CA2819391C - Method for manufacturing of slurry for production of battery film - Google Patents
Method for manufacturing of slurry for production of battery film Download PDFInfo
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- CA2819391C CA2819391C CA2819391A CA2819391A CA2819391C CA 2819391 C CA2819391 C CA 2819391C CA 2819391 A CA2819391 A CA 2819391A CA 2819391 A CA2819391 A CA 2819391A CA 2819391 C CA2819391 C CA 2819391C
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- 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
- H01M4/36—Selection of substances as active materials, active masses, active liquids
- H01M4/362—Composites
- H01M4/364—Composites as mixtures
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- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/05—Accumulators with non-aqueous electrolyte
- H01M10/052—Li-accumulators
- H01M10/0525—Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodes; Lithium-ion batteries
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- H01M10/058—Construction or manufacture
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- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/04—Processes of manufacture in general
- H01M4/0402—Methods of deposition of the material
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- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/04—Processes of manufacture in general
- H01M4/0402—Methods of deposition of the material
- H01M4/0404—Methods of deposition of the material by coating on electrode collectors
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- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/04—Processes of manufacture in general
- H01M4/043—Processes of manufacture in general involving compressing or compaction
- H01M4/0435—Rolling or calendering
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- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/04—Processes of manufacture in general
- H01M4/0471—Processes of manufacture in general involving thermal treatment, e.g. firing, sintering, backing particulate active material, thermal decomposition, pyrolysis
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- 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
- H01M4/131—Electrodes based on mixed oxides or hydroxides, or on mixtures of oxides or hydroxides, e.g. LiCoOx
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- 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
- H01M4/136—Electrodes based on inorganic compounds other than oxides or hydroxides, e.g. sulfides, selenides, tellurides, halogenides or LiCoFy
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- 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
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- 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
- H01M4/1391—Processes of manufacture of electrodes based on mixed oxides or hydroxides, or on mixtures of oxides or hydroxides, e.g. LiCoOx
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- 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
- H01M4/1391—Processes of manufacture of electrodes based on mixed oxides or hydroxides, or on mixtures of oxides or hydroxides, e.g. LiCoOx
- H01M4/13915—Processes of manufacture of electrodes based on mixed oxides or hydroxides, or on mixtures of oxides or hydroxides, e.g. LiCoOx containing halogen atoms, e.g. LiCoOxFy
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- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/36—Selection of substances as active materials, active masses, active liquids
- H01M4/48—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
- H01M4/485—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of mixed oxides or hydroxides for inserting or intercalating light metals, e.g. LiTi2O4 or LiTi2OxFy
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- H01M4/48—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
- H01M4/50—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of manganese
- H01M4/505—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of manganese of mixed oxides or hydroxides containing manganese for inserting or intercalating light metals, e.g. LiMn2O4 or LiMn2OxFy
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- H01M4/36—Selection of substances as active materials, active masses, active liquids
- H01M4/48—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
- H01M4/52—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron
- H01M4/525—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron of mixed oxides or hydroxides containing iron, cobalt or nickel for inserting or intercalating light metals, e.g. LiNiO2, LiCoO2 or LiCoOxFy
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- H—ELECTRICITY
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- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/36—Selection of substances as active materials, active masses, active liquids
- H01M4/58—Selection of substances as active materials, active masses, active liquids of inorganic compounds other than oxides or hydroxides, e.g. sulfides, selenides, tellurides, halogenides or LiCoFy; of polyanionic structures, e.g. phosphates, silicates or borates
- H01M4/5825—Oxygenated metallic salts or polyanionic structures, e.g. borates, phosphates, silicates, olivines
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- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/62—Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
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- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/62—Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
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- 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
- H01M4/62—Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
- H01M4/621—Binders
- H01M4/622—Binders being polymers
- H01M4/623—Binders being polymers fluorinated polymers
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- 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
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- 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
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P70/00—Climate change mitigation technologies in the production process for final industrial or consumer products
- Y02P70/50—Manufacturing or production processes characterised by the final manufactured product
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- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T29/00—Metal working
- Y10T29/49—Method of mechanical manufacture
- Y10T29/49002—Electrical device making
- Y10T29/49108—Electric battery cell making
- Y10T29/49115—Electric battery cell making including coating or impregnating
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- Materials Engineering (AREA)
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- Composite Materials (AREA)
- Crystallography & Structural Chemistry (AREA)
- Battery Electrode And Active Subsutance (AREA)
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Abstract
Description
BATTERY FILM
Technical field The present invention relates to method for manufacturing of a slurry for production of a battery film. More specifically, the present invention relates to a method for generating a slurry for application of anode and cathode materials in batteries, in addition to a method for manufacturing of cathodes and anodes for lithium batteries and a method for manufacturing of a lithium battery cell.
Background technique A lithium battery is made from three main components: anode, cathode and electrolyte.
Anode and cathode normally consist of metal foils which are covered by a thin layer of a powder mixture, active materials, which are bound together by a binder. The binders function is to glue the powder particles together and glue these firmly to the metal foil. The binder must be flexible and chemically stable towards the electrolyte.
A typical anode consist of a copper foil which is covered by a thin layer (40 ¨ 100 microns) with graphite powder, carbon, which is tied together by means of the plastic material PVDF
(polyvinylidene fluoride).
A typical cathode consist of an aluminum foil which is coated by a thin layer (40-100 microns) of lithium metal oxide which is bound together by the plastic material PVDF.
A typical electrolyte is a mixture of a lithium salt such as lithium hexafluorophosphate (LiPF6), lithium tetrafluorophosphate (LiPF4), lithium hexafluoroarsenate (LiAsF6), lithium perchlorate (LiC104), Lithium tetrafluoroborate (LiBF4), and lithium triflate (LiCF3S03) and organic carbonates, for instance EC (ethylene carbonate), DEC (diethyl carbonate) and DMC(dimethyl carbonate).
The most common manufacturing process for making a battery film for lithium ion batteries is to blend active materials and PVDF, and mix this into a solvent dissolving the PVDF. The purpose to dissolve the binder is to disperse the material evenly between the particles in the powder mixture in order to secure a good binding between these. This mixture is then applied
The most common solvent in order to dissolve PVDF is NMP (N- Methyl-Pyrrolidone), which is both a toxic and environmentally harmful chemical. There are a variety of alternative solvents, but most of them have in common that they are either toxic, liable to catch fire or unfavorable relating to the chemical structure of the finished battery.
Consequently, it is important that the solvent is fully removed from the battery film during production and that the evaporation of NMP is controlled with regards to the environmental requirements. The process of removing the last remnants of the solvent (down to ppm level) from the battery film is a demanding process which is both energy- and space demanding and make substantial demands from the technical equipment.
There are waterborne manufacturing processes in which the powder is mixed with water to form a paste or thin slurry. The disadvantage of using water is the relatively energy demanding process to evaporate the water so that the dried battery film must be completely free from water so that the battery shall operate.
From US 2005/0271797 Al it is known that a production process for a lithium battery consisting of the steps of a) prepare an EC (ethylene carbonate) solution by loosening EC-crystals in a suitable solvent, (b) then dissolve a binder in a suitable solvent in order to make a binder solution and then add and mix sufficiently an active electrode material and an electric conductive material of a wanted composition into the binder solution, (c) add a defined amount of the EC mixture prepared in step (a) into the binder solution from step (b), blend the mixture of EC solution and the binder solution sufficiently so that the slurry in form of an electrode binder can be coated onto an electrode, (e) coat a collector with the slurry, (f) dry the paste layer at a given temperature, and complete the electrode production by pressing a dried electrode structure at a given pressure after the slurry has dried. The process described in US 2005/0271797 Al also comprises mixing a solvent together with an ethylene carbonate plus insert a second solvent to a binder solution together with an active material for then subsequently to add a given amount of the solvent mixed with ethylene carbonate to the mixture of the binder solution with the other solvent. Thus the process comprises the application of at least one solvent for generating the slurry.
Summary of the invention There is a purpose with the present invention to provide a method for manufacturing of slurry for application onto cathode and anode materials in batteries, a method for manufacturing of cathodes and anodes for lithium batteries plus a method for manufacturing of a lithium ion battery cell, where the above mentioned problems are solved.
More exactly, the present invention is stating a method for manufacturing slurry for coating of electrodes for use in lithium ion battery. The method comprises steps of:
a) Mixing active materials with a binder into a binder solution, and b) Adding an organic carbonate to a binder solution to generate the slurry.
According to one aspect of the invention, the mixing process is executed according to the steps a) and b), wherein the above step b) is carried out at temperature above the melting temperature of the organic carbonate (C).
According to another aspect of the invention the active materials (A) are adapted to an anode and a cathode.
In accordance with yet another aspect of the invention is the active cathode material is selected from the group of: LiCo02, LiFePat, LiMn204, LiNi02, Li2FePO4F, LiCowNiii3jMni/302, and Li(LiaNixMnyCoz) and the active anode material is selected from the group comprising LiC6, Li4Ti5012,Si (Li4,4Si) and Ge (Li4,4Ge).
In accordance with an additional aspect of the invention, the binder is a polyvinyl fluoride and the organic carbonate is selected from the group comprising ethylene carbonate, dimethyl carbonate and diethyl carbonate.
The present invention also discloses a method for manufacturing of electrodes for a lithium battery cell, the method comprising steps of:
a) Mixing active materials with a binder into a binder solution, b) Adding an organic carbonate to generate slurry;
The process is also characterized by the fact that step d further may comprise a parallel step of recovery 4 where gases from the organic carbonate is collected for re-use. The collected organic carbonate can be condensed, filtered and cleaned before being used again.
In another implementation step e) comprises one or more sub-steps of:
i) rolling the electrode material, ii) baking the electrode material, and iii) finishing the electrode material for use in the lithium battery cell.
In accordance with another aspect of the available invention, the active materials are adjusted for one anode and one cathode respectively, and the active cathode material may be selected from a group comprising LiCo02, LiFePO4, LiMn204, LiNi02, Li2FePO4F, LiComNiii3Mni/302, and Li(LiaNiõMnyCoz) and the active anode material selected from a group comprising LiC6, Li4Ti5012, Si(Li4,4Si) and Ge(Li4,4Ge).
In accordance with an aspect from the available invention, then the binder is a polyvinylidene fluoride.
In another aspect of the present invention, the organic carbonate can be selected from the group comprising ethylene carbonate, diethyl carbonate and dimethyl carbonate.
In another aspect of the invention, a method for generating a lithium battery cell is provided, wherein the method at least comprises the steps of:
a) generating a slurry for coating of electrodes for use in lithium ion batteries, where the slurry comprises active materials, binder and an additional diluting agent (thinner)/organic carbonate(C), where the diluting agent/organic carbonate(C) consists of a component in an electrolyte material for a manufactured lithium battery cell, wherein, the above step a) is carried out at temperature above melting temperature of thinner/organic carbonate(C);
The present invention also relates to slurry comprising active material (A), binder (B) and organic carbonate (C) obtained by method as disclosed herein.
The present invention also relates to an electrode(s) for a lithium battery cell, obtained by the method as disclosed herein.
The present invention also relates to a lithium ion battery cell obtained by the method as disclosed herein.
Further aspects and characteristics of the available invention are brought forward by the belonging independent patent claims.
Detailed description of the invention In the following text, the available invention will be described along with support from the accompanying figure.
It shall be understood that according to the invention, the foil that is normally used as cathodes and anodes also may comprise materials similar to fabrics or more generally, any conductive conductor which is compatible with the methods according to the available invention.
First, there will be a description of general implementation of the invention, followed by examples of the methods that will be shown.
As indicated introductorily, there exists a desire to change the process of manufacturing the slurry for coating of battery electrodes for lithium batteries.
Lithium ion batteries normally consist of three active elements, namely anode, cathode and an electrolyte. As indicated above, it is the purpose of the available invention to find an alternative to the disadvantageous use of solvents for coating of the electrode foils.
The slurry that is applied to the electrode foils must have the correct body and viscosity so that the active layer that is applied to the electrodes will have a correct dry film thickness and homogeneity.
In order to be able to form a paste or thinly liquid slurry from binder, such as PVDF and powder in the form of active materials, a liquid needs to be added. By using a liquid which is entered as a component in the finished battery it is not necessary that the liquid is removed completely. In the event the liquid is removed completely, this component will still have to be added at a later stage. According to the execution of the available invention, a method for manufacturing of the slurry for coating of battery electrodes is provided, wherein the slurry,
In general, the process for manufacturing of slurry according to the available invention can be described with support from figure 1. Active materials A which will be constituent parts in the final slurry, will be mixed with a binder B in a first homogenization step 1.
In order to obtain correct viscosity and consistency of the slurry a solvent C is added. It is in accordance with the present invention that the solvent C represents a component of the final lithium ion battery cell.
After the homogenization step, the slurry attains the desired body/viscosity and the electrode material D can be coated with the slurry. The method for coating may be in the form of extruding, rolling or tape casting, or other suitable methods for coating known from the industry.
Step 3 in the method comprises evaporation of the thinner which was added to the homogenization process 1. The applied slurry will consequently change from being viscous slurry to become a more solid material.
In parallel with step 3, there may be an active recycling step 4 which recycles the thinner that evaporates.
The step 5 is the step following steps 3 and 4, and is a step where the electrode material with the applied coating is rolled.
The step 6 comprises baking of the rolled electrode. This baking will among other things, secure that the binder adheres sufficiently to the active electrode materials and to the electrode foil.
The final step 7 comprises further finishing of the lithium ion batteries.
It shall be understood that manufacturing according to the steps 1 to 7 may be run consecutively and continuously, so that when step 1 is finished and a batch from step 1 moves onto step 2, then new materials can be added to homogenization of step 1. The same is valid for all the following steps, so that a manufacturing process can run continuously.
= CA 02819391 2015-04-29 =
In this example, in accordance with the present invention, the materials that will be used in the manufacturing of a lithium ion battery cell will comprise the following.
The anode, that is the negative electrode, consists of a copper foil. This copper foil shall be coated with an active material, generally in the form of a graphite powder (LiC6). Further, other active materials such as titanate (Li4Ti5012), Si(Li4,4S1) or Ge(Li4,4Ge) can be used as active anode material. The graphite powder shall be applied to the copper foil. In order for such a coating process to be successful and to obtain a homogeneous surface then the graphite powder must be mixed with PVDF. The PVDF and the graphite powder must consequently be given a viscosity which is suitable for coating. To attain the required viscosity an organic carbonate, such as ethylene carbonate (EC) C is added and blended. This blending step corresponds to the homogenization step 1 according to the general process description. The mixture may be heated to a temperature above the melting point of the thinner/Ethylene Carbonate (C), i.e. the ingredient that was blended in order to give the right viscosity. The temperature may well be above the melting point of the thinner/EC and the temperature can be either above or below the melting point of the binder.
The cathode, i.e. the positive electrode consists of an aluminum foil. This aluminum foil shall be coated by an active material in the form of a lithium metal oxide. The lithium metal oxide shall be coated on the copper foil, so that such a coating process shall be successful and provides for a homogeneous surface. The lithium metal oxide A is mixed with PVDF. The PVDF and lithium metal oxide must consequently be given a viscosity suitable for coating.
Therefore, to attain the desired viscosity, an organic carbonate such as Ethylene Carbonate (EC) C is added and the mixture is blended. This step of the mixing corresponds with the homogenization step 1 according to the general process description The following steps for cathode and anode follow generally the same process as described in figure 1.
Another performance specification according to the available invention The instant invention is described with additional example as follows:
The anode, which is the positive electrode, consists of a copper foil. This copper foil shall typically be coated by an active material in the form of a graphite powder.
Thus the process preparing the anode is according to the description above.
The cathode, which is the positive electrode, consists of an aluminum foil.
This aluminum foil shall be coated by an active material in the form of a metal oxide such like one of Lithium cobalt oxide (LiCo02), a polyanion such like Lithium iron phosphate (LiFePO4) or a lithium manganese oxide (LiMn204). Further cathode materials are found in the not supplementary group i.e., LiNi02, Li2FePO4F, LiCo113Ni11302 and Li (LiaNixMnyCoz)02. For simplicity, the term metal oxide will be used in the following for these mentioned phosphates/
oxides.
The metal oxide shall be coated on the copper foil. In order for such a coating process to be successful and obtain a homogeneous surface, the metal oxide A must be mixed [1] with a binder B, for instance PVDF and the metal oxide must in addition be given a viscosity suitable for coating. Therefore, to attain the desired viscosity, an organic carbonate such as ethylene carbonate (EC) C or diethyl carbonate is added to the mixture and blended. This mixing step corresponds to the homogenization step [1] according to the general process description.
The following steps for cathode and anode will roughly follow the same process as described in figure 1.
It shall be understood that a number of binders and active raw materials can be combined, where the central issue is that the thinner/organic carbonate (C) shall be a component in the final battery.
It is therefore understood that, there is no need to remove the last remaining concentration of the thinner/organic carbonate (C), thus saving energy.
Following is the description of the electrolyte and the properties associated with the materials composing the parts of the electrolyte. The electrolyte in a normal battery essentially consists of organic carbonates such as EC (ethylene carbonate) or diethyl carbonate.
The EC which is most commonly used is a waxy material which melts at approximately 40 C and is then a liquid with low viscosity. EC is not poisonous. It is without smell and is only flammable at high temperatures (above 140 C).
According to an aspect of the invention, the desired viscosity of this slurry may be generated by mixing the binder B (such as PVDF), the powder A (active, materials) and molten EC C.
5 The amount of EC is adjusted according to the desired viscosity of the mixture.
This mixture is homogenized 1 vigorously at a temperature above the melting point of EC and at any temperature above or below the melting point of the binder (for example at approx.
180 C for PVDF). The particles with the binder will then because of the vigorous mixture be dispersed between all the particles in the mixture.
The consequent rolling 5 of the battery film will press the particles together and will improve the binding between the particles.
The EC- vapor which is formed by drying of the battery film can be condensed, filtered and reused in the process. EC is a harmless liquid with few health and environmental impacts.
The list of numerals and alphabetic representation is given below:
I:
A: Active materials, such as graphite and lithium oxide B: Binder, for example PVDF
C: Thinner according to the available invention, an electrolyte component such as organic carbonates D: Leading foil, such as aluminum foil, copper foil, aluminum canvas and copper canvas among others
Claims (12)
a) mixing active materials with a binder to obtain a mixture, and b) adding an organic carbonate to the mixture to generate the slurry, wherein the step (b) is carried out at temperature above the melting temperature of the organic carbonate and characterized in that the active material for anode is selected from the group consisting of Li4Ti5O12, Si(Li4.4Si), and Ge(Li4.4Ge).
a) mixing active materials with a binder to obtain a mixture, b) adding an organic carbonate to the mixture to generate a slurry, wherein the step (b) is carried out at temperature above the melting temperature of the organic carbonate and wherein the active material for cathode is selected from the group consisting of LiCoO2, LiFePO4, LiMn2O4, LiNiO2, Li2FePO4F, and LiCo1/3Ni1/3Mn1/3O2;
and the active material for anode is selected from the group consisting of Li4Ti5O12, Si(Li4.4Si), and Ge(Li4.4Ge);
c) coating electrode material with the slurry, d) drying the coating on the electrode material by drying the organic carbonate, and e) surface treatment of the slurry so that the electrode is prepared for use in the lithium battery cell;
wherein the step d) comprises a parallel recycling step, wherein the organic carbonate is collected for re-use.
i) rolling the electrode material;
ii) baking the electrode material; and iii) finishing the electrode material for use in the lithium battery cell.
a) manufacturing of electrodes by the method as claimed in claim 4, wherein the electrodes are an anode and a cathode, b) arranging the cathode and the anode in layers with lithium ion permeable membranes in between, c) arranging the cathode, the anode and the permeable membranes in a house with openings, and d) filling an electrolyte into the house, wherein the electrolyte comprises lithium containing salts and the organic carbonate.
wherein the active material for anode is selected from the group consisting of Li4Ti5O12, Si(Li4.4Si), and Ge(Li4.4Ge); wherein the binder is polyvinylidene fluoride;
and wherein the organic carbonate is selected from the group consisting of ethylene carbonate, dimethyl carbonate, and diethyl carbonate.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NO20101514 | 2010-10-28 | ||
| NO20101514A NO333181B1 (en) | 2010-10-28 | 2010-10-28 | Process for producing slurry for production of battery film |
| PCT/IB2011/054738 WO2012056389A1 (en) | 2010-10-28 | 2011-10-24 | Method for manufacturing of slurry for production of battery film |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2819391A1 CA2819391A1 (en) | 2012-05-03 |
| CA2819391C true CA2819391C (en) | 2017-07-18 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA2819391A Active CA2819391C (en) | 2010-10-28 | 2011-10-24 | Method for manufacturing of slurry for production of battery film |
Country Status (9)
| Country | Link |
|---|---|
| US (2) | US9324998B2 (en) |
| EP (1) | EP2633583B1 (en) |
| JP (1) | JP6158707B2 (en) |
| CN (1) | CN103460492A (en) |
| BR (1) | BR112013010447A2 (en) |
| CA (1) | CA2819391C (en) |
| NO (1) | NO333181B1 (en) |
| SG (1) | SG190071A1 (en) |
| WO (1) | WO2012056389A1 (en) |
Families Citing this family (9)
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| KR102295365B1 (en) | 2014-12-31 | 2021-08-31 | 삼성전자주식회사 | Composite anode active material, preparing method thereof, anode and lithium secondary battery comprising the same |
| JP6206439B2 (en) * | 2015-04-06 | 2017-10-04 | トヨタ自動車株式会社 | Method for producing non-aqueous electrolyte secondary battery |
| CN108630898A (en) * | 2017-03-20 | 2018-10-09 | 索尼公司 | The preparation method of lithium ion battery negative electrode, thus obtained cathode pole piece and the lithium ion battery comprising it |
| KR102837094B1 (en) * | 2020-05-08 | 2025-07-23 | 주식회사 엘지에너지솔루션 | Negative electrode, method for preparing the negative electrode, secondary battery, and method for preparing the secondary battery |
| EP4347540A4 (en) | 2021-05-25 | 2025-12-31 | ionobell Inc | SILICON MATERIAL AND MANUFACTURING PROCESS |
| US11799075B2 (en) | 2021-10-12 | 2023-10-24 | Ionobell, Inc. | Silicon battery and method for assembly |
| US11945726B2 (en) | 2021-12-13 | 2024-04-02 | Ionobell, Inc. | Porous silicon material and method of manufacture |
| WO2024010903A1 (en) | 2022-07-08 | 2024-01-11 | Ionobell, Inc. | Electrode slurry and method of manufacture |
| CN115458709B (en) * | 2022-09-22 | 2025-09-19 | 三一红象电池有限公司 | Nonaqueous electrode plate and preparation method thereof |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62213064A (en) * | 1986-03-14 | 1987-09-18 | Showa Denko Kk | Lithium-alloy negative electrode and its manufacture |
| JPH0367614A (en) | 1989-08-07 | 1991-03-22 | Bridgestone Corp | Tire vulcanizing jig in precuring method |
| JP2721467B2 (en) * | 1993-02-25 | 1998-03-04 | キヤノン株式会社 | Lithium battery material recovery method |
| JPH07105940A (en) * | 1993-10-01 | 1995-04-21 | Matsushita Electric Ind Co Ltd | Non-aqueous electrolyte battery |
| JPH09167614A (en) | 1995-12-15 | 1997-06-24 | Yuasa Corp | Manufacture of composite electrode |
| JPH11250892A (en) * | 1998-02-26 | 1999-09-17 | Yuasa Corp | Battery |
| JP4226704B2 (en) * | 1998-11-05 | 2009-02-18 | 株式会社クレハ | Non-aqueous electrochemical element electrode binder solution, electrode mixture, electrode and electrochemical element |
| DE19952335B4 (en) * | 1999-10-29 | 2007-03-29 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | In electrochemical components usable pasty mass, thus formed layers, films, laminations and rechargeable electrochemical cells and methods for producing the layers, films and laminations |
| US7491467B2 (en) * | 2002-12-17 | 2009-02-17 | Mitsubishi Chemical Corporation | Negative electrode for nonaqueous electrolyte secondary battery and nonaqueous electrolyte secondary battery using the same |
| JP4077432B2 (en) | 2003-07-07 | 2008-04-16 | Tdk株式会社 | Electrochemical element |
| DE10352063B4 (en) | 2003-11-07 | 2013-01-03 | Dilo Trading Ag | Lithium polymer cell, process for their preparation and lithium polymer battery system with it |
| CN1691375A (en) * | 2004-04-30 | 2005-11-02 | 中国电子科技集团公司第十八研究所 | A kind of manufacturing method of electrode containing auxiliary binder |
| KR100583672B1 (en) * | 2004-06-07 | 2006-05-26 | 한국전기연구원 | Manufacturing method of high power pole plate for lithium secondary battery |
| TWI338403B (en) * | 2005-09-29 | 2011-03-01 | Lg Chemical Ltd | Electrode with enhanced performance and electrochemical device comprising the same |
| JP2010064022A (en) * | 2008-09-11 | 2010-03-25 | Nissan Motor Co Ltd | Solvent recovery system and solvent recovery method |
| KR101578706B1 (en) * | 2008-12-05 | 2015-12-18 | 삼성에스디아이 주식회사 | Cathode and lithium battery employing it |
| TWI411149B (en) * | 2008-12-31 | 2013-10-01 | Ind Tech Res Inst | Lithium battery and fabrication method thereof |
| US9893377B2 (en) * | 2009-09-25 | 2018-02-13 | Kabushiki Kaisha Toshiba | Nonaqueous electrolyte battery, battery pack and vehicle |
-
2010
- 2010-10-28 NO NO20101514A patent/NO333181B1/en not_active IP Right Cessation
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2011
- 2011-10-24 CA CA2819391A patent/CA2819391C/en active Active
- 2011-10-24 CN CN2011800632082A patent/CN103460492A/en active Pending
- 2011-10-24 SG SG2013033139A patent/SG190071A1/en unknown
- 2011-10-24 US US13/882,501 patent/US9324998B2/en active Active
- 2011-10-24 BR BR112013010447A patent/BR112013010447A2/en not_active Application Discontinuation
- 2011-10-24 EP EP11793868.8A patent/EP2633583B1/en active Active
- 2011-10-24 JP JP2013535558A patent/JP6158707B2/en active Active
- 2011-10-24 WO PCT/IB2011/054738 patent/WO2012056389A1/en not_active Ceased
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Also Published As
| Publication number | Publication date |
|---|---|
| NO333181B1 (en) | 2013-03-25 |
| EP2633583B1 (en) | 2018-08-29 |
| WO2012056389A1 (en) | 2012-05-03 |
| US20160365568A1 (en) | 2016-12-15 |
| CA2819391A1 (en) | 2012-05-03 |
| JP2013545234A (en) | 2013-12-19 |
| US9324998B2 (en) | 2016-04-26 |
| SG190071A1 (en) | 2013-06-28 |
| BR112013010447A2 (en) | 2016-12-06 |
| JP6158707B2 (en) | 2017-07-05 |
| US10153482B2 (en) | 2018-12-11 |
| US20130219704A1 (en) | 2013-08-29 |
| EP2633583A1 (en) | 2013-09-04 |
| NO20101514A1 (en) | 2012-04-30 |
| CN103460492A (en) | 2013-12-18 |
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