EP2719002A1 - Elektrodenmaterialien für elektrische zellen - Google Patents
Elektrodenmaterialien für elektrische zellenInfo
- Publication number
- EP2719002A1 EP2719002A1 EP12797243.8A EP12797243A EP2719002A1 EP 2719002 A1 EP2719002 A1 EP 2719002A1 EP 12797243 A EP12797243 A EP 12797243A EP 2719002 A1 EP2719002 A1 EP 2719002A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- polymer
- formula
- units
- substituted
- ethylene glycol
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
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Classifications
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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
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/05—Accumulators with non-aqueous electrolyte
- H01M10/052—Li-accumulators
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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
- H01M4/13—Electrodes for accumulators with non-aqueous electrolyte, e.g. for lithium-accumulators; Processes of manufacture thereof
- H01M4/137—Electrodes based on electro-active polymers
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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
- H01M4/13—Electrodes for accumulators with non-aqueous electrolyte, e.g. for lithium-accumulators; Processes of manufacture thereof
- H01M4/139—Processes of manufacture
- H01M4/1399—Processes of manufacture of electrodes based on electro-active polymers
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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
- H01M4/60—Selection of substances as active materials, active masses, active liquids of organic compounds
- H01M4/602—Polymers
- H01M4/604—Polymers containing aliphatic main chain polymers
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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
- H01M4/62—Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
- H01M4/624—Electric conductive fillers
- H01M4/625—Carbon or graphite
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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
- H01M2220/00—Batteries for particular applications
- H01M2220/20—Batteries in motive systems, e.g. vehicle, ship, plane
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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
- H01M4/38—Selection of substances as active materials, active masses, active liquids of elements or alloys
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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
- H01M4/38—Selection of substances as active materials, active masses, active liquids of elements or alloys
- H01M4/381—Alkaline or alkaline earth metals elements
- H01M4/382—Lithium
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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
- H01M4/62—Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
- H01M4/621—Binders
- H01M4/622—Binders being 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
Definitions
- Electrode materials for electrical cells are Electrode materials for electrical cells
- the present invention relates to electrode materials for electrical cells comprising as component (A) at least one polymer containing polymer chains consisting of identical or different monomer units selected from the group consisting of substituted and unsubstituted vinyl units and substituted and unsubstituted C 2 -C 10 -alkylene glycol units, and containing at least one monomer unit -M1 - comprising at least one thiolate group -S ⁇ or at least one end of a disulfide or Polysulfidmaschine - (S) m-, wherein m is an integer from 2 to 8, and wherein the thiolate group or the one end of the disulphide or polysulphide bridge is - (S) m - in each case directly bonded to a carbon atom of the monomer unit -M1 -, and as component (B) carbon in a modification which has at least 60% sp 2 - comprises hybridized C atoms. Furthermore, the present invention relates to electrical cells containing the electrode material according
- Secondary batteries, accumulators, rechargeable batteries or "rechargeable batteries” are only a few embodiments for storing and using electrical energy after production because of their significantly better power density, they have recently deviated from the water-based secondary batteries and developed such batteries.
- conventional Li-ion batteries which have a carbon anode and a metal oxide-based cathode, are limited in their energy density New dimensions in energy density have been attributed to lithium In lithium-sulfur cells, sulfur in the sulfur cathode is reduced via polysulfide ions to S 2_ , which are oxidized again during the loading of the cell to form sulfur-sulfur bonds.
- the problem is the solubility of polysulfides, for example L12S4 and L12S6, which are soluble in the solvent and can migrate to the anode.
- the consequences can include: loss of capacity and deposition of electrically insulating material on the electrode.
- the migration of the polysulfide ions from cathode to anode can ultimately lead to a discharge of the affected cell and to cell death in the battery.
- This unwanted migration of polysulfide ions is also referred to in English as a "shuttle", a term also used in the context of the present invention as a shuttle
- This shuttle a term also used in the context of the present invention as a shuttle
- Liu describes the use of polyorganodisulfides as materials for solid redox polymerization electrodes (M. Liu et al, J. Electrochem.Soc, 1991, 138, 1896-1901, U.S. 5,162,175).
- the electrode is used in rechargeable cells together with polymeric electrolytes.
- the operation of the cell requires high temperatures of 80 to 130 ° C, and the specific capacities achieved are very low.
- an electrode material for an electric cell comprising (A) polymer containing polymer chains formed from identical or different monomer units selected from the group consisting of substituted and unsubstituted vinyl units and substituted and unsubstituted C 2 -C 10 -alkylene glycol units, and at least one monomer unit
- -M1 - containing at least one thiolate -S - or at least one end of a disulfide or Polysulfidmaschine - (S) m -, wherein m is an integer from 2 to 8, and wherein the thiolate or the one end of the disulfide - or polysulfide bridge - (S) m - each directly to a carbon atom of the monomer unit -M1 - is bound,
- the polymer contained in the electrode material according to the invention contains polymer chains which are formed from identical or different monomer units selected from the group consisting of substituted and unsubstituted vinyl units and substituted and unsubstituted C 2 -C 10 -alkylene glycol units and contain at least one monomer unit - M1 -, the at least one thiolate group -S ⁇ or at least one end of a disulfide or polysulfide bridge - (S) m - comprises, wherein m is an integer from 2 to 8, and wherein the thiolate group or one end of the disulfide or polysulfide bridge - ( S) m - each directly to a carbon atom of the monomer unit -M1 - is bound.
- this polymer is also called polymer (A) or component (A) for short.
- Polymer (A) preferably contains more than 50% by weight, preferably more than 80% by weight, in particular more than 95% by weight, of polymer chains described above which contain at least one monomer unit M 1 -.
- the polymer chains of the polymer contained in the electrode material of the present invention are formed of the same or different monomer units selected from the group consisting of substituted and unsubstituted vinyl units and substituted and unsubstituted C 2 -C 10 alkylene glycol units.
- polymer (A) may also be a mixture of two different polymers prepared separately from one another, which are then mixed intensively, for example with the aid of an extruder, and are generally referred to as polymer blends.
- Substituted and unsubstituted vinyl units in polymer chains or the olefinically unsaturated compounds which can be used for this purpose in a polymerization are generally known to the person skilled in the art.
- the vinyl unit -CH 2 -CHCl- derives from the monomer vinyl chloride or the vinyl unit -Ch -CHPh- from the monomer styrene.
- polymer chains with substituted and unsubstituted C 2 -C 10 -alkylene glycol units and the monomers customarily used for this purpose in a corresponding polymerization are likewise known to the person skilled in the art.
- the ethylene glycol unit -CH 2 -CH 2 -O- is derived from the monomer ethylene oxide
- the butylene glycol unit -CH 2 -CH 2 -CH 2 -CH 2 -O- is derived from the monomer tetrahydrofuran
- the substituted ethylene glycol unit is -CH 2 -CH (CH 2 Cl) - O- is derived from the monomer epichlorohydrin
- the substituted propylene glycol moiety - CH2-C (CH2Cl) 2 -CH2-0- is derived from the monomer bis-chloromethyl-oxacyclobutane.
- the polymer chains of the polymer (A) contain at least one monomer unit -M1 - comprising at least one thiolate group -S ⁇ or at least one end of a disulphide or polysulphide bridge - (S) m-, wherein m is an integer from 2 to 8, preferably from 2 to 4, in particular 2, and wherein the thiolate group or the one end of the disulfide or polysulfide bridge - (S) m - is in each case directly bonded to a carbon atom of the monomer unit -M1 -.
- the negative charge of the thiolate group -S ⁇ is preferably neutralized by a metal cation Met + .
- Met + is alkali metal cations, half equivalents of alkaline earth metal dications or one half equivalent of zinc dication, more preferably Li + , Na + , V2 Mg ++ or V2 Zn ++ , especially Li + .
- At least 60% preferably at least equal
- the monomer unit 80%, more preferably at least 95 to at most 100% of the monomer units from which the polymer chains of the polymer (A) are formed, the monomer unit
- the monomer unit -M1 - can be illustrated by the following examples, which are derived from vinyl units or C 2 -C 10 -alkylene glycol units:
- the monomer units -M1- with thiolate group could be polymerized directly into the polymer chain by polymerization of the corresponding monomers, wherein in the corresponding monomers the sulfur-containing group would preferably be used in a form capped with a protective group, following the polymerization would be removed.
- the sulfur-containing group would preferably be used in a form capped with a protective group, following the polymerization would be removed.
- substitution with suitable sulfur nucleophiles known to the person skilled in the art and possibly subsequent reactions may produce the monomer units M 1 - on an existing polymer chain.
- Monomers which can be converted into polymers and whose halogen atoms can be converted into the monomer units -M1 - by subsequent reactions of the finished polymer in so-called polymer-analogous reactions are, for example:
- the electrode material according to the invention is characterized in that in the polymer chains of the polymer (A) the monomer unit -M1 - represents a substituted vinyl unit of the formula (I) and / or the formula (II)
- the electrode material is characterized in that the second end of the di- or polysulfide bridge is - (S) m - part of a further monomer unit -M1 - which is either in the same polymer chain as the first monomer unit -M1 - in another polymer chain of the polymer (A).
- the electric cell electrode material of the present invention further contains carbon in a modification comprising at least 60% sp 2 -hybridized C atoms, preferably from 75% to 100% sp 2 -hybridized C atoms. In the context of the present invention, this carbon is also called carbon (B) or component (B) for short and is known as such.
- the carbon (B) is an electrically conductive modification of carbon.
- carbon (B) may be selected from graphite, carbon black, carbon nanotubes, graphene or mixtures of at least two of the foregoing.
- data in% refers to the total carbon (B) which, together with polymer (A), contained in the electrode material, including any impurities, and denote weight percent.
- carbon (B) is carbon black.
- Carbon black may, for example, be chosen from lampblack, furnace black, flame black, thermal black, acetylene black, carbon black and furnace carbon black.
- Carbon black may contain impurities, for example hydrocarbons, in particular aromatic hydrocarbons, or oxygen-containing compounds or oxygen-containing groups, for example OH groups.
- sulfur or iron-containing impurities in carbon black are possible.
- carbon (B) is partially oxidized carbon black.
- carbon (B) is carbon nanotubes.
- Carbon nanotubes carbon nanotubes, in short CNT or English carbon nanotubes), for example single-walled carbon nanotubes (SW CNT) and preferably multi-walled carbon nanotubes (MW CNT), are known per se , A process for their preparation and some properties are described, for example, by A. Jess et al. in Chemie Ingenieurtechnik 2006, 78, 94 - 100.
- carbon nanotubes have a diameter in the range of 0.4 to 50 nm, preferably 1 to 25 nm.
- carbon nanotubes have a length in the range of 10 nm to 1 mm, preferably 100 nm to 500 nm.
- Carbon nanotubes can be prepared by methods known per se.
- a volatile carbon-containing compound such as methane or carbon monoxide, acetylene or ethylene, or a mixture of volatile carbon-containing compounds such as synthesis gas in the presence of one or more reducing agents such as hydrogen and / or another gas such For example, decompose nitrogen.
- Another suitable gas mixture is a mixture of carbon monoxide with ethylene.
- Suitable decomposition temperatures are for example in the range of 400 to 1000 ° C, preferably 500 to 800 ° C.
- Suitable pressure conditions for the decomposition are, for example, in the range of atmospheric pressure to 100 bar, preferably up to 10 bar.
- Single- or multi-walled carbon nanotubes can be obtained, for example, by decomposition of carbon-containing compounds in the arc, in the presence or absence of a decomposition catalyst.
- the decomposition of volatile carbon-containing compounds or carbon-containing compounds in the presence of a decomposition catalyst for example Fe, Co or preferably Ni.
- graphene is understood as meaning almost ideal or ideally two-dimensional hexagonal carbon crystals, which are constructed analogously to individual graphite layers.
- carbon (B) is selected from graphite, graphene, activated carbon and especially carbon black.
- Carbon (B) may be present, for example, in particles having a diameter in the range of 0.1 to 100 ⁇ m, preferably 2 to 20 ⁇ m.
- the particle diameter means the average diameter of the secondary particles, determined as volume average.
- carbon (B), and especially carbon black has a BET surface area in the range of 20 to 1500 m 2 / g measured according to ISO 9277.
- At least two, for example two or three different types of carbon (B) are mixed.
- Different types of carbon (B) may differ, for example, in terms of particle diameter or BET surface area or level of contamination.
- carbon (B) is selected as a combination of two different carbon blacks.
- the electrode material according to the invention for an electrical cell contains, in addition to polymer (A) and carbon (B), optionally elemental sulfur. Elemental sulfur, also called sulfur (C) or component (C) in the context of the present invention, is known as such.
- the electrode material according to the invention contains
- the electrode material according to the invention is characterized in that the mass ratio between polymer (A) and elemental sulfur (C) is in the range of 1 to 100 to 100 to 1, preferably 1 to 10 to 10 to 1, especially 1 to 2 to 2 to 1.
- electrode material contains in the range from 20 to 80% by weight, preferably 30 to 70% by weight, of sulfur, determined by elemental analysis, the sulfur comprising both component (A) and component ( C).
- electrode material according to the invention contains in the range from 0.1 to 40% by weight of carbon (B), preferably from 1 to 30% by weight.
- This carbon can also be determined, for example, by elemental analysis, whereby it must be taken into account in the evaluation of the elemental analysis that carbon is also introduced into the electrode material according to the invention via polymer (A), and optionally further sources.
- the electrode material according to the invention for an electrical cell contains polymer (A) and carbon (B) optionally at least one further polymer as a binder, which is also referred to as binder (D) in the context of the present invention.
- Binder (D) is mainly used for the mechanical stabilization of inventive electrode material.
- binder (D) is selected from organic (co) polymers.
- suitable organic (co) polymers may be halogenated or halogen-free.
- PEO polyethylene oxide
- cellulose carboxymethylcellulose
- polyvinyl alcohol polyethylene
- polypropylene polytetrafluoroethylene
- polyacrylonitrile-methyl methacrylate copolymers polyethylene
- polypropylene polytetrafluoroethylene
- polyacrylonitrile-methyl methacrylate copolymers styrene-butadiene copolymers
- tetrafluoroethylene-hexafluoropropylene copolymers vinylidene fluoride-hexafluoropropylene copolymers (PVdF-HFP)
- Vinylidene fluoride-tetrafluoroethylene copolymers perfluoroalkyl vinyl ether copolymers, ethylene-tetrafluoroethylene copolymers, vinylidene fluoride-ch
- Suitable binders are in particular polyvinyl alcohol and halogenated (co) polymers, for example polyvinyl chloride or polyvinylidene chloride, in particular fluorinated (co) polymers such as polyvinyl fluoride and in particular polyvinylidene fluoride and polytetrafluoroethylene.
- the average molecular weight M w of binder (D) can be chosen within wide limits, suitable, for example, 20,000 g / mol to 1. 000,000 g / mol.
- the electrode material according to the invention contains in the range from 0.1 to 10% by weight of binder, preferably 1 to 8% by weight and particularly preferably 3 to 6% by weight, based on the total mass of the components (A ), (B), (C) and (D).
- Binder (D) can be incorporated by various methods into electrode material according to the invention. For example, it is possible to dissolve soluble binders (D) such as polyvinyl alcohol in a suitable solvent or solvent mixture, for example, water / isopropanol is suitable for polyvinyl alcohol, and to prepare a suspension with the other constituents of the electrode material. After application to a suitable substrate, the solvent or solvent mixture is removed, for example vaporized, and an electrode is obtained from the electrode material according to the invention.
- suitable solvent for polyvinylidene fluoride is NMP.
- binders (D) for example polytetrafluoroethylene or tetrafluoroethylene-hexafluoropropylene copolymers
- a suspension of particles of the relevant binder (D) and the other constituents of the electrode material is prepared and processed as described above Electrode.
- Inventive electrode materials are particularly suitable as or for the production of electrodes, in particular for the production of electrodes of lithium-containing batteries.
- the present invention relates to the use of electrode materials according to the invention as or for the production of electrodes for electrical cells.
- a further subject of the present invention are electrical cells containing at least one electrode which has been produced from or using at least one electrode material according to the invention.
- the respective electrode is the cathode.
- that electrode is referred to as the cathode, which has a reducing effect during unloading (working).
- electrode material according to the invention is processed into electrodes, for example in the form of endless belts, which are processed by the battery manufacturer.
- Electrodes produced from electrode material according to the invention may have, for example, thicknesses in the range from 20 to 500 ⁇ m, preferably 40 to 200 ⁇ m. They may be, for example, rod-shaped, in the form of round, elliptical or square columns or cuboidal or as flat electrodes.
- electrical cells according to the invention contain, in addition to electrode material according to the invention, at least one electrode which is metallic. magnesium, metallic aluminum, metallic zinc, metallic sodium or preferably metallic lithium.
- electrical cells according to the invention described above comprise, in addition to inventive electrode material, a liquid electrolyte which contains a lithium-containing electrolyte salt.
- electrical cells according to the invention contain, in addition to inventive electrode material and another electrode, in particular an electrode containing metallic lithium, at least one nonaqueous solvent which may be liquid or solid at room temperature, preferably liquid at room temperature , and is preferably selected from polymers, cyclic or non-cyclic ethers, cyclic or non-cyclic acetals, cyclic or non-cyclic organic carbonates and ionic liquids.
- a nonaqueous solvent which may be liquid or solid at room temperature, preferably liquid at room temperature , and is preferably selected from polymers, cyclic or non-cyclic ethers, cyclic or non-cyclic acetals, cyclic or non-cyclic organic carbonates and ionic liquids.
- suitable polymers are in particular polyalkylene glycols, preferably P0IV-C1-C4-alkylene glycols and in particular polyethylene glycols.
- Polyethylene glycols may contain up to 20 mol% of one or more C 1 -C 4 -alkylene glycols in copolymerized form.
- Polyalkylene glycols are preferably polyalkylene glycols double-capped with methyl or ethyl.
- the molecular weight M w of suitable polyalkylene glycols and especially of suitable polyethylene glycols may be at least 400 g / mol.
- the molecular weight M w of suitable polyalkylene glycols and in particular of suitable polyethylene glycols may be up to 5,000,000 g / mol, preferably up to 2,000,000 g / mol
- non-cyclic ethers are, for example, diisopropyl ether, di-n-butyl ether, 1, 2-dimethoxyethane, 1, 2-diethoxyethane, preference is 1, 2-dimethoxyethane.
- Suitable cyclic ethers are tetrahydrofuran and 1,4-dioxane.
- non-cyclic acetals are, for example, dimethoxymethane, diethoxymethane, 1,1-dimethoxyethane and 1,1-diethoxyethane.
- Suitable cyclic acetals are 1, 3-dioxane and in particular 1, 3-dioxolane.
- non-cyclic organic carbonates examples include dimethyl carbonate, ethyl methyl carbonate and diethyl carbonate.
- suitable cyclic organic carbonates are compounds of the general formulas (X) and (XI)
- R 1 , R 2 and R 3 may be identical or different and selected from hydrogen and C 1 -C 4 -alkyl, for example methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec. Butyl and tert-butyl, preferably R 2 and R 3 are not both tert-butyl.
- R 1 is methyl and R 2 and R 3 are each hydrogen or R 1 , R 2 and R 3 are each hydrogen.
- Another preferred cyclic organic carbonate is vinylene carbonate, formula (XII).
- the solvent or solvents are used in the so-called anhydrous state, i. with a water content in the range of 1 ppm to 0.1 wt .-%, determined for example by Karl Fischer titration.
- electrochemical cells according to the invention comprise one or more conductive salts, preference being given to lithium salts.
- suitable lithium salts are LiPF 6, LiBF 4, LiCI0 4, LiAsF 6, L1CF3SO3, LiC (C n F 2n + IS02) 3, lithium imides such as LiN (C n F 2n + IS02) 2, where n is an integer in the range 1-20 LiN (SO 2 F) 2, Li 2 SiFe, LiSbF 6, LiAICU, and salts of the general formula (C n F 2n + i SO 2) m X Li, where m is defined as follows:
- m 3 if X is chosen from carbon and silicon.
- Preferred conducting salts are selected from LiC (CF 3 SO 2 ) 3 , LiN (CF 3 SO 2 ) 2 , LiPF 6 , LiBF 4 ,
- electrochemical cells according to the invention contain one or more separators, by means of which the electrodes are mechanically separated.
- Suitable separators are polymer films, in particular porous polymer films, which are unreactive with respect to metallic lithium and to lithium sulfides and lithium polysulfides.
- Particularly suitable materials for separators are polyolefins, in particular film-shaped porous polyethylene and film-shaped porous polypropylene.
- Polyolefin separators particularly polyethylene or polypropylene, may have a porosity in the range of 35 to 45%. Suitable pore diameters are for example in the range from 30 to 500 nm.
- separators made of PET particles filled with inorganic particles may have a porosity in the range of 40 to 55%. Suitable pore diameters are for example in the range of 80 to 750 nm.
- Inventive electrical cells are characterized by particularly high capacity, high performance even after repeated charging and greatly delayed cell death.
- Electric cells according to the invention are very well suited for use in automobiles, aircraft, electric motor-driven two-wheeled vehicles, for example pedelecs, ships or stationary energy storage devices. Such uses are another object of the present invention
- Another object of the present invention is also a polymer containing polymer chains which are formed from substituted and / or unsubstituted, preferably substituted Ethylenglyco- leinRIC as monomer units, wherein more than 95% of these monomer units, up to 100%, of a monomer unit -M1 ', which represents a substituted ethylene glycol unit of the formula (III') and / or of the formula (IV),
- the polymer according to the invention consists of more than 50% by weight, preferably more than 80% by weight, in particular more than 95% by weight to not more than 100% by weight, of the above-described polymer chains which are built up to more than 95% to at most 100% of monomer units of the formula (III ') and / or of the formula (IV).
- the polymer according to the invention is outstandingly suitable as polymer (A) in the above-described electrode material for electric cells according to the invention.
- a further subject matter of the present invention is also a process for preparing a polymer comprising polymer chains which are formed from substituted and / or unsubstituted ethylene glycol units as monomer units, where more than 95% of these monomer units, up to 100%, of a monomer unit, M1 '-, which represents a substituted ethylene glycol unit of the formula (III') and / or the formula (IV), preferably of the formula (IV),
- the linear polyepichlorohydrins used in process step a), which have a molecular weight M w of 100,000 g / mol to 3,000,000 g / mol, are known to the person skilled in the art and can be purchased. Accordingly, the average degree of polymerisation o in formula (V) for these polymers ranges from about 1000 to about 33000.
- process step a) of the process according to the invention it is possible to use as strong aqueous protic acid, for example hydrochloric acid, sulfuric acid, hydrobromic acid or perchloric acid. Hydrochloric acid is particularly preferably used as the strong aqueous protic acid.
- the polar aprotic solvent which can be used in process step a) of the process according to the invention is, for example, dimethylformamide, N-methyl-2-pyrrolidone, dimethyl sulfoxide, diethyl carbonate or tetramethylurea. It is particularly preferred to use dimethylformamide as the polar aprotic solvent.
- the thiourea is usually used at least in stoichiometric amounts based on the number of chlorine atoms to be substituted.
- the ratio of thiourea to the chlorine atoms to be substituted is preferably at least 2 to 1, particularly preferably at least 4 to 1.
- the ratio of thiourea to the chlorine atoms to be substituted is not more than 10 to 1, preferably not more than 8 to 1, in particular not more than 6 to 1.
- Process step a) of the process according to the invention is carried out at a temperature of more than 100 ° C. and a pressure of more than 1 atm.
- process step a) of the process according to the invention is carried out at a temperature of not more than 250.degree.
- the reaction is carried out in a pressure vessel at a temperature between 140 and 160 ° C.
- the reaction time in process step a) usually depends on the reaction temperature and the desired conversion of the reaction. Preferably, the reaction is carried out for a period of 1 day to 5 days.
- process step b) optionally the polymer obtained in process step a) containing monomer units with isothiuronium salt groups of the formula (VI) with aqueous base in the presence of a phase transfer catalyst with elimination of urea and formation of a polymer containing substituted ethylene glycol units of formula (III ') reacted with Met equal to H.
- aqueous bases preference is given to using aqueous solutions of alkali metal hydroxides or alkaline earth metal hydroxides, in particular of alkali metal hydroxides.
- Phase transfer catalysts are generally known to the person skilled in the art.
- tetraalkylammonium salts in particular tetraalkylammonium halides, are preferably used as phase transfer catalysts.
- process step b) the polymer from process step a) is reacted with aqueous sodium hydroxide solution in the presence of catalytic amounts of tetrabutylammonium iodide.
- the reaction is preferably carried out in a temperature range from 50 to 100 ° C.
- the polymer obtained in process step b) is reacted with an oxidizing agent to form a polymer containing substituted ethylene glycol units of the formula (IV) where n is 1, in each case two ethylene glycol units of the formula (IV) having a disulfide bridge. S2-, wherein these two ethylene glycol units of the formula (IV) are either in the same polymer chain or in two different polymer chains.
- oxidizing agents for the oxidative coupling of two thiol groups -SH to a disulfide bridge -SS-, in principle all oxidizing agents known to those skilled in the art can be used.
- oxidizing agents are, for example, iodine, bromine, p-benzoquinone, iron (III) chloride or red blood lye salt.
- iodine in process step c) is particularly preferred.
- the polymer obtained in process step c) is optionally reacted with elemental sulfur to form a polysulfide-bridged polymer containing substituted ethylene glycol units of the formula (IV) wherein in each case two ethylene glycol units of the formula (IV) have a polysulfide bridge (S. ) n - (S) n -, where n + n is an integer from 3 to 8, and the two ethylene glycol units of formula (IV) are either in the same polymer chain or in two different polymer chains.
- the reaction of the polymer obtained in process step c) with elemental sulfur is preferably carried out at temperatures above the melting point of sulfur ( ⁇ -Se: 1 19.6 ° C.), more preferably in a temperature range from 150 to 170 ° C.
- the electrode material according to the invention allows the production of electrical cells with a high specific capacity, in particular with the addition of elemental sulfur (component (C)), while at the same time an increased life, especially at temperatures below 30 ° C, is achieved.
- component (C) elemental sulfur
- the invention is illustrated by the following, but not limiting examples of the invention.
- the resulting solid was filtered off and washed with water (200 ml), hydrochloric acid (2M, 100 ml), and water (200 ml).
- the hydrous solid was frozen at -30 ° C and dried for 48 h on the lyophile. It 5.3 g of a colorless powder could be isolated. The characterization was done by elemental analysis and ATR-IR.
- the precipitate was filtered off and washed with EtOH (100 mL), water (200 mL), hydrochloric acid (2 M, 100 mL) and water (200 mL).
- EtOH 100 mL
- hydrochloric acid 2 M, 100 mL
- water 200 mL
- the hydrous solid was frozen at -30 ° C and dried for 48 h on the lyophile. It was possible to isolate 2.5 g of a colorless solid (P1). The characterization was done by elemental analysis and ATR-IR.
- the mixture was transferred to a stainless steel grinding vessel and then a ball mill (Powertept 6 from Fritsch) was used, stirring for 30 min at 300 rpm with stainless steel balls. After dispersion, a very homogeneous ink with a creamy consistency was obtained. The ink was sprayed by airbrush on a vacuum table (temperature: 75 ° C) on aluminum foil (thickness: 30 ⁇ ). Nitrogen was used for spraying. A solids loading of 4 mg / cm 2 was achieved. Thereafter, the one-side coated aluminum foil was carefully laminated between two rubber rollers. It was chosen a small contact pressure, so that the coating remained porous. Thereafter, the unilaterally coated aluminum foil was thermally treated in a drying oven at a temperature of 40.degree.
- Electrochemical cells according to FIG. 1 were built for the electrochemical characterization of the electrode material according to the invention produced from the inventive polymer P1 and the cathode K1 produced therefrom.
- the following components were used in addition to the cathodes produced in II.
- Anode Li foil, 50 ⁇ thick,
- Electrolyte 8% by weight LiTFSI (LiN (S0 2 CF 3 ) 2 ), 46% by weight 1, 3-dioxolane and 46% by weight 1, 2-dimethoxyethane
- FIG. 1 shows the schematic structure of a disassembled electrochemical cell for testing electrode materials according to the invention.
- FIG. 1 The explanations in FIG. 1 mean:
- the electrochemical cell according to the invention showed a resting potential of 2.45 volts. During discharge (C / 5), the cell potential dropped to 2.2 to 2.3 volts (1st plateau) and then to 2.0 to 2.1 volts (2nd plateau). The cell was discharged to 1.8V and then charged. During charging, the cell potential increased to 2.2 volts and the cell was charged to reach 2.5 volts. This was followed by a one-hour charging step at 2.5 volts. Thereafter, the unloading process started again. The produced electrochemical cell according to the invention reached more than 30 cycles with very little capacity loss.
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Abstract
Description
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Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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EP12797243.8A EP2719002A4 (de) | 2011-06-09 | 2012-06-06 | Elektrodenmaterialien für elektrische zellen |
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EP11169298 | 2011-06-09 | ||
EP12797243.8A EP2719002A4 (de) | 2011-06-09 | 2012-06-06 | Elektrodenmaterialien für elektrische zellen |
PCT/IB2012/052831 WO2012168862A1 (de) | 2011-06-09 | 2012-06-06 | Elektrodenmaterialien für elektrische zellen |
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EP2719002A1 true EP2719002A1 (de) | 2014-04-16 |
EP2719002A4 EP2719002A4 (de) | 2015-03-18 |
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EP12797243.8A Withdrawn EP2719002A4 (de) | 2011-06-09 | 2012-06-06 | Elektrodenmaterialien für elektrische zellen |
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WO (1) | WO2012168862A1 (de) |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3594355A (en) * | 1969-10-29 | 1971-07-20 | Hercules Inc | Water-soluble isothiuronium salts of epihalohydrin polymers |
US6403255B1 (en) * | 1999-12-13 | 2002-06-11 | Bar Ilan University | Polyvinyl mercaptan redox material for cathodes in non-aqueous batteries |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
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US5162175A (en) | 1989-10-13 | 1992-11-10 | Visco Steven J | Cell for making secondary batteries |
JP3116451B2 (ja) * | 1991-09-24 | 2000-12-11 | 松下電器産業株式会社 | 可逆性電極 |
US6200704B1 (en) * | 1998-09-01 | 2001-03-13 | Polyplus Battery Company, Inc. | High capacity/high discharge rate rechargeable positive electrode |
US6652440B1 (en) * | 1999-05-04 | 2003-11-25 | Moltech Corporation | Electroactive polymers of high sulfur content for use in electrochemical cells |
JP4208451B2 (ja) * | 2001-10-16 | 2009-01-14 | 日立マクセル株式会社 | ポリ硫化カーボンおよびそれを用いた非水電解質電池 |
WO2007102705A1 (en) * | 2006-03-07 | 2007-09-13 | Hee Jung Kim | Anion receptor and electrolyte using the same |
-
2012
- 2012-06-06 WO PCT/IB2012/052831 patent/WO2012168862A1/de active Application Filing
- 2012-06-06 EP EP12797243.8A patent/EP2719002A4/de not_active Withdrawn
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3594355A (en) * | 1969-10-29 | 1971-07-20 | Hercules Inc | Water-soluble isothiuronium salts of epihalohydrin polymers |
US6403255B1 (en) * | 1999-12-13 | 2002-06-11 | Bar Ilan University | Polyvinyl mercaptan redox material for cathodes in non-aqueous batteries |
Non-Patent Citations (2)
Title |
---|
M. Okawara ET AL: "Chemical Modification of Polyvinyl Chloride and Related Polymers" In: "Modification of Polymers", 10. Juni 1980 (1980-06-10), AMERICAN CHEMICAL SOCIETY, WASHINGTON, D.C., XP055168339, ISBN: 978-0-84-120686-1 Bd. 121, Seiten 41-57, DOI: 10.1021/bk-1980-0121.ch004, * Seite 51 - Seite 56 * * |
See also references of WO2012168862A1 * |
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WO2012168862A1 (de) | 2012-12-13 |
EP2719002A4 (de) | 2015-03-18 |
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