WO2009012899A1 - Elektroden und lithium-ionen-zellen mit neuartigem elektrodenbinder - Google Patents

Elektroden und lithium-ionen-zellen mit neuartigem elektrodenbinder Download PDF

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Publication number
WO2009012899A1
WO2009012899A1 PCT/EP2008/005673 EP2008005673W WO2009012899A1 WO 2009012899 A1 WO2009012899 A1 WO 2009012899A1 EP 2008005673 W EP2008005673 W EP 2008005673W WO 2009012899 A1 WO2009012899 A1 WO 2009012899A1
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WO
WIPO (PCT)
Prior art keywords
electrode according
electrode
lithium
matrix
polysaccharide
Prior art date
Application number
PCT/EP2008/005673
Other languages
German (de)
English (en)
French (fr)
Inventor
Nikolaus Stefan Hochgatterer
Stefan Koller
Mario Rene Schweiger
Martin Winter
Calin Wurm
Arno Perner
Thomas Wöhrle
Original Assignee
Varta Microbattery Gmbh
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Varta Microbattery Gmbh filed Critical Varta Microbattery Gmbh
Priority to EP08784714A priority Critical patent/EP2179464B1/de
Priority to JP2010517292A priority patent/JP2010534392A/ja
Priority to ES08784714T priority patent/ES2378006T3/es
Priority to CN200880100231A priority patent/CN101796675A/zh
Priority to US12/668,916 priority patent/US9653733B2/en
Priority to AT08784714T priority patent/ATE538510T1/de
Publication of WO2009012899A1 publication Critical patent/WO2009012899A1/de

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Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/62Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
    • H01M4/621Binders
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00Secondary cells; Manufacture thereof
    • H01M10/05Accumulators with non-aqueous electrolyte
    • H01M10/052Li-accumulators
    • H01M10/0525Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodes; Lithium-ion batteries
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/36Selection of substances as active materials, active masses, active liquids
    • H01M4/48Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
    • H01M4/52Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron
    • H01M4/525Selection 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
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/62Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
    • H01M4/621Binders
    • H01M4/622Binders being polymers
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10Energy storage using batteries

Definitions

  • Electrodes and lithium-ion cells with novel electrode binder 5 are Electrodes and lithium-ion cells with novel electrode binder 5
  • the present invention relates to an electrode, in particular for a lithium-ion battery, a battery comprising at least one such electrode and a new use of a polysaccharide.
  • Galvanic elements such as lithium-ion cells typically have composite electrodes containing particles of electrochemically active ingredients, a binder and current collectors.
  • the binder ensures the mechanical stability of the electrode, in particular it is to ensure the contact of the particles with each other and with the current collector. Decontacting both between individual electrochemically active particles and between the particles and the current collector can occur, for example, due to gassing in the electrode as a result of electrolyte decomposition or due to the electrochemically induced volumetric dynamics of an electrode. Decontamination is often associated with creeping capacity losses, which can ultimately lead to uselessness of the affected electrode.
  • Binders based on fluorinated polymers and copolymers are known from the prior art, in particular based on polyvinylidene fluorides (PVdF) and polyvinylidene fluoride-hexafluoropropylene (PVdF-HFP). Electrodes with such binders are described, for example, in EP 1 261 048 and in US Pat. No. 5,296,318.
  • Electrodes with a binder based on styrene-butadiene rubber are known.
  • sodium carboxymethyl cellulose is used to adjust the viscosity.
  • the polymers or copolymers used as binders usually form a matrix in which the electrochemically active materials are finely dispersed.
  • electrochemically active materials such as, for example, graphite are generally completely insoluble in the polymers or copolymers mentioned. They do not enter into a firm bond with the binder matrix. Rather, a connection takes place physically, for example via adhesion forces, or mechanically. Capacitance losses as a result of decontacting are often measurable already after a few charge and discharge cycles with such electrodes.
  • the capacitive performance should decrease less as the age of the battery decreases, as is the case with known batteries.
  • An electrode according to the invention is particularly suitable for a lithium-ion battery.
  • a lithium-ion battery is a lithium-based electrochemical power source that is rechargeable unlike many conventional batteries.
  • Lithium ion batteries exist in various embodiments.
  • a further development is, for example, the lithium-polymer battery, in which in particular a polymer-based electrolyte is used.
  • An electrode according to the invention comprises a matrix based on at least one polysaccharide as well as particles of at least one electrochemically active material which are embedded in the matrix.
  • the electrode is essentially free of synthetic polymer compounds.
  • electrodes known from the prior art always have binders of synthetic polymers, such as the fluoropolymers mentioned, or the styrene-butadiene rubber known from EP 14 89 673.
  • binders of synthetic polymers such as the fluoropolymers mentioned, or the styrene-butadiene rubber known from EP 14 89 673.
  • binders can be completely replaced by a binder based on a biopolymer, namely on the basis of at least one polysaccharide.
  • an electrode according to the invention means that they are contained at most in very small amounts which are not sufficient per se to be able to perform a binder function, for example in amounts of less than 0.1% by weight (based on the solids content of the electrode.)
  • An electrode according to the invention is particularly preferably completely free of synthetic polymer compounds.
  • synthetic polymer compounds refers to polymer compounds which are not preparable by modification of natural polymers but are in particular fully synthetic Examples of synthetic polymer compounds in the context of the present application are in particular substituted and unsubstituted polyolefins or silicones.
  • the matrix of an electrode according to the invention which is based on at least one polysaccharide, forms a three-dimensional structure within which the electrochemically active particles are preferably distributed homogeneously.
  • matrix thus simply denotes a material in which particles of one or more further materials are embedded.
  • electrochemically active material in the present case is to be understood as meaning a material which is directly involved in the electrochemical processes in the electrode according to the invention, in particular a material which is capable of reversibly incorporating and displacing lithium ions.
  • an electrode according to the invention is characterized in that at least a part of the particles is connected to the matrix via covalent bonds.
  • covalent bond is to be understood as meaning, in particular, a chemical bond formed by a condensation reaction, particularly preferably a condensation reaction with elimination of water Embodiments functional groups that can undergo condensation reactions together (which will be discussed later).
  • the covalent bonding between the particles and the matrix results in a particularly strong and durable electrode structure that can withstand the internal mechanical stresses during charge and discharge processes excellently. This has a particularly advantageous effect on the life of an electrode according to the invention.
  • At least a portion of the particles comprise or at least partially consist of a carbon-based, lithium-intercalating material.
  • a carbon-based, lithium-intercalating material is preferably graphite.
  • Suitable non-carbon-based lithium-intercalating materials can also be used in the context of the present invention. These can be used both in combination with a carbon-based lithium intercalating material and alone.
  • Suitable carbon-based and non-carbon-based lithium intercalating materials are known in principle to the person skilled in the art and require no further explanation. It is preferred that at least some of the particles of the carbon-based, lithium-intercalating material have an average particle size between 1 ⁇ m and 50 ⁇ m, in particular between 4 ⁇ m and 30 ⁇ m. 5
  • At least a part of the particles comprises (or at least partly consists of) a metal and / or a metal which can form an alloy with lithium. This also applies in particular if the electrode according to the invention is a negative electrode.
  • At least a portion of the particles of the metal and / or the semimetal has an average particle size of less than 15 microns.
  • the metal and / or semimetal mentioned are in particular aluminum, silicon, antimony, tin, cobalt or a mixture thereof.
  • a tin / antimony or a tin-cobalt mixture is particularly preferred.
  • An electrode according to the invention can be based exclusively on the abovementioned carbon-based, lithium-intercalating material or on a metal and / or semimetal which can form an alloy with lithium.
  • an electrode according to the invention comprises both particles with a carbon-based, lithium-intercalating material and also particles which comprise a metal and / or semimetal.
  • the mixing ratio between the particles of the carbon-based, lithium-intercalating material and the particles comprising a metal and / or a semi-metal in these cases is particularly preferably between 1: 1 and 9: 1.
  • An electrode according to the invention has, in preferred embodiments, a particle comprising metal and / or a semimetal whose surface is at least partially oxidized. 5
  • Metallic and semi-metallic particles may have OH groups (hydroxyl groups) on their surface when the surface is at least partially oxidized. This case can occur in particular when the particles are brought into contact with water.
  • About sol-0 che OH groups can connect more substances with suitable functional groups in principle to the surface of the metallic or semi-metallic particles, in particular by a condensation reaction with dehydration. Again, this is the preferred way to form the above-mentioned covalent bonding of the particles to the matrix.
  • metallic or semi-metallic particles for example particles of a tin-antimony alloy or of silicon, can be introduced together with a matrix-forming polysaccharide in water or in an aqueous solution (a solids content of between 15 and 45% by weight is preferred).
  • surfactants may be added in minor amounts.
  • the particles can oxidize superficially and OH groups can form on the surface. With the matrix-forming polysaccharide can then take place the already mentioned several times condensation reaction.
  • an electrode according to the invention comprises particles which at least partially, preferably completely, consist of lithium cobalt oxide. This is the case in particular when the electrode according to the invention is a positive electrode. Since particles based on lithium cobalt oxide (Li
  • Polysaccharides which are suitable according to the invention are, in particular, polysaccharides modified with reactive groups, where the reactive groups are, in particular, functional groups which can enter into a condensation reaction with OH groups.
  • the reactive groups are particularly preferably hydroxyl, carboxyl, carboxylate, carbonyl, cyano, sulfonic acid, halocarbonyl, carbamoyl, thiol and / or amino groups.
  • the matrix of an electrode according to the invention consists at least partially of a polysaccharide having 50 to 10,000 monosaccharide units.
  • the matrix of an electrode according to the invention consists at least partially, preferably completely, of a cellulose derivative.
  • the cellulose derivative is present in a salt-like form, in particular as alkali metal, alkaline earth metal or ammonium salt.
  • Cellulose is an unbranched polysaccharide, which is usually formed from several 100 to 10,000 ß-D-glucose molecules, the latter linked via ß (1, 4) -glucosidic bonds.
  • ZeIIu- Loose is insoluble in water and in most organic solvents. Therefore, according to the invention, in particular water-soluble or at least water-swellable derivatives of cellulose are preferred.
  • the matrix is based on a cellulose derivative of the following formula:
  • R includes, in particular, at least one member selected from the group consisting of H, (CH 2) n OH, (CH 2) n O (CH 2) n CH 3, (CH 2) n CO (CH 2) n CH 3, (CH 2) n CHO, (CH 2 ) n COOH, (CHz) n N (COOMe) 2 , (CH 2 ) n CH 3 , (CH 2 ) n CN and (CH 2 ) n COOMe, where Me is Li 1 Na, K, Rb, Cs or Ca, n can assume values between 1 and 10 and at least 1 R is not equal to H.
  • An electrode according to the invention particularly preferably has a matrix which is based on at least one carboxyalkyl cellulose, preferably carboxymethyl cellulose and / or carboxyethyl cellulose, in particular carboxymethyl cellulose.
  • Carboxymethylcelluloses are known derivatives of cellulose in which at least a part of the OH groups of the cellulose is linked as ether with a carboxymethyl group.
  • carboxymethyl cellulose cellulose is usually converted in a first step in reactive alkali cellulose and then reacted with chloroacetic acid to carboxymethyl cellulose. The cellulose structure is retained in this procedure.
  • carboxyalkylcelluloses are generally relatively soluble in water.
  • An electrode according to the invention particularly preferably has a matrix based on sodium carboxyalkyl cellulose, in particular based on sodium carboxymethyl cellulose.
  • cellulose derivatives used according to the invention have a degree of substitution between 0.5 and 3, in particular between 0.8 and 1, 6.
  • the degree of substitution indicates the average number of modified hydroxyl groups per monosaccharide unit in a cellulose derivative. Since three hydroxyl groups are available for a reaction in the cellulose per monosaccharide unit, the maximum achievable degree of substitution in the present case is 3.
  • an electrode according to the invention has a conductivity improver.
  • Carbon black, graphite or a mixture of both are particularly suitable as conductivity improvers.
  • an electrode according to the invention usually has a current collector, in particular a metallic current collector. If the electrode according to the invention is a negative electrode, current collectors made of copper are preferred. In the case of a positive electrode, aluminum current collectors are preferred.
  • an electrode according to the invention has, as the at least one polysaccharide, a cellulose derivative, this is preferably present in a proportion of between 1% by weight and 15% by weight, in particular between 2% by weight and 8% by weight containing the electrode (in each case based on the solids content of the electrode).
  • an electrode according to the invention may comprise an organic electrolyte with a lithium-based conductive salt, for example lithium tetrafluoroborate.
  • a battery in particular a lithium-ion battery, which comprises at least one electrode according to the invention.
  • a battery according to the invention preferably has a single cell with at least one positive and at least one negative electrode, between which a separator is arranged.
  • a battery according to the invention has a plurality of individual cells.
  • Both the at least one positive and the at least one negative electrode can be electrodes according to the invention, ie electrodes having a matrix based on at least one polysaccharide.
  • a polysaccharide as binder for electrochemically active electrode materials is the subject of the present invention.
  • conventional binders can be completely replaced by binders based on at least one polysaccharide.
  • the at least one polysaccharide is used as binder in electrode compositions that are free of synthetic polymer compounds.
  • a negative electrode 8% by weight of sodium carboxymethylcellulose (Walocell® CRT10G) are introduced into water and brought to complete swelling.
  • the electrode paste thus obtained is knife-coated onto a copper foil with a thickness of 200 ⁇ m.
  • Negative electrodes prepared in this way are characterized in 3-electrode Swagelok-type cells with 6 fleece separators (Freudenberg 2190) and a CeIgard 2400 against lithium (as a positive electrode).
  • the electrolyte mixture used is a standard mixture of fluorinated conductive salts in organic solvents.
  • the discharge capacities C D of the tin-antimony-copper electrodes produced, based on the electrode active mass, are shown in FIG. 1 as a function of the number of cycles n.
  • the discharge, carried out at room temperature, is carried out with a current of the size 1C (950 mA / g).
  • Curve 1 characterizes the anode material made with the new binder system.
  • Curve 2 shows in comparison the capacity and its decrease with the number of cycles of a comparable anode, in which 8 wt .-% PVdF-HFP copolymer processed in NMP instead of the sodium carboxymethyl cellulose used in the invention were used. 5
  • silicon-graphite composite anodes 8% by weight sodium carboxymethylcellulose (Walocell® ® CRT2000PPA12) ser be entered and in water 0 brought to swell fully. Furthermore, 20% nanoparticulate silicon (Nanostructured and Amorphous Materials Los Alamos) and 5% carbon nanofibers (Electro vac AG, LHT-XT) are sequentially introduced and highly energetically dispersed. 5% conductive black (Super P) and 62% graphite (natural graphite, potato shaped) are finally introduced and dispersed.
  • the electrode paste thus obtained is knife-coated onto a copper foil (Schlenk) in the thickness of 200 ⁇ m.
  • the anodes are characterized in 3-electrode Swagelok-type cells with 6 fleece separators (Freudenberg 2190) and a Celgard 2400 against lithium.
  • the electrolyte mixture is a standard mixture of fluorinated conductive salts in organic solvents.
  • the discharge capacities C D of the silicon-graphite anodes produced in this way are shown relative to the electrode active mass as a function of the number of cycles n.
  • the discharge, carried out at room temperature, is carried out with a current of the size 1C (1250 mA / g).
  • Curve 1 shows the course of the discharge capacity of the anode with increasing number of cycles n produced with the new binder.
  • Curve 2 shows in comparison the capacity and its decrease with increasing number of cycles of an anode, in the production of which 4% by weight of styrene butadiene rubber (SBR) as binder and 4% Na-carboxymethylcellulose as dispersant were used.
  • SBR styrene butadiene rubber
  • Curve 3 describes the capacitive characteristic of a silicon-graphite composite anode in which 10 weight percent PVdF-HFP copolymer processed as a carrier polymer was used in NMP.
PCT/EP2008/005673 2007-07-25 2008-07-11 Elektroden und lithium-ionen-zellen mit neuartigem elektrodenbinder WO2009012899A1 (de)

Priority Applications (6)

Application Number Priority Date Filing Date Title
EP08784714A EP2179464B1 (de) 2007-07-25 2008-07-11 Elektroden und lithium-ionen-zellen mit neuartigem elektrodenbinder
JP2010517292A JP2010534392A (ja) 2007-07-25 2008-07-11 電極、および新規電極結合剤を備えるリチウムイオン電池
ES08784714T ES2378006T3 (es) 2007-07-25 2008-07-11 Electrodos y celdas de iones de litio con novedoso ligante de electrodos
CN200880100231A CN101796675A (zh) 2007-07-25 2008-07-11 具有新型电极粘合剂的电极和锂离子电池
US12/668,916 US9653733B2 (en) 2007-07-25 2008-07-11 Electrodes and lithium-ion cells with a novel electrode binder
AT08784714T ATE538510T1 (de) 2007-07-25 2008-07-11 Elektroden und lithium-ionen-zellen mit neuartigem elektrodenbinder

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE102007036653A DE102007036653A1 (de) 2007-07-25 2007-07-25 Elektroden und Lithium-Ionen-Zellen mit neuartigem Elektrodenbinder
DE102007036653.3 2007-07-25

Publications (1)

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WO2009012899A1 true WO2009012899A1 (de) 2009-01-29

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US (1) US9653733B2 (und)
EP (1) EP2179464B1 (und)
JP (1) JP2010534392A (und)
KR (1) KR20100034007A (und)
CN (1) CN101796675A (und)
AT (1) ATE538510T1 (und)
DE (1) DE102007036653A1 (und)
ES (1) ES2378006T3 (und)
WO (1) WO2009012899A1 (und)

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DE102010039416A1 (de) 2010-08-17 2012-02-23 Varta Micro Innovation Gmbh Flexible Batterieelektroden und ihre Herstellung
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ES2378006T3 (es) 2012-04-04
DE102007036653A1 (de) 2009-02-05
US20100239915A1 (en) 2010-09-23
US9653733B2 (en) 2017-05-16
EP2179464A1 (de) 2010-04-28
ATE538510T1 (de) 2012-01-15
CN101796675A (zh) 2010-08-04

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