperatures of the ultracapacitor without substantial degradation. Moreover in those embodiments where the sealant contacts the separators, it should be capable of flowing through the thickness of the separator layers. Once cured, the sealant should be substantially impermeable to the flow or passage of electrolyte.

Heat-curable sealants may be used in some embodiments. Moisture-cured sealants or externally-cured materials may be used. Other embodiments may use air-curable or pressure-sensitive sealants, such as “hot melt” glues. Illustrative sealants include those based on acrylic, ethylene such as ethylene vinyl acetate (EVA) copolymer, silicone, rubber, epoxy materials, or combinations of these materials. Commercial examples include the materials commonly referred to as “hot glues.”

The sealants are usually in the form of liquids, pastes, or solids. A sealant may be applied to one or both of the facing surfaces of the separators or other surfaces. Many techniques are available for applying sealant. Known application techniques include the use of a spatula, brush, roller, spray, or glue gun. As one example, a bead, strip or “ring” of sealant is applied along the peripheral area 68 of one of the separator layers. Alternatively, individual droplets of sealant can be deposited at sites in the peripheral area 68 with the droplets flowing and covering the peripheral area 68 upon the application of pressure, vacuum and/or heat. As yet another alternative, at least one of the separator layers 18 can be pre-impregnated with sealant. All of these techniques cause the sealant to form a continuous layer. In general, the particular method of deposition is not critical, as long as the sealant is applied to locations where it will eventually form a seal after pressure or vacuum is released. The ultracapacitor becomes sealed by a barrier which is perpendicular to the horizontal capacitor layers which are encased in the barrier.

A compressive force is applied to promote the flow of the sealant—especially in the case of sealant compositions with very high softening points or glass transition temperatures, such as the EVA based types. Compression can be applied indirectly to the sealant through upper ultracapacitor layers by means of the mechanical press 50 of FIG. 3 . Other devices to seal an ultracapacitor include an hydraulic press or pneumatic press or any device for applying compressive force. The press 50 of FIG. 3 includes structural frame 70 and adjustable beam 72 . The length of beam 72 moves in a direction perpendicular to the base portion of the structural frame as controlled by the selective action of hand lever 74 and gears 76 and 78 . Compression element 80 is detachably attached as the base of beam 72 . Bottom surface 82 can be similar in shape to the peripheral area of the top planar surface of ultracapacitor 40 . The force applied by the press should be sufficient to cause the sealant to become substantially fluid, to flow and form a continuous bead or strip around the peripheral area of the layer on which it is deposited. Thus, the particular press force depends in large part on the nature of the sealant. In general, the pressure will be in the range of about 1 psi to about 1,000 psi and preferably, in the range of about 10 psi to about 100 psi. A lower press force will be suitable for lower viscosity sealants and a higher press force will be required for higher viscosity materials.

The sealant can be heated while being compressed. Heating enhances the flow characteristics of the sealant. Heating temperature should be sufficient to soften the sealant. Preferably, the temperature is high enough to melt the sealant. For a sealant made from an EVA based material, a suitable temperature will be in the range of about 100° C. to about 300° C.

Heat is applied to the sealant in the press 50 of FIG. 3 by means of a standard electrical heating element that is encased within element 80 and is connected to an electrical outlet by way of cord 82 . The bottom surface 84 of element 80 has a shape that aligns with sealant-containing peripheral regions of ultracapacitor 10 . Thus, when compression element 80 is lowered for compression of the ultracapacitor through membrane 64 , heat is transmitted primarily to the sealant containing regions.

A vacuum can be applied to press together the layers of the ultracapacitor and to evacuate ambient gasses from the internal region of the cell structure. In FIG. 3 , vacuum tube 60 is connected to a vacuum source through vacuum valve 88 with backfill vacuum tube 86 . When vacuum is applied, the collapsible membrane 64 is positioned over recess 52 . The membrane 64 maintains the vacuum within the recess and transmits the applied compressive force to the layers of the ultracapacitor. The membrane 64 is heat-resistant to a temperature of about 400° C. The amount of vacuum applied ranges from about 700 mm mercury to 0.1 mm mercury. A typical vacuum pressure is in the range of about 500 mm mercury to about 0.1 mm mercury.

In operation, the applied vacuum pressure draws collapsible membrane 64 tightly against the top of ultracapacitor 10 , compressing the individual layers of the ultracapacitor against platform layer 58 while the action of compression element 80 presses against sealant-containing regions to induce sealant 46 , 48 to permeate the peripheral regions of separator layers 18 . The sealant contacts substantially aligned peripheral areas 60 of the facing surfaces of conductive layers 22 and 24 . As the sealant cures or solidifies, it forms a strong bond to join layers 22 and 24 . After sealing is complete, compression element 80 is retracted and the ultracapacitor is allowed to cool.

The following example is illustrative of the invention.

EXAMPLE

This example shows that improvement in electrolyte conductivity can be achieved with mixed solvent systems. Conductivity data of 1M tetraethylammonium tetraflouroborate ((Et) 4 NBF 4 ) were experimentally developed for various solvent combinations and are summarized in Table 1. In the Table PC, GBL, EC, and DMC stand for propylene carbonate, γ-butyrolactone, ethylene carbonate and dimethyl carbonate, respectively. The ratios in brackets are expressed in volume (ml) except for ethylene carbonate which is expressed in weight (g) since it is a solid at room temperature.

TABLE 1
Electrolyte Conductivity for 1 Molar (Et) 4 NBF 4
Solutions at room temperature
			Ratio	Ratio
	Mixture	Conductivity,	to pure	to pure
Mixture	Ratio	mS/cm	PC	GBL
PC	Pure	12.65	1	0.72
PC + EC	1:1	15.58	1.23	0.88
PC + GBL	1:1	15.91	1.26	0.90
GBL + DMC*	1:1	16.00	1.26	0.91
PC + DMC*	1:1	16.18	1.28	0.92
GBL	Pure	17.63	1.39	1
GBL + EC	1:1	17.95	1.42	1.02
GBL + EC + DMC	2:2:1	19.76	1.56	1.12
GBL + EC + DMC	1:1:1	20.16	1.59	1.14
*Solvents are saturated at 1 Molar or lower (Et) 4 NBF 4 at room temperature, therefore, data are for saturated solutions.
PC = Propylene Carbonate
EC = Ethylene Carbonate (solid at room temperature, but liquid in above solutions)
DMC = Dimethyl Carbonate
GBL = gamma Butyrolactone

As shown in Table 1, the mixed solvent systems provide more than 50% higher conductivity than conventional PC solvent. Moreover, the ternary solvent system with γ-butyrolactone, ethylene carbonate and dimethyl carbonate is significantly more conductive than corresponding binary systems for 1M (Et) 4 NBF 4 . Thus, the internal resistance of nonaqueous ultracapacitors can be greatly reduced, which in turn improves power and energy performance of ultracapacitor devices and reduces materials cost.

Claims

1. An ultracapacitor comprising at least one cell, said cell comprising:two solid, nonporous current collectors, two porous electrodes separating said current collectors, a porous separator between said electrodes and an electrolyte occupying pores in said electrodes and separator, wherein said electrolyte comprises (i) a cyclic carbonate solvent and (ii) a cyclic ester solvent and an electrolyte salt, wherein the electrolyte salt comprises a hexasubstituted guanidinium salt.

2. The ultracapacitor of claim 1, wherein said electrolyte comprises at least one additional aprotic organic solvent.

3. The ultracapacitor of claim 2, wherein said at least one additional aprotic organic solvent comprises a chain carbonate.

4. The ultracapacitor of claim 3, wherein said at least one additional aprotic organic solvent comprises dimethyl carbonate.

5. A stack of ultracapacitor cells, comprising at least one of the cells of claim 4.

6. A stack of ultracapacitor cells, comprising at least one of the cells of claim 3.

7. The ultracapacitor of claim 2, wherein said cyclic carbonate solvent is propylene carbonate, said cyclic ester solvent is γ-butyrolactone, said at least one additional aprotic organic solvent is dimethyl carbonate.

8. A stack of ultracapacitor cells, comprising at least one of the cells of claim 7.

9. A stack of ultracapacitor cells, comprising at least one of the cells of claim 2.

10. The ultracapacitor of claim 2, wherein a ratio by volume of the cyclic carbonate solvent to the cyclic ester solvent to the at least one additional aprotic organic solvent is between 2:2:1 and 1:1:2.

11. The ultracapacitor of claim 1, wherein said cyclic carbonate solvent comprises propylene carbonate.

12. A stack of ultracapacitor cells, comprising at least one of the cells of claim 11.

13. The ultracapacitor of claim 1, wherein said cyclic ester solvent comprises γ-butyrolactone.

14. A stack of ultracapacitor cells, comprising at least one of the cells of claim 13.

15. The ultracapacitor of claim 1, wherein said current collectors comprise an aluminum substrate.

16. A stack of ultracapacitor cells, comprising at least one of the cells of claim 15.

17. The ultracapacitor of claim 1, wherein said electrodes comprise carbon.

18. A stack of ultracapacitor cells, comprising at least one of the cells of claim 17.

19. The ultracapacitor of claim 1, wherein said separator is polypropylene or cellulosic tissue material.

20. A stack of ultracapacitor cells, comprising at least one of the cells of claim 19.

21. The ultracapacitor of claim 1, comprising a plurality of electrodes separating said current collectors.

22. A stack of ultracapacitor cells, comprising at least one of the cells of claim 21.

23. A stack of ultracapacitor cells, comprising at least one of the cells of claim 1.

24. The ultracapacitor of claim 1, wherein a ratio by volume of the cyclic carbonate solvent to the cyclic ester solvent is between 2:1 and 1:2.

25. An ultracapacitor comprising at least one cell, said cell comprising:two solid, nonporous current collectors, two porous electrodes separating said current collectors, a porous separator between said electrodes, an electrolyte occupying pores in said electrodes and a separator, wherein said electrolyte comprises propylene carbonate, γ-butyrolactone, dimethyl carbonate and tetraethylammonium tetraflouroborate salt.

26. A stack of ultracapacitor cells, comprising at least one of the cells of claim 25.

27. A method of making an ultracapacitor, comprising:(A) providing a multilayer cell comprising two solid, nonporous current collectors; two porous electrodes separating said current collectors; a porous separator between said electrodes and an electrolyte occupying pores in said electrodes and separator, and an electrolyte salt; and (B) sealing said cell to form said ultracapacitor, wherein said electrolyte comprises propylene carbonate, γ-butyrolactone, dimethyl carbonate and tetraethylammonium tetraflouroborate salt.

28. A method of making a stack of ultracapacitor cells, comprising:(A) providing in stacked relationship, a plurality of bipolar double layer ultracapacitor cells, at least one comprising porous, oppositely charged electrodes with ionically charged separator disposed between said electrodes; (B) providing a non-porous current collector between each cell with each current collector having adjoining polarized electrodes of different cells bonded thereto; (C) saturating said electrodes and separators with an electrolyte comprising a cyclic carbonate solvent and a cyclic ester solvent and a hexasubstituted guanidinium; and (D) sealing said cells, current collectors and separators to form said stack of ultracapacitor cells.

29. The method of claim 28, wherein said electrolyte comprises at least one additional aprotic organic solvent.

30. The method of claim 29, wherein said at least one additional aprotic organic solvent comprises a chain carbonate.

31. The method of claim 29, wherein said at least one additional aprotic organic solvent comprises dimethyl carbonate.

32. The method of claim 29, wherein said electrolyte comprises propylene carbonate, γ-butyrolactone, and dimethyl carbonate.

33. The method of claim 29, wherein said electrolyte comprises propylene carbonate, γ-butyrolactone, and dimethyl carbonate.

34. The method of claim 28, wherein said cyclic carbonate solvent comprises propylene carbonate.

35. The method of claim 28, wherein said cyclic ester solvent comprises γ-butyrolactone.

36. A method of making an ultracapacitor, comprising:(A) providing a multilayer cell comprising two solid, nonporous current collectors; two porous electrodes separating said current collectors; a porous separator between said electrodes and an electrolyte occupying pores in said electrodes and separator, wherein said electrolyte comprises a cyclic carbonate solvent and a cyclic ester solvent and a hexasubstituted guanidinium salt; and (B) sealing said cell to form said ultracapacitor.

37. The method of claim 36, wherein said electrolyte comprises (iii) at least one additional aprotic organic solvent.

38. The method of claim 37, wherein said at least one additional aprotic organic solvent comprises a chain carbonate.

39. The method of claim 37, wherein said at least one additional aprotic organic solvent comprises dimethyl carbonate.

40. The method of claim 37, wherein a ratio by volume of the cyclic carbonate solvent to the cyclic ester solvent to the at least one additional aprotic organic solvent is between 2:2:1 and 1:1:2.

41. The method of claim 36, wherein said cyclic carbonate solvent comprises propylene carbonate.

42. The method of claim 36, wherein said cyclic ester solvent comprises γ-butyrolactone.

43. The method of claim 36, wherein a ratio by volume of the cyclic carbonate solvent to the cyclic ester solvent is between 2:1 and 1:2.