WO2024042888A1 - 非水電解質二次電池 - Google Patents

非水電解質二次電池 Download PDF

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Publication number
WO2024042888A1
WO2024042888A1 PCT/JP2023/025310 JP2023025310W WO2024042888A1 WO 2024042888 A1 WO2024042888 A1 WO 2024042888A1 JP 2023025310 W JP2023025310 W JP 2023025310W WO 2024042888 A1 WO2024042888 A1 WO 2024042888A1
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Prior art keywords
negative electrode
secondary battery
less
electrolyte secondary
silicon
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English (en)
French (fr)
Japanese (ja)
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基浩 坂田
陽祐 佐藤
真仁 大塚
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Panasonic Intellectual Property Management Co Ltd
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Panasonic Intellectual Property Management Co Ltd
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Priority to JP2024542630A priority Critical patent/JPWO2024042888A1/ja
Priority to US19/103,651 priority patent/US20260051507A1/en
Priority to EP23857005.5A priority patent/EP4579835A4/en
Priority to CN202380060405.1A priority patent/CN119895607A/zh
Publication of WO2024042888A1 publication Critical patent/WO2024042888A1/ja
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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
    • H01M4/628—Inhibitors, e.g. gassing inhibitors, corrosion inhibitors
    • 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
    • H01M10/0525—Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodes; Lithium-ion batteries
    • 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
    • H01M10/42—Methods or arrangements for servicing or maintenance of secondary cells or secondary half-cells
    • H01M10/4235—Safety or regulating additives or arrangements in electrodes, separators or electrolyte
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/13—Electrodes for accumulators with non-aqueous electrolyte, e.g. for lithium-accumulators; Processes of manufacture thereof
    • H01M4/133—Electrodes based on carbonaceous material, e.g. graphite-intercalation compounds or CFx
    • 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
    • H01M4/134—Electrodes based on metals, Si or alloys
    • 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
    • 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
    • H01M4/366—Composites as layered products
    • 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
    • H01M4/386—Silicon or alloys based on silicon
    • 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
    • H01M4/48—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
    • H01M4/52—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron
    • H01M4/525—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron of mixed oxides or hydroxides containing iron, cobalt or nickel for inserting or intercalating light metals, e.g. LiNiO2, LiCoO2 or LiCoOxFy
    • 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
    • H01M4/58—Selection of substances as active materials, active masses, active liquids of inorganic compounds other than oxides or hydroxides, e.g. sulfides, selenides, tellurides, halogenides or LiCoFy; of polyanionic structures, e.g. phosphates, silicates or borates
    • H01M4/583—Carbonaceous material, e.g. graphite-intercalation compounds or CFx
    • H01M4/587—Carbonaceous material, e.g. graphite-intercalation compounds or CFx for inserting or intercalating light metals
    • 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
    • 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
    • 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 disclosure relates to a non-aqueous electrolyte secondary battery.
  • Patent Document 1 describes a silicon-containing material that includes porous carbon and silicon and is applicable to negative electrodes for secondary batteries, including silicon containing 15% by mass or more and 85% by mass or less, and 0.05cm 3 /g or more and 0.05% by mass or more and 0.05cm 3 /g or more. Materials are disclosed that have a nitrogen-inaccessible volume of 5 cm 3 /g or less and a particle skeletal density of 1.5 g/cm 3 or more and 2.2 g/cm 3 or less. Patent Document 1 attempts to realize a battery with high capacity, high durability, and high output by optimizing the true density and pore state of a silicon-containing material.
  • a negative electrode using a silicon-containing material is effective in increasing the capacity of a battery, but the silicon-containing material has a large volume change due to charging and discharging, and there are problems with durability (charge-discharge cycle characteristics). For this reason, in conventional techniques including Patent Document 1, it is common to use a larger amount of graphite as a negative electrode active material than the silicon-containing material, and it is not easy to achieve both high capacity and high durability.
  • a nonaqueous electrolyte secondary battery is a nonaqueous electrolyte secondary battery including a positive electrode, a negative electrode, and a nonaqueous electrolyte, and the positive electrode includes a lithium-containing transition metal composite oxide and a lithium-containing transition metal composite oxide.
  • sulfonic acid compound present on the particle surface of the object is a compound represented by formula (I),
  • A is a Group 1 or Group 2 element
  • R is a hydrocarbon group
  • n is 1 or 2
  • the negative electrode has a negative electrode mixture layer containing a silicon-containing material as a negative electrode active material.
  • the proportion of the silicon-containing material in the substance is 50% by mass or more, and the value obtained by dividing the volumetric capacity of the negative electrode mixture layer by the porosity is 48.0mAh/cc ⁇ % or less.
  • cycle characteristics can be improved in a high capacity non-aqueous electrolyte secondary battery containing a silicon-containing material.
  • FIG. 1 is a cross-sectional view of a non-aqueous electrolyte secondary battery that is an example of an embodiment.
  • the present inventors found that the volume specific capacity and porosity of the negative electrode mixture layer containing silicon-containing materials It was found that the relationship between A negative electrode in which the proportion of silicon-containing material in the negative electrode active material is 50% by mass or more generally has a large capacity drop due to charging and discharging, but when the volume specific capacity of the negative electrode mixture layer is divided by the porosity It has been found that by controlling the value (volume specific volume/porosity) to 48.0 mAh/cc ⁇ % or less, such capacity reduction can be highly suppressed.
  • the porosity in the present disclosure means the proportion of voids between negative electrode active material particles in the mixture layer, and voids within the active material particles are not counted in the porosity.
  • Batteries using negative electrodes containing a large amount of silicon-containing material have been thought to be difficult to use, for example, as batteries for in-vehicle applications or power storage applications, from the viewpoint of cycle characteristics. If the excess voids are introduced into the negative electrode mixture layer and the volume specific volume/porosity is controlled to 48.0 mAh/cc ⁇ % or less, it is possible to achieve both high capacity and high durability. In other words, in a non-aqueous electrolyte secondary battery that contains a large amount of silicon-containing material, such as the proportion of silicon-containing material in the negative electrode active material being 50% by mass or more, the volume ratio/porosity may reach a boundary of 48.0 mAh/cc.%. The cycle characteristics are specifically improved.
  • volume specific volume/porosity of the negative electrode mixture layer is 48.0 mAh/cc ⁇ % or less, a sufficient movement path for cations in the negative electrode is secured, and as a result, non-uniformity of battery reactions is suppressed, and as a result, the cycle It is thought that the characteristics will be greatly improved.
  • the sulfonic acid compound represented by the above formula (I) exist on the particle surface of the lithium-containing transition metal composite oxide used as the positive electrode active material, a non-woven fabric with higher capacity and excellent initial charge/discharge efficiency can be obtained. It has become clear that a water electrolyte secondary battery can be realized. This is considered to be because the reaction resistance at the positive electrode was reduced by the function of the sulfonic acid compound, making it possible to increase the depth of charge and discharge. On the other hand, if the depth of charging and discharging becomes deeper due to the reduction in reaction resistance, there is a concern that the cycle characteristics will deteriorate.
  • non-aqueous electrolyte secondary battery a cylindrical battery in which a wound electrode body 14 is housed in a cylindrical outer can 16 with a bottom is exemplified.
  • the non-aqueous electrolyte secondary battery according to the present disclosure may be, for example, a prismatic battery with a prismatic exterior can, a coin-shaped battery with a coin-shaped exterior can, and a laminate sheet containing a metal layer and a resin layer.
  • a pouch-type battery may be provided with an exterior body made up of.
  • the electrode body is not limited to a wound type electrode body, and may be a laminated type electrode body in which a plurality of positive electrodes and a plurality of negative electrodes are alternately laminated with separators interposed therebetween.
  • FIG. 1 is a cross-sectional view of a nonaqueous electrolyte secondary battery 10 that is an example of an embodiment.
  • the non-aqueous electrolyte secondary battery 10 includes a wound electrode body 14, a non-aqueous electrolyte, and an outer can 16 that houses the electrode body 14 and the non-aqueous electrolyte.
  • the electrode body 14 includes a positive electrode 11 , a negative electrode 12 , and a separator 13 , and has a wound structure in which the positive electrode 11 and the negative electrode 12 are spirally wound with the separator 13 in between.
  • the outer can 16 is a bottomed cylindrical metal container with an open end in the axial direction, and the opening of the outer can 16 is closed by a sealing member 17 .
  • the sealing body 17 side of the battery will be referred to as the upper side
  • the bottom side of the outer can 16 will be referred to as the lower side.
  • the non-aqueous electrolyte has lithium ion conductivity.
  • the non-aqueous electrolyte may be a liquid electrolyte (electrolyte solution) or a solid electrolyte.
  • the liquid electrolyte includes a non-aqueous solvent and an electrolyte salt dissolved in the non-aqueous solvent.
  • a non-aqueous solvent for example, esters, ethers, nitriles, amides, mixed solvents of two or more of these, and the like are used.
  • nonaqueous solvents include ethylene carbonate (EC), ethylmethyl carbonate (EMC), dimethyl carbonate (DMC), diethyl carbonate (DEC), and mixed solvents thereof.
  • the non-aqueous solvent may contain a halogen-substituted product (for example, fluoroethylene carbonate) in which at least a portion of hydrogen in these solvents is replaced with a halogen atom such as fluorine.
  • a halogen-substituted product for example, fluoroethylene carbonate
  • a lithium salt such as LiPF 6 is used as the electrolyte salt.
  • the solid electrolyte for example, a solid or gel polymer electrolyte, an inorganic solid electrolyte, etc.
  • an inorganic solid electrolyte materials known for use in all-solid lithium ion secondary batteries and the like (for example, oxide-based solid electrolytes, sulfide-based solid electrolytes, halogen-based solid electrolytes, etc.) can be used.
  • the polymer electrolyte includes, for example, a lithium salt and a matrix polymer, or a nonaqueous solvent, a lithium salt, and a matrix polymer.
  • the matrix polymer for example, a polymer material that absorbs a non-aqueous solvent and gels is used. Examples of polymer materials include fluororesins, acrylic resins, polyether resins, and the like.
  • the positive electrode 11, the negative electrode 12, and the separator 13 that constitute the electrode body 14 are all long strip-shaped bodies, and are wound in a spiral shape so that they are alternately stacked in the radial direction of the electrode body 14.
  • the negative electrode 12 is formed to be one size larger than the positive electrode 11 in order to prevent precipitation of lithium. That is, the negative electrode 12 is formed longer than the positive electrode 11 in the length direction and the width direction.
  • the separators 13 are formed to be at least one size larger than the positive electrode 11, and for example, two separators 13 are arranged so as to sandwich the positive electrode 11 therebetween.
  • the electrode body 14 has a positive electrode lead 20 connected to the positive electrode 11 by welding or the like, and a negative electrode lead 21 connected to the negative electrode 12 by welding or the like.
  • Insulating plates 18 and 19 are arranged above and below the electrode body 14, respectively.
  • the positive electrode lead 20 passes through the through hole of the insulating plate 18 and extends toward the sealing body 17, and the negative electrode lead 21 passes through the outside of the insulating plate 19 and extends toward the bottom of the outer can 16.
  • the positive electrode lead 20 is connected by welding or the like to the lower surface of the internal terminal plate 23 of the sealing body 17, and the cap 27, which is the top plate of the sealing body 17 and electrically connected to the internal terminal plate 23, serves as a positive electrode terminal.
  • the negative electrode lead 21 is connected to the bottom inner surface of the outer can 16 by welding or the like, and the outer can 16 serves as a negative electrode terminal.
  • a gasket 28 is provided between the outer can 16 and the sealing body 17 to ensure airtightness inside the battery.
  • the outer can 16 is formed with a grooved part 22 that supports the sealing body 17 and has a part of the side surface protruding inward.
  • the grooved portion 22 is preferably formed in an annular shape along the circumferential direction of the outer can 16, and supports the sealing body 17 on its upper surface.
  • the sealing body 17 is fixed to the upper part of the outer can 16 by the grooved part 22 and the open end of the outer can 16 which is crimped to the sealing body 17 .
  • the sealing body 17 has a structure in which an internal terminal plate 23, a lower valve body 24, an insulating member 25, an upper valve body 26, and a cap 27 are laminated in order from the electrode body 14 side.
  • Each member constituting the sealing body 17 has, for example, a disk shape or a ring shape, and each member except the insulating member 25 is electrically connected to each other.
  • the lower valve body 24 and the upper valve body 26 are connected at their respective central portions, and an insulating member 25 is interposed between their respective peripheral portions.
  • the positive electrode 11, negative electrode 12, and separator 13 that make up the electrode body 14 will be explained in detail, particularly the positive electrode active material that makes up the positive electrode 11, and the negative electrode active material that makes up the negative electrode 12.
  • the positive electrode 11 includes a positive electrode core 30 and a positive electrode mixture layer 31 provided on the positive electrode core 30.
  • a metal foil such as aluminum that is stable in the potential range of the positive electrode 11, a film with the metal disposed on the surface, or the like can be used.
  • the positive electrode mixture layer 31 contains a positive electrode active material, a conductive agent, and a binder, and is preferably provided on both surfaces of the positive electrode core 30 except for the portion to which the positive electrode lead 20 is connected.
  • the positive electrode 11 is formed by applying a positive electrode mixture slurry containing a positive electrode active material, a conductive agent, and a binder to the surface of the positive electrode core 30, drying the coating film, and then compressing it to form the positive electrode mixture layer 31. It can be produced by forming on both sides of the positive electrode core body 30.
  • Examples of the conductive agent included in the positive electrode mixture layer 31 include carbon black such as acetylene black and Ketjen black, graphite, carbon nanotubes (CNT), carbon nanofibers, and carbon materials such as graphene.
  • Examples of the binder included in the positive electrode mixture layer 31 include fluorine-containing resins such as polytetrafluoroethylene (PTFE) and polyvinylidene fluoride (PVDF), polyacrylonitrile (PAN), polyimide, acrylic resin, and polyolefin. . Further, these resins, carboxymethyl cellulose (CMC) or a salt thereof, polyethylene oxide, etc. may be used in combination.
  • the content of the conductive agent and the binder is, for example, 0.1% by mass or more and 5% by mass or less with respect to the mass of the negative electrode mixture layer 31, respectively.
  • the positive electrode 11 includes a lithium-containing transition metal composite oxide and a sulfonic acid compound present on the particle surface of the composite oxide.
  • the lithium-containing transition metal composite oxide with a sulfonic acid compound attached to the particle surface functions as a positive electrode active material.
  • the sulfonic acid compound is a compound represented by formula (I). In the formula, A is a Group 1 or Group 2 element, R is a hydrocarbon group, and n is 1 or 2.
  • the sulfonic acid compound represented by formula (I) functions specifically when applied to the particle surface of the lithium-containing transition metal oxide to form the positive electrode 11. reduce the reaction resistance in As a result, it becomes possible to increase the depth of charging and discharging, and further increase in capacity can be achieved.
  • the sulfonic acid compound exhibits the effect even in a very small amount, it is preferably present on the particle surface of the composite oxide in an amount of 0.01% by mass or more based on the lithium-containing transition metal composite oxide.
  • the content of the sulfonic acid compound is more preferably 0.05% by mass or more, particularly preferably 0.10% by mass or more, based on the lithium-containing transition metal composite oxide.
  • the upper limit of the content of the sulfonic acid compound is not particularly limited, but from the viewpoint of achieving both output characteristics and cycle characteristics, 2.0% by mass is preferable with respect to the lithium-containing transition metal composite oxide, and 1.5% by mass is preferable. More preferably, 1.0% by mass is particularly preferred.
  • the sulfonic acid compound is present in an amount of, for example, 0.05% by mass or more and 1.50% by mass or less, or 0.1% by mass or more and 1.0% by mass or less based on the lithium-containing transition metal composite oxide. .
  • the positive electrode active material may have as a main component composite particles that are a lithium-containing transition metal composite oxide with a sulfonic acid compound attached to the particle surface, and may be substantially composed only of the composite particles.
  • the positive electrode active material may contain a composite oxide other than the composite particles or other compounds as long as the purpose of the present disclosure is not impaired.
  • a composite oxide without a sulfonic acid compound attached to the particle surface may be included as part of the positive electrode active material.
  • the lithium-containing transition metal oxide preferably has a layered rock salt structure.
  • the layered rock salt structure of the lithium-containing transition metal oxide include a layered rock salt structure belonging to space group R-3m, a layered rock salt structure belonging to space group C2/m, and the like.
  • a layered rock salt structure belonging to space group R-3m is preferred from the viewpoint of high capacity and stability of crystal structure.
  • the layered rock salt structure of the lithium-containing transition metal oxide includes a transition metal layer, a Li layer, and an oxygen layer.
  • the lithium-containing transition metal oxide is a composite oxide containing metal elements such as Co, Mn, Ni, and Al in addition to Li.
  • Metal elements constituting the lithium-containing transition metal oxide include, for example, Mg, Al, Ca, Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Ga, Ge, Y, Zr, Sn. , Sb, W, Pb, and Bi. Among these, it is preferable to contain at least one selected from Co, Ni, and Mn.
  • suitable composite oxides include composite oxides containing Ni, Co, and Mn, and composite oxides containing Ni, Co, and Al.
  • the lithium-containing transition metal oxide is preferably 50 mol% or more, more preferably 70 mol% or more, particularly preferably 80 mol%, based on the total number of moles of metal elements excluding Li. Contains the above amount of Ni. Further, the effect of adding a sulfonic acid compound is more remarkable when a lithium-containing transition metal oxide with a high Ni content is used.
  • the Ni content may be 85 mol% or more, or 90 mol% or more with respect to the total number of moles of metal elements excluding Li.
  • the upper limit of the Ni content is, for example, 95 mol%.
  • a suitable lithium-containing transition metal oxide is a composite oxide containing Ni, Co, and Al, as described above.
  • the Al content is 4 mol% or more and 15 mol% or less, and the Co content is 1.5 mol% or less. If the Al content is within this range, the crystal structure will be stabilized and the cycle characteristics will be improved.
  • Co may not be substantially added, battery performance is improved by adding a small amount of Co.
  • M1 is Mn, Fe, Ti, Si, Nb, It is a composite oxide represented by at least one element selected from Zr, Mo, and Zn.
  • M1 is Mn.
  • the content of the elements constituting the lithium-containing transition metal composite oxide is measured using an inductively coupled plasma emission spectrometer (ICP-AES), an electron beam microanalyzer (EPMA), an energy dispersive X-ray analyzer (EDX), etc. can be measured.
  • ICP-AES inductively coupled plasma emission spectrometer
  • EPMA electron beam microanalyzer
  • EDX energy dispersive X-ray analyzer
  • a lithium-containing transition metal composite oxide is, for example, a secondary particle formed by agglomerating a plurality of primary particles.
  • the volume-based median diameter (D50) of the composite oxide is not particularly limited, but is, for example, 3 ⁇ m or more and 30 ⁇ m or less, preferably 5 ⁇ m or more and 25 ⁇ m or less.
  • the D50 of the composite oxide means the D50 of the secondary particles.
  • D50 means a particle size at which the cumulative frequency is 50% from the smallest particle size in the volume-based particle size distribution, and is also called the median diameter.
  • the particle size distribution of the composite oxide (the same applies to the negative electrode active material) can be measured using a laser diffraction type particle size distribution measuring device (for example, MT3000II manufactured by Microtrac Bell Co., Ltd.) using water as a dispersion medium.
  • a laser diffraction type particle size distribution measuring device for example, MT3000II manufactured by Microtrac Bell Co., Ltd.
  • the average particle size of the primary particles constituting the lithium-containing transition metal composite oxide is, for example, 0.05 ⁇ m or more and 1 ⁇ m or less.
  • the average particle diameter of the primary particles is calculated by averaging the diameters of the circumscribed circles of the primary particles extracted by analyzing a scanning electron microscope (SEM) image of a cross section of the secondary particles.
  • the sulfonic acid compound present on the particle surface of the lithium-containing transition metal composite oxide is a compound represented by formula (I).
  • A is a Group 1 or Group 2 element
  • R is a hydrocarbon group
  • n is 1 or 2.
  • A is preferably a Group 1 element.
  • Li or Na is more preferred, and Li is particularly preferred.
  • R is preferably an alkyl group.
  • the number of carbon atoms in the alkyl group is preferably 5 or less, more preferably 3 or less. From the viewpoint of reducing reaction resistance, etc., a suitable example of R is an alkyl group having 3 or less carbon atoms, and among them, a methyl group is preferable.
  • a part of hydrogen bonded to carbon may be substituted with fluorine.
  • n in formula (I) is preferably 1.
  • sulfonic acid compounds include lithium methanesulfonate, lithium ethanesulfonate, lithium propanesulfonate, sodium methanesulfonate, sodium ethanesulfonate, magnesium methanesulfonate, lithium fluoromethanesulfonate, and the like.
  • at least one selected from the group consisting of lithium methanesulfonate, lithium ethanesulfonate, and sodium methanesulfonate is preferred, and lithium methanesulfonate is particularly preferred.
  • the sulfonic acid compound exists homogeneously over the entire particle surface of the lithium-containing transition metal composite oxide.
  • the presence of the sulfonic acid compound on the particle surface of the composite oxide can be confirmed by Fourier transform infrared spectroscopy (FT-IR).
  • FT-IR Fourier transform infrared spectroscopy
  • a positive electrode active material containing lithium methanesulfonate has absorption peaks around 1238 cm ⁇ 1 , 1175 cm ⁇ 1 , 1065 cm ⁇ 1 , and 785 cm ⁇ 1 , for example.
  • the peaks around 1238 cm ⁇ 1 , 1175 cm ⁇ 1 , and 1065 cm ⁇ 1 are peaks caused by SO stretching vibrations derived from lithium methanesulfonate.
  • the peak around 785 cm ⁇ 1 is a peak resulting from CS stretching vibration derived from lithium methanesulfonate.
  • positive electrode active materials containing sulfonic acid compounds other than lithium methanesulfonate can also be confirmed from the absorption peak derived from the sulfonic acid compound in the infrared absorption spectrum.
  • the presence of a sulfonic acid compound on the particle surface of a lithium-containing transition metal composite oxide can also be confirmed by ICP, atomic absorption spectrometry, X-ray photoelectron spectroscopy (XPS), synchrotron radiation XRD measurement, TOF-SIMS, etc. .
  • a positive electrode active material that is an example of an embodiment can be manufactured by the following method. Note that the manufacturing method described here is just an example, and the method for manufacturing the positive electrode active material is not limited to this method.
  • Metal oxides can be prepared by, for example, adding an alkaline solution such as sodium hydroxide dropwise to a solution of metal salts containing Ni, Al, Co, Mn, etc. while stirring the solution, and adjusting the pH to an alkaline side (for example, 8.5 to 12.5%). 5 or less), a composite hydroxide containing metal elements such as Ni, Al, Co, and Mn is precipitated (co-precipitated), and the composite hydroxide can be synthesized by heat treatment.
  • the heat treatment temperature is not particularly limited, but is, for example, 300°C or higher and 600°C or lower.
  • lithium compound examples include Li 2 CO 3 , LiOH, Li 2 O 2 , Li 2 O, LiNO 3 , LiNO 2 , Li 2 SO 4 , LiOH ⁇ H 2 O, LiH, and LiF.
  • the metal oxide and the lithium compound are mixed such that, for example, the molar ratio of the metal element in the metal oxide to Li in the lithium compound is 1:0.98 or more and 1:1.1 or less. Note that when mixing the metal oxide and the lithium compound, other metal raw materials may be added as necessary.
  • the mixture of metal oxide and lithium compound is fired, for example, in an oxygen atmosphere.
  • the mixture may be fired through multiple heating processes.
  • the firing step includes, for example, a first temperature raising step of increasing the temperature from 450° C. to 680° C. at a temperature increasing rate of 1.0° C./min or more and 5.5° C./min or less, and 0.1° C./min.
  • a second heating step is included in which the temperature is raised to a temperature exceeding 680° C. at a heating rate of 3.5° C./min or less.
  • the maximum temperature of the firing step may be set to 700° C. or higher and 850° C. or lower, and the temperature may be maintained at this temperature for 1 hour or more and 10 hours or less.
  • the fired product (lithium-containing transition metal composite oxide) is washed with water and dehydrated to obtain a cake-like composition.
  • This cleaning step removes remaining alkaline components. Washing with water and dehydration can be performed by conventionally known methods.
  • the cake-like composition is dried to obtain a powder-like composition.
  • the drying step may be performed under a vacuum atmosphere. An example of the drying conditions is at a temperature of 150° C. or higher and 400° C. or lower for 0.5 hours or more and 15 hours or less.
  • the sulfonic acid compound is added, for example, to the cake-like composition obtained in the washing step or the powder-like composition obtained in the drying step.
  • a sulfonic acid solution may be added instead of or together with the sulfonic acid compound.
  • the sulfonic acid compound may be added as an aqueous dispersion.
  • the sulfonic acid solution is an aqueous solution of sulfonic acid.
  • the concentration of sulfonic acid in the sulfonic acid solution is, for example, 0.5% by mass or more and 40% by mass or less.
  • the negative electrode 12 includes a negative electrode core 40 and a negative electrode mixture layer 41 provided on the negative electrode core 40.
  • a metal foil such as copper that is stable in the potential range of the negative electrode 12, a film with the metal disposed on the surface, or the like can be used.
  • the negative electrode mixture layer 41 contains a negative electrode active material and a binder, and is provided on both sides of the negative electrode core 40 except for the portion to which the negative electrode lead 21 is connected.
  • the negative electrode 12 is made by applying a negative electrode mixture slurry containing a negative electrode active material and a binder to the surface of the negative electrode core 40, drying the coating film, and then compressing the negative electrode mixture layer 41 to the negative electrode core. It can be produced by forming it on both sides of 40.
  • the binder contained in the negative electrode mixture layer 41 fluororesin, PAN, polyimide, acrylic resin, polyolefin, etc. can be used as in the case of the positive electrode 11, but styrene-butadiene rubber (SBR) is preferably used.
  • the negative electrode mixture layer 41 preferably contains CMC or a salt thereof, polyacrylic acid (PAA) or a salt thereof, polyvinyl alcohol (PVA), or the like. Among these, it is preferable to use SBR, CMC or a salt thereof, and PAA or a salt thereof in combination.
  • the content of the binder is, for example, 0.1% by mass or more and 5% by mass or less with respect to the mass of the negative electrode mixture layer 41.
  • the negative electrode mixture layer 41 may contain a conductive agent such as CNT.
  • the negative electrode mixture layer 41 contains a silicon-containing material as a negative electrode active material.
  • the proportion of the silicon-containing material in the negative electrode active material is 50% by mass or more.
  • Silicon-containing materials can absorb more Li ions than carbon-based active materials such as graphite, which are commonly used as negative electrode active materials, so increasing the content of silicon-containing materials can increase the capacity of batteries. It is possible to aim for As will be described in detail later, simply increasing the content of the silicon-containing material will significantly reduce the cycle characteristics.
  • volume specific capacity/porosity the value obtained by dividing the volume specific capacity of the negative electrode mixture layer 41 by the porosity (hereinafter referred to as "volume specific capacity/porosity") ) is 48.0mAh/cc ⁇ % or less.
  • the proportion (content) of the silicon-containing material in the negative electrode active material is preferably 60% by mass or more, more preferably 70% by mass or more, particularly preferably 80% by mass or more, and may be 90% by mass or more. .
  • the upper limit of the content of the silicon-containing material is not particularly limited, and may be 100% by mass.
  • An example of a suitable range for the content of the silicon-containing material is 70 to 100% by mass of the negative electrode active material, more preferably 80% by mass or more and 100% by mass or less.
  • the negative electrode mixture layer 41 may contain substantially only a silicon-containing material as a negative electrode active material, but may also contain a carbon material in an amount of 50% by mass or less.
  • the carbon material that functions as the negative electrode active material is, for example, at least one selected from the group consisting of natural graphite, artificial graphite, soft carbon, and hard carbon.
  • at least artificial graphite such as massive artificial graphite (MAG) and graphitized mesophase carbon microbeads (MCMB), natural graphite such as flaky graphite, lumpy graphite, and earthy graphite, or a mixture thereof is used as the carbon material. It is preferable.
  • the volume-based D50 of the carbon material is, for example, 1 ⁇ m or more and 30 ⁇ m or less, preferably 5 ⁇ m or more and 25 ⁇ m or less.
  • Soft carbon and hard carbon are classified as amorphous carbon in which the graphite crystal structure is not developed. More specifically, it means a carbon component having a d(002) plane spacing of 0.342 nm or more as determined by X-ray diffraction. Soft carbon is also called easily graphitizable carbon, and is carbon that is more easily graphitized by high-temperature treatment than hard carbon. Hard carbon is also called non-graphitizable carbon. Note that, in view of the configuration of the present invention, it is not necessary to clearly distinguish between soft carbon and hard carbon. Graphite and at least one amorphous carbon of soft carbon and hard carbon may be used together as the negative electrode active material.
  • the negative electrode mixture layer 41 has a volume specific capacity/porosity of 48.0 mAh/cc ⁇ % or less.
  • the voids between the particles of the negative electrode active material are considered to be the main movement paths for Li ions that move within the negative electrode mixture layer 41 during charging and discharging, and the value of the volume specific capacity/porosity of the negative electrode mixture layer 41 is If it is 48.0 mAh/cc ⁇ % or less, it is considered that a sufficient movement path for Li ions is secured. Further, if it is 48.0 mAh/cc ⁇ % or less, it is considered that the influence of expansion of the silicon-containing material during charging can be sufficiently alleviated. If the volume specific capacity/porosity is 48.0 mAh/cc ⁇ % or less, for these reasons, the capacity decrease due to charging and discharging is highly suppressed, and the cycle characteristics are greatly improved.
  • the cycle characteristics of the non-aqueous electrolyte secondary battery 10 change greatly when the volume specific capacity/porosity of the negative electrode mixture layer 41 reaches 48.0 mAh/cc.%, so for example, the cycle characteristics of the battery performance, etc. From this point of view, the volume specific capacity/porosity is controlled to be 45.0 mAh/cc ⁇ % or less.
  • An example of a suitable volume specific capacity/porosity is 45.0 mAh/cc ⁇ % or less, or 40.0 mAh/cc ⁇ % or less.
  • the lower limit of the volume specific capacity/porosity of the negative electrode mixture layer 41 is not particularly limited, but if it is too small, the cycle characteristic improvement effect will reach a ceiling, so it is preferably 25.0 mAh/cc ⁇ %. More preferably, it is 30.0mAh/cc ⁇ %. If the volume specific capacity/porosity of the negative electrode mixture layer 41 is 48.0mAh/cc.% or less, 25.0mAh/cc.% or more, or 30.0Ah/cc.% or more, high capacity and high Achieves a higher level of durability.
  • the volume specific capacity of the negative electrode mixture layer is measured by the following method.
  • the battery to be evaluated is dismantled, the negative electrode plate is cut out, and a monopolar cell is fabricated using metal Li as the counter electrode and ionic liquid as the electrolyte.
  • (2) Charge the unipolar cell at 0.1C in a temperature environment of 25°C until the cell voltage reaches 5mV, rest for 20 minutes, and then discharge at 0.1C until the cell voltage reaches 1.0V. , find the discharge capacity (C).
  • the porosity of the negative electrode mixture layer 41 is preferably 25% or more, more preferably 35% or more, or 40% or more. As described above, the porosity refers to the proportion of voids between the negative electrode active material particles in the negative electrode mixture layer 41, and voids within the active material particles are not included in the porosity.
  • the porosity of the negative electrode mixture layer 41 is controlled so that the volumetric capacity/porosity ratio becomes a desired value, and changes depending on, for example, the compression conditions of the negative electrode mixture layer 41 during manufacture of the negative electrode 12. Generally, when the compression force of the negative electrode mixture layer 41 is decreased, the porosity increases, and when the compression force is increased, the porosity decreases.
  • the porosity of the negative electrode mixture layer 41 can also be controlled by the particle size distribution of the negative electrode active material.
  • the upper limit of the porosity of the negative electrode mixture layer 41 is not particularly limited, but if the porosity is made too high, the cycle characteristic improvement effect will reach a ceiling, so it is preferably 65%, more preferably 60%, Or 55%. If the porosity of the negative electrode mixture layer 41 is 25% or more and 65% or less, or 60% or less, both high capacity and high durability can be achieved to a higher degree.
  • the porosity of the negative electrode mixture layer is measured using a mercury porosimeter.
  • a mercury porosimeter (1) After discharging the battery to be evaluated to 2.5V, disassemble the battery, cut out the negative electrode plate, and insert a plurality of negative electrode plates as samples into a measurement cell of a mercury porosimeter.
  • the density of the negative electrode mixture layer 41 is preferably 1.5 g/cc or less, more preferably 1.2 g/cc or less. In this case, the effect of improving cycle characteristics becomes more significant.
  • the lower limit of the density is preferably 0.65 g/cc from the viewpoint of achieving both high capacity and high durability.
  • An example of a suitable range for the density of the negative electrode mixture layer 41 is 0.65 g/cc or more and 1.5 g/cc or less, or 0.72 g/cc or more and 1.2 g/cc or less. When the materials used are the same, the density of the negative electrode mixture layer 41 becomes lower as the porosity increases.
  • the density of the negative electrode mixture layer is measured by the following method. (1) After discharging the battery to be evaluated to 2.5V, disassemble the battery and cut out the negative electrode plate, wash it by immersing it in DMC, vacuum dry it at 100°C for 5 hours, and then ) to measure. (2) After peeling off the negative electrode mixture layer from the negative electrode plate and performing ultrasonic cleaning, the mass (Wc) of the negative electrode core is measured.
  • the particle expansion coefficient of the silicon-containing material is preferably 3.0 times or less.
  • the particle expansion rate of the silicon-containing material is preferably 3.0 times or less from the viewpoint of improving cycle characteristics, but if the particle expansion rate becomes too small, the capacity tends to decrease. Therefore, the particle expansion coefficient of the silicon-containing material is preferably 1.1 times or more.
  • An example of a suitable range for the particle expansion coefficient is 1.1 times or more and 3.0 times or less, more preferably 1.3 times or more and 2.1 times or less. If the particle expansion coefficient of the silicon-containing material is within the range, it becomes easy to achieve both high capacity and high durability.
  • the particle expansion coefficient of silicon-containing materials is measured by the method described below.
  • the battery to be evaluated is disassembled, the negative electrode plate is cut out, and a monopolar cell is fabricated using metal Li as the counter electrode and an ionic liquid as the electrolyte, with the particle cross section of the silicon-containing material exposed.
  • the expansion rate of the negative electrode mixture layer 41 depends on the expansion rate and amount of the negative electrode active material.
  • the expansion coefficient of the negative electrode mixture layer 41 is preferably 1.5 times or less. In this case, the effect of improving cycle characteristics becomes more significant.
  • the lower limit of the expansion coefficient of the negative electrode mixture layer 41 is not particularly limited, but is 1.1 times as an example.
  • An example of a suitable range for the expansion coefficient of the negative electrode mixture layer 41 is 1.1 times or more and 1.5 times or less, more preferably 1.2 times or more and 1.4 times or less. If the expansion coefficient of the negative electrode mixture layer 41 is within this range, it becomes easy to achieve both high capacity and high durability.
  • the expansion coefficient of the negative electrode mixture layer is measured by the following method.
  • the battery to be evaluated is dismantled, the negative electrode plate is cut out, and a monopolar cell is fabricated using metal Li as the counter electrode and ionic liquid as the electrolyte.
  • the silicon-containing material may be any material containing Si, and examples thereof include silicon alloys, silicon compounds, and composite materials containing Si. Among these, composite materials containing Si are preferred.
  • the D50 of silicon-containing materials is generally lower than that of graphite.
  • the volume-based D50 of the silicon-containing material is, for example, 1 ⁇ m or more and 20 ⁇ m or less, or 1 ⁇ m or more and 15 ⁇ m or less. Note that one type of silicon-containing material may be used alone, or two or more types may be used in combination.
  • Suitable silicon-containing materials are composite particles comprising an ion-conducting phase and a Si phase dispersed within the ion-conducting phase.
  • the ion conductive phase is, for example, at least one selected from the group consisting of a silicate phase, a carbon phase, a silicide phase, and a silicon oxide phase.
  • the silicide phase is a phase of a compound consisting of Si and an element more electropositive than Si, and examples thereof include NiSi, Mg 2 Si, TiSi 2 and the like.
  • the Si phase is formed by dispersing Si in the form of fine particles.
  • the ion conductive phase is a continuous phase composed of aggregation of particles finer than the Si phase.
  • the average value of the size of the Si phase is preferably 1 nm or more and 200 nm or less, more preferably 1 nm or more and 100 nm or less.
  • the average size of the Si phase may be, for example, 1 nm or more and 10 nm or less.
  • the above composite material may have a conductive layer covering the surface of the ion conductive phase.
  • the conductive layer is made of a material having higher conductivity than the ion conductive layer, and forms a good conductive path in the negative electrode mixture layer 41.
  • the conductive layer is, for example, a carbon film made of a conductive carbon material.
  • carbon black such as acetylene black and Ketjen black, graphite, amorphous carbon with low crystallinity (amorphous carbon), etc. can be used.
  • the thickness of the conductive layer is preferably 1 nm or more and 200 nm or less, or 5 nm or more and 100 nm or less, in consideration of ensuring conductivity and diffusibility of Li ions into the inside of the particles.
  • the thickness of the conductive layer can be measured by observing the cross section of the composite material using a SEM or a transmission electron microscope (TEM).
  • the ion conductive phase may contain at least one element selected from the group consisting of Group 1 and Group 2 elements of the periodic table.
  • the ion conductive layer may be a Li-doped silicon oxide phase.
  • the ion conductive phase is selected from the group consisting of B, Al, Zr, Nb, Ta, V, Y, Ti, P, Bi, Zn, Sn, Pb, Sb, Co, Er, F, W, and lanthanoids. It may contain at least one kind.
  • An example of a suitable composite material containing Si has a sea-island structure in which fine Si is substantially uniformly dispersed in an amorphous silicon oxide phase, and has the general formula SiO x (0 ⁇ x ⁇ 2) as a whole.
  • This is a composite particle represented.
  • the main component of silicon oxide may be silicon dioxide.
  • the silicon oxide phase may be doped with Li.
  • the content ratio (x) of oxygen to Si is, for example, 0.5 ⁇ x ⁇ 2.0, preferably 0.8 ⁇ x ⁇ 1.5.
  • a suitable composite material containing Si is a composite particle having a sea-island structure in which fine Si is substantially uniformly dispersed in an amorphous silicate phase.
  • a preferred silicate phase is a lithium silicate phase containing Li.
  • the lithium silicate phase is, for example, a complex oxide phase represented by the general formula Li 2z SiO (2+z) (0 ⁇ z ⁇ 2).
  • Li 4 SiO 4 is an unstable compound and exhibits alkalinity when reacting with water, so it may alter Si and cause a decrease in charge/discharge capacity.
  • a suitable composite material containing Si is a composite particle having a sea-island structure in which fine Si is substantially uniformly dispersed in a carbon phase.
  • the carbon phase is an amorphous carbon phase.
  • the carbon phase may contain a crystalline phase component, it is preferable that the carbon phase contains more amorphous phase components.
  • the amorphous carbon phase is composed of, for example, a carbon material having an average interplanar spacing of (002) planes of more than 0.34 nm as measured by X-ray diffraction.
  • the composite material containing a carbon phase may have a conductive layer separate from the carbon phase, or may not have the conductive layer.
  • a porous sheet having ion permeability and insulation properties is used.
  • porous sheets include microporous thin films, woven fabrics, and nonwoven fabrics.
  • Suitable materials for the separator 13 include polyolefins such as polyethylene and polypropylene, cellulose, and the like.
  • the separator 13 may have a single layer structure or a multilayer structure. Further, a resin layer with high heat resistance such as aramid resin may be formed on the surface of the separator 13.
  • a filler layer containing an inorganic filler may be formed at the interface between the separator 13 and at least one of the positive electrode 11 and the negative electrode 12.
  • the inorganic filler include oxides and phosphoric acid compounds containing metal elements such as Ti, Al, Si, and Mg.
  • the filler layer can be formed by applying a slurry containing the filler to the surface of the positive electrode 11, the negative electrode 12, or the separator 13.
  • the nonaqueous electrolyte secondary battery 10 with the above configuration has a charging upper limit voltage of 4.2V and a cutoff voltage of 2.0V. That is, the nonaqueous electrolyte secondary battery 10 is preferably charged and discharged in a voltage range of 2.0V or more and 4.2V or less. More preferably, charging and discharging is controlled within a voltage range of 2.5V or more and 4.2V or less. In this case, it is possible to achieve both high capacity and high durability.
  • a positive electrode mixture slurry is prepared using N-methyl-2-pyrrolidone (NMP) as a dispersion medium.
  • NMP N-methyl-2-pyrrolidone
  • a positive electrode mixture slurry is applied onto the positive electrode core made of aluminum foil, the coating film is dried and compressed, and then the positive electrode core is cut into a predetermined electrode size, and the positive electrode mixture is coated on both sides of the positive electrode core.
  • a positive electrode on which the agent layer was formed was obtained. Note that an exposed portion in which the surface of the positive electrode core was exposed was provided in a part of the positive electrode.
  • a silicon-containing material composite particles having a sea-island structure in which fine Si is almost uniformly dispersed in a carbon phase (average size of Si phase: 5 nm, D50: 10 ⁇ m, true density: 1.5 g/cc) are used. there was.
  • the silicon-containing material sodium carboxymethyl cellulose (CMC-Na), and a dispersion of styrene-butadiene rubber (SBR) were mixed at a solid content mass ratio of 100:1:1.
  • SBR styrene-butadiene rubber
  • the negative electrode mixture slurry is applied to both sides of a negative electrode core made of copper foil, and after the coating film is dried, the coating film is compressed using a roller and cut into a predetermined electrode size to form the negative electrode core.
  • a negative electrode was obtained in which negative electrode mixture layers were formed on both sides. Note that an exposed portion in which the surface of the negative electrode core was exposed was provided in a part of the negative electrode.
  • Non-aqueous electrolyte 1.2 mol of LiPF 6 was added to a mixed solvent of ethylene carbonate (EC), methyl ethyl carbonate (MEC), and dimethyl carbonate (DMC) mixed at a volume ratio of 3:3:4 (25°C).
  • EC ethylene carbonate
  • MEC methyl ethyl carbonate
  • DMC dimethyl carbonate
  • a non-aqueous electrolyte solution was prepared by dissolving the solution at a concentration of 1/liter.
  • test cell non-aqueous electrolyte secondary battery
  • Leads were attached to the positive electrode and the negative electrode, respectively, and the positive and negative electrodes were spirally wound through a separator to obtain a wound electrode body.
  • the electrode body was housed in a cylindrical outer can with a bottom, and the negative electrode lead was welded to the inner surface of the bottom of the outer can, and the positive electrode lead was welded to the internal terminal plate of the sealing body. Thereafter, the non-aqueous electrolyte was poured into the outer can, and the opening edge of the outer can was caulked and fixed to the sealing body to produce a cylindrical test cell.
  • the particle expansion rate of the silicon-containing material, the density of the negative electrode mixture layer, and the expansion rate of the negative electrode mixture layer were measured by the above method, the particle expansion rate was 1.78 times, and the density of the negative electrode mixture layer was 0.
  • the expansion rate was 864 g/cc, which was 1.27 times that of the negative electrode mixture layer.
  • the above test cell was evaluated for initial charge/discharge efficiency and cycle characteristics (capacity retention rate) by the following method, and the evaluation results are shown in Table 1.
  • the same evaluation was performed for each test cell of Examples and Comparative Examples described below, and the evaluation results are shown in Table 1 together with the physical properties of the negative electrode.
  • Examples 1 to 10 are labeled A1 to A10
  • Comparative Examples 1 to 6 are labeled B1 to B6.
  • the capacity retention rate of each test cell shown in Table 1 is a relative value when the capacity retention rate of the test cell of Example 1 (A1) is set to 100.
  • Capacity retention rate (%) (100th cycle discharge capacity ⁇ 1st cycle discharge capacity) x 100
  • Examples 2 to 10 A negative electrode and a non-aqueous electrolyte were prepared in the same manner as in Example 1, except that the compression conditions of the negative electrode mixture layer were changed and the volume specific capacity/porosity values of the negative electrode mixture layer were set to the values shown in Table 1. A second battery was produced and the performance evaluation described above was performed.
  • test cells of the examples have higher capacity retention rates after the cycle test than the test cells of Comparative Examples 1 to 6, and have excellent cycle characteristics.
  • test cells of Examples have higher initial charge/discharge efficiency than the test cells of Comparative Examples 5 and 6.
  • lithium methanesulfonate is applied to the positive electrode, but if a sulfonic acid compound is not used, the charge/discharge efficiency decreases.
  • a sulfonic acid compound is applied to the positive electrode, and the volume specific capacity/porosity of the negative electrode mixture layer is By controlling this to 48.0 mAh/cc ⁇ % or less, it is possible to improve the charging/discharging efficiency and achieve both high capacity and high durability.
  • Configuration 1 A non-aqueous electrolyte secondary battery comprising a positive electrode, a negative electrode, and a non-aqueous electrolyte
  • the positive electrode includes a lithium-containing transition metal composite oxide and a sulfonic acid compound present on the particle surface of the composite oxide,
  • the sulfonic acid compound is a compound represented by formula (I),
  • A is a Group 1 or Group 2 element
  • R is a hydrocarbon group
  • n is 1 or 2
  • the negative electrode has a negative electrode mixture layer containing a silicon-containing material as a negative electrode active material, the proportion of the silicon-containing material in the negative electrode active material is 50% by mass or more, and the volume ratio of the negative electrode mixture layer is
  • a non-aqueous electrolyte secondary battery whose capacity divided by porosity is 48.0 mAh/cc ⁇ % or less.
  • Configuration 2 The non-aqueous electrolyte secondary according to Configuration 1, wherein the sulfonic acid compound is present in an amount of 0.1% by mass or more and 1.0% by mass or less based on the lithium-containing transition metal composite oxide. battery.
  • Configuration 3 The nonaqueous electrolyte secondary battery according to Configuration 1 or Configuration 2, wherein A in formula (I) is Li or Na.
  • Configuration 4 The nonaqueous electrolyte secondary battery according to any one of configurations 1 to 3, wherein R in formula (I) is an alkyl group having 3 or less carbon atoms.
  • Configuration 5 The nonaqueous electrolyte secondary battery according to any one of configurations 1 to 4, wherein the negative electrode mixture layer has a density of 1.5 g/cc or less.
  • Configuration 6 The nonaqueous electrolyte secondary battery according to any one of configurations 1 to 5, wherein the proportion of the silicon-containing material in the negative electrode active material is 70% by mass or more.
  • Configuration 7 The nonaqueous electrolyte secondary battery according to any one of configurations 1 to 6, wherein the silicon-containing material has a particle expansion coefficient of 3.0 times or less.
  • Configuration 8 The non-aqueous electrolyte secondary battery according to any one of configurations 1 to 7, wherein the expansion coefficient of the negative electrode mixture layer is 1.5 times or less.
  • Configuration 9 Any of configurations 1 to 8, wherein the negative electrode mixture layer contains at least one carbon material selected from the group consisting of natural graphite, artificial graphite, soft carbon, and hard carbon as the negative electrode active material.
  • Configuration 10 The silicon-containing material includes an ion-conducting phase and a Si phase dispersed in the ion-conducting phase, and the ion-conducting phase is a group consisting of a silicate phase, a carbon phase, a silicide phase, and a silicon oxide phase.
  • Configuration 12 The non-aqueous electrolyte secondary battery according to any one of Configurations 1 to 11, wherein charging and discharging are controlled in a voltage range of 2.0 V or more and 4.2 V or less.
  • Non-aqueous electrolyte secondary battery 11 positive electrode, 12 negative electrode, 13 separator, 14 electrode body, 16 outer can, 17 sealing body, 18, 19 insulating plate, 20 positive electrode lead, 21 negative electrode lead, 22 grooved part, 23 internal terminal Plate, 24 lower valve body, 25 insulating member, 26 upper valve body, 27 cap, 28 gasket, 30 positive electrode core, 31 positive electrode mixture layer, 40 negative electrode core, 41 negative electrode mixture layer

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