CA2189100C - Porous nickel electrode substrate - Google Patents

Porous nickel electrode substrate Download PDF

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Publication number
CA2189100C
CA2189100C CA002189100A CA2189100A CA2189100C CA 2189100 C CA2189100 C CA 2189100C CA 002189100 A CA002189100 A CA 002189100A CA 2189100 A CA2189100 A CA 2189100A CA 2189100 C CA2189100 C CA 2189100C
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CA
Canada
Prior art keywords
nickel
substrate
core
porous
substrate according
Prior art date
Legal status (The legal status 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 status listed.)
Expired - Fee Related
Application number
CA002189100A
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French (fr)
Other versions
CA2189100A1 (en
Inventor
Victor Alexander Ettel
John Ambrose
Kirt Kenneth Cushnie
James Alexander Evert Bell
Vladimir Paserin
Peter Joseph Kalal
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Vale Canada Ltd
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Vale Canada Ltd
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Publication date
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Publication of CA2189100A1 publication Critical patent/CA2189100A1/en
Application granted granted Critical
Publication of CA2189100C publication Critical patent/CA2189100C/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/64Carriers or collectors
    • H01M4/70Carriers or collectors characterised by shape or form
    • H01M4/72Grids
    • H01M4/74Meshes or woven material; Expanded metal
    • H01M4/745Expanded metal
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/64Carriers or collectors
    • H01M4/66Selection of materials
    • H01M4/665Composites
    • H01M4/667Composites in the form of layers, e.g. coatings
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/64Carriers or collectors
    • H01M4/70Carriers or collectors characterised by shape or form
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/64Carriers or collectors
    • H01M4/70Carriers or collectors characterised by shape or form
    • H01M4/80Porous plates, e.g. sintered carriers
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/64Carriers or collectors
    • H01M4/70Carriers or collectors characterised by shape or form
    • H01M4/80Porous plates, e.g. sintered carriers
    • H01M4/806Nonwoven fibrous fabric containing only fibres
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M2004/026Electrodes composed of, or comprising, active material characterised by the polarity
    • H01M2004/029Bipolar electrodes
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/64Carriers or collectors
    • H01M4/66Selection of materials
    • H01M4/668Composites of electroconductive material and synthetic resins
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/64Carriers or collectors
    • H01M4/70Carriers or collectors characterised by shape or form
    • H01M4/80Porous plates, e.g. sintered carriers
    • H01M4/808Foamed, spongy materials
    • 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
    • Y02E60/10Energy storage using batteries
    • 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T29/00Metal working
    • Y10T29/49Method of mechanical manufacture
    • Y10T29/49002Electrical device making
    • Y10T29/49108Electric battery cell making
    • Y10T29/49114Electric battery cell making including adhesively bonding
    • 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T29/00Metal working
    • Y10T29/49Method of mechanical manufacture
    • Y10T29/49002Electrical device making
    • Y10T29/49108Electric battery cell making
    • Y10T29/49115Electric battery cell making including coating or impregnating

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Composite Materials (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Cell Electrode Carriers And Collectors (AREA)
  • Battery Electrode And Active Subsutance (AREA)

Abstract

A porous nickel electrode substrate having a central high conductivity core sandwiched between two layers of porous conductive material such as nickel foam or nickel felt. The porous conductive material is plated with nickel and then sintered.
By selectively controlling the plating of nickel on the porous material, variable conductivities may be designed into the substrate.

Description

~'' ;; ..

POROUS NICKEL ELECTRODE SUBSTRATE
TEC>ERVICAL FIELD
The instant invention relates to battery electrodes in general, and more particularly, to a porous nickel electrode substrate having variable conductivity and reduced weight.
BACKGROUND ART
Due to increasing political and environmental pressures, electric vehicles ("EV's") are being championed as a means for reducing vehicle borne pollutants. The main recognized weakness of EV's are their battery systems. Much research is being conducted to raise the energy density and reduce the weight of existing and promising battery systems.
An EV battery must allow sufficient driving range between recharges, have low maintenance, give adequate acceleration and permit safe rapid recharging, both when needed by the user and during regenerative braking. The cost of the battery and any replacements) that may be required during the life of the vehicle must also be low enough to make the non-polluting EV an attractive choice for the consumer.
-2- 2 1 8 ~ ~ ~ ~ PC-4132/
For example, in 1991 an attempt to define the above criteria was made by the United States Advanced Battery Consortium (USABC):

Mi Term Long Term Specific Energy, Wh/kg 80_100 200 Specific Power, W/kg 150-200 400 Cycle Life, 80% DOD cycles600 1000 Ultimate Price, $/kWh < $150 < $100 Recharge Time < 6 hrs 3-6 hrs Fast Recharge 40-80% SOC 40-80%
SOC

in < 15 min. in < 15 min.

Operating Environment -30 to 65C -40 to A better touchstone than the separate cost of kWh and cycle life criteria is the combination thereof. That is, the battery cost per distance (mile or kilometer) over the life of the vehicle. It is ultimately a long battery life that will drive the economics of EV's.
Many batteries today meet or excel in some of the above criteria but fail or are marginal in others. For example, lead acid batteries excel in cost per kWh, are marginal in the cycle life criterion, and are insufficient in energy density which affects driving range.
Nickel cadmium and nickel metal hydride batteries offer fair to good energy density and other performance properties, but currently fail to meet the cost per kWh criteria because of their high manufacturing costs. Cost of primary materials is not unacceptably high. For example, the traditional design of a NiCd battery with a sintered nickel plaque positive electrode and a pasted negative electrode usually contains (per kWh of capacity) about 4.5 pounds (2 kg) of nickel in the active mass and about 5.5 pounds (2.5 kg) in the current distributing plaque. Ten pounds (4.5 kg) of nickel metal corresponds to around $40 per kWh. Eight pounds (3.7 kg) of cadmium per kWh corresponds to only $17 per kWh. Yet the price of a manufactured NiCd battery is over $500 per kWh, as compared to the price of comparable lead acid battery of only $150/kWh.
The difference between the cost of these batteries ($350/kWh) is much more than the difference in the cost of materials because it reflects the complicated, Labor intensive process of making NiCd batteries incorporating sintered electrodes as compared to the simple, high speed grid production and pasting of lead acid batteries.
Similar high speed pasting of nickel batteries is possible when using nickel foam or similar substrates developed for this specific purpose and manufactured in large volume to reduce cost. Large cost savings may be realized by reducing the number of operations required in electrode manufacture and/or simplifying them.
Another expensive operation that raises the cost of NiCd batteries is attaching electrode tabs to the porous sheets by welding. This is usually done after pasting the electrode strip and cutting it into individual electrodes. To successfully weld a tab to the porous sheet, the weld area must be cleaned of active mass. Furthermore, the weld joint is a point of weakness and the unavoidable vibrations during vehicle use may result in weld break and premature electrode failure.
A similar undesirable task is welding porous sheets to the non-porous central foil in manufacturing of bipolar electrodes.
SUMMARY OF THE INVENTION
Accordingly, there is provided a porous nickel electrode substrate especially suited for electric vehicle battery plates. The substrate comprises a central high conductivity core laminated on both sides with a porous layer consisting of -3a-nickel foam or nickel felt. The design results in enhanced performance with a concomitant reduction in weight when compared to conventional electrodes made with plated porous central sheets.
Thus, the invention provides an electrode substrate comprising a central eletrically conductive core, a porous electically conductive material attached to the core, the porous electrically conductive material selected from the group consisting of nickel foam and nickel felt formed by the decomposition of nickel tetracarbonyl, and the electrical conductivity of the substrate varying from the top of the substrate to the bottom of the substrate.
BRIEF DESCRIPTION OF THE DRAWINGS
Figure 1 is a plan view of an embodiment of the invention.
Figure 2 is a side view of an embodiment of the invention.
Figure 3 is a plan view of an embodiment of the invention.
Figure 4 is a representative view taken along lines 4-4 of Figure 2.
PREFERRED MODE FOR CARRYING OUT THE INVENTION
The instant invention relates to a porous nickel substrate with engineered variable conductivity suitable for manufacturing EV battery plates with enhanced performance and minimized weight.
-4- ~ ~ ~ ~ ~ ~ 0 PC-4132/
Figure 1 shows a porous electrode substrate 10 consisting of a high conductivity core 12 laminated on both sides with a layer of porous conductive material 14 such as nickel plated foam or nickel plated felt.
The central core 12 provides mechanical strength and electrical S conductivity whereas the two porous layers 14 distribute the electrical current throughout the active mass to be embedded therein.
By separating mechanical strength and electrical conductivity into two discrete yet related functions, it is possible to use a central core 12 with lower nickel density and lower cost without compromising the conductivity and strength of the electrode. The requisite strength and conductivity is provided by the central core 12 which can be manufactured more economically than the conventional porous sheets produced by plating pure nickel. The core 12 can be a sheet of reticulated expanded mesh 16, a solid or perforated plate 18 (See Figure 3), or a conductive plastic such as polypropylene/carbon black composite. More particularly, the electrically conductive core 12 may be made from nickel plated steel, nickel, or copper.
The central core 12 may incorporate one or more solid sections 20 to permit cutting out electrodes (transversely or longitudinally) with tabs 22 formed from these sections 20. The central core 12 may also have variable conductivity to provide high conductivity at the top section of the electrode substrate 10 which carries most of the electrode current and with reduced material density at the bottom part, which carries very little current and where high conductivity is not needed.
The composite substrate 10 can be produced by laminating two sheets of a porous organic material 14 (polyurethane foam, polyester felt, etc.) over the central expanded or perforated strip 16 followed by nickel plating and sintering of the plated composite. Another method of producing such a structure is to produce the two porous nickel structures first, sandwiching them about the central core 12 and sintering the combination together.
Electrolytic (e.g. U.S. patents 4,978,431; 5,098,544 and 5,374,491), carbonyl (US patent 4,957,543), or physical vapor deposition ("PVD") plating processes may be used to coat the porous material 14. In addition, a mechanical joining method such as gluing, resistance welding, etc. may be used to bond the material 14 to the central core 12.
An object of this invention is an efficient method of manufacturing a -5- 2' 8 ~ 1 C~ G PC-4132/
continuous strip of porous substrate that can be pasted and stamped into complete electrode substrates ready for pasting and assembling into cells and batteries.
Monopolar electrodes can also be equipped with a current distributing grid in the upper section of the electrode which has to carry much higher currents than the bottom section. In the case of a negative electrode, a copper cored substrate 10 can be used to further increase electrode conductivity and performance under high drain (acceleration) or rapid charge.
This process can also be used to produce bipolar electrodes with a solid sheet in the middle and porous sheets such as nickel foam or nickel felt on both sides, or a sandwich of solid sheet and porous nickel felt or foam.
It has been determined that gluing porous substrate layers 14 (e.g.
polyurethane foam or suitable felts) to a central core 12 made from a strip of expanded metal grid attached to a continuous solid section 20, followed by plating using the carbonyl method and annealing, produces an integral structure which permits pasting and cutting into finished electrodes.
Similarly, gluing sheets of polymeric foam (or suitable polymeric, carbon or other felt 14) to the opposite sides of a center core sheet 12 permits producing, after plating and annealing, an integral substrate for a bipolar electrode.
It is also possible to join certain foams and felts to the core 12 mesh by processes other than gluing, e.g. needling or thermal bonding.
An alternate method for producing the substrates 10 involves sintering separately produced porous nickel structures together with a central sheet of expanded or perforated metal, or other suitable material, optionally equipped with solid strip to form the tabs 22 after punching out the finished electrodes.
Bipolar electrodes can also be produced by sintering or otherwise attaching porous structures to both sides of a solid sheet.
In both cases, the strength of the laminated structures can be improved by applying a layer of easily sinterable powder (such as INCO~ type T-110) to the future interface.
A custom electrode structure may be obtained by controlled density variation of the nickel foam or nickel felt using the carbonyl plating process. In this process, nickel deposition is achieved by thermal decomposition of nickel tetracarbonyl on a porous substrate such as polyurethane foam or polyester felt 14. Because the ---8 9 ~ O O PC-4132/
deposition rate is a function of temperature, it is possible to program the plating process so that it produces a controlled variation in temperature of the substrate 10 as it passes through the plating zone and hence controlled variation in nickel density and concomitantly conductivity. Electrodes with controlled and variable conductivity can be manufactured from the continuous strip of the substrate material.
Figure 2 is a cross-sectional view of an electrode substrate 10 having a sandwiched sintered layer 14 enveloping an expanded mesh 16 core 12. Figure 4 is a representative view taken along lines 4-4 of Figure 2.
Figure 3 depicts a core 12 made from a solid nickel plate 18 enveloped by a porous conductive layer 14 prior to plating and sintering.
A number of examples were made in accordance with the teachings of the instant invention:
1. Foam-mesh sandwich was prepared using nickel mesh from Expanded Metal Corp., 0.006 inch (0.15 mm) thick, density 490 g/m2, and two layers of polyurethane foam (each approx. 1.7 mm thick, 80 pores per inch [31.5 pores per cm]) glued to the mesh using Halltech~" 7191 temperature glue. The foam-mesh composite was plated with nickel by the carbonyl process, then sintered at 1000°C in a reducing atmosphere.
2. Expanded metal foil from Delker Corp., with solid metal section (0.010 inch [0.25 mm] thick, 250 g/m ), was used to prepare another sample. Polyurethane foam was again glued to both sides and the composite substrate was plated with nickel, then sintered at 1000°C.
3. A layer of carbon pitch fiber felt (1.7 mm thick, sheet density 2 oz/yd2 [67.5 g/m~]) was glued to both sides of Expanded Metal Corp. nickel mesh, carbonyl plated with nickel and sintered at 1000°C.
4. 0.005 inch (0.12 mm) thick nickel foil was used to prepare a composite substrate by gluing a 1.7 mm thick sheet of 110 ppi polyurethane foam to both sides, plating with nickel and sintering at 1000°C.

-." _~_ ~ ~ ~ ~ ~ ~ ~~ PC-4132/
While in accordance with the provisions of the statute, there are illustrated and described herein specific embodiments of the invention, those skilled in the art will understand that changes may be made in the form of the invention covered by the claims and that certain features of the invention may sometimes be used to advantage without a corresponding use of the other features.

Claims (13)

1. An electrode substrate comprising a central electrically conductive core, a porous electrically conductive material attached to the core, the porous electrically conductive material selected from the group consisting of nickel foam and nickel felt formed by the decomposition of nickel tetracarbonyl, and the electrical conductivity of the substrate varying from the top of the substrate to the bottom of the substrate.
2. The substrate according to claim 1 wherein the core is expended metal.
3. The substrate according to claim 1 wherein the core is a plate.
4. The substrate according to claim 1 wherein the core is perforated.
5. The substrate according to claim 1 including a tab connected to the core.
6. The substrate according to claim 1 wherein the core is selected from the group consisting of steel, nickel plated steel nickel, copper and conductive plastic.
7. The substrate according to claim 1 wherein the substrate is sintered.
8. The substrate according to claim 1 including nickel powder.
9. The substrate according to claim 1 wherein the porous material is glued to the core.
10. A process for varying the conductivity of an electrode substrate, the process comprising:
1) providing an electrically conductive core having opposing sides, 2) affixing at least one porous layer to each side of the core, the porous layer selected from the group consisting of foam and felt, 3) depositing nickel from the decomposition of nickel tetracarbonyl directly onto each porous layer, 4) causing the concentration of the nickel deposit from step 3) to vary along the substrate, and 5) sintering the nickel deposit.
11. The process according to claim 10 wherein nickel powder is added to the substrate prior to sintering.
12. The process according to claim 10 wherein a tab is formed from the core.
13. The process according to claim 10 wherein the core is selected from the group consisting of plate, foil, mesh and expanded metal.
CA002189100A 1996-02-15 1996-10-29 Porous nickel electrode substrate Expired - Fee Related CA2189100C (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US08/601,738 1996-02-15
US08/601,738 US5700363A (en) 1996-02-15 1996-02-15 Porous nickel electrode substrate

Publications (2)

Publication Number Publication Date
CA2189100A1 CA2189100A1 (en) 1997-08-16
CA2189100C true CA2189100C (en) 2000-02-08

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CA002189100A Expired - Fee Related CA2189100C (en) 1996-02-15 1996-10-29 Porous nickel electrode substrate

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US (1) US5700363A (en)
EP (1) EP0790656B1 (en)
JP (1) JP3321011B2 (en)
CA (1) CA2189100C (en)
DE (1) DE69704892T2 (en)

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US20070063368A1 (en) * 2004-02-23 2007-03-22 Nike, Inc. Fluid-filled bladder incorporating a foam tensile member
US20070178988A1 (en) * 2006-02-01 2007-08-02 Nike, Inc. Golf clubs and golf club heads including cellular structure metals and other materials
US7941941B2 (en) 2007-07-13 2011-05-17 Nike, Inc. Article of footwear incorporating foam-filled elements and methods for manufacturing the foam-filled elements
CN105027242A (en) * 2012-09-06 2015-11-04 “能源及电动汽车合作项目”有限责任公司 High-power electric double-layer capacitor
DE102017209960A1 (en) * 2017-06-13 2018-12-13 Robert Bosch Gmbh Method for producing an electrode, in particular for a battery
JP7220313B2 (en) * 2021-02-01 2023-02-09 本田技研工業株式会社 Electrodes and storage devices
KR102886417B1 (en) * 2025-07-09 2025-11-14 주식회사 한울인터내셔널 Method for manufacturing a conductive sponge and conductive sponge manufactured thereby

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JP3509031B2 (en) * 1993-12-10 2004-03-22 片山特殊工業株式会社 Method for manufacturing porous metal body with lead and porous metal body with lead manufactured by the method

Also Published As

Publication number Publication date
JP3321011B2 (en) 2002-09-03
DE69704892D1 (en) 2001-06-28
US5700363A (en) 1997-12-23
EP0790656B1 (en) 2001-05-23
CA2189100A1 (en) 1997-08-16
EP0790656A1 (en) 1997-08-20
DE69704892T2 (en) 2002-04-18
JPH09231978A (en) 1997-09-05

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