1. Field of the Invention
The present invention relates generally to an electrochemical cell. More particularly, the present invention relates to an electrochemical cell having a stack holder that keeps the electrodes in proper electrochemical alignment with each other, even as their dimensions change during cell discharge.
2. Description of Related Art
A typical electrochemical cell that is used to power implantable medical devices is comprised of a casing housing an anode and a cathode. The anode and cathode are separated from each other, typically by enclosing at least one of them within an envelope or bag of insulative separator material. The separator material is typically provided as a thin porous sheet material that is saturated with electrolyte and allows the transport of ions in the electrolyte there through. The anode and cathode are generally formed as one or more respective plates of anode and cathode active material. The plates are then aligned face-to-face with each other to form an electrode assembly or electrode stack within the cell casing. In order to maximize discharge efficiency and stabilize the location of the electrodes within the casing, it is preferable that the electrode assembly be tightly fitted within the walls of the casing while occupying as much internal volume as possible.
During cell discharge, the thicknesses of the plates of cathode active material and anode active material change. The thicknesses of the cathode plates increase while those of the anode decrease. In some cells, the total thickness of the electrode assembly decreases continuously throughout discharge. This occurs because the rate of cathode thickness increase due to lithium intercalation is smaller than the rate of lithium consumption at the anode. As the overall electrode assembly thickness decreases, the electrodes may become loosely held or confined within the casing. There may eventually be sufficient space inside the casing for the electrode assembly to move around within it. This condition is disadvantageous. As the electrodes move, they may no longer be directly opposite each other in their original face-to-face orientation. Misalignment may result in an increase in cell resistance between the cathode and anode, thereby causing lower pulse voltages, faster cell polarization, cell voltage fluctuations, and in general, more delivered capacity variation.
What is needed is an electrochemical cell comprising an electrode assembly having an anode and a cathode that are tightly held together in their original face-to-face alignment throughout the entire discharge life of the cell.
The present invention meets this need by providing an electrochemical cell comprising a conductive casing housing an electrode assembly. The casing comprises a side wall structure extending to an open end closed by a lid. The electrode assembly comprises a cathode of at least a first plate of cathode active material, an anode of at least a first plate of anode active material, and a separator disposed at an intermediate location between the plates of cathode active material and anode active material. The cell further includes a stack holder surrounding the electrode assembly. The stack holder may be formed as a bag that envelopes the electrode assembly. Alternatively, the stack holder may be formed as a band disposed around a perimeter of the electrode assembly. In embodiments in which both plates of the anode and cathode active materials are enclosed by separators, the stack holder may be formed by joining the separators along their respective perimeters that contact each other.
The stack holder is preferably made of an elastic material. In that manner, as the volume of the electrode assembly varies during cell discharge, the volume encircled within or surrounded by the stack holder varies a like amount. In particular, as the circumference of the electrode assembly decreases, the circumference encircled or surrounded within the stack holder also decreases, thus maintaining the desired face-to-face alignment between the anode and cathode plates.
Either or both of the anode and cathode may be comprised of a plurality of plates of their respective electrode active materials. The cell may be provided in either a case-positive or case-negative configuration. Each of the respective plates of electrode active material may be enveloped in its own separator, with the entire electrode assembly then being encircled by the stack holder. In that respect, the stack holder is a component or part that is separate or in addition to that portion of the separator material disposed at an intermediate location between the opposite polarity electrodes.
The foregoing and additional objects, advantages, and characterizing features of the present invention will become increasingly more apparent upon a reading of the following detailed description together with the included drawings.
The present invention will be described by reference to the following drawings, in which like numerals refer to like elements, and in which:
The present invention will be described in connection with preferred embodiments, however, it will be understood that there is no intent to limit the invention to the embodiments described. On the contrary, the intent is to cover all alternatives, modifications, and equivalents as may be included within the spirit and scope of the invention as defined by the appended claims.
Turning first to
The electrode assembly or electrode stack 20 comprises a cathode 22 and an anode 24 housed within the casing 12. The cathode 22 is comprised of opposed plates 26 of cathode active material sandwiching a cathode current collector 34. Suitable cathode active materials include fluorinated carbon, silver vanadium oxide, copper silver vanadium oxide, Ag2O, Ag2O2, CuF2, Ag2CrO4, MnO2, V2O5, MnO2, TiS2, Cu2S, FeS, FeS2, copper oxide, copper vanadium oxide, and mixtures thereof. Suitable cathode current collector materials are selected from the group consisting of stainless steel, titanium, tantalum, platinum, gold, aluminum, cobalt nickel alloys, nickel-containing alloys, highly alloyed ferritic stainless steel containing molybdenum and chromium, and nickel-, chromium- and molybdenum-containing alloys.
The anode 24 is comprised of a plate 28 of anode active material contacting one side of an anode current collector 30. The other, bare side of the anode current collector 30 resides adjacent to the casing major face wall 14. That's because only anode material directly facing the cathode participates in cell discharge. For a primary cell, lithium and its alloys and intermetallic compounds, for example, Li—Si, Li—Al, Li—B and Li—Si—B alloys, are preferred for the anode active material. For a secondary cell, the anode is of a carbonaceous material, for example graphite, that is capable of intercalating and de-intercalating lithium ions. Preferably, the anode is a thin metal sheet or foil of lithium metal or graphite, pressed or rolled on a metallic anode current collector selected from titanium, titanium alloy, nickel, copper, tungsten or tantalum. The anode current collector 30 includes a grounding tab 32 that is joined to the major face wall 14 of the casing 12.
Referring to
Seal 40 is preferably a glass-to-metal seal comprised of a ferrule 44 joined to the lid 42, and a bead 46 of fused glass bonded within the annulus between the ferrule 44 and the terminal pin 38. The ferrule 44 can be made of titanium although molybdenum, aluminum, nickel alloy and stainless steel are also suitable. The glass is of a corrosion resistant type having up to about 50% by weight silicon such as CABAL 12, TA 23, FUSITE 425 or FUSITE 435. Although the cell 10 shown in
Cell 10 is further comprised of a first separator enveloping at least one of the cathode 22 and the anode 24. In the case-negative cell design shown in
The separators 48, 50 are of an electrically insulative material that is chemically unreactive with the anode and cathode active materials and both chemically unreactive with and insoluble in the electrolyte. In addition, the separator material has a degree of porosity sufficient to allow flow there through of the electrolyte during the electrochemical reaction of the cell. Illustrative separator materials include fabrics woven from fluoropolymeric fibers including polyvinylidine fluoride, polyethylenetetrafluoroethylene, and polyethylenechlorotrifluoroethylene used either alone or laminated with a fluoropolymeric microporous film, non-woven glass, polypropylene, polyethylene, glass fiber materials, ceramics, polytetrafluoroethylene membrane commercially available under the designation ZITEX (Chemplast Inc.), polypropylene membrane commercially available under the designation CELGARD (Celanese Plastic Company, Inc.) and a membrane commercially available under the designation DEXIGLAS (C. H. Dexter, Div., Dexter Corp.).
The cell 10 is thereafter filled with the electrolyte solution and hermetically sealed such as by close-welding a stainless steel ball over the second opening in the lid 42 serving as a fill-hole. The electrolyte serves as a medium for migration of ions between the anode 24 and the cathode 22 during the electrochemical reactions of the cell. For both a primary and a secondary cell chemistry, electrochemical reaction at the electrodes involves conversion of ions in atomic or molecular forms which migrate from the anode 24 to the cathode 22. A suitable electrolyte has an inorganic, ionically conductive salt dissolved in a nonaqueous solvent, and more preferably, the electrolyte includes an ionizable lithium salt dissolved in a mixture of aprotic organic solvents comprising a low viscosity solvent and a high permittivity solvent. The inorganic, ionically conductive salt serves as the vehicle for migration of the anode ions to intercalate or react with the cathode active materials. Suitable lithium salts include LiPF6, LiBF4, LiAsF6, LiSbF6, LiClO4, LiO2, LiAlCl4, LiGaCl4, LiC(SO2CF3)3, LiN(SO2CF3)2, LiSCN, LiO3SCF3, LiC6F5SO3, LiO2CCF3, LiSO6F, LiB(C6H5)4, LiCF3SO3, and mixtures thereof.
Low viscosity solvents useful with the present invention include esters, linear and cyclic ethers and dialkyl carbonates such as tetrahydrofuran (THF), methyl acetate (MA), diglyme, trigylme, tetragylme, dimethyl carbonate (DMC), 1,2-dimethoxyethane (DME), 1,2-diethoxyethane (DEE), 1-ethoxy, 2-methoxyethane (EME), ethyl methyl carbonate (EMC), methyl propyl carbonate, ethyl propyl carbonate, diethyl carbonate (DEC), dipropyl carbonate, and mixtures thereof, and high permittivity solvents include cyclic carbonates, cyclic esters and cyclic amides such as propylene carbonate (PC), ethylene carbonate (EC), butylene carbonate, acetonitrile, dimethyl sulfoxide, dimethyl formamide, dimethyl acetamide, γ-valerolactone, γ-butyrolactone (GBL), N-methyl-pyrrolidinone (NMP), and mixtures thereof.
In order to maintain the electrode plates 26 and 28 in proper electrochemical face-to-face alignment with each other during cell discharge, a stack holder 52 according to the present invention surrounds the electrode assembly 20. Referring to FIG. 1, in one embodiment the stack holder 52 is formed as a bag that encloses or envelopes the electrode assembly 20 to maintain proper face-to-face electrochemical alignment between the anode and cathode plates. The stack holder 52 covers the outwardly facing side walls of the electrode assembly as well as the opposed ends adjacent to the casing bottom wall 18 and the lid 42.
Referring next to
In that respect,
It will also be apparent to those skilled in the art that while three stack holders are shown in
The stack holders 52, 54, 54A and 54B may be made of the same materials used for the separators 48 and 50. In one preferred embodiment, the holder material is an elastic material capable of accommodating an initial expansion of the cathode that may occur at the early stage of cell discharge, and subsequent shrinkage of the electrode stack 20 during later stages of cell discharge. The term elastic is defined as a material that is capable of quickly recovering its original size and shape after a deformation force is removed.
Suitable materials that are also useful for the stack holders 52, 54, 54A and 54B are the same materials that are used for separators 48, 50 and include fabrics woven from fluoropolymeric fibers including polyvinylidine fluoride, polyethylenetetrafluoroethylene, and polyethylenechlorotrifluoroethylene used either alone or laminated with a fluoropolymeric microporous film, non-woven glass, polypropylene, polyethylene, glass fiber materials, ceramics, polytetrafluoroethylene membrane commercially available under the designation ZITEX (Chemplast Inc.), polypropylene membrane commercially available under the designation CELGARD (Celanese Plastic Company, Inc.) and a membrane commercially available under the designation DEXIGLAS (C. H. Dexter, Div., Dexter Corp.). These materials can be provided in a bi-layer or tri-layer construction. An example is a tri-layer polymeric material of polypropylene/polyethylene/polyethylene (PP/PE/PE).
In fabrication, the stack holder material may be wrapped around the electrode assembly and held under tension in a fixture to provide constrictive forces against the electrode plates 26 and 28. The stack holder material may be heat sealed in a manner similar to that used to fabricate individual electrode plate separators 48 and 50.
As long as they are elastic, the stack holders may also be made from non-porous materials that are not typically used to construct cell separators. Examples are polyimide tape and polypropylene tape. The difference between these tapes and the previously mentioned separator materials is that the former are non-porous and contain adhesives. As used herein, the term “porous” refers to a material that has sufficient permeability to permit an acceptable degree of ion flow there through to support electrochemical discharge. On the other hand, a non-porous material may have some permeability, but not to a degree sufficient to permit ion flow to sustain an electrochemical discharge.
In other embodiments, either or both of the anode and cathode may be comprised of a plurality of plates of their respective electrode active materials. Each of the respective plates of electrode active material may be enveloped in its own separator, with the entire electrode assembly being further encircled by an elastic stack holder. One exemplary cell comprised of multiple electrode plates is shown in
It is noted that the exemplary cells 10, 11 and 13 of respective
In one preferred embodiment, separators 48 and 50 are joined to each other by a heat seal 60. For the sake of clarity of illustration, heat seal 60 is depicted as being relatively thick compared to respective electrode plates 26 and 28. It is to be understood that the respective separators 48 and 50 for electrodes 26 and 28 are in closer contact with each other than is shown in
It is, therefore, apparent that an electrochemical cell is provided with a stack holder that surrounds the electrode assembly or stack thereof. The stack holder maintains the desired face-to-face electrical alignment between the opposite polarity electrode plates as the cell is discharged. While this invention has been described in conjunction with preferred embodiments thereof, it is evident that many alternatives, modifications, and variations will be apparent to those skilled in the art. Accordingly, the present invention is intended to embrace all such alternatives, modifications and variations that fall within the broad scope of the appended claims.
This application claims priority from U.S. Provisional Application Ser. No. 60/974,496, filed Sep. 24, 2007.
Number | Date | Country | |
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60974496 | Sep 2007 | US |