WO2007116244A2 - Method of fabricating electrodes with low contact resistance for batteries and double-layer capacitors - Google Patents
Method of fabricating electrodes with low contact resistance for batteries and double-layer capacitors Download PDFInfo
- Publication number
- WO2007116244A2 WO2007116244A2 PCT/IB2006/004045 IB2006004045W WO2007116244A2 WO 2007116244 A2 WO2007116244 A2 WO 2007116244A2 IB 2006004045 W IB2006004045 W IB 2006004045W WO 2007116244 A2 WO2007116244 A2 WO 2007116244A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- carbon
- current collector
- electrode
- electrodes
- layer
- Prior art date
Links
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 12
- 239000003990 capacitor Substances 0.000 title claims abstract description 11
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 96
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 61
- 239000002245 particle Substances 0.000 claims abstract description 29
- 230000010287 polarization Effects 0.000 claims abstract description 7
- 238000005304 joining Methods 0.000 claims abstract 3
- 238000000034 method Methods 0.000 claims description 54
- 239000011888 foil Substances 0.000 claims description 37
- 229910052751 metal Inorganic materials 0.000 claims description 37
- 239000002184 metal Substances 0.000 claims description 37
- 239000011230 binding agent Substances 0.000 claims description 15
- 239000003575 carbonaceous material Substances 0.000 claims description 8
- 238000005096 rolling process Methods 0.000 claims description 6
- 239000000843 powder Substances 0.000 claims description 5
- 238000003825 pressing Methods 0.000 claims description 4
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 claims description 2
- 229910044991 metal oxide Inorganic materials 0.000 claims description 2
- 150000004706 metal oxides Chemical class 0.000 claims description 2
- 229910052976 metal sulfide Inorganic materials 0.000 claims description 2
- 239000000654 additive Substances 0.000 claims 1
- 230000000996 additive effect Effects 0.000 claims 1
- 238000007788 roughening Methods 0.000 claims 1
- 238000007569 slipcasting Methods 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
- 239000010410 layer Substances 0.000 description 36
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 30
- 229910052782 aluminium Inorganic materials 0.000 description 29
- 239000010439 graphite Substances 0.000 description 16
- 229910002804 graphite Inorganic materials 0.000 description 16
- 238000000576 coating method Methods 0.000 description 12
- 239000011248 coating agent Substances 0.000 description 10
- 239000004411 aluminium Substances 0.000 description 9
- 239000005030 aluminium foil Substances 0.000 description 9
- 238000005516 engineering process Methods 0.000 description 7
- 238000005259 measurement Methods 0.000 description 7
- 238000010892 electric spark Methods 0.000 description 6
- 239000007769 metal material Substances 0.000 description 6
- 239000002002 slurry Substances 0.000 description 6
- 239000007772 electrode material Substances 0.000 description 4
- 239000004744 fabric Substances 0.000 description 4
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 4
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 239000002482 conductive additive Substances 0.000 description 3
- 229910052802 copper Inorganic materials 0.000 description 3
- 239000010949 copper Substances 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 229910001416 lithium ion Inorganic materials 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 2
- 239000006230 acetylene black Substances 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 238000005266 casting Methods 0.000 description 2
- 229910001651 emery Inorganic materials 0.000 description 2
- 238000004146 energy storage Methods 0.000 description 2
- 238000005530 etching Methods 0.000 description 2
- 229910052744 lithium Inorganic materials 0.000 description 2
- 239000004810 polytetrafluoroethylene Substances 0.000 description 2
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- 150000003568 thioethers Chemical class 0.000 description 2
- 238000001771 vacuum deposition Methods 0.000 description 2
- 238000003466 welding Methods 0.000 description 2
- HBBGRARXTFLTSG-UHFFFAOYSA-N Lithium ion Chemical compound [Li+] HBBGRARXTFLTSG-UHFFFAOYSA-N 0.000 description 1
- 239000002033 PVDF binder Substances 0.000 description 1
- 239000011149 active material Substances 0.000 description 1
- 238000004873 anchoring Methods 0.000 description 1
- 230000003466 anti-cipated effect Effects 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000010406 cathode material Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 238000010891 electric arc Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- 239000011229 interlayer Substances 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000005240 physical vapour deposition Methods 0.000 description 1
- 229920005596 polymer binder Polymers 0.000 description 1
- 239000002491 polymer binding agent Substances 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 238000009958 sewing Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/13—Electrodes for accumulators with non-aqueous electrolyte, e.g. for lithium-accumulators; Processes of manufacture thereof
- H01M4/139—Processes of manufacture
- H01M4/1393—Processes of manufacture of electrodes based on carbonaceous material, e.g. graphite-intercalation compounds or CFx
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
- H01G11/22—Electrodes
- H01G11/26—Electrodes characterised by their structure, e.g. multi-layered, porosity or surface features
- H01G11/28—Electrodes characterised by their structure, e.g. multi-layered, porosity or surface features arranged or disposed on a current collector; Layers or phases between electrodes and current collectors, e.g. adhesives
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
- H01G11/22—Electrodes
- H01G11/30—Electrodes characterised by their material
- H01G11/32—Carbon-based
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
- H01G11/66—Current collectors
- H01G11/70—Current collectors characterised by their structure
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
- H01G11/84—Processes for the manufacture of hybrid or EDL capacitors, or components thereof
- H01G11/86—Processes for the manufacture of hybrid or EDL capacitors, or components thereof specially adapted for electrodes
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/13—Electrodes for accumulators with non-aqueous electrolyte, e.g. for lithium-accumulators; Processes of manufacture thereof
- H01M4/133—Electrodes based on carbonaceous material, e.g. graphite-intercalation compounds or CFx
-
- 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
-
- 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
- Y02E60/13—Energy storage using capacitors
Definitions
- This invention relates to a method of fabricating the electrodes for batteries and double-layer capacitors (EDLC). More particularly, the invention relates to a method of fabricating electrodes for batteries and double-layer capacitors or hybrid devices with low contact (or interfacial) resistance between the electrode material and metal current collector.
- Double-layer capacitors also referred to as electrochemical double layer capacitors
- EDLC EDLC
- supercapacitors are energy storage devices requiring very low inner resistance in order to provide the high power output. Therefore, all contributions to the impedance must be reduced including the contact resistance between the polarizing nanoporous carbon electrode and metal current collector. This is also very important in battery technology, such as lithium primary or secondary batteries, wherein carbon or carbon-containing polarizing electrodes have contact planes with metal current collectors.
- the electrodes are typically made of powdered carbonaceous materials, e.g. nanoporous carbon powder in EDLC or carbon based (e.g. graphite) powder in Li- ion batteries, or comprised as electrically conductive additives, e.g.
- a significant problem is that typically there is a very poor adhesion between carbon particles and metal foil, such as when the aluminum foil is used as a current collector. Besides, the aluminum foil is covered with a native insulating oxide film about 5 nm thick. Poor adhesion as well as the insulating film can increase a contact (or interfacial) resistance between the electrode material and metal current collector resulting in degraded performance of energy storage device. What is needed is a low cost method for forming low contact resistance contact between the metal current collector and carbon-containing electrode.
- An object of the present invention is to develop a low-cost but still effective method of fabricating the electrodes for batteries, double-layer capacitors or hybrid devices with low contact resistance between the metal current collector and carbon-containing electrode.
- An example of hybrid device is supercapacitor/Li-ion battery.
- nanoporous carbon powder pressed or rolled with a binder as is used in EDLC technology or composite which includes active materials (for example oxides, sulfides), binder and conductive additives (for example carbon, black) as is used in battery technology.
- active materials for example oxides, sulfides
- binder for example carbon, black
- U.S. Pat. No. 5,907,472 discloses a method to lower the internal resistance of an EDLC by the use of aluminum-impregnated carbon cloth electrodes.
- the carbon cloth used in such electrodes tends to be somewhat costly.
- carbon cloth is inherently too thick (300 microns or more) to provide the very low resistivity needed.
- 6,447,555 discloses a method for reducing the contact resistance between the aluminum current collectors and their respective polarizing electrodes via the granular carbon.
- hard amorphous granular carbon is made to penetrate into the surface of the aluminum collector.
- Granular carbon is sprayed and pressed against the surface using a roller by some other method. As a result, the hard granular carbon penetrates through the oxide film into the surface of the aluminum foil.
- the metal current collector should preferably have a rough surface.
- carbon particles should preferably project slightly from the surface of the metal material, hi addition, for EDLC, a layer of nano- porous carbon with a binder (a polarizing electrode) can be fixed firmly to the roughened surface, and the contact resistance of the surface can thus be reduced by ca. 2.5 times as compared with the plain aluminum foil.
- a layer of nano- porous carbon with a binder a polarizing electrode
- U.S. Pat. Nos. 6,493,210 and 6,808,845 to Nonaka, et al. disclose a method for producing a valve metal material for electrodes by driving or squeezing numerous carbon particles into the surface thereof.
- Two methods can be employed in accordance with the invention.
- a mixture of valve metal powder and carbon powder is heated near its melting point and pressurized in a container to make an ingot so that the carbon powder may be contained in the valve metal ingot.
- a second method includes a carbon-powder driving step wherein carbon particles are driven into the surface of a valve metal material by pressurizing carbon particles dispersed on the surface of the valve metal material.
- Pressing using dies or rollers may be employed to drive powder of carbon particles into a valve metal sheet, then, carbon particles being fixed in the surface of the valve metal sheet with the particle exposed on the surface.
- the valve metal material Prior to pressing the valve metal material may preferably be roughened or electrochemically etched on the surface, particularly be made porous in a thin layer of the surface, facilitating carbon particles to engage and embed in the porous surface layer effectively.
- carbon particles can be pressed and fitted in the surface of the valve metal material and fixed.
- This invention was used by the authors to reduce the contact resistance between metal current collectors and electrodes in both lithium ion secondary batteries and EDLC. The batteries exhibited excellent high-rate performance, and the resistance of EDLC electrodes was reduced by 2-3-fold.
- Pat. No. 6,631,074 disclose an EDLC having low-resistance carbon powder electrodes. Their method includes the steps of: preparing a first slurry that includes conducting carbon powder and a binder; applying the first slurry to the bare aluminum surface of the foil (a current collector plate); drying the applied first slurry to form a primary coating; preparing a second slurry that includes nano-porous carbon powder, a solvent and a binder; and applying the second slurry to the primary coating.
- the primary coating preferably comprises a highly conducting carbon powder (e.g., graphite) in large proportion and a polymer binder.
- the surface of the aluminum foil can be corona treated, or mechanically or chemically modified to promote wettability and adhesion.
- Other possible methods of making the carbon electrodes include employing perforated foil collector plates or screens.
- the primary coating is then applied using a slurry transfer apparatus such as a reverse comma coat system and other methods such as slot coating. Gravure, extrusion, flexographic or roll coating methods may
- the thickness of the resulting primary coating is about 4 to 6 ⁇ m.
- the primary coating reduces the interfacial resistance and serves as a seed coat for a secondary coating with a layer of nano-porous carbon material that serves as a double layer electrode.
- An EDLC made in accordance with the above-described method had a capacitance of about 2,650 to 2,700 F and an impedance.of less than 0.6 mOhm. This corresponds to an RC-constant value of ca. 1.6 s, though the authors targeted to the value as low as 0.5 s.
- U.S. Pat. No. 6,831,826 to Iwaida, et al. discloses a method for reducing the contact resistance between the sheet-shaped carbon electrodes and aluminum foil (current collector) by attaching the electrodes to the foil surface through a conductive adhesive.
- the laminating step is performed by attaching the sheet-shaped electrodes while applying the conductive adhesive with a thickness of 10 micron or less to the surface of the conductive foil by using a gravure coater. It is preferred that the adhered portions of the foil surface are made rough in advance by an etching treatment or the like.
- Fig. 1 is a schematic drawing of electric-spark method to fuse the carbon particles into a metal foil: 1 - electric-spark machine; 2 - carbon rod; 3 - metal foil (current collector).
- Fig. 2 shows a cross-sectional view of a metal foil (current collector) doped with carbon particles, which are or embedded into the metal surface: 1 - one-side doping; 2 - two-side doping.
- Fig. 3 shows a cross-sectional view of a one-side gradient electrode fabricated in accordance with a method presented in this invention: 1 - metal current collector; 2 - a layer of graphite particles fused or embedded into the metal surface; 3 - a nano-porous carbon electrode comprising an activated carbon powder and a binder.
- Fig. 4 illustrates a magnified view (observed with microscope) of the metal surface with carbon particles fused thereon.
- Fig. 5 illustrates a method for measuring the resistivity of electrodes wherein a constant current passes across the aluminium current collector, the electrode and platinum foil pressed on top, and the voltage drop between two foils is measured by a high-resistance voltmeter.
- the method of electrode fabrication includes fabrication of the metallic current collector and polarization electrode.
- the surface of the metallic foil is preliminary treated chemically or mechanically with the goal of increasing the surface area or providing a rough surface.
- an initial layer of carbon materials is disposed (Fig.4).
- highly conductive carbon particles e.g. graphite particles
- a carbon rod being used as one of two electrodes and the foil as the other electrode.
- a second layer of carbon material with high conductivity is coated onto the first layer of carbon material, which has been fused into the metal foil.
- a polarizing electrode is rolled, or pressed, or cast (Fig. 3), or spread on the current collector coated with carbon material made in the previous steps.
- the polarizing electrode is fabricated, for example, from nano-porous carbon powder and a binder (as in EDLC technology), or from metal oxide/sulphide powder, a conductive additive such as a graphite powder, and a binder (as in lithium battery technology).
- a short-term electric spark between a carbon rod and aluminum foil is formed by moving the carbon rod back and forth near the surface of the foil (Fig. 1).
- an electrical spark or arc is initiated between the carbon rod and the aluminum surface.
- the spark melts the aluminum metal locally, and carbon particles detach from the rod and fuse into the metal surface (Fig. 2).
- Either the carbon rod or metal foil can move horizontally so that the electric-spark machine acts as a "sewing machine” forming a stitch of carbon particles fused into metal surface (Fig. 4).
- carbon particles project from the surface of metal foil to increase the contact area between this first layer of conductive carbon particles and the second layer of carbon- containing electrode.
- the metal foil can be roughened either mechanically or chemically. This can be accomplished, for example, by rolling the metal foil with emery paper or by etching the foil chemically or electrochemically, or by any other common method that increases the surface area of the metal foil.
- an interlayer of highly conductive carbon powder such as graphite powder or acetylene black
- graphite powder or acetylene black can be applied on the first layer of carbon particles fused into the metal current collector followed by pressing, rolling or spreading the second layer of polarizing electrode onto the surface thus formed. Due to this embodiment the electrical contact between the first layer, which is fused into the metal current collector, and the second layer, which is the polarizing electrode of the battery or EDLC, can further be improved.
- the aluminium foil with the thickness 20 microns was pressed with a copper plate with the frame from stainless steel with a rectangular window 35 x 45 mm.
- an electro spark device which included a positive electrode from graphite rod and negative electrode of aluminium foil, the aluminium foil was doped with the particles of graphite over the windows of the frame.
- the current of the process was 0.6 A.
- the duration was 6 minutes.
- a layer of graphite was fused into the surface of the aluminium.
- the thickness of this graphite layer was 3-5 microns.
- a suspension of nano-porous carbon powder with PVDF binder was coated.
- the concentration of the binder was 10%.
- the method of coating was casting. After drying, and following forge-rolling, the thickness of the nano-porous carbon was approximately 100 micron.
- the resistance of electrode that was fabricated by the method described above was measured. The method of the resistance measurement used is described below. A scheme of this method is shown in Fig. 5. Results of the measurements are presented in Table 1, line 1.
- Aluminum foil having a thickness of 60 microns was passed through rolls several times with emery paper to roughen the surface. Thereafter, the aluminium foil was pressed with a copper plate with the frame of stainless steel, with a rectangular window 35 x 45 mm. Using an electro-spark device that included a positive electrode comprising a graphite rod and a negative electrode that comprised said aluminium foil, the roughened aluminium foil was doped with particles of graphite over the windows of the frame. The electrical current of the doping process was between 0.6 A and 1.0 A. The duration of the process was 7 minutes. The resulting layer of the graphite was fused into the surface of the aluminium. The thickness of this graphite layer was 3-5 micron.
- a suspension of nano-porous carbon powder with PTFE binder was disposed onto the aluminium current collector with the graphite layer that was fused into the surface of the aluminium.
- the concentration of the binder was 7%.
- the method of coating was casting. After drying, and following forge-rolling, the thickness of the nano-porous carbon layer was approximately 100 microns.
- the resistance of electrode that was fabricated by the method described above was measured. The method of the resistance measurement is described below. A scheme depicting the method is presented in Fig. 5. Results of the measurement are presented in the Table 1, line 2.
- the resulting thickness of the nano-porous carbon was approximately 100 microns.
- the resistance of the electrode that was fabricated by the method describe above was measured. The method used for the resistance measurement is described below. A scheme of the method is shown in Fig. 5. Results of the measurement are presented in Table 1, line 3. [0031]
- the electrical resistances of nano-porous carbon electrodes made in accordance with the present invention were measured by determining the voltage drop across the electrode using a 4-connection circuit as presented in Fig. 5. A platinum foil pressed to the upper surface of the electrode as in Fig. 5 was used as an electrical contact when a constant current was passed through the electrode.
- the contact resistance reduces to ca. 0.6 ⁇ .cm 2 but it is still rather high for EDLC application. This is supposedly due to the existence of a native insulating oxide film on the aluminum surface.
- the resistivity can be lowered as compared with the method of vacuum deposition of the aluminum, and can reach 0.03
Landscapes
- Engineering & Computer Science (AREA)
- Power Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Electrochemistry (AREA)
- Manufacturing & Machinery (AREA)
- Electric Double-Layer Capacitors Or The Like (AREA)
- Secondary Cells (AREA)
- Cell Electrode Carriers And Collectors (AREA)
- Battery Electrode And Active Subsutance (AREA)
Abstract
A method of fabricating low-contact resistance electrodes for batteries and double-electric layer capacitors including the steps of providing a current collector and a polarization electrode, placing a plurality of highly electrically conductive carbon particles into a surface of the current collector to form a first carbon comprising layer, and joining the electrode to the surface of the current collector.
Description
METHOD OF FABRICATING ELECTRODES WITH LOW CONTACT RESISTANCE FOR BATTERIES AND DOUBLE-LAYER CAPACITORS
FIELD OF THE INVENTION
[0001] This invention relates to a method of fabricating the electrodes for batteries and double-layer capacitors (EDLC). More particularly, the invention relates to a method of fabricating electrodes for batteries and double-layer capacitors or hybrid devices with low contact (or interfacial) resistance between the electrode material and metal current collector.
BACKGROUND
[0002] Double-layer capacitors, also referred to as electrochemical double layer capacitors
(EDLC) or supercapacitors, are energy storage devices requiring very low inner resistance in order to provide the high power output. Therefore, all contributions to the impedance must be reduced including the contact resistance between the polarizing nanoporous carbon electrode and metal current collector. This is also very important in battery technology, such as lithium primary or secondary batteries, wherein carbon or carbon-containing polarizing electrodes have contact planes with metal current collectors. The electrodes are typically made of powdered carbonaceous materials, e.g. nanoporous carbon powder in EDLC or carbon based (e.g. graphite) powder in Li- ion batteries, or comprised as electrically conductive additives, e.g. carbon black or graphite powder in various cathode materials based on non-conducting oxides or sulfides. [0003] A significant problem is that typically there is a very poor adhesion between carbon particles and metal foil, such as when the aluminum foil is used as a current collector. Besides, the aluminum foil is covered with a native insulating oxide film about 5 nm thick. Poor adhesion as well as the insulating film can increase a contact (or interfacial) resistance between the electrode material and metal current collector resulting in degraded performance of energy storage device. What is needed is a low cost method for forming low contact resistance contact between the metal current collector and carbon-containing electrode.
SUMMARY OF THE INVENTION
[0004] An object of the present invention is to develop a low-cost but still effective method of fabricating the electrodes for batteries, double-layer capacitors or hybrid devices with low contact resistance between the metal current collector and carbon-containing electrode. An
example of hybrid device is supercapacitor/Li-ion battery. This is another object of the present invention to develop a gradient electrode material, which comprises at least two different layers: the first layer is a highly conductive carbon material, e.g. graphite or pyrocarbon, fused into the metal current collector, e.g. aluminum foil, and the second layer is a polarizing carbon-containing electrode, e.g. a nanoporous carbon powder pressed or rolled with a binder as is used in EDLC technology or composite which includes active materials (for example oxides, sulfides), binder and conductive additives (for example carbon, black) as is used in battery technology.
DESCRIPTION OF RELATED ART
[0005] U.S. Pat. No. 5,907,472 (Farahmandi et al.) discloses a method to lower the internal resistance of an EDLC by the use of aluminum-impregnated carbon cloth electrodes. However, the carbon cloth used in such electrodes tends to be somewhat costly. And as an electrode material, carbon cloth is inherently too thick (300 microns or more) to provide the very low resistivity needed. Thus, it would be advantageous to have a method and/or apparatus for lowering the internal resistance of double layer capacitors that does not rely on carbon cloth. [0006] U.S. Pat. No. 6,447,555 (Okamura, et al.) discloses a method for reducing the contact resistance between the aluminum current collectors and their respective polarizing electrodes via the granular carbon. In accordance with the invention, hard amorphous granular carbon is made to penetrate into the surface of the aluminum collector. Granular carbon is sprayed and pressed against the surface using a roller by some other method. As a result, the hard granular carbon penetrates through the oxide film into the surface of the aluminum foil. The metal current collector should preferably have a rough surface. In particular, carbon particles should preferably project slightly from the surface of the metal material, hi addition, for EDLC, a layer of nano- porous carbon with a binder (a polarizing electrode) can be fixed firmly to the roughened surface, and the contact resistance of the surface can thus be reduced by ca. 2.5 times as compared with the plain aluminum foil.
[0007] U.S. Pat. Nos. 6,493,210 and 6,808,845 to Nonaka, et al. disclose a method for producing a valve metal material for electrodes by driving or squeezing numerous carbon particles into the surface thereof. Two methods can be employed in accordance with the invention. In a first method, a mixture of valve metal powder and carbon powder is heated near its melting point and pressurized in a container to make an ingot so that the carbon powder may be contained in the valve metal ingot. A second method includes a carbon-powder driving step wherein carbon particles are driven into the surface of a valve metal material by pressurizing carbon particles
dispersed on the surface of the valve metal material. Pressing using dies or rollers may be employed to drive powder of carbon particles into a valve metal sheet, then, carbon particles being fixed in the surface of the valve metal sheet with the particle exposed on the surface. Prior to pressing the valve metal material may preferably be roughened or electrochemically etched on the surface, particularly be made porous in a thin layer of the surface, facilitating carbon particles to engage and embed in the porous surface layer effectively. In either of the two methods, carbon particles can be pressed and fitted in the surface of the valve metal material and fixed. This invention was used by the authors to reduce the contact resistance between metal current collectors and electrodes in both lithium ion secondary batteries and EDLC. The batteries exhibited excellent high-rate performance, and the resistance of EDLC electrodes was reduced by 2-3-fold.
[0008] U.S. Pat. Nos. 6,627,252, 6,643,119 and 6,804,108 (Nanjundiah, et al.), and U.S.
Pat. No. 6,631,074 ( Bendale, et al.) disclose an EDLC having low-resistance carbon powder electrodes. Their method includes the steps of: preparing a first slurry that includes conducting carbon powder and a binder; applying the first slurry to the bare aluminum surface of the foil (a current collector plate); drying the applied first slurry to form a primary coating; preparing a second slurry that includes nano-porous carbon powder, a solvent and a binder; and applying the second slurry to the primary coating. The primary coating preferably comprises a highly conducting carbon powder (e.g., graphite) in large proportion and a polymer binder. Prior to the coating process, the surface of the aluminum foil can be corona treated, or mechanically or chemically modified to promote wettability and adhesion. Other possible methods of making the carbon electrodes include employing perforated foil collector plates or screens. The primary coating is then applied using a slurry transfer apparatus such as a reverse comma coat system and other methods such as slot coating. Gravure, extrusion, flexographic or roll coating methods may
also be used. The thickness of the resulting primary coating is about 4 to 6 μm. The primary
coating reduces the interfacial resistance and serves as a seed coat for a secondary coating with a layer of nano-porous carbon material that serves as a double layer electrode. An EDLC made in accordance with the above-described method had a capacitance of about 2,650 to 2,700 F and an impedance.of less than 0.6 mOhm. This corresponds to an RC-constant value of ca. 1.6 s, though the authors targeted to the value as low as 0.5 s.
[0009] U.S. Pat. No. 6,831,826 to Iwaida, et al. discloses a method for reducing the contact resistance between the sheet-shaped carbon electrodes and aluminum foil (current collector) by attaching the electrodes to the foil surface through a conductive adhesive. In accordance with the invention, the laminating step is performed by attaching the sheet-shaped electrodes while applying the conductive adhesive with a thickness of 10 micron or less to the surface of the conductive foil by using a gravure coater. It is preferred that the adhered portions of the foil surface are made rough in advance by an etching treatment or the like. [0010] U.S. Pat. Nos. 6,602,742 and 6,697,249 to Maletin, et al. disclose a method to reduce the contact resistance in EDLC devices due to covering the carbonaceous electrode with a thin aluminum layer using the plasma activated physical vapor deposition of aluminum in high vacuum followed by welding this layer to the aluminum current collector. Such a technology provides very low contact resistance (see Table 1 below) resulting in very low RC-constant values (about 0.3 s); however, this is a labor- intensive and expensive technology.
DESCRIPTION QF THE FIGURES
[0011 ] A fuller understanding of the present invention and the features and benefits thereof will be accomplished upon review of the following detailed description together with the accompanying drawings, in which:
[0012] Fig. 1 is a schematic drawing of electric-spark method to fuse the carbon particles into a metal foil: 1 - electric-spark machine; 2 - carbon rod; 3 - metal foil (current collector).
[0013] Fig. 2 shows a cross-sectional view of a metal foil (current collector) doped with carbon particles, which are or embedded into the metal surface: 1 - one-side doping; 2 - two-side doping.
[0014] Fig. 3 shows a cross-sectional view of a one-side gradient electrode fabricated in accordance with a method presented in this invention: 1 - metal current collector; 2 - a layer of graphite particles fused or embedded into the metal surface; 3 - a nano-porous carbon electrode comprising an activated carbon powder and a binder. [0015] Fig. 4 illustrates a magnified view (observed with microscope) of the metal surface with carbon particles fused thereon.
[0016] Fig. 5 illustrates a method for measuring the resistivity of electrodes wherein a constant current passes across the aluminium current collector, the electrode and platinum foil pressed on top, and the voltage drop between two foils is measured by a high-resistance voltmeter.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS [0017] To achieve the objectives of the present invention the general method for fabricating an electrode can be described as follows:
[0018] The method of electrode fabrication includes fabrication of the metallic current collector and polarization electrode. The surface of the metallic foil is preliminary treated chemically or mechanically with the goal of increasing the surface area or providing a rough surface.
[0019] In the next step, on the surface of the metallic current collector an initial layer of carbon materials is disposed (Fig.4). For this purpose, highly conductive carbon particles, e.g. graphite particles, are fused or embedded into the metal foil (current collector) using an electric spark or electric arc deposition, a carbon rod being used as one of two electrodes and the foil as the other electrode.
[0020] A second layer of carbon material with high conductivity is coated onto the first layer of carbon material, which has been fused into the metal foil.
[0021] hi the next step, a polarizing electrode is rolled, or pressed, or cast (Fig. 3), or spread on the current collector coated with carbon material made in the previous steps. The polarizing electrode is fabricated, for example, from nano-porous carbon powder and a binder (as in EDLC technology), or from metal oxide/sulphide powder, a conductive additive such as a graphite powder, and a binder (as in lithium battery technology). [0022] In an electric-spark technique, which can preferably be employed in this embodiment, a short-term electric spark between a carbon rod and aluminum foil is formed by moving the carbon rod back and forth near the surface of the foil (Fig. 1). Upon close approach, an electrical spark or arc is initiated between the carbon rod and the aluminum surface. [0023] The spark melts the aluminum metal locally, and carbon particles detach from the rod and fuse into the metal surface (Fig. 2). Either the carbon rod or metal foil can move
horizontally so that the electric-spark machine acts as a "sewing machine" forming a stitch of carbon particles fused into metal surface (Fig. 4).
[0024] The diameter of carbon particles fused into the metal current collector surface
should preferably be in the range of 0.01 to 50 μm, more preferably, in the range of 0.1 to 10 μm.
It is also preferable that carbon particles project from the surface of metal foil to increase the contact area between this first layer of conductive carbon particles and the second layer of carbon- containing electrode. To further increase the contact area and to improve "the anchoring affect" the metal foil can be roughened either mechanically or chemically. This can be accomplished, for example, by rolling the metal foil with emery paper or by etching the foil chemically or electrochemically, or by any other common method that increases the surface area of the metal foil.
[0025] As another embodiment of this invention, an interlayer of highly conductive carbon powder, such as graphite powder or acetylene black, can be applied on the first layer of carbon particles fused into the metal current collector followed by pressing, rolling or spreading the second layer of polarizing electrode onto the surface thus formed. Due to this embodiment the electrical contact between the first layer, which is fused into the metal current collector, and the second layer, which is the polarizing electrode of the battery or EDLC, can further be improved. [0026] The present invention is described in more detail below by examples. It should be understood, however, that the present invention is not limited to these examples but can as well be embodied in other forms and devices without departing from the scope and spirit of the invention.
EXAMPLE 1.
[0027] The aluminium foil with the thickness 20 microns was pressed with a copper plate with the frame from stainless steel with a rectangular window 35 x 45 mm. With the help of an electro spark device, which included a positive electrode from graphite rod and negative electrode
of aluminium foil, the aluminium foil was doped with the particles of graphite over the windows of the frame. The current of the process was 0.6 A. The duration was 6 minutes. As a result, a layer of graphite was fused into the surface of the aluminium. The thickness of this graphite layer was 3-5 microns. Onto the aluminium current collector with the graphite layer that was fused into the surface of the aluminium, a suspension of nano-porous carbon powder with PVDF binder was coated. The concentration of the binder was 10%. The method of coating was casting. After drying, and following forge-rolling, the thickness of the nano-porous carbon was approximately 100 micron. The resistance of electrode that was fabricated by the method described above was measured. The method of the resistance measurement used is described below. A scheme of this method is shown in Fig. 5. Results of the measurements are presented in Table 1, line 1.
EXAMPLE 2.
[0028] Aluminum foil having a thickness of 60 microns was passed through rolls several times with emery paper to roughen the surface. Thereafter, the aluminium foil was pressed with a copper plate with the frame of stainless steel, with a rectangular window 35 x 45 mm. Using an electro-spark device that included a positive electrode comprising a graphite rod and a negative electrode that comprised said aluminium foil, the roughened aluminium foil was doped with particles of graphite over the windows of the frame. The electrical current of the doping process was between 0.6 A and 1.0 A. The duration of the process was 7 minutes. The resulting layer of the graphite was fused into the surface of the aluminium. The thickness of this graphite layer was 3-5 micron.
[0029] A suspension of nano-porous carbon powder with PTFE binder was disposed onto the aluminium current collector with the graphite layer that was fused into the surface of the aluminium. The concentration of the binder was 7%. The method of coating was casting. After drying, and following forge-rolling, the thickness of the nano-porous carbon layer was
approximately 100 microns. The resistance of electrode that was fabricated by the method described above was measured. The method of the resistance measurement is described below. A scheme depicting the method is presented in Fig. 5. Results of the measurement are presented in the Table 1, line 2.
EXAMPLE 3.
[0030] The surface of an aluminium foil strip with thickness 60 micron was treated as described in Example 2. Thereafter, the aluminium foil was pressed with a copper plate and the surface of the aluminium foil was doped as described in Examples 1 and 2. The current of the doping process was between 0.6. A and 1.0 A. The duration of the process was 8 minutes. The thickness of the resulting graphite layer that was fused into the surface of the aluminium was 3-5 micron. Thereafter, a thin layer (1-2 micron) of acetylene black was disposed onto the surface. Thereafter, onto the fabricated surface that included aluminium and two layers of carbon, a suspension of nano-porous carbon powder with PTFE binder (7%) was coated using the method of forge-rolling. The resulting thickness of the nano-porous carbon was approximately 100 microns. The resistance of the electrode that was fabricated by the method describe above was measured. The method used for the resistance measurement is described below. A scheme of the method is shown in Fig. 5. Results of the measurement are presented in Table 1, line 3. [0031] The electrical resistances of nano-porous carbon electrodes made in accordance with the present invention (Examples 1-3) were measured by determining the voltage drop across the electrode using a 4-connection circuit as presented in Fig. 5. A platinum foil pressed to the upper surface of the electrode as in Fig. 5 was used as an electrical contact when a constant current was passed through the electrode. The contributions to the total electrode resistance from different components, namely; from the contact resistance between the collector foil and carbon electrode, RAI/C, from the carbon electrode itself, Rc, and from the contact resistance between the
carbon electrode and platinum foil, Rpt/c, were eliminated by measuring the total resistance at various electrode thickness and replacing the aluminum collector foil with another platinum foil. The results of measurements are listed in Table 1, below, wherein some known methods of electrode fabrication are also presented for comparison purposes.
Table 1. Resistivity of carbon electrodes fabricated by different methods
The results presented in Table 1 show that the plain Al foil leads, as can be anticipated,
provides to very high contact resistance (ca. 2 Ω.cm2). If the contact area is increased due to using
a grid or roughened metal collector surface, the contact resistance reduces to ca. 0.6 Ω.cm2 but it is
still rather high for EDLC application. This is supposedly due to the existence of a native insulating oxide film on the aluminum surface.
It is possible to reduce the contact resistance if use the vacuum deposition of the Al in the surface of carbon polarization electrode and follow the welding the Al which was deposited to the aluminum foil - current collector. However this method is very expensive and labor-intensive.
If the electrodes are made using the method of the present invention, the resistivity can be lowered as compared with the method of vacuum deposition of the aluminum, and can reach 0.03
Ω.cm2. The simplicity and cost efficiency of the present invention are evident, and the resulting
reduced cost and labor required in the fabrication of supercapacitors are a substantial advantage of the present invention.
It is to be understood that while the invention has been described in conjunction with the preferred specific embodiments thereof, that the foregoing description, as well as the examples which follow, are intended to illustrate and not limit the scope of the invention. Other aspects, advantages and modifications within the scope of the invention will be apparent to those skilled in the art to which the invention pertains.
Claims
1. A method of fabricating low-contact resistance electrodes for batteries and double-electric layer capacitors, comprising the steps of: providing a current collector and a polarization electrode; introducing a plurality of highly electrically conductive carbon particles into a surface said current collector to form a first carbon comprising layer, and joining said electrode to said surface of said current collector.
2. The method of claim 1, wherein said current collector comprises a metal foil.
3. The method of claim 2, wherein a plurality of highly electrically conductive carbon particles is fused into said metal foil.
4. The method of claim 3, wherein an electrical spark or an electrical arc is used for said fusing.
5. The method of claim 1, wherein said electrode is a carbon comprising electrode.
6. The method of claim 2, further comprising the step of roughening the surface of said metal foil by a mechanical or chemical method before said joining.
7. The method of claim 1, wherein said carbon particles have an average diameter within the range 0.01 - 50 μm.
8. The method of claim 1, wherein said polarization electrode comprises a carbon- comprising material and a binder.
9. The method of claim 1, wherein said polarization electrode is produced from nanoporous carbon-comprising powder with a binder applied on said first carbon comprising layer by rolling, pressing or slip casting.
10. The method of claim 1 wherein said polarization electrode comprises a metal oxide or sulfide mixed with an electrically conducting additive and a binder.
1 1. A battery or double-electric layer capacitor, comprising: a first and second current collector having first and second electrodes coupled thereto, wherein at least one of said current collectors includes a plurality of highly electrically conductive carbon particles in a surface said current collector.
12. The method of claim 1, wherein at least one of said electrodes are carbon comprising electrodes.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
UA200506296 | 2005-06-25 | ||
UAA200506296A UA90448C2 (en) | 2005-06-25 | 2005-06-25 | Method for manufacturing electrodes with a low contact resistance for batteries and capacitors with a double electric layer |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2007116244A2 true WO2007116244A2 (en) | 2007-10-18 |
WO2007116244A3 WO2007116244A3 (en) | 2009-12-17 |
Family
ID=38581451
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/IB2006/004045 WO2007116244A2 (en) | 2005-06-25 | 2006-06-23 | Method of fabricating electrodes with low contact resistance for batteries and double-layer capacitors |
Country Status (2)
Country | Link |
---|---|
UA (1) | UA90448C2 (en) |
WO (1) | WO2007116244A2 (en) |
Cited By (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2011149807A3 (en) * | 2010-05-27 | 2012-03-01 | Corning Incorporated | Multi-layered electrode for ultracapacitors |
EP2525377A1 (en) * | 2011-05-19 | 2012-11-21 | Yunasko Limited | Current collector and method of its fabrication |
CN103178269A (en) * | 2013-03-06 | 2013-06-26 | 长春吉大科诺科技有限责任公司 | Modification processing method of lithium ion battery anode current collector aluminum foil |
CN103177883A (en) * | 2013-03-06 | 2013-06-26 | 长春吉大科诺科技有限责任公司 | Method for modifying electric spark embedded carbon on surface of current collector of supercapacitor |
CN103199261A (en) * | 2013-03-06 | 2013-07-10 | 长春吉大科诺科技有限责任公司 | Modification method of negative current collector copper foil of lithium ion battery |
CN103198929A (en) * | 2013-03-06 | 2013-07-10 | 长春吉大科诺科技有限责任公司 | Electrode plate of electric double layer capacitor (EDLC) and preparation method thereof |
FR2990050A1 (en) * | 2012-04-25 | 2013-11-01 | Yunasko Ltd | ELECTROCHEMICAL CAPACITOR WITH DOUBLE ELECTRIC LAYER AND METHOD OF MANUFACTURING THE SAME |
WO2014090892A1 (en) * | 2012-12-12 | 2014-06-19 | Varta Microbattery Gmbh | Composite material, method for the production thereof, system produced therefrom and application of same |
US8840687B2 (en) | 2010-08-23 | 2014-09-23 | Corning Incorporated | Dual-layer method of fabricating ultracapacitor current collectors |
US9209464B2 (en) | 2009-09-24 | 2015-12-08 | Corning Incorporated | Current collectors having textured coating |
CN105603372A (en) * | 2015-12-22 | 2016-05-25 | 长春吉大科诺科技有限责任公司 | Electromagnetic drive type graphite inlaying probe adopting arc sputtering |
CN105914054A (en) * | 2016-05-25 | 2016-08-31 | 长春吉大科诺科技有限责任公司 | Automatic current collector double-sided modification device |
CN107221456A (en) * | 2017-06-30 | 2017-09-29 | 北方民族大学 | A kind of aviation is with mixing carbon-based super capacitor of nickel and preparation method thereof |
US10522300B2 (en) | 2015-05-26 | 2019-12-31 | National Research Council Of Canada | Metallic surface with karstified relief, forming same, and high surface area metallic electrochemical interface |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9524830B2 (en) * | 2011-12-02 | 2016-12-20 | Yuriy Maletin | Method for selecting nanoporous carbon material for polarizable electrode, method for manufacturing such polarizable electrodes and method for manufacturing electrochemical double layer capacitor |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5262255A (en) * | 1991-01-30 | 1993-11-16 | Matsushita Electric Industrial Co., Ltd. | Negative electrode for non-aqueous electrolyte secondary battery |
US6524707B1 (en) * | 1999-07-09 | 2003-02-25 | Powerstor Corporation | Carbon-bonded metal structures and methods of fabrication |
US6631074B2 (en) * | 2000-05-12 | 2003-10-07 | Maxwell Technologies, Inc. | Electrochemical double layer capacitor having carbon powder electrodes |
-
2005
- 2005-06-25 UA UAA200506296A patent/UA90448C2/en unknown
-
2006
- 2006-06-23 WO PCT/IB2006/004045 patent/WO2007116244A2/en active Application Filing
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5262255A (en) * | 1991-01-30 | 1993-11-16 | Matsushita Electric Industrial Co., Ltd. | Negative electrode for non-aqueous electrolyte secondary battery |
US6524707B1 (en) * | 1999-07-09 | 2003-02-25 | Powerstor Corporation | Carbon-bonded metal structures and methods of fabrication |
US6631074B2 (en) * | 2000-05-12 | 2003-10-07 | Maxwell Technologies, Inc. | Electrochemical double layer capacitor having carbon powder electrodes |
Cited By (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9209464B2 (en) | 2009-09-24 | 2015-12-08 | Corning Incorporated | Current collectors having textured coating |
CN102906838A (en) * | 2010-05-27 | 2013-01-30 | 康宁股份有限公司 | Multi-layered electrode for ultracapacitors |
JP2013527619A (en) * | 2010-05-27 | 2013-06-27 | コーニング インコーポレイテッド | Multi-layer electrode for ultracapacitor |
WO2011149807A3 (en) * | 2010-05-27 | 2012-03-01 | Corning Incorporated | Multi-layered electrode for ultracapacitors |
US8687346B2 (en) | 2010-05-27 | 2014-04-01 | Corning Incorporated | Multi-layered electrode for ultracapacitors |
US8840687B2 (en) | 2010-08-23 | 2014-09-23 | Corning Incorporated | Dual-layer method of fabricating ultracapacitor current collectors |
EP2525377A1 (en) * | 2011-05-19 | 2012-11-21 | Yunasko Limited | Current collector and method of its fabrication |
FR2990050A1 (en) * | 2012-04-25 | 2013-11-01 | Yunasko Ltd | ELECTROCHEMICAL CAPACITOR WITH DOUBLE ELECTRIC LAYER AND METHOD OF MANUFACTURING THE SAME |
WO2014090892A1 (en) * | 2012-12-12 | 2014-06-19 | Varta Microbattery Gmbh | Composite material, method for the production thereof, system produced therefrom and application of same |
CN105122504A (en) * | 2012-12-12 | 2015-12-02 | 瓦尔达微电池有限责任公司 | Composite material, method for the production thereof, system produced therefrom and application of same |
CN103198929A (en) * | 2013-03-06 | 2013-07-10 | 长春吉大科诺科技有限责任公司 | Electrode plate of electric double layer capacitor (EDLC) and preparation method thereof |
CN103199261A (en) * | 2013-03-06 | 2013-07-10 | 长春吉大科诺科技有限责任公司 | Modification method of negative current collector copper foil of lithium ion battery |
CN103177883A (en) * | 2013-03-06 | 2013-06-26 | 长春吉大科诺科技有限责任公司 | Method for modifying electric spark embedded carbon on surface of current collector of supercapacitor |
CN103178269A (en) * | 2013-03-06 | 2013-06-26 | 长春吉大科诺科技有限责任公司 | Modification processing method of lithium ion battery anode current collector aluminum foil |
CN103198929B (en) * | 2013-03-06 | 2016-12-28 | 长春吉大科诺科技有限责任公司 | A kind of super capacitor electrode sheet and preparation method thereof |
US10522300B2 (en) | 2015-05-26 | 2019-12-31 | National Research Council Of Canada | Metallic surface with karstified relief, forming same, and high surface area metallic electrochemical interface |
CN105603372A (en) * | 2015-12-22 | 2016-05-25 | 长春吉大科诺科技有限责任公司 | Electromagnetic drive type graphite inlaying probe adopting arc sputtering |
CN105914054A (en) * | 2016-05-25 | 2016-08-31 | 长春吉大科诺科技有限责任公司 | Automatic current collector double-sided modification device |
CN107221456A (en) * | 2017-06-30 | 2017-09-29 | 北方民族大学 | A kind of aviation is with mixing carbon-based super capacitor of nickel and preparation method thereof |
CN107221456B (en) * | 2017-06-30 | 2020-04-28 | 北方民族大学 | Aviation nickel-doped carbon-based super capacitor and preparation method thereof |
Also Published As
Publication number | Publication date |
---|---|
UA90448C2 (en) | 2010-05-11 |
WO2007116244A3 (en) | 2009-12-17 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US20090130564A1 (en) | Method of fabrication electrodes with low contact resistance for batteries and double layer capacitors | |
WO2007116244A2 (en) | Method of fabricating electrodes with low contact resistance for batteries and double-layer capacitors | |
US6191935B1 (en) | Electric double-layer capacitor having hard granular carbon material penetrating into the aluminum collector electrodes | |
JP5791613B2 (en) | Current collector with satin coating | |
JP4406667B2 (en) | High performance double layer capacitors with composite electrodes of aluminum and carbon | |
US7623339B2 (en) | Electrochemical device | |
TWI601330B (en) | Electrode material and energy storage apparatus | |
US9105406B2 (en) | Graphene electrolytic capacitor | |
US20080151472A1 (en) | Electrochemical double layer capacitor | |
WO2005036574A1 (en) | Electrode for electric double layer capacitor, method for producing same, electric double layer capacitor, and conductive adhesive | |
KR20060119817A (en) | Method for producing electrochemical capacitor electrode | |
WO2011149807A2 (en) | Multi-layered electrode for ultracapacitors | |
JP3534031B2 (en) | Method for manufacturing electrode for battery / capacitor | |
WO2004055844A1 (en) | Polarizable electrode for electric double layer capacitor, method for manufacturing same and electric double layer capacitor | |
JP2003234254A (en) | Electrical double layer capacitor using carbon nano-tube | |
TW201232582A (en) | Dual-layer method of fabricating ultracapacitor current collectors | |
JP4095145B2 (en) | Electrode manufacturing method | |
JP2000269095A (en) | Electrode for electric double-layer capacitor | |
JP2007180251A (en) | Manufacturing method and manufacturing apparatus of electrode for electrochemical capacitor | |
JP5328734B2 (en) | Electrode manufacturing method, power storage device and electrode | |
JPH10177935A (en) | Electric double-layered capacitor and its manufacture | |
JPH10223487A (en) | Electrode for electric double layer capacitor and electric double layer capacitor | |
JP2000286167A (en) | Manufacture of electrode for battery and capacitor | |
EP4293693A1 (en) | Capacitor | |
KR102016520B1 (en) | Super capacitor with high voltage and method for manufacturing the same |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
WWW | Wipo information: withdrawn in national office |
Country of ref document: DE |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 06851086 Country of ref document: EP Kind code of ref document: A2 |
|
122 | Ep: pct application non-entry in european phase |
Ref document number: 06851086 Country of ref document: EP Kind code of ref document: A2 |