WO1991011033A1 - Electrochemical cathode and materials therefor - Google Patents

Electrochemical cathode and materials therefor Download PDF

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Publication number
WO1991011033A1
WO1991011033A1 PCT/US1991/000158 US9100158W WO9111033A1 WO 1991011033 A1 WO1991011033 A1 WO 1991011033A1 US 9100158 W US9100158 W US 9100158W WO 9111033 A1 WO9111033 A1 WO 9111033A1
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WO
WIPO (PCT)
Prior art keywords
forming
electrochemical cathode
silver
cathode
electrochemical
Prior art date
Application number
PCT/US1991/000158
Other languages
French (fr)
Inventor
Bhaskara M. L. Rao
Original Assignee
Alupower, Inc.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Alupower, Inc. filed Critical Alupower, Inc.
Priority to JP91504365A priority Critical patent/JPH05505492A/en
Publication of WO1991011033A1 publication Critical patent/WO1991011033A1/en

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Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/86Inert electrodes with catalytic activity, e.g. for fuel cells
    • H01M4/88Processes of manufacture
    • H01M4/8803Supports for the deposition of the catalytic active composition
    • H01M4/8807Gas diffusion layers
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/86Inert electrodes with catalytic activity, e.g. for fuel cells
    • H01M4/88Processes of manufacture
    • H01M4/8825Methods for deposition of the catalytic active composition
    • H01M4/8842Coating using a catalyst salt precursor in solution followed by evaporation and reduction of the precursor
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/86Inert electrodes with catalytic activity, e.g. for fuel cells
    • H01M4/88Processes of manufacture
    • H01M4/8878Treatment steps after deposition of the catalytic active composition or after shaping of the electrode being free-standing body
    • H01M4/8882Heat treatment, e.g. drying, baking
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/86Inert electrodes with catalytic activity, e.g. for fuel cells
    • H01M4/88Processes of manufacture
    • H01M4/8878Treatment steps after deposition of the catalytic active composition or after shaping of the electrode being free-standing body
    • H01M4/8896Pressing, rolling, calendering
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/86Inert electrodes with catalytic activity, e.g. for fuel cells
    • H01M4/96Carbon-based electrodes
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/86Inert electrodes with catalytic activity, e.g. for fuel cells
    • H01M2004/8678Inert electrodes with catalytic activity, e.g. for fuel cells characterised by the polarity
    • H01M2004/8689Positive electrodes
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/30Hydrogen technology
    • Y02E60/50Fuel cells

Definitions

  • This invention relates to a process for manufacturing
  • Metal/air batteries produce electricity by electrochemically coupling in a cell a reactive metallic anode to an air cathode through a suitable electrolyte.
  • an air cathode is a typically sheetlike member having opposite surfaces respectively exposed to the atmosphere and to an aqueous
  • the air cathode must be permeable to air but substantially hydrophobic ⁇ 2& (so that aqueous electrolyte will not seep or leak through it)/ and must incorporate an electrically conductive element for external circuitry.
  • the air cathode is commonly constituted of active carbon (with or without an added
  • dissociation-promoting catalyst containing a finely divided - " hydrophobic polymeric material and incorporating a metal screen as the conductive element.
  • anode metals are used including iron/ zinc/ magnesium/ aluminum/ alloys of aluminum/ etc. Alloys of aluminum and magnesium are considered especially advantageous for particular applications owing to low cost , light weight and ability to function as anodes in metal/air batteries using neutral electrolytes/ such as sea water or other aqueous saline solutions.
  • Metal/air batteries have an essentially infinite shelf-storage life rendering them very suitable for standby or emergency uses in that the metal-air battery may be activated by addition of electrolyte.
  • an air cathode comprised of a sheetlike laminate including first and second layers having opposed major surfaces/ respectively/ exposed for contact with a liquid electrolyte and with air/ and having facing major surfaces.
  • the second layer is permeable to air but not to a liquid electrolyte.
  • a current-collecting layer is in contact with the first layer and is connected to external electrical circuitry.
  • the first layer of the cathode is comprised of a nonwoven fibrous web/ preferably of conductive carbon fibers/ impregnated with a mixture of carbon particles and a nonfibrous polymeric substance for holding the carbon particles in the web.
  • the facing major surfaces of the first and second layers are bonded together by heat seal coating material distributed on facing major surfaces in manner to provide an array or network of areas free of coating material extending substantially uniformly thereover with the coating material being distributed as a multiplicity of spaced-apart dots, or as a mesh having coating-material-free interstices. Coating-free spaces maintains sufficient unclogged pores in the second layer to enable the air cathode to function as intended/ yet with effective lamination of , 5 the layers to each other and/or to the current-collecting means/ such as a layer of metal mesh interposed between and coextensive with the first and second layer.
  • An object of the present invention is to provide an improved cathode for electrochemical cells.
  • Another object of the present invention is to provide an 25 improved electrochemical cathode for electrochemical cells providing improved electrochemical characteristics.
  • a further object of the present invention is to provide an improved electrochemical cathode for electrochemical cells exhibiting improved retention of the catalyst in systems using alkaline electrolytes.
  • Still another object of the present invention is to provide a novel process for producing an improved cathode for electrochemical cells-
  • Yet another object of the present invention is to provide a novel process for producing an improved cathode for electrochemical cells exhibiting improved electrochemical characteristics/ such as improved corrosion resistance.
  • an electrochemical cathode for an electrochemical cell comprised of a current collecting layer or substrate laminated between layers of a nonwoven conductive fibrous web, preferably of conductive carbon fibers, impregnated with a mixture of silver-containing carbon particles and a nonfibrous polymeric substance/ and optionally with a hydrophobic microporous film or layer disposed on one of the layers of the nonwoven conductive fibrous web as well as the product produced thereby.
  • FIGURE 1 is a schematic elevational sectional view of an electrochemical metal/air battery incorporating an electrochemical cathode of one embodiment of the present invention
  • FIGURE 2 is a schematic exploded view of the embodiment of an electrochemical cathode of Figure 1;
  • FIGURE 3 is a schematic exploded view of another embodiment of an electrochemical cathode/ such as for a lithium battery/ of the present invention
  • FIGURE 4 is a graph illustrating improved performance achieved by the use of silver-containing carbon particles in a air cathode.
  • a metal/air battery/ generally indicated as 10 comprised of a housing 12 defining a chamber 14 for receiving a liquid electrolyte 16,' such as an aqueous solution of sodium chloride; an air cathode, generally indicated as 18, and a metal anode 20.
  • the anode 20 is connected by line 22 to a light bulb 24 connected by line 26 including a switch 28 to the air cathode 18.
  • the housing 12 defines a large vertical aperture 30 for receiving the air cathode 18 in liquid-tight fashion with the periphery of the air cathode 18 sealed to the periphery of the aperture 30 of the housing 12.
  • the air cathode 18 is a laminate structure comprised of a metal mesh substrate 32, reactive layers 34 laminated to the mesh substrate 32 and a hydrophobic microporous layer 36 mounted to the outer reactive layer 34.
  • the metal mesh 32 is the current collector of the metal/air battery 10, and is formed of a suitable metallic material, such as nickel, stainless steel and the like/ formed for example by expanded metal techniques and includes an upwardly extending tab portion 38 for connection to line 26.
  • the anode 20/ may be formed of a suitable anodic material/ such as aluminum/ magnesium or the like/ and is illustrated as being disposed in a top 40 of the housing 12 in the form of a plate member extending vertically into the chamber 14 including the electrolyte 16.
  • the anode 20 is longitudinally disposed with reference to the housing 12 and is spaced apart in parallelled relationship to the air cathode 18 a distance sufficient to form a gap therebetween for the electrolyte 16.
  • the general arrangement of the metal/air battery 10 may be substantially the same as that of one of the cells of the plural-cell battery/ such as described in U.S. Patent No. 4/626/482 hereby incorporated by reference.
  • FIG 3/ there is illustrated an electrochemical cathode/ generally indicated as 42/ constituting another embodiment of the present invention and a laminate structure comprised of the metal mesh substrate 32 laminated between an inner reactive layer 34 and an outer reactive layer 34 without any hydrophobic microporous layer mounted to an outer reactive layer 34.
  • the reactive layer 34 is comprised of a conductive nonwoven fibrous web impregnated with a mixture of silver-containing carbon particles and a nonfibrous polymeric substance for holding the carbon particles in the web.
  • Other substances e.g. catalyst may also be included in the impregnating mixture.
  • the nonwoven fibrous web of the present invention is preferably formed of electrically conductive carbon fibers having a length of from about 1.25 to 3.20 cm. and a diameter of from about 5.0 to 15.0 u.
  • the carbon content of such carbon fibers is preferably at least about 90 weight percent exhibiting a resistance of less than about 20 ohms/sq. meters.
  • the conductive nonwoven fibrous web is formed into a thickness of from 0.125 to 0.5 mm. exhibiting a pore volume of at least about 90 percent/ to provide a high pick-up of the impregnation mixture whether in suspension or in a coating format.
  • the impregnation mixture should increase the basic weight of the conductive nonwoven fibrous web by about 20 to 120
  • the impregnation mixture/ in the form of a suspension or coating/ is comprised of silver-containing carbon particles/ generally in the form of silver-containing carbon black/ a nonfibrous adhesive polymeric material to bind the carbon particles to the web and a dispersion or mixing agents.
  • the carbon particles are preferably of small size/ expressed as surface area (m. /g.)/ generally in excess of 1000/ and preferably greater than about 1250, such as Black Pearls 2000, available from Cabot Corporation having a mean particle diameter of 0.015 u.
  • An aqueous slurry of the carbon particles is admixed with a solution of water soluble silver salt, such as silver nitrate preferably in an amount to be quantitatively absorbed by the carbon particles.
  • the quantity of silver adsorbed by carbon is a formation of the structure of the carbon particles and generally is time dependent capable of being accelerated by heating the admixture. While the mechanism of silver adsorption is not completely understood, nor is the present invention to be limited thereby, it is believed that silver is fixed to the carbon by 1) ion exchange by carboxylic groups, 2) electrochemical reduction of silver ions by carbon. As readily appreciated, other mechanisms may occur to effect silver adsorption in the carbon particles. Silver adsorption may be quantitatively effected and determined by the formation of silver chloride precipitate (silver chloride) results once a maximum capacity of adsorption of silver is exceeded in the preparation of the silver-containing carbon slurry.
  • silver chloride precipitate silver chloride
  • the nonfibrous adhesive polymeric materials include the polytetrafluoroethylenes, such as Teflon® T-30, a registered trademark of duPont.
  • the dispersion or mixing agents include the sodium salt of polymeric naphthalene sulfonic acid and those included with the polytetrafluoroethyene (PTFE).
  • PTFE polytetrafluoroethyene
  • the nonfibrous adhesive polymeric material and dispersing and/or mixing agents are added subsequent to the slurry of silver containing carbon particles.
  • the conductive nonwoven web of carbon fibers is impregnated by immersion/ coating extrusion or the like/ with the aqueous suspension of the impregnation mixture of the silver containing-carbon particles, nonfibrous polymeric substance and/or other desired nonfibrous ingredients.
  • the impregnated conductive nonwoven fibrous web is dried at a temperature of from about 65 to 205°C, a temperature below the sintering temperature of the binder material, i.e. the PTFE/ and a temperature high enough to ensure substantially complete moisture removal.
  • the microporous or hydrophobic layer 36 is a film or web permeable to air but impermeable to the solvent of the electrolyte system to prevent or minimize penetration of the electrolyte through the air cathode to the exterior of the metal/air battery 10 with concomitant disappearance of active interface sites.
  • the hydrophobic layer 36 is laminated on the reactive layer 34 for intended use particularly in conjunction with liquid electrolytes. It has been found that a film of polymeric hydrophobic material/ such as films of polytetrafluoroethylene of a thickness of from 2 to 10 mils embossed with mesh of a netted configuration of 0.85 to 3.175mm. diameter provides particularly desirable hydrophobic properties while concomitantly providing for effective diffusion of a gaseous fuel.
  • Embossing of the polymeric hydrophobic layer may be readily effected by passage through an embossing roller assembly maintained at a temperature of from 65 to 150°C-, generally at a temperature to compact the film at the contact points or areas of the embossing roll.
  • Wire mesh used to form the current collector layer has been found effective in embossing the polymeric hydrophobic layer.
  • the layers of the air cathode laminate 18 are bonded by a discontinuous heat seal coating applied to the reactive layers as a discontinuous dot matrix system or an interposed layer of meshed coating material to be subsequently heated and subjected to a pressure step during passage of the air cathode laminate through a pressure roller system (not shown). Bonding of a reactive layer to the metal mesh substrate is particularly effectively performed by passing the metal mesh substrate 38 through a liquid solution and then dried, or dispersion of a sealing material prior to lamination with a reactive layer 34.
  • the sealing material is a Teflon® dispersion in water.
  • the reactive layers 34 with seal coating either applied as a dot pattern on inner facing major surfaces surfaces or heat seal netting material (not shown) interposed are juxtaposed to the current collecting substrate 32 in a "sandwich" of layers/ and the sandwich subjected to bonding heat and pressure sufficient to activate the heat seal coating to bond the reactive layers 34 to the metal substrate 32.
  • the materials of the electrochemical cathode are selected such that activation temperatures of the heat-seal coating to bond the layers does not damage any layers or component substance/ generally a temperature less than 120°C
  • the hydrophyllic layer 36 may be simultaneously laminated to one of the reactive layers 34 as part of the laminate sandwich/ or in a separate but like bonding step. Once the layers are bonded/ the resulting laminate is cut to size to provide the individu electrochemical cathodes.
  • Increased silver adsorption is achieved by effecting the u of hydrogen peroxide, hydrazine, formaldehyde or like reduci agents or by the oxidizing of the carbon, such as with pero disulfate in the preparation of the carbon particle slurry pri to admixture with the silver containing solution.
  • a conductive nonwoven web of carbon fibers (Internation Paper Company), is introduced into a continuous web machine t effect coating and drying operations.
  • the impregnated mixtur (silver-containing carbon/Teflon®) is comprised of 45 gms. of aqueous dispersion of Black Pearls (carbon) 2000 (15% solids) i 300 grams of deionized water to which is added 158 gms. of silver nitrate. Thereafter, 180 gms. of 10% Daxad (sodium sal of polymerized naphthalure sulfuric acid) is added followed the addition of 36 gms. Teflon® T-30 (60% solids). Impregnatio is effected to provide an add-on of 75 GSM.

Abstract

There is disclosed a process for producing an electrochemical cathode (18) for an electrochemical cell (10) comprised of a current collecting layer or substrate (32) laminated to a layer of a nonwoven conductive fibrous web (34), preferably of conductive carbon fibers, impregnated with a mixture of silver-containing carbon particles and a nonfibrous polymeric substance, and optionally with a hydrophobic microporous film (36) or layer disposed on one of the layers of the nonwoven conductive fibrous web (34), as well as the product produced thereby.

Description

ELECTROCHEMICAL CATHODE AND MATERIALS THEREFOR
BACKGROUND OF THE INVENTION
(1) Field of the Invention
This invention relates to a process for manufacturing
5 electrodes and electrodes produced thereby/ and more particularly to a process for manufacturing electrochemical cathodes for use in electrochemical cells and electrochemical cathodes produced thereby.
(2) Description of the Prior Art
10 Metal/air batteries produce electricity by electrochemically coupling in a cell a reactive metallic anode to an air cathode through a suitable electrolyte. As is well known in the art/ an air cathode is a typically sheetlike member having opposite surfaces respectively exposed to the atmosphere and to an aqueous
15 electrolyte of the cell/ in which (during cell operation) atmospheric oxygen dissociates while metal of the anode oxidizes providing a usable electric current flow through external circuitry connected between the anode and cathode. The air cathode must be permeable to air but substantially hydrophobic ~2& (so that aqueous electrolyte will not seep or leak through it)/ and must incorporate an electrically conductive element for external circuitry.
In present-day commercial practice/ the air cathode is commonly constituted of active carbon (with or without an added
25 dissociation-promoting catalyst) containing a finely divided - " hydrophobic polymeric material and incorporating a metal screen as the conductive element. A variety of anode metals are used including iron/ zinc/ magnesium/ aluminum/ alloys of aluminum/ etc. Alloys of aluminum and magnesium are considered especially advantageous for particular applications owing to low cost , light weight and ability to function as anodes in metal/air batteries using neutral electrolytes/ such as sea water or other aqueous saline solutions. Metal/air batteries have an essentially infinite shelf-storage life rendering them very suitable for standby or emergency uses in that the metal-air battery may be activated by addition of electrolyte.
In copending application Serial No. 07/070/183/ there is disclosed an air cathode comprised of a sheetlike laminate including first and second layers having opposed major surfaces/ respectively/ exposed for contact with a liquid electrolyte and with air/ and having facing major surfaces. The second layer is permeable to air but not to a liquid electrolyte. A current-collecting layer is in contact with the first layer and is connected to external electrical circuitry. The first layer of the cathode is comprised of a nonwoven fibrous web/ preferably of conductive carbon fibers/ impregnated with a mixture of carbon particles and a nonfibrous polymeric substance for holding the carbon particles in the web.
The facing major surfaces of the first and second layers are bonded together by heat seal coating material distributed on facing major surfaces in manner to provide an array or network of areas free of coating material extending substantially uniformly thereover with the coating material being distributed as a multiplicity of spaced-apart dots, or as a mesh having coating-material-free interstices. Coating-free spaces maintains sufficient unclogged pores in the second layer to enable the air cathode to function as intended/ yet with effective lamination of , 5 the layers to each other and/or to the current-collecting means/ such as a layer of metal mesh interposed between and coextensive with the first and second layer.
In copending application Serial No. 07/287/482/ filed December 20/ 1988/ there is disclosed a process for forming an
10 improved air cathode and the resulting air cathode comprised of an electrochemical cell comprised of a current collecting layer or substrate laminated between layers of a nonwoven conductive fibrous web/ preferably of conductive carbon fibers/ impregnated with a mixture of carbon particles and a nonfibrous polymeric
15 substance, and optionally with a hydrophobic microporous film or layer disposed on one of the layers of the nonwoven conductive fibrous web as well as the product produced thereby.
While such an air cathode have been effective, there is a continuing desire to increase current densities at cost effective
20 processing, etc. of such air cathode.
Objects of the Invention
An object of the present invention is to provide an improved cathode for electrochemical cells.
Another object of the present invention is to provide an 25 improved electrochemical cathode for electrochemical cells providing improved electrochemical characteristics. A further object of the present invention is to provide an improved electrochemical cathode for electrochemical cells exhibiting improved retention of the catalyst in systems using alkaline electrolytes. Still another object of the present invention is to provide a novel process for producing an improved cathode for electrochemical cells-
Yet another object of the present invention is to provide a novel process for producing an improved cathode for electrochemical cells exhibiting improved electrochemical characteristics/ such as improved corrosion resistance.
SUMMARY OF THE INVENTION
These and other objects of the present invention are achieved by a process for producing an electrochemical cathode for an electrochemical cell comprised of a current collecting layer or substrate laminated between layers of a nonwoven conductive fibrous web, preferably of conductive carbon fibers, impregnated with a mixture of silver-containing carbon particles and a nonfibrous polymeric substance/ and optionally with a hydrophobic microporous film or layer disposed on one of the layers of the nonwoven conductive fibrous web as well as the product produced thereby.
Brief Description of the Drawings
Other features and advantages of the present invention will become more readily apparent from the following detailed description when taken with the accompanying drawings wherein; —
FIGURE 1 is a schematic elevational sectional view of an electrochemical metal/air battery incorporating an electrochemical cathode of one embodiment of the present invention; FIGURE 2 is a schematic exploded view of the embodiment of an electrochemical cathode of Figure 1;
FIGURE 3 is a schematic exploded view of another embodiment of an electrochemical cathode/ such as for a lithium battery/ of the present invention; and FIGURE 4 is a graph illustrating improved performance achieved by the use of silver-containing carbon particles in a air cathode.
Detailed Description of the Invention
Referring now to FIGURE 1/ there is illustrated a metal/air battery/ generally indicated as 10 comprised of a housing 12 defining a chamber 14 for receiving a liquid electrolyte 16,' such as an aqueous solution of sodium chloride; an air cathode, generally indicated as 18, and a metal anode 20. The anode 20 is connected by line 22 to a light bulb 24 connected by line 26 including a switch 28 to the air cathode 18. The housing 12 defines a large vertical aperture 30 for receiving the air cathode 18 in liquid-tight fashion with the periphery of the air cathode 18 sealed to the periphery of the aperture 30 of the housing 12. Closing of the switch 28 closes an electrical circuit formed between the air cathode 18 and the anode 20 via the electrolyte 16 thereby illuminating the light bulb 24. The air cathode 18 is a laminate structure comprised of a metal mesh substrate 32, reactive layers 34 laminated to the mesh substrate 32 and a hydrophobic microporous layer 36 mounted to the outer reactive layer 34. The metal mesh 32, is the current collector of the metal/air battery 10, and is formed of a suitable metallic material, such as nickel, stainless steel and the like/ formed for example by expanded metal techniques and includes an upwardly extending tab portion 38 for connection to line 26. The anode 20/ may be formed of a suitable anodic material/ such as aluminum/ magnesium or the like/ and is illustrated as being disposed in a top 40 of the housing 12 in the form of a plate member extending vertically into the chamber 14 including the electrolyte 16. The anode 20 is longitudinally disposed with reference to the housing 12 and is spaced apart in parallelled relationship to the air cathode 18 a distance sufficient to form a gap therebetween for the electrolyte 16. The general arrangement of the metal/air battery 10 may be substantially the same as that of one of the cells of the plural-cell battery/ such as described in U.S. Patent No. 4/626/482 hereby incorporated by reference.
In Figure 3/ there is illustrated an electrochemical cathode/ generally indicated as 42/ constituting another embodiment of the present invention and a laminate structure comprised of the metal mesh substrate 32 laminated between an inner reactive layer 34 and an outer reactive layer 34 without any hydrophobic microporous layer mounted to an outer reactive layer 34. Such embodiment of the present invention finds application in the lithium battery art. The reactive layer 34 is comprised of a conductive nonwoven fibrous web impregnated with a mixture of silver-containing carbon particles and a nonfibrous polymeric substance for holding the carbon particles in the web. Other substances e.g. catalyst, may also be included in the impregnating mixture. The nonwoven fibrous web of the present invention is preferably formed of electrically conductive carbon fibers having a length of from about 1.25 to 3.20 cm. and a diameter of from about 5.0 to 15.0 u. The carbon content of such carbon fibers is preferably at least about 90 weight percent exhibiting a resistance of less than about 20 ohms/sq. meters.
The conductive nonwoven fibrous web is formed into a thickness of from 0.125 to 0.5 mm. exhibiting a pore volume of at least about 90 percent/ to provide a high pick-up of the impregnation mixture whether in suspension or in a coating format. The impregnation mixture should increase the basic weight of the conductive nonwoven fibrous web by about 20 to 120
2 g./m as a function of solids content of the impregnation suspension or coating and pore volume of the conductive nonwoven fibrous web/ and provide a front-to-back (F/B) electrical conductivity of less than about 1 ohm.
The impregnation mixture/ in the form of a suspension or coating/ is comprised of silver-containing carbon particles/ generally in the form of silver-containing carbon black/ a nonfibrous adhesive polymeric material to bind the carbon particles to the web and a dispersion or mixing agents. The carbon particles are preferably of small size/ expressed as surface area (m. /g.)/ generally in excess of 1000/ and preferably greater than about 1250, such as Black Pearls 2000, available from Cabot Corporation having a mean particle diameter of 0.015 u.
An aqueous slurry of the carbon particles is admixed with a solution of water soluble silver salt, such as silver nitrate preferably in an amount to be quantitatively absorbed by the carbon particles. The quantity of silver adsorbed by carbon is a formation of the structure of the carbon particles and generally is time dependent capable of being accelerated by heating the admixture. While the mechanism of silver adsorption is not completely understood, nor is the present invention to be limited thereby, it is believed that silver is fixed to the carbon by 1) ion exchange by carboxylic groups, 2) electrochemical reduction of silver ions by carbon. As readily appreciated, other mechanisms may occur to effect silver adsorption in the carbon particles. Silver adsorption may be quantitatively effected and determined by the formation of silver chloride precipitate (silver chloride) results once a maximum capacity of adsorption of silver is exceeded in the preparation of the silver-containing carbon slurry.
The nonfibrous adhesive polymeric materials include the polytetrafluoroethylenes, such as Teflon® T-30, a registered trademark of duPont. The dispersion or mixing agents include the sodium salt of polymeric naphthalene sulfonic acid and those included with the polytetrafluoroethyene (PTFE). Generally, the nonfibrous adhesive polymeric material and dispersing and/or mixing agents are added subsequent to the slurry of silver containing carbon particles. The conductive nonwoven web of carbon fibers is impregnated by immersion/ coating extrusion or the like/ with the aqueous suspension of the impregnation mixture of the silver containing-carbon particles, nonfibrous polymeric substance and/or other desired nonfibrous ingredients.
The impregnated conductive nonwoven fibrous web is dried at a temperature of from about 65 to 205°C, a temperature below the sintering temperature of the binder material, i.e. the PTFE/ and a temperature high enough to ensure substantially complete moisture removal.
The microporous or hydrophobic layer 36 is a film or web permeable to air but impermeable to the solvent of the electrolyte system to prevent or minimize penetration of the electrolyte through the air cathode to the exterior of the metal/air battery 10 with concomitant disappearance of active interface sites. The hydrophobic layer 36 is laminated on the reactive layer 34 for intended use particularly in conjunction with liquid electrolytes. It has been found that a film of polymeric hydrophobic material/ such as films of polytetrafluoroethylene of a thickness of from 2 to 10 mils embossed with mesh of a netted configuration of 0.85 to 3.175mm. diameter provides particularly desirable hydrophobic properties while concomitantly providing for effective diffusion of a gaseous fuel. Embossing of the polymeric hydrophobic layer may be readily effected by passage through an embossing roller assembly maintained at a temperature of from 65 to 150°C-, generally at a temperature to compact the film at the contact points or areas of the embossing roll. Wire mesh used to form the current collector layer has been found effective in embossing the polymeric hydrophobic layer.
As disclosed in the aforementioned copending application, the layers of the air cathode laminate 18 are bonded by a discontinuous heat seal coating applied to the reactive layers as a discontinuous dot matrix system or an interposed layer of meshed coating material to be subsequently heated and subjected to a pressure step during passage of the air cathode laminate through a pressure roller system (not shown). Bonding of a reactive layer to the metal mesh substrate is particularly effectively performed by passing the metal mesh substrate 38 through a liquid solution and then dried, or dispersion of a sealing material prior to lamination with a reactive layer 34.
In this aspect of the present invention/ the sealing material is a Teflon® dispersion in water.
The reactive layers 34 with seal coating either applied as a dot pattern on inner facing major surfaces surfaces or heat seal netting material (not shown) interposed are juxtaposed to the current collecting substrate 32 in a "sandwich" of layers/ and the sandwich subjected to bonding heat and pressure sufficient to activate the heat seal coating to bond the reactive layers 34 to the metal substrate 32. The materials of the electrochemical cathode are selected such that activation temperatures of the heat-seal coating to bond the layers does not damage any layers or component substance/ generally a temperature less than 120°C The hydrophyllic layer 36 may be simultaneously laminated to one of the reactive layers 34 as part of the laminate sandwich/ or in a separate but like bonding step. Once the layers are bonded/ the resulting laminate is cut to size to provide the individu electrochemical cathodes.
Increased silver adsorption is achieved by effecting the u of hydrogen peroxide, hydrazine, formaldehyde or like reduci agents or by the oxidizing of the carbon, such as with pero disulfate in the preparation of the carbon particle slurry pri to admixture with the silver containing solution.
The process of the present invention is set forth in t following specific examples which are intended to be mere illustrative and the present invention is intended not to limited thereto.
EXAMPLE
A conductive nonwoven web of carbon fibers (Internation Paper Company), is introduced into a continuous web machine t effect coating and drying operations. The impregnated mixtur (silver-containing carbon/Teflon®) is comprised of 45 gms. of aqueous dispersion of Black Pearls (carbon) 2000 (15% solids) i 300 grams of deionized water to which is added 158 gms. of silver nitrate. Thereafter, 180 gms. of 10% Daxad (sodium sal of polymerized naphthalure sulfuric acid) is added followed the addition of 36 gms. Teflon® T-30 (60% solids). Impregnatio is effected to provide an add-on of 75 GSM. The resulti impregnated layers and fine nickel mesh (Delker) precoated wi an adhesive are passed through an oven maintained at temperature of from 90 to 150°C. and thence web and passe through laminating rolls at nip pressure of 690 kgs. per line cm. at a temperature of 120°C to form an electrochemic cathode suitable for use in an electrochemical battery. While the invention has been described in connection with an exemplary embodiment thereof, it will be understood that many modifications will be apparent to those of ordinary skill in the art; and that this application is intended to cover any adaptations of variations thereof. Therefore, it is manifestly intended that this invention be only limited by the claims and the equivalents thereof.

Claims

WHAT IS CLAIMED
1. A process for forming an electrochemical cathode, which comprises:
(a) admixing a slurry of carbon particles with a solution of silver salt to form a slurry of silver-containing carbon particles.
(b) impregnating a conductive nonwoven fibrous web with a dispersion comprised of silver-containing carbon particles and a nonfibrous polymeric material for holding said silver-containing carbon particles to said web; and (c) laminating a current collecting substrate to said impregnated web to form said electrochemical cathode.
2. The process for forming an electrochemical cathode as defined in Claim 1 wherein concentration of said silver salt in said solution is in an amount sufficient to form a silver precipitate after step (a).
3. The process for forming an electrochemical cathode as defined in Claim 1 wherein said slurry of silver-containing carbon particles includes a reducing agent.
4. The process for forming an electrochemical cathode as defined in Claim 1/ and further including the steps of forming and drying a sandwich of said current collecting substrate and said layers of said impregnated web prior to step c).
5. The process for forming an electrochemical cathode as defined in Claim 2 wherein drying is effected at a temperature of from 90 to 150°C.
6. The process for forming an electrochemical cathode as defined in Claim 1/ 2 or 3 wherein said current collecting substrate is coated with a polytetrafluoroethylene dispersion.
7. The process for forming an electrochemical cathode as defined in Claim 6 , wherein laminating is effected at a temperature of about 65 to about 205°C.
8. The process for forming an electrochemical cathode as defined in Claim 1 wherein said nonfibrous polymeric material is polytetrafluoroethylene.
9. The process for forming an electrochemical cathode as defined in Claim 3 and further including a polymeric film in said sandwich in contact with one of said layers of said impregnated web.
10. The process for forming an electrochemical cathode as defined in Claim 4 and further including a polymeric film in said sandwich in contact with one of said layers of said impregnated web.
11. The process for forming an electrochemical cathode as defined in Claim 4 or 5 wherein step b) is effected with an embossing roller in contact with said polymeric film.
12. The process for forming an electrochemical cathode as defined in Claim 4 or 5 wherein said current collecting substrate is coated with a polytetrafluoroethylene dispersion prior to step c).
13. The process for forming an electrochemical cathode as defined in Claim 8 wherein drying is effected at a temperature of from 90 to 150°C. -
14. The process for forming an electrochemical cathode as defined in Claim 11 wherein step c) is effected with an embossing roller in contact with said polymeric film.
PCT/US1991/000158 1990-01-08 1991-01-08 Electrochemical cathode and materials therefor WO1991011033A1 (en)

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Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH04162365A (en) * 1990-10-25 1992-06-05 Tanaka Kikinzoku Kogyo Kk Method for preparing electrode of fuel cell
US5439758A (en) * 1992-10-02 1995-08-08 Voltek, Inc. Electrochemical power generating system
US5415949A (en) * 1992-10-02 1995-05-16 Voltek, Inc. Metal-air cell and power system using metal-air cells
GB9324101D0 (en) * 1993-11-23 1994-01-12 Johnson Matthey Plc Improved manufacture of electrodes
US5650241A (en) * 1994-09-09 1997-07-22 Mcgee; Richard L. Metal-air cell battery
US6054228A (en) * 1996-06-06 2000-04-25 Lynntech, Inc. Fuel cell system for low pressure operation
US6194099B1 (en) 1997-12-19 2001-02-27 Moltech Corporation Electrochemical cells with carbon nanofibers and electroactive sulfur compounds
US6368751B1 (en) 1999-10-08 2002-04-09 Reves, Inc. Electrochemical electrode for fuel cell
US6632557B1 (en) * 1999-10-26 2003-10-14 The Gillette Company Cathodes for metal air electrochemical cells
WO2001071826A2 (en) * 2000-03-22 2001-09-27 Sarnoff Corporation Battery and circuitry assembly
US6921606B2 (en) * 2002-04-16 2005-07-26 Gore Enterprise Holdings, Inc. Composite films for electrochemical devices
US20070259234A1 (en) * 2006-05-06 2007-11-08 David Chua Metal-air semi-fuel cell with an aqueous acid based cathode
CN101197444B (en) * 2006-12-08 2010-06-16 比亚迪股份有限公司 Air electrode, and method and device for producing the same
ATE518267T1 (en) * 2006-12-27 2011-08-15 Eveready Battery Inc METHOD FOR PRODUCING AN ELECTROCHEMICAL CELL HAVING A CATALYTIC ELECTRODE
KR101008400B1 (en) * 2007-09-27 2011-01-14 한국전력공사 Electrode for ion sorption, electosorption purifying device of using the same and method for manufacturing the electrode for ion sorption
US8123577B2 (en) 2008-07-09 2012-02-28 Argopower, Llc Autonomous vehicle with fuel cell and autonomous flushing system
CN101702454B (en) * 2009-10-29 2011-06-01 黑龙江慧能绿色能源科技开发有限公司 Zinc ion battery and manufacturing method thereof
US9525197B2 (en) * 2011-10-10 2016-12-20 Toyota Motor Europe Nv/Sa Stable non-aqueous electrolyte promoting ideal reaction process in rechargeable lithium-air batteries
CA3011823A1 (en) 2015-01-21 2016-07-28 Swes Technology KFT. Cathode arrangement, energy cell comprising the same, method for manufacturing the cathode arrangement, and arrangement for processing hydrogen gas

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3682707A (en) * 1970-01-12 1972-08-08 Westinghouse Electric Corp Stabilization of silver catalyst in an air diffusion electrode
US4885217A (en) * 1987-07-06 1989-12-05 Alupower, Inc. Air cathodes and materials therefor
US4906535A (en) * 1987-07-06 1990-03-06 Alupower, Inc. Electrochemical cathode and materials therefor

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4293396A (en) * 1979-09-27 1981-10-06 Prototech Company Thin carbon-cloth-based electrocatalytic gas diffusion electrodes, and electrochemical cells comprising the same
FR2468219A1 (en) * 1979-10-18 1981-04-30 Alsthom Cgee METHOD FOR THE CONTINUOUS PRODUCTION BY PAPER TECHNIQUE OF POROUS THIN STRIPS AND PRODUCTS OBTAINED, ESPECIALLY ELECTRODES FOR FUEL CELLS
US4569924A (en) * 1982-12-30 1986-02-11 Ozin Geoffrey A Metal carbon catalyst preparation
DE3303779A1 (en) * 1983-02-04 1984-08-16 Hoechst Ag, 6230 Frankfurt METHOD FOR PRODUCING A CATALYTICALLY EFFECTIVE ELECTRODE MATERIAL FOR OXYGEN CONSUMPTION ELECTRODES
US4615954A (en) * 1984-09-27 1986-10-07 Eltech Systems Corporation Fast response, high rate, gas diffusion electrode and method of making same

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3682707A (en) * 1970-01-12 1972-08-08 Westinghouse Electric Corp Stabilization of silver catalyst in an air diffusion electrode
US4885217A (en) * 1987-07-06 1989-12-05 Alupower, Inc. Air cathodes and materials therefor
US4906535A (en) * 1987-07-06 1990-03-06 Alupower, Inc. Electrochemical cathode and materials therefor

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of EP0510107A4 *

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EP0510107A1 (en) 1992-10-28
CA2072088A1 (en) 1991-07-09
EP0510107A4 (en) 1993-03-17
AU7242591A (en) 1991-08-05
JPH05505492A (en) 1993-08-12
MX166747B (en) 1993-02-01
US5053375A (en) 1991-10-01

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