Abstract:
A new sandwich cathode design is provided comprising a cathode active material provided in at least two different thicknesses. The different thickness cathode structures are then individually pressed on opposite sides of a current collector so that both are in direct contact with the substrate. Preferably, the cathode structure on the side facing the anode is of a lesser thickness than that on the opposite side of the current collector. Such an exemplary cathode design might look like: SVO(x)/current collector/SVO(y)/current collector/SVO(z), wherein x, y and z represent thicknesses and wherein x and z are lesser than y.
Abstract:
A single phase silver vanadium oxide prepared from a mixture of a decomposable silver salt and vanadium oxide first heated at about 2° C. to about 40° C. above the decomposition temperature of the mixture followed by a second heating in a temperature range of about 490° C. to about 520° C. is described. The silver vanadium oxide material is coupled with a lithium anode and activated with a nonaquecus electrolyte to provide an improved high energy density electrochemical cell having increased pulse voltages and a reduction in voltage delay.
Abstract:
A secondary electrochemical cell comprising a medium rate electrode region intended to be discharged under a substantially constant drain and a high rate electrode region intended to be pulse discharged, is described. Both electrode regions share a common anode and are activated with the same electrolyte.
Abstract:
An electrochemical cell of either a primary or a secondary chemistry, is described. In either case, the cell has a negative electrode of lithium or of an anode material which is capable of intercalating and de-intercalating lithium coupled with a positive electrode of a cathode active material. A phosphonate compound is mixed with either the anode material or the cathode active material prior to contact with its current collector. The resulting electrode couple is activated by a non-aqueous electrolyte. The electrolyte flows into and throughout the electrodes causing the phosphonate additive to dissolve in the electrolyte. The phosphonate solute is then able to contact the lithium to provide an electrically insulating and ionically conducting passivation layer thereon.
Abstract:
An alkali metal, solid cathode, non-aqueous electrochemical cell capable of delivering high current pulses, rapidly recovering its open circuit voltage and having high current capacity, is described. The stated benefits are realized by the addition of at least one organic sulfate additive to an electrolyte comprising an alkali metal salt dissolved in a mixture of a low viscosity solvent and a high permittivity solvent. A preferred solvent mixture includes propylene carbonate, 1,2-dimethoxyethane and a sulfate additive having at least one unsaturated hydrocarbon containing a C(sp or sp2)-C(sp3) bond unit having the C(sp3) carbon directly connected to the —OSO3— functional group.
Abstract:
An alkali metal, solid cathode, nonaqueous electrochemical cell capable of delivering high current pulses, rapidly recovering its open circuit voltage and having high current capacity, is described. The stated benefits are realized by the addition of at least one organic sulfite additive to an electrolyte comprising an alkali metal salt dissolved in a mixture of a low viscosity solvent and a high permittivity solvent. A preferred solvent mixture includes propylene carbonate, dimethoxyethane and a sulfite additive having at least one unsaturated hydrocarbon containing a C(sp2 or sp3)—C(sp3) bond unit having the C(sp3) carbon directly connected to the —OSO2— functional group.
Abstract:
Cobalt-based alloys are provided for use as a positive electrode current collector in a solid cathode, nonaqueous liquid electrolyte, alkali metal anode active electrochemical cell. The cobalt-based alloys are characterized by chemical compatibility with aggressive cell environments, high corrosion resistance and resistance to fluorination and passivation at elevated temperatures, thus improving the longevity and performance of the electrochemical cell. The cell can be of either a primary or a secondary configuration.
Abstract:
A lithium ion electrochemical cell having high charge/discharge capacity, long cycle life and exhibiting a reduced first cycle irreversible capacity, is described. The stated benefits are realized by the addition of at least one phosphate additive to an electrolyte comprising an alkali metal salt dissolved in a solvent mixture that includes ethylene carbonate, dimethyl carbonate, ethylmethyl carbonate and diethyl carbonate. The preferred additive is an alkyl phosphate compound.
Abstract:
An autoclavable elctrochemical cell which may be used in an implantable medical device. The anode active material is lithium or other material from groups IA and IIA of the Periodic Table and having a melting point greater than about 150 degrees C. The cathode active material is silver vanadium oxide or other metal oxide or carbon monoflouride. The solvent for the electrolyte has a boiling point greater than about 100 degrees C. and a dielectric constant greater than about 5 so that the cell may be dimensionally and chemically stable during repeated exposures of about one hour each to the autoclaving temperatures.
Abstract:
A solid cathode liquid organic electrolyte alkali metal high rate cell wherein a combination of an elongated alkali metal anode and elongated solid cathode with separator therebetween is wound to form an anode-cathode subassembly having a jellyroll type configuration and wherein the combination is shaped so that the resulting sub-assembly has a substantially rectangular cross-section, the shaping of the combination being done either simultaneously with or subsequent to the winding thereof. The anode-cathode sub-assembly is placed in a conductive cell casing of prismatic shape having opposed flat faces, a lead of either the anode or cathode is attached to the cell casing depending upon whether case positive or case negative electrical configuration is desired and a lead of the other of the anode or cathode is connected to an electrical connector means extending through the casing in an insulated manner. Liquid electrolyte is introduced to the anode-cathode sub-assembly in the casing whereupon the casing then is sealed closed. The foregoing provides a new and improved prismatic high rate battery which significantly reduces the time required to manufacture the cell stack assembly while maintaining the requisite performance, safety and reliability standards in operation.