WO2009081704A1 - リチウム電池正極用複合材料 - Google Patents
リチウム電池正極用複合材料 Download PDFInfo
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- WO2009081704A1 WO2009081704A1 PCT/JP2008/071958 JP2008071958W WO2009081704A1 WO 2009081704 A1 WO2009081704 A1 WO 2009081704A1 JP 2008071958 W JP2008071958 W JP 2008071958W WO 2009081704 A1 WO2009081704 A1 WO 2009081704A1
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- positive electrode
- lithium battery
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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
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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
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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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- 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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- 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
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M2004/021—Physical characteristics, e.g. porosity, surface area
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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
- H01M2004/026—Electrodes composed of, or comprising, active material characterised by the polarity
- H01M2004/028—Positive electrodes
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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
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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
- the present invention relates to a composite material for a lithium battery positive electrode composed of composite particles containing positive electrode active material particles and fibrous carbon, a method for producing the same, and a positive electrode and a battery using the lithium battery positive electrode composite material.
- a battery is indispensable as an auxiliary power source, and a high output battery capable of following the sudden start and rapid acceleration of an automobile is desired.
- a battery having a high energy density is desired from the viewpoint of weight load on the vehicle and improvement in fuel consumption. From such a background, a lithium ion secondary battery that has the highest energy density among the secondary batteries and can exhibit high output is promising.
- an electrode is composed of a positive electrode including a lithium ion-containing oxide and a negative electrode including a carbon substance.
- a positive electrode since the conductivity of the lithium ion-containing oxide (positive electrode active material) itself is low, a conductive material such as carbon black or carbon fiber is added to improve the conductivity.
- VGCF registered trademark
- carbon nanotubes having a fiber diameter of nano-order by a gas phase method have been developed for carbon fibers, and application to battery applications is being studied.
- Patent Document 1 discloses an example in which a positive electrode is produced by applying a paste formed by mixing a positive electrode active material, carbon nanotubes, graphite and a binder.
- Patent Document 2 a spherical positive electrode active material having a particle size of 5 to 30 ⁇ m and a carbon nanofiber are mixed with a centrifugal ball mill while applying mechanically strong shearing force, and the carbon nanofiber is cut and adhered to the active material surface. Attempts have been made.
- Patent Document 3 discloses a composite for a lithium battery positive electrode in which a positive electrode active material obtained by mixing and firing a transition metal compound and a lithium compound and a conductive auxiliary agent such as carbon powder are spray-dried to form a composite. A method for manufacturing the material is disclosed.
- the present invention provides a lithium battery excellent in high-speed discharge characteristics, has a sufficiently secured Li diffusion path, and has high conductivity, a lithium battery positive electrode composite material, a method for producing the same, and the lithium battery positive electrode composite material A positive electrode and a battery are provided.
- the present inventors perform spray granulation using a slurry in which positive electrode active material particles and fibrous carbon are sufficiently dispersed in a solvent, whereby the positive electrode active material particles are held by the fibrous carbon. Granules were obtained, and this granulated product was found to be a composite material for positive electrodes excellent in high-speed discharge characteristics, and the present invention was completed.
- the composite material for a lithium battery positive electrode of the present invention is a composite material for a lithium battery positive electrode composed of composite particles containing positive electrode active material particles and fibrous carbon, and the composite particles include the positive electrode active material particles.
- the composite particles include the positive electrode active material particles.
- this invention relates to the positive electrode and battery using the composite material for lithium battery positive electrodes of the said invention.
- the method for producing a composite material for a lithium battery positive electrode of the present invention is a method for producing a composite material for a lithium battery positive electrode composed of composite particles containing positive electrode active material particles and fibrous carbon, Step 1 for obtaining a slurry containing the positive electrode active material particles and the fibrous carbon in a dispersed state, and spray granulation using the slurry obtained in the step 1, and the positive electrode active material particles and the fibrous carbon Is a method for producing a composite material for a lithium battery positive electrode.
- the lithium battery positive electrode composite material of the present invention (hereinafter sometimes simply referred to as “positive electrode composite material”) is a lithium battery positive electrode composite material composed of composite particles including positive electrode active material particles and fibrous carbon.
- the positive electrode active material particles are a composite material for a lithium battery positive electrode in which the fibrous carbon is held.
- the positive electrode active material particles are held by fibrous carbon refers to a state in which the positive electrode active material particles contained in the composite particles are held by the fibrous carbon and the shape of the composite particles is maintained. This can be confirmed by the method described later.
- the composite material for positive electrode of the present invention since the positive electrode active material particles are held by fibrous carbon, a conductive network is constructed in all the positive electrode active material particles, and the composite material for positive electrodes has very high conductivity. Can be provided. In addition, since a fine space is easily formed by the entanglement of fibrous carbon, lithium ions can be smoothly diffused through the gap, so that it is considered that a positive electrode composite material excellent in high-speed discharge can be provided. Furthermore, when the net made of fibrous carbon wraps the positive electrode active material, the net is rich in flexibility, so that it is possible to suppress the spherical structure from being crushed and collapsed by the press when manufacturing the electrode. . For this reason, the composite material for positive electrode according to the present invention can reduce the internal resistance of the battery as compared with the conventional one, and thus it is considered that a lithium battery excellent in high-speed discharge characteristics can be provided.
- the composite particle of the composite material for a lithium battery positive electrode of the present invention preferably has a form in which at least a part of fibrous carbon is present in the gap between the positive electrode active material particles, and a part of the fibrous carbon is positive electrode active material particle. More preferably, the carbon atoms are present in the gaps and have a form in which the fibrous carbon wraps the positive electrode active material particles in a network. Such a form can be confirmed by observation with a scanning electron microscope, as shown in Examples described later.
- any conventionally known material can be used as the material of the positive electrode active material particles.
- a Li / Mn composite oxide such as LiMn 2 O 4
- a Li / Co composite oxide such as LiCoO 2 , LiNiO 2, etc. of Li ⁇ Ni-based composite oxide
- Li ⁇ Fe-based composite oxides such as LiFeO 2, Li x CoO 2, Li x NiO 2, MnO 2, LiMnO 2, Li x Mn 2 O 4, Li x Mn 2-y O 4 , ⁇ -V 2 O 5 , TiS 2 and the like can be mentioned.
- lithium manganate such as LiMn 2 O 4
- lithium cobaltate such as LiCoO 2
- lithium nickelate such as LiNiO 2
- LiMn 2 O More preferred is lithium manganate such as 4 .
- the average agglomerated particle size of the positive electrode active material particles is preferably 0.1 ⁇ m or more, more preferably 0.3 ⁇ m or more, and further preferably 0.5 ⁇ m, from the viewpoints of safety and stability of the positive electrode active material and cycle characteristics.
- the thickness is preferably 10 ⁇ m or less, more preferably 5 ⁇ m or less, and still more preferably 2 ⁇ m or less.
- the average aggregate particle diameter of the positive electrode active material particles is preferably 0.1 to 10 ⁇ m, more preferably 0.3 to 5 ⁇ m, and even more preferably 0.5 to 2 ⁇ m.
- the positive electrode active material is held by the fibrous carbon while the fibrous carbons are intertwined.
- the fibrous carbon has a small fiber diameter and a long fiber length.
- the aspect ratio (L / W) of the fiber diameter (W) to the fiber length (L) of the fibrous carbon is preferably 50 or more, more preferably 100 or more, and still more preferably 200 or more.
- the aspect ratio (L / W) is preferably 50 to 20000, more preferably 100 to 5000, and still more preferably 200 to 1000.
- the fibrous carbon has a structure that is easily entangled, and the fiber length of the fibrous carbon is preferably 50 nm or more, more preferably 500 nm or more, and further preferably 1 ⁇ m or more.
- the fiber length of the fibrous carbon is preferably 50 ⁇ m or less, more preferably 30 ⁇ m or less, and even more preferably 10 ⁇ m or less. It is.
- the fiber length of the fibrous carbon is preferably 50 nm to 50 ⁇ m, more preferably 500 nm to 30 ⁇ m, and even more preferably 1 ⁇ m to 10 ⁇ m.
- the ratio of the fiber carbon fiber length to the average aggregate particle size (active material particle size) of the positive electrode active material particles (fiber length of the fibrous carbon / active material particle size) holds the positive electrode active material in the fibrous carbon. In view of the above, it is preferably 1 or more, more preferably 2 or more, and still more preferably 3 or more.
- the ratio between the fiber length of the fibrous carbon and the active material particle size is preferably 500 or less, more preferably 100 or less, and still more preferably 20 or less. Taking these viewpoints together, the ratio of the fibrous carbon fiber length to the active material particle size is preferably 1 to 500, more preferably 2 to 100, and even more preferably 3 to 20.
- the fibrous carbon has a structure that is easily entangled, and from the viewpoint of establishing a conductive path by making more contact with the surface of the positive electrode active material, the fiber diameter of the fibrous carbon is 1 to 1000 nm. Preferably, it is 1 to 500 nm, more preferably 1 to 100 nm, still more preferably 1 to 50 nm.
- the fibrous carbon it is easy to form the above-mentioned preferred aspect ratio, fiber length, and fiber diameter, and a granulated product in which the positive electrode active material particles are held by the fibrous carbon is easily obtained by spray granulation (described later). From the viewpoint, it is possible to use fibrous carbon made of a polymer represented by polyacrylonitrile (PAN), and pitch-based fibrous carbon made of pitch.
- PAN polyacrylonitrile
- carbon nanotubes graphite sheet, ie graphene sheet
- a cylinder Merists Engineering Volume I, P651, Fuji Techno System Co., Ltd.
- VGCF vapor-grown fibrous carbon
- hydrocarbon gas as a raw material : Registered carbon
- arc discharge method laser evaporation method
- chemical vapor deposition method etc.
- carbon nanotubes is preferably used.
- fibrous carbon having a small fiber diameter is preferable, and VGCF and carbon nanotubes are preferably used.
- carbon nanotubes are preferably used.
- the carbon nanotube is, for example, an arc discharge method in which a graphite electrode is evaporated by arc discharge under an atmospheric gas such as He, Ar, CH 4 , or H 2 , and graphite containing a metal catalyst such as Ni, Co, Y, or Fe.
- An arc discharge method in which electrodes are evaporated by arc discharge, a YAG laser is applied to graphite mixed with a metal catalyst such as Ni—Co, Pd—Rd, and the laser is sent to an electric furnace heated to about 1200 ° C. with an Ar air stream.
- the aspect ratio of the carbon nanotube for example, the smaller the concentration ratio of the hydrocarbon (benzene or the like) and the atmospheric gas such as hydrogen gas, the smaller the diameter of the generated carbon nanotube and the larger the aspect ratio.
- the shorter the reaction time the thinner the carbon nanotubes that are produced, and the higher the aspect ratio.
- a carbon material that assists conductivity may be blended.
- a carbon material include graphite and carbon black. Among these, it is preferable to use carbon black.
- Carbon black is produced by any of the following methods: thermal black method, decomposition method such as acetylene black method, channel black method, gas furnace black method, oil furnace black method, pine smoke method, lamp black method, etc.
- thermal black method decomposition method such as acetylene black method, channel black method, gas furnace black method, oil furnace black method, pine smoke method, lamp black method, etc.
- furnace black and acetylene black are preferably used from the viewpoint of conductivity. These may be used alone or in combination of two or more.
- DBP absorption of carbon black from the viewpoint of suitably assist the conductivity of the fibrous carbon is preferably 40 ⁇ 300cm 3 / 100g, and more preferably 80 ⁇ 200cm 3 / 100g.
- a carbon material other than fibrous carbon such a carbon material may be added to a dispersion of fibrous carbon and used to be combined with the positive electrode active material particles together with the fibrous carbon.
- particles obtained by spray granulation from a dispersion of fibrous carbon and a positive electrode active material and a carbon material may be mixed and used for the purpose of improving the conductivity between the granulated products.
- the blending amount of the carbon material other than fibrous carbon is preferably 0 to 20 parts by weight, more preferably 100 parts by weight with respect to 100 parts by weight of the positive electrode active material, from the viewpoint of maintaining the shape of the granulated product while assisting conductivity.
- the amount is 0 to 10 parts by weight, more preferably 0 to 5 parts by weight.
- the total blending amount of the carbon material is preferably based on 100 parts by weight of the positive electrode active material from the viewpoint of reducing the volume resistance of the positive electrode composite material. It is 0.02 parts by weight or more, more preferably 0.1 parts by weight or more, and further preferably 0.5 parts by weight or more. Moreover, from a viewpoint of raising the energy density of the composite material for positive electrodes, Preferably it is 30 weight part or less, More preferably, it is 20 weight part or less, More preferably, it is 10 weight part or less. Taking these viewpoints together, the total amount of fibrous carbon and carbon material other than fibrous carbon is preferably 0.02 to 30 parts by weight, more preferably 0.1 to 20 parts by weight, and 0.5 to 10 parts. Part by weight is more preferred.
- the volume resistance of the positive electrode composite material of the present invention is preferably 0 to 3 ⁇ ⁇ cm, more preferably 0 to 2 ⁇ ⁇ cm, further preferably 0 to 1.5 ⁇ ⁇ cm, from the viewpoint of imparting sufficient conductivity in the positive electrode. preferable.
- the composite material for positive electrode of the present invention micropores are easily formed due to the gap between the portions where the fibrous carbon is entangled and the gap between the positive electrode active materials.
- the total pore volume of 0.01 to 1 ⁇ m is preferably 0.3 ml / g or more and more preferably 0.4 ml / g or more from the viewpoint of smooth movement of Li. .
- the total pore volume of 0.01 to 1 ⁇ m is preferably 0.8 ml / g or less, and more preferably 0.6 ml / g or less.
- the manufacturing method of the composite material for a lithium battery positive electrode of the present invention will be described.
- the manufacturing method of the composite material for lithium battery positive electrodes of this invention is a suitable method for manufacturing the composite material for lithium battery positive electrodes of this invention mentioned above, it abbreviate
- the method for producing a composite material for a lithium battery positive electrode of the present invention is a method for producing a composite material for a lithium battery positive electrode composed of composite particles containing positive electrode active material particles and fibrous carbon.
- Step 2 is included.
- a slurry is obtained that contains positive electrode active material particles and fibrous carbon dispersed in a solvent.
- the fibrous carbon in which the fibers are intertwined and aggregated in the form of a thread ball is dispersed in a solvent to a dispersion state as described later (preferably dispersed using a dispersant).
- a slurry in which fibrous carbon and positive electrode active material particles are uniformly mixed is formed and spray-dried to construct spherical composite particles having the positive electrode active material and the fibrous carbon. It is preferable to do so.
- fibrous carbon dispersed in the positive electrode active material is entangled, so that the positive electrode active material in the vicinity is preferably held by the fibrous carbon, and is held in an encapsulated state to be spherical particles More preferably, is formed.
- the fibrous carbon the same carbon fibers as those in the above-described composite material for a lithium battery positive electrode of the present invention can be used.
- VGCF and carbon nanotubes are preferably used, and carbon nanotubes are more preferable.
- the amount of fibrous carbon added in the slurry is preferably 0.01 parts by weight or more, more preferably 0.1 parts by weight with respect to 100 parts by weight of the positive electrode active material. Above, more preferably 0.5 parts by weight or more. Further, from the viewpoint of coverage on the surface of the positive electrode active material, it is preferably 15 parts by weight or less, more preferably 10 parts by weight or less, and still more preferably 5 parts by weight or less. Taking these viewpoints together, the amount of fibrous carbon added to the slurry is preferably 0.01 to 15 parts by weight, more preferably 0.1 to 10 parts by weight, and even more preferably 0.5 to 5 parts by weight.
- the positive electrode composite material is produced mainly by two steps, preferably three steps.
- a slurry containing positive electrode active material particles and fibrous carbon dispersed in a solvent is obtained.
- the state in which the positive electrode active material particles and the fibrous carbon are dispersed means that when the slurry is sampled and diluted to a predetermined concentration and the average particle size is measured with a particle size distribution measuring device without delay, the average particle size is measured.
- the positive electrode active material particles and the fibrous carbon are dispersed in a state in which the fibrous carbon is dispersed in a solvent using a dispersant and then the positive electrode active material, and in some cases other than the fibrous carbon.
- An example is a method of irradiating ultrasonic waves by adding the carbon material.
- Step 2 spray granulation is performed using the slurry obtained in Step 1 to obtain a granulated product containing positive electrode active material particles and fibrous carbon.
- the slurry is sprayed to generate spherical droplets, and then the solvent is evaporated by heat and dried to form a spherical granulated powder, so-called spray granulation is performed.
- Step 2 or after Step 2 it is preferable to obtain a composite particle by removing the dispersant from the granulated product as [Step 3] which is an optional step.
- a step of mixing a carbon material other than fibrous carbon may be added.
- N-methyl-2-pyrrolidone NMP, boiling point 202 ° C.
- dimethylformamide DMF, boiling point 153 ° C.
- dimethylacetamide Boiling point 165 ° C.
- water Boiling point 100 ° C.
- Methyl ethyl ketone Boiling point 79.5 ° C.
- tetrahydrofuran Boiling point 66 ° C.
- acetone boiling point 56.3 ° C.
- ethanol Boiling point 78.3 ° C.
- ethyl acetate Boiling point 76.8 ° C.
- Water is preferably used from the viewpoint of cost and ease of dispersion of fibrous carbon.
- the amount of the solvent used in step 1 is 60 with respect to 100 parts by weight of the positive electrode active material from the viewpoint of sufficiently dispersing the fibrous carbon and setting the viscosity to be sufficient for spray granulation which is step 2. It is preferably at least 100 parts by weight, more preferably at least 200 parts by weight. Moreover, from a viewpoint of productivity, 3000 weight part or less is preferable, 2000 weight part or less is more preferable, 1500 weight part or less is still more preferable.
- a dispersant can be used, and as the dispersant used in that case, an anionic, nonionic or cationic surfactant, or a polymer dispersant can be used.
- Fibrous carbon is a fine carbon fiber having a diameter of 1000 nm or less, and has a structure in which a network of carbon hexagonal mesh surfaces extends in a cylindrical shape.
- a dispersant having a good structure and affinity those having an aromatic functional group similar in size and shape to the carbon hexagonal network surface, and having an alicyclic compound as a functional group unit
- the dispersant is preferable because it has a property of being easily adsorbed on fibrous carbon. That is, the dispersant to be used preferably has a functional group containing an aromatic ring and / or an aliphatic ring.
- polymer dispersant a polycarboxylic acid polymer dispersant having a plurality of carboxyl groups in the molecule and a polyamine polymer dispersant having a plurality of amino groups in the molecule
- a polymer dispersant having a plurality of amide groups in the molecule and a polymer dispersant containing a plurality of polycyclic aromatic compounds in the molecule are preferred.
- polycarboxylic acid polymer dispersant examples include poly (meth) acrylic acid and its derivatives.
- the derivative include a copolymer of (meth) acrylic acid and (meth) acrylic acid ester, a copolymer of (meth) acrylic acid and maleic anhydride, and an amidated or esterified product thereof.
- examples thereof include a copolymer of (meth) acrylic acid and maleic acid, and a comb polymer having a (meth) acrylic acid unit.
- (meth) acrylic acid refers to acrylic acid or methacrylic acid.
- polyamine polymer dispersant examples include polyalkyleneamine and derivatives thereof, polyallylamine and derivatives thereof, polydiallylamine and derivatives thereof, poly N, N-dimethylaminoethyl methacrylate and derivatives thereof, and polyesters to be grafted onto the above polyamines.
- Type polymer and the like examples include polyalkyleneamine and derivatives thereof, polyallylamine and derivatives thereof, polydiallylamine and derivatives thereof, poly N, N-dimethylaminoethyl methacrylate and derivatives thereof, and polyesters to be grafted onto the above polyamines.
- Type polymer and the like examples include polyalkyleneamine and derivatives thereof, polyallylamine and derivatives thereof, polydiallylamine and derivatives thereof, poly N, N-dimethylaminoethyl methacrylate and derivatives thereof, and polyesters to be grafted onto the above polyamines.
- Type polymer and the like examples include polyalkyleneamine and derivatives thereof, poly
- polymer dispersant having a plurality of amide groups in the molecule examples include polyamides obtained by condensation reaction and derivatives thereof, polyvinylpyrrolidone and derivatives thereof, poly N, N-dimethylacrylamide and derivatives thereof, and polyesters and derivatives thereof.
- examples thereof include a comb-type polymer grafted with polyalkylene glycol.
- polymer dispersant containing a polycyclic aromatic compound examples include copolymers of various monomers with vinyl monomers having a pyrene or quinacridone skeleton.
- dispersants can be used alone or in admixture of two or more dispersants.
- a preferable addition amount is 0.05 to 20% by weight, more preferably 0.05 to 10% by weight with respect to the slurry from the viewpoint of lowering the slurry viscosity while suitably dispersing the slurry. %.
- the dispersant remains in the composite material for positive electrode of the present invention, it itself becomes a resistance component, which may hinder the high-speed discharge performance of the battery. Accordingly, it is preferable to remove the dispersant as in Step 3 described in detail later.
- the removal method a method of removing the dispersant by washing and a method of decomposing by the heat treatment are mainly used. From such a viewpoint, it is preferable to use a surfactant as a dispersant that is easy to wash.
- a nonionic surfactant is more preferable from the viewpoint that it can be completely decomposed by heat treatment and can be vaporized without leaving counter ions.
- the blending amount of the dispersant in step 1 is preferably 1 part by weight or more, more preferably 5 parts by weight or more, and more preferably 10 parts by weight or more with respect to 100 parts by weight of the fibrous carbon. preferable. Further, from the viewpoint of reducing the load in the dispersant removing step, which is step 3, it is preferably 200 parts by weight or less, more preferably 150 parts by weight or less and even more preferably 100 parts by weight or less. Taking these viewpoints together, the blending amount of the dispersant is preferably 1 to 200 parts by weight, more preferably 5 to 150 parts by weight, and still more preferably 10 to 100 parts by weight.
- fibrous carbon such as carbon nanofibers is generally aggregated in the form of yarn balls, but it is preferable to disintegrate mechanically to some extent and disaggregate before dispersing it with a dispersant.
- a dry pulverizer specifically, an impact pulverizer such as a rotor speed mill and a hammer mill, a dry rolling ball mill, a dry vibration ball mill, a dry planetary mill
- a dry medium pulverizer such as a medium stirring mill
- an airflow pulverizer such as a jet mill
- a method using an impact pulverizer such as a rotor speed mill or a hammer mill is preferable from the viewpoint of appropriate pulverization.
- step 1 it is preferable to disperse the fibrous carbon in a solvent using a dispersant.
- the dispersant is added to the slurry, or before or after the addition, preferably after. It is more preferable to forcibly disperse using a disperser.
- the disperser include an ultrasonic disperser, a stirring disperser, a high-speed rotary shear disperser, a mill disperser, a high-pressure jet disperser, and the like. Sonic dispersers and high-pressure jet dispersers are preferably used.
- the fibrous carbon is dispersed in the solvent by the step 1, and the average aggregate particle diameter of the fibrous carbon at that time is preferably 0.1 to 40 ⁇ m from the viewpoint of loosening the fibrous carbon to the single fiber, and 1 to 10 ⁇ m is more preferable, and 0.1 to 5 ⁇ m is still more preferable.
- the solid content concentration of the slurry obtained in step 1 is preferably 1% by weight or more from the viewpoint of increasing the productivity of spray granulation in the next step. 2% by weight or more is more preferable, and 5% by weight or more is more preferable. Moreover, from a viewpoint which makes the particle size of the granulated material obtained at the process 2 into a preferable range, 60 weight% or less is preferable, 50 weight% or less is more preferable, and 40 weight% or less is still more preferable. Taking these viewpoints together, the solid content concentration of the slurry is preferably 1 to 60% by weight, more preferably 2 to 50% by weight, and even more preferably 5 to 40% by weight.
- the viscosity of the slurry obtained in step 1 is preferably 5000 mPa ⁇ s or less, more preferably 1000 mPa ⁇ s or less, and more preferably 100 mPa ⁇ s, from the viewpoint of controlling the particle size of the granulated product obtained in step 2 within a preferable range. The following is more preferable.
- step 2 spray granulation is performed using the slurry obtained in step 1.
- spray granulation is performed in which the slurry is formed into droplets using a nozzle, an atomizer, etc., and dried in a very short time.
- a method such as a spray freeze-drying method in which the droplets are frozen in a short time and then dried under reduced pressure, or a spray pyrolysis method in which spray drying and baking are combined can be used. Of these, the spray drying method is preferred.
- the drying temperature of the droplets obtained by spraying is preferably dried at a temperature at which the fibrous carbon or other carbon material is not combusted.
- the drying temperature is preferably 400 ° C. or lower, and 300 ° C. or lower. Is more preferable.
- the average agglomerated particle diameter of the granulated product in step 2 is preferably 20 ⁇ m or less, more preferably 15 ⁇ m or less, and more preferably 10 ⁇ m or less from the viewpoint of improving the insertion / desorption ability of Li and maintaining the smoothness of the coating film. Further preferred.
- 1 micrometer or more is preferable from a viewpoint of reducing the quantity of a binder, 3 micrometers or more are more preferable, and 5 micrometers or more are still more preferable. Taking these viewpoints together, the average aggregate particle size of the granulated product is preferably 1 to 20 ⁇ m, more preferably 3 to 15 ⁇ m, and even more preferably 5 to 10 ⁇ m.
- Step 3 is effective when a dispersant added to disperse the fibrous carbon is contained in the particles obtained in Step 2. If the dispersant remains, the dispersant becomes a resistance component, which not only hinders the high-speed discharge characteristics of the battery, but also the generation of gas due to decomposition in the battery and the charge / discharge cycle characteristics. It becomes a decrease factor. Therefore, it is necessary to remove the remaining dispersant, and this process is step 3.
- Specific methods include two methods: (1) a method of removing the dispersant by washing with a solvent capable of dissolving it, and (2) a method of removing the dispersant by decomposition and vaporization by heat treatment.
- the method (1) is preferable because it can be applied to most dispersants, and the method (2) is preferable because it is a lower cost and higher productivity method than the method (1).
- the heating temperature is preferably 100 ° C. or higher, more preferably 150 ° C. or higher, from the viewpoint of efficiently decomposing the dispersant. Moreover, from a viewpoint which does not decompose fibrous carbon, 400 degrees C or less is preferable and 300 degrees C or less is more preferable.
- the shape of the composite material for a positive electrode obtained by the above steps 1 to 3 is a spherical shape, but it is not always possible to obtain only a true spherical shape.
- Particles that can be obtained by spray granulation such as those that are distorted, partly dented, chipped, or agglomerated by aggregation of several spherical particles, can be obtained.
- carbon fiber with a large fiber diameter is contained as the fibrous carbon, a carbon fiber having a form protruding from the spherical particle surface can be obtained.
- the average aggregate particle diameter of the composite particles obtained through the step 3 is preferably 1 ⁇ m or more, more preferably 3 ⁇ m or more, and more preferably 5 ⁇ m or more from the viewpoint of reducing the amount of the binder when producing a coating film as the positive electrode of the battery. Is more preferable. Moreover, from the viewpoint of the surface property of the positive electrode obtained using the composite particles, it is preferably 20 ⁇ m or less, more preferably 15 ⁇ m or less, and even more preferably 10 ⁇ m or less. Taking these viewpoints together, the average aggregate particle size of the composite particles is preferably 1 to 20 ⁇ m, more preferably 3 to 15 ⁇ m, and even more preferably 5 to 10 ⁇ m.
- the lithium battery positive electrode of the present invention comprises the positive electrode composite material and the binder described above. Moreover, the lithium battery of this invention is equipped with the positive electrode formed by containing the composite material for positive electrodes mentioned above and a binder. That is, the lithium battery positive electrode and the lithium battery of the present invention are not limited at all with respect to other constituent requirements as long as the above-described positive electrode composite material is used as the positive electrode material.
- the binder any conventional binder such as polyvinylidene fluoride, polyamideimide, polytetrafluoroethylene, polyethylene, polypropylene, and polymethyl methacrylate can be used.
- the use of the battery using the positive electrode composite material of the present invention is not particularly limited, but can be used for electronic devices such as notebook computers, electronic book players, DVD players, portable audio players, video movies, portable TVs, and mobile phones.
- it can be used for consumer devices such as cordless vacuum cleaners, cordless electric tools, batteries for electric vehicles, hybrid cars, etc., and auxiliary power sources for fuel cell vehicles.
- cordless vacuum cleaners cordless electric tools
- batteries for electric vehicles hybrid cars, etc.
- auxiliary power sources for fuel cell vehicles Among these, it is suitably used as a battery for automobiles that require particularly high output.
- Example Examples and the like specifically showing the present invention will be described below.
- the evaluation item in an Example etc. measured as follows.
- DBP absorption amount DBP absorption amount was measured based on JIS K 6217-4.
- the length of the line segment means that for each of the 30 fibrous carbons, the normal line of one of the two curves drawn by the contour in the length direction of the fibrous carbon image is the two normal lines. This is the length of the line segment cut out by the curve.
- Aspect ratio of fibrous carbon It was determined by dividing the fiber length of fibrous carbon by the fiber diameter.
- volume resistance In the method of JIS K 1469, the amount of powder sample was changed to 0.3 g, the pressure at the time of powder compression was changed to 100 kg / cm 2, and the electric resistance value of the compressed powder sample compressed into a cylindrical shape was The volume resistivity (electrical resistivity) was calculated using the following equation 1 from the measured resistance value. Specifically, 0.3 g of a powder sample is filled in a cylindrical container composed of an insulating cylinder (made of Bakelite, outer diameter 28 mm, inner diameter 8 mm) and ( ⁇ ) electrode, and the insulating cylindrical container packed with the sample (+ ) The electrode was inserted and the powder sample was sandwiched, and placed on the press machine base.
- a force of 100 kg / cm 2 was applied to the sample in the cylindrical container by a press machine and compressed.
- the (+) electrode and the ( ⁇ ) electrode were connected to a digital multimeter measurement input cable, and the electrical resistance value was measured after 3 minutes from the start of compression.
- ⁇ S / h ⁇ R (Formula 1)
- ⁇ the electrical resistivity ( ⁇ ⁇ cm)
- S the cross-sectional area (cm 2 ) of the sample
- h the filling height (cm) of the sample
- R the electrical resistance value ( ⁇ ).
- the ( ⁇ ) electrode used was made of battery grade brass, the electrode surface was a 7.8 ⁇ 1 mm ⁇ , pedestal electrode with a 5 mm height projection, and the (+) electrode was a battery grade yellow It was made of copper, and the electrode surface was a rod-like electrode having a length of 7.8 ⁇ 1 mm ⁇ and a length of 60 mm.
- Pore volume Using a mercury intrusion pore distribution measuring device (pore sizer 9320, manufactured by Shimadzu Corporation), the total pore volume in the range of 0.01 to 1 ⁇ m was measured, and the obtained value was used as the pore volume. The capacity.
- the particle size distribution after irradiation with ultrasonic waves for 3 minutes was measured with a relative refractive index of 1.5 in the memory 7 of the apparatus, and the volume median particle size (D50) at this time was measured under the condition (2) above.
- the ratio was calculated by dividing this by the average agglomerated particle size of the substance and multiplying this by 100. In the present invention, a state in which this ratio is within 130% is defined as a dispersed state.
- a coating paste 10 parts by weight of hard carbon, 9.3 parts by weight of 12% by weight polyvinylidene fluoride (PVDF) in N-methylpyrrolidone and 8.5 parts by weight of N-methylpyrrolidone were uniformly mixed to prepare a coating paste.
- the paste was uniformly coated on a copper foil (thickness 18 ⁇ m) used as a current collector with a coater (YBA type baker applicator), and dried under reduced pressure (100 to 300 mmHg) at 80 ° C. over 12 hours. . After drying, it was cut into a predetermined size (20 mm ⁇ 15 mm) and molded into a uniform film thickness with a press machine to obtain a test negative electrode.
- PVDF polyvinylidene fluoride
- the thickness of the negative electrode layer at this time was 25 ⁇ m.
- Celguard # 2400 manufactured by Celguard
- the electrolytic solution an ethylene carbonate: diethyl carbonate (1: 1 vol%) solution of 1 mol / L LiPF 6 was used.
- the test cell was assembled in a glove box under an argon atmosphere. After the test cell was assembled, it was left at 25 ° C. for 24 hours, and then the internal resistance characteristics were evaluated.
- Example 1 0.375 parts by weight of a nonionic dispersant having a phenyl group as a functional group (Emulgen A-90 manufactured by Kao) was added to 100 parts by weight of water and dissolved. 0.375 parts by weight of carbon nanotubes having a fiber diameter of 20 nm, a fiber length of 5 ⁇ m, and an aspect ratio of 250 were added to the solution, and ultrasonically dispersed until the average aggregate particle diameter of the carbon nanotubes reached 3 ⁇ m.
- a nonionic dispersant having a phenyl group as a functional group Emulgen A-90 manufactured by Kao
- the average aggregate particle size 2 [mu] m (primary particle size 25 nm)
- the average aggregate particle size 2 [mu] m (primary particle size 25 nm)
- 7.5 parts by weight of lithium manganate having an average agglomerated particle size of 1.2 ⁇ m was added, and further ultrasonic dispersion was performed for 2 minutes.
- the obtained dispersion was spray-dried at a hot air temperature of 135 ° C. using a spray dryer (SD-1000 manufactured by Tokyo Rika Kikai Co., Ltd.).
- the obtained composite material for positive electrode is shown in FIG.
- the obtained composite material for positive electrode was confirmed by the method shown in (9) above.
- the positive electrode active material particles were composite particles held by carbon nanotubes. More specifically, as shown in FIG. The nanotubes existed in the gaps between the positive electrode active material particles, and the carbon nanotubes had a form in which the positive electrode active material particles were wrapped in a network.
- Example 2 1.5 g of granules containing the dispersant obtained by spray-drying in the same manner as in Example 1 were heated in an electric furnace at 200 ° C. for 10 hours to decompose and remove the dispersant.
- the obtained composite material for positive electrode is shown in FIG.
- the obtained composite material for positive electrode was confirmed by the method shown in the above (9).
- the positive electrode active material particles were composite particles held by carbon nanotubes. More specifically, as shown in FIG. The nanotubes existed in the gaps between the positive electrode active material particles, and the carbon nanotubes had a form in which the positive electrode active material particles were wrapped in a network.
- Example 3 The composite material for positive electrode was prepared in the same manner as in Example 1 except that the amount of nonionic dispersant having a phenyl group as a functional group was 0.15 parts by weight and the amount of carbon nanotubes was 0.15 parts by weight. Obtained.
- the obtained composite material for positive electrode is shown in FIG. 3, the physical properties are shown in Table 1, and the internal resistance during battery production is shown in Table 2.
- the obtained composite material for positive electrode was confirmed by the method shown in (9) above.
- positive electrode active material particles were composite particles held by carbon nanotubes. More specifically, as shown in FIG. The nanotubes existed in the gaps between the positive electrode active material particles, and the carbon nanotubes had a form in which the positive electrode active material particles were wrapped in a network.
- Example 4 Example 1 except that VGCF (0.225 parts by weight) having a fiber diameter of 120 nm, a fiber length of 10 ⁇ m, and an aspect ratio of 83 was used instead of the carbon nanotubes, and the amount of the dispersant used was 0.225 parts by weight.
- the composite material for positive electrodes was obtained by the same method.
- FIG. 4 shows the obtained composite material for positive electrode
- Table 1 shows the physical properties
- Table 2 shows the internal resistance during battery production.
- the obtained composite material for positive electrode was confirmed by the method shown in (9) above.
- the positive electrode active material particles were composite particles held by VGCF.
- the VGCF had a form in which the positive electrode active material particles were wrapped in a network.
- Example 1 instead of using 0.375 parts by weight of carbon nanotubes, 0.375 parts by weight of carbon black was used, except that the total amount of carbon black was 0.525 parts by weight. 1 was used to obtain a composite material for positive electrode. Table 1 shows the physical properties of the obtained composite material for positive electrode, and Table 2 shows the internal resistance during battery production.
- Comparative Example 2 In Example 1, the same amount of carbon nanotubes, carbon black, and lithium manganate were mixed with a magnetic stirrer without adding a dispersant, and a slurry was prepared. A composite material was obtained. Table 1 shows the physical properties of the obtained composite material for positive electrode. In Examples 1 to 4, the ratios obtained by the method shown in (8) above for the state of the dispersion before spray drying were all within 130%, but in Comparative Example 2, the ratios were It was 400% and could not be said to be in a dispersed state. Further, the composite material for positive electrode of Comparative Example 2 was confirmed by the method shown in (9) above. As a result, one composite particle was composed of positive carbon active material particles in which fibrous carbon almost disappeared and aggregated fibrous carbon particles. Therefore, the positive electrode active material particles were not composite particles held by fibrous carbon (carbon nanotubes).
- the lithium battery positive electrode composite materials of Examples 1 to 4 have low volume resistance and sufficient pore capacity, so that lithium ion migration is thought to be smooth during battery discharge. It is done.
- the internal resistance was able to be made smaller as a characteristic at the time of battery preparation.
- the composite material for a lithium battery positive electrode (Comparative Example 1) obtained without using fibrous carbon has a large volume resistance, insufficient pore capacity, and a large internal resistance during battery production. became.
- the lithium battery positive electrode composite material (Comparative Example 2) obtained by spray granulation using a slurry with insufficient dispersion of fibrous carbon the positive electrode active material particles are not held by the carbon nanotubes. Volume resistance was large.
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Abstract
Description
以下、本発明を具体的に示す実施例等について説明する。なお、実施例等における評価項目は下記のようにして測定を行った。
DBP吸収量は、JIS K 6217-4に基づいて測定した。
レーザー回折/散乱式粒度分布測定装置LA920(堀場製作所製)を用い、水を分散媒とし、超音波3分照射後の粒度分布を相対屈折率1.5で測定したときの体積中位粒径(D50)の値を繊維状炭素、カーボンブラックの平均凝集粒径、正極活物質、工程2における造粒物、及び工程3を経て得られた複合粒子の平均凝集粒径とした。
電界放出形走査電子顕微鏡(日立製S-4000)により撮影した倍率10000~50000倍のSEM像から、一次粒子50個を抽出し、それらの直径の平均値を一次粒子径とした。ただし、前記直径とは、(長軸径+短軸径)/2で算出される値で、着目するカーボンブラックのSEM像を2本の平行線ではさんだ時、その2本の平行線の間隔が最小となるときの間隔を短軸径、この平行線に直角な方向の2本の平行線でこのカーボンブラックのSEM像をはさんだ時、その2本の平行線の間隔を長軸径とする。
電界放出形走査電子顕微鏡(日立製S-4000)により撮影した倍率2000~50000倍のSEM像から、繊維状炭素30個を抽出し、以下のように測定した線分の長さの平均値を繊維径とし、繊維の長さの平均値を繊維長とした。ここで、前記線分の長さとは、30個の繊維状炭素のそれぞれについて、繊維状炭素の画像の長さ方向の輪郭が描く2本の曲線の一方の曲線の法線が、これら2本の曲線に切り取られる線分の長さをいう。
繊維状炭素の繊維長を繊維径で除することで求めた。
JIS K 1469の方法において、粉体試料量を0.3g、粉体圧縮時圧力を100kg/cm2に変更して、円筒状に圧縮した圧縮粉体試料の電気抵抗値を測定し、測定抵抗値より下記の式1を用いて体積抵抗率(電気抵抗率)を算出した。具体的には、絶縁性円筒(ベークライト製、外径28mm、内径8mm)と(-)電極からなる円筒容器に粉体試料を0.3g充填し、試料を詰めた絶縁性円筒容器に(+)電極を挿入して粉体試料を挟み、プレス機架台上に設置した。プレス機により円筒容器内の試料に100kg/cm2の力を加え、圧縮した。(+)電極と(-)電極をデジタルマルチメーターの測定用入力ケーブルに接続し、圧縮開始から3分経過後、電気抵抗値を測定した。
ここで、ρは電気抵抗率(Ω・cm)、Sは試料の断面積(cm2)、hは試料の充填高さ(cm)、Rは電気抵抗値(Ω)である。
水銀圧入式細孔分布測定装置(ポアサイザー9320、島津製作所製)を用いて、0.01~1μmの範囲の細孔容量の合計を測定し、得られた値を細孔容量とした。
レーザー回折/散乱式粒度分布測定装置LA920(堀場製作所製)に、スラリーと同一の溶媒120mLを添加し、攪拌循環(循環レベル4)させた。そこに、サンプリングしたスラリー(溶媒中に正極活物質粒子と繊維状炭素とを含有するスラリー)を滴下し、装置のセル内のレーザーの透過率が75~95%の範囲になるようスラリー濃度を調節した。そして、装置のメモリ7で超音波3分照射後の粒度分布を相対屈折率1.5で測定し、このときの体積中位粒径(D50)を上記(2)の条件で測定した正極活物質の平均凝集粒径で除して、これに100を乗じて比率を算出した。本発明では、この比率が130%以内になるような状態を分散状態とする。
正極活物質と繊維状炭素とを有する一粒の複合粒子を、600℃1時間加熱したとき、当該一粒の複合粒子が、複数の複合粒子に崩壊するか、又は繊維状炭素がほぼ消失した正極活物質粒子に崩壊した場合、当該一粒の複合粒子中の正極活物質粒子は繊維状炭素により保持されていたものとする。すなわち、600℃1時間加熱した複合粒子を電界放出形走査電子顕微鏡(日立製S-4000)により撮影し、倍率1000~50000倍のSEM画像を目視観察する。観察の結果、繊維状炭素がほぼ消失した正極活物質粒子のみ観察される場合、正極活物質粒子に繊維状炭素が絡んだ複合粒子のみ観察される場合、さらには、繊維状炭素がほぼ消失した正極活物質粒子と正極活物質粒子に繊維状炭素が絡んだ複合粒子の両方が観察される場合を正極活物質粒子が繊維状炭素により保持されていたものとする。一方、繊維状炭素がほぼ消失した正極活物質粒子と凝集した繊維状炭素の粒子が観察される場合、正極活物質粒子が繊維状炭素により保持されていなかったものとする。
表2に示す配合比にて正極用複合材料、カーボンブラック、12重量%ポリフッ化ビニリデン(PVDF)のNメチルピロリドン溶液、Nメチルピロリドンを均一に混合し、塗工用ペーストを調製した。当該ペーストをコーター(YBA型ベーカーアプリケーター)にて集電体として用いたアルミニウム箔(厚さ20μm)上に均一に塗工(乾燥後に0.009g/cm2)し、80℃にて12時間以上かけて減圧(100~300mmHg)乾燥した。乾燥後、所定の大きさ(20mm×15mm)に切断し、アルミニウム箔を含む全体の厚さが55μmになるようにプレス機で均一膜厚に成型して、試験用正極とした。
後述する実施例3,4および比較例1により得られたリチウムイオン二次電池の内部抵抗を評価した。まず、0.2Cの定電流で4.0Vまで充電した後、4.0Vで定電位充電を1時間行うことにより、各電池を満充電の約60%の充電状態に調整した。そして、5Cの定電流値で30秒間放電を行い、電位降下値を測定した。この電位降下値を放電電流値で除した値を電池の内部抵抗値として、得られたリチウムイオン二次電池の内部抵抗を評価した。表2には比較例1の内部抵抗値を100とした場合の実施例3,4の内部抵抗値の相対値を示す。
水100重量部にフェニル基を官能基にもつノニオン型分散剤(花王製エマルゲンA-90)を0.375重量部添加し溶解させた。その溶液に繊維径20nm、繊維長5μm、アスペクト比250のカーボンナノチューブを0.375重量部添加し、カーボンナノチューブの平均凝集粒径が3μmになるまで超音波分散した。このカーボンナノチューブ分散液に超音波を照射しながら、平均凝集粒径2μm(一次粒子径25nm)、DBP吸収量155cm3/100gのカーボンブラックを0.15重量部添加し1分間超音波照射した後、平均凝集粒径1.2μmのマンガン酸リチウム7.5重量部を添加し、更に超音波による分散を2分行った。得られた分散液を噴霧乾燥機(東京理化器械製SD-1000)を用いて熱風温度135℃で噴霧乾燥した。得られた顆粒6gを円筒ろ紙にいれ、ソックスレー抽出機で、400mlのエタノールにより、8時間抽出し、顆粒に残留している分散剤を除去した。得られた正極用複合材料を図1に、物性を表1に示す。得られた正極用複合材料は、上記(9)に示す方法で確認したところ、正極活物質粒子がカーボンナノチューブにより保持された複合粒子であり、より詳細には、図1に示すように、カーボンナノチューブが正極活物質粒子間隙に存在するとともに、カーボンナノチューブが正極活物質粒子を網目状に包み込んだ形態を有していた。
実施例1と同じ要領で噴霧乾燥して得た、分散剤が含有した顆粒1.5gを電気炉で200℃、10時間加熱し、分散剤を分解気化させ除去した。得られた正極用複合材料を図2に、物性を表1に示す。得られた正極用複合材料は、上記(9)に示す方法で確認したところ、正極活物質粒子がカーボンナノチューブにより保持された複合粒子であり、より詳細には、図2に示すように、カーボンナノチューブが正極活物質粒子間隙に存在するとともに、カーボンナノチューブが正極活物質粒子を網目状に包み込んだ形態を有していた。
フェニル基を官能基にもつノニオン型分散剤の使用量を0.15重量部、カーボンナノチューブの使用量を0.15重量部にしたこと以外は、実施例1と同じ手法で正極用複合材料を得た。得られた正極用複合材料を図3に、物性を表1、電池作製時の内部抵抗を表2に示す。得られた正極用複合材料は、上記(9)に示す方法で確認したところ、正極活物質粒子がカーボンナノチューブにより保持された複合粒子であり、より詳細には、図3に示すように、カーボンナノチューブが正極活物質粒子間隙に存在するとともに、カーボンナノチューブが正極活物質粒子を網目状に包み込んだ形態を有していた。
カーボンナノチューブの代わりに、繊維径120nm、繊維長10μm、アスペクト比83のVGCF(0.225重量部)を用い、分散剤の使用量を0.225重量部としたこと以外は、実施例1と同じ手法により正極用複合材料を得た。得られた正極用複合材料を図4に、物性を表1、電池作製時の内部抵抗を表2に示す。得られた正極用複合材料は、上記(9)に示す方法で確認したところ、正極活物質粒子がVGCFにより保持された複合粒子であり、より詳細には、図4に示すように、VGCFが正極活物質粒子間隙に存在するとともに、VGCFが正極活物質粒子を網目状に包み込んだ形態を有していた。
実施例1において、カーボンナノチューブ0.375重量部を使用する代わりに、カーボンブラック0.375重量部を使用することで、カーボンブラックの合計量を0.525重量部としたこと以外は、実施例1と同じ手法により正極用複合材料を得た。得られた正極用複合材料の物性を表1、電池作製時の内部抵抗を表2に示す。
実施例1において、分散剤を加えずに、同量のカーボンナノチューブ、カーボンブラック、及びマンガン酸リチウムをマグネチックスターラーにより混合して、スラリーを調製したこと以外は、実施例1と同じ手法により正極用複合材料を得た。得られた正極用複合材料の物性を表1に示す。なお、実施例1~4では、噴霧乾燥前の分散液の状態について、上記(8)に示す方法で求めた比率が何れも130%以内であったが、この比較例2では、当該比率が400%であり、分散状態とはいえなかった。また、比較例2の正極用複合材料は、上記(9)に示す方法で確認したところ、一粒の複合粒子が、繊維状炭素がほぼ消失した正極活物質粒子と凝集した繊維状炭素の粒子とに崩壊したため、正極活物質粒子が繊維状炭素(カーボンナノチューブ)により保持された複合粒子ではなかった。
Claims (20)
- 正極活物質粒子と繊維状炭素とを含む複合粒子から構成されるリチウム電池正極用複合材料であって、
前記複合粒子は、前記正極活物質粒子が前記繊維状炭素により保持されている形態を有するリチウム電池正極用複合材料。 - 前記複合粒子は、前記繊維状炭素の少なくとも一部が前記正極活物質粒子間隙に存在する形態を有する請求項1に記載のリチウム電池正極用複合材料。
- 前記複合粒子は、前記繊維状炭素の一部が前記正極活物質粒子間隙に存在するとともに、前記繊維状炭素が前記正極活物質粒子を網目状に包み込んだ形態を有する請求項1又は2に記載のリチウム電池正極用複合材料。
- 前記正極活物質粒子の平均凝集粒径が、0.1~10μmである請求項1~3のいずれか1項に記載のリチウム電池正極用複合材料。
- 前記繊維状炭素の繊維径が、1~1000nmである請求項1~4のいずれか1項に記載のリチウム電池正極用複合材料。
- 前記繊維状炭素が、カーボンナノチューブである請求項1~5のいずれか1項に記載のリチウム電池正極用複合材料。
- 前記複合粒子は、溶媒中に前記正極活物質粒子と前記繊維状炭素とが分散した状態で含まれるスラリーから噴霧造粒により得られる請求項1~6のいずれか1項に記載のリチウム電池正極用複合材料。
- 前記複合粒子は、前記溶媒中にて前記繊維状炭素が分散剤により分散されている前記スラリーから噴霧造粒により得られる請求項7に記載のリチウム電池正極用複合材料。
- 前記複合粒子は、前記噴霧造粒で得られた造粒物から前記分散剤を除去して得られる請求項8に記載のリチウム電池正極用複合材料。
- 前記分散剤が、芳香族環及び/又は脂肪族環を含む官能基を有する請求項8又は9に記載のリチウム電池正極用複合材料。
- 請求項1~10のいずれか1項に記載のリチウム電池正極用複合材料、及びバインダーを含有してなるリチウム電池正極。
- 請求項1~10のいずれか1項に記載のリチウム電池正極用複合材料、及びバインダーを含有してなる正極を備えるリチウム電池。
- 正極活物質粒子と繊維状炭素とを含む複合粒子から構成されるリチウム電池正極用複合材料の製造方法であって、
溶媒中に前記正極活物質粒子と前記繊維状炭素とが分散した状態で含まれるスラリーを得る工程1と、
前記工程1で得たスラリーを用いて噴霧造粒して、前記正極活物質粒子と前記繊維状炭素とを含有する造粒物を得る工程2とを含むリチウム電池正極用複合材料の製造方法。 - 前記工程1において、前記スラリーがさらに分散剤を含有する請求項13に記載のリチウム電池正極用複合材料の製造方法。
- 前記工程2で得た造粒物は、前記正極活物質粒子が前記繊維状炭素により保持されている造粒物である請求項13又は14に記載のリチウム電池正極用複合材料の製造方法。
- 前記工程2において、又は前記工程2の後に、前記造粒物から前記分散剤を除去して複合粒子を得る工程3をさらに含む請求項14又は15に記載のリチウム電池正極用複合材料の製造方法。
- 前記正極活物質の平均凝集粒径が、0.1~10μmである請求項13~16のいずれか1項に記載のリチウム電池正極用複合材料の製造方法。
- 前記繊維状炭素の繊維径が、1~1000nmである請求項13~17のいずれか1項に記載のリチウム電池正極用複合材料の製造方法。
- 前記繊維状炭素が、カーボンナノチューブである請求項13~18のいずれか1項に記載のリチウム電池正極用複合材料の製造方法。
- 前記分散剤が、芳香族環及び/又は脂肪族環を含む官能基を有する請求項14~19のいずれか1項に記載のリチウム電池正極用複合材料の製造方法。
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CN113793939A (zh) * | 2021-09-24 | 2021-12-14 | 鹤壁市诺信电子有限公司 | 一种超低温高倍率锂离子电池及其制备方法 |
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WO2022130553A1 (ja) * | 2020-12-17 | 2022-06-23 | 株式会社 東芝 | 電極、二次電池及び電池パック |
JP7463558B2 (ja) | 2020-12-17 | 2024-04-08 | 株式会社東芝 | 負極、二次電池及び電池パック |
Also Published As
Publication number | Publication date |
---|---|
EP2228856A4 (en) | 2012-01-25 |
US20100248034A1 (en) | 2010-09-30 |
CN101919089A (zh) | 2010-12-15 |
CN101919089B (zh) | 2014-04-16 |
KR20100095473A (ko) | 2010-08-30 |
KR101267351B1 (ko) | 2013-05-24 |
EP2228856A1 (en) | 2010-09-15 |
US8426064B2 (en) | 2013-04-23 |
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