US20100136426A1 - Resistance-stabilizing additives for electrolyte - Google Patents
Resistance-stabilizing additives for electrolyte Download PDFInfo
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- US20100136426A1 US20100136426A1 US12/683,514 US68351410A US2010136426A1 US 20100136426 A1 US20100136426 A1 US 20100136426A1 US 68351410 A US68351410 A US 68351410A US 2010136426 A1 US2010136426 A1 US 2010136426A1
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/05—Accumulators with non-aqueous electrolyte
- H01M10/056—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes
- H01M10/0564—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes the electrolyte being constituted of organic materials only
- H01M10/0566—Liquid materials
- H01M10/0567—Liquid materials characterised by the additives
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- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/10—Energy storage using batteries
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- the present invention generally relates to an electrochemical cell and, more particularly, to an additive in an electrolyte for a battery.
- IMDs Implantable medical devices detect and treat a variety of medical conditions in patients.
- IMDs include implantable pulse generators (IPGs) or implantable cardioverter-defibrillators (ICDs) that deliver electrical stimuli to tissue of a patient.
- ICDs typically comprise, inter alia, a control module, a capacitor, and a battery that are housed in a hermetically sealed container.
- the control module signals the battery to charge the capacitor, which in turn discharges electrical stimuli to tissue of a patient.
- the battery includes a case, a liner, and an electrode assembly.
- the liner surrounds the electrode assembly to prevent the electrode assembly from contacting the inside of the case.
- the electrode assembly comprises an anode and a cathode with a separator therebetween.
- In the case wall or cover is a fill port or tube that allows introduction of electrolyte into the case.
- the electrolyte is a medium that facilitates ionic transport and forms a conductive pathway between the anode and cathode.
- An electrochemical reaction between the electrodes and the electrolyte causes charge to be stored on each electrode.
- the electrochemical reaction also creates a solid electrolyte interphase (SEI) or passivation film on a surface of an anode such as a lithium anode.
- SEI solid electrolyte interphase
- passivation film is ionically conductive and prevents parasitic loss of lithium.
- the passivation film increases internal resistance which reduces the power capability of the battery. It is
- FIG. 1 is a cutaway perspective view of an implantable medical device (IMD);
- IMD implantable medical device
- FIG. 2 is a cutaway perspective view of a battery in the IMD of FIG. 1 ;
- FIG. 3 is an enlarged view of a portion of the battery depicted in FIG. 2 and designated by line 4 .
- FIG. 4 is a cross-sectional view of an anode and a passivation film
- FIG. 5 is graph that compares discharge and resistance for a conventional and exemplary additive in an electrolyte
- FIG. 6 is graph that compares resistance over time for exemplary additives to an electrolyte
- FIG. 7 is a flow diagram for forming an electrolyte for a battery.
- FIG. 8 is a flow diagram for autoclaving a battery.
- the present invention is directed to an additive for an electrolyte.
- the additive stabilizes resistance of the battery during storage, thermal processing, and throughout discharge.
- a resistance-stabilizing additive is defined as one or more chemical compounds, added to an electrolyte, that causes a battery to exhibit low resistance (i.e. generally below 500 ohm centimeter (cm) 2 ) throughout the battery's useful life.
- the additive is characterized by an electron withdrawing group.
- Exemplary chemical compounds containing electron withdrawing group include 2,2,2-trifluoroacetamide, and benzoyl acetone.
- an organic acid serves as a resistance-stabilizing additive.
- Exemplary organic acids include benzoic acids, carboxylic acids, malic acid, tetramethylammonium (TMA) hydrogen phthalate and hexafluoroglutaric acid.
- a battery that includes an exemplary additive may be autoclaved at 125° C. for a half an hour, defined as one cycle, performed three times without adversely affecting the battery.
- the additives may be used in low, medium, or high capacity batteries.
- FIG. 1 depicts an implantable medical device (IMD) 10 .
- IMD 10 includes a case 50 , a control module 52 , a battery 54 (e.g. organic electrolyte battery) and capacitor(s) 56 .
- Control module 52 controls one or more sensing and/or stimulation processes from IMD 10 via leads (not shown).
- Battery 54 includes an insulator 58 disposed therearound. Battery 54 charges capacitor(s) 56 and powers control module 52 .
- FIGS. 2 and 3 depict details of an exemplary organic electrolyte battery 54 .
- Battery 54 includes a case 70 , an anode 72 , separators 74 , a cathode 76 , a liquid electrolyte 78 , and a feed-through terminal 80 .
- Cathode 76 is wound in a plurality of turns, with anode 72 interposed between the turns of the cathode winding.
- Separator 74 insulates anode 72 from cathode 76 windings.
- Case 70 contains the liquid electrolyte 78 to create a conductive path between anode 72 and cathode 76 .
- Electrolyte 78 which includes an additive, serves as a medium for migration of ions between anode 72 and cathode 76 during an electrochemical reaction with these electrodes.
- Anode 72 is formed of a material selected from Group IA, IIA or IIIB of the periodic table of elements (e.g. lithium, sodium, potassium, etc.), alloys thereof or intermetallic compounds (e.g. Li—Si, Li—B, Li—Si—B etc.).
- Anode 72 comprises an alkali metal (e.g. lithium, etc.) in metallic or ionic form.
- Cathode 76 may comprise metal oxides (e.g. vanadium oxide, silver vanadium oxide (SVO), manganese dioxide (MnO 2 ) etc.), carbon monofluoride and hybrids thereof (e.g., CF x +MnO 2 ), combination silver vanadium oxide (CSVO) or other suitable compounds.
- metal oxides e.g. vanadium oxide, silver vanadium oxide (SVO), manganese dioxide (MnO 2 ) etc.
- carbon monofluoride and hybrids thereof e.g., CF x +MnO 2
- Electrolyte 78 chemically reacts with anode 72 to form an ionically conductive passivation film 82 on anode 72 , as shown in FIG. 4 .
- Electrolyte 78 includes a base liquid electrolyte composition and at least one resistance-stabilizing additive selected from Table 1 presented below.
- the base electrolyte composition typically comprises 1.0 molar (M) lithium tetrafluoroborate (1-20% by weight), gamma-butyrolactone (50-70% by weight), and 1,2-dimethoxyethane (30-50% by weight).
- resistance-stabilizing additives are directed to chemical compounds that include electron withdrawing groups.
- An exemplary chemical compound with an electron withdrawing group includes 2,2,2-trifluoroacetamide.
- the additive is a proton donor such as an organic acid.
- organic acid is benzoic acid (e.g. 3-hydroxy benzoic acid or 2-4 hydroxy benzoic acid etc.). Every combination of benzoic acid and hydroxyl benzoic acids that exists may be used as a resistance-stabilizing additive composition.
- Malic acid and tetramethylammonium hydrogen phthalate are other organic acids that may serve as a resistance-stabilizing additive.
- Tables 1 and 2 list some exemplary resistance-stabilizing additives. In particular, Table 1 ranks each additive as to its effectiveness with a rank of 1 being the highest or best additive and rank 6 being the lowest ranked additive. Table 1 also briefly describes the time period in which battery 54 , which included the specified additive in the electrolyte 78 , exhibited resistance-stabilizing characteristics.
- the listed additives may be added to the base electrolyte composition in the range of about 0.001M to 0.5M.
- an additive composition comprises a first additive that exhibits substantially superior resistance-stabilizing characteristics at the BOL whereas a second additive exhibits substantially superior resistance-stabilizing characteristics at the EOL.
- a first resistance-stabilizing additive exhibits a substantially superior resistance-stabilizing characteristics at the BOL whereas a second resistance-stabilizing additive exhibits average resistance-stabilizing characteristics at the EOL.
- a first resistance-stabilizing additive exhibits substantially superior resistance-stabilizing characteristics at the EOL whereas a second resistance-stabilizing additive exhibits average resistance-stabilizing characteristics at the BOL.
- each additive is combined with the electrolyte 78 through dissolution or other suitable means.
- FIGS. 5-6 graphically depict the resistance-stabilizing superiority of electrolyte 78 over a control electrolyte 88 .
- Electrolyte 78 includes 2,2,2-trifluoroacetamide as the resistance-stabilizing additive and the base electrolyte composition previously described.
- Control electrolyte 88 is the base electrolyte composition without any additive.
- Passivation layer 82 initially possesses similar discharge to passivation layer formed by control electrolyte 88 . However, later in the discharge (e.g. about 0.90 ampere ⁇ hour(Ah)), the passivation layer formed by control electrolyte 88 exhibits resistance that substantially increases.
- electrolyte 78 that includes the additive causes battery 54 to exhibit resistance that remains substantially below the resistance of control electrolyte 88 late in discharge.
- electrolyte 78 results in battery 54 having 30 ohms lower resistance than control electrolyte 88 , as show in FIG. 5 .
- a recommended replacement time (RRT) signal may be generated.
- desirable resistance is kept low as long as possible to increase efficiency of battery 54 .
- FIG. 7 depicts a method for forming a resistance-stabilizing additive composition.
- a first resistance stabilizing additive is selected.
- the first resistance stabilizing additive is combined with a second resistance stabilizing additive to create a resistance stabilizing composition.
- FIG. 8 depicts a method for autoclaving battery cell 54 .
- Battery cell 54 is inserted into a chamber of an autoclave at operation 300 .
- Battery cell 54 includes an electrolyte and a first resistance-stabilizing additive combined with the electrolyte.
- heat is applied to the chamber of the autoclave.
- the autoclaving process occurs at a temperature of 125° C. for a half an hour per cycle.
- the autoclave cycle is repeated at least three times. After three cycles of autoclaving, battery cell 54 adequately operates.
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Abstract
A resistance-stabilizing additive to an electrolyte for a battery cell in an implantable medical device is presented. At least one resistance-stabilizing additive is selected from a group comprising an electron withdrawing group, an aromatic diacid salt, an inorganic salt, an aliphatic organic acid, an aromatic diacid, and an aromatic monoacid.
Description
- This application is related to, and claims the benefit of, U.S. patent application Ser. No. 10/876,003 filed Feb. 13, 2003 entitled “Liquid Electrolyte For An Electrochemical Cell, Electrochemical Cell And Implantable Medical Device”, which is incorporated herein by reference in its entirety.
- The present invention generally relates to an electrochemical cell and, more particularly, to an additive in an electrolyte for a battery.
- Implantable medical devices (IMDs) detect and treat a variety of medical conditions in patients. IMDs include implantable pulse generators (IPGs) or implantable cardioverter-defibrillators (ICDs) that deliver electrical stimuli to tissue of a patient. ICDs typically comprise, inter alia, a control module, a capacitor, and a battery that are housed in a hermetically sealed container. When therapy is required by a patient, the control module signals the battery to charge the capacitor, which in turn discharges electrical stimuli to tissue of a patient.
- The battery includes a case, a liner, and an electrode assembly. The liner surrounds the electrode assembly to prevent the electrode assembly from contacting the inside of the case. The electrode assembly comprises an anode and a cathode with a separator therebetween. In the case wall or cover is a fill port or tube that allows introduction of electrolyte into the case. The electrolyte is a medium that facilitates ionic transport and forms a conductive pathway between the anode and cathode. An electrochemical reaction between the electrodes and the electrolyte causes charge to be stored on each electrode. The electrochemical reaction also creates a solid electrolyte interphase (SEI) or passivation film on a surface of an anode such as a lithium anode. The passivation film is ionically conductive and prevents parasitic loss of lithium. However, the passivation film increases internal resistance which reduces the power capability of the battery. It is desirable to reduce internal resistance associated with the passivation film for a battery.
- The present invention will become more fully understood from the detailed description and the accompanying drawings, wherein:
-
FIG. 1 is a cutaway perspective view of an implantable medical device (IMD); -
FIG. 2 is a cutaway perspective view of a battery in the IMD ofFIG. 1 ; -
FIG. 3 is an enlarged view of a portion of the battery depicted inFIG. 2 and designated byline 4. -
FIG. 4 is a cross-sectional view of an anode and a passivation film; -
FIG. 5 is graph that compares discharge and resistance for a conventional and exemplary additive in an electrolyte; -
FIG. 6 is graph that compares resistance over time for exemplary additives to an electrolyte; -
FIG. 7 is a flow diagram for forming an electrolyte for a battery; and -
FIG. 8 is a flow diagram for autoclaving a battery. - The following description of embodiments is merely exemplary in nature and is in no way intended to limit the invention, its application, or uses. For purposes of clarity, the same reference numbers are used in the drawings to identify similar elements.
- The present invention is directed to an additive for an electrolyte. The additive stabilizes resistance of the battery during storage, thermal processing, and throughout discharge. A resistance-stabilizing additive is defined as one or more chemical compounds, added to an electrolyte, that causes a battery to exhibit low resistance (i.e. generally below 500 ohm centimeter (cm)2) throughout the battery's useful life. In one embodiment, the additive is characterized by an electron withdrawing group. Exemplary chemical compounds containing electron withdrawing group include 2,2,2-trifluoroacetamide, and benzoyl acetone. In another embodiment, an organic acid serves as a resistance-stabilizing additive. Exemplary organic acids include benzoic acids, carboxylic acids, malic acid, tetramethylammonium (TMA) hydrogen phthalate and hexafluoroglutaric acid.
- A battery that includes an exemplary additive may be autoclaved at 125° C. for a half an hour, defined as one cycle, performed three times without adversely affecting the battery. The additives may be used in low, medium, or high capacity batteries.
-
FIG. 1 depicts an implantable medical device (IMD) 10. IMD 10 includes acase 50, acontrol module 52, a battery 54 (e.g. organic electrolyte battery) and capacitor(s) 56.Control module 52 controls one or more sensing and/or stimulation processes fromIMD 10 via leads (not shown).Battery 54 includes aninsulator 58 disposed therearound.Battery 54 charges capacitor(s) 56 andpowers control module 52. -
FIGS. 2 and 3 depict details of an exemplaryorganic electrolyte battery 54.Battery 54 includes acase 70, ananode 72,separators 74, acathode 76, aliquid electrolyte 78, and a feed-through terminal 80.Cathode 76 is wound in a plurality of turns, withanode 72 interposed between the turns of the cathode winding.Separator 74insulates anode 72 fromcathode 76 windings.Case 70 contains theliquid electrolyte 78 to create a conductive path betweenanode 72 andcathode 76.Electrolyte 78, which includes an additive, serves as a medium for migration of ions betweenanode 72 andcathode 76 during an electrochemical reaction with these electrodes. -
Anode 72 is formed of a material selected from Group IA, IIA or IIIB of the periodic table of elements (e.g. lithium, sodium, potassium, etc.), alloys thereof or intermetallic compounds (e.g. Li—Si, Li—B, Li—Si—B etc.).Anode 72 comprises an alkali metal (e.g. lithium, etc.) in metallic or ionic form. -
Cathode 76 may comprise metal oxides (e.g. vanadium oxide, silver vanadium oxide (SVO), manganese dioxide (MnO2) etc.), carbon monofluoride and hybrids thereof (e.g., CFx+MnO2), combination silver vanadium oxide (CSVO) or other suitable compounds. -
Electrolyte 78 chemically reacts withanode 72 to form an ionicallyconductive passivation film 82 onanode 72, as shown inFIG. 4 .Electrolyte 78 includes a base liquid electrolyte composition and at least one resistance-stabilizing additive selected from Table 1 presented below. The base electrolyte composition typically comprises 1.0 molar (M) lithium tetrafluoroborate (1-20% by weight), gamma-butyrolactone (50-70% by weight), and 1,2-dimethoxyethane (30-50% by weight). In one embodiment, resistance-stabilizing additives are directed to chemical compounds that include electron withdrawing groups. An exemplary chemical compound with an electron withdrawing group includes 2,2,2-trifluoroacetamide. In another embodiment, the additive is a proton donor such as an organic acid. One type of organic acid is benzoic acid (e.g. 3-hydroxy benzoic acid or 2-4 hydroxy benzoic acid etc.). Every combination of benzoic acid and hydroxyl benzoic acids that exists may be used as a resistance-stabilizing additive composition. Malic acid and tetramethylammonium hydrogen phthalate are other organic acids that may serve as a resistance-stabilizing additive. - Tables 1 and 2 list some exemplary resistance-stabilizing additives. In particular, Table 1 ranks each additive as to its effectiveness with a rank of 1 being the highest or best additive and rank 6 being the lowest ranked additive. Table 1 also briefly describes the time period in which
battery 54, which included the specified additive in theelectrolyte 78, exhibited resistance-stabilizing characteristics. -
TABLE 1 List of exemplary additive resistance-stabilizing additives Chemical Exemplary additive Rank class compound Chemical Structure Notes 3 Aromatic diacid salts Tetramethyl- ammonium (TMA) hydrogen phthalate Battery exhibited excellent resistance- stabilizing characteristic during storage Battery exhibited good to neutral resistance- stabilizing characteristic during discharge 6 Inorganic acid salts Tetrabutyl- ammonium (TBA) hydrogen sulfate Battery exhibited good resistance- stabilizing characteristic during storage Battery exhibited neutral resistance- stabilizing characteristic during discharge 5 Aliphatic organic acids Phosphonoacetic acid Battery exhibited excellent resistance- stabilizing characteristic during storage Battery exhibited good to neutral resistance- stabilizing characteristic during discharge 1 (*) 2,2,2- Trifluoroacetamide Battery exhibited excellent resistance- stabilizing characteristic during storage and discharge (*) Trifluoromethyl vinyl acetate Battery exhibited very good resistance- stabilizing characteristic during discharge 4 Aromatic diacids Phthalic acid Battery exhibited good resistance- stabilizing characteristic during storage and discharge (*) Benzoylacetone Battery exhibited good resistance- stabilizing characteristic during storage and discharge (*) Benzoyltrifluoro- acetone Battery exhibited good resistance- stabilizing characteristic during storage and discharge 2 Aromatic mono- acids Benzoic acid Battery exhibited excellent resistance- stabilizing characteristic during storage and discharge
(*) These compounds include a chemical structure that is characterized by one or more electron-withdrawing groups (e.g. —CF3, —C6H5 located one or two carbon atoms from a double-bonded oxygen atom (i.e. a ketone group)). Additionally, the listed additives may be added to the base electrolyte composition in the range of about 0.001M to 0.5M. - Table 2 lists exemplary additive compositions that are mixed with the base electrolyte composition to produce effective resistance-stabilization in
battery 54. Effective additive compositions are based upon additives that exhibit superior resistance-stabilizing characteristics either at the beginning of life (BOL) or at the end of life (EOL) ofbattery 54. In one embodiment, an additive composition comprises a first additive that exhibits substantially superior resistance-stabilizing characteristics at the BOL whereas a second additive exhibits substantially superior resistance-stabilizing characteristics at the EOL. In another embodiment, a first resistance-stabilizing additive exhibits a substantially superior resistance-stabilizing characteristics at the BOL whereas a second resistance-stabilizing additive exhibits average resistance-stabilizing characteristics at the EOL. In still yet another embodiment, a first resistance-stabilizing additive exhibits substantially superior resistance-stabilizing characteristics at the EOL whereas a second resistance-stabilizing additive exhibits average resistance-stabilizing characteristics at the BOL. Generally, each additive is combined with theelectrolyte 78 through dissolution or other suitable means. -
TABLE 2 Exemplary resistance-stabilizing composition additives Additive compositions Quantity of each additive TMA hydrogen phthalate + About 0.001 M to about 0.5M 2,2,2-Trifluoroacetamide TMA hydrogen phthalate + About 0.001 M to about 0.5M Trifluoromethyl vinyl acetate TMA hydrogen phthalate + About 0.001 M to about 0.5M Acetone TMA hydrogen phthalate + About 0.001 M to about 0.05M Xylitol Phosphonoacetic acid + About 0.001 M to about 0.5M 2,2,2-Trifluoroacetamide Phosphonoacetic acid + About 0.001 M to about 0.5M Trifluoromethyl vinyl acetate Phosphonoacetic acid + About 0.001 M to about 0.5M Acetone Phosphonoacetic acid + About 0.001 M to about 0.5M Xylitol -
FIGS. 5-6 graphically depict the resistance-stabilizing superiority ofelectrolyte 78 over acontrol electrolyte 88.Electrolyte 78 includes 2,2,2-trifluoroacetamide as the resistance-stabilizing additive and the base electrolyte composition previously described.Control electrolyte 88 is the base electrolyte composition without any additive.Passivation layer 82 initially possesses similar discharge to passivation layer formed bycontrol electrolyte 88. However, later in the discharge (e.g. about 0.90 ampere·hour(Ah)), the passivation layer formed bycontrol electrolyte 88 exhibits resistance that substantially increases. In contrast,electrolyte 78 that includes the additive causesbattery 54 to exhibit resistance that remains substantially below the resistance ofcontrol electrolyte 88 late in discharge. For example,electrolyte 78 results inbattery 54 having 30 ohms lower resistance thancontrol electrolyte 88, as show inFIG. 5 . - If the resistance increases in the area between 1 and 1.2 Ah of the curve and
IMD 10 records the voltage after a high current event (e.g. telemetry event etc.), a recommended replacement time (RRT) signal may be generated. Preferably, desirable resistance is kept low as long as possible to increase efficiency ofbattery 54. -
FIG. 7 depicts a method for forming a resistance-stabilizing additive composition. Atoperation 200, a first resistance stabilizing additive is selected. Atoperation 210, the first resistance stabilizing additive is combined with a second resistance stabilizing additive to create a resistance stabilizing composition. -
FIG. 8 depicts a method for autoclavingbattery cell 54.Battery cell 54 is inserted into a chamber of an autoclave atoperation 300.Battery cell 54 includes an electrolyte and a first resistance-stabilizing additive combined with the electrolyte. Atblock 310, heat is applied to the chamber of the autoclave. Generally, the autoclaving process occurs at a temperature of 125° C. for a half an hour per cycle. The autoclave cycle is repeated at least three times. After three cycles of autoclaving,battery cell 54 adequately operates. - The following patent application is incorporated by reference in its entirety. Co-pending U.S. patent application Ser. No. XXXXXXXX, entitled “ELECTROLYTE ADDITIVE FOR PERFORMANCE STABILITY OF BATTERIES”, filed by Kevin Chen, Donald Merritt and Craig Schmidt and assigned to the same Assignee of the present invention, describes resistance-stabilizing additives for electrolyte.
- Although various embodiments of the invention have been described and illustrated with reference to specific embodiments thereof, it is not intended that the invention be limited to such illustrative embodiments. For example, while an additive composition is described as a combination of two additives, it may also include two or more additives selected from Table 1. The description of the invention is merely exemplary in nature and, thus, variations that do not depart from the gist of the invention are intended to be within the scope of the invention. Such variations are not to be regarded as a departure from the spirit and scope of the invention.
Claims (40)
1. A resistance-stabilizing additive for an electrolyte of a battery cell in an implantable medical device (IMD) comprising:
at least one chemical compound selected from a chemical class consisting of an electron withdrawing group, an aromatic diacid salt, an inorganic salt, an aliphatic organic acid, an aromatic diacid, and an aromatic monoacid.
2. The additive of claim 1 wherein the electron-withdrawing group selected from one of trifluoromethylvinyl acetate and 2,2,2-trifluoroacetamide.
3. The additive of claim 1 , wherein aromatic monoacid comprises benzoic acid.
4. The additive of claim 1 , wherein the benzoic acid includes fluorinated benzoic acid.
5. The additive of claim 1 , wherein the benzoic acid being one of 3-hydroxy benzoic acid and 2-4 hydroxy benzoic acid.
6. The additive of claim 1 , wherein the organic acid selected from a group comprising carboxylic acid, benzoic acid, and hexafluoroglutaric acid.
7. An additive to an electrolyte for use in a battery cell in an IMD, the additive comprising:
an electron-withdrawing group.
8. The additive of claim 6 wherein the electron-withdrawing group selected from one of trifluoromethylvinyl acetate and 2,2,2-trifluoroacetamide.
9. An additive to an electrolyte for use in a battery cell in an IMD, the additive being at least one of tetramethyl ammonium (TMA) hydrogen phthalate, tetrabutyl-ammonium (TBA) hydrogen sulfate, phosphonoacetic acid, 2,2,2-trifluoroacetamide, trifluoromethyl vinyl acetate, phthalic acid, benzoylacetone, benzoltrifluoroactone, and benzoic acid.
10. An additive composition for an electrolyte in a battery cell for an IMD comprising:
a first resistance-stabilizing additive; and
a second resistance-stabilizing additive combined with the first resistance-stabilizing additive.
11. The additive composition of claim 10 , the first resistance-stabilizing additive being at least one of TMA hydrogen phthalate, TBA hydrogen sulfate, phosphonoacetic acid, 2,2,2-trifluoroacetamide, trifluoromethyl vinyl acetate, phthalic acid, benzoylacetone, benzoltrifluoroactone, and benzoic acid.
12. The additive composition of claim 10 , the second resistance-stabilizing additive being at least one of TMA hydrogen phthalate, TBA hydrogen sulfate, phosphonoacetic acid, 2,2,2-trifluoroacetamide, trifluoromethyl vinyl acetate, phthalic acid, benzoylacetone, benzoltrifluoroactone, and benzoic acid.
13. The additive composition of claim 10 , further comprising:
a third resistance-stabilizing additive, the third resistance-stabilizing additive being at least one of TMA hydrogen phthalate, TBA hydrogen sulfate, phosphonoacetic acid, 2,2,2-trifluoroacetamide, trifluoromethyl vinyl acetate, phthalic acid, benzoylacetone, benzoltrifluoroactone, and benzoic acid.
14. A method for forming an additive composition for an electrolyte in a battery cell for an IMD, the method comprising:
selecting a first resistance-stabilizing additive; and
combining a second resistance-stabilizing additive with the first resistance-stabilizing additive to form a resistance-stabilizing composition.
15. The method of claim 14 , further comprising:
combining the resistance-stabilizing composition with a base electrolyte composition for the battery cell.
16. The method of claim 14 , the first resistance-stabilizing additive being at least one of TMA hydrogen phthalate, TBA hydrogen sulfate, phosphonoacetic acid, 2,2,2-trifluoroacetamide, trifluoromethyl vinyl acetate, phthalic acid, benzoylacetone, benzoltrifluoroactone, and benzoic acid.
17. The method of claim 14 , the second resistance-stabilizing additive being at least one of TMA hydrogen phthalate, TBA hydrogen sulfate, phosphonoacetic acid, 2,2,2-trifluoroacetamide, trifluoromethyl vinyl acetate, phthalic acid, benzoylacetone, benzoltrifluoroactone, and benzoic acid.
18. An electrolyte comprising a base liquid electrolyte composition and a resistance-stabilizing additive distinct from the base liquid electrolyte composition, wherein the resistance-stabilizing additive comprises at least one chemical compound selected from a chemical class consisting of a compound comprising an electron withdrawing group, an aromatic diacid salt, an inorganic salt, an aliphatic organic acid, an aromatic diacid, and an aromatic monoacid.
19. The electrolyte of claim 18 , wherein the resistance-stabilizing additive comprises a compound comprising an electron-withdrawing group that is selected from one of trifluoromethylvinyl acetate and 2,2,2-trifluoroacetamide.
20. The electrolyte of claim 18 , wherein the resistance-stabilizing additive comprises an aromatic monoacid that comprises a benzoic acid.
21. The electrolyte of claim 20 , wherein the benzoic acid includes fluorinated benzoic acid.
22. The electrolyte of claim 20 , wherein the benzoic acid is selected from one of 3-hydroxy benzoic acid and 2-4 hydroxy benzoic acid.
23. The electrolyte of claim 18 , wherein the resistance-stabilizing additive comprises an organic acid that is selected from a group comprising carboxylic acid, benzoic acid, and hexafluoroglutaric acid.
24. An electrolyte comprising a base liquid electrolyte composition and a resistance-stabilizing additive distinct from the base liquid electrolyte composition, wherein the resistance-stabilizing additive comprises a compound having an electron-withdrawing group.
25. The electrolyte of claim 24 , wherein the compound having an electron-withdrawing group comprises 2,2,2-trifluoroacetamide.
26. An electrolyte comprising a base liquid electrolyte composition and a resistance-stabilizing additive distinct from the base liquid electrolyte composition, wherein the resistance-stabilizing additive comprises at least one of tetramethyl ammonium (TMA) hydrogen phthalate, tetrabutyl-ammonium (TBA) hydrogen sulfate, phosphonoacetic acid, 2,2,2-trifluoroacetamide, trifluoromethyl vinyl acetate, phthalic acid, benzoylacetone, benzoyltrifluoroacetone, and benzoic acid.
27. An electrolyte comprising:
a base liquid electrolyte composition;
a first resistance-stabilizing additive; and
a second resistance-stabilizing additive combined with the first resistance-stabilizing additive;
wherein the first and second resistance-stabilizing additives are distinct from the base liquid electrolyte composition.
28. The electrolyte of claim 27 , the first resistance-stabilizing additive being at least one of TMA hydrogen phthalate, TBA hydrogen sulfate, phosphonoacetic acid, 2,2,2-trifluoroacetamide, trifluoromethyl vinyl acetate, phthalic acid, benzoylacetone, benzoyltrifluoroacetone, and benzoic acid.
29. The electrolyte of claim 27 , the second resistance-stabilizing additive being at least one of TMA hydrogen phthalate, TBA hydrogen sulfate, phosphonoacetic acid, 2,2,2-trifluoroacetamide, trifluoromethyl vinyl acetate, phthalic acid, benzoylacetone, benzoyltrifluoroacetone, and benzoic acid.
30. The electrolyte of claim 27 , further comprising:
a third resistance-stabilizing additive, the third resistance-stabilizing additive being at least one of TMA hydrogen phthalate, TBA hydrogen sulfate, phosphonoacetic acid, 2,2,2-trifluoroacetamide, trifluoromethyl vinyl acetate, phthalic acid, benzoylacetone, benzoyltrifluoroacetone, and benzoic acid.
31. A method for forming an electrolyte in a battery cell for an implantable medical device, the method comprising:
selecting a first resistance-stabilizing additive;
combining a second resistance-stabilizing additive with the first resistance-stabilizing additive to form a resistance-stabilizing composition; and
combining the resistance-stabilizing composition with a base electrolyte composition for the battery cell.
32. The method of claim 31 , the first resistance-stabilizing additive being at least one of TMA hydrogen phthalate, TBA hydrogen sulfate, phosphonoacetic acid, 2,2,2-trifluoroacetamide, trifluoromethyl vinyl acetate, phthalic acid, benzoylacetone, benzoyltrifluoroacetone, and benzoic acid.
33. The method of claim 31 , the second resistance-stabilizing additive being at least one of TMA hydrogen phthalate, TBA hydrogen sulfate, phosphonoacetic acid, 2,2,2-trifluoroacetamide, trifluoromethyl vinyl acetate, phthalic acid, benzoylacetone, benzoyltrifluoroacetone, and benzoic acid.
34. A battery comprising an electrode assembly and an electrolyte, wherein the electrolyte comprises a liquid electrolyte and a resistance-stabilizing additive distinct from the liquid electrolyte, wherein the resistance-stabilizing additive comprises at least one chemical compound selected from a compound comprising an electron withdrawing group, an aromatic diacid salt, an inorganic salt, an aliphatic organic acid, an aromatic diacid, an aromatic monoacid, and combinations thereof.
35. The battery of claim 34 , wherein the resistance-stabilizing additive comprises compound comprising an electron-withdrawing group.
36. An implantable medical device comprising the battery of claim 34 .
37. A battery comprising an electrode assembly and an electrolyte, wherein the electrolyte comprises a liquid electrolyte and a resistance-stabilizing additive distinct from the liquid electrolyte, the additive being at least one of TMA hydrogen phthalate, TBA hydrogen sulfate, phosphonoacetic acid, 2,2,2-trifluoroacetamide, trifluoromethyl vinyl acetate, phthalic acid, benzoylacetone, benzoyltrifluoroacetone, and benzoic acid.
38. An implantable medical device comprising the battery of claim 37 .
39. A battery comprising an electrode assembly and an electrolyte, wherein the electrolyte comprises a liquid electrolyte and a resistance-stabilizing additive composition distinct from the liquid electrolyte, the additive composition comprising:
a first resistance-stabilizing additive; and
a second resistance-stabilizing additive combined with the first resistance-stabilizing additive.
40. An implantable medical device comprising the battery of claim 39 .
Priority Applications (1)
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US12/683,514 US20100136426A1 (en) | 2006-01-31 | 2010-01-07 | Resistance-stabilizing additives for electrolyte |
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US11/344,376 US7807300B2 (en) | 2006-01-31 | 2006-01-31 | Resistance-stabilizing additives for electrolyte |
US12/683,514 US20100136426A1 (en) | 2006-01-31 | 2010-01-07 | Resistance-stabilizing additives for electrolyte |
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US11/344,376 Continuation US7807300B2 (en) | 2001-05-30 | 2006-01-31 | Resistance-stabilizing additives for electrolyte |
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US11/344,376 Expired - Fee Related US7807300B2 (en) | 2001-05-30 | 2006-01-31 | Resistance-stabilizing additives for electrolyte |
US12/683,514 Abandoned US20100136426A1 (en) | 2006-01-31 | 2010-01-07 | Resistance-stabilizing additives for electrolyte |
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US7807300B2 (en) | 2010-10-05 |
US20070178378A1 (en) | 2007-08-02 |
WO2007089978A3 (en) | 2007-10-04 |
EP1992039A2 (en) | 2008-11-19 |
WO2007089978A2 (en) | 2007-08-09 |
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