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1. WO2007089970 - AUTOCLAVE IMPLANTABLE BATTERY

Note: Text based on automatic Optical Character Recognition processes. Please use the PDF version for legal matters

[ EN ]

AUTOCLAVE IMPLANTABLE BATTERY

FIELD OF THE INVENTION

The present invention generally relates to an electroclienncal cell and, more particularly, to an additive in an electrolyte for a battery.

BACKGROUND OF THE INVENTION

implantable medical devices (IMDs) detect and treat a variety of medical conditions in patients. IMDs include implantable puise generators (IPGs) or implantable cardioverter-defibrillators (ICDs) that deliver electrical stimuli to tissue of a patient. IGDs typically comprise, inter alia, a control module, a capacitor, ami 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 discbarges 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 ύ\m on a surface of an anode such as a lithium aaode. The passivation film is ionicaiiy 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.

BRIEF DESCRIPTION OF THE DRAWINGS

The present invention will, become more fully understood .from the detailed description and the accompanying drawings, wherein:

Figure 1 is a cutaway perspective view of an implantable medical device (IMD); Figure 2 is a cutaway perspective view of a battery in the IMD of Figure 1;

Figure 3 is an enlarged view of a portion of the battery depicted in Figure 2 and designated by line 4.

Figure 4 is a cross-sectional view of an anode and a passivation film;

Figure 5 is graph that compares discharge and resistance for a conventional and exemplary additive in an electrolyte;

Figure 6 is graph that compares resistance over time for exemplary additives to an electrolyte;

Figure 7 is a flow diagram for forming an electrolyte for a battery; and

Figure 8 is a flow diagram for autøclavmg a battery.

DETAILED DESCRIPTION

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 identity 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 characterised by an electron withdrawing group. Exemplary chemical compounds containing electron withdrawing group include 2,2,2,-trifiuoroacetarmde, arid benzoyl acetone. In another embodiment, an organic acid serves as a resistance-stabilizing additive. Exemplary organic ackfs include benzoic acids, carboxyiic acids, malic acid, tetramethylammoiuum (TMA)) hydrogen phthalate and hexaϊluoroglutaric acid.

A battery that includes an exemplary additive may be autoclaved at 125 ºC for a half an hoar, defined as one cycle, performed three times without adversely affecting the battery. The additives may be used in low, medium, or high capacity batteries.

Figure 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.

Figures 2 and 3 depict details of an exemplary organic electrolyte batten 54.

Battery 54 includes a case 70, an anode 72, separators 74, a cathode 76, a liquid electrolyte 7% 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 intermetaille 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 (MnGa) etc.), carbon monofluoride and hybrids thereof (e.g., CFx+MnO2), combination silver vanadium oxide (CSVO) or other suitable compounds.

Electrolyte 78 chemically reacts with anode 72 to form an ioaicaily conductive passivation film 82 on anode 72, as shown in Figure 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 tetrafiuoroborate (1-20% by weight), gamma-butyroiactone (50-70% by weight), and 1,2-dϊmethoxyethane (30-50% by weight). In one embodiment, resistance-stabilizing additives are directed to chemical compounds that include electron

withdrawing groups. An exemplary dierøica! 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. Maisc acid and tetcsmethyI ammonium hydrogen phthaiate 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.

(*)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-beaded 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) of battery 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 the electrolyte 78 through dissolution or other suitable means.


Figures 5-6 graphically depict the resistance -stsbilizing superiority of electrolyte 78 over a control electrolyte 88. Electrolyte 78 includes 2,2,2-trifluoroacetamicb as the resistance-stabilising 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. In contrast 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. For example, electrolyte 78 results in battery 54 having 30 ohms lower resistance than control electrolyte 88, as show in Figure 5.

If the resistance increases in the area between 1 and 1.2 Ah of the curve and IMD 1.0 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 of battery 54.

Figure 7 depicts a method for forming a resistance-stabilizing additive

composition. At operation 200, a first resistance stabilizing additive is selected. At operation 210, the first resistance stabilizing additive is combined with a seeoad resistance stabilizing additive to create a resistance stabilizing composition.

Figure 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. At block 310, beat is applied to the chamber of the autoclave. Generally, the autociaving process occurs at a temperature of 125ºC for a half an hour per cycle. The autoclave cycle is repeated at least three times. After three cycles of autoclaving, battery cell 54 adequ ately 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 STABILlTY 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 thai 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 natwre 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.